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691 results for “plant traits”
Evolutionary divergence of potential drought adaptations between two subspecies of an annual plant: Are trait combinations facilitated, independent, or constrained?
<p><b><span>Premise</span></b><span>: Whether drought-adaptation mechanisms tend to evolve together, evolve independently, and/or evolve constrained by genetic architecture is incompletely resolved, particularly for water relations traits besides gas exchange. We addressed this issue in two subspecies of </span><i>Clarkia xantiana</i><span> (Onagraceae), California winter annuals that separated approximately 65,000 years ago and are adapted, partly by differences in flowering time, to native ranges differing in precipitation.</span></p> <p><b><span>Methods: </span></b><span>In these subspecies and in recombinant inbred lines (RILs) from a cross between them we scored traits related to drought adaptation (timing of seed germination and of flowering; succulence; pressure-volume curve parameters) in common environments.</span></p> <p><b><span>Results: </span></b><span>The subspecies native to more arid environments (<i>parviflora</i>) exhibited slower seed germination in saturated conditions, earlier flowering, and greater succulence, likely indicating superior drought avoidance, drought escape, and dehydration resistance via water storage, respectively. The other subspecies (<i>xantiana</i>) had lower osmotic potential at full turgor and lower water potential at turgor loss, implying superior dehydration tolerance. Genetic correlations among RILs suggest facilitated evolution of some trait combinations and independence of others. Where genetic correlations exist, subspecies differences fell along them, with the exception of differences in succulence and turgor loss point. In that case, subspecies difference overcame genetic correlations, possibly reflecting strong selection and/or antagonistic genetic correlations with other traits. </span></p> <p><b><span>Conclusions:</span></b><span> <i>Clarkia xantiana </i>subspecies' differ in multiple mechanisms of drought adaptation. Genetic architecture generally does not seem to have constrained the evolution of these mechanisms, and it may have facilitated the evolution of some of trait combinations. </span></p>
Data from: Spatiotemporal variation in the role of floral traits in shaping tropical plant-pollinator interactions
<p>Supplementary datasets for <strong>Klomberg <em>et al.</em> 2021 Spatiotemporal variation in the role of floral traits in shaping tropical plant-pollinator interactions</strong><strong>.</strong> <em>Ecology Letters.</em></p> <p>All related information can be found in the cited paper.</p> <p>When using the dataset for anything, cite the Klomberg <em>et al. </em>paper.</p> <p>For additional information, refer to the paper or write to robert.tropek@gmail.com</p>
How detritivores, plant traits and time modulate coupling of leaf versus woody litter decomposition rates across species
<p>1. Plant functional traits are increasingly used to understand ecological relationships and (changing) ecosystem functions. For understanding ecosystem-level biogeochemistry, we need to understand how (much) traits co-vary between different plant organs across species, and its implications for litter decomposition. However, we do not know how the degree of synchronous variation in decomposition rates between organs across species could be influenced by different keystone invertebrates decomposing different senesced plant organs, especially in warm-climate forests. Here we asked whether interspecific patterns in wood and leaf decomposition rates and in the spectra of resource economics traits underpinning them, co-vary across woody species; and how (much) the keystone invertebrate decomposers of the litter of these organs enhance or lower such co-variation of decomposition rates through time. </p> <p>2. We addressed these questions through an 18-month "common-garden" decomposition experiment using leaf, twig and branch litter of 41 woody species in two distant subtropical forest sites in east China. We quantified the effects of leaf, twig, and branch functional traits and their respective key invertebrates (moth larvae, termites) on the decomposition rates of those organs. </p> <p>3. Interspecific variation in wood traits was partly decoupled from that in leaf traits across species, while strong coupling was found between twigs and branches. The co-variation between leaf and woody organ decomposition rates was altered dynamically through the shifting activities of the key decomposers, which created non-linear relationships of invertebrate litter consumption as a function of species rankings along the resource economic trait spectra of leaves and branches.</p> <p>4. The deviations from coupling of decomposition rates between organs were likely caused by combinations of three mechanisms: (1) (de-)coupling between organs of other traits, not commonly considered in resource economics spectra (e.g., resins) (2) leaf and wood decomposers having specific diet requirements, and (3) temporal patterns of the decomposers' activity.</p> <p>5. Synthesis. Our study highlights the importance of considering the different ways by which invertebrate detritivores drive decomposition processes through time. Under the ongoing biodiversity decline, future research would benefit from a better understanding of the role of the dynamic interactions between detritivore activities and plant functional traits on the carbon turnover in ecosystems.</p>
