Land use and climatic factors structure regional patterns in soil microbial communities

Although patterns are emerging for macroorganisms, we have limited understanding of the factors determining soil microbial community composition and productivity at large spatial extents. The overall objective of this study was to discern the drivers of microbial community composition at the extent...

Full description

Saved in:
Bibliographic Details
Published inGlobal ecology and biogeography Vol. 19; no. 1; pp. 27 - 39
Main Authors Drenovsky, Rebecca E., Steenwerth, Kerri L., Jackson, Louise E., Scow, Kate M.
Format Journal Article
LanguageEnglish
Published Oxford, UK Oxford, UK : Blackwell Publishing Ltd 2010
Blackwell Publishing Ltd
Blackwell Publishing
Wiley Subscription Services, Inc
Subjects
Online AccessGet full text

Cover

Loading…
Abstract Although patterns are emerging for macroorganisms, we have limited understanding of the factors determining soil microbial community composition and productivity at large spatial extents. The overall objective of this study was to discern the drivers of microbial community composition at the extent of biogeographical provinces and regions. We hypothesized that factors associated with land use and climate would drive soil microbial community composition and biomass. Great Basin Province, Desert Province and California Floristic Province, California, USA. Using phospholipid fatty acid analysis, we compared microbial communities across eight land-use types sampled throughout the State of California, USA (n= 1117). The main factor driving composition and microbial biomass was land-use type, especially as related to water availability and disturbance. Dry soils were more enriched in Gram-negative bacteria and fungi, and wetter soils were more enriched in Gram-positive, anaerobic and sulphate-reducing bacteria. Microbial biomass was lowest in ecosystems with the wettest and driest soils. Disturbed soils had less fungal and more Gram-positive bacterial biomass than wildland soils. However, some factors known to influence microbial communities, such as soil pH and specific plant taxa, were not important here. Distinct microbial communities were associated with land-use types and disturbance at the regional extent. Overall, soil water availability was an important determinant of soil microbial community composition. However, because of the inclusion of managed and irrigated agricultural ecosystems, the effect of precipitation was not significant. Effects of environmental and management factors, such as flooding, tillage and irrigation, suggest that agricultural management can have larger effects on soil microbial communities than elevation and precipitation gradients.
AbstractList Aim  Although patterns are emerging for macroorganisms, we have limited understanding of the factors determining soil microbial community composition and productivity at large spatial extents. The overall objective of this study was to discern the drivers of microbial community composition at the extent of biogeographical provinces and regions. We hypothesized that factors associated with land use and climate would drive soil microbial community composition and biomass. Location  Great Basin Province, Desert Province and California Floristic Province, California, USA. Methods  Using phospholipid fatty acid analysis, we compared microbial communities across eight land‐use types sampled throughout the State of California, USA ( n = 1117). Results  The main factor driving composition and microbial biomass was land‐use type, especially as related to water availability and disturbance. Dry soils were more enriched in Gram‐negative bacteria and fungi, and wetter soils were more enriched in Gram‐positive, anaerobic and sulphate‐reducing bacteria. Microbial biomass was lowest in ecosystems with the wettest and driest soils. Disturbed soils had less fungal and more Gram‐positive bacterial biomass than wildland soils. However, some factors known to influence microbial communities, such as soil pH and specific plant taxa, were not important here. Main conclusions  Distinct microbial communities were associated with land‐use types and disturbance at the regional extent. Overall, soil water availability was an important determinant of soil microbial community composition. However, because of the inclusion of managed and irrigated agricultural ecosystems, the effect of precipitation was not significant. Effects of environmental and management factors, such as flooding, tillage and irrigation, suggest that agricultural management can have larger effects on soil microbial communities than elevation and precipitation gradients.
Aim Although patterns are emerging for macroorganisms, we have limited understanding of the factors determining soil microbial community composition and productivity at large spatial extents. The overall objective of this study was to discern the drivers of microbial community composition at the extent of biogeographical provinces and regions. We hypothesized that factors associated with land use and climate would drive soil microbial community composition and biomass. Location Great Basin Province, Desert Province and California Floristic Province, California, USA. Methods Using phospholipid fatty acid analysis, we compared microbial communities across eight land-use types sampled throughout the State of California, USA (n= 1117). Results The main factor driving composition and microbial biomass was land-use type, especially as related to water availability and disturbance. Dry soils were more enriched in Gram-negative bacteria and fungi, and wetter soils were more enriched in Gram-positive, anaerobic and sulphate-reducing bacteria. Microbial biomass was lowest in ecosystems with the wettest and driest soils. Disturbed soils had less fungal and more Gram-positive bacterial biomass than wildland soils. However, some factors known to influence microbial communities, such as soil pH and specific plant taxa, were not important here. Main conclusions Distinct microbial communities were associated with land-use types and disturbance at the regional extent. Overall, soil water availability was an important determinant of soil microbial community composition. However, because of the inclusion of managed and irrigated agricultural ecosystems, the effect of precipitation was not significant. Effects of environmental and management factors, such as flooding, tillage and irrigation, suggest that agricultural management can have larger effects on soil microbial communities than elevation and precipitation gradients. [PUBLICATION ABSTRACT]
Although patterns are emerging for macroorganisms, we have limited understanding of the factors determining soil microbial community composition and productivity at large spatial extents. The overall objective of this study was to discern the drivers of microbial community composition at the extent of biogeographical provinces and regions. We hypothesized that factors associated with land use and climate would drive soil microbial community composition and biomass. Great Basin Province, Desert Province and California Floristic Province, California, USA. Using phospholipid fatty acid analysis, we compared microbial communities across eight land-use types sampled throughout the State of California, USA (n= 1117). The main factor driving composition and microbial biomass was land-use type, especially as related to water availability and disturbance. Dry soils were more enriched in Gram-negative bacteria and fungi, and wetter soils were more enriched in Gram-positive, anaerobic and sulphate-reducing bacteria. Microbial biomass was lowest in ecosystems with the wettest and driest soils. Disturbed soils had less fungal and more Gram-positive bacterial biomass than wildland soils. However, some factors known to influence microbial communities, such as soil pH and specific plant taxa, were not important here. Distinct microbial communities were associated with land-use types and disturbance at the regional extent. Overall, soil water availability was an important determinant of soil microbial community composition. However, because of the inclusion of managed and irrigated agricultural ecosystems, the effect of precipitation was not significant. Effects of environmental and management factors, such as flooding, tillage and irrigation, suggest that agricultural management can have larger effects on soil microbial communities than elevation and precipitation gradients.
Aim Although patterns are emerging for macroorganisms, we have limited understanding of the factors determining soil microbial community composition and productivity at large spatial extents. The overall objective of this study was to discern the drivers of microbial community composition at the extent of biogeographical provinces and regions. We hypothesized that factors associated with land use and climate would drive soil microbial community composition and biomass. Location Great Basin Province, Desert Province and California Floristic Province, California, USA. Methods Using phospholipid fatty acid analysis, we compared microbial communities across eight land‐use types sampled throughout the State of California, USA (n= 1117). Results The main factor driving composition and microbial biomass was land‐use type, especially as related to water availability and disturbance. Dry soils were more enriched in Gram‐negative bacteria and fungi, and wetter soils were more enriched in Gram‐positive, anaerobic and sulphate‐reducing bacteria. Microbial biomass was lowest in ecosystems with the wettest and driest soils. Disturbed soils had less fungal and more Gram‐positive bacterial biomass than wildland soils. However, some factors known to influence microbial communities, such as soil pH and specific plant taxa, were not important here. Main conclusions Distinct microbial communities were associated with land‐use types and disturbance at the regional extent. Overall, soil water availability was an important determinant of soil microbial community composition. However, because of the inclusion of managed and irrigated agricultural ecosystems, the effect of precipitation was not significant. Effects of environmental and management factors, such as flooding, tillage and irrigation, suggest that agricultural management can have larger effects on soil microbial communities than elevation and precipitation gradients.
Although patterns are emerging for macroorganisms, we have limited understanding of the factors determining soil microbial community composition and productivity at large spatial extents. The overall objective of this study was to discern the drivers of microbial community composition at the extent of biogeographical provinces and regions. We hypothesized that factors associated with land use and climate would drive soil microbial community composition and biomass. Great Basin Province, Desert Province and California Floristic Province, California, USA. Using phospholipid fatty acid analysis, we compared microbial communities across eight land-use types sampled throughout the State of California, USA ( = 1117). The main factor driving composition and microbial biomass was land-use type, especially as related to water availability and disturbance. Dry soils were more enriched in Gram-negative bacteria and fungi, and wetter soils were more enriched in Gram-positive, anaerobic and sulphate-reducing bacteria. Microbial biomass was lowest in ecosystems with the wettest and driest soils. Disturbed soils had less fungal and more Gram-positive bacterial biomass than wildland soils. However, some factors known to influence microbial communities, such as soil pH and specific plant taxa, were not important here. Distinct microbial communities were associated with land-use types and disturbance at the regional extent. Overall, soil water availability was an important determinant of soil microbial community composition. However, because of the inclusion of managed and irrigated agricultural ecosystems, the effect of precipitation was not significant. Effects of environmental and management factors, such as flooding, tillage and irrigation, suggest that agricultural management can have larger effects on soil microbial communities than elevation and precipitation gradients.
