scholarly journals Temperature-dependent sex-biased embryo mortality in a bird

2008 ◽  
Vol 275 (1652) ◽  
pp. 2703-2706 ◽  
Author(s):  
Yvonne A Eiby ◽  
Jessica Worthington Wilmer ◽  
David T Booth

Sex ratios have important evolutionary consequences and are often biased by environmental factors. The effect of developmental temperature on offspring sex ratios has been widely documented across a diverse range of taxa but has rarely been investigated in birds and mammals. However, recent field observations and artificial incubation experiments have demonstrated that the hatching sex ratio of a megapode, the Australian brush-turkey ( Alectura lathami ), varied with incubation temperature; more females hatched at high incubation temperatures and more males hatched at low temperatures. Here, we investigated the causes of this temperature-dependent sex-biasing system. Molecular sexing of chicks and embryos confirmed that male embryo mortality was greater at high temperatures while female embryo mortality is greater at low temperatures, with mortality in both sexes similar at intermediate incubation temperatures. Temperature-dependent sex-biased embryo mortality represents a novel mechanism of altering sex ratios in birds. This novel mechanism, coupled with the unique breeding biology of the brush-turkey, offers a potentially unparalleled opportunity in which to investigate sex allocation theory in birds.

1999 ◽  
Vol 77 (9) ◽  
pp. 1465-1473 ◽  
Author(s):  
Matthew H Godfrey ◽  
Adriana F D'Amato ◽  
Maria  Marcovaldi ◽  
N Mrosovsky

Like all other species of sea turtle, the hawksbill turtle (Eretmochelys imbricata) exhibits temperature-dependent sexual differentiation, with high incubation temperatures producing females and low temperatures producing males. Relatively little is known about the sex ratios of hatchlings produced by nesting populations of hawksbill turtles. Here we estimate the overall seasonal sex ratios of hatchling hawksbill turtles produced in Bahia, Brazil, during 6 nesting seasons, based on incubation durations, pivotal temperature, and pivotal incubation duration. The overall sex ratio of hatchlings produced in Bahia from 1991-1992 through 1996-1997 was estimated to be >90% female, which is more female-biased than estimated sex ratios of hatchling loggerhead turtles from Bahia and Florida, U.S.A. The biological and conservation implications of skewed sex ratios are discussed.


2021 ◽  
Author(s):  
◽  
Kelly Maree Hare

<p>The conditions under which reptilian eggs are incubated affect survival probability and physiological attributes of the progeny. The egg-laying skink, Oligosoma suteri, is the only endemic oviparous lizard in New Zealand. No controlled laboratory incubation had previously been undertaken, and thus no information was available on the requirements for successful captive incubation. I studied the effects of incubation regime on the eggs and hatchlings of O. suteri to four months of age. Oligosoma suteri eggs (n = 174) were randomly distributed among three constant incubation temperatures (18°C, 22°C and 26°C) and two water potentials (-120 kPa and -270 kPa). Hatching success and hatchling survival were greatest at 22°C and 26°C, with hatchlings from 18°C incubation suffering from physical abnormalities. Incubation regime and maternal influence did not affect sex of individuals, with equal sex ratios occurring from each incubation treatment. Hatchlings from the 22°C and -120 kPa incubation treatments were larger, for most measurements, and warmer incubation temperatures resulted in increased growth rates. Juveniles from 22°C and 26°C and individuals with greater mass per unit length (condition index) sprinted faster over 0.25 m. Sprint speed was positively correlated with ambient temperature. At four months of age sprint speed decreased in 18°C individuals and individuals incubated at 26°C and -270 kPa compared to their performance at one month. The results suggest that the most successful captive incubation regime for O. suteri is 22°C and -120 kPa. This study also shows that temperature-dependent sex determination does not occur in O. suteri, but that fitness traits are influenced by incubation temperature.</p>


1977 ◽  
Author(s):  
K. Breddin ◽  
H.J. Krzywanek

ADP-, collagen and epinephrine-induced aggregation change markedly if citrate blood or PRP are kept at different incubation temperatures or/and if the time interval between blood sampling and testing varies. With a growing time interval the response of PRP to ADP, collagen or epinephrine increases. Desaggregation after ADP-aggregation decreases with time. If PRP is incubated at 4°C or 10°C aggregation is increased in comparison with room temperature. At 37°C aggregation is markedly inhibited. This inhibitory effect is almost fully reversible several hours after blood sampling. Corresponding results were obtained with PAT III, measuring spontaneous aggregation tendency. Morphologic platelet changes show some correlation with the time and temperature dependent changes of the aggregation pattern. In clinical studies the time interval between blood sampling and testing and the incubation temperature of PRP should be strictly controlled. If enhanced platelet aggregation is to be studied the time interval between venepuncture and performance of the test should be 30 - 60 min for ADP-or collagen-induced aggregation and between 90 and 360 min for PAT III. PRP should always be kept at 20 - 25°C.


