Application of a model of scale dependence to quantify scale domains in open predation experiments

We use a model of open predation experiments to define scale domains that differ in terms of the controlling processes and scale dependence of predator impacts. For experimental arenas that are small compared to the movements of the prey (small scale domain) the model predicts that predator impacts are scale independent and controlled by prey movements. For arenas of intermediate scale we predict that predator impacts are scale dependent and controlled by both prey movements and direct predation, and for the largest scale domain we predict weak scale dependence and predation control.
We propose that the scale‐domain concept is useful when designing and interpreting field experiments. As an illustration we apply the concept to experiments examining predator effects on the stream benthos. First, we test two key assumptions of the underlying model: that area‐specific prey migration rates decrease with increasing size of experimental arenas and that predation rates are independent of arena size. For this purpose we used published estimates of prey emigration and predator consumption rates for nine studies examining the effects of stream predators on benthic prey. We found that prey per capita emigration rates but not predation rates decreased with increasing arena length.
Second, we demonstrate a method for identifying the scale domain of real experiments. The model of predation experiments was parameterized using experimental data and the expected spatial and temporal scale dependence of predator impacts on prey in these experiments was simulated. The simulations suggest that the studies conducted in the largest arenas (length 15–35 m) should be classified as large‐scale, consumption‐controlled experiments, whereas the experiments conducted in smaller arenas (length 1.5–6 m) should be classified as small or intermediate‐scale. We also attempted to determine the scale domain of the experiments in a large data set, including results from most published stream predation experiments. The majority of arenas used in these experiments (73%) were smaller than 1 m in length. Our data on the scale dependence of predation and prey migration rate suggest that experiments in this scale range (<1 m) should be classified as small‐scale, movement‐controlled experiments for most prey taxa.     

Metapopulation structure and habitat quality in modelling dispersal in the butterfly Iolana iolas

Quantifying dispersal is fundamental to understanding the effects of fragmentation on populations. Although it has been shown that patch and matrix quality can affect dispersal patterns, standard metapopulation models are usually based on the two basic variables, patch area and connectivity. In 2004 we studied migration patterns among 18 habitat patches in central Spain for the butterfly Iolana iolas, using mark–release–recapture methods. We applied the virtual migration (VM) model and estimated the parameters of emigration, immigration and mortality separately for males and females. During parameter estimation and model simulations, we used original and modified patch areas accounting for habitat quality with three different indices. Two indices were based on adult and larval resources (flowers and fruits) and the other one on butterfly density. Based on unmodified areas, our results showed that both sexes were markedly different in their movements and mortality rates. Females emigrated more frequently from patches, but males that emigrated were estimated to move longer daily dispersal distances and suffer higher mortality than females during migration. Males were more likely to emigrate from small than from large patches, but patch area had no significant effect on female emigration. The effects of area on immigration rate and the within-patch mortality were similar in both sexes. Based on modified areas, the estimated parameter values and the model simulation results were similar to those estimated using the unmodified patch areas. One possible reason for the failure to significantly improve the parameter estimates of the VM model is the fact that resource quantity and butterfly population sizes were strongly correlated with patch area. Our results suggest that the standard VM modelling approach, based on patch area and connectivity, can provide a realistic picture of the movement patterns of I. iolas .     

Implications of empirical data quality to metapopulation model parameter estimation and application

Parameter estimation is a critical step in the use of any metapopulation model for predictive purposes. Typically metapopulation studies assume that empirical data are of good quality and any errors are so insignificant that they can be ignored. However, three types of errors occur commonly in metapopulation data sets. First, patch areas can be mis-estimated. Second, unknown habitat patches may be located within or around the study area. Third, there may be false zeros in the data set, that is, some patches were observed to be empty while there truly was a population in the patch. This study investigates biases induced into metapopulation model parameter estimates by these three types of errors. It was found that mis-estimated areas influence the scaling of extinction risk with patch area; extinction probabilities for large patches become overestimated. Missing patches cause overestimation of migration distances and colonization ability of the species. False zeros can affect very strongly all model components, the extinction risk in large patches, intrinsic extinction rates in general, migration distances and colonization ability may become all overestimated. Biases in parameter estimates translate into corresponding biases in model predictions, which are serious particularly if metapopulation persistence becomes overestimated. This happens for example when the migration capability of the species is overestimated. Awareness of these biases helps in understanding seemingly anomalous parameter estimation results. There are also implications for field work: it may be reasonable to allocate effort so that serious errors in data are minimized. It is particularly important to avoid observing false zeros for large and/or isolated patches.     

