A342-1219-10M-L TEXAS AGRICULTURAL EXPERIMENT STATION AGRICULTURAL AND MECHANICAL COLLEGE OF TEXAS W. B. BIZZELL, Presiden! BULLETIN NO. 256 DECEMBER, 1919 DIVISION OF ENTOMOLOGY TI-IE COWPEA WEEVIL B. YOUNGBLOOD, DIRECTOR, COLLEGE STATION, muzos COUNTY, TRXAB STATION STAFFT ADMINISTRATION B. YOUNGBLOOD, M. S. Director A. B. CONNER B. S., Vice Director J. M. Jonas, A. M.. Assistant Director CnAs. A. FELKEH, Chief Clerk A. S. WARE, Secretary . .............................. .., Executive Assistant i CHARLES Sosoux, Technical Assistant VETERINARY SCIENCE *M. FRANCIS, D. V. M., Chief H. Scumnr, D. V. S., Veterinarian D. H. BENNETT, V. M. D., Veterinarian CHEMISTRY _ G. S. FRAPS, Ph. D., Chief; State Chemist S. E. AsRURY. M. S., Assistant Chemist S. LOMANXTZ, B. S., Assistant Chemist F. B. SCHILLI\G. B. S., Assistant Chemist J. B. SMITH, B. S., Assistant Chemist HORTICULTURE H. NESS, M. S.. Chief W. S. Horcniuss, Horticulturist ANIMAL INDUSTRY J. M. JONES, A. M., Chief; Sheep and Goat Investigations _ IJ. C. BURNS, B. S., Animal Husbandman in Charge of Beef Cattle Investigations (on leave) R. M. Smnwoon, B. S., Poultryman J. B. McNULTY, B. S., Dairyman O. E. McComn 1.1., B. S., Animal Husband- man in Charge of Swine Investigations G. R. WARREN, B.S., Assistant Animal Hus- ENTOMOLOGY M. C. TANQUARY, Ph. D., Chief; State Ento- mologist H. J. REINHARD, B. S., Entomologist H. B. P\RKS, B. S., Apiculturist ———, Assistant Entomologist AGRONOMY A. B. CoNNER, B. S., Chief A. H. Lemma, B. S., Agronomist '. W. GEYER, B. S., Agronomist . H. LAUDE, M. S., Agronomist PLANT PATHOLOGY AND PHYSIOLDGV J. J. TAUBENHAUS, Ph. D., Chief FEED CONTROL SERVIC F. D. FULLER, M. S., Chief J AMES SULLIVAN, Executive Secretary FORESTRY E. O. SIECKE, B. S., Chief; State Forester PLANT BREEDING E. P. HUMRERT, Ph. D., Chief FARM AND RANCH ECONOMICS H. M. ELIOT, M. A., Chief SOIL SURVEY **\V. T. CARTER, JR., B. S., Chief J. F. S-rRoun, Soil Surveyor bandman T. M. BUSHNELL, B. S., Soil Surveyor R. A. BRRwFR, B. S., Assistant Animal Hus- W- B. FRANCIS. B- $-. $01! 511F178!!!" bandman _ SUBSTATIONS No. l. Beeville, Bee County No. 8. Lubbock, Lubbock County l. E. COWART, M. S., Superintendent Troup, Smith County W. S. Horcnmss, Superintendent Angleton, Brazoria County . REYNOLDS, M. S., Superintendent 3. B 4. Beaumont, Jetferson County A. H. PRINCE, B. S., Superintendent l. T Temple, Bell County _ . Kmnoucn, B. S., Superintendent Danton, Denton County C. H. MCDOWELL, B. S., Superintendent No. 7. Spur, Dickens County R. E. DICKSON, B. S., Superintendent _ As of December 1, 1919. R. E. KARPER, B. S., Superintendent D. L. JONES. Scientific Assistant G. M. Rows, Forest Nursergman and Ir- rigationist No. 9. Pecos, Reeves County J. W. JACKSON, B. S., Superintendent No. 10. (Feeding and Breeding Subltatlnm, College Station, Brazos County -—-———-i-—, Superintendent E. CAMERON, Scientific Assistant No. ll. Nacogdoches, Nacozdochel County G. T. McNizss, Superintendent "No. 12. Chilllcothe, Hardeman County A. B. CRON, B. S., S u erintendent V. E. HAFNER, B. S., cientific Assistant No. l4. Sonora, Sutton-Edwgrdl COlllfleI E. M. PETERS, B. S., Superintendent In cooperation with School of Agriculture, A. & M. College of Texas. ‘In cooperation wlth the School of Veterinary Medicine, A. 8c M. College 0t Texas. "In cooperation with the United States Department of Agriculture. CONTENTS. PAGE Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .. 9 History . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2 . . . . . . . . . . . . . . . . . . . . . 9 Distribution . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11 Systematic Position . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .. 11 Allied Species . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .. 13 _Gommon Names... . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .. 13 Economic Importance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .. 13 Food Plants . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .. 1.4 Methods of Study . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .. 14 Life History . . . . . . . .1 . . . . . . . .2 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 14 Egg . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .. 15 Embryology . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .. 15 Hatching . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .. 15 Duration of Egg Stage . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 21 ’ Larva . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .... . . . . Description . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .‘ . . . . . . . . 23 Duration of Larval Stage . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .. 23 Pupa . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .' . . . . . . . . . . . . . . . . . . . . 30 Description . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .. 3O Duration of Pupal Stage . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .. 3O Adults . . . . . . . . . . . . . . . . . ..4 . . . . . ... . . . . . . . . . . . . . . . . . . . . . .. 3'7 Description . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .. 37 Feeding Habits . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .. 38 Average Eggs per Female . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .. 39 Period from Last Oviposition to Death of Female . . . . . . . . . . . . . . 39 Difference in Death Rate of Sexes . . . . . . . . . . . . . . . . . . . . . . . . . .. 40 Length of Life of Unmated Adults . . . . . . . . . . . . . . . . . . . . . . . . .. 40 Length of Life of Mated Adults . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 44 Proportion of Sexes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .. 49 Location of Food . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .. 5O Adaptive Capacity . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .. 51 Copulation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .. 51 Period Between Maturity and Copulation . . . . . . . . . . . . . . . . . . . .. 52 Fertility . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .. 52 Oviposition . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .. 52 Age at Beginning of Oviposition . . . . . . . . . . . . . . . . . . . . . . . . . . .. 53 Period of Oviposition . . . . . . . . . i . . . . . . . . . . . . . . . . . . . . . . . . . . . . 53 Rate of Oviposition . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .. 58 Generation Series . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .. 78 Protection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .. 78 Mortality . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Q . . . . . . . . . . . . 80 4 CONTENTS. PAGE Natural Control . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .. 80 Parasite of Larva . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 80 Parasite of Egg . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .. 81 Remedial Measures . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .. 83- Harvesting . . . . . . . . . . . . . . . . . . .A . . . . . . . . . . . . . . . . . . . . . . . . . . . . 83 Storage . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 83 Fumigation With Carbon Bisulphide . . . . . . . . . . . . . . . . . . . . . . . .. 84 Heat . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .. 86 Effect of Heat 0n Germination . . . . . . . . . . . . . . . . . . . . . . . . . . . . .. 89 Summary . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . , . . . . . . . . . . . . . . . .. 90 Literature Cited . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .. 90 Bibliography . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .. 91 ILLUSTRATIONS. PLATES. PAGE Laboratory where the life history studies were conducted . . . . .. 14 Cowpeas showing extreme Weevil infestation. Egg details are shown . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .. 16 Cowpea Weevil: larva above, pupa below . . . . . . . . . . . . . . . . .. 23 Cowpea Weevil: adults shoiving variation in size of sex; females above and males bellow . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 38 Parasites: adult larval parasit (a), larval and pupal stage (b), ' and adult egg parasite (c) . . . . . . . . . . . . . . . .., . . . . . . . . .. 81 Fumigator: left, general view; right, detail of door construction 85 FIGURES. World distribution of the Cowpea Weevil . . . . . . . . . . . . . . . . . . . 10 Distribution of the Cowpea Weevil in the United States . . . . . . . 12 Generation Series Studies . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .. '79 [Blank Page in Original Bulletin] TABLES. PAGE Table N0. 1.—Egg Measurements . . . . . . . . . . . . . . . . . . . . . . . . . . .. 15 Table No. 2.—Duration of the Egg Stage . . . . . . . . . . . . . . . . . . .. 16 Table No. 3.—Yearl_v Variation in Duration of Egg Stage . . . . . . . 22 Table No. i-Summary of Duration of the Egg Stage . . . . . . . .. 22 Table No. 5.—Efi’eot of ‘fllemperature on Duration of Egg Stage. . 23 Table No. 6.—Duration of Larval Stage . . . . . . . . . . . . . . . . . . . . .. 23 Table N o. 7.—Yearly Variation in Duration of the Larval Stage. . 29 Table No. 8.——Summary of Duration of the Larval Stage . . . . . .. 29 Table N0. 9.—Efl’ect of Temperature on Length of Larval Stage. . 29 Table No. 10.—Measurements of Pupa . . . . . . . . . . . . . . . . . . . . . . .. 30 Table No. 11.—+Duration of Pupal Stage . . . . . . . . . . . . . . . . . . . . . .. 31 Table No. 12.—Yearly Variation in Duration of Pupal Stage . . .. 36 Table No. 13.—S11mmary of Duration of the Pupal Stage T . . . . . . .. 37 Table N0. 14.—Efl’ect of Temperature on Length of Pupal Stage. 3'7’ Table No. 15.—-Summary of Development of the Cowpea Weevil. . . 3'7 Table No. 16.——Average Eggs per Female . . . . . . . . . . . . . . . . . . . . .. 39 Table No. 1'7.—Average Ilime-Between Oviposition and Death. . .. 40 Table No. 18.——Differenoe in Death Rate of Sexes . . . . . . . . . . . . . .. 110 Table No. 19.——Length of Life of Unmated Adults . . . . . . . . . . . . .. 41 Table No. 20.——Length of Life of Mated Adults . . . . . . . . . . . . . . .. 45 Table No. 2l.—Proportion of Sexes . . . . . . . . . . . . . . . . . . . . . . . . . . . 50 Table No. 22.-—Period of Oviposition . . . . . . . . . . . . . . . . . . . . . . . . .. 54 Table No. 23.——-Rate of Oviposition . . . . . . . . . . . . . . . . . . . . . . . . . .. 60 Table N 0. 24.—Fumigation With Carbon Bisulphide . . . . . . . . . . . .. 85 Table N o. 25.—Efl.’ect of Heat on Eg'g, Larval, and Pupal Stages. . 86 Table No. 26.—-Effeot of Heat on Germination . . . . . . . . . . . . . . . . .. 89 [Blank Page in Original Bulletin] BULLETIN N0. 256. DECEMBER, 1919. THE COWPEA WEEVIL *F. B. PAnnocK. H. J. REINHARD. INTRODUCTION. Most Texans who have ever grown cowpeas are familiar with the cowpea Weevil in at least one of its stages. This insect seems to be present in every garden and field in the State, wherever any variety of cowpea is grown. It is a very serious pest, and it is often dreaded ' by those who are growing the cowpea for table use. The climatic conditions of the State are especially favorable for the development of the weevil as the mild winters result in a low mortality of the insect in stored peas, and since the weevil is not generally attached by ene— mies, its control must depend almost entirely upon the efforts of the grower. _ The studies recorded in this bulletin were begun by the senior author in March, 1915, and continued throughout the year. During the spring and summer of 1916, the life history notes were taken by O. K. Court- ney, then Assistant Entomologist. The junior author is responsible for notes made since September, 1916. HISTORY. This insect was first described by Fabricus (1) in 1792 from material collected in Santa Cruz, West Indies. The specimens described were in his collection at that time, but the date of collection is not given. The original home of this species is very much in doubt for it was noted at widely different localities at about the same time. It was undoubtedly of tropical origin, however, since its spread has been more or less confined to the tropical and semitropical regions. The next mention of this species was in 1.795 by Olivier (2) when he records it as occurring in peas in “Carolina,” which was quite probably Carolina in Spain, although this cannot be said positively. In 1801, the species was again listed by Fabricus (3) in a revision of entomology. The first mention of this species in the United States was by Say (4) in 1824, recording a specimen from New Orleans, Louisiana. In 1872, Horn (6) in his “Revision of the Bruchidae of the United States,” gives the distribution of this species as “West Indies Islands and the Southern States.” It was not, however, until 1885 ('7) that the insect attracted attention as an economic pest. In that year, black-eyed “table beans” from Texas, which were very badly infested with the cowpea ‘Chief, Division of Entomology; State Entomologist; resigned September 15,. 1919. TEXAS AGRICULTURAL EXPERIMENT STATION. 415w? QSmBQO 23 iv zofinnffiwmmh tic?» A 25F; . é“ ‘I -. J3 s w? THE COWPEA WEEVIL. 11 weevil, B. quadrimaculatus, were exhibited at the Cotton Exposition in Atlanta, Georgia. It was not until 1893 (8) that this species again attracted attention, being found in large numbers in beans exhibited by Brazil and Vene- zuela at the World’s Fair in Chicago. At this time the Bureau of Entomology records the species as “common in Southern States.” The same year the Weevil was reported from Delaware (9) in peas that had been purchased from North Carolina. It was also introduced into New York that year (10) in peas sent from the South, the exact locality of the origin of the peas not being given. The following year it was reported from Georgia, Mississippi, Alabama, and Texas. Hamilton (1.1) in his “Distribution of Coleoptera” lists southern France and - Ethiopia as the habitat of this species. In 1895 it Was reported from Ames, Iowa (12) in seed purchased from Virginia. In 1896 Chit- tenden (13) added British Honduras, Mexico, and Italy, to the dis- tribution of the pest and the following year he added the East Indies and Sierra Leone to its domain. Finally in 1916, a report from Wis- consin indicated the presence of the cowpea weevil in the Northwest, where it had been introduced from the South in seed. DISTRIBUTION. In Figure 1 is shown the distribution of the cowpea weevil, as indi- cated in the available references on this species, but from all the available information it is impossible to ascertain the date of the en- trance of this species into the United States or the exact place and manner of its introduction. Nor can the spread of the species be traced from state to state, though it is certain that it is confined by the range of its only food plant, the cowpea, to the Southern States. (See Figure 2.) The weevil has been introduced many times with seed into the Northern States, but. has not become established in such locations, and it does not even occur in California or other Western States. SYSTEMATIC POSITION. In his original description, Fabricus places this species in the genus Bruchus, erected by Linnaeus in 1767’. Fabricus defined the genus as follows: Palpi aequales, filiformes; maxilla vnembrancea, bilfida; labiwm aczcminatzrm; antennae filiformes. Say in 1824 lists B. quadrimrzculatus in the Curculiomides although no reason is given for changing from the arrangement of Fabricus. In LeConte’s revision (5) of this Work in 1853 he criticizes the “unnatural classification of this family.” Horn, in 187.2, places this species in the genus Bruchus, in his revision o-f the Bruchidae of theUnited States. In 1894-, Hamil- ton in his “Catalogue of Coleoptera,” lists quadrimaculatus in the genus Bruchus, of the family’ Bruchidae. Chittenden, in 1897, places quadri- maculaius in the genus Bruchus. Blatchley, in 1910, in his “Coleoptera of Indiana,” places quad/rinmculatus‘ in the genus Bmchus of the family Bruchida-e. 12 TEXAS AGRICULTURAL EXPERIMENT STATION. @865 @829 2w 5 mzxé, Asgaao s: u. =as=figummm d wpzmwm THE COWPEA WEEVIL. 13 ALLIED SPECIES. The most closely related species,both from the anatomical and his- torical standpoint, i.s B. chmensis Linn. This species is separated from quadrimaculatzas as follows: b. Median basal thoracic lobe with elevated ivory-like spgce: chinensis. bb. Median basal thoracic lobe with whitish hairs only: quadri- maculatus. These species are confused very often by those who are not specialists in this group. Both of these species feed extensively on the cowpea, and their life history, habits, and control are quite similar. Horn (6) gives the following points wherein B. quadrimaculatus differs from chinensis: - “The thorax is broader, the sides distinctly arcuate, the basal lobe not eburneous. The scutellum is fiat and with a median line. The elytra are longer, and differently spotted and the abdomen is evenly clothed with cinereous pubescence. This species is also larger and much less robust.” COLIMON NAME. The usual name that has been applied to the insect in previous literature is the “four spotted bean weevil.” In 1897, Chittenden says, the above name (the cowpea weevil), which is proposed for Bruchus chineensis, will sufficiently distinguish it from B. quadrimaculatus, since the latter is already known as the “four spotted bean weevil.” When the studies here recorded were begun on the weevils infesting cowpeas in this State, it was thought that B. ch/inensis was by far the more abundant species. Collections, however, made over a period of three years from all sections of the State show that quadrimaculatus is much the more common. Bruchus quadrimaculatus was used in all of the experiments. For our purpose in Texas, then, in spite of the fact that the double use of aicommon name may prove confusing, the cowpea weevil must be known as B. quadrimaculatus. ‘ ECONOMIC IMPORTANCE. In view of the fact that the cowpea is grown very extensively in Texas, that human food as well as stock food is concerned, and that the weevil is present in every section where the cowpea is grown, it becomes evident that the damage done by this insect is very great and materially affects the agricultural economy of the State. The pest became of paramount importance when the treatment of the black-eyed cowpea for export trade was commenced. 'I‘his variety of cowpea is especially sus- ceptible to infestation by the weevil, and very few cowpeas are harvested which are not infested. The treatment of such cowpeas presented a very difficult problem and they were therefore, even after treatment, unfit for human consumption. The keeping of cowpea seed has always been a very diflicult problem, since the germination percentage of weevil-infested seed is always very low. The importance of the weevil in Texas is indeed very great although it is difficult to place a money '14; Texas AGRICULTURAL EXPERIMENT STATION. value on the damage done. The cowpea is an important crop, but its value in the State is limited by the work of the weevil. There is hardly a grower Who does not have to reckon with. the ravages of this pest. when considering the production of cowpeas. U FOOD PLANTS. The primary food plant for this insect, as the common name indi- cates, is the cowpea. Apparently all varieties of cowpeas are attacked and the insect shows no preference for any particular variety. It has been repeatedly bred in the following varieties of cowpeas: Black-eyed, Old Bokhara, Chinese Red,_Clii11ese~ Yellow, Red Ripper, Iron, Speckled Cowder, Whippoorwill, Tinkles Holstein, New Era, and Lady Pea. The cowpea weevil has not been observed to feed upon any plant except the cowpea. Laboratory experiments have failed t0 establish any of the following as food plants for this insect: Navy beans, Mexican Frijole, Lima or butter beans, soy beans, yellow string beans, castor beans, and peanuts. Oviposition proceeded without reduction or delay, but in each case the eggs either tailed to hatch or the young larvae perished before entrance into the substituted food supply was ac- complished. The active feeding period is confined to the larval stage and it is doubtful if any other plants can be added to the cowpea, as a food for this insect. IVIETHODS OF STUDY. For the detailed observations on the life history of the weevil, vials 2524100 mm. were used. A pair of weevils were placed in these with ample peas for oviposition for a 24-hour period. The Chinese Red cowpea was used because any eggs on them were easy to observe. The peas with eggs upon them were removed each day and observations were made on the hatching of the egg, the pupation of the larvae, and the emergence of the adult. The laboratory, in which all life history observations were made, is shown in Plate 1.. No heat was available in the laboratory so that conditions were very similar to warehouse or storage conditions. Temperature records were obtained by the use of a recording thermograph placed close to the vials containing the weevils in any stage. In some phases of the work, humidity records were obtained also. by the use of a. hygro-thermograph. Seasonal’ notes were made in the field on the Agronomy Farm and in the experimental plats of the Division of Entomology. LIFE HISTORY. The life history of the cowpea weevil has been mentioned by a few of the early writers in a very indefinite way. In 1891, Slingerland (10) made some laboratory notes on the egg stage and the habits of the adults. In 1895, Osborn (12) describe-d all the stages and deter- mined the length of the egg stage. Later papers on weevils assume that the life history of B. quadrimaculatus is very much like that of chinensis, obteciits, or pest. In the following pages are given the re- sults of our detailed observations on all phases of its life history. wimfim fimvogfioww Qrmwm $5 Him wfiwfioww wffifimm émwm oosmcgmm. THE CowPnA WEEVIL. 