Sex Determination and Sex Ratios of Pacific Leatherback Turtles, Dermochelys coriacea

Copeia ◽  
1998 ◽  
Vol 1998 (2) ◽  
pp. 291 ◽  
Author(s):  
Christopher A. Binckley ◽  
James R. Spotila ◽  
Kathryne S. Wilson ◽  
Frank V. Paladino
2021 ◽  
Vol 112 (2) ◽  
pp. 155-164
Author(s):  
Suzanne Edmands

Abstract Rising global temperatures threaten to disrupt population sex ratios, which can in turn cause mate shortages, reduce population growth and adaptive potential, and increase extinction risk, particularly when ratios are male biased. Sex ratio distortion can then have cascading effects across other species and even ecosystems. Our understanding of the problem is limited by how often studies measure temperature effects in both sexes. To address this, the current review surveyed 194 published studies of heat tolerance, finding that the majority did not even mention the sex of the individuals used, with <10% reporting results for males and females separately. Although the data are incomplete, this review assessed phylogenetic patterns of thermally induced sex ratio bias for 3 different mechanisms: sex-biased heat tolerance, temperature-dependent sex determination (TSD), and temperature-induced sex reversal. For sex-biased heat tolerance, documented examples span a large taxonomic range including arthropods, chordates, protists, and plants. Here, superior heat tolerance is more common in females than males, but the direction of tolerance appears to be phylogenetically fluid, perhaps due to the large number of contributing factors. For TSD, well-documented examples are limited to reptiles, where high temperature usually favors females, and fishes, where high temperature consistently favors males. For temperature-induced sex reversal, unambiguous cases are again limited to vertebrates, and high temperature usually favors males in fishes and amphibians, with mixed effects in reptiles. There is urgent need for further work on the full taxonomic extent of temperature-induced sex ratio distortion, including joint effects of the multiple contributing mechanisms.


Ecosphere ◽  
2011 ◽  
Vol 2 (7) ◽  
pp. art84 ◽  
Author(s):  
Scott R. Benson ◽  
Tomoharu Eguchi ◽  
Dave G. Foley ◽  
Karin A. Forney ◽  
Helen Bailey ◽  
...  

2004 ◽  
Vol 118 (1) ◽  
pp. 72 ◽  
Author(s):  
Donald F. McAlpine ◽  
Stan A. Orchard ◽  
Kelly A. Sendall ◽  
Rod Palm

Marine turtles in British Columbia have previously been considered off course stragglers. Here we document 20 new reports for Green Turtles, Chelonia mydas, and Leatherback Turtles, Dermochelys coriacea, for the province. Until recently there had been no concerted effort to acquire data on marine turtle abundance or frequency off British Columbia. Observations presented here allow a reassessment of marine turtle status in British Columbia waters. We suggest Green Turtles and Leatherbacks should be considered rare vagrants and uncommon seasonal residents, respectively, off British Columbia and that they are a natural part of the British Columbia marine environment.


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

2000 ◽  
Vol 23 (1) ◽  
pp. 97-103 ◽  
Author(s):  
Lincoln S. Rocha ◽  
André Luiz P. Perondini

In sciarid flies, the control of sex determination and of the progeny sex ratio is exercised by the parental females, and is based on differential X-chromosome elimination in the initial stages of embryogenesis. In some species, the females produce unisexual progenies (monogenic females) while in others, the progenies consist of males and females (digenic females). The sex ratio of bisexual progenies is variable, and departs considerably from 1:1. Bradysia matogrossensis shows both monogenic and digenic reproduction. In a recently established laboratory strain of this species, 15% of the females were digenic, 10% produced only females, 13% produced only males, and 62% produced progenies with one predominant sex (33% predominantly of female and 29% predominantly male progenies). These progeny sex ratios were maintained in successive generations. Females from female-skewed progenies yielded female- and male-producing daughters in a 1:1 ratio. In contrast, daughters of females from male-skewed progenies produce bisexual or male-skewed progenies. The X-chromosome of B. matogrossensis shows no inversion or other gross aberration. These results suggest that the control of the progeny sex ratio (or differential X-chromosome elimination) involves more than one locus or, at least, more than one pair of alleles. The data also suggest that, in sciarid flies, monogeny and digeny may share a common control mechanism.


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