Selection in monoculture vs. mixture alters plant metabolic fingerprints

Aims In grassland biodiversity experiments, positive biodiversity effects on primary productivity increase over time. Recent research has shown that differential selection in monoculture and mixed-species communities leads to the rapid emergence of monoculture and mixture types, adapted to their own biotic community. We used eight plant species selected for 8 years in such a biodiversity experiment to test if monoculture and mixture types differed in metabolic profiles using infrared spectroscopy.Methods Fourier transform infrared spectroscopy (FTIR) was used to assess metabolic fingerprints of leaf samples of 10 individuals of each species from either monocultures or mixtures. The FTIR spectra were analyzed using multivariate procedures to assess (i) whether individuals within species could be correctly assigned to monoculture or mixture history based on the spectra alone and (ii) which parts of the spectra drive the group assignment, i.e. which metabolic groups were subject to differential selection in monocultures vs. mixtures.Important findings Plant individuals within each of the eight species could be classified as either from monoculture or mixture selection history based on their FTIR spectra. Different metabolic groups were differentially selected in the different species; some of them may be related to defense of pathogens accumulating more strongly in monocultures than in mixtures. The rapid selection of the monoculture and mixture types within the eight study species could have been due to a sorting-out process based on large initial genetic or epigenetic variation within the species.     

Plant density affects measures of biodiversity effects

Aim s: We tested for the effect of final sowing plant density (i.e. density of established seedlings) on the values of biodiversity effects [transgressive overyielding, net effect, complementarity effect (CE) and selection effect (SE), trait-dependent complementarity and dominance effect] in a glasshouse pot experiment.Methods: We conducted a single-season (4 months) glasshouse experiment. Species monocultures and mixtures containing up to four common meadow species from different functional groups were sown and subsequently thinned to five density levels (8–128 individuals per pot, i.e. 200–3200 individuals m ?2). Community functioning was characterized by yield (both living and dead biomass) of all constituent species.Important Findings: Our results show that plant density (final sowing density in our case, but this finding can be generalized) affects the yields of both monocultures and mixtures. As these and their relationships are the basis for calculation of biodiversity effects, these effects also varied along the density gradient. Net biodiversity effect, CE and SE all increased with density. The net biodiversity effect and the CE switched from negative to quite positive in the four-species mixture. Using Fox's tripartite partitioning, trait-dependent complementarity was minor in comparison to the dominance effect. One of our experimental species did not follow the density-productivity relationship, called constant final yield (CFY), which was reflected in the biodiversity measures. The shape of the density-productivity relationship for experimental species affects also the values of biodiversity indices, particularly when species do not follow the CFY relationship. According to our data and recent simulation experiments, the values of commonly used biodiversity effects can be rather misleading if a species has, e.g. a unimodal dependence of yield for the density gradient and the density level used in the experiment is higher than the peak density.     

Overyielding in grassland communities: testing the sampling effect hypothesis with replicated biodiversity experiments

We derive and test some assumptions and predictions of the Sampling Effect Hypothesis (SEH) by examining the relationship between the traits of species in monoculture and their relative abundance in mixture, and by comparing polyculture performance with single-species plots. Although we found a positive relationship between production in monoculture and dominance in mixtures as predicted by the SEH, the relationship had low explanatory power. Counter to predictions, the species with the highest monoculture biomass were not able to strongly dominate all mixtures; instead the dominance of these species decreased with increasing species richness. On average, polycultures did not achieve greater biomass than (transgressively overyield) the species in each mixture, or at each site, that was most productive in monoculture. However, mixture yields did transgressively overyield both the monoculture biomass of the dominant species in the mixtures, and the weighted average of all monocultures (non-transgressive overyielding), both of which were positively related to increasing species richness. The varying responses of different overyielding tests resulted because resource partitioning and positive interactions were often counter-balanced by selection for species with lower biomass than the highest-yielding monocultures. Judging whether or not mixtures overyield therefore depends in part upon which species is the basis for comparison. We present a new general framework for overyielding analysis where every monoculture provides a potential comparison and from which the most relevant tests can be selected.     

