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Nat Commun
2018 Dec 11;91:5149. doi: 10.1038/s41467-018-07592-1.
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Functional biodiversity loss along natural CO2 gradients.
Teixidó N
,
Gambi MC
,
Parravacini V
,
Kroeker K
,
Micheli F
,
Villéger S
,
Ballesteros E
.
Abstract
The effects of environmental change on biodiversity are still poorly understood. In particular, the consequences of shifts in species composition for marine ecosystem function are largely unknown. Here we assess the loss of functional diversity, i.e. the range of species biological traits, in benthic marine communities exposed to ocean acidification (OA) by using natural CO2 vent systems. We found that functional richness is greatly reduced with acidification, and that functional loss is more pronounced than the corresponding decrease in taxonomic diversity. In acidified conditions, most organisms accounted for a few functional entities (i.e. unique combination of functional traits), resulting in low functional redundancy. These results suggest that functional richness is not buffered by functional redundancy under OA, even in highly diverse assemblages, such as rocky benthic communities.
Fig. 1. Species and functional diversity changes among pH zones. a Barplots show species richness (Sp), number of functional entities (unique trait combinations, FE) and functional richness (volume filled by each assemblage in the four dimensions of the functional space, Vol. 4D). Values are expressed as a relative percentage of the value for the total pool and are displayed above the bars. b Functional space filled by the functional entities (FEs) present in species assemblages from each pH condition. Axes (PCoA1 and PCoA2) represent the first two dimensions of the 4D functional space. Principal coordinate analysis (PCoA) was computed on functional-trait values. Number of species = 72; number of FEs = 68
Fig. 2. Overall distribution of FE abundance across the functional space. Each point represents a functional entity (i.e. unique combination of functional attributes) and the size of the circles is proportional to the relative cover of the species belonging to a certain functional entity. Number of species = 72; number of FEs = 68
Fig. 4. Taxonomic and functional biodiversity loss along the pH gradient. The ambient pH zone is characterized by a mosaic of strategies, from ‘faster’ to ‘slower’ life histories, from encrusting to massive and erect forms, including a variety of sizes, both photosynthetic autotrophy and heterotrophy (including filter feeders and grazers/herbivores), and the presence of calcareous skeletons. The low pH zone is mainly characterized by fleshy morphologies, seasonal population dynamics, fast growth and is mainly composed of non-calcareous organisms, where photosynthetic autotrophy is the major energetic resource. The conditions in low pH zones are used to represent atmospheric carbon dioxide concentration values under future climatic conditions with a decrease in surface pH from −0.14 to −0.4 pH units under IPCC RCP2.6 and RCP8.5 by 2100 relative to 1870. The extreme low pH zone is dominated by encrusting-fleshy forms, ‘fast' growth, non-calcareous organisms and photosynthetic autotrophy as the only energetic resource. The encrusting red form is Hildenbrandia crouaniorum, a non-calcareous, perennial red algae. This extreme low pH zone is used to represent more extreme scenarios based on high CO2 emissions or the more distant future by 2500. See Table 1 for names of selected species supporting ecological functions
Alsterberg,
Consumers mediate the effects of experimental ocean acidification and warming on primary producers.
2013, Pubmed
Alsterberg,
Consumers mediate the effects of experimental ocean acidification and warming on primary producers.
2013,
Pubmed
Balvanera,
Quantifying the evidence for biodiversity effects on ecosystem functioning and services.
2006,
Pubmed
Baselga,
Historical legacies in world amphibian diversity revealed by the turnover and nestedness components of Beta diversity.
2012,
Pubmed
Boyd,
Experimental strategies to assess the biological ramifications of multiple drivers of global ocean change-A review.
2018,
Pubmed
Caldeira,
Oceanography: anthropogenic carbon and ocean pH.
2003,
Pubmed
Cardinale,
Biodiversity loss and its impact on humanity.
2012,
Pubmed
D'agata,
Unexpected high vulnerability of functions in wilderness areas: evidence from coral reef fishes.
2016,
Pubmed
Darling,
Evaluating life-history strategies of reef corals from species traits.
2012,
Pubmed
Dirzo,
Defaunation in the Anthropocene.
2014,
Pubmed
Doney,
Ocean acidification: the other CO2 problem.
2009,
Pubmed
,
Echinobase
Duffy,
The functional role of biodiversity in ecosystems: incorporating trophic complexity.
2007,
Pubmed
Díaz,
Functional traits, the phylogeny of function, and ecosystem service vulnerability.
2013,
Pubmed
Feely,
Impact of anthropogenic CO2 on the CaCO3 system in the oceans.
2004,
Pubmed
Gattuso,
OCEANOGRAPHY. Contrasting futures for ocean and society from different anthropogenic CO₂ emissions scenarios.
2015,
Pubmed
Ghedini,
Trophic compensation reinforces resistance: herbivory absorbs the increasing effects of multiple disturbances.
2015,
Pubmed
Hall-Spencer,
Volcanic carbon dioxide vents show ecosystem effects of ocean acidification.
2008,
Pubmed
,
Echinobase
Isbell,
Linking the influence and dependence of people on biodiversity across scales.
2017,
Pubmed
Kroeker,
Impacts of ocean acidification on marine organisms: quantifying sensitivities and interaction with warming.
2013,
Pubmed
Kroeker,
Community dynamics and ecosystem simplification in a high-CO2 ocean.
2013,
Pubmed
,
Echinobase
Kroeker,
Divergent ecosystem responses within a benthic marine community to ocean acidification.
2011,
Pubmed
Laliberté,
Land-use intensification reduces functional redundancy and response diversity in plant communities.
2010,
Pubmed
Laliberté,
A distance-based framework for measuring functional diversity from multiple traits.
2010,
Pubmed
Linares,
Persistent natural acidification drives major distribution shifts in marine benthic ecosystems.
2015,
Pubmed
Loreau,
Biodiversity and ecosystem functioning: current knowledge and future challenges.
2001,
Pubmed
McGill,
Rebuilding community ecology from functional traits.
2006,
Pubmed
Mouillot,
Functional over-redundancy and high functional vulnerability in global fish faunas on tropical reefs.
2014,
Pubmed
Mouillot,
Rare species support vulnerable functions in high-diversity ecosystems.
2013,
Pubmed
Mouillot,
A functional approach reveals community responses to disturbances.
2013,
Pubmed
Naeem,
The functions of biological diversity in an age of extinction.
2012,
Pubmed
Oliver,
Biodiversity and Resilience of Ecosystem Functions.
2015,
Pubmed
Pacella,
Seagrass habitat metabolism increases short-term extremes and long-term offset of CO2 under future ocean acidification.
2018,
Pubmed
Parravicini,
Global mismatch between species richness and vulnerability of reef fish assemblages.
2014,
Pubmed
Poore,
Global patterns in the impact of marine herbivores on benthic primary producers.
2012,
Pubmed
Teixidó,
Impacts on coralligenous outcrop biodiversity of a dramatic coastal storm.
2013,
Pubmed
Teixidó,
Functional biodiversity loss along natural CO2 gradients.
2018,
Pubmed
,
Echinobase
Villéger,
New multidimensional functional diversity indices for a multifaceted framework in functional ecology.
2008,
Pubmed
Villéger,
The multidimensionality of the niche reveals functional diversity changes in benthic marine biotas across geological time.
2011,
Pubmed
Vizzini,
Ocean acidification as a driver of community simplification via the collapse of higher-order and rise of lower-order consumers.
2017,
Pubmed