Deserts have always amazed researchers due to their high diversity of habitats, where plant and animal species have been able to adapt and diversify, even when these areas impose several constraints on an organism's activity patterns. In particular, deserts support several lizard species adapted to the thermal and water restrictions found in such biomes. Although several studies have attempted to understand how lizard species might respond to water deficits or droughts in deserts, few have addressed how these responses might vary along a latitudinal gradient. This raises the question of whether physiological buffering of the organism or the climatic environment affects water loss in lizards. Here, we used six populations of Urosaurus ornatus to test whether water loss is influenced more by the intrinsic physiology of the lizard or by the climatic niche. We found that water loss is primarily influenced by the climatic niche of the lizard. However, future studies should focus on how microclimatic variables can influence water loss in organisms found across large latitudinal gradients.
{"title":"The Shape of Water: Physiological Adaptations to Habitat Aridity in the Ornate Tree Lizard (Urosaurus ornatus).","authors":"Jhan C Salazar, Donald B Miles","doi":"10.1093/icb/icae061","DOIUrl":"10.1093/icb/icae061","url":null,"abstract":"<p><p>Deserts have always amazed researchers due to their high diversity of habitats, where plant and animal species have been able to adapt and diversify, even when these areas impose several constraints on an organism's activity patterns. In particular, deserts support several lizard species adapted to the thermal and water restrictions found in such biomes. Although several studies have attempted to understand how lizard species might respond to water deficits or droughts in deserts, few have addressed how these responses might vary along a latitudinal gradient. This raises the question of whether physiological buffering of the organism or the climatic environment affects water loss in lizards. Here, we used six populations of Urosaurus ornatus to test whether water loss is influenced more by the intrinsic physiology of the lizard or by the climatic niche. We found that water loss is primarily influenced by the climatic niche of the lizard. However, future studies should focus on how microclimatic variables can influence water loss in organisms found across large latitudinal gradients.</p>","PeriodicalId":54971,"journal":{"name":"Integrative and Comparative Biology","volume":null,"pages":null},"PeriodicalIF":2.2,"publicationDate":"2024-09-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141285388","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}
Many coastal marine species have discontinuous distributions or genetic breakpoints throughout their geographical ranges. These spatial and genetic disjunctions occur in species that span limited to broad dispersal potential. Thus, the mechanisms that underlie these disjunctions remain speculative or incompletely known, particularly on small spatial scales where long-term historical processes are unlikely to be the only mechanism contributing to disjunction. Rather, ecological or oceanographic factors may be important. To identify key drivers of coastal disjunctions, we reviewed publications investigating spatial and genetic disjunctions in coastal marine species and visually summarized where and why they are thought to occur. The most frequently cited mechanisms implicated in causing disjunctions include historical processes, oceanographic features, heterogeneous habitat, species introductions, and limited larval dispersal capacities. However, the relative importance of each of these processes varies depending on the spatial scales investigated. Furthermore, locations associated with disjunctions for a suite of species are typically associated with multiple processes that maintain these disjunctions. This study provides a non-exhaustive synthesis of disjunctions in coastal marine species by visualizing where they occur, exploring underlying mechanisms, and investigating biases in how the scientific community studies this phenomenon.
