Pub Date : 2014-04-01DOI: 10.1016/j.jphysparis.2014.10.001
Nelson A. Velásquez
Geographic variation of traits may represent the first step for evolutionary divergence potentially leading to speciation. Signals are behavioral traits of particular interest for the study of variation at a geographic scale. The anuran acoustic communication system represents an excellent model for studies of this kind, because their vocalizations play a main role in reproduction and the extant variation in this system may determine the evolution of this group. This review is committed to studies on geographic variation of acoustic communication systems in anurans, focusing on temporal and spectral characteristics of signals, environmental constraints affecting them and sound producing and receiving organs. In addition to the review of the literature on these topics, I highlight the deficit of investigation in some areas and propose alternative directions to overcome these drawbacks. Further, I propose the four-eyed frog, Pleurodema thaul, as an excellent model system to study geographic variation using a wide spectrum of approaches.
{"title":"Geographic variation in acoustic communication in anurans and its neuroethological implications","authors":"Nelson A. Velásquez","doi":"10.1016/j.jphysparis.2014.10.001","DOIUrl":"10.1016/j.jphysparis.2014.10.001","url":null,"abstract":"<div><p>Geographic variation of traits may represent the first step for evolutionary divergence potentially leading to speciation. Signals are behavioral traits of particular interest for the study of variation at a geographic scale. The anuran acoustic communication system represents an excellent model for studies of this kind, because their vocalizations play a main role in reproduction and the extant variation in this system may determine the evolution of this group. This review is committed to studies on geographic variation of acoustic communication systems in anurans, focusing on temporal and spectral characteristics of signals, environmental constraints affecting them and sound producing and receiving organs. In addition to the review of the literature on these topics, I highlight the deficit of investigation in some areas and propose alternative directions to overcome these drawbacks. Further, I propose the four-eyed frog, <em>Pleurodema thaul</em>, as an excellent model system to study geographic variation using a wide spectrum of approaches.</p></div>","PeriodicalId":50087,"journal":{"name":"Journal of Physiology-Paris","volume":"108 2","pages":"Pages 167-173"},"PeriodicalIF":0.0,"publicationDate":"2014-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.jphysparis.2014.10.001","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"32856413","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2014-04-01DOI: 10.1016/j.jphysparis.2014.07.005
Ana Carolina Pereira, Alejo Rodríguez-Cattáneo, Angel A. Caputi
This is a first communication on the self-activation pattern of the electrosensory lobe in the pulse weakly electric fish Gymnotus omarorum. Field potentials in response to the fish’s own electric organ discharge (EOD) were recorded along vertical tracks (50 μm step) and on a transversal lattice array across the electrosensory lobe (resolution 50 μm × 100 μm). The unitary activity of 82 neurons was recorded in the same experiments. Field potential analysis indicates that the slow electrosensory path shows a characteristic post-EOD pattern of activity marked by three main events: (i) a small and early component at about 7 ms, (ii) an intermediate peak about 13 ms and (iii) a late broad component peaking after 20 ms. Unit firing rate showed a wide range of latencies between 3 and 30 ms and a variable number of spikes (median 0.28 units/EOD). Conditional probability analysis showed monomodal and multimodal post-EOD histograms, with the peaks of unit activity histograms often matching the timing of the main components of the field potentials. Monomodal responses were sub-classified as phase locked monomodal (variance smaller than 1 ms), early monomodal (intermediate variance, often firing in doublets, peaking range 10–17 ms) and late monomodal (large variance, often firing two spikes separated about 10 ms, peaking beyond 17 ms). The responses of multimodal units showed that their firing probability was either enhanced, or depressed just after the EOD. In this last (depressed) subtype of unit the probability stepped down just after the EOD. Early inhibition and the presence of early phase locked units suggest that the observed pattern may be influenced by a fast feed forward inhibition. We conclude that the ELL in pulse gymnotiformes is activated in a complex sequence of events that reflects the ELL network connectivity.
