PeerJ Preprints: Zoologyhttps://peerj.com/preprints/index.atom?journal=peerj&subject=3100Zoology articles published in PeerJ PreprintsDevelopment and application of a robotic zebra finch (RoboFinch) to study multimodal cues in vocal communicationhttps://peerj.com/preprints/28004v32019-12-302019-12-30Ralph SimonJudith VarkevisserEzequiel MendozaKlaus HochradelConstance ScharffKatharina RiebelWouter Halfwerk
Understanding animal behaviour through psychophysical experimentation is often limited by insufficiently realistic stimulus representation. Important physical dimensions of signals and cues, especially those that are outside the spectrum of human perception, can be difficult to standardize and control separately with currently available recording and displaying techniques (e.g. video displays). Accurate stimulus control is in particular important when studying multimodal signals, as spatial and temporal alignment between stimuli is often crucial. Especially for audiovisual presentations, some of these limitations can be circumvented by the employment of animal robots that are superior to video presentations in all situations requiring realistic 3D presentations to animals. Here we report the development of a robotic zebra finch, called RoboFinch, and how it can be used to study vocal learning in a songbird, the zebra finch.
Understanding animal behaviour through psychophysical experimentation is often limited by insufficiently realistic stimulus representation. Important physical dimensions of signals and cues, especially those that are outside the spectrum of human perception, can be difficult to standardize and control separately with currently available recording and displaying techniques (e.g. video displays). Accurate stimulus control is in particular important when studying multimodal signals, as spatial and temporal alignment between stimuli is often crucial. Especially for audiovisual presentations, some of these limitations can be circumvented by the employment of animal robots that are superior to video presentations in all situations requiring realistic 3D presentations to animals. Here we report the development of a robotic zebra finch, called RoboFinch, and how it can be used to study vocal learning in a songbird, the zebra finch.The châtelperronian Neandertals of Cova Foradada (Calafell, Spain) used Iberian imperial eagle phalanges for symbolic purposeshttps://peerj.com/preprints/271332019-11-022019-11-02Antonio Rodríguez-HidalgoJuan Ignacio MoralesArtur CebriáLloyd A. CourtenayJuan L. Fernández-MarchenaGala García García-ArgudoJuan MarínPalmira SaladiéMaria SotoJosé-Miguel TejeroJosep-María Fullola
Evidence for the symbolic behavior of Neandertals in the use of personal ornaments is relatively scarce. Eagle talons, which were presumably used as pendants, stand out due to their abundance. This phenomenon seems to appear concentrated in a specific area of Southwestern Europe during a span of ca. 80 Ka. Here we present the analysis of one eagle pedal phalange recovered from the Châtelperronian layer of Foradada Cave (Spain). Our research broadens the known geographical and temporal range of this aspect of Neandertal symbolic behavior, by providing the first documentation of its use among Neandertals in Iberia, as well as of its oldest use in the peninsula. The recurrent appearance of large raptor talons throughout the Neandertal timeframe, including their presence among the last Neandertal populations, raises the question of the survival of some cultural elements of the Middle Paleolithic into the transitional Middle to Upper Paleolithic assemblages.
