AbstractNest microclimates influence embryonic development and survival in many lineages, including reptiles with temperature-dependent sex determination. These microclimates are dependent on physical drivers and biological processes, such as embryonic metabolism, that generate heat. The flatback turtle (Natator depressus) has among the largest hatchlings of the seven extant sea turtle species, making it an excellent candidate for quantifying the contribution of embryonic metabolism to the nest microclimate. Consequently, we measured embryonic metabolic rates, development rates, and the relationship between temperature and sex determination for a N. depressus population nesting at Cemetery Beach in Western Australia, a mainland beach characterized by high sand temperatures. Total oxygen consumed at 29.5°C during an average 52-d incubation period was 2,622 mL, total carbon dioxide produced was 1,886 mL, and estimated embryonic heat production reached 38 mW at 90% of development. Adjustment of metabolic rates to 32°C and 34°C increased peak heat production by 18% and 27%, respectively. The pivotal temperature (TPIV) producing an equal sex ratio was 30.3°C, mixed sexes were produced between 29.3°C and 31.2°C, and only females were produced above 31.2°C. The TPIV was similar (within 0.2°C) to that of an island rookery within the same genetic stock (North West Shelf), but the peak development rate (2.5% d-1) was estimated to be achieved at a temperature ~2.5°C higher (34.7°C) than the island rookery. Our results add to a growing consensus that thermal thresholds vary among sea turtle populations, even within the same genetic stock. Furthermore, we show that metabolic heat will have an appreciable impact on the nest microclimate, which has implications for embryonic survival and fitness under a future climate with warmer sand temperatures.
{"title":"Metabolic Rates and Thermal Thresholds of Embryonic Flatback Turtles (<i>Natator depressus</i>) from the North West Shelf of Australia.","authors":"Malindi Gammon, Blair Bentley, Sabrina Fossette, Nicola Mitchell","doi":"10.1086/716848","DOIUrl":"https://doi.org/10.1086/716848","url":null,"abstract":"<p><p>AbstractNest microclimates influence embryonic development and survival in many lineages, including reptiles with temperature-dependent sex determination. These microclimates are dependent on physical drivers and biological processes, such as embryonic metabolism, that generate heat. The flatback turtle (<i>Natator depressus</i>) has among the largest hatchlings of the seven extant sea turtle species, making it an excellent candidate for quantifying the contribution of embryonic metabolism to the nest microclimate. Consequently, we measured embryonic metabolic rates, development rates, and the relationship between temperature and sex determination for a <i>N. depressus</i> population nesting at Cemetery Beach in Western Australia, a mainland beach characterized by high sand temperatures. Total oxygen consumed at 29.5°C during an average 52-d incubation period was 2,622 mL, total carbon dioxide produced was 1,886 mL, and estimated embryonic heat production reached 38 mW at 90% of development. Adjustment of metabolic rates to 32°C and 34°C increased peak heat production by 18% and 27%, respectively. The pivotal temperature (<i>T</i><sub>PIV</sub>) producing an equal sex ratio was 30.3°C, mixed sexes were produced between 29.3°C and 31.2°C, and only females were produced above 31.2°C. The <i>T</i><sub>PIV</sub> was similar (within 0.2°C) to that of an island rookery within the same genetic stock (North West Shelf), but the peak development rate (2.5% d<sup>-1</sup>) was estimated to be achieved at a temperature ~2.5°C higher (34.7°C) than the island rookery. Our results add to a growing consensus that thermal thresholds vary among sea turtle populations, even within the same genetic stock. Furthermore, we show that metabolic heat will have an appreciable impact on the nest microclimate, which has implications for embryonic survival and fitness under a future climate with warmer sand temperatures.</p>","PeriodicalId":54609,"journal":{"name":"Physiological and Biochemical Zoology","volume":"94 6","pages":"429-442"},"PeriodicalIF":1.6,"publicationDate":"2021-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39467088","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Theoretical models about the relationship between food restriction and individual differences in risk-taking behavior (i.e., boldness) have led to conflicting predictions: some models predict that food restriction increases boldness, while other models predict that food restriction decreases boldness. This discrepancy may be partially attributable to an underappreciation for animals’ complex physiological responses to food restriction. To understand the proximate mechanisms mediating state-dependent boldness, we used freshwater snails (Helisoma trivolvis) to examine the relationships among food availability, body condition, boldness (latency to reemerge from shell and exploration), and mRNA expression of three genes (adenosine monophosphate–activated protein kinase [AMPK], molluscan insulin-like peptide [MIP], and serotonin receptor [5-HT]) involved in maintaining energy homeostasis during periods of moderate food restriction. Latency to reemerge and exploratory behavior decreased over time, but fed snails were bolder than fasted snails, suggesting that food restriction reduces bold behavior. Although food restriction decreased body condition, there was not a relationship between body condition and latency to reemerge from shell. However, expression of MIP was positively correlated with latency to reemerge from shell. Furthermore, AMPK was positively correlated with MIP and negatively correlated with body condition and 5-HT. Therefore, individual differences in physiological responses to food restriction, not overall body condition per se, appear to be more closely associated with state-dependent bold behavior. Finally, snails that experienced a novel assay environment returned to their initial “shy” behavior, suggesting that habituation to the assay environment may contribute to snails expressing bolder behavior over time.
