The data from this study, describes embryo development in Golden king crab, Lithodes aequispinus. Six female multiparous golden king crab were captured from the Aleutian Islands, Alaska, and mated in the laboratory. Their embryos were photographed and staged on average once every 9 days throughout embryogenesis.

Juvenile red and blue king crabs (Paralithodes camtschaticus and P. platypus) were exposed to three pH levels: ambient (pH 8.1), pH 7.8, and pH 7.5 for three weeks. Oxygen consumption and feeding ration were determined immediately after exposure to treatment water and after three weeks exposure. Growth can be calculated from the wet mass observations.

This data set is the results of a laboratory experiment. Juvenile red king crab and Tanner crab were reared in individual containers for nearly 200 days in flowing control (pH 8.0), pH 7.8, and pH 7.5 seawater at ambient temperatures (range 4.4-11.9 C). Survival, growth, and morphology were measured throughout the experiment. At the end of the experiment, calcium concentration was measured in each crab and the dry mass and condition index of each crab were determined.

This dataset contains data from a series of experiments that determined the upper thermal tolerance of early benthic stage red and blue king crabs. Experiments included determining the temperature at which 50% of crabs died after 24 hour exposure, determining the effect of temperature on feeding ration, and the effects of temperature on long-term growth and mortality.

This data set is from a series of laboratory experiments examining the interactions between red and blue king crabs and habitat. We examined how density and predator presence affect habitat choice by red and blue king crabs. Further experiments determined how temperature and habitat affect predation by year-1 red king crab on year-0 blue king crab. Finally, long-term interaction experiments examined how habitat and density affected growth, survival, and intra-guild interactions between red and blue king crab.

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).

This is data from a laboratory experiment in which blue king crab juveniles were held at three different pHs (ambient, pH 7.8, and pH 7.5) for a year. Growth, survival, and morphology were recorded.

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.

This data is from an experiment designed to test the viability of using hatchery reared crab to supplement wild stocks and to determine the optimal density for future releases. Crab were released by divers into 5 x 5 m quadrats marked with ground line at three densities: 25, 50, and 75 m-2. Researchers monitored the crab density inside the plots, in order to estimate survival, as well as outside the plots, to estimate crab movement. In addition, they determined predator densities and performed tethering experiments on red king crab to see if predator density or predation risk differed among the density treatments.

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.