Evidence for the symbolic behavior of Neandertals in the use of personal ornaments is relatively scarce. Eagle talons, which were presumably used as pendants, stand out due to their abundance. This phenomenon seems to appear concentrated in a specific area of Southwestern Europe during a span of ca. 80 Ka. Here we present the analysis of one eagle pedal phalange recovered from the Châtelperronian layer of Foradada Cave (Spain). Our research broadens the known geographical and temporal range of this aspect of Neandertal symbolic behavior, by providing the first documentation of its use among Neandertals in Iberia, as well as of its oldest use in the peninsula. The recurrent appearance of large raptor talons throughout the Neandertal timeframe, including their presence among the last Neandertal populations, raises the question of the survival of some cultural elements of the Middle Paleolithic into the transitional Middle to Upper Paleolithic assemblages.Comparative studies of Echinometra mathaei species complex (Echinoidea: Camarodonta: Echinometridae) from two sites in Western Visayas, Philippines (Taklong Island, Guimaras and Nabas, Aklan)https://peerj.com/preprints/279862019-10-282019-10-28Joseph Ricky TamayoMaria Celia D Malay
Echinometra mathaei is a species complex with its constituent reproductively-isolated species informally called A, B, C and D based on studies done in Okinawa and the Red Sea. Little research has been done on this genus, and to our knowledge no studies have been done on the E. mathaei complex in the Philippines. To help clarify species delineations in the E. mathaei complex, a comparative study was done between two localities in Western Visayas, Philippines: the Taklong Island National Marine Reserve, in Nueva Valencia, Guimaras and Barangay Unidos in Nabas, Aklan. Morphological characteristics (spine color, milled rings, and skin around the peristome) and tubefeet and gonad spicules were observed. Two or possibly three species of Echinometra were found in the two sites based on their morphology and spicules, namely: Echinometra sp. A, Echinometra sp. C, and Echinometra affinity C, which resembles sp. C but differs in the milled rings and gonad spicules. Echinometra sp. C and E. affinity C cannot be distinguished on the basis of field-visible characters, thus the two morphs are referred to as Echinometra VC for the purpose of field surveys. Echinometra VC and Echinometra sp. A exhibited differences in abundance (VC was much more common) and microhabitat (VC was restricted to rocky shores and never observed in coral communities). To study the abundance and distribution of Echinometra VC, 50 m by 2 m belt transects were surveyed along the rocky shores of both sites: two parallel transects (at 0 m and at 0.9 m) and a perpendicular transect (only in Nabas), each with three replicates. The transect data showed that the mean densities for 0 m and 0.9 m in Nabas are significantly higher in Taklong yielding p-values of 0.001 and 0.002, respectively, when analyzed using t-test.Of the two sites, only Nabas showed a significant difference between the mean densities at 0 m and 0.9 m, with the mean density at 0.9 m significantly higher than that of 0 m yielding a p-value of 0.02 when analyzed using two-sample t-test. A Poisson regression on the perpendicular transect data from Nabas showed a trend of increasing Echinometra density with increasing distance from the shore. In the future, DNA barcoding and cross-fertilization studies should be performed in order to confirm the species of Echinometra observed. Many factors can affect the density and distribution of Echinometra, so further studies must be conducted to explain observed differences in their distribution and abundance.
Echinometra mathaei is a species complex with its constituent reproductively-isolated species informally called A, B, C and D based on studies done in Okinawa and the Red Sea. Little research has been done on this genus, and to our knowledge no studies have been done on the E. mathaei complex in the Philippines. To help clarify species delineations in the E. mathaei complex, a comparative study was done between two localities in Western Visayas, Philippines: the Taklong Island National Marine Reserve, in Nueva Valencia, Guimaras and Barangay Unidos in Nabas, Aklan. Morphological characteristics (spine color, milled rings, and skin around the peristome) and tubefeet and gonad spicules were observed. Two or possibly three species of Echinometra were found in the two sites based on their morphology and spicules, namely: Echinometra sp. A, Echinometra sp. C, and Echinometra affinity C, which resembles sp. C but differs in the milled rings and gonad spicules. Echinometra sp. C and E. affinity C cannot be distinguished on the basis of field-visible characters, thus the two morphs are referred to as Echinometra VC for the purpose of field surveys. Echinometra VC and Echinometra sp. A exhibited differences in abundance (VC was much more common) and microhabitat (VC was restricted to rocky shores and never observed in coral communities). To study the abundance and distribution of Echinometra VC, 50 m by 2 m belt transects were surveyed along the rocky shores of both sites: two parallel transects (at 0 m and at 0.9 m) and a perpendicular transect (only in Nabas), each with three replicates. The transect data showed that the mean densities for 0 m and 0.9 m in Nabas are significantly higher in Taklong yielding p-values of 0.001 and 0.002, respectively, when analyzed using t-test.Of the two sites, only Nabas showed a significant difference between the mean densities at 0 m and 0.9 m, with the mean density at 0.9 m significantly higher than that of 0 m yielding a p-value of 0.02 when analyzed using two-sample t-test. A Poisson regression on the perpendicular transect data from Nabas showed a trend of increasing Echinometra density with increasing distance from the shore. In the future, DNA barcoding and cross-fertilization studies should be performed in order to confirm the species of Echinometra observed. Many factors can affect the density and distribution of Echinometra, so further studies must be conducted to explain observed differences in their distribution and abundance.Endless forms of sexual selectionhttps://peerj.com/preprints/275842019-10-012019-10-01Willow R LindsayStaffan AnderssonBadreddine BererhiJacob HöglundArild JohnsenCharlotta KvarnemoErica H LederJan T LifjeldCalum E NinnesMats OlssonGeoff A ParkerTommaso PizzariAnna QvarnströmRebecca J SafranOla SvenssonScott Edwards