Does functional redundancy exist?

Functional redundancy has often been assumed as an intuitive null hypothesis in biodiversity experiments, but theory based on the classical Lotka-Volterra competition model shows that functional redundancy sensu stricto is incompatible with stable coexistence. Stable coexistence requires differences between species which lead to functional complementarity and differences between the yields of mixtures and monocultures. Only a weaker version of functional redundancy, i.e. that mixture yields lie within the range of variation of monoculture yields, is compatible with stable coexistence in Lotka-Volterra systems. Spatial and temporal environmental variability may provide room for functional redundancy at small spatial and temporal scales, but is not expected to do so at the larger scales at which environmental variations help maintain coexistence. Neutral coexistence of equivalent competitors, non-linear per capita growth rates, and lack of correlation between functional impact and biomass may provide the basis for the existence of functional redundancy in natural ecosystems. Overall, there is a striking parallel between the conditions that allow stable coexistence and those that allow overyielding.     

一年生和多年生豆禾混播草地超产与多样性效应的比较

为了测度一年生和多年生豆禾混播草地的超产效应与植物多样性效应的关系, 明确一年生和多年生混播草地的高产优势, 探索豆禾混播草地多样性效应和超产效应对其生态功能的响应机制, 于2013-2015年在新疆伊犁地区昭苏盆地开展了3年的牧草产量观测试验。该试验设置3种牧草混播种类和混播比例, 分别为一年生豆禾混播草地(2种牧草混播, AM2)和多年生豆禾混播草地(2种牧草混播, PM2; 4种牧草混播, PM4; 6种牧草混播, PM6), 豆禾混播比例分别为6:4、5:5和4:6。结果表明: 1) 2013、2014年和3年平均值AM2的超产幅度小于PM2和PM6, 2015年AM2的超产幅度大于PM2、PM4和PM6; 混播群落生产力与群落组分中生产力最高产物种单产以及各组分种平均单产的差值表现出相似的规律。2) 2013、2014年和3年平均值AM2的互补效应大于PM2、PM4和PM6, AM2的选择效应则远小于互补效应, PM2、PM4和PM6的互补效应则比较稳定。3)物种丰富度和物种均匀度与牧草产量(群落生产力)大部分情况下呈单峰的“饱和上升型”模式, 分别在4种牧草混播和豆禾混播比例为5:5时, 具有较高生产力。4)多年生豆禾混播草地的互补效应、选择效应和多样性净效应均随生长年限的延长而呈下降趋势, 也导致了超产幅度、超产效应及其稳定性的下降。由此可见, 在建植初期, 互补效应和选择效应共同主导了多年生豆禾混播草地的超产效应, 而随着生长年限的延长, 选择效应则成为主要影响因素; 一年生豆禾混播草地的超产效应则一直受互补效应的影响。     

Light partitioning in experimental grass communities

Through complementary use of canopy space in mixtures, aboveground niche separation has the potential to promote species coexistence and increase productivity of mixtures as compared to monocultures. We set up an experiment with five perennial grass species which differed in height and their ability to compete for light to test whether plants partition light under conditions where it is a limiting resource, and if this resource partitioning leads to increased biomass production in mixtures (using relative yield-based methods). Further, we present the first application of a new model of light competition in plant communities. We show that under conditions where biomass production was high and light a limiting resource, only a minority of mixtures outperformed monocultures and overyielding was slight. The observed overyielding could not be explained by species differences in canopy structure and height in monoculture and was also not related to changes in the canopy traits of species when grown in mixture rather than monoculture. However, where overyielding occurred, it was associated with higher biomass density and light interception. In the new model of competition for light, greater light use complementarity was related to increased total energy absorption. Future work should address whether greater canopy space-filling is a cause or consequence of overyielding.     