{"title":"Mind the Gap: A Review of Disjunctions in Coastal Marine Species.","authors":"Veronica Pagowski, Fiorenza Micheli","doi":"10.1093/icb/icae099","DOIUrl":"10.1093/icb/icae099","url":null,"abstract":"<p><p>Many coastal marine species have discontinuous distributions or genetic breakpoints throughout their geographical ranges. These spatial and genetic disjunctions occur in species that span limited to broad dispersal potential. Thus, the mechanisms that underlie these disjunctions remain speculative or incompletely known, particularly on small spatial scales where long-term historical processes are unlikely to be the only mechanism contributing to disjunction. Rather, ecological or oceanographic factors may be important. To identify key drivers of coastal disjunctions, we reviewed publications investigating spatial and genetic disjunctions in coastal marine species and visually summarized where and why they are thought to occur. The most frequently cited mechanisms implicated in causing disjunctions include historical processes, oceanographic features, heterogeneous habitat, species introductions, and limited larval dispersal capacities. However, the relative importance of each of these processes varies depending on the spatial scales investigated. Furthermore, locations associated with disjunctions for a suite of species are typically associated with multiple processes that maintain these disjunctions. This study provides a non-exhaustive synthesis of disjunctions in coastal marine species by visualizing where they occur, exploring underlying mechanisms, and investigating biases in how the scientific community studies this phenomenon.</p>","PeriodicalId":54971,"journal":{"name":"Integrative and Comparative Biology","volume":null,"pages":null},"PeriodicalIF":2.2,"publicationDate":"2024-09-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141545564","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}
Emily R Lancaster, Damian C Brady, Markus Frederich
As global temperatures continue to rise, accurate predicted species distribution models will be important for forecasting the movement of range-shifting species. These predictions rely on measurements of organismal thermal tolerance, which can be measured using classical threshold concepts such as Arrhenius break temperatures and critical thermal temperatures, or through ecologically relevant measurements such as the temperature at which reproduction and growth occur. Many species, including invasive species, exhibit thermal plasticity, so these thresholds may change based on ambient temperature, life stage, and measurement techniques. Here, we review thermal thresholds for 15 invertebrate species invasive to the Gulf of Maine. The high degree of variability within a species and between applied conceptual frameworks suggests that modeling the future distribution of these species in all ecosystems, but especially in the rapidly warming northwest Atlantic and Gulf of Maine, will be challenging. While each of these measurement techniques is valid, we suggest contextualization and integration of threshold measurements for accurate modeling.
{"title":"In Hot Water: Current Thermal Threshold Methods Unlikely to Predict Invasive Species Shifts in NW Atlantic.","authors":"Emily R Lancaster, Damian C Brady, Markus Frederich","doi":"10.1093/icb/icae102","DOIUrl":"10.1093/icb/icae102","url":null,"abstract":"<p><p>As global temperatures continue to rise, accurate predicted species distribution models will be important for forecasting the movement of range-shifting species. These predictions rely on measurements of organismal thermal tolerance, which can be measured using classical threshold concepts such as Arrhenius break temperatures and critical thermal temperatures, or through ecologically relevant measurements such as the temperature at which reproduction and growth occur. Many species, including invasive species, exhibit thermal plasticity, so these thresholds may change based on ambient temperature, life stage, and measurement techniques. Here, we review thermal thresholds for 15 invertebrate species invasive to the Gulf of Maine. The high degree of variability within a species and between applied conceptual frameworks suggests that modeling the future distribution of these species in all ecosystems, but especially in the rapidly warming northwest Atlantic and Gulf of Maine, will be challenging. While each of these measurement techniques is valid, we suggest contextualization and integration of threshold measurements for accurate modeling.</p>","PeriodicalId":54971,"journal":{"name":"Integrative and Comparative Biology","volume":null,"pages":null},"PeriodicalIF":2.2,"publicationDate":"2024-09-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141592194","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}
Potential effects of climate change include greater extremes of temperature and increased severity of storms. Many plants have evolved to resist the challenges of winter (freezing, dehydration, and wind) in a process known as cold hardening. Sensing reducing temperatures, they make structural changes at the cellular level to increase their mechanical resistance and prevent damage. Previous work on this topic, though extensive, has been conducted under laboratory conditions rather than in the field, and while many workers have observed changes to cell wall thickness and composition, which imply increased mechanical strength, few have actually measured strength or any other parameter describing structural integrity. This paper describes experiments on a model system designed to measure the structural integrity of leaf laminae from plants growing naturally in the field over extended periods, allowing seasonal variations to be captured. Standard engineering properties-tensile strength and fracture toughness-were measured for leaves of Griselinia littoralis on 19 separate occasions over a 12-month period. Toughness (rather than strength) was found to be the controlling mechanical property. Toughness values were found to change significantly during the year, by more than a factor of 2. Toughness correlated strongly with average daily soil temperature, but with a lag of about 1-2 weeks, suggesting that this is the time needed for structural adjustments to take place. Highest toughness values occurred in winter, confirming cold hardening. Increasing temperature in the spring was associated with decreasing toughness, but in the summer, when highest temperatures occurred, toughness increased again. This apparent "hot hardening" may be a response to dehydration. Results imply that a given leaf is able to both increase and decrease its toughness in response to temperature changes, demonstrating excellent plasticity of response. This case study of a single species establishes a method of reliably measuring changes in a plant's structural integrity due to cold hardening and other seasonal variations, which may be used to investigate the effects of climate change and other variables.
