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J.E. Hines

Publications and source records attributed to J.E. Hines.

At least 73 records · Page 4Linked to original sources

Disentangling sampling and ecological explanations underlying species-area relationships

We used a probabilistic approach to address the influence of sampling artifacts on the form of species-area relationships (SARs). We developed a model in which the increase in observed species richness is a function of sampling effort exclusively. We assumed that effort depends on area sampled, and we generated species-area curves under that model. These curves can be realistic looking. We then generated SARs from avian data, comparing SARs based on counts with those based on richness estimates. We used an approach to estimation of species richness that accounts for species detection probability and, hence, for variation in sampling effort. The slopes of SARs based on counts are steeper than those of curves based on estimates of richness, indicating that the former partly reflect failure to account for species detection probability. SARs based on estimates reflect ecological processes exclusively, not sampling processes. This approach permits investigation of ecologically relevant hypotheses. The slope of SARs is not influenced by the slope of the relationship between habitat diversity and area. In situations in which not all of the species are detected during sampling sessions, approaches to estimation of species richness integrating species detection probability should be used to investigate the rate of increase in species richness with area.

Maryland

Influence of behavioural tactics on recruitment and reproductive trajectory in the kittiwake

Many studies have provided evidence that, in birds, inexperienced breeders have a lower probability of breeding successfully. This is often explained by lack of skills and knowledge, and sometimes late laying dates in the first breeding attempt. There is growing evidence that in many species with deferred reproduction, some prebreeders attend breeding places, acquire territories and form pairs. Several behavioural tactics assumed to be associated with territory acquisition have been described in different species. These tactics may influence the probability of recruiting in the breeding segment of the population, age of first breeding, and reproductive success in the first breeding attempt. Here we addressed the influence of behaviour ('squatting') during the prebreeding period on demographic parameters (survival and recruitment probability) in a long-lived colonial seabird species: the kittiwake. We also investigated the influence of behaviour on reproductive trajectory. Squatters have a higher survival and recruitment probability, and a higher probability of breeding successfully in the first breeding attempt in all age-classes where this category is represented. The influence of behaviour is mainly expressed in the first reproduction. However, there is a relationship between breeding success in the first occasion and subsequent occasions. The influence of breeding success in the first breeding attempt on the rest of the trajectory may indirectly reflect the influence of behaviour on breeding success in the first occasion. The shape of the reproductive trajectory is influenced by behaviour and age of first breeding. There is substantial individual variation from the mean reproductive trajectory, which is accounted for by heterogeneity in performance among individuals in the first attempt, but there is no evidence of individual heterogeneity in the rate of change over time in performance in subsequent breeding occasions

Book chapter

Investigations of potential bias in the estimation of lambda using Pradel's (1996) model for capture-recapture data

Pradel's (1996) temporal symmetry model permitting direct estimation and modelling of population growth rate, lambda sub i provides a potentially useful tool for the study of population dynamics using marked animals. Because of its recent publication date, the approach has not seen much use, and there have been virtually no investigations directed at robustness of the resulting estimators. Here we consider several potential sources of bias, all motivated by specific uses of this estimation approach. We consider sampling situations in which the study area expands with time and present an analytic expression for the bias in lambda hat sub i. We next consider trap response in capture probabilities and heterogeneous capture probabilities and compute large-sample and simulation-based approximations of resulting bias in lambda hat sub i. These approximations indicate that trap response is an especially important assumption violation that can produce substantial bias. Finally, we consider losses on capture and emphasize the importance of selecting the estimator for lambda sub i that is appropriate to the question being addressed. For studies based on only sighting and resighting data, Pradel's (1996) lambda hat prime sub i is the appropriate estimator.