Overyielding in experimental grassland communities – irrespective of species pool or spatial scale

In a large integrated biodiversity project (‘The Jena Experiment’ in Germany) we established two experiments, one with a pool of 60 plant species that ranged broadly from dominant to subordinate competitors on large 20 × 20 m and small 3.5 × 3.5 m plots (= main experiment), and one with a pool of nine potentially dominant species on small 3.5 × 3.5 m plots (= dominance experiment). We found identical positive species richness–aboveground productivity relationships in the main experiment at both scales. This result suggests that scaling up, at least over the short term, is appropriate in interpreting the implications of such experiments for larger‐scale patterns. The species richness–productivity relationship was more pronounced in the experiment with dominant species (46.7 and 82.6% yield increase compared to mean monoculture, respectively). Additionally, transgressive overyielding occurred more frequently in the dominance experiment (67.7% of cases) than in the main experiment (23.4% of cases). Additive partitioning and relative yield total analyses showed that both complementarity and selection effects contributed to the positive net biodiversity effect.     

Effect of functional group richness and species richness in manipulated productivity–diversity studies: a glasshouse pot experiment

Species and functional group (grasses, legumes, creeping nonlegume forbs, rosette nonlegume forbs) richness of species assemblages composed of 16 species from four functional plant groups were manipulated to evaluate the productivity-diversity relationships in a greenhouse pot experiment. Pots were filled with sand, and supplied at two levels of nutrients. The plants were grown in monocultures, two, four, eight and 16 species mixtures. Individual two, four, and eight species mixtures differed in the richness of functional groups. Although the two characteristics of biodiversity, i.e. species and functional group richness, were necessarily correlated, it was shown that it is possible to separate their effect statistically, and also test for their common effect without pronounced loss of test power. There was a pronounced increase of average aboveground biomass and a mild increase in belowground biomass with biodiversity. The effect of functional group richness was more pronounced than the effect of the number of species. By using the method of Loreau and Hector (Nature 411 (2001) 72), selection and complementarity effects were statistically separated, and the overyielding index was calculated as a ratio of the productivity of a mixture to the productivity of its most productive component (to demonstrate transgressive overyielding). Positive values of complementarity and transgressive overyielding were both found, particularly in some rich communities and under high nutrient levels. Complementarity significantly increased only with functional group richness and mainly under high nutrients in the belowground biomass. Some species, when grown in monocultures, had decreased productivity under higher nutrients, and thus were more productive in mixtures than in monocultures. It seems that those species suffered from too high nutrient levels when grown in monocultures, but not in the presence of other species, which were able to use the nutrients in high concentrations and effectively decrease the nutrient levels. As a consequence, mixtures of high diversity were always more productive under high nutrients. The difference in species proportions between high and low nutrients, characterized by chord distance, increased with species richness. The relative change in productivity decreased with the number of functional groups. This suggests that species richness might lead to stabilization of aggregate characteristics (like total productivity) under changing environmental conditions by changing the proportions of individual species.     

Effects of plant species richness on stand structure and productivity

Aims Aboveground biomass production commonly increases with species richness in plant biodiversity experiments. Little is known about the direct mechanisms that cause this result. We tested if by occupying different heights and depths above and below ground, and by optimizing the vertical distribution of leaf nitrogen, species in mixtures can contribute to increased resource uptake and, thus, increased productivity of the community in comparison with monocultures.Methods We grew 24 grassland plant species, grouped into four nonoverlapping species pools, in monoculture and 3- and 6-species mixture in spatially heterogeneous and uniform soil nutrient conditions. Layered harvests of above- and belowground biomass, as well as leaf nitrogen and light measurements, were taken to assess vertical canopy and root space structure.Important findings The distribution of leaf mass was shifted toward greater heights and light absorption was correspondingly enhanced in mixtures. However, only some mixtures had leaf nitrogen concentration profiles predicted to optimize whole-community carbon gain, whereas in other mixtures species seemed to behave more 'selfish'. Nevertheless, even in these communities, biomass production increased with species richness. The distribution of root biomass below ground did not change from monocultures to three- and six-species mixtures and there was also no indication that mixtures were better than monocultures at extracting heterogeneously as compared to homogeneously distributed soil resources. We conclude that positive biodiversity effect on aboveground biomass production cannot easily be explained by a single or few common mechanisms of differential space use. Rather, it seems that mechanisms vary with the particular set of species combined in a community.     

