Guillaume Poncelet, Lucia Parolini, Sebastian M. Shimeld
Sea squirts (Tunicata) are chordates and develop a swimming larva with a small and defined number of individually identifiable cells. This offers the prospect of connecting specific stimuli to behavioral output and characterizing the neural activity that links these together. Here, we describe the development of a microfluidic chip that allows live larvae of the sea squirt Ciona intestinalis to be immobilized and recorded. By generating transgenic larvae expressing GCaAMP6m in defined cells, we show that calcium ion levels can be recorded from immobilized larvae, while microfluidic control allows larvae to be exposed to specific waterborne stimuli. We trial this on sea water carrying increased levels of carbon dioxide, providing evidence that larvae can sense this gas.
{"title":"A microfluidic chip for immobilization and imaging of Ciona intestinalis larvae","authors":"Guillaume Poncelet, Lucia Parolini, Sebastian M. Shimeld","doi":"10.1002/jez.b.23267","DOIUrl":"10.1002/jez.b.23267","url":null,"abstract":"<p>Sea squirts (Tunicata) are chordates and develop a swimming larva with a small and defined number of individually identifiable cells. This offers the prospect of connecting specific stimuli to behavioral output and characterizing the neural activity that links these together. Here, we describe the development of a microfluidic chip that allows live larvae of the sea squirt <i>Ciona intestinalis</i> to be immobilized and recorded. By generating transgenic larvae expressing GCaAMP6m in defined cells, we show that calcium ion levels can be recorded from immobilized larvae, while microfluidic control allows larvae to be exposed to specific waterborne stimuli. We trial this on sea water carrying increased levels of carbon dioxide, providing evidence that larvae can sense this gas.</p>","PeriodicalId":15682,"journal":{"name":"Journal of experimental zoology. Part B, Molecular and developmental evolution","volume":"342 7","pages":"443-452"},"PeriodicalIF":1.8,"publicationDate":"2024-06-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/jez.b.23267","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141283805","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}
Žiga Fišer, Hana Whitehorn, Tia Furness, Peter Trontelj, Meredith Protas
Similar phenotypes can evolve repeatedly under the same evolutionary pressures. A compelling example is the evolution of pigment loss and eye loss in cave-dwelling animals. While specific genomic regions or genes associated with these phenotypes have been identified in model species, it remains uncertain whether a bias towards particular genetic mechanisms exists. An isopod crustacean, Asellus aquaticus, is an ideal model organism to investigate this phenomenon. It inhabits surface freshwaters throughout Europe but has colonized groundwater on multiple independent occasions and evolved several cave populations with distinct ecomorphology. Previous studies have demonstrated that three different cave populations utilized common genetic regions, potentially the same genes, in the evolution of pigment and eye loss. Expanding on this, we conducted analysis on two additional cave populations, distinct either phylogenetically or biogeographically from those previously examined. We generated F2 hybrids from cave × surface crosses and tested phenotype-genotype associations, as well as conducted complementation tests by crossing individuals from different cave populations. Our findings revealed that pigment loss and orange eye pigment in additional cave populations were associated with the same genomic regions as observed in the three previously tested cave populations. Moreover, the lack of complementation across all cross combinations suggests that the same gene likely drives pigment loss. These results substantiate a genetic bias in the recurrent evolution of pigment loss in this model system. Future investigations should focus on the cause behind this bias, possibly arising from allele recruitment from ancestral surface populations' genetic variation or advantageous allele effects via pleiotropy.
