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1.
The number of animals in a population is conventionally estimated by capture–recapture without modelling the spatial relationships between animals and detectors. Problems arise with non‐spatial estimators when individuals differ in their exposure to traps or the target population is poorly defined. Spatially explicit capture–recapture (SECR) methods devised recently to estimate population density largely avoid these problems. Some applications require estimates of population size rather than density, and population size in a defined area may be obtained as a derived parameter from SECR models. While this use of SECR has potential benefits over conventional capture–recapture, including reduced bias, it is unfamiliar to field biologists and no study has examined the precision and robustness of the estimates. We used simulation to compare the performance of SECR and conventional estimators of population size with respect to bias and confidence interval coverage for several spatial scenarios. Three possible estimators for the sampling variance of realised population size all performed well. The precision of SECR estimates was nearly the same as that of the null‐model conventional population estimator. SECR estimates of population size were nearly unbiased (relative bias 0–10%) in all scenarios, including surveys in randomly generated patchy landscapes. Confidence interval coverage was near the nominal level. We used SECR to estimate the population of a species of skink Oligosoma infrapunctatum from pitfall trapping. The estimated number in the area bounded by the outermost traps differed little between a homogeneous density model and models with a quadratic trend in density or a habitat effect on density, despite evidence that the latter models fitted better. Extrapolation of trend models to a larger plot may be misleading. To avoid extrapolation, a large region of interest should be sampled throughout, either with one continuous trapping grid or with clusters of traps dispersed widely according to a probability‐based and spatially representative sampling design.  相似文献   

2.
Borchers DL  Efford MG 《Biometrics》2008,64(2):377-385
Live-trapping capture-recapture studies of animal populations with fixed trap locations inevitably have a spatial component: animals close to traps are more likely to be caught than those far away. This is not addressed in conventional closed-population estimates of abundance and without the spatial component, rigorous estimates of density cannot be obtained. We propose new, flexible capture-recapture models that use the capture locations to estimate animal locations and spatially referenced capture probability. The models are likelihood-based and hence allow use of Akaike's information criterion or other likelihood-based methods of model selection. Density is an explicit parameter, and the evaluation of its dependence on spatial or temporal covariates is therefore straightforward. Additional (nonspatial) variation in capture probability may be modeled as in conventional capture-recapture. The method is tested by simulation, using a model in which capture probability depends only on location relative to traps. Point estimators are found to be unbiased and standard error estimators almost unbiased. The method is used to estimate the density of Red-eyed Vireos (Vireo olivaceus) from mist-netting data from the Patuxent Research Refuge, Maryland, U.S.A. Estimates agree well with those from an existing spatially explicit method based on inverse prediction. A variety of additional spatially explicit models are fitted; these include models with temporal stratification, behavioral response, and heterogeneous animal home ranges.  相似文献   

3.
We have evaluated techniques of estimating animal density through direct counts using line transects during 1988–92 in the tropical deciduous forests of Mudumalui Sanctuary in southern India for four species of large herbivorous mammals, namely, chital (Axis axis). sambar (Cervus unicolor). Asian elephant (Elephas maximus) and gaur (Bos gaurus) Density estimates derived from the Fourier Series and the Half-Normal models consistently had the lowest coefficient of variation. These two models also generated similar mean density estimates. For the Fourier Series estimator, appropriate cut-off widths for analyzing line transect data for the four species are suggested. Grouping data into various distance classes did not produce any appreciable differences in estimates of mean density or their variances, although model fit is generally better when data arc placed in fewer groups. The sampling effort needed to achieve a desired precision (coefficient of variation) in the density estimate is derived. A sampling effort of 800 km of transects returned a 10% coefficient of variation on estimate for ehital; for the other species a higher effort was needed to achieve this level of precision. There was no statistically significant relationship between detectability of a group and the size of the group for any species. Density estimates along roads were generally significantly different from those in the interior of the forest, indicating that road-side counts many not be appropriate for most species.  相似文献   