{"title":"The slow pathway in the electrosensory lobe of Gymnotus omarorum: Field potentials and unitary activity","authors":"Ana Carolina Pereira, Alejo Rodríguez-Cattáneo, Angel A. Caputi","doi":"10.1016/j.jphysparis.2014.07.005","DOIUrl":"10.1016/j.jphysparis.2014.07.005","url":null,"abstract":"<div><p>This is a first communication on the self-activation pattern of the electrosensory lobe in the pulse weakly electric fish <span><em>Gymnotus</em><em> omarorum</em></span>. Field potentials in response to the fish’s own electric organ discharge (EOD) were recorded along vertical tracks (50<!--> <!-->μm step) and on a transversal lattice array across the electrosensory lobe (resolution 50<!--> <!-->μm<!--> <!-->×<!--> <!-->100<!--> <!-->μm). The unitary activity of 82 neurons was recorded in the same experiments. Field potential analysis indicates that the slow electrosensory path shows a characteristic post-EOD pattern of activity marked by three main events: (i) a small and early component at about 7<!--> <!-->ms, (ii) an intermediate peak about 13<!--> <!-->ms and (iii) a late broad component peaking after 20<!--> <!-->ms. Unit firing rate showed a wide range of latencies between 3 and 30<!--> <!-->ms and a variable number of spikes (median 0.28<!--> <!-->units/EOD). Conditional probability analysis showed monomodal and multimodal post-EOD histograms, with the peaks of unit activity histograms often matching the timing of the main components of the field potentials. Monomodal responses were sub-classified as phase locked monomodal (variance smaller than 1<!--> <!-->ms), early monomodal (intermediate variance, often firing in doublets, peaking range 10–17<!--> <!-->ms) and late monomodal (large variance, often firing two spikes separated about 10<!--> <!-->ms, peaking beyond 17<!--> <span>ms). The responses of multimodal units showed that their firing probability was either enhanced, or depressed just after the EOD. In this last (depressed) subtype of unit the probability stepped down just after the EOD. Early inhibition and the presence of early phase locked units suggest that the observed pattern may be influenced by a fast feed forward inhibition. We conclude that the ELL in pulse gymnotiformes is activated in a complex sequence of events that reflects the ELL network connectivity.</span></p></div>","PeriodicalId":50087,"journal":{"name":"Journal of Physiology-Paris","volume":"108 2","pages":"Pages 71-83"},"PeriodicalIF":0.0,"publicationDate":"2014-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.jphysparis.2014.07.005","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"32557035","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2014-04-01DOI: 10.1016/j.jphysparis.2014.10.002
Daniel E. Olazábal
Parental behavior is commonly displayed by progenitors. However, other individuals, genetically related (e.g. siblings, aunts, uncles) or not with the newborns, also display parental behavior (commonly called alloparental, or adoptive behavior). I hypothesize that species that live in family or social groups where other non-reproductive members (males and females) take care of infants, have brain adaptations to promote or facilitate that behavioral response. The present work revises the evidence supporting the hypothesis that high density of oxytocin receptors (OXTR) in the nucleus accumbens (NA) is one of those adaptations. All species known to have high NA OXTR show not only female, but also male alloparental care. Therefore, I predict that high NA OXTR could be present in all species in which juvenile and adult male alloparental behavior have been observed. Strategies to test this and other alternative working hypothesis and its predictions are presented.