Interactions between protea plants and their animal mutualists and antagonists are structured more by energetic than morphological trait matching
<p class="MsoNormal"><span>Traits mediate mutualistic and antagonistic interactions between plants and animals, and should thus be useful for predicting trophic species interactions. Studies to date have examined the importance of morphological trait matching for plant-animal interactions, but have rarely explored the extent to which these interactions are shaped by matching between energetic provisions of plants and energetic demands of animals.</span></p> <p class="MsoNormal"><span>We tested whether energetic and/or morphological trait matching shapes interactions between <em>Protea</em> plant species and their interacting animal mutualists and antagonists in the Cape Floristic Region, South Africa.</span></p> <p class="MsoNormal"><span>We recorded interactions between 22 <em>Protea</em> species, pollinating insects, and vertebrates as well as seed predators (endophagous insect larvae in protea cones) at 21 study sites. To relate species interactions to matching trait pairs, we measured key morphological traits (shape and size of flower heads and seed cones, and mouth part length as well as body length) and quantified the animals' energetic demands (metabolic rate) together with the plants' energetic provisions (nectar sugar amount, seed-to-cone mass ratio). We calculated log ratios of both energetic and morphological traits between animals and plants as predictor variables for the number of observed interactions between <em>Protea</em> species and their animal interaction partners.</span></p> <p class="MsoNormal"><span>For both mutualistic and antagonistic interactions, we found significant effects of morphological and energetic trait ratios on the interactions between plants and animals. Trait ratios accounted for 11% to 22% of the variation in species interactions. Consistent with energetic trait matching, we found a hump-shaped relationship between interaction frequency and log ratios of energetic traits of animals and plants, indicating that interactions were most frequent at intermediate log ratios between energetic demand and provision. Effects of morphological trait ratios on interactions were statistically supported in most cases but were variable in the magnitude and shape of the predicted relationships. </span></p> <p><span>Across animal taxa and interaction types, energetic traits had more consistent effects on interactions between plants and animals than morphological traits. This suggests that energy can function as an important interaction currency and facilitate the understanding and prediction of trophic species interactions.</span></p>
Data for the article: Coupling of leaf elemental traits with root fungal community composition reveals a plant resource acquisition strategy in a desert ecosystem
<p><em>Purpose</em>: Plant-associated microbes enhance nutrient access and stress tolerance of the host species, and therefore, are crucial for plant traits and resource strategies. However, the links between aboveground plant traits and belowground microbes related to plant resource strategies under stressful conditions remain poorly understood.</p> <p><em>Methods</em>: We tested the relationships between leaf traits linked to water (carbon isotopic composition, δ<sup>13</sup>C) and nutrient use (elemental concentrations and stoichiometry) with microbial compositions in roots and rhizospheres of two dominant species (<em>Artemisia ordosica</em> and <em>Leymus secalinus</em>) in the Mu Us Desert, northern China.</p> <p><em>Results</em>: <em>L. secalinus</em> exhibited higher Mg and Mn concentrations, N:P ratios, stoichiometric flexibility, and root fungi:bacteria ratios, but lower foliar K and Ca concentrations and δ<sup>13</sup>C values than <em>A. ordosica</em>. The leaf N:P of <em>L. secalinus</em> increased with the root fungi:bacteria ratios, whereas the leaf N:P of <em>A. ordosica</em> decreased with the root fungi:bacteria ratios. The plant elemental levels (P, N, K, Ca, Mn, and δ<sup>13</sup>C) of <em>L. secalinus</em> but not <em>A. ordosica</em> were significantly related to their root fungal composition. Additionally, the random forest model identified four key fungal families in predicting leaf elemental traits for both plant species.</p> <p><em>Conclusion</em>: The results suggested tight coupling and coordination between leaf elemental traits and root microbial compositions (especially fungal communities) related to plant resource acquisition strategies. By regulating aboveground and belowground feedback loops through trait flexibility and root microbial compositions, the studied plant species can sustain their resource strategies under stressful environmental conditions.</p>
Eco-evolutionary contributions to community trait change in floating aquatic plants