15 From these results it is evident that thelife history of the cowpea Weevil is not composed of definite seasonal broods. The records show that there is a continuous breeding when food is available, and at this ' locality there is seldom a cessation of activity. Climatic conditions ‘undoubtedly do restrict the abundance of individuals at certain. seasons. The generation series was conducted to determine the number of gen- erations of the weevils that may normally occur in a period of twelve months. The Egg. The outline of the egg is generally ovate, varying somewhat at times. Its length is usually one and one-third times its breadth, the posterior end broadly rounded, the anterior end tapering, giving the semblance of a point when viewed with the unaided eye. Under the microscope it likewise appears rounded but much less broad than the posterior end. Viewed laterally the egg is convex in outline, higher at the posterior, sloping sharply toward the anterior end. The whole under surface of the egg is attached to the pea. except in some abnormal cases when the female is nearing the end of her quota of eggs. Apparently the supply of sticky material withwhich the eggs are glued to the peas is exhausted and in such cases the eggs are insecurely fastened to the pea, either on the end or the side. Such eggs have never been observed to hatch. When first laid the egg is glistening white, jellylike, translucent mass, but soon hardens on exposure to the air. The sur- face is perfectly smooth and shining. Plate II‘ shows details of the eggs when deposited under natural conditions. The size of the egg varies greatly; measurements of the greatest length and width of eggs gave the figures in Table 1. Table 1.—Egg Measurements. Length Width 1 . . . . . . . . . . . . . . . . . . . . . . .. 1.98 mm. 1.38 mm 2 . . . . . . . . . . . . . . . . . . . . . . .. 2.64 mm. 1.44 mm 3 . . . . . . . . . . . . . . . . . . . . . . .. 2.40 mm. 1.35 mm 4 . . . . . . . . . . . . . . . . . . . . . . .. 2.63 mm. 1.45 mm 5 . . . . . . . . . . . . . . . . . . . . . . .. 2.40 mm. 1.37 mm 6 . . . . . . . . . . . . . . . . . . . . . . .. 2.59 mm. 1.46 mrn 7 . . . . . . . . . . . . . . . . . . . . . . .. 2.48 mm; 1.80 mm 8 . . . . . . . . . . . . . . . . . . . . . . .. 2.49 ‘mm. _ 1.54 mm 9 . . . . . . . . . . . . . . . . . . . . . . .. 2.57 mm. 1.45 mm 10 . . . . . . . . . . . . . . . . . . . . . . .. 2.40 mm. 1.39 mm 11 . . . . . . . . . . . . . . . . . . . . . . .. 2.40 mm. 1.45 mm 12 . . . . . . . . . . . . . . . . . . . . . . .. 2.40 mm. 1.36 mm 13 . . . . . . . . . . . . . . . . . . . . . . .. 2.64 mm. 1.35 mm 14 . . . . . . . . . . . . . . . . . . . . . . .. 2.53 mm. 1.47 mm 15 . . . . . . . . . . . . . . . . . . . . . . .. 2.40 mm. 1.34 mm Embry0Z0gy.——As the developing embryonic larva increases in size, its movements can be very readily detected through the upper part of the egg shell, which remains white and translucent until it is hatched. When matured, with its brown head appearing as a tiny speck near the broader end of the egg, the larva soon begins to eat its way through the egg shell. Hatchmg.—The exit is always made 011 the side of the egg which is attached or glued to the pea. The larva, having eaten through the 16 TEXAS AGRICULTURAL EXPERIMENT STATION. shell of the egg and reached the surface of the pea, continues to eat its way into the pea Without any apparent delay. The exit hole in the egg shell and the entrance aperture into the pea are very tiny and can hardly be distinguished Without magnification. The hole in the egg shell and the entrance hole in the pea, are very nearly round and have a smooth edge. The exit hole in the egg shell is always at the broad end of the egg, the aperture by which the larva gains entrance into the pea always appearing directly beneath it. 7 As soon as hatching begins, the color of the egg is changed materially. It first becomes mottled ivith dark yellowish opaque spots, because as the larva feeds, many small particles of food, together with the excreted material, are pushed back under the egg shell. By the time the larva has completely entered the pea, the entire space beneath the egg shell is filled with this material and the egg then is a uniform yellow or straw color, and is wholly opaque. g _ The length of the hatching period varies considerably, depending upon the temperature and the hardness or dryness of the peas. In fresh‘ peas the period of hatching may comprise only the short period of an hour or two, while several days may elapse before the larva suc- ceeds in entering dried and hardened peas. Table 2.—Duration of the Egg Stage. _ Temperature Laid Hatched Period ‘ Max. Min. Mean Nov. 7 . . . . . . . . . . . . 6 81 66 76.0 Nov. 8 . . . . . . . . . . .. 6 81 66 75.0 ' Nov. 9 . . . . . . . . . . . . 6 82 66 75. 1 Nov. 10 . . . . . . . . . . . . 6 83 74 76.2 Nov. 11 . . . . . . . . . . .. _ 6 83 , 74 75.4 Nov. 12 . . . . . . . . . . . . 6 83 64 64.2 Nov. 12 . . . . . . . . . . . . 4 83 64 77.2 Nov. 17 . . . . . . . . . . . . 8 83 54 70.2 Nov. 18 . . . . . . . . . . . . 8 84 57 69.7 Nov. 18 . . . . . . . . . . .. 7 82 57 68.5 Nov. 19 . . . . . . . . . . .. 7 84 57 69.5 Nov. 20 . . . . . . . . . . . . 7 84 57 70.8 Nov. 21 . . . . . . . . . . . . 7 86 57 72.0 Nov. 22 . . . . . . . . . . . . 7 87 58 73.5 Nov. 23 . . . . . . . . . . . . 7 87 66 75.7 Nov. 24 . . . . . . . . . . . . 7 87 66 76.3 Nov. 25 . . . . . . . . . . . . 7 87 66 76.0 Nov. 26 . . . . . . . . . . . . 7 87 66 65.5 Nov. 27 . . . . . . . . . . . . 7 87 66 76.2 Nov. 28 . . . . . . . . . . . . 7 87 66 76. 1 Nov. 29 . . . . . . . . . . . . 7 82 66 76.1 Nov. 29 . . . . . . . . . . . . 6 82 70 75.6 Nov. 30 . . . . . . . . . . . . 6 82 70 76.0 Dec. . . . . . . . . . . . . 6 86 68 76. 5 Dec. 3 . . . . . . . . . . . . 7 86 68 77.0 Dee. 3 . . . . . . . . . . . . 6 8b 68 76.7 Dec. 4 . . . . . . . . . . . . 6 86 67 76.8 Dec. 5 . . . . . . . . . . . . 6 86 67 76.5 Dec. 6 . . . . . . . . . . . . 6 86 67 77.5 Dec. 7 . . . . . . . . . . . . 6 85 67 77.6 Dec. 8 . . . . . . . . . . . . 6 85 67 77.3 Dec. . . . . . . . . . . . . 6 85 67 76.2 Dee. 10 . . . . . . . . . . .. 6 85 57 75.7 Dec. 11 . . . . . . . . . . .. 6 83 50 74.9 Dec. 12 . . . . . . . . . . .. 6 83 43 71.8 Dee. 13 . . . . . . . . . . .. 6 83 43 69.1 Jan. 4 . . . . . . . . . _ . . 27 83 29 55.8 Jan 5 . . . . . . . . . . . . 27 83 29 55.4 Jan 6 . . . . . . . . . . . . 27 79 29 55.6 Jan 7 . . . . . . . . . . . . 27 79 29 55.6 Jan 8 . . . . . . . . . . . . 27 79 29 55.4 Jan 7 . . . . . . . . . . . . 25 79 29 55.2 Jan 7 . . . . . . . . . . . . 24 79 29 55.2 Jan. 7 . . . . . . . . . . .. 23 79 29 55.3 Plate II. Cowpeas showing extreme weevil infestation. Egg details are shown. [Blank Page in Original Bulletin] THE COWPEA WEEVIL. Table 2.——Duration of the Egg Stage.-—Continued. 17 Temperature Laid Hatched Period _ hdax hdny hdean 79 29 55.0 79 29 54.0 79 29 54.2 79 29 55.5 79 29 55.8 79 29 ' 56.4 79 22 54.0 79 29 53.4 79 29 57.9 79 22 58.5 79 45 61.0 79 45 61.8 ' . 79 45 62.0 . 79 22 53.1 . 79 22 60.5 . 79 22 53.4 . 79 22 53.2 . 79 22 51.9 . 78 26 54.5 . 78 26 54.3 . 81 38 57.8 . . 81 39 59.3 . . 81 39 59.3 . . 81 39 59.7 ; . 81 39 59.3 . . 86 39 59.3 . . 86 39 61.2 . . 86 39 61.7 . . 86 39 61.4 . . . 86 39 63.2 . . 86 44 64.2 . .1 86 44 64.1 . . 86 44 69.2 . . 89 44 68.0 . . 89 44 68.2 . . 89 48 70.9 . . 89 48 70.7 . . 89 48 64.0 . . 89 48 68.8 . . 89 48 -69.9 . ' 86 48 69.4 . ' 86 48 68.4 . 1 86 48 67.0 . ' 86 40 65.4 . ' 86 40 64.2 . 1 86 40 64.1 . ' 83 40 64.4 . ' 83 40 64.0 . 1 83 40 ~64.1 ' ' 83 40 62.3 1 ‘ 83 40 63.7 ' 1 83 40 64.1 ' ' 83 40 65.0 ‘ ' 83 40 65.0 Apfll 7 . . . . . . . . . . . .. Aprfl15 8 83 40 64.5 Aprfl 8 . . . . . . . . . . . .. Aprfl16 . . . . . . . . . . .. 8 83 40 66.2 Apfll10 . . . . . . . . . . . .. Apfll16 . . . . . . . . . . .. 6 83 53 70.4 Aprfl . . . . . . . . . . . H AprU17 . . . . . . . . . . .. 6 85 56 71.1 Apfl]12 . . . . . . . . . . . .. Aprfl18 . . . . . . . . . . .. 6 87 56 71.5 Apfil13 . . . . . . . . . . . .. Apfil20 . . . . . . . . . . .. 7 87 56 72.7 Apflll . . . . . . . . . . . .. Aprfl21 . . . . . . . . . . .. 7 87 56 72.5 Aprfl15 . . . . . . . . . . . .. Aprfl . . . . . . . . . . .. 7 87 56 71.5 Apflllfi . . . . . . . . . . . .. AprU2 . . . . . . . . . . .. 7 87 58 71.4 Apfil17 . . . . . . . . . . . .. Aprfl24 . . . . . . . . . . .. 7 87 58 73.4 Apfll18 . . . . . . . . . . . .. Aprfl . . . . . . . . . . . .. 7 87 58 75.0 Apfll19 . . . . . . . . . . . .. Apfll25 . . . . . . . . . . .. 6 87 58 74.8 Apfil20 . . . . . . . . . . . .. Apfil26 . . . . . . . . . . .. 6 87 58 74.0 Apfll21 . . . . . . . . . . . H Aprfl . . . . . . . . . . .. 8 87 52 71.6 Apfil22 . . . . . . . . . . . . .. A rfl30 . . . . . . . . . . .. 8 87 52 70.8 Apfil23 . . . . . . . . . . . .. ay 1 . . . . . . . . . . .. 8 87 52 70.4 Apfil2 . . . . . . . . . . . .. hday 3 . . . . . . . . . . .. 9 87 52 70.5 AprH25 . . . . . . . . . . . . .. hday 4 . . . . . . . . . . .. 9 87 52 69.7 Apfll26 . . . . . . . . . . . .. hday 4 . . . . . . . . . . .. 8 86 52 69.2 AprH2 . . . - . . . . . . . . . A. hday 4 . . . . . . . . . . .. 7 86 52 68.2 Apfll28 . . . . . . . . . . . . .. hday 4 . . . . . . . . . . .. 6 86 54 68.8 A fil30 . . . . . . . . . . . .. hday 6 . . . . . . . . . . .. 6 94 65 73.9 ay . . . . . . . . . . . .. hday 6 . . . . . . . . . . .. 5 94 65 74.2 Lday 2 . . . . . . . . . . . . .. hday 8 . . . . . . . . . . .. 6 99 65 77.7 a 18 TEXAS AGRICULTURAL EXPERIMENT STATION. Table 2.—Duration of the Egg Stage.-—Continued. _ Temperature Laid Hatched Perlod Max Min. Mean 1916 May 3 . . . . . . . . . . . .. May 8 . . . . . . . . . . . . 5 99 66 79.2 May 4 . . . . . . . . . . . . . . May 9 . . . . . . . . . . . . 5 100 73 82. 1 May 5 . . . . . . . . . . . . . May 10 . . . . . . . . . . . . 5 100 74 86.3 May 6 . . . . . . . . . . . .. May 11 . . . . . . . . . . . . 5 100 76- 87.6 May 7...._. . . . . . . .. May 12 . . . . . . . . . . .. 5 100 80 88.6 May 8 . . . . . . . . . . . . .. May 13 . . . . . . . . . . . . 5 100 80 89.2 May 9 . . . . . . . . . . . . . . May 14 . . . . . . . . . . .. 5 98 8O 88.9 May 10 . . . . . . . . . . . .. May 15 . . . . . . . . . . .. 5 98 80 88.7 May 11 . . . . . . . . . . . .. May 16 . . . . . . . . . . .. 5 97 74 88.4 May 12 . . . . . . . . . . . .. May 19 . . . . . . . . . . .. 7 97 70 84.7 May 13 . . . . . . . . . . . . . May 20 . . . . . . . . . . . . 7 97 70 82.5 May 14 . . . . . . . . . . . .. May 21 . . . . . . . . . . .. 7 97 70 81.1 May 15 . . . . . . . . . . . .. May 22 . . . . . . . . . . .. 7 97 70 80.3 May 16 . . . . . . . . . . . .. May 23 . . . . . . . . . . .. 7 91 70 79.1 May 17 . . . . . . . . . . . .. May 24 . . . . . . . . . . .. 7 91 70 78.7 May 18 . . . . . . . . . . . .. May 24 . . . . . . . . . . .. 6 91 70 78.5 May 19 . . . . . . . . . . . . . May 25 . . . . . . . . . . .. 6 91 71 79.1 May 2O . . . . . . . . . . . .. May 26 . . . . . . . . . . .. 6 91 71 80.2 May 21 . . . . . . . . . . . . . May 27 . . . . . . . . . . .. 6 89 71 81.8 May 22 . . . . . . . . . . . . . May 26 . . . . . . . . . . . . 4 89 71 80.0 May 23 . . . . . . . . . . . .. May 28 . . . . . . . . . . .. 5 89 71 80.9 May 24 . . . . . . . . . . . . . May 29 . . . . . . . . . . . . 5 89 73 80.5 May 25 . . . . . . . . . . . . . May 30 . . . . . . . . . . . . 5 89 73 80.7 May 26 . . . . . . . . . . . .. May 31 . . . . . . . . . . .. 5 94 73 81.0 May 27 . . . . . . . . . . . .. June 1 . . . . . . . . . . .. 5 94 73 81.6 May 28 . . . . . . . . . . . . . June 2 . . . . . . . . . . . . 5 94 73 82.0. May 29 . . . . . . . . . . . .. June 2 . . . . . . . . . . .. 4 94 74 82.5 May 30 . . . . . . . . . . . . . June 3 . . . . . . . . . . . . 4 94 77 83.5 May 31 . . . . . . . . . . . .. June 4 . . . . . . . . . . .. 4 91 77 84.3 June 1 . . . . . . . . . . . .. June 5 . . . . . . . . . . .. 4 92 78 84.1 June 2 . . . . . . . . . . . .. June 6 . . . . . . . . . . .. 4 93 78 84.2 June 3 . . . . . . . . . . . .. June 7.. 4 94 78 84.8 June 4 . . . . . . . . . . . . .. June 8 . . . . . . . . . . .. 4 94 71 84.8 June 5 . . . . . . . . . . . .. June 9 . . . . . . . . . . .. 4 94 71 82.4 June 6 . . . . . . . . . . . .. June 10 . . . . . . . . . . .. 4 94 71 81.7 June 7 . . . . . . . . . . . .. June 11 . . . . . . . . . . .. 4 90 71 81.6 June 8 . . . . . . . . . . . . .. June 12 . . . . . . . . . . .. 4 90 72 81.5 June .9 . . . . . . . . . . . . . . June 13 . . . . . . . . . . . . 4 90 73 83.6 June 10 . . . . . . . . . . . .. June 14 . . . . . . . . . . .. 4 9O 76 84.0 June 11 . . . . . . . . . . . .. June 15 . . . . . . . . . . .. 4 9O 76 83.7 June 12 . . . . . . . . . . . .. June 16 . . . . . . . . . . .. 4 90 72 83.3 June 13 . . . . . . . . . . . .. June 17 . . . . . . . . . . .. 4 90 72 82.0 June 14 . . . . . . . . . . . . .. June 18 . . . . . . . . . . .. 4 89 72 82.0 June 15 . . . . . . . . . . . .. June 19 . . . . . . . . . . .. 4 89 72 81.0 June 16 . . . . . . . . . . . . .. June 20 . . . . . . . . . . .. 4 91 74 80.5 June 17 . . . . . . . . . . . . .. June 21 . . . . . . . . . . .. 4 95 75 81.7 June 18 . . . . . . . . . . . .. June 22 . . . . . . . . . . .. 4 95 75 83.0 June 19 . . . . . . . . . . . .. June 23 . . . . . . . . . . .. 4 95 75 84.5 June 2O . . . . . . . . . . . .. June 24 . . . . . . . . . . .. 4 95 78 ‘ 85.5 June 21 . . . . . . . . . . . . .. June 25 . . . . . . . . . . .. 4 95 80 86.2 June 22 . . . . . . . . . . . . . June 26 . . . . . . . . . . . . 4 95 80 86.7 June 23 . . . . . . . . . . . . . June 27 . . . . . . . . . . . . 4 95 80 86.7 June 24 . . . . . . . . . . . . . une 28 . . . . . . . . . . . . 4 95 75 87.7 June 25 . . . . . . . . . . . . . . June 29 . . . . . . . . . . . . 4 95 75 87.5 June 26 . . . . . . . . . . . . . June 30 . . . . . . . . . . . . 4 95 75 86.2 June 27 . . . . . . . . . . . . .. July 1 . . . . . . . . . . .. 4 95 75 85.2 June 28 . . . . . . . . . . . .. July 2 . . . . . . . . . . .. 4 93 76 84.0 June'29 . . . . . . . . . . . .. July‘ 3 . . . . . . . . . . .. 4 93 77 84.2 June 30 . . . . . . . . . . . . .. July 4 . . . . . . . . . . .. 4 93 76 84.5 July 1 . . . . . . . . . . . . . July 5 . . . . . . . . . . . . 4 95 76 84.7 July 2 . . . . . . . . . . . .. July 6 . . . . . . . . . . .. 4 95 76 85.2 July 3 . . . . . . . . . . . .. July 7 . . . . . . . . . . .. 4 97 76 85.5 July 4 . . . . . . . . . . . . .. July 8 . . . . . . . . . . .. 4 a 99 77 86.5 July 5 . . . . . . . . . . . .. July 9 . . . . . . . . . . .. 4 99 79 88.0 July 6 . . . . . . . . . . . . . July 10 . . . . . . . . . . .. 4 99 79 88.5 July 7 . . . . . . . . . . . .. July 11 . . . . . . . . . . .. 4 99 79 89.2 July 8 . . . . . . . . . . . . .. July 12 . . . . . . . . . . .. 4 98 79 89.0 July 9 . . . . . . . . . . . .. July 13 . . . . . . . . . . .. 4 98 79 85.2 July 10 . . . . . . . . . . . .. July 14 . . . . . . . . . . .. 4 97 79 87.0 July 11 . . . . . . . . . . . .. July 15 . . . . . . . . . . .. 4 95 80 86.5 July 12 . . . . . . . . . . . .. July 16 . . . . . . . . . . .. 4 97 79 86.2 Julv 13 . . . . . . . . . . . .. July 17 . . . . . . . . . . .. 4 98 79 87.0 July 14 . . . . . . . . . . . .. July 18 . . . . . . . . . . .. 4 99 78 87.5 July 15 . . . . . . . . . . . .. July 19 . . . . . . . . . . .. 4 99 78 88.2 July 16 . . . . . . . . . . . .. July 20.. 4 99 78 87.7 July 17 . . . . . . . . . . . .. July 21 . . . . . . . . . . .. 4 99 78 88.0 July 18 . . . . . . . . . . . .. July 22 . . . . . . . . . . .. 4 97 80 87.7 July 19 . . . . . . . . . . . .. July 23 . . . . . . . . . . .. 4 97 80 88.2 July 20 . . . . . . . . . . . .. July 24 . . . . . . . . . . .. 4 99 80 88.2 I THE COWPEA WEEVIL. Table 2.—Duration 9f "the Egg Staga-Continued. 19 Tempera Lvrc Laid Hatched Period -— hdax A111. hdcan 4 99 80 88.5 4 99 78 89.0 4 99 78 87.7 4 98 78 87.5 4 97 78 86.7 4 97 78 86.2 4 97 78 86.0 4 97 78 86.0 4 97 78 86.5 4 97 79 86.5 4 97 79 87.5 4 97 79 88.0 4 97 79 88.2 4 96 79 86.5 4 96 79 85.5 4 95 79 85.5 4 95 79 84.2 4 95 79 84.7 4 94 78 85.0 4 95 78 85.0 4 96 80 85.7 4 95 79 87.0 4 95 79 87.2 4 95 75 87.0 4 95 75 85.7 4 95 75 85.5 4 94 75 85.7 4 100 80 85.7 4 100 80 87.7 4 100 80 88.5 4 100 79 88.7 4 97 73 88.2 4 96 70 85.7 4 93 70 84.2 4 93 70’ 83.0 4 94 70 83.2 4 94 75 84.2 4 97 77 85.0 4 97 77 86.0 4 97 77 86.0 4 97 78 86.5 ' 4 97 79 87.2 3 97 80 87.0 4 97 80 88.2 4 97 80 88.5 4 101 80 88.5 4 101 80 89.0 4 101 80 89.5 4 101 80 89.2 4 99 80 89.0 3 97 70 88.5 4 97 78 88.2 4 97 73 87.5 4 97 70 85.7 5 99 67 82.4 5 99 67 81.4 5 99 67 80.0 5 99 67 79.6 5 99 67 80.2 4 91 68 80.5 4 91 69 80.0 4 91 70 80.5 5 91 70 81.0 5 105 70 80.2 5 105 71 80.2 5 105 60 83.4 6 105 57 79.3 6 105 57 76.6 6 95 57 76.4 6 85 57 74.0 6 89 57 72.6 6 89 59 73.5 5 89 54 74.0 5 89 66 77.0 5 90 66 77.7 4 90 66 77.7 4 91 69 78.0 4 94 68 79.3 4 94 68 81.0 TEXAS ‘AGRICULTURAL EXPERIMENT STATION. 20 Table 2.—Duration of the Egg Stage.-—-Continued. _ Temperature Laid Hatched Penod Max Min. Mean 1916 Oct. 8 . . . . . . . . . . . . . . Oct 12 . . . . . . . . . . . . 4 94 68 80.0 Oct. 9 . . . . . . . . . . . . . Oct 13 . . . . . . . . . . . . 4 94 68 79.5 Oct. 1O . . . . . . . . . . . . . Oct 14 . . . . . . . . . . . . 4 9O 68 79. 7 Oct. 11 . . . . . . . . . . . . . Oct 15 . . . . . . . . . . . . 4 90 68 79.7 Oct. 12 . . . . . . . . . . . . . Oct 16 . . . . . . . . . . . . 4 9O 65 80.0 Oct. 13.. Oct 18 . . . . . . . . . . . . 5 90 61 78.8 Oct. 14 . . . . . . . . . . . . . Oct 22 . . . . . . . . . . . . 8 87 41 70. 6 Oct. 15 . . . . . . . . . . . . . . Oct 23 . . . . . . . . . . . . 8 87 41 68.6 Oct. 16 . . . . . . . . . . . . . Oct 25 . . . . . . . . . . . . 9 95 41 69.0 Oct. 17 . . . . . . . . . . . . . Oct 27 . . . . . . . . . . . . 10 95 41 68.4 Oct. 18 . . . . . . . . . . . . . Oct 28 . . . . . . . . . . . . 10 95 41 68.1 Oct. 19 . . . . . . . . . . . . . Oct 28 . . . . . . . . . . . . 9 95 41 68.3 Oct. 20 . . . . . . . . . . . . . . Oct 29 . . . . . . . . . . . . 9 95 41 68.5 Oct. 21 . . . . . . . . . . . . . Oct 29 . . . . . . . . . . . . 8 95 52 69.3 Oct 22 . . . . . . . . . . . . . . Oct 30 . . . . . . . . . . . . 8 . 95 53 71.3 Oct 23 . . . . . . . . . . . . . Oct 3O . . . . . . . . . . . . 7 95 53 72.4 Oct 24 . . . . . . . . . . . . . Nov 1 . . . . . . . . . . . . 8 9O 53 74. 6 Oct 25 . . . . . . . . . . . . . . Nov 2 . . . . . . . . . . . . 8 9O 53 74.1 Oct 26 . . . . . . . . . . . . . Nov 2 . . . . . . . . . . . . 7 90 53 74.0 Oct 27 . . . . . . . . . . . . . Nov 2 . . . . . . . . . . . . 6 9O ‘ 56 75.6 Oct 28 . . . . . . . . . . . . . Nov 3 . . . . . . . . . . . . 6 9O 6O 76.2 Oct 29 . . . . . . . . . . . . . Nov 4 . . . . . . . . . . . . 6 9O 6O 77.6 Oct 3O . . . . . . . . . . . . . Nov 5 . . . . . . . . . . . . 6 89 6O 77.4 Oct 31 . . . . . . . . . . . . . Nov 6 . . . . . . . . . . . . 6 89 60 76.6 Nov 1 . . . . . . . . . . . . . Nov 7 . . . . . . . . . . . . 6 89 60 75.1 Nov 2 . . . . . . . . . . . . . Nov 8 . . . . . . . . . . . . 6 87 6O _ 75.5 Nov 3 . . . . . . . . . . . .. Nov 11 . . . . . . . . . . .. 8 87 51 74.5 Nov 4 . . . . . . . . . . . .. Nov 12 . . . . . . . . . . .. 8 87 51 73.8 Nov 5 . . . . . . . . . . . .. Nov 16 . . . . . . . . . . .. 11 87 33 68.1 Nov 6 . . . . . . . . . . . .. Nov 19 . . . . . . . . . . .. 13 89 33 66.0 Nov 7 . . . . . . . . . . . .. Nov 20 . . . . . . . . . . .. 13 93 33 65.6 Nov. 8 . . . . . . . . . . . .. Nov 21 . . . . . . . . . . . . 13 94 33 65.4 Nov. 9 . . . . . . . . . . . . . Nov 25 . . . . . . . . . . . . 16 94 33 64.6 Nov. 10 . . . . . . . . . . . .. Nov 26 . . . . . . . . . . .. 16 94 33 64.1 Nov. 11 . . . . . . . . . . . .. Nov 27 . . . . . . . . . . .. 16 94 33 64.0 Nov. 12 . . . . . . . . . . . .. Nov 28 . . . . . . . . . . .. 16 94 33 63.7 Nov. 13 . . . . . . . . . . . . . Nov 29 . . . . . . . . . . .. 16 98 33 63.1 Nov. 14 . . . . . . . . . . . . . Nov 29 . . . . . . . . . . . . 15 98 33 63.0 Nov. 15 . . . . . . . . . . . .. Nov 3O . . . . . . . . . . .. 15 98 39 65.3 Nov. 16 . . . . . . . . . . . . . Nov 3O . . . . . . . . . . . . 14 98 44 66.7 Nov. 17 . . . . . . . . . . . .. Dec 1 . . . . . . . . . . .. 14 98 44 68.1 Nov._ 18 . . . . . . . . . . . .. Dec 1 . . . . . . . . . . . . 13 98 44 68.3 Nov. 19 . . . . . . . . . . . . . Dec 2 . . . . . . . . . . . . 13 98 44 69.0 Nov. 20 . . . . . . . . . . . . . Dec 3 . . . . . . . . . . . . 13 98 44 69.3 Nov. 21 . . . . . . . . . . . .. Dec 4 . . . . . . . . . . . . 13 98 44 69.8 Nov. 22 . . . . . . . . . . . . . Dec 5 . . . . . . . . . . .. 13 101 44 69.3 Nov. 23 . . . . . . . . . . . . . Dec 5 . . . . . . . . . . . . 12 101 44 72.0 Nov. 24 . . . . . . . . . . . . . Dec 6 . . . . . . . . . . .. 12 101 44 73.0 Nov. 25 . . . . . . . . . . . . . Dec 6 . . . . . . . . . . .. 11 101 44 73.6 Nov 26. Dec 6 . . . . . . . . . . .. 10 101 48 74.5 Nov. 27 . . . . . . . . . . . .. Dec 6 . . . . . . . . . . .. 9 101 48 75.6 Nov 28 . . . . . . . . . . . .. Dec 6 . . . . . . . . . . .. 8 101 48 77.1 Nov 29 . . . . . . . . . . . .. Dec 7 . . . . . . . . . . .. 8 101 48 79.6 Nov 3O . . . . . . . . . . . . . Dec 8 . . . . . . . . . . . . 8 101 48 79.3 Dec 1 . . . . . . . . . . . . . Dec 8 . . . . . . . . . . . . 7 101 38 80.0 Dec 2 . . . . . . . . . . . . . Dec 11 . . . . . . . . . . .. 9 101 38 75.2 Dec 3 . . . . . . . . . . . .. Dec 15 . . . . . . . . . . .. 12 101 34 69.5 Dec 4 . . . . . . . . . . . .. Dec 2O . . . . . . . . . . .. 16 101 32 66.2 Dec 5 . . . . . . . . . . . . . Dec 26 . . . . . . . . . . . . 21 99 28 61.9 Dec 6 . . . . . . . . . . . . . Dec 27 . . . . . . . . . . . . 21 9O 28 61.0 Dec 7 . . . . . . . . . . . .. Jan 1, 1917 . . . . . . .. 25 90 28 60.3 Dec 8 . . . . . . . . . . . . . Jan 2 . . . . . . . . . . . . 25 89 28 59.3 Dec 9 . . . . . . . . . . . . . Jan 2 . . . . . . . . . . . . _ 24 92 28 58.9 Dec 10 . . . . . . . . . . . . . Jan 3 . . . . . . . . . . . . 24 92 28 59.9 Dec 1 1 . . . . . . . . . . . . . Jan 3 . . . . . . . . . . . . 23 92 28 59. 6 Dec 12 . . . . . . . . . . . .. Jan 4 . . . . . . . . . . .. 23 92 28 60.1 Dec 13 . . . . . . . . . . . . . Jan 4 . . . . . . . . . . . . 22 92 28 60.4 Dec 14 . . . . . . . . . . . .. Jan 4 . . . . . . . . . . .. 21 92 28 60.5 Dec 15 . . . . . . . . . . . .. Jan 5 . . . . . . . . . . .. 21 92 28 61.6 Dec 16 . . . . . . . . . . . .. Jan 5 . . . . . . . . . . .. 20 92 28 61.2 Dec 17 . . . . . . . . . . . .. Jan 5 . . . . . . . . . . .. 19 92 28 61.4 Dec 18 . . . . . . . . . . . .. Jan 6 . . . . . . . . . . .. 19 92 28 58.6 Dec 19 . . . . . . . . . . . .. Jan 7 . . . . . . . . . . .. 19 92 28 , 61.7 Dec . . . . . . . . . . . . .. Jan 7 . . . . . . . . . . .. 18 92 28 62.4 Dec 22 . . . . . . . . . . . . . Jan 7 . . . . . . . . . . . . 16 92 38 63.0 Dec 23 . . . . . . . . . . . . . Jan 8 . . . . . . . . . . .. 16 92 46 64.4 ~ Dec. 24 . . . . . . . . . . . .. Jan 8 . . . . . . . . . . .. 15 92 46 65.5 Dec. 25 . . . . . . . . . . . .. Jan 8 . . . . . . . . . . .. 14 92 46 65.9 Dec. 26 . . . . . . . . . . . .. Jan. 9 . . . . . . . . . . .. 14 93 46 66.2 , THE COWPEA WEEvIL. 21 Table 2.—Duration of the Egg Stage.—Continued. Temperature Laid Hatched Perod Max. Min. Mean 1916 Dec. 27 . . . . . . _ . . . . .. Jan 9 . . . . . . . . . . . . 13 93 46 66.0 Dec. 2 . . . . . . . . . . . .. Jan 9 . . . . . . . . . . .. 12 93 46 63.6 Dec. 29 . . . . . . . . . . . .. Jan 10 . . . . . . . . . . .. 