TY - JOUR A1 - Wright, Justin P. A1 - Ames, Gregory M. A1 - Mitchelll, Rachel M. T1 - The more things change, the more they stay the same? When is trait variability important for stability of ecosystem function in a changing environment JF - Philosophical transactions of the Royal Society of London : B, Biological sciences N2 - The importance of intraspecific trait variability for community dynamics and ecosystem functioning has been underappreciated. There are theoretical reasons for predicting that species that differ in intraspecific trait variability will also differ in their effects on ecosystem functioning, particularly in variable environments. We discuss whether species with greater trait variability are likely to exhibit greater temporal stability in their population dynamics, and under which conditions this might lead to stability in ecosystem functioning. Resolving this requires us to consider several questions. First, are species with high levels of variation for one trait equally variable in others? In particular, is variability in response and effects traits typically correlated? Second, what is the relative contribution of local adaptation and phenotypic plasticity to trait variability? If local adaptation dominates, then stability in function requires one of two conditions: (i) individuals of appropriate phenotypes present in the environment at high enough frequencies to allow for populations to respond rapidly to the changing environment, and (ii) high levels of dispersal and gene flow. While we currently lack sufficient information on the causes and distribution of variability in functional traits, filling in these key data gaps should increase our ability to predict how changing biodiversity will alter ecosystem functioning. KW - biodiversity KW - intraspecific variation KW - ecosystem function KW - functional traits KW - phenotypic plasticity Y1 - 2016 U6 - https://doi.org/10.1098/rstb.2015.0272 SN - 0962-8436 SN - 1471-2970 VL - 371 PB - Royal Society CY - London ER - TY - JOUR A1 - Weithoff, Guntram A1 - Rocha, Marcia R. A1 - Gaedke, Ursula T1 - Comparing seasonal dynamics of functional and taxonomic diversity reveals the driving forces underlying phytoplankton community structure JF - Freshwater biology N2 - In most biodiversity studies, taxonomic diversity is the measure for the multiplicity of species and is often considered to represent functional diversity. However, trends in taxonomic diversity and functional diversity may differ, for example, when many functionally similar but taxonomically different species co-occur in a community. The differences between these diversity measures are of particular interest in diversity research for understanding diversity patterns and their underlying mechanisms. We analysed a temporally highly resolved 20-year time series of lake phytoplankton to determine whether taxonomic diversity and functional diversity exhibit similar or contrasting seasonal patterns. We also calculated the functional mean of the community in n-dimensional trait space for each sampling day to gain further insights into the seasonal dynamics of the functional properties of the community. We found an overall weak positive relationship between taxonomic diversity and functional diversity with a distinct seasonal pattern. The two diversity measures showed synchronous behaviour from early spring to mid-summer and a more complex and diverging relationship from autumn to late winter. The functional mean of the community exhibited a recurrent annual pattern with the most prominent changes before and after the clear-water phase. From late autumn to winter, the functional mean of the community and functional diversity were relatively constant while taxonomic diversity declined, suggesting competitive exclusion during this period. A further decline in taxonomic diversity concomitant with increasing functional diversity in late winter to early spring is seen as a result of niche diversification together with competitive exclusion. Under these conditions, several different sets of traits are suitable to thrive, but within one set of functional traits only one, or very few, morphotypes can persist. Taxonomic diversity alone is a weak descriptor of trait diversity in phytoplankton. However, the combined analysis of taxonomic diversity and functional diversity, along with the functional mean of the community, allows for deeper insights into temporal patterns of community assembly