INFLUENCE OF DATE OF OVIPOSITION ON EGG HATCHING AND EMBRYO SURVIVAL IN THE RED TURNIP BEETLE, ENTOMOSCELIS AMERICANA (COLEOPTERA: CHRYSOMELIDAE)

1984 ◽  
Vol 116 (4) ◽  
pp. 645-652 ◽  
Author(s):  
G. H. Gerber

AbstractEmbryological development and hatching for the red turnip beetle, Entomoscelis americana Brown, were studied at 20 °C. In eggs kept at this temperature for > 12 days, embryological development proceeded until a late stage embryo was formed, at which time the embryo entered diapause for the winter. The time required for 50% of the eggs to reach the late embryo stage was estimated to be 11 days. The late embryo stage was not reached before winter in eggs kept at 20 °C for < 11 days, but most of them survived and hatched. Embryogenesis proceeded normally after winter without any apparent adverse effects, and hatching was delayed by the amount of time required to complete embryogenesis. Although it was not essential for the eggs to reach the late embryo stage to overwinter successfully and hatch, a critical minimum stage of development had to be reached during embryogenesis for the eggs to survive. The critical minimum stage of development occurred in the germ band formation stage and was reached during the first 1.5 days of embryogenesis. Most of the eggs laid from 1 to 15 September 1980 and kept outdoors reached the late embryo stage before winter and hatched the next spring; those laid from 15 September to 15 October reached the critical minimum stage of development before winter and also hatched successfully; and those laid after 15 October did not hatch, because they apparently had not reached the critical minimum stage. An evaluation of the data for the eggs kept outdoors and of atmospheric air temperature data suggested that embryo death due to eggs not reaching the critical minimum stage of development before winter normally should not be an important factor in the population dynamics of E. americana in the rapeseed- and canola-growing areas of western Canada. The ecological significance of the data is discussed.

1967 ◽  
Vol 99 (9) ◽  
pp. 952-971 ◽  
Author(s):  
P. W. Riegert

AbstractA brief historical review of the occurrence of the clear-winged grasshopper, Camnula pellucida (Scudd.), is presented as well as recent information pertaining to the biology of its various life stages. In the egg stage, diapause is more successfully terminated by chilling at 5 °C for 70 days than at either 0 or −7 °C. Embryological development proceeded very favourably at incubation temperatures of 30 °C while 35 °C produced excessive mortality especially to pre-blastokinesis embryos. Most embryos in eggs of this species reach the same pre-blastokinesis stage of development more consistently every year than do those of other pest species of grasshopper in Saskatchewan. Thirty days of chilling at −12, −18, and −23 °C reduced the viability of the eggs by about 10, 20, and 50% respectively. Exposure to −29 °C killed all eggs in 3.5 to 5 hours.The phototactic and thermokinetic reactions of nymphs and adults, leading to aggregation, basking, and dispersal, are discussed and compared with those of other species. Details of nymphal migrations are described and related to such meteorological factors as wind, temperature, and position of the sun. Some further details of mating and oviposition are described, especially aggregation on egg beds and oviposition in stubble fields. Observations of predation by sandhill cranes and skunks are also recorded.


PLoS Biology ◽  
2011 ◽  
Vol 9 (7) ◽  
pp. e1001115 ◽  
Author(s):  
Hannah S. Seidel ◽  
Michael Ailion ◽  
Jialing Li ◽  
Alexander van Oudenaarden ◽  
Matthew V. Rockman ◽  
...  

1990 ◽  
Vol 122 (2) ◽  
pp. 329-341 ◽  
Author(s):  
Christian Hébert ◽  
Conrad Cloutier

AbstractRelationships between temperature and development rates of eggs and larvae of Winthemia fumiferanae Toth. were experimentally determined, using the spruce budworm as host. Hatching of parasitoid eggs was triggered by host pupation. The median time required to complete egg development at different temperatures was estimated from distributions of percentage development success of the parasitoid over time between egg deposition and host pupation. For parasitoid eggs that had sufficient time to hatch, detachment from the host before pupation was the most important cause of mortality at 15 °C or higher, but was negligible below this temperature. A curvilinear model describing egg development rate as a function of temperature was used to simulate the development of W. fumiferanae eggs in the field. The relationship between larval development rate and temperature also was modelled, and the variability described. Simulations initiated by host pupation-driven egg hatching, and terminated with prepupal drop to the ground, are presented and discussed with respect to the appropriateness of using host pupation as an indicator of parasitoid egg hatching in the field.


1973 ◽  
Vol 30 (6) ◽  
pp. 799-810 ◽  
Author(s):  
Peter J. Colby ◽  
L. T. Brooke

Embryonic development of lake herring (Coregonus artedii) was observed in the laboratory at 13 constant temperatures from 0.0 to 12.1 C and in Pickerel Lake (Washtenaw County, Michigan) at natural temperature regimes. Rate of development during incubation was based on progression of the embryos through 20 identifiable stages.An equation was derived to predict development stage at constant temperatures, on the general assumption that development stage [Formula: see text] is a function of time (days, D) and temperature (T). The equation should also be useful in interpreting estimates from future regressions that include other environmental variables that affect egg development.A second regression model, derived primarily for fluctuating temperatures, related development rate for stage [Formula: see text], expressed as the reciprocal of time, to temperature (x). The generalized equation for a development stage is:[Formula: see text]In general, time required for embryos to reach each stage of development in Pickerel Lake agreed closely with the time predicted from this equation, derived from our laboratory observations. Hatching time was predicted within 1 day in 1969 and within 2 days in 1970.We used the equations derived with the second model to predict the effect of the super-imposition of temperature increases of 1 and 2 C on the measured temperatures in Pickerel Lake. Conceivably, hatching dates could be affected sufficiently to jeopardize the first feeding of lake herring through loss of harmony between hatching date and seasonal food availability.


