Kapsenberg Lydia

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Last Name
Kapsenberg
First Name
Lydia
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Now showing 1 - 3 of 3
  • Dataset
    Shell length data of mussel larvae grown in static and fluctuating pH treatments
    (Biological and Chemical Oceanography Data Management Office (BCO-DMO). Contact: bco-dmo-data@whoi.edu, 2021-01-21) Kapsenberg, Lydia
    Mussel larvae of Mytilus galloprovincialis were grown in static and fluctuating pH treatments in a flow-through seawater system. pH was modified with CO2 gas. D-veliger larvae were collected for shell length measurements on various days per experiment. Shell length was determined using microscope photography and analysis in ImageJ. For a complete list of measurements, refer to the full dataset description in the supplemental file 'Dataset_description.pdf'. The most current version of this dataset is available at: https://www.bco-dmo.org/dataset/751282
  • Dataset
    Developmental morphology data of mussel larvae grown in static and fluctuating pH treatments
    (Biological and Chemical Oceanography Data Management Office (BCO-DMO). Contact: bco-dmo-data@whoi.edu, 2021-01-22) Kapsenberg, Lydia
    Mussel larvae of Mytilus galloprovincialis were grown in static and fluctuating pH treatments in a flow-through seawater system. pH was modified with CO2 gas. Larvae were collected on day 3 (D-veliger stage) and staged for developmental success and morphology, using microscope photography. For a complete list of measurements, refer to the full dataset description in the supplemental file 'Dataset_description.pdf'. The most current version of this dataset is available at: https://www.bco-dmo.org/dataset/751232
  • Dataset
    Biological data of mussel larvae treated with fluorescent dyes and grown in two pH treatments.
    (Biological and Chemical Oceanography Data Management Office (BCO-DMO). Contact: bco-dmo-data@whoi.edu, 2021-01-22) Kapsenberg, Lydia
    Mussel larvae of Mytilus galloprovincialis were grown in two pH treatments (pH 8.1 and 7.4). Larvae were collected for biological measurements of shell field development and calcification at 35 hours post-fertilization (hpf, trochophore stage). Calcein dye was added to the cultures prior to the start of calcification. Calcofluor is live dye and so was added to sampled larvae at 35 hpf for immediate imaging. Confocal microscopy was used for 3D imaging of larvae. Images were processed in ImageJ. Shell field area was determined as the area stained by calcofluor, on one valve. Calcification area was determined as the area stained by calcein, on one valve. For a complete list of measurements, refer to the full dataset description in the supplemental file 'Dataset_description.pdf'. The most current version of this dataset is available at: https://www.bco-dmo.org/dataset/751258