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Marianne L. Riedman

Publications and source records attributed to Marianne L. Riedman.

4 recordsLinked to original sources
USGS2003

Individual variation in prey selection by sea otters: Patterns, causes and implications

1. Longitudinal records of prey selection by 10 adult female sea otters on the Monterey Peninsula, California, from 1983 to 1990 demonstrate extreme inter-individual variation in diet. Variation in prey availability cannot explain these differences as the data were obtained from a common spatial-temporal area. 2. Individual dietary patterns persisted throughout our study, thus indicating that they are life-long characteristics. 3. Individual dietary patterns in sea otters appear to be transmitted along matrilines, probably by way of learning during the period of mother-young association. 4. Efficient utilization of different prey types probably requires radically different sensory/motor skills, each of which is difficult to acquire and all of which may exceed the learning and performance capacities of any single individual. This would explain the absence of generalists and inertia against switching, but not the existence of alternative specialists. 5. Such individual variation might arise in a constant environment from frequency-dependent effects, whereby the relative benefit of a given prey specialization depends on the number of other individuals utilizing that prey. Additionally, many of the sea otter's prey fluctuate substantially in abundance through time. This temporal variation, in conjunction with matrilineal transmission of foraging skills, may act to mediate the temporal dynamics of prey specializations. 6. Regardless of the exact cause, such extreme individual variation in diet has broad ramifications for population and community ecology. 7. The published literature indicates that similar patterns occur in many other species.

Journal of Animal Ecology↗
USGS1995

Repertoire, structure, and individual variation of vocalizations in the sea otter

Vocalizations of the California sea otter ( Enhydra lutris nereis ) were recorded from wild and captive adults and young and analyzed spectrographically. Parameters measured from the sonagrams included fundamental frequency, duration, maximum frequency, intercall interval, and the location and amplitude of energy peaks. We identified 10 basic vocal categories, one of which consisted of graded signals. The contexts for each call, when known or suspected, are described. Discriminant analysis of the spectrographic parameters for the scream call showed significant differences among individuals for adult females and young. Using only the parameters quantified, each call was assigned correctly to the individual that produced it with 80% accuracy for mothers and 75% for young, thus, indicating that the potential exists for individual vocal recognition in the sea otter. The sea otter's vocal repertoire is similar in complexity to that of certain pinnipeds, but may be less complex than that of several species of social cetaceans and primates. In general, the sea otter's vocal patterns have characteristics thought to be most suitable for short-range communication among familiar individuals.

Journal of Mammalogy↗
USGS1994

Breeding patterns and reproductive success of California sea otters

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.

California↗