Aim Although patterns are emerging for macroorganisms, we have limited understanding of the factors determining soil microbial community composition and productivity at large spatial extents. The overall objective of this study was to discern the drivers of microbial community composition at the extent of biogeographical provinces and regions. We hypothesized that factors associated with land use and climate would drive soil microbial community composition and biomass. Location Great Basin Province, Desert Province and California Floristic Province,California, USA. Methods Using phospholipid fatty acid analysis, we compared microbial communities across eight land-use types sampled throughout the State of California, USA (n = 1117). Results The main factor driving composition and microbial biomass was landuse type, especially as related to water availability and disturbance. Dry soils were more enriched in Gram-negative bacteria and fungi, and wetter soils were more enriched in Gram-positive, anaerobic and sulphate-reducing bacteria. Microbial biomass was lowest in ecosystems with the wettest and driest soils. Disturbed soils had less fungal and more Gram-positive bacterial biomass than wildland soils. However, some factors known to influence microbial ommunities, such as soil pH and specific plant taxa, were not important here. Main conclusions Distinct microbial communities were associated with landuse types and disturbance at the regional extent. Overall, soil water availability was an important determinant of soil microbial community composition. However, because of the inclusion of managed and irrigated agricultural ecosystems, the effect of precipitation was not significant. Effects of environmental and management factors, such as flooding, tillage and irrigation, suggest that agricultural management can have larger effects on soil microbial communities than elevation and precipitation gradients.
Although patterns are emerging for macroorganisms, we have limited understanding of the factors determining soil microbial community composition and productivity at large spatial extents. The overall objective of this study was to discern the drivers of microbial community composition at the extent of biogeographical provinces and regions. We hypothesized that factors associated with land use and climate would drive soil microbial community composition and biomass.AIMAlthough patterns are emerging for macroorganisms, we have limited understanding of the factors determining soil microbial community composition and productivity at large spatial extents. The overall objective of this study was to discern the drivers of microbial community composition at the extent of biogeographical provinces and regions. We hypothesized that factors associated with land use and climate would drive soil microbial community composition and biomass.Great Basin Province, Desert Province and California Floristic Province, California, USA.LOCATIONGreat Basin Province, Desert Province and California Floristic Province, California, USA.Using phospholipid fatty acid analysis, we compared microbial communities across eight land-use types sampled throughout the State of California, USA (n = 1117).METHODSUsing phospholipid fatty acid analysis, we compared microbial communities across eight land-use types sampled throughout the State of California, USA (n = 1117).The main factor driving composition and microbial biomass was land-use type, especially as related to water availability and disturbance. Dry soils were more enriched in Gram-negative bacteria and fungi, and wetter soils were more enriched in Gram-positive, anaerobic and sulphate-reducing bacteria. Microbial biomass was lowest in ecosystems with the wettest and driest soils. Disturbed soils had less fungal and more Gram-positive bacterial biomass than wildland soils. However, some factors known to influence microbial communities, such as soil pH and specific plant taxa, were not important here.RESULTSThe main factor driving composition and microbial biomass was land-use type, especially as related to water availability and disturbance. Dry soils were more enriched in Gram-negative bacteria and fungi, and wetter soils were more enriched in Gram-positive, anaerobic and sulphate-reducing bacteria. Microbial biomass was lowest in ecosystems with the wettest and driest soils. Disturbed soils had less fungal and more Gram-positive bacterial biomass than wildland soils. However, some factors known to influence microbial communities, such as soil pH and specific plant taxa, were not important here.Distinct microbial communities were associated with land-use types and disturbance at the regional extent. Overall, soil water availability was an important determinant of soil microbial community composition. However, because of the inclusion of managed and irrigated agricultural ecosystems, the effect of precipitation was not significant. Effects of environmental and management factors, such as flooding, tillage and irrigation, suggest that agricultural management can have larger effects on soil microbial communities than elevation and precipitation gradients.MAIN CONCLUSIONSDistinct microbial communities were associated with land-use types and disturbance at the regional extent. Overall, soil water availability was an important determinant of soil microbial community composition. However, because of the inclusion of managed and irrigated agricultural ecosystems, the effect of precipitation was not significant. Effects of environmental and management factors, such as flooding, tillage and irrigation, suggest that agricultural management can have larger effects on soil microbial communities than elevation and precipitation gradients.
ABSTRACT Aim  Although patterns are emerging for macroorganisms, we have limited understanding of the factors determining soil microbial community composition and productivity at large spatial extents. The overall objective of this study was to discern the drivers of microbial community composition at the extent of biogeographical provinces and regions. We hypothesized that factors associated with land use and climate would drive soil microbial community composition and biomass. Location  Great Basin Province, Desert Province and California Floristic Province, California, USA. Methods  Using phospholipid fatty acid analysis, we compared microbial communities across eight land‐use types sampled throughout the State of California, USA (n= 1117). Results  The main factor driving composition and microbial biomass was land‐use type, especially as related to water availability and disturbance. Dry soils were more enriched in Gram‐negative bacteria and fungi, and wetter soils were more enriched in Gram‐positive, anaerobic and sulphate‐reducing bacteria. Microbial biomass was lowest in ecosystems with the wettest and driest soils. Disturbed soils had less fungal and more Gram‐positive bacterial biomass than wildland soils. However, some factors known to influence microbial communities, such as soil pH and specific plant taxa, were not important here. Main conclusions  Distinct microbial communities were associated with land‐use types and disturbance at the regional extent. Overall, soil water availability was an important determinant of soil microbial community composition. However, because of the inclusion of managed and irrigated agricultural ecosystems, the effect of precipitation was not significant. Effects of environmental and management factors, such as flooding, tillage and irrigation, suggest that agricultural management can have larger effects on soil microbial communities than elevation and precipitation gradients.
Author Scow, Kate M.
Drenovsky, Rebecca E.
Steenwerth, Kerri L.
Jackson, Louise E.
AuthorAffiliation 1 Biology Department, John Carroll University, 20700 North Park Boulevard, University Heights, OH 44118 USA
2 USDA/ARS, Crops Pathology and Genetics Research Unit, Davis, CA 95616, USA
3 Department of Land, Air and Water Resources, University of California, Davis, One Shields Avenue, Davis, CA 95616 USA
AuthorAffiliation_xml – name: 3 Department of Land, Air and Water Resources, University of California, Davis, One Shields Avenue, Davis, CA 95616 USA
– name: 2 USDA/ARS, Crops Pathology and Genetics Research Unit, Davis, CA 95616, USA
– name: 1 Biology Department, John Carroll University, 20700 North Park Boulevard, University Heights, OH 44118 USA
Author_xml – sequence: 1
  givenname: Rebecca E.
  surname: Drenovsky
  fullname: Drenovsky, Rebecca E.
– sequence: 2
  givenname: Kerri L.
  surname: Steenwerth
  fullname: Steenwerth, Kerri L.
– sequence: 3
  givenname: Louise E.
  surname: Jackson
  fullname: Jackson, Louise E.
– sequence: 4
  givenname: Kate M.
  surname: Scow
  fullname: Scow, Kate M.
