Pub Date : 2024-09-01Epub Date: 2023-07-12DOI: 10.1007/s00359-023-01651-9
Evangeline M Rose, Chelsea M Haakenson, Aliyah Patel, Shivika Gaind, Benjamin D Shank, Gregory F Ball
Birdsong is a relatively well-studied behavior, both due to its importance as a model for vocal production learning and as an intriguing complex social behavior. Until the last few decades, work on birdsong focused almost exclusively on males. However, it is now widely accepted that female song not only exists, but is fairly common throughout the oscine passerines. Despite this, and the large number of researchers who have begun exploring female song in the field, researchers in the lab have been slow to adopt model species with female song. Studying female song in the lab is critical for our understanding of sex-specific factors in the physiology controlling this fascinating behavior. Additionally, as a model for vocal production learning in humans, understanding the mechanistic and neuroendocrine control of female song is clearly important. In this study, we examined the red-cheeked cordon bleu (RCCB), an Estrildid finch species with extensive female song. Specifically, we found that there were no significant sex differences in circulating levels of testosterone and progesterone, nor in song production rate. There were no significant differences in cell densities in the three nuclei of the song control system we examined. Additionally, the volume of the robust nucleus of the arcopallium was not significantly different and we report the smallest sex difference in HVC yet published in a songbird. Finally, we demonstrated similar levels of motor driven immediate early gene expression in both males and females after song production.
{"title":"Song system neuroanatomy, and immediate early gene expression in a finch species with extensive male and female song.","authors":"Evangeline M Rose, Chelsea M Haakenson, Aliyah Patel, Shivika Gaind, Benjamin D Shank, Gregory F Ball","doi":"10.1007/s00359-023-01651-9","DOIUrl":"10.1007/s00359-023-01651-9","url":null,"abstract":"<p><p>Birdsong is a relatively well-studied behavior, both due to its importance as a model for vocal production learning and as an intriguing complex social behavior. Until the last few decades, work on birdsong focused almost exclusively on males. However, it is now widely accepted that female song not only exists, but is fairly common throughout the oscine passerines. Despite this, and the large number of researchers who have begun exploring female song in the field, researchers in the lab have been slow to adopt model species with female song. Studying female song in the lab is critical for our understanding of sex-specific factors in the physiology controlling this fascinating behavior. Additionally, as a model for vocal production learning in humans, understanding the mechanistic and neuroendocrine control of female song is clearly important. In this study, we examined the red-cheeked cordon bleu (RCCB), an Estrildid finch species with extensive female song. Specifically, we found that there were no significant sex differences in circulating levels of testosterone and progesterone, nor in song production rate. There were no significant differences in cell densities in the three nuclei of the song control system we examined. Additionally, the volume of the robust nucleus of the arcopallium was not significantly different and we report the smallest sex difference in HVC yet published in a songbird. Finally, we demonstrated similar levels of motor driven immediate early gene expression in both males and females after song production.</p>","PeriodicalId":54862,"journal":{"name":"Journal of Comparative Physiology A-Neuroethology Sensory Neural and Behavioral Physiology","volume":" ","pages":"735-749"},"PeriodicalIF":1.9,"publicationDate":"2024-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9761542","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"心理学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-09-01Epub Date: 2024-03-12DOI: 10.1007/s00359-024-01696-4
Kendra C Buresch, Noelle D Huget, William C Brister, Elaine Y Zhou, Abraham S Lineaweaver, Chloe Rifai, Jinyang Hu, Zoe E Stevenson, Jean G Boal, Roger T Hanlon
Octopuses integrate visual, chemical and tactile sensory information while foraging and feeding in complex marine habitats. The respective roles of these modes are of interest ecologically, neurobiologically, and for development of engineered soft robotic arms. While vision guides their foraging path, benthic octopuses primarily search "blindly" with their arms to find visually hidden prey amidst rocks, crevices and coral heads. Each octopus arm is lined with hundreds of suckers that possess a combination of chemo- and mechanoreceptors to distinguish prey. Contact chemoreception has been demonstrated in lab tests, but mechanotactile sensing is less well characterized. We designed a non-invasive live animal behavioral assay that isolated mechanosensory capabilities of Octopus bimaculoides arms and suckers to discriminate among five resin 3D-printed prey and non-prey shapes (all with identical chemical signatures). Each shape was introduced inside a rock dome and was only accessible to the octopus' arms. Octopuses' responses were variable. Young octopuses discriminated the crab prey shape from the control, whereas older octopuses did not. These experiments suggest that mechanotactile sensing of 3D shapes may aid in prey discrimination; however, (i) chemo-tactile information may be prioritized over mechanotactile information in prey discrimination, and (ii) mechanosensory capability may decline with age.
