Assessing the condition of walleye pollock Theragra chalcogramma (Pallas) larvae using muscle-based flow cytometric cell cycle analysis

Flow cytometric cell cycle analysis was used to determine the fraction of muscle cells in the S and G2 phases of the cell cycle, which were used as covariates with temperature and standard length, in a laboratory-developed model to assess the physiological condition of wild walleye pollock, Theragra chalcogramma, larvae. The assay was calibrated to the range of temperatures larvae are likely to encounter in the eastern Bering Sea, and it was sensitive to changes in condition within 3 days of starvation. The S and G2 phases of the cell cycle gave an indication of larval walleye pollock condition. Healthy larvae had a larger fraction of cells in the S phase than G2 phase, and unhealthy larvae had a larger fraction of cells in the G2 phase than the S phase. Validation tests showed that the model classified 75% to 83% of the larvae correctly. The assessment of the condition of walleye pollock larvae collected from the southeastern Bering Sea in 2007 indicated that unhealthy larvae were located on the continental shelf (6%), and this may be due in part to the coldest temperatures occurring there and less abundant prey. In the continental slope/ocean basin waters, where prey levels were higher and temperatures warmest, no larvae in unhealthy condition were found.

Research Highlights
► The S and G2 phases of the cell cycle indicated larval walleye pollock condition.
► Validation tests showed that the model classified 75% to 83% of the larvae correctly.
► Unhealthy larvae were located on the continental shelf of the southeast Bering Sea.