Search USGS⌕ Search

USGS · 1008133

Breeding patterns and reproductive success of California sea otters

Abstract

Following commercial exploitation in the eighteenth and nineteenth centuries, sea otter ( Enhydra lutris ) populations in Alaska, British Columbia, and Washington recovered at 17-20% a year, yet the California population increased at only 5% a year. This slow rate of increase is perplexing, given that unoccupied and apparently favorable habitats occur throughout the sea otter's California range, and higher growth rates occurred among northern sea otter populations. Better knowledge of the demography of the California population is important in understanding these disparate population growth rates. We studied the reproductive biology and behavior of 53 tagged female sea otters from 1985 to 1991 in Monterey Bay, California. During the study, 136 pups were born to these females. Observations of each female enabled us to determine exact or estimated pup birth dates, which we used to calculate lengths of gestation, pup dependency, and reproductive cycle. Seasonal trends in pupping, in the proportion of adult females with pups, and in pup separations from their mothers were relatively uniform throughout the year. The average interval between separation from pup and subsequent birth was 198 days, the interbirth interval was 407 days, and estimated birth rate was 0.90/year for all adult females. For females that pupped annually (did not lose undetected newborns), the average interbirth interval was 342 days, given an estimated birth rate of 1.07/year. Length of the reproductive cycle increased with increasing length of prior pup dependency. However, the interval between separation from pup and subsequent birth was delayed among females that prematurely lost their pups. The average length of dependency for pups that survived to weaning was 166 days, but ranged from 120 to 280 days. The maximum preweaning survival rate was 0.60-0.65, less than values measured or inferred for some Alaskan populations. Most pups that did not survive to weaning were lost within a month of birth. The probability of successfully weaning pups and the length of dependency increased ( P = 0.077) with mothers' ages, thus indicating that reproductive success may increase among females with greater mothering experience. The high preweaning pup mortality we observed probably accounts for much of the relatively slow growth rate of the California sea otter population.

Explore related subjects

90° N90° S · 180° W ← longitude → 180° E
Source-reported bounding extent: 36.59490298566752° to 36.97023271761633° latitude; -122.10609399826899° to -121.78989896317114° longitude. This indicates report coverage, not an exact sampling location. View area on OpenStreetMap.

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Marianne L. Riedman, James A. Estes, Michelle M. Staedler, Alisa A. Giles, David R. Carlson. 1994. Breeding patterns and reproductive success of California sea otters. https://doi.org/10.2307/3809308

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related USGS reports

Duck nesting response to experimental management of upland habitats in California

Habitat loss and limited upland nesting cover likely constrain waterfowl productivity in intensively managed wetland landscapes in California, USA. We evaluated whether experimental manipulations of upland habitats, including the seeding of native plants, dense nesting cover, or cereal grains, could enhance nesting vegetation and improve duck nest density and nest survival in a Mediterranean climate. During 2008 to 2013, we used a before-after-control-impact (BACI) experimental design within 15 upland grassland fields (each 12–28 ha in size) at a state wildlife area to evaluate habitat management treatment effects on nest site vegetation, vegetation structure, and reproductive performance of mallard ( Anas platyrhynchos ) and gadwall ( Mareca strepera ). The BACI design allowed vegetation and duck nesting responses in treated fields to be compared to untreated control fields both before and after treatment implementation. Prior to treatment implementation, all study fields consisted of upland grasslands dominated primarily by non-native annual grasses typical of Mediterranean-climate ecosystems in California. Relative to control fields, we observed only limited improvement to duck nest success in fields seeded with cereal grains and dense nesting cover, whereas fields seeded with native plants showed persistently lower duck nest survival. Vegetation composition after treatment application shifted rapidly from plants that were purposefully seeded to non-native grasses (e.g., Italian ryegrass [ Lolium multiflorum ]) by the second and third years after treatment. Vegetation structural metrics (i.e., visual obstruction height, lateral density, and canopy density) also showed limited or no improvement attributable to the experimental treatments. Across nearly all treatment and control fields, duck nest densities increased during the first several years following treatment implementation but later declined towards pre-treatment levels by the fourth year after treatment. However, mallard nest densities increased much more markedly in native fields than in control fields in the early post-treatment years but declined again in later post-treatment years, suggesting limited long-term benefit. Clutch size, nest initiation date, and egg hatching success were not affected by treatments. Our results indicate that vegetation management and direct seeding had limited short-term and no measurable long-term benefits to the vegetation's structure, duck nesting densities, or duck nest survival, and upland habitat conditions showed little sustained improvement during later breeding seasons (years 2–4 post-treatment). Upland restoration efforts in agricultural landscapes may need more continued, multi-year habitat management to improve nesting conditions for waterfowl over the long-term.

California↗

Beginning with a single step: A social theory of change for managing chronic wasting disease

Emerging wildlife diseases, like chronic wasting disease (CWD), not only lead to changing dynamics within the ecology of the susceptible species but also to changes within interrelated social and management systems. Chronic wasting disease has proven challenging to manage partially because the best management practices (BMP) available have conflicted with historical cervid management paradigms. In support of CWD management decisions, we conducted an expert elicitation investigation of potential intervention strategies that experts believed would positively affect CWD management. The most prioritized intervention was “understanding audiences, outreach, and engagement with public.” Using the most prioritized intervention theme, we continued the expert elicitation process to develop a social theory of change that describes the expected results of implementing the intervention theme. The results chain describes a process of conducting social science investigation to gather evidence and understand the situation and use the gathered evidence to support the selection of appropriate behavior change strategies and pathways prior to implementing a desired CWD management action. The produced social theory of change provides CWD managing organizations with a framework for evaluating efforts to engage with the public about the actions they are taking and working to increase support or participation.

Journal of Wildlife Management↗

White light reduces flight height of birds in low-density migration corridor

Artificial light at night (ALAN) has been shown to influence the behavior of migratory birds, yet how different light spectra modulate these effects remains unclear. We conducted a field experiment for 31 nights at a remote site in northern Colorado, USA, using 2 800-W light-emitting diode (LED) floodlights with white, red, amber, and blue lighting treatments during fall migration in 2023 and 2024. Using a vertical-looking radar system, we quantified avian in-flight responses in migration traffic rate, flight height, and flight direction between paired control periods with no light and periods with lighting treatments. Although we found no effects of our treatments on migration traffic rate and weak effects on flight direction, we found that broad-spectrum white light with emissions across a 400–600 nm spectrum reduced mean avian flight height by an estimated 22.57 m (±10.53 SE) compared to dark periods, and this response was stronger than red and blue lighting treatments. Our ability to detect behavior changes from a point source in a rural, low-density migration system supports the notion that the effects of artificial light at night on bird behavior may be more pervasive than is often recognized, and that this varies by ALAN spectra. Beyond providing insight into avian orientation and in-flight behavior, our results have implications for future research, the conservation management of artificial light at night, and lighting designs that minimize effects on migratory birds.

Colorado↗