{"title":"Evidence for tactile 3D shape discrimination by octopus.","authors":"Kendra C Buresch, Noelle D Huget, William C Brister, Elaine Y Zhou, Abraham S Lineaweaver, Chloe Rifai, Jinyang Hu, Zoe E Stevenson, Jean G Boal, Roger T Hanlon","doi":"10.1007/s00359-024-01696-4","DOIUrl":"10.1007/s00359-024-01696-4","url":null,"abstract":"<p><p>Octopuses integrate visual, chemical and tactile sensory information while foraging and feeding in complex marine habitats. The respective roles of these modes are of interest ecologically, neurobiologically, and for development of engineered soft robotic arms. While vision guides their foraging path, benthic octopuses primarily search \"blindly\" with their arms to find visually hidden prey amidst rocks, crevices and coral heads. Each octopus arm is lined with hundreds of suckers that possess a combination of chemo- and mechanoreceptors to distinguish prey. Contact chemoreception has been demonstrated in lab tests, but mechanotactile sensing is less well characterized. We designed a non-invasive live animal behavioral assay that isolated mechanosensory capabilities of Octopus bimaculoides arms and suckers to discriminate among five resin 3D-printed prey and non-prey shapes (all with identical chemical signatures). Each shape was introduced inside a rock dome and was only accessible to the octopus' arms. Octopuses' responses were variable. Young octopuses discriminated the crab prey shape from the control, whereas older octopuses did not. These experiments suggest that mechanotactile sensing of 3D shapes may aid in prey discrimination; however, (i) chemo-tactile information may be prioritized over mechanotactile information in prey discrimination, and (ii) mechanosensory capability may decline with age.</p>","PeriodicalId":54862,"journal":{"name":"Journal of Comparative Physiology A-Neuroethology Sensory Neural and Behavioral Physiology","volume":" ","pages":"815-823"},"PeriodicalIF":1.9,"publicationDate":"2024-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140112162","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"心理学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-09-01Epub Date: 2023-09-29DOI: 10.1007/s00359-023-01675-1
Vladimir V Popov, Dmitry I Nechaev, Alexander Ya Supin, Evgeniya V Sysueva
Short-latency auditory-evoked potentials (AEPs) were recorded non-invasively in the bottlenose dolphin Tursiops truncatus. The stimuli were two sound clicks that were played either monaurally (both clicks to one and the same acoustic window) or dichotically (the leading stimulus (masker) to one acoustic window and the delayed stimulus (test) to the other window). The ratio of the levels of the two stimuli was 0, 10, or 20 dB (at 10 and 20 dB, the leading stimulus was of a higher level). The inter-stimulus intervals (ISIs) varied from 0.15 to 10 ms. The test response magnitude was assessed by correlation analysis as a percentage of the control (non-masked) response. At monaural stimulation, the test response was of a constant magnitude (5-6% of the control) at ISIs of 0.15-0.3 ms and recovered at longer ISIs. At dichotic stimulation, the deepest suppression of the test response occurred at ISIs of 0.5-0.7 ms. The response was slightly suppressed at short ISIs (0.15-0.3 ms) and recovered at ISIs longer than 0.5-0.7 ms. The relation of parameters of the forward masking to echolocation in dolphins is discussed.