2017 ◽  
Vol 284 (1848) ◽  
pp. 20162576 ◽  
Author(s):  
Graeme C. Hays ◽  
Antonios D. Mazaris ◽  
Gail Schofield ◽  
Jacques-Olivier Laloë

For species with temperature-dependent sex determination (TSD) there is the fear that rising temperatures may lead to single-sex populations and population extinction. We show that for sea turtles, a major group exhibiting TSD, these concerns are currently unfounded but may become important under extreme climate warming scenarios. We show how highly female-biased sex ratios in developing eggs translate into much more balanced operational sex ratios so that adult male numbers in populations around the world are unlikely to be limiting. Rather than reducing population viability, female-biased offspring sex ratios may, to some extent, help population growth by increasing the number of breeding females and hence egg production. For rookeries across the world ( n = 75 sites for seven species), we show that extreme female-biased hatchling sex ratios do not compromise population size and are the norm, with a tendency for populations to maximize the number of female hatchlings. Only at extremely high incubation temperature does high mortality within developing clutches threaten sea turtles. Our work shows how TSD itself is a robust strategy up to a point, but eventually high mortality and female-only hatchling production will cause extinction if incubation conditions warm considerably in the future.


1994 ◽  
Vol 143 (2) ◽  
pp. 279-289 ◽  
Author(s):  
D Crews ◽  
J M Bergeron

Abstract In many turtles the temperature during the middle of incubation determines the gonadal sex of the hatchling. In the red-eared slider turtle (Trachemys scripta), an incubation temperature of 26 °C results in all male offspring, whereas an incubation temperature of 31 °C results in all female offspring; at temperatures intermediate to these (e.g. 29, 29·2, 29·4 °C) a mixed sex ratio is obtained. Administration of exogenous oestrogens will overcome the effects of an all-male producing incubation temperature to cause female sex determination, whereas administration of exogenous dihydrotestosterone (DHT) or testosterone to eggs incubating at an all-female temperature will have no discernible effect. Administration of DHT will cause male sex determination only if administered at intermediate incubation temperatures whereas administration of testosterone to eggs incubating at all male-producing and male-biased intermediate temperatures results in a significant number of female offspring, an effect presumably due to aromatization of testosterone to oestradiol (OE2), Since testosterone serves as the precursor to both DHT and OE2, being metabolized by reductase and aromatase respectively, three experiments were conducted to determine whether various putative reductase and aromatase inhibitors would overcome the effect of incubation temperature. First, while administration of testosterone to eggs incubating at all male-producing and male-biased intermediate temperatures produced females in a dose- and temperature-dependent manner, significant numbers of intersex individuals resulted from high dosage testosterone treatment to eggs incubating at a female-biased intermediate temperature. The reductase inhibitors 4MA and MK906 were capable of producing female offspring if administered at intermediate temperatures, but not in a dose-dependent fashion. Administration of the aromatase inhibitors CGS16949A and CGS20267 resulted in male offspring at both female-biased intermediate and at all female-producing temperatures in a dose-dependent fashion. Second, similar findings were obtained with combined doses of testosterone and reductase or aromatase inhibitors. Combined treatment of eggs at male-biased intermediate incubation temperatures with testosterone and reductase inhibitor resulted in female hatchlings, whereas combined treatment of testosterone and aromatase inhibitor at both female-biased intermediate and at all female-producing temperatures resulted in male hatchlings. Finally, treatment with reductase inhibitor and aromatase inhibitor combined resulted in only male offspring at all incubation temperatures with the exception of the all-female incubation temperature; in the latter instance almost all offspring were female. These studies indicate that in the red-eared slider turtle (i) male and female sex determination are independent cascades residing equally in each individual and regulated by incubation temperature, (ii) steroid hormones are involved in temperature-dependent sex determination, and (iii) testosterone plays a pivotal role in this process. The data also suggest that aromatase and oestrogen receptors may be involved in the initiation of an ovary determining cascade and that reductase and androgen receptors may be involved in the initiation of a testis determining cascade. Journal of Endocrinology (1994) 143, 279–289


1991 ◽  
Vol 69 (10) ◽  
pp. 2693-2696 ◽  
Author(s):  
Thane Wibbels ◽  
Flavius C. Killebrew ◽  
David Crews

Sex determination was investigated in Cagle's map turtle, Graptemys caglei, which has a restricted distribution which is the southernmost of all Graptemys species. This species exhibits temperature-dependent sex determination, with high incubation temperatures producing only females and low temperatures producing only males. The estimated pivotal temperature (approximately 30.0 °C) is higher than those reported for other species of Graptemys in North America; however, the interspecific variations in pivotal temperature are small (approximately 0.5–1.0 °C). Temperature appears to affect the ovarian or testicular nature of the gonads in an "all or none" fashion, but exerts a graded effect on the length of ovaries. In addition, temperature appears to exert a graded effect on the regression of the oviducts in males. The occurrence of temperature-dependent sex determination in this species is also of conservational importance, since alterations to a single river system could potentially impact the reproductive success of this species by changing nest temperatures and, thus, population sex ratio(s).