4.
ABSTRACT Estimation of abundance is important for assessing population responses to management actions. Accurate abundance estimates are particularly critical for monitoring temporal variation following reintroductions when the management goal is to attain population sizes capable of sustaining harvest. Numerous reintroductions have taken place in the Great Lakes region of North America, including efforts to restore extirpated fishers (Martes pennanti) and American martens (M. americana). We used a DNA-based noninvasive hair-snaring method based on one trap design and trapping -grid configuration, and evaluated capture—mark—recapture (CMR) analytical approaches to simultaneously estimate population size for co-distributed fishers and American martens in a 671-km2 area of the Ottawa National Forest in the western Upper Peninsula of Michigan, USA. We included harvest as a final recapture period to increase probability of recapture and to evaluate potential violations of geographic closure assumptions. We used microsatellite markers to identify target species, eliminate congener species, and provide individual identity for estimation of abundance. Population estimates for fishers and martens on the study area ranged from 35 to 60 and 8 to 28, respectively. Estimators incorporating harvest data resulted in up to a 40% increase in abundance estimates relative to estimators without harvest. We considered population estimates not including harvest data the most appropriate for the study due to timing of sampling and environmental factors, but inclusion of harvested individuals was shown to be useful as a means to detect violations of the assumption of geographic closure. We suggest improvements on future CMR sampling designs for larger landscape scales of relevance to management through incorporation of habitat or historical harvest data. Noninvasive genetic methods that simultaneously estimate the numerical abundance of co-distributed species can greatly decrease assessment costs relative to traditional methods, and increase resulting demographic and ecological information.  相似文献   

5.
Finding practical ways to robustly estimate abundance or density trends in threatened species is a key facet for effective conservation management. Further identifying less expensive monitoring methods that provide adequate data for robust population density estimates can facilitate increased investment into other conservation initiatives needed for species recovery. Here we evaluated and compared inference-and cost-effectiveness criteria for three field monitoring-density estimation protocols to improve conservation activities for the threatened Komodo dragon (Varanus komodoensis). We undertook line-transect counts, cage trapping and camera monitoring surveys for Komodo dragons at 11 sites within protected areas in Eastern Indonesia to collect data to estimate density using distance sampling methods or the Royle–Nichols abundance induced heterogeneity model. Distance sampling estimates were considered poor due to large confidence intervals, a high coefficient of variation and that false absences were obtained in 45 % of sites where other monitoring methods detected lizards present. The Royle–Nichols model using presence/absence data obtained from cage trapping and camera monitoring produced highly correlated density estimates, obtained similar measures of precision and recorded no false absences in data collation. However because costs associated with camera monitoring were considerably less than cage trapping methods, albeit marginally more expensive than distance sampling, better inference from this method is advocated for ongoing population monitoring of Komodo dragons. Further the cost-savings achieved by adopting this field monitoring method could facilitate increased expenditure on alternative management strategies that could help address current declines in two Komodo dragon populations.  相似文献   

6.
Density estimation in live-trapping studies   总被引:3,自引:0,他引:3  
Murray Efford 《Oikos》2004,106(3):598-610
Unbiased estimation of population density is a major and unsolved problem in animal trapping studies. This paper describes a new and general method for estimating density from closed-population capture–recapture data. Many estimators exist for the size (N) and mean capture probability ( p ) of a closed population. These statistics suffer from an unknown bias due to edge effect that varies with trap layout and home range size. The mean distance between successive captures of an individual (     ) provides information on the scale of individual movements, but is itself a function of trap spacing and grid size. Our aim is to define and estimate parameters that do not depend on the trap layout. In the new method, simulation and inverse prediction are used to estimate jointly the population density (D) and two parameters of individual capture probability, magnitude (g0) and spatial scale (σ), from the information in     , p and     . The method uses any configuration of traps (e.g. grid, web or line) and any choice of closed-population estimator. It is assumed that home ranges have a stationary distribution in two dimensions, and that capture events may be simulated as the outcome of competing Poisson processes in time. The method is applied to simulated and field data. The estimator appears unusually robust and free from bias.  相似文献   

7.
In a Costa Rican tropical lower montane rain forest the wood densities of canopy tree species are related to the windiness of their preferred habitats, and to their abilities to tolerate shade. Shade-intolerant species tend to have less dense wood than shade-tolerant species from the same habitat. Species characteristic of windy sites tend to have denser wood than species characteristic of sheltered habitats. Stand mean wood density, the average of species’ wood densities weighted by their proportional contributions to stand basal area, increases with exposure to the wind. These trends in wood density should at least partially counteract the damaging effects of wind on exposed sites. Since investment in wood must come at the expense of growth elsewhere, such trends in wood density may help explain the small stature of elfin forest and montane thicket formations in tropical mountains.  相似文献   