{"title":"Monaural and dichotic forward masking in the dolphin's auditory system.","authors":"Vladimir V Popov, Dmitry I Nechaev, Alexander Ya Supin, Evgeniya V Sysueva","doi":"10.1007/s00359-023-01675-1","DOIUrl":"10.1007/s00359-023-01675-1","url":null,"abstract":"<p><p>Short-latency auditory-evoked potentials (AEPs) were recorded non-invasively in the bottlenose dolphin Tursiops truncatus. The stimuli were two sound clicks that were played either monaurally (both clicks to one and the same acoustic window) or dichotically (the leading stimulus (masker) to one acoustic window and the delayed stimulus (test) to the other window). The ratio of the levels of the two stimuli was 0, 10, or 20 dB (at 10 and 20 dB, the leading stimulus was of a higher level). The inter-stimulus intervals (ISIs) varied from 0.15 to 10 ms. The test response magnitude was assessed by correlation analysis as a percentage of the control (non-masked) response. At monaural stimulation, the test response was of a constant magnitude (5-6% of the control) at ISIs of 0.15-0.3 ms and recovered at longer ISIs. At dichotic stimulation, the deepest suppression of the test response occurred at ISIs of 0.5-0.7 ms. The response was slightly suppressed at short ISIs (0.15-0.3 ms) and recovered at ISIs longer than 0.5-0.7 ms. The relation of parameters of the forward masking to echolocation in dolphins is discussed.</p>","PeriodicalId":54862,"journal":{"name":"Journal of Comparative Physiology A-Neuroethology Sensory Neural and Behavioral Physiology","volume":" ","pages":"751-759"},"PeriodicalIF":1.9,"publicationDate":"2024-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"41160301","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"心理学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-09-01Epub Date: 2024-03-23DOI: 10.1007/s00359-024-01694-6
Cristián Gutiérrez-Ibáñez, Douglas R Wylie
For most quadrupeds, locomotion involves alternating movements of the fore- and hindlimbs. In birds, however, while walking generally involves alternating movements of the legs, to generate lift and thrust, the wings are moved synchronously with each other. Neural circuits in the spinal cord, referred to as central pattern generators (CPGs), are the source of the basic locomotor rhythms and patterns. Given the differences in the patterns of movement of the wings and legs, it is likely that the neuronal components and connectivity of the CPG that coordinates wing movements differ from those that coordinate leg movements. In this study, we used in vitro preparations of embryonic chicken spinal cords (E11-E14) to compare the neural responses of spinal CPGs that control and coordinate wing flapping with those that control alternating leg movements. We found that in response to N-methyl-D-aspartate (NMDA) or a combination of NMDA and serotonin (5-HT), the intact chicken spinal cord produced rhythmic outputs that were synchronous both bilaterally and between the wing and leg segments. Despite this, we found that this rhythmic output was disrupted by an antagonist of glycine receptors in the lumbosacral (legs), but not the brachial (wing) segments. Thus, our results provide evidence of differences between CPGs that control the wings and legs in the spinal cord of birds.
{"title":"Investigation of central pattern generators in the spinal cord of chicken embryos.","authors":"Cristián Gutiérrez-Ibáñez, Douglas R Wylie","doi":"10.1007/s00359-024-01694-6","DOIUrl":"10.1007/s00359-024-01694-6","url":null,"abstract":"<p><p>For most quadrupeds, locomotion involves alternating movements of the fore- and hindlimbs. In birds, however, while walking generally involves alternating movements of the legs, to generate lift and thrust, the wings are moved synchronously with each other. Neural circuits in the spinal cord, referred to as central pattern generators (CPGs), are the source of the basic locomotor rhythms and patterns. Given the differences in the patterns of movement of the wings and legs, it is likely that the neuronal components and connectivity of the CPG that coordinates wing movements differ from those that coordinate leg movements. In this study, we used in vitro preparations of embryonic chicken spinal cords (E11-E14) to compare the neural responses of spinal CPGs that control and coordinate wing flapping with those that control alternating leg movements. We found that in response to N-methyl-D-aspartate (NMDA) or a combination of NMDA and serotonin (5-HT), the intact chicken spinal cord produced rhythmic outputs that were synchronous both bilaterally and between the wing and leg segments. Despite this, we found that this rhythmic output was disrupted by an antagonist of glycine receptors in the lumbosacral (legs), but not the brachial (wing) segments. Thus, our results provide evidence of differences between CPGs that control the wings and legs in the spinal cord of birds.