and niche diversification. KW - algae KW - biodiversity KW - functional traits KW - seasonality KW - time series Y1 - 2015 U6 - https://doi.org/10.1111/fwb.12527 SN - 0046-5070 SN - 1365-2427 VL - 60 IS - 4 SP - 758 EP - 767 PB - Wiley-Blackwell CY - Hoboken ER - TY - JOUR A1 - Wacker, Alexander A1 - Marzetz, Vanessa A1 - Spijkerman, Elly T1 - Interspecific competition in phytoplankton drives the availability of essential mineral and biochemical nutrients JF - Ecology : a publication of the Ecological Society of America N2 - The underlying mechanisms and consequences of competition and diversity are central themes in ecology. A higher diversity of primary producers often results in higher resource use efficiency in aquatic and terrestrial ecosystems. This may result in more food for consumers on one hand, while, on the other hand, it can also result in a decreased food quality for consumers; higher biomass combined with the same availability of the limiting compound directly reduces the dietary proportion of the limiting compound. Here we tested whether and how interspecific competition in phytoplankton communities leads to changes in resource use efficiency and cellular concentrations of nutrients and fatty acids. The measured particulate carbon : phosphorus ratios (C:P) and fatty acid concentrations in the communities were compared to the theoretically expected ratios and concentrations of measurements on simultaneously running monocultures. With interspecific competition, phytoplankton communities had higher concentrations of the monounsaturated fatty acid oleic acid and also much higher concentrations of the ecologically and physiologically relevant long-chain polyunsaturated fatty acid eicosapentaenoic acid than expected concentrations based on monocultures. Such higher availability of essential fatty acids may contribute to the positive relationship between phytoplankton diversity and zooplankton growth, and may compensate limitations by mineral nutrients in higher trophic levels. KW - biodiversity KW - C:P ratio KW - competition KW - eicosapentaenoic acid KW - elemental composition KW - EPA KW - food quality KW - minerals KW - phosphorus KW - polyunsaturated fatty acids KW - PUFA KW - resource use efficiency Y1 - 2015 U6 - https://doi.org/10.1890/14-1915.1 SN - 0012-9658 SN - 1939-9170 VL - 96 IS - 9 SP - 2467 EP - 2477 PB - Wiley CY - Washington ER - TY - JOUR A1 - Venail, Patrick A1 - Gross, Kevin A1 - Oakley, Todd H. A1 - Narwani, Anita A1 - Allan, Eric A1 - Flombaum, Pedro A1 - Isbell, Forest A1 - Joshi, Jasmin Radha A1 - Reich, Peter B. A1 - Tilman, David A1 - van Ruijven, Jasper A1 - Cardinale, Bradley J. T1 - Species richness, but not phylogenetic diversity, influences community biomass production and temporal stability in a re-examination of 16 grassland biodiversity studies JF - Functional ecology : an official journal of the British Ecological Society N2 - Hundreds of experiments have now manipulated species richness (SR) of various groups of organisms and examined how this aspect of biological diversity influences ecosystem functioning. Ecologists have recently expanded this field to look at whether phylogenetic diversity (PD) among species, often quantified as the sum of branch lengths on a molecular phylogeny leading to all species in a community, also predicts ecological function. Some have hypothesized that phylogenetic divergence should be a superior predictor of ecological function than SR because evolutionary relatedness represents the degree of ecological and functional differentiation among species. But studies to date have provided mixed support for this hypothesis. Here, we reanalyse data from 16 experiments that have manipulated plant SR in grassland ecosystems and examined the impact on above-ground biomass production over multiple time points. Using a new molecular phylogeny of the plant species used in these experiments, we quantified how the PD of plants impacts average community biomass production as well as the stability of community biomass production through time. Using four complementary analyses, we show that, after statistically controlling for variation in SR, PD (the sum of branches in a molecular phylogenetic tree connecting all species in a community) is neither related to mean community biomass nor to the temporal stability of biomass. These results run counter to past claims. However, after controlling for SR, PD was positively related to variation