BackLink https://www.ncbi.nlm.nih.gov/pubmed/24443643$$D View this record in MEDLINE/PubMed
BookMark eNqNkktv1DAUhSNURB_wE4BISKibGfyOLSEkKGUGMYJFqcrOchxn8JDEg-3A9N_XaUp4LGi9caTz-UT33HOY7XWuM1mWQzCH6bzYzCFhbMYR5nMEgJgDQDib7-5lB5OwN32jL_vZYQgbAAAllD3I9hEhBDOCD7KLleqqvA8mH27d2FZFq_Na6eh8yEP0vY69N7k3a-s61eRbFaPxXchtlwdnm7y12rvSJkm7tu07G60JD7P7tWqCeXRzH2Xn704_nyxnq0-L9yevVzPNOGIzVPNKY20Mo0VdYaGwECXRSkFRQUVUVWhWYlpWNUdAAKOF0SWndYEpKzjg-Ch7Nfpu-7I1lTZd9KqRW58G8ZfSKSv_Vjr7Va7dD4m5gFywZPD8xsC7770JUbY2aNM0qjOuD5IwQonAJIHH_wWhSKcADKLb0TQ65RRhdjuKClRAnIZN6LN_0I3rfVrJQBFEMIJ8MHzyZyBTEr9WngA-AmlrIXhTTwgEcmiX3MihOHIokRzaJa_bJXe_w56eahtTX9wQrW3uYvByNPhpG3N55x_Lxekbcj3b4_H5JqR2Ts8JIICmgJI-G3UbotlNuvLfJCtwQeXFx4UUy7cFXn44kzDxT0e-Vk6qtbdBnp8hADGAKXMMKb4CIKEKqA
CODEN GEBIFS
CitedBy_id crossref_primary_10_1007_s40333_021_0022_4
crossref_primary_10_1002_ecy_1829
crossref_primary_10_1111_1462_2920_16146
crossref_primary_10_1590_S0100_204X2011001200012
crossref_primary_10_1186_s12898_018_0214_8
crossref_primary_10_1007_s42832_020_0030_x
crossref_primary_10_1111_jbi_12806
crossref_primary_10_1007_s11270_017_3595_y
crossref_primary_10_1007_s10980_014_9996_z
crossref_primary_10_1016_S1002_0160_19_60836_2
crossref_primary_10_1038_s41467_023_37937_4
crossref_primary_10_1007_s00374_021_01599_5
crossref_primary_10_3390_agronomy13102613
crossref_primary_10_1016_j_ejsobi_2018_07_003
crossref_primary_10_1007_s11368_018_2022_3
crossref_primary_10_1177_1178636118810366
crossref_primary_10_1016_j_scitotenv_2024_173630
crossref_primary_10_1893_0005_3155_90_2_112
crossref_primary_10_1016_j_soilbio_2020_107951
crossref_primary_10_1007_s00374_011_0623_8
crossref_primary_10_1016_j_ejsobi_2012_07_002
crossref_primary_10_1016_j_envpol_2016_03_057
crossref_primary_10_5194_bg_18_5085_2021
crossref_primary_10_1007_s00248_013_0195_2
crossref_primary_10_1016_j_apsoil_2021_104311
crossref_primary_10_1016_j_pedobi_2011_08_001
crossref_primary_10_1016_j_scitotenv_2023_167454
crossref_primary_10_1016_j_ecoleng_2017_03_010
crossref_primary_10_1016_j_catena_2016_08_012
crossref_primary_10_1016_j_ecolind_2022_108852
crossref_primary_10_1007_s00248_021_01746_3
crossref_primary_10_1016_j_chemgeo_2012_05_021
crossref_primary_10_1007_s10533_021_00856_x
crossref_primary_10_1139_cjss_2024_0082
crossref_primary_10_1016_j_geodrs_2018_e00173
crossref_primary_10_1016_j_apsoil_2019_05_021
crossref_primary_10_1007_s11104_015_2511_8
crossref_primary_10_1016_j_jenvman_2017_11_067
crossref_primary_10_3389_fgene_2019_01344
crossref_primary_10_1093_femsre_fuaa053
crossref_primary_10_1111_1462_2920_14990
crossref_primary_10_1038_s41598_022_06560_6
crossref_primary_10_1016_j_still_2019_05_015
crossref_primary_10_1016_j_envpol_2019_06_082
crossref_primary_10_1038_s41598_020_74193_8
crossref_primary_10_1111_mec_12854
crossref_primary_10_1016_j_jclepro_2021_127991
crossref_primary_10_1016_j_soilbio_2012_08_023
crossref_primary_10_1016_j_apsoil_2020_103623
crossref_primary_10_1016_j_actao_2018_10_003
crossref_primary_10_3832_ifor3231_013
crossref_primary_10_1038_ismej_2012_48
crossref_primary_10_1088_2515_7620_ad5b3e
crossref_primary_10_1007_s11104_018_3823_2
crossref_primary_10_1016_j_apsoil_2010_11_006
crossref_primary_10_1016_j_soilbio_2014_09_027
crossref_primary_10_1038_hdy_2014_91
crossref_primary_10_1016_j_scitotenv_2024_171246
crossref_primary_10_1002_mbo3_256
crossref_primary_10_1016_j_soilbio_2015_12_016
crossref_primary_10_1016_j_scitotenv_2023_168353
crossref_primary_10_1002_mbo3_255
crossref_primary_10_3390_f14101980
crossref_primary_10_1016_j_pedobi_2018_02_002
crossref_primary_10_1016_j_soilbio_2015_04_013
crossref_primary_10_1016_j_still_2021_105197
crossref_primary_10_1016_j_scitotenv_2019_135494
crossref_primary_10_1016_j_soilbio_2014_04_010
crossref_primary_10_1016_j_apsoil_2019_08_012
crossref_primary_10_1016_j_soilbio_2022_108573
crossref_primary_10_1016_j_catena_2024_108667
crossref_primary_10_1016_j_soilbio_2024_109424
crossref_primary_10_1016_j_pedobi_2022_150821
crossref_primary_10_1094_PBIOMES_11_22_0092_R
crossref_primary_10_3390_agronomy10070971
crossref_primary_10_1002_ldr_3803
crossref_primary_10_1016_j_catena_2017_09_030
crossref_primary_10_1016_j_apsoil_2015_06_011
crossref_primary_10_1093_femsec_fiy224
crossref_primary_10_1002_ldr_4576
crossref_primary_10_1016_j_scitotenv_2023_163455
crossref_primary_10_1016_j_geoderma_2023_116429
crossref_primary_10_3389_fmicb_2014_00681
crossref_primary_10_1016_j_pedobi_2013_12_006
crossref_primary_10_1128_aem_01161_24
crossref_primary_10_5194_se_9_1157_2018
crossref_primary_10_1016_j_soilbio_2014_10_028
crossref_primary_10_1038_srep18496
crossref_primary_10_1016_j_apsoil_2016_03_013
crossref_primary_10_5194_essd_14_4339_2022
crossref_primary_10_1007_s00248_021_01740_9
crossref_primary_10_1016_j_scitotenv_2023_166713
crossref_primary_10_1016_j_baae_2019_03_001
crossref_primary_10_1016_j_jhazmat_2022_130241
crossref_primary_10_1111_j_1466_8238_2010_00628_x
crossref_primary_10_1186_s40793_022_00409_1
crossref_primary_10_1007_s13157_018_1020_y
crossref_primary_10_1016_j_soilbio_2020_108072
crossref_primary_10_1021_acs_jafc_1c00210
crossref_primary_10_3390_su10041095
crossref_primary_10_1016_j_soilbio_2013_12_003
crossref_primary_10_1016_j_scitotenv_2021_145780
crossref_primary_10_1111_ecog_01226
crossref_primary_10_1371_journal_pone_0252216
crossref_primary_10_1016_j_envpol_2023_122840
crossref_primary_10_3389_fmicb_2022_968551
crossref_primary_10_1016_j_soilbio_2016_02_021
crossref_primary_10_1016_j_soilbio_2012_04_001
crossref_primary_10_1093_femsec_fix116
crossref_primary_10_13005_bbra_3096
crossref_primary_10_1016_j_gecco_2022_e02162
crossref_primary_10_3389_fenvs_2023_1137845
crossref_primary_10_1016_j_agee_2011_12_014
crossref_primary_10_3389_fmicb_2022_865184
crossref_primary_10_3354_meps13086
crossref_primary_10_1016_j_apsoil_2016_07_003
crossref_primary_10_1038_s41598_018_30005_8
crossref_primary_10_1029_2020JG006115
crossref_primary_10_5194_bg_12_6751_2015
crossref_primary_10_1016_j_soilbio_2015_09_002
crossref_primary_10_1016_j_agee_2025_109513
crossref_primary_10_3390_agronomy11010173
crossref_primary_10_1128_AEM_05005_11
crossref_primary_10_1016_j_apsoil_2022_104793
crossref_primary_10_1016_j_soilbio_2016_11_011
crossref_primary_10_1371_journal_pone_0130672
crossref_primary_10_1093_femsec_fix109
crossref_primary_10_1007_s00442_014_3136_y
crossref_primary_10_1016_j_soilbio_2024_109621
crossref_primary_10_3389_fmicb_2019_02277
crossref_primary_10_1186_s40168_020_00858_1
