Michael A. Litzow

Sea ice retreat alters the biogeography of the Bering Sea continental shelf.

Seasonal ice cover creates a pool of cold bottom water on the eastern Bering Sea continental shelf each winter. The southern edge of this cold pool, which defines the ecotone between arctic and subarctic communities, has retreated approximately 230 km northward since the early 1980s. Bottom trawl surveys of fish and invertebrates in the southeastern Bering Sea (1982-2006) show a coincident reorganization in community composition by latitude. Survey catches show community-wide northward distribution shifts, and the area formerly covered by the cold pool has seen increases in total biomass, species richness, and average trophic level as subarctic fauna have colonized newly favorable habitats. Warming climate has immediate management implications, as 57% of variability in commercial snow crab (Chionoecetes opilio) catch is explained by winter sea ice extent. Several measures of community distribution and structure show linear relationships with bottom temperature, suggesting warming climate as the primary cause of changing biogeography. However, residual variability in distribution not explained by climate shows a strong temporal trend, suggesting that internal community dynamics also contribute to changing biogeography. Variability among taxa in their response to temperature was not explained by commercial status or life history traits, suggesting that species-specific responses to future warming will be difficult to predict.

INCREASED SPATIAL VARIANCE ACCOMPANIES REORGANIZATION OF TWO CONTINENTAL SHELF ECOSYSTEMS

Phase transitions between alternate stable states in marine ecosystems lead to disruptive changes in ecosystem services, especially fisheries productivity. We used trawl survey data spanning phase transitions in the North Pacific (Gulf of Alaska) and the North Atlantic (Scotian Shelf) to test for increases in ecosystem variability that might provide early warning of such transitions. In both time series, elevated spatial variability in a measure of community composition (ratio of cod [Gadus sp.] abundance to prey abundance) accompanied transitions between ecosystem states, and variability was negatively correlated with distance from the ecosystem transition point. In the Gulf of Alaska, where the phase transition was apparently the result of a sudden perturbation (climate regime shift), variance increased one year before the transition in mean state occurred. On the Scotian Shelf, where ecosystem reorganization was the result of persistent overfishing, a significant increase in variance occurred three years before the transition in mean state was detected. However, we could not reject the alternate explanation that increased variance may also have simply been inherent to the final stable state in that ecosystem. Increased variance has been previously observed around transition points in models, but rarely in real ecosystems, and our results demonstrate the possible management value in tracking the variance of key parameters in exploited ecosystems.

Reassessing regime shifts in the North Pacific: incremental climate change and commercial fishing are necessary for explaining decadal‐scale biological variability

In areas of the North Pacific that are largely free of overfishing, climate regime shifts - abrupt changes in modes of low-frequency climate variability - are seen as the dominant drivers of decadal-scale ecological variability. We assessed the ability of leading modes of climate variability [Pacific Decadal Oscillation (PDO), North Pacific Gyre Oscillation (NPGO), Arctic Oscillation (AO), Pacific-North American Pattern (PNA), North Pacific Index (NPI), El Niño-Southern Oscillation (ENSO)] to explain decadal-scale (1965-2008) patterns of climatic and biological variability across two North Pacific ecosystems (Gulf of Alaska and Bering Sea). Our response variables were the first principle component (PC1) of four regional climate parameters [sea surface temperature (SST), sea level pressure (SLP), freshwater input, ice cover], and PCs 1-2 of 36 biological time series [production or abundance for populations of salmon (Oncorhynchus spp.), groundfish, herring (Clupea pallasii), shrimp, and jellyfish]. We found that the climate modes alone could not explain ecological variability in the study region. Both linear models (for climate PC1) and generalized additive models (for biology PC1-2) invoking only the climate modes produced residuals with significant temporal trends, indicating that the models failed to capture coherent patterns of ecological variability. However, when the residual climate trend and a time series of commercial fishery catches were used as additional candidate variables, resulting models of biology PC1-2 satisfied assumptions of independent residuals and out-performed models constructed from the climate modes alone in terms of predictive power. As measured by effect size and Akaike weights, the residual climate trend was the most important variable for explaining biology PC1 variability, and commercial catch the most important variable for biology PC2. Patterns of climate sensitivity and exploitation history for taxa strongly associated with biology PC1-2 suggest plausible mechanistic explanations for these modeling results. Our findings suggest that, even in the absence of overfishing and in areas strongly influenced by internal climate variability, climate regime shift effects can only be understood in the context of other ecosystem perturbations.

Fishing through (and up) Alaskan food webs

We used a 112-year time series of Alaskan fishery catches to test competing hypotheses concerning trends in mean catch trophic level, a widely used indicator of fisheries sustainability. We found that mean trophic level has generally remained steady or increased in recent decades on Alaska-wide and regional scales, indicating stable catches of high trophic level taxa. During historical periods of declining mean trophic level, catches of upper trophic level taxa either increased or remained steady, contrary to the predictions of the “fishing down the food web” hypothesis. Further, a climate index was highly correlated (r = 0.69–0.97) with mean trophic level and (or) the related fisheries in balance (FIB) index across climate regime shifts in the 1940s and 1970s, indicating that climate effects, particularly on high trophic level taxa, can act as the major driver of variability in these parameters. These results provide a contrast to the view of ubiquitous declines in mean trophic level of fishery catches, ...