12 94 46 66.9 Dee. 30 . . . . . . . . . . . .. Jan 11 . . . . . . . . . . .. 12 94 44 68.6 Deleéli; . . . . . . . . . . . .. Jan. 12 . . . . . . . . . . .. 12 94 44 67.8 Jan. . . . . . . . . . . . .. Jan 12 . . . . . . . . . . .. 11 94 44 69.0 Jan 2 . . . . . . . . . . . .. Jan 21 . . . . . . . . . . .. 19 94 30 56._4 Jan 3 . . . . . . . . . . . .. Jan 25 . . . . . . . . . . .. 22 94 30 55.0 Jan 4 . . . . . . . . . . . . . Jan 29 . . . . . . . . . . . . 25 94 30 55.2 Jan 5 . . . . . . . . . . . .. Jan 30 . . . . . . . . . . .. 25 100 30 54.6 Jan 6 . . . . . . . . . . . .. Jan 31 . . . . . . . . . . . .. 25 100 3O 55.4 Jan 7 . . . . . . . . . . . .. Feb 1 . . . . . . . . . . . . 25 100 30 56.4 Jan 8 . . . . . . . . . . . . . Feb 2 . . . . . . . . . . . . 25 100 25 55. 9 Jan 9 . . . . . . . . . . . . . Feb 8 . . . . . . . . . . . . 3O 100 25 53.9 Jan 10 . . . . . . . . . . . .. Feb 13 . . . . . . . . . . .. 34 100 25 52.7 Jan 11 . . . . . . . . . . . .. Feb 15 . . . . . . . . . . .. 35 100 25 51.4 Jan 12 . . . . . . . . . . . . . Feb 18 . . . . . . . . . . . . 37 100 25 53.2 Jan 20 . . . . . . . . . . . . _ Feb 18 . . . . . . . . . . . . 29 100 25 57.0 Jan 21 . . . . . . . . . . . .. Feb 18 . . . . . . . . . . .. 28 100 25 57.1 Jan 24 . . . . . . . . . . . . . . Feb 18 . . . . . . . . . . . . 25 100 25 57.2 Jan 25 . . . . . . . . . . . . . Feb 18 . . . . . . . . . . . . 24 100 25 57.6 Jan 26 . . . . . . . . . . . . . Feb 19 . . . . . . . . . . . . 24 100 25 61.0 Jan 27 . . . . . . . . . . . .. Feb 19 . . . . . . . . . . .. 23 100 25 61.0 Jan 28 . . . . . . . . . . . . . Feb 19 . . . . . . . . . . . . 22 100 25 58.0 Jan 29 . . . . . . . . . . . . . Feb 20 . . . . . . . . . . . . 22 100 25 08.4 Jan 30 . . . . . . . . . . . . . Feb 21 . . . . . . . . . . . . 22 103 ~25 58.5 Jan 31 . . . . . . . . . . . . . Feb 22 . . . . . . . . . . . . 22 103 25 57.9 Feb 2 . . . . . . . . . . . . . Feb 22 . . . . . . . . . . . . 20 103 30 56. 6 Feb 4 . . . . . . . . . . . . . Feb 2% . . . . . . . . . . . . 19 103 30 59.4 Feb 5 . . . . . . . . . . . . . Feb 23 . . . . . . . . . . . . 18 103 36 60.4 Feb 6 . . . . . . . . . . . . . Feb 24 . . . . . . . . . . . . 18 103 40 61.3 Feb 7 . . . . . . . . . . . . . Feb 24 . . . . . . . . . . . . 17 103 41 62.2 Feb 8 . . . . . . . . . . . . . Feb 24 . . . . . . . . . . . . 16 103 41 63.2 Feb 9 . . . . . . . . . . . . . Feb 24 . . . . . . . . . . . . 15 103 41 63.9 Feb 10 . . . . . . . . . . . . . Feb 24 . . . . . . . . . . . . 14 103 41 63.7 Feb 11 . . . . . . . . . . . . . Feb 25 . . . . . . . . . . . . 14 103 41 64.9 Feb 12 . . . . . . . . . . . . . Feb 25 . . . . . . . . . . . . 13 103 42 65.0 Feb 13 . . . . . . . . . . . . . Feb 25 . . . . . . . . . . . . 12 103 44 66.1 Feb 14 . . . . . . . . . . . . . Feb 25 . . . . . . . . . . . . 11 103 44 67.9 Feb 15 . . . . . . . . . . . . . Feb 25 . . . . . . . . . . . . 10 103 44 69.2 Feb 16 . . . . . . . . . . . . . . Feb 26' . . . . . . . . . . . 10 103 44 70.9 Feb 17 . . . . . . . . . . . . . Feb 26 . . . . . . . . . . . . 9 103 54 72.6 Feb 18 . . . . . . . . . . . . . Feb 26 . . . . . . . . . . . . 8 103 54 75.2 Feb 19 . . . . . . . . . . . .. Feb 27 . . . . . . . . . . .. 8 103 54 77.0 Feb 20 . . . . . . . . . . . . . Feb 28 . . . . . . . . . . . . 8 103 33 79.3 Feb 21 . . . . . . . . . . . .. Mar 6 . . . . . . . . . . . . 13 102 33 69.5 Feb 22 . . . . . . . . . . . . . Mar 9 . . . . . . . . . . . . 15 102 33 68.4 Feb 23 . . . . . . . . . . . .. Mar 11 . . . . . . . . . . .. 16 102 33 67.3 Feb 24 . . . . . . . . . . . .. Mar 13 . . . . . . . . . . . . 17 102 33 67.5 Feb 25 . . . . . . . . . . . .. Mar 14 . . . . . . . . . . .. 17 102 33 61.5 Duration- 0f Egg Stage. Detailed observations have been made on the eggs of about 350 weevils covering a period of almost one and, one-half years. The records were made in the laboratory- Where only natural temperature conditions prevailed throughout the entire time. A thermograph was used to record the existing temperatures during the period of observa- tions. The results of the observations are shown in Table 2. For each period the single highest temperature and the single lowest temperature of the entire period are given. The mean temperature is the average of the mean daily temperatures during the period. The shortest period observed, 4 days, occurred frequently during the warmer portions of 1916. In fact, every period during June, July, and August, 191.6, was four days. The mean temperature necessary for this short period ranges from 81 to 89.2 degrees F. During the 22 TEXAS AGRICULTURAL EXPERIMENT STATION. period of three months when there was an unbroken record of four days for the length of the egg stage, the mean temperature was 85.8 degrees F. In one instance a period of four days occurred with a mean temperature for the period of only 80 degrees F. The longest period of ‘the egg stage recorded was from January 12 to February 19, 1917', a period of 37 days. During this period the lowest temperature recorded was 25 degrees F. and the mean temperature for the period was 53.9 degrees F. The yearly variations in the duration of the egg stage are shown in Table 3. The mean temperature evidently does not have positive in- fluence upon the duration 0f the egg stage and in such cases continued low temperature influence is evident. Tab‘e 3.——Yearly Variation inYDuration of Egg Stage. Period, Temperature, Date Days - ean November, 1915 . . . . . . . . . . . . . . . . . . . 6.5 l 75.6 ~ November, 1916 . . . . . . . . . . . . . . . . . . III 12.0 ; 70.0 December, 1915 . . . . . . . . . . . . . . . . . . . .l 17.4 I so. 1 December, 1916 . . . . . . . . . . . . . . . . . . . . 17.5 I 63.9 January, 1916 . . . . . . . . . . . . . . . . . . . . . .. 22.2 53.8 January, 1917 . . . . . . . . . . . . . . . . . . . . . . 25.2 56.5 February, 1916 . . . . . . . . . . . . . . . . . . . . . 19.4 60.4 14. 5 l 68.2 February, 1917 . . . . . . . . . . . . . . . . . . . . . In Table 4 is given a summary of the duration of the egg stage during the summer months and during the winter months. The aver- age period during the warmest months was about 5 days and during the coldest months the average period was about 15 days. The period during the summer months is quite constant, but during the fall the period increases slowly. During the winter the period is quite variable, probably due to the variations in temperature at that season of the ' year in this locality. Table 4.—Summary of Duration of the Egg Stage. . Collections Month Average Shortest Longest of Eggs Period Period Period Observed Days Days Days June, 1916 . . . . . . . . . . . . . . . . . . . . . . . . 5 5 5 26 July, 1916 . . . . . . . . . . . . . . . . . . . . . . .. 5 5 5 26 August, 1916 . . . . . . . . . . . . . . . . . . . . . . 5 5 5 25 September, 1916 . . . . . . . . . . . . . . . . . . . 5 4 7 30 November, 1916 . . . . . . . . . . . . . . . . . . . 12.7 7 17 29 December, 1916 . . . . . . . . . . . . . . . . . . . 18.5 8 25 30 January, 1917. . . . . . . . . . . . . . . . . . . . . . 25.5 12 37 22 February, 1917 . . . . . . . . . . . . . . . . . . .. 14.8 8 19 22 There is quite a close relationship between the duration oi: the egg stage and existing temperatures. This effect is shown in Table 5. The low temperature at which the vitality of the eggs is destroyed was not determined. 1 [Blank Page in Original Bulletin] ’ .3015 £95 miona QQPEA 315w?» swmfioO A: 35% THE COWPEA W EEVIL. a 23 Table 5.—Efi'ect of Temperature on Duration of Egg Stage. Avera e Daily Month Perio , Temperature, . . Days Degrees F. June, 1916 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 86 5 87 August, 1916 . . . . . . . . . . . . ' 5 86 September, 1916 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5.6 83.5 November, 1916 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12.7 68.5 December, 1916 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .. 18.5 y 64.6 January, 1917 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .. 25.5 60.3 February, 1917 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .. 14.8 62 Larva. Descripti0nQ~The larva of B. qaadrimacalatus is a fleshy grub; its body is fusiform. and yellowish-white in color; its head small and brownish; its trophi dark brown. The length varies from 1 to 5 mm. depending upon the inolt; the larva is strongly curved when in natural position, the posterior end being considerably larger and tapering abruptly to a blunt point on the anal extremity. Head small, wider than long, light in color; antennae rudimentary; eye spots well defined. Thoracic segments distinct, prothorax slightly larger; no bristles or hairs present. Views of the larva are shown in Plate III. Duration 0f Larval Stage. Exact records were made on the duration of the larval stage of the cowpea weevil for a period of almost one and one-half years. These observations were made in the laboratory Where only natural tempera- ture conditions prevailed throughout the entire time. A thermograph was used to record the existing temperatures during the" period of observation. The records made in‘ these observations are given in Table 6. For each period are given its single highest temperature and its single lowest temperature. The mean temperature given is the average of the mean daily temperatures during the period. Normal dry peas were the only food of the larvae. Table 6.—Duration of Larval Stage. _ Temperature Hatched Pupated Period _ Max. Min. I .Mean 1915 Nov. . . . . . . . . . . . . . Nov 20 . . . . . . . . . . . . 18 84 57 73.3 Nov 2 . . . . . . . . . . . .. Nov. 20 . . . . . . . . . . .. 18 84 57 73.3 ’ Nov 2 . . . . . . . . . . . .. Nov. 21 . . . . . . . . . . .. 19 86 57 73.3 Nov 4 . . . . . . . . . . . .. Nov 22 . . . . . . . . . . .. 18 87 57 73.4 Nov 4 . . . . . . . . . . . .. Nov 24 . . . . . . . . . . .. 20 87 57 73.6 Nov 5 . . . . . . . . . . . .. Nov 24 . . . . . . . . . . .. 19 87 57 73.6 Nov 5 . . . . . . . . . . . . . Nov 25 . . . . . . . . . . . . 20 87 57 73.9 i Nov 6 . . . . . . . . . . . . . Nov 26 . . . . . . . . . . .. 20 87 57 73.7 Nov 7 . . . . . . . . . . . .. Nov 26 . . . . . . . . . . .. 19 87 57 73.5 Nov 8 . . . . . . . . . . . .. Nov 27 . . . . . . . . . . .. 19 87 57 73.3 Nov . . . . . . . . . . . . . Nov 28 . . . . . . . . . . . . 19 87 57 73.7 Nov 10 . . . . . . . . . . . .. Nov 28 . . . . . . . . . . .. 18 87 57 73.4 Nov 11 . . . . . . . . . . . .. Nov 29 . . . . . . . . . . .. 18 87 57 73.3 Nov 12 . . . . . . . . . . . .. Dec. 1 . . . . . . . . . . .. 19 87 57 73.6 Nov 12 . . . . . . . . . . . .. Dec. 4 . . . . . . . . . . .. 22 87 57 74.2 Nov 16 . . . . . . . . . . . . .. Dec 3 . . . . . . . . . . .. 17 87 66 76.0 Nov 17 . . . . . . . . . . . .. Dec 4 . . . . . . . . . . .. 17 87 66 76.5 Nov 18 . . . . . . . . . . . .. Dec 3 . . . . . . . . . . .. 15 87 66 76.5 24 TEXAS AGRICULTURAL EXPERIMENT STATION. Table 6.—Duration of Larval stagger-Continued. _ Temperature Hatched Pupated Penod _ hdax Alum hdean 16 87 66 76.5 16 87 66 76.3 15 87 66 76.3 15 87 66 71.2 13 86 66 84.0 14 86 66 76.5 15 86 66 76.4 15 86 57 76.4 15 86 50 75.9 34 86 29 61.5 37 86 29 61.1 37 86 29 61.1 39 86 29 61.5 39 86 29 61.3 40 85 29 59.5 53 85 22 56.7 73 83 22 55.5 74 83 22 55.2 74 83 22 54.9 74 83 22 54.9 81 83 22 57.0 88 86 22 55.7 86 86 22 55.2 83 81 22 55.8 72 86 22 57.1 72 86 22 56.9 72 86 22 56.6 70 88 22 56.6 72 86 22 55.1 71 86 22 55.5 71 88 22 54.9 68 86 22 56.7 37 80 22 50.7 39 80 22 50.9 60 86 22 58.0 68 86 22 56.9 70 86 22 56.6 69 86 22 56.5 71 88 22 56.4 61 88 22 58.8 59 89 22 59.3 51 89 26 60.2 48 89 27 60.1 50 89 38 56.3 36 89 39 66.6 35 89 39 67.5 37 89 39 66.1 37 89 39 66.2 36 89 39 66.3 32 89 44 67.5 33 89 40 66.1 31 89 40 66.7 28 89 40 66.0 26 89 40 67.1 26 89 40 67.4 26 89 40 67.5 26 89 40 67.6 25 87 40 67.2 24 87 40 66.7 26 87 40 67.8 26 87 40 68.7 28 87 40 68.4 28 87 40 68.2 27 87 40 68.3 24 87 44 69.3 23 87 52 71.0 23 87 52 1 71.5 23 87 52 71.5 22 87 52 71.8 23 91 52 72.0 22 91 52 71.9 21 91 52 71.7 21 91 52 71.7 20 91 52 71.4 20 91 52 71.4 21 94 52 71.9 Aprfl16 . . . . . . . . . . . .. hday 6 . . . . . . . . . . .. 20 94 52 72.5 THE OQWPEA WVEEVIL. Table 6.—Duration of Lz-lrval Stage.-—Continued. 25 Temperature Hatched Pupated Period hdax hdhn hdean 1916 Aprfl16 . . . . . . . . . . . .. hday 7 . . . . . . . . . . .. 21 96 52 73.0 AprU17 . . . . . . . . . . . .. hday 7 . . . . . . . . . . .. 20 96 52 73.6 Aprfl18 . . . . . . . . . . . .. hday 7 . . . . . . . . . . .. 19 96 52 74.0 Aprfl2O . . . . . . . . . . . . .. hday 8 . . . . . . . . . . .. 18 99 52 74.2 Apfil21 . . . . . . . . . . . .. hday 8 . . . . . . . . . . .. 17 99 52 74.3 Aprfl22. . . . . . . . . . . .. hday 9 . . . . . . . . . . .. 17 100 52 75.4 Apfll23 . . . . . . . . . . . .. hday 9 . . . . . . . . . . .. 16 100 52 75.5 Aprfl24 . . . . . . . . . . . .. hday 9 . . . . . . . . . . .. 15 100 52 75.6 Apfl125 . . . . . . . . . . . . .. hflay 10 . . . . . . . . . . .. 15 100 52 76.4 ' 16 100 52 77.2 ' 15 100 52 76.6 13 100 59 79.5 13 100 60 81.5 13 100 65 83.0 14 100 66 85.1 14 100 70 85.8 15 100 70 84.6 18 100 70 84.0 18 100 70 84.0 17 100 70 84.3 17 100 70 84.3 16 100 70 84.1 16 100 70 84.1 16 98 70 83.5 17 98 70 82.8 17 97 70 82.4 16 97 70 82.0 16 97 70 81.4 16 97 70 80.9 16 97 70 80.4 16 94 70 80.4 13 94 71 80.4 13 94 71 81.1 13 94 71 81.6 13 94 71 81.7 12 94 71 82.0 12 94 73 82.2 12 94 73 82.2 12 94 73 82.6 11 94 73 82.8 11 94 73 82.8 11 94 73 83.0 11 94 71 83.5 11 94 71 83.2 11 94 71 83.1 11 94 71 83.6 11 94 71 83.3 11 94 71 83.5 11 94 71 83.2 11 94 71 83.2 11* Q4 71 83.0 11 94 71 82.6 11 90 71 82.3 11 90 72 81.8 12 95 72 82.5 12 95 72 83.0 12 95 72 .83.0 12 95 72 83.1 12 95 72 83.3 12 95 72 83.9 12 95 72 84.1 12 95 74 84.5 12 95 75 85.0 12 95 75 85.3 12 95 75 85.5 12 95 75 85.7 11 95 75 85.9 11 95 75 85.6 10 95 75 85.7 10 95 75 85.6 10 95 75 85.3 10 97 75 85.2 10 99 76 85.3 10 99 76 85.8 10 99 76 86.2 10 99 76 86.7 10 99 76 87.2 10 99 76 87.2 10 99 77 87.3 26 TEXAS AGRICULTURAL EXPERIMENT STATION. Table 6.—Duration of Larval Stage. _ - Temperature matched Pupated Penod _ Max Mm. Mean 1916 . July 5 . . . . . . . . . . . .. July 15 . . . . . . . . . . .. 10 99 79 87.5 July 6 . . . . . . . . . . . .. July 16 . . . . . . . . . . .. 1O 99 79 87.6 July 7 . . . . . . . . . . . .. July 17 . . . . . . . . . . . . 10 99 79 87.8 July 8 . . . . . . . . . . . . . July 18 . . . . . . . . . . . . 10 99 78 87.8 July 9 . . . . . . . . . . . .. July 19 . . . . . . . . . . .. 10 99 78 87.6 July 1O . . . . . . . . . . . .. July 0 . . . . . . . . . . .. 10 99 78 87.4 July 11 . . . . . . . . . . . .. July 20 . . . . . . . . . . . . 9 99 78 87.2 July 12 . . . . . . . . . . . .. July 22 . . . . . . . . . . . . 10 99 78 87.3 July 14 . . . . . . . . . . . .. July 23 . . . . . . . . . . . . 9 99 78 88.0 July 15 . . . . . . . . . . . . . July 24 . . . . . . . . . . .. 9 99 78 87.0 July l6 . . . . . . . . . . . .. July 27 . . . . . . . . . . .. 11 99 78 88.0 July 17 . . . . . . . . . . . .. July 27 . . . . . . . . . . . . 10 99 78 88.1 July 18 . . . . . . . . . . . .. July 28 . . . . . . . . . . .. 10 99 78 87.7 July 19.. July 28 . . . . . . . . . . .. 9 99 78 87.6 July 2O . . . . . . . . . . . .. July 29 . . . . . . . . . . .. 9 99 78 87.7 July 21 . . . . . . . . . . . .. July 3O . . . . . . . . . . .. 9 99 78 87.7 July 22 . . . . . . . . . . . . .. July 31 . . . . . . . . . . .. 9 99 78 87.0 July 23 . . . . . . . . . . . .. Aug. 1 . . . . . . . . . . .. 9 99 78 86.6 July 24 . . . . . . . . . . . .. Aug. 2 . . . . . . . . . . .. 9 99 78 87.1 July 25 . . . . . . . . . . . .. Aug. 3 . . . . . . . . . . .. 9 99 78 86.8 July 26 . . . . . . . . . . . .. Aug. 4 . . . . . . . . . . .. 9 99 78 86.6 July 27 . . . . . . . . . . . . .. Aug. 5 . . . . . . . . . . .. 9 99 78 86.8 July 28 . . . . . . . . . . . .. Aug. 6 . . . . . . . . . . .. 9 97 78 87.3 July 29 . . . . . . . . . . . .. Aug. 8 . . . . . . . . . . .. 1O 97 78 86.6 July 30 . . . . . . . . . . . . . Aug. 9 . . . . . . . . . . . . 10 97 78 86.5 July 31 . . . . . . . . . . . .. Aug 10 . . . . . . . . . . . . 10 97 78 86.6 Aug. 1 . . . . . . . . . . . .. Aug 11 . . . . . . . . . . .. 10 97 79 6.2 Aug. 2 . . . . . . . . . . . . . Aug 12 . . . . . . . . . . . . 10 97 79 5.9 Aug. 3 . . . . . . . . . . . . . Aug 13 . . . . . . . . . . . . 10 96 79 85.8 Aug. 4. . . . . . . . . . . . . Aug 14 . . . . . . . . . . . . 10 96 79 85.7 Aug. 5 . . . . . . . . . . . . .. Aug 16 . . . . . . . . . . . . 11 496 79 85.7 Aug. 6 . . . . . . . . . . . .. Aug 17 . . . . . . . . . . .. 11 96 75 85.5 Aug. 7 . . . . . . . . . . . . . Aug 17 . . . . . . . . . . .. 10 96 75 86.0 Aug. 8 . . . . . . . . . . . . . Aug 18 . . . . . . . . . . . . . 10 96 75 85.8 Aug 9 . . . . . . . . . . . . . Aug 19 . . . . . . . . . . . . 10 96 75 85.8 Aug 10 . . . . . . . . . . . .. Aug 20 . . . . . . . . . . .. 10 96 75 86.0 Aug 11 . . . . . . . . . . . .. Aug 20 . . . . . . . . . . .. 9 96 75 86.2 Aug 12 . . . . . . . . . . . . . Aug. 21 . . . . . . . . . . . . 9 100 75 86.4 Aug 13 . . . . . . . . . . . .. Aug 22 . . . . . . . . . . .. 9 100 75 87.0 Aug 14 . . . . . . . . . . . . . Aug. 25 . . . . . . . . . . . . 11 100 73 86.9 Aug 15.- . . . . . . . . . . . . Aug. 26 . . . . . . . . . . . . 11 100 70 86.3 Aug 16 . . . . . . . . . . . . . Aug. 28 . . . . . . . . . . . . 12 100 70 85.8 Aug 17 . . . . . . . . . . . .. Aug. 29 . . . . . . . . . . .. 12 100 70 85.7 Aug 18 . . . . . . . . . . . . . Aug. 30 . . . . . . . . . . . . 12 100 7O 86.0 Aug 19 . . . . . . . . . . . .. Aug 31 . . . . . . . . . . .. 12 100 70 86.0 Aug. 20 . . . . . . . . . . . . . Sept 1 . . . . . . . . . . . . 12 100 7O 86.0 Aug. 21 . . . . . . . . . . . . . Sept 2 . . . . . . . . . . . . 12 97 70 85.9 Aug 22 . . . . . . . . . . . .. Sept 2 . . . . . . . . . . .. 11 97 70 85.4 Aug. 23 . . . . . . . . . . . . . Sept 3 . . . . . . . . . . . . 11 97 70 85.4 Aug. 25 . . . . . . . . . . . . . Sept 5 . . . . . . . . . . . . 11 97 70 85.7 Aug 26 . . . . . . . . . . . .. Sept 7 . . . . . . . . . . .. 12 97 75 86.4 Aug. 27 . . . . . . . . . . . . . Sept 8 . . . . . . . . . . . . 12 101 77 86.9 Aug. 28 . . . . . . . . . . . . . Sept. 10 . . . . . . . . . . . . 13 101 77 87.7 Aug. 29 . . . . . . . . . . . . . Sept. 11 . . . . . . . . . . . . 13 101 77 87.7 Aug. 30 . . . . . . . . . . . . . Sept. 11 . . . . . . . . . . . . 12 101 78 88.0 Sept. 1 . . . . . . . . . . . . . Sept. 12 . . . . . . . . . . . . 11 101 80 80.3 Sept. 2 . . . . . . . . . . . . . Sept. 13 . . . . . . . . . . . . 11 101 79 88.5 Sept. 3 . . . . . . . . . . . . . Sept. 14 . . . . . . . . . . . . 11 101 78 88.5 Sept. 4 . . . . . . . . . . . . . Sept. 14 . . . . . . . . . . . . 1O 101 78 88.6 Sept. 4.‘ . . . . . . . . . . . . Sept. 16 . . . . . . . . . . . . 12 101 70 88 4 Sept. 6 . . . . . . . . . . . . . Sept. 17 . . . . . . . . . . . . 11 101 70 86.7 Sept. 7, . . . . . . . . . . . . . Sept. 18 . . . . . . . . . . . . 11 101 67 85.7 Sept. 8 . . . . . . . . . . . . . Sept. 19 . . . . . . . . . . . . 11 99 67 85.2 Sept. 9 . . . . . . . . . . . . . Sept. 2O . . . . . . . . . . . . 11 99 67 84.1 Sept. 10 . . . . . . . . . . . . . Sept. 23 . . . . . . . . . . . . 13 99 67 83.0 Sept. 11 . . . . . . . . . . . . . Sept. 24 . . . . . . . . . . . . 13 99 67 82.4 Sept. 12 . . . . . . . . . . . . . Sept. 25 . . . . . . . . . . . . 13 99 67 81.8 Sept. 12 . . . . . . . . . . . . . Sept. 27 . . . . . . . . . . . . 15 105 67 81 . 5 Sept. 14 . . . . . . . . . . . . . Sept. 28 . . . . . . . . . . . . 14 105 67 81.2 Sept. 15 . . . . . . . . . . . . . Sept 3O . . . . . . . . . . . . 15 105 57 80.7 Sept. 16 . . . . . . . . . . . .. Oct 2 . . . . . . . . . . .. 16 105 57 78.7 Sept. 18 . . . . . . . . . . . . . Oct 3 . . . . . . . . . . . . 15 105 57 78.6 Sept. 19 . . . . . . . . . . . . . Oct 4 . . . . . . . . . . . . 15 105 57 78:2 Sept. 2O . . . . . . . . . . . . . Oct 5 . . . . . . . . . . . . 15 105 57 78.2 Sept. 21 . . . . . . . . . . . . . Oct 6 . . . . . . . . . . . . 15 105 57 78.0 Sept. 22 . . . . . . . . . . . . . Oct 7 . . . . . . . . . . . . 15 105 57 77.8 Sept. 22 . . . . . . . . . . . . . Oct 8 . . . . . . . . . . . . 16 105 57 77.6 Sept. 23 . . . . . . . . . . . . . Oct 8 . . . . . . . . . . . . 15 105 57 77.6 Sept 24 . . . . . . . . . . . . . . Oct 9 . . . . . . . . . . . . 15 105 57 77.6 THE COWPEA WYEEVIL. Table 6.—Duration of Larval Stage.—Continued. 2'7 _ Temperature Hatched Pupated Penod Max Min. Mean 1916 . Sept. 26 . . . . . . . . . . . . . Oct. 11 . . . . . . . . . . . . 15 105 57 77. 6 Sept. 27 . . . . . . . . . . . . . Oct. 12 . . . . . . . . . . . . 15 95 57 77. 5 Sept. 28 . . . . . . . . . . . . . Oct. 13 . . . . . . . . . . . . 15 94 57 76. 8 Sept. 29 . . . . . . . . . . . . . Oct. 13 . . . . . . . . . . . . 14 94 57 76.1 Oct. 1 . . . . . . . . . . . . . Oct. 14 . . . . . . . . . . . . 1'3 94 64 77. 5 Oct. 2 . . . . . . . . . . . . . Oct. 15 . . . . . . . . . . . . 13 94 66 78. 6 Oct. 3 . . . . . . . . . . . . . Oct. 16 . . . . . . . . . . . . 13 94 65 79. O Oct. 4 . . . . . . . . . . . . . Oct. 17 . . . . . . . . . . . . 13 94 65 78.9 Oct. 5 . . . . . . . . . . . . . Oct. 18 . . . . . . . . . . . . 13 94 61 78.6 Oct. 6 . . . . . . . . . . . .. Oct. 21 . . . . . . . . . . . . 15 94 61 76.1 Oct. 6 . . . . . . . . . . . . . Oct 22 . . . . . . . . . . . . 16 94 41 75.0 Oct. 7 . . . . . . . . . . . . . Oct 23 . . . . . . . . . . . . 16 94 41 74. 2 Oct. 8 . . . . . . . . . . . . . Oct. 25 . . . . . . . . . . . . 17 95 41 74.4 Oct. 8 . . . . . . . . . . . . . Oct. 28 . . . . . . . . . . . . 20 95 41 73. 6 Oct. 9 . . . . . . . . . . . . . Oct 29 . . . . . . . . . . . . 20 95 41 73. 1 Oct. 10 . . . . . . . . . . . . . Oct 30 . . . . . . . . . . . . 20 95 41 72. 5 Oct. 11 . . . . . . . . . . . . . Oct 31 . . . . . . . . . . . . 20 95 41 72 6 Oct. 12 . . . . . . . . . . . . . Nov. 1 . . . . . . . . . . . . 20 95 41 73. 0 Oct. 13 . . . . . . . . . . . . . Nov 4 . . . . . . . . . . . . 22 95 41 72.9 Oct. 14 . . . . . . . . . . . . . Nov 5 . . . . . . . . . . . . 22 95 41 72.5» Oct. 15.. . . . . . . . .. Nov 5 . . . . . . . . . . . . 21 95 41 72.1 Oct. 16 . . . . . . . . . . . . . Nov 6 . . . . . . . . . . . . 21 95 41 72.1 Oct. 18 . . . . . . . . . . . . . Nov 16 . . . . . . . . . . . . 29 95 33 70.1 Oct. 22 . . . . . . . . . . . .. Nov 18 . . . . . . . . . . . . 27 95 33 70.0- Oct. 23 . . . . . . . . . . . .. Nov 20 . . . . . . . . . . . . 28 95 33 70.3 Oct. 25 . . . . . . . . . . . . . Nov 24 . . . . . . . . . . . . 30 94 33 69.7 Oct. 27 . . . . . . . . . . . .. Nov 25 . . . . . . . . . . . . 