Interspecific Neighbor Interactions Promote the Positive Diversity-Productivity Relationship in Experimental Grassland Communities

Because the frequency of heterospecific interactions inevitably increases with species richness in a community, biodiversity effects must be expressed by such interactions. However, little is understood how heterospecific interactions affect ecosystem productivity because rarely are biodiversity ecosystem functioning experiments spatially explicitly manipulated. To test the effect of heterospecific interactions on productivity, direct evidence of heterospecific neighborhood interaction is needed. In this study we conducted experiments with a detailed spatial design to investigate whether and how heterospecific neighborhood interactions promote primary productivity in a grassland community. The results showed that increasing the heterospecific: conspecific contact ratio significantly increased productivity. We found there was a significant difference in the variation in plant height between monoculture and mixture communities, suggesting that height-asymmetric competition for light plays a central role in promoting productivity. Heterospecific interactions make tall plants grow taller and short plants become smaller in mixtures compared to monocultures, thereby increasing the efficiency of light interception and utilization. Overyielding in the mixture communities arises from the fact that the loss in the growth of short plants is compensated by the increased growth of tall plants. The positive correlation between species richness and primary production was strengthened by increasing the frequency of heterospecific interactions. We conclude that species richness significantly promotes primary ecosystem production through heterospecific neighborhood interactions.     

Genotypic diversity effects on biomass production in native perennial bioenergy cropping systems

The perennial grass species that are being developed as biomass feedstock crops harbor extensive genotypic diversity, but the effects of this diversity on biomass production are not well understood. We investigated the effects of genotypic diversity in switchgrass (Panicum virgatum) and big bluestem (Andropogon gerardii) on perennial biomass cropping systems in two experiments conducted over 2008–2014 at a 5.4‐ha fertile field site in northeastern Illinois, USA. We varied levels of switchgrass and big bluestem genotypic diversity using various local and nonlocal cultivars – under low or high species diversity, with or without nitrogen inputs – and quantified establishment, biomass yield, and biomass composition. In one experiment (‘agronomic trial’), we compared three switchgrass cultivars in monoculture to a switchgrass cultivar mixture and three different species mixtures, with or without N fertilization. In another experiment (‘diversity gradient’), we varied diversity levels in switchgrass and big bluestem (1, 2, 4, or 6 cultivars per plot), with one or two species per plot. In both experiments, cultivar mixtures produced yields equivalent to or greater than the best cultivars. In the agronomic trial, the three switchgrass mixture showed the highest production overall, though not significantly different than best cultivar monoculture. In the diversity gradient, genotypic mixtures had one‐third higher biomass production than the average monoculture, and none of the monocultures were significantly higher yielding than the average mixture. Year‐to‐year variation in yields was lowest in the three‐cultivar switchgrass mixtures and Cave‐In‐Rock (the southern Illinois cultivar) and also reduced in the mixture of switchgrass and big bluestem relative to the species monocultures. The effects of genotypic diversity on biomass composition were modest relative to the differences among species and genotypes. Our findings suggest that local genotypes can be included in biomass cropping systems without compromising yields and that genotypic mixtures could help provide high, stable yields of high‐quality biomass feedstocks.     

Evidence for rapid evolution in a grassland biodiversity experiment

In long‐term grassland experiments, positive biodiversity effects on plant productivity commonly increase with time. Subsequent glasshouse experiments showed that these strengthened positive biodiversity effects persist not only in the local environment but also when plants are transferred into a common environment. Thus, we hypothesized that community diversity had acted as a selective agent, resulting in the emergence of plant monoculture and mixture types with differing genetic composition. To test our hypothesis, we grew offspring from plants that were grown for eleven years in monoculture or mixture environments in a biodiversity experiment (Jena Experiment) under controlled glasshouse conditions in monocultures or two‐species mixtures. We used epiGBS, a genotyping‐by‐sequencing approach combined with bisulphite conversion, to provide integrative genetic and epigenetic (i.e., DNA methylation) data. We observed significant divergence in genetic and DNA methylation data according to selection history in three out of five perennial grassland species, namely Galium mollugo, Prunella vulgaris and Veronica chamaedrys, with DNA methylation differences mostly reflecting the genetic differences. In addition, current diversity levels in the glasshouse had weak effects on epigenetic variation. However, given the limited genome coverage of the reference‐free bisulphite method epiGBS, it remains unclear how much of the differences in DNA methylation was independent of underlying genetic differences. Our results thus suggest that selection of genetic variants, and possibly epigenetic variants, caused the rapid emergence of monoculture and mixture types within plant species in the Jena Experiment.     

