The impacts of climate change and the socioecological challenges they present are ubiquitous and increasingly severe. Practical efforts to operationalize climate-responsive design and management in the global network of marine protected areas (MPAs) are required to ensure long-term effectiveness for safeguarding marine biodiversity and ecosystem services. Here, we review progress in integrating climate change adaptation into MPA design and management and provide eight recommendations to expedite this process. Climate-smart management objectives should become the default for all protected areas, and made into an explicit international policy target. Furthermore, incentives to use more dynamic management tools would increase the climate change responsiveness of the MPA network as a whole. Given ongoing negotiations on international conservation targets, now is the ideal time to proactively reform management of the global seascape for the dynamic climate-biodiversity reality.

The endangered leatherback turtle is a large, highly migratory marine predator that inexplicably relies upon a diet of low-energy gelatinous zooplankton. The location of these prey may be predictable at large oceanographic scales, given that leatherback turtles perform long distance migrations (1000s of km) from nesting beaches to high latitude foraging grounds. However, little is known about the profitability of this migration and foraging strategy. We used GPS location data and video from animal-borne cameras to examine how prey characteristics (i.e., prey size, prey type, prey encounter rate) correlate with the daytime foraging behavior of leatherbacks ( n = 19) in shelf waters off Cape Breton Island, NS, Canada, during August and September. Video was recorded continuously, averaged 1:53 h per turtle (range 0:08–3:38 h), and documented a total of 601 prey captures. Lion's mane jellyfish ( Cyanea capillata ) was the dominant prey (83–100%), but moon jellyfish ( Aurelia aurita ) were also consumed. Turtles approached and attacked most jellyfish within the camera's field of view and appeared to consume prey completely. There was no significant relationship between encounter rate and dive duration ( p = 0.74, linear mixed-effects models). Handling time increased with prey size regardless of prey species ( p = 0.0001). Estimates of energy intake averaged 66,018 kJ•d −1 but were as high as 167,797 kJ•d −1 corresponding to turtles consuming an average of 330 kg wet mass•d −1 (up to 840 kg•d −1 ) or approximately 261 (up to 664) jellyfish•d -1 . Assuming our turtles averaged 455 kg body mass, they consumed an average of 73% of their body mass•d −1 equating to an average energy intake of 3–7 times their daily metabolic requirements, depending on estimates used. This study provides evidence that feeding tactics used by leatherbacks in Atlantic Canadian waters are highly profitable and our results are consistent with estimates of mass gain prior to southward migration.

Nine prey species (n = 7431) were fed to four captive female Steller sea lions ( Eumetopias jubatus (Schreber, 1776)) in 11 feeding trials over 75 days to investigate the effectiveness of different methods used to determine diet from prey hard remains. Trials aimed to replicate short (1–2 days) and long feeding bouts, and consisted of single species and mixed daily diets. Overall, 25.2% ± 22.2% (mean ± SD, range 0%–83%) otoliths were recovered, but recovery rates varied by species (ANOVA, P = 0.01) and were linearly related to otolith robustness (R2 = 0.88). Squid beaks were recovered at higher frequencies (mean 96%) than the otoliths of all species. Enumerating both non-otolith skeletal structures and otoliths (together termed bones) increased species recovery rates by twofold, on average (P < 0.001), with increases up to 2.5 times for Pacific herring ( Clupea pallasii Valenciennes in Cuvier and Valenciennes, 1847) and 3–4 times for salmonids. Using bones reduced interspecific differences (P = 0.08), but recovery varied among sea lions. Bones were distributed over more scats per meal (mean 2.9 scats, range 0–5) than otoliths (mean 1.9 scats, range 0–4). In three different 15-day mixed diet trials, biomass reconstruction (BR) indices performed better than frequency of occurrence indices in predicting diet fed. Applying our experimentally derived numerical correction factors (to account for species differences in complete prey digestion) further improved BR estimates, resulting in all 12 unweighted comparisons within 5% (for otoliths) and 12% (for bones) of the actual diet fed.

Reliable estimates of diets are vital to monitor impacts of sea lion populations on their ecosystems and their interactions with fisheries, and to understand the role of food to animal nutrition and health. Approaches include using (1) prey remnants in stomach contents, spews and scats; (2) prey DNA in scats; (3) fatty acid signatures in blubber; and (4) stable isotope ratios in predator's tissue. Each methodology has particular advantages and limitations, many of which can be assessed and improved through controlled captive feeding trials. Analysis of prey remnants from captive sea lion scats have shown significant variability in digestion between and within prey species, which, coupled with preferential regurgitation and enumeration biases, can confound accurate diet quantification, but does not prevent spatial or temporal comparisons. Correction for partial digestion and use of additional structures besides otoliths can provide reliable prey size estimates. Prey DNA can be consistently isolated from soft remains in scats from captive sea lions, and with further development this approach may allow quantification of diet. Genetic methods can be expensive and representative of only one to two