<p>An entire community of organisms may become modified when its environment changes. These modifications can happen through physiological process (plasticity), evolutionary processes (adaptation) or shifts in species composition (sorting). The outcome of these three sources of change constitutes the community's phenotypic response, but how they combine to drive community trait dynamics is not currently well understood. We have conducted a community selection experiment in which communities of short-lived floating aquatic plants were grown in a range of stressful conditions, and measured changes in their body size. Determinants of phenotypic change were assessed with a full community reciprocal transplant which led to estimates of the contributions of plasticity, adaptation, and sorting. Species were modified during the experiment by both plasticity and adaptation, but in either case the magnitude and direction of change differed among species. Sorting and adaptation were of equal magnitude, but tended to act in opposite directions: in conditions where species with large fronds prevailed, each species evolved smaller fronds, and vice versa. We conclude that community trait dynamics cannot be understood simply by extrapolating the adaptive response of any single species to the whole community.</p>
Mapping trait versus species turnover reveals spatiotemporal variation in functional redundancy and network robustness in a plant‐pollinator community
<p>1. Functional overlap among species (redundancy) is considered important in shaping competitive and mutualistic interactions that determine how communities respond to environmental change. Most studies view functional redundancy as static, yet traits within species – which ultimately shape functional redundancy – can vary over seasonal or spatial gradients. We therefore have limited understanding of how trait turnover within and between species could lead to changes in functional redundancy or how loss of traits could differentially impact mutualistic interactions depending on where and when the interactions occur in space and time.</p> <p>2. Using an Arctic bumblebee community as a case study, and 1,277 individual measures from 14 species over three annual seasons, we quantified how inter- and intraspecific body-size turnover compared to species turnover with elevation and over the season. Coupling every individual and their trait with a plant visitation, we investigated how grouping individuals by a morphological trait or by species identity altered our assessment of network structure and how this differed in space and time. Finally, we tested how the sensitivity of the network in space and time differed when simulating extinction of nodes representing either morphological trait similarity or traditional species groups. This allowed us to explore the degree to which trait-based groups increase or decrease interaction redundancy relative to species-based nodes.</p> <p>3. We found that i) groups of taxonomically and morphologically similar bees turn over in space and time independently from each other, with trait turnover being larger over the season; ii) networks composed of nodes representing species versus morphologically similar bees were structured differently; and iii) simulated loss of bee trait groups caused faster coextinction of bumblebee species and flowering plants than when bee taxonomic groups were lost. Crucially, the magnitude of these effects varied in space and time, highlighting the importance of considering spatiotemporal context when studying the relative importance of taxonomic and trait contributions to interaction network architecture.</p> <p>4. Our finding that functional redundancy varies spatiotemporally demonstrates how considering the traits of individuals within networks is needed to understand the impacts of environmental variation and extinction on ecosystem functioning and resilience.</p>
A direct comparison of ecological theories for predicting the relationship between plant traits and growth
<p>Despite long-standing theory for classifying plant ecological strategies, limited data directly links organismal traits to whole-plant growth rates. We compared trait-growth relationships based on three prominent theories: growth analysis, Grime's competitive-stress tolerant-ruderal (CSR) triangle, and the leaf economics spectrum (LES). Under these schemes, growth is hypothesized to be predicted by traits related to relative biomass investment, leaf structure or gas exchange, respectively. We also considered traits not included in these theories, but that might provide potential alternative best predictors of growth. In phylogenetic analyses of 30 diverse milkweeds (<em>Asclepias</em> spp.) and 21 morphological and physiological traits, growth rate (total biomass produced per day) varied 50-fold and was best predicted by biomass allocation to leaves (as predicted by growth analysis) and the CSR traits of leaf size and leaf dry matter content. Total leaf area and plant height were also excellent predictors of whole-plant growth rate. Despite two LES traits correlating with growth (mass-based leaf nitrogen and area-based leaf phosphorus contents), these were in the opposite direction predicted by LES, such that higher N and P contents corresponded to slower growth. The remaining LES traits (e.g., leaf gas exchange) were not predictive of plant growth rates. Overall, differences in growth rate were driven more by whole-plant characteristics such as biomass fractions and total leaf area than individual leaf-level traits such as photosynthetic rate or specific leaf area. Our results are most consistent with classical growth analysis - combining leaf traits with whole-plant allocation to best predict growth. However, given that destructive biomass measures are often not feasible, applying easy-to-measure leaf traits associated with the CSR classification appear more predictive of whole plant growth than LES traits. Testing the generality of this result across additional taxa would further improve our ability to predict whole-plant growth from functional traits across scales.</p>
