Giants on the landscape: modelling the abundance of megaherbivorous dinosaurs of the Morrison Formation (Late Jurassic,western USA)

The ecosystem impact of megaherbivorous dinosaurs of the Morrison Formation would have depended on their abundance (number of animals per unit of habitat area) on the landscape. We constrain Morrison megaherbivore abundance by modelling dinosaur abundance in terms of carrying capacity (K), average body mass (ABM) and animal's energy needs. Two kinds of model are presented: ‘demand-side’ models that estimate K in terms of the aggregate energy demand of the dinosaur community, and ‘supply-side’ models that estimate K in terms of retrodicted primary productivity. Baseline values of K, ABM and energy needs for the models are further derived from comparisons with modern large herbivores, and from the composition of the megaherbivore fauna from a particular stratigraphic interval of the Morrison, but in all models a broad range of fractions and multiples of these baseline parameters are considered. ‘Best-guess’ estimates of Morrison megaherbivore abundance suggest an upper limit of a few hundred animals across all taxa and size classes per square kilometre, and up to a few tens of individuals of large subadults and adults.     

Environmental and resource burdens associated with world biofuel production out to 2050: footprint components from carbon emissions and land use to waste arisings and water consumption

Environmental or ‘ecological’ footprints have been widely used in recent years as indicators of resource consumption and waste absorption presented in terms of biologically productive land area [in global hectares (gha)] required per capita with prevailing technology. In contrast, ‘carbon footprints’ are the amount of carbon (or carbon dioxide equivalent) emissions for such activities in units of mass or weight (like kilograms per functional unit), but can be translated into a component of the environmental footprint (on a gha basis). The carbon and environmental footprints associated with the world production of liquid biofuels have been computed for the period 2010–2050. Estimates of future global biofuel production were adopted from the 2011 International Energy Agency (IEA) ‘technology roadmap’ for transport biofuels. This suggests that, although first generation biofuels will dominate the market up to 2020, advanced or second generation biofuels might constitute some 75% of biofuel production by 2050. The overall environmental footprint was estimated to be 0.29 billion (bn) gha in 2010 and is likely to grow to around 2.57 bn gha by 2050. It was then disaggregated into various components: bioproductive land, built land, carbon emissions, embodied energy, materials and waste, transport, and water consumption. This component‐based approach has enabled the examination of the Manufactured and Natural Capital elements of the ‘four capitals’ model of sustainability quite broadly, along with specific issues (such as the linkages associated with the so‐called energy–land–water nexus). Bioproductive land use was found to exhibit the largest footprint component (a 48% share in 2050), followed by the carbon footprint (23%), embodied energy (16%), and then the water footprint (9%). Footprint components related to built land, transport and waste arisings were all found to account for an insignificant proportion to the overall environmental footprint, together amounting to only about 2%     

Long‐distance signals influence assessment of close range mating displays in the field cricket,Gryllus integer

Male sexual displays often include components detected across long distances, and those perceived only at close range. Understanding what information females gain from each component of a complex display and how they use these signals to make decisions are questions of major interest in sexual selection research. We evaluated content‐based hypotheses (‘redundant signals’ and ‘multiple messages’) for the courtship displays of field crickets (Gryllus integer) by measuring female responses to males' long‐distance calling song (calls) and close‐range chemical cues. Females' responses to a male's calls and chemical cues were uncorrelated, supporting the ‘multiple messages’ hypothesis. We also tested the ‘inter‐signal interaction’ hypothesis by investigating how long‐distance calls influence evaluation of close‐range courtship. The relationship between long‐ and close‐range signals was complex and conditional: females accepted close‐range courtship more quickly after exposure to attractive calling song than they did after exposure to either unattractive calling song or silence, and unattractive calls were no more or less effective than silence. This inter‐signal interaction could affect our understanding of mate choice in species with multiple mating signals because it implies that females may save time and energy by not assessing the close‐range signals of attractive long‐distance signalers. © 2010 The Linnean Society of London, Biological Journal of the Linnean Society, 2010, 100 , 856–865.     