29 94 33 69.2‘ Oct. 28 . . . . . . . . . . . . . Nov 25 . . . . . . . . . . . . 28 94 33 69.5- Oct. 28 . . . . . . . . . . . . . Nov 26 . . . . . . . . . . . . 29 94 33 69.4 Oct. 29 . . . . . . . . . . . . . Nov. 26 . . . . . . . . . . . . 28 94 33 69.3» Oct. 29 . . . . . . . . . . . . . Nov. 27 . . . . . . . . . . . . 29 98 33 69. 2 Oct. 30 . . . . . . . . . . . . . Nov 28 . . . . . . . . . . . . 29 98 33 68.5 Oct. 30 . . . . . . . . . . . . . Nov. 28 . . . . . . . . . . . . 29 98 33 68.5 Nov 1 . . . . . . . . . . . . . Nov. 29 . . . . . . . . . . . . 28 98 33 68. 1 Nov 2 . . . . . . . . . . . . . Nov. 30 . . . . . . . . . . . . 28 98 33 68.0 Nov 2 . . . . . . . . . . . . . Dec 1 . . . . . . . . . . . . 29 98 33 68.3 Nov 2 . . . . . . . . . . . . . Dec 3 . . . . . . . . . . . . 31 98 33 68.7 Nov 4 . . . . . . . . . . . . . Dec 4 . . . . . . . . . . . . 30 98 33 68.4 Nov 4 . . . . . . . . . . . . . Dec 5 . . . . . . . . . . . . 31 101 33 68. 9' Nov 5 . . . . . . . . . . . . . . Dec 6 . . . . . . . . . . . . 31 101 33 69. 5~ Nov 7 . . . . . . . . . . . . . Dec 7 . . . . . . . . . . . . 3O 101 33 69. 5 Nov 7 . . . . . . . . . . . . . Dec 8 . . . . . . . . . . . . 31 101 33 69.91 Nov 8 . . . . . . . . . . . . . Dec 11 . . . . . . . . . . .. 33 101 ' 33 69.1 Nov 11 . . . . . . . . . . . .. Dec 12 . . . . . . . . . . . . 31 101 33 68. 5- Nov 12 . . . . . . . . . . . . . Dec 17 . . . . . . . . . . . . 35 101 32 66. 8- Nov. 16 . . . . . . . . . . . . . Dec 24 . . . . . . . . . . . . 38 1E1 28 65.5 Nov. 19 . . . . . . . . . . . .. Dec. 25 . . . . . . . . . . . . 36 101 28 62.8 Nov. 20 . . . . . . . . . . . .. Jan 2 . . . . . . . . . . . . 43 101 28 65.7 6 96 75 86.8 Aug 12 . . . . . . . . . . . .. Aug 18 . . . . . . . . . . .. 6 96 75 86.3 Aug 13 . . . . . . . . . . . .. Aug 19 . . . . . . . . . . .. 6 96 75 86.1 Aug 14 . . . . . . . . . . . .. Aug 2O . . . . . . . . . . .. 6 95 75 86.2 Aug 16 . . . . . . . . . . . .. Aug. 20 . . . . . . . . . . .. 4 94 75 85.7 Aug 17 . . . . . . . . . . . .. Aug. 21 . . . . . . . . . . .. 4 100 8O 85.7 Aug 17.. Aug 22 . . . . . . . . . . .. 5 100 80 86.8 Aug 18.. Aug 23 . . . . . . . . . . .. 5 100 80 88.0 Aug 19 . . . . . . . . . . . .. Aug. 25 . . . . . . . . . . .. 6 100 73 87.8 Aug 20 . . . . . . . . . . . . . Aug. 26 . . . . . . . . . . . . 6 100 7O 87.0 Aug. 20 . . . . . . . . . . . . . . Aug. 27 . . . . . . . . . . . . 6 100 7O 86.2 Aug. 21 . . . . . . . . . . . . . Aug. 27 . . . . . . . . . . . . 6 97 70 86. 1 Aug. 22 . . . . . . . . . . . . . Aug. 28'. . . . . . . . . . . . 6 96 70 84.6 Aug. 25 . . . . . . . . . . . .. Aug. 31 . . . . . . . . . . .. ’ 6 97 7O 84.0 Aug. 26 . . . . . . . . . . . .. Aug. 31 . . . . . . . . . . .. 5 97 75 84.4 Aug. 28 . . . . . . . . . . . . . Sept. 1 . . . . . . . . . . . . 4 97 77 86.2 Aug 29 . . . . . . . . . . . .. Sept 2 . . . . . . . . . . .. 4 97 78 86.0 Aug 30 . . . . . . . . . . . .. Sept 4 . . . . . . . . . . .. 5 97 78 86.8 Aug. 31 . . . . . . . . . . . .. Sept 4 . . . . . . . . . . .. 4 97 79 87.2 Sept 1 . . . . . . . . . . . . . Sept 5 . . . . . . . . . . . . 4 97 80 87. 5 Sept. 2 . . . . . . . . . . . .. Sept 5 . . . . . . . . . . .. 3 97 8O 88.0 Sept. 2 . . . . . . . . . . . .. Sept 6 . . . . . . . . . . .. 4 97 80 88.2 Sept. 3 . . . . . . . . . . . .. Sept 7 . . . . . . . . . . .. 4 97 8O 88.5 TEXAS AGRICULTURAL EXPERIMENT STATION. 34 Table 11.—Duration of Pupal Stage.—-Continued. _ Temperature Pupated Emerged Perlod _ Max Mm. Mean 1916 Sept. 5 . . . . . . . . . . . . . Sept. 10 . . . . . . . . . . . . 5 101 8O 89.2 Sept 7 . . . . . . . . . . . . . Sept. 11 . . . . . . . . . . . . 4 101 80 89.0 Sept 8 . . . . . . . . . . . . . Sept. 12 . . . . . . . . . . . . 4 99 80 89.0 Sept 10 . . . . . . . . . . . . . Sept. 13 . . . . . . . . . . . . 3 97 79 88.0 Sept 11 . . . . . . . . . . . . . Sept. 14 . . . . . . . . . . . . 3 96 78 88.0 Sept 11 . . . . . . . . . . . . . Sept. 14 . . . . . . . . . . . . 3 96 78 88.0 Sept 12 . . . . . . . . . . . . . Sept. 17 . . . . . . . . . . . . 5 97 70 84.2 Sept 13 . . . . . . . . . . . .. Sept. 18 . . . . . . . . . . . . 5 99 67 82.2 Sept 14 . . . . . . . . . . . . . Sept. 19 . . . . . . . . . . . . 5 99 67 81.2 Sept 14 . . . . . . . . . . . . . Sept. 20 . . . . . . . . . . . . 6 99 67 80.8 Sept 16 . . . . . . . . . . . . . Sept. 20 . . . . . . . . . . . . 4 99 67 79.4 Sept 17 . . . . . . . . . . . . . Sept. 22 . . . . . . . . . . . . 5 99 67 80.2 Sept 18 . . . . . . . . . . . . . Sept. 24 . . . . . . . . . . . . 6 91 68 80.5 Sept 19 . . . . . . . . . . . . . Sept. 26 . . . . . . . . . . . . 7 91 69 80. 5 Sept 20 . . . . . . . . . . . . . Sept. 27 . . . . . . . . . . . . 7 105 70 80.2 Sept 23 . . . . . . . . . . . . . Sept. 28 . . . . . . . . . . . . 5 105 71 80.2 Sept. . . . . . . . . . . . . . Sept. 29 . . . . . . . . . . . . 5 105 60 85.2 Sept. 25 . . . . . . . . . . . . . Sept. 29 . . . . . . . . . . . . 4 105 60 83. 7 Sept 27 . . . . . . . . . . . . . Oct. 4 . . . . . . . . . . . . 7 95 57 77.7 Sept 28 . . . . . . . . . . . . . Oct". 5 . . . . . . . . . . . . 7 89 57 74.5 Sept 30 . . . . . . . . . . . . . Oct. 7 . . . . . . . . . . . . 7 89 59 74.1 Oct. 2 . . . . . . . . . . . . . Oct. 7 . . . . . . . . . . . . 5 89 64 77. 0 Oct. 3 . . . . . . . . . . . . . Oct. 8 . . . . . . . . . . . . 5 90 66 77.6 Oct. 4 . . . . . . . . . . . . . Oct. 9 . . . . . . . . . . . . 5 91 66 78.0 Oct. 5 . . . . . . . . . . . . . Oct. 11 . . . . . . . . . . . . 6 94 68 79.0 Oct. 6 . . . . . . . . . . . . . Oct. 11 . . . . . . . . . . . . 5 94 68 79.2 Oct. 7 . . . . . . . . . . . . . Oct. 12 . . . . . . . . . . . . 5 94 68 79.4 Oct. ' 8 . . . . . . . . . . . . . Oct. 13 . . . . . . . . . . . . 5 94 68 79.6 Oct. L8 . . . . . . . . . . . . . , Oct. 13 . . . . . . . . . . . . 5 94 68 79.6 Oct. 9 . . . . . . . . . . . . . Oct. 14 . . . . . . . . . . . . 5 94 68 79. 8 Oct. 11 . . . . . . . . . . . . . Oct. 16 . . . . . . . . . . . . 5 90 65 79.6 Oct. 12 . . . . . . . . . . . . . Oct. 17 . . . . . . . . . . . . 5 90 65 79.2 ~Oct. 13 . . . . . . . . . . . . . Oct. 17 . . . . . . . . . . . . 4 90 65 79.5 -Oct. 13 . . . . . . . . . . . . . Oct. 19 . . . . . . . . . . . . 6 90 60 76. 5 Oct.‘ 14 . . . . . . . . . . . .. Oct. 23 . . . . . . . . . . . . 9 87 41 70.0 ~Oct.j15 . . . . . . . . . . . . . Oct. 24 . . . . . . . . . . . . 9 95 41 68.7 OctJ 16 . . . . . . . . . . . . . Oct. 24 . . . . . . . . . . . . 8 95 41 67.6 Oct] 17 . . . . . . . . . . . . . Oct. 28 . . . . . . . . . . . . 11 95 41 68.8 Oct] 18 . . . . . . . . . . . . . Oct. 29 . . . . . . . . . . . . 11 95 41 68. 6 Oct.; 21 . . . . . . . . . . . . . Oct. 29 . . . . . . . . . . . . 8 95 52 69. 3 Octal 22 . . . . . . . . . . . . . Oct. 30 . . . . . . . . . . . . 8 95 53 71.3 Octx, 23 . . . . . . . . . . . . . Oct. 31 . . . . . . . . . . . . 8 95 53 73. 1 Oct. 25 . . . . . . . . . . . . . Nov. 1 . . . . . . . . . . . . 7 92 53 73.8 Oct. [.28 . . . . . . . . . . . . . Nov. 2 . . . . . . . . . . . . 5 90 60 76.7 Oct. [29 . . . . . . . . . . . . . Nov. 4 . . . . . . . . . . . . 6 90 60 76.8 ~Oct. 30 . . . . . . . . . . . . . Nov. 4 . . . . . . . . . . . . 5 89 60 77.0 ~Oct. 31 . . . . . . . . . . . . . ‘Nov. 8 . . . . . . . . . . . . 8 89 60 76.6 .Nov. 1 . . . . . . . . . . . . . Nov. 8 . . . . . . . . . . . . 7 89 60 75. 7 .Nov. 4 . . . . . . . . . . . . . Nov. 12 . . . . . . . . . . . . 8 87 54 74.0 iNov. 5 . . . . . . . . . . . . . Nov. 12 . . . . . . . . . . . . 7 87 51 72.8 Nov. 5 . . . . . . . . . . . . . Nov. 21 . . . . . . . . . . . . 16 94 33 67. 5 Nov. f 6 . . . . . . . . . . . . . Nov. 21 . . . . . . . . . . . . »15 94 33 66.8 Nov. 16 . . . . . . . . . . . . . Dec 2 . . . . . . . . . . . . 16 98 44 67.8 Nov. 18 . . . . . . . . . . . . . Dec 3 . . . . . . . . . . . . 15 94 44 69.0 Nov. 20 . . . . . . . . . . . . . Dec 5 . . . . . . . . . . . . 15 101 44 76.6 Nov. 24 . . . . . . . . . . . . . Dec 5 . . . . . . . . . . . . 11 101 44 71.6 Nov. 25 . . . . . . . . . . . . . Dec 6 . . . . . . . . . . . . 11 101 44 73.7 Nov. 25 . . . . . . . . . . . . . Dec 12 . . . . . . . . . . . . 17 101 44 72.2 Nov. 26 . . . . . . . . . . . . . Dec 8 . . . . . . . . . . . . 12 101 48 75.8 Nov. 26 . . . . . . . . . . . . . Dec. 9 . . . . . . . . . . . . 13 101 38 75.4 Nov. 27‘ . . . . . . . . . . . . . Dec 9 . . . . . . . . . . . . 12 101 38 76.3 Nov. 28 . . . . . . . . . . . . . Dec 1O . . . . . . . . . . .. 12 101 38 75.5 Nov. 28 . . . . . . . . . . . . . Dec 10 . . . . . . . . . . . . 12 101 38 75.5 .Nov. 29 . . . . . . . . . . . . . Dec 14 . . . . . . . . . . . . 15 101 32 77.8 Nov. 30 . . . . . . . . . . . .. Dec 17 . . . . . . . . . . .. 17 101 32 73.9 Dec. 1 . . . . . . . . . . . . . Dec 18 . . . . . . . . . . . . 17 101 34 68.1 Dec. 3 . . . . . . . . . . . . . Dec 24 . . . . . . . . . . . . 21 101 28 63.1 Dec. 4 . . . . . . . . . . . . . Dec 25 . . . . . . . . . . . . 21 101 28 62.7 Dec. 5 . . . . . . . . . . . . . Dec 25 . . . . . . . . . . . . 20 99 28 61.2 Dec. 6 . . . . . . . . . . . . . Dec 31 . . . . . . . . . . . . 25 90 28 61.2 Dec. 7 . . . . . . . . . . . . . Jan. 1 . . . . . . . . . . . . 25 90 28 59. 8 Dec. 8 . . . . . . . . . . . . . an. 3 . . . . . . . . . . . . 26 92 28 60.0 Decx 11 . . . . . . . . . . . . . Jan. 5 . . . . . . . . . . . . 25 92 28 58. 6 Dec. 12 . . . . . . . . . . . . . Jan 7 . . . . . . . . . . . . 26 92 28 59.3 Dec. 17 . . . . . . . . . . . .. Jan 9 . . . . . . . . . . . . 23 92 28 59.6 Dec. . . . . . . . . . . . . . Jan. 18 . . . . . . . . . . . . 25 92 30 59.0 Dec. 25 . . . . . . . . . . . . . Jan. 26. _. . . . . . . . . . . 32 92 30 57.4 THE COWPEA YVEEVIL. 35 Table lL-Duration of Pupal Stage.-——Continued. . Temperature Pupated Emerged Period _ Max Mm. Mean 1917 an. 2 . . . . . . . . . . . .. Jan. 27 . . . . . . . . . . . . 25 94 3O 55. 6 Jan. 2 . . . . . . . . . . . .. Jan. 29 . . . . . . . . . . .. 27 94 3O 56.0 Jan 2 . . . . . . . . . . . .. Feb. 2 . . . . . . . . . . . . 31 100 25 57.0 Jan 3 . . . . . . . . . . . . . Feb. 5 . . . . . . . . . . . . 33 100 25 58.4 Jan 4 . . . . . . . . . . . . . Feb. 10 . . . . . . . . . . .. 37 100 25 60.6 Jan 5 . . . . . . . . . . . .. Feb. 11 . . . . . . . . . . .. 37 100 25 60. 6 Jan 6 . . . . . . . . . . . .. Feb. 13. . . . . . . . . . .. 38 100 25 60.0 Jan 6 . . . . . . . . . . . .. Feb. 15 . . . . . . . . . . .. 40 100 25 60.2 Jan 7 . . . . . . . . . . . .. Feb. 15 . . . . . . . . . . .. 39 100 25 59. 9 Jan 7 . . . . . . . . . . . . . Feb. 18 . . . . . . . . . . .. 42 100 25 59.8 Jan 10 . . . . . . . . . . . .. Feb. 16 . . . . . . . . . . .. 37 100 25 63.0 Jan 11 . . . . . . . . . . . .. Feb. 18 . . . . . . . . . . .. 38 100 25 60.5 Jan 26 . . . . . . . . . . . . . Feb. 20 . . . . . . . . . . . . 25 100 25 65. 6 Jan 27 . . . . . . . . . . . .. Feb. 17 . . . . . . . . . . .. 21 100 25 69.5 Jan 27 . . . . . . . . . . . . . Mar. 6 . . . . . . . . . . . . 38 103 25 56.0 Jan 28 . . . . . . . . . . . . . Feb. 21 . . . . . . . . . . . . 24 100 25 53.0 Jan 29 . . . . . . . . . . . . . Feb. 21 . . . . . . . . . . . . 23 100 25 53. 0 Jan 29 . . . . . . . . . . . . . Feb. 22 . . . . . . . . . . . . 24 103 25 53.1 Jan 30 . . . . . . . . . . . . . Feb. 22 . . . . . . . . . . . . 23 103 25 52.0 Jan 30 . . . . . . . . . . . . . Feb. 23 . . . . . . . . . . . . 24 103 25 53. 0 Jan 31 . . . . . . . . . . . . . Feb. 25 . . . . . . . . . . . . 25 103 25 55.4 Feb. 6 . . . . . . . . . . . . . Feb. 25 . . . . . . . . . . . . 19 103 4O 57.8 Feb 13 . . . . . . . . . . . . .. Feb. 27 . . . . . . . . . . . . 14 103 41 58.2 Feb 17 . . . . . . . . . . . . . Mar. 1 . . . . . . . . . . . . 12 103 41 65.8 Feb 20 . . . . . . . . . . . . . Mar. 7 . . . . . . . . . . . . 15 103 33 64. 5 Feb 21 . . . . . . . . . . . . . Mar. 11 . . . . . . . . . . . . 18 103 33 65.2 Feb 24 . . . . . . . . . . . . . Mar. 15 . . . . . . . . . . . . 19 102 33 66.3 Feb 25 . . . . . . . . . . . . . Mar. 13 . . . . . . . . . . . . 16 102 33 66.4 Feb 25 . . . . . . . . . . . . . Mar. 13 . . . . . . . . . . . . 16 102 33 66.4 Feb 26 . . . . . . . . . . . .. Mar. 15 . . . . . . . . . . .. 17 102 33 61.3 Feb 26 . . . . . . . . . . . .. Mar. 15 . . . . . . . . . . .. 17 102 33 61.3 Feb 26 . . . . . . . . . . . . . Mar. 19 . . . . . . . . . . . . 21 ,102 33 66.1 Feb 26 . . . . . . . . . . . . . Mar. 23 . . . . . . . . . . . . 25 102 33 67. 6 Feb 27 . . . . . . . . . . . . . Mar. 14 . . . . . . . . . . . . 15 100 33 67.3 Feb 28 . . . . . . . . . . . . . Mar. 14 . . . . . . . . . . . . 14 91 33 64. O Feb 28 . . . . . . . . . . . . . Mar. 16 . . . . . . . . . . . . 16 92 33 64. 5 Feb 28 . . . . . . . . . . . . . Mar. 16 . . . . . . . . . . . . 16 .92 33 64.5 Feb 28 . . . . . . . . . . . . . Mar. 17 . . . . . . . . . . . . 17 92 33 65.3 Feb 28 . . . . . . . . . . . . . Mar. 17 . . . . . . . . . . . . 17 92 33 65.3 Mar 1 . . . . . . . . . . . . . Mar. 16 . . . . . . . . . . . . 15 92 33 63. 8 Mar 1 . . . . . . . . . . . . . Mar. 20 . . . . . . . . . . . . 19 92 33 63.6 Mar 2 . . . . . . . . . . . . . Mar. 17 . . . . . . . . . . . . 15 92 33 63.5 Mar 2 . . . . . . . . . . . .. Mar. 18 . . . . . . . . . . .. l6 92 33 63.2 Mar 2 . . . . . . . . . . . . . Mar. 18 . . . . . . . . . . . . 16 92' 33 63.2 Mar 2 . . . . . . . . . . . . . Mar. 20 . . . . . . . . . . . . 18 92 33 64.0 Mar 2 . . . . . . . . . . . . . Mar. 20 . . . . . . . . . . . . 18 92 33 64.0 Mar 2 . . . . . . . . . . . . . Mar. 20 . . . . . . . . . . . . 18 92 33 64.0 Mar 3 . . . . . . . . . . . . . Mar. 20 . . . . . . . . . . . . 17 92 33 63.8 Mar 3 . . . . . . . . . . . .. Mar. 21 . . . . . . . . . . .. 18 92 33 64.3 Mar 4 . . . . . . . . . . . . . Mar. 21 . . . . . . . . . . . . 17 92 33 64.7 Mar 6 . . . . . . . . . . . .. Mar. 21 . . . . . . . . . . .. 15 92 47 66.4 Mar 8 . . . . . . . . . . . . . Mar. 22 . . . . . . . . . . . . 14 99 49 66. 3 Mar 8 . . . . . . . . . . . . . Mar. 22 . . . . . . . . . . . . 14 99 49 66.3 Mar. 11 . . . . . . . . . . . . . Mar. 25 . . . . . . . . . . . . 14 99 49 69.1 Mar. 12 . . . . . . . . . . . . . Mar. 26 . . . . . . . . . . . . 14 99 49 69.2 Mar. 14 . . . . . . . . . . . . . Mar. 26 . . . . . . . . . . . . 12 99 49 70.0 Mar. 15 . . . . . . . . . . . . . . Mar. 26 . . . . . . . . . . . . ll 99 49 69.4 Mar. 15 . . . . . . . . . . . . . . Mar. 29 . . . . . . . . . . . . 14 99 49 67.4 Mar. 16 . . . . . . . . . . . .. Mar. 28 . . . . . . . . . . . . 12 99 49 68.2 Mar. 16 . . . . . . . . . . . .. Mar. 28 . . . . . . . . . . .. 12 99 49 68.2 Mar. 19 . . . . . . . . . . . .. Mar. 31 . . . . . . . . . . .. 12 99 50 70.0 Mar. 20 . . . . . . . . . . . . . Mar. 30 . . . . . . . . . . . . 10 99 50 69.7 Mar. 20 . . . . . . . . . . . . . Mar. 31 . . . . . . . . . . . . ll 99 50 69.9 Mar. 20 . . . . . . . . . . . . . Mar. 31 . . . . . . . . . . . . 11 99 50 69. 9 Mar. 20 . . . . . . . . . . . . .. M31‘. 31 . . . . . . . . . . .. 11 99 5O 69.9 Mar. 2O . . . . . . . . . . . . . Aprll 1 . . . . . . . . . . . . 12 99 50 75. 7 Mar. 20 . . . . . . . . . . . . . Aprll 6 . . . . . . . . . . . . 17 102 5O 71,2 Mar. 21 . . . . . . . . . . . . . Mar. 30 . . . . . . . . . . . . 9 99 50 69.6 Mar. 21 . . . . . . . . . . . .. Mar. 31 . . . . . . . . . . . . 10 99 50 70.9 Mar. 21 . . . . . . . . . . . . . . April 2 . . . . . . . . . . . . 12 102 50 71.7 Mar. 21 . . . . . . . . . . . .. Aprll 4 . . . . . . . . . . .. 14 102 50 71.3 Mar. 22 . . . . . . . . . . . . . M31‘. 31 . . . . . . . . . . . . 9 99 50 69.1 Mar. 22 . . . . . . . . . . . . . Aprgl 4 . . . . . . . . . . . . 13 102 50 70_ 0 Mar. 22 . . . . . . . . . . . . . . Aprll 6 . . . . . . . . . . . . 15 102 50 70. 0 Mar. 24 . . . . . . . . . . . . . . Aprll 5 . . . . . . . . . . . . 12 102 5O 74,8 Mar. 24 . . . . . . . . . . . . . . Aprll 5 . . . . . . . . . . . . 12 102 5O 74, 8 Mar. 24 . . . . . . . . . . . . . . Apryl 6 . . . . . . . . . . . . 13 102 50 62. 5 Mar. 25 . . . . . . . . . . . . . . Aprgl 5 . . . . . . . . . . . . ll 102 50 69.7 Mar. 25 . . . . . . . . . . . . . Aprll 7 . . . . . . . . . . . . 13 102 50 62.2 36 TEXAS AGRICULTURAL EXPERIMENT STATION.‘ Table 11.—Duration of Pupal Stage-Continued. _ Temperature Pupated Emerged Period _ _ Max. Min. Mean Mar. 25 . . . . . . . . . . . . . April 10 . . . . . . . . . . . . 16 102 50 69.5 Mar. 26 . . . . . .‘ . . . . . .. April 6 . . . . . . . . . . . . 11 102 50 69.2 Mar. 26 . . . . . . . . . . . . . April 8 . . . . . . . . . . . . 13 ' 102 50 69.5 Mar. 26 . . . . . . . . . . . .. April 15 . . . . . . . . . . 20 102 5O 69.1 Mar. 27. .5 . . . . . . . . . . . April 7 . . . . . . . . . . . . 11 102 50 70.1 Mar. 28 . . . . . . . . . . . .. April 10 . . . . . . . . . . .. 13 102 51 70.7 Mar. 29 . . . . . . . . . . . .. April 10 . . . . . . . . . . .. 12 102 51 71.5 Mar. 30 . . . . . . . . . . . .. April 10 . . . . . . . . . . .. 11 102 51 70.7 Mar. 3O . . . . . . . . . . . .. April 12 . . . . . . . . . . .. 13 102 51 70.0 Mar. 3O . . . . . . . . . . . .. April 14 . . . . . . . . . . . . 15 102 51 70. 1 Mar. 31 . . . . . . . . . . . .. April16 . . . . . . . . . . .. 16 102 51 %.0 April 5,3 . . . . . . . . . . . .. April 19 . . . . . . . . . . .. 16 90 51 .9 The shortest pupal period of three days occurred three times in November, 1915, once in March, 191.6, and four times in September, 1916. During November this period occurred with a mean tempera- ture of 76.9 degrees F. This period in March occurred with a mean temperature of but 741.11 degrees F. The maximum temperature of the period was 89 degrees F. and the minimum was 60 degrees F. In September, when the pupal stage was but three days, the mean tempera- ture was 87.6 degrees F. The longest pupal period of 53 days occurred from January 5 to February 27, 1916. During this period the mean temperature was 54.8 degrees; the lowest temperature of the period was 22 degrees. = The yearly variation in the duration of the pupal stage is shown in Table 12. The mean temperature of the period does not have a positive effect upon its length. The average length of periods is in- fluenced by a severe low temperature or a fexv days of warm weather. Table 12.—Yearly Variation in Duration of Pupal Stage. _ Period Mean Date (Days) Temperature _ (Degrees) November, 1915 . . . . . . . . . . . . . . .. 5.6 75.8 November, 1916 . . . . . . . . . . . . . . . . 12.8 72.3 December, 1915 . . . . . . . . . . . . . . . . 28.1 60.5 December, 1916. ._ . . . . . . . . . . . . .. 23.8 58.9 January, 1916 . . . . . . . . . . . . . . . . .. 41.1 54.4 January, 1917 . . . . . . . . . . . . . . . . .. 31 . 1 57.5 February, 1916 . . . . . . . . . . . . . . . .. ' 28.0 61.4 February, 1917 . . . . . . . . . . . . . . . . . 18. 1 66. 7 A summary of the duration of the pupal stage during the representa- tive summer months and winter months is given in Table 13. During the warmest months of the year in this locality the pupal stage com- prised an average of days. During the coldest months of the year the average pupal stage was 21.2 days. The pupal stage was quite variable throughout each month while the observations were being made. THE CowrsA WVEEVIL. 37 Table 13.—Summary of Duration of Pupal Stage. Number Average Shortest Longest Collections Month Period Period Period Observed i June . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5. 8 4 8 34 July . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5. 5 3 7 32 ;_ August . . . . . . . . . . . . . . . . . . . . . . . . . . . 5. 5 4 7 28 ._"September . . . . . . . . . . . . . . . . . . . . . . . . 4.4 3 7 25 ; November . . . . . . . . . . . . . . . . . . . . . . . . 8.3 4 17 | 48 QDecember . . . . . . . . . . . . . . . . . . . . . . . . 24. 8 4 53 ' 24 é-January . . . . . . . . . . . . . . . . . . . . . . . . . . . - 33.3 24 53 27 i February . . . . . . . . . . . . . . . . . . . . . . . . .i 19.3 12 53 23 t. E; quite noticeable. The relation of temperature t0 the duration of the pupal stage is‘ The results of the observations are shown in Table 14. Table 14.—Effect of Temperature on Length of Pupal Stage. ‘i Avera e Mean Month Perio , Daily i Days Temperature - June . . . . . . . . . . . . . . . . . . . . . . . . . . 5. 8 86 July . . . . . . . . . . . . . . . . . . . . . . . . . . . .5. 5 87 August . . . . . . . . . . . . . . . . . . . . . . . . 5 . 5 86 September . . . . . . . . . . . . . . . . . . . . . 4. 4 83 November . . . . . . . . . . . . . . . . . . . ..\ 8.3 71.8 December . . . . . . . . . . . . . . . . . . . . . . 24. 8 62.2 January . . . . . . . . . . . . . . . . . . . . . . . 33. 3 58. 5 February . . . . . . . . . . . . . . . . . . . . . . 19. 3 58. 5 Summaryrdlrom the tables given which show the length of the egg, Zplarval, and pupal stage, it is evident that the length of these periods jvaries greatly with the seasons of the year. jyeach stage combined, may consume about 16 days, however, this total [was never obtained in any single generation. were combined, 1'78 days would be required, but no single generation Econsumed this much time. The shortest periods of If all of the long periods Table 15.—-Summary of Development of Cowpea Weevil. g “Elongate oval, moderately shining. p hitish pubescence. ~ Elytra ferruginous or pale brown with large lat- lral spot and apex broadly bla.ck. Head dark brown or black, densely Egg, Larva, Pupa, Total Days Days Days Days K ortest . . . . . . . . . . . . . . . . . . . . . . .. 4 9 3 ‘ 16 ngést . . . . . . . . . . . . . . . . . . . . . . . . . . 37 88 53 178 Adults. Descripti0n.