Literature review of elasmobranch bycatch and retention rate

To address growing concern over the effects of fisheries non-target catch on elasmobranchs worldwide, the accurate reporting of elasmobranch catch is essential. This requires data on a combination of measures, including reported landings, retained and discarded non-target catch, and post-discard survival. Identification of the factors influencing discard vs. retention is needed to improve catch estimates and to determine wasteful fishing practices. To do this we compared retention rates of elasmobranch non-target catch in a broad subset of fisheries throughout the world by taxon, fishing country, and gear. A regression tree and random forest analysis indicated that taxon was the most important determinant of retention in this dataset, but all three factors together explained 59% of the variance. Estimates of total elasmobranch removals were calculated by dividing the FAO global elasmobranch landings by average retention rates and suggest that total elasmobranch removals may exceed FAO reported landings by as much as 400%. This analysis is the first effort to directly characterize global drivers of discards for elasmobranch non-target catch. Our results highlight the importance of accurate quantification of retention and discard rates to improve assessments of the potential impacts of fisheries on these species.

Otolith microstructure and trace elemental concentrations in juvenile Pacific bluefin tuna (Thunnus orientalis) caught off of Southern California in 2012

We combined longitudinal analyses of otolith microstructure and trace elemental composition in ~ age 1-2 Pacific bluefin tuna (PBT, n = 24) for inferring the arrival of individuals in the California Current Large Marine Ecosystem (CCLME). Element:Ca ratios in transverse otolith sections (9-12 rows, triplicate ablations from coreprimordium to edge, ø50 µm) were quantified for eight elements: Li, Mg, Mn, Co, Cu, Zn, Sr, and Ba, which was followed by microstructure analysis to provide age estimates corresponding to each ablation spot. Age estimates from otoliths ranged from 328 to 498 days post hatch. The combined elemental signatures of four elements (Ba, Mg, Co, Cu) showed a significant increase at the otolith edge in approximately half of the individuals (30-60 days prior to catch). Given the different oceanographic properties of oligotrophic open Pacific vs. high nutrient, upwelling CCLME waters, this signal is consistent with the entry of the fish into the CCLME, which was estimated to occur primarily in July after a transoceanic migration of ~1.5-2.0 months.