{"title":"Genetic bias in repeated evolution of pigment loss in cave populations of the Asellus aquaticus species complex","authors":"Žiga Fišer, Hana Whitehorn, Tia Furness, Peter Trontelj, Meredith Protas","doi":"10.1002/jez.b.23256","DOIUrl":"10.1002/jez.b.23256","url":null,"abstract":"<p>Similar phenotypes can evolve repeatedly under the same evolutionary pressures. A compelling example is the evolution of pigment loss and eye loss in cave-dwelling animals. While specific genomic regions or genes associated with these phenotypes have been identified in model species, it remains uncertain whether a bias towards particular genetic mechanisms exists. An isopod crustacean, <i>Asellus aquaticus</i>, is an ideal model organism to investigate this phenomenon. It inhabits surface freshwaters throughout Europe but has colonized groundwater on multiple independent occasions and evolved several cave populations with distinct ecomorphology. Previous studies have demonstrated that three different cave populations utilized common genetic regions, potentially the same genes, in the evolution of pigment and eye loss. Expanding on this, we conducted analysis on two additional cave populations, distinct either phylogenetically or biogeographically from those previously examined. We generated F2 hybrids from cave × surface crosses and tested phenotype-genotype associations, as well as conducted complementation tests by crossing individuals from different cave populations. Our findings revealed that pigment loss and orange eye pigment in additional cave populations were associated with the same genomic regions as observed in the three previously tested cave populations. Moreover, the lack of complementation across all cross combinations suggests that the same gene likely drives pigment loss. These results substantiate a genetic bias in the recurrent evolution of pigment loss in this model system. Future investigations should focus on the cause behind this bias, possibly arising from allele recruitment from ancestral surface populations' genetic variation or advantageous allele effects via pleiotropy.</p>","PeriodicalId":15682,"journal":{"name":"Journal of experimental zoology. Part B, Molecular and developmental evolution","volume":"342 6","pages":"425-436"},"PeriodicalIF":1.8,"publicationDate":"2024-06-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/jez.b.23256","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141198917","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}
{"title":"In the Spotlight—Established researcher","authors":"Janine M. Ziermann-Canabarro","doi":"10.1002/jez.b.23257","DOIUrl":"10.1002/jez.b.23257","url":null,"abstract":"","PeriodicalId":15682,"journal":{"name":"Journal of experimental zoology. Part B, Molecular and developmental evolution","volume":"342 6","pages":"417-418"},"PeriodicalIF":1.8,"publicationDate":"2024-05-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141081680","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":"In the Spotlight: Established researcher","authors":"Virginia Abdala","doi":"10.1002/jez.b.23258","DOIUrl":"10.1002/jez.b.23258","url":null,"abstract":"","PeriodicalId":15682,"journal":{"name":"Journal of experimental zoology. Part B, Molecular and developmental evolution","volume":"342 5","pages":"389-390"},"PeriodicalIF":2.2,"publicationDate":"2024-05-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141065725","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}
Astrid K. Lisondro-Arosemena, María José Salazar-Nicholls, Karen M. Warkentin
Egg dehydration can kill terrestrial frog embryos, and this threat is increasing with climate change and deforestation. In several lineages that independently evolved terrestrial eggs, and retained aquatic tadpoles, embryos accelerate hatching to escape from drying eggs, entering the water earlier and less developed. However, the cues that stimulate drying-induced early hatching are unknown. Ammonia is a toxic, water-soluble metabolic waste that accumulates within eggs as embryos develop and concentrates as eggs dehydrate. Thus, increasing ammonia concentration may be a direct threat to embryos in drying eggs. We hypothesized that it could serve as a cue, stimulating embryos to hatch and escape. The embryos of red-eyed treefrogs, Agalychnis callidryas, hatch early to escape from many threats, including dehydration, and are known to use mechanosensory, hypoxia, and light cues. To test if they also use high ammonia as a cue to hatch, we exposed stage-matched pairs of hatching-competent, well-hydrated sibling embryos to ammonia and control solutions in shallow water baths and recorded their behavior. Control embryos remained unhatched while ammonia-exposed embryos showed a rapid, strong hatching response; 95% hatched, on average in under 15 min. This demonstrates that elevated ammonia can serve as a hatching cue for A. callidryas embryos. This finding is a key step in understanding the mechanisms that enable terrestrial frog embryos to escape from egg drying, opening new possibilities for integrative and comparative studies on this growing threat.