-—The cowpea weevil is very closely related to a few ‘ther species of weevils and can hardly be distinguished from them by ose not familiar with technical details. Any popular description that , ight be given would hardly allow the proper diagnosis of the exact ecies of weevil infesting cowpeas or other stored products. The most comprehensive technical description of this species is that y Horn, which is given herewith as it occurred in his paper (6) : Beneath equally clothed with 38 Texas AGRICULTURAL EXPERIMENT STATION. punctured, front sub-carinate. Antennae as long as head and thorax, serrate in both sexes, four basal joints pale rufous, outer joints dark and nearly black. Thorax trapezoidal, broader at base than long, sides distinctly arcuate, base trisinuate, basal lobe emarginate and clothed with whitish hairs; color variable from ferruginous to black, coarsely punctured, sub-granulate and feebly shining, sparsely clothed with cinereous hair. Scutellum with median impressed line and clothed with whitish hair. Elytra broader at base than thorax and longer than wide, sides feebly areuate, humeri moderately prominent; striate, striae punctured, intervals fiat densely punetulate; color ferruginous with large lateral spot and apex. black, clothed with whitish and cinereous pubescence. Pygidium nearly black with median line of whitish pubescence. Body beneath pieeous densely punctulate and sparsely but evenly clothed with cinerous hairs; abdomen pale brown. Anterior and middle legs pale rufous, hind legs pale brown. Hind femora armed with an acute tooth on the inner side and a broad triangular tooth on the outer side. Length .12-.18 inch; 3-4.5 mm.” Most of the specimens are nearly black with four spots of pale brown A on the wing covers. Many of these spots are outlined with a band of white. In nearly all specimens the wing covers are clothed with fine hairs. Sometimes the color of the spot is hidden by a patch of very fine hairs. In Plate IV is shown a series of adult weevils. From this plate it is possible to distinguish the difference in the size of the males and females. It will also be seen that there is a variation in the size of a sex. As a rule the females are much larger than the males, but it is possible to find males that are larger than females. The plates will also show a variation in the color pattern of the wing covers. By selection it was possible to produce individuals of either sex with an absence of spots and with brown wing covers. Feeding Ilabits of Adults. The cowpea weevil has not been observed to feed on any solid food in the adult stage, and the cowpea is injured only by the feeding larva. Observations show that the adult wreevil never attacks cowpeas directly, except when emerging, it sometimes gnaws its way through the thin shell covering the exit of the larval burrow. Frequently the adults re- enter the larval burrows in the peas and die, giving rise to an erroneous popular opinion that they feed upon the peas. In the field the adults feed almost exclusively upon nectar secreted by the nectaries located at the base of the green pods. A few adults have been collected from the blossoms of cowpeas. None were observed to visit blossoms of other plants with any regularity. The adults are egregious in feed- ing. Invariably single individuals were found feeding; occasionally two or three were observed at the base of the same pod, but they never fed in large numbers. The weevils, while feeding, are very active, and seek shelter very quickly upon the slightest disturbance. mans H4. Océwmw 3423:“ @5218 wwosmsm Dec 17 . . . . . . . . . . . . .. Jan. 1O . . . . . . . . . . .. 15 Jan 17 . . . . . . . . . . .. 31 . ec 18 . . . . . . . . . . . . .. Jan. 16 . . . . . . . . . . .. 29 Jan 12 . . . . . . . . . . .. 25 {Dec 19 . . . . . . . . . . . . .. Jan. 13 . . . . . . . . . . .. 25 Jan 13 . . . . . . . . . . .. 25 93cc 2O . . . . . . . . . . . . . . Jan. 22 . . . . . . . . . . . . 33 Jan 19 . . . . . . . . . . . . 3O r‘ ec 21 . . . . . . . . . . . . .. Jan. 13 . . . . . . . . . . .. 23 Jan 12 . . . . . . . . . . .. 22 j ec 22 . . . . . . . . . . . . .. Jan. 18 . . . . . . . . . . .. 27 Jan 19 . . . . . . . . . . .. 28 5 ec 23 . . . . . . . . . . . . . . Jan 21 . . . . . . . . . . . . 29 Jan 27 . . . . . . . . . . . . 35 tDec 24 . . . . . . . . . . . . . . Jan 19 . . . . . . . . . . . . 34 Jan 27 . . . . . . . . . . . . 34 Q ec 25 . . . . . . . . . . . . .. Jan 19 . . . . . . . . . . .. 32 Jan 19 . . . . . . . . . . .. 32 “Dec 26 . . . . . . . . . . . . . . Jan 11 . . . . . . . . . . . . 32 Jan 29 . . . . . . . . . . . . 32 iDec 27 . . . . . . . . . . . . . . Jan 21 . . . . . . . . . . . . 25 Jan 2O . . . . . . . . . . . . 24 fDec 3O . . . . . . . . . . . . . . Jan 19 . . . . . . . . . . . . 2O Jan. 2O . . . . . . . . . . . . 21 1917 1133‘ 2 """"""""" ""123 §3":::::"::: 33 "lit 2%.::"::::"" g2 Qan 3 . . . . . . . . . . . . . . Jan 29 . . . . . . . . . . . . 26 Feb 5 . . . . . . . . . . . . 33 Jan 4 . . . . . . . . . . . . . . Feb 11 . . . . . . . . . . . . 38 Feb 7 . . . . . . . . . . . . 34 Jan b . . . . . . . . . . . . . . Feb 5 . . . . . . . . . . . . 3O Jan 28 . . . . . . . . . . . . 22 plan 7 . . . . . . . . . . . . . . Feb 3 . . . . . . . . . . . . 27 Feb 24 . . . . . . . . . . . . 48 flan 8 . . . . . . . . . . . . . . Feb 1O . . . . . . . . . . . . 29 Feb 19 . . . . . . . . . . . . 4O ’ an 9 . . . . . . . . . . . . . . Feb 18 . . . . . . . . . . . . 4O Feb 2O . . . . . . . . . . . . 42 iJan 1O . . . . . . . . . . . .‘. . Feb 16 . . . . . . . . . . . . 37 Feb 21 . . . . . . . . . . . . 42 Jan 11 . . . . . . . . . . . . . . Feb 17 . . . . . . . . . . . . 37 Feb 27 . . . . . . . . . . . . 37 Jan 12 . . . . . . . . . . . . . . Feb 9 . . . . . . . . . . . . 28 Feb 22 . . . . . . . . . . . . 41 Jan 13 . . . . . . . . . . . . . . Feb . . . . . . . . . . . . 23 Mar . . . . . . . . . . . . 5O Jan l7 . . . . . . . . . . . . . . Feb 19 . . . . . . . . . . . . 33 Feb 22 . . . . . . . . . . . . 36 Jan 18 . . . . . . . . . . . . . . Feb 13 . . . . . . . . . . . . 26 Feb 27 . . . . . . . . . . . . 4O Jan 19 . . . . . . . . . . . . . . Feb 21 . . . . . . . . . . . . 33 Feb 13 . . . . . . . . . . . . 25 Jan 2O . . . . . . . . . . . . . . Feb 22 . . . . . . . . . . . . 33 Feb 24 . . . . . . . . . . . . 35 Jan 21 . . . . . ., . . . . . . . Feb 16 . . . . . . . . . . . . 26 Feb 22 . . . . . . . . . . . . 33 Jan 23 . . . . . . . . . . . . . . Feb 22 . . . . . . . . . . . . 30 Feb 21 . . . . . . . . . . . . 29 Jan 25 . . . . . . . . . . . . . . Feb 14 . . . . . . . . . . . . 20 Feb 22 . . . . . . . . . . . . 28 Jan 26 . . . . . . . . . . . . . . Feb 21 . . . . . . . . . . . . 26 Feb 25 . . . . . . . . . . . . 3O Jan 27 . . . . . . . . . . . . . . Feb 26 . . . . . . . . . . . . 3O Feb 24 . . . . . . . . . . . . 28 Jan 28 . . . . . . . . . . . . . . Feb 27 . . . . . . . . . . . . 3O Feb 26 . . . . . . . . . . . . 29 Jan 29 . . . . . . . . . . . . . . Feb 27 . . . . . . . . . . . . 29 Feb 26 . . . . . . . . . . . . 28 léan. 3O . . . . . . -. . . . . . . . Feb. 28 . . . . . . . . . . . . 29 Mar. 3 . . . . . . . . . . . . 31 131L112 . . . . . . . . . . . . .. Feb. 28 . . . . . . . . . . .. 26 Feb. 26 . . . . . . . . . . .. 24 l. E1 5 _ Temperature apparently is an important factor in the length of the life period. When the temperature drops there is a corresponding in- Qcrease in the length of the life period. The fatal lOW temperature has Linot been determined. Proportion of Sexes. o Of the 2942 individuals which emerged in the laboratory from Jan- .f11ary, 1916, to May, 1917, 1494, or slightly more than 50 per cent., ‘were males, while 1448, a little less than 5O per cent, were females. {Table 21 shows the proportion of sexes by months. It is interesting Etc note that the numbers are very nearly equal throughout the entire eperiod. There is a slight increase in females during the cold period and males are more abundant during the warmer period. In the field the proportion of sexes is likewise very nearly equal. Out of 243 Eweevils collected at various dates during the summer of 1916, 117, or 50 _ TEXAS AGRICULTURAL EXPERIMENT STATION. about 48 per cent., were females; 126, slightly less than 52 per cent, were males. The male is readily attracted to the female, and in the; field the active female is usually attended by one and occasionally by’ several. Of the inactive weevils or those in places of hiding, approxi-f mately an equal number of males and females Were collected. 5 Table 21.—-Proportion of Sexes. i Number Mean Mean Date Emerged Males Females Temp. Humidity f 1916 January . . . . . . . . . . . . . . . . . . . . . . . 77 36 41 56.9 78.9 February . . . . . . . . . . . . . . . . . . . . . . 34 14 20 55.0 66.7 March . . . . . . . . . . . . . . . . . . . . . . . . . 140 73 67 66.4 61.8 A ril . . . . . . . . . . . . . . . . . . . . . . . . .. 125 61 64 68.9 73.0 ay . . . . . . . . . . . . . . . . . . . . . . . . .. 350 190 160 79. 6 71.7 June . . . . . . . . . . . . . . . . . . . . . . . . .. 284 146 138 86. 0 71.0 J y . . . . . . . . . . . . . . . . . . . . . . . . .. 201 111 0 87.0 69.0 August . . . . . . . . . . . . . . . . . . . . . . 194 98 96 86.0 68.5 September . . . . . . . . . . . . . . . . . . . . . 226 122 104 83. 5 63.0 October . . . . . . . . . . . . . . . . . . . . . . . . ' 209 105 104 73. 0 63. 5 November . . . . . . . . . . . . . . . . . . . . . 96 49 47 68. 5 69. 5 December . . . . . . . . . . . . . . . . . . . . . . 175 91 84 64. 6 64. 5 1917 . . January . . . . . . . . . . . . . . . . . . . . . . . 87 35 52 60.3 70.9 February . . . . . . . . . . . . . . . . . . . . . . 194 93 101 62.0 58.7 March . . . . . . . . . . . . . . . . . . . . . . . . . 330 165 165 68. 7 63 .0 April . . . . . . . . . . . . . . . . . . . . . . . . . . 220 105 115 71.4 63.7 n: Location of Food. The adult Weevil has fully developed wings but cannot be considered a strong flier. If disturbed it Will take to flight very readily, but the distance of a continuous flight has rarely been observed to exceed 100 yards and is usually much shorter. By intermittent flights, the weevil is able to cover considerable distance, and doubtless flight is an im- portant means of dissemination in the field. The most isolated patches of cowpeas are usually found to be infested with the insect. The cowpeas grown on the experimental plats of the Division of Entomology were infested during the summers of 1915, 1916, and 1917, notwith- standing the fact that no other cowpeas were growing nearer than a mile away. The infestation was particularly severe during the sum- mer of 1916. Owing‘ to a lack of rain, the cowpeas in the immediate vicinity were to a large extent a failure, and the weevils seemed there- fore to concentrate on the cowpeas growing on the experimental plats; these cowpeas had been irrigated and produced a normal growth. No migration in pronounced numbers has been observed to take place, as is often the case with other insects. If the food is depleted the num- ber of weevils gradually‘ decreases, but as long as any cowpeas remain in the field, a few isolated individuals can usually be found, and weevils have been collected in patches after the peas have been har- vested. In confinement the weevil is likewise very aggressive in its search for food, peas left exposed in the laboratory were discovered and attacked with an uncanny precision. Even a single isolated pea in the most remote corner or nook if accessible to the weevil is attacked and will soon have eggs adhering to it. ‘Mating; is conducive to a more insistent search for food. THE OowPEA “TEEVIL. - 51 Adaptive Capacity. There is a very little flexibility in the habits of this insect to adapt itself to a strange environment. This is particularly true with respect "to its food plant. Changing the food from one variety of cowpea to another did not apparently affect the weevil, but When a nearly ‘related food plant, such as certain varieties of beans, navy, and lima, Were repeatedly tried, the Weevil could not complete its life cycle. In all experiments egg deposition took place readily enough, as has been elsewhere stated. The eggs hatched in a large percentage of cases, but the larvae could not subsist in the substituted food, and all were dead Within three days after hatching. In the field the cowpea Weevil has not been collected consistently on any plant except cowpeas. When the food is removed the weevils probably disseminate from that point ‘to other patches of cowpeas, instead of attacking other plants groxving adjacent to infested patches. The weevil is restricted to the coWpea as a food plant. Copulatioiz. Copulation is generally of short duration, rarely comprising more than three or four minutes. In the laboratory on September 8, 1916, ten pairs of weevils were timed While copulating. The average time Was three minutes and twenty seconds. The male normally is ag- gressive and insistent and continues to follow the female about very closely. The attraction of the male to virgin females two or three days old is much more pronounced than to the newly emerged indi- viduals. When the female is in a receptive mood she remains very quiet; usually is motionless and exhibits no excitement, while the male appears to be very nervous. At the beginning of coitu the male strokes the female with his antennae. Without exception the female makes the initial attempt at release; the male appearing helpless to extricate himself. The separation is accomplished by the female’s pushing against the male with her hind legs, a few vigorous backward strokes usually suificing. The male during this time remains perfectly quiet. Some- times, however, several minutes are required before the separation is completed. In the laboratory copulation took place freely in any. temperature sufficient to maintain activity among‘ the weevils. The total number of eopulations occurring during the life of a female varies under different conditions. As many as three often occur and have been observed at various times in the life history studies on the insect. Intermating is a com- mon occurrence. The female Will readily unite with any male, at a propitious time even if she has already mated to another male. The male is no more pronounced in his instinct for choosing a mate and will unite with any female regardless of any previous mating with other individuals. The total number of females that a single male can fertilize has been determined by laboratory experiments. The average of ten males mated in each case to virgin females, resulted in eight females fertilized in five days. Sometimes mating will take place after the male is no longer capable of fertilizing the female. The average time that these "males lived was seven days. 52 TEXAS AGRICULTURAL EXPERIMENT STATION. Period Between Maturity and Copulation. The period between maturity and copulation is very short. On August 20, 1916, in the laboratory, Courtney noted a pair of weevils in copulation one minute after they had emerged. This was doubtless "an extreme case and does not occur frequently. During the warm season when the activity of the weevils is at a maximum, the actual time which elapses between maturity and copulation ranges from five minutes, which was frequently observed in the laboratory throughout the summer of 1916, to a maximum that is determined only by the ability of the male to come into contact with the female. It might be said that the insect is ready to mate and begin reproduction almost immediately after maturity and emergence. The average time occur- ring between maturity‘ and copulation was not definitely determined, but it is safe to assume that it is not over 24 hours and probably less. In Table 23 it will be noted that egg deposition took place invariably on the day following mating, over the entire period. No eggs were deposited by an unmated female. Fertility. One mating is sufiicient to fertilize the entire egg quota of the female. If the male dies or is removed after copulation has taken place, all the eggs deposited by the female are fertile and will hatch, However, successive matings seem to stimulate the female to further egg deposition. The per cent. of normally deposited eggs that were unfertile or that did not hatch, over the entire period of the life history notes, was very small, in fact, it could well be considered negligible. Sometimes the egg is insecurely stuck to the pea and is brushed off, or it may be stuck at only one side or on the end and lifted away from the surface of the pea. These eggs were not observed to hatch. All experiments conducted in the laboratory attempting to induce unmated females to deposit eggs produced negative results. Oviposition. Oviposition is usually a short simple process. The female crawls about the seed in search of a favorable place for egg deposition. When the pea has been selected, the female explores the surface with her antennae. She stops and remains quiet for a few moments. The tip ofthe abdomen, which is protruded, is then bent well under the body and rubbed on the surface and immediately a clear sticky fluid is exuded; the egg follows shortly and is placed in the midst of this material which soon hardens and attaches the egg firmly to the surface of the pea. Sometimes the female turns about and examines the egg with her antennae. The entire operation is often completed within a minute. Sometimes after resting a few seconds, the female repeats the operation; usually, however, three or four minutes, often a much longer time elapses between deposition of eggs. When the supply of seed is abundant one egg is usually placed on a pea, but very often two or three, and occasionally more may be found on a single pea. When the supply of seed is small, however, or the infestation of weevils great, THE OowPEA WEEVIL. 53 very often a single seed containing twenty or thirty eggs may be found. On October 19, 1916, a medium sized cowpea of the Chinese Red variety was found in the field, with forty-founeggs adhering to it. The minimum average mean temperature at which oviposition took place was 33 degrees F. Only a few eggs were deposited in a tempera- ture below 5O degrees. When the temperature drops below '70 degrees there is, however, a noticeable decrease in oviposition. The optimum temperature for oviposition ranges between 85 and 95 degrees F. Fe- males will oviposit on any foreign objects if cowpeas are inaccessible. Frequently the eggs adhered to the sides of the vials. Temperature greatly influences the rate of oviposition and the total number of eggs deposited. The average number of eggs produced per female for the year 1916 was '73. The average mean temperature for the year was 72.9 degrees F. i Age at Beginning of Oviposition. The age at which the female begins ovipositing varies greatly with the season. The relationship of temperature to the age at beginning of oviposition is very pronounced. In Table 23 the daily egg produc- tion with the maximum, minimum, and mean daily temperature and humidity, is given. The longest period recorded, 1G days, occurred but once. Female No. 371, mated on January 10, 1917, deposited her first eggs on January 26, 1917. During this period the mean temperature ranged from a maximum of 76 degrees to a minimum of 30 degrees F., with a daily mean average of 53 degrees F. A period of from 3 to 5 days occurred frequently during the winter months of December, Jan- uary, and February of both 1916 and 1917. When the mean tempera- ture was 65 degrees F. or above, oviposition invariably took place on the same day that mating occurred. p Throughout the summer months of 1916 frequent observations were made in the laboratory, in which cases the female began oviposition‘ in from 3 to 5 minutes after mating. On October 16, 1915, Courtney noted an extreme case, a female depositing an egg in less than one minute after mating. ‘The average period is much longer. In a temperature of 70 degrees F. or above, the female will always begin oviposition within a period of 24 hours if she has been mated with an active male. When a female has been mated and does not have - access to cowpeas the time until oviposition begins is much prolonged. On September 12, 1916, fifteen females were placed in separate empty vials and the average time until eggs were deposited on the sides of the vials was slightly over three days. Showing that the female can con- trol, within certain limits, the time at which oviposition begins. Period 0f O/viposition. The length of the period of oviposition, from October 1, 1915, to February 1, 1917, is given in Table The period ranges from a minimum of 4 "days, which occurred frequently throughout the warm months, to a maximum of 34 day's, which was noted on January 10, 1917’. This long period occurred but once in the entire stuiilies. The daily mean temperature for this period ranged from 34 to 83 degrees Q34 TEXAS idGRICULTURAL EXPERIMENT STATION. ~F'., with an average mean temperature of slightly less than 56 degrees F. Eggs were deposited over a period of 28 days by three females during December, 1916. In a warm temperature activity is much more pro- nounced and the rate of oviposition is larger. When a female has laid her entire quota of eggs she becomes sluggish and usually dies in a few days. This greatly decreases the period for the warm months. In the cold season when the mean temperature is 50 degrees F. or below, activity is likely to cease altogether, and the weevils will seem dead t0 all outward appearances. ‘With a rise in temperature, however, they quickly resume a normal activity and egg laying continues. Within certain limits the length of the period of oviposition varies in direct proportion to the concurrent temperature. Table 22.——Period of Oviposition. _ ’ ' _ Temperature First Egg Last Egg Period, - _ c Days Max. Min. Mean 1915 Oct 1 . . . . . . . . . . . . . Oct. . . . . . . . . . . . . 9 85 69 77.3 Oct 7 . . . . . . . . . . . . . Oct. 15 . . . . . . . . . . . . 9 86 7O 78. 6 Oct 7 . . . . . . . . . . . . . Oct. 12 . . . . . . . . . . . . 6 85 69 79.3 Oct 15.- . . . . . . . . . . . . Oct. 21 . . . . . . . . . . . . 7 85 70 78.3 Oct 15 . . . . . . . . . . . . . Oct. 19 . . . . . . . . . . . . 5 85 70 79.6 Oct 17 . . . . . . . . . . . . . Oct- 26 . . . . . . . . . . . . 10 85 68 75.5 Oct 18 . . . . . . . . . . . . . Oct. 23 . . . . . . . . . . . . 6 84 68 76.2 Oct 19 . . . . . . . . . . . . . Oct. 30 . . . . . . . . . . . . 12 83 68 74.4 Oct 20 . . . . . . . . . . . . . Oct. 29 . . . . . . . . . . . . 1 78 68 73.9 Oct 22 . . . . . . . . . . . . . Oct. 29 . . . . . . . . . . . . 78 68 73.6 Oct 24 . . . . . . . . . . . . . Nov. 2 . . . . . . . . . . . . 10 8O 69 74. 9 Oct 24 . . . . . . . . . . . . . Nov. 2 . . . . . . . . . . . . 10 80 69 74.9 Oct 25 . . . . . . . . . . . . . Nov. 1 . . . . . . . . . . . . 8 79 71 74.7 Oct 26 . . . . . . . . . . . . . Oct 31 . . . . . . . . . . . . 6 79 72 75. 0 Oct 27 . . . . . . . . . . . . . Oct 3O . . . . . . . . . . . . 4 79 72 75.3 Oct 28 . . . . . . . . . . . . . Nov 2 . . . . . . . . . . . . 6 80 72 76.3 Oct 29 . . . . . . . . . . . . . Nov 4 . . . . . . . . . . . . 7 81 66 75.5 Oct 30 . . . . . . . . . . . . . Nov 7 . . . . . . . . . . . . 9 81 66 75.4 Nov 1 . . . . . . . . . . . . .. Nov 8 . . . . . . . . . . .. 8 81 66 75.6 Nov 3 . . . . . . . . . . . . . Nov . . . . . . . . . . . . 7 82 66 75. 8 Nov 4 . . . . . . . . . . . .. Nov 11 . . . . . . . . . . . . 8 83 66 75.8 Nov 8 . . . . . . . . . . . . . Nov 11 . . . . . . . . . . . . 4 83 76 78.2 Nov 8 . . . . . . . . . . . . . Nov . . . . . . . . . . .. 1 8O 77 79. 5 Nov 10 . . . . . . . . . . . .. Nov 16 . . . . . . . . . . .. 7 83 57 68.8 Nov 10 . . . . . . . . . . . .. Nov 21 . . . . . . . . . . .. 12 86 57 72.0 Nov 11 . . . . . . . . . . . .. Nov 21 . . . . . . . . . . .. 