In recent years, the field of sexual selection has exploded, with advances in theoretical and empirical research complementing each other in exciting ways. This perspective piece is the product of a “stock-taking” workshop on sexual selection and conflict. Our aim is to identify and deliberate on outstanding questions and to stimulate discussion rather than provide a comprehensive overview of the entire field. These questions are organized into four thematic sections we deem essential to the field. First we focus on the evolution of mate choice and mating systems. Variation in mate quality can generate both competition and choice in the opposite sex, with implications for the evolution of mating systems. Limitations on mate choice may dictate the importance of direct vs. indirect benefits in mating decisions and consequently, mating systems, especially with regard to polyandry. Second, we focus on how sender and receiver mechanisms shape signal design. Mediation of honest signal content likely depends on integration of temporally variable social and physiological costs that are challenging to measure. We view the neuroethology of sensory and cognitive receiver biases as the main key to signal form and the ‘aesthetic sense’ proposed by Darwin. Since a receiver bias is sufficient to both initiate and drive ornament or armament exaggeration, without a genetically correlated or even coevolving receiver, this may be the appropriate ‘null model’ of sexual selection. Thirdly, we focus on the genetic architecture of sexually selected traits. Despite advances in modern molecular techniques, the number and identity of genes underlying performance, display and secondary sexual traits remains largely unknown. In-depth investigations into the genetic basis of sexual dimorphism in the context of long-term field studies will reveal constraints and trajectories of sexually selected trait evolution. Finally, we focus on sexual selection and conflict as drivers of speciation. Population divergence and speciation are often influenced by an interplay between sexual and natural selection. The extent to which sexual selection promotes or counteracts population divergence may vary depending on the genetic architecture of traits as well as the covariance between mating competition and local adaptation. Additionally, post-copulatory processes, such as selection against heterospecific sperm, may influence the importance of sexual selection in speciation. We propose that efforts to resolve these four themes can catalyze conceptual progress in the field of sexual selection, and we offer potential avenues of research to advance this progress.
In recent years, the field of sexual selection has exploded, with advances in theoretical and empirical research complementing each other in exciting ways. This perspective piece is the product of a “stock-taking” workshop on sexual selection and conflict. Our aim is to identify and deliberate on outstanding questions and to stimulate discussion rather than provide a comprehensive overview of the entire field. These questions are organized into four thematic sections we deem essential to the field. First we focus on the evolution of mate choice and mating systems. Variation in mate quality can generate both competition and choice in the opposite sex, with implications for the evolution of mating systems. Limitations on mate choice may dictate the importance of direct vs. indirect benefits in mating decisions and consequently, mating systems, especially with regard to polyandry. Second, we focus on how sender and receiver mechanisms shape signal design. Mediation of honest signal content likely depends on integration of temporally variable social and physiological costs that are challenging to measure. We view the neuroethology of sensory and cognitive receiver biases as the main key to signal form and the ‘aesthetic sense’ proposed by Darwin. Since a receiver bias is sufficient to both initiate and drive ornament or armament exaggeration, without a genetically correlated or even coevolving receiver, this may be the appropriate ‘null model’ of sexual selection. Thirdly, we focus on the genetic architecture of sexually selected traits. Despite advances in modern molecular techniques, the number and identity of genes underlying performance, display and secondary sexual traits remains largely unknown. In-depth investigations into the genetic basis of sexual dimorphism in the context of long-term field studies will reveal constraints and trajectories of sexually selected trait evolution. Finally, we focus on sexual selection and conflict as drivers of speciation. Population divergence and speciation are often influenced by an interplay between sexual and natural selection. The extent to which sexual selection promotes or counteracts population divergence may vary depending on the genetic architecture of traits as well as the covariance between mating competition and local adaptation. Additionally, post-copulatory processes, such as selection against heterospecific sperm, may influence the importance of sexual selection in speciation. We propose that efforts to resolve these four themes can catalyze conceptual progress in the field of sexual selection, and we offer potential avenues of research to advance this progress.What do we mean by the directions “cranial” and “caudal” on a vertebra?https://peerj.com/preprints/274372019-09-302019-09-30Michael P TaylorMatthew J Wedel
In illustrating vertebrae, it is important to consistently depict their orientation, so we can objectively assess and compare the slope of the neural arch, neural canal, or articular surfaces. However, differing vertebral shapes across taxa and across regions of the spinal column make it difficult to maintain consistency, or even define what we mean by the directions “cranial” and “caudal”. Consequently, characters such as “Neural arch slopes cranially 30° relative to the vertical” are disputable rather than objective measurements. Cranial and caudal are defined as directed along the horizontal axis, but several different notions of “horizontal” are possible:
1. Long axis of centrum is horizontal. This is appealing for elongate vertebrae such as sauropod cervicals, but is not always well defined, and is difficult to determine for craniocaudally short vertebrae such as most caudals.
