Fish size and habitat depth relationships in headwater streams

Summary Surveys of 262 pools in 3 small streams in eastern Tennessee demonstrated a strong positive relationship between pool depth and the size of the largest fish within a pool (P<0.001). Similarly, the largest colonizers of newly-created deep pools were larger than the colonizers of shallow pools. We explored the role of predation risk in contributing to the bigger fish — deeper habitat pattern, which has been noted by others, by conducting five manipulative field experiments in two streams. Three experiments used stoneroller minnows (Campostoma anomalum); one used creek chubs (Semotilus atromaculatus); and one used striped shiners (Notropis chrysocephalus). The stoneroller experiments showed that survival of fish approximately 100 mm in total length (TL) was much lower in shallow pools (10 cm deep) than in deep (40 cm maximum) pools (19% versus 80% survival over 12 d in one experiment) and added cover markedly increased stoneroller survival in shallow pools (from 49% to 96% in an 11-d experiment). The creek chub experiment showed that, as for stonerollers, pool depth markedly influenced survival: the chubs survived an average of 4.9 d in shallow pools and >10.8 d in deep pools. In the striped shiner experiment in shallow artificial streamside troughs, no individuals 75–100 mm TL survived as long as 13 d, where-as smaller (20–25 mm) fish had 100% survival over 13 d. The results of the experiments show that predation risk from wading/diving animals (e.g., herons and raccoons) is much higher for larger fishes in shallow water than for these fishes in deeper water or for smaller fish in shallow water. We discuss the role of predation risk from two sources (piscivorous fish, which are more effective in deeper habitats, and diving/wading predators, which are more effective in shallow habitats) in contributing to the bigger fish — deeper habitat pattern in streams.     

Habitat selection and subsequent reproductive success in the beaugregory damselfish

Synopsis Male beaugregory damselfish,Stegastes leucostictus, were provided with three types of artificial breeding structures to determine if they change habitats based on past or future reproductive payoffs. All three site types quickly lured males away from their natural sites. In comparison to those living on natural sites, those using artificial sites were less likely to move to different areas and had a higher reproductive success. When given no choice, male reproductive success was correlated to structural type. A second experiment provided males with an additional structure after using the intermediate quality type for 2 months. Males would often initially use both sites but would eventually shift their spawning activity to the new site if it was of the same quality or better than the old one. However, males would not move if the new site was of inferior quality. When given a new site identical to the initial one, approximately half of the males shifted to the new site. There was no evidence that reproductive performance influenced a male's decision to use a new site.     

The first born,their dispersal,and vole cycles

Summary On the basis of some empirical data and the existing theory of vole cycles, a new hypothesis is proposed. It explains cyclicity as an effect of obligatory dispersal of the first seasonal cohort of young (Y1) from their natal (optimal) habitats into vacant (suboptimal) habitats. This behaviour could evolve, because it increases contribution of genetic lineages with dispersing Y1, to subsequent generation. It is assumed that the dispersal of Y1 is common among vole species, it does not change during consecutive phases of the cycle, and it does not vary between cyclic and non-cyclic populations. It results in multiannual cycles only under a certain set of spatial and climatic conditions, which are discussed in a paper. Otherwise it results in annual dynamics.     

Discovery of isolated patches ofIcerya purchasi byRodolia cardinalis: A field study

The discovery of isolated patches of prey by the natural enemies of the cottony-cushion scaleIcerya purchasi Maskell was tested in the field on potted plants ofAcacia baileyana and citrus between November and February in South Australia. The survival of scales to adults in patches in the 4 fortnightly releases (cohort sets) was not significantly different between location-1 (under anAcacia tree harbouring scales and its natural enemies) and location-2 (about 500 m away from the nearest host plant of the scale). The temporal distribution of mortality in the scale cohorts was described by the Weibull model. The proportion of scales surviving at the 2 locations (on the 3^rd & 6^th fornight) was not significantly different suggesting that the total effect of all the mortality factors on the scales at the 2 locations was the same. The trends in prey patches destroyed in time could be explained from the period of activity of the natural enemies in the field.Rodolia cardinalis (Mulsant) had discovered the prey patches within a fortnight of the release of scale crawlers. The results substantiate earlier reports thatRodolia can find and destroy isolated scale colonies.      

Controlled experiments of habitat fragmentation: a simple computer simulation and a test using small mammals

Habitat fragmentation involves a reduction in the effective area available to a population and the imposition of hard patch edges. Studies seeking to measure effects of habitat fragmentation have compared populations in fragments of different size to estimate and area effect but few have examined the effect of converting open populations to closed ones (an effect of edges). To do so requires a shift in spatial scope-from comparison of individual fragments to that of fragmented versus unfragmented landscapes. Here we note that large-scale, controlled studies of habitat fragmentation have rarely been performed and are needed. In making our case we develop a simple computer simulation model based on how individual animals with home ranges are affected by the imposition of habitat edges, and use it to predict population-level responses to habitat fragmentation. We then compare predictions of the model with results from a field experiment on Peromyscus and Microtus. Our model treats the case where home ranges/territories fall entirely within or partially overlap with that of sample areas in continuous landscapes, but are restricted to areas within habitat fragments in impacted landscapes. Results of the simulations demonstrate that the imposition of hard edges can produce different population abundances for similar-sized areas in continuous and fragmented landscapes. This edge effect is disproportionately greater in small than large fragments and for species with larger than smaller home ranges. These predictions were generally supported by our field experiment. We argue that large-scale studies of habitat fragmentation are sorely needed, and that control-experiment contrasts of fragmented and unfragmented microlandscapes provide a logical starting point.     