in community biomass over time due to an increase in the variances of individual species, but this relationship was not strong enough to influence community stability. In contrast to the non-significant relationships between PD, biomass and stability, our analyses show that SR per se tends to increase the mean biomass production of plant communities, after controlling for PD. The relationship between SR and temporal variation in community biomass was either positive, non-significant or negative depending on which analysis was used. However, the increases in community biomass with SR, independently of PD, always led to increased stability. These results suggest that PD is no better as a predictor of ecosystem functioning than SR.Synthesis. Our study on grasslands offers a cautionary tale when trying to relate PD to ecosystem functioning suggesting that there may be ecologically important trait and functional variation among species that is not explained by phylogenetic relatedness. Our results fail to support the hypothesis that the conservation of evolutionarily distinct species would be more effective than the conservation of SR as a way to maintain productive and stable communities under changing environmental conditions. KW - biodiversity KW - community biomass KW - data synthesis KW - ecosystem functioning KW - grasslands KW - phylogenetic diversity KW - relatedness KW - stability Y1 - 2015 U6 - https://doi.org/10.1111/1365-2435.12432 SN - 0269-8463 SN - 1365-2435 VL - 29 IS - 5 SP - 615 EP - 626 PB - Wiley-Blackwell CY - Hoboken ER - TY - JOUR A1 - Soliveres, Santiago A1 - Maestre, Fernando T. A1 - Ulrich, Werner A1 - Manning, Peter A1 - Boch, Steffen A1 - Bowker, Matthew A. A1 - Prati, Daniel A1 - Delgado-Baquerizo, Manuel A1 - Quero, Jose L. A1 - Schöning, Ingo A1 - Gallardo, Antonio A1 - Weisser, Wolfgang W. A1 - Müller, Jörg A1 - Socher, Stephanie A. A1 - Garcia-Gomez, Miguel A1 - Ochoa, Victoria A1 - Schulze, Ernst-Detlef A1 - Fischer, Markus A1 - Allan, Eric T1 - Intransitive competition is widespread in plant communities and maintains their species richness JF - Ecology letters N2 - Intransitive competition networks, those in which there is no single best competitor, may ensure species coexistence. However, their frequency and importance in maintaining diversity in real-world ecosystems remain unclear. We used two large data sets from drylands and agricultural grasslands to assess: (1) the generality of intransitive competition, (2) intransitivity-richness relationships and (3) effects of two major drivers of biodiversity loss (aridity and land-use intensification) on intransitivity and species richness. Intransitive competition occurred in >65% of sites and was associated with higher species richness. Intransitivity increased with aridity, partly buffering its negative effects on diversity, but was decreased by intensive land use, enhancing its negative effects on diversity. These contrasting responses likely arise because intransitivity is promoted by temporal heterogeneity, which is enhanced by aridity but may decline with land-use intensity. We show that intransitivity is widespread in nature and increases diversity, but it can be lost with environmental homogenisation. KW - Aridity KW - biodiversity KW - coexistence KW - drylands KW - land use KW - mesic grasslands KW - rock-paper-scissors game Y1 - 2015 U6 - https://doi.org/10.1111/ele.12456 SN - 1461-023X SN - 1461-0248 VL - 18 IS - 8 SP - 790 EP - 798 PB - Wiley-Blackwell CY - Hoboken ER - TY - JOUR A1 - Socher, Stephanie A. A1 - Prati, Daniel A1 - Boch, Steffen A1 - Müller, Jörg A1 - Klaus, Valentin H. A1 - Hölzel, Norbert A1 - Fischer, Markus T1 - Direct and productivity-mediated indirect effects of fertilization, mowing and grazing on grassland species richness JF - The journal of ecology N2 - Recent declines in biodiversity have given new urgency to questions about the relationship between land-use change, biodiversity and ecosystem processes. Despite the existence of a large body of research on the effects of land use on species richness, it is unclear whether the effects of land use on species richness are principally direct or indirect, mediated by concomitant changes in ecosystem processes. Therefore, we compared the direct effects of land use (fertilization, mowing and grazing) on species richness with indirect ones (mediated via grassland productivity) for grasslands in central Europe. We measured the richness and