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Relationships between biological soil crusts, bacterial diversity and abundance, and ecosystem functioning: Insights from a semi‐arid Mediterranean environment

Identifieur interne : 001400 ( Istex/Corpus ); précédent : 001399; suivant : 001401

Relationships between biological soil crusts, bacterial diversity and abundance, and ecosystem functioning: Insights from a semi‐arid Mediterranean environment

Auteurs : Andrea P. Castillo-Monroy ; Matthew A. Bowker ; Fernando T. Maestre ; Susana Rodríguez-Echeverría ; Isabel Martinez ; Claudia E. Barraza-Zepeda ; Cristina Escolar

Source :

RBID : ISTEX:6102DD18FAAE1430A1BEBF989DE7475F1C664473

English descriptors

Abstract

Questions: To what degree do biological soil crusts (BSCs), which are regulators of the soil surface boundary, influence associated microbial communities? Are these associations important to ecosystem functioning in a Mediterranean semi‐arid environment?

Url:
DOI: 10.1111/j.1654-1103.2010.01236.x

Links to Exploration step

ISTEX:6102DD18FAAE1430A1BEBF989DE7475F1C664473

Le document en format XML

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<forename type="first">Susana</forename>
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<forename type="first">Claudia E.</forename>
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<p>Questions: To what degree do biological soil crusts (BSCs), which are regulators of the soil surface boundary, influence associated microbial communities? Are these associations important to ecosystem functioning in a Mediterranean semi‐arid environment?</p>
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<p>Location: Gypsum outcrops near Belmonte del Tajo, Central Spain.</p>
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<p>Methods: We sampled a total of 45 (50 cm × 50 cm) plots, where we estimated the cover of every lichen and BSC‐forming lichen species. We also collected soil samples to estimate bacterial species richness and abundance, and to assess different surrogates of ecosystem functioning. We used path analysis to evaluate the relationships between the richness/abundance of above‐ and below‐ground species and ecosystem functioning.</p>
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<p>Results: We found that the greatest direct effect upon the ecosystem function matrix was that of the biological soil crust (BSC) richness matrix. A few bacterial species were sensitive to the lichen community, with a disproportionate effect of Collema crispum and Toninia sedifolia compared to their low abundance and frequency. The lichens Fulgensia subbracteata and Toninia spp. also had negative effects on bacteria, while Diploschistes diacapsis consistently affected sensitive bacteria, sometimes positively. Despite these results, very few of the BSC effects on ecosystem function could be ascribed to changes within the bacterial community.</p>
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<p>Conclusion: Our results suggest the primary importance of the richness of BSC‐forming lichens as drivers of small‐scale changes in ecosystem functioning. This study provides valuable insights on semi‐arid ecosystems where plant cover is spatially discontinuous and ecosystem function in plant interspaces is regulated largely by BSCs.</p>
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<affiliation xml:id="a2" countryCode="PT">
<unparsedAffiliation>Centre for Functional Ecology, Department of Life Science. FCTUC, University of Coimbra, 3001‐455 Coimbra, Portugal</unparsedAffiliation>
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<affiliation xml:id="a3" countryCode="CL">
<unparsedAffiliation>Laboratorio de Microbiología, Departamento de Biología, Facultad de Ciencias, Universidad de La Serena, Casilla 599, La Serena, Chile</unparsedAffiliation>
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<keyword xml:id="k1">DGGE analyses</keyword>
<keyword xml:id="k2">Ecosystem functioning</keyword>
<keyword xml:id="k3">Enzyme activity</keyword>
<keyword xml:id="k4">Partial Mantel test</keyword>
<keyword xml:id="k5">Semi‐arid ecosystem</keyword>
<keyword xml:id="k6">Soil bacteria</keyword>
</keywordGroup>
<supportingInformation>
<p>
<b>Appendix S1.</b>
Example DGGE profile. Each lane (1–7) represents a soil sample. Each band represents a bacterial strain. The number of bands was defined as the bacterial richness of each sample. Each strain was labelled with a number follow by a sequential letter (e.g. 1A, 1B … 2A, 2B … 3A, 3B … etc.). Lane M contains the DGGE marker.</p>
