Literature DB >> 20380210

A mechanistic basis for underyielding in phytoplankton communities.

Andrea Schmidtke1, Ursula Gaedke, Guntram Weithoff.   

Abstract

Species richness has been shown to increase biomass production of plant communities. Such overyielding occurs when a community performs better than its component monocultures due to the complementarity or dominance effect and is mostly detected in substrate-bound plant communities (terrestrial plants or submerged macrophytes) where resource use complementarity can be enhanced due to differences in rooting architecture and depth. Here, we investigated whether these findings are generalizeable for free-floating phytoplankton with little potential for spatial differences in resource use. We performed aquatic microcosm experiments with eight phytoplankton species belonging to four functional groups to determine the manner in which species and community biovolume varies in relation to the number of functional groups and hypothesized that an increasing number of functional groups within a community promotes overyielding. Unexpectedly, we did not detect overyielding in any algal community. Instead, total community biovolume tended to decrease with an increasing number of functional groups. This underyielding was mainly caused by the negative dominance effect that originated from a trade-off between growth rate and final biovolume. In monoculture, slow-growing species built up higher biovolumes than fast-growing ones, whereas in mixture a fast-growing but low-productive species monopolized most of the nutrients and prevented competing species from developing high biovolumes expected from monocultures. Our results indicated that the magnitude of the community biovolume was largely determined by the identity of one species. Functional diversity and resource use complementarity were of minor importance among free-floating phytoplankton, possibly reflecting the lack of spatially heterogeneous resource distribution. As a consequence, biodiversity-ecosystem functioning relationships may not be easily generalizeable from substrate-bound plant to phytoplankton communities and vice versa.

Mesh:

Year:  2010        PMID: 20380210     DOI: 10.1890/08-2370.1

Source DB:  PubMed          Journal:  Ecology        ISSN: 0012-9658            Impact factor:   5.499


  14 in total

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Authors:  Erik Sperfeld; Andrea Schmidtke; Ursula Gaedke; Guntram Weithoff
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Authors:  Michael P Carey; David H Wahl
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4.  Interplay between r- and K-strategists leads to phytoplankton underyielding under pulsed resource supply.

Authors:  Lydia A Papanikolopoulou; Evangelia Smeti; Daniel L Roelke; Panayiotis G Dimitrakopoulos; Giorgos D Kokkoris; Daniel B Danielidis; Sofie Spatharis
Journal:  Oecologia       Date:  2018-01-03       Impact factor: 3.225

5.  Biomass and lipid production of dinoflagellates and raphidophytes in indoor and outdoor photobioreactors.

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Journal:  Microorganisms       Date:  2022-04-14

7.  Phytoplankton assemblage characteristics in recurrently fluctuating environments.

Authors:  Daniel L Roelke; Sofie Spatharis
Journal:  PLoS One       Date:  2015-03-23       Impact factor: 3.240

8.  Per capita interactions and stress tolerance drive stress-induced changes in biodiversity effects on ecosystem functions.

Authors:  Jan M Baert; Colin R Janssen; Koen Sabbe; Frederik De Laender
Journal:  Nat Commun       Date:  2016-08-18       Impact factor: 14.919

9.  Toward an Ecologically Optimized N:P Recovery from Wastewater by Microalgae.

Authors:  Tânia V Fernandes; María Suárez-Muñoz; Lukas M Trebuch; Paul J Verbraak; Dedmer B Van de Waal
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10.  Biodiversity increases the productivity and stability of phytoplankton communities.

Authors:  Alina A Corcoran; Wiebke J Boeing
Journal:  PLoS One       Date:  2012-11-16       Impact factor: 3.240

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