2. Articular surfaces of centrum are vertical. Difficult to determine when dealing with facets that are concave or (worse) convex; and ambiguous for “keystoned” vertebrae in which the facets are not parallel.
3. Neural canal is horizontal. Anatomically informative, but difficult to determine in vertebrae that have not been fully prepared or CT-scanned, and impossible to see in lateral view. Ambiguous for vertebrae where the dorsal and ventral margins of the canal are not straight or not parallel.
4. Similarity in articulation (“horizontal” is defined as a line joining the same point on two similarly oriented copies of the same vertebra when optimally articulated). This is less intuitive than definitions 1–3, but takes the entire vertebra into account.
We advocate explicitly stating a definition and using it consistently. In most cases, definition 3 (“Neural canal is horizontal”) best reflects anatomical and developmental realities, and it is therefore preferred. Low-tech techniques can be used to determine neural canal orientation with adequate precision for most purposes.
In illustrating vertebrae, it is important to consistently depict their orientation, so we can objectively assess and compare the slope of the neural arch, neural canal, or articular surfaces. However, differing vertebral shapes across taxa and across regions of the spinal column make it difficult to maintain consistency, or even define what we mean by the directions “cranial” and “caudal”. Consequently, characters such as “Neural arch slopes cranially 30° relative to the vertical” are disputable rather than objective measurements. Cranial and caudal are defined as directed along the horizontal axis, but several different notions of “horizontal” are possible:1. Long axis of centrum is horizontal. This is appealing for elongate vertebrae such as sauropod cervicals, but is not always well defined, and is difficult to determine for craniocaudally short vertebrae such as most caudals.2. Articular surfaces of centrum are vertical. Difficult to determine when dealing with facets that are concave or (worse) convex; and ambiguous for “keystoned” vertebrae in which the facets are not parallel.3. Neural canal is horizontal. Anatomically informative, but difficult to determine in vertebrae that have not been fully prepared or CT-scanned, and impossible to see in lateral view. Ambiguous for vertebrae where the dorsal and ventral margins of the canal are not straight or not parallel.4. Similarity in articulation (“horizontal” is defined as a line joining the same point on two similarly oriented copies of the same vertebra when optimally articulated). This is less intuitive than definitions 1–3, but takes the entire vertebra into account.We advocate explicitly stating a definition and using it consistently. In most cases, definition 3 (“Neural canal is horizontal”) best reflects anatomical and developmental realities, and it is therefore preferred. Low-tech techniques can be used to determine neural canal orientation with adequate precision for most purposes.How to make new discoveries in (human) anatomyhttps://peerj.com/preprints/279802019-09-242019-09-24Mathew John Wedel
Despite the perception that human anatomy is a completed science, new discoveries continue to be reported. Some merely expand the previously known range of human variation, but others are gross structures present in most people, which simply escaped detection until recently. An analysis of recent discoveries suggests several avenues along which new discoveries might be sought:
1. Anatomically complex regions with multiple potential distractors: the anterolateral ligament of the knee escaped widespread appreciation until 2013, probably because the human knee is a forbiddingly complex structure that is rarely dissected completely, and several superficially similar structures are present in the same area.