The ‘n’ effect in molecular recognition

The cooperativity which exists in crystal melting and many biological molecular recognition phenomena arises from extended arrays of weak interactions. We present a correlation between the melting temperature of a crystal and the intermolecular energy (which is evident only when compounds possessing several or many internal rotors are excluded). The correlation is used as the basis for a model of crystal melting which is capable of estimating the melting temperature of crystals. This model provides the basis for an understanding of the sharpness of the crystal melting transition for organic and inorganic substances. The cooperativity illustrated by the extended arrays of weak interactions, or the ‘n’ effect, is extended to analogous order/disorder transitions in biological systems, such as the ‘melting’ of DNA and RNA duplexes, providing insights into the physical properties of these structures.     

Does the presence of grassy strips and landscape grain affect the spatial distribution of aphids and their carabid predators?

• 1 We investigated, over the course of 2 years, the spatial distribution and abundance of two species of aphid, Metopolophium dirhodum and Sitobion avenae, and predatory species of carabid. This was undertaken in 24 wheat fields in ‘coarse‐grain’ and ‘fine‐grain’ landscapes in western France. A greater percentage of the latter landscape was covered by hedgerows and grassland and the total area covered by fields and the average size of the fields were smaller.
• 2 The effects on aphid abundance of the distance from field margins, the presence of grassy strips and carabid abundance were determined in both landscapes.
• 3 Both aphid species were more abundant in the ‘fine‐grain’ landscape, which may have been a result of the higher density of semi‐natural elements. In both types of landscape, the total numbers of aphids were negatively correlated with the distance from the field margin. This may have been because aphids were dispersing from overwintering sites in field margins. The abundance of M. dirhodum was strongly negatively correlated with the presence of grassy strips in the ‘coarse‐grain’ landscape, although there were no such significant correlations for either of the aphid species in the ‘fine‐grain’ landscape.
• 4 Aphid and carabid abundances were negatively correlated in the ‘fine‐grain’ and positively in ‘coarse‐grain’ landscape.
• 5 The results obtained in the present study emphasize the importance of semi‐natural areas in agricultural landscapes in shaping the spatial distribution of aphids and carabid beetles, their natural enemies, at different spatial scales.

     

Symbiont community diversity is more variable in corals that respond poorly to stress

Coral reefs are declining globally as climate change and local water quality press environmental conditions beyond the physiological tolerances of holobionts—the collective of the host and its microbial symbionts. To assess the relationship between symbiont composition and holobiont stress tolerance, community diversity metrics were quantified for dinoflagellate endosymbionts (Family: Symbiodiniaceae) from eight Acropora millepora genets that thrived under or responded poorly to various stressors. These eight selected genets represent the upper and lower tails of the response distribution of 40 coral genets that were exposed to four stress treatments (and control conditions) in a 10‐day experiment. Specifically, four ‘best performer’ coral genets were analyzed at the end of the experiment because they survived high temperature, high pCO₂, bacterial exposure, or combined stressors, whereas four ‘worst performer’ genets were characterized because they experienced substantial mortality under these stressors. At the end of the experiment, seven of eight coral genets mainly hosted Cladocopium symbionts, whereas the eighth genet was dominated by both Cladocopium and Durusdinium symbionts. Symbiodiniaceae alpha and beta diversity were higher in worst performing genets than in best performing genets. Symbiont communities in worst performers also differed more after stress exposure relative to their controls (based on normalized proportional differences in beta diversity), than did best performers. A generalized joint attribute model estimated the influence of host genet and treatment on Symbiodiniaceae community composition and identified strong associations among particular symbionts and host genet performance, as well as weaker associations with treatment. Although dominant symbiont physiology and function contribute to host performance, these findings emphasize the importance of symbiont community diversity and stochasticity as components of host performance. Our findings also suggest that symbiont community diversity metrics may function as indicators of resilience and have potential applications in diverse disciplines from climate change adaptation to agriculture and medicine.     