Book chapter

Forest fragmentation and bird community dynamics: Inference at regional scales

With increasing fragmentation of natural areas and a dramatic reduction of forest cover in several parts of the world, quantifying the impact of such changes on species richness and community dynamics has been a subject of much concern. Here, we tested whether in more fragmented landscapes there was a lower number of area-sensitive species and higher local extinction and turnover rates, which could explain higher temporal variability in species richness. To investigate such potential landscape effects at a regional scale, we merged two independent, large-scale monitoring efforts: the North American Breeding Bird Survey (BBS) and the Land Use and Land Cover Classification data from the U.S. Geological Survey. We used methods that accounted for heterogeneity in the probability of detecting species to estimate species richness and temporal changes in the bird communities for BBS routes in three mid-Atlantic U.S. states. Forest breeding bird species were grouped prior to the analyses into area-sensitive and non-area-sensitive species according to previous studies. We tested predictions relating measures of forest structure at one point in time (1974) to species richness at that time and to parameters of forest bird community change over the following 22-yr-period (1975–1996). We used the mean size of forest patches to characterize landscape structure, as high correlations among landscape variables did not allow us to disentangle the relative roles of habitat fragmentation per se and habitat loss. As predicted, together with lower species richness for area-sensitive species on routes surrounded by landscapes with lower mean forest-patch size, we found higher mean year-to-year rates of local extinction. Moreover, the mean year-to-year rates of local turnover (proportion of locally new species) for area-sensitive species were also higher in landscapes with lower mean forest-patch size. These associations were not observed for the non-area-sensitive species group. These results suggest that landscape structure may influence forest bird communities at regional scales through its effects on the total number of species but also on the temporal rates of change in community composition. Evidence for higher rates of local extinction and turnover in more fragmented landscapes suggests that bird communities function as metapopulations at a regional scale, and points out the importance of colonizations and recolonizations from surrounding landscapes to local community dynamics. Further, our results illustrate that the methods used to estimate the community parameters can be a powerful statistical tool in addressing questions relative to the dynamics of communities.

Ecology

Estimation of species richness and parameters reflecting community dynamics using data from ecological monitoring programs

Although many ecological monitoring programs are now in place, the use of resulting data to draw inferences about changes in biodiversity is problematic. The difficulty arises because of the inability to count all animals present in any sampled area. This inability results not only in underestimation of species richness but also in potentially misleading comparisons of species richness over time and space. We recommend the use of probabilistic estimators for estimating species richness and related parameters (e.g., rate of change in species richness, local extinction probability, local turnover, local colonization) when animal detection probabilities are <1. We illustrate these methods using data from the North American Breeding Bird Survey obtained along survey routes in Maryland. We also introduce software to implement these estimation methods.

Book chapter

Regional patterns in proportion of bird species detected in the North American Breeding Bird Survey

Counts from the North American Breeding Bird Survey (BBS) underestimate species richness. We use capture-recapture methods to estimate species richness from BBS count data collected in 1996 and show that detection probabilities demonstrate clear regional patterns. Capture-recapture methods should be used to estimate species richness from count data, and failure to use estimation procedures for species richness could result in biased estimates of spatial change in species richness.

Book chapter

Modeling avian detection probabilities as a function of habitat using double-observer point count data

Point counts are a controversial sampling method for bird populations because the counts are not censuses, and the proportion of birds missed during counting generally is not estimated. We applied a double-observer approach to estimate detection rates of birds from point counts in Maryland, USA, and test whether detection rates differed between point counts conducted in field habitats as opposed to wooded habitats. We conducted 2 analyses. The first analysis was based on 4 clusters of counts (routes) surveyed by a single pair of observers. A series of models was developed with differing assumptions about sources of variation in detection probabilities and fit using program SURVIV. The most appropriate model was selected using Akaike's Information Criterion. The second analysis was based on 13 routes (7 woods and 6 field routes) surveyed by various observers in which average detection rates were estimated by route and compared using a t-test. In both analyses, little evidence existed for variation in detection probabilities in relation to habitat. Double-observer methods provide a reasonable means of estimating detection probabilities and testing critical assumptions needed for analysis of point counts.

Book chapter

A double-observer approach for estimating detection probability and abundance from point counts