above-ground biomass in 150 grassland plots in 3 regions of Germany (the so-called Biodiversity Exploratories). We used univariate and structural equation models to examine direct and indirect land-use effects. The direct effects of mowing (-0.37, effect size) and grazing (0.04) intensity on species richness were stronger compared with the indirect effects of mowing (-0.04) and grazing (-0.01). However, the strong negative effect of fertilization (-0.23) on species richness was mainly indirect, mediated by increased productivity compared with the weak direct negative effect (-0.07). Differences between regions in land-use effects showed five times weaker negative effects of mowing (-0.13) in the region with organic soils (Schorfheide-Chorin), strong overall negative effects of grazing (-0.29) for the region with organic soils opposed to a similar strong positive effect (0.30) in the Hainich-Dun region, whereas the Schwabische Alb region displayed a five times weaker positive effect (0.06) only. Further, fertilization effects on species richness were positive (0.03) for the region with organic soils compared to up to 25 times stronger negative effects in the other two regions. Synthesis. Our results clearly show the importance of studying both direct and indirect effects of land-use intensity. They demonstrate the indirect nature, via productivity, of the negative effect of fertilization intensity on plant species richness in the real-world context of management-induced gradients of intensity of fertilization, mowing and grazing. Finally, they highlight that careful consideration of regional environments is necessary before attempting to generalize land-use effects on species diversity. KW - biodiversity KW - determinants of plant community diversity and structure KW - ecosystem functioning KW - functional plant group KW - land use KW - productivity KW - species richness KW - structural equation modelling Y1 - 2012 U6 - https://doi.org/10.1111/j.1365-2745.2012.02020.x SN - 0022-0477 VL - 100 IS - 6 SP - 1391 EP - 1399 PB - Wiley-Blackwell CY - Hoboken ER - TY - JOUR A1 - Schwarzer, Christian A1 - Heinken, Thilo A1 - Luthardt, Vera A1 - Joshi, Jasmin Radha T1 - Latitudinal shifts in species interactions interfere with resistance of southern but not of northern bog-plant communities to experimental climate change JF - The journal of ecology N2 - The persistence of species under changed climatic conditions depends on adaptations and plastic responses to these conditions and on interactions with their local plant community resulting in direct and indirect effects of changed climatic conditions. Populations at species' range margins may be especially crucial in containing a gene pool comprising adaptations to extreme climatic conditions. Many species of northern European bog ecosystems reach their southern lowland range limit in central Europe. In a common-garden experiment, we experimentally assessed the impact of projected climatic changes on five bog-plant species (including peat moss Sphagnum magellanicum) sampled along a latitudinal gradient of 1400km from Scandinavia to the marginal lowland populations in Germany. Populations were cultivated in monocultures and in experimental communities composed of all five species from their local community, and exposed to five combinations of three climate treatments (warming, fluctuating water-tables, fertilization) in a southern common garden. Whereas most monocultures showed a decreasing biomass production from southern to northern origins under southern environmental conditions, in the experimental mixed-species communities, an increasing biomass production towards northern communities was observed together with a shift in interspecific interactions along the latitudinal gradient. While negative dominance effects prevailed in southern communities, higher net biodiversity effects were observed in northern subarctic communities. The combined effects of climate treatments increased biomass production in monocultures of most origins. In communities, however, overall the treatments did not result in significantly changed biomass production. Among individual treatments, water-table fluctuations caused a significant decrease in biomass production, but only in southern communities, indicating higher vulnerability to changed climatic conditions. Here, negative effects of climate treatments on graminoids were not compensated by the slightly increased growth of peat