Environmental heterogeneity increases complementarity in experimental grassland communities

Previous grassland biodiversity experiments were carried out in uniform environments. It is conceivable, however, that biodiversity effects on community characteristics such as primary productivity might be enhanced under more realistic levels of environmental heterogeneity, if this allows complementary resource use by different species in mixture. Therefore, we would expect larger complementarity effects between species in a heterogeneous environment than in a uniform environment. We tested these hypotheses with experiments in four non-overlapping species pools containing the three functional groups grasses, herbs and legumes. We established all species in monoculture, 3- and 6-species mixture on plots with horizontally heterogeneous or uniform distribution of the same total amount of soil nutrients. The positive net biodiversity effects on aboveground biomass production were similar in both heterogeneous and uniform environment. When the net biodiversity effects were partitioned into components, however, it became clear that in the heterogeneous environment they were due to increased complementarity among species whereas in the uniform environment dominance of species with high monoculture yield played also an important role.     

Exotic tree seedlings are much more competitive than natives but show underyielding when growing together

Aims Invasive species continue to be a worldwide threat to ecosystems mainly as a cause for biodiversity loss. Forest ecosystems, for example, are subject to a change in species composition due to the invasion of exotic species. Specifying the attributes that cause the strong competitiveness of several exotic species may improve the ability to understand and effectively manage plant invasions in the future. In this study the following hypotheses were tested: (1) biomass production of below- and aboveground plant components of the exotic tree species is higher than that of the natives, resulting in a higher competitiveness of the exotics; (2) the exclusion of root competition has a positive effect on the biomass production of the inferior native species; and (3) mixtures of native and exotic species yield a higher biomass production than the respective monocultures.Methods A pot experiment, containing about 2000 tree seedlings, was established. We investigated the biomass productivity and growth reactions of two native (Quercus robur L., Carpinus betulus L.) and two exotic tree species (Prunus serotina Ehrh., Robinia pseudoacacia L.) in different intra- and interspecific, competitive situations with and without the influence of root competition.Important findings The biomass production of both exotic species was significantly higher and led to a strong competitive advantage, resulting in a biomass decrease of the less competitive native species. The high belowground biomass of both exotic species had a negative effect on the biomass production. The competitive pressure of exotic tree seedlings on the native ones was largely driven by root competition. Furthermore, mixtures of native and exotic tree species had a higher productivity than their growth in monocultures would have predicted. Competition was lower for exotic species in mixtures with the less productive native species compared to the competition in monocultures or in mixture with the other highly productive exotic species. Accordingly, both highly competitive exotic species produced less biomass in mixture with each other compared to monocultures. Despite the significantly higher biomass of P. serotina in all mixtures and in monoculture, R. pseudoacacia seemed to be the dominating species. Due to its strong root competition, R. pseudoacacia significantly reduced the biomass production of P. serotina .     

Colonization sequence influences selection and complementarity effects on biomass production in experimental algal microcosms

Species extinction and immigration are both common in natural communities and the sequence with which species are lost from or added to communities may be crucial to community structure. We experimentally addressed this issue by growing six green algal species in monocultures and all possible two-species mixtures, with two colonization sequences for each mixture. Both convergence and divergence in community structure were observed. The compositions containing particularly productive species were more likely to converge, while those comprising of species with similar monoculture yields were more likely to diverge. The species mixtures with high-yielding initial and low-yielding invading species produced more biomass than monocultures, but mixtures with the opposite assembly order produced only the same level of biomass as monocultures did. To address the diversity–ecosystem functioning issue, we estimate complementarity effect by relative yield total (RYT) and selection effect by the correlation between species' monoculture yields and their relative yields in mixtures, respectively. We found overall negative complementarity and positive selection effect in mixtures with high-yielding species as initial colonizers, but positive complementarity and negative selection effect in mixtures with low-yielding initial species. Nonetheless, because we used only up to two species in each microcosm, our results are limited in addressing the relationship between species diversity and ecosystem functioning. Future research should study the effects of immigration history with many more species involved in community assembly.     