{"title":"Comparative analysis of oxytocin receptor density in the nucleus accumbens: An adaptation for female and male alloparental care?","authors":"Daniel E. Olazábal","doi":"10.1016/j.jphysparis.2014.10.002","DOIUrl":"10.1016/j.jphysparis.2014.10.002","url":null,"abstract":"<div><p>Parental behavior is commonly displayed by progenitors. However, other individuals, genetically related (e.g. siblings, aunts, uncles) or not with the newborns, also display parental behavior (commonly called alloparental, or adoptive behavior). I hypothesize that species that live in family or social groups where other non-reproductive members (males and females) take care of infants, have brain adaptations to promote or facilitate that behavioral response. The present work revises the evidence supporting the hypothesis that high density of oxytocin receptors (OXTR) in the nucleus accumbens (NA) is one of those adaptations. All species known to have high NA OXTR show not only female, but also male alloparental care. Therefore, I predict that high NA OXTR could be present in all species in which juvenile and adult male alloparental behavior have been observed. Strategies to test this and other alternative working hypothesis and its predictions are presented.</p></div>","PeriodicalId":50087,"journal":{"name":"Journal of Physiology-Paris","volume":"108 2","pages":"Pages 213-220"},"PeriodicalIF":0.0,"publicationDate":"2014-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.jphysparis.2014.10.002","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"32856867","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2014-04-01DOI: 10.1016/j.jphysparis.2014.05.004
Lidia Szczupak
The review proposes a comparison between recurrent inhibition in motor systems of vertebrates and the leech nervous system, where a detailed cellular and functional analysis has been accomplished. A comparative study shows that recurrent inhibition is a conserved property in motor systems of phylogenetically distant species. Recurrent inhibition has been extensively characterized in the spinal cord of mammals, where Renshaw cells receive excitatory synaptic inputs from motoneurons (MNs) and, in turn, exert an inhibitory effect on the MNs. In the leech, a recurrent inhibitory circuit has been described, centered around a pair of nonspiking (NS) neurons. NS are linked to every excitatory MN through rectifying electrical junctions. And, in addition, the MNs are linked to the NS neurons through hyperpolarizing chemical synapses. Functional analysis of this leech circuit showed that heteronymous MNs in the leech are electrically coupled and this coupling is modulated by the membrane potential of NS neurons. Like Renshaw cells, the membrane potential of NS neurons oscillates in phase with rhythmic motor patterns. Functional analysis performed in the leech shows that NS influences the activity of MNs in the course of crawling suggesting that the recurrent inhibitory circuit modulates the motor performance.
{"title":"Recurrent inhibition in motor systems, a comparative analysis","authors":"Lidia Szczupak","doi":"10.1016/j.jphysparis.2014.05.004","DOIUrl":"10.1016/j.jphysparis.2014.05.004","url":null,"abstract":"<div><p>The review proposes a comparison between recurrent inhibition in motor systems of vertebrates and the leech nervous system, where a detailed cellular and functional analysis has been accomplished. A comparative study shows that recurrent inhibition is a conserved property in motor systems of phylogenetically distant species. Recurrent inhibition has been extensively characterized in the spinal cord of mammals, where Renshaw cells receive excitatory synaptic inputs from motoneurons (MNs) and, in turn, exert an inhibitory effect on the MNs. In the leech, a recurrent inhibitory circuit has been described, centered around a pair of nonspiking (NS) neurons. NS are linked to every excitatory MN through rectifying electrical junctions. And, in addition, the MNs are linked to the NS neurons through hyperpolarizing chemical synapses. Functional analysis of this leech circuit showed that heteronymous MNs in the leech are electrically coupled and this coupling is modulated by the membrane potential of NS neurons. Like Renshaw cells, the membrane potential of NS neurons oscillates in phase with rhythmic motor patterns. Functional analysis performed in the leech shows that NS influences the activity of MNs in the course of crawling suggesting that the recurrent inhibitory circuit modulates the motor performance.</p></div>","PeriodicalId":50087,"journal":{"name":"Journal of Physiology-Paris","volume":"108 2","pages":"Pages 148-154"},"PeriodicalIF":0.0,"publicationDate":"2014-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.jphysparis.2014.05.004","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"32374786","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2014-04-01DOI: 10.1016/j.jphysparis.2014.05.006
Mariana Lozada, Paola D’Adamo
In this paper we review several studies on Vespulagermanica behavioral plasticity while relocating a food source in natural environments. This exotic social wasp, which has become established in many parts of the world, displays diverse cognitive abilities when foraging. Given its successful invasiveness worldwide, our initial hypothesis was that this species has great behavioral plasticity, which enables it to face environmental uncertainty. In our work we have analyzed foraging behavior associated with undepleted resources. Throughout several experiments, rapid learning was observed in this species; after few learning experiences they associate diverse contextual cues with a food source. However, by exploring wasp behavior when food suddenly disappeared, either because it had been removed or displaced, we found that they continued searching over a no longer rewarding site for a considerable period of time, suggesting that past experience can hinder new learning. Particularly surprising is the fact that when food was displaced nearby, wasps persisted in searching over the empty dish, ignoring the presence of food close by. We propose that this species could be a suitable model for studying cognitive plasticity in relation to environmental uncertainty.
