Reconciling competing ecological explanations for sexual segregation in ungulates

Sexual segregation in ungulates has important conservation and theoretical implications, but despite numerous studies, the impetus for this behavioral pattern remains a topic of debate. Sexual segregation hypotheses can be broadly grouped into social and ecological explanations, but only ecological explanations can adequately describe why sexes use different areas and habitats. The reproductive strategy hypothesis (RSH) and forage selection hypothesis (FSH) are leading ecological explanations, and although both have received support in the literature, neither the collective basis for that support nor overlap between these hypotheses has been adequately evaluated. This review analyzed seasonal sex comparisons of habitat forage quantity (n=66), quality (n=67), and diet (n=63) from peer-reviewed studies of north temperate ruminants to test predictions of each hypothesis. Empirical data supported predictions of the RSH, but did not support two of three key predictions of the FSH. Males used habitats with greater forage quantity significantly more than females. But, contrary to predictions of the FSH, females did not use habitats with superior forage quality nor consume higher-quality diets more than males. Sexes typically used habitats and consumed diets of similar quality, and when differences were reported, males used higher-quality habitats significantly more than females. Results refute FSH arguments that differences in dietary requirements associated with sexual dimorphism are a universal explanation for sexual segregation in ungulates, but the physiological mechanism on which the FSH is predicated may explain why males consume poorer-quality diets when high-quality forage is scarce. The FSH, therefore, operates at a proximate level because it explains diet and habitat selection by males under certain environmental conditions, but multiple environmental factors may influence sexual segregation, and no single proximate explanation adequately describes this behavioral pattern. The RSH explains sexual segregation as the evolutionary response to differences in reproductive strategies: males choose habitats to maximize energy gains in preparation for rut, and females select habitats with combinations of resources that contribute to offspring survival. Consequently, the RSH provides an ultimate explanation that can be used to explain and interpret studies of sexual segregation in ungulates.     

Species-specific defense strategies of vegetative versus reproductive blades of the Pacific kelps <Emphasis Type="Italic">Lessonia nigrescens</Emphasis> and <Emphasis Type="Italic">Macrocystis integrifolia</Emphasis>

Chemical defense is assumed to be costly and therefore algae should allocate defense investments in a way to reduce costs and optimize their overall fitness. Thus, lifetime expectation of particular tissues and their contribution to the fitness of the alga may affect defense allocation. Two brown algae common to the SE Pacific coasts, Lessonia nigrescens Bory and Macrocystis integrifolia Bory, feature important ontogenetic differences in the development of reproductive structures; in L. nigrescens blade tissues pass from a vegetative stage to a reproductive stage, while in M. integrifolia reproductive and vegetative functions are spatially separated on different blades. We hypothesized that vegetative blades of L. nigrescens with important future functions are more (or equally) defended than reproductive blades, whereas in M. integrifolia defense should be mainly allocated to reproductive blades (sporophylls), which are considered to make a higher contribution to fitness. Herein, within-plant variation in susceptibility of reproductive and vegetative tissues to herbivory and in allocation of phlorotannins (phenolics) and N-compounds was compared. The results show that phlorotannin and N-concentrations were higher in reproductive blade tissues for both investigated algae. However, preferences by amphipod grazers (Parhyalella penai) for either tissue type differed between the two algal species. Fresh reproductive tissue of L. nigrescens was more consumed than vegetative tissue, while the reverse was found in M. integrifolia, thus confirming the original hypothesis. This suggests that future fitness function might indeed be a useful predictor of anti-herbivore defense in large, perennial kelps. Results from feeding assays with artificial pellets that were made with air-dried material and extract-treated Ulva powder indicated that defenses in live algae are probably not based on chemicals that can be extracted or remain intact after air-drying and grinding up algal tissues. Instead, anti-herbivore defense against amphipod mesograzers seems to depend on structural traits of living algae.     

