RESUMEN
The process of testicular maturation in relation to intrapuparial development was studied in the sheep nasal bot fly, Oestrus ovis L. (Diptera: Oestridae). After formation of the puparium during larval-pupal apolysis and the cryptocephalic pupal stage (approximately 24-72 h), spermatogonia had undergone mitotic divisions and sperm cysts had been formed. Five days after pupariation, spermatogonia transformed into primary spermatocytes during the phanerocephalic pupal stage, and secondary spermatocytes first appeared during the pupal-adult apolysis. Secondary spermatocytes began undergoing the second meiotic division by day 8 (transparent-eye pharate adult stage). By days 9 and 10, round spermatids were present and began to elongate by day 11. By day 12, the first bundles of tailed spermatozoa had appeared. By day 15 (the yellow-orange eye pharate adult stage), round, elongated, tailed and bundled spermatids were predominant and by day 17 differentiating spermatids occupied nearly 35% of the testicular cavity, and 60% was occupied by free sperm. By day 21 (the red-brown eye pharate adult stage), spermatozoa colonized the seminal vesicle. At emergence (approximately day 22), a complement of free sperm occupied the testis and the seminal vesicle, but groups of developing cells frequently remained in certain zones. Spermatogenesis was carried out after pupariation and spermiogenesis occurred during the pharate adult stage. After emergence, males possessed fully formed spermatozoa ready for ejaculation.
Asunto(s)
Dípteros/crecimiento & desarrollo , Enfermedades de las Cabras/parasitología , Espermatogénesis/fisiología , Testículo/crecimiento & desarrollo , Animales , Dípteros/fisiología , Cabras , Histocitoquímica , Masculino , Testículo/fisiologíaRESUMEN
Observations of fly strikes or larvipositions (n=68 in 21 days of observation) were carried out in a herd of goats during the spring in Baja California Sur, Mexico in order to identify the climatic conditions favoring larviposition activity of gravid Oestrus ovis L. flies, as well as to investigate whether a mixture of some potentially useful compounds was involved in this behavior. Hand-caught, tethered flies (n=43) were either exposed or unexposed to a combination of carbon dioxide, humidity, 1-octen-3-ol, butyric, propionic, acetic acid and acetone released from movable sheep and goat dummies under open field and cage conditions. Fly strikes occurred at temperatures greater than 20 degrees C, but mainly between 25 and 28 degrees C and from 116 to 838W m(-2) of solar irradiance. Few or no strikes were seen under moderate or strong wind, but did occur in a wide range of relative humidity. The chemicals applied did not improve the capacity of animal dummies to induce the flies to larviposit, but very irregular behavior was observed. Fourteen larvipositions were made on the dummies lacking chemical stimuli, so visual ability and movement by the dummies was very important in stimulation of the flies. Temperature appeared to be the main factor determining fly activity, but wind and solar irradiance also played important roles. Characteristics of O. ovis larviposition are discussed.
Asunto(s)
Dípteros/fisiología , Infestaciones Ectoparasitarias/veterinaria , Animales , Femenino , Enfermedades de las Cabras , Cabras , Larva/fisiología , Postura , Embarazo , TemperaturaRESUMEN
The phenology of intrapuparial development in Oestrus ovis L. is described, based on 302 specimens collected from the head cavities of goats and reared in the laboratory at a photoperiod of 12:12 (L:D) h and 32 and 16 degrees C. Dissection and histology of puparia at pupariation and at 3, 6, 9, 12, 15, 18, 21, 24, 30, 36, 42, 48, 66, and 72 h after pupariation and every day of the intra-puparial period showed that pupariation was achieved in approximately 12 h in heavily pigmented larvae (range, 2-46 h in postfeeding period). Larval-pupal apolysis began immediately after pupariation and was completed by 18-36 h after pupariation (prepupal period). The cryptocephalic pupa was found from this time to the 5th d, when head eversion occurred. Pupal-adult apolysis was initiated before head eversion and completed by day 7. The pharate adult presented progressive coloration in compound eyes (transparent, white, yellow, orange, red, brown, silver) while integumental pigmentation and sclerotization were in progress. Adult emergence occurred at 22 and 23 d in males and females, respectively. Changes in the weekly puparial weight of specimens reared under both field and laboratory conditions was described. It was concluded that although the intra-puparial development of O. ovis displayed some unique characteristics, it was essentially similar to other cyclorraphous flies. The actual pupal period of O. ovis lasted from the 2-7 d post-pupariation, whereas approximately two-thirds of the intra-puparial period was used for the maturation of the pharate adult.
Asunto(s)
Dípteros/crecimiento & desarrollo , Enfermedades de las Cabras/parasitología , Miasis/veterinaria , Animales , Cabras , Larva , Miasis/parasitología , Pupa/crecimiento & desarrolloRESUMEN
Microanatomical characteristics and the size of the ovaries of Oestrus ovis L. during development were related to the intrapuparial-phenological stadia. Mature 3rd instars were collected from the head cavities of slaughtered goats, and pupae were reared under laboratory conditions. The length of freshly dissected ovaries and follicles were measured daily after pupal-adult apolysis to emergence. Ovarian tissue was stained using the PAS-Picroindigocarmine techniques. Oocyte development was classified according to a six-stage scale previously used in oestrid species. Shortly after pupal-adult apolysis, the single primary follicle is still unseparated from the germarium. In early white-eyed pharate adults, the primary follicle of stage 1 separates from the germarium, the nurse cells and oocyte are surrounded by a layer of cuboidal follicular cells, and the remaining oogonia degenerate. Oocytes in stage 2 initiate yolk deposition becoming ovoid, and this occurs when pharate adults have white-yellow to orange eyes. Oocytes in stage 3 are mainly vitellogenic, during the orange to red-eye stage. In stage 4, oocytes complete vitellogenesis and nurse cells degenerate when pupae achieve 90-96% of development. Mature oocytes of stage 5 can be found at emergence. Ovaries and ovarioles increase in size because of yolk deposition. O. ovis begins oogenesis as pharate adults, whereas vitellogenesis occurs during 55-96% of pupal development. Females emerge with one life-long complement of eggs ready to be fertilized, similar to other species of the Family Oestridae.