Inferring landscape resistance to gene flow when genetic drift is spatially heterogeneous

In connectivity models, land cover types are assigned cost values characterizing their resistance to species movements. Landscape genetic methods infer these values from the relationship between genetic differentiation and cost distances. The spatial heterogeneity of population sizes, and consequently genetic drift, is rarely included in this inference although it influences genetic differentiation. Similarly, migration rates and population spatial distributions potentially influence this inference. Here, we assessed the reliability of cost value inference under several migration rates, population spatial patterns and degrees of population size heterogeneity. Additionally, we assessed whether considering intra-population variables, here using gravity models, improved the inference when drift is spatially heterogeneous. We simulated several gene flow intensities between populations with varying local sizes and spatial distributions. We then fit gravity models of genetic distances as a function of (i) the ‘true’ cost distances driving simulations or alternative cost distances, and (ii) intra-population variables (population sizes, patch areas). We determined the conditions making the identification of the ‘true’ costs possible and assessed the contribution of intra-population variables to this objective. Overall, the inference ranked cost scenarios reliably in terms of similarity with the ‘true’ scenario (cost distance Mantel correlations), but this ‘true’ scenario rarely provided the best model goodness of fit. Ranking inaccuracies and failures to identify the ‘true’ scenario were more pronounced when migration was very restricted (<4 dispersal events/generation), population sizes were most heterogeneous and some populations were spatially aggregated. In these situations, considering intra-population variables helps identify cost scenarios reliably, thereby improving cost value inference from genetic data.     

How does adaptive consumer movement affect population dynamics in consumer-resource metacommunities with homogeneous patches?

This article uses simple models to explore the impact of adaptive movement by consumers on the population dynamics of a consumer-resource metacommunity consisting of two identical patches. Consumer-resource interactions within a patch are described by the Rosenzweig-MacArthur predator-prey model, and these dynamics are assumed to be cyclic in the absence of movement. The per capita movement rate from one patch to the other is an increasing function of the difference between the per capita birth minus death rate in the destination patch and that in the currently occupied patch. Several variations on this model are considered. Results show that adaptive movement frequently creates anti-phase cycles in the two patches; these suppress the predator-prey cycle and lead to low temporal variation of the total population sizes of both species. Paradoxically, even when movement is very sensitive to the fitness difference between patches, perfect synchrony of patches is often much less likely than in comparable systems with random movement. Under these circumstances adaptive movement of consumers often generates differences in the average properties of the two patches. In addition, mean global densities and responses to global perturbations often differ greatly from similar systems with no movement or random movement.     

Metapopulation dynamics of the bog fritillary butterfly: movements between habitat patches

Recent studies on metapopulation dynamics have emphasized the need for improved methods for quantifying individual movements between local populations and habitat patches. In this paper, we report on a 6-yr study in which a network of 12 habitat patches occupied by the bog fritillary, Proclossiana eunomia , was surveyed, with special focus on quantifying movements between the habitat patches. We applied the Virtual Migration model which has been designed to estimate survival and migration parameters in a metapopulation of several connected local populations. The model was parameterized using mark-release-recapture data collected during 6 yr. Generally, the estimated parameter values indicated a high level of movements, with roughly half of butterfly-days spent outside the natal patch. Mortality within patches was higher in males than in females. Females tended to be more mobile and spent more time outside their natal patch than males. Further analysis of the MRR data shows that in this protandrous species males tend to move very little between habitat patches before substantial numbers of females have emerged.     

