This dataset is from a field experiment that examined how juvenile flatfish distribution changed with worm tube heterogeneity, i.e. density and patchiness.

This dataset is from laboratory experiments testing the onset and ontogenetic changes in habitat selection of pre- and post-settling northern rock sole (NRS) larvae, and from field surveys investigating settlement patterns of NRS.

This dataset is from an experiment where northern rock sole larvae were reared in the laboratory to measure growth, condition, development and settlement parameters across four temperatures (2, 4, 7 and 10C).

The importance of high relief structure containing biotic habitat to rockfish and other species remains largely unknown. This data set was created to examine the importance of this habitat for Pacific ocean perch, northern rockfish, and dusky rockfish. These data were derived from four research cruises that occurred between May 2012 and December 2014. During the cruises, video data was recorded of habitat associations, plankton samples were collected, temperature profiles were recorded, and several types of biological samples were taken from trawl captured rockfish. These data will be recorded in several tables in an access database and video files will also be available.

Juvenile rockfish were observed amongst coral, sponge, cobble, and gravel habitats. Rockfish utilized coral habitats more than any other, while gravel was the least utilized. Sponge and cobble habitat utilization was intermediate to coral and gravel. Predation of young-of-the-year rockfish by sculpin predators was greatest in gravel habitats and lowest in coral habitats.

This dataset is from field surveys that examined depth distribution, habitat association, and growth of newly settled Tanner crab at 4 sites around the eastern end of Kodiak Island, Alaska.

To study the effects of ocean acidification we examined the effects of ocean acidification on the larval stages of the economically important southern Tanner crab, Chionoecetes bairdi. Ovigerous females were reared in one of 3 treatments: control (ambient pH ~8.1), pH 7.8, and pH 7.5 for 2 years. Larvae in year 1 were from oocytes developed in the field whereas larvae in year 2 were from oocytes developed under acidified conditions. Larvae hatched each year, were also exposed to 3 pH treatments to examine starvation-survival, morphology, condition, and calcium/magnesium content. Approximately 300 larvae were stocked in multiple treatments for testing the effect of pH. Hatching success was measured as the total % of larval hatched from a full clutch while duration was the number of days over which hatching occurred. Hatching success did not differ among treatments in 2012 but varied between 46 to 87% in 2013 dependent on pH treatment. Larval mass was highest in pH 7.8 in 2012 and lowest in the control, however in 2013 the highest larval mass was in the control water. There were only small (not significant) changes in magnesium or calcium content among treatments in 2012 however, the reduction in both minerals at higher pH was greater in 2013. There was higher percent carbon and nitrogen contents in pH 7.5 larvae in 2013. The morphology of Tanner crab larval was assessed from 200 larvae stocked in multiple 2 L beakers. There was no effect of treatment on larval morphometrics. In 2012 and 2013, we examined if embryos developed under acidified conditions affected larval morphology by assessing 15 newly hatched larvae from each treatment. There was again no effect of treatment on larval morphometrics. Starvation survival experiments were performed in 1 L sized PVC inserts. In both years larvae from embryos that developed in pH 7.5 water survived about 3 days longer than those that developed in control water. However, in 2012 larvae from embryos that had developed in pH 7.8 water were similar to control larvae whereas in 2013 they were intermediate between the control and pH 7.5 larvae. The overall effects of treatment at the larval stage appeared to be better condition and initial survival at lower pH, however multiple years of treatment led to lower survival.

Region(s) of distribution of Tubenose Poacher (Pallasina barbata) (Steindachner, 1876) in the Arctic as digitized for U.S. Geological Survey Scientific Investigations Report 2016-5038. For details on the project and purpose, see the report at https://doi.org/10.3133/sir20165038. Complete metadata for the collection of species datasets is in the metadata document "Dataset_for_Alaska_Marine_Fish_Ecology_Catalog.xml" at https://doi.org/10.5066/F7M61HD7. Source(s) for this digitized data layer are listed in the metadata Process Steps section. Note that the original source may show an extended area; some datasets were limited to the published map boundary. Distributions of marine fishes are shown in adjacent Arctic seas where reliable data are available. The data were clipped to show only the marine distribution areas although some species also may have an inland presence.

Region(s) of distribution of Tubenose Poacher (Pallasina barbata) (Steindachner, 1876) in the Arctic as digitized for U.S. Geological Survey Scientific Investigations Report 2016-5038. For details on the project and purpose, see the report at https://doi.org/10.3133/sir20165038. Complete metadata for the collection of species datasets is in the metadata document "Dataset_for_Alaska_Marine_Fish_Ecology_Catalog.xml" at https://doi.org/10.5066/F7M61HD7. Source(s) for this digitized data layer are listed in the metadata Process Steps section. Note that the original source may show an extended area; some datasets were limited to the published map boundary. Distributions of marine fishes are shown in adjacent Arctic seas where reliable data are available. The data were clipped to show only the marine distribution areas although some species also may have an inland presence.

This data set describes the holding temperatures and developmental stages of larvae of red and blue king crab (Paralithodes camtschaticus and P. platypus) reared to the first crab stage at the Kodiak Laboratory.