8.
Assessing species richness of small mammal communities is an important research objective for many live-trapping studies designed to assess or monitor biological diversity. We tested the effectiveness and efficiency of various trap densities for determining estimates and counts of small mammal species richness. Trapping was conducted in grassland habitats in northeastern Kansas during spring and fall of 2002 and 2003. Estimates and counts of species richness were higher at increased trap densities. This effect appeared to be primarily due to the higher number of individuals sampled at higher trap densities. At least 3 nights duration was needed to produce a stable estimate of species richness for the range of trap densities tested (9–144 trap stations/ha). Higher trap densities generally reached stable richness estimates in fewer nights than low density trapping arrangements. Given that counts and estimates of species richness were influenced by trap density and sampling duration, it is critical that these parameters are selected to most effectively meet research objectives.  相似文献   

9.
Although dramatic amphibian declines have been documented worldwide, only few of such events have been quantitatively documented for the tropical forests of South America. This is due partly to the fact that tropical amphibians are patchily distributed and difficult to detect. We tested three methods often used to monitor population trends in amphibian species in a remote lowland tropical forest of French Guiana. These methods are capture-mark-recapture (CMR), estimation of the number of calling males with repeated counts data and distance sampling, and rates of occupancy inferred by presence/absence data. We monitored eight diurnal, terrestrial amphibian species including five Dendrobatidae and three Bufonidae. We found that CMR, the most precise way of estimating population size, can be used only with two species in high density patches where the recapture rate is high enough. Only for one of the species (Dendrobates tinctorius), a low coefficient of variation (CV = 0.19) can be achieved with 15 to 20 capture events. For dendrobatid species with day-calling males, audio surveys yield a better probability of detection with only 8 audio surveys needed; quantitative estimates can be achieved by computing the number of calling males inferred from audio counts or distance sampling analysis. We therefore suggest that an efficient monitoring protocol for Neotropical amphibian species should include a combination of sighting and audio techniques, and we discuss the need of implementing a large-scale monitoring in order to provide a baseline for comparison with future changes.  相似文献   

10.
The probability of long‐term persistence of a population is strongly determined by adult survival rates, but estimates of survival are currently lacking for most species of birds in the tropical Andes, a global biodiversity hotspot. We calculated apparent survival rates of birds in the Ecuadorian tropical Andes using a moderately long‐term (11 yr) capture–recapture dataset from three habitats that varied in how much they had been modified by human activities (native forest, introduced forest, and shrubs). We fit mark–recapture models for 28 species with habitat as a covariable. For all species, recapture rates between sampling sessions were low and varied from 0.04 for Rainbow Starfrontlets (Coeligena iris) to 0.41 for Stripe‐headed Brushfinches (Arremon assimilis) when averaged across all occupied habitats. Annual survival rates varied from 0.07 for Black‐crested Warblers (Margarornis squamiger) to 0.75 for Violet‐throated Metaltails (Metallura baroni). We found no significant differences in survival rates either among habitats or species grouped by habitat specialization. Because we found similar survival rates in native forest and human‐modified habitats, our results support those of recent studies concerning the potential value of secondary habitats for the conservation of some species of birds in the tropics. However, our conclusions are tempered by the uncertainty around the estimates of survival rates. Despite the relatively long‐term nature of our study, obtaining survival estimates for bird species in this region was challenging, and either more years of study or modification of field protocols may be needed to obtain more precise survival estimates.  相似文献   

11.
This study examined temporal variation in population dynamics and size structuring of two cyprinid minnows, Pseudobarbus afer and Barbus anoplus, in relation to their proximate physical habitats. Population estimates were determined using three‐pass depletion sampling during both summer and winter. The habitats were characterised by seasonal variation in all physico‐chemical conditions and spatial variation in substrata compositions. Whereas significant differences in population size were noted between seasons for B. anoplus, no differences were found between seasons for density and capture probability for either species. An increase in boulders was associated with increase in population size and density for P. afer; for B. anoplus, increased percentages of bedrock and bank vegetation were associated with an increase in population size and probability of capture, respectively. According to Canonical Correspondence Analysis, size structuring in P. afer was explained predominantly by seasonality, with smaller length classes associated with the seasonal variable of summer, while larger length classes were associated with pH that was higher in winter. By comparison, for B. anoplus, the habitat variables – bank vegetation and bedrock – accounted for much of the explained variance for size structuring. Recruitment appeared to be the major driver of size structuring for the two species; refugia, especially boulders and bank vegetation, also appeared to be important. Overall, the two species were adapted to the headwater streams that were generally variable in environmental conditions. Potential invasions by non‐native invasive fishes that occur within the mainstream habitats threaten these two species. Efforts should continue to protect these minnows from such invasions by constructing barriers to upstream migration of non‐native fishes into these headwater habitats.  相似文献   