crossref_primary_10_3389_fmicb_2023_1208971
crossref_primary_10_1002_ece3_3708
crossref_primary_10_1111_j_1469_8137_2012_04233_x
crossref_primary_10_1007_s42729_023_01332_1
crossref_primary_10_1016_j_apsoil_2016_05_003
crossref_primary_10_1111_ejss_13049
crossref_primary_10_1007_s00248_011_9878_8
crossref_primary_10_1002_jobm_201300744
crossref_primary_10_1029_2020JG005838
crossref_primary_10_12688_f1000research_28450_1
crossref_primary_10_1111_ejss_13040
crossref_primary_10_3389_fmicb_2015_00031
crossref_primary_10_1002_agg2_20063
crossref_primary_10_55643_fcaptp_4_45_2022_3782
crossref_primary_10_1007_s00248_023_02180_3
crossref_primary_10_1007_s11442_021_1880_6
crossref_primary_10_1016_j_soilbio_2015_08_010
crossref_primary_10_1515_agri_2016_0006
crossref_primary_10_1093_jpe_rtab106
crossref_primary_10_1016_j_scitotenv_2021_145298
crossref_primary_10_1002_jsfa_5547
crossref_primary_10_1002_saj2_20201
crossref_primary_10_1093_femsec_fiz063
crossref_primary_10_1111_geb_13017
crossref_primary_10_1016_j_apsoil_2024_105747
crossref_primary_10_1016_j_scitotenv_2021_146148
crossref_primary_10_1016_j_gca_2021_11_014
crossref_primary_10_1016_j_still_2025_106465
crossref_primary_10_1016_j_catena_2024_108006
crossref_primary_10_1016_j_apsoil_2016_01_003
crossref_primary_10_1002_ecy_1883
crossref_primary_10_1007_s11368_021_03037_3
crossref_primary_10_1016_j_geoderma_2019_01_020
crossref_primary_10_1007_s00374_016_1171_z
crossref_primary_10_1007_s00248_021_01908_3
crossref_primary_10_3390_f14050971
crossref_primary_10_1111_ejss_13143
crossref_primary_10_1016_j_apsoil_2022_104467
crossref_primary_10_1016_j_envres_2025_120863
crossref_primary_10_1007_s00248_019_01401_y
crossref_primary_10_1093_femsle_fnab010
crossref_primary_10_1016_j_envres_2023_115470
crossref_primary_10_31545_intagr_155096
crossref_primary_10_1016_j_ecolind_2019_105919
crossref_primary_10_1007_s13157_012_0343_3
crossref_primary_10_1093_femsec_fiaa041
crossref_primary_10_1128_AEM_01856_15
crossref_primary_10_1590_1678_992x_2022_0139
crossref_primary_10_1071_SR19377
crossref_primary_10_3390_soilsystems5020024
crossref_primary_10_1128_AEM_01010_21
crossref_primary_10_1016_j_scitotenv_2024_176778
crossref_primary_10_1371_journal_pone_0050597
crossref_primary_10_1007_s10924_022_02683_z
crossref_primary_10_1016_j_soilbio_2017_12_016
crossref_primary_10_3390_agriculture15050496
crossref_primary_10_5194_bg_11_7097_2014
crossref_primary_10_1007_s40415_019_00557_8
crossref_primary_10_1093_femsec_fiw212
crossref_primary_10_1007_s12275_016_6526_5
crossref_primary_10_1007_s11104_024_06809_1
crossref_primary_10_1016_j_scitotenv_2016_04_122
crossref_primary_10_1016_j_catena_2015_03_016
crossref_primary_10_1016_j_apsoil_2021_104220
crossref_primary_10_1016_j_jhazmat_2023_131359
crossref_primary_10_1007_s13199_021_00787_z
crossref_primary_10_1016_j_catena_2021_105678
crossref_primary_10_1016_j_envc_2024_101045
crossref_primary_10_1371_journal_pone_0111667
crossref_primary_10_1038_ismej_2010_130
crossref_primary_10_1016_j_geomorph_2013_09_015
crossref_primary_10_4141_cjps_2015_013
crossref_primary_10_1016_j_soilbio_2014_06_014
crossref_primary_10_1111_ejss_12551
crossref_primary_10_1038_srep25815
crossref_primary_10_5194_bg_12_2585_2015
crossref_primary_10_1002_ldr_3521
crossref_primary_10_1186_1472_6785_13_46
crossref_primary_10_3390_su141610307
crossref_primary_10_1016_j_soilbio_2016_09_007
crossref_primary_10_1007_s00374_019_01390_7
crossref_primary_10_1007_s41748_024_00552_4
crossref_primary_10_1016_j_apsoil_2021_104351
crossref_primary_10_1371_journal_pone_0173901
crossref_primary_10_1016_j_catena_2023_107348
crossref_primary_10_1016_j_marpolbul_2017_06_044
crossref_primary_10_1002_mbo3_676
crossref_primary_10_5194_bg_17_3183_2020
crossref_primary_10_3389_fmicb_2021_673810
crossref_primary_10_1007_s10457_010_9332_9
crossref_primary_10_1007_s11356_022_22178_7
crossref_primary_10_1016_j_scitotenv_2022_153075
crossref_primary_10_1016_j_agee_2012_01_022
crossref_primary_10_1038_srep16587
crossref_primary_10_3390_f14010038
crossref_primary_10_1016_j_scitotenv_2020_144442
crossref_primary_10_1556_0088_2019_00024
crossref_primary_10_1007_s40974_020_00158_2
crossref_primary_10_1155_2022_2429826
crossref_primary_10_1016_S1002_0160_20_60038_8
crossref_primary_10_1002_eap_2325
crossref_primary_10_3390_f15040581
crossref_primary_10_1111_jbi_13109
crossref_primary_10_3389_fsufs_2021_664359
crossref_primary_10_1016_j_ecolind_2019_04_083
crossref_primary_10_1002_ldr_3188
crossref_primary_10_1007_s00374_016_1097_5
crossref_primary_10_1111_geb_12070
crossref_primary_10_1111_rec_13156
crossref_primary_10_1016_j_emcon_2022_02_003
crossref_primary_10_3390_agriculture12060782
crossref_primary_10_1016_j_jia_2023_06_031
crossref_primary_10_1016_j_apsoil_2016_11_005
crossref_primary_10_1016_j_scitotenv_2016_05_073
crossref_primary_10_1016_j_apsoil_2016_11_008
Cites_doi 10.1021/jf00104a043
10.1016/S0038-0717(00)00067-5
10.1007/978-3-642-75115-8_2
10.1016/S0016-7061(03)00046-6
10.1016/j.pedobi.2006.03.003
10.1128/aem.63.4.1531-1542.1997
10.2307/1940179
10.1046/j.1462-2920.2003.00404.x
10.1038/nature03073
10.1073/pnas.0507535103
10.1038/nrmicro1341
10.1016/j.soilbio.2004.05.002
10.1017/CBO9780511615146
10.1111/j.0021-8901.2004.00938.x
10.1016/j.soilbio.2005.09.027
10.1007/s003740050496
10.2136/sssaj2005.0160
10.1111/j.1469-8137.1990.tb00374.x
10.2136/sssaj1997.03615995006100020015x
10.1046/j.1365-2699.1998.252166.x
10.1016/S0038-0717(03)00028-2
10.2136/sssaj2001.651118x
10.1016/S0038-0717(03)00120-2
10.2307/1943519
10.1128/AEM.72.5.3357-3366.2006
10.1111/j.1461-0248.2006.00931.x
10.1016/0038-0717(94)00140-V
10.1016/S0016-7061(97)00032-3
10.1007/s10530-004-3856-8
10.1073/pnas.0608361104
10.1126/science.1153475
10.1046/j.1365-2699.2001.00563.x
10.1016/S0269-7491(01)00211-1
10.1007/s002489900087
10.1016/j.soilbio.2005.12.005
10.1111/j.1365-2699.2008.01931.x
10.1128/AEM.01809-07
10.3733/ca.v059n03p176
10.1007/s002489900082
10.1016/j.soilbio.2003.08.018
10.1038/nature01548
10.1016/S0038-0717(99)00016-4
ContentType Journal Article
Copyright Copyright 2010 Blackwell Publishing
2009 Blackwell Publishing Ltd
2009 Blackwell Publishing Ltd 2009
Copyright_xml – notice: Copyright 2010 Blackwell Publishing
– notice: 2009 Blackwell Publishing Ltd
– notice: 2009 Blackwell Publishing Ltd 2009
DBID FBQ
BSCLL
AAYXX
CITATION
NPM
7QG
7SN
7SS
7ST
7U6
C1K
M7N
7X8
7S9
L.6
5PM
DOI 10.1111/j.1466-8238.2009.00486.x
DatabaseName AGRIS
Istex
CrossRef
PubMed
Animal Behavior Abstracts