moss that benefited from interspecific interactions only in northern communities.Synthesis. We conclude that shifting interactions within multispecies communities caused pronounced responses to changed climatic conditions in wetland communities of temperate southern marginal, but not of northern subarctic origin. Therefore, future models investigating the impacts of climate change on plant communities should consider geographical variation in species interactions an important factor influencing community responses to changed climatic conditions. KW - additive partitioning of biodiversity effects KW - biodiversity KW - ecosystem services KW - ecosystem stability KW - intraspecific divergence KW - multifactorial environmental change KW - nitrogen deposition KW - northern peatlands KW - Sphagnum magellanicum KW - wetland ecosystems Y1 - 2013 U6 - https://doi.org/10.1111/1365-2745.12158 SN - 0022-0477 SN - 1365-2745 VL - 101 IS - 6 SP - 1484 EP - 1497 PB - Wiley-Blackwell CY - Hoboken ER - TY - JOUR A1 - Rottstock, Tanja A1 - Joshi, Jasmin Radha A1 - Kummer, Volker A1 - Fischer, Markus T1 - Higher plant diversity promotes higher diversity of fungal pathogens, while it decreases pathogen infection per plant JF - Ecology : a publication of the Ecological Society of America N2 - Fungal plant pathogens are common in natural communities where they affect plant physiology, plant survival, and biomass production. Conversely, pathogen transmission and infection may be regulated by plant community characteristics such as plant species diversity and functional composition that favor pathogen diversity through increases in host diversity while simultaneously reducing pathogen infection via increased variability in host density and spatial heterogeneity. Therefore, a comprehensive understanding of multi-host multi-pathogen interactions is of high significance in the context of biodiversity-ecosystem functioning. We investigated the relationship between plant diversity and aboveground obligate parasitic fungal pathogen ("pathogens" hereafter) diversity and infection in grasslands of a long-term, large-scale, biodiversity experiment with varying plant species (1-60 species) and plant functional group diversity (1-4 groups). To estimate pathogen infection of the plant communities, we visually assessed pathogen-group presence (i.e., rusts, powdery mildews, downy mildews, smuts, and leaf-spot diseases) and overall infection levels (combining incidence and severity of each pathogen group) in 82 experimental plots on all aboveground organs of all plant species per plot during four surveys in 2006. Pathogen diversity, assessed as the cumulative number of pathogen groups on all plant species per plot, increased log-linearly with plant species diversity. However, pathogen incidence and severity, and hence overall infection, decreased with increasing plant species diversity. In addition, co-infection of plant individuals by two or more pathogen groups was less likely with increasing plant community diversity. We conclude that plant community diversity promotes pathogen-community diversity while at the same time reducing pathogen infection levels of plant individuals. KW - biodiversity KW - ecosystem processes KW - ecosystem services KW - grasslands KW - multi-host-multi-pathogen interactions KW - obligate parasitic fungal pathogens KW - pathogen diversity KW - pathogen proneness KW - pathogen transmission KW - plant functional types Y1 - 2014 SN - 0012-9658 SN - 1939-9170 VL - 95 IS - 7 SP - 1907 EP - 1917 PB - Wiley CY - Washington ER - TY - JOUR A1 - Rojas-Jimenez, Keilor A1 - Grossart, Hans-Peter A1 - Cordes, Erik A1 - Cortés, Jorge T1 - Fungal Communities in Sediments Along a Depth Gradient in the Eastern Tropical Pacific JF - Frontiers in Microbiology N2 - Deep waters represent the largest biome on Earth and the largest ecosystem of Costa Rica. Fungi play a fundamental role in global biogeochemical cycling in marine sediments, yet, they remain little explored. We studied fungal diversity and community composition in several marine sediments from 16 locations sampled along a bathymetric gradient (from a depth of 380 to 3,474 m) in two transects of about 1,500 km length in the Eastern Tropical Pacific (ETP) of Costa Rica. Sequence analysis of the V7-V8 region of the 18S rRNA gene obtained from sediment cores revealed the presence of 787 fungal amplicon sequence variants (ASVs). On average, we detected a richness of 75 