Drift and settlement of stream insects in a complex hydraulic environment

1. The hydraulic and geomorphic characteristics of stream patches are often associated with distinctive assemblages or densities of stream invertebrates, and it is routinely presumed that these patterns reflect primarily species‐specific habitat requirements. An alternative hypothesis is that such patterns may be influenced by constraints on movement, such as the results of departure and settlement processes. We describe a manipulative experiment that examined how the hydraulic environments created by topographic bedforms influenced the drift behaviour and potential settlement sites for two species of mayfly (Baetis rhodani and Ecdyonurus torrentis). These species are common in the drift and often co‐occur in streams, but differ in their small‐scale distribution patterns, body shape and movement behaviour. 2. Flume experiments were carried out to determine how the hydraulic environments conditioned by a step bedform influence the behaviour of mayflies in the drift (swimming, posturing, tumbling), and the consequences of those behaviours (drift distance and time), compared to drift over a plane bed. The ramped step in the flume mimicked step bedforms that are common in coarse‐grained, high‐gradient streams. In contrast to the plane bed, a zone of recirculating flow was created downstream of the step, above which flow was faster and more turbulent. Uniform flows are used in most flume studies of drift; our approach is novel in recreating a complex hydraulic environment characteristic of stream channels. 3. Both species had some behavioural control over drift, and drift distances and times were shorter for live larvae than for dead larvae over the plane bed. The step had no impact on drift time or distance for live Baetis, but dead larvae were trapped in the flow separation eddy and drift time increased accordingly. Some Ecdyonurus also became trapped in the eddy, but live larvae drifted farther than dead larvae, and farther over the step than the plane bed. 4. Whilst in the drift, larvae altered their behaviour according to the ambient hydraulic environment, but in a species‐specific manner. Over the plane bed, Baetis had occasional swimming bursts, but primarily postured (maintained a stable body orientation), whereas Ecdyonurus spent roughly equal time posturing and swimming. In the more turbulent flows generated by the step, Baetis spent proportionately more time swimming, whereas Ecdyonurus spent more time posturing and often tumbling as body orientation became unstable. 5. In a high‐gradient stream, Baetis was more abundant close to steps than in plane bed patches with less complex flow, whereas the opposite pattern held for Ecdyonurus. Thus, the small‐scale distribution patterns of these species within streams correspond to their drift behaviours and ability to access various hydraulic patch types in our flume. These results are consistent with the hypothesis that constraints on movement and settlement may be important driver of distribution patterns within streams.     

Migration of the clouded Apollo butterfly Parnassius mnemosyne in a network of suitable habitats – effects of patch characteristics

The clouded Apollo Parnassius mnemosyne is a food plant specialist with short but frequent movements between habitat patches. The short average dispersal distances suggest that the probability of colonisation of vacant patches decreases rapidly as the distance between the source and target patches increases, which means that a dense habitat network is needed for the conservation of the species. Both emigration rate and the number of immigrants varied among patches and were not affected only by isolation but also by several other patch characteristics. The model that explained most of the variation in emigration rates among patches included patch area and the number of conspecifics. The area and the population density of the target patch had significant effects on the number of arriving immigrants. Thus, the colonisation of vacant patches is dependent on these patch characteristics. Generally, emigration rates were lower and residence times longer in large patches with many conspecifics. Butterfly density was the most important single factor explaining the variation in the number of immigrants among patches, although the positive effect of the area of the target patch was also significant. As a consequence of the marked positive density dependence caused by conspecific attraction, small patches with higher than average butterfly density, receive more immigrants than could be expected based on the patch area only. Due to conspecific attraction, per capita immigration rates are higher in small than large patches. Thus, immigration may have a more significant effect on the local dynamics of small than large populations.     

Do all inter-patch movements represent dispersal? A mixed kernel study of butterfly mobility in fragmented landscapes

1. In times of ongoing habitat fragmentation, the persistence of many species is determined by their dispersal abilities. Consequently, understanding the rules underlying movement between habitat patches is a key issue in conservation ecology. 2. We have analysed mark-release-recapture (MRR) data on inter-patches movements of the Dusky Large Blue butterfly Maculinea nausithous in a fragmented landscape in northern Bavaria, Germany. The aim of the analysis was to quantify distance dependence of dispersal as well as to evaluate the effect of target patch area on immigration probability. For statistical evaluation, we apply a 'reduced version' of the virtual migration model (VM), only fitting parameters for dispersal distance and immigration. In contrast to other analyses, we fit a mixed dispersal kernel to the MRR data. 3. A large fraction of recaptures happened in other habitat patches than those where individuals were initially caught. Further, we found significant evidence for the presence of a mixed dispersal kernel. The results indicate that individuals follow different strategies in their movements. Most movements are performed over small distances, nonetheless involving travelling between nearby habitat patches (median distance c. 480 m). A small fraction (c. 0·025) of the population has a tendency to move over larger distances (median distance c. 3800 m). Further, immigration was positively affected by patch area (I～A(ζ) ), with the scaling parameter ζ = 0·5. 4. Our findings should help to resolve the long-lasting dispute over the suitability of the negative exponential function vs. inverse-power one for modelling dispersal. Previous studies on various organisms found that the former typically gives better overall fit to empirical distance distributions, but that the latter better represents long-distance movement probabilities. As long-distance movements are more important for landscape-level effects and thus, e.g. for conservation-oriented analyses like PVAs, fitting inverse-power kernels has often been preferred. 5. We conclude that the above discrepancy may simply stem from the fact that recorded inter-patch movements are an outcome of two different processes: daily routine movements and genuine dispersal. Consequently, applying mixed dispersal kernels to disentangle the two processes is recommended.     

