USGS Science⌕ Search

SEARCH · USGS Science

Results for “The R Journal”

Search indexed USGS publications on groundwater, aquifers, geologic maps, mineral resources and earthquakes. Explore source records by subject and place.

Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.

At least 415 records · Page 23Linked to original sources
USGS2010

Modeling distribution of dispersal distances in male white-tailed deer

Dispersal distances and their distribution pattern are important to understanding such phenomena as disease spread and gene flow, but oftentimes dispersal characteristics are modeled as a fixed trait for a given species. We found that dispersal distributions differ for spring and autumn dispersals of yearling male white-tailed deer (Odocoileus virginianus) but that combined data can be adequately modeled based on a log-normal distribution. We modeled distribution of dispersal distances from 3 distinct populations in Pennsylvania and Maryland, USA, based on the relationship between percent forest cover and mean dispersal distance and the relationship between mean and variance of dispersal distances. Our results suggest distributions of distances for dispersing yearling male white-tailed deer can be modeled by simply measuring a readily obtained landscape metric, percent forest cover, which could be used to create generalized spatially explicit disease or gene.

Journal of Wildlife Management↗
USGS2010

Habitat use by female mallards in the lower Mississippi alluvial valley

Mallard ( Anas platyrhynchos ) populations in the lower Mississippi Alluvial Valley (LMAV), USA, historically averaged 1.6 million and represented the largest concentrations of wintering mallards in North America. Effective management of this wintering population requires current information on use of habitats. Accordingly, we employed radiotelemetry techniques to assess proportional use of habitats by female mallards during winters 2004-2005 and 2005-2006. We divided winters into 4 time periods defined by hunting seasons (FIRST, SPLIT, SECOND, and POST) and recorded diurnal and nocturnal locations. We examined variations in proportional use of habitats and use of areas closed to hunting due to effects of age (immature or ad), winter (2004-2005 or 2005-2006), time period (SECOND or POST), individual female, and all potential interactions of these effects, using locations recorded during the latter 2 time periods. We found that diurnal and nocturnal proportional use of habitats varied inconsistently among time periods and winters. Mean proportional use of forested wetlands ranged from 0.475 to 0.816 and from 0.428 to 0.764 during diurnal and nocturnal sampling periods, respectively. Diurnal proportional use of areas closed to hunting varied inconsistently among time periods and winters. Mean proportional use of areas closed to hunting ranged from 0.183 to 0.423 during diurnal sampling periods. Nocturnal use of areas closed to hunting varied inconsistently among female ages and time periods and among female ages and winters. Mean proportional use of areas closed to hunting ranged from 0.211 to 0.445 during nocturnal sampling periods. Our research suggests that forested wetlands in the LMAV provide important wintering habitats for female mallards; continued restoration and establishment of these habitats should benefit female mallards.

Journal of Wildlife Management↗
USGS1969

Establishing hunting regulations and allowable harvest of mallards in the United States

As a major part of establishing hunting regulations each year in the United States, data for the mallard ( Anas platyrhynchos ) are examined extensively to estimate the effect of various harvest strategies on the breeding population the following spring. This requires estimates of the breeding-population level and of the production, harvest, and mortality rates. Predictions made at the time hunting regulations are established have been in general agreement with more reliable estimates made after the hunting season when data from banding, kill, and wing surveys are available.

Journal of Wildlife Management↗
USGS1979

The composite dynamic method as evidence for age-specific waterfowl mortality

For the past 25 years estimation of mortality rates for waterfowl has been based almost entirely on the composite dynamic life table. We examined the specific assumptions for this method and derived a valid goodness of fit test. We performed this test on 45 data sets representing a cross section of banded sampled for various waterfowl species, geographic areas, banding periods, and age/sex classes. We found that: (1) the composite dynamic method was rejected (P <0.001) in 37 of the 45 data sets (in fact, 29 were rejected at P <0.00001) and (2) recovery and harvest rates are year-specific (a critical violation of the necessary assumptions). We conclude that the restrictive assumptions required for the composite dynamic method to produce valid estimates of mortality rates are not met in waterfowl data. Also we demonstrate that even when the required assumptions are met, the method produces very biased estimates of age-specific mortality rates. We believe the composite dynamic method should not be used in the analysis of waterfowl banding data. Furthermore, the composite dynamic method does not provide valid evidence for age-specific mortality rates in waterfowl.

Journal of Wildlife Management↗
USGS1975

Gut morphology of mallards in relation to diet quality

Digestive organ lengths, weights, and volumes in each of three groups of mallards ( Anas platyrhynchos ) were determined at the end of a 21-day period, during which one group was starter (control diet), another group was fed whole corn (low fiber content), and the third fed alfalfa pellets (high fiber content) to demonstrate the adaptive efficiency of the waterfowl diets of varying quality. Food consumption by the alfalfa-fed ducks was significantly gr 0.01) than the other two groups. All digestive organs of the alfalfa-fed ducks were significan (P < 0.01) than those of the corn- and turkey starter-fed ducks at the end of the study. It is that mallards can adapt rapidly to fibrous, relatively indigestible foods. This ability may hav value when higher quality foods are unavailable or when food habits change rapidly duritions.

