Ants of Three Adjacent Habitats of a Transition Region Between the Cerrado and Caatinga Biomes: The Effects of Heterogeneity and Variation in Canopy Cover

Habitat heterogeneity and complexity associated with variations in climatic conditions are important factors determining the structure of ant communities in different terrestrial ecosystems. The objective of this study was to describe the horizontal and vertical distribution patterns of the ant community associated with three adjacent habitats in a transition area between the Cerrado and Caatinga biomes at the Pandeiros River, state of Minas Gerais, Brazil. We tested the following hypotheses: (1) the richness and composition of ant species and functional group structure changes between different habitats and strata; (2) habitats with higher tree species richness and density support higher ant species richness; and (3) habitats with lower variation in canopy cover support higher ant species richness. Sampling was conducted in three adjacent habitats and at three vertical strata. Ant species richness was significantly different among vertical strata. Ant species composition was different among both habitats and vertical strata and functional group structure was divergent among habitats. Partitioning of the diversity revealed that the diversity for the three components was statistically different from the one expected by the null model; α and β ₂ were higher and β ₁ was lower than the values expected by chance. Tree density and variation in canopy cover negatively affected ant species richness. The occurrence of different species and the changing of functional group structures in different habitats and strata suggest an ecological–evolutionary relationship between ants and their habitats and emphasize the need to implement local conservation strategies in the ecotones between biomes.     

The analysis of stratified 2 x 2 contingency tables

We consider the problem of testing for independence against the consistent superiority of one treatment over another when the response variable is binary and is compared across two treatments in each of several strata. Specifically, we consider the randomized clinical trial setting. A number of issues arise in this context. First, should tables be combined if there are small or zero margins? Second, should one assume a common odds ratio across strata? Third, if the odds ratios differ across strata, then how does the standard test (based on a common odds ratio) perform? Fourth, are there other analyzes that are more appropriate for handling a situation in which the odds ratios may differ across strata? In addressing these issues we find that the frequently used Cochran–Mantel–Haenszel test may have a poor power profile, despite being optimal when the odds ratios are common. We develop novel tests that are analogous to the Smirnov, modified Smirnov, convex hull, and adaptive tests that have been proposed for ordered categorical data. (© 2006 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)     

Species Turnover and Vertical Partitioning of Ant Assemblages in the Brazilian Amazon: A Comparison of Forests and Savannas1

We measured beta diversity, or turnover in species composition, of ant assemblages inhabiting patches of forest and savanna (cerrado) near Alter do Chão, in the Brazilian Amazon. In addition, we assessed vertical partitioning of these assemblages by comparing the ground and lower vegetation strata within each habitat. Ants attracted to sardine baits were collected along transects in 39 savanna and 34 forest sites scattered over a 16 km × 16 km landscape. There were about twice as many species in the forest as in the savanna, and within both habitats, we collected more species on the ground than in the vegetation. Similar results were obtained when analyzing data at the level of individual transects, indicating that ant species richness is affected by both habitat and strata. About two‐thirds of the species recorded in the savanna were also found in the forest. Within both habitats, a large proportion of the species found in the least species‐rich stratum (vegetation) were also found in the richer one (ground). However, ordination analysis, using data from individual transects, revealed that different habitats and strata can be clearly discriminated from each other in terms of their ant species composition. Each habitat and stratum had a number of characteristic (indicator) species which, although generally not exclusive to that particular habitat and stratum, predominated there. Our findings indicate that habitat and strata specialization is an important factor governing the organization of ant communities in Amazonia.     