Area-dependent migration by ringlet butterflies generates a mixture of patchy population and metapopulation attributes

Interpretation of spatially structured population systems is critically dependent on levels of migration between habitat patches. If there is considerable movement, with each individual visiting several patches, there is one ”patchy population”; if there is intermediate movement, with most individuals staying within their natal patch, there is a metapopulation; and if (virtually) no movement occurs, then the populations are separate (Harrison 1991, 1994). These population types actually represent points along a continuum of much to no mobility in relation to patch structure. Therefore, interpretation of the effects of spatial structure on the dynamics of a population system must be accompanied by information on mobility. We use empirical data on movements by ringlet butterflies, Aphantopus hyperantus, to investigate two key issues that need to be resolved in spatially-structured population systems. First, do local habitat patches contain largely independent local populations (the unit of a metapopulation), or merely aggregations of adult butterflies (as in patchy populations)? Second, what are the effects of patch area on migration in and out of the patches, since patch area varies considerably within most real population systems, and because human landscape modification usually results in changes in habitat patch sizes? Mark-release-recapture (MRR) data from two spatially structured study systems showed that 63% and 79% of recaptures remained in the same patch, and thus it seems reasonable to call both systems metapopulations, with some capacity for separate local dynamics to take place in different local patches. Per capita immigration and emigration rates declined with increasing patch area, while the resident fraction increased. Actual numbers of emigrants either stayed the same or increased with area. The effect of patch area on movement of individuals in the system are exactly what we would have expected if A. hyperantus were responding to habitat geometry. Large patches acted as local populations (metapopulation units) and small patches simply as locations with aggregations (units of patchy populations), all within 0.5 km². Perhaps not unusually, our study system appears to contain a mixture of metapopulation and patchy-population attributes.     

Prior knowledge about spatial pattern affects patch assessment rather than movement between patches in tactile-feeding mallard

1. Heterogeneity in food abundance allows a forager to concentrate foraging effort in patches that are rich in food. This might be problematic when food is cryptic, as the content of patches is unknown prior to foraging. In such case knowledge about the spatial pattern in the distribution of food might be beneficial as this enables a forager to estimate the content of surrounding patches. A forager can benefit from this pre-harvest information about the food distribution by regulating time in patches and/or movement between patches. 2. We conducted an experiment with mallard Anas platyrhynchos foraging in environments with random, regular, and clumped spatial configurations of full and empty patches. An assessment model was used to predict the time in patches for different spatial distributions, in which a mallard is predicted to remain in a patch until its potential intake rate drops to the average intake rate that can be achieved in the environment. A movement model was used to predict lengths of interpatch movements for different spatial distributions, in which a mallard is predicted to travel to the patch where it expects the highest intake rate. 3. Consistent with predictions, in the clumped distribution mallard spent less time in an empty patch when the previously visited neighbouring patch had been empty than when it had been full. This effect was not observed for the random distribution. This shows that mallard use pre-harvest information on spatial pattern to improve patch assessment. Patch assessment could not be evaluated for the regular distribution. 4. Movements that started in an empty patch were longer than movements that started in a full patch. Contrary to model predictions this effect was observed for all spatial distributions, rather than for the clumped distribution only. In this experiment mallard did not regulate movement in relation to pattern. 5. An explanation for the result that pre-harvest information on spatial pattern affected patch assessment rather than movement is that mallard move to the nearest patch where the expected intake rate is higher than the critical value, rather than to the patch where the highest intake rate is expected.     