2. Common characters of other taxa expressed as rare variants in humans: vagus nerve fibers to the trachea and esophagus are typically incorporated into the recurrent laryngeal nerve in humans, but form a separate pararecurrent nerve in some other mammals, and rarely in humans.
3. Replaced peripheral nerves: nerve fibers from the 4th lumbar spinal level to the leg are usually incorporated into the femoral nerve, but in rare cases become part of the obturator nerve. In such cases, the posterior branch of the saphenous nerve appears to have been replaced by the obturator nerve. Similar replacements in other regions of the body are underexplored.
Most recent discoveries fall into a perceptual blind spot: medical students dissecting human cadavers have the opportunity to find these structures, but usually lack the expertise to recognize or preserve them. In contract, surgeons have the necessary expertise, but rarely have the opportunity to open people up sufficiently to identify or trace these structures.
If new discoveries remain to be made even in the well-trod ground of human anatomy, then many more surely await discovery in extant and extinct non-humans, and these guidelines may prove useful in other taxa as well.
Despite the perception that human anatomy is a completed science, new discoveries continue to be reported. Some merely expand the previously known range of human variation, but others are gross structures present in most people, which simply escaped detection until recently. An analysis of recent discoveries suggests several avenues along which new discoveries might be sought:1. Anatomically complex regions with multiple potential distractors: the anterolateral ligament of the knee escaped widespread appreciation until 2013, probably because the human knee is a forbiddingly complex structure that is rarely dissected completely, and several superficially similar structures are present in the same area.2. Common characters of other taxa expressed as rare variants in humans: vagus nerve fibers to the trachea and esophagus are typically incorporated into the recurrent laryngeal nerve in humans, but form a separate pararecurrent nerve in some other mammals, and rarely in humans.3. Replaced peripheral nerves: nerve fibers from the 4th lumbar spinal level to the leg are usually incorporated into the femoral nerve, but in rare cases become part of the obturator nerve. In such cases, the posterior branch of the saphenous nerve appears to have been replaced by the obturator nerve. Similar replacements in other regions of the body are underexplored.Most recent discoveries fall into a perceptual blind spot: medical students dissecting human cadavers have the opportunity to find these structures, but usually lack the expertise to recognize or preserve them. In contract, surgeons have the necessary expertise, but rarely have the opportunity to open people up sufficiently to identify or trace these structures.If new discoveries remain to be made even in the well-trod ground of human anatomy, then many more surely await discovery in extant and extinct non-humans, and these guidelines may prove useful in other taxa as well.Neural canal ridges: A novel osteological correlate of post-cranial neurology in dinosaurshttps://peerj.com/preprints/279672019-09-172019-09-17Jessie AtterholtMathew J Wedel
Bony ridges occur on the walls of the neural canal in caudal vertebrae of numerous sauropod dinosaurs. These neural canal ridges (NCRs) are anteroposteriorly elongated but do not extend to the ends of the canal. To date, we have observed NCRs in caudal vertebrae of Alamosaurus, Apatosaurus, Astrophocaudia,Brontomerus, Camarasaurus, and Diplodocus.
Numerous similar structures occur in extant vertebrates: (1) Neurocentral joints are ventral to NCRs in sauropod caudal vertebrae, and NCRs occur in unfused juvenile arches. Hypothesis rejected. (2) Attachment scars from ligamentum flavum occur at the ends of the dorsal roof of the canal, not the midpoint of the lateral edges, and this mammalian ligament was probably absent in dinosaurs. Hypothesis rejected. (3) Smooth ridges separate the spinal cord from the dorsal spinal vein and paramedullary airways in some crocodilians and birds, respectively. However, these septa persist to the ends of the canal, giving it an 8-shape, unlike the discrete NCRs of dinosaurs. Hypothesis rejected. (4) Bony attachments for denticulate ligaments occur in some non-mammalian vertebrates. The dura mater around the spinal cord fuses to the periosteum of the neural canal in non-mammals, so the denticulate ligaments that support the spinal cord can leave ossified attachment scars. These spinal cord supports have been identified in teleosts, salamanders, and a juvenile lizard, and they are the best match for the morphology of the NCRs in sauropod vertebrae.
