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Realistic changes in seaweed biodiversity affect multiple ecosystem functions on a rocky shore
Given current threats to biodiversity, understanding the effects of diversity changes on the functions and services associated with intact ecosystems is of paramount importance. However, limited realism in most biodiversity studies makes it difficult to link the large and growing body of evidence fo...
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Published in: | Ecology (Durham) 2013-09, Vol.94 (9), p.1944-1954 |
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container_end_page | 1954 |
container_issue | 9 |
container_start_page | 1944 |
container_title | Ecology (Durham) |
container_volume | 94 |
creator | Bracken, Matthew E. S Williams, Susan L |
description | Given current threats to biodiversity, understanding the effects of diversity changes on the functions and services associated with intact ecosystems is of paramount importance. However, limited realism in most biodiversity studies makes it difficult to link the large and growing body of evidence for important functional consequences of biodiversity change to real-world losses of biodiversity. Here, we explored two methods of incorporating realism into biodiversity research: (1) the use of two-, five-, and eight-species assemblages that mimicked those that we observed in surveys of seaweed biodiversity patterns on a northern California (USA) rocky shore and the explicit comparison of those assemblages to random assemblages compiled from the same local species pool; and (2) the measurement of two fundamental ecosystem functions, nitrate uptake and photosynthesis, both of which contribute to growth of primary producers. Specifically, we measured nitrate uptake rates of seaweed assemblages as a function of initial nitrate concentrations and photosynthetic rates as a function of irradiance levels for both realistic and random assemblages of seaweeds. We only observed changes in ecosystem functioning along a richness gradient for realistic assemblages, and both maximum nitrate uptake rates (
V
max
) and photosynthetic light use efficiency values (α
P
=
P
max
/
I
K
) were higher in realistic assemblages than in random assemblages. Furthermore, the parameter affected by changes in richness depended on the function being measured. Both
V
max
and α
P
declined with increasing richness in nonrandom assemblages due to a combination of species identity effects (for
V
max
) and overyielding effects (for both
V
max
and α
P
). In contrast, neither nitrate uptake efficiency values (α
N
=
V
max
/
K
s
), nor maximum photosynthetic rates (
P
max
) changed along the gradient in seaweed species richness. Furthermore, overyielding was only evident in realistic assemblages, and the parameters exhibiting overyielding, including
V
max
, α
N
,
P
max
, and α
P
, changed along a gradient in species richness. Our results suggest that in realistic assemblages of species (1) some functions may be maximized at low levels of species richness, and (2) it is not only diversity, per se, that is important for sustaining multiple ecosystem functions, but also the range of diversity values in an ecosystem. |
doi_str_mv | 10.1890/12-2182.1 |
format | article |
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V
max
) and photosynthetic light use efficiency values (α
P
=
P
max
/
I
K
) were higher in realistic assemblages than in random assemblages. Furthermore, the parameter affected by changes in richness depended on the function being measured. Both
V
max
and α
P
declined with increasing richness in nonrandom assemblages due to a combination of species identity effects (for
V
max
) and overyielding effects (for both
V
max
and α
P
). In contrast, neither nitrate uptake efficiency values (α
N
=
V
max
/
K
s
), nor maximum photosynthetic rates (
P
max
) changed along the gradient in seaweed species richness. Furthermore, overyielding was only evident in realistic assemblages, and the parameters exhibiting overyielding, including
V
max
, α
N
,
P
max
, and α
P