Ecology Abstracts
Entomology Abstracts (Full archive)
Environment Abstracts
Sustainability Science Abstracts
Environmental Sciences and Pollution Management
Algology Mycology and Protozoology Abstracts (Microbiology C)
MEDLINE - Academic
AGRICOLA
AGRICOLA - Academic
PubMed Central (Full Participant titles)
DatabaseTitle CrossRef
PubMed
Entomology Abstracts
Ecology Abstracts
Environment Abstracts
Sustainability Science Abstracts
Animal Behavior Abstracts
Environmental Sciences and Pollution Management
Algology Mycology and Protozoology Abstracts (Microbiology C)
MEDLINE - Academic
AGRICOLA
AGRICOLA - Academic
DatabaseTitleList CrossRef
Entomology Abstracts

AGRICOLA
PubMed

MEDLINE - Academic
Ecology Abstracts

AGRICOLA
Database_xml – sequence: 1
  dbid: NPM
  name: PubMed
  url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed
  sourceTypes: Index Database
– sequence: 2
  dbid: FBQ
  name: AGRIS
  url: http://www.fao.org/agris/Centre.asp?Menu_1ID=DB&Menu_2ID=DB1&Language=EN&Content=http://www.fao.org/agris/search?Language=EN
  sourceTypes: Publisher
DeliveryMethod fulltext_linktorsrc
Discipline Ecology
Environmental Sciences
EISSN 1466-8238
1466-822X
EndPage 39
ExternalDocumentID PMC3891896
2848252511
24443643
10_1111_j_1466_8238_2009_00486_x
GEB486
40405783
ark_67375_WNG_9HD73HKS_1
US201301713315
Genre article
Journal Article
GeographicLocations California
USA, California
GeographicLocations_xml – name: California
– name: USA, California
GrantInformation_xml – fundername: NIEHS NIH HHS
  grantid: P42 ES004699
– fundername: National Institute of Environmental Health Sciences : NIEHS
  grantid: P42 ES004699-24 || ES
GroupedDBID -~X
.3N
.GA
.Y3
0R~
10A
1OC
29I
31~
33P
4.4
50Y
51W
51X
52M
52N
52O
52P
52S
52T
52W
52X
5GY
5HH
5LA
5VS
702
7PT
8-0
8-1
8-3
8-4
8-5
8UM
930
A03
AAEVG
AAHBH
AAHHS
AAHKG
AAHQN
AAISJ
AAKGQ
AAMNL
AANHP
AANLZ
AASGY
AAXRX
AAYCA
AAZKR
ABBHK
ABCQN
ABCUV
ABEML
ABLJU
ABPLY
ABPPZ
ABPVW
ABSQW
ABTLG
ABXSQ
ACAHQ
ACBWZ
ACCFJ
ACCZN
ACHIC
ACPOU
ACPRK
ACRPL
ACSCC
ACSTJ
ACXBN
ACXQS
ACYXJ
ADBBV
ADEOM
ADIZJ
ADKYN
ADMGS
ADNMO
ADOZA
ADULT
ADXAS
ADZMN
ADZOD
AEEZP
AEIGN
AEIMD
AENEX
AEQDE
AEUPB
AEUYR
AFAZZ
AFBPY
AFEBI
AFFPM
AFGKR
AFRAH
AFWVQ
AFZJQ
AGHNM
AGUYK
AHBTC
AHXOZ
AILXY
AITYG
AIURR
AIWBW
AJBDE
ALMA_UNASSIGNED_HOLDINGS
ALUQN
ALVPJ
AMBMR
AMYDB
ANHSF
AQVQM
ASPBG
ATUGU
AUFTA
AVWKF
AZFZN
BDRZF
BFHJK
BMNLL
BMXJE
BRXPI
BY8
CAG
CBGCD
COF
CS3
CUYZI
D-E
D-F
DCZOG
DEVKO
DPXWK
DR2
DRFUL
DRSTM
EBS
ECGQY
EJD
F00
F01
F04
FBQ
FEDTE
G-S
GODZA
GTFYD
HF~
HGD
HGLYW
HQ2
HTVGU
HVGLF
HZI
IHE
IPSME
IX1
JAAYA
JBMMH
JBS
JEB
JENOY
JHFFW
JKQEH
JLS
JLXEF
JPM
JST
LATKE
LC2
LC3
LEEKS
LH4
LITHE
LOXES
LP6
LP7
LUTES
LW6
LYRES
MEWTI
MRFUL
MRSTM
MSFUL
MSSTM
MXFUL
MXSTM
N9A
OIG
P2W
P4D
Q11
QB0
ROL
RX1
SA0
SUPJJ
TN5
UB1
UPT
VQP
W99
WIH
WIK
WQJ
WXSBR
XG1
ZZTAW
~KM
ADACV
AEUQT
AFPWT
BSCLL
DOOOF
EQZMY
ESX
JSODD
WRC
AAMMB
AEFGJ
AEYWJ
AGQPQ
AGXDD
AGYGG
AIDQK
AIDYY
AAYXX
CITATION
NPM
7QG
7SN
7SS
7ST
7U6
C1K
M7N
7X8
7S9
L.6
5PM
ID FETCH-LOGICAL-c6826-2f8dc3cee657fd39a399b4caa19d1a4ad7c6b35bdf82090ec9ecb85f735678083
IEDL.DBID DR2
ISSN 1466-822X
IngestDate Thu Aug 21 18:32:38 EDT 2025
Fri Jul 11 09:12:56 EDT 2025
Fri Jul 11 18:30:47 EDT 2025
Fri Jul 11 00:30:19 EDT 2025
Fri Jul 11 01:29:33 EDT 2025
Fri Jul 25 03:34:34 EDT 2025
Mon Jul 21 05:53:07 EDT 2025
Thu Apr 24 23:00:04 EDT 2025
Tue Jul 01 01:46:02 EDT 2025
Wed Jan 22 17:09:17 EST 2025
Thu Jul 03 21:09:23 EDT 2025
Wed Oct 30 09:46:07 EDT 2024
Thu Apr 03 09:42:50 EDT 2025
IsDoiOpenAccess false
IsOpenAccess true
IsPeerReviewed true
IsScholarly true
Issue 1
Keywords microbial biomass
disturbance
PLFA
soil microbial community
California
water
Language English
License http://onlinelibrary.wiley.com/termsAndConditions#vor
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-c6826-2f8dc3cee657fd39a399b4caa19d1a4ad7c6b35bdf82090ec9ecb85f735678083
Notes http://dx.doi.org/10.1111/j.1466-8238.2009.00486.x
ArticleID:GEB486
istex:87F1DC4FED9DD21EC54AB6C649B9BEBF06AB4C12
ark:/67375/WNG-9HD73HKS-1
ObjectType-Article-1
SourceType-Scholarly Journals-1
content type line 14
ObjectType-Article-2
ObjectType-Feature-1
content type line 23
ObjectType-Feature-2
OpenAccessLink https://www.ncbi.nlm.nih.gov/pmc/articles/3891896
PMID 24443643
PQID 1242432186
PQPubID 24069
PageCount 13
ParticipantIDs pubmedcentral_primary_oai_pubmedcentral_nih_gov_3891896
proquest_miscellaneous_46454934
proquest_miscellaneous_1999970612
proquest_miscellaneous_1826585236
proquest_miscellaneous_1272713678
proquest_journals_1242432186
pubmed_primary_24443643
crossref_primary_10_1111_j_1466_8238_2009_00486_x
crossref_citationtrail_10_1111_j_1466_8238_2009_00486_x
wiley_primary_10_1111_j_1466_8238_2009_00486_x_GEB486
jstor_primary_40405783
istex_primary_ark_67375_WNG_9HD73HKS_1
fao_agris_US201301713315
ProviderPackageCode CITATION
AAYXX
PublicationCentury 2000
PublicationDate 2010
2010-01
20100101
January 2010
2010-01-00
2010-Jan
PublicationDateYYYYMMDD 2010-01-01
PublicationDate_xml – year: 2010
  text: 2010
PublicationDecade 2010
PublicationPlace Oxford, UK
PublicationPlace_xml – name: Oxford, UK
– name: England
– name: Oxford
PublicationTitle Global ecology and biogeography
PublicationTitleAlternate Glob Ecol Biogeogr
PublicationYear 2010
Publisher Oxford, UK : Blackwell Publishing Ltd
Blackwell Publishing Ltd
Blackwell Publishing
Wiley Subscription Services, Inc
Publisher_xml – name: Oxford, UK : Blackwell Publishing Ltd
– name: Blackwell Publishing Ltd
– name: Blackwell Publishing
– name: Wiley Subscription Services, Inc
References Calderón, F.J., Jackson, L.E., Scow, K.M. & Rolston, D.E. (2000) Microbial responses to simulated tillage in cultivated and uncultivated soils. Soil Biology and Biochemistry, 32, 1547-1559.
Jackson, L.E., Calderón, F.J., Steenwerth, K.L., Scow, K.M. & Rolston, D.E. (2003) Responses of soil microbial processes and community structure to tillage events and implications for soil quality. Geoderma, 114, 305-317.
Martiny, J.B.H., Bohannan, B.J.M., Brown, J.H., Colwell, R.K., Fuhrman, J.A., Green, J.L., Horner-Devine, M.C., Kane, M., Krumins, J.A., Kuske, C.R., Morin, P.J., Naeem, S., Øvreås, L., Reysenbach, A.L., Smith, V.H. & Staley, J.T. (2006) Microbial biogeography: putting microorganisms on the map. Nature Reviews Microbiology, 4, 102-112.
Ramsey, P.W., Rillig, M.C., Feris, K.P., Holben, W.E. & Gannon, J.E. (2006) Choice of methods for soil microbial community analysis: PLFA maximizes power compared to CLPP and PCR-based approaches. Pedobiologia, 50, 275-280.