{"title":"Elevated ammonia cues hatching in red-eyed treefrogs: A mechanism for escape from drying eggs","authors":"Astrid K. Lisondro-Arosemena, María José Salazar-Nicholls, Karen M. Warkentin","doi":"10.1002/jez.b.23253","DOIUrl":"10.1002/jez.b.23253","url":null,"abstract":"<p>Egg dehydration can kill terrestrial frog embryos, and this threat is increasing with climate change and deforestation. In several lineages that independently evolved terrestrial eggs, and retained aquatic tadpoles, embryos accelerate hatching to escape from drying eggs, entering the water earlier and less developed. However, the cues that stimulate drying-induced early hatching are unknown. Ammonia is a toxic, water-soluble metabolic waste that accumulates within eggs as embryos develop and concentrates as eggs dehydrate. Thus, increasing ammonia concentration may be a direct threat to embryos in drying eggs. We hypothesized that it could serve as a cue, stimulating embryos to hatch and escape. The embryos of red-eyed treefrogs, <i>Agalychnis callidryas</i>, hatch early to escape from many threats, including dehydration, and are known to use mechanosensory, hypoxia, and light cues. To test if they also use high ammonia as a cue to hatch, we exposed stage-matched pairs of hatching-competent, well-hydrated sibling embryos to ammonia and control solutions in shallow water baths and recorded their behavior. Control embryos remained unhatched while ammonia-exposed embryos showed a rapid, strong hatching response; 95% hatched, on average in under 15 min. This demonstrates that elevated ammonia can serve as a hatching cue for <i>A. callidryas</i> embryos. This finding is a key step in understanding the mechanisms that enable terrestrial frog embryos to escape from egg drying, opening new possibilities for integrative and comparative studies on this growing threat.</p>","PeriodicalId":15682,"journal":{"name":"Journal of experimental zoology. Part B, Molecular and developmental evolution","volume":"342 5","pages":"406-411"},"PeriodicalIF":2.2,"publicationDate":"2024-05-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140851108","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}
<p></p><p>Ingo is a Guest Coeditor of this special issue on <i>Aquatic Models for Biomedical Evo-Devo</i>.</p><p>Website: https://www.fishevodevogeno.org/</p><p>Google scholar page: https://scholar.google.com/citations?user=xVw8dCAAAAAJ</p><p>I studied biology at the University of Konstanz, Germany, and worked as an undergraduate on my first comparative fish genomics projects in the group of Axel Meyer with two fantastic postdocs at the time: John S. Taylor, now faculty at the University of Victoria, Canada, and Walter Salzburger, now faculty at the University of Basel, Switzerland. For my doctoral work, I joined Manfred Schartl and Jean-Nicolas Volff at the University of Würzburg, also in Germany, studying the functional genetic impacts of whole genome duplications on the evolution of vertebrate pigmentation. For my postdoc, I worked in the group of John H. Postlethwait at the University of Oregon in Eugene. John's group had just started to use spotted gar as a genomic outgroup to the teleost fishes and the teleost genome duplication. There, I began developing spotted gar as a developmental and functional genomic model system for vertebrate biology and EvoDevo – work that continues in my laboratory at Michigan State University.</p><p>I grew up in provincial Germany as the son of a high school chemistry and physics teacher and a pharmaceutical technician, so I was exposed to the natural sciences early on. Starting in elementary school, I developed a passion for reading about dinosaurs and prehistoric people, years before <i>Jurassic Park</i> made paleontology cool. Thus, although I didn't know the term then, I had an early appreciation for macroevolution. In high school, I kept all kinds of aquarium fishes (can you ever have too many tanks?), while reading about Darwin's <i>Voyage of the Beagle</i>, evolution, and genetics. This fascination kept going and was a reason I chose the University of Konstanz for undergraduate studies because of its strong curricular