The canopy beetle faunas of Gondwanan element trees in Chilean temperate rain forests

Aim To describe the coleopteran fauna occurring in canopies of temperate Gondwanan tree species in terms of their diversity and guild and taxonomic structures, and to test the proposition that this structuring reflects the Gondwanan origins of this fauna. Location The Andes and the coastal cordillera of temperate Chile. Methods Canopy fogging was used to sample beetles from 29 trees. The samples were statistically described using S_chao and the Simpson diversity index D. Cluster analyses and multi‐dimensional scaling (MDS) were performed. The taxonomic and guild structures of the Chilean coleopteran fauna were compared quantitatively with those found in other parts of the world using homogeneity chi‐square and t‐tests. Results A collection of 25,497 beetle specimens was obtained primarily from Nothofagus dombeyi, Nothofagus obliqua and Araucaria araucana. The specimens collected were distributed between 485 morphospecies and included 107 putative, new generic‐level taxa and 223 apparently undescribed species. Estimates of the size of the canopy beetle fauna showed that 600+ species were likely to be present. The communities found on a tree species differed markedly between years. MDS plots showed less community divergence between tree species for predators than for phytophages and xylophages. The guild structure was similar to that found on Australian ‘Gondwanan’ trees but differed significantly from the community structures found on ‘Laurasian’ tropical and temperate trees in supporting fewer phytophages and saprophages, but more xylophages. The predator guild showed a different pattern, with tropical faunas differing from those of more temperate regions, irrespective of hemisphere, as did the distribution of superfamilies. Main conclusions The beetle fauna found in the canopies of N. dombeyi, N. obliqua and A. araucana was large (600+ species), with about half of the species undescribed. S_chao was found to vary with sample size and to give lower estimates of S than species attenuation curves, raising the possibility that the two methods are estimating the sizes of different statistical communities. It is possible that the attenuation curve is estimating the number of species to be found on a particular tree species, while S_chao is estimating the ‘carrying capacity’ for beetle species of individual trees, and this varies from tree to tree. Care also needs to be taken in experimental design when monitoring temporal changes in forest insect communities given the difference in communities found between years in this study. The proportions of phytophages, saprophages and xylophages resemble those of a ‘Gondwanan’ rain forest from Australia and differ significantly from those of tropical and temperate ‘Laurasian’ forests.     

Geographical gradients of species richness: a test of the water‐energy conjecture of Hawkins et al. (2003) using European data for five taxa

Aims We present an analysis of grid‐based species‐richness data for European plants, mammals, birds, amphibians and reptiles, designed to test the proposition of Hawkins et al. (2003a ) that the single best factor describing richness variation switches from the water regime to the energy regime in the mid‐latitudes and that the ‘breakpoint’ is related to the physiological character of the taxa. We go on to develop subregional models showing the extent to which regional model fits vary as a function of the extent of the study system, and compare the relative performance of ‘water’, ‘energy’ and ‘water–energy’ models of richness for southern, northern and pan‐European models. Location Western Europe. Methods We use atlas data comprising species range data for 187 species of mammals, 445 species of breeding birds, 58 amphibians, 91 reptiles and 2362 plant species, inserted into a c. 50 × 50 km grid cell system. We used 11 modelled climate variables, averaged for the period 1961–90. Statistical analyses were carried out using generalized additive models (GAMs), with splines simplified to a maximum of four degrees of freedom, and we tested for spatial autocorrelation using Moran's I values obtained at 10 different distance intervals. We selected favoured models on the grounds of deviance explained combined with a simple parsimony criterion, such that we selected either: (1) the best two‐variable energy, water or water–energy model, or (2) a four‐variable water–energy model, where the latter improved on the best two‐variable model by a minimum of 5% deviance explained. Results Threshold energy values, at which richness shows a transition from an increasing to a decreasing function of annual solar radiation, were identified for all taxa apart from reptiles. We found conditional support for the switch from dominance of water variables (southern models) to energy variables (northern models). Our favoured models switched between ‘water’ and ‘energy’ for mammals, and between ‘energy’ and ‘water–energy’ for birds, depending on whether we used data of pan‐European extent, southern or northern subsets. Deviance explained in our favoured models varied from 15% (birds, southern Europe) to 72% (amphibians, northern Europe), i.e. ranging from very poor to good fits with the data. Comparison with previous work indicates that our models are generally consistent with (if sometimes weaker than) previous findings. Main conclusions Our models are incomplete representations of factors influencing macro‐scale richness patterns across Europe, taking no explicit account of, for example, topographic variation, human influences or long‐term climatic variation. However, with the exception of birds, for which only the northern model attains over one‐third deviance explained, the models show that climate can account for meaningful proportions of the deviance. We find general support for considering water and energy regimes together in modelling species richness, and for the proposition that water is more limiting in southern Europe and energy in the north. Our analyses demonstrate the sensitivity of model outcomes to the geographical location and extent of the study system, illustrating that simple curve‐fitting exercises like these, particularly if based on regions with the complex history and geography characteristic of Europe, are unlikely to provide the basis for global, predictive models. However, such exercises may be of value in detecting which aspects of water and energy regimes may be of most importance in refining independently generated global models for regional application.     