<p>
<b>Appendix S2.</b>
Results of effects of community structure in BSC‐forming lichens upon the presence and absence of underlying soil bacterial taxa. NMDS: non‐metric multidimensional scaling analysis was performed; Bact: different bacterial strains found in our samples; Acno:
<i>Acarospora nodulosa</i>
; Plsq:
<i>Placidium squamulosum</i>
; Plpi:
<i>Placidium pilosellum</i>
; Cla:
<i>Cladonia convoluta</i>
; Coll:
<i>Collema crispum</i>
; Dd:
<i>Diploschistes diacapsis</i>
; End:
<i>Endocarpon pusillum</i>
; Fg:
<i>Fulgensia subbracteata</i>
; Lepra:
<i>Lepraria crassissima</i>
; Psgl:
<i>Psora globifera</i>
; Psde:
<i>Psora decipiens</i>
; Pssa:
<i>Psora savizcii</i>
; Sqca:
<i>Squamarina cartilaginea</i>
; Scle:
<i>Squamarina lentigera</i>
; Toal:
<i>Toninia albilabra</i>
; Tose:
<i>Toninia sedifolia</i>
; Toto:
<i>Toninia toniniana</i>
.</p>
<p>
<b>Appendix S3.</b>
Frequency and cover of lichens forming biological soil crusts in the study area. Cover data represent means±SD (
<i>n</i>
=45). Data from Maestre, F.T., Escolar, C., Martinez, I. and Escudero, A. 2008. Are soil lichen communities structured by biotic interactions? A null model analysis.
<i>Journal of Vegetation Science</i>
19: 261–266.</p>
<p>
<b>Appendix S4.</b>
Lichen substances identified in biological soil crust‐forming lichens found in our study area.</p>
<p>Please note: Wiley‐Blackwell are not responsible for the content or functionality of any supporting materials supplied by the authors. Any queries (other than missing material) should be directed to the corresponding author for the article.</p>
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<abstractGroup>
<abstract type="main" xml:lang="en">
<title type="main">Abstract</title>
<p>
<b>Questions: </b>
To what degree do biological soil crusts (BSCs), which are regulators of the soil surface boundary, influence associated microbial communities? Are these associations important to ecosystem functioning in a Mediterranean semi‐arid environment?</p>
<p>
<b>Location: </b>
Gypsum outcrops near Belmonte del Tajo, Central Spain.</p>
<p>
<b>Methods: </b>
We sampled a total of 45 (50 cm × 50 cm) plots, where we estimated the cover of every lichen and BSC‐forming lichen species. We also collected soil samples to estimate bacterial species richness and abundance, and to assess different surrogates of ecosystem functioning. We used path analysis to evaluate the relationships between the richness/abundance of above‐ and below‐ground species and ecosystem functioning.</p>
<p>
<b>Results: </b>
We found that the greatest direct effect upon the ecosystem function matrix was that of the biological soil crust (BSC) richness matrix. A few bacterial species were sensitive to the lichen community, with a disproportionate effect of
<i>Collema crispum</i>
and
<i>Toninia sedifolia</i>
compared to their low abundance and frequency. The lichens
<i>Fulgensia subbracteata</i>
and
<i>Toninia</i>
spp. also had negative effects on bacteria, while
<i>Diploschistes diacapsis</i>
consistently affected sensitive bacteria, sometimes positively. Despite these results, very few of the BSC effects on ecosystem function could be ascribed to changes within the bacterial community.</p>
<p>
<b>Conclusion: </b>
Our results suggest the primary importance of the richness of BSC‐forming lichens as drivers of small‐scale changes in ecosystem functioning. This study provides valuable insights on semi‐arid ecosystems where plant cover is spatially discontinuous and ecosystem function in plant interspaces is regulated largely by BSCs.</p>
</abstract>
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<p>
<b>Castillo‐Monroy, A.P.</b>
(corresponding author:
<email normalForm="andrea.castillo@urjc.es">andrea.castillo@urjc.es</email>
),
<b>Bowker, M.A.</b>
(
<email normalForm="matthew.bowker@nau.edu">matthew.bowker@nau.edu</email>
),
<b>Maestre, F.T.</b>
(
<email normalForm="fernando.maestre@urjc.es">fernando.maestre@urjc.es</email>
),
<b>Martinez, I.</b>
(
<email normalForm="isabel.martinez@escet.urjc.es">isabel.martinez@escet.urjc.es</email>
) &
<b>Escolar, C.</b>
(
<email normalForm="cristina.escolar@urjc.es">cristina.escolar@urjc.es</email>
): Área de Biodiversidad y Conservación, Departamento de Biología y Geología, Escuela Superior de Ciencias Experimentales y Tecnología, Universidad Rey Juan Carlos, 28933 Móstoles, Spain