Whittaker, R.H. (1956) Vegetation of the Great Smoky Mountains. Ecological Monographs, 23, 41-78.
Borcard, D., Legendre, P. & Drapeau, P. (1992) Partialling out the spatial component of ecological variation. Ecology, 73, 1045-1055.
Batten, K.M., Scow, K.M., Davies, K.F. & Harrison, S.P. (2006) Two invasive plants alter soil microbial community composition in serpentine grasslands. Biological Invasions, 8, 217-230.
Buckley, D.H. & Schmidt, T.M. (2003) Diversity and dynamics of microbial communities in soils from agro-ecosystems. Environmental Microbiology, 5, 441-452.
Dowling, N.J.E., Widdel, F. & White, D.C. (1986) Phospholipid ester-linked fatty acid biomarkers of acetate-oxidizing sulfate-reducers and other sulfide-forming bacteria. Journal of General Microbiology, 132, 1815-1826.
Hickman, J.C. (ed.) (1993) The Jepson manual: higher plants of California. University of California Press, Berkeley, CA.
Heikkinen, R.K., Luoto, M., Virkkala, R. & Rainio, K. (2004) Effects of habitat cover, landscape structure and spatial variables on the abundance of birds in an agricultural-forest mosaic. Journal of Applied Ecology, 41, 824-835.
Bossio, D.A. & Scow, K.M. (1998) Impacts of carbon and flooding on soil microbial communities: phospholipid fatty acid profiles and substrate utilization patterns. Microbial Ecology, 35, 265-278.
Whittaker, R.J., Willis, K.J. & Field, R. (2001) Scale and species richness: towards a general, hierarchical theory of species diversity. Journal of Biogeography, 28, 453-470.
Drenovsky, R.E., Elliott, G.N., Graham, K.J. & Scow, K.M. (2004) Comparison of phospholipid fatty acid (PLFA) and total soil fatty acid methyl esters (TSFAME) for characterizing soil microbial communities. Soil Biology and Biochemistry, 36, 1793-1800.
Calderón, F.J., Jackson, L.E., Scow, K.M. & Rolston, D.E. (2001) Short-term dynamics of nitrogen, microbial activity, and phospholipid fatty acids after tillage. Soil Science Society of America Journal, 65, 118-126.
Steenwerth, K.L., Jackson, L.E., Carlisle, E.A. & Scow, K.M. (2006) Microbial communities of a native perennial bunchgrass do not respond consistently across a gradient of land-use intensification. Soil Biology and Biochemistry, 38, 1797-1811.
Wardle, D.A. (2006) The influence of biotic interactions on soil biodiversity. Ecology Letters, 9, 870-886.
Nordby, H.E., Nemec, S. & Nagy, S. (1981) Fatty acids and sterols associated with citrus root mycorrhizae. Journal of Agricultural and Food Chemistry, 29, 396-401.
Bossio, D.A., Scow, K.M., Gunapala, N. & Graham, K.J. (1998) Determinants of soil microbial communities: effects of agricultural management, season, and soil type on phospholipid fatty acid profiles. Microbial Ecology, 36, 1-12.
Steenwerth, K.L., Jackson, L.E., Calderón, F.J., Stromber, M.R. & Scow, K.M. (2003) Soil microbial community composition and land use history in cultivated and grassland ecosystems of coastal California. Soil Biology and Biochemistry, 35, 489-500.
McCulley, R.L. & Burke, I.C. (2004) Microbial community composition across the Great Plains: landscape versus regional variability. Soil Science Society of America Journal, 68, 106-115.
Kourtev, P.S., Ehrenfeld, J.G. & Häggblom, M. (2003) Experimental analysis of the effect of exotic and native plant species on the structure and function of soil microbial communities. Soil Biology and Biochemistry, 35, 895-905.
O'Brien, E.M. (1998) Water-energy dynamics, climate, and prediction of woody plant species richness: an interim general model. Journal of Biogeography, 25, 379-398.
Lepš, J. & Šmilauer, P. (2003) Multivariate analysis of ecological data using CANOCO. Cambridge University Press, Cambridge.
Vetaas, O.R. & Ferrer-Castán, D. (2008) Patterns of woody plant species richness in the Iberian Peninsula: environmental range and spatial scale. Journal of Biogeography, 35, 1863-1878.
Stevenson, B.A., Sparling, G.P., Schipper, L.A., Degens, B.P. & Duncan, L.C. (2004) Pasture and forest soil microbial communities show distinct patterns in their catabolic respiration responses at a landscape scale. Soil Biology and Biochemistry, 36, 49-55.
Fierer, N. & Jackson, R.B. (2006) The diversity and biogeography of soil bacterial communities. Proceedings of the National Academy of Sciences USA, 103, 626-631.
Kieft, T.L., Wilch, E., O'Connor, K., Ringelberg, D.B. & White, D.C. (1997) Survival and phospholipid fatty acid profiles of surface and subsurface bacteria in natural sediment microcosms. Applied and Environmental Microbiology, 63, 1531-1542.
Evans, D.G. & Miller, M.H. (1990) The role of the external mycelial network in the effect of soil-disturbance upon the vesicular - arbuscular mycorrhizal colonization of maize. New Phytologist, 114, 65-71.
Sylvia, D.M., Fuhrmann, J.J., Hartel, P.G. & Zuberer, D.A. (2005) Principles and applications of soil microbiology, 2nd edn. Pearson Prentice Hall, Upper Saddle River, NJ.
Kreft, H. & Jetz, W. (2007) Global patterns and determinants of vascular plant diversity. Proceedings of the National Academy of Sciences USA, 104, 5925-5930.
Zogg, G.P., Zak, D.R., Ringelberg, D.B., Macdonald, N.W., Pregitzer, K.S. & White, D.C. (1997) Compositional and functional shifts in microbial communities because of soil warming. Soil Science Society of America Journal, 61, 475-481.
Green, J.L., Bohannan, B.J.M. & Whitaker, R.J. (2008) Microbial biogeography: from taxonomy to traits. Science, 320, 1039-1043.
Steinberger, Y., Zelles, L., Bai, Q.Y., von Lutzow, M. & Munch, J.C. (1999) Phospholipid fatty acid profiles as indicators for the microbial community structure in soils along a climatic transect in the Judean Desert. Biology and Fertility of Soils, 28, 292-300.
Horner-Devine, M.C., Lage, M., Hughes, J.B. & Bohannan, B.J.M. (2004) A taxa-area relationship for bacteria. Nature, 432, 750-753.
Drenovsky, R.E., Duncan, R.A. & Scow, K.M. (2005a) Soil sterilization and organic carbon, but not microbial inoculants, change microbial communities in replanted peach orchards. California Agriculture, 59, 176-181.
Petersen, S.O., Debosz, K., Schjonning, P., Christensen, B.T. & Elmholt, S. (1997) Phospholipid fatty acid profiles and C availability in wet-stable macro-aggregates from conventionally and organically farmed soils. Geoderma, 78, 181-196.
Curtis, J.T. (1959) The vegetation of Wisconsin: an ordination of plant communities. University of Wisconsin Press, Madison, WI.
Bååth, E., Frostegård, Å., Pennanen, T. & Fritze, H. (1995) Microbial community structure and pH response in relation to soil organic matter quality in wood-ash fertilized, clear-cut or burned coniferous forest soils. Soil Biology and Biochemistry, 27, 229-240.
Córdova-Kreylos, A.L., Cao, Y.P., Green, P.G., Hwang, H.M., Kuivila, K.M., LaMontagne, M.G., Van De Werfhorst, L.C., Holden, P.A. & Scow, K.M. (2006) Diversity, composition, and geographical distribution of microbial communities in California salt marsh sediments. Applied and Environmental Microbiology, 72, 3357-3366.
Lal, R. (2002) Soil carbon dynamics in cropland and rangeland. Environmental Pollution, 116, 353-362.
Zhang, W.J., Rui, W.Y., Tu, C., Diab, H.G., Louws, F.J., Mueller, J.P., Creamer, N., Bell, M., Wagger, M.G. & Hu, S. (2005) Responses of soil microbial community structure and diversity to agricultural deintensification. Pedosphere, 15, 440-447.
Bardgett, R.D., Lovell, R.D., Hobbs, P.J. & Jarvis, S.C. (1999) Seasonal changes in soil microbial communities along a fertility gradient of temperate grasslands. Soil Biology and Biochemistry, 31, 1021-1030.
De Deyn, G., Raaijmakers, C., Zoomer, H., Berg, M., De Ruiter, P., Verhoef, H., Bezemer, T. & Van der Putten, W. (2003) Soil invertebrate fauna enhances grassland succession and diversity. Nature, 422, 711-713.
Findlay, R.H., Yeates, C., Hullar, M.A.J., Stahl, D.A. & Kaplan, L.A. (2008) Biome-level biogeography of streambed microbiota. Applied and Environmental Microbiology, 74, 3014-3021.