</p>","PeriodicalId":54862,"journal":{"name":"Journal of Comparative Physiology A-Neuroethology Sensory Neural and Behavioral Physiology","volume":" ","pages":"801-814"},"PeriodicalIF":1.9,"publicationDate":"2024-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11384640/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140195102","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"心理学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-09-01Epub Date: 2024-06-18DOI: 10.1007/s00359-024-01710-9
Monika Stengl
Jürgen Boeckh, a respected pioneer of insect olfaction died shortly after his beloved wife Vera Boeckh, née von Zwehl, who pioneered insect vision. Both met in 1958, at the Zoological Institute in Munich. There, Jürgen worked in the group of his PhD advisor Dietrich Schneider, while Vera finished her PhD with Werner Jacobs before she joined the group of Hansjochem Autrum. There, Vera characterized the spectral sensitivity of bee photoreceptors, laying the physiological foundation of Karl von Frisch´s behavioral experiments with bee color vision. Meanwhile, Jürgen focused on the physiological characterization of insect antennal olfactory sensilla. In 1962 Vera and Jürgen married in Munich. Sadly, but characteristic of German woman at these times, Vera´s career ended after her marriage, while Jürgen moved with his mentor Schneider to the Max Planck Institute of Behavioral Physiology in Seewiesen near Munich, which became a famous cradle of insect neuroethology. Vera accompanied and supported her husband Jürgen´s career during his scientific Wanderschaft which ended in 1969, when Jürgen received a full professorship at the University of Regensburg. There, Jürgen became an accomplished German professor, focusing on insect olfaction from peripheral sensory transduction to information processing in the brain´s antennal lobe. After Jürgens retirement in 2000 they moved to Hopfen, Enzensberg near Füssen, where they enjoyed happy years together, before especially Vera´s health deteriorated. Both died shortly after one another during the Corona pandemic. We lost a remarkable couple of insect scientists that will be remembered as pioneers of sensory physiology and neuroethology.
{"title":"Jürgen Boeckh (1934-2023) and Vera Boeckh, née von Zwehl (1928-2022): pioneers of sensory physiology and neuroethology.","authors":"Monika Stengl","doi":"10.1007/s00359-024-01710-9","DOIUrl":"10.1007/s00359-024-01710-9","url":null,"abstract":"<p><p>Jürgen Boeckh, a respected pioneer of insect olfaction died shortly after his beloved wife Vera Boeckh, née von Zwehl, who pioneered insect vision. Both met in 1958, at the Zoological Institute in Munich. There, Jürgen worked in the group of his PhD advisor Dietrich Schneider, while Vera finished her PhD with Werner Jacobs before she joined the group of Hansjochem Autrum. There, Vera characterized the spectral sensitivity of bee photoreceptors, laying the physiological foundation of Karl von Frisch´s behavioral experiments with bee color vision. Meanwhile, Jürgen focused on the physiological characterization of insect antennal olfactory sensilla. In 1962 Vera and Jürgen married in Munich. Sadly, but characteristic of German woman at these times, Vera´s career ended after her marriage, while Jürgen moved with his mentor Schneider to the Max Planck Institute of Behavioral Physiology in Seewiesen near Munich, which became a famous cradle of insect neuroethology. Vera accompanied and supported her husband Jürgen´s career during his scientific Wanderschaft which ended in 1969, when Jürgen received a full professorship at the University of Regensburg. There, Jürgen became an accomplished German professor, focusing on insect olfaction from peripheral sensory transduction to information processing in the brain´s antennal lobe. After Jürgens retirement in 2000 they moved to Hopfen, Enzensberg near Füssen, where they enjoyed happy years together, before especially Vera´s health deteriorated. Both died shortly after one another during the Corona pandemic. We lost a remarkable couple of insect scientists that will be remembered as pioneers of sensory physiology and neuroethology.</p>","PeriodicalId":54862,"journal":{"name":"Journal of Comparative Physiology A-Neuroethology Sensory Neural and Behavioral Physiology","volume":" ","pages":"825-833"},"PeriodicalIF":1.9,"publicationDate":"2024-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11384639/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141421849","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"心理学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-09-01Epub Date: 2024-02-28DOI: 10.1007/s00359-024-01693-7