Macroinvertebrate colonization and breakdown of leaves in an astatic pond in south India

Macroinvertebrate colonization and breakdown of Pongamia pinnata and Morinda tinctoria leaves were studied in an astatic pond in Madura College, Madurai. Morinda tinctoria leaves broke down fasterthan the leaves of P. pinnata. Breakdown capacities of astatic pond cannot be attributed to colonization of macroinvertebrates. Instead, microbial processing, and abiotic fragmentation are suggested as factors controlling breakdown rates. Tanypus sp (midgelarva) was abundant in leaf bags during the experimental period. This midge-larva appeared to use litter accumulations as a microhabitat that provided shelter and a rich supply of food in the form of organic matter Their abundance and regular occurrence of two leaves suggest that midge larvae enhance leaf fragmentation and possibly mediate the incorporation of organic matter in pond sediments once the plant tissue is sufficiently macerated.     

Antimony uptake by <Emphasis Type="Italic">Zea mays</Emphasis> (L.) and <Emphasis Type="Italic">Helianthus annuus</Emphasis> (L.) from nutrient solution

We investigated the extent of Sb uptake by maize (Zea mays) and sunflower (Helianthus annuus) from nutrient solutions containing concentrations from 3 to 24 mg/L of potassium antimonate, with the aim of determining the potential of Sb to enter the food chain. The maximum shoot Sb concentrations in Z. mays and H. annuus were 41 mg/kg and 77 mg/kg dry weight, respectively. There was no significant difference in Sb uptake between species. The average bioaccumulation coefficients (the plant/solution concentration quotients) were 1.02 and 1.93 for Z. mays and H. annuus, respectively. Phosphate addition did not affect plant growth or Sb uptake. Antimony uptake by both Z. mays and H. annuus is unlikely to pose a health risk to animals and humans.     

Importance of movement constraints in habitat selection studies

The aim of this study is to empirically illustrate the importance of taking movement constraints into account when testing for habitat selection with telemetry data. Global Positioning System relocations of two Scandinavian brown bears were used to compare the results of two different tests of habitat selection by the bears within their home range. Both relied on the comparison of observed dataset with datasets simulated under the hypothesis of random habitat use. The first analysis did not take movement constraints into account (simulations were carried out by randomly distributing a set of points in the home range) whereas the second analysis accounted for these constraints (simulations were carried out by building random trajectories in the home range). The results for the two analyses showed contrasted results. Therefore, not accounting for movement constraints in analyses may result in a misleading biological interpretation. Autocorrelation between relocations is not undesirable: it contains information about ecological processes that should be integrated in habitat selection analyses.     

Toward a complete soil C and N cycle: incorporating the soil fauna

Increasing pressures on ecosystems through global climate and other land-use changes require predictive models of their consequences for vital processes such as soil carbon and nitrogen cycling. These environmental changes will undoubtedly affect soil fauna. There is sufficient evidence that soil fauna have significant effects on all of the pools and fluxes in these cycles, and soil fauna mineralize more N than microbes in some habitats. It is therefore essential that their role in the C and N cycle be understood. Here we introduce a new framework that attempts to reconcile our current understanding of the role of soil fauna within the C and N cycle with biogeochemical models and soil food web models. Using a simple stoichiometric approach to integrate our understanding of N mineralization and immobilization with the C:N ratio of substrates and faunal life history characteristics, as used in food web studies, we consider two mechanisms through which soil fauna can directly affect N cycling. First, fauna that are efficient assimilators of C and that have prey with similar C:N ratios as themselves, are likely to contribute directly to the mineral N pool. Second, fauna that are inefficient assimilators of C and that have prey with higher C:N ratios than themselves are likely to contribute most to the dissolved organic matter (DOM) pool. Different groups of fauna are likely to contribute to these two pathways. Protists and bacteria-feeding nematodes are more likely to be important for N mineralization through grazing on microbial biomass, while the effects of enchytraeids and fungal-feeding microarthropods are most likely to be important for DOM production. The model is consistent with experimental evidence and, despite its simplicity, provides a new framework in which the effects of soil fauna on pools and fluxes can be understood. Further, the model highlights our gaps in knowledge, not only for effects of soil fauna on processes, but also for understanding of the soil C and N cycle in general.     