Faunal influences on New Zealand seed dispersal characteristics

A range of distinctive dispersal features have been recognised within the New Zealand flora, and a wide range of fauna are involved in the dispersal of seed in New Zealand, either by consuming fruit or seed, or as transporters of adhesive seed. In this study the composition of New Zealand’s zoochorous fauna (except insects) was examined using both trait matching within environmental, morphological and behavioural variables, and compared to the trait pattern of the groups of plant species they disperse. The importance of the different dispersal groups to the plant species they disperse varies with habitat, landform, region of New Zealand, foraging behaviour, and morphology. Over half of New Zealand’s vertebrate fauna are involved in fruit dispersal, though only 6% are considered frugivorous—the remainder include varying quantities of insects and other plant material in their diets. Flighted species are over-represented in wooded environments and higher strata and flightless species predominate in low alpine and grassland habitats. The frugivore-fruiting plant interaction group shows some indications of ecological generalism as frugivorous species consume a range of fruit sizes across all vegetation strata and fruit-bearing plants have lower species diversity and occupy a wide range of habitats. Granivores are over-represented in wetland habitats and the eastern South Island. The importance of species which unintentionally disperse adhesive seed depends on whether they are volant (higher importance in coastal environments) or flightless (higher importance dry grasslands and in low alpine areas). A subgroup of birds, such as the ratite Apteryx spp. and the now extinct Dinornithiform moa, with loose feathers (“velcro” species) are over-represented in lower vegetation strata and this matches the zone where many attachment-dispersed plant species present their seed.     

Differences in trait compositions between rocky natural and artificial habitats

Question: What are the differences in trait compositions that enable native plants to colonise comparable natural and man‐made habitats? Are these traits independent of phylogenetic relationships between species? Location: Czech Republic. Methods: The relative importance of biological, ecological and distributional traits of native species was studied, using a dataset of 75 species growing in rock and wall habitats in the Czech Republic. Species preferences for individual habitats due to climatic conditions and proportions of different vegetation types in their surroundings were partialled out using partial canonical correspondence analysis. The pattern of plant traits along a gradient from natural rock habitats to secondary wall habitats was analysed using regression trees and generalized linear models with and without phylogenetic correction. Results: The most common native species colonising rock habitats are phanerophytes, mostly woody juveniles, with a CSR life strategy and most are adapted to epizoochory. Summer green leaves, annual life span, CR life strategy, reproduction mostly by seeds and dispersal by ants are all traits positively associated with the ability of species to colonise wall habitats. These species are also characterised by their high demand for nutrients, temperature, base‐rich substrates and light. Biological and ecological traits are more important for colonising new habitats than traits related to species dispersal ability or phylogenetic relationships between species. Biological and ecological traits alone explained 29.3% of variability in the species dataset, while dispersal characteristics and phylogeny alone explained 9.1% and 4.8%, respectively. Conclusions: We outline how the process of environmental filtering determines native species assemblages and identify a set of species traits that enable them to persist in particular habitats. We conclude that although urbanisation generally results in loss of natural habitats, there are new, man‐made habitats potentially suitable for native species.     

An analysis of fish distribution in Kainji lake Nigeria

The distribution of fish in the three major habitats (inshore, surface and bottom) in Kainji Lake was studied using gill-nets in graded fleets each consisting of seven nets with mesh sizes ranging from 5 cm to 18 cm. No significant difference was observed in the annual yields of fish in the three habitats. Three of the nine major families, however, gave higher yields in selected habitats. Characidae and Cichlidae were most abundant in the shore and surface and Bagridae in the shore and bottom. Catches of the Cichlidae in the surface were limited to areas where the mean depth was below 7 meters. Analysis of variance showed no significant difference in the overall yields of fish among sampling areas located within the major strata of the lake. Although a general trend was observed in the seasonal yields of fish, with higher yields during low water, the variations were not significant either for the overall annual yields or among sets. The implications of these findings in relation to the mode of life of the major fish species and the stability of the fish population are discussed.     

Characterizing the microhabitats of exotic species in Illinois shale barrens

Like native species, exotics form part of the mosaic structure of plant communities. However, their role in these communities is unclear. Thus, we ask, are invading exotic species present in recognizable microhabitats within plant communities? We compared the microhabitat of exotic species and random locations to determine if exotic plants occupied a recognizable subset of habitats within three barren communities. Fourteen exotic species were identified. The factors that characterized their habitats varied between barrens and among species. Considered as a group, exotic microhabitats comprised a subset of available habitats within the barrens, specifically, edge habitats rather than the open conditions of the barrens interior. Soil properties such as low temperature or neutral pH, and high litter or woody species cover, were common factors associated with the occurrence of exotics. Individual exotic species occupied different habitats within those identified for exotics as a group, but the range of variation between the different species was not generally significant. Within each barren, exotics occupied a distinct subset of microhabitats. This distribution suggests that exotics are not widely dispersed within these areas. Site conditions may be restricting the establishment of exotics to specific microhabitats, and in addition, some exotics may be altering the microhabitats that they colonize. Therefore, management efforts toward maintaining open conditions in the barrens may also discourage further encroachment by exotics into these areas.     