Michael Tea, Yihang Kevin Pan, Joshua G R Lister, Steve F Perry, Kathleen M Gilmour
Zebrafish (Danio rerio) are unusual in having two paralogues of the serotonin re-uptake transporter (Sert), slc6a4a (serta) and slc6a4b (sertb), the transporter that serves in serotonin re-uptake from a synapse into the pre-synaptic cell or in serotonin uptake from the extracellular milieu into cells in the peripheral tissues. To address a knowledge gap concerning the specific roles of these paralogues, we used CRISPR/Cas9 technology to generate zebrafish knockout lines predicted to lack functional expression of Serta or Sertb. The consequences of loss-of-function of Serta or Sertb were assessed at the gene expression level, focusing on the serotonergic signalling pathway, and at the behaviour level, focusing on aggression. Whereas serta mRNA was expressed in all tissues examined, with high expression in the heart, gill and brain, only the brain displayed substantial sertb mRNA expression. In both serta-/- and sertb-/- fish, changes in transcript abundances of multiple components of the serotonin signalling pathway were detected, including proteins involved in serotonin synthesis (tph1a, tph1b, tph2, ddc), packaging (vmat2) and degradation (mao), and serotonin receptors (htr1aa, htr1ab). Using a mirror aggression test, serta-/- male but not female fish exhibited greater aggression than wildtype fish. However, both male and female sertb-/- fish displayed less aggression than their wildtype counterparts. These differences in behaviour between serta-/- and sertb-/- individuals hold promise for increasing our understanding of the neurophysiological basis of aggression in zebrafish.
斑马鱼(Danio rerio)有两个不同寻常的血清素再摄取转运体(Sert)的旁系亲属,即slc6a4a(serta)和slc6a4b(sertb),它们是血清素从突触再摄取到突触前细胞或从细胞外环境摄取到外周组织细胞的转运体。为了填补有关这些旁系物特定作用的知识空白,我们利用 CRISPR/Cas9 技术生成了斑马鱼基因敲除系,预测它们缺乏 Serta 或 Sertb 的功能表达。我们在基因表达水平(侧重于血清素能信号通路)和行为水平(侧重于攻击行为)上评估了 Serta 或 Sertb 功能缺失的后果。Serta mRNA在所有受检组织中均有表达,在心脏、鳃和大脑中的表达量较高,而只有大脑中有大量的Sertb mRNA表达。在 serta-/- 和 sertb-/- 鱼体内,检测到血清素信号通路中多种成分的转录本丰度发生了变化,包括参与血清素合成(tph1a、tph1b、tph2、ddc)、包装(vmat2)和降解(mao)的蛋白质,以及血清素受体(htr1aa、htr1ab)。通过镜像攻击测试,serta-/-雄鱼(而非雌鱼)比野生型鱼表现出更强的攻击性。然而,与野生型鱼类相比,sertb-/-雄鱼和雌鱼的攻击性都较低。serta-/-和sertb-/-个体之间的这些行为差异有望加深我们对斑马鱼攻击行为神经生理基础的了解。
{"title":"Effects of serta and sertb knockout on aggression in zebrafish (Danio rerio).","authors":"Michael Tea, Yihang Kevin Pan, Joshua G R Lister, Steve F Perry, Kathleen M Gilmour","doi":"10.1007/s00359-024-01693-7","DOIUrl":"10.1007/s00359-024-01693-7","url":null,"abstract":"<p><p>Zebrafish (Danio rerio) are unusual in having two paralogues of the serotonin re-uptake transporter (Sert), slc6a4a (serta) and slc6a4b (sertb), the transporter that serves in serotonin re-uptake from a synapse into the pre-synaptic cell or in serotonin uptake from the extracellular milieu into cells in the peripheral tissues. To address a knowledge gap concerning the specific roles of these paralogues, we used CRISPR/Cas9 technology to generate zebrafish knockout lines predicted to lack functional expression of Serta or Sertb. The consequences of loss-of-function of Serta or Sertb were assessed at the gene expression level, focusing on the serotonergic signalling pathway, and at the behaviour level, focusing on aggression. Whereas serta mRNA was expressed in all tissues examined, with high expression in the heart, gill and brain, only the brain displayed substantial sertb mRNA expression. In both serta<sup>-/-</sup> and sertb<sup>-/-</sup> fish, changes in transcript abundances of multiple components of the serotonin signalling pathway were detected, including proteins involved in serotonin synthesis (tph1a, tph1b, tph2, ddc), packaging (vmat2) and degradation (mao), and serotonin receptors (htr1aa, htr1ab). Using a mirror aggression test, serta<sup>-/-</sup> male but not female fish exhibited greater aggression than wildtype fish. However, both male and female sertb<sup>-/-</sup> fish displayed less aggression than their wildtype counterparts. These differences in behaviour between serta<sup>-/-</sup> and sertb<sup>-/-</sup> individuals hold promise for increasing our understanding of the neurophysiological basis of aggression in zebrafish.</p>","PeriodicalId":54862,"journal":{"name":"Journal of Comparative Physiology A-Neuroethology Sensory Neural and Behavioral Physiology","volume":" ","pages":"785-799"},"PeriodicalIF":1.9,"publicationDate":"2024-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139984548","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"心理学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-07-01Epub Date: 2023-08-16DOI: 10.1007/s00359-023-01667-1