Periphyton responds differentially to nutrients recycled in dissolved or faecal pellet form by the snail grazer Theodoxus fluviatilis

1. We aimed to separate the effects of grazers on periphyton via grazing from that of nutrient recycling from their faecal pellets. 2. We set up three different experimental treatments (snails/no snails/faecal pellets) and sampled over 16 days. The ‘snail’ treatment contained a low density (snail biomass c. 14 g^?2) of the gastropod grazer Theodoxus fluviatilis and the ‘faecal pellet’ treatment received the same amount of faecal pellets as were produced in the ‘snail’ treatment. Whereas the ‘faecal pellet’ treatment provided extra nutrients to periphyton from the faeces, the ‘snail’ treatment provided nutrients in the form of both faeces and in excreta. There was also direct grazing on periphyton in the ‘snail’ treatment. The ‘no snail’ was not grazed and received no nutrients in faeces or excreta. 3. We measured periphyton C, N and P content, chlorophyll‐a (chl‐a), primary production, bacterial biomass, bacterial production and bacterial respiratory activity. In the water column we measured dissolved inorganic N and soluble reactive P. 4. Snails increased the amount of dissolved inorganic N in the water. On day 16, the periphyton N : P ratio in the ‘faecal pellet’ treatment was lower, and periphyton P content was higher, than in the other two treatments. N : P ratios decreased over time in the ‘faecal pellet’ treatment. Primary and bacterial production were positively correlated in all treatments. 5. Algal chl‐a and primary production of periphyton per unit area and periphyton chl‐a : C ratios increased over the 16 day in the ‘snail’ treatment, and thus excretion of dissolved N by snails had a stronger positive effect on the periphyton community than N and P in faecal pellets. 6. Our data show that excretion and egestion can have different effects on periphyton, probably because of the higher proportion of dissolved N in excreta and the higher proportion of P recycled in faecal pellets. The relative effect of nutrients recycled in egesta or in excretions, probably depends on the form of nutrient limitation of the periphyton. Further, the different components of the periphyton matrix could react differently to the different forms of nutrient recycling. 7. We conclude that direct grazing effects are less important than nutrient effects when nutrients are limiting and grazing pressure is low. Further, the spatial separation of different grazing effects can lead to differences in periphyton production and nutrient stoichiometry. This might be an explanation for the patchiness of periphyton in nature.     

Palaeontology., adaptation and community ecology: A response to Walter and Pater son (1994)

Abstract This paper challenges Walter and Paterson's (1994) assertion that the community concept ought to be abandoned because of recent palaeontological evidence pointing to the ‘individualistic’ nature of biological communities. The ‘individualistic’ versus ‘superorganismic’ community concepts might provide good grist for the philosophical mill, but have little practical relevance to contemporary community ecology. Ecologists define communities in terms of current species distributions and interactions, and seek to integrate the roles of both biotic and abiotic factors influencing species distributions. There is no assumption of tight co-evolution among component species; Walter and Paterson confuse ‘organization’ with ‘co-adaptation’. Nor, contrary to the authors’ claims, is there an implicit assumption that all community patterns are caused by competition. For most ecologists, the ‘competition debate’ ended a decade ago. Walter and Paterson's view that competition is rarely, if ever, important in structuring communities is not even held by the main protaganists of the ‘competition is not so important’ school of the 1980s, and is in direct contradiction of the extensive, more recent literature on the subject. It entirely ignores plant ecology. Many of Walter and Paterson's misunderstandings appear to arise from the false premise that explanation of adaptation should be the ultimate goal of any ecological discipline. The authors are hostile to community ecology because, if communities are individualistic, then little light can be shed on species adaptations. Fortunately, most ecologists are not so preoccupied with adaptation.     