Resampling alpine herbarium records reveals changes in plant traits over space and time - dataset
<p><strong>Data overview:</strong></p> <p>These data correspond to the analyses conducted for the article "Resampling alpine herbarium records reveals changes in plant traits over space and time" by Francesca Jaroszynska, Christian Rixen, Sarah Woodin, Jonathan Lenoir and Sonja Wipf, in Journal of Ecology</p> <p><strong>Metadata for jaroszynska_herbarium_traits_data.csv:</strong></p> <p>date = date; date of collection</p> <p>time = factor; time of collection (historical or recent)</p> <p>elevation = numerical; elevation in metres above sea level of the sample collection site</p> <p>selevation = numerical; scaled <em>elevation</em></p> <p>selevation2 = numerical; elevation in metres above sea level of sample collection site (elevation/1000).</p> <p>sSlope = numerical; scaled slope (slope/10)</p> <p>slope = numerical; computed slope based on elevation</p> <p>trait = string; name of the measured trait</p> <ul> <li> <p>crFlowerN = numerical; Cardamine resedifolia; number of flowers</p> </li> <li> <p>crHeight = numerical; Cardamine resedifolia; plant height</p> </li> <li> <p>crLeafL = numerical; Cardamine resedifolia; length of longest leaf</p> </li> <li> <p>crRosetteLeafN = numerical; Cardamine resedifolia; number of leaves in rosette</p> </li> <li> <p>paBasalLeafL = numerical; Poa alpina; basal leaf length</p> </li> <li> <p>paInflorescenceL = numerical; Poa alpina; inflorescence length</p> </li> <li> <p>paHeight = numerical; Poa alpina; plant height</p> </li> <li> <p>pvInfL = numerical; Polygonum viviparum; length of inflorescence</p> </li> <li> <p>pvLA = numerical; Polygonum viviparum; leaf area (length x width)</p> </li> <li> <p>pvLeafL = numerical; Polygonum viviparum; leaf length</p> </li> <li> <p>pvRepH= numerical; Polygonum viviparum; plant height</p> </li> <li> <p>rgFlowerStemL = numerical; Ranunculus glacialis; flowering stem length</p> </li> <li> <p>rgLeafStemL = numerical; Ranunculus glacialis; petiole length</p> </li> <li> <p>rgLeafW = numerical; Ranunculus glacialis; leaf width</p> </li> <li> <p>rgFlowerN = integer; Ranunculus glacialis; number of flowers</p> </li> </ul> <p> </p> <p>traitGroup = factor; the group to which each trait belongs (VegHeight = vegetative height, ReprHeight = reproductive height, ReprOut = reproductive output, PhotoCap = photosynthetic capacity)</p> <p>value = numerical; value of the trait measured</p> <p>species = factor; species code (car_res = Cardamine resedifolia, ran_glac = Ranunculus glacialis, pol_viv = Polygonum viviparum, poa_alp = Poa alpina)</p> <p>transect = string; transect along which the herbarium sample was taken</p> <p>confidence = factor; reliability of the metadata associated with the herbarium sample, assigned by the authors Jaroszynska and Wipf (low, medium, high)</p> <p>northness = numerical; northness</p> <p>eastness = numerical; eastness</p> <p>observer = string; botanist who conducted the collection</p> <p>sheet = string; unique identifier for the collection sheet</p> <p> </p> <p><strong>Metadata for jaroszynska_climate_traits_data.csv:</strong></p> <p>year = year; year of sample collection</p> <p>Month = integer; month of sample colection</p> <p>Temperature = numerical; monthly average temperature (ºC)</p> <p>Precipitation = numerical; monthly total precipitation (mm)</p> <p>yearMonth = string; year.month</p> <p>season = factor; season associated to the corresponding month (spring, summer, autumn, winter)</p> <p>timePeriod = factor; climate period referring to the time before, after, or during the baseline reference period (see article for further details)</p> <p>meanAnnTemp = numerical; mean annual temperature (ºC)</p> <p>sumAnnPrecip = numerical; total annual precipitation (mm)</p> <p>meanSeaTemp = numerical; mean seasonal temperature (ªC)</p> <p>sumSeaPrecip = numerical; total seasonal precipitation (mm)</p> <p>meanRefTemp = numerical; mean seasonal temperature for reference period (ªC)</p> <p>temp_anomaly = numerical; temerature anomaly from the reference period (ªC)</p> <p>lagMonths = string; used in seasonal calculation</p> <p>seasonal_precip = numerical; seasonal precipitation (mm)</p> <p>precip_anomaly = numerical; seasonal precipitation anomaly (mm)</p>
Dataset related to article: Differential effect of climate of origin and cultivation climate on structural and biochemical plant traits
<p><span>Exploring patterns and causes of intraspecific trait variation is crucial for a better understanding of the effects of climate change on plant populations and ecosystems. However, our current understanding of the intraspecific trait variation is mainly based on structural (morphological) traits, and we have limited knowledge on patterns and causes of variation in biochemical traits (e.g., leaf pigments), which are also crucial for plant adaptation. As a result, we also do not know how similar the climatic effects on structural versus biochemical traits are. </span></p> <p><span>Using plant traits from 110 genotypes representing 11 <em>Festuca</em> <em>rubra</em> populations grown in 4 different climates, we studied trait covariation among structural traits (linked to fitness, resource use, gas exchange, and reproduction) and biochemical traits (linked to photosynthesis, photoprotection, and oxidative stress). We also disentangled the relative role of the climate of origin and the climate of cultivation in the structural versus biochemical traits and tested for adaptive plasticity in the traits. </span></p> <p><span>We found that 1) biochemical traits did not covary with structural traits and represent independent '<em>photoharvesting</em> – <em>photoprotection</em>' strategy dimension of functional variation; 2) interactive effects of climate of origin and cultivation were more pronounced for biochemical than structural traits</span>. 