Functions of NCRs remain obscure. Denticulate ligaments are largest in regions of the vertebral column that experience strong lateral flexion. The hypothesis that NCRs supported the spinal cord of sauropods during lateral tail-whipping is attractive, but inconsistent with our recent discovery of NCRs in a hadrosaur caudal. NCRs are a new osteological correlate of the peripheral nervous system in dinosaurs, and highlight the need for more study in this area.
Bony ridges occur on the walls of the neural canal in caudal vertebrae of numerous sauropod dinosaurs. These neural canal ridges (NCRs) are anteroposteriorly elongated but do not extend to the ends of the canal. To date, we have observed NCRs in caudal vertebrae of Alamosaurus, Apatosaurus, Astrophocaudia,Brontomerus, Camarasaurus, and Diplodocus.Numerous similar structures occur in extant vertebrates: (1) Neurocentral joints are ventral to NCRs in sauropod caudal vertebrae, and NCRs occur in unfused juvenile arches. Hypothesis rejected. (2) Attachment scars from ligamentum flavum occur at the ends of the dorsal roof of the canal, not the midpoint of the lateral edges, and this mammalian ligament was probably absent in dinosaurs. Hypothesis rejected. (3) Smooth ridges separate the spinal cord from the dorsal spinal vein and paramedullary airways in some crocodilians and birds, respectively. However, these septa persist to the ends of the canal, giving it an 8-shape, unlike the discrete NCRs of dinosaurs. Hypothesis rejected. (4) Bony attachments for denticulate ligaments occur in some non-mammalian vertebrates. The dura mater around the spinal cord fuses to the periosteum of the neural canal in non-mammals, so the denticulate ligaments that support the spinal cord can leave ossified attachment scars. These spinal cord supports have been identified in teleosts, salamanders, and a juvenile lizard, and they are the best match for the morphology of the NCRs in sauropod vertebrae.Functions of NCRs remain obscure. Denticulate ligaments are largest in regions of the vertebral column that experience strong lateral flexion. The hypothesis that NCRs supported the spinal cord of sauropods during lateral tail-whipping is attractive, but inconsistent with our recent discovery of NCRs in a hadrosaur caudal. NCRs are a new osteological correlate of the peripheral nervous system in dinosaurs, and highlight the need for more study in this area.Barnacle recruit density and size increase from high to middle intertidal elevations in wave-exposed habitats on the Atlantic coast of Nova Scotiahttps://peerj.com/preprints/279662019-09-172019-09-17Ricardo A Scrosati
Barnacle recruitment is often studied in rocky intertidal habitats due to the relevant role that barnacles can play in intertidal communities. In 2014, barnacle (Semibalanus balanoides) recruitment was measured at high elevations in wave-exposed intertidal habitats on the NW Atlantic coast in Nova Scotia, Canada. Values were considerably lower than previously reported for middle elevations in wave-exposed intertidal habitats on the NE Atlantic and NE Pacific coasts. To determine if such differences in recruitment may have resulted from elevation influences, I did a field experiment in 2019 in wave-exposed intertidal habitats in Nova Scotia to test the hypothesis that recruitment is higher at middle than at high elevations, based on known environmental differences between both elevation zones. Based on data from three locations spanning 158 km of the Nova Scotia coast, barnacle recruitment was, on average, nearly 200 % higher (and recruits were larger) at middle than at high elevations. However, even with this increase, barnacle recruitment on this NW Atlantic coast is still lower than for comparable habitats on the NE Atlantic and NE Pacific coasts, and also lower than previously reported for wave-exposed locations farther south on the NW Atlantic coast, in Maine, USA. Therefore, barnacle recruitment in wave-exposed intertidal environments in Nova Scotia appears to be only moderate relative to other shores. This difference in the supply of barnacle recruits might influence the intensity of interspecific interactions involving barnacles.