Components of partial resistance to Septoria nodorum in winter wheat

Components of partial resistance to Septoria nodorum were investigated in 10 cultivars of winter wheat having similar field resistances. The components measured were infection frequency, latent period, size, shape and rate of growth of lesions, spore production and its rate of increase. Latent period was found to be lognormally distributed. Some of the components of resistance were found to be significantly different between cultivars. Cluster analysis also showed that cultivars could be distinguished on the basis of their components of resistance. Principal components analysis indicated that resistance could be broken down into four underlying factors, three of which could be readily interpreted. The measurements of the components of resistance were combined in a model, the r-index, based on Van der Plank's r. The amount of variation between cultivars cast some doubt on the predictive value of the index but all the cultivar values were well within the range bounded by two ‘synthetic’ cultivars made up of combinations of either the most resistant or the most susceptible components. It is considered that the r-index has potential in screening for field resistance. The possibility of incorporating the most resistant-type components into one cultivar is discussed. The use of cultivar mixtures containing cultivars having similar field resistances is also discussed in the light of the variability found in this study.     

Archaeal and bacterial communities in geochemically diverse hot springs of Yellowstone National Park, USA

Microbiological and geochemical surveys were conducted at three hot springs (Obsidian Pool, Sylvan Spring, and ‘Bison Pool’) in Yellowstone National Park (Wyoming, USA). Microbial community structure was investigated by polymerase chain reaction (PCR) amplification of 16S rRNA gene sequences from DNA extracted from sediments of each hot spring, followed by molecular cloning. Both bacterial and archaeal DNA was retrieved from all samples. No Euryarchaea were found, but diverse Crenarchaea exist in all three pools, particularly affiliating with deep‐branching, but uncultivated organisms. In addition, cloned DNA affiliating with the Desulphurococcales and Thermoproteales was identified, but the distribution of taxa differs in each hot spring. The bacterial community at all three locations is dominated by members of the Aquificales and Thermodesulfobacteriales, indicating that the ‘knallgas’ reaction (aerobic hydrogen oxidation) may be a central metabolism in these ecosystems. To provide geochemical context for the microbial community structures, energy‐yields for a number of chemolithoautotrophic reactions are provided for >80 sampling sites in Yellowstone, including Obsidian Pool, Sylvan Spring, and ‘Bison Pool’. This energy profile shows that the knallgas reaction is just one of many exergonic reactions in the Yellowstone hot springs, that energy‐yields for certain reactions can vary substantially from one site to the next, and that few of the demonstrated exergonic reactions are known to support microbial metabolism.     

The balance between the foliage projective covers of overstorey and understorey strata in Australian vegetation

Foliage Projective Cover of the overstorey (canopy) of a‘climax’community appears to reach an equilibrium value determined largely by the prevailing climate. Overstorey FPC decreases in‘climax’communities in a graded series from humid to arid regions. Understorey cover (of all strata below the canopy) in‘climax’communities attains a balance with overstorey FPC. Disturbance (gaps, microhabitats, fire, overgrazing, invasion of woody weeds, etc.) may reduce the overstorey cover which will be compensated by an increase in understorey cover. Secondary succession back to the‘climax’structure will follow a path maintaining an inverse linear relationship between understorey cover and overstorey cover. At the same time, species diversity appears to decrease as overstorey cover increases.     

Four decades of old field vegetation development and the role of Celastrus orbiculatus in the northeastern United States

Abstract. This paper describes four decades of in situ vegetation change in a post-agricultural site in southern New England where the role of the introduced vine, Celastrus orbiculatus, has drastically modified the course of vegetation development. An initial perennial forb-grassland community was replaced by two strikingly different physiognomic vegetation types-an early hardwood forest and a vine community occupying the same site 40 yr later. This ecological phenomenon was unpredictable since Celastrus was not recorded at the site until the 1970s. Within the young hardwood forest dominated by Prunus serotina and Acer rubrum, a few old field species (five) persist, whereas 17 forest herbs have become established. Typical forest shrubs are rare or absent. The Celastrus-dominated vine community has suppressed or eliminated pre-existing growth to form a relatively stable community where a forest vegetation is the regional vegetation type. Celastrus also appears to be facilitating a native vine (Vitis labrusca) by forming a ‘ladder’ for its advance. Although A. rubrum and Quercus spp. could ultimately dominate the forest community, the contiguous and aggressive nature of Celastrus makes predictions questionable. This long-term study highlights the unpredictable nature of old field succession and the role of an exotic species in threatening the natural vegetation development.     