{"title":"Seasonal Variations in the Toughness of Leaves: A Case Study Using Griselinia littoralis.","authors":"David Taylor","doi":"10.1093/icb/icae004","DOIUrl":"10.1093/icb/icae004","url":null,"abstract":"<p><p>Potential effects of climate change include greater extremes of temperature and increased severity of storms. Many plants have evolved to resist the challenges of winter (freezing, dehydration, and wind) in a process known as cold hardening. Sensing reducing temperatures, they make structural changes at the cellular level to increase their mechanical resistance and prevent damage. Previous work on this topic, though extensive, has been conducted under laboratory conditions rather than in the field, and while many workers have observed changes to cell wall thickness and composition, which imply increased mechanical strength, few have actually measured strength or any other parameter describing structural integrity. This paper describes experiments on a model system designed to measure the structural integrity of leaf laminae from plants growing naturally in the field over extended periods, allowing seasonal variations to be captured. Standard engineering properties-tensile strength and fracture toughness-were measured for leaves of Griselinia littoralis on 19 separate occasions over a 12-month period. Toughness (rather than strength) was found to be the controlling mechanical property. Toughness values were found to change significantly during the year, by more than a factor of 2. Toughness correlated strongly with average daily soil temperature, but with a lag of about 1-2 weeks, suggesting that this is the time needed for structural adjustments to take place. Highest toughness values occurred in winter, confirming cold hardening. Increasing temperature in the spring was associated with decreasing toughness, but in the summer, when highest temperatures occurred, toughness increased again. This apparent \"hot hardening\" may be a response to dehydration. Results imply that a given leaf is able to both increase and decrease its toughness in response to temperature changes, demonstrating excellent plasticity of response. This case study of a single species establishes a method of reliably measuring changes in a plant's structural integrity due to cold hardening and other seasonal variations, which may be used to investigate the effects of climate change and other variables.</p>","PeriodicalId":54971,"journal":{"name":"Integrative and Comparative Biology","volume":null,"pages":null},"PeriodicalIF":2.2,"publicationDate":"2024-09-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11406155/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140061375","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Insects must fly in highly variable natural environments filled with gusts, vortices, and other transient aerodynamic phenomena that challenge flight stability. Furthermore, the aerodynamic forces that support insect flight are produced from rapidly oscillating wings of time-varying orientation and configuration. The instantaneous flight forces produced by these wings are large relative to the average forces supporting body weight. The magnitude of these forces and their time-varying direction add another challenge to flight stability, because even proportionally small asymmetries in timing or magnitude between the left and right wings may be sufficient to produce large changes in body orientation. However, these same large-magnitude oscillating forces also offer an opportunity for unexpected flight stability through nonlinear interactions between body orientation, body oscillation in response to time-varying inertial and aerodynamic forces, and the oscillating wings themselves. Understanding the emergent stability properties of flying insects is a crucial step toward understanding the requirements for evolution of flapping flight and decoding the role of sensory feedback in flight control. Here, we provide a brief review of insect flight stability, with some emphasis on stability effects brought about by oscillating wings, and present some preliminary experimental data probing some aspects of flight stability in free-flying insects.
