Net Biodiversity Effect Research Articles

Overyielding and stable species coexistence

The concept of overyielding originated in plant sciences in the 1950s and 1960s and was widely used in the following decades to assess whether mixtures of plants performed better than expected when compared with monocultures. Overyielding has re-emerged in the last few years as an important method in the analysis of biodiversity experiments (Hector, 1998; Loreau, 1998; Loreau et al., 2001, 2002; Hooper et al., 2005) and other new research areas (Bernasconi et al., 2003). Biodiversity experiments manipulate community diversity (while holding other factors constant) to investigate impacts on ecosystem functioning. Previously, use of the overyielding concept has been limited mainly to the analysis of community ecology experiments on species interactions and in agricultural research, particularly intercropping. However, there has been relatively little work that assesses the overyielding concept in the context of community ecology theory. Loreau (2004) used the classical Lotka–Volterra competition model to investigate overyielding and functional redundancy of species in the context of theory on the stable coexistence of species (Fig. 1). In this issue, Beckage & Gross (pp. 140–148) also use Lotka–Volterra competition models to assess the frequency and degree of overyielding of theoretical communities.

Species abundances influence the net biodiversity effect in mixtures of two plant species

Species abundances (evenness or identity of the dominant species in mixtures) usually are not rigorously controlled when testing relationships between plant production and species richness and may be highly dynamic in disturbed or early successional communities. Changes in species abundances may affect the yield of mixtures relative to yields expected from species monocultures [the net biodiversity effect (NBE)] by changing how species that differ in function are distributed in the plant community. To test the prediction that variation in species abundances affects the NBE via changes in the expression of functional differences among species (the complementarity effect), we grew perennial grasses and forbs in field plots in central Texas, USA, as equal-density monocultures and two-species mixtures in which relative abundances of species were varied. Function should differ more consistently between species of different growth forms than of the same growth form. We predicted, therefore, that the complementarity effect and influence of species abundances on the NBE would be more pronounced in grass/forb mixtures than in mixtures with species of the same growth form (grass/grass and forb/forb mixtures). The NBE varied with species evenness in two of the six species pairs studied and with identity of the dominant species in a third species combination. The NBE was sensitive to species proportions in both grass/grass and grass/forb assemblages. In all combinations in which the NBE differed with either evenness or identity of the dominant species, the variation resulted largely from change in the complementarity effect. Our results suggest that the NBE of mixtures is sensitive to effects of species ratios on complementarity.

Effects of macroalgal species identity and richness on primary production in benthic marine communities

Plant biodiversity can enhance primary production in terrestrial ecosystems, but biodiversity effects are largely unstudied in the ocean. We conducted a series of field and mesocosm experiments to measure the relative effects of macroalgal identity and richness on primary productivity (net photosynthetic rate) and biomass accumulation in hard substratum subtidal communities in North Carolina, USA. Algal identity consistently and strongly affected production; species richness effects, although often significent, were subtle. Partitioning of the net biodiversity effect indicated that complementarity effects were always positive and species were usually more productive in mixtures than in monoculture. Surprisingly, slow growing species performed relatively better in the most diverse treatments than the most productive species, thus selection effects were consistently negative. Our results suggest that several basic mechanisms underlying terrestrial plant biodiversity effects also operate in algal-based marine ecosystems, and thus may be general.

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

AbstractIn 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.

Ecosystem recovery after climatic extremes enhanced by genotypic diversity.

Contemporary climate change is characterized both by increasing mean temperature and increasing climate variability such as heat waves, storms, and floods. How populations and communities cope with such climatic extremes is a question central to contemporary ecology and biodiversity conservation. Previous work has shown that species diversity can affect ecosystem functioning and resilience. Here, we show that genotypic diversity can replace the role of species diversity in a species-poor coastal ecosystem, and it may buffer against extreme climatic events. In a manipulative field experiment, increasing the genotypic diversity of the cosmopolitan seagrass Zostera marina enhanced biomass production, plant density, and faunal abundance, despite near-lethal water temperatures due to extreme warming across Europe. Net biodiversity effects were explained by genotypic complementarity rather than by selection of particularly robust genotypes. Positive effects on invertebrate fauna suggest that genetic diversity has second-order effects reaching higher trophic levels. Our results highlight the importance of maintaining genetic as well as species diversity to enhance ecosystem resilience in a world of increasing uncertainty.