Predicting immigration of two species in contrasting landscapes: effects of scale, patch size and isolation

Migration is a key process for spatially structured populations. We examined how a variety of patch based metrics commonly used to predict the number of immigrants to a habitat patch performed based on data from three different years, in two distinct insect systems. The first system was an herbivorous beetle inhabiting patches of its host plant within a 'typical' patch network. In this system there were numerous patches located relatively close to one another, given the beetle's dispersal ability. The second system consisted of a butterfly inhabiting a series of 17 subalpine meadows. Here, the patches were arranged in a linear fashion and were more distant from each other. Overall, we found that the best models incorporating aspects of patch size and/or isolation explained a large (30–40%) amount of deviance in immigration, but there were considerable differences between the systems. For the first system, we found that metrics including the size of the target patch explained the highest proportion of deviance in immigrant numbers, while metrics based only on interpatch distances explained very little deviance. The situation was reversed for the second system. Metrics including the size of the target patch explained little deviance, while metrics based on the distance between patches explained the bulk of deviance in the number of immigrants. The results of our study show that the effects of patch size and isolation on the number of immigrants are highly important, but dependent on spatial scale, the organism studied, and how it responds to the spatial arrangement of patches. Correspondingly, there will be no single generalized metric to predict immigration for all cases. Given the dependency of the results on the system studied, we recommend that future studies provide explicit data on habitat areas and dispersal distance relative to interpatch distance to allow for meaningful comparison among organisms and systems.     

Spatial and temporal variation in patch occupancy and population density in a model system of an arctic Collembola species assemblage

We employed an experimental model system to investigate the mechanisms underlying patterns of patch occupancy and population density in a high arctic assemblage of Collembola species inhabiting a sedge tussock landscape on Svalbard. The replicate model systems consisted of 5 cores of the tussocks (habitat patches) imbedded in a barren matrix. Four of the patches were open so that animals could migrate between them, while there was one closed patch per system to test the effect of migration on extinction rate. There were model systems of two types: one with long and one with short inter‐patch distances to test the effect of patch isolation on colonisation and extinction rates. Each of the four most common collembolan species at the field site were introduced to two open patches per system (source patches), with the other two functioning as colonisation patches for the species. The experiment was run in an ecotrone over three identical, simulated arctic summers separated by winters of 3 weeks. Six replicates of systems with short and long inter‐patch distances were sampled at the end of each summer. The species varied markedly in their performance in both open arenas and closed patches, indicating differential responses to patch humidity, consistent with their differential distribution along the moisture gradient in the field site. The extinction – colonisation dynamics differed markedly between species as predicted from our field studies. This could partly be ascribed to differential dispersal and colonisation ability, but also to different tolerance to spatially variable patch quality and/or tendency for aggregative behaviour. Three of the species exhibited dynamics that superficially resemble what could be expected from classical metapopulation dynamics. However, there was a striking discrepancy between what would be expected from the effect of migration on the extinction rate of isolated patches (in particular closed patches) and the observed rates. Thus, metapopulation processes, such as stochastic colonisation and extinction events due to demographic stochasticity, were relatively unimportant compared to other sources of spatial variability among which subtle differences in patch quality are probably most important. We discuss the value of combining field studies with model system experiments, in particular when habitat quality cannot easily be measured in the field. However, our field and laboratory studies also emphasise the need for a thorough knowledge of species‐specific life history traits for making biologically sound interpretations based on both observational and experimental data.     

The drift distances and time spent in the drift by freshwater shrimps, Gammarus pulex, in a small stony stream, and their implications for the interpretation of downstream dispersal