{"title":"Learning in an exotic social wasp while relocating a food source","authors":"Mariana Lozada, Paola D’Adamo","doi":"10.1016/j.jphysparis.2014.05.006","DOIUrl":"10.1016/j.jphysparis.2014.05.006","url":null,"abstract":"<div><p>In this paper we review several studies on <em>Vespula</em> <em>germanica</em> behavioral plasticity while relocating a food source in natural environments. This exotic social wasp, which has become established in many parts of the world, displays diverse cognitive abilities when foraging. Given its successful invasiveness worldwide, our initial hypothesis was that this species has great behavioral plasticity, which enables it to face environmental uncertainty. In our work we have analyzed foraging behavior associated with undepleted resources. Throughout several experiments, rapid learning was observed in this species; after few learning experiences they associate diverse contextual cues with a food source. However, by exploring wasp behavior when food suddenly disappeared, either because it had been removed or displaced, we found that they continued searching over a no longer rewarding site for a considerable period of time, suggesting that past experience can hinder new learning. Particularly surprising is the fact that when food was displaced nearby, wasps persisted in searching over the empty dish, ignoring the presence of food close by. We propose that this species could be a suitable model for studying cognitive plasticity in relation to environmental uncertainty.</p></div>","PeriodicalId":50087,"journal":{"name":"Journal of Physiology-Paris","volume":"108 2","pages":"Pages 187-193"},"PeriodicalIF":0.0,"publicationDate":"2014-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.jphysparis.2014.05.006","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"32422545","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2014-04-01DOI: 10.1016/j.jphysparis.2014.07.001
Eliana M. Canero, Gabriela Hermitte
The ability to stay alert to subtle changes in the environment and to freeze, fight or flight in the presence of predators requires integrating sensory information as well as triggering motor output to target tissues, both of which are associated with the autonomic nervous system. These reactions, which are commonly related to vertebrates, are the fundamental physiological responses that allow an animal to survive danger. The circulatory activity in vertebrates changes in opposite phases. The stage where circulatory activity is high is termed the “fight or flight stage”, while the stage where circulatory activity slows down is termed the “rest and digest stage”. It may be assumed that highly evolved invertebrates possess a comparable response system as they also require rapid cardiovascular and respiratory regulation to be primed when necessary. However, in invertebrates, the body plan may have developed such a system very differently. Since this topic is insufficiently studied, it is necessary to extend studies for a comparative analysis. In the present review, we use our own experimental results obtained in the crab Neohelice granulata and both older and newer findings obtained by other authors in decapod crustaceans as well as in other invertebrates, to compare the pattern of change in circulatory activity, especially in the “fight or flight” stage. We conclude that the main features of neuroautonomic regulation of the cardiac function were already present early in evolution, at least in highly evolved invertebrates, although conspicuous differences are also evident.