Sergio Hidalgo, Joanna C Chiu
Organisms adapt to unfavorable seasonal conditions to survive. These seasonal adaptations rely on the correct interpretation of environmental cues such as photoperiod, and temperature. Genetic studies in several organisms, including the genetic powerhouse Drosophila melanogaster, indicate that circadian clock components, such as period and timeless, are involved in photoperiodic-dependent seasonal adaptations, but our understanding of this process is far from complete. In particular, the role of temperature as a key factor to complement photoperiodic response is not well understood. The development of new sequencing technologies has proven extremely useful in understanding the plastic changes that the clock and other cellular components undergo in different environmental conditions, including changes in gene expression and alternative splicing. This article discusses the integration of photoperiod and temperature for seasonal biology as well as downstream molecular and cellular pathways involved in the regulation of physiological adaptations that occur with changing seasons. We focus our discussion on the current understanding of the involvement of the molecular clock and the circadian clock neuronal circuits in these adaptations in D. melanogaster.
{"title":"Integration of photoperiodic and temperature cues by the circadian clock to regulate insect seasonal adaptations.","authors":"Sergio Hidalgo, Joanna C Chiu","doi":"10.1007/s00359-023-01667-1","DOIUrl":"10.1007/s00359-023-01667-1","url":null,"abstract":"<p><p>Organisms adapt to unfavorable seasonal conditions to survive. These seasonal adaptations rely on the correct interpretation of environmental cues such as photoperiod, and temperature. Genetic studies in several organisms, including the genetic powerhouse Drosophila melanogaster, indicate that circadian clock components, such as period and timeless, are involved in photoperiodic-dependent seasonal adaptations, but our understanding of this process is far from complete. In particular, the role of temperature as a key factor to complement photoperiodic response is not well understood. The development of new sequencing technologies has proven extremely useful in understanding the plastic changes that the clock and other cellular components undergo in different environmental conditions, including changes in gene expression and alternative splicing. This article discusses the integration of photoperiod and temperature for seasonal biology as well as downstream molecular and cellular pathways involved in the regulation of physiological adaptations that occur with changing seasons. We focus our discussion on the current understanding of the involvement of the molecular clock and the circadian clock neuronal circuits in these adaptations in D. melanogaster.</p>","PeriodicalId":54862,"journal":{"name":"Journal of Comparative Physiology A-Neuroethology Sensory Neural and Behavioral Physiology","volume":" ","pages":"585-599"},"PeriodicalIF":1.9,"publicationDate":"2024-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11057393/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10402461","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"心理学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-07-01Epub Date: 2023-09-11DOI: 10.1007/s00359-023-01673-3
Bettina Fishman, Eran Tauber
Seasonal adaptation in animals is a complex process that involves genetic, epigenetic, and environmental factors. The present review explores recent studies on epigenetic mechanisms implicated in seasonal adaptation in animals. The review is divided into three main sections, each focusing on a different epigenetic mechanism: DNA methylation, histone modifications, and non-coding RNA. Additionally, the review delves into the current understanding of how these epigenetic factors contribute to the regulation of circadian and seasonal cycles. Understanding these molecular mechanisms provides the first step in deciphering the complex interplay between genetics, epigenetics, and the environment in driving seasonal adaptation in animals. By exploring these mechanisms, a better understanding of how animals adapt to changing environmental conditions can be achieved.