Stochastic determinants of assemblage patterns in coral reef fishes: a quantification by means of two models

Synopsis One perspective emphasizing the importance of stochastic processes in determining coral reef fish assemblages implies that there is little organization in species richness, abundance structure, and spatial distribution. We examine the degree to which this perspective is correct by analyzing distribution of fishes on a collection of patch reefs (Discovery Bay, Jamaica). We ask the question whether these patches accumulate species and individuals in a manner consistent with stochastic expectations. To address this question we use two conceptual models, each permitting a different insight. One assumes that fish are distributed stochastically on patches while the other assumes presence of restrictions on fish distribution due to habitat structure. For each conceptual model we use two types of benchmark: we compare observed patterns to those predicted by theoretical models, and we also compare observed patterns to those obtained from a random reallocation of fish individuals to patches. We found that the conceptual model assuming stochastic processes appeared to provide weaker explanation of patterns than the conceptual model that includes restrictions due to habitat structure. Further, and more importantly, we found that (i) the community is shaped by a mixture of stochastic and non-stochastic mechanisms, and (ii) the stochastic assembly processes decrease in importance for species restricted to fewer microhabitat types and sites. Our study therefore indicates that patches do accumulate individuals and species in a manner consistent with stochastic expectations, however, this applies primarily to the habitat generalists (unrestricted species). By the same token, increased habitat specialization by some species imposes constraints on the stochastic model such that it eventually fails.     

Topography of the enteric nervous system in Peyer's patches of the porcine small intestine

The mechanisms of intercommunication between the immune and nervous systems are not fully understood. In the case of the intestine, the enteric nervous system is involved in the regulation of immune responses. It was therefore decided to employ immunohistochemical techniques to investigate the structural organization of the enteric nervous system in Peyer's patches of the porcine small intestine. Using antibodies against various nervous system-specific markers (protein gene product 9.5, neuron-specific enolase, neurofilament 200, S-100 protein and the glial fibrillary acidic protein), an intimate and specific structural association could be demonstrated between enteric nerves and the compartments of Peyer's patches: follicles, interfollicular regions and domes. Peyer's patches have a close topographical relationship to the two submucosal plexuses. Enteric nerves are located around the follicle in the interfollicular area — the so-called traffic area-and in the dome area, which plays an important role in the uptake and presentation of antigens.     

Effects of pond size and consequent predator density on two species of tadpoles

Experimental ponds were used as a model system of habitat patches to study the effect of habitat size on the relative growth performance of tadpoles of Bufo americanus and Pseudacris triseriata, and on colonization by predatory insects. Three pond depths and surface areas were habitat size treatments in a replicated, factorial experiment. Tadpoles of both species were astablished together at a single density and ponds were left open to natural colonization by aquatic insects. Pond area had a significant effect on the multivariate response of P. triseriata larval period, survival, and metamorphic mass. P. triseriata survived better relative to B. americanus in larger ponds. However, increasing pond area led to greater incidence of predacious beetle larvae (Dytiscus, Coleoptera: Dytiscidae). Dytiscus larvae had a significant negative effect on the survival of P. triseriata and led to reduced P. triseriata survival relative to B. americanus in colonized ponds. The results suggest that habitat size can influence community structure by altering the distribution of predation among habitat patches.     

Aggregation and the maintenance of genetic diversity: An individual-based cellular model

Summary A cellular model, where each individual is explicitly defined, is used to describe a population of a mycophagous species ofDrosophila. Patches represent single fungal fruiting bodies which are only available as oviposition sites for a single fly generation. Standard competition equations are used to describe the interaction between larval genotypes at each patch. Dispersal of adults is obligatory and uses a simple model of patch choice to produce aggregated arrivals of adults at fresh patches. The degree to which aggregation of adults and eggs can promote coexistence of genotypes in a one-locus, two-allele system with dominance is explored. When both phenotypes (A- andaa) are aggregated, a polymorphism can be maintained for over 1000 generations even when the selective disadvantage of one phenotype (aa) is great. This model enhances the degree of polymorphism in a population, using aggregation. It does not preclude the operation of other methods which enhance the coexistence of genotypes. Therefore, it is acting to augment the degree of polymorphism maintained in species which exploit patchy and ephemeral habitats, including allDrosophila and a wide range of other organisms.     

Spectral regions in which aquatic insects see reflected polarized light

For diverse water insects (species of Hydrophilidae, Hadraenidae, Dytiscidae, Haliplidae and aquatic Heteroptera), the attractiveness of an artificial water surface was found to vary when the polarization of the reflected light, the property by which these insects identify water, was abolished in different regions of the spectrum. The sensitivity maxima of their reflection-polarization visual systems (max(POL)) thus determined were in various spectral regions, between < 360 nm (UV) and ca. 550 nm (yellow-green). Species with max(POL) at the short-wavelength end of the spectrum would be able to identify bodies of water by polarization regardless of whether the subsurface reflection was bright or dark; nevertheless, this group includes forms that avoid water with a bright subsurface because of the intensity of the reflected light. Species with max(POL) in the long-wavelength region fail to use certain bodies of water with a bright subsurface as habitats because the light they reflect at the longer wavelengths is insufficiently polarized. That the POL system of a species has a large max could affect habitat choice; on the other hand, it could also be that systems operating in the long-wavelength region were produced in the course of adaptation to the light conditions in or above the habitat.Abbreviations max(POL) spectral sensitivity maximum for polarization vision