11 86 57 71.5 Nov 12 . . . . . . . . . . . .. Nov 19 . . . . . . . . . . .. 8 84 57 70.3 Nov 13 . . . . . . . . . . . .. Nov 19 . . . . . . . . . . .. 7 84 57 70.8 Nov 14 . . . . . . . . . . . .. Nov 19 . . . . . . . . . . .. 6 87 57 71.1 Nov 15 . . . . . . . . . . . .. Nov 21 . . . . . . . . . . .. 7 86 57 73.0 Nov 16 . . . . . . . . . . . .. Nov 21 . . . . . . . . . . .. 6 86 58 74.2 Nov 17 . . . . . . . . . . . .. Nov. 21 . . . . . . . . . . .. 5 86 69 75.6 Nov 18 . . . . . . . . . . . .. Nov 21 . . . . . . . . . . .. 4 86 69 75.4 Nov 19 . . . . . . . . . . . .. rNov 24 . . . . . . . . . . .. 6 87 66 75.6 Nov 2O . . . . . . . . . . . .. Nov 26 . . . . . . . . . . .. 7 87 66 76.2 ‘Nov 21 . . . . . . . . . . . .. Nov 26 . . . . . . . . . . .. 6 87 66 76.1 Nov 22 . . . . . . . . . . . .. Nov 28 . . . . . . . . . . .. 7 87 66 76.1 Nov 23 . . . . . . . . . . . . . Dec 1 . . . . . . . . . . . . 9 86 66 76.7 Nov 24 . . . . . . . . . . . .. Nov 30 . . . . . . . . . . .. 7 82 70 76.0 Nov 25 . . . . . . . . . . . . . Nov 3O . . . . . . . . . . . . 6 82 70 76.5 ' Nov 26 . . . . . . . . . . . . . Dec 2 . . . . . . . . . . . . 7 86 68 77.0 Nov 27 . . . . . . . . . . . . . Dec 2 . . . . . . . . . . . . 6 86 68 76.7 Nov 28 . . . . . . . . . . . . . Dec 6 . . . . . . . . . . . . 9 86 68 77.1 Nov 29 . . . . . . . . . . . . . Dec 5 . . . . . . . . . . . . 7 86 67 77.1 Nov 30 . . . . . . . . . . . . . Dec 5 . . . . . . . . . . . . 6 86 .67 77.5 Dec 1 . . . . . . . . . . . . . Dec 5 . . . . . . . . . . . . 5 86 68 77.8 Dec 2 . . . . . . . . . . . . . Dec 8 . . . . . . . . . . . . 7 85 68 76.7 Dec 3 . . . . . . . . . . . . . Dec . . . . . . . . . . . . 7 85 68 75.7 Dec 4 . . . . . . . . . . . . . Dec 14 . . . . . . . . . . . . 11 85 43 67.7 Dec 5 . . . . . . . . . . . .. Dec 1O . . . . . . . . . . .. 6 85 43 75.0 Dec 6 . . . . . . . . . . . . . Dec 18 . . . . . . . . . . . . 11 83 39 74.6 Dec 7 . . . . . . . . . . . . . Dec 27 . . . . . . . . . . . . 21 83 35 56.5 Dec 8 . . . . . . . . . . . . . Dec 23 . . . . . . . . . . . . 16 83 35 56.8 Dec 9 . . . . . . . . . . . . . . Jan 8 . . . . . . . . . . . . 31 83 29 64.5 Dec 10 . . . . . . . . . . . . . Jan 11 . . . . . . . . . . . . 33 83 29 56.0 Dec 13 . . . . . . . . . . . . . Jan. 11 . . . . . . . . . . . . 3O 79 29 55. 5 THE COWPEA W EEVIL. 55 Table 22.—Period of Oviposition.—Continued. Temperature First Egg Last Egg Period, _ Days Max Min. Mean 1915 Dec. 14 . . . . . . . . . . .. Jan 9 . . . . . . . . . . .. 27 79 29 62.6 Dec 14 . . . . . . . . . . . .. Jan 5 . . . . . . . . . . .. 23 74 29 54.5 Dec 14 . . . . . . . . . . . .. Jan 5 . . . . . . . . . . .. 23 74 29 54.5 Dec 15 . . . . . . . . . . . .. Jan 9 . . . . . . . . . . .. 26 74 29 54.9 Dec 16 . . . . . . . . . . . .. Jan 5 . . . . . . . . . . .. 21 74 29 54.3 Dec 22 . . . . . . . . . . . .. Jan 11 . . . . . . . . . . .. 21 79 29 56.3 Dec 23 . . . . . . . . . . . . . Jan . . . . . . . . . . . . 15 79 29 57. 0 Dec 21 . . . . . . . . . . . .. Jan 11 . . . . . . . . . . .. 22 79 29 56.0 Dec 27 . . . . . . . . . . . . . Jan. 6 . . . . . . . . . . .. 11 79 29 58.5 Dec 27 . . . . . . . . . . . .. Jan. 11 . . . . . . . . . . .. 16 79 29 58.1 Dec 28 . . . . . . . . . . . .. Jan. 5 . . . . . . . . . . .. 9 75 29 56.6 Dec 31 . . . . . . . . . . . .. Jan. 11 . . . . . . . . . . .. 12 79 30 62.3 1916 Jan. 1 . . . . . . . . . . . .. Jan 11 . . . . . . . . . . .. 11 79 45 62.7 Jan. 4 . . . . . . . . . . . .. Jan 12 . . . . . . . . . . .. 9 79 45 62.0 Jan. 12 . . . . . . . . . . . .. Jan 21 . . . . . . . . . . .. 1O 79 22 48.0 Jan. 2O . . . . . . . . . . . .. Jan 21 . . . . . . . . . . .. 2 71 38 59.0 Jan. 21 . . . . . . . . . . . .. Feb 20 . . . . . . . . . . .. 31 80 26 54.7 Jan. 26 . . . . . . . . . . . .. Feb 21 . . . . . . . . . . .. 27 8O 26 54.2 Jan. 26 . . . . . . . . . . . .. Jan. 26 . . . . . . . . . . .. 1 73 59 66.0 Feb. 11 . . . . . . . . . . . .. Feb. 24 . . . . . . . . . . .. 14 80 39 58.8 Feb. 17 . . . . . . . . . . . .. Mar. 8 . . . . . . . . . . .. 21 84 39 60.8 Mar. 7 . . . . . . . . . . . .. Mar 19 . . . . . . . . . . .. 13 86 39 66.0 Mar. 7 . . . . . . . . . . . .. Mar. 19 . . . . . . . . . . . . 13 86 39 66.0 Mar. 9 . . . . . . . . . . . .. Mar. 17 . . . . . . . . . . . . 9 86 44 64.1 Mar 10 . . . . . . . . . . . .. Mar. 21 . . . . . . . . . . .. 12 88 44 67.6 Mar. 10 . . . . . . . . . . . .. Mar. 19 . . . . . . . . . . . . 1O 86 44 66.0. Mar 17 . . . . . . . . . . . . . Mar. 3O . . . . . . . . . . . . 14 89 45 69.3 Mar 20 . . . . . . . . . . . .. Mar. 31 . . . . . . . . . . . . 12 89 48 70.4 Mar 21 . . . . . . . . . . . . . Mar. 31 . . . . . . . . . . . . 11 89 48 70.1 Mar 23 . . . . . . . . . . . .. April 4 . . . . . . . . . . .. 13 86 48 67.5 Mar 24 . . . . . . . . . . . .. April 4 . . . . . . . . . . . . 12 86 48 67.1 Mar 29 . . . . . . . . . . . . . April 22 . . . . . . . . . . . . 25 87 4O 68.1 Mar 3O . . . . . . . . . . . . . April 12 . . . . . . . . . . . . 14 83 55 64.7 April 2 . . . . . . . . . . . . . pril 14 . . . . . . . . . . . . 13 83 4O 64.8 - April 4 . . . . . . . . . . . . . April 16 . . . . . . . . . . . . 13 83 40 65. 7 April 7 . . . . . . . . . . . . . April 19 . . . . . . . . . . . . 13 87 4O 66. 6 April 8 . . . . . . . . . . . . . pril 1 . . . . . . . . . . . . 12 87 40 _ 67. 6 April 11 . . . . . . . . . . . . . April 20 . . . . . . . . . . . . 10 87 53 72. 3 April 12 . . . . . . . . . . . . . April 21 . . . . . . . . . . . . 10 87 56 72.8 April 13 . . . . . . . . . . . . . April 23 . . . . . . . . . . . . 11 87 56 72.9 April 14 . . . . . . . . . . . . . April 23 . . . . . . . . . . . . 10 87 56 72.6 April 15 . . . . . . . . . . . . . April 23 . . . . . . . . . . . . 9 87 - 56 72. 1 April 17 . . . . . . . . . . . . . pril 23 . . . . . . . . . . . . 7 87 58 73.4 April 18 . . . . . . . . . . . . . April 3O . . . . . . . . . . . . 13 87 52 71.9 April 19 . . . . . . . . . . . . . April 25 . . . . . . . . . . . . 7 87 58 74. 5 April 21 . . . . . . . . . . . . . April 30 . . . . . . . . . . . . 10 87 52 70.7 April 22 . . . . . . . . . . . . . May 4 . . . . . . . . . . . . 13 87 52 71.3 April 24 . . . . . . . . . . . . . May 3 . . . . . . . . . . . . 10 87 52 70.4 April 25 . . . . . . . . . . . . . May 4 . . . . . . . . . . . . 10 87 52 70.3 April 26 . . . . . . . . . . . . . May 6 . . . . . . . . . . . . 11 94 52 72.2 April 27 . . . . . . . . . . . . . May 7 . . . . . . . . . . . . 11 96 52 73.2 April 29 . . . . . . . . . . . . . May 6 . . . . . .~ . . . . . . 8 94 54 74.0 May 2 . . . . . . . . .. . May 8 . . . . . . . . . . .. 7 99 65 79.4 May 3 . . . . . . . . . . . .. May 8 . . . . . . . . . . .. 6 99 65 81.0 May 5 . . . . . . . . . . . .. May 5 . . . . . . . . . . .. 1 91 73 82.0 May 5 . . . . . . . . . . . .. May 13 . . . . . . . . . . .. 9 " 100 73 87.3 May 6 . . . . . . . . . . . .. May 13 . . . . . . . . . . .. 8 100 74 88.0 May 8 . . . . . . . . . . . .. May 14 . . . . . . . . . . .. 7 100 8O 89.0 May 9 . . . . . . . . . . . .. May 18 . . . . . . . . . . .. 10 100 70 86.1 May 1O . . . . . . . . . . . .. May 19 . . . . . . . . . . .. 10 98 70 84.4 May 12 . . . . . . . . . . . . .. May 22 . . . . . . . . . . .. 11 97 70 82.4 May 13 . . . . . . . . . . . .. ay 1 . . . . . . . . . . .. 9 97 70 82.1 May l5 . . . . . . . . . . . .. May 25 . . . . . . . . . . .. 11 97 70 81. 1 May 16 . . . . . . . . . . . .. May 16 . . . . . . . . . . .. 1 97 74 85.5 May 17 . . . . . . . . . . . . . May 25 . . . . . . . . . . .. 9 91 70 79.1 May 18 . . . . . . . . . . . . .. May 25 . . . . . . . . . . .. 8 91 70 79.0 May 19 . . . . . . . . . . . .. May 24 . . . . . . . . . . . . 6 91 7O 79. 1 May 20 . . . . . . . . . . . .. May 27 . . . . . . . . . . . . 8 91 71 80.6 May 22 . . . . . . . . . . . .. May 29 . . . . . . . . . . . . 8 87 71 80.5 May 23 . . . . . . . . . . . . . May 30 . . . . . . . . . . . . 8 89 71 80.8 May 24 . . . . . . . . . . . . . . May 29 . . . . . . . . . . . . 6 89 71 80.5 May 25 . . . . . . . . . . . . . May 30 . . . . . . . . . . . . 6 89 73 80.8 May 26 . . . . . . . . . . . . . une 2 . . . . . . . . . . . . 8 94 73 82.3 May 27 . . . . . . . . . . . . . June 2 . . . . . . . . . . . . 7 94 73 82.1 May 29 . . . . . . . . . . . .. June 5 . . . . . . . . . . . . 8 94 73 83.3 ‘ ay 30 . . . . . . . . . . . .. June 5 . . . . . . . . . . .. 7 94 74 83.8 _ May 31 . . . . . . . . . . . .. June 4 . . . . . . . . . . .. 5 94 77 ' 84.6 56 TEXAS AGRICULTURAL EXPERIMENT STATION. Table 22.—Period of Oviposition.—Continued. _ Temperature Flrst Egg Last Egg Period, Days Max Min. Mean 1916 June 1 . . . . . . . . . . . .. June 6.. 6 93 77 84.3 June 3 . . . . . . . . . . . .. June 8 . . . . . . . . . . .. 6 93 71 83.3 June 5 . . . . . . . . . . . .. une 12 . . . . . . . . . . .. 8 94 71 83.0 June 5 . . . . . . . . . . . .. June 11 . . . . . . . . . . .. 7 94 71 82.8 June 6 . . . . . . . . . . . .. June 13 . . . . . . . . . . .. 8 94 71 82.8 June 7 . . . . . . . . . . . .. June 13 . . . . . . . . . . .. 7 94 71 82.3 June 8 . . . . . . . . . . . .. June 14 . . . . . . . . . . .. 7 90 71 82.4 June 9 . . . . . . . . . . . . . June 14 . . . . . . . . . . . . 6 90 72 83.5 June 1O . . . . . . . . . . . . . June 15 . . . . . . . . . . . . 6 9O 73 84.0 June 12 . . . . . . . . . . . .. June 17 . . . . . . . . . . .. 6 90 72 82.1 June 14 . . . . . . . . . . . .. June 19 . . . . . . . . . . .. 6 90 72 81.8 June 15 . . . . . . . . . . . .. June 21 . . . . . . . . . . .. 7 95 72 82.1 June 16 . . . . . . . . . . . .. June 20 . . . . . . . . . . .. 5 95 72 81.1 June 17 . . . . . . . . . . . .. June 23 . . . . . . . . . . . . 7 95 75 83.4 June 20 . . . . . . . . . . . . . June 25 . . . . . . . . . . . . 6 95 75 86.1 June 21 . . . . . . . . . . . . . June 25 . . . . . . . . . . . . 5 95 78 86.8 June 22 . . . . . . . . . . . . . June 28 . . . . . . . . . . . . 7 95 75 86.8 v June 23 . . . . . . . . . . . . . June 29 . . . . . . . . . . . . 7 95 75 87.3 June 24 . . . . . . . . . . . . . June 29 . . . . . . . . . . . . 6 95 75 86.7 June 25 . . . . . . . . . . . .. June 25 . . . . . . . . . . .. 1 95 81 88.0 June 26 . . . . . . . . . . . . . July 2 . . . . . . . . . . . . 7 95 75 85.4 June 27 . . . . . . . . . . . .. July 2 . . . . . . . . . . .. 6 95 75 85.1 ' June 28 . . . . . . . . . . . .. July 5 . . . . . . . . . . .. 8 95 75 84.6 June 29 . . . . . . . . . . . .. July 5 . . . . . . . . . . .. 7 95 76 84.5 June 30 . . . . . . . . . . . .. July 5 . . . . . . . . . . .. 6 95 76 84.5 July 1 . . . . . . . . . . . .. July 5 . . . . . . . . . . .. 5 95 76 84.8 July 3 . . . . . . . . . . . .. July 9 . . . . . . . . . . .. 7 99 76 87.1 July 4 . . . . . . . . . . . .. July 8 . . . . . . . . . . .. 5 99 76 87.2 July 6‘ . . . . . . . . . . . .. July 11 . . . . . . . . . . .. 6 99 79 88.5 July 7 . . . . . . . . . . . .. July 12 . . . . . . . . . . .. 6 99 79 88.3 July 8 . . . . . . . . . . . . . .July 13 . . . . . . . . . . .. 6 99 79 87.8 July 10 . . . . . . . . . . . .. .July 16 . . . . . . . . . . .. 7 98 79 87.1 July 11 . . . . . . . . . . . .. July 15 . . . . . . . . . . .. 5 97 79 86.6 July 12 . . . . . . . . . . . .. July 15 . . . . . . . . . . .. 4 95 80 86.2 July 13 . . . . . . . . . . . .. July 17 . . . . . . . . . . .. 5 98 79 87.4 July 14 . . . . . . . . . . . .. July 21 . . . . . . . . . . .. 8 99 78 87.5 July 15 . . . . . . . . . . . .. July 19 . . . . . . . . . . .. 5 99 78 87.8 July 17 . . . . . . . . . . . .. July 22 . . . . . . . . . . .. 6 99 78 88.3 July 18 . . . . . . . . . . . .. July 23 . . . . . . . . . . .. 6 99 78 87.8 July 19 . . . . . . . . . . . .. July 24 . . . . . . . . . . .. 6 99 80 88.1 J uly 20 . . . . . . . . . . . . . July 24 . . . . . . . . . . . 5 99 80 88. 6 July 21 . . . . . . . . . . . .. July 24 . . . . . . . . . . .. 4 99 8O 88.6 July 22 . . . . . . . . . . . .. July 26 . . . . . . . . . . .. 5 99 80 88.2 July 24 . . . . . . . . . . . .. July 29 . . . . . . . . . . .. .6 99 80 87.6 July 25 . . . . . . . . . . . .. July 28 . . . . . . . . . . .. 4 98 80 87.0 July 26 . . . . . . . . . . . .. July 30 . . . . . . . . . . .. 5 97 80 86.0 July 27 . . . . . . . . . . . .. July 31 . . . . . . . . . . .. 5 97 78 86.0 July 28 . . . . . . . . . . . .. Aug. 3 . . . . . . . . . . .. 7 97 79 86.8 July 29 . . . . . . . . . . . .. Aug. 3 . . . . . . . . . . .. 6 97 79 86.9 July 31 . . . . . . . . . . . .. Aug. 5 . . . . . . . . . . . . 6 97 79 87.3 Aug. 1 . . . . . . . . . . . . . Aug. 7 . . . . . . . A. . . . 7 97 79 86.9 Aug. 3 . . . . . . . . . . . . . Aug. 9 . . . . . . . . . . . . 7 97 79 86.0 Aug. 4 . . . . . . . . . . . .. Aug 10 . . . . . . . . . . .. 7 96 78 85.3 Aug. -5 . . . . . . . . . . . . . Aug 10 . . . . . . . . . . . . 6 96 78 84.9 Aug. 7 . . . . . . . . . . . .. Aug 12 . . . . . . . . . . .. 6 95 78 85.3 Aug 9. . . . . . . . . . . . . Aug 12 . . . . . . . . . . .. 4 94 80 85.2 Aug 11 . . . . . . . . . . . . . Aug. 17 . . . . . . . . . . . . 7 96 75 87. 1 Aug 12 . . . . . . . . . . . . . Aug 16 . . . . . . . . . . . . 5 96 79 87. 1 Aug 12 . . . . . . . . . . . .. Aug 18 . . . . . . . . . . .. 7 96 75 86.2 Aug. 14 . . . . . . . . . . . . . Aug 23 . . . . . . . . . . . . 10 ‘ 100 75 87. 1 Aug. 15 . . . . . . . . . . . .. Aug 20 . . . . . \ . . . . . .. 6 95 75 85.8 Aug. 16 . . . . . . . . . . . .. Aug 22 . . . . . . . . . . .. 7 100 75 87.1 Aug. 17 . . . . . . . . . . . . . Aug. 23 . . . . . . . . . . . . 7 100 75 87.2 Aug. 18 . . . . . . . . . . . . . Aug. 24 . . . . . . . . . . . . 7 100 79 87.5 Aug. 19 . . . . . . . . . . . . . Aug. 24 . . . . . . . . . . . . 6 100 79 87.7 Aug. 21 . . . . . . . . . . . . . Aug. 26 . . . . . . . . . . . . 6 100_ 70 86.0 Aug. 22 . . . . . . . . . . . . . Aug. 27 . . . . . . . . . . . . 6 97 70 84.6 Aug. 23 . . . . . . . . . . . . . Aug. 29 . . . . . . . . . . . . 7 96 70 84.0 Aug. 24 . . . . . . . . . . . . . Aug. 27 . . . . . . . . . . . . 4 93 70 83.0 Aug. 25 . . . . . . . . . . . . . Sept. 2 . . . . . . . . . . . . 9 97 70 85.0 Aug. 26 . . . . . . . . . . . . . . Sept. 2 . . . . . . . . . . . . 8 97 70 85.3 Aug. 28 . . . . . . . . . . . . . Sept. 3 . . . . . . . . . . . . 7 97 77 87.5 Aug. 29 . . . . . . . . . . . . . Sept. 4 . . . . . . . . . . . . 7 97 77 86.8 Aug. 30 . . . . . . . . . . . . . Sept. 4 . . . . . . . . . . . . 6 97 77 87.0 Sept. 1 . . . . . . . . . . . .. Sept. 7 . . . . . . . . . . .. 7 97 79 88.0 Sept 2 . . . . . . . . . . . . . Sept. 8 . . . . . . . . . . . . 7 101 80 88.7 Sept 3 . . . . . . . . . . . . . Sept 7 . . . . . . . . . . . . 5 97 80 88.6 Sept 4 . . . . . . . . . . . .. Sept 12 . . . . . . . . . . .. 9 101 80 88.7 Sept 5 . . . . . . . . . . . . . Sept 11 . . . . . . . . . . .. 7 101 80 88.8 THE OOWPEA WEEVIL. Table 22.—Period of Ovipositiom-Continued.‘ 57 _ Temperature Flrst Egg Last Egg Period, . _ Days Max Mm. Mean 1916 Sept. 6 . . . . . . . . . . . . . Sept. 11 . . . . . . . . . . . . . 6 101 80 89.0 Sept. 7 . . . . . . . . . . . . . Sept. 12 . . . . . . . . . . . . 6 101 80 88.8 Sept. 8 . . . . . . . . . . . . . Sept. 15 . . . . . . . . . . . . 8 101 73 87.3 Sept. 9 . . . . . . . . . . . . . Sept. 13 . . . . . . . . . . . . 5 99 79 88.4 Sept. 10 . . . . . . . . . . . . . Sept. 14 . . . . . . . . . . . . 5 97 78 87.6 Sept. 11 . . . . . . . . . . . . . . Sept. 21 . . . . . . . . . . . . 11 99 67 82. 8 Sept. 12 . . . . . . . . . . . .. Sept. 17 . . . . . . . . . . . . 6 97 7O 83.3 Sept. 13 . . . . . . . . . . . . . Sept. 20 . . . . . . . . . . . . 8 99 67 81.7 Sept. 14 . . . . . . . . . . . . . Sept. 20 . . . . . . . . . . . . 7 99 67 80.8 Sept. 15 . . . . . . . . . . . . . Sept. 23 . . . . . . . . . . . . 9 99 67 80.2 Sept. 16 . . . . . . . . . . . . . Sept. 21 . . . . . . . . . . . . 6 99 67 79.8 Sept. 17 . . . . . . . . . . . . . Sept. 22 . . . . . . . . . . . . 6 99 67 80. 1 Sept. 18 . . . . . . . . . . . . . Sept. 25 . . . . . . . . . . . . 8 99 67 80.8 Sept. 19 . . . . . . . . . . . . . Sept. 25 . . . . . . . . . . . . 7 91 68 80.5 Sept. 20 . . . . . . . . . . . . . Sept. 25 . . . . . . . . . . . . 6 91 69 81.0 Sept. 22 . . . . . . . . . . . . . Sept. 29 . . . . . . . . . . . . 8 105 60 81.2 Sept. 23 . . . . . . . . . . . . . Sept. 28 . . . . . . . . . . . . 6 105 70 82.8 Sept. 24 . . . . . . . . . . . . . Oct. 1 . . . . . . . . . . . . 8 105 57 77.8 Sept. 25 . . . . . . . . . . . . . Oct. 6 . . . . . . . . . . . . 12 105 57 77. 2 Sept. 26 . . . . . . . . . . . . . Oct. 4 . . . . . . . . . . . . 9 105 57 76.5 Sept. 27 . . . . . . . . . . . . . Oct. 3 . . . . . . . . . . . . 7 105 57 76.1 Sept 28 . . . . . . . . . . . . . Oct. 5 . . . . . . . . . . . . 8 95 57 74.8 Sept 29 . . . . . . . . . . . . . Oct. 7 . . . . . . . . . . . . 9 89 57 73.9 Sept 30 . . . . . . . . . . . . . Oct. 7 . . . . . . . . . . . . 8 89 57 74.5 Oct. 1 . . . . . . . . . . . . . Oct. 8 . . . . . . . . . . . . 8 90 59 75.8 Oct. 3 . . . . . . . . . . . . . Oct. 9 . . . . . . . . . . . . 7 91 66 78.5 Oct. 4 . . . . . . . . . . . . . Oct. 9 . . . . . . . . . . . . 6 91 66 78.7 Oct. 5 . . . . . . . . . . . . . Oct. 12 . . . . . . . . . . . . 8 94 66 78.7 Oct. 6 . . . . . . . . . . . . . Oct. 12 . . . . . . . . . . . . 7 94 68 78.9 Oct. 7 . . . . . . . . . . . . . Oct. 14 . . . . . . . . . . . . 8 94 68 79.7 Oct. 8 . . . . . . . . . . . . . Oct. 13 . . . . . . . . . . . . 6 94 68 80.0 Oct. 9 . . . . . . . . . . . . . Oct. 15 . . . . . . . . . . . . 7 94 l 68 80.0 Oct. 10 . . . . . . . . . . . . . Oct. 19 . . . . . . . . . . . . 10 94 60 76.4 Oct. ll . . . . . . . . . . . . . Oct. 18 . . . . . . . . . . . . c8 90 61 76.8 Oct. 12 . . . . . . . . . . . . . Oct. 18 . . . . . . . . . . . . 7 90 61 76.6 Oct. 13 . . . . . . . . . . . . . Oct. 22 . . . . . . . . . . . . 10 9O 41 71.3 Oct. 14 . . . . . . . . . . . .. Oct. 22 . . . . . . . . . . .. 9 90 41 70.1 Oct. 15 . . . . . . . . . . . . . Oct. 26 . . . . . . . . . . . . 12 95 41 69.9 Oct. 16 . . . . . . . . . . . .. Oct. 30 . . . . . . . . . . .. 15 95 41 70.3 Oct. 17 . . . . . . . . . . . . . Oct. 30 . . . . . . . . . . . . 14 95 41 69.9 Oct. 18 . . . . . . . . . . . .. Oct. 3O . . . . . . . . . . .. 13 95 41 70.2 Oct. 19 . . . . . . . . . . . . . Oct. 31 . . . . . . . . . . . . 13 95 41 70.7 Oct. 20 . . . . . . . . . . . . . Nov. 1 . . . . . . . . . . .. 13 95 41 71.5 Oct. 21 . . . . . . . . . . . . . Nov. 1 . . . . . . . . . . . . 12 95 41 72.3 Oct. 22 . . . . . . . . . . . .. Oct. 31 . . . . . . . . . . .. 10 95 52 73.1 Oct. 23 . . . . . . . . . . . . . Nov. 2 . . . . . . . . . . . . 11 95 53 73. 5 Oct. 24 . . . . . . . . . . . . . Nov. 1 . . . . . . . . . . . . 9 95 53 74.8 Oct. 25 . . . . . . . . . . . . . Nov. 5 . . . . . . . . . . . . 12 92 53 74.8 Oct. 26 . . . . . . . . . . . . . Nov. 9 . . . . . . . . . . . . 15 92 53 74.8 Oct. 27 . . . . . . . . . . . . . Nov. 5 . . . . . . . . . . . . 10 92 53 75.3 Oct. 28 . . . . . . . . . . . . . Nov. 4 . . . . . . . . . . . . 8 90 56 75.2 . Oct. 29 . . . . . . . . . . . . . Nov. 5 . . . . . . . . . . . . 8 90 60 76.3 Oct 30 . . . . . . . . . . . . . Nov. 7 . . . . . . . . . . . . 9 90 60 76.4 Oct 31 . . . . . . . . . . . . . Nov. 10 . . . . . . . . . . . . 11 89 60 74.6 Nov 1 . . . . . . . . . . . . . Nov. 9 . . . . . . . . . . . . 9 89 58 75. 7 Nov 2 . . . . . . . . . . . .. Nov. l0 . . . . . . . . . . .. 9 89 51 74.5 Nov 3 . . . . . . . . . . . .. Nov. l1 . . . . . . . . . . .. 9 87 51 74.0 Nov 4 . . . . . . . . . . . .. Nov. 11 . . . . . . . . . . .. 8 87 51 74.0 Nov 5 . . . . . . . . . . . .. Nov. 19 . . . . . . . . . . .. 15 89 33 67.0 Nov 6 . . . . . . . . . . . . . Nov. 23 . . . . . . . . . . . . 18 94 33 66.6 Nov 7 . . . . . . . . . . . .. Nov 21 . . . . . . . . . . .. 15 94 33 66.6 Nov 8 . . . . . . . . . . . . . Nov. 28 . . . . . . . . . . . . 21 98 33 65.2 Nov 9 . . . . . . . . . . . . . Nov. 30 . . . . . . . . . . . . 22 98 33 65.8 Nov 10 . . . . . . . . . . . .. Nov. 28 . . . . . . . . . . . . 19 94 33 63.6 Nov 12 . . . . . . . . . . . . . Dec l . . . . . . . . . . . . 20 98 33 65.8 Nov 15 . . . . . . . . . . . . . Nov. 28 . . . . . . . . . . . . 14 94 33 64.1 Nov 15 . . . . . . . . . . . . . Nov 28 . . . . . . . . . . .. 14 94 33 64. 1 Nov. 19 . . . . . . . . . . . . . Dec 4 . . . . . . . . . . . . 16 98 44 70. 5 Nov. 20 . . . . . . . . . . . . . Dec 4 . . . . . . . . . . . . 15 98 44 70.6 Nov 21 . . . . . . . . . . . . . Dec 3 . . . . . . . . . . .. 13 98 44 69.2 Nov 23 . . . . . . . . . . . . . Dec 7 . . . . . . . . . . . . 15 101 44 72.8 Nov. 24 . . . . . . . . . . . . . Dec 6 . . . . . . . . . . . . 13 101 44 74.0 Nov 26 . . . . . . . . . . . . . Dec 8 . . . . . . . . . . . . 13 101 44 75.3 Nov 28 . . . . . . . . . . . . . Dec 10 . . . . . . . . . . . . 13 101 38 75.0 gov 3O . . . . . . . . . . . . . Dec 8 . . . . . . . . . . . . 9 101 48 78.4 ec. 1 . . . . . . . . . . . . . Dec 14 . . . . . . . . . . . . 14 101 32 70.1 Dec 2 . . . . . . . . . . . .. Dec 12 . . . . . . . . . . . . 11 101 34 71.7 Dec 3 . . . . . . . . . . . . . Dec 16 . . . . . . . . . . . . 14 101 32 67.7 Dec. 4 . . . . . . . . . . . . . Dec 17 . . . . . . . . . . . . 14 101 32 67.0 58 TEXAS AGRICULTURAL EXPERIMENT STATION. Table 22.—Period of Oviposition.—Continued. _ Temperature Period, _ Days Max. Min. Mean Dec. 29 101 28 62. 5 Dec. 24 99 28 61.6 Dec. 28 92 28 60. 9 Dec. 28 9O 28 60. 8 Dec. 24 92 28 60.0 Dec. 24 92 ' 28 60.0 Dec. 25 92 28 60.8 Dec. 15 89 28 58.9 Dec. 22 92 28 60. 9 Dec. 21 92 28 61.0 Dec. 21 92 28 61.3 Dec. 23 93 28 63.0 Dec. 20 94 46 66.4 Dec. 17 93 46 66. 4 Dec. 17 93 46 66.4 Dec. 17 94 46 67.3 Dec. 15 92 46 66. 1 Dec. 15 93 46 67. 1 Dec. 18 94 44 67.0 Dec. 18 94 44 67.0 Dec. 15 94 46 67.2 Jan. 11 94 44 69. 6 Jan. 11 94 44 69.6 Jan. 10 95 44 68. 8 Jan. 24 » 94 30- 56. O Jan. 24 94 30 55. 7 Jan. 22 94 3O 55.0 Jan. 22 100 3O 55.5 Jan. 34 100 25 56. 5 Jan. 24 100 25 57. 5 Jan. 26 100 25 57.4 Jan. 82 40 56.3 Jan. 20 100 25 58. 1 Jan. 24 100 25 57.4 Jan. 19 100 25 57.7 Jan. 27 103 25 61.2 Jan. 20 100 25 57. 1 Jan. 23 100 25 58.6 Jan. 25 103 25 61.0 Jan. 24 103 25 60. 1 Rate 0f Oviposition. The rate of oviposition is shown in Table. 23. The maximum num- ber of eggs produced in 24 hours was 58, by female N0. 