3) T<span>rait plasticity was affected by the climate of origin (</span>precipitation and temperature as well as their interaction<span>); 4) </span><em>F. rubra</em> showed both adaptive and mal-adaptive plasticity, and adaptiveness depended upon trait type, cultivation climate, and climate of origin.</p> <p><span>Overall, our results suggest that structural and biochemical plant traits respond differentially to climate and thus the response of one group of traits cannot be predicted from the other. Responses are also strongly determined by interactions between the climate of origin and cultivation. Thus, more studies on variation in biochemical traits, their correspondence to other traits, and their variation with climate are needed. </span></p>
Altered trait covariances between invasive and native ranges of a global plant invader
<p>Increasing evidence suggests that invasive populations adapt to novel environments rapidly, and the ability to rapidly adapt depends on genetically-based trait variation and covariation. However, few studies have investigated the trait covariance in the native and invasive ranges. Such investigation will give a more comprehensive picture of how historical contingency and adaptation shape invasiveness, contributing to the prediction of future invasion dynamics.</p> <p>Here, we collected seven and nine populations alongside latitudes from invasive and native ranges of a global invasive plant, <em>Spartina alterniflora</em>, and planted them in two common gardens at the southernmost and northernmost sites of the invasive range. We measured plant traits, including the first flowering time, plant height, and seed set, and analyzed how these traits varied with garden sites and populations' origin latitudes and how their covariance changed between ranges.</p> <p>We found that plants flowered later, grew taller, and set more seeds in the high-latitude garden than in the low-latitude one. The growth and expression of genetic variation of traits appeared to be limited by high ambient temperature in the low-latitude garden. In the high-latitude garden, the flowering time of populations showed clinal variation for both invasive and native populations, whereas the plant height and seed set showed clinal variation only for native or invasive populations. From the native to the invasive range, the flowering time and seed set developed negative genetic covariance, and flowering time and plant height changed from negative genetically correlated to uncorrelated.</p> <p>Our results suggested that <em>S. alterniflora</em> has experienced rapid adaptation to clinal and local conditions over the 40-year invasion. Such geographic-scale rapid adaptation appeared to have benefited from previously identified genetic admixture that has released the trait covariance. Our study highlights the importance of integrating full-range geographical surveys with introduction history to understand the potential and mechanisms of trait evolution during invasion.</p>
The data table of eleven invasive species in Hungary and Romania: Invasive species' cover, invasive species' traits, basic characteristics, trait composition, functional diversity indices and soil parameters of recipient plant communities
<p>We studied 11 widespread herbaceous invasive alien species of East-Central Europe and their 16 impact metrics (resident plant communities' ecological characteristics, trait composition, functional diversity, and soil parameters) by sampling invaded and similar, uninvaded sites (space-for-time substitution method). Our aim was to (1) investigate the detailed ecological impacts of invasive plants on native plant communities; (2) explore the type of cover-impact relationships across impact metrics and their consistency across species; (3) study whether the cover-impact relationship depends on functional traits of invasive species. We present the data table with the 11 invasive species: the status of the sites (invaded, uninvaded), the cover of invasive species at plot level, the invasive species traits (lifespan, height, SLA, seed mass, clonal spread, flowering duration), community characteristics (species richness and diversity, native vegetation cover and bare ground cover at plot level), trait composition of native plant communities (native vegetation height, CWM height, CWM SLA, CWM seed mass, CWM clonal spread), functional diversity (functional richness, functional evenness, functional divergence, functional distance, RaoQ) and soil properties (N, P, organic C, pH).</p>
Plant functional traits predict heterogeneous distributional shifts in response to climate change