Barnacle recruitment is often studied in rocky intertidal habitats due to the relevant role that barnacles can play in intertidal communities. In 2014, barnacle (Semibalanus balanoides) recruitment was measured at high elevations in wave-exposed intertidal habitats on the NW Atlantic coast in Nova Scotia, Canada. Values were considerably lower than previously reported for middle elevations in wave-exposed intertidal habitats on the NE Atlantic and NE Pacific coasts. To determine if such differences in recruitment may have resulted from elevation influences, I did a field experiment in 2019 in wave-exposed intertidal habitats in Nova Scotia to test the hypothesis that recruitment is higher at middle than at high elevations, based on known environmental differences between both elevation zones. Based on data from three locations spanning 158 km of the Nova Scotia coast, barnacle recruitment was, on average, nearly 200 % higher (and recruits were larger) at middle than at high elevations. However, even with this increase, barnacle recruitment on this NW Atlantic coast is still lower than for comparable habitats on the NE Atlantic and NE Pacific coasts, and also lower than previously reported for wave-exposed locations farther south on the NW Atlantic coast, in Maine, USA. Therefore, barnacle recruitment in wave-exposed intertidal environments in Nova Scotia appears to be only moderate relative to other shores. This difference in the supply of barnacle recruits might influence the intensity of interspecific interactions involving barnacles.Broad similarities in shoulder muscle architecture and organization across two amniotes: Implications for reconstructing non-mammalian synapsidshttps://peerj.com/preprints/279502019-09-102019-09-10Philip Fahn-LaiAndrew A BiewenerStephanie E Pierce
The evolution of upright limb posture in mammals may have enabled modifications of the forelimb for diverse locomotor ecologies. A rich fossil record of non-mammalian synapsids holds the key to unraveling the transition from “sprawling” to “erect” limb function in the precursors to mammals, but a detailed understanding of muscle functional anatomy is a necessary prerequisite to reconstructing postural evolution in fossils. Here we characterize the gross morphology and internal architecture of muscles crossing the shoulder joint in two morphologically-conservative extant amniotes that form a phylogenetic and morpho-functional bracket for non-mammalian synapsids: the Argentine black and white tegu Salvator merianaeand the Virginia opossum Didelphis virginiana. By combining traditional physical dissection of cadavers with non-destructive three-dimensional digital dissection, we find striking similarities in muscle organization and architectural parameters. Despite the wide phylogenetic gap between our study species, distal muscle attachments are notably similar, while differences in proximal muscle attachments are driven by modifications to the skeletal anatomy of the pectoral girdle that are well-documented in transitional synapsid fossils. Further, correlates for force production (PCSA, physiological cross-sectional area), muscle gearing (pennation), and working range (fascicle length) are statistically indistinguishable for an unexpected number of muscles. Functional tradeoffs between force production and working range reveal muscle specializations that may facilitate increased girdle mobility, weight support, and active stabilization of the shoulder in the opossum—a possible signal of postural transformation. Together, these results create a foundation for reconstructing the musculoskeletal anatomy of the non-mammalian synapsid pectoral girdle with greater confidence, as we demonstrate by inferring shoulder muscle PCSAs in the fossil non-mammalian cynodont Massetognathus pascuali.
The evolution of upright limb posture in mammals may have enabled modifications of the forelimb for diverse locomotor ecologies. A rich fossil record of non-mammalian synapsids holds the key to unraveling the transition from “sprawling” to “erect” limb function in the precursors to mammals, but a detailed understanding of muscle functional anatomy is a necessary prerequisite to reconstructing postural evolution in fossils. Here we characterize the gross morphology and internal architecture of muscles crossing the shoulder joint in two morphologically-conservative extant amniotes that form a phylogenetic and morpho-functional bracket for non-mammalian synapsids: the Argentine black and white tegu Salvator merianaeand the Virginia opossum Didelphis virginiana. By combining traditional physical dissection of cadavers with non-destructive three-dimensional digital dissection, we find striking similarities in muscle organization and architectural parameters. Despite the wide phylogenetic gap between our study species, distal muscle attachments are notably similar, while differences in proximal muscle attachments are driven by modifications to the skeletal anatomy of the pectoral girdle that are well-documented in transitional synapsid fossils. Further, correlates for force production (PCSA, physiological cross-sectional area), muscle gearing (pennation), and working range (fascicle length) are statistically indistinguishable for an unexpected number of muscles. Functional tradeoffs between force production and working range reveal muscle specializations that may facilitate increased girdle mobility, weight support, and active stabilization of the shoulder in the opossum—a possible signal of postural transformation. Together, these results create a foundation for reconstructing the musculoskeletal anatomy of the non-mammalian synapsid pectoral girdle with greater confidence, as we demonstrate by inferring shoulder muscle PCSAs in the fossil non-mammalian cynodont Massetognathus pascuali.Call overlapping signals sexual status in Darwin’s frogshttps://peerj.com/preprints/279432019-09-072019-09-07Jose M SerranoNoé GuzmánMario PennaMarco A MéndezClaudio Soto-Azat
Background. In animal reproductive contexts, calling behaviour is mostly performed by males but in species in which females call, it is not known how vocal interaction occurs between sexes, particularly when sexual dimorphism in signals is low, as in cases in which call repertoire is identical but acoustic properties differ. In Darwin’s frog (Rhinoderma darwinii), a species in which males brood larvae inside their vocal sacs, females have higher dominant frequency and shorter calls and notes than males. Since in this species males persist calling after getting pregnant with larvae, different vocal interaction patterns are expected to occur among animals having dissimilar reproductive status.