{"title":"Bold Behavior Is Associated with Genes That Regulate Energy Use but Does Not Covary with Body Condition in Food-Restricted Snails.","authors":"Christopher G Goodchild, Sarah E DuRant","doi":"10.1086/716431","DOIUrl":"https://doi.org/10.1086/716431","url":null,"abstract":"Theoretical models about the relationship between food restriction and individual differences in risk-taking behavior (i.e., boldness) have led to conflicting predictions: some models predict that food restriction increases boldness, while other models predict that food restriction decreases boldness. This discrepancy may be partially attributable to an underappreciation for animals’ complex physiological responses to food restriction. To understand the proximate mechanisms mediating state-dependent boldness, we used freshwater snails (Helisoma trivolvis) to examine the relationships among food availability, body condition, boldness (latency to reemerge from shell and exploration), and mRNA expression of three genes (adenosine monophosphate–activated protein kinase [AMPK], molluscan insulin-like peptide [MIP], and serotonin receptor [5-HT]) involved in maintaining energy homeostasis during periods of moderate food restriction. Latency to reemerge and exploratory behavior decreased over time, but fed snails were bolder than fasted snails, suggesting that food restriction reduces bold behavior. Although food restriction decreased body condition, there was not a relationship between body condition and latency to reemerge from shell. However, expression of MIP was positively correlated with latency to reemerge from shell. Furthermore, AMPK was positively correlated with MIP and negatively correlated with body condition and 5-HT. Therefore, individual differences in physiological responses to food restriction, not overall body condition per se, appear to be more closely associated with state-dependent bold behavior. Finally, snails that experienced a novel assay environment returned to their initial “shy” behavior, suggesting that habituation to the assay environment may contribute to snails expressing bolder behavior over time.","PeriodicalId":54609,"journal":{"name":"Physiological and Biochemical Zoology","volume":"94 6","pages":"366-379"},"PeriodicalIF":1.6,"publicationDate":"2021-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39380701","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Armand A Cann, Rebecca R Weber, Leigh Anne Harden, Daniel Thompson, Jeremy Nadolski, Jenna Mattes, Alexandra Karwowska, Sumaiya Shahjahan, Joseph R Milanovich
AbstractConservation translocations are important in maintaining viable wildlife populations of vulnerable species within their indigenous ranges. To be effective, population restoration efforts (e.g., head start programs) must consider the species' life history, regional ecology, and physiology and the health status of wild and translocated populations. The decline of Blanding's turtles (Emydoidea blandingii) has prompted the initiation of head start programs, but the health and short-term survival of head-started juveniles released to the wild is largely unknown. From May to October 2016 and 2017, we radio tracked captive-reared, recently released juvenile Blanding's turtles and monitored their survivorship and monthly physiological health. We aimed to (1) compare physiological metrics of juveniles before and after release from captivity and between head-started cohorts, (2) identify seasonal trends in physiological metrics of recently released juveniles, (3) compare physiological metrics of recently released and formerly released juveniles, and (4) identify predictors of juvenile survivorship after release from captivity. Juvenile short-term survival was low compared with other studies. Most physiological metrics did not change after release from captivity, negating significant juvenile stress before or after release. Physiological metrics for recently released cohorts varied seasonally, suggesting that these juveniles were likely in good health. Some physiological metrics differed between recently released and formerly released juveniles, demonstrating a potential postrelease acclimatization period. Finally, no physiological metrics significantly predicted survival, but surviving juveniles had a higher percentage of fat. In all, juvenile deaths were not due to poor turtle health but rather to predation from human-subsidized mesocarnivores. Therefore, head-started juvenile Blanding's turtles released in suburban areas may benefit from antipredator training and mesocarnivore control at release sites.