1. The objectives were (i) to determine experimentally and to model the relationship between mean water velocity and both the mean distance travelled, and the mean time spent, in the drift by freshwater shrimps, Gammarus pulex; (ii) to develop a drift distance–water velocity model from the experimental study, and validate it with field data; (iii) to examine the relationship between drift rate, water velocity and benthic density with the latter expressed as a mean value for the whole stream and a mean value corrected for the distance travelled in the drift. 2. In field experiments at 10 water velocities (0.032–0.962 m s^?1), the significant relationship between the mean drift distance and mean water velocity was described both by a power function (power, 0.96) and a linear relationship. The mean drift time was fairly constant at 8.3 s (95% CL ± 0.4). A simple model estimated the drift distance and time spent in the drift by different percentages of the drifting invertebrates. This model predicted correctly the positive relationship between drift rate and water velocity for field data over a year. 3. The relationship between drift rate per hour and the independent variables, water velocity and benthic density, was well described by a multiple‐regression model. Adding temperature and date did not improve model fit. Variations in water velocity and benthic density explained 96% of the variation in nocturnal drift rate (65% to velocity, 31% to benthic density), but only 40% of the variation in diurnal drift rate (29% to velocity, 11% to benthic density). Correcting benthic density for the drift distances did not improve model fit. 4. The significance of this study is that it developed models to predict drift distances and time, values being similar to those obtained in another, larger stream. It also illustrated the importance of spatial scale in the interpretation of drift by showing that when drift distances were taken into account, the impact of drift on the population was higher (4–10% lost day^?1) than when drift distances were ignored (usually < 3% lost day^?1), especially at a local level.     

Patch Choice Decisions among Ifaluk Fishers

Studies of patch choice decisions among human foragers have failed to explain why foragers do not exclusively exploit the patch with the highest mean profitability. One possible explanation is that profitability rankings are likely to vary daily; however, this instability is not captured when profitabilities are calculated as a sampled average over a longer time span. Here I present data on the patch choice decisions of Ifaluk fishers to evaluate whether men are responding to daily variation in the profitability of their primary fishing patch. Results show that men choose to fish most frequently in the patch with the highest mean profitability. Men fish in alternative patches (alternative from the most profitable patch) when, on that morning or the previous day, return rates in the most profitable patch are lower than the overall mean per capita return rate of alternative patches. Results also indicate that when fishers pursue alternative patches after fishing in the patch with the highest profitability, their mean per capita return rates are generally higher in the alternative patches exploited. However, variance in the profitability of the most profitable patch cannot explain why men exploit two patches, the Nine-mile reef and the dogtoothed tuna patch, which on average have very low profitability. These results and directions for future research are discussed. [Keywords: human behavioral ecology, patch choice decisions, Micronesia]     

The relative importance of drift causes for stream insect herbivores across a canopy gradient

A key attribute of riverine food webs is the downstream movement of invertebrates via the water column, or invertebrate drift. Causes of drift include benthic predation, food limitation, and perhaps passive entry, which may occur when invertebrates lose their purchase on stream substrate. However, the relative importance of drift causes is unknown, as is whether the relative importance of drift causes varies across space. Combining observational data on invertebrate herbivore and predator guild densities with in‐stream experiments, we evaluated the relative importance of benthic predation, food limitation, and passive entry as proximate causes of drift for the herbivore guild across the canopy gradient of a montane stream. We found that 1) benthic predation and food limitation were both more important as causes of herbivore drift than passive entry; 2) drift caused by food limitation did not vary with riparian canopy, whereas herbivore density decreased with increasing riparian canopy, and 3) per capita drift increased linearly with increasing density, while per capita drift decreased in a negative hyperbolic fashion with increasing food, indicating that herbivore drift is proportional to herbivore density, and inversely proportional to food. We conclude that invertebrate herbivore drift was overwhelmingly an active process to improve fitness, and that herbivore food did not vary across the canopy gradient, likely because increased herbivory from larger herbivore populations at sunnier sites prevented food from accumulating.     

A stochastic model of the distribution of unequal competitors between resource patches

We present a stochastic model of individuals' movements between two patches of resources. The population is made up of two types of individual with differing competitive abilities, and two types of movements occur, with individuals moving either to increase their intake rate or at random. Several previous models have used simulations to evaluate the likely distribution of individuals. We instead derive equations for the equilibrium distribution of the population, which can be solved numerically. This avoids the need to choose an initial distribution for the population, and enables us to obtain the probability with which rare events occur. This may not be possible when simulations are used, since a rare event may not occur at all. We find that when random movements are rare, an increase in the rate of random movements out of a patch can increase the number of individuals on that patch. We consider an approximation to the model with rare random movements, which provides an explanation for this phenomenon.     