Immune defense and reproductive pace of life in Peromyscus mice

Immune activity is variable within and among vertebrates despite the potentially large fitness costs of pathogens to their hosts. From the perspective of life history theory, immunological variability may be the consequence of counterbalancing investments in immune defense against other expensive physiological processes, namely, reproduction. In the present study, we tested the hypothesis that immune defense among captive-bred, disease-free Peromyscus mice would be influenced by their reproductive life history strategies. Specifically, we expected that small species that reproduce prolifically and mature rapidly (i.e., fast pace of life) would favor inexpensive, nonspecific immune defenses to promote reproductive proclivity. Alternatively, we expected that large species that mature slowly and invest modestly in reproduction over multiple events (i.e., slow pace of life) would favor developmentally expensive, specific immune defenses and avoid cheap, nonspecific ones because such defenses are predisposed to self-damage. We found that species exhibited either strong ability to kill (gram-negative) bacteria, a developmentally inexpensive defense, or strong ability to produce antibodies against a novel protein, a developmentally expensive defense, but not both. Cell-mediated inflammation also varied significantly among species, but in a unique fashion relative to bacteria killing or antibody production; wound healing was comparatively similar among species. These results indicate that Peromyscus species use immune strategies that are constrained to a dominant axis, but this axis is not determined solely by reproductive pace of life. Further comparisons, ideally with broader phylogenetic coverage, could identify what ecological and evolutionary forces produce the pattern we detected. Importantly, our study indicates that species may not be differentially immunocompetent; rather, they use unique defense strategies to prevent infection.     

Antagonistic interactions between plant competition and insect herbivory

Interspecific competition between plants and herbivory by specialized insects can have synergistic effects on the growth and performance of the attacked host plant. We tested the hypothesis that competition between plants may also negatively affect the performance of herbivores as well as their top-down effect on the host plant. In such a case, the combined effects of competition and herbivory may be less than expected from a simple multiplicative response. In other words, competition and herbivory may interact antagonistically. In a greenhouse experiment, Poa annua was grown in the presence or absence of a competitor (either Plantago lanceolata or Trifolium repens), as well as with or without a Poa-specialist aphid herbivore. Both competition and herbivory negatively affected Poa growth. Competition also reduced aphid density on Poa. This effect could in part be explained by changes in the biomass and the nitrogen content of Poa shoots. In treatments with competitors, reduced aphid densities alleviated the negative effect of herbivory on above- and belowground Poa biomass. Hence, we were able to demonstrate an antagonistic interaction between plant-plant interspecific competition and herbivory. However, response indices suggested that antagonistic interactions between competition and herbivory were contingent on the identity of the competitor. We found the antagonistic effect only in treatments with T. repens as the competitor. We conclude that both competitor identity and the herbivore's ability to respond with changes in its density or activity to plant competition affect the magnitude and direction (synergistic vs. antagonistic) of the interaction between competition and herbivory on plant growth.     

A meta‐analysis of functional group responses to forest recovery outside of the tropics

Both active and passive forest restoration schemes are used in degraded landscapes across the world to enhance biodiversity and ecosystem service provision. Restoration is increasingly also being implemented in biodiversity offset schemes as compensation for loss of natural habitat to anthropogenic development. This has raised concerns about the value of replacing old‐growth forest with plantations, motivating research on biodiversity recovery as forest stands age. Functional diversity is now advocated as a key metric for restoration success, yet it has received little analytical attention to date. We conducted a meta‐analysis of 90 studies that measured differences in species richness for functional groups of fungi, lichens, and beetles between old‐growth control and planted or secondary treatment forests in temperate, boreal, and Mediterranean regions. We identified functional‐group–specific relationships in the response of species richness to stand age after forest disturbance. Ectomycorrhizal fungi averaged 90 years for recovery to old‐growth values (between 45 years and unrecoverable at 95% prediction limits), and epiphytic lichens took 180 years to reach 90% of old‐growth values (between 140 years and never for recovery to old‐growth values at 95% prediction limits). Non‐saproxylic beetle richness, in contrast, decreased as stand age of broadleaved forests increased. The slow recovery by some functional groups essential to ecosystem functioning makes old‐growth forest an effectively irreplaceable biodiversity resource that should be exempt from biodiversity offsetting initiatives.