{"title":"Physiological Health and Survival of Captive-Reared and Released Juvenile Blanding's Turtles.","authors":"Armand A Cann, Rebecca R Weber, Leigh Anne Harden, Daniel Thompson, Jeremy Nadolski, Jenna Mattes, Alexandra Karwowska, Sumaiya Shahjahan, Joseph R Milanovich","doi":"10.1086/716832","DOIUrl":"https://doi.org/10.1086/716832","url":null,"abstract":"<p><p>AbstractConservation translocations are important in maintaining viable wildlife populations of vulnerable species within their indigenous ranges. To be effective, population restoration efforts (e.g., head start programs) must consider the species' life history, regional ecology, and physiology and the health status of wild and translocated populations. The decline of Blanding's turtles (<i>Emydoidea blandingii</i>) has prompted the initiation of head start programs, but the health and short-term survival of head-started juveniles released to the wild is largely unknown. From May to October 2016 and 2017, we radio tracked captive-reared, recently released juvenile Blanding's turtles and monitored their survivorship and monthly physiological health. We aimed to (1) compare physiological metrics of juveniles before and after release from captivity and between head-started cohorts, (2) identify seasonal trends in physiological metrics of recently released juveniles, (3) compare physiological metrics of recently released and formerly released juveniles, and (4) identify predictors of juvenile survivorship after release from captivity. Juvenile short-term survival was low compared with other studies. Most physiological metrics did not change after release from captivity, negating significant juvenile stress before or after release. Physiological metrics for recently released cohorts varied seasonally, suggesting that these juveniles were likely in good health. Some physiological metrics differed between recently released and formerly released juveniles, demonstrating a potential postrelease acclimatization period. Finally, no physiological metrics significantly predicted survival, but surviving juveniles had a higher percentage of fat. In all, juvenile deaths were not due to poor turtle health but rather to predation from human-subsidized mesocarnivores. Therefore, head-started juvenile Blanding's turtles released in suburban areas may benefit from antipredator training and mesocarnivore control at release sites.</p>","PeriodicalId":54609,"journal":{"name":"Physiological and Biochemical Zoology","volume":"94 6","pages":"411-428"},"PeriodicalIF":1.6,"publicationDate":"2021-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39454370","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Christopher Dwane, Simon D Rundle, Oliver Tills, Enrico L Rezende, Juan Galindo, Emilio Rolán-Alvarez, Manuela Truebano
AbstractThermal stress is a potentially important selective agent in intertidal marine habitats, but the role that thermal tolerance might play in local adaptation across shore height has been underexplored. Northwest Spain is home to two morphologically distinct ecotypes of the periwinkle Littorina saxatilis, separated by shore height and subject to substantial differences in thermal stress exposure. However, despite other biotic and abiotic drivers of ecotype segregation being well studied, their thermal tolerance has not been previously characterized. We investigated thermal tolerance across multiple life history stages by employing the thermal death time (TDT) approach to determine (i) whether the two ecotypes differ in thermal tolerance and (ii) how any differences vary with life history stage. Adults of the two ecotypes differed in their thermal tolerance in line with their shore position: the upper-shore ecotype, which experiences more extreme temperatures, exhibited greater endurance of thermal stress compared with the lower-shore ecotype. This difference was most pronounced at the highest temperatures tested. The proximate physiological basis for these differences is unknown but likely due to a multifarious interaction of traits affecting different parts of the TDT curve. Differences in tolerance between ecotypes were less pronounced in early life history stages but increased with ontogeny, suggesting partial divergence of this trait during development. Thermal tolerance could potentially play an important role in maintaining population divergence and genetic segregation between the two ecotypes, since the increased thermal sensitivity of the lower-shore ecotype may limit its dispersal onto the upper shore and so restrict gene flow.
