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Growth and potential yield of perch (Perca spp.) in selected areas of Lake Baikal and the Laurentian Great Lakes
We compared growth, mortality, and potential yield of Eurasian perch (Perca fluviatilis) from Chivirkui Bay in Lake Baikal with that of yellow perch (P. flavescens) from three areas of the Laurentian Great Lakes --Chequamegon Bay in Lake Superior, northeastern Lake Ontario, and southwestern Lake Erie. Graded mesh gill nets were fished in August to sample perch in lakes Baikal (1993), Ontario (1985-93), and Erie (1994). Bottom trawls were fished in July-August to sample perch in Lake Superior (1973-93). Adult yellow perch from the Laurentian Great Lakes were heavier at most lengths than adult Eurasian perch from Lake Baikal. The increase in body weight per unit increase in length was greatest in Lake Erie. Total annual mortality of perch was low in Lake Baikal (0.31), intermediate in lakes Superior (0.41) and Ontario (0.54), and high in Lake Erie (0.66). Annual fishing mortality (u) for perch in Lake Baikal was 60%-70% lower than that for perch in the Great Lakes. At ages 1-3, perch in Lake Erie were longer than those in lakes Baikal, Superior, and Ontario but at ages 4-9 perch in Lake Baikal were longer than those in the other lakes. Although Eurasian perch in Lake Baikal were longer at age 4 and older, growth in length, as measured by the Brody growth coefficient, K, was lower there than in the other lakes and was similar to that in Lake Superior; yellow perch in Lake Erie grew the fastest. Yield-per-recruit was lowest in Lake Erie and highest in Lake Superior. Potential yield was influenced by growth rates and fishing mortality.
Ecology of Siberian Taimen Hucho taimen in the Lake Baikal Basin
Taimen Hucho taimen historically inhabited most tributaries and littoral areas of Lake Baikal, in south central Siberia, where they supported subsistence and commercial fisheries. Logging, pollution, and overfishing have caused dramatic population declines or local extinction of most stocks. Most of what is known about this species has been published in eastern journals and therefore is not readily available to western scientists. New data collected during the 1980s and 1990s have been combined with other reports to provide an overview of the biology and life history of this species. Taimen are long-lived fish and can reach ages of 29 years and sizes up to 60 kg. Populations can either be strictly riverine or anadromous. Adults from both life histories ascend rivers in spring to spawn and feed, and less extensive migrations occur in fall to prey on spawning omul ( Coregonus autumnalis migratorius ). Principal food items for age 1 and 2 taimen are macroinvertebrates, but young taimen quickly become piscivorous at age 2 when they consume mainly black Baikal grayling ( Thymallus arcticus baicalensis ), and sculpins ( Taracottus kneri, Cottus kesslerij ). Males reach sexual maturity at ages 7 to 8 and later for females at ages 8 to 9. Average egg production per female was about 22,000 eggs. Parasite burdens are heavy but composed of few species and mediated by prey items consumed. This fish is a highly-specialized predator and plays an indispensable role in the structure of fish communities in mountains and foothills. Taimen conservation in the Baikal region is impossible without adoption and implementation of a dedicated rehabilitation program that includes the protection of remaining populations and habitat, and possibly introduction of hatchery-reared fish in selected areas where habitat remains, but parental stocks are low.
American badgers selectively excavate burrows in areas used by black-footed ferrets: implications for predator avoidance
We evaluated how American badgers ( Taxidea taxus ) might exert selective pressure on black-footed ferrets ( Mustela nigripes ) to develop antipredator defenses. In a colony of black-tailed prairie dogs ( Cynomys ludovicianus ) in South Dakota, badgers concentrated their activities where burrow openings and prairie dogs were abundant, a selective behavior that was exhibited by ferrets in the same colony. Badgers excavated burrows more often when in areas recently used by a ferret, suggesting that badgers hunt ferrets or steal prey from ferrets, or both. We also conducted an analysis of survival studies for ferrets and Siberian polecats ( M. eversmanii ) released onto prairie dog colonies. This polecat is the ferret's ecological equivalent but evolved without a digging predator. Badgers accounted for 30.0% of predation on polecats and 5.5% of predation on ferrets. In contrast, both polecats and ferrets have evolutionary experience with canids, providing a plausible explanation for the similar relative impact of coyotes ( Canis latrans ) on them (65.0% and 67.1% of predation, respectively). We hypothesize that ferrets and badgers coexist because ferrets are superior at exploitation competition and are efficient at avoiding badgers, and badgers are superior at interference competition.