Methodology. To explore the mechanisms underlying vocal recognition among the different sexual status of R. darwinii, we recorded natural duets between non-pregnant males (NPM), pregnant males (PM) and females (F) and evaluated their evoked vocal response to natural playback stimuli of each sexual status from November to February 2015-2016 in Chiloé island, Chile. Call rate, phase angles, sound pressure level (SPL), number of overlapping calls and delay of overlapping calls were measured to determine differential responses between natural duets and in response to stimuli consisting of natural calls of individuals of different sexual status.
Results. Spontaneous duet interactions occurred mainly between males and no clear differences between duets were detected. In playbacks, call ratios in response to calls of different sexual status were similar. Females decreased their SPL in response to F calls, while F and PM had longer call delays and lower call overlaps between each other. Major differences were observed in call overlap, as the occurrence of this phenomenon was larger in playback experiments than during natural duets. The number of calls overlapped during natural duets was fewer (10.9 %) than during playback experiments (36.8 %).
Conclusions. Our results suggest that in R. darwinii, PM and F signalize their sexual status by decreasing their call overlap and that NPM respond indistinctly to the other sexual status. In general, these differences in selective call overlap between Darwin's frogs arise as a novel mechanism for signal recognition between animal vocal interactions.
Background. In animal reproductive contexts, calling behaviour is mostly performed by males but in species in which females call, it is not known how vocal interaction occurs between sexes, particularly when sexual dimorphism in signals is low, as in cases in which call repertoire is identical but acoustic properties differ. In Darwin’s frog (Rhinoderma darwinii), a species in which males brood larvae inside their vocal sacs, females have higher dominant frequency and shorter calls and notes than males. Since in this species males persist calling after getting pregnant with larvae, different vocal interaction patterns are expected to occur among animals having dissimilar reproductive status.Methodology. To explore the mechanisms underlying vocal recognition among the different sexual status of R. darwinii, we recorded natural duets between non-pregnant males (NPM), pregnant males (PM) and females (F) and evaluated their evoked vocal response to natural playback stimuli of each sexual status from November to February 2015-2016 in Chiloé island, Chile. Call rate, phase angles, sound pressure level (SPL), number of overlapping calls and delay of overlapping calls were measured to determine differential responses between natural duets and in response to stimuli consisting of natural calls of individuals of different sexual status.Results. Spontaneous duet interactions occurred mainly between males and no clear differences between duets were detected. In playbacks, call ratios in response to calls of different sexual status were similar. Females decreased their SPL in response to F calls, while F and PM had longer call delays and lower call overlaps between each other. Major differences were observed in call overlap, as the occurrence of this phenomenon was larger in playback experiments than during natural duets. The number of calls overlapped during natural duets was fewer (10.9 %) than during playback experiments (36.8 %).Conclusions. Our results suggest that in R. darwinii, PM and F signalize their sexual status by decreasing their call overlap and that NPM respond indistinctly to the other sexual status. In general, these differences in selective call overlap between Darwin's frogs arise as a novel mechanism for signal recognition between animal vocal interactions.