{"title":"New evidence on an old question: Is the “fight or flight” stage present in the cardiac and respiratory regulation of decapod crustaceans?","authors":"Eliana M. Canero, Gabriela Hermitte","doi":"10.1016/j.jphysparis.2014.07.001","DOIUrl":"10.1016/j.jphysparis.2014.07.001","url":null,"abstract":"<div><p>The ability to stay alert to subtle changes in the environment and to freeze, fight or flight in the presence of predators requires integrating sensory information as well as triggering motor output to target tissues, both of which are associated with the autonomic nervous system. These reactions, which are commonly related to vertebrates, are the fundamental physiological responses that allow an animal to survive danger. The circulatory activity in vertebrates changes in opposite phases. The stage where circulatory activity is high is termed the “fight or flight stage”, while the stage where circulatory activity slows down is termed the “rest and digest stage”. It may be assumed that highly evolved invertebrates possess a comparable response system as they also require rapid cardiovascular and respiratory regulation to be primed when necessary. However, in invertebrates, the body plan may have developed such a system very differently. Since this topic is insufficiently studied, it is necessary to extend studies for a comparative analysis. In the present review, we use our own experimental results obtained in the crab <em>Neohelice granulata</em> and both older and newer findings obtained by other authors in decapod crustaceans as well as in other invertebrates, to compare the pattern of change in circulatory activity, especially in the “fight or flight” stage. We conclude that the main features of neuroautonomic regulation of the cardiac function were already present early in evolution, at least in highly evolved invertebrates, although conspicuous differences are also evident.</p></div>","PeriodicalId":50087,"journal":{"name":"Journal of Physiology-Paris","volume":"108 2","pages":"Pages 174-186"},"PeriodicalIF":0.0,"publicationDate":"2014-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.jphysparis.2014.07.001","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"32679169","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2014-04-01DOI: 10.1016/j.jphysparis.2014.08.004
Martín Roberto Ramallo , Leonel Morandini , Felipe Alonso , Agustina Birba , Cecilia Tubert , Ana Fiszbein , Matías Pandolfi
Sociobiology, the study of social behavior, calls for a laboratory model with specific requirements. Among the most obvious is the execution of social interactions that need to be readily observable, quantifiable and analyzable. If, in turn, one focuses on the neuroendocrinological basis of social behavior, restrictions grow even tighter. A good laboratory model should then allow easy access to its neurological and endocrine components and processes. During the last years, we have been studying the physiological foundation of social behavior on what we believe fits all the aforementioned requirements: the so called “chanchita”, Cichlasoma dimerus. This Neotropical cichlid fish exhibits biparental care of the eggs and larvae and presents a hierarchical social system, established and sustained through agonistic interactions. The aim of the current article is to review new evidence on chanchita’s social and reproductive behavior.
{"title":"The endocrine regulation of cichlids social and reproductive behavior through the eyes of the chanchita, Cichlasoma dimerus (Percomorpha; Cichlidae)","authors":"Martín Roberto Ramallo , Leonel Morandini , Felipe Alonso , Agustina Birba , Cecilia Tubert , Ana Fiszbein , Matías Pandolfi","doi":"10.1016/j.jphysparis.2014.08.004","DOIUrl":"10.1016/j.jphysparis.2014.08.004","url":null,"abstract":"<div><p>Sociobiology, the study of social behavior, calls for a laboratory model with specific requirements. Among the most obvious is the execution of social interactions that need to be readily observable, quantifiable and analyzable. If, in turn, one focuses on the neuroendocrinological basis of social behavior, restrictions grow even tighter. A good laboratory model should then allow easy access to its neurological and endocrine components and processes. During the last years, we have been studying the physiological foundation of social behavior on what we believe fits all the aforementioned requirements: the so called “chanchita”, <em>Cichlasoma dimerus.</em> This Neotropical cichlid fish exhibits biparental care of the eggs and larvae and presents a hierarchical social system, established and sustained through agonistic interactions. The aim of the current article is to review new evidence on chanchita’s social and reproductive behavior.</p></div>","PeriodicalId":50087,"journal":{"name":"Journal of Physiology-Paris","volume":"108 2","pages":"Pages 194-202"},"PeriodicalIF":0.0,"publicationDate":"2014-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.jphysparis.2014.08.004","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"32616478","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2014-04-01DOI: 10.1016/j.jphysparis.2014.04.006
F. Guidobaldi , I.J. May-Concha , P.G. Guerenstein
Several blood-feeding (hematophagous) insects are vectors of a number of diseases including dengue, Chagas disease and leishmaniasis which persistently affect public health throughout Latin America. The vectors of those diseases include mosquitoes, triatomine bugs and sandflies. As vector control is an efficient way to prevent these illnesses it is important to understand the sensory biology of those harmful insects. We study the physiology of the olfactory system of those insects and apply that knowledge on the development of methods to manipulate their behavior. Here we review some of the latest information on insect olfaction with emphasis on hematophagous insects. The insect olfactory sensory neurons are housed inside hair-like organs called sensilla which are mainly distributed on the antenna and mouthparts. The identity of many of the odor compounds that those neurons detect are already known in hematophagous insects. They include several constituents of host (vertebrate) odor, sex, aggregation and alarm pheromones, and compounds related to egg-deposition behavior. Recent work has contributed significant knowledge on how odor information is processed in the insect first odor-processing center in the brain, the antennal lobe. The quality, quantity, and temporal features of the odor stimuli are encoded by the neural networks of the antennal lobe. Information regarding odor mixtures is also encoded. While natural mixtures evoke strong responses, synthetic mixtures that deviate from their natural counterparts in terms of key constituents or proportions of those constituents evoke weaker responses. The processing of olfactory information is largely unexplored in hematophagous insects. However, many aspects of their olfactory behavior are known. As in other insects, responses to relevant single odor compounds are weak while natural mixtures evoke strong responses. Future challenges include studying how information about odor mixtures is processed in their brain. This could help develop highly attractive synthetic odor blends to lure them into traps.