<b>Rodríguez‐Echeverría, S.</b>
(
<email normalForm="susanare@ci.uc.pt">susanare@ci.uc.pt</email>
): Centre for Functional Ecology, Department of Life Science. FCTUC, University of Coimbra, 3001‐455 Coimbra, Portugal

<b>Barraza‐Zepeda, C.E.</b>
(
<email normalForm="claudiabarraz@gmail.com">claudiabarraz@gmail.com</email>
): Laboratorio de Microbiología, Departamento de Biología, Facultad de Ciencias, Universidad de La Serena, Casilla 599, La Serena, Chile
Current Address: Colorado Plateau Research Station, P.O. Box 5614, ARD Building, Northern Arizona University, Flagstaff, AZ 86011, USA</p>
</note>
<note xml:id="fn2">
<p>Co‐ordinating Editor: Alicia Acosta</p>
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<title>Relationships between biological soil crusts, bacterial diversity and abundance, and ecosystem functioning: Insights from a semi‐arid Mediterranean environment</title>
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<titleInfo type="abbreviated" lang="en">
<title>Biological soil crusts, bacterial diversity and abundance, and ecosystem functioning</title>
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<title>Relationships between biological soil crusts, bacterial diversity and abundance, and ecosystem functioning: Insights from a semi‐arid Mediterranean environment</title>
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<affiliation>Área de Biodiversidad y Conservación, Departamento de Biología y Geología, Escuela Superior de Ciencias Experimentales y Tecnología, Universidad Rey Juan Carlos, 28933 Móstoles, Spain</affiliation>
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<role>
<roleTerm type="text">author</roleTerm>
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<affiliation>Centre for Functional Ecology, Department of Life Science. FCTUC, University of Coimbra, 3001‐455 Coimbra, Portugal</affiliation>
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<roleTerm type="text">author</roleTerm>
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<name type="personal">
<namePart type="given">Isabel</namePart>
<namePart type="family">Martinez</namePart>
<affiliation>Área de Biodiversidad y Conservación, Departamento de Biología y Geología, Escuela Superior de Ciencias Experimentales y Tecnología, Universidad Rey Juan Carlos, 28933 Móstoles, Spain</affiliation>
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<name type="personal">
<namePart type="given">Claudia E.</namePart>
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<affiliation>Laboratorio de Microbiología, Departamento de Biología, Facultad de Ciencias, Universidad de La Serena, Casilla 599, La Serena, Chile</affiliation>
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<name type="personal">
<namePart type="given">Cristina</namePart>
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<affiliation>Área de Biodiversidad y Conservación, Departamento de Biología y Geología, Escuela Superior de Ciencias Experimentales y Tecnología, Universidad Rey Juan Carlos, 28933 Móstoles, Spain</affiliation>
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<edition>Received 7 September 2010, Accepted 5 November 2010</edition>
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<abstract>Questions: To what degree do biological soil crusts (BSCs), which are regulators of the soil surface boundary, influence associated microbial communities? Are these associations important to ecosystem functioning in a Mediterranean semi‐arid environment?</abstract>
<abstract>Location: Gypsum outcrops near Belmonte del Tajo, Central Spain.</abstract>
<abstract>Methods: We sampled a total of 45 (50 cm × 50 cm) plots, where we estimated the cover of every lichen and BSC‐forming lichen species. We also collected soil samples to estimate bacterial species richness and abundance, and to assess different surrogates of ecosystem functioning. We used path analysis to evaluate the relationships between the richness/abundance of above‐ and below‐ground species and ecosystem functioning.</abstract>
<abstract>Results: We found that the greatest direct effect upon the ecosystem function matrix was that of the biological soil crust (BSC) richness matrix. A few bacterial species were sensitive to the lichen community, with a disproportionate effect of Collema crispum and Toninia sedifolia compared to their low abundance and frequency. The lichens Fulgensia subbracteata and Toninia spp. also had negative effects on bacteria, while Diploschistes diacapsis consistently affected sensitive bacteria, sometimes positively. Despite these results, very few of the BSC effects on ecosystem function could be ascribed to changes within the bacterial community.</abstract>
