scholarly journals Population viability at extreme sex-ratio skews produced by temperature-dependent sex determination

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.

2021 ◽  
Author(s):  
Ellen Porter ◽  
David T Booth ◽  
Col J Limpus

All sea turtles exhibit temperature-dependent sex-determination, where warmer temperatures produce mostly females and cooler temperatures produce mostly males. As global temperatures continue to rise, sea turtle sex-ratios have become increasingly female-biased, threatening the long-term viability of many populations. Nest temperatures are dependent on sand temperature, and heavy rainfall events reduce sand temperatures for a brief period. However, it is unknown whether these short-term temperature drops are large and long enough to produce male hatchlings. To discover if short-term temperature drops within the sex-determining period can lead to male hatchling production, we exposed green and loggerhead turtle eggs to short-term temperature drops conducted in constant temperature rooms. We dropped incubation temperature at four different times during the sex-determining period for a duration of either 3 or 7 days to mimic short-term drops in temperature caused by heavy rainfall in nature. Some male hatchlings were produced when exposed to temperature drops for as little as 3 days, but the majority of male production occurred when eggs were exposed to 7 days of lowered temperature. More male hatchlings were produced when the temperature drop occurred during the middle of the sex-determining period in green turtles, and the beginning and end of the sex-determining period in loggerhead turtles. Inter-clutch variation was evident in the proportion of male hatchlings produced, indicating that maternal and or genetic factors influence male hatchling production. Our findings have management implications for the long-term preservation of sea turtles on beaches that exhibit strongly female-biased hatchling sex-ratios.


2021 ◽  
pp. 1-9
Author(s):  
Horacio Merchant-Larios ◽  
Verónica Díaz-Hernández ◽  
Diego Cortez

The discovery in mammals that fetal testes are required in order to develop the male phenotype inspired research efforts to elucidate the mechanisms underlying gonadal sex determination and differentiation in vertebrates. A pioneer work in 1966 that demonstrated the influence of incubation temperature on sexual phenotype in some reptilian species triggered great interest in the environment’s role as a modulator of plasticity in sex determination. Several chelonian species have been used as animal models to test hypotheses concerning the mechanisms involved in temperature-dependent sex determination (TSD). This brief review intends to outline the history of scientific efforts that corroborate our current understanding of the state-of-the-art in TSD using chelonian species as a reference.


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

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).


2015 ◽  
Vol 45 ◽  
pp. 125-130
Author(s):  
Ayrton Vollet-Neto ◽  
Charles Fernando dos Santos ◽  
Leandro Rodrigues Santiago ◽  
Denise de Araujo Alves ◽  
Júlia Pinheiro de Figueiredo ◽  
...  

The sex determination system in the eusocial stingless bees (Apidae, Meliponini) is based on the combination of alleles at the complementary sex determination (CSD) locus. In this system, males are haploid and females are diploid. However, diploid males can develop from fertilized eggs when they are homozygous at single or multiple sex loci. The production of such males can negatively affect population viability, since they are usually infertile or inviable. Moreover, when they are viable but infertile, or siring sterile triploid offspring, this could cause another load on the population, leading the fertilized offspring of other females to be only haploid males or triploid sterile daughters. In this context, our aim was to verify whether diploid males of the stingless bee Scaptotrigonadepilis do in fact join reproductive aggregations. We showed that of 360 marked males from two different colonies, five were participating in a reproductive aggregation ca. 20 meters from their natal colonies. Using microsatellites markers, it was confirmed that three of these five males were diploid. They were captured in the mating aggregations when they were 15 to 20 days old. Further research is necessary to determine the mating success of stingless bee diploid males under natural conditions and to determine their impact on stingless bee population extinction risks.


2021 ◽  
Author(s):  
◽  
Nicola J Nelson

<p>Juveniles resulting from artificially induced and incubated eggs are often used to found or augment populations of rare reptiles, but both procedures may compromise the health of hatchlings or their fitness in natural environments. I aimed to test whether these procedures affected size or performance of juvenile tuatara, Sphenodon punctatus, New Zealand reptiles with temperature-dependent sex determination (TSD). Size and performance are phenotypic traits likely to influence fitness and eventual lifetime reproductive success, and are thus important measures of the suitability of artificial induction and incubation techniques for conservation management. I incubated 320 tuatara eggs artificially at 18, 21 and 22ºC; 52% of these were obtained by induction, the remainder were collected from natural nests. An additional 25 natural nests were left intact for investigation of TSD and effects of incubation temperature in nature. Juveniles from all incubation regimes were kept for ten months post-hatching in similar rearing conditions and sexed by laparoscopy. Induced eggs were significantly smaller than naturally laid eggs, and resulted in significantly smaller hatchlings, even when variation among clutches was accounted for. Incubation temperature did not greatly influence size at hatching, but was an important determinant of size by ten months of age; initial egg mass was the most important factor affecting size of hatchlings. Data indicate that TSD occurs in nature. The sex of hatchlings from 21 nests was investigated: 10 nests produced 100% male hatchlings, 4 nests produced 100% female hatchlings, and only 7 nests produced mixed sex ratios which ranged from 11% to 88% males. Sex of juveniles was related to temperature with a larger proportion of males produced in warmer nests. The overall percentage of male hatchlings in natural nests was 64%. Hatching success was 65% from natural nests during the 1998/99 season. Incubation temperatures throughout the year ranged from 2.9 to 34.4ºC. Global warming is likely to skew the hatchling sex ratio towards males if female tuatara are unable to select nest sites according to environmental cues. Evidence from size patterns of tuatara incubated in natural nests supports differential fitness models for the adaptive significance of TSD. The evaluation of artificial incubation as a conservation management tool demonstrated that it is a procedure that benefits conservation as it can be used reliably to produce founders; hatching success was 94% during this study. The sex ratio of artificially incubated juveniles can be easily manipulated; the pivotal temperature lies between 21 and 22ºC. Constant artificial incubation conditions resulted in larger juveniles by ten months of age than those from natural incubation. Naturally incubated juvenile tuatara, however, were faster for their size, their reaction norm to predator stimuli was to run, and they were possibly more aggressive, suggesting naturally incubated juveniles could survive better in nature. No firm conclusions can be reached on the quality of artificially incubated juvenile tuatara because further research will be required to establish the relevance of performance test results in nature and consequences of incubation regimes in the longer term with respect to relative fitness of individuals.</p>


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