{"title":"Morphology and physiology of the olfactory system of blood-feeding insects","authors":"F. Guidobaldi , I.J. May-Concha , P.G. Guerenstein","doi":"10.1016/j.jphysparis.2014.04.006","DOIUrl":"10.1016/j.jphysparis.2014.04.006","url":null,"abstract":"<div><p>Several blood-feeding (hematophagous) insects are vectors of a number of diseases including dengue, Chagas disease and leishmaniasis which persistently affect public health throughout Latin America. The vectors of those diseases include mosquitoes, triatomine bugs and sandflies. As vector control is an efficient way to prevent these illnesses it is important to understand the sensory biology of those harmful insects. We study the physiology of the olfactory system of those insects and apply that knowledge on the development of methods to manipulate their behavior. Here we review some of the latest information on insect olfaction with emphasis on hematophagous insects. The insect olfactory sensory neurons are housed inside hair-like organs called sensilla which are mainly distributed on the antenna and mouthparts. The identity of many of the odor compounds that those neurons detect are already known in hematophagous insects. They include several constituents of host (vertebrate) odor, sex, aggregation and alarm pheromones, and compounds related to egg-deposition behavior. Recent work has contributed significant knowledge on how odor information is processed in the insect first odor-processing center in the brain, the antennal lobe. The quality, quantity, and temporal features of the odor stimuli are encoded by the neural networks of the antennal lobe. Information regarding odor mixtures is also encoded. While natural mixtures evoke strong responses, synthetic mixtures that deviate from their natural counterparts in terms of key constituents or proportions of those constituents evoke weaker responses. The processing of olfactory information is largely unexplored in hematophagous insects. However, many aspects of their olfactory behavior are known. As in other insects, responses to relevant single odor compounds are weak while natural mixtures evoke strong responses. Future challenges include studying how information about odor mixtures is processed in their brain. This could help develop highly attractive synthetic odor blends to lure them into traps.</p></div>","PeriodicalId":50087,"journal":{"name":"Journal of Physiology-Paris","volume":"108 2","pages":"Pages 96-111"},"PeriodicalIF":0.0,"publicationDate":"2014-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.jphysparis.2014.04.006","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"32347729","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2014-04-01DOI: 10.1016/j.jphysparis.2014.08.002
Florencia Scarano, Daniel Tomsic
Historically, arthropod behavior has been considered to be a collection of simple, automaton-like routines commanded by domain-specific brain modules working independently. Nowadays, it is evident that the extensive behavioral repertoire of these animals and its flexibility necessarily imply far more complex abilities than originally assumed. For example, even what was thought to be a straightforward behavior of crabs, the escape response to visual danger stimuli, proved to involve a number of sequential stages, each of which implying decisions made on the bases of stimulus and contextual information. Inspired in previous observations on how the stimulus trajectory can affect the escape response of crabs in the field, we investigated the escape response to images of objects approaching directly toward the crab (looming stimuli: LS) or moving parallel to it (translational stimuli: TS) in the laboratory. Computer simulations of moving objects were effective to elicit escapes. LS evoked escapes with higher probability and intensity (speed and distance of escape) than TS, but responses started later. In addition to the escape run, TS also evoked a defensive response of the animal with its claws. Repeated presentations of TS or LS were both capable of inducing habituation. Results are discussed in connection with the possibilities offered by crabs to investigate the neural bases of behaviors occurring in the natural environment.
