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Environmental Treatments (environmental + treatment)
Selected AbstractsA rating scale for wildness and ease of handling laboratory mice: results for 21 inbred strains tested in two laboratoriesGENES, BRAIN AND BEHAVIOR, Issue 2 2003D. Wahlsten Rating scales for difficulty in capturing and holding mice were devised that proved to be easy to use and highly sensitive to differences among mouse strains on the A and B priority lists of the Mouse Phenome Project. The simplicity of the scales makes it feasible to rate wildness during behavioral test sessions without adding much to testing time or distracting the technician from the principal task at hand. Overall wildness and placidity ratings obtained by combining capture and hold ratings provide a good impression of the difficulties encountered while working with lab mice in the course of complex experiments. Ratings of 21 inbred strains during the course of 15 behavioral tests in two laboratories demonstrated that the SPRET/Ei, PERA/Ei, CAST/Ei and SWR/J strains were particularly difficult to handle. The NOD/LtJ strain posed no special challenge in the Edmonton laboratory but was very difficult to handle in the Portland lab. The rating scales should be useful for judging the difficulties in working with novel targeted or induced mutations in mice as well as effects of a variety of environmental treatments or drugs. [source] Response of beech (Fagus sylvatica) to elevated CO2 and N: Influence on larval performance of the gypsy moth Lymantria dispar (Lep., Lymantriidae)JOURNAL OF APPLIED ENTOMOLOGY, Issue 9-10 2001M. W. Henn Two-year-old beech seedlings were kept from germination to bioassays with Lymantriadispar under the following conditions: ambient CO2/low N, elevated CO2/low N, ambient CO2/elevated N, and elevated CO2/elevated N. The effect of these growing conditions of the trees on the performance of the defoliator L. dispar was studied 2 years after initiating the tree cultivation. The developmental success of third-instar larvae of L. dispar was characterized by the weight gained, percentage of weight gain, relative growth rate (RGR), relative consumption rate (RCR), and efficiency of conversion of ingested food into body substance (ECI). Contrary to our expectations, additional N-fertilization did not increase and elevated CO2 did not delay larval growth rate. However, the environmental treatments of the beech seedlings were found to affect the larval performance. Larvae consumed significantly higher amounts of foliage (RCR) on beech trees under controlled conditions (ambient CO2 and low N) compared to those under elevated CO2 and enhanced N. The opposite was true for ECI. The lowest efficacy to convert consumed food to body substance was observed under control conditions and the highest when the larvae were kept on beech trees grown under elevated CO2 and additional N-fertilization. These opposite effects resulted in the weight gain-based parameters (absolute growth, percentage of growth, and RGR) of the gypsy moth larvae remaining unaffected. The results indicate that the gypsy moth larvae are able to change their ECI and RCR to obtain a specific growth rate. This is discussed as an adaptation to specific food qualities. [source] Ecosystem properties determined by plant functional group identityJOURNAL OF ECOLOGY, Issue 2 2010Jennie R. McLaren Summary 1.,Ecosystem properties may be determined by the number of different species or groups of species in a community, the identity of those groups, and their relative abundance. The mass ratio theory predicts that the effect of species or groups of species on ecosystem properties will be dependent on their proportional abundance in a community. 2.,Single plant functional groups (graminoids, legumes, non-leguminous forbs) were removed from a natural grassland in northern Canada to examine the role of group identity in determining both ecosystem properties and biomass compensation by remaining species. Removals were conducted across two different environmental treatments (fertilization and fungicide) to examine the context dependency of functional group identity effects. 3.,The degree of biomass compensation in the first 4 years after removal was influenced by the identity of the functional group removed and also of those remaining. When graminoids were removed, none of the remaining functional groups compensated for the loss of biomass. Graminoids partially compensated for the removal of forbs or legumes, with the degree of compensation depending on environmental treatments. 4.,Light interception, soil moisture and soil nutrients were all influenced by functional group identity, with graminoids having a greater impact than expected based on their biomass contribution to the community. Legumes, in contrast, had very little effect on any of the ecosystem properties measured. 5.,For most ecosystem properties measured, the role of plant functional groups was not context dependent; functional groups had the same effect on ecosystem properties regardless of fertilization or fungicide treatments. 6.,Synthesis. We have shown that the effects of losing a functional group do not solely depend on the group's dominance. In this northern grassland, there are greater effects of losing graminoids than one would predict based on their biomass contributions to the community, and functional group identity plays a critical role in determining the effects of diversity loss. [source] Genetic identity of interspecific neighbours mediates plant responses to competition and environmental variation in a species-rich grasslandJOURNAL OF ECOLOGY, Issue 5 2007JASON D. FRIDLEY Summary 1Although outbreeding populations of many grassland plants exhibit substantial genetic and phenotypic variation at fine spatial scales (< 100 m2), the implications of local genetic diversity for community structure are poorly understood. Genetic diversity could contribute to local species diversity by mediating the effects of competition between species and by enhancing species persistence in the face of environmental variation. 