fungal ASVs per sample. Ascomycota represented the most abundant phylum with Saccharomycetes constituting the dominant class. Three ASVs accounted for ca. 63% of all fungal sequences: the yeast Metschnikowia (49.4%), Rhizophydium (6.9%), and Cladosporium (6.7%). We distinguished a cluster composed mainly by yeasts, and a second cluster by filamentous fungi, but we were unable to detect a strong effect of depth and the overlying water temperature, salinity, dissolved oxygen (DO), and pH on the composition of fungal communities. We highlight the need to understand further the ecological role of fungi in deep-sea ecosystems. KW - deep-sea KW - aquatic fungi KW - biodiversity KW - Metschnikowia KW - Costa Rica Y1 - 2020 U6 - https://doi.org/10.3389/fmicb.2020.575207 SN - 1664-302X VL - 11 PB - Frontiers Media CY - Lausanne ER - TY - JOUR A1 - Mooij, Wolf M. A1 - Trolle, Dennis A1 - Jeppesen, Erik A1 - Arhonditsis, George B. A1 - Belolipetsky, Pavel V. A1 - Chitamwebwa, Deonatus B. R. A1 - Degermendzhy, Andrey G. A1 - DeAngelis, Donald L. A1 - Domis, Lisette Nicole de Senerpont A1 - Downing, Andrea S. A1 - Elliott, J. Alex A1 - Fragoso Jr, Carlos Ruberto A1 - Gaedke, Ursula A1 - Genova, Svetlana N. A1 - Gulati, Ramesh D. A1 - Håkanson, Lars A1 - Hamilton, David P. A1 - Hipsey, Matthew R. A1 - ‘t Hoen, Jochem A1 - Hülsmann, Stephan A1 - Los, F. Hans A1 - Makler-Pick, Vardit A1 - Petzoldt, Thomas A1 - Prokopkin, Igor G. A1 - Rinke, Karsten A1 - Schep, Sebastiaan A. A1 - Tominaga, Koji A1 - Van Dam, Anne A. A1 - Van Nes, Egbert H. A1 - Wells, Scott A. A1 - Janse, Jan H. T1 - Challenges and opportunities for integrating lake ecosystem modelling approaches JF - Aquatic ecology N2 - A large number and wide variety of lake ecosystem models have been developed and published during the past four decades. We identify two challenges for making further progress in this field. One such challenge is to avoid developing more models largely following the concept of others ('reinventing the wheel'). The other challenge is to avoid focusing on only one type of model, while ignoring new and diverse approaches that have become available ('having tunnel vision'). In this paper, we aim at improving the awareness of existing models and knowledge of concurrent approaches in lake ecosystem modelling, without covering all possible model tools and avenues. First, we present a broad variety of modelling approaches. To illustrate these approaches, we give brief descriptions of rather arbitrarily selected sets of specific models. We deal with static models (steady state and regression models), complex dynamic models (CAEDYM, CE-QUAL-W2, Delft 3D-ECO, LakeMab, LakeWeb, MyLake, PCLake, PROTECH, SALMO), structurally dynamic models and minimal dynamic models. We also discuss a group of approaches that could all be classified as individual based: super-individual models (Piscator, Charisma), physiologically structured models, stage-structured models and traitbased models. We briefly mention genetic algorithms, neural networks, Kalman filters and fuzzy logic. Thereafter, we zoom in, as an in-depth example, on the multi-decadal development and application of the lake ecosystem model PCLake and related models (PCLake Metamodel, Lake Shira Model, IPH-TRIM3D-PCLake). In the discussion, we argue that while the historical development of each approach and model is understandable given its 'leading principle', there are many opportunities for combining approaches. We take the point of view that a single 'right' approach does not exist and should not be strived for. Instead, multiple modelling approaches, applied concurrently to a given problem, can help develop an integrative view on the functioning of lake ecosystems. We end with a set of specific recommendations that may be of help in the further development of lake ecosystem models. KW - aquatic KW - food web dynamics KW - plankton KW - nutrients KW - spatial KW - lake KW - freshwater KW - marine KW - community KW - population KW - hydrology KW - eutrophication KW - global change KW - climate warming KW - fisheries KW - biodiversity KW - management KW - mitigation KW - adaptive processes KW - non-linear dynamics KW - analysis KW - bifurcation KW - understanding KW - prediction KW - model limitations KW - model integration Y1 - 2010 U6 - https://doi.org/10.1007/s10452-010-9339-3 SN - 1573-5125 SN - 1386-2588 VL - 44 SP - 633 EP - 667 PB - Springer Science + Business Media B.V. CY - Dordrecht ER -