Journal of Wildlife Management↗
USGS1977

Organochlorine and mercury residues in canvasback duck eggs, 1972-73

Eggs of canvasback ducks (Aythya valisineria) from several major breeding areas were analyzed for organochlorine and mercury residues. Polychlorinated biphenyls (PCBs) were detected in 96 of 97 eggs, in concentrations up to 29 ppm (wet wt.). DDE occurred in 79 percent of the samples with a maximum residue of 12 ppm (wet wt.). DDT, DDD, dieldrin, hexachlorobenzene, cis-chlordane, heptachlor epoxide, and oxychlordane were detected less frequently. Mercury was detected in only 6 of 34 eggs analyzed. Most of the eggs contained concentrations of organochlorines and mercury below levels known to cause adverse effects on avian survival or reproduction.

Journal of Wildlife Management↗
USGS1974

Feeding Ecology of Breeding Blue-Winged Teals

A 5-year investigation of factors influencing the selection of foods consumed by blue-winged teals ( Anas discors ) during the breeding season in the glaciated prairie region of south-central North Dakota showed that birds first arriving on the breeding grounds consumed a diet consisting of 45 percent invertebrates. The proportion of animal foods in the diet increased to 95 percent at the onset of the nesting season. The quality and quantity of foods selected at any given time were influenced by the biological demands and morphological adaptations of the bird, the behavior and ecology of the invertebrates selected as foods, and the general nature of the aquatic ecosystems as determined by the hydrology and geology of the area and modified by land use and weather. Feeding activities changed significantly when food availability within the aquatic ecosystem changed. During the spring and early summer, temporary and seasonal wetlands, if not severely disturbed, were of paramount importance to breeding blue-winged teals since they provided abundant and readily available, high protein, animal foods. Later in the summer when seasonal wetlands began to dry up, insects began to emerge in the semipermanent ponds and lakes, and feeding intensity shifted to these more permanent waters. This trend, however, was often reversed temporarily during the early summer following heavy precipitation that refilled shallow water areas and again stimulated invertebrate development.

North Dakota↗
USGS1984

Estimating the effect of hunting on annual survival rates of adult mallards

Management programs for waterfowl populations include rationale for, and establishment of, hunting regulations. These programs rest partially on the results of scientific studies on the effect of harvest rates on annual survival rates. The evidence of this relationship has changed markedly since the mid-1970's, and it is not widely believed that a largely compensatory relationship exists between hunting mortality and other forms of mortality for the mallard ( Anas platyrhynchos ). This paper employs a general probabilistic model formulated to include a parameter (b) representing a continuum between complete compensation (b=0) and total additivity (b=1). Maximum likelihood estimates of this parameter were computer for 47 data sets of adult mallards banded throughout North American before hunting commenced. We found additional evidence of a highly compensatory mortality process for adult male mallards, while the evidence for adults female mallards remains inconclusive. Effective harvest, land acquisition, and land management programs depend upon additional information on the chronology and mechanisms underlying a compensatory mortality process.

Journal of Wildlife Management↗
USGS1984

Comparative ability of northern pintails, gadwalls, and northern shovelers to metabolize foods

Feeding trials were used to compare the ability of northern pintails ( Anas acuta ), gadwalls ( A. strepera ), and northern shovelers ( A. clypeata ) to metabolize energy from a turkey starter ration, alfalfa pellets, and common barnyardgrass ( Echinochloa crusgalli ) seeds. No differences (P > 0.05) were detected among the three species for any of the three foods (kg body weight/day basis), for dry matter intake (DMI), body weight gain (BWG), apparent metabolizable energy (AME), or metabolized energy (MEE) on any given diet consumed in quantities large enough to promote body weight gain. The AME content of alfalfa was 57% less than the value for turkey starter and 50% less than for barnyardgrass seeds. All three species metabolized more energy and gained weight faster when fed turkey starter. Energy modeling may be facilitated if additional research verifies that all species of dabbling ducks have equal ability to obtain energy from foods available to them in the wild. Behavioral and morphological factors may be more important in defining feeding niches than digestive physiology, at least for the three duck species tested, at the time of year of the experiments, and within the limits of the quality of foods used.

Journal of Wildlife Management↗
USGS1988

Survival of juvenile ring-necked ducks on wetlands of different pH

Brood and duckling survival of ring-necked ducks ( Aythya collaris ) was examined in relation to wetland water chemistry in eastcentral Maine during 1983-85. Daily survival rates (DSR) of broods and ducklings were determined for 381 ducklings from 64 broods by counts of each brood at 6-10-day intervals during broodrearing. Twelve of 64 females lost entire broods. Only 176 of 381 (46%) ducklings survived to fledge. Brood survival for the 45-day rearing period was 0.7731; duckling survival was 0.3707. Young ducklings ( ≤ 24 days) survived at a lower rate (0.9750/day) than older ( ≥ 25 days) ducklings (0.9818/day) ( P = 0.002). Survival rates of broods and ducklings did not differ among wetlands of high and low alkalinities. Brood survival did not differ among wetlands of different pH, but DSR of ducklings was lower (0.9763/day) on low-pH (<6.0) wetlands than on high-pH ( ≥ 6.1) wetlands (0.9816/day) ( P = 0.049). Class IIb-III (25-45 days old) ducklings from the lowest-pH wetlands(<5.5) had the lowest DSR (0.9752) while Class IIb-III ducklings from the highest-pH wetlands (>6.5) had the highest DSR (0.9856) ( P = 0.009).

Maine↗