{"title":"Divergence in Thermal Physiology Could Contribute to Vertical Segregation in Intertidal Ecotypes of <i>Littorina saxatilis</i>.","authors":"Christopher Dwane, Simon D Rundle, Oliver Tills, Enrico L Rezende, Juan Galindo, Emilio Rolán-Alvarez, Manuela Truebano","doi":"10.1086/716176","DOIUrl":"https://doi.org/10.1086/716176","url":null,"abstract":"<p><p>AbstractThermal stress is a potentially important selective agent in intertidal marine habitats, but the role that thermal tolerance might play in local adaptation across shore height has been underexplored. Northwest Spain is home to two morphologically distinct ecotypes of the periwinkle <i>Littorina saxatilis</i>, separated by shore height and subject to substantial differences in thermal stress exposure. However, despite other biotic and abiotic drivers of ecotype segregation being well studied, their thermal tolerance has not been previously characterized. We investigated thermal tolerance across multiple life history stages by employing the thermal death time (TDT) approach to determine (i) whether the two ecotypes differ in thermal tolerance and (ii) how any differences vary with life history stage. Adults of the two ecotypes differed in their thermal tolerance in line with their shore position: the upper-shore ecotype, which experiences more extreme temperatures, exhibited greater endurance of thermal stress compared with the lower-shore ecotype. This difference was most pronounced at the highest temperatures tested. The proximate physiological basis for these differences is unknown but likely due to a multifarious interaction of traits affecting different parts of the TDT curve. Differences in tolerance between ecotypes were less pronounced in early life history stages but increased with ontogeny, suggesting partial divergence of this trait during development. Thermal tolerance could potentially play an important role in maintaining population divergence and genetic segregation between the two ecotypes, since the increased thermal sensitivity of the lower-shore ecotype may limit its dispersal onto the upper shore and so restrict gene flow.</p>","PeriodicalId":54609,"journal":{"name":"Physiological and Biochemical Zoology","volume":"94 6","pages":"353-365"},"PeriodicalIF":1.6,"publicationDate":"2021-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39342590","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
AbstractThe received wisdom on how activity affects energy expenditure is that the more activity is undertaken, the more calories will have been burned by the end of the day. Yet traditional hunter-gatherers, who lead physically hard lives, burn no more calories each day than Western populations living in labor-saving environments. Indeed, there is now a wealth of data, both for humans and other animals, demonstrating that long-term lifestyle changes involving increases in exercise or other physical activities do not result in commensurate increases in daily energy expenditure (DEE). This is because humans and other animals exhibit a degree of energy compensation at the organismal level, ameliorating some of the increases in DEE that would occur from the increased activity by decreasing the energy expended on other biological processes. And energy compensation can be sizable, reaching many hundreds of calories in humans. But the processes that are downregulated in the long-term to achieve energy compensation are far from clear, particularly in humans-we do not know how energy compensation is achieved. My review here of the literature on relevant exercise intervention studies, for both humans and other species, indicates conflict regarding the role, if any, of basal metabolic rate (BMR) or low-level activity such as fidgeting play, particularly once changes in body composition are factored out. In situations where BMR and low-level activity are not major components of energy compensation, what then drives it? I discuss how changes in mitochondrial efficiency and changes in circadian fluctuations in BMR may contribute to our understanding of energy management. Currently unexplored, these mechanisms and others may provide important insights into the mystery of how energy compensation is achieved.
{"title":"The Mystery of Energy Compensation.","authors":"Lewis G Halsey","doi":"10.1086/716467","DOIUrl":"https://doi.org/10.1086/716467","url":null,"abstract":"<p><p>AbstractThe received wisdom on how activity affects energy expenditure is that the more activity is undertaken, the more calories will have been burned by the end of the day. Yet traditional hunter-gatherers, who lead physically hard lives, burn no more calories each day than Western populations living in labor-saving environments. Indeed, there is now a wealth of data, both for humans and other animals, demonstrating that long-term lifestyle changes involving increases in exercise or other physical activities do not result in commensurate increases in daily energy expenditure (DEE). This is because humans and other animals exhibit a degree of energy compensation at the organismal level, ameliorating some of the increases in DEE that would occur from the increased activity by decreasing the energy expended on other biological processes. And energy compensation can be sizable, reaching many hundreds of calories in humans. But the processes that are downregulated in the long-term to achieve energy compensation are far from clear, particularly in humans-we do not know how energy compensation is achieved. My review here of the literature on relevant exercise intervention studies, for both humans and other species, indicates conflict regarding the role, if any, of basal metabolic rate (BMR) or low-level activity such as fidgeting play, particularly once changes in body composition are factored out. In situations where BMR and low-level activity are not major components of energy compensation, what then drives it? I discuss how changes in mitochondrial efficiency and changes in circadian fluctuations in BMR may contribute to our understanding of energy management. Currently unexplored, these mechanisms and others may provide important insights into the mystery of how energy compensation is achieved.</p>","PeriodicalId":54609,"journal":{"name":"Physiological and Biochemical Zoology","volume":"94 6","pages":"380-393"},"PeriodicalIF":1.6,"publicationDate":"2021-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39422114","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Iván Beltrán, Constant Perry, Faustine Degottex, Martin J Whiting
AbstractThermal conditions during embryonic development affect offspring phenotype in ectotherms. Therefore, rising environmental temperatures can have important consequences for an individual's fitness. Nonetheless, females have some capacity to compensate for potential negative consequences that adverse developmental environments may have on their offspring. Recent studies show that oviparous reptiles exhibit behavioral plasticity in nest site selection, which can buffer their embryos against high incubation temperatures; however, much less is known about these responses in viviparous reptiles. We subjected pregnant viviparous skinks, Saiphos equalis, to current or projected midcentury (2050) temperatures to test (i) how elevated temperatures affect female thermoregulatory and foraging behavior; (ii) whether temperatures experienced by females during pregnancy negatively affect the morphology, performance, and behavior of hatchlings; and (iii) whether behavioral thermoregulation during pregnancy is costly to females. Females from the elevated temperature treatment compensated by going deeper belowground to seek cooler temperatures and eating less, and they consequently had a lower body mass relative to snout-to-vent length (condition estimator) compared with females from the current thermal treatment. The temperatures experienced by females in the elevated temperature treatment were high enough to affect foraging and locomotor performance but not the morphology and growth rate of hatchlings. By seeking cooler temperatures, mothers can mitigate some of the effects of high temperatures on their offspring (e.g., reduced body size and growth). However, this protective behavior of females may come at an energetic cost to them. This study adds to growing evidence of lizards' vulnerability to global warming, particularly during reproduction when females are already paying a substantial cost.