focus on molecular biology. Working as an undergraduate researcher in the Meyer Lab and being surrounded by an international crew of world-class molecular evolutionary biologists around me – who even used fish models to answer big questions about the deep evolutionary history of vertebrates – was immensely thrilling. Comparing sequences from diverse organisms and reconstructing their evolutionary change across phylogenies, I could practically look back in time! I knew I had found my path. However, sequencing DNA and analyzing genetic information on the computer was not enough for me. Fondly remembering my childhood fish breeding projects and the beauty of watching fish embryos grow, I successively added developmental biology to my research portfolio. The name of my research group, the <i>Fish Evo Devo Geno Lab</i>, reflects this multipronged approach.</p><p>Observing the elegance of developmental processes in many different fish species is my happy place. How could anyone ever just want to
Ingo是本期 "生物医学进化论的水生模型 "特刊的客座联合编辑。网站:https://www.fishevodevogeno.org/Google 学术网页:https://scholar.google.com/citations?user=xVw8dCAAAAAJI 在德国康斯坦茨大学攻读生物学,本科时曾在阿克塞尔-迈耶(Axel Meyer)的小组与当时两位出色的博士后一起从事我的第一个比较鱼类基因组学项目:约翰-泰勒(John S. Taylor,现任加拿大维多利亚大学教师)和沃尔特-萨尔茨伯格(Walter Salzburger,现任瑞士巴塞尔大学教师)。博士期间,我加入了德国维尔茨堡大学的曼弗雷德-沙特尔(Manfred Schartl)和让-尼古拉斯-沃尔夫(Jean-Nicolas Volff)的团队,研究全基因组复制对脊椎动物色素进化的功能性遗传影响。博士后期间,我在尤金俄勒冈大学约翰-H-波斯特斯韦特(John H. Postlethwait)小组工作。当时约翰的研究小组刚刚开始将斑鲤作为长尾鱼类和长尾鱼类基因组复制的基因组外群。在那里,我开始将斑点叉尾鮰作为脊椎动物生物学和进化论的发育和功能基因组模型系统进行开发,我在密歇根州立大学的实验室继续这项工作。我在德国外省长大,父亲是中学化学和物理教师,母亲是制药技师,因此我很早就接触到自然科学。从小学开始,我就热衷于阅读有关恐龙和史前人类的书籍,这比《侏罗纪公园》让古生物学变酷还要早几年。因此,虽然当时我还不知道这个词,但我很早就对宏观进化有了认识。高中时,我饲养了各种各样的鱼类(鱼缸再多也不为过),同时阅读了达尔文的《小猎犬号航行记》、进化论和遗传学方面的书籍。这种痴迷一直持续到现在,这也是我选择康斯坦茨大学攻读本科的原因之一,因为该校的分子生物学课程重点突出。在迈耶实验室担任本科生研究员,身边围绕着一群世界一流的分子进化生物学家--他们甚至用鱼类模型来解答脊椎动物深层进化史的重大问题--让我感到无比兴奋。比较来自不同生物的序列,重建它们在不同系统发育过程中的进化变化,我几乎可以回望过去!我知道自己找到了方向。然而,DNA测序和在电脑上分析遗传信息对我来说还远远不够。回想起儿时的养鱼计划和观察鱼胚胎成长的美好时光,我陆续将发育生物学加入了我的研究领域。我的研究小组名为 "鱼类进化发育基因实验室"(Fish Evo Devo Geno Lab),反映了这种多管齐下的研究方法。怎么会有人只想研究一种生物呢?在我的研究生涯中,我研究过斑马鱼、青鳉、慈鲷、鸭嘴鱼和剑尾鱼、鳉鱼、嘎尔鱼、弓鳍鱼等等,更不用说我们还分析了所有的鱼类基因组。在我看来,这正是进化胚胎学研究的核心所在--能够欣赏、研究,有时甚至解开 "无穷无尽的最美形态 "的一些机制基础。与此同时,由于没有一个实验室能保留所有的模式生物,也没有一个实验室能成为所有必要方法的专家,因此比较进化胚胎学研究本质上是合作性的,而且我强烈认为,它还特别具有开放性思维和开阔性思维。随着基因组学、基因组编辑、转基因、体内成像以及包括人工智能在内的计算技术的惊人进步,我们显然将迎来一个伟大的时代。大量的相关数据需要在不同的研究生物体中进行功能测试,以便在基因型和表型之间建立实际的因果联系--自然,EvoDevo 研究将引领这一潮流。由于我们这个领域的跨学科性质,您可能会发现自己经常处于这样的境地--无论是在研究生院、在会议上,还是在您新加入的系里--您的思维方式、想法和研究被认为超出了我们旨在整合的任何专业学科的主流。让您的 EvoDevo 研究既能吸引基础研究,也能吸引更多的应用和生物医学资助机制。保持自信,胸怀大局,相信自己有能力超越个别研究领域的知识孤岛和障眼法。幸运的是,随着泛美进化发育生物学学会和欧洲进化发育生物学学会在过去20年中的成立,我个人认为这是我的知识家园,我们现在有很多机会在我们热闹的社区中建立联系,共同倡导EvoDevo思想。快来加入我们吧
{"title":"In the Spotlight—Established researcher","authors":"Ingo Braasch","doi":"10.1002/jez.b.23254","DOIUrl":"https://doi.org/10.1002/jez.b.23254","url":null,"abstract":"<p></p><p>Ingo is a Guest Coeditor of this special issue on <i>Aquatic Models for Biomedical Evo-Devo</i>.</p><p>Website: https://www.fishevodevogeno.org/</p><p>Google scholar page: https://scholar.google.com/citations?user=xVw8dCAAAAAJ</p><p>I studied biology at the University of Konstanz, Germany, and worked as an undergraduate on my first comparative fish genomics projects in the group of Axel Meyer with two fantastic postdocs at the time: John S. Taylor, now faculty at the University of Victoria, Canada, and Walter Salzburger, now faculty at the University of Basel, Switzerland. For my doctoral work, I joined Manfred Schartl and Jean-Nicolas Volff at the University of Würzburg, also in Germany, studying the functional genetic impacts of whole genome duplications on the evolution of vertebrate pigmentation. For my postdoc, I worked in the group of John H. Postlethwait at the University of Oregon in Eugene. John's group had just started to use spotted gar as a genomic outgroup to the teleost fishes and the teleost genome duplication. There, I began developing spotted gar as a developmental and functional genomic model system for vertebrate biology and EvoDevo – work that continues in my laboratory at Michigan State University.