<p>Climate change is causing the rapid redistribution of vegetation as plant species move to track their climatic optima. Despite a global trend of upward movement in latitude and elevation, there is extensive heterogeneity among species and locations, with few emerging generalizations. Greater generalization may be achieved by considering multidimensional changes in species' distributions as well as incorporating ecologically relevant functional traits into studies of range shifts.</p> <p>To better understand how recent changes in climate are influencing the elevational distribution of plant species and how species' functional traits mediate distributional changes, we resampled a 2,438-meter elevation transect spanning a distance of 16 kilometers which encompasses desert scrub, pinyon-juniper woodland, chaparral, and coniferous forest plant communities.</p> <p>Over the last 42 years, total perennial cover and species' average cover increased at lower elevations and decreased at higher elevations while the average elevational leading-edge increased 116 m and the elevational rear edge decreased 84 m. Notably, these changes were mediated by species' functional traits, where species exhibiting more conservative traits (lower SLA, greater δ13C, larger seed mass) and taller height shifted upward in their leading-edge range limit, average elevation, and trailing edge range limit, while declining in abundance at the median and trailing edge of their range. Species possessing more acquisitive traits (higher SLA, lower δ13C, smaller seed mass) and shorter height shifted downward and increased in abundance at their trailing edge, with increases in their total range size.</p> <p>Our results provide clear evidence that heterogeneous range dynamics under recent climate change can be generalized by considering ecologically relevant plant functional traits, and how they respond to localized climate exposure. Further, by documenting changes across a steep ecological gradient comprising a large aridity gradient, we show divergent patterns for plants occupying contrasting positions along the global spectrum of plant form and function, which provides critical insight into how trait-mediated changes under increasing aridity will impact ecosystem functioning.</p>
Seed size, seed dispersal traits, and plant dispersion patterns for native and introduced grassland plants
<p>Most terrestrial plants disperse by seeds, yet the relationship between seed mass, seed dispersal traits, and plant dispersion is poorly understood. We quantified seed traits for 48 species of native and introduced plants from grasslands of western Montana, USA, to investigate the relationships between seed traits and plant dispersion patterns. Additionally, because the linkage between dispersal traits and dispersion patterns might be stronger for actively dispersing species, we compared these patterns between native and introduced plants. Finally, we evaluated the efficacy of a global trait database, the TRY plant traits database, versus locally collected data for examining these questions.</p> <p>This archive contains species-level data used in analyses, including species metadata (origin, growth form), mean values of measured seed traits (size metrics and type of dispersal structures), two metrics of dispersion (local and broad scales, respectively) derived from grassland surveys in the study region, and information on the seed mass accessed from the TRY traits database. Note that the latter seed mass data could not be included in the archive, but can be acquired directly from the TRY plant traits database (<a href="https://www.try-db.org/TryWeb/Home.php">https://www.try-db.org/TryWeb/Home.php</a>).</p>
Stronger effect of individual species' traits than shading on aquatic plant community productivity and interspecific competition
<p>Competition is one of the major factors structuring plant communities. Species with similar traits generally compete more intensely and have more similar yield than functionally dissimilar species, which often respond differently to environmental change. Little is known about how the interacting species' traits influence the effect of environmental change on interspecific competition. However, theory predicts that environmental change should lead to more asymmetric competition, by favouring the species best adapted to the particular environmental change. Here we used a mesocosm experiment with three common aquatic plant species from the Baltic Sea (Northern Europe), to test how community productivity and competition asymmetry were affected by functional dissimilarity, individual species' traits, and a common stressor: shading. Competition asymmetry was defined as the absolute difference in reductions in yield relative to monocultures of two interacting species. Community productivity decreased and competition asymmetry increased with functional dissimilarity of the interacting species, possibly explained by the traits of the superior species, which had higher specific leaf area, maximum canopy height, and primary production rate than the subordinate species. Community productivity was not affected by shading, contrary to our expectation, while competition asymmetry was higher in shaded than ambient conditions. Individual species yield depended on species identity and species combination. Only the shortest species was negatively affected by shading. Thus, by favouring tall-growing species, shading can alter interspecific competition. Together, these findings suggest that non-random species loss following environmental change can be caused by competitive exclusion, in addition to a direct effect of abiotic filtering.</p>
Variation and association of leaf traits for desert plants in the arid area, northwest China