<abstract>Conclusion: Our results suggest the primary importance of the richness of BSC‐forming lichens as drivers of small‐scale changes in ecosystem functioning. This study provides valuable insights on semi‐arid ecosystems where plant cover is spatially discontinuous and ecosystem function in plant interspaces is regulated largely by BSCs.</abstract>
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<topic>Ecosystem functioning</topic>
<topic>Enzyme activity</topic>
<topic>Partial Mantel test</topic>
<topic>Semi‐arid ecosystem</topic>
<topic>Soil bacteria</topic>
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<note type="content"> Appendix S1. Example DGGE profile. Each lane (1–7) represents a soil sample. Each band represents a bacterial strain. The number of bands was defined as the bacterial richness of each sample. Each strain was labelled with a number follow by a sequential letter (e.g. 1A, 1B … 2A, 2B … 3A, 3B … etc.). Lane M contains the DGGE marker. Appendix S2. Results of effects of community structure in BSC‐forming lichens upon the presence and absence of underlying soil bacterial taxa. NMDS: non‐metric multidimensional scaling analysis was performed; Bact: different bacterial strains found in our samples; Acno: Acarospora nodulosa; Plsq: Placidium squamulosum; Plpi: Placidium pilosellum; Cla: Cladonia convoluta; Coll: Collema crispum; Dd: Diploschistes diacapsis; End: Endocarpon pusillum; Fg: Fulgensia subbracteata; Lepra: Lepraria crassissima; Psgl: Psora globifera; Psde: Psora decipiens; Pssa: Psora savizcii; Sqca: Squamarina cartilaginea; Scle: Squamarina lentigera; Toal: Toninia albilabra; Tose: Toninia sedifolia; Toto: Toninia toniniana. Appendix S3. Frequency and cover of lichens forming biological soil crusts in the study area. Cover data represent means±SD (n=45). Data from Maestre, F.T., Escolar, C., Martinez, I. and Escudero, A. 2008. Are soil lichen communities structured by biotic interactions? A null model analysis. Journal of Vegetation Science 19: 261–266. Appendix S4. Lichen substances identified in biological soil crust‐forming lichens found in our study area. Please note: Wiley‐Blackwell are not responsible for the content or functionality of any supporting materials supplied by the authors. Any queries (other than missing material) should be directed to the corresponding author for the article. Appendix S1. Example DGGE profile. Each lane (1–7) represents a soil sample. Each band represents a bacterial strain. The number of bands was defined as the bacterial richness of each sample. Each strain was labelled with a number follow by a sequential letter (e.g. 1A, 1B … 2A, 2B … 3A, 3B … etc.). Lane M contains the DGGE marker. Appendix S2. Results of effects of community structure in BSC‐forming lichens upon the presence and absence of underlying soil bacterial taxa. NMDS: non‐metric multidimensional scaling analysis was performed; Bact: different bacterial strains found in our samples; Acno: Acarospora nodulosa; Plsq: Placidium squamulosum; Plpi: Placidium pilosellum; Cla: Cladonia convoluta; Coll: Collema crispum; Dd: Diploschistes diacapsis; End: Endocarpon pusillum; Fg: Fulgensia subbracteata; Lepra: Lepraria crassissima; Psgl: Psora globifera; Psde: Psora decipiens; Pssa: Psora savizcii; Sqca: Squamarina cartilaginea; Scle: Squamarina lentigera; Toal: Toninia albilabra; Tose: Toninia sedifolia; Toto: Toninia toniniana. Appendix S3. Frequency and cover of lichens forming biological soil crusts in the study area. Cover data represent means±SD (n=45). Data from Maestre, F.T., Escolar, C., Martinez, I. and Escudero, A. 2008. Are soil lichen communities structured by biotic interactions? A null model analysis. Journal of Vegetation Science 19: 261–266. Appendix S4. Lichen substances identified in biological soil crust‐forming lichens found in our study area. Please note: Wiley‐Blackwell are not responsible for the content or functionality of any supporting materials supplied by the authors. Any queries (other than missing material) should be directed to the corresponding author for the article. Appendix S1. Example DGGE profile. Each lane (1–7) represents a soil sample. Each band represents a bacterial strain. The number of bands was defined as the bacterial richness of each sample. Each strain was labelled with a number follow by a sequential letter (e.g. 1A, 1B … 2A, 2B … 3A, 3B … etc.). Lane M contains the DGGE marker. Appendix S2. Results of effects of community structure in BSC‐forming lichens upon the presence and absence of underlying soil bacterial taxa. NMDS: non‐metric multidimensional scaling analysis was performed; Bact: different bacterial strains found in