9 research outputs found

    Trophic interactions of Bathyraja trachura and sympatric fishes

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    Quantifying deep-sea food webs can be resource intensive due to the difficulties of sampling fishes from the deep sea. The diet of fishes is often quantified through stomach content analysis, through this method has many sampling constraints, and it can be difficult to obtain sufficient samples for an in-depth study. This study attempts to fill a critical data gap by determining the diet and trophic level of the deep-sea Roughtail Skate, Bathyraja trachura, using traditional stomach content analysis. This study also attempts to determine the validity and accuracy of stable isotope analysis in the continental slope fishes of the deep-sea of the eastern North Pacific, as an alternative method to determine trophic level in fishes. The Roughtail Skate is an abundant deep-sea skate in the eastern North Pacific. Little is known about the diet of this skate, which is landed as by-catch in commercial bottom trawls. Skates were collected between 2005 and 2008 from fishery-independent trawl surveys of the continental slope and outer shelf. Geometric Index of Importance (GII) values indicated that crustaceans (71.4%), fishes (17.8%), polychaetes (4.3%), and cephalopods (3.7%) were the most important prey groups in the diet. Diet differed significantly with total length, but not with sex. Larger individuals (by total length) had significantly higher trophic level values, and year and latitude explained variation in the diet for three prey categories. In this study, fishes and invertebrates collected from the continental slope (1,000 m depth) of the eastern North Pacific were analyzed using stable isotope analysis (SIA). The carbon and nitrogen stable isotope results were used to construct dual isotope plots to investigate the trophic relationships of this deep-sea community. The plots indicated a decoupling of the benthic and pelagic food webs, with the benthic food web being isotopically enriched. Stomach and isotope samples were collected from 32 Roughtail Skates (Bathyraja trachura) to determine the validity and accuracy of SIA in determining the trophic levels of the skates. A linear regression analysis indicated that nitrogen values from SIA and trophic levels calculated from stomach content analysis, when plotted against skate total length, exhibited similar variation and patterns, although only the stomach content analysis yielded significant results (stomach content: p=0.020, r2=0.168; stable isotope: p=0.077, r2=0.101)

    High-resolution volumetric imaging constrains compartmental models to explore synaptic integration and temporal processing by cochlear nucleus globular bushy cells

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    Globular bushy cells (GBCs) of the cochlear nucleus play central roles in the temporal processing of sound. Despite investigation over many decades, fundamental questions remain about their dendrite structure, afferent innervation, and integration of synaptic inputs. Here, we use volume electron microscopy (EM) of the mouse cochlear nucleus to construct synaptic maps that precisely specify convergence ratios and synaptic weights for auditory- nerve innervation and accurate surface areas of all postsynaptic compartments. Detailed biophysically-based compartmental models can help develop hypotheses regarding how GBCs integrate inputs to yield their recorded responses to sound. We established a pipeline to export a precise reconstruction of auditory nerve axons and their endbulb terminals together with high-resolution dendrite, soma, and axon reconstructions into biophysically-detailed compartmental models that could be activated by a standard cochlear transduction model. With these constraints, the models predict auditory nerve input profiles whereby all endbulbs onto a GBC are subthreshold (coincidence detection mode), or one or two inputs are suprathreshold (mixed mode). The models also predict the relative importance of dendrite geometry, soma size, and axon initial segment length in setting action potential threshold and generating heterogeneity in sound-evoked responses, and thereby propose mechanisms by which GBCs may homeostatically adjust their excitability. Volume EM also reveals new dendritic structures and dendrites that lack innervation. This framework defines a pathway from subcellular morphology to synaptic connectivity, and facilitates investigation into the roles of specific cellular features in sound encoding. We also clarify the need for new experimental measurements to provide missing cellular parameters, and predict responses to sound for further in vivo studies, thereby serving as a template for investigation of other neuron classes

    High-resolution volumetric imaging constrains compartmental models to explore synaptic integration and temporal processing by cochlear nucleus globular bushy cells

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    Globular bushy cells (GBCs) of the cochlear nucleus play central roles in the temporal processing of sound. Despite investigation over many decades, fundamental questions remain about their dendrite structure, afferent innervation, and integration of synaptic inputs. Here, we use volume electron microscopy (EM) of the mouse cochlear nucleus to construct synaptic maps that precisely specify convergence ratios and synaptic weights for auditory nerve innervation and accurate surface areas of all postsynaptic compartments. Detailed biophysically based compartmental models can help develop hypotheses regarding how GBCs integrate inputs to yield their recorded responses to sound. We established a pipeline to export a precise reconstruction of auditory nerve axons and their endbulb terminals together with high-resolution dendrite, soma, and axon reconstructions into biophysically detailed compartmental models that could be activated by a standard cochlear transduction model. With these constraints, the models predict auditory nerve input profiles whereby all endbulbs onto a GBC are subthreshold (coincidence detection mode), or one or two inputs are suprathreshold (mixed mode). The models also predict the relative importance of dendrite geometry, soma size, and axon initial segment length in setting action potential threshold and generating heterogeneity in sound-evoked responses, and thereby propose mechanisms by which GBCs may homeostatically adjust their excitability. Volume EM also reveals new dendritic structures and dendrites that lack innervation. This framework defines a pathway from subcellular morphology to synaptic connectivity, and facilitates investigation into the roles of specific cellular features in sound encoding. We also clarify the need for new experimental measurements to provide missing cellular parameters, and predict responses to sound for further in vivo studies, thereby serving as a template for investigation of other neuron classes
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