<p><span>Characterizing variation and association of plant traits is critical for understanding plant adaptation strategies and community assembly mechanisms. However, little is known about the leaf trait variations of desert plants and their association with different life forms. We used principal component analysis, Pearson's correlation, phylogenetic independent contrasts, linear mixed model, and variance decomposition to explore the variation and association of 10 leaf traits in 22 desert plants in the arid area of northwest China. We found that: (1) the contribution of interspecific variation to the overall variation was greater than the intraspecific variation of all the studied leaf traits; (2) intraspecific and interspecific variation in leaf traits differed among life forms. Some leaf traits, such as tissue density of shrubs and specific leaf area of herbs, exhibited greater intraspecific than interspecific variation, while other traits exhibited the inverse; (3) desert shrubs corroborate the leaf economic spectrum hypothesis and had a fast acquisitive resource strategy, but herbs may not conform to this hypothesis; (4) there were trade‐offs between leaf traits, which were mediated by phylogeny. Overall, our results suggest that interspecific variation of leaf traits significantly contributes to the total leaf traits variation in desert plants. However, intraspecific variation should not be overlooked. There are contrasts in the resource acquisition strategies between plants life forms. Our results support understanding of the mechanisms underlying community assembly in arid regions and suggest that future works may focus on the variation and association of plant traits at both intra‐ and interspecific scales.</span></p>
Linking trait network parameters with plant growth across light gradients and seasons
<p>1. Reduced light availability induced by eutrophication has dramatically affected the growth of submerged macrophytes and caused their rapid decline globally in lakes. Functional traits have usually been used to predict ecological processes and explain plant adaptation. Trait networks, which are constructed from a series of nodes (traits) and edges (trait-trait correlations), can reveal complex relationships among traits. Plant traits belonging to different organs are considered relevant for overall plant performance. Therefore, variation in trait network topology at the whole-plant level can better reflect plant adaptation and response to environments than traditional methods, but the mechanisms underlying the decline of plants from a trait network perspective are not well understood.</p> <p>2. In this study, based on a one-year manipulation experiment for <em>Potamogeton maackianus</em> cultured with four levels of light intensity, we constructed trait networks from 20 traits belonging to different organs.</p> <p>3. Our results showed that trait network connectivity decreases in harsh environments, probably due to increased trait modules responding independently to stress. Network connectivity was positively related to the plant relative growth rate (RGR), as high trait connectivity and coordination should be beneficial for plants to acquire and transport resources efficiently across the whole plant. Additionally, we found that specific stem length, leaf:root mass ratios, and leaf total nonstructural carbohydrates were hub traits with high connectivity. These hub traits expressed high phenotypic plasticity, had close links with plant growth, and consistently held their higher importance within the network across light gradients or seasons.</p> <p>4. We found that low phenotypic integration in stressful environments may constrain plant growth, which can provide important implications for understanding plant adaptation strategies to low-light stress and even predicting community dynamics in the context of global environmental change.</p>
Effects of long-term mowing on leaf- and root-associated bacterial community structures are linked to functional traits in 11 plant species from a temperate steppe
<ol> <li><span>Long-term mowing can cause morphological stuntedness of plants, thus reducing grassland productivity and exacerbating grassland degradation. Although plant microbiomes can enhance plant resistance against disturbance, considerable uncertainty exists regarding how mowing and mowing-induced plant trait plasticity affect plant microbiomes in natural grasslands. </span></li> <li><span>Here we examined the responses of leaf-/root-associated bacterial (LAB/RAB) communities of 11 dominant herbaceous perennials (6 replicates per species) to a 17-year mowing treatment in a temperate grassland. We also measured leaf/root physiological and morphological traits and analyzed the relationships among mowing practice, bacterial community structures, and leaf/root trait parameters. </span></li> <li><span>We found that both leaf and root functional traits showed interspecific variations (variations across different plant species), while only the leaf traits exhibited intraspecific variation (treatment-induced variations within plant species) between the treatments. Similarly, the LAB community structure was more sensitive to mowing but less influenced by host species identity, compared to the RAB community. The RAB community structure was primarily shaped by host species identity, while mowing was a secondary influencing factor. </span></li> <li> <span>The different patterns of LAB and RAB communities in response to mowing could be specifically explained by the inter-/intraspecific