Kennedy, A.C. & Schillinger, W.F. (2006) Soil quality and water intake in traditional-till vs. no-till paired farms in Washington's Palouse region. Soil Science Society of America Journal, 70, 940-949.
White, D.C., Bobbie, R.J., Nickels, J.S., Fazio, S.D. & Davis, W.M. (1980) Nonselective biochemical methods for the determination of fungal mass and community structure in estuarine detrital microflora. Botanica Marina, 23, 239-250.
Bossio, D.A., Fleck, J.A., Scow, K.M. & Fujii, R. (2006) Alteration of soil microbial communities and water quality in restored wetlands. Soil Biology and Biochemistry, 38, 1223-1233.
2006; 70
2007; 104
2005a; 59
2006; 72
1986; 132
2006; 38
2004; 68
2002; 116
2008; 35
2008; 74
2003; 114
2005b
1990
1995; 27
2004; 36
1985
2003; 5
1988
2004; 41
1997; 61
2006; 50
1997; 63
1999; 28
1980; 23
2006; 9
2003; 35
2006; 8
1995
2006
1981; 29
2005
1993
2006; 4
2003
2001; 28
2002
2008; 320
1959
1992; 73
1998; 25
2001; 65
1990; 114
2004; 432
2000; 32
1956; 23
1997; 78
1999; 31
2005; 15
2003; 422
1998; 36
2006; 103
1998; 35
e_1_2_7_5_1
e_1_2_7_3_1
e_1_2_7_9_1
e_1_2_7_7_1
e_1_2_7_17_1
e_1_2_7_15_1
Curtis J.T. (e_1_2_7_14_1) 1959
e_1_2_7_13_1
e_1_2_7_11_1
e_1_2_7_45_1
e_1_2_7_47_1
e_1_2_7_49_1
e_1_2_7_28_1
Sylvia D.M. (e_1_2_7_51_1) 2005
Dowling N.J.E. (e_1_2_7_16_1) 1986; 132
e_1_2_7_50_1
e_1_2_7_25_1
e_1_2_7_31_1
e_1_2_7_52_1
e_1_2_7_23_1
e_1_2_7_21_1
e_1_2_7_35_1
e_1_2_7_56_1
McCulley R.L. (e_1_2_7_37_1) 2004; 68
e_1_2_7_39_1
White D.C. (e_1_2_7_54_1) 1980; 23
e_1_2_7_6_1
e_1_2_7_4_1
O'Leary W.M. (e_1_2_7_41_1) 1988
e_1_2_7_8_1
e_1_2_7_18_1
Kroppenstedt R.M. (e_1_2_7_33_1) 1985
e_1_2_7_40_1
e_1_2_7_2_1
e_1_2_7_42_1
e_1_2_7_12_1
e_1_2_7_44_1
e_1_2_7_10_1
e_1_2_7_46_1
e_1_2_7_48_1
e_1_2_7_27_1
e_1_2_7_29_1
Hickman J.C. (e_1_2_7_26_1) 1993
Pinkart H.C. (e_1_2_7_43_1) 2002
Drenovsky R.E. (e_1_2_7_19_1) 2005
e_1_2_7_30_1
e_1_2_7_53_1
e_1_2_7_24_1
e_1_2_7_32_1
e_1_2_7_55_1
e_1_2_7_22_1
e_1_2_7_34_1
e_1_2_7_20_1
e_1_2_7_36_1
e_1_2_7_59_1
e_1_2_7_38_1
Wilkinson S.G. (e_1_2_7_57_1) 1988
Zhang W.J. (e_1_2_7_58_1) 2005; 15
References_xml – reference: Petersen, S.O., Debosz, K., Schjonning, P., Christensen, B.T. & Elmholt, S. (1997) Phospholipid fatty acid profiles and C availability in wet-stable macro-aggregates from conventionally and organically farmed soils. Geoderma, 78, 181-196.
– reference: Steinberger, Y., Zelles, L., Bai, Q.Y., von Lutzow, M. & Munch, J.C. (1999) Phospholipid fatty acid profiles as indicators for the microbial community structure in soils along a climatic transect in the Judean Desert. Biology and Fertility of Soils, 28, 292-300.
– reference: Drenovsky, R.E., Duncan, R.A. & Scow, K.M. (2005a) Soil sterilization and organic carbon, but not microbial inoculants, change microbial communities in replanted peach orchards. California Agriculture, 59, 176-181.
– reference: Horner-Devine, M.C., Lage, M., Hughes, J.B. & Bohannan, B.J.M. (2004) A taxa-area relationship for bacteria. Nature, 432, 750-753.
– reference: Lepš, J. & Šmilauer, P. (2003) Multivariate analysis of ecological data using CANOCO. Cambridge University Press, Cambridge.
– reference: Lal, R. (2002) Soil carbon dynamics in cropland and rangeland. Environmental Pollution, 116, 353-362.
– reference: Bossio, D.A., Scow, K.M., Gunapala, N. & Graham, K.J. (1998) Determinants of soil microbial communities: effects of agricultural management, season, and soil type on phospholipid fatty acid profiles. Microbial Ecology, 36, 1-12.
– reference: Zogg, G.P., Zak, D.R., Ringelberg, D.B., Macdonald, N.W., Pregitzer, K.S. & White, D.C. (1997) Compositional and functional shifts in microbial communities because of soil warming. Soil Science Society of America Journal, 61, 475-481.
– reference: De Deyn, G., Raaijmakers, C., Zoomer, H., Berg, M., De Ruiter, P., Verhoef, H., Bezemer, T. & Van der Putten, W. (2003) Soil invertebrate fauna enhances grassland succession and diversity. Nature, 422, 711-713.
– reference: Evans, D.G. & Miller, M.H. (1990) The role of the external mycelial network in the effect of soil-disturbance upon the vesicular - arbuscular mycorrhizal colonization of maize. New Phytologist, 114, 65-71.
– reference: Vetaas, O.R. & Ferrer-Castán, D. (2008) Patterns of woody plant species richness in the Iberian Peninsula: environmental range and spatial scale. Journal of Biogeography, 35, 1863-1878.
– reference: Jackson, L.E., Calderón, F.J., Steenwerth, K.L., Scow, K.M. & Rolston, D.E. (2003) Responses of soil microbial processes and community structure to tillage events and implications for soil quality. Geoderma, 114, 305-317.
– reference: Zhang, W.J., Rui, W.Y., Tu, C., Diab, H.G., Louws, F.J., Mueller, J.P., Creamer, N., Bell, M., Wagger, M.G. & Hu, S. (2005) Responses of soil microbial community structure and diversity to agricultural deintensification. Pedosphere, 15, 440-447.
– reference: Nordby, H.E., Nemec, S. & Nagy, S. (1981) Fatty acids and sterols associated with citrus root mycorrhizae. Journal of Agricultural and Food Chemistry, 29, 396-401.
– reference: Whittaker, R.H. (1956) Vegetation of the Great Smoky Mountains. Ecological Monographs, 23, 41-78.
– reference: Findlay, R.H., Yeates, C., Hullar, M.A.J., Stahl, D.A. & Kaplan, L.A. (2008) Biome-level biogeography of streambed microbiota. Applied and Environmental Microbiology, 74, 3014-3021.
– reference: Hickman, J.C. (ed.) (1993) The Jepson manual: higher plants of California. University of California Press, Berkeley, CA.
– reference: O'Brien, E.M. (1998) Water-energy dynamics, climate, and prediction of woody plant species richness: an interim general model. Journal of Biogeography, 25, 379-398.
– reference: Bossio, D.A., Fleck, J.A., Scow, K.M. & Fujii, R. (2006) Alteration of soil microbial communities and water quality in restored wetlands. Soil Biology and Biochemistry, 38, 1223-1233.
– reference: Kreft, H. & Jetz, W. (2007) Global patterns and determinants of vascular plant diversity. Proceedings of the National Academy of Sciences USA, 104, 5925-5930.
– reference: Batten, K.M., Scow, K.M., Davies, K.F. & Harrison, S.P. (2006) Two invasive plants alter soil microbial community composition in serpentine grasslands. Biological Invasions, 8, 217-230.
– reference: Green, J.L., Bohannan, B.J.M. & Whitaker, R.J. (2008) Microbial biogeography: from taxonomy to traits. Science, 320, 1039-1043.
– reference: White, D.C., Bobbie, R.J., Nickels, J.S., Fazio, S.D. & Davis, W.M. (1980) Nonselective biochemical methods for the determination of fungal mass and community structure in estuarine detrital microflora. Botanica Marina, 23, 239-250.
– reference: Steenwerth, K.L., Jackson, L.E., Calderón, F.J., Stromber, M.R. & Scow, K.M. (2003) Soil microbial community composition and land use history in cultivated and grassland ecosystems of coastal California. Soil Biology and Biochemistry, 35, 489-500.