12.
热带雨林木质藤本植物叶片性状及其关联   总被引:2,自引:0,他引:2  
热带雨林中木质藤本植物较为丰富。随着全球气候变化加剧,木质藤本植物的丰富度具有不断增加的趋势,有可能对热带森林的结构、功能和动态产生重要影响。然而,目前对木质藤本响应环境变化的机制所知甚少。本研究以13个科20种热带雨林常见木质藤本植物为材料,测定了冠层叶片的17个形态特征及结构性状,并分析了性状间的相互关系。结果表明,叶片相对含水量的种间变异最小(变异系数为5%),而上表皮厚度的种间变异最大(变异系数为80%),其它性状的种间变异系数为24%~61%。木质藤本植物的叶脉密度、叶片密度均与气孔密度呈显著正相关,叶片干物质含量与比叶面积呈显著负相关。与相同生境的树木相比,木质藤本的叶面积更小、气孔密度和叶片密度更低、比叶面积更高,但两种植物类群的叶片横切面组织结构厚度无显著差异。研究结果对理解木质藤本植物的生态适应性具有重要意义。  相似文献   

13.
We developed a capture-mark-recapture protocol for measuring the population density (D) of ship rats (Rattus rattus) in forest. Either mesh cage traps or Elliott box traps were set at each of six sites (48 traps per site for 5 nights) in the Orongorongo Valley on two occasions in autumn 2003. Cage traps only were set at three sites in autumn 2004. Rats were caught much more readily in cage traps than in Elliott traps and none were recaptured in Elliott traps. Additional food, bedding and trap covers reduced mortality and interference with traps. To estimate density we fitted a spatial detection model; this method avoids the need to estimate effective trapping area. Estimates were based on both a model assuming equal capture probability (Dˆ0) and a model incorporating temporal and individual variation (Dˆth). Our target for precision was CV(Dˆ) ≤ 20%, but when data were pooled from multiple sites with cage traps, CV(Dˆth) was ~30%. Estimated density of rats (Dˆth) was 5 ha-1in 2003 and 9 ha-1 in 2004; these estimates did not differ significantly. The overall capture index in 2004 was 3 rats per 00 corrected trap-nights on snap-trap lines set after live trapping. House mice were caught in both types of live trap, but at rates high enough for density estimation only where Elliott traps were used. Field estimates of detection functions for rats captured with cage traps allowed us to simulate the performance of alternative trapping systems. We predict that a 64-trap layout at three sites with five trapping occasions would yield acceptable precision of Dˆth (20–23%) at the observed rat densities. Our use of Dˆth was conservative; slightly higher precision may be achieved by assuming constant trappability ( Dˆ0), and future work may justify this assumption.  相似文献   

14.
Capture-mark-recapture (CMR) is commonly used in conservation biology, but rarely used to study non-native species in freshwater habitats. The power of CMR lies in the ability to go beyond simple density estimates and to quantify invasion dynamics and vital population parameters. I applied CMR to a population of the non-native Chinese mystery snail (Cipangopaludina chinensis, Viviparidae) in a 1.46 ha pond on Long Island, NY to estimate population size and survival probability in the waterbody and to uncover potential mechanisms for enormous differences in introduction success within and between waterbodies (observed densities range <1–40 individuals m?2). The C. chinensis population increased from approximately 150 to nearly 970 individuals from 2010 to 2012. Daily capture probabilities were low (<0.2) for snails of all sizes. Daily survival probabilities were size-dependent (almost 1.0 for snails larger than 30 mm shell length, and decreasing below that threshold), suggesting size-dependent mortality. This study highlights the ease of applying CMR to C. chinensis and its potential for other non-native species. Traditional survey methods such as density estimates with transects or quadrats cannot document increasing population sizes or size-specific mortality factors, which are essential for understanding introduction success and dynamics.  相似文献   