Although point counts are frequently used in ornithological studies, basic assumptions about detection probabilities often are untested. We apply a double-observer approach developed to estimate detection probabilities for aerial surveys (Cook and Jacobson 1979) to avian point counts. At each point count, a designated 'primary' observer indicates to another ('secondary') observer all birds detected. The secondary observer records all detections of the primary observer as well as any birds not detected by the primary observer. Observers alternate primary and secondary roles during the course of the survey. The approach permits estimation of observer-specific detection probabilities and bird abundance. We developed a set of models that incorporate different assumptions about sources of variation (e.g. observer, bird species) in detection probability. Seventeen field trials were conducted, and models were fit to the resulting data using program SURVIV. Single-observer point counts generally miss varying proportions of the birds actually present, and observer and bird species were found to be relevant sources of variation in detection probabilities. Overall detection probabilities (probability of being detected by at least one of the two observers) estimated using the double-observer approach were very high (>0.95), yielding precise estimates of avian abundance. We consider problems with the approach and recommend possible solutions, including restriction of the approach to fixed-radius counts to reduce the effect of variation in the effective radius of detection among various observers and to provide a basis for using spatial sampling to estimate bird abundance on large areas of interest. We believe that most questions meriting the effort required to carry out point counts also merit serious attempts to estimate detection probabilities associated with the counts. The double-observer approach is a method that can be used for this purpose.

The Auk

Estimation of contributions to population growth: A reverse-time capture-recapture approach

We consider methods for estimating the relative contributions of different demographic components, and their associated vital rates, to population growth. We identify components of the population at time i (including a component for animals not in the population at i ). For each such component we ask the following question: “What is the probability that an individual randomly selected from the population at time i + 1 was a member of this component at i ?” The estimation methods for these probabilities (γ i ) are based on capture–recapture studies of marked animal populations and use reverse-time modeling. We consider several different sampling situations and present example analyses for meadow voles, Microtus pennsylvanicus. The relationship between these γ i parameters and elasticities (and other parameters based on projection matrix asymptotics) is noted and discussed. We conclude by suggesting that model-based asymptotics be viewed as demographic theory and that direct estimation approaches be used to test this theory with data from sampled populations with marked animals.

Ecology

Relative species richness and community completeness: avian communities and urbanization in the mid-Atlantic states

The idea that local factors govern local richness has been dominant for years, but recent theoretical and empirical studies have stressed the influence of regional factors on local richness. Fewer species at a site could reflect not only the influence of local factors, but also a smaller regional pool. The possible dependency of local richness on the regional pool should be taken into account when addressing the influence of local factors on local richness. It is possible to account for this potential dependency by comparing relative species richness among sites, rather than species richness per se. We consider estimation of a metric permitting assessment of relative species richness in a typical situation in which not all species are detected during sampling sessions. In this situation, estimates of absolute or relative species richness need to account for variation in species detection probability if they are to be unbiased. We present a method to estimate relative species richness based on capture-recapture models. This approach involves definition of a species list from regional data, and estimation of the number of species in that list that are present at a site-year of interest. We use this approach to address the influence of urbanization on relative richness of avian communities in the Mid-Atlantic region of the United States. There is a negative relationship between relative richness and landscape variables describing the level of urban development. We believe that this metric should prove very useful for conservation and management purposes because it is based on an estimator of species richness that both accounts for potential variation in species detection probability and allows flexibility in the specification of a 'reference community.' This metric can be used to assess ecological integrity, the richness of the community of interest relative to that of the 'original' community, or to assess change since some previous time in a community.

Delaware, Maryland, New Jersey, New York, Pennsylv

Simultaneous use of mark-recapture and radiotelemetry to estimate survival, movement, and capture rates

Biologists often estimate separate survival and movement rates from radio-telemetry and mark-recapture data from the same study population. We describe a method for combining these data types in a single model to obtain joint, potentially less biased estimates of survival and movement that use all available data. We furnish an example using wood thrushes ( Hylocichla mustelina ) captured at the Piedmont National Wildlife Refuge in central Georgia in 1996. The model structure allows estimation of survival and capture probabilities, as well as estimation of movements away from and into the study area. In addition, the model structure provides many possibilities for hypothesis testing. Using the combined model structure, we estimated that wood thrush weekly survival was 0.989 ± 0.007 ( ± SE). Survival rates of banded and radio-marked individuals were not different ( α [ S radioed , S banded ] =log[ S radioed / S banded ]=0.0239 ± 0.0435). Fidelity rates (weekly probability of remaining in a stratum) did not differ between geographic strata ( Ψ = 0.911 ± 0.020; α [ Ψ 11 , Ψ 22 ]=0.0161 ± 0.047), and recapture rates ( p = 0.097 ± 0.016) banded and radio-marked individuals were not different ( α [ P radioed , P banded ]=0.145 ± 0.655). Combining these data types in a common model resulted in more precise estimates of movement and recapture rates than separate estimation, but ability to detect stratum or mark-specific differences in parameters was week. We conducted simulation trials to investigate the effects of varying study designs on parameter accuracy and statistical power to detect important differences. Parameter accuracy was high (relative bias [RBIAS] <2 %) and confidence interval coverage close to nominal, except for survival estimates of banded birds for the 'off study area' stratum, which were negatively biased (RBIAS -7 to -15%) when sample sizes were small (5-10 banded or radioed animals 'released' per time interval). To provide adequate data for useful inference from this model, study designs should seek a minimum of 25 animals of each marking type observed (marked or observed via telemetry) in each time period and geographic stratum.