{"title":"Behavioral Thermoregulation by Mothers Protects Offspring from Global Warming but at a Cost.","authors":"Iván Beltrán, Constant Perry, Faustine Degottex, Martin J Whiting","doi":"10.1086/715976","DOIUrl":"https://doi.org/10.1086/715976","url":null,"abstract":"<p><p>AbstractThermal conditions during embryonic development affect offspring phenotype in ectotherms. Therefore, rising environmental temperatures can have important consequences for an individual's fitness. Nonetheless, females have some capacity to compensate for potential negative consequences that adverse developmental environments may have on their offspring. Recent studies show that oviparous reptiles exhibit behavioral plasticity in nest site selection, which can buffer their embryos against high incubation temperatures; however, much less is known about these responses in viviparous reptiles. We subjected pregnant viviparous skinks, <i>Saiphos equalis</i>, to current or projected midcentury (2050) temperatures to test (i) how elevated temperatures affect female thermoregulatory and foraging behavior; (ii) whether temperatures experienced by females during pregnancy negatively affect the morphology, performance, and behavior of hatchlings; and (iii) whether behavioral thermoregulation during pregnancy is costly to females. Females from the elevated temperature treatment compensated by going deeper belowground to seek cooler temperatures and eating less, and they consequently had a lower body mass relative to snout-to-vent length (condition estimator) compared with females from the current thermal treatment. The temperatures experienced by females in the elevated temperature treatment were high enough to affect foraging and locomotor performance but not the morphology and growth rate of hatchlings. By seeking cooler temperatures, mothers can mitigate some of the effects of high temperatures on their offspring (e.g., reduced body size and growth). However, this protective behavior of females may come at an energetic cost to them. This study adds to growing evidence of lizards' vulnerability to global warming, particularly during reproduction when females are already paying a substantial cost.</p>","PeriodicalId":54609,"journal":{"name":"Physiological and Biochemical Zoology","volume":"94 5","pages":"302-318"},"PeriodicalIF":1.6,"publicationDate":"2021-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1086/715976","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39185183","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Kim Birnie-Gauvin, Martin H Larsen, Kathryn S Peiman, Jonathan D Midwood, Alexander D M Wilson, Steven J Cooke, Kim Aarestrup
AbstractEarly-life experiences can shape life histories and population dynamics of wild animals. To examine whether stressful stimuli experienced in early life resulted in carryover effects in later life stages, we conducted several experimental manipulations and then monitored wild fish with passive integrated transponder tags during juvenile out-migration and adult return migration. In total, 3,217 juvenile brown trout (Salmo trutta) were subjected to one of six manipulations: chase to exhaustion, thermal challenge, food deprivation, low-concentration cortisol injection, high-concentration cortisol injection, and sham injection, plus a control group. Cortisol and food deprivation treatments were previously shown to have short-term effects on juveniles, such as lower survival to out-migration and changes in migration timing. However, it remained unknown whether any of the six manipulations had effects that carried over into the adult phase. We therefore investigated whether these extrinsic manipulations, as well as intrinsic factors (size and condition), affected probability of return as adults and time spent at sea. Of the 1,273 fish that out-migrated, 146 returned as adults. We failed to detect any effect of treatments on return rates, while high-concentration cortisol weakly affected time spent at sea in one tagging event. We also found that juvenile condition was positively correlated to likelihood of adult return in only one tagging event. Overall, our findings did not identify either intrinsic factors or extrinsic stressful early-life experiences that have strong effects on fish that survive to adulthood. This suggests that some species may be more resilient than others to stressful stimuli encountered early in life.