The virtual eco-costs ‘99 A single LCA-based indicator for sustainability and the eco-costs-value ratio (EVR) model for economic allocation

In literature, many models (qualitatively as well as quantitatively) can be found to cope with the problem of communicating results of LCA analyses with decision takers. In a previous article of this Journal, an LCA-based single indicator for emissions is proposed: the ‘virtual pollution prevention costs ‘99’ (Vogtländer et al. 2000a). In this article, a single LCA-based indicator for sustainability is proposed. It builds on the virtual pollution prevention costs ‘99 for emissions, and adds the other two main aspects of sustainability: material depletion and energy consumption. This single indicator, the ‘virtual eco-costs ‘99’, is the sum of the marginal prevention costs of:

Material depletion, applying ‘material depletion costs’, to be reduced by recycling

Energy consumption, applying ‘eco-costs of energy’ being the price of renewable energy

Toxic emissions, applying the ‘virtual pollution prevention costs ‘99’

The calculation model includes ‘direct’ as well as ‘indirect’ environmental impacts. The main groups of ‘indirect’ components in the life cycle of products and services are:

Labour (the environmental impacts of office heating, lighting, computers, commuting, etc.)

production assets (equipment, buildings, transport vehicles, etc.)

To overcome allocation problems of the indirect components of complex product-service systems, a methodology of economic allocation has been developed, based on the so called Eco-costs/ Value Ratio (EVR) model. This EVR calculation model appears to be a practical and powerful tool to assess the sustainability of a product, a service, or a product-service combination.     

Recognizing cross‐ecosystem responses to changing temperatures: soil warming impacts pelagic food webs

The energy and materials that move across ecosystem boundaries influence food web structure and key ecosystem functions. Despite the acknowledged importance of such ecological subsidies, surprisingly little information is available regarding the role of environmental temperature in influencing subsidy quality and the response of the recipient ecosystem. We evaluated the impacts of temperature‐mediated changes in leaves from deciduous trees, an important subsidy from terrestrial to freshwater ecosystems, on both the producer‐based and detritivore‐based components of a pelagic pond food web in a field mesocosm experiment. We hypothesized that variation in leaf chemistry driven by increased soil temperature would alter both the quality of leaf subsidies and the pond response. We collected red maple Acer rubrum leaves from heated and ambient temperature plots from the long‐term soil warming experiment at the Harvard Experimental Forest and added them to 167‐l field mesocosms containing established plankton communities, creating ‘no leaf’, ‘ambient leaf’ and ‘heated leaf’ treatments during autumn 2012. We then monitored physical, chemical, and biological responses to treatments until the mesocosms froze six weeks later. Experimental soil warming altered the chemical composition of deciduous leaves, the physical and chemical environment of the aquatic ecosystems to which leaves were added, and the pelagic pond food webs as measured by community composition. Compared to leaves from ambient‐temperature soils, leaves from warmed soils initially resulted in lower water column phosphorus and dissolved organic carbon, reducing bacterial densities. However, the diminished carbon and phosphorus resulting from soil warming also increased light availability that ultimately stimulated cladoceran zooplankton relative to ambient‐temperature leaves. Our results suggest that changes in temperature can alter ecological subsidies in unanticipated ways, and suggest that accurately predicting the potential consequences of climate change will require conducting research across ecosystem boundaries.     

Component analysis and modelling of the movement process: Analysis of simple tracks

The construction of a general model of animal movement using the ‘experimental components' approach ofC. S. Holling is proposed. The process of ‘movement’ is interpreted very generally as any displacement of the whole organism in space. The rationale for modelling such processes rests upon the idea that there is a basic “canonical” pattern of movement characteristic of a species moving in a homogeneous environment, which pattern is overlaid by the various directional stimuli present in more usual heterogeneous environments. The ‘canonical movement model’ is a necessary first step in construction of more realistic representations. We suggest it can be made using six components viz. the initial heading of the animal, the mean and variance of the angular displacements made by the animal as it moves, the mean and variance of the speed of the animal, and a term for the continuity of the movement. We have measured all these components in the field for the two-dimensional movement of the inter-tidal snail, Polinices incei and these results are presented here. Difficulties inherent in the measure ment of angular displacement in particular are discussed and means of resolving them proposed. The shortcomings involved in the measurements and techniques for their more detailed representation and the next steps in the proposed modelling sequence are discussed.     