251, on Sep- tember 12, 1916. This maximum occurred but a single time during the entire studies. From 50 to 55 eggs for a 24-hour period occurred frequently during the warm months. Generally the maximum number of eggs for a. 24-hour period is deposited immediately after mating. In a few instances thelfemalc deposited her entire egg quota during the first day after mating, and during the summer, it frequently happened that she deposited all her eggs in the first two or three days. During the second 24-hour period the number is reduced by about one-third. In the succeeding periods there is a considerable fluctuation in the number of eggs deposited. In a few instances, usually during the cold periods, more eggs Were deposited on the fourth and fifth day than on the preceding; days. During the warm season, however, the decline in rate of oviposition after three days is very abrupt. Temperature has a very important influence as will be seen from Table 23. In cold weather the period of oviposition greatly increased, while the rate of oviposition suffers a corresponding decrease. No regularity appears in the number of eggs deposited for any given period. In fact, the num- THE CowPEA ll/VEEVIL. 59 ber of eggs deposited depends directly upon the prevailing temperature for the period. The female may begin oviposition "with a single egg and gradually 0r suddenly increase this t0 many times the number. Sometimes two weeks or more may pass after mating before a single egg is deposited, and occasionally it happens that the female will not deposit any eggs during the period of her life. 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THE COWPEA W EEVIL. ‘Q m n m mm m m mm m m m > mdwdmow dm "w ' dwo'd ‘N mcmm :12 ‘monhmnwgvw$$g£wg£gwwmEw§§aEwwww E : vmwmwomwhwmo>mwvwhowowQm~¢ohwNm E E NmmmmvmwNwm¢Nm¢m~ ¢mmmmmmmmNmmw 5 I I X ooooooooommooohom~mwo~@mmwwoNmm w wooooooouwmmwowwmnwmhbmmmmwwwwm 2 v-(Fewn-iaww v-l 899 ' ' . : : : . °° mg - I - oooo WS ‘ @:”N” qgg - bmcbv-uwfl vgg _ _ _ ZOBCOPCQNM %£ .....'III°°°w°“*“ mg - -----;;:oow:¢2omm Q9 -I - Ioomwmvommm wg _:ooom2mmohm “Q IIIIIIII..I°°°N22°2“°” 817g I I I I I I I :ooo\no§q=:a-~wooN mg ____:mvmmmmm¢Nwoommwv~m~oo 69$ ' ' I I Z zOOv-iefiOhwmlflfiOOOwhlfiflOtflQOfi 3% ;2NmmwhmmmNmmooomvhwmc~o My _;~m¢vw~2oowowvoo~oo§oo~o~ 9% :2mwoN¢ohoNw~moooo~m—o~ooo gg :@2W€OWHW®HONmfiNOOOmNMMNH 7% I222~VOHNN~OHMOOOOOQfimNNHOOO (egg fl§goomhmovomo~mo v _ -‘: _ _ _ _ _ as w¢N>m~wo~m~m~~ocooooooooo v-lv-lFi . . . . 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' : . : l: L!) LO LO UULO L!) LO g wwmmmommma~m¢Nm~ 3 2 mmmwmwwvvmwmwwww : -v-> E . 0 E mhwNmmm~w~o~ww>> Q 2 mmwvmmmwvvwwmmww E Q fi, Q ssssssssssssssss 2 .- o I III II II ‘*3 . - I - u - I I - w . ... .. .. Q :::.:::::::: 1~=dzN www/N E32 dNw/N flaw/N I1 www Nww Nw/w www www www hww www www Nww Nww www whw whw whw Nhw Nhw whw www www www www I! BwQ wtwNEswN ohsfifiomfioh. .w@ncScoU|lcoN:moci/O we BmMN‘wN 03mm. 78 Texas AGRICULTURAL EXPERIMENT STATION. Generation Series. In March, 1916, notes were begun on the number of generations that are produced in a year under natural conditions. These notes were made vsdthout interruption until March, 1917, and appear in detail in Fig. 3. Two pairs of weevils, Nos. 1 and 2, were mated March 14, 1916, and the first weevils of the first eggs and the last weevils of the last eggs are represented by the A and B series, respectively. A1 and B1 indicate origin from the pair No. 1; F1, F2, F3, etc., represent the filial generation. The last number to the right indicates the collection of eggs from which the next generation was produced. This number, ~ in case of the first we-evils of the first eggs, would of course always be one as will be seen in the A series in Fig. 3. In the last weevils of the last eggs produced, however, the number varies from 3 to 11 because all the pairs do not produce the same number of collections of eggs even under the same conditions. Two pairs of weevils were used for two reasons: to insure completion of notes for an entire year, and to check the results. The above explanation applies to pair No. 2 also. It will be seen in the chart that under the best conditions, by mating the first female of each generation, nearly ten generations became pos- sible in a year; and under the most adverse conditions, by mating the last female of each generation, eight generations might be produced. According to the average, it is safe to assume that normally nine gen- erations are produced in a year in this locality. Protection. While the egg adheres to the external surface it is nevertheless pro- tected to some degree by its semi-translucent color, which is not readily observed on any of the light colored or mottled varieties of cowpeas. The eggs are often placed in a depression or among other irregularities on the surface of the peas. As has been stated, when the egg is de- posited it is covered by a sticky fluid secreted by the female, which hardens on exposure, forming a hard shell coating for the egg. Doubt- less this affords much protection from crushing as the peas are Ihoved about. The entire under surface of the egg is glued securely to the pea, and the larva’s access to the food supply is thus insured. The larva enters the pea from the under side of the egg, and matures wholly within the pea, which affords an excellent protection against parasites. climatic conditions, or similar influences. Adults protect themselves in several ways~—feigning death being the most common. Upon the slightest disturbance, they immediately drop and remain motionless, sometimes feigning death. for three or four minutes. The weevils can run rapidlyr, and in nature it is difficult to follow an individual which has been disturbed. They seek shelter quickly and are greatly aided in this respect by their inconspicuous brownish- black markings. Flight is another important protection. The weevil will take to the wing very quickly if disturbed, and while it cannot be classed as a strong flier, it is able to fly rapidly for short distances. This without doubt enables it to elude many of its enemies. 79' THE COWPEA XVEEVIL. .2 QQVMWQ W\.Q .N\ Q \Q\I\NY .8 QQnPFQ w\.w\m\ w. \.mm\\v\ W\.%.N\.\< wk NEQ W\.N\.Q\ Q \WL.\NY wxwxwx? .w\.\\.N\..QK W\.%\.Q\Q 3x $x 3 Evnwmww wl .N\.Q. v.m|.\ N% wkgx? w\.w\.Q\..Qk w\.\N.% Q fi Q -2 \\.w\.nwk w\.\.N\-Q 3% wlwfi Q :W\\v\ w\.%\§\§\ w\.\N.m.§\ w\\\.Q\.Qm\ WFRAWUQM dwflvfiaw wwiww confifiwcwfi m\ .w.w\.>\ w» M.N\..Qm $9.9. Q VmkN% wiwmw? w\.\w.m.wk Qxmwfi Q \N1v\ N‘ W\.N.N\.>\ w\.\.w\wk w\.\\.Q\ Q |flw|v\\% wxmww Q \~:\ \v\ W\.N. Q\ .>\ Smévu.» 8-9m Q hewww QQNM .3 w\NN.%..QK wk -% Q \.WU\NY w\.\-%\.>\ QQYQFQM w\ W6, Q “wk... W\..N-Q Q Gui? wxmwmr? m\.\-® .\\ W\.%N.%..Qk\W\%.mr.Qk 3mm .§\ W\-\.m. Wk w\. 3% - Q aw ~% W\.\ -%$< W\.m.m..m¢ W\.\\ K Q \..m.\wv\ wxvm§ w\.\-m..ku.% wxnxn Q Nwzw w\.\\.m Q C“ \v.\ .m 259.; 9.5m .>\ QM...“ w» w,\.V\.k Q m Qwfi W\.\\.\.>\ WFQN Q.» Qw..-» .Q \$|\NV\ w\.~-@.>\ Qwwww . 3.3.x w fiwm 3i N -2 wxwvwww wfiww Q \.~.»\€\ 36R .2 3635mm 33¢ Q wll i W\.Q\.N..Q.w “$3 ..\. “Qfi wXMNw .\< wbfi WWW . w\-N-w w és 8.3. w .>\ Q5 w Mm. wR WW .Q QQNQ w\.w.w.>\ 3S w“. $m%& \.NI\NY. w\.\\-w-§\ W\qQ\.W.|.Q% w\$\.|fi Q QWSQ wxwwq \ NM§Y w\.w.w..>\ Q\.N.W.>\ w\.w.w...wm\w\.wwwmw Ssvwi Q Qh .3 $3 .m w §QNm w\.w.m.>\ wt fiw QQR. Q \QNW\ >32 wvfiwwx 8mm.» Q QQUQQ w\.&\-m,|.Q EOEY - 80 TEXAS AGRICULTURAL EXPERIMENT STATION. Mortality. The rate of mortality resulting from adverse climatic conditions, is very low. While the fatal low temperature has not been determined, the adult weevils exposed to freezing temperatures revived apparently unaffected. Peas containing eggs, developing larvae in all stages and pupaewere likewise exposed to the lowest temperatures d.uring the win- ters of 1916 and 1917. No appreciable increase in the rate of mortality resulted; in fact, it was no greater than normally occurred, as shown in the life history notes taken over the entire period. At no time during the warm season does the heat become sufficiently intense to destroy the developing weevils within the peas. Many in- fested peas containing larvae and pupae that had been exposed to the direct rays of the sun and the hottest weather occurring during the summer. of 1916 and 1917, were taken into the laboratory, and the adult weevils rarely failed to emerge. Both adult weevils and developing larvae and pupae appear to be very little aifected by a high or low humidity produced by artificial means. Excessive rainfall probably destroys a number of the adults, but_ there is no increase in mortality of the immature forms unless the peas are submerged for a long time. NATURAL CONTROL. Parasites. The larva of Britclzus quacZr-irnz/aculzztits is attacked by a parasite, Bruchobius laticeps Ashmead.*- This species was described in Proc. Nat. Mus, Vol. ~15, p. 7250, and. the original description is given below: Female.——Type, length about 2.5 mm. Green, with brassy tinges; head wider than thorax, head and thorax, including pleurae and pro- podeum, with coarse thimble-like punctures, those on the mesonotum so coarse as to somewhat resemble irregular reticulations; antennae 13-jointed, honey color, with three ring joints, the third subquadrate; first joint of funicle almost twice as long as pedicel, the following joints almost subequal in length, the second joint of funicle about two—thirds as long as first; pronotum sharply truncate anteriorly; propodeum com- pletely covered with thimble-like punctures, with lateral folds, the spiracles large, elongate-ovate, situated basad; marginal vein short, about one-third as long as submarginal; postmarginal slightly longer than marginal; stigmal and marginal subequal in length; femora and bases of tibiae reddish-honey color; rest of tibiae and tarsi whitish; abdomen about as long as head and thorax combined. Male. iLength about 1.75 mm. Similar to the female; antennae with two ring joints, the third being elongated into a joint of the tunicle, being as long as the pedicel, but not as long as the following joint of the funicle; abdomen with a large basal white spot. The type material consists of four females and four males and is labeled “Washington, D. C, Nov. 12, 1896”; bred from Bruchus quadri- maculatus. (F. C‘. Pratt, collector.) *Detern1ined through the kindness of Dr. L. O. Howard. 7 n . . w 3x5 “ , i: Qrwwra 1Z2 25:“ 5: 2mm k it wwwpw Emma can Q Z2 Aov wfimwwwm w? £51m 9E IV‘ IN y\|n. '1. ‘a, v This parasite was first observed in the laboratory in August, 1916, in some cowpeas heavily infested with the weevil, and collected during July in the field at College Station, Texas. This parasite is shown in Plate V (a) ; the males are on the right and the females 0n the left of the photograph. The parasites were numerous and examination at that time showed at least 1O per cent. of the weevil larvae parasitized. Efforts to collect adult parasites in the field, however, resulted in the ' taking of only a few specimens. This parasite was also observed in infested cowpeas collected at Lubbock, Texas. During the summer of 1917 no parasites were found at College Station, Texas. although care- _ful search was made for them. As efforts to induce oviposition by adult parasites proved unsuccessful, complete life history notes were not made. The eggs are doubtless placed on the weevil larva or in the larval burrow by means of a strong ovipositor with which the female is equipped. The egg stage was not observed. After hatching, the tiny parasite larva attaches itself to the weevil larva and feeds externally. This is shown in Plate V (b) at the left side 0f the photograph. The parasite increases in size very rapidly and the host is usually not killed until it is nearly developed. By the time it is fully matured and ready for pupation the entire body of the host, except the head, has usually been consumed. Pupation takes place within the larval burrow of the weevil. The adult parasite emerges through a round hole similar to the weevil’s exit, except it is much smaller. One parasite larva was observed to pupate September 23, 1916, and emerged as an adult October 1, 1916. The importance of Bruchobius Zaticeps Ashmead, as a natural control, is questionable. Though it undoubtedly destroys many weevil larvae, it does not appear to be abundant enough to produce an appreciable reduction in the number of weevils in this locality.‘ “THE OowPEA WEEVIL. l A 81 Egg Parasite. The most important natural enemy of Bruchus quadrimaculatus is Uscana scmi_fzam4lpenn,1's Girault,* a minute egg parasite which destroys the weevil eggs in great numbers. The adult parasite is shown enlarged in Plate V (c). The description of this species is given as it originally appeared in Trans. Amer. Ent. Soc., Vol. 37, pp. 23-24. Uscana, semifumipenazis Girault. Female.—Length, 0.80 mm. Moderately small, visible easily to the naked eye, but not casually even to the trained eye. General color tawny yellow, the abdomen usually deep black, in some specimens vary- ing to dusky yellowish, the legs dusky excepting the pallid yellow knees, the tarsi (excepting the very slightly dusky terminal joint) and the cephalic and intermediate tibiae; antennae dusky to pallid yellow; eyes bright pinkish red; wings hyaline excepting the" proximal halves of the fore wings, that portion proximad of the discal end of the venation, which is distinctly though not pronouncedly, fumated; the fumated area. extends to a point opposite the end of the stigmal knob and its *Determined through the kindness of Dr. L. O. Howard. 82 TEXAS AGRICULTURAL EXPERIMENT STATION. distal bounding line is nearly straight. Venation dusky. Body sculp- ture inconspicuous. Colors of legs somewhat variable. Tegulae dusky yellowish. l Fore Wings with short marginal fringes along the cephalic margin, which gradually slightly lengthen along the apex, becoming twice longer at the disto-caudal apex of the wing, then gradually shortening again caudad and proximad ; the longest cilia are not more than an eighth of the greatest Wing width, which is near to, but not at the apex. The discal ciliation is short and moderately close, arranged in about from 16 to 20 lines across the Widest portion of the wing. Marginal vein broad, straight, twice the length of the stigmal and nearly a half shorter . than the submarginal vein, truncate distad; submarginal vein narrow, straight, but distad Where it curves cephalo-distad to join the marginal, abruptly broader but not quite so broad as the latter. Oaudal wings normal, the blade moderate in Width, acuminate, the marginal cilia normal, those of the caudal margin as usual much longer, here grad- ually lengthening distad where they are distinctly longer than the greatest wing width, those of the cephalic margin usual, short; discal ciliation of the caudal Wings consisting of three longitudinal lines of cilia, the cephalic two paired, slightly converging distad, originating at the apex of the marginal vein or nearly, the caudal line slightly fainter, originating farther proximad, gradually converging on the others to- ward the apex, nearer to, but not on, the caudal wing margin. Antennae short and moderately stout, the club forming half of their length, the scape short, not as long as the club, cylindrical, curved, the pedicel shorter than the scape, not much longer than wide, conic to subquadrate, subequal in length to the proximal club joint; ring joint minute, flat, abruptly narrower than the pedicel or club; the three club joints distinct, the intermediate joint l.ongest and widest (base), the apical joint small, conic, acute; the club itself pointed conic-ovate in shape. Pubescence of the antennae sparse, consisting of scattered long hairs, mostly on the club. , From 30 specimens, g inch objective, 1 inch optic, Bausch and Lomb. M aZe.~—-The same; the antennal club shorter, not as pointed. From 13 specimens, §- inch objective, 1 inch optic, Bausch and Lomb. Described from 13 males and 30 females mounted in balsam and forming ‘a series of slides in the collections of the Bureau of Entomology, U. S. Department of Agriculture, kindly loaned for study by Dr. L. O. Howard and labelled as follows: ‘A‘Bred from Bean-weevil parasite material from Beeville, Texas.—Honolulu, Haxvaii, October 30, 1909, D. T. Fullowayn” Habitat.—-United States: Beeville, Texas. This tiny insect, which is scarcely visible to the unaided eye, deposits its egg inside the weevil egg. The parasite larva feeds upon the con- tents of the weevil egg, which furnishes a sufficient food supply to reach maturity. The adult parasite emerges from the host egg through a minute round aperture, usually at the broad end of the egg. The parasitized weevil egg first appears reddish yellow and grad- ually turning darker as the‘ parasitedevelops, finally takes on a shiny black color. The eggs on both the pods and seed are attacked, and where they are grouped together it is unusual to find normal eggs on the same seed with those that have been parasitized. One seed with THE OowPEA WEEVIL. 83 twelve and another with eight parasitized eggs Were collected, the num- bers ranging from three to five were much more common. This parasite was first observed in the field in October, 1916, and at that time appeared to be very abundant. Out of a total of 1621 Weevil eggs examined during October, 1916, 1098, or over 67 per cent., were parasitized, and 554. were normal. Without question, this species, the importance of which is indicated by the above figures, is the most effective factor in reducing the natural increase of the pea Weevil in this locality. REMEDIAL MEASURES. Harvesting. Proper harvesting of the cowpea crop will result in a reduction of from 50 to 90 per cent. of the infestation of weevils. Where the crop is permitted to remain in the field after it is fully matured, the tips of the dry pods usually part sufficiently to expose the first two or three seeds to weevil attack. Examination of a field of cowpeas in this con- dition in October, 1916, showed that over 90 per cent. of the peas thus exposed were infested by the weevil. The adult prefers to confine its attack to the exposed seeil; obviously, if the crop is harvested at the proper time, that is, before the pods open and the seeds are exposed, the infestation can be materially checked. This may necessitate sev- eral pickings and thus increase the cost of harvesting, but the reduction in injury to the crop will more than justify the additional expenditure of time and. labor. Experiments conducted with the proper harvesting of cowpeas in ‘accordance with the recommendations given above, showed that 100 per cent. weevil free seed could be obtained. Where the operations are carried on in a commercial way, however, an infestation of from 2 to 5 per cent. may result from eggs that are deposited on the pods. This cannot be eliminated because this insect cannot be combated by any direct control measures in the field. It is therefore important to re- member that proper harvesting is not recommended as a complete control measure for the weevil. ln this connection, the crop should be treated with either carbon bisulphide or heat as soon as possible after it is har- vested in order to destroy any weevils not eliminated by precautions taken in harvesting the crop. Sltorage. No matter how efiiciently the preventive measures have been carried out, complete success depends upon the proper storage, since cowpeas are always subject to reinfestation with the weevil. The popular belief that “processed” (heated or furnigated) cowpeas will not become re- infested, is erroneous. The cowpea weevil has been repeate-dlyr bred. in hard,- dry, processed cowpeas, and apparently experienced no (lifficulty, except that the period of development was greatly prolonged. R-egard- less of the method employed in destroying the weevils in infested seed, it should always be stored in a weevil-proof bin or other containers. Seed in sacks is subject to infestation and should never be kept in this condition exposed to the weevil. This was determined in an ex- 8a TEXAS AGRICULTURAL EXPERIMENT STATION. perimental Way by exposing uninfested peas in a canvas sack to weevils. Oviposition took place readily on the outside of the sack, and the larvae succeeded in working through and infesting the seed within. Weevil-proof bins constructed of tightly-fitted matched lumber, or tight- ffitted metal containers have proved to be the most satisfactory method of storing seed. The cost of such equipment varies with the size and quality. The prevention of weevil injury makes it an economical investment. Fumigation With- Carbon Bisulphide. Carbon bisulphide, which has been extensively used against insects which infest stored seed, is, when properly used, one of the cheapest and most effective methods of controlling the cowpea weevil. Chem- ically pure liquid carbon bisulphide is colorless and completely volatile, though the usual commercial product is yellowish in color because of the presence of excess sulphur. It has a strong disagreeable odor and evaporates rapidly on being exposed. The fumes of carbon bisulphide are over twice as heavy as air and therefore will diffuse rapidly down- ward. This is an important point to remember in the application of this material. It should always be exposed above the seed to be treated. The rapidity of irolatilization depends upon the surface of liquid exposed to the air. Since rapid evaporation is desirable because the material is an effective insecticide only in the gas form, the liquid should always be exposed in large shallow containers to expedite evaporation. The fumes have such penetrative power that it is possible to use this material for treating seed in large quantities. Since it is confined space and not the contents that determines the dosage, the seed to be treated should be placed in as small a space as possible. Tempe-rature has an important influence upon the effectiveness of carbon bisulphide fumes, and unless the fumigation is conducted under favorable conditions with respect to this factor, the results obtained will not be satisfactory. The effectiveness of the fumes is materially reduced at temperatures below 6O degrees F. Temperature governs the amount of carbon bisulphide gas that is necessary to saturate the air. The higher the temperature, the more carbon bisulphide is necessary to saturate it, within certain limits. Evaporation of the liquid takes place more slowly in lower temperatures, and more time will therefore be required for the total dosage to become effective. It has been found that active insects are more susceptible than inactive ones to the effects of the gas, and insect activity varies directly with the increase of temperature within certain limits. Though the fumes from carbon bisulphide are highly inflammable, and under certain conditions explosive, there is practically no danger involved, if the proper precautions are taken. There must be no fire or. source of fire near, while the fumigation is being done. If the ' va or is sufficiently dense, an ex losion mi ht result from even a small P . P g source of fire like a lighted cigar, or a spark from an electric light or fan. In a temperature above 297 degrees F, the fumes may ignite without the presence of flame. The extensive discussion of the danger of the use of carbon bisulphide as a fumigant has resulted in a popular opinion that many accidents occur “bygitsuse. jyhenjhevpfdargigziil-k . éofiuzrflwcoo poem we Zmwww 3w: W33,» fiiwcww “$3 "powwwmizh A> 35L THE OowrEA WEEviL. 