Convergent Evolution towards High Net Carbon Gain Efficiency Contributes to the Shade Tolerance of Palms (Arecaceae)

Most palm species occur in the shaded lower strata of tropical rain forests, but how their traits relate to shade adaptation is poorly understood. We hypothesized that palms are adapted to the shade of their native habitats by convergent evolution towards high net carbon gain efficiency (CGE_n), which is given by the maximum photosynthetic rate to dark respiration rate ratio. Leaf mass per area, maximum photosynthetic rate, dark respiration and N and P concentrations were measured in 80 palm species grown in a common garden, and combined with data of 30 palm species growing in their native habitats. Compared to other species from the global leaf economics data, dicotyledonous broad-leaved trees in tropical rainforest or other monocots in the global leaf economics data, palms possessed consistently higher CGE_n, achieved by lowered dark respiration and fairly high foliar P concentration. Combined phylogenetic analyses of evolutionary signal and trait evolution revealed convergent evolution towards high CGE_n in palms. We conclude that high CGE_n is an evolutionary strategy that enables palms to better adapt to shady environments than coexisting dicot tree species, and may convey advantages in competing with them in the tropical forest understory. These findings provide important insights for understanding the evolution and ecology of palms, and for understanding plant shade adaptations of lower rainforest strata. Moreover, given the dominant role of palms in tropical forests, these findings are important for modelling carbon and nutrient cycling in tropical forest ecosystems.     

Diel movement of smallmouth yellowfish Labeobarbus aeneus in the Vaal River,South Africa

Diel movements of Orange–Vaal smallmouth yellowfish Labeobarbus aeneus (Burchell, 1822) in the Vaal River, South Africa, were determined by externally attaching radio transmitters to 11 adult fish and manually tracking them between March and May 2012. Twenty-four radio telemetry monitoring surveys produced 2 304 diel tracks. At night, yellowfish displayed a preference for slow shallow (<0.3?m s?1, <0.5?m) and fast shallow habitats (>0.3?m s?1, <0.3?m), whereas by day they avoided these habitats, preferring fast deep areas (>0.3?m s?1, >0.3?m). The average total distance of 272?m moved per 24-hour period was three times greater than the diel range, and the average maximum displacement per minute was significantly higher in daytime (4?m) than at night (1.5?m). These findings suggest that L. aeneus is active primarily during the day in fast-flowing, deeper waters, and relatively inactive at night, when it occupies shallower habitats. This behaviour should be further explored to identify causal mechanisms underlying the diel habitat shifts in this species such as water temperature, foraging tactics and/or predator avoidance.     

The impact of encroachment of mangroves into saltmarshes on saltwater mosquito habitats

Will mangrove encroachment into saltmarshes affect saltwater mosquito habitats? To address this, we synthesized information from two perspectives: 1) at a detailed level, the immature mosquito habitat within mangroves; 2) at a more general or regional level, changes due to mangrove expansion into saltmarshes. This is a synthesis of two research projects. One showed that mosquito larval habitats in mangroves are complex, related to the detailed interactions between topography and tidal patterns and that not all parts of a mangrove forest are suitable habitat. The other, based on remote sensing and analysis of rainfall data, showed that mangrove encroachment in eastern Australia is related to both climate and human land use over several decades (1972–2004). An important question emerged: when mangroves encroach into saltmarshes will they displace saltmarsh immature mosquito habitats or will they replace them with mangrove ones? There is no simple answer: it will vary with climate change and sea level scenario and how these affect the system. We conclude that mosquito management, which is locally implemented, needs to be integrated with land use planning systems, which often operate at a more general level.     

