Maternally derived yolk hormones vary in follicles of the painted turtle, Chrysemys picta (original) (raw)
Related papers
Biology of Reproduction, 1999
Incubation temperature determines gonadal sex in the redeared slider turtle, Trachemys scripta. However, little is known about the long-term effects of incubation temperature on traits other than gonadal sex in this species. To investigate the hypothesis that incubation temperature (independent of gonadal sex) influences sex steroid levels after hatching, we incubated eggs of the red-eared slider turtle at three temperatures (26, 28.6, and 31؇C). We then measured plasma levels of dihydrotestosterone, estradiol, progesterone, and testosterone in 6-wkold males from 26؇C and 28.6؇C eggs, and in 6-wk-old females from 28.6؇C and 31؇C eggs. We found that dihydrotestosterone levels were not influenced by incubation temperature or gonadal sex. However, progesterone levels were significantly higher in males from 26؇C eggs than in males from 28.6؇C eggs. In contrast, testosterone levels did not differ between males from 26؇C versus males from 28.6؇C eggs, but they were significantly higher in females from 28.6؇C than in females from 31؇C eggs. Progesterone and testosterone levels did not differ between males and females from 28.6؇C eggs. Temperature also influenced estradiol levels in both sexes, but the effects were enigmatic. We conclude that incubation temperature has lasting effects on sex steroid levels even after hatching.
Embryonic sex steroid hormones accumulate in the eggshell of loggerhead sea turtle (Caretta caretta
Steroids hormones such as estradiol-17b (E2) and testosterone (T) are involved in gonadal differentiation of oviparous animals with temperature-dependent sex determination (TSD), and are greatly distributed. This hypothesizes that these embryonic steroid hormones probably accumulate in the eggshell throughout blood or/and chorioallantoic fluid in sea turtle species with TSD, producing females at higher temperature. To demonstrate this hypothesis, concentrations of E2 and T in the blood plasma from the hatchling loggerhead sea turtle (Caretta caretta) and in their eggshells were measured by radioimmunoassay. In the present study we propose that both concentrations of E2 and T in the blood plasma are correlated with amounts of these sex steroids in the eggshell. Moreover, contents of E2 in the eggshell showed a significant positive correlation with mean incubation temperatures during a thermosensitive period in the experimental nests, whereas T contents in the eggshell did not. Taken together, these findings indicated that embryonic E2 and T that accumulated in the eggshell can be extracted and measured. Furthermore, the present study suggested that contents of E2 in the eggshell may differ between male and female, and monitoring of these steroids is a useful method to identify the sex of loggerhead sea turtle hatchling.
General and comparative …, 2002
This study investigates the potential effects of maternally derived hormones present in the yolk of reptile eggs. Specifically, we ask when are these hormones utilized by developing red-eared slider turtles (Trachemys scripta elegans), a species with temperaturedependent sex determination (TSD). Eggs were incubated at 27°C, a male-producing temperature, and at 31°C, a female-producing temperature. Concentrations of progesterone, testosterone, and 17b-estradiol were measured at four points during development: at oviposition, at the start of the temperature sensitive period (TSP), at the end of the TSP, and at hatching. No effects of incubation temperature on yolk hormone concentrations were detected. The highest concentrations of all three hormones were measured at oviposition. Hormone-specific patterns of decline occurred throughout development. Each hormone declined between oviposition and the early TSP. Although estradiol was present in detectable quantities at oviposition, it was virtually undetectable by the early TSP. Testosterone showed no further decline after the early TSP. Progesterone continued to decline between the early and post-TSP. These results demonstrate that maternally derived yolk hormones decline at different rates. Alternative explanations for the disappearance of these yolk hormones are presented.
Synergism between temperature and estradiol: A common pathway in turtle sex determination?
Journal of Experimental Zoology, 1991
In many reptiles, the temperature at which the eggs are incubated determines the sex of the hatchlings. Administration of estradiol will counteract the masculinizing effects of a male-producing temperature, resulting in female hatchlings. To address whether temperature and estrogen are biologically equivalent, two experiments were conducted with the red-eared slider turtle, Trachemys scripta. In the first experiment, varying dosages of estrogen were administered at Stage 17 (the middle of the temperature-sensitive window) to eggs maintained at two temperatures, 26°C (which normally produces all males) and 28.2"C (which produces mostly males but lies at the threshold of the transition from male-to female-producing temperatures). Results indicate that estrogen and temperature exert a synergistic effect on sex determination. In the second experiment, estrogen was administered at different stages of embryonic development. The results indicate an estrogen-sensitive period ranging from Stage 14 through Stage 21, a period similar to the temperature-sensitive period for this species. The results of these experiments are consistent with the hypothesis that temperature and estradiol act in a common pathway in temperature-dependent sex determination.