</p><p>I grew up in provincial Germany as the son of a high school chemistry and physics teacher and a pharmaceutical technician, so I was exposed to the natural sciences early on. Starting in elementary school, I developed a passion for reading about dinosaurs and prehistoric people, years before <i>Jurassic Park</i> made paleontology cool. Thus, although I didn't know the term then, I had an early appreciation for macroevolution. In high school, I kept all kinds of aquarium fishes (can you ever have too many tanks?), while reading about Darwin's <i>Voyage of the Beagle</i>, evolution, and genetics. This fascination kept going and was a reason I chose the University of Konstanz for undergraduate studies because of its strong curricular focus on molecular biology. Working as an undergraduate researcher in the Meyer Lab and being surrounded by an international crew of world-class molecular evolutionary biologists around me – who even used fish models to answer big questions about the deep evolutionary history of vertebrates – was immensely thrilling. Comparing sequences from diverse organisms and reconstructing their evolutionary change across phylogenies, I could practically look back in time! I knew I had found my path. However, sequencing DNA and analyzing genetic information on the computer was not enough for me. Fondly remembering my childhood fish breeding projects and the beauty of watching fish embryos grow, I successively added developmental biology to my research portfolio. The name of my research group, the <i>Fish Evo Devo Geno Lab</i>, reflects this multipronged approach.</p><p>Observing the elegance of developmental processes in many different fish species is my happy place. How could anyone ever just want to ","PeriodicalId":15682,"journal":{"name":"Journal of experimental zoology. Part B, Molecular and developmental evolution","volume":"342 3","pages":"121-122"},"PeriodicalIF":2.2,"publicationDate":"2024-04-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/jez.b.23254","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140814166","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}
Patricia N. Schneider, Frauke Seemann, Matthew P. Harris, Ingo Braasch
{"title":"Trawling aquatic life for new models in biomedical research and evolutionary developmental biology","authors":"Patricia N. Schneider, Frauke Seemann, Matthew P. Harris, Ingo Braasch","doi":"10.1002/jez.b.23255","DOIUrl":"https://doi.org/10.1002/jez.b.23255","url":null,"abstract":"","PeriodicalId":15682,"journal":{"name":"Journal of experimental zoology. Part B, Molecular and developmental evolution","volume":"342 3","pages":"123-125"},"PeriodicalIF":2.2,"publicationDate":"2024-04-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/jez.b.23255","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140814167","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}
Evolutionary developmental biology (Evo-Devo) is flourishing in Latin America, particularly Argentina, where researchers are leveraging this integrative field to unlock the secrets of the region's remarkable biodiversity. A recent symposium held at the 5th Argentinean Meeting on Evolutionary Biology (RABE V) showcased a vibrant Evo-Devo community and the diversity of its research endeavors. The symposium included 3 plenary talks, 3 short talks, and 12 posters, and spanned a range of organisms and approaches. Interestingly, the symposium highlighted a prevalence of “top-down” Evo-Devo studies in the region, where researchers first analyze existing diversity and then propose potential developmental mechanisms. This approach, driven in part by financial constraints and the region's historical focus on natural history, presents a unique opportunity to bridge disciplines like comparative biology, paleontology, and botany. The symposium's success underscores the vital role of Evo-Devo in Latin America, not only for advancing our understanding of evolution but also for providing valuable tools to conserve and manage the region's irreplaceable biodiversity. As Evo-Devo continues to grow in Latin America, fostering collaboration and knowledge exchange within the region and beyond will be crucial for realizing the full potential of this transformative field.
