scholarly journals Temperature-dependent sex determination in the Kemp’s ridley sea turtle: effects of incubation temperatures on sex ratios

2012 ◽  
Vol 19 (2) ◽  
pp. 123-128 ◽  
Author(s):  
AM LeBlanc ◽  
T Wibbels ◽  
D Shaver ◽  
JS Walker
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.


2021 ◽  
Vol 288 (1943) ◽  
pp. 20202819
Author(s):  
Sarah L. Whiteley ◽  
Arthur Georges ◽  
Vera Weisbecker ◽  
Lisa E. Schwanz ◽  
Clare E. Holleley

Sex determination and differentiation in reptiles is complex. Temperature-dependent sex determination (TSD), genetic sex determination (GSD) and the interaction of both environmental and genetic cues (sex reversal) can drive the development of sexual phenotypes. The jacky dragon ( Amphibolurus muricatus ) is an attractive model species for the study of gene–environment interactions because it displays a form of Type II TSD, where female-biased sex ratios are observed at extreme incubation temperatures and approximately 50 : 50 sex ratios occur at intermediate temperatures. This response to temperature has been proposed to occur due to underlying sex determining loci, the influence of which is overridden at extreme temperatures. Thus, sex reversal at extreme temperatures is predicted to produce the female-biased sex ratios observed in A. muricatus . The occurrence of ovotestes during development is a cellular marker of temperature sex reversal in a closely related species Pogona vitticeps . Here, we present the first developmental data for A. muricatus , and show that ovotestes occur at frequencies consistent with a mode of sex determination that is intermediate between GSD and TSD. This is the first evidence suggestive of underlying unidentified sex determining loci in a species that has long been used as a model for TSD.


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.


2018 ◽  
Vol 222 (1) ◽  
pp. jeb190215 ◽  
Author(s):  
Melanie D. Massey ◽  
Sarah M. Holt ◽  
Ronald J. Brooks ◽  
Njal Rollinson

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.


2007 ◽  
Vol 4 (2) ◽  
pp. 176-178 ◽  
Author(s):  
Rajkumar S Radder ◽  
Alexander E Quinn ◽  
Arthur Georges ◽  
Stephen D Sarre ◽  
Richard Shine

An individual's sex depends upon its genes (genotypic sex determination or GSD) in birds and mammals, but reptiles are more complex: some species have GSD whereas in others, nest temperatures determine offspring sex (temperature-dependent sex determination). Previous studies suggested that montane scincid lizards ( Bassiana duperreyi , Scincidae) possess both of these systems simultaneously: offspring sex is determined by heteromorphic sex chromosomes (XX–XY system) in most natural nests, but sex ratio shifts suggest that temperatures override chromosomal sex in cool nests to generate phenotypically male offspring even from XX eggs. We now provide direct evidence that incubation temperatures can sex-reverse genotypically female offspring, using a DNA sex marker. Application of exogenous hormone to eggs also can sex-reverse offspring (oestradiol application produces XY as well as XX females). In conjunction with recent work on a distantly related lizard taxon, our study challenges the notion of a fundamental dichotomy between genetic and thermally determined sex determination, and hence the validity of current classification schemes for sex-determining systems in reptiles.


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.


2013 ◽  
Vol 280 (1772) ◽  
pp. 20132460 ◽  
Author(s):  
Timothy S. Mitchell ◽  
Jessica A. Maciel ◽  
Fredric J. Janzen

Evolutionary theory predicts that dioecious species should produce a balanced primary sex ratio maintained by frequency-dependent selection. Organisms with environmental sex determination, however, are vulnerable to maladaptive sex ratios, because environmental conditions vary spatio-temporally. For reptiles with temperature-dependent sex determination, nest-site choice is a behavioural maternal effect that could respond to sex-ratio selection, as mothers could adjust offspring sex ratios by choosing nest sites that will have particular thermal properties. This theoretical prediction has generated decades of empirical research, yet convincing evidence that sex-ratio selection is influencing nesting behaviours remains absent. Here, we provide the first experimental evidence from nature that sex-ratio selection, rather than only viability selection, is probably an important component of nest-site choice in a reptile with temperature-dependent sex determination. We compare painted turtle ( Chrysemys picta ) neonates from maternally selected nest sites with those from randomly selected nest sites, observing no substantive difference in hatching success or survival, but finding a profound difference in offspring sex ratio in the direction expected based on historical records. Additionally, we leverage long-term data to reconstruct our sex ratio results had the experiment been repeated in multiple years. As predicted by theory, our results suggest that sex-ratio selection has shaped nesting behaviour in ways likely to enhance maternal fitness.


1985 ◽  
Vol 63 (11) ◽  
pp. 2543-2547 ◽  
Author(s):  
Lin Schwarzkopf ◽  
Ronald J. Brooks

Temperature-dependent sex determination was studied in a northern population of painted turtles (Chrysemys picta) in both laboratory and field. Eggs incubated at constant temperatures of 30 and 32 °C produced females only, whereas those kept at 22, 24, and 26 °C produced males only. Both sexes occurred at 20 and 28 °C. The threshold temperatures (temperatures producing 50% males) were estimated to be 27.5 and 20.0 °C, and were similar to those reported for more southerly populations of C. picta. In both 1983 (a relatively warm summer) and 1984 (an average summer), temperatures in natural nests regularly fluctuated above and below both threshold temperatures. Mean nest temperatures were warmer in 1983 than in 1984, but were not useful to predict nest sex ratios. Mean nest temperatures were not similar to constant temperatures in their effect on sex ratio. Sex ratios in nests could be described best by the total number of hours for which the temperature at each nest was intermediate to the two threshold temperatures. Sex ratios (proportion male) of hatchlings in 1983 and 1984 were similar and female biased (0.12 and 0.13, respectively).


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