{"title":"No Evidence for Long-Term Carryover Effects in a Wild Salmonid Fish.","authors":"Kim Birnie-Gauvin, Martin H Larsen, Kathryn S Peiman, Jonathan D Midwood, Alexander D M Wilson, Steven J Cooke, Kim Aarestrup","doi":"10.1086/716000","DOIUrl":"https://doi.org/10.1086/716000","url":null,"abstract":"<p><p>AbstractEarly-life experiences can shape life histories and population dynamics of wild animals. To examine whether stressful stimuli experienced in early life resulted in carryover effects in later life stages, we conducted several experimental manipulations and then monitored wild fish with passive integrated transponder tags during juvenile out-migration and adult return migration. In total, 3,217 juvenile brown trout (<i>Salmo trutta</i>) were subjected to one of six manipulations: chase to exhaustion, thermal challenge, food deprivation, low-concentration cortisol injection, high-concentration cortisol injection, and sham injection, plus a control group. Cortisol and food deprivation treatments were previously shown to have short-term effects on juveniles, such as lower survival to out-migration and changes in migration timing. However, it remained unknown whether any of the six manipulations had effects that carried over into the adult phase. We therefore investigated whether these extrinsic manipulations, as well as intrinsic factors (size and condition), affected probability of return as adults and time spent at sea. Of the 1,273 fish that out-migrated, 146 returned as adults. We failed to detect any effect of treatments on return rates, while high-concentration cortisol weakly affected time spent at sea in one tagging event. We also found that juvenile condition was positively correlated to likelihood of adult return in only one tagging event. Overall, our findings did not identify either intrinsic factors or extrinsic stressful early-life experiences that have strong effects on fish that survive to adulthood. This suggests that some species may be more resilient than others to stressful stimuli encountered early in life.</p>","PeriodicalId":54609,"journal":{"name":"Physiological and Biochemical Zoology","volume":"94 5","pages":"319-329"},"PeriodicalIF":1.6,"publicationDate":"2021-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1086/716000","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39201472","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Natalie M Claunch, Matthew Holding, J Tony Frazier, Emma M Huff, Richard B Schonour, Ben Vernasco, Ignacio T Moore, Darin R Rokyta, Emily N Taylor
AbstractVenom is an integral feeding trait in many animal species. Although venom often varies ontogenetically, little is known about the proximate physiological mediators of venom variation within individuals. The glucocorticoid hormone corticosterone (CORT) can alter the transcription and activation of proteins, including homologues of snake venom components such as snake venom metalloproteinases (SVMPs) and phospholipase A2 (PLA2). CORT is endogenously produced by snakes, varies seasonally and also in response to stress, and is a candidate endogenous mediator of changes in venom composition and functional activity. Here, we tested the hypothesis that CORT induces changes in snake venom by sampling the venom of wild adult rattlesnakes before and after they were treated with either empty (control) or CORT-filled (treatment) Silastic implants. We measured longitudinal changes in whole-venom composition, whole-venom total protein content, and enzymatic activity of SVMP and PLA2 components of venom. We also assessed the within-individual repeatability of venom components. Despite successfully elevating plasma CORT in the treatment group, we found no effect of CORT treatment or average plasma CORT level on any venom variables measured. Except for total protein content, venom components were highly repeatable within individuals ([Formula: see text]). Our results indicate that the effects of CORT, a hormone commonly associated with stress and metabolic functions, in adult rattlesnake venom are negligible. Our findings bode well for venom researchers and biomedical applications that rely on the consistency of venoms produced from potentially stressed individuals and provide an experimental framework for future studies of proximate mediators of venom variation across an individual's life span.
