13 research outputs found

    Development of form and function in peripheral auditory structures of the zebrafish (Danio rerio)

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    Investigations of the development of auditory form and function have, with a few exceptions, thus far been largely restricted to birds and mammals, making it difficult to postulate evolutionary hypotheses. Teleost fishes represent useful models for developmental investigations of the auditory system due to their often extensive period of posthatching development and the diversity of auditory specializations in this group. Using the auditory brainstem response and morphological techniques we investigated the development of auditory form and function in zebrafish ~Danio rerio) ranging in size from 10 to 45 mm total length. We found no difference in auditory sensitivity, response latency, or response amplitude with development, but we did find an expansion of maximum detectable frequency from 200 Hz at 10 mm to 4000 Hz at 45 mm TL. The expansion of frequency range coincided with the development of Weberian ossicles in zebrafish, suggesting that changes in hearing ability in this species are driven more by development of auxiliary specializations than by the ear itself. We propose a model for the development of zebrafish hearing wherein the Weberian ossicles gradually increase the range of frequencies available to the inner ear, much as middle ear development increases frequency range in mammals

    The Modular Optical Underwater Survey System

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    The Pacific Islands Fisheries Science Center deploys the Modular Optical Underwater Survey System (MOUSS) to estimate the species-specific, size-structured abundance of commercially-important fish species in Hawaii and the Pacific Islands. The MOUSS is an autonomous stereo-video camera system designed for the in situ visual sampling of fish assemblages. This system is rated to 500 m and its low-light, stereo-video cameras enable identification, counting, and sizing of individuals at a range of 0.5–10 m. The modular nature of MOUSS allows for the efficient and cost-effective use of various imaging sensors, power systems, and deployment platforms. The MOUSS is in use for surveys in Hawaii, the Gulf of Mexico, and Southern California. In Hawaiian waters, the system can effectively identify individuals to a depth of 250 m using only ambient light. In this paper, we describe the MOUSS’s application in fisheries research, including the design, calibration, analysis techniques, and deployment mechanism

    Co-occurring ocean biogeochemical changes to the year 2100 under the RCP85.

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    <p>For these plots, we separated absolute changes shown in <a href="http://www.plosbiology.org/article/info:doi/10.1371/journal.pbio.1001682#pbio-1001682-g002" target="_blank">Figure 2A–D</a> between those that will be positive (i.e., cooling, basification, oxygenation, and productivity increase; Plots A–E) and negative (i.e., warming, acidification, oxygen depletion, and primary food reduction; Plots F–J). Resulting absolute changes were scaled between 0 and 1 (Plots B–E, G–J), 0 being zero absolute change and 1 being the extreme 97.5% observed value globally. The resulting scaled scores from each variable were added to provide a global composite map of co-occurring positive (Plot A) and negative (Plot F) changes in ocean biogeochemistry. These cumulative change maps ranged from 4 (i.e., the maximum predicted change in all four parameters occurred in that cell) to 0 (i.e., no negative or positive change in any of the four parameters occurred in that cell). The results for the RCP45 at the ocean surface and both RCPs for the seafloor are presented in the Supporting Information section.</p

    Accuracy and precision on future ocean biogeochemical projections.

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    <p>Plots A–D refer to sea-surface parameters; plots E–H to seafloor parameters. These plots illustrate the number of 1 km<sup>2</sup> cells by their projected change to the year 2100 under the RCP45 (blue lines), RCP85 (red lines), errors in accuracy (green lines), and precision (purple lines). Accuracy was defined as the difference between multimodel average projections and actual data and precision as the standard deviation among the projections of all models. Comparison of these frequency distributions illustrates that errors in accuracy and precision are insufficient to offset projected changes in surface temperature, oxygen, and pH. Note that in those cases, accuracy (green lines) is centered to zero, meaning that for the great majority of cells the multimodel average prediction was identical to actual observations. Errors in precision were often larger, but they are added to both sides of the projections, meaning that they will broaden expected projections but will not reverse them. However, in the case of surface productivity and all parameters at the seafloor, errors in accuracy and precision were larger than the projected change, highlighting the need for caution in those cases. Further details are presented in <a href="http://www.plosbiology.org/article/info:doi/10.1371/journal.pbio.1001682#pbio.1001682.s004" target="_blank">Table S2</a>; the performance of individual models is shown in <a href="http://www.plosbiology.org/article/info:doi/10.1371/journal.pbio.1001682#pbio.1001682.s003" target="_blank">Table S1</a>.</p

    Exposure of the world's oceans to co-occurring changes in ocean biogeochemistry to the year 2100.

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    <p>(A–B) are the cumulative percentage of cells globally exposed to the composite score of co-occurring ocean biogeochemistry changes (see <a href="http://www.plosbiology.org/article/info:doi/10.1371/journal.pbio.1001682#pbio-1001682-g003" target="_blank">Figure 3</a> for details). (A) is for negative and (B) for the positive biogeochemistry changes. (C–D) is the discrimination of total ocean cells globally exposed to negative (C) and positive (D) changes in each variable and the composite score.</p

    Future biogeochemistry change in the world's oceans.

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    <p>Plots A–D show the spatial difference between future (i.e., the average from 2091 to 2100) and contemporary (i.e., the average from years 1996 to 2005) values under the RCP85 scenario (decadal averages were chosen to minimize aliasing by interannual variability; beside each color scale we provide the absolute change, whereas the numbers on top indicate the rescaled values; complete results for the RCP85 and RCP45 for the ocean surface and floor are shown in <a href="http://www.plosbiology.org/article/info:doi/10.1371/journal.pbio.1001682#pbio.1001682.s002" target="_blank">Figure S2</a>). Plots E–H show the global average change relative to contemporary values under the RCP45 and RCP85 at the ocean surface and seafloor; semitransparent lines are the projections for individual models.</p
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