Predicting ecosystem stability from community composition and biodiversity

As biodiversity is declining at an unprecedented rate, an important current scientific challenge is to understand and predict the consequences of biodiversity loss. Here, we develop a theory that predicts the temporal variability of community biomass from the properties of individual component species in monoculture. Our theory shows that biodiversity stabilises ecosystems through three main mechanisms: (1) asynchrony in species’ responses to environmental fluctuations, (2) reduced demographic stochasticity due to overyielding in species mixtures and (3) reduced observation error (including spatial and sampling variability). Parameterised with empirical data from four long‐term grassland biodiversity experiments, our prediction explained 22–75% of the observed variability, and captured much of the effect of species richness. Richness stabilised communities mainly by increasing community biomass and reducing the strength of demographic stochasticity. Our approach calls for a re‐evaluation of the mechanisms explaining the effects of biodiversity on ecosystem stability.     

资源互补效应对多样性-生产力关系的影响

许多有关物种多样性-生态系统功能关系的观察、理论和实验研究都表明, 在局域尺度范围内, 植物种多样性对生态系统生产力存在正效应。 然而, 对于促成这种关系的潜在生态学机制却缺乏足够的了解。 该实验利用9种一年生栽培牧草, 采用各物种单播及混播的方法, 构建不同多样性梯度的实验群落, 对物种多样性与生态系统生产力的关系及资源互补效应对系统生产力的影响进行了研究。 结果表明, 在一年生植物群落内,植物种多样性在一定程度内对系统生产力存在正效应, 物种多样性与生产力呈二次函数关系, 关系式为y = -98.449x² + 1 039.2 x - 42.407, (R² = 0.423 1)。 各物种在资源利用、生长速度和竞争能力等功能特征方面存在较大差异, 最高产物种和最低产物种间产量相差5.8倍。 在同一多样性梯度内, 不同物种组合的群落间生产力和互补效应也存在较大差异, 说明物种的成分对生态系统生产力也有重要影响。 同时,在混播群落中程度不同地存在着资源的互补性利用, 说明物种多样性对系统生产力有增强作用, 但相关分析表明, 互补效应和物种多样性间不存在显著相关关系。互补效应的4种计算方法所反映的资源互补程度有所不同, 每种方法各有利弊, 在对系统的多样性效应作用机制进行评价时, 应根据具体情况, 同时采用几种方法, 以利于对资源互补效应做出恰当的估测。     

Partitioning the effects of algal species identity and richness on benthic marine primary production

Influential research in terrestrial habitats indicates that several ecosystem processes are related to plant biodiversity, yet these links remain poorly studied in marine ecosystems. We conducted one field and one mesocosm experiment to quantify the relative effects of macroalgal species identity and richness on primary production in coral reef macroalgal communities off the north coast of Jamaica. We measured production as the net accumulation of algal biomass in the absence of consumers and as photosynthetic rate using oxygen probes in sealed aquaria. We used two recently developed techniques to attribute deviations in expected relative yield to components associated with species identity or diversity and then to further partition diversity effects into mechanistic components based on dominance, trait-dependent complementarity, and trait-independent complementarity. Our results indicate that algal identity had far greater effects on absolute net growth and photosynthesis than richness. The most diverse mixture of macroalgae did not outperform the most productive monoculture or the average monoculture in either measure of primary production (i.e. we did not find evidence of either transgressive or non-transgressive overyielding). Trait-independent complementarity effects were positive but dominance and trait-dependent complementarity were both negative and became stronger when richness was increased. Thus the potentially positive influence of species interactions and niche partitioning on production were negated by dominance and other negative selection effects. These results demonstrate that the counteracting influence of component effects can diminish the net richness effects on production. This could explain frequently observed weak net richness effects in other aquatic and terrestrial systems and suggests that life history tradeoffs greatly reduce the potential for ecologically relevant plant biodiversity effects on ecosystem properties.     

