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Geology topics

Michelle Kissling

Publications and source records attributed to Michelle Kissling.

3 recordsLinked to original sources

Kittlitz’s murrelet seasonal distribution and post-breeding migration from the Gulf of Alaska to the Arctic Ocean

Kittlitz’s Murrelets ( Brachyramphus brevirostris ) nest during summer in glaciated or recently deglaciated (post-Wisconsin) landscapes. They forage in adjacent marine waters, especially those influenced by glacial meltwater. Little is known of their movements and distribution outside the breeding season. To identify post-breeding migrations of murrelets, we attached satellite transmitters to birds (n = 47) captured at sea in the Gulf of Alaska and Aleutian Islands during May – July 2009 – 15 and tracked 27 birds that migrated from capture areas. Post-breeding murrelets migrated toward the Bering Sea, with short periods of movement (median 2 d) separated by short stopovers (median 1 d). Travel speeds averaged 79.4 km d-1 (83.5 SD, 449.1 maximum). Five Kittlitz’s Murrelets tagged in Prince William Sound in May migrated to the Bering Sea by August and four continued north to the Arctic Ocean, logging 2500 – 4000 km of travel. Many birds spent 2‒3 weeks with little movement along coasts of the Alaska Peninsula or eastern Bering Sea during late August through September, also the pre-basic molt period. Ship-based surveys, many of which were conducted concurrently with our telemetry studies, confirmed that substantial numbers of Kittlitz’s Murrelets migrate into the Arctic Ocean during autumn. They also revealed that some birds spend winter and spring in the Bering Sea in association with ice-edge, polynya, or marginal ice zone habitats before returning to summer breeding grounds. We conclude that this species is best characterized as a sub-Arctic and Arctic species, which has implications for future risk assessments and threat mitigation.

Alaska

Estimating Pacific walrus abundance and survival with multievent mark-recapture models

Arctic marine ecosystems are undergoing rapid physical and biological change associated with climate warming and loss of sea ice. Sea ice loss will impact many species through altered spatial and temporal availability of resources. In the Bering and Chukchi Seas, the Pacific walrus Odobenus rosmarus divergens is one species that could be impacted by rapid environmental change, and thus, population assessments are needed to monitor changes in the status of this ecologically and culturally important marine mammal. We conducted a 5 yr genetic mark-recapture study to estimate demographic parameters for the Pacific walrus. We developed a Bayesian multievent mark-recapture model to estimate walrus survival and abundance while accounting for age misclassification. We estimated the probability of juvenile annual survival as 0.63 (95% credible interval [CrI]: 0.39-0.87) and adult female annual survival as 0.90 (95% CrI: 0.74-1.00). We estimated total abundance as 257 193 (95% CrI: 171 138-366 366). We provide the first estimate of total Pacific walrus abundance since an aerial survey in 2006, which generated a substantially less precise total population size estimate (129 000; 95% CI: 55 000-507 000). The emerging ecosystem state in the northern Bering and Chukchi Seas will likely result in a decline in Pacific walrus abundance, but there is substantial uncertainty regarding the magnitude of the anticipated decline. Our demographic estimates provide critical information to evaluate future population trends of this subsistence resource vital to communities that border the Bering and Chukchi Seas in the USA and Russia.

Alaska

Trends and carrying capacity of sea otters in Southeast Alaska

Sea otter populations in Southeast Alaska (SEAK) have increased dramatically from fewer than 500 translocated animals in the late 1960s. The recovery of sea otters to ecosystems from which they had been absent has affected coastal food webs, including commercially important fisheries, and thus information on expected growth and equilibrium abundances can help inform resource management. We compile available survey data for SEAK and fit a Bayesian state-space model to estimate past trends and current abundance. Our model improves upon previous analyses by partitioning and quantifying sources of estimation error, accounting for over-dispersion of aerial count data, and providing realistic measurements of uncertainty around point estimates of abundance at multiple spatial scales. We also provide the first estimates of carrying capacity (K) for SEAK, at both regional and sub-regional scales, and analyze growth rates, current population status and expected future trends. At the regional scale, the population increased from 13,221 otters in 2003 (95% credible interval 9,990 – 16,828) to 25,584 otters in 2011 (CI95 18,739 – 33,163). The average annual growth rate in southern SEAK (7.8%) was higher than northern SEAK (2.7%); however, growth varied at the sub-regional scale and there was a negative relationship between growth rates and the number of years sea otters were present in an area. Local populations vary in terms of current densities and expected future growth: the mean estimated density at K was 4.2 (1.58) sea otters per km2 of habitat (defined as the sub-tidal benthos between 0-40m depth) and current densities correspond on average to 50% of projected equilibrium values (range = 1% to 97%) with the earliest-colonized sub-regions tending to be closer to K. Assuming a similar range of equilibrium densities for currently un-occupied habitats in SEAK, the projected value of K for all of SEAK is 74,650 sea otters (CI95 =36,778–136,506). Future analyses can improve upon the precision of K estimates by employing more frequent surveys at index sites and incorporating environmental covariates into the process model to generate habitat-specific estimates of equilibrium density.

Alaska