{"title":"5th Argentinean Meeting on Evolutionary Biology (RABE V): Report on the “Evo-Devo” Extended Symposium","authors":"Eduardo E. Zattara, Marina M. Strelin","doi":"10.1002/jez.b.23252","DOIUrl":"10.1002/jez.b.23252","url":null,"abstract":"<p>Evolutionary developmental biology (Evo-Devo) is flourishing in Latin America, particularly Argentina, where researchers are leveraging this integrative field to unlock the secrets of the region's remarkable biodiversity. A recent symposium held at the 5th Argentinean Meeting on Evolutionary Biology (RABE V) showcased a vibrant Evo-Devo community and the diversity of its research endeavors. The symposium included 3 plenary talks, 3 short talks, and 12 posters, and spanned a range of organisms and approaches. Interestingly, the symposium highlighted a prevalence of “top-down” Evo-Devo studies in the region, where researchers first analyze existing diversity and then propose potential developmental mechanisms. This approach, driven in part by financial constraints and the region's historical focus on natural history, presents a unique opportunity to bridge disciplines like comparative biology, paleontology, and botany. The symposium's success underscores the vital role of Evo-Devo in Latin America, not only for advancing our understanding of evolution but also for providing valuable tools to conserve and manage the region's irreplaceable biodiversity. As Evo-Devo continues to grow in Latin America, fostering collaboration and knowledge exchange within the region and beyond will be crucial for realizing the full potential of this transformative field.</p>","PeriodicalId":15682,"journal":{"name":"Journal of experimental zoology. Part B, Molecular and developmental evolution","volume":"342 4","pages":"335-341"},"PeriodicalIF":2.2,"publicationDate":"2024-04-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140842332","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}
Wolves howl and dogs bark, both are able to produce variants of either vocalization, but we see a distinct difference in usage between wild and domesticate. Other domesticates also show distinct changes to their vocal output: domestic cats retain meows, a distinctly subadult trait in wildcats. Such differences in acoustic output are well-known, but the causal mechanisms remain little-studied. Potential links between domestication and vocal output are intriguing for multiple reasons, and offer a unique opportunity to explore a prominent hypothesis in domestication research: the neural crest/domestication syndrome hypothesis. This hypothesis suggests that in the early stages of domestication, selection for tame individuals decreased neural crest cell (NCCs) proliferation and migration, which led to a downregulation of the sympathetic arousal system, and hence reduced fear and reactive aggression. NCCs are a transitory stem cell population crucial during embryonic development that tie to diverse tissue types and organ systems. One of these neural-crest derived systems is the larynx, the main vocal source in mammals. We argue that this connection between NCCs and the larynx provides a powerful test of the predictions of the neural crest/domestication syndrome hypothesis, discriminating its predictions from those of other current hypotheses concerning domestication.