Invasiveness,invasibility and the role of environmental stress in the spread of non-native plants

Invasion ecology, the study of how organisms spread in habitats to which they are not native, asks both about the invasiveness of species and the invasibility of habitats: Which species are most likely to become invasive? Which habitats are most susceptible to invasion? To set the stage for considering these questions with regard to plants, we offer a two-way classification of nativeness and invasiveness that distinguishes natives, non-invasive non-natives and invasive non-natives. We then consider the current state of knowledge about invasiveness and invasibility. Despite much investigation, it has proven difficult to identify traits that consistently predict invasiveness. This may be largely because different traits favour invasiveness in different habitats. It has proven easier to identify types of habitats that are relatively invasible, such as islands and riverbanks. Factors thought to render habitats invasible include low intensities of competition, altered disturbance regimes and low levels of environmental stress, especially high resource availability. These factors probably often interact; the combination of altered disturbance with high resource availability may particularly promote invasibility. When biotic factors control invasibility, non-natives that are unlike native species may prove more invasive; the converse may also be true. We end with a simple conceptual model for cases in which high levels of environmental stress should and should not reduce invasibility. In some cases, it may be possible to manipulate stress to control biological invasions by plants.     

Important foliar traits depend on species-grouping: analysis of a remnant temperate forest at the Keerqin Sandy Lands, China

Foliar traits are often interpreted to reflect strategies for coping with water and nutrient supply limitations. In this study, we measured several important leaf traits for 147 species sampled from a remnant, temperate deciduous broad-leaved forest in Keerqin Sandy Lands, Northeast China to test whether these traits are ‘invariant’ or dependent on water supply limitations. Our data show that average specific leaf area (SLA), nitrogen (N) and phosphorus (P) concentrations, leaf C/N, C/P and N/P were 273 cm²?g^?1, 18.1 mg?g^?1, 1.60 mg?g^?1, 28.2, 343 and 12.4, respectively. However, most of these traits were significantly different (P?<?0.05) for different species groupings based on growth forms, phylogenetic history, photosynthetic pathways, or habitats. SLA was positively correlated with leaf P concentration across the broad spectrum of 118 species and most species functional groupings. However, SLA was not correlated with N concentration across all species or within each species functional group. SLA and N and P concentrations in dry habitats were lower than those in wet habitats, whereas leaf C/N, C/P, and N/P had the opposite trend both across all species and within major species functional groupings (herb, monocots and C3 species). Our data indicate that SLA vs. leaf N and SLA vs. P relationships may be regulated differentially for different species functional groupings and that water limitation may have a greater influence than nutrient limitation for plant growth.     

Vegetation structure and pollination in the Venezuelan Central Plain

Classes of pollination agents and pollination system specificities were evaluated according to the vegetation structure in the Venezuelan Central Plain. Two main questions were examined: (i) Do the frequencies of pollination categories estimated at plant species level differ from those estimated considering plant abundance? and (ii) Does plant abundance differ according to categories of pollination in the context of each vegetation attribute? The frequencies of classes of pollination agents and systems of pollination specificity were estimated at plant species and plant abundance level for the community, habitats, life-forms, strata, horizontal disposition, and season. Besides, plant abundance of each category of pollination agent classes and systems of pollination specificity were statistically compared. Most of the comparisons between the frequency of plant species and plant abundance were non-significant (58.3%). The multivariate classifications of life-forms and habitats according to pollination agent classes using plant species and plant abundance separately are very similar. In both analyses, perennial herbs come out as a separate group, which is associated with a comparable frequency distribution of pollination agent classes. The frequency distributions of polyphilous, oligophilous, and monophilous species were statistically higher for plant abundance than for plant species in the disturbed area and in the lowest stratum (D), which is primarily associated with the relation between life-forms and vegetation strata. The average values of abundance for wind-pollinated plants were found to be larger than those for other categories of pollination systems specificity and pollination agent classes, respectively, in the forest–savanna transition and overall community. All anemephilous species have clumped distribution and plant abundance was higher in this case than what was found with the other categories of pollination specificity with clumped distribution. Estimates of pollination agent classes at plant species level proved to be a practical method to estimate pollination frequency, mainly for those studies related to the floristic composition of the community. The large values of abundance for wind-pollinated species are in concordance with the savanna–forest mosaic vegetation growing in the Venezuelan Central Plain, but are in contrast with the comparatively low percentage of wind-pollinated species recorded.     