{"title":"Escape response of the crab Neohelice to computer generated looming and translational visual danger stimuli","authors":"Florencia Scarano, Daniel Tomsic","doi":"10.1016/j.jphysparis.2014.08.002","DOIUrl":"10.1016/j.jphysparis.2014.08.002","url":null,"abstract":"<div><p>Historically, arthropod behavior has been considered to be a collection of simple, automaton-like routines commanded by domain-specific brain modules working independently. Nowadays, it is evident that the extensive behavioral repertoire of these animals and its flexibility necessarily imply far more complex abilities than originally assumed. For example, even what was thought to be a straightforward behavior of crabs, the escape response to visual danger stimuli, proved to involve a number of sequential stages, each of which implying decisions made on the bases of stimulus and contextual information. Inspired in previous observations on how the stimulus trajectory can affect the escape response of crabs in the field, we investigated the escape response to images of objects approaching directly toward the crab (looming stimuli: LS) or moving parallel to it (translational stimuli: TS) in the laboratory. Computer simulations of moving objects were effective to elicit escapes. LS evoked escapes with higher probability and intensity (speed and distance of escape) than TS, but responses started later. In addition to the escape run, TS also evoked a defensive response of the animal with its claws. Repeated presentations of TS or LS were both capable of inducing habituation. Results are discussed in connection with the possibilities offered by crabs to investigate the neural bases of behaviors occurring in the natural environment.</p></div>","PeriodicalId":50087,"journal":{"name":"Journal of Physiology-Paris","volume":"108 2","pages":"Pages 141-147"},"PeriodicalIF":0.0,"publicationDate":"2014-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.jphysparis.2014.08.002","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"32666525","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2014-04-01DOI: 10.1016/j.jphysparis.2014.08.009
Leonel Gómez-Sena, Federico Pedraja , Juan I. Sanguinetti-Scheck , Ruben Budelli
Weakly electric fish can sense electric signals produced by other animals whether they are conspecifics, preys or predators. These signals, sensed by passive electroreception, sustain electrocommunication, mating and agonistic behavior. Weakly electric fish can also generate a weak electrical discharge with which they can actively sense the animate and inanimate objects in their surroundings. Understanding both sensory modalities depends on our knowledge of how pre-receptorial electric images are formed and how movements modify them during behavior. The inability of effectively measuring pre-receptorial fields at the level of the skin contrasts with the amount of knowledge on electric fields and the availability of computational methods for estimating them. In this work we review past work on modeling of electric organ discharge and electric images, showing the usefulness of these methods to calculate the field and providing a brief explanation of their principles. In addition, we focus on recent work demonstrating the potential of electric image modeling and what the method has to offer for experimentalists studying sensory physiology, behavior and evolution.
{"title":"Computational modeling of electric imaging in weakly electric fish: Insights for physiology, behavior and evolution","authors":"Leonel Gómez-Sena, Federico Pedraja , Juan I. Sanguinetti-Scheck , Ruben Budelli","doi":"10.1016/j.jphysparis.2014.08.009","DOIUrl":"10.1016/j.jphysparis.2014.08.009","url":null,"abstract":"<div><p>Weakly electric fish can sense electric signals produced by other animals whether they are conspecifics, preys or predators. These signals, sensed by passive electroreception, sustain electrocommunication, mating and agonistic behavior<span>. Weakly electric fish can also generate a weak electrical discharge with which they can actively sense the animate and inanimate objects in their surroundings. Understanding both sensory modalities depends on our knowledge of how pre-receptorial electric images are formed and how movements modify them during behavior<span>. The inability of effectively measuring pre-receptorial fields at the level of the skin contrasts with the amount of knowledge on electric fields and the availability of computational methods for estimating them. In this work we review past work on modeling of electric organ discharge and electric images, showing the usefulness of these methods to calculate the field and providing a brief explanation of their principles. In addition, we focus on recent work demonstrating the potential of electric image modeling and what the method has to offer for experimentalists studying sensory physiology, behavior and evolution.</span></span></p></div>","PeriodicalId":50087,"journal":{"name":"Journal of Physiology-Paris","volume":"108 2","pages":"Pages 112-128"},"PeriodicalIF":0.0,"publicationDate":"2014-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.jphysparis.2014.08.009","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"32686688","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}