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Gary C. White

Publications and source records attributed to Gary C. White.

42 records · Page 3Linked to original sources

Problems in estimating age-specific survival rates from recovery data of birds ringed as young

(1) The life table model is frequently employed in the analysis of ringer samples of young in bird populations. The basic model is biologically unrealistic and of little use in making inferences concerning age-specific survival probabilities. (2) This model rests on a number of restrictive assumptions, the failure of which causes serious biases. Several important assumptions are not met with real data and the estimators of age-specific survival are not robust enough to these failures. (3) Five major problems in the use of the life table method are reviewed. Examples are provided to illustrate several of the problems involved in using this method in making inferences about survival rates and its age-specific nature. (4) We conclude that this is an invalid procedure and it should not be used. Furthermore, ringing studies involving only young birds are pointless as regards survival estimation because no valid method exists for estimating age-specific or time-specific survival rates from such data. (5) In our view, inferences about age-specific survival rates are possible only if both young and adult (or young, subadult and adult) age classes are ringed each year for k years ( k ≥ 2).

Journal of Animal Ecology

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

Density estimation of small-mammal populations using a trapping web and distance sampling methods

Distance sampling methodology is adapted to enable animal density (number per unit of area) to be estimated from capture-recapture and removal data. A trapping web design provides the link between capture data and distance sampling theory. The estimator of density is D = M t+1 f(0) , where M t+1 is the number of individuals captured and f(0) is computed from the M t+1 distances from the web center to the traps in which those individuals were first captured. It is possible to check qualitatively the critical assumption on which the web design and the estimator are based. This is a conceptual paper outlining a new methodology, not a definitive investigation of the best specific way to implement this method. Several alternative sampling and analysis methods are possible within the general framework of distance sampling theory; a few alternatives are discussed and an example is given.

Ecology

Capture-recapture and removal methods for sampling closed populations

The problem of estimating animal abundance is common in wildlife management and environmental impact asessment. Capture-recapture and removal methods are often used to estimate population size. Statistical Inference From Capture Data On Closed Animal Populations, a monograph by Otis et al. (1978), provides a comprehensive synthesis of much of the wildlife and statistical literature on the methods, as well as some extensions of the general theory. In our primer, we focus on capture-recapture and removal methods for trapping studies in which a population is assumed to be closed and do not treat open-population models, such as the Jolly-Seber model, or catch-effort methods in any detail. The primer, written for students interested in population estimation, is intended for use with the more theoretical monograph.

Report

Statistical inference from capture data on closed animal populations

The estimation of animal abundance is an important problem in both the theoretical and applied biological sciences. Serious work to develop estimation methods began during the 1950s, with a few attempts before that time. The literature on estimation methods has increased tremendously during the past 25 years (Cormack 1968, Seber 1973). However, in large part, the problem remains unsolved. Past efforts toward comprehensive and systematic estimation of density (D) or population size (N) have been inadequate, in general. While more than 200 papers have been published on the subject, one is generally left without a unified approach to the estimation of abundance of an animal population This situation is unfortunate because a number of pressing research problems require such information. In addition, a wide array of environmental assessment studies and biological inventory programs require the estimation of animal abundance. These needs have been further emphasized by the requirement for the preparation of Environmental Impact Statements imposed by the National Environmental Protection Act in 1970. This publication treats inference procedures for certain types of capture data on closed animal populations. This includes multiple capture-recapture studies (variously called capture-mark-recapture, mark-recapture, or tag-recapture studies) involving livetrapping techniques and removal studies involving kill traps or at least temporary removal of captured individuals during the study. Animals do not necessarily need to be physically trapped; visual sightings of marked animals and electrofishing studies also produce data suitable for the methods described in this monograph. To provide a frame of reference for what follows, we give an exampled of a capture-recapture experiment to estimate population size of small animals using live traps. The general field experiment is similar for all capture-recapture studies (a removal study is, of course, slightly different). A typical field experiment is the following: a number of traps are positioned in the area to be studied, say 144 traps in a 12 X 12 grid, 7 m apart. At the beginning of the study (j=1) a sample size of n 1 is taken from the population, the animals are tagged and marked for future identification, and then returned to the population, usually at the same point where they were trapped. After allowing time of the marked and unmarked animals to mix, a second sample (j=2, often the following day) or n 2 animals is then taken.the second sample normally contains both marked and unmarked animals. The unmarked animals are marked and all captured animals are released back into the population. This procedure continues for t periods where t ≥ 2. The animals should be marked in such a way that the capture-recapture history of each animal caught during the study is known. In practice, toes are often clipped to uniquely identify individual animals (Taber and Cowan 1969) or serially numbered tags are sometimes used on larger animals. Such capture studies are classified by 2 schemes that are directly related to what class of models are appropriate and what parameters can be estimated. The first classification addresses the subject of closure. Closure usually means the size of the population is constant over the priod of investigation, i.e., no recruitment (birth or immigration) or losses (death or emigration). This is a strong assumption and, of course, never completely true in a natural biological population. For greater generality, we define closure to mean there are no unknown changes to the initial population. In practice, this means known losses (trap death), or deliberate removals) do not violate our definition of closure. If the study is properly designed, closure can be met at least approximately. Open or nonclosed populations explicitly allow for one or more types of recruitment or losses to operate during the course of the experiment (Jolly 1965, Seber 1965, Robson 1969, Pollock 1975). Only closed populations will be considered in this monograph. The second classification depends on the type of data collected with 2 possibilities occurring (Pollock 1974, unpublished doctoral dissertation, Cornell University, Ithaca, New York): (1) only information on the recovery of marked animals is available for each sampling occasion, j, j=1, 2, ... t. (2) information on both marked and unmarked animals is available for each sampling occasion, j, j=1, 2, ... t. In case (1), population size (N) is not identifiable, however, other parameters can be estimated (Brownie et al. 1978). In case (2), N can be estimated using a wide variety of approaches depending upon what we wish to assume. Only case (2) will be dealt with here.

Wildlife Monographs