{"title":"Biomechanics of Insect Flight Stability and Perturbation Response.","authors":"Tyson L Hedrick, Emily Blandford, Haithem E Taha","doi":"10.1093/icb/icae076","DOIUrl":"10.1093/icb/icae076","url":null,"abstract":"<p><p>Insects must fly in highly variable natural environments filled with gusts, vortices, and other transient aerodynamic phenomena that challenge flight stability. Furthermore, the aerodynamic forces that support insect flight are produced from rapidly oscillating wings of time-varying orientation and configuration. The instantaneous flight forces produced by these wings are large relative to the average forces supporting body weight. The magnitude of these forces and their time-varying direction add another challenge to flight stability, because even proportionally small asymmetries in timing or magnitude between the left and right wings may be sufficient to produce large changes in body orientation. However, these same large-magnitude oscillating forces also offer an opportunity for unexpected flight stability through nonlinear interactions between body orientation, body oscillation in response to time-varying inertial and aerodynamic forces, and the oscillating wings themselves. Understanding the emergent stability properties of flying insects is a crucial step toward understanding the requirements for evolution of flapping flight and decoding the role of sensory feedback in flight control. Here, we provide a brief review of insect flight stability, with some emphasis on stability effects brought about by oscillating wings, and present some preliminary experimental data probing some aspects of flight stability in free-flying insects.</p>","PeriodicalId":54971,"journal":{"name":"Integrative and Comparative Biology","volume":null,"pages":null},"PeriodicalIF":2.2,"publicationDate":"2024-09-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141428369","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}
Caleb J Axelrod, Ellen M Urquhart, Pria N Mahabir, Bruce A Carlson, Swanne P Gordon
Traits often do not evolve in isolation or vary independently of other traits. Instead, they can be affected by covariation, both within and across species. However, the importance of within-species trait covariation and, critically, the degree to which it varies between species has yet to be thoroughly studied. Brain morphology is a trait of great ecological and behavioral importance, with regions that are hypothesized to vary in size based on behavioral and cognitive demands. Sizes of brain regions have also been shown to covary with each other across various taxa. Here, we test the degree to which covariation in brain region sizes within species has been conserved across 10 teleost fish species. These 10 species span five orders, allowing us to examine how phylogenetic proximity influences similarities in intraspecific trait covariation. Our results showed a trend that similar patterns of brain region size covariation occur in more closely related species. Interestingly, there were certain brain region pairs that showed similar levels of covariation across all species regardless of phylogenetic distance, such as the telencephalon and optic tectum, while others, such as the olfactory bulb and the hypothalamus, varied more independently. Ultimately, the patterns of brain region covariation shown here suggest that evolutionary mechanisms or constraints can act on specific brain regions independently, and that these constraints can change over evolutionary time.
{"title":"Diversity of Intraspecific Patterns of Brain Region Size Covariation in Fish.","authors":"Caleb J Axelrod, Ellen M Urquhart, Pria N Mahabir, Bruce A Carlson, Swanne P Gordon","doi":"10.1093/icb/icae075","DOIUrl":"10.1093/icb/icae075","url":null,"abstract":"<p><p>Traits often do not evolve in isolation or vary independently of other traits. Instead, they can be affected by covariation, both within and across species. However, the importance of within-species trait covariation and, critically, the degree to which it varies between species has yet to be thoroughly studied. Brain morphology is a trait of great ecological and behavioral importance, with regions that are hypothesized to vary in size based on behavioral and cognitive demands. Sizes of brain regions have also been shown to covary with each other across various taxa. Here, we test the degree to which covariation in brain region sizes within species has been conserved across 10 teleost fish species. These 10 species span five orders, allowing us to examine how phylogenetic proximity influences similarities in intraspecific trait covariation. Our results showed a trend that similar patterns of brain region size covariation occur in more closely related species. Interestingly, there were certain brain region pairs that showed similar levels of covariation across all species regardless of phylogenetic distance, such as the telencephalon and optic tectum, while others, such as the olfactory bulb and the hypothalamus, varied more independently. Ultimately, the patterns of brain region covariation shown here suggest that evolutionary mechanisms or constraints can act on specific brain regions independently, and that these constraints can change over evolutionary time.</p>","PeriodicalId":54971,"journal":{"name":"Integrative and Comparative Biology","volume":null,"pages":null},"PeriodicalIF":2.2,"publicationDate":"2024-09-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141421909","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}
Cities, through the generation of urban heat islands, provide a venue for exploring contemporary convergent evolution to climatic warming. We quantified how repeatable the evolution of heat tolerance, cold tolerance, and body size was among diverse lineages in response to urban heat islands. Our study revealed significant shifts toward higher heat tolerance and diminished cold tolerance among urban populations. We further found that the magnitude of trait divergence was significantly and positively associated with the magnitude of the urban heat island, suggesting that temperature played a major role in the observed divergence in thermal tolerance. Despite these trends, the magnitude of trait responses lagged behind environmental warming. Heat tolerance responses exhibited a deficit of 0.84°C for every 1°C increase in warming, suggesting limits on adaptive evolution and consequent adaptational lags. Other moderators were predictive of greater divergence in heat tolerance, including lower baseline tolerance and greater divergence in body size. Although terrestrial species did not exhibit systematic shifts toward larger or smaller body size, aquatic species exhibited significant shifts toward smaller body size in urban habitats. Our study demonstrates how cities can be used to address long-standing questions in evolutionary biology regarding the repeatability of evolution. Importantly, this work also shows how cities can be used as forecasting tools by quantifying adaptational lags and by developing trait-based associations with responses to contemporary warming.
