Pacific Lampreys Entosphenus tridentatus are declining in the Columbia River basin as well as in much of their broader range. To mitigate for reductions in abundance, strategies such as hatchery propagation and captive rearing of lamprey larvae are currently being considered. We conducted a series of experiments using captive larval Pacific Lampreys at Eagle Creek National Fish Hatchery to investigate the effect of different food types and different food concentrations on the growth of larvae. In our first experiment, we evaluated the growth of larvae (TL range, 59–145 mm) given four different food types (algae, leaves, yeast–larval fish food, and salmon carcass analogs) and a control group that was not fed. Assimilation of food types was evaluated by tracking unique stable isotope signatures of δ13C and δ15N within larval tissues. Results from experiment 1 indicated that lampreys fed a diet of salmon carcass analog or algae had positive growth (up to 0.16 mm/d and 42% proportional change in length) over approximately 6 months. Isotopic analyses of larval tissues showed unique signatures that matched those of their specific food treatment. Based on the results of experiment 1, we conducted a second experiment to evaluate the growth of larvae fed four different quantities of salmon carcass analog. Results from this experiment indicated larval growth rate increased with increasing rations of food, but positive growth was observed in all feeding treatments. The highest dose of salmon carcass analog resulted in the highest growth (up to 0.15 mm/d and 36% proportional change in length) over 6 months. We successfully reared larval Pacific Lampreys in captivity with minimal mortality and positive growth, which highlights the potential to use captive rearing and propagation as a conservation tool for this ecologically and culturally important species.

Native lamprey populations are declining worldwide. In the Pacific Northwest focus on conservation and management of these ecologically and culturally important species has increased. Concern has emerged regarding the effects of sampling and handling of lamprey, with little to no attention given to the larval lifestage. We monitored the survival of larval Pacific Lamprey Entosphenus tridentatus and Lampetra spp. after backpack electrofishing, deepwater electrofishing and suction-pumping, anesthesia, and handling. We performed survival trials on wild-caught lamprey (n = 15 larvae in each trial) collected from the Clackamas River drainage in Oregon, USA, coupled with control group trials from lamprey sourced from a hatchery (n = 10 larvae). Short-term (96 h) survival was >98% with only one observed mortality. Delayed mortality (1 wk) was observed for four individuals that had fungus; two of those were positive for the bacteria Aeromonas hyrdrophila. We recorded blood hematocrit as a secondary measure of stress. The baseline, nonstressed larvae hematocrit levels did not differ from those of fish that had undergone stress through electrofishing, suction-pumping, and handling without anesthesia. Electrofishing, suction-pumping, and anesthesia showed no short-term negative effects on larval lamprey although potential long-term effects remain unstudied. These techniques appear to provide efficient and relatively safe methods for collecting and surveying larval lamprey.

Climate models suggest that by 2100, maximum temperatures where many larval Pacific lamprey, Entosphenus tridentatus, rear now may approach 27–31 °C. Little information exists on whether larval Pacific lamprey can tolerate these temperatures. We used acclimated chronic exposure (ACE) and direct acute exposure (DAE) experiments to determine the water temperature that is lethal to larval Pacific lamprey and whether sublethal water temperatures influence larval burrowing behavior. After 30 days in ACE experiments, all larvae survived in temperatures averaging ≤ 27.7 °C, no larvae survived in temperatures averaging ≥ 30.7 °C and the ultimate upper incipient lethal temperature (UILT) was estimated to be 29.2 °C. After seven days in DAE experiments, all larvae survived in 27.1 °C, only larvae acclimated to 23.3 °C survived in 29.1 °C, and no larvae survived in temperatures ≥ 30.6 °C. Using a time to death analysis, estimates of the UILTs ranged from 27.5 to 30.2 °C and the ultimate UILT was estimated to be > 28.3 °C. Using a percent mortality analysis, estimates of the ultimate UILT were not definitive but indicated it may be > 30.2 °C. To burrow, larvae reared for 30 days at temperatures averaging 26.9–27.7 °C exhibited more total time, active time, and stops than those reared for 30 days at temperatures averaging 22.3–23.9 °C. Our findings suggest that larval Pacific lamprey may be resilient to the most likely temperature increase scenarios predicted by climate models. However, they may be vulnerable to the high-temperature increase scenarios and, relatively high but sublethal temperatures may impact the behavior, and ultimately survival, of larval Pacific lamprey.