Journal of Wildlife Management

Monitoring survival rates of landbirds at varying spatial scales: An application of the MAPS Program

Survivorship is a primary demographic parameter affecting population dynamics, and thus trends in species abundance. The Monitoring Avian Productivity and Survivorship (MAPS) program is a cooperative effort designed to monitor landbird demographic parameters. A principle goal of MAPS is to estimate annual survivorship and identify spatial patterns and temporal trends in these rates. We evaluated hypotheses of spatial patterns in survival rates among a collection of neighboring sampling sites, such as within national forests, among biogeographic provinces, and between breeding populations that winter in either Central or South America, and compared these geographic-specific models to a model of a common survival rate among all sampling sites. We used data collected during 1992-1995 from Swainson's Thrush (Cathorus ustulatus) populations in the western region of the United States. We evaluated the ability to detect spatial and temporal patterns of survivorship with simulated data. We found weak evidence of spatial differences in survival rates at the local scale of 'location,' which typically contained 3 mist-netting stations. There was little evidence of differences in survival rates among biogeographic provinces or between populations that winter in either Central or South America. When data were pooled for a regional estimate of survivorship, the percent relative bias due to pooling 'locations' was <1%. With the pooled data, we estimated a 44% annual regional survival rate; this low estimated survival rate was likely due to the presence of transients in the population (Rosenberg and others 1999). Using simulated data, we found that power to detect spatial differences increased considerably with number of years and spatial scale, the latter reflecting larger sample size. Detection of trends at smaller spatial scales required > 12 years of monitoring. Detection of spatial patterns and temporal trends in survival rates from local to regional scales will provide important information for management and future research directed toward conservation of landbirds.

Book chapter

A removal model for estimating detection probabilities from point-count surveys

We adapted a removal model to estimate detection probability during point count surveys. The model assumes one factor influencing detection during point counts is the singing frequency of birds. This may be true for surveys recording forest songbirds when most detections are by sound. The model requires counts to be divided into several time intervals. We used time intervals of 2, 5, and 10 min to develop a maximum-likelihood estimator for the detectability of birds during such surveys. We applied this technique to data from bird surveys conducted in Great Smoky Mountains National Park. We used model selection criteria to identify whether detection probabilities varied among species, throughout the morning, throughout the season, and among different observers. The overall detection probability for all birds was 75%. We found differences in detection probability among species. Species that sing frequently such as Winter Wren and Acadian Flycatcher had high detection probabilities (about 90%) and species that call infrequently such as Pileated Woodpecker had low detection probability (36%). We also found detection probabilities varied with the time of day for some species (e.g. thrushes) and between observers for other species. This method of estimating detectability during point count surveys offers a promising new approach to using count data to address questions of the bird abundance, density, and population trends.

Book chapter

Estimates of population change in selected species of tropical birds using mark-recapture data

The population biology of tropical birds is known for a only small sample of species; especially in the Neotropics. Robust estimates of parameters such as survival rate and finite rate of population change (A) are crucial for conservation purposes and useful for studies of avian life histories. We used methods developed by Pradel (1996, Biometrics 52:703-709) to estimate A for 10 species of tropical forest lowland birds using data from a long-term (> 20 yr) banding study in Panama. These species constitute a ecologically and phylogenetically diverse sample. We present these estimates and explore if they are consistent with what we know from selected studies of banded birds and from 5 yr of estimating nesting success (i.e., an important component of A). A major goal of these analyses is to assess if the mark-recapture methods generate reliable and reasonably precise estimates of population change than traditional methods that require more sampling effort.