our samples; Acno: Acarospora nodulosa; Plsq: Placidium squamulosum; Plpi: Placidium pilosellum; Cla: Cladonia convoluta; Coll: Collema crispum; Dd: Diploschistes diacapsis; End: Endocarpon pusillum; Fg: Fulgensia subbracteata; Lepra: Lepraria crassissima; Psgl: Psora globifera; Psde: Psora decipiens; Pssa: Psora savizcii; Sqca: Squamarina cartilaginea; Scle: Squamarina lentigera; Toal: Toninia albilabra; Tose: Toninia sedifolia; Toto: Toninia toniniana. Appendix S3. Frequency and cover of lichens forming biological soil crusts in the study area. Cover data represent means±SD (n=45). Data from Maestre, F.T., Escolar, C., Martinez, I. and Escudero, A. 2008. Are soil lichen communities structured by biotic interactions? A null model analysis. Journal of Vegetation Science 19: 261–266. Appendix S4. Lichen substances identified in biological soil crust‐forming lichens found in our study area. Please note: Wiley‐Blackwell are not responsible for the content or functionality of any supporting materials supplied by the authors. Any queries (other than missing material) should be directed to the corresponding author for the article. Appendix S1. Example DGGE profile. Each lane (1–7) represents a soil sample. Each band represents a bacterial strain. The number of bands was defined as the bacterial richness of each sample. Each strain was labelled with a number follow by a sequential letter (e.g. 1A, 1B … 2A, 2B … 3A, 3B … etc.). Lane M contains the DGGE marker. Appendix S2. Results of effects of community structure in BSC‐forming lichens upon the presence and absence of underlying soil bacterial taxa. NMDS: non‐metric multidimensional scaling analysis was performed; Bact: different bacterial strains found in our samples; Acno: Acarospora nodulosa; Plsq: Placidium squamulosum; Plpi: Placidium pilosellum; Cla: Cladonia convoluta; Coll: Collema crispum; Dd: Diploschistes diacapsis; End: Endocarpon pusillum; Fg: Fulgensia subbracteata; Lepra: Lepraria crassissima; Psgl: Psora globifera; Psde: Psora decipiens; Pssa: Psora savizcii; Sqca: Squamarina cartilaginea; Scle: Squamarina lentigera; Toal: Toninia albilabra; Tose: Toninia sedifolia; Toto: Toninia toniniana. Appendix S3. Frequency and cover of lichens forming biological soil crusts in the study area. Cover data represent means±SD (n=45). Data from Maestre, F.T., Escolar, C., Martinez, I. and Escudero, A. 2008. Are soil lichen communities structured by biotic interactions? A null model analysis. Journal of Vegetation Science 19: 261–266. Appendix S4. Lichen substances identified in biological soil crust‐forming lichens found in our study area. Please note: Wiley‐Blackwell are not responsible for the content or functionality of any supporting materials supplied by the authors. Any queries (other than missing material) should be directed to the corresponding author for the article. Appendix S1. Example DGGE profile. Each lane (1–7) represents a soil sample. Each band represents a bacterial strain. The number of bands was defined as the bacterial richness of each sample. Each strain was labelled with a number follow by a sequential letter (e.g. 1A, 1B … 2A, 2B … 3A, 3B … etc.). Lane M contains the DGGE marker. Appendix S2. Results of effects of community structure in BSC‐forming lichens upon the presence and absence of underlying soil bacterial taxa. NMDS: non‐metric multidimensional scaling analysis was performed; Bact: different bacterial strains found in our samples; Acno: Acarospora nodulosa; Plsq: Placidium squamulosum; Plpi: Placidium pilosellum; Cla: Cladonia convoluta; Coll: Collema crispum; Dd: Diploschistes diacapsis; End: Endocarpon pusillum; Fg: Fulgensia subbracteata; Lepra: Lepraria crassissima; Psgl: Psora globifera; Psde: Psora decipiens; Pssa: Psora savizcii; Sqca: Squamarina cartilaginea; Scle: Squamarina lentigera; Toal: Toninia albilabra; Tose: Toninia sedifolia; Toto: Toninia toniniana. Appendix S3. Frequency and cover of lichens forming biological soil crusts in the study area. Cover data represent means±SD (n=45). Data from Maestre, F.T., Escolar, C., Martinez, I. and Escudero, A. 2008. Are soil lichen communities structured by biotic interactions? A null model analysis. Journal of Vegetation Science 19: 261–266. Appendix S4. Lichen substances identified in biological soil crust‐forming lichens found in our study area. Please note: Wiley‐Blackwell are not responsible for the content or functionality of any supporting materials supplied by the authors. Any queries (other than missing material) should be directed to the corresponding author for the article.Supporting Info Item: Supporting info item - </note>
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