Evaluation of macrofaunal effects on leaf litter breakdown rates in aquatic and terrestrial habitats

Abstract Decomposition of the organic matter is a key process in the functioning of aquatic and terrestrial ecosystems, although different factors influence processing rates between and within these habitats. Most patterns were described for temperate regions, with fewer studies in tropical, warmer sites. In this study, we carried out a factorial experiment to compare processing rates of mixed species of leaf litter between terrestrial and aquatic habitats at a tropical site, using ?ne and coarse mesh cages to allow or prevent colonization by macroinvertebrates. The experiment was followed for 10 weeks, and loss of leaf litter mass through time was evaluated using exponential models. We found no interaction between habitat and mesh size and leaf litter breakdown rates did not differ between ?ne and coarse mesh cages, suggesting that macroinvertebrates do not influence leaf litter decomposition in either habitat at our studied site. Leaf breakdown rates were faster in aquatic than in terrestrial habitats and the magnitude of these differences were comparable to studies in temperate regions, suggesting that equivalent factors can influence between‐habitat differences detected in our study.     

Deciphering the distribution of the savanna biome

? We aimed to identify the limits of savanna across Africa, Australia and South America. We based our investigation on the rich history of hypotheses previously examined: that the limits of savanna are variously determined by rainfall, rainfall seasonality, soil fertility and disturbance. ? We categorized vegetation on all continents as 'savanna' (open habitats with a C(4) grass layer) or 'not-savanna' (closed habitats with no C(4) grass layer) and used a combination of statistical approaches to examine how the presence of savanna varied as a function of five environmental correlates. ? The presence of savanna is constrained by effective rainfall and rainfall seasonality. Soil fertility is regionally important, although the direction of its effect changes relative to rainfall. We identified three continental divergences in the limits of savanna that could not be explained by environment. ? Climate and soils do not have a deterministic effect on the distribution of savanna. Over the range of savanna, some proportion of the land is always 'not-savanna'. We reconciled previous contradictory views of savanna limits by developing a new conceptual framework for understanding these limits by categorizing environmental factors into whether they had a positive or negative effect on woody growth and the frequency of disturbance.     

A survey and GIS-based estimate of the breeding population of Great Snipe Gallinago media in Central Norway

Capsule By using a GIS-model to identify suitable breeding habitats for Great Snipe in Central Norway, we estimated a total of 276 leks holding approximately 2700 males.

Aim To estimate the size of the Great Snipe population in central parts of the species remaining breeding areas in Western Europe.

Methods GIS-analysis identified an area of 528?km² as suitable habitat for Great Snipe in the total study area (22?000?km²). Complete surveys were made in 8% of these habitats by using a subset of 53 sampling areas.

Results A total of 28 Great Snipe leks were found within the sampling areas. Ten of these were found in previously known lek areas, while 18 leks were found in areas with no previous knowledge of leks. Extrapolating the lek density and the lek size found in the surveyed areas, resulted in a total estimate of 276 Great Snipe leks holding approximately 2700 lekking males. The leks were found on open fens along the forest edge and were mainly situated on base-rich bedrocks. Mean altitude of the leks was 570?m.

Conclusion The total population of Great Snipe in Norway was previously assumed to comprise 5000–15?000 lekking males or ‘pairs'. By extrapolating the densities of leks found in Central Norway to a national scale, we expect the true breeding population of Great Snipe to be approximately 13?500 males. Changes in the elevation of the tree limit and increased overgrowth, as a result of reduced grazing pressure and/or global warming, are possible threats that may reduce the availability of preferred Great Snipe habitats and increase population fragmentation.     

Comparative analysis of environmental sequences: potential and challenges

Environmental sequencing, also dubbed metagenomics, is increasingly being used to obtain insights into organismal communities in diverse habitats, and has a variety of potential applications foreseeable in biotechnology and medicine. The first public large-scale data provide already a wealth of information hidden in vast amounts of fragmented pieces of DNA from unknown species residing in these environments. Comparative sequence analysis is essential for the interpretation of such data. However, different layers of complexity that are intrinsic to each sample require the establishment of some baselines for comparison: how to normalize for the differences in phylogenetic and functional diversity, how to avoid biases from incomplete data, and how to deal with differences in species dominance or genome sizes? Here we discuss a few of these items and delineate some simple discriminative sequence properties for four distinct habitats.     