variations of the related leaf and root traits. The LAB community was strongly correlated with the leaf traits which exhibited mowing-induced plasticity (intraspecific variation), with the correlations with nitrogen resorption efficiency and aboveground dry weight being the greatest. The root traits were important indicators of bacterial community structure in the root compartment across the hosts, rather than between the treatments. Root tissue density</span> <span>showed the strongest interspecific variation, and was identified as an overwhelming driver of the RAB community. The shifts in LAB/RAB communities under mowing were largely attributed to the increased proportions of Actinobacteria. The high mowing sensitivity of the LAB community was associated with the enrichment of soil-derived Actinobacteria in leaves under mowing. Actinobacteria were also the main keystone taxa in the bacterial community networks under mowing.</span> </li> <li><span>Our results demonstrate that the magnitude of plant-associated microbial community response to long-term mowing is plant compartment- and trait-variation-dependent, and advance our understanding of the leaf/root microbiome-trait relationships in complex plant communities.</span></li> </ol>
Plant trait responses to variation in N and P availability
<ol> <li><span>Global change drivers such as eutrophication and plant invasions will create novel environments for many plant species. Through adaptive trait plasticity plants may maintain their performance under these novel conditions and may outcompete those showing low adaptive trait plasticity. In a greenhouse study, we determined if plasticity in traits is adaptive or maladaptive in endangered, non-endangered and invasive plant species in response to variation of nitrogen (N) and phosphorus (P) availability (N:P ratios 1.7, 15 and 135) and whether plastic trait responses are adaptive and/or costly for fitness (i.e. biomass). </span></li> <li><span>Species choice comprised 17 species from three functional groups (legumes, non-legume forbs and grasses), either classified as endangered, non-endangered or invasive. After two months plants were harvested and nine traits related to carbon assimilation and nutrient uptake were measured (leaf area, SLA, LDMC, SPAD, RMR, root length, SRL, root surface area and PME activity).</span></li> <li> <span>We found more traits responding plastically to variation in P than in N. Plasticity only created costs when P was varied. Plasticity in traits was mostly adaptively neutral towards fitness, with plasticity in three traits being similarly adaptive across all species groups: SPAD (as a measure of chlorophyll content, adaptive to N and P limitation), leaf area and root surface area (adaptive to P limitation). We found little differences in trait plasticity between endangered, non-endangered and invasive species.</span> </li> <li> <em><span>Synthesis</span></em><span>. Along a gradient from N limitation, balanced N:P supply and P limitation we found that the type of fluctuating nutrient (i.e. if N or P is varied) is decisive for the adaptive value of a trait. Variation in P availability (from balanced supply to P limitation) created both a stronger reduction in fitness as well as created plasticity costs in more traits than variation in N availability (from balanced supply to N limitation). However, the patterns observed in our study may change if nutrient availability is altered, either by nutrient inputs or by a shift in nutrient availabilities, e.g. by decreasing N input as foreseen by European Legislation, but without simultaneously decreasing P input. </span> </li> </ol>
Data from: Phenotypic clines in herbivore resistance and reproductive traits in wild plants along an agricultural gradient
<p>The conversion of natural landscapes to agriculture is a leading cause of biodiversity loss worldwide. While many studies examine how landscape modification affects species diversity, a trait-based approach can provide new insights into species responses to environmental change. Wild plants persisting in heavily modified landscapes provide a unique opportunity to examine species' responses to land use change. Trait expression within a community plays an important role in structuring species interactions, highlighting the potential implications of landscape mediated trait changes on ecosystem functioning. Here we test the effect of increasing agricultural landscape modification on defensive and reproductive traits in three commonly occurring Brassicaceae species to evaluate plant responses to landscape change. We collected seeds from populations at spatially separated sites with variation in surrounding agricultural land cover and grew them in a greenhouse common garden, measuring defensive traits through an herbivore no-choice bioassay as well as reproductive traits such as flower size and seed set. In two of the three species, plants originating from agriculturally dominant landscapes expressed a consistent reduction in flower size and herbivore leaf consumption. One species also showed reduced fitness associated with increasingly agricultural landscapes. These findings suggest that wild plants are responding to landscape modification, highlighting that species diversity alone does not fully capture the effects of land use change. </p>
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Annotated Behaviour and Observability Dataset (ABODe)
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