1991 ◽  
Vol 18 (2) ◽  
pp. 225 ◽  
Author(s):  
M Palmer-Allen ◽  
F Beynon ◽  
a Georges

Eastern long-necked turtles, Chelodina longicollis, are known to lack heteromorphic sex chromosomes and to lack temperature-dependent sex determination when incubated under constant conditions. This study determined whether sex ratios of hatchlings emerging from natural nests of C. longicollis were different from that expected from constant temperature experiments. Temperatures in the eight nests monitored varied considerably each day (by 1.7-12.6�C), with eggs at the top of the nest experiencing the greatest variation (mean range 9.0�C) and eggs at the bottom experiencing least variation (mean range 5.3�C). Temperatures experienced by the top and bottom eggs differed by as much as 5.7�C at any one time. No monotonic seasonal trend was evident, but rainfall caused a sharp drop in nest temperatures. Sex ratios in hatchlings from 14 field nests of C. longicollis did not differ significantly from 1:1, a result in agreement with previous studies conducted at constant incubation temperatures in the laboratory.


1992 ◽  
Vol 70 (2) ◽  
pp. 391-394 ◽  
Author(s):  
Cory R. Etchberger ◽  
Michael A. Ewert ◽  
Beth A. Raper ◽  
Craig E. Nelson

The sex of painted turtles (Chrysemys picta) is determined by the incubation temperature of the egg. At high temperatures (> 30 °C), all females are produced, with a transition to all males at most lower temperatures (24–27 °C). However, two of three previous studies have reported that some females also result when incubation temperatures are low (20–22 °C). In this study C. picta eggs were incubated at low temperatures (21.5 and 22.5 °C); however, macroscopic and histological examination of both embryos and hatchlings did not confirm these reports. Thus, C. picta has, at least typically, the pattern of sex determination that is most common among the genera to which it is most closely allied.


1995 ◽  
Vol 73 (11) ◽  
pp. 2091-2097 ◽  
Author(s):  
Vanessa Lewis-Winokur ◽  
Robert M. Winokur

Eggs of captive desert tortoises. Gopherus agassizi, incubated at six temperatures (25, 27, 28, 29, 29.4, and 31 °C) produced 107 specimens. Eggs incubated at 31 °C resulted in a male to female sex ratio of 5:7; all other incubation temperatures resulted in males only. Histological examination of gonads revealed that the testes of newly hatched to 3-month-old individuals showed incomplete and poorly developed seminiferous tubules. Female gonads showed a thickened cortex. Incubation times were longer at lower temperatures. Both hatching success and hatchling survivorship were lower at lower incubation temperatures. We confirm that temperature-dependent sex determination occurs in desert tortoises and that the pivotal temperature is between 31 and 32 °C.


1996 ◽  
Vol 149 (3) ◽  
pp. 457-463 ◽  
Author(s):  
D Crews ◽  
A R Cantú ◽  
J M Bergeron

Abstract This study addressed the hypothesis that, in the red-eared slider turtle, Trachemys scripta, non-aromatizable androgens are the physiological equivalent of temperature in determining male development. In the first experiment, eggs were treated in the middle of the temperature-sensitive period with 1·0 or 10·0 μg androsterone, 5α-dihydrotestosterone, 3α-androstanediol, or 3β-androstanediol, while at an all-male, male-biased, or one of two female-biased incubation temperatures. In the second experiment, eggs were treated with the same dosages of dihydrotestosterone at different stages of embryonic development while at a male-biased, threshold, or a female-biased incubation temperature. Results of experiment one indicated that hormone-induced masculinization is specific to non-aromatizable androgens. Results of experiment two indicated that the sensitivity to dihydrotestosterone corresponds to the temperature-sensitive window during development. Further, there is a dose–response relationship but no apparent synergism between exogenous dihydrotestosterone and incubation temperature. When considered with other research, it is suggested that non-aromatizable androgens and their products are involved in the initiation of male sex determination whereas oestrogens and their aromatizable androgen precursors are involved in the initiation of female sex determination. Journal of Endocrinology (1996) 149, 457–463


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