{"title":"Epigenetics and seasonal timing in animals: a concise review.","authors":"Bettina Fishman, Eran Tauber","doi":"10.1007/s00359-023-01673-3","DOIUrl":"10.1007/s00359-023-01673-3","url":null,"abstract":"<p><p>Seasonal adaptation in animals is a complex process that involves genetic, epigenetic, and environmental factors. The present review explores recent studies on epigenetic mechanisms implicated in seasonal adaptation in animals. The review is divided into three main sections, each focusing on a different epigenetic mechanism: DNA methylation, histone modifications, and non-coding RNA. Additionally, the review delves into the current understanding of how these epigenetic factors contribute to the regulation of circadian and seasonal cycles. Understanding these molecular mechanisms provides the first step in deciphering the complex interplay between genetics, epigenetics, and the environment in driving seasonal adaptation in animals. By exploring these mechanisms, a better understanding of how animals adapt to changing environmental conditions can be achieved.</p>","PeriodicalId":54862,"journal":{"name":"Journal of Comparative Physiology A-Neuroethology Sensory Neural and Behavioral Physiology","volume":" ","pages":"565-574"},"PeriodicalIF":1.9,"publicationDate":"2024-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11226475/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10555261","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"心理学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-07-01Epub Date: 2023-10-18DOI: 10.1007/s00359-023-01674-2
Theresa S E Floessner, Elena Dalla Benetta, Domien G M Beersma, Roelof A Hut
The circadian clock times physiological and behavioural processes and resets on a daily basis to synchronize with the environment. The involvement of the circadian clock in photoperiodic time measurement synchronising annual rhythms is still under debate and different models have been proposed explaining their integration. Insects overcome unfavourable conditions in diapause, a form of dormancy. A latitudinal cline in diapause induction in the parasitoid wasp Nasonia vitripennis as well as a difference in circadian light sensitivity between north and south provide us with additional evidence that the circadian system of Nasonia is involved in photoperiodic time measurement and that latitude-specific seasonality drives adaptive evolution in photoperiodism partly through adaptation responses in the circadian system. We tested diapause induction in a range of T-cycles and photoperiods and found diapause induction in short photoperiods in all T-cycles in the northern line but in the southern line, diapause only occurred in T-cycles close to 24 h. Due to a lower light sensitivity in the southern line, a wider distribution of phase angles of entrainment can be expected at a specific T-cycle duration, while the range of entrainment will decrease. Taking these oscillator properties into account, our data can be explained by an external coincidence model involving a single oscillator with a light-sensitive phase that drives annual timing of diapause in Nasonia vitripennis.
