Dataset: Survival of larval Strongylocentrotus purpuratus under ocean warming and food availability scenarios

Forty S. purpuratus were collected from kelp forests between 2.2 – 8.8 meters from Carpinteria Reef in the Santa Barbara Channel, California in June 2022. Before spawning, individuals were held at 13°C for 4 weeks at UC Davis Bodega Marine Laboratory and were fed 20 grams of Urchinomics Inc. kelp-based pelleted food every other day. 

A homogeneous pool of fertilized embryos were assigned to temperature treatments. Spawning was induced by injecting of 1–2 mL of 0.5 M KCl. Female urchins were placed upside down over 250 mL beakers filled with filtered to 0.1 µm seawater (FSW) at ambient temperature. Eggs were allowed to collect at the bottom of beakers. Sperm was collected dry from the aboral surface and placed on ice in 2.0 mL microcentrifuge tubes until use. Gamete quality was visually inspected with eggs assessed for shape, color, and uniform size and sperm for motility. Eggs from four females were pooled and rinsed before being fertilized by sperm from four males. Approximately equal proportions of gametes from each individual within each sex were represented.  Successful fertilization was determined by 95% of eggs having a fertilization envelope with no polyspermy. Fertilized eggs were rinsed three times with FSW to remove excess sperm to prevent polyspermy. Approximately 2800 embryos (concentration of ~5.5 embryos mL^-1) were placed in each 500 mL glass bottles filled with FSW and placed on roller tables to suspend larvae (Karelitz et al. 2020).

Roller agitation tables were constructed to provide water movement for larval sea urchin cultures. Rollers on free moving axles kept larval culture bottles rotating to prevent larvae from settling to the bottom.  Bottles were partially submerged in water baths heated or chilled using Heater/Chillers (TECO US Inc. TK-500) to maintain target temperatures. Embryos were initially stocked in bottles with ambient temperature (16°C) FSW to minimize temperature shock but immediately placed into water baths to allow embryos to acclimate to target temperatures. Each of the 24 temperature x food treatments had four replicate bottles for a total of 96 bottles. Larvae were fed daily starting at 4 days post-fertilization (when larvae were observed to be competent to feed) and water changes and feeding were conducted every 2 days.

Larval sampling was conducted every two days to estimate changes in larval density, morphometry, and competency, in conjunction with water changes and feedings. Larval densities were quantified by concentrating larval cultures to 100 mL and counting the number of larvae found in five 1 mL subsamples. Density counts continued until larvae showed signs of metamorphosis, as determined by the presence of a rudiment and exposed tube feet.