2We assayed the performance of three genotypes each of a dominant tussock grass (Koeleria macrantha [Ledeb.] J.A. Schultes) and dominant sedge (Carex caryophyllea Lat.) derived from a single 10 × 10 m quadrat within a limestone grassland in Derbyshire, UK. Genotypes were grown in monoculture and grass,sedge mixtures of different genetic composition in two environments of contrasting fertility. Species mixtures also included one genotype of the subordinate forb Campanula rotundifolia L. 3When grown without neighbours, intraspecific genotypes responded similarly to environmental treatments. One genotype of the sedge performed worse in both environments than the other two sedge genotypes. 4When grown in species mixtures, genotype performance was significantly influenced by the genetic identity of the neighbouring species for both the sedge and the grass. At high fertility, differential genotype performance was not sufficient to alter the expectation of competitive exclusion of the sedge by the grass. However, at low fertility, the competitive dominant depended on the genetic identity of both the grass and the sedge. In addition, each genotype of the grass performed best next to a different genotype of the sedge, and the identity of the best genotype pairings switched with environment. 5Performance of a single genotype of the subordinate Campanula was not predictable by fertility alone, but by how fertility interacted with different neighbouring genotypes of both the grass and the sedge. 6Results support the hypothesis that the genetic identity of interspecific neighbours influences plant performance in multispecies assemblages and mediates species' responses to environmental variation. Such interactions could be a key factor in the contribution of local intraspecific genetic diversity to species diversity. [source] Intensity and Importance of Competition for a Grass (Festuca rubra) and a Legume (Trifolium pratense) Vary with Environmental ChangesJOURNAL OF INTEGRATIVE PLANT BIOLOGY, Issue 12 2008Junyan Zhang Abstract How plant competition varies across environmental gradients has been a long debate among ecologists. We conducted a growth chamber experiment to determine the intensity and importance of competition for plants grown in changed environmental conditions. Festuca rubra and Trifolium pratense were grown in monoculture and in two- and/or three-species mixtures under three environmental treatments. The measured competitive variations in terms of growth (height and biomass) were species-dependent. Competition intensity for Festuca increased with decreased productivity, whilst competition importance displayed a humpback response. However, significant response was detected in neither competition intensity nor importance for Trifolium. Intensity and importance of competition followed different response patterns, suggesting that they may not be correlated along an environmental gradient. The biological and physiological variables of plants play an important role to determine the interspecific competition associated with competition intensity and importance. However, the competitive feature can be modified by multiple environmental changes which may increase or hinder how competitive a plant is. [source] Does disturbance, competition or resource limitation underlie Hieracium lepidulum invasion in New Zealand?AUSTRAL ECOLOGY, Issue 3 2010Mechanisms of establishment, functional differentiation among invasive, native species, persistence Abstract The processes underlying plant invasions have been the subject of much ecological research. Understanding mechanisms of plant invasions are difficult to elucidate from observations, yet are crucial for ecological management of invasions. Hieracium lepidulum, an asteraceous invader in New Zealand, is a species for which several explanatory mechanisms can be raised. Alternative mechanisms, including competitive dominance, disturbance of resident vegetation allowing competitive release or nutrient resource limitation reducing competition with the invader are raised to explain invasion. We tested these hypotheses in two field experiments which manipulated competitive, disturbance and nutrient environments in pre-invasion and post-invasion vegetation. H. lepidulum and resident responses to environmental treatments were measured to allow interpretation of underlying mechanisms of establishment and persistence. We found that H. lepidulum differed in functional response profile from native species. We also found that other exotic invaders at the sites were functionally different to H. lepidulum in their responses. These data support the hypothesis that different invaders use different invasion mechanisms from one another. These data also suggest that functional differentiation between invaders and native resident vegetation may be an important contributing factor allowing invasion. H. lepidulum appeared to have little direct competitive effect on post-invasion vegetation, suggesting that competition was not a dominant mechanism maintaining its persistence. There was weak support for disturbance allowing initial establishment of H. lepidulum in pre-invasion vegetation, but disturbance did not lead to invader dominance. Strong support for nutrient limitation of resident species was provided by the rapid competitive responses with added nutrients despite presence of H. lepidulum. Rapid competitive suppression of H. lepidulum once nutrient limitation was alleviated suggests that nutrient limitation may be an important process allowing the invader to dominate. Possible roles of historical site degradation and/or invader-induced soil chemical/microbial changes in nutrient availability are discussed. 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