, changed along a gradient in species richness. Our results suggest that in realistic assemblages of species (1) some functions may be maximized at low levels of species richness, and (2) it is not only diversity, per se, that is important for sustaining multiple ecosystem functions, but also the range of diversity values in an ecosystem.</description><identifier>ISSN: 0012-9658</identifier><identifier>EISSN: 1939-9170</identifier><identifier>DOI: 10.1890/12-2182.1</identifier><identifier>PMID: 24279266</identifier><identifier>CODEN: ECGYAQ</identifier><language>eng</language><publisher>Washington, DC: Ecological Society of America</publisher><subject>Algae ; Animal and plant ecology ; Animal, plant and microbial ecology ; Animals ; Aquatic ecology ; Biodiversity ; Biological and medical sciences ; Bodega Marine Reserve, California, USA ; Coasts ; Ecological function ; ecosystem function ; Ecosystem studies ; Ecosystems ; Fundamental and applied biological sciences. Psychology ; General aspects ; Geological Phenomena ; Light ; Marine ecology ; Marine ecosystems ; Nitrates ; nonrandom ; Oxygen ; Photosynthesis ; Plant growth ; random ; realistic ; rocky intertidal ; Sea water ecosystems ; seaweed ; Seaweed - classification ; Seaweeds ; Species ; Species diversity ; Species Specificity ; Synecology</subject><ispartof>Ecology (Durham), 2013-09, Vol.94 (9), p.1944-1954</ispartof><rights>Copyright © 2013 Ecological Society of America</rights><rights>2013 by the Ecological Society of America</rights><rights>2014 INIST-CNRS</rights><rights>Copyright Ecological Society of America Sep 2013</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a6014-e90aa5af3224b8f2eaba1fcadf3977408a6b728a2a6b897553bc514e294b0c203</citedby><cites>FETCH-LOGICAL-a6014-e90aa5af3224b8f2eaba1fcadf3977408a6b728a2a6b897553bc514e294b0c203</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/23597317$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/23597317$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>314,780,784,27924,27925,58238,58471</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=27761581$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24279266$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Shanks, AL</contributor><creatorcontrib>Bracken, Matthew E. S</creatorcontrib><creatorcontrib>Williams, Susan L</creatorcontrib><title>Realistic changes in seaweed biodiversity affect multiple ecosystem functions on a rocky shore</title><title>Ecology (Durham)</title><addtitle>Ecology</addtitle><description>Given current threats to biodiversity, understanding the effects of diversity changes on the functions and services associated with intact ecosystems is of paramount importance. However, limited realism in most biodiversity studies makes it difficult to link the large and growing body of evidence for important functional consequences of biodiversity change to real-world losses of biodiversity. Here, we explored two methods of incorporating realism into biodiversity research: (1) the use of two-, five-, and eight-species assemblages that mimicked those that we observed in surveys of seaweed biodiversity patterns on a northern California (USA) rocky shore and the explicit comparison of those assemblages to random assemblages compiled from the same local species pool; and (2) the measurement of two fundamental ecosystem functions, nitrate uptake and photosynthesis, both of which contribute to growth of primary producers. Specifically, we measured nitrate uptake rates of seaweed assemblages as a function of initial nitrate concentrations and photosynthetic rates as a function of irradiance levels for both realistic and random assemblages of seaweeds. We only observed changes in ecosystem functioning along a richness gradient for realistic assemblages, and both maximum nitrate uptake rates (
V
max
) and photosynthetic light use efficiency values (α
P
=
P
max
/
I
K
) were higher in realistic assemblages than in random assemblages. Furthermore, the parameter affected by changes in richness depended on the function being measured. Both
V
max
and α
P
declined with increasing richness in nonrandom assemblages due to a combination of species identity effects (for
V
max
) and overyielding effects (for both
V
max
and α
P
). In contrast, neither nitrate uptake efficiency values (α
N
=
V
max
/
K
s
), nor maximum photosynthetic rates (
P
max
) changed along the gradient in seaweed species richness. Furthermore, overyielding was only evident in realistic assemblages, and the parameters exhibiting overyielding, including
V
max
, α
N
,
P
max
, and α
P