Moss Communities and Their Characteristics in Ice-free Areas of the Windmill Islands,Wilkes Land,Continental Antarctica

The moss vegetation of the Windmill Islands can be classified into the following seven communities: 1.Grimmia antarctici community; 2. G. antarctici-Ceratodon purpureus community; 3. Bryum pseudotriquetrum community; 4. G. antarctici-B, pseudotriquetrum community; 5. Ceratodon purpureus community; 6. C. purpureus-G, antarctici community; 7. C. purpureus B. pseudotriquetrum community. Communities 1, 3, 4 and 7 occur in wet habitats while communities 5 and 6 are found in rather dry habitats, community 2 distributes between dry and wet habitats. Microtopography governs the distribution of water supply and therefore community types. Stable moss communities usually form moss hummocks and hollows. Species composition, colour and height of the hummocks determines the vertical structure of the moss community layers with 2-3 strata being discernible and level structure forming mosaic. Other phytocoenological characteristics of the moss communities, such as the dense moss cushions, asexual reproduction (although antheridia or archegonia have been found in each of the species), abundance of epiphytic algae and lichens growing on the surface of moss hummocks, the colour change of some species in different habitats, appear related to moisture availability, light intensity, wind exposure and temperature.     

Taxonomy of estuarine invertebrates in Australia

An Australian estuary is primarily a marine-dominated environment, subjected to major salinity changes only after heavy rains and during flood conditions. In southeastern Australia estuarine biota are similar to those in shallow coastal bays and some of the coastal lagoons, and most taxonomic studies on estuarine fauna have occurred in this region. Several major surveys of estuarine and coastal bays have been undertaken in Australia during the past three decades and these surveys have largely provided the material for taxonomic studies of the major groups of macrobenthos. All these studies have revealed a diverse and abundant benthic macrobenthos. The composition of estuarine invertebrate fauna is compared with open exposed coasts, including fauna found in soft strata and on hard strata. Australia has a limited specialized estuarine biota much of which is restricted to particular habitats, and a highly diverse marine community which thrives in the sheltered protected waters of estuaries and the associated soft sediments. Currently, interactive computer-based keys are being developed which should greatly assist the student and the benthic ecologist to identify the fauna and prevent potential loss of data. Some aspects of the current debate of the level of taxonomic resolution required to answer various ecological questions are discussed. Finally, some comments are suggested as to future directions in which taxonomists and estuarine ecologists should proceed in order to be able to detect changes or losses of estuarine biodiversity and the loss of the associated biological information which may be critical in understanding the functioning of the estuarine ecosystem.     

Increasing arboreality with altitude: a novel biogeographic dimension

Biodiversity is spatially organized by climatic gradients across elevation and latitude. But do other gradients exist that might drive biogeographic patterns? Here, we show that rainforest''s vertical strata provide climatic gradients much steeper than those offered by elevation and latitude, and biodiversity of arboreal species is organized along this gradient. In Philippine and Singaporean rainforests, we demonstrate that rainforest frogs tend to shift up in the rainforest strata as altitude increases. Moreover, a Philippine-wide dataset of frog distributions shows that frog assemblages become increasingly arboreal at higher elevations. Thus, increased arboreality with elevation at broad biogeographic scales mirrors patterns we observed at local scales. Our proposed ‘arboreality hypothesis’ suggests that the ability to exploit arboreal habitats confers the potential for larger geographical distributions because species can shift their location in the rainforest strata to compensate for shifts in temperature associated with elevation and latitude. This novel finding may help explain patterns of species richness and abundance wherever vegetation produces a vertical microclimatic gradient. Our results further suggest that global warming will ‘flatten’ the biodiversity in rainforests by pushing arboreal species towards the cooler and wetter ground. This ‘flattening’ could potentially have serious impacts on forest functioning and species survival.