{"title":"Experimental Manipulation of Corticosterone Does Not Affect Venom Composition or Functional Activity in Free-Ranging Rattlesnakes.","authors":"Natalie M Claunch, Matthew Holding, J Tony Frazier, Emma M Huff, Richard B Schonour, Ben Vernasco, Ignacio T Moore, Darin R Rokyta, Emily N Taylor","doi":"10.1086/714936","DOIUrl":"https://doi.org/10.1086/714936","url":null,"abstract":"<p><p>AbstractVenom is an integral feeding trait in many animal species. Although venom often varies ontogenetically, little is known about the proximate physiological mediators of venom variation within individuals. The glucocorticoid hormone corticosterone (CORT) can alter the transcription and activation of proteins, including homologues of snake venom components such as snake venom metalloproteinases (SVMPs) and phospholipase A<sub>2</sub> (PLA<sub>2</sub>). CORT is endogenously produced by snakes, varies seasonally and also in response to stress, and is a candidate endogenous mediator of changes in venom composition and functional activity. Here, we tested the hypothesis that CORT induces changes in snake venom by sampling the venom of wild adult rattlesnakes before and after they were treated with either empty (control) or CORT-filled (treatment) Silastic implants. We measured longitudinal changes in whole-venom composition, whole-venom total protein content, and enzymatic activity of SVMP and PLA<sub>2</sub> components of venom. We also assessed the within-individual repeatability of venom components. Despite successfully elevating plasma CORT in the treatment group, we found no effect of CORT treatment or average plasma CORT level on any venom variables measured. Except for total protein content, venom components were highly repeatable within individuals ([Formula: see text]). Our results indicate that the effects of CORT, a hormone commonly associated with stress and metabolic functions, in adult rattlesnake venom are negligible. Our findings bode well for venom researchers and biomedical applications that rely on the consistency of venoms produced from potentially stressed individuals and provide an experimental framework for future studies of proximate mediators of venom variation across an individual's life span.</p>","PeriodicalId":54609,"journal":{"name":"Physiological and Biochemical Zoology","volume":"94 5","pages":"286-301"},"PeriodicalIF":1.6,"publicationDate":"2021-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1086/714936","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39101679","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
AbstractBasal metabolic rate (BMR) represents the lowest level of aerobic metabolism in a resting, postabsorptive endotherm as measured within the thermoneutral zone. By contrast, maximal metabolic rate ([Formula: see text]max) reflects the upper limit of aerobic metabolism achieved during intensive exercise. As BMR and [Formula: see text]max define the boundaries of the possible levels of aerobic metabolism expressed by a normothermic individual, a key question is whether BMR and [Formula: see text]max are correlated. In the present study, we took repeated paired measurements of thermoneutral resting metabolic rate (RMRt) and [Formula: see text]max on 165 white-footed mice (Peromyscus leucopus). Over a single summer (May-October), repeatability (R ± SE) was low but statistically significant ([Formula: see text]) for both RMRt and [Formula: see text]max ([Formula: see text] for RMRt; [Formula: see text] for [Formula: see text]max). Willingness to run during the forced-exercise trials was also significantly repeatable ([Formula: see text]). At the residual level (within individual), RMRt and [Formula: see text]max tended to be positively correlated ([Formula: see text], [Formula: see text]), suggesting the presence of correlated phenotypic plasticity. By contrast, RMRt and [Formula: see text]max were significantly negatively correlated at the among-individual level ([Formula: see text]). To the extent that variation in RMRt reflects variation in BMR, the negative among-individual correlation does not corroborate the idea that a costly metabolic machinery is needed to support a high [Formula: see text]max. Future research should investigate the (genetic) relationship between RMRt (and BMR) and other energetically expensive behaviors and activities to better understand how energy is allocated within individuals.
{"title":"Individual (Co)variation in Resting and Maximal Metabolic Rates in Wild Mice.","authors":"Alyssa Fiedler, Vincent Careau","doi":"10.1086/716042","DOIUrl":"https://doi.org/10.1086/716042","url":null,"abstract":"<p><p>AbstractBasal metabolic rate (BMR) represents the lowest level of aerobic metabolism in a resting, postabsorptive endotherm as measured within the thermoneutral zone. By contrast, maximal metabolic rate ([Formula: see text]max) reflects the upper limit of aerobic metabolism achieved during intensive exercise. As BMR and [Formula: see text]max define the boundaries of the possible levels of aerobic metabolism expressed by a normothermic individual, a key question is whether BMR and [Formula: see text]max are correlated. In the present study, we took repeated paired measurements of thermoneutral resting metabolic rate (RMR<sub>t</sub>) and [Formula: see text]max on 165 white-footed mice (<i>Peromyscus leucopus</i>). Over a single summer (May-October), repeatability (<i>R</i> ± SE) was low but statistically significant ([Formula: see text]) for both RMR<sub>t</sub> and [Formula: see text]max ([Formula: see text] for RMR<sub>t</sub>; [Formula: see text] for [Formula: see text]max). Willingness to run during the forced-exercise trials was also significantly repeatable ([Formula: see text]). At the residual level (within individual), RMR<sub>t</sub> and [Formula: see text]max tended to be positively correlated ([Formula: see text], [Formula: see text]), suggesting the presence of correlated phenotypic plasticity. By contrast, RMR<sub>t</sub> and [Formula: see text]max were significantly negatively correlated at the among-individual level ([Formula: see text]). To the extent that variation in RMR<sub>t</sub> reflects variation in BMR, the negative among-individual correlation does not corroborate the idea that a costly metabolic machinery is needed to support a high [Formula: see text]max. Future research should investigate the (genetic) relationship between RMR<sub>t</sub> (and BMR) and other energetically expensive behaviors and activities to better understand how energy is allocated within individuals.