, changed along a gradient in species richness. Our results suggest that in realistic assemblages of species (1) some functions may be maximized at low levels of species richness, and (2) it is not only diversity, per se, that is important for sustaining multiple ecosystem functions, but also the range of diversity values in an ecosystem.</description><subject>Algae</subject><subject>Animal and plant ecology</subject><subject>Animal, plant and microbial ecology</subject><subject>Animals</subject><subject>Aquatic ecology</subject><subject>Biodiversity</subject><subject>Biological and medical sciences</subject><subject>Bodega Marine Reserve, California, USA</subject><subject>Coasts</subject><subject>Ecological function</subject><subject>ecosystem function</subject><subject>Ecosystem studies</subject><subject>Ecosystems</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>General aspects</subject><subject>Geological Phenomena</subject><subject>Light</subject><subject>Marine ecology</subject><subject>Marine ecosystems</subject><subject>Nitrates</subject><subject>nonrandom</subject><subject>Oxygen</subject><subject>Photosynthesis</subject><subject>Plant growth</subject><subject>random</subject><subject>realistic</subject><subject>rocky intertidal</subject><subject>Sea water ecosystems</subject><subject>seaweed</subject><subject>Seaweed - classification</subject><subject>Seaweeds</subject><subject>Species</subject><subject>Species diversity</subject><subject>Species Specificity</subject><subject>Synecology</subject><issn>0012-9658</issn><issn>1939-9170</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><recordid>eNqN0U2LFDEQBuBGFHddPfgDlIAIepg1X51OjjKsH7AgiB68GKozFTdjT2dM0q79780w4w7ICuZShzz1JkU1zWNGz5k29BXjC840P2d3mlNmhFkY1tG7zSml9caoVp80D3Je03qY1PebEy55Z7hSp83XjwhDyCU44q5g_IaZhJFkhGvEFelDXIWfmHIoMwHv0RWymYYStgMSdDHPueCG-Gl0JcQxkzgSICm67zPJVzHhw-aehyHjo0M9az6_ufi0fLe4_PD2_fL15QJU_dICDQVowQvOZa89R-iBeQcrL0zXSapB9R3XwGvVpmtb0buWSeRG9tRxKs6aF_vcbYo_JszFbkJ2OAwwYpyyZVJxoQxV_0Ol5kwZ01b67C-6jlMa6yBVCcVbLqSu6uVeuRRzTujtNoUNpNkyanf7sYzb3X4sq_bpIXHqN7i6kX8WUsHzA4DsYPAJRhfy0XWdYq3eBbV7dx0GnP_9or1YfuGUCSMNM1LWvif7vnUuMR1zRWs6wbrjyFDmbRwtZrh1jFvUzZPblbflVxG_Af3Fxh4</recordid><startdate>201309</startdate><enddate>201309</enddate><creator>Bracken, Matthew E. S</creator><creator>Williams, Susan L</creator><general>Ecological Society of America</general><general>ECOLOGICAL SOCIETY OF AMERICA</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QG</scope><scope>7SN</scope><scope>7SS</scope><scope>7ST</scope><scope>7T7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>K9.</scope><scope>P64</scope><scope>RC3</scope><scope>SOI</scope><scope>7TN</scope><scope>7U6</scope><scope>F1W</scope><scope>H95</scope><scope>L.G</scope><scope>7X8</scope></search><sort><creationdate>201309</creationdate><title>Realistic changes in seaweed biodiversity affect multiple ecosystem functions on a rocky shore</title><author>Bracken, Matthew E. S ; Williams, Susan L</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a6014-e90aa5af3224b8f2eaba1fcadf3977408a6b728a2a6b897553bc514e294b0c203</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Algae</topic><topic>Animal and plant ecology</topic><topic>Animal, plant and microbial ecology</topic><topic>Animals</topic><topic>Aquatic ecology</topic><topic>Biodiversity</topic><topic>Biological and medical sciences</topic><topic>Bodega Marine Reserve, California, USA</topic><topic>Coasts</topic><topic>Ecological function</topic><topic>ecosystem function</topic><topic>Ecosystem studies</topic><topic>Ecosystems</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>General aspects</topic><topic>Geological Phenomena</topic><topic>Light</topic><topic>Marine ecology</topic><topic>Marine ecosystems</topic><topic>Nitrates</topic><topic>nonrandom</topic><topic>Oxygen</topic><topic>Photosynthesis</topic><topic>Plant growth</topic><topic>random</topic><topic>realistic</topic><topic>rocky intertidal</topic><topic>Sea water ecosystems</topic><topic>seaweed</topic><topic>Seaweed - classification</topic><topic>Seaweeds</topic><topic>Species</topic><topic>Species diversity</topic><topic>Species Specificity</topic><topic>Synecology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bracken, Matthew E. S</creatorcontrib><creatorcontrib>Williams, Susan L</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Animal Behavior Abstracts</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Environment Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>Environment Abstracts</collection><collection>Oceanic Abstracts</collection><collection>Sustainability Science Abstracts</collection><collection>ASFA: Aquatic Sciences and Fisheries