General and Comparative Endocrinology, 1997
Reptile embryos with temperature sex determination have a thermosensitive period (TSP). The finding that exogenous estradiol (E2) overcomes the effect of malepromoting temperature led to the idea that temperature may regulate estrogen concentration in the gonad during TSP. Since interspecific variations in TSP and in the effect of exogenous E2 exist, we undertook a study in the olive ridley Lepidochelys olivacea. Four parameters were correlated: the TSP (time dimension), the thermosensitive stages (rate of development), gonad development (histological aspect), and the estradiol response. Two kinds of experiments were performed: (1) Eggs were shifted once, at different stages of development, from a male-promoting temperature to a female-temperature (or vice versa) for the remainder of development. (2) Eggs at male-promoting temperature were treated once with 6 or 12 mg of estradiol (E2) at various times of incubation. Sex ratio was established around hatching in each experimental series. We found that the temporal dimension of the TSP was around 7 days (Days 20-27 of incubation) at a male-promoting or a female-promoting temperature. The rate of development of the whole embryo and gonadal growth was faster at femalepromoting temperature than at male-promoting temperature. Formation of the genital ridge began at stage 21-22 and histological differentiation of the gonads occurred around stage 26-27. Although these stages coincided with the TSP, at male-promoting temperature the thermo-sensitive stages occurred earlier (from stages 20-21 to stages 23-24) than at female-promoting temperature (from stages 23-24 to stages 26-27). Thus, at male promoting-temperature, sex was determined in embryos with incipient or undifferentiated gonads. In contrast, E2 treatment continued to feminize the gonads of embryos at a male-promoting temperature beyond the TSP up to stage 25-26, but the E2-induced ovaries were significantly smaller than temperature-induced ovaries. It is suggested that the doses of E2 used were higher than the concentration of endogenous E2 required for normal sex determination. The lack of correlation between sex determination and gonad differentiation suggests that irreversible molecular processes underlying sex determination occur earlier at male-than at female-promoting temperature. Results suggest that the male sex may be the default state and that the female condition must be imposed upon it. r 1997 Academic Press Sexual differentiation of the gonads is dependent on incubation temperature in five sea turtle species: Eretmochelys imbricata , Lepidochelys olivacea Caretta caretta Mrosovsky, 1980, 1982), Chelonia mydas Limpus, 1980, Morreale et al., 1982), and Dermochelys coriacea . Pivotal temperatures (temperature during incubation at constant temperature which gives 50% individuals of each sexual
Concentrations of steroid hormones in layers and biopsies of chelonian egg yolks
General and Comparative …, 2001
The actions of circulating hormones, although relatively well understood for adults, are largely unknown for their developing embryos. Transfer of maternal hormones to the egg is known to occur in oviparous species, and recently the presence of hormonally heterogeneous yolk layers has been described in two avian species. To investigate the possibility of a similar phenomenon occurring in chelonian species, egg yolk layers were analyzed in the painted turtle (Chrysemys picta marginata) and the redeared slider turtle (Trachemys scripta elegans), two species that exhibit temperature-dependent sex determination. There was a similar pattern of hormonally heterogeneous yolk layers in both species: concentrations of progesterone and testosterone were significantly higher in the external yolk layer while concentrations of 17-estradiol were significantly higher in the intermediate and internal layers. This pattern of hormone deposition concurs with previously published studies of plasma hormone profiles from females of temperate-zone turtle species. Yolks of freshly laid eggs were also sampled using a biopsy technique to examine the concordance of early yolk hormone concentrations and offspring sex. No relationship was found between yolk hormone concentrations and individual offspring sex. Previous work showing that maternally derived yolk estradiol concentrations are correlated with female-biased sex ratios was, however, replicated. These findings suggest that off-spring sex is influenced, in part, by the maternal hormone environment.
Marine Biology, 2002
We collected data on plasma levels of testosterone+5a-dihydrotestosterone (T+DHT) and corticosterone (CORT) from adult female green sea turtles (Chelonia mydas) from southern Queensland during distinct stages of their reproductive cycle. Those females capable of breeding in a given year had elevated plasma steroid levels (T+DHT 0.91±0.08; CORT 1.05±0.29 ng/ml), associated with follicular development, until courtship began in October. At the beginning of the nesting season in November plasma levels of CORT were related to when the female first nested (r 2=0.06; F=10.45; P=0.01). However, they were not correlated with the number of clutches a female laid in that season (F=3.65; P=0.08). We repeatedly sampled 23 turtles over the nesting season and profiled changes in steroids immediately following oviposition of each clutch. Levels of T+DHT (range 0.41–0.58 ng/ml) and CORT (range 2.13–2.81 ng/ml) were similar through the early stages of the nesting season and inter-nesting period, and declined to near basal levels (T+DHT 0.37±0.03 and CORT 1.85±ng/ml) following the last clutch for the season. Steroid hormone levels were also low (T+DHT 0.38±0.16; CORT 0.46±0.21 ng/ml) in four independent post-breeding (atretic) females; samples for these females were taken at a time when body condition was presumably at the lowest for the season. Subtle changes in the nesting environment, such as variation in nesting habitat or the time of night that nesting occurred, were associated with a small and slow CORT increase. We suggest CORT is increased in nesting females to assist in lipid transfer to prepare the ovarian follicles and/or the reproductive organs for ovulation.