Mortality of Siberian polecats and black-footed ferrets released onto prairie dog colonies
Black-footed ferrets ( Mustela nigripes ) likely were extirpated from the wild in 1985–1986, and their repatriation depends on captive breeding and reintroduction. Postrelease survival of animals can be affected by behavioral changes induced by captivity. We released neutered Siberian polecats ( M. eversmanii ), close relatives of ferrets, in 1989–1990 on black-tailed prairie dog ( Cynomys ludovicianus ) colonies in Colorado and Wyoming initially to test rearing and reintroduction techniques. Captive-born polecats were reared in cages or cages plus outdoor pens, released from elevated cages or into burrows, and supplementally fed or not fed. We also translocated wild-born polecats from China in 1990 and released captive-born, cage-reared black-footed ferrets in 1991, the 1st such reintroduction of black-footed ferrets. We documented mortality for 55 of 92 radiotagged animals in these studies, mostly due to predation (46 cases). Coyotes ( Canis latrans ) killed 31 ferrets and polecats. Supplementally fed polecats survived longer than nonprovisioned polecats. With a model based on deaths per distance moved, survival was highest for wild-born polecats, followed by pen-experienced, then cage-reared groups. Indexes of abundance (from spotlight surveys) for several predators were correlated with mortality rates of polecats and ferrets due to those predators. Released black-footed ferrets had lower survival rates than their ancestral population in Wyoming, and lower survival than wild-born and translocated polecats, emphasizing the influence of captivity. Captive-born polecats lost body mass more rapidly postrelease than did captive-born ferrets. Differences in hunting efficiency and prey selection provide further evidence that these polecats and ferrets are not ecological equivalents in the strict sense.
Monitoring boreal forest leaf area index across a Siberian burn chronosequence: A MODIS validation study
Landscapes containing differing amounts of ecological disturbance provide an excellent opportunity to validate and better understand the emerging Moderate Resolution Imaging Spectrometer (MODIS) vegetation products. Four sites, including 1‐year post‐fire coniferous, 13‐year post‐fire deciduous, 24‐year post‐fire deciduous, and >100 year old post‐fire coniferous forests, were selected to serve as a post‐fire chronosequence in the central Siberian region of Krasnoyarsk (57.3°N, 91.6°E) with which to study the MODIS leaf area index (LAI) and vegetation index (VI) products. The collection 4 MODIS LAI product correctly represented the summer site phenologies, but significantly underestimated the LAI value of the >100 year old coniferous forest during the November to April time period. Landsat 7‐derived enhanced vegetation index (EVI) performed better than normalized difference vegetation index (NDVI) to separate the deciduous and conifer forests, and both indices contained significant correlation with field‐derived LAI values at coniferous forest sites ( r 2 = 0.61 and r 2 = 0.69, respectively). The reduced simple ratio (RSR) markedly improved LAI prediction from satellite measurements ( r 2 = 0.89) relative to NDVI and EVI. LAI estimates derived from ETM+ images were scaled up to evaluate the 1 km resolution MODIS LAI product; from this analysis MODIS LAI overestimated values in the low LAI deciduous forests (where LAI<5) and underestimated values in the high LAI conifer forests (where LAI>6). Our results indicate that further research on the MODIS LAI product is warranted to better understand and improve remote LAI quantification in disturbed forest landscapes over the course of the year.