15.
The ratio of juvenile to adult birds in mist‐net samples is used to monitor avian productivity, but whether it is a “true” estimate of per capita productivity or an index proportional to productivity depends on whether capture probability is not age‐dependent (true estimate) or age difference in capture probability is consistent among years (index). Better understanding of the processes affecting age‐ and year‐specific capture probabilities is needed to advance the application of constant‐effort mist‐netting for monitoring and conservation, particularly in many tropical settings where capture rates are often low. We ranked members of the avian community by capture frequencies, determined if temporary emigration influenced the availability of birds to be captured, and assessed the distribution of birds relative to mist‐nets and the parity between capture‐based productivity estimates and number of fledglings in nest plots in a tropical dry forest in Puerto Rico in 2009 and 2010. Few captures characterized the community of 25 resident species and, when estimable, capture probabilities were low, particularly for juveniles (typically < 0.1). Negative trends in capture probability, temporary emigration, and the distribution of birds suggest that avoidance of mist‐nets influenced capture rates in our study. Increasing mist‐net coverage or moving mist‐nets between sampling periods could increase capture rates. The number of fledglings observed in nest plots (25 ha/plot) did not correlate well with capture‐derived estimates (20 ha/net stations), suggesting the presence of immigrants or failure to find all nests. Our results suggest that indices of breeding productivity from mist‐netting data may track temporal changes in productivity, but such data likely do not reflect “true” productivity in most cases unless age‐specific differences in capture probability are incorporated into estimates. Pilot studies should be conducted to evaluate capture rates and the spatial extent sampled by mist‐nets to improve sampling design and inferences before informing decisions.  相似文献   

16.
Estimating density of elusive carnivores with capture–recapture analyses is increasingly common. However, providing unbiased and precise estimates is still a challenge due to uncertainties arising from the use of (1) bait or lure to attract animals to the detection device and (2) ad hoc boundary-strip methods to compensate for edge effects in area estimation. We used photographic-sampling data of the Malagasy civet Fossa fossana collected with and without lure to assess the effects of lure and to compare the use of four density estimators which varied in methods of area estimation. The use of lure did not affect permanent immigration or emigration, abundance and density estimation, maximum movement distances, or temporal activity patterns of Malagasy civets, but did provide more precise population estimates by increasing the number of recaptures. The spatially-explicit capture–recapture (SECR) model density estimates ±SE were the least precise as they incorporate spatial variation, but consistent with each other (Maximum likelihood-SECR = 1.38 ± 0.18, Bayesian-SECR = 1.24 ± 0.17 civets/km2), whereas estimates relying on boundary-strip methods to estimate effective trapping area did not incorporate spatial variation, varied greatly and were generally larger than SECR model estimates. Estimating carnivore density with ad hoc boundary-strip methods can lead to overestimation and/or increased uncertainty as they do not incorporate spatial variation. This may lead to inaction or poor management decisions which may jeopardize at-risk populations. In contrast, SECR models free researchers from making subjective decisions associated with boundary-strip methods and they estimate density directly, providing more comparable and valuable population estimates.  相似文献   

17.
Wildlife managers are urgently searching for improved sociodemographic population assessment methods to evaluate the effectiveness of implemented conservation activities. These need to be inexpensive, appropriate for a wide spectrum of species and straightforward to apply by local staff members with minimal training. Furthermore, conservation management would benefit from single approaches which cover many aspects of population assessment beyond only density estimates, to include for instance social and demographic structure, movement patterns, or species interactions. Remote camera traps have traditionally been used to measure species richness. Currently, there is a rapid move toward using remote camera trapping in density estimation, community ecology, and conservation management. Here, we demonstrate such comprehensive population assessment by linking remote video trapping, spatially explicit capture–recapture (SECR) techniques, and other methods. We apply it to three species: chimpanzees Pan troglodytes troglodytes, gorillas Gorilla gorilla gorilla, and forest elephants Loxodonta cyclotis in Loango National Park, Gabon. All three species exhibited considerable heterogeneity in capture probability at the sex or group level and density was estimated at 1.72, 1.2, and 1.37 individuals per km2 and male to female sex ratios were 1:2.1, 1:3.2, and 1:2 for chimpanzees, gorillas, and elephants, respectively. Association patterns revealed four, eight, and 18 independent social groups of chimpanzees, gorillas, and elephants, respectively: key information for both conservation management and studies on the species' ecology. Additionally, there was evidence of resident and nonresident elephants within the study area and intersexual variation in home range size among elephants but not chimpanzees. Our study highlights the potential of combining camera trapping and SECR methods in conducting detailed population assessments that go far beyond documenting species diversity patterns or estimating single species population size. Our study design is widely applicable to other species and spatial scales, and moderately trained staff members can collect and process the required data. Furthermore, assessments using the same method can be extended to include several other ecological, behavioral, and demographic aspects: fission and fusion dynamics and intergroup transfers, birth and mortality rates, species interactions, and ranging patterns.  相似文献   