Maternally derived sex steroid hormones impact sex ratios of loggerhead sea turtles
An optimal sex ratio is arguably one of the most important demographic traits of species. Rising global temperatures threaten temperature-dependent sex determination (TSD) species with extreme sex ratio bias and ultimately extinction. Because sex steroid hormones can impact sex determination in TSD reptiles, variation in their maternal transfer within the egg yolk may form a buffer mechanism against raising temperatures. We tested this hypothesis by quantifying the effect of maternal oestradiol (E2) and testosterone (T) on offspring sex in a threatened TSD population of loggerhead sea turtles (Caretta caretta). Circulating levels of E2 and T in nesting females, in egg yolks at oviposition and in neonates were measured. Immediately after oviposition, nests were relocated into an in situ experimental hatchery where temperatures were controlled by standardising the incubation depth. We used affinity propagation clustering on hormone profiles guided by incubation duration, to sex indivi...
General and comparative …, 1996
triol treatment also resulted in cranially hypertrophied In many turtles the temperature during the middle of oviducts at all incubation temperatures in a dose-depenincubation determines the gonadal sex of the hatchling. dent manner, whereas animals treated with estradiol-Sex steroid hormones have been implicated in tempera-17b and estrone had normal oviducts. These results supture-dependent sex determination in the red-eared slider port the hypothesis that estrogens are involved in the turtle, Trachemys scripta; nonaromatizable androgens final common pathway of female sex determination in are involved in male sex determination and estrogens this species. ᭧ 1996 Academic Press, Inc. and aromatizable androgens in female sex determination. Administration of exogenous estradiol-17b to eggs incubating at a temperature that normally produces only In many reptiles gonadal sex is determined by the males can overcome the effect of temperature and result temperature of the incubating egg, a process known as in all offspring being female. Further, estradiol-17b and temperature-dependent sex determination (TSD). In the incubation temperature synergize to produce a greater red-eared slider turtle (Trachemys scripta), incubation of feminizing effect at intermediate incubation temperaeggs at relatively low temperatures (e.g., 20 -28.6Њ) retures that produce mixed sex ratios. This study demonsults in only male hatchlings, whereas relatively high strates that, in the red-eared slider, there is a complex temperatures (e.g., 29.6 -35Њ) results in only female interaction between incubation temperature, different hatchlings; when eggs are incubated at temperatures estrogens, and the dosage effect of each hormone. There intermediate to these, varying sex ratios are produced are changes in potency of different estrogens with incu- . Sex steroid hormones appear to be bation temperature such that estriol is more potent than the physiological equivalent of incubation temperature estrone and estradiol-17b at 26Њ (an all-male producing and both male-and female-producing incubation temincubation temperature), estrone and estriol are equipoperatures and exogenous steroids exert their effects tent to each other and more potent than estradiol-17b at during the mid-trimester of development (Crews et al., . Estrogens and aromatizable biased sex ratio), and estradiol-17b is more potent than androgens induce female sex determination, whereas estrone and estriol at 29Њ (an incubation temperature nonaromatizable androgens induce male sex determithat produced equal numbers of males and females).
Copeia, 2015
The Pascagoula Map Turtle (Graptemys gibbonsi) is a narrowly endemic species found only in the Pascagoula River drainage in Mississippi. It is among the most poorly known turtle species because of research taxonomic biases and this species' relatively recent recognition as a unique taxon. A recent petition requested protective status for G. gibbonsi under the U.S. Endangered Species Act. We describe population parameters, quantitatively assess sexual dimorphism of G. gibbonsi, and document hormone secretion patterns from the Chickasawhay and Leaf rivers in Mississippi. We demonstrate a significant male-skewed sex ratio and a female-biased size dimorphism in both carapace length and height. Males showed a bimodal peak of plasma testosterone in fall and spring, consistent with the pattern shown by many other southeastern turtles with late summer-fall spermatogenesis and mating during spring and fall. Females did not show seasonal variation in estradiol secretion, an unexpected result that was possibly due to our small sample size of females, none of which were gravid when captured. Although this observation may be due to our limited capacity to sample females, given the reproductive issues reported for Graptemys flavimaculata from the same drainage (e.g., reproductive hormone abnormalities, low nesting frequency and success), this finding warrants concern and necessitates additional research. Finally, in order to put our hormone data in context, we briefly review hormone and reproductive patterns in southeastern U.S. turtles. Our review includes the timing of follicular enlargement, ovulation and nesting, clutch frequency, and estradiol cycles. The review for male turtles includes details on the spermatogenic cycle, spermiation, and the timing and frequency of testosterone peaks.