Effects of total resources, resource ratios, and species richness on algal productivity and evenness at both metacommunity and local scales

The study of the interrelationship between productivity and biodiversity is a major research field in ecology. Theory predicts that if essential resources are heterogeneously distributed across a metacommunity, single species may dominate productivity in individual metacommunity patches, but a mixture of species will maximize productivity across the whole metacommunity. It also predicts that a balanced supply of resources within local patches should favor species coexistence, whereas resource imbalance would favor the dominance of one species. We performed an experiment with five freshwater algal species to study the effects of total supply of resources, their ratios, and species richness on biovolume production and evenness at the scale of both local patches and metacommunities. Generally, algal biovolume increased, whereas algal resource use efficiency (RUE) and evenness decreased with increasing total supply of resources in mixed communities containing all five species. In contrast to predictions for biovolume production, the species mixtures did not outperform all monocultures at the scale of metacommunities. In other words, we observed no general transgressive overyielding. However, RUE was always higher in mixtures than predicted from monocultures, and analyses indicate that resource partitioning or facilitation in mixtures resulted in higher-than-expected productivity at high resource supply. Contrasting our predictions for the local scale, balanced supply of resources did not generally favor higher local evenness, however lowest evenness was confined to patches with the most imbalanced supply. Thus, our study provides mixed support for recent theoretical advancements to understand biodiversity-productivity relationships.     

Small scale genotypic richness stabilizes plot biomass and increases phenotypic variance in the invasive grass Phalaris arundinacea

Aims We aim to understand how small-scale genotypic richness and genotypic interactions influence the biomass and potential invasiveness of the invasive grass, Phalaris arundinacea under two different disturbance treatments: intact plots and disturbed plots, where all the native vegetation has been removed. Specifically, we address the following questions (i) Does genotypic richness increase biomass production? (ii) Do genotypic interactions promote or reduce biomass production? (iii) Does the effect of genotypic richness and genotypic interactions differ in different disturbance treatments? Finally (iv) Is phenotypic variation greater as genotypic richness increases?Methods We conducted a 2-year common garden experiment in which we manipulated genotype richness using eight genotypes planted under both intact and disturbed conditions in a wetland in Burlington, Vermont (44°27′23″N, 73°11′29″W). The experiment consisted of a randomized complete block design of three blocks, each containing 20 plots (0.5 m 2) per disturbed treatment. We calculated total plot biomass and partitioned the net biodiversity effect into three components: dominance effect, trait-dependent complementarity and trait-independent complementarity. We calculated the phenotypic variance for each different genotype richness treatment under the two disturbance treatments.Important findings Our results indicate that local genotypic richness does not increase total biomass production of the invasive grass P. arundinacea in either intact or disturbed treatments. However, genotypic interactions underlying the responses showed very different patterns in response to increasing genotypic richness. In the intact treatment, genotypic interactions resulted in the observed biomass being greater than the predicted biomass from monoculture plots (e.g., overyielding) and this was driven by facilitation. However, facilitation was reduced as genotypic richness increased. In the disturbed treatment, genotypic interactions resulted in underyielding with observed biomass being slightly less than expected from the performance of genotypes in monocultures; however, underyielding was reduced as genotypic richness increased. Thus, in both treatments, higher genotypic richness resulted in plot biomass nearing the additive biomass from individual monocultures. In general, higher genotypic richness buffered populations against interactions that would have reduced biomass and potentially spread. Phenotypic variance also had contrasting patterns in intact and disturbed treatments. In the intact treatment, phenotypic variance was low across all genotypic richness levels, while in the disturbed treatment, phenotypic variance estimates increased as genotypic richness increased. Thus, under the disturbed treatment, plots with higher genotypic richness had a greater potential response to selection. Therefore, limiting the introduction of new genotypes, even if existing genotypes of the invasive species are already present, should be considered a desirable management strategy to limit the invasive behavior of alien species.