Eye Optics in Semiaquatic Mammals for Aerial and Aquatic Vision

2018 ◽  
Vol 92 (3-4) ◽  
pp. 117-124
Author(s):  
Alla M. Mass ◽  
Alexander Ya Supin

Based on anatomical measurements of refractive structures in the eye, the positions of focused images were computed for several groups of semiaquatic mammals: rodents, a nonpinniped semiaquatic carnivore (the sea otter), and pinniped carnivores (seals, sea lions, and the walrus). In semiaquatic rodents, eye optics enable emmetropia in the air but cause substantial hypermetropia in the water. In semiaquatic carnivores, there are several mechanisms for amphibious vision that focus images on the retina in both air and water. These mechanisms include the potential for a substantial change in the lens shape of sea otters and the presence of the corneal emmetropic window in pinnipeds. The results suggest that several groups of mammals that independently adapted to aquatic environments vary in how their visual systems adapted to aquatic vision.

2020 ◽  
Author(s):  
Gisela Heckel ◽  
◽  
M.G. Ruiz Mar ◽  
Y. Schramm ◽  
U. Gorter

Marine mammals are a group of charismatic megafauna, capable of awakening fascination in most people, which makes them especially visible when natural resources or ecosystems are exploited, as is the case with the generation of energy using the sea. There are 131 species of marine mammals in the world, including whales, dolphins, sea lions, seals, walruses, sea otters, polar bears, manatees and dugongs. Mexico’s marine environment is megadiverse, with 38 cetacean species (eight mysticeti or baleen whale species, 30 odontoceti or toothed whale species, dolphins and porpoises), four pinnipeds (two seal species and two sea lion species), one sea otter sub-species and one manatee subspecies (


2020 ◽  
Vol 655 ◽  
pp. 123-137
Author(s):  
TM Grimes ◽  
MT Tinker ◽  
BB Hughes ◽  
KE Boyer ◽  
L Needles ◽  
...  

Protective legislation and management have led to an increase in California’s sea otter Enhydra lutris nereis population. While sea otter recovery has been linked to ecosystem benefits, sea otter predation may negatively affect commercially valuable species. Understanding the potential influence of sea otters is of particular importance as their range expands into estuaries that function as nurseries for commercially valuable species like Dungeness crab Metacarcinus magister. We consider how sea otter predation has affected the abundance and size of juvenile Dungeness crab in Elkhorn Slough, California, USA, and analyzed cancrid crab abundance and size across 4 California estuaries with and without sea otters to understand how biotic and abiotic factors contribute to observed variation in crab size and abundance. We compared trends in southern sea otters relative to Dungeness crab landings in California to assess whether increasing sea otter abundance have negatively impacted landings. In Elkhorn Slough, juvenile Dungeness crab abundance and size have declined since 2012, coinciding with sea otter population growth. However, the impact of sea otters on juvenile Dungeness crab size was habitat-specific and only significant in unvegetated habitat. Across estuaries, we found that cancrid crab abundance and size were negatively associated with sea otter presence. While abiotic factors varied among estuaries, these factors explained little of the observed variation in crab abundance or size. Although we found evidence that sea otters can have localized effects on cancrid crab populations within estuaries, we found no evidence that southern sea otters, at recent population sizes, have negatively impacted Dungeness crab landings in California from 2000-2014.


Oryx ◽  
2021 ◽  
pp. 1-6
Author(s):  
Igor Popov ◽  
Alexey Scopin

Abstract We describe the population of the Еndangered sea otter Enhydra lutris on Urup Island, one of the main wildlife refuges in the southern Kuril Islands of Russia. We reviewed historical and local reports of the sea otter, identified its habitat around the island, and surveyed the coastal waters of the island in 2019. Sea otters were numerous on Urup Island in the past but were hunted excessively and almost exterminated by the 1950s. Since then, sea otter populations have increased, and as the island is almost uninhabited we expected otters to be numerous. This was not the case, and we estimated the total population to be 363 ± SE 126 individuals. Our observation of two skinned carcasses on the shore suggests the low numbers are a result of poaching for the illegal fur trade. The case of Urup Island demonstrates that sea otters require active conservation, as even on a remote island they remain threatened. Establishment of protected areas would be an effective conservation measure for this species, although the suppression of demand for sea otter fur is of the greatest importance.


Science ◽  
2020 ◽  
Vol 368 (6496) ◽  
pp. 1243-1247 ◽  
Author(s):  
Edward J. Gregr ◽  
Villy Christensen ◽  
Linda Nichol ◽  
Rebecca G. Martone ◽  
Russell W. Markel ◽  
...  

Predator recovery often leads to ecosystem change that can trigger conflicts with more recently established human activities. In the eastern North Pacific, recovering sea otters are transforming coastal systems by reducing populations of benthic invertebrates and releasing kelp forests from grazing pressure. These changes threaten established shellfish fisheries and modify a variety of other ecosystem services. The diverse social and economic consequences of this trophic cascade are unknown, particularly across large regions. We developed and applied a trophic model to predict these impacts on four ecosystem services. Results suggest that sea otter presence yields 37% more total ecosystem biomass annually, increasing the value of finfish [+9.4 million Canadian dollars (CA$)], carbon sequestration (+2.2 million CA$), and ecotourism (+42.0 million CA$). To the extent that these benefits are realized, they will exceed the annual loss to invertebrate fisheries (−$7.3 million CA$). Recovery of keystone predators thus not only restores ecosystems but can also affect a range of social, economic, and ecological benefits for associated communities.


2020 ◽  
Vol 7 ◽  
Author(s):  
Melissa A. Miller ◽  
Megan E. Moriarty ◽  
Laird Henkel ◽  
Martin Tim Tinker ◽  
Tristan L. Burgess ◽  
...  