Abstracts</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) 1: Biological Sciences & Living Resources</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Professional</collection><collection>MEDLINE - Academic</collection><jtitle>Ecology (Durham)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bracken, Matthew E. S</au><au>Williams, Susan L</au><au>Shanks, AL</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Realistic changes in seaweed biodiversity affect multiple ecosystem functions on a rocky shore</atitle><jtitle>Ecology (Durham)</jtitle><addtitle>Ecology</addtitle><date>2013-09</date><risdate>2013</risdate><volume>94</volume><issue>9</issue><spage>1944</spage><epage>1954</epage><pages>1944-1954</pages><issn>0012-9658</issn><eissn>1939-9170</eissn><coden>ECGYAQ</coden><abstract>Given current threats to biodiversity, understanding the effects of diversity changes on the functions and services associated with intact ecosystems is of paramount importance. However, limited realism in most biodiversity studies makes it difficult to link the large and growing body of evidence for important functional consequences of biodiversity change to real-world losses of biodiversity. Here, we explored two methods of incorporating realism into biodiversity research: (1) the use of two-, five-, and eight-species assemblages that mimicked those that we observed in surveys of seaweed biodiversity patterns on a northern California (USA) rocky shore and the explicit comparison of those assemblages to random assemblages compiled from the same local species pool; and (2) the measurement of two fundamental ecosystem functions, nitrate uptake and photosynthesis, both of which contribute to growth of primary producers. Specifically, we measured nitrate uptake rates of seaweed assemblages as a function of initial nitrate concentrations and photosynthetic rates as a function of irradiance levels for both realistic and random assemblages of seaweeds. We only observed changes in ecosystem functioning along a richness gradient for realistic assemblages, and both maximum nitrate uptake rates (
V
max
) and photosynthetic light use efficiency values (α
P
=
P
max
/
I
K
) were higher in realistic assemblages than in random assemblages. Furthermore, the parameter affected by changes in richness depended on the function being measured. Both
V
max
and α
P
declined with increasing richness in nonrandom assemblages due to a combination of species identity effects (for
V
max
) and overyielding effects (for both
V
max
and α
P
). In contrast, neither nitrate uptake efficiency values (α
N
=
V
max
/
K
s
), nor maximum photosynthetic rates (
P
max
) changed along the gradient in seaweed species richness. Furthermore, overyielding was only evident in realistic assemblages, and the parameters exhibiting overyielding, including
V
max
, α
N
,
P
max
, and α
P
, changed along a gradient in species richness. Our results suggest that in realistic assemblages of species (1) some functions may be maximized at low levels of species richness, and (2) it is not only diversity, per se, that is important for sustaining multiple ecosystem functions, but also the range of diversity values in an ecosystem.</abstract><cop>Washington, DC</cop><pub>Ecological Society of America</pub><pmid>24279266</pmid><doi>10.1890/12-2182.1</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record> |
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ispartof | Ecology (Durham), 2013-09, Vol.94 (9), p.1944-1954 |
issn | 0012-9658 1939-9170 |
language | eng |
recordid | cdi_crossref_primary_10_1890_12_2182_1 |
source | JSTOR Archival Journals and Primary Sources Collection; Wiley-Blackwell Read & Publish Collection |
subjects | Algae Animal and plant ecology Animal, plant and microbial ecology Animals Aquatic ecology Biodiversity Biological and medical sciences Bodega Marine Reserve, California, USA Coasts Ecological function ecosystem function Ecosystem studies Ecosystems Fundamental and applied biological sciences. Psychology General aspects Geological Phenomena Light Marine ecology Marine ecosystems Nitrates nonrandom Oxygen Photosynthesis Plant growth random realistic rocky intertidal Sea water ecosystems seaweed Seaweed - classification Seaweeds Species Species diversity Species Specificity Synecology |
title | Realistic changes in seaweed biodiversity affect multiple ecosystem functions on a rocky shore |
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