7 research outputs found

    Appendix A. Sensitivity test of peak velocities on nutrient distribution.

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    Sensitivity test of peak velocities on nutrient distribution

    DataSheet_1_Effect of Mytilus coruscus selective filtration on phytoplankton assemblages.docx

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    The feeding selectivity of bivalves can play an important role in shaping the structure of phytoplankton communities of natural waters. This could be particularly true in waters with intensive bivalves farming, like Sungo Bay, Northern China. Understanding the role of bivalve feeding behavior is important for assessing how the dense cultivation of bivalves may affect phytoplankton community composition and food web structure in farm areas. In this study, we investigated the feeding selectivity of blue mussel Mytilus coruscus on natural phytoplankton assemblages in Sungo Bay using both optical microscopy and HPLC-pigment analysis. Results showed that cryptophytes dominated the phytoplankton community and made up 66.1% of the total phytoplankton abundance. A comparison of phytoplankton composition between natural and filtered seawater showed that M. coruscus preferred cryptophytes and dinoflagellates than Chaetoceros spp. and Skeletonema spp. Cryptophytes were not detected in gut contents by microscopic observation, while their marker pigment alloxanthin was present, suggesting they were also consumed by M. coruscus and can be readily digested. This highlights the shortcomings of microscopic methods and the significance of HPLC-pigment analysis in obtaining a comprehensive understanding of feeding selectivity of bivalves. The proportions of Chaetoceros spp. and Skeletonema spp. in gut contents were significantly lower than their proportions in the seawater, and contrastingly, the proportions of Cocconeis spp. and Pinnularia spp. showed opposite patterns. The marker pigments prasinoxanthin and zeaxanthin were detected in the gut of M. coruscus indicating that picophytoplankton (e.g., prasinophytes and Synechococcus) are also food sources for this bivalve. This information furthers our understanding of bivalve aquaculture and environment interactions.</p

    Relationships between the mean annual sea surface temperature and the growth performance index (Φ′).

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    <p>This index issued from the Arrhenius model was given for populations sampled in (1) Vigo, (2) Ile de Re, (3) Bay of Brest, (4) Bay of Seine, (5) Plymouth, (6) Holyhead, (7) Scarborough, (8) Campbell Town, (9) Austevoll, (10) Bessaker, (11) Bronnoysund, and (12) Traena.</p

    Summary growth data.

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    <p>Von Bertalanffy growth parameters and index of growth performance (Φ′) were fitted from growth data of each study station (in brackets, the limits of the asymptotic 95% confidence interval). Maximum daily growth, MDG (in µm d<sup>−1</sup>), was averaged on the ten highest successive increments (± standard error).</p

    Relationships between the mean annual sea surface temperature and the daily growth parameters.

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    <p>This is shown for A) the maximum numbers of growth days (MNG); and B) the variation in the number of growth days with increasing age (Ω in d y<sup>−1</sup>) for populations sampled in (1) Vigo, (2) Ile de Re, (3) Bay of Brest, (4) Bay of Seine, (5) Plymouth, (6) Holyhead, (7) Scarborough, (8) Campbell Town, (9) Austevoll, (10) Bessaker, (11) Bronnoysund, and (12) Traena.</p

    Variation in mean daily shell growth throughout life (black line) for each sampled population.

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    <p>Gray vertical bars represent the 95% confidence interval of each mean value. The numbers in each graph indicate the annual number of growth days. (1) Vigo, (2) Ile de Re, (3) Bay of Brest, (4) Bay of Seine, (5) Plymouth, (6) Holyhead, (7) Scarborough, (8) Campbell Town, (9) Austevoll, (10) Bessaker, (11) Bronnoysund, and (12) Traena.</p

    Description of the 12 sampled stations.

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    <p>Main geographic characteristics of the study stations are detailed (latitude, longitude, annual average temperature and chlorophyll <i>a</i> concentrations) as the number of individuals used for estimating parameters of the von Bertalanffy growth model and used for estimating the mean growth trajectory and the maximum age observed in the two analyses.</p
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