Isolation determines patterns of species presence in highly fragmented landscapes

In fragmented landscapes, changes in habitat availability, patch size, shape and isolation may affect survival of local populations. Proposing efficient conservation strategies for such species relies initially on distinguishing the particular effects of those factors. To address these issues, we investigated the occurrence of 3 bird species in fragmented Brazilian Atlantic Forest landscapes. Playback techniques were used to collect presence/absence data of these species inside 80 forest patches, and incidence models were used to infer their occupancy pattern from landscape spatial structure. The relative importance of patch size, shape and surrounding forest cover and isolation was assessed using a model selection approach based on maximum likelihood estimation. The presence of all species was in general positively affected by the amount of surrounding habitat and negatively affected by inter‐patch distances. The joint effects of patch size and the surrounding landscape characteristics were important determinants of occupancy for two species. The third species was affected only by forest cover and mean patch isolation. Our results suggest that local species presence is in general more influenced by the isolation from surrounding forests than by patch size alone. We found evidence that, in highly fragmented landscapes, birds that can not find patches large enough to settle may be able to overcome short distances through the matrix and include several nearby patches within their home‐ranges to complement their resource needs. In these cases, patches must be defined as functionally connected habitat networks rather than mere continuous forest segments. Bird conservation strategies in the Atlantic forest should focus on increasing patch density and connectivity, in order to implement forest networks that reduce the functional isolation between large remnants with remaining core habitat.     

Between‐Patch Bird Movements within a High‐Andean Polylepis Woodland/Matrix Landscape: Implications for Habitat Restoration

The movement ability of species in fragmented landscapes must be considered if habitat restoration strategies are to allow maximum benefit in terms of increased or healthier wildlife populations. We studied movements of a range of bird species between woodland patches within a high‐altitude Polylepis/matrix landscape in the Cordillera Vilcanota, Peru. Movement rates between Polylepis patches differed across guilds, with arboreal omnivores, arboreal sally‐strikers and nectarivores displaying the highest movement rates, and understorey guilds and arboreal sally‐gleaners the lowest movement rates. Birds tend to avoid flights to more distant neighboring patches, especially when moving from patches which were themselves isolated. The decline in bird flight frequencies with increasing patch isolation followed broken‐stick models most closely, and while we suggest that there is evidence for a decline in between‐patch movements over distances of 30–210 m, there was great variability in movement rates across individual patches. This variability is presumably a result of complex interactions between patch size, quality and configuration, and flight movement patterns of individual bird species. Our study does, however, highlight the contribution small woodland patches make toward fragmented Polylepis ecosystem functioning, and we suggest that, where financial resources permit, small patch restoration would be an important compliment to the restoration of larger woodland patches. Most important is that replanting takes place within 200 m or so of existing larger patches. This will be especially beneficial in allowing more frequent use of woodland elements within the landscape and in improving the total area of woodland patches that are functionally connected.     

Three ways of assessing metapopulation structure in the butterfly Plebejus argus

1. Three independent methods were used to investigate population structure in the butterfly Plebejus argus . First, migration and dispersal ability were measured by mark–release–recapture in seven adjacent habitat patches, and by release of butterflies in unoccupied habitat. Secondly, colonization of newly created habitat was observed over 7 years. Finally, genetic differentiation of local populations within a metapopulation was investigated. Sampled local populations included parts of the mark–release–recapture study area.
2. Plebejus argus is relatively sedentary: the maximum movement detected was 395 m, and only 2% of individuals moved further than 100 m between recaptures on different days. None the less, adjacent local populations in the mark–release–recapture study area were linked by occasional migration, with ≈ 1.4% of individuals moving between patches separated by 13–200 m.
3. Despite low mobility, observed colonizations occurred rapidly over distances of 1 km. Because P. argus occurs at high population densities, 1.4% migration can generate enough migrants to colonize newly suitable habitat quickly at this spatial scale.
4. Mark–release–recapture data were used to predict that there would be limited genetic differentiation through drift between local populations at this spatial scale. The prediction was supported by allele frequency data for the same local populations.
5. Genetic differentiation often indicates higher levels of migration than are revealed by the movements of marked individuals. This study shows that when experimental releases and extensive marking are undertaken in areas that are large relative to most movements, indirect measures of gene flow and direct measures of dispersal can concur.
6. Evidence from the three different approaches was complementary, indicating that P. argus occurs as metapopulations within the study area.