{"title":"Physiology Evolves Convergently but Lags Behind Warming in Cities.","authors":"Sarah E Diamond, Logan R Kolaske, Ryan A Martin","doi":"10.1093/icb/icae034","DOIUrl":"10.1093/icb/icae034","url":null,"abstract":"<p><p>Cities, through the generation of urban heat islands, provide a venue for exploring contemporary convergent evolution to climatic warming. We quantified how repeatable the evolution of heat tolerance, cold tolerance, and body size was among diverse lineages in response to urban heat islands. Our study revealed significant shifts toward higher heat tolerance and diminished cold tolerance among urban populations. We further found that the magnitude of trait divergence was significantly and positively associated with the magnitude of the urban heat island, suggesting that temperature played a major role in the observed divergence in thermal tolerance. Despite these trends, the magnitude of trait responses lagged behind environmental warming. Heat tolerance responses exhibited a deficit of 0.84°C for every 1°C increase in warming, suggesting limits on adaptive evolution and consequent adaptational lags. Other moderators were predictive of greater divergence in heat tolerance, including lower baseline tolerance and greater divergence in body size. Although terrestrial species did not exhibit systematic shifts toward larger or smaller body size, aquatic species exhibited significant shifts toward smaller body size in urban habitats. Our study demonstrates how cities can be used to address long-standing questions in evolutionary biology regarding the repeatability of evolution. Importantly, this work also shows how cities can be used as forecasting tools by quantifying adaptational lags and by developing trait-based associations with responses to contemporary warming.</p>","PeriodicalId":54971,"journal":{"name":"Integrative and Comparative Biology","volume":null,"pages":null},"PeriodicalIF":2.2,"publicationDate":"2024-09-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140867699","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}
Dylan K Wainwright, George V Lauder, Bradford J Gemmell
The scales and skin mucus of bony fishes are both proposed to have a role in beneficially modifying the hydrodynamics of water flow over the body surface. However, it has been challenging to provide direct experimental evidence that tests how mucus and fish scales change the boundary layer in part due to the difficulties in working with live animal tissue and difficulty directly imaging the boundary layer. In this manuscript, we use direct imaging and flow tracking within the boundary layer to compare boundary layer dynamics over surfaces of fish skin with mucus, without mucus, and a flat control surface. Our direct measurements of boundary layer flows for these three different conditions are repeated for two different species, bluegill sunfish (Lepomis macrochirus) and blue tilapia (Oreochromis aureus). Our goals are to understand if mucus and scales reduce drag, shed light on mechanisms underlying drag reduction, compare these results between species, and evaluate the relative contributions to hydrodynamic function for both mucus and scales. We use our measurements of boundary layer flow to calculate shear stress (proportional to friction drag), and we find that mucus reduces drag overall by reducing the velocity gradient near the skin surface. Both bluegill and tilapia showed similar patterns of surface velocity reduction. We also note that scales alone do not appear to reduce drag, but that mucus may reduce friction drag up to 50% compared to scaled surfaces without mucus or flat controls.