We compiled findings from 15 years (1998–2012) of southern sea otter (Enhydra lutris nereis) necropsies, incorporating data from 560 animals. Sensitive diagnostic tests were used to detect biotoxins, bacteria, parasites and fungi. Methods to classify primary and contributing causes of death (COD) and sequelae utilized an updated understanding of health risks affecting this population. Several interesting patterns emerged, including identification of coastal regions of high mortality risk for sea otter mortality due to shark bite, cardiomyopathy, toxoplasmosis, sarcocystosis, acanthocephalan peritonitis and coccidioidomycosis. We identified demographic attributes that enhanced the risk of disease in relation to age, sex, and reproductive stage. Death due to white shark (Carcharodon carcharias) bite increased dramatically during the study period and was the most common primary COD. However, when primary and contributing COD were combined, the most prevalent COD was infectious disease (affecting 63% of otters), especially fatal infections by acanthocephalans (Profilicollis spp.) and protozoa (e.g., Sarcocystis neurona and Toxoplasma gondii). Fatal bacterial infections were also extremely common as a primary process or a sequela, affecting 68% of examined otters. Substantial advances were made in identifying sea otters that died following exposure to the pervasive marine neurotoxin domoic acid (DA), and DA intoxication was conservatively estimated as a primary or contributing COD for 20% of otters. Cardiomyopathy was also highly prevalent as a primary or contributing COD (41%) and exhibited significant associations with DA intoxication and protozoal infection. For adult and aged adult females in late pup care through post-weaning at the time of death, 83% had end lactation syndrome (ELS) as a primary or contributing COD. This comprehensive longitudinal dataset is unique in its depth and scope. The large sample size and extensive time period provided an opportunity to investigate mortality patterns in a changing environment and identify spatial and temporal disease “hot spots” and emerging threats. Our findings will help improve estimates of population-level impacts of specific threats and optimize conservation and environmental mitigation efforts for this threatened species.


1958 ◽  
Vol 15 (1) ◽  
pp. 5-17 ◽  
Author(s):  
Gordon C. Pike ◽  
Brian E. Maxwell

The abundance and distribution of the northern sea lion, Eumetopias jubata, in British Columbia are described chiefly on the basis of a survey conducted during the summer of 1956. Results of surveys and censuses made in the years 1913, 1916, 1938 and 1955 are included for comparison. Most major rookeries and hauling-out sites were visited in 1956. Some which were missed were surveyed by aircraft in 1957.The numbers of sea lions in British Columbia are estimated to be 11,000–12,000 in 1956–57. They have apparently changed little since 1913 and 1916 when the population is estimated less reliably to have been 12,000–13,000. Some changes have occurred in their distribution, mainly as a result of organized destruction of concentrations centred near to fishing areas. Numbers in the Sea Otter Group have been reduced to about one-quarter of their former abundance. Numbers on the Cape St. James rookery, where the population has seldom been molested, have doubled.Present rookeries include: Triangle, Sartine, and Beresford Islands, in the Scott Island group; Kerouard Islands off Cape St. James; and North Danger Rocks. The Virgin and Pearl Rocks in the Sea Otter Group are no longer rookeries. Sartine Island and North Danger Rocks are recorded for the first time as rookeries. The Scott Islands and Kerouard Islands rookeries accommodate approximately 70% of the entire population, and 90% of the pups during the summer breeding season.Destruction of approximately 1,000 sea lions annually, when many of these are pups, is shown to be ineffective in substantially reducing the total population. Where efforts are concentrated in one area such as the Sea Otter Group, however, a local population can be greatly reduced and pupping curtailed or stopped.Pups are born from late May until late June. Soon after giving birth, the cows are serviced by the harem bulls. The harem structure, which averages about 10 cows per harem bull on the rookeries, begins to disintegrate near the end of July when pups take to the water and dominant bulls are replaced by reserve bulls. Some cows, probably not more than 25% at any one time, may forgo the normal annual pregnancy and continue to nurse a pup for more than a year.It is calculated that more than 70% of the sexually mature females in this population are pregnant in any one year. Natural mortality among the pups appears to be slight, but severe storms in some years may cause heavy pup mortality and constitute an important check on population growth.


1995 ◽  
Vol 73 (6) ◽  
pp. 1161-1169 ◽  
Author(s):  
Daniel H. Monson ◽  
Anthony R. DeGange

Radiotelemetry methods were used to examine the demographic characteristics of sea otters inhabiting the leading edge of an expanding population on Kodiak Island, Alaska. Fifteen male and 30 female sea otters were instrumented and followed from 1986 to 1990. Twenty-one percent of females were sexually mature (had pupped) at age 2, 57% by age 3, 88% by age 4, and 100% by age 5. Fifteen females produced 26 pups, an overall reproduction rate of 94% for mature females. The reproduction rate was 17, 45, 66, and 100% for 2-, 3-, 4-, and 5-year-olds, respectively. Eighty-five percent of observed pups survived to weaning (120 days), and the percentage of pups weaned ranged from 34% for pups of 2-year-olds to 100% for pups of 5-year-olds. At least three of four known pup losses occurred within a month of parturition. The mean pup dependency period for weaned pups was 153 days and the mean gestation period was 218 days. No synchrony in pupping activity was observed. Mean annual survival of adults was high. Estimates of survival ranged from 89 to 96% for females and 86 to 91% for males. Human harvest was the primary source of known mortality of adults. Our estimates of reproductive rates and survival of adults are at the high end of those reported for sea otters, but preweaning survival stands out as being particularly high. Abundant food resources and the availability of protected water presumably contributed to the high reproductive success observed in this recently established sea otter population.


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