{"title":"Variation in photoperiod response corresponds to differences in circadian light sensitivity in northern and southern Nasonia vitripennis lines.","authors":"Theresa S E Floessner, Elena Dalla Benetta, Domien G M Beersma, Roelof A Hut","doi":"10.1007/s00359-023-01674-2","DOIUrl":"10.1007/s00359-023-01674-2","url":null,"abstract":"<p><p>The circadian clock times physiological and behavioural processes and resets on a daily basis to synchronize with the environment. The involvement of the circadian clock in photoperiodic time measurement synchronising annual rhythms is still under debate and different models have been proposed explaining their integration. Insects overcome unfavourable conditions in diapause, a form of dormancy. A latitudinal cline in diapause induction in the parasitoid wasp Nasonia vitripennis as well as a difference in circadian light sensitivity between north and south provide us with additional evidence that the circadian system of Nasonia is involved in photoperiodic time measurement and that latitude-specific seasonality drives adaptive evolution in photoperiodism partly through adaptation responses in the circadian system. We tested diapause induction in a range of T-cycles and photoperiods and found diapause induction in short photoperiods in all T-cycles in the northern line but in the southern line, diapause only occurred in T-cycles close to 24 h. Due to a lower light sensitivity in the southern line, a wider distribution of phase angles of entrainment can be expected at a specific T-cycle duration, while the range of entrainment will decrease. Taking these oscillator properties into account, our data can be explained by an external coincidence model involving a single oscillator with a light-sensitive phase that drives annual timing of diapause in Nasonia vitripennis.</p>","PeriodicalId":54862,"journal":{"name":"Journal of Comparative Physiology A-Neuroethology Sensory Neural and Behavioral Physiology","volume":" ","pages":"667-676"},"PeriodicalIF":1.9,"publicationDate":"2024-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11226509/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"49685236","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"心理学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-07-01Epub Date: 2023-07-24DOI: 10.1007/s00359-023-01660-8
Francesca Sara Colizzi, David Martínez-Torres, Charlotte Helfrich-Förster
The pea aphid, Acyrthosiphon pisum, is a paradigmatic photoperiodic species that exhibits a remarkable annual life cycle, which is tightly coupled to the seasonal changes in day length. During spring and summer, characterised by longer days, aphid populations consist exclusively of viviparous females that reproduce parthenogenetically. When autumn comes and the days shorten, aphids switch their reproductive mode and generate males and oviparous sexual females, which mate and produce cold-resistant eggs that overwinter and survive the unfavourable season. While the photoperiodic responses have been well described, the nature of the timing mechanisms which underlie day length discrimination are still not completely understood. Experiments from the 1960's suggested that aphids rely on an 'hourglass' clock measuring the elapsed time during the dark night by accumulating a biochemical factor, which reaches a critical threshold at a certain night length and triggers the switch in reproduction mode. However, the photoperiodic responses of aphids can also be attributed to a strongly dampened circadian clock. Recent studies have uncovered the molecular components and the location of the circadian clock in the brain of the pea aphid and revealed that it is well connected to the neurohormonal system controlling aphid reproduction. We provide an overview of the putative mechanisms of photoperiodic control in aphids, from the photoreceptors involved in this process to the circadian clock and the neuroendocrine system.
{"title":"The circadian and photoperiodic clock of the pea aphid.","authors":"Francesca Sara Colizzi, David Martínez-Torres, Charlotte Helfrich-Förster","doi":"10.1007/s00359-023-01660-8","DOIUrl":"10.1007/s00359-023-01660-8","url":null,"abstract":"<p><p>The pea aphid, Acyrthosiphon pisum, is a paradigmatic photoperiodic species that exhibits a remarkable annual life cycle, which is tightly coupled to the seasonal changes in day length. During spring and summer, characterised by longer days, aphid populations consist exclusively of viviparous females that reproduce parthenogenetically. When autumn comes and the days shorten, aphids switch their reproductive mode and generate males and oviparous sexual females, which mate and produce cold-resistant eggs that overwinter and survive the unfavourable season. While the photoperiodic responses have been well described, the nature of the timing mechanisms which underlie day length discrimination are still not completely understood. Experiments from the 1960's suggested that aphids rely on an 'hourglass' clock measuring the elapsed time during the dark night by accumulating a biochemical factor, which reaches a critical threshold at a certain night length and triggers the switch in reproduction mode. However, the photoperiodic responses of aphids can also be attributed to a strongly dampened circadian clock. Recent studies have uncovered the molecular components and the location of the circadian clock in the brain of the pea aphid and revealed that it is well connected to the neurohormonal system controlling aphid reproduction. We provide an overview of the putative mechanisms of photoperiodic control in aphids, from the photoreceptors involved in this process to the circadian clock and the neuroendocrine system.</p>","PeriodicalId":54862,"journal":{"name":"Journal of Comparative Physiology A-Neuroethology Sensory Neural and Behavioral Physiology","volume":" ","pages":"627-639"},"PeriodicalIF":1.9,"publicationDate":"2024-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11226554/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9860940","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"心理学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}