</p>","PeriodicalId":54609,"journal":{"name":"Physiological and Biochemical Zoology","volume":"94 5","pages":"338-352"},"PeriodicalIF":1.6,"publicationDate":"2021-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1086/716042","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39271280","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Celiwe A Ngcamphalala, Michelle Bouwer, Susan W Nicolson, André Ganswindt, Andrew E McKechnie
AbstractNoninvasive measurement of stress-related alterations in fecal glucocorticoid metabolite (fGCM) concentrations has considerable potential for quantifying physiological responses to very hot weather in free-ranging birds, but practical considerations related to sampling will often make this method feasible only for habituated study populations. Here we evaluate an alternate approach, the use of experimentally manipulated thermal environments for evaluating stress responses to high environmental temperatures in wild-caught birds housed in captivity. Using an enzyme immunoassay utilizing antibodies against 5ß-pregnane-3α,11ß,21-triol-20-one-CMO∶BSA (tetrahydrocorticosterone), we quantified fGCMs in captive individuals of three southern African arid-zone species (southern pied babblers [Turdoides bicolor], white-browed sparrow-weavers [Plocepasser mahali], and southern yellow-billed hornbills [Tockus leucomelas]) experiencing daily air temperature maxima (Tmax) ranging from 30°-32°C to 42°-44°C. For none of the three species did Tmax emerge as a significant predictor of elevated fGCM concentrations, and no stress response to simulated hot weather was evident. The apparent lack of a stress response to Tmax = 42°C in captive southern pied babblers contrasts with linear increases in fGCMs at Tmax > 38°C in free-ranging conspecifics. The lack of an effect of Tmax on fGCM levels may potentially be explained by several factors, including differences in operative temperatures and the availability of water and food between free-ranging and captive settings or the stress effect of captivity itself. Our results suggest that experimental manipulations of thermal environments experienced by wild-caught captive birds have limited usefulness for testing hypotheses concerning the effects of hot weather events on fGCM (and, by extension, glucocorticoid) concentrations.
{"title":"Experimental Manipulation of Air Temperature in Captivity Appears Unsuitable for Evaluating Fecal Glucocorticoid Metabolite Responses of Wild-Caught Birds to Heat Exposure.","authors":"Celiwe A Ngcamphalala, Michelle Bouwer, Susan W Nicolson, André Ganswindt, Andrew E McKechnie","doi":"10.1086/716043","DOIUrl":"https://doi.org/10.1086/716043","url":null,"abstract":"<p><p>AbstractNoninvasive measurement of stress-related alterations in fecal glucocorticoid metabolite (fGCM) concentrations has considerable potential for quantifying physiological responses to very hot weather in free-ranging birds, but practical considerations related to sampling will often make this method feasible only for habituated study populations. Here we evaluate an alternate approach, the use of experimentally manipulated thermal environments for evaluating stress responses to high environmental temperatures in wild-caught birds housed in captivity. Using an enzyme immunoassay utilizing antibodies against 5ß-pregnane-3α,11ß,21-triol-20-one-CMO∶BSA (tetrahydrocorticosterone), we quantified fGCMs in captive individuals of three southern African arid-zone species (southern pied babblers [<i>Turdoides bicolor</i>], white-browed sparrow-weavers [<i>Plocepasser mahali</i>], and southern yellow-billed hornbills [<i>Tockus leucomelas</i>]) experiencing daily air temperature maxima (<i>T</i><sub>max</sub>) ranging from 30°-32°C to 42°-44°C. For none of the three species did <i>T</i><sub>max</sub> emerge as a significant predictor of elevated fGCM concentrations, and no stress response to simulated hot weather was evident. The apparent lack of a stress response to <i>T</i><sub>max</sub> = 42°C in captive southern pied babblers contrasts with linear increases in fGCMs at <i>T</i><sub>max</sub> > 38°C in free-ranging conspecifics. The lack of an effect of <i>T</i><sub>max</sub> on fGCM levels may potentially be explained by several factors, including differences in operative temperatures and the availability of water and food between free-ranging and captive settings or the stress effect of captivity itself. Our results suggest that experimental manipulations of thermal environments experienced by wild-caught captive birds have limited usefulness for testing hypotheses concerning the effects of hot weather events on fGCM (and, by extension, glucocorticoid) concentrations.</p>","PeriodicalId":54609,"journal":{"name":"Physiological and Biochemical Zoology","volume":"94 5","pages":"330-337"},"PeriodicalIF":1.6,"publicationDate":"2021-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1086/716043","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39208934","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}