The effects of shrimps on benthic material in a Brazilian island stream

1. Shrimps are abundant in many tropical coastal streams. Studies in Central America and the Caribbean have demonstrated the importance of shrimps in removing sediments and altering the composition of the benthos. Previous work in our study area showed that ephemeropterans and not shrimps were important in removing benthic material. 2. Here we used an experimental exclusion to test the hypothesis that shrimps exert strong influence on sediment dynamics with direct and indirect effects on the benthic algal and faunal community at a site where they are the predominant element of macrofauna. We used electricity to exclude Macrobrachium olfersi and Potimirim glabra from small quadrats (0.135 m²) for 34 days in a stream located at Ilha Grande, Rio de Janeiro state, Brazil. We analysed benthic sediment dynamics and community colonisation during this period on artificial substrates in electrified and not‐electrified quadrats. 3. Significantly higher sediment accrual had occurred in the electrified treatment after 14 days and persisted for the 34‐day course of the experiment; substrates protected from shrimps contained about four times as much ash‐free dry mass (AFDM) as those of the controls. After 34 days, significantly more pennate diatoms were present in the exclusion treatment, but chlorophyll was not significantly different between treatments. Densities of baetid ephemeropteran nymphs were significantly higher in the presence of shrimps. 4. We attribute all these effects to the atyid P. glabra, the more abundant and active shrimp observed in the control treatment. Our results suggest that atyid shrimps played an important role related to sediment removal on hard substrate by direct ingestion and ‘bioturbation’. They reduced certain components of the periphyton (pennate diatoms) without affecting primary production (chlorophyll a). The activity of these shrimps on periphyton affected also faunal components such as baetid ephemeropterans and seems to determine the composition of the benthic community.     

Multivariate analysis of a fine-scale breeding bird atlas using a geographical information system and partial canonical correspondence analysis: environmental and spatial effects

Aim To assess the relative roles of environment and space in driving bird species distribution and to identify relevant drivers of bird assemblage composition, in the case of a fine‐scale bird atlas data set. Location The study was carried out in southern Belgium using grid cells of 1 × 1 km, based on the distribution maps of the Oiseaux nicheurs de Famenne: Atlas de Lesse et Lomme which contains abundance for 103 bird species. Methods Species found in < 10% or > 90% of the atlas cells were omitted from the bird data set for the analysis. Each cell was characterized by 59 landscape metrics, quantifying its composition and spatial patterns, using a Geographical Information System. Partial canonical correspondence analysis was used to partition the variance of bird species matrix into independent components: (a) ‘pure’ environmental variation, (b) spatially‐structured environmental variation, (c) ‘pure’ spatial variation and (d) unexplained, non‐spatial variation. Results The variance partitioning method shows that the selected landscape metrics explain 27.5% of the variation, whilst ‘pure’ spatial and spatially‐structured environmental variables explain only a weak percentage of the variation in the bird species matrix (2.5% and 4%, respectively). Avian community composition is primarily related to the degree of urbanization and the amount and composition of forested and open areas. These variables explain more than half of the variation for three species and over one‐third of the variation for 12 species. Main conclusions The results seem to indicate that the majority of explained variation in species assemblages is attributable to local environmental factors. At such a fine spatial resolution, however, the method does not seem to be appropriated for detecting and extracting the spatial variation of assemblages. Consequently, the large amount of unexplained variation is probably because of missing spatial structures and ‘noise’ in species abundance data. Furthermore, it is possible that other relevant environmental factors, that were not taken into account in this study and which may operate at different spatial scales, can drive bird assemblage structure. As a large proportion of ecological variation can be shared by environment and space, the applied partitioning method was found to be useful when analysing multispecific atlas data, but it needs improvement to factor out all‐scale spatial components of this variation (the source of ‘false correlation’) and to bring out the ‘pure’ environmental variation for ecological interpretation.