{"title":"Hydrodynamic Function of the Slimy and Scaly Surfaces of Teleost Fishes.","authors":"Dylan K Wainwright, George V Lauder, Bradford J Gemmell","doi":"10.1093/icb/icae066","DOIUrl":"10.1093/icb/icae066","url":null,"abstract":"<p><p>The scales and skin mucus of bony fishes are both proposed to have a role in beneficially modifying the hydrodynamics of water flow over the body surface. However, it has been challenging to provide direct experimental evidence that tests how mucus and fish scales change the boundary layer in part due to the difficulties in working with live animal tissue and difficulty directly imaging the boundary layer. In this manuscript, we use direct imaging and flow tracking within the boundary layer to compare boundary layer dynamics over surfaces of fish skin with mucus, without mucus, and a flat control surface. Our direct measurements of boundary layer flows for these three different conditions are repeated for two different species, bluegill sunfish (Lepomis macrochirus) and blue tilapia (Oreochromis aureus). Our goals are to understand if mucus and scales reduce drag, shed light on mechanisms underlying drag reduction, compare these results between species, and evaluate the relative contributions to hydrodynamic function for both mucus and scales. We use our measurements of boundary layer flow to calculate shear stress (proportional to friction drag), and we find that mucus reduces drag overall by reducing the velocity gradient near the skin surface. Both bluegill and tilapia showed similar patterns of surface velocity reduction. We also note that scales alone do not appear to reduce drag, but that mucus may reduce friction drag up to 50% compared to scaled surfaces without mucus or flat controls.</p>","PeriodicalId":54971,"journal":{"name":"Integrative and Comparative Biology","volume":null,"pages":null},"PeriodicalIF":2.2,"publicationDate":"2024-09-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141288966","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}
{"title":"Motherhood and Academia: Tradeoffs.","authors":"Andrea L Liebl, Chloe C Josefson","doi":"10.1093/icb/icae150","DOIUrl":"https://doi.org/10.1093/icb/icae150","url":null,"abstract":"","PeriodicalId":54971,"journal":{"name":"Integrative and Comparative Biology","volume":null,"pages":null},"PeriodicalIF":2.2,"publicationDate":"2024-09-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142127411","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}
Endothermic species have evolved strategies to maximize survival in highly variable or extreme environments. Birds are exemplary as they are among the most widely distributed endotherms on the planet, living in all manner of inhospitable environments. As an example, winter in temperate regions is characterized by cold temperatures and low food availability. Some birds have evolved to tolerate these conditions by seasonally increasing thermogenic capacity, increasing heterothermy, and displaying highly flexible phenotypes. Other species have evolved to avoid the inhospitable conditions of winter altogether by migrating—again requiring a unique set of physiological adaptations that allow success in this challenging endeavor. In these examples and in many others, the organismal requirements for success share similarities, but the underlying mechanisms, physiological requirements, and selection on those traits can differ significantly, as can their ecological and evolutionary impacts. In recent years, a suite of novel and established tools has become widely available and more accessible, allowing insights into long-standing questions. Genomic tools, new approaches to measure organismal performance, the use of citizen science data, easier access to metabolite assays or hormone detection, to name a few, have spurred rapid advances in our understanding of avian physiology. These new tools have been leveraged to investigate important questions regarding avian responses to our rapidly changing climate in an attempt to understand species resilience and limits.
{"title":"Recent advances in the mechanistic understanding of avian responses to environmental challenges","authors":"Alexander R Gerson, Cory Elowe, Maria Stager","doi":"10.1093/icb/icae147","DOIUrl":"https://doi.org/10.1093/icb/icae147","url":null,"abstract":"Endothermic species have evolved strategies to maximize survival in highly variable or extreme environments. Birds are exemplary as they are among the most widely distributed endotherms on the planet, living in all manner of inhospitable environments. As an example, winter in temperate regions is characterized by cold temperatures and low food availability. Some birds have evolved to tolerate these conditions by seasonally increasing thermogenic capacity, increasing heterothermy, and displaying highly flexible phenotypes. Other species have evolved to avoid the inhospitable conditions of winter altogether by migrating—again requiring a unique set of physiological adaptations that allow success in this challenging endeavor. In these examples and in many others, the organismal requirements for success share similarities, but the underlying mechanisms, physiological requirements, and selection on those traits can differ significantly, as can their ecological and evolutionary impacts. In recent years, a suite of novel and established tools has become widely available and more accessible, allowing insights into long-standing questions. Genomic tools, new approaches to measure organismal performance, the use of citizen science data, easier access to metabolite assays or hormone detection, to name a few, have spurred rapid advances in our understanding of avian physiology. These new tools have been leveraged to investigate important questions regarding avian responses to our rapidly changing climate in an attempt to understand species resilience and limits.","PeriodicalId":54971,"journal":{"name":"Integrative and Comparative Biology","volume":null,"pages":null},"PeriodicalIF":2.6,"publicationDate":"2024-08-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142190683","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}