{"title":"The domestication of the larynx: The neural crest connection","authors":"Raffaela Lesch, W. Tecumseh Fitch","doi":"10.1002/jez.b.23251","DOIUrl":"10.1002/jez.b.23251","url":null,"abstract":"<p>Wolves howl and dogs bark, both are able to produce variants of either vocalization, but we see a distinct difference in usage between wild and domesticate. Other domesticates also show distinct changes to their vocal output: domestic cats retain meows, a distinctly subadult trait in wildcats. Such differences in acoustic output are well-known, but the causal mechanisms remain little-studied. Potential links between domestication and vocal output are intriguing for multiple reasons, and offer a unique opportunity to explore a prominent hypothesis in domestication research: the neural crest/domestication syndrome hypothesis. This hypothesis suggests that in the early stages of domestication, selection for tame individuals decreased neural crest cell (NCCs) proliferation and migration, which led to a downregulation of the sympathetic arousal system, and hence reduced fear and reactive aggression. NCCs are a transitory stem cell population crucial during embryonic development that tie to diverse tissue types and organ systems. One of these neural-crest derived systems is the larynx, the main vocal source in mammals. We argue that this connection between NCCs and the larynx provides a powerful test of the predictions of the neural crest/domestication syndrome hypothesis, discriminating its predictions from those of other current hypotheses concerning domestication.</p>","PeriodicalId":15682,"journal":{"name":"Journal of experimental zoology. Part B, Molecular and developmental evolution","volume":"342 4","pages":"342-349"},"PeriodicalIF":2.2,"publicationDate":"2024-04-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/jez.b.23251","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140581138","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}
The chin, a distinguishing feature of Homo sapiens, has sparked ongoing debates regarding its evolutionary origins and adaptive significance. We contend that these controversies stem from a fundamental disagreement about what constitutes a well-defined biological trait, a problem that has received insufficient attention despite its recognized importance in biology. In this paper, we leverage paleoanthropological research on the human chin to investigate the general issue of character or trait identification. First, we examine four accounts of the human chin from the existing literature: the mandibular differential growth byproduct, the bony prominence, the inverted T-relief, and the symphyseal angle. We then generalize from these accounts and propose a three-stage framework for the process of character identification: description, detection, and justification. We use this framework to reinterpret the four accounts, elucidating key points of contention surrounding the chin as well as other morphological characters. We show that debates over the chin carry broad and important biological implications that extend beyond this trait and that are not mere semantic issues of definition.
下巴是智人的一个显著特征,它的进化起源和适应意义引发了持续不断的争论。我们认为,这些争论源于对什么是定义明确的生物特征的根本分歧,尽管这一问题在生物学中的重要性已得到公认,但却没有得到足够的重视。在本文中,我们利用古人类学对人类下巴的研究来探讨性格或特征识别的一般问题。首先,我们研究了现有文献中关于人类下巴的四种描述:下颌差异生长副产品、骨突、倒 T 形凸起和骨骺角。然后,我们从这些描述中进行归纳,提出了特征识别过程的三阶段框架:描述、检测和论证。我们利用这一框架重新解释了这四种说法,阐明了围绕下巴和其他形态特征的关键争议点。我们表明,关于下巴的争论具有广泛而重要的生物学意义,这些意义超出了这一特征的范围,也不仅仅是定义的语义问题。
{"title":"What is a trait? Lessons from the human chin","authors":"Andra Meneganzin, Grant Ramsey, James DiFrisco","doi":"10.1002/jez.b.23249","DOIUrl":"10.1002/jez.b.23249","url":null,"abstract":"<p>The chin, a distinguishing feature of <i>Homo sapiens</i>, has sparked ongoing debates regarding its evolutionary origins and adaptive significance. We contend that these controversies stem from a fundamental disagreement about what constitutes a well-defined biological trait, a problem that has received insufficient attention despite its recognized importance in biology. In this paper, we leverage paleoanthropological research on the human chin to investigate the general issue of character or trait identification. First, we examine four accounts of the human chin from the existing literature: the mandibular differential growth byproduct, the bony prominence, the inverted T-relief, and the symphyseal angle. We then generalize from these accounts and propose a three-stage framework for the process of character identification: description, detection, and justification. We use this framework to reinterpret the four accounts, elucidating key points of contention surrounding the chin as well as other morphological characters. We show that debates over the chin carry broad and important biological implications that extend beyond this trait and that are not mere semantic issues of definition.</p>","PeriodicalId":15682,"journal":{"name":"Journal of experimental zoology. Part B, Molecular and developmental evolution","volume":"342 2","pages":"65-75"},"PeriodicalIF":2.2,"publicationDate":"2024-03-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/jez.b.23249","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140287563","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}