85 volved is understood, however, and the proper precautions in its use are observed, the likelihood of any accident is removed. The experiments giving the best results were conducted in a mean average temperature ranging from 75 to 81 degrees F. This work was done in the fumigation house shown in Plate V1’. The inside measurements of this building are 8 feet by 8 feet by 8 feet, giving it a contents of 512i cubic feet. It is tightly constructed throughout with matched lumber. The sides and ceiling within are lined with beaver board. The floor is constructed with a double layer of matched lumber, and covered with a heavy coat of paint to make it impervious. The total cost of material and construction was $70.00. Table 24.—Fumigation with Carbon Bisulphide. E Temperature Humidity .,_., q; d.) Charge Exposure '9 wt ‘O 1,000 Cu.Ft. § E _ _ g g 5 Z Max. Min. Mean Max. Min. Mean m x 9 pounds, . . . . 24 hours. . . . . E 43 88 63 75.5 58 44 51.0 0 100 9 pounds. . . . . 24 hours . . . . . . L 474 88 63 75.5 58 44 51.0 0 100 9 ounds. . . .. 24 hours. . .. . . P 134 88 63 75.5 58 44 51.0 0 100 C ec . . . . . . .. Untreated.... E 28 88 63 75.5 58 44 51.0 92.5 Check . . . . . . . . Untreated. . . . L 130 88 63 75.5 58 44 51.0 100.0 . Check . . . . . . . . Untreated. . . . P 60 88 63 75. 5 58 44 51.0 100.0 . .. . . 6 pounds. . . .. 24 hours. . . . . E 133 94 63 78.5 54 13 33.5 0 100 6 pounds. . . . . 24 hours... . . . L 246 94 63 78.5 54 13 33.5 0 100 6 pounds. . . .. 24 hours. . . . . P 67 94 63 78.5 54 13 33.5 0 100 Check . . . . . . . . Untreated. . . . E 38 94 63 78. 5 54 13 33.5 92.1 . . . . . Check . . . . . . . . Untreated. . . . - L 116 94 63 78.5 54 13 33. 5 100 . . . . . Check . . . . . . . . Untreated. . . . P 106 94 63 78. 5 54 13 33.5 100 . . . . . 4 pounds. . . . . 24 hours. . . . . E 44 99 63 81 58 36 47 0 100 4 pounds. . . . . 24 hours. . .. . . L 470 99 63 81 58 36 47 0 100 4 pounds. . . . . 24 hours... . . . P 267 99 63 81 58 ‘ 36 47 O 100 Check . . . . . . . . Untreated. . . . E 48 99 63 81 58 36 47 89.8 . . . . . Check . . . . . . . . Untreated. . . . L 50 99 63 81 58 .36 47 98.0 . . . . . Check . . . . . . . . Untreated. . . . P 47 99 63 81 58 36 47 100. O . . . . . The advantages of fumigating in a building of this ‘type are many, and few of the most important ones may be mentioned here. First: it is cheaper because a large quantity of seed may be treated in a single operation with the same dosage of carbon bisulphide. Second: the building can be utilized for the storage of treated seed; it is particularly adaptable for this purpose because it is Weevil-proof and treated seed will not become reinfested. Third: the results obtained are more sat- isfactory because leakage is reduced to a minimum. Temperature re- mains nearer the normal, which is desirable to get the best penetration of the fumes. The results that were obtained from experiments conducted in this fumigator are given in detail in Table 24. The different- stages in which the weevil was exposed are represented by E for eggs, L for larvae, and P for pupae. The temperature and relative humidity were taken by a recording hygro-thermograph placed on the floor beside the exposed cowpeas. It should always be remembered that the treated cowpeas are subject to reinfestation if they are not stored properly in weevil-proof containers or bins. 86 TEXAS AGRICULTURAL EXPERIMENT STATION. H eat. It is a. long-established fact that heat is a satisfactory insecticide where it can be employed economically. It is particularly applicable to species oi’ insects attacking stored grains which are not seriously affected by temperatures sufficiently high so as to destroy the insects and not injure the texture or the germination of the seed. Table 25.—Efl'ect of Heat on Egg Stage. Temp. Exposure Age Per Cent Per_ Cent Temp. Exposure Age Per Cent Per Cent (degrees)! (IIIIIL) (days) Emerged Killed (degrees) (m1n.) (days) ‘Emerged Killed | < l 12O 5 1 85 15 12O 10 1 0 100 120 5 2 80 2O 12O 1O 2 65 35 120 5 3 9O 1O 12O 10 3 75 25 120 5 4 85 15 12O 10 4 60 4O 12O 5 5 85 15 12O 10 5 75 25 126 5 1 75 25 126 1O 1 0 lOO 126 5 2 95 5 126 1O 2 4O 60 126 5 3 6O 4O 126 1O 3 85 15 126 5 4 55 45 126 1O 4 60 4O 126 5 5 6O 4O 126 1O 5 4O 60 130 5 1 8O 20 130 10 1 1O 9O 130 5 2 3O 70 130 1O 2 45 55 130 5 3 9O 1O 13O 1O 3 65 35 130 5 4 7O 3O 130 1O 4 45 55 130 5 5 85 15 130 1O 5 35 65 136 5 1 25 75 136 1O 1 O 10O 136 5 2 25 75 136 1O 2 O lOO 136 5 3 10O 136 1O 3 5 95 136 5 4 55 45 136 10 4 2O 80 136 5 5 6 0 136 10 5 0 100 140 5 1 O lOO 140 1O 1 O 10O 140 5 2 O lOO 140 10 2 O lOO 140 5 3 5 5 140 1O 3 0 10O 140 5 4 O 1OO 140 1O 4 O 10O 140 5 5 5 95 140 1O 5 O 10O 146 5 1 O 10O 146 1O 1 O 10O 146 5 2 O 10O 146 1O 2 O 10O 146 5 3 O 10O 146 10 3 O 10O 146 5 4 O lOO 146 1O 4 O 10O 146 5 5 0 lOO 146 1O 5 O 10O 150 5 1 O lOO 15O 1O 1 O lOO 15O 5 2 O lOO 150 1O 2 0 lOO 15O 5 3 O lOO 15O 10 3 O 10O 15O 5 4 O 1OO 15O 1O 4 0 10O 150 5 5 O 1OO 15O 1O 5 _ O 10O Effect of Heat on Larval Stage. Temp. Exposure Age Per Cent Per_ Cent Temp. Exposure Age Per Cent Per Cent (degrees) (m1n.) (days) Emerged Killed (degrees) (min.) (days) Emerged Killed 12O 5 1 85 15 12O 1O 1 90 1O 12O 5 2 9O 1O 12O 10 2 85 15 120 5 3 90 1O 12O 1O 3 9O 10 12O 5 4 7 3O 12O 1O 4 8O 2O 12O 5 5 10O O 12O 1O 5 10O O 12O 5 6 95 5 12O 1O 6 75 25 120 5 7 76 24 12O 1O 7 95 5 120 5 8 75 25 12O 1O 8 85 15 12O 5 9 95 a 12O 10 9 9O 1O 12O 5 1O 85 15 12O 1O 1O 8O 20 12O 5 over 1O 85 15 12O 1O over 1O 9O 1O 126 5 1 85 15 126 1O 1 15 85 126 5 2 7O 3O 126 1O 2 10O 126 5 3 8O 2O 126 1O 3 15 85 126 5 4 8O 2O 126 1O 4 80 2O 126 5 5 8O 20 126 1O 5 55 45 126 5 6 5 45 126 1O 6 ' 2O 8O 126 5 7 10O O 126 1O 7 6O 4O 126 5 8 95 5 126 1O 8 91 9 126 5 9 75 25 126 1O 9 85 15 126 5 1O 95 5 126 1O 1O 95 THE OOWPEA XVEEvIL. 87 Effect of Heat on Larval Stage-—C0ntinued. 1d an Temp. Exposure Age Per Cent Per_ Cent Temp. Expqsure Age Per Cent Per_ Cent (degrees) (min) (days) Emerged Kxlled (degrees) (m1n,) (days) Emerged Kllled 126 5 over 10 75 25 126 10 over 10 85 15 130 5 80 2O 130 10 1 O 100 130 5 85 15 130 10 2 25 75 130 5 3 75 25 130 10 3 0 1OO 130 5 4 8O 20 130 10 4 80 20 130 5 5 100 0 130 1O 5 1O 9O 130_ 5 6 85 15 130 10 6 0 100 130 5 7 85 15 130 1O 7 1O 9O 130 5 8 81 19 130 10 8 15 85 130 5 9 85 15 130 10 9 1O 9O 130 5 1O 80 20 130 1O 10 7O 3O 130 5 over 1O 100 O 130 1O over 1O 100 0 136 5 1 3O 7O 136 1O 1 0 100 136 5 2 2O 80 136 10 2 0 100 136 5 3 O 1OO 136 10 3 O 100 136 5 4 25 75 136 1O 4 0 100 136 5 5 5O 5O 136 10 5 O 100 136 5 6 67 33 136 1O 6 O lOO 136 5 7 70 30 136 10 7 O 100 136 5 8 50 5O 136 10 8 O 100 136 5 9 95 136 1O 9 0 100 136 5 1O 100 O 136 1O 1O 3Q’ 7O 136 5 over 1O 100 _ 136 1O over 10 75 25 140 5 1 O 100 14O 10 1 O 100 140 5 2 O 100 140 1O 2 O 100 140 5 3 5 95 140 1O 3 0 100 140 5 4 0 100 140 1O 4 O 100 140 5 5 O 100 140 10 5 O 100 140 5 6 0 100 140 1O 6 0 100 140 5 7 15 85 140 10 7 O 100 140 5 8 0 100 140 1O 8 O 100 140 5 9 10 9O 140 10 9 O 100 140 5 10 0 100 140 10 10 0 100 140 5 over 1O O 1OO 140 10 over 10 O 1()O _146 5 1 O 100 146 10 1 O 100 146 5 2 0 100 146 1O 2 O 100 146 5 3 O lOO 146 1O 3 0 100 146 5 4 0 100 146 l0 4 O 100 146 5 5 0 100 146 10 5 0 100 146 5 6 5 95 146 10 6 O 100 146 5 7 0 100 146 10 7 0 100 146 5 8 0 100 146 1O 8 O 1OO 146 5 9 O 100 146 1O 9 O 100 146 5 1O 0 lOO 146 1O 1O 0 100 146 5 over 1O 0 100 146 10 over 1O O 100 150 5 1 0 100 150 10 1 O 100 150 5 2 O 100 150 1O 2 O 100 150 5 3 0 100 150 1O 3 O 100 150 5 4 0 100 150 1O 4 O 100 150 5 5 0 100 150 10 5 0 100 150 5 6 0 100 150 10 6 0 100 150 5 7 0 100 150 1O 7 0 100 150 5 8 0 100 150 10 8 O 100 150 5 9 0 100 150 10 9 0 100 150 5 1O O 100 150 1O 10 ' 0 100 150 5 over 10 O lOO 150 10 over 10 0 100 Effect of Heat on Pupal Stage. l X I Temp. ‘Expqsure Age \Per Cent Per_ Cent Temp. Expqsure Age Per Cent Per_ Cent (degrees)i (m1n.) (days) ‘iEmerged Kllled (degrees) (m1n.) (days) Emergedi Kllled i , ‘ ‘ 12o 5 1 l s5 15 120 10 1 90 i 10 120 5 2 100 O 120 10 2 85 15 120 5 3 95 5 120 10 3 90 10 120 5 4 100 O 120 1O 4 lOO 0 120 5 5 90 1O 120 10 5 100 0 120 5 over 5 100 1 0 120 10 over 5 85 ' 15 126 5 1 95 5 126 1O 1 95 5 126 5 2 90 1O 126 10 2 90 i 10 126 5 3 95 5 126 1O 3 86 14 12s 5 4 75 25 12s 10 4 s5 i 15 126 5 5 9O 1O 126 10 5 90. 1O 126 5 over 5 85 15 126 10 over 5 80 2O 88 TEXAS AGRICULTURAL EXPERIMENT STATION. Effect of Heat on Pupal Stage-Continued. Temp. Exposure Age Per Cent Per_Cent Temp. Exposure Age Per Cent Per Cent (degrees) (min) (days) Emerged Killed (degrees) (m1n.) (days) Emerged Killed 130 5 1 100 0 130 10 1 90 10 130 5 2 90 1O 130 10 2 35 65 130 5 3 90 10 130 10 3 25 75 130 5 4 90 1O 130 10 4 80 20 130 5 5 85 15 130 l0 5 85 15 130 5 over 5 95 130 10 over 5 95 5 136 5 1 85 15 136 10 1 10 90 136 5 2 20 136 10 2 35 65 136 5 3 100 136 10 3 0 100 136 5 4 100 0 136 10 4 22 78 136 5 5 85 15 136 10 5 85 15 136 5 over 5 55 136 1O over 5 5 95 140 5 1 100 140 1O 1 O ~ 100 140 5 2 6O 4 140 10 2 O 100 140 5 3 35 65 140 10 3 0 100 140 5 4 5O 50 140 1O 4 O 100 140 5 5 0 100 140 1O 5 O 100 140 5 over 5 0 100 140 1O over 5 O 100 146 5 1 . 0 100 146 1O 1 0 100 146 5 2 5 146 l0 2 0 100 146 5 3 0 100 146 1O 3 O 100 146 5 4 0 100 146 1O 4 0 lOO 146 5 5 0 100 146 1O 5 0 100 146 5 over 5 0 100 146 1O over 5 0 100 150 5 1 O 100 150 10 1 O 100 150 5 2 0 100 150 1O 2 O 100 150 5 3 0 100 150 1O 3 O 100 150 5 4 O 100 150 1O 4 O 100 150 5 O 100 150 10 0 100 150 5 over 5 0 100 150 1O over 5 0 100 A series of experiments to determine the effect of heat on the various stages of the cowpea weevil were conducted and the results are given in detail in Table 25. All this work was done under laboratory con- ditions and every possible precaution was taken to obtain results un- influenced by other factors. A double-lined, two-hole Boss oven with a tight-fitting base to prevent undue circulation of air, was used. The bottom of the oven was lined with a sheet of asbestos to insure a more uniform temperature from the source of heat applied beneath it. With this arrangement the temperature within the oven could be held prac- tically constant, at most varying not more than one degree. Only dry heat was employed, the source being a gas flame. The temperatures were recorded from a thermometer suspended on a level with the infested cowpeas exposed in thin wire baskets.- Cowpeas containing a normal moisture content were used in all cases. It will be noted that only short time exposures were used with a large variation in temperature. This was done for two reasons: first, it was found by preliminary experiments, that a sufficiently high temperature and short exposure could be employed to kill the weevil without seriously affecting the germination of the seed; second. if heat is to be employed for weevil control in a commercial way, it appears very desirable to turn over the produce in as short time as possible. i In order to determine the exact temperature which will destroy all stages of the weevil, the eggs, larvae, and pupae at a difference in age of 24 hours, were exposed. It was found that greater mortality occurred in the younger material, the resistance to withstand heat increasing with age. Referring to Table .25, it will be noted that no temperature for either a five or ten minute exposure produced satisfactory results under 140 degrees F. At a temperature of 140 degrees F. for ten THE CowrEA WEEVIL. 89 minutes exposure the point at which nearly all weevil life is destroyed is being approached; in fact, no emergence took place in any stage at this temperature and exposure. However, a temperature of 146 degrees F. for five minutes’ exposure did not destroy all the developing weevils, but when the exposure was increased to ten minutes all the weevils in each stage were destroyed. It should be remembered that since these experiments were conducted under most favorable conditions, which might not be readily duplicated in a practical way, due allowance must be made for variations in results obtained. The germination of the seed is not affected by this temperature and it is advisable to increase the exposure to twenty or thirty minutes in all cases where the tempera- ture cannot be held constant and large quantities of cowpeas are being treated. Efiect of Heat 0n Germination. Uninfested cowpeas of the same lot used in the experiments on heat control, were exposed in a similar man.ner for five and ten minutes’ exposures to temperatures ranging from 120 to 200 degrees F. In order to obtain complete information relative to the effect of heat on the seed, they were planted in» the field and notes were taken on the character of plants produced, While the per cent. of germination was obtained. The results are given in Table 26. It will be noted that the per cent. of germination did not seem to be seriously affected at any temperature under 190 degrees F, though weak plants occurred con- sistently from exposure to a temperature of 1'? 0 degrees F. Everything below 150 degrees F. with four exceptions produced normal and vigor- ous plants. Table 26.—Effect of Heat on Germination. Temperature, Exposure, Number Number Per Cent Degrees Min. Planted Germ. Strong Weak Germ. 120 . . . . . . . . . . . . . . . . . 5 2O 2O 2O O lOO 120 . . . . . . . . . . . . . . . .. 10 20 19 19 0 95 126 . . . . . . . . . . . . . . . .. 20 18 18 0 90 126 . . . . . . . . . . . . . . . .. 10 20 20 20 0 100 130 . . . . . . . . . . . . . . . .. 20 20 20 0 100 130 . . . . . . . . . . . . . . . . . 1O 2O 2O 19 1 100 136 . . . . . . . . . . . . . . . .. 20 18 18 0 90 136 . . . . . . . . . . . . . . . .. 10 20 19 18 1 95 140 . . . . . . . . . . . . . . . .. 20 20 20 0 100 14O . . . . . . . . . . . . . . . . . 1O 2O 18 17 1 9O 146 . . . . . . . . . . . . . . . .. 20 19 19 1 95 146 . . . . . . . . . . . . . . . .. 10 20 20 20 0 100 150 . . . . . . . . . . . . . . . . . 2O 19 19 O 95 150 . . . . . . . . . . . . . . . . . 1O 2O 2O 2O O IOO 156 . . . . . . . . . . . . . . . .. 20 20 18 2 100 156 . . . . . . . . . . . . . . . .. 10 20 20 19 1 100 160 . . . . . . . . . . . . . . . .. 20 20 20 0 100 160 . . . . . . . . . . . . . . . .. 10 20 19 19 0 95 166 . . . . . . . . . . . . . . . .. 20 19 18 1 95 166 . . . . . . . . . . . . . . . .. 10 20 18 18 0 90 170 . . . . . . . . . . . . . . . . . 5 2O 2O 17 3 1OO 170 . . . . . . . . . . . . . . . .. 10 20 17 15 2 85 180 . . . . . . . . . . . . . . . .. 5 20 19 17 2 95 180 . . . . . . . . . . . . . . . .. 10 20 18 16 2 90 186 . . . . . . . . . . . . . . . .. 5 20 19 17 2 95 186 . . . . . . . . . . . . . . . .. 10 20 18 16 2 90 190 . . . . . . . . . . . . . . . .. 5 20 18 15 3 90 190 . . . . . . . . . . . . . . . .. 10 20 17 15 2 85 196 . . . . . . . . . . . . . . . .. 5 20 19 16 3 95 I96 . . . . . . . . . . . . . . . .. 10 20 16 14 2 80 . . . . . . . . . . . . . . . .. 5 20 13 8 5 65 200 . . . . . . . . . . . . . . . .. 10 20 13 8 5 65 9O TEXAS AGRICULTURAL EXPERIMENT STATIoN. SUMMARY. The most common species of Weevil infesting cowpeas in Texas is Bruchus quadrvlnzaculcttus Fabr. It is found in all localities of this State where cowpeas are grown. The climatic conditions of Texas are especially favorable for the development of this insect. All varieties- of cowpeas grown in this locality are subject to attack, and no preference is shown by the Weevil to any particular variety. The annual loss in Texas to the cowpea crop, resulting from this insect, is very great. _ Under favorable conditions the life cycle from egg deposition to- emergence of the adult may be completed in less than three weeks. The weevil is very prolific. An average of 106 eggs have been produced by females during the warm season. Temperature has a positive influence on the rate of oviposition and the length of the various stages of the Weevil. In stored seed breeding is practically continuous throughout the year. Most WQQVIIS undoubtedly hibernate in stored seed. Nine generations of weevils occur in a year at College Station. Three .natural enemies of the immature stages of the weevil were found: a predacious mite, a chalcid, and an egg parasite. The weevil, however, is not sufliciently checked by its natural enemies, and remedial and artificial control measures must be employed. Proper harvesting will greatly reduce the initial infestation of the field. To prevent seed from becoming reinfested it must be stored in tight bins or containers. The weevil can be destroyed in any stage by heating the infested seed to a temperature of 1~3l~6 degrees F. for an exposure of fifteen minutes, which will not affect the germination of the seed. Fumigation with carbon bisulphide is an effective means of destroying the cowpea weevil and, used at the rate of four pounds for a thousand cubic feet of space with. a 24-hour exposure, it will kill the insect in all of its stages. Fumigated and “processed” or heated seed is always subject‘ to rein— festation by the weevil. LITERATURE CITED. (1) 1792. Fabricus, Ento. Syst. I, 2, p. 371. Original description with habitat. (2) 1795. Olivier, Historie Naturelle des Insects, IV, '79, p. 19. Habitat. (3) 1801. Fabricus, Syst. El., II, p. 398. Description. (4) 1824. Say, Entomology, I, p. 259. Specimens taken at New Orleans. Habitat includes Santa Cruz. (5) ' 1853. Le Conte, Revision of Say Entomology, I, p. 259. Crit- icizes systematic position of species. (6) 1872. Horn, Trans. Am. Ent. Soc, IV, p. 318. ,Technical description of species. ('7) 1885._ Riley and Howard, Insect Life, V, p. 165. Infested ' table beans from Texas. (8) 1893. Riley, C. V., Insect Life, VI, 3, p. 220. In beans from Brazil and Venezuela at V\7orld’s Fair. (9) 1893. Beckwith, M. H., Del. Bull. 21, p. 10. In peas from North Carolina. THE CoWPEA WVEEVIL. 91 (10) 1893. Slingerland, M. V ., Psyche, VI, p. 447. Introduced in peas from the South. (11) 1894. Hamilton, John, Trans. Am. Ent. Soc., XXI, p. 400. Records species. (12) 1895. Osborn and Mally, Ia. Sta. Bull. 32, p. 161. Descrip- tion of stages. _ (13) 1896. Chittenden, F. H., Bur. Ent. Bull..8 n. s., p. 27. Dis- tribution. BIBLIOGRAPHY. Ashmead, Wm. H. 1894. Notes on Insects Found in Mississippi. Ins. Life, vol. V.II, No. 3, p. 246. Found in cotton blooms. Bandi, F. 1890. Dent. Ent. Zeit., p. 338. Records localities. Beckwith, M. H. 1893. Del. Bull. 21, p. 10. Weevils in North Caro- lina cowpeas determine-d to be B. quadrimaculatus. Remedy is carbon bisulphide. Blatchley, W. S. 1910. Coleoptera o1’ Indiana, p. 1237. Listed. Chittenden, F. H. 1896. Insects Injurious to Vegetables, pp. 105-107. Description, occurrence, habits, life history. Effect of carbon bisulphide on larvae and pupae. Effect on germination. Chittenden, F. H. 1897. Some Little-known Insects Affecting Stored Vegetable Products, U. S. D. A. Div. Ent. Bull. 8 (n. s.), p. 27. Occurrence, distribution, and parasitic enemies. Chittenden, F. H. 1898. Insects Injurious to Beans. U. S. D. A. Yearbook, 1898, p. 245. Distribution, history, and remedy are iven. Chittgenden, F. H. 1898. Yearbook U. S. D. A._, 1898, p. 247. Pre- dacious mites of coWpea weevil are given. Chittenden, F. H. 1912. The Cowpea Weevil. U. S. D. A. Bur. Ent. Bull. 96, pt. 6, pp. 83-94. Species just mentioned. Currie, R. P. 1905. Cat. of the Exhibit of Eco. Ent. at the Lewis & Clark Centennial Exposition. U. D. A. Bur. Ent. Bull. 53, p. 50. Refers to Chittenden, in U. S. Yearbook, 1898. Duvel, J. W. F. 1905.’ Cold Storage for Cowpeas. U. S. D. A. Bur. Ent. Bull. 54, pp. 49-54. Cold as a preventive measure. Fabricus. 1792. 96 Bastrichus Ento. Syst, vol. I, pt. 2, p. 371. De- scription given. Fabricus. 1801. Brychus. Syst. El., II, p. 398. Description given. Fink, D. E. 1914. Ammonia Gas as a Fumigant. Jr. E0. Ent., VII (1914), 1, p. 149. Experiments on CoWpea Weevil. ' Hamilton, John, 1894. Distribution of Coleoptera. Trans. Am. Ent. Soc., XXI, p. 400. Records B. quadrimaculatus. Horn, Geo. H. 1872. Revision of the Bruchidac of the U. S. Trans. Amer. Ent. Soc., vol. IV, p. 318. Technical description of struct- ural characters. Variations mentioned. Difference between B. scutellaris and B. quadrimaculatus. Krall, J. A. 1914. The Cowpea Weevil. Okla. Sta. Cir. 31, p. 8. Notes on controlling the coWpea Weevil. . Le Conte, J. L. 1853. Revision of Say Entomology, I, p. 259. Criticizes systematic position of species. _ O’Kane, Wj C. 1912. Injurious Insects, p. 366. Habits and Life History. Remedy given. 92 ‘Fnxxs AGRICULTURAL EXPERIMENT STATION. Olivier. 1795. Historic. N aturelle des Insects, vol. IV, No. '79, p. 19. Distribution. v Osborn, H., and Mally, C. W. 1895. Entomological Work for 1895. Iowa Sta. Bull. 32, pp. 161-407, pl. 1, fig. II. Description. Ex- periments With carbon bisulphide. Pettit, R. H. 1910. Mich. Exp. Sta. Bull. 258. Injury and remedy are given. Price, R. H. 1894. Insects Injurious to Stored Grains. Texas Bull. 31, p. 466. Occurrence, injury and tests of preventives. Quaintance, A. L. 1896. Insects Injurious to Stored Grain. Fla. Bull. 36, p. 3'71. Brief notes on distribution, life history, and habits. Riley and Howard. 1893. Food-plants of N. Am. Species of Bruchus. Insect Life, vol. V, p. 165. Notes on species. Riley, C. V. 1894. Insects Which Occurred in Grain and Other Stored Vegetable Products at the World’s Fair. Insect Life, vol. VI, No. 3, p. 220. Common in the Southern States. In beans from Brazil and Venezuela. Sanborn, C. E. 1914. Garden and Crop Pests. Okla. Sta. Bull. 100, p. 12. Description and remedies are given. Sanderson, D. W. 1912. Insect Pests of F. O. & G., p. 312. De- scription, occurence, life history, and remedial measures. Say, Thos. 1859. American Entomology, vol. I, p. 259. Distribution. Skaife, S. H. 1918. Pea and Bean Weevils, Bull. 12, Union of S. A. Dept. of Agr. Brief account. Slingerland, M. V. 1893. B. quadrimaculatus Fabn, Psyche, vol. VI, p. 447. Occurrence, and life history are given. Steadman, J. M. 1895. Insects Injurious to Stored Grain. Ala. College Sta. Bull. 61, p. 51. Mentions occurrence. Titus and Pratt. 1904. Cat. of Exhibit of Eco. Ent. at the La. Ex- position. U. S. D. A. Bur. Ent. Bull. 4'7, p. 86. -Refers to Chittenden, U. S. Yearbook, 1898. Urich, F. W. 1918. The Black-eye Pea Weevil. Bull. Dept. Agr., Trinidad, pt. 1, vol. XVII. Complete account as Pachymerus.