Book chapter

Annual survival of Snail Kites in Florida: Radio telemetry versus capture-resighting data

We estimated annual survival of Snail Kites ( Rostrhamus sociabilis ) in Florida using the Kaplan-Meier estimator with data from 271 radio-tagged birds over a three-year period and capture-recapture (resighting) models with data from 1,319 banded birds over a six-year period. We tested the hypothesis that survival differed among three age classes using both data sources. We tested additional hypotheses about spatial and temporal variation using a combination of data from radio telemetry and single- and multistrata capture-recapture models. Results from these data sets were similar in their indications of the sources of variation in survival, but they differed in some parameter estimates. Both data sources indicated that survival was higher for adults than for juveniles, but they did not support delineation of a subadult age class. Our data also indicated that survival differed among years and regions for juveniles but not for adults. Estimates of juvenile survival using radio telemetry data were higher than estimates using capture-recapture models for two of three years (1992 and 1993). Ancillary evidence based on censored birds indicated that some mortality of radio-tagged juveniles went undetected during those years, resulting in biased estimates. Thus, we have greater confidence in our estimates of juvenile survival using capture-recapture models. Precision of estimates reflected the number of parameters estimated and was surprisingly similar between radio telemetry and single-stratum capture-recapture models, given the substantial differences in sample sizes. Not having to estimate resighting probability likely offsets, to some degree, the smaller sample sizes from our radio telemetry data. Precision of capture-recapture models was lower using multistrata models where region-specific parameters were estimated than using single-stratum models, where spatial variation in parameters was not taken into account.

The Auk

Estimating rates of local species extinction, colonization and turnover in animal communities

Species richness has been identified as a useful state variable for conservation and management purposes. Changes in richness over time provide a basis for predicting and evaluating community responses to management, to natural disturbance, and to changes in factors such as community composition (e.g., the removal of a keystone species). Probabilistic capture-recapture models have been used recently to estimate species richness from species count and presence-absence data. These models do not require the common assumption that all species are detected in sampling efforts. We extend this approach to the development of estimators useful for studying the vital rates responsible for changes in animal communities over time; rates of local species extinction, turnover, and colonization. Our approach to estimation is based on capture-recapture models for closed animal populations that permit heterogeneity in detection probabilities among the different species in the sampled community. We have developed a computer program, COMDYN, to compute many of these estimators and associated bootstrap variances. Analyses using data from the North American Breeding Bird Survey (BBS) suggested that the estimators performed reasonably well. We recommend estimators based on probabilistic modeling for future work on community responses to management efforts as well as on basic questions about community dynamics.

Ecological Applications

Size-sex variation in survival rates and abundance of pig frogs, Rana grylio, in northern Florida wetlands

During 1991-1993, we conducted capture-recapture studies on pig frogs, Rana grylio, in seven study locations in northcentral Florida. Resulting data were used to test hypotheses about variation in survival probability over different size-sex classes of pig frogs. We developed multistate capture-recapture models for the resulting data and used them to estimate survival rates and frog abundance. Tests provided strong evidence of survival differences among size-sex classes, with adult females showing the highest survival probabilities. Adult males and juvenile frogs had lower survival rates that were similar to each other. Adult females were more abundant than adult males in most locations at most sampling occasions. We recommended probabilistic capture-recapture models in general, and multistate models in particular, for robust estimation of demographic parameters in amphibian populations.

Journal of Herpetology

Stochastic seasonality and nonlinear density-dependent factors regulate population size in an African rodent

Ecology has long been troubled by the controversy over how populations are regulated. Some ecologists focus on the role of environmental effects, whereas others argue that density-dependent feedback mechanisms are central. The relative importance of both processes is still hotly debated, but clear examples of both processes acting in the same population are rare. Keyfactor analysis (regression of population changes on possible causal factors) and time-series analysis are often used to investigate the presence of density dependence, but such approaches may be biased and provide no information on actual demographic rates. Here we report on both density-dependent and density-independent effects in a murid rodent pest species, the multimammate rat Mastomys natalensis (Smith, 1834), using statistical capture-recapture models. Both effects occur simultaneously, but we also demonstrate that they do not affect all demographic rates in the same way. We have incorporated the obtained estimates of demographic rates in a population dynamics model and show that the observed dynamics are affected by stabilizing nonlinear density-dependent components coupled with strong deterministic and stochastic seasonal components.

Nature