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Fraser River sockeye salmon: data synthesis and cumulative impacts

Fraser River sockeye salmon: data synthesis and cumulative impacts

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examples illustrate this problem -- the collapse of Canada's Northern cod populations inthe early 1990s <strong>and</strong> the virtual disappearance of California sardine in the 1960s -- both ofwhich fueled long debates about the relative importance of fishing, environmentalchanges, <strong>and</strong> government regulations in causing those collapses.The <strong>sockeye</strong> stocks within the <strong>Fraser</strong> Basin have widely varying life history, genetic <strong>and</strong> habitatcharacteristics that create different levels of vulnerability to the stressors each stock encounters(described in Nelitz et al. 2011). Effects of stressors on survival at any life history stage dependon both the magnitude of the stress <strong>and</strong> the vulnerability of the <strong>salmon</strong>. Characteristics that varyacross stocks include: spawning habitat (inlets, outlets, lake shore, flow rates, substrateconditions, environmental conditions), nursery lakes (area, size, productivity, temperature, icebreak-up, duration of rearing), smolt out-migration (distance, timing, temperatures, arrival atestuary, residence time in estuary), coastal migration (timing, duration, route), <strong>and</strong> adultmigration (return route, age of return, timing, estuary residence time, timing of upstreammigration, upstream distances <strong>and</strong> duration, river temperatures <strong>and</strong> other environmentalcharacteristics, pre-spawn mortality rates). Many <strong>Fraser</strong> <strong>sockeye</strong> stocks are strongly cyclical(e.g., Late Shuswap, Quesnel, Scotch) whereas others are less so. Once mobile, each <strong>salmon</strong> hasa recurring choice – eat or hide. Sockeye stocks (<strong>and</strong> sub-populations within each stock) havedeveloped complicated <strong>and</strong> varying life histories that include moving between ranges of habitatsvarying in the risks they represent (Christensen <strong>and</strong> Trites 2011, pg. 5). Finally, we are observinglarge scale effects of climate change in both freshwater <strong>and</strong> marine environments, withinfluences on many of the above attributes <strong>and</strong> their interactive relationships.3.2 Unknowns, Unknowables, Knowledge Gaps, <strong>and</strong> Data LimitationsGiven all of the above challenges, what can fisheries science achieve that is helpful to both theCohen Commission <strong>and</strong> fisheries managers? First, science can test hypotheses, rejecting thosethat are unlikely or false. Even with considerable gaps in <strong>data</strong> <strong>and</strong> underst<strong>and</strong>ing, <strong>and</strong> mostlyindirect evidence, contrasts over space <strong>and</strong> time in both <strong>salmon</strong> stock productivity <strong>and</strong> thepotential stressors allow us to judge certain stressors to be unlikely to have been the primaryfactors causing declines in <strong>sockeye</strong> productivity or abundance. Other factors may be possible oreven likely, provided that they fulfill most or all of various criteria (i.e., have a plausiblemechanism by which survival could be affected; have generally exposed <strong>Fraser</strong> <strong>sockeye</strong> toincreased stress over the period of productivity declines; correlate over space, time <strong>and</strong> stockswith variations in productivity; <strong>and</strong> (ideally) have other corroborating evidence from cause-effectstudies). The procedure by which we evaluate alternative hypotheses is described below insection 3.3. Two key principles are: 1) hypotheses can be rejected as false or unlikely, but cannotbe accepted as true (only relatively more likely); <strong>and</strong> 2) correlation does not equal causation (one14

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