Parasitology ◽  
1921 ◽  
Vol 13 (4) ◽  
pp. 327-347 ◽  
Author(s):  
N. Cunliffe ◽  
G. H. F. Nuttall

1. Copulation between individuals of the two species O. moubata, and O. savignyi may occur, and the stimulus of coition may induce oviposition, the eggs being non-fertile.2. There is no evidence of parthenogenesis in this species, nor do these ticks undergo ecdysis after reaching maturity.3. An increase in temperature of 8° C. from 22° C. (a) doubles the.rate of oviposition, (b) decreases the fertility of the eggs by 30 per cent., (c) reduces the longevity of the female tick from 715 to 397 days, i.e. by 40 per cent, and (d) approximately halves the period required for metamorphosis, under laboratory conditions. Under these conditions at 37° C., reproduction is inhibited, and the longevity of the female is reduced by 80 per cent.4. An individual may undergo from four to eight ecdyses before reaching maturity, the great majority of the males appearing after the fifth ecdysis and the females about equally after the fifth and sixth ecdyses.5. Engorgement can take place one or two days after emergence, at any stage, the average time required being three-quarters of an hour. There is great variation in the extent of engorgement at each stage, but this is not correlated with the ecdysis period. The largest meal may be taken either before or after an individual reaches maturity.6. Moisture has an adverse influence on the vitality of the individual, excess of moisture inhibiting growth.7. An approximation to the stage of development attained can be made after the study of the structure of the hypostome, leg and spiracle. The larval and first four nymphal stages are fairly well differentiated, much more so than the later stages, but variation due to nutrition requires further study.


1948 ◽  
Vol 80 (1-12) ◽  
pp. 83-88 ◽  
Author(s):  
H. W. Moore

A study of embryological development in grasshopper eggs was made as a part of a general study of the effect of weather on the seasonal development of grasshoppers. The variation in the stage of development in which eggs of Melanoplus bivittatus (Say), Melanoplus mexicanus mexicanus (Sauss.), and Camnula pellucida (Scud.) entered the winters of 1941 to 1947 in different areas of the Prairie Region of Canada is presented in the following paper.


2004 ◽  
Vol 55 (5) ◽  
pp. 589 ◽  
Author(s):  
K. L. Bayliss ◽  
J. M. Wroth ◽  
W. A. Cowling

Several species of lupin (Lupinus spp.) are grown in Australia as crop and pasture plants. Lupin breeding, and legume breeding in general, is constrained by the inability to produce doubled haploid (DH) plants, which would accelerate the selection and release of new varieties. This technology is still in the developmental phase for legumes, although other major grain crops such as wheat, barley, and canola successfully use DHs on a commercial scale. A new, reproducible method of microspore culture that leads to cell division and pro-embryos in lupin is reported here. Microspores at the late uninucleate stage of development are mechanically isolated from lupin buds and embryogenesis induced by a combined heat shock and sucrose starvation stress treatment. Addition of further components to the growth medium promotes division of up to 50% of microspores to ≥16 cells within 24 h. Further development of these multicellular structures or pro-embryos appears to be limited by the rigid outer exine layer, which needs to rupture for continued cell division to the globular embryo stage. Further research is required to break this barrier to development of haploid lupin embryos.


Author(s):  
E.M. Koloskova ◽  
◽  
V.A. Ezerskii ◽  
T.P. Trubitsina ◽  
◽  
...  

The survival rate of rabbit embryos microinjected by the plasmid form of CRISPR/Cas9 components specific to the sour whey protein gene was evaluated. At high concentrations of plasmid components, embryo survival decreased slightly, possibly because the WAP gene does not belong to the housekeeping genes. After microinjection of a genetic construct with a sequence of green fluorescent protein under a cytomegalovirus promoter, the embryo survival significantly decreased. This is most likely due to the superexpression of GFP at the 2-16 cell stage of development.


2020 ◽  
Vol 98 (11) ◽  
Author(s):  
Peter J Hansen

Abstract Typically, bovine embryos are transferred into recipient females about day 7 after estrus or anticipated ovulation, when the embryo has reached the blastocyst stage of development. All the biological and technical causes for failure of a female to produce a blastocyst 7 d after natural or artificial insemination (AI) are avoided when a blastocyst-stage embryo is transferred into the female. It is reasonable to expect, therefore, that pregnancy success would be higher for embryo transfer (ET) recipients than for inseminated females. This expectation is not usually met unless the recipient is exposed to heat stress or is classified as a repeat-breeder female. Rather, pregnancy success is generally similar for ET and AI. The implication is that either one or more of the technical aspects of ET have not yet been optimized or that underlying female fertility that causes an embryo to die before day 7 also causes it to die later in pregnancy. Improvements in pregnancy success after ET will depend upon making a better embryo, improving uterine receptivity, and forging new tools for production and transfer of embryos. Key to accelerating progress in improving pregnancy rates will be the identification of phenotypes or phenomes that allow the prediction of embryo competence for survival and maternal capacity to support embryonic development.


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