18.
Collisions and electrocutions at power lines are thought to kill large numbers of birds in the United States annually. However, existing estimates of mortality are either speculative (for electrocution) or based on extrapolation of results from one study to all U.S. power lines (for collision). Because national-scale estimates of mortality and comparisons among threats are likely to be used for prioritizing policy and management strategies and for identifying major research needs, these estimates should be based on systematic and transparent assessment of rigorously collected data. We conducted a quantitative review that incorporated data from 14 studies meeting our inclusion criteria to estimate that between 12 and 64 million birds are killed each year at U.S. power lines, with between 8 and 57 million birds killed by collision and between 0.9 and 11.6 million birds killed by electrocution. Sensitivity analyses indicate that the majority of uncertainty in our estimates arises from variation in mortality rates across studies; this variation is due in part to the small sample of rigorously conducted studies that can be used to estimate mortality. Little information is available to quantify species-specific vulnerability to mortality at power lines; the available literature over-represents particular bird groups and habitats, and most studies only sample and present data for one or a few species. Furthermore, additional research is needed to clarify whether, to what degree, and in what regions populations of different bird species are affected by power line-related mortality. Nonetheless, our data-driven analysis suggests that the amount of bird mortality at U.S. power lines is substantial and that conservation management and policy is necessary to reduce this mortality.  相似文献   

19.
Surveying plant diversity in arid desert areas is extremely difficult because of the harsh climate, hostile terrain, lack of roads, and insecurity, which is why it is particularly important to improve the sampling efficiency, but few relevant studies have been done. The performance of non-parametric estimators was assessed with first-hand field data to determine (a) the threshold of the proportion of uniques (number of species that occur in exactly one plot divided by the number of species sampled) that involves the least sampling effort and (b) the method of locating plots to obtain a more reliable estimate of species richness. The study area (Gurbantunggut desert, China) was divided into five sub-regions based on variation in physical environment and vegetation. The following common correction factors were selected: ACE, Chao1, Bootstrap, Chao2, ICE, Jack1, and Jack2. The estimates for each sub-region (partition) and for the entire region (without partition), the threshold of proportion of uniques, and the method of determining sampling locations (including prior sampling of plots that show large differences in habitats) were compared in terms of their ability to predict the number of species more accurately. We found that ACE and Chao1 (which use abundance data) showed more biased estimates than the other factors (incidence data), and best estimator is Jack1. Species richness was significantly underestimated for the region, but the non-parametric estimators could estimate the species richness for each sub-region reliably. Sampling locations affected the performance of non-parametric estimators significantly. The threshold of minimum sampling was 15% and that of uniques was 30%; the two were able to limit the bias within 5 and 10%, respectively. It is concluded that the non-parametric estimators can estimate the plant diversity of arid deserts reliably from the data on incidence. The study area (on the scale of a region) should be partitioned to improve the performance of the non-parametric estimators. The plots with larger differences in habitats should be sampled more extensively based on the threshold of the proportion of uniques.  相似文献   

20.
Ideas on the spatial variation of biodiversity often imply a causal link between the abundance and species richness of organisms. We investigated this ‘more individuals hypothesis’ using light‐trapping data of three unrelated groups of moths (Arctiidae, Geometridae and Pyraloidea) from the Ecuadorian Andes. We analyzed environmental correlates of specimen densities found in different habitats, finding effects of temperature, moonlight, forest succession, elevation and season. We corrected abundance data for light‐trapping artefacts, and we measured species diversity with various metrics known to be unbiased by undersampling. We found significant positive correlations between abundance and species diversity for all three taxonomic groups. We discuss implications for a general evaluation of species‐energy theory as well as for a better understanding of ecological processes in montane habitats of the Andes.  相似文献   

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