– reference: Bardgett, R.D., Lovell, R.D., Hobbs, P.J. & Jarvis, S.C. (1999) Seasonal changes in soil microbial communities along a fertility gradient of temperate grasslands. Soil Biology and Biochemistry, 31, 1021-1030.
– reference: Dowling, N.J.E., Widdel, F. & White, D.C. (1986) Phospholipid ester-linked fatty acid biomarkers of acetate-oxidizing sulfate-reducers and other sulfide-forming bacteria. Journal of General Microbiology, 132, 1815-1826.
– reference: Heikkinen, R.K., Luoto, M., Virkkala, R. & Rainio, K. (2004) Effects of habitat cover, landscape structure and spatial variables on the abundance of birds in an agricultural-forest mosaic. Journal of Applied Ecology, 41, 824-835.
– reference: Kourtev, P.S., Ehrenfeld, J.G. & Häggblom, M. (2003) Experimental analysis of the effect of exotic and native plant species on the structure and function of soil microbial communities. Soil Biology and Biochemistry, 35, 895-905.
– reference: Martiny, J.B.H., Bohannan, B.J.M., Brown, J.H., Colwell, R.K., Fuhrman, J.A., Green, J.L., Horner-Devine, M.C., Kane, M., Krumins, J.A., Kuske, C.R., Morin, P.J., Naeem, S., Øvreås, L., Reysenbach, A.L., Smith, V.H. & Staley, J.T. (2006) Microbial biogeography: putting microorganisms on the map. Nature Reviews Microbiology, 4, 102-112.
– reference: McCulley, R.L. & Burke, I.C. (2004) Microbial community composition across the Great Plains: landscape versus regional variability. Soil Science Society of America Journal, 68, 106-115.
– reference: Buckley, D.H. & Schmidt, T.M. (2003) Diversity and dynamics of microbial communities in soils from agro-ecosystems. Environmental Microbiology, 5, 441-452.
– reference: Steenwerth, K.L., Jackson, L.E., Carlisle, E.A. & Scow, K.M. (2006) Microbial communities of a native perennial bunchgrass do not respond consistently across a gradient of land-use intensification. Soil Biology and Biochemistry, 38, 1797-1811.
– reference: Borcard, D., Legendre, P. & Drapeau, P. (1992) Partialling out the spatial component of ecological variation. Ecology, 73, 1045-1055.
– reference: Fierer, N. & Jackson, R.B. (2006) The diversity and biogeography of soil bacterial communities. Proceedings of the National Academy of Sciences USA, 103, 626-631.
– reference: Kieft, T.L., Wilch, E., O'Connor, K., Ringelberg, D.B. & White, D.C. (1997) Survival and phospholipid fatty acid profiles of surface and subsurface bacteria in natural sediment microcosms. Applied and Environmental Microbiology, 63, 1531-1542.
– reference: Bååth, E., Frostegård, Å., Pennanen, T. & Fritze, H. (1995) Microbial community structure and pH response in relation to soil organic matter quality in wood-ash fertilized, clear-cut or burned coniferous forest soils. Soil Biology and Biochemistry, 27, 229-240.
– reference: Drenovsky, R.E., Elliott, G.N., Graham, K.J. & Scow, K.M. (2004) Comparison of phospholipid fatty acid (PLFA) and total soil fatty acid methyl esters (TSFAME) for characterizing soil microbial communities. Soil Biology and Biochemistry, 36, 1793-1800.
– reference: Whittaker, R.J., Willis, K.J. & Field, R. (2001) Scale and species richness: towards a general, hierarchical theory of species diversity. Journal of Biogeography, 28, 453-470.
– reference: Calderón, F.J., Jackson, L.E., Scow, K.M. & Rolston, D.E. (2000) Microbial responses to simulated tillage in cultivated and uncultivated soils. Soil Biology and Biochemistry, 32, 1547-1559.
– reference: Kennedy, A.C. & Schillinger, W.F. (2006) Soil quality and water intake in traditional-till vs. no-till paired farms in Washington's Palouse region. Soil Science Society of America Journal, 70, 940-949.
– reference: Wardle, D.A. (2006) The influence of biotic interactions on soil biodiversity. Ecology Letters, 9, 870-886.
– reference: Bossio, D.A. & Scow, K.M. (1998) Impacts of carbon and flooding on soil microbial communities: phospholipid fatty acid profiles and substrate utilization patterns. Microbial Ecology, 35, 265-278.
– reference: Sylvia, D.M., Fuhrmann, J.J., Hartel, P.G. & Zuberer, D.A. (2005) Principles and applications of soil microbiology, 2nd edn. Pearson Prentice Hall, Upper Saddle River, NJ.
– reference: Córdova-Kreylos, A.L., Cao, Y.P., Green, P.G., Hwang, H.M., Kuivila, K.M., LaMontagne, M.G., Van De Werfhorst, L.C., Holden, P.A. & Scow, K.M. (2006) Diversity, composition, and geographical distribution of microbial communities in California salt marsh sediments. Applied and Environmental Microbiology, 72, 3357-3366.
– reference: Ramsey, P.W., Rillig, M.C., Feris, K.P., Holben, W.E. & Gannon, J.E. (2006) Choice of methods for soil microbial community analysis: PLFA maximizes power compared to CLPP and PCR-based approaches. Pedobiologia, 50, 275-280.
– reference: Calderón, F.J., Jackson, L.E., Scow, K.M. & Rolston, D.E. (2001) Short-term dynamics of nitrogen, microbial activity, and phospholipid fatty acids after tillage. Soil Science Society of America Journal, 65, 118-126.
– reference: Curtis, J.T. (1959) The vegetation of Wisconsin: an ordination of plant communities. University of Wisconsin Press, Madison, WI.
– reference: Stevenson, B.A., Sparling, G.P., Schipper, L.A., Degens, B.P. & Duncan, L.C. (2004) Pasture and forest soil microbial communities show distinct patterns in their catabolic respiration responses at a landscape scale. Soil Biology and Biochemistry, 36, 49-55.
– volume: 74
  start-page: 3014
  year: 2008
  end-page: 3021
  article-title: Biome‐level biogeography of streambed microbiota
  publication-title: Applied and Environmental Microbiology
– volume: 78
  start-page: 181
  year: 1997
  end-page: 196
  article-title: Phospholipid fatty acid profiles and C availability in wet‐stable macro‐aggregates from conventionally and organically farmed soils
  publication-title: Geoderma
– year: 2005
– volume: 28
  start-page: 453
  year: 2001
  end-page: 470
  article-title: Scale and species richness: towards a general, hierarchical theory of species diversity
  publication-title: Journal of Biogeography
– volume: 25
  start-page: 379
  year: 1998
  end-page: 398
  article-title: Water–energy dynamics, climate, and prediction of woody plant species richness: an interim general model
  publication-title: Journal of Biogeography
– volume: 41
  start-page: 824
  year: 2004
  end-page: 835
  article-title: Effects of habitat cover, landscape structure and spatial variables on the abundance of birds in an agricultural‐forest mosaic
  publication-title: Journal of Applied Ecology
– volume: 104
  start-page: 5925
  year: 2007
  end-page: 5930
  article-title: Global patterns and determinants of vascular plant diversity
  publication-title: Proceedings of the National Academy of Sciences USA
– volume: 32
  start-page: 1547
  year: 2000
  end-page: 1559
  article-title: Microbial responses to simulated tillage in cultivated and uncultivated soils
  publication-title: Soil Biology and Biochemistry
– volume: 103
  start-page: 626
  year: 2006
  end-page: 631
  article-title: The diversity and biogeography of soil bacterial communities
  publication-title: Proceedings of the National Academy of Sciences USA
– volume: 72
  start-page: 3357
  year: 2006
  end-page: 3366
  article-title: Diversity, composition, and geographical distribution of microbial communities in California salt marsh sediments
  publication-title: Applied and Environmental Microbiology
– volume: 29
  start-page: 396
  year: 1981
  end-page: 401
  article-title: Fatty acids and sterols associated with citrus root mycorrhizae
  publication-title: Journal of Agricultural and Food Chemistry
– volume: 38
  start-page: 1223
  year: 2006
  end-page: 1233
  article-title: Alteration of soil microbial communities and water quality in restored wetlands
  publication-title: Soil Biology and Biochemistry
– volume: 432
  start-page: 750
  year: 2004
  end-page: 753
  article-title: A taxa–area relationship for bacteria
  publication-title: Nature
– volume: 116
  start-page: 353
  year: 2002
  end-page: 362
  article-title: Soil carbon dynamics in cropland and rangeland
  publication-title: Environmental Pollution
– volume: 422
  start-page: 711
  year: 2003
  end-page: 713
  article-title: Soil invertebrate fauna enhances grassland succession and diversity
  publication-title: Nature
– volume: 50
  start-page: 275
  year: 2006
  end-page: 280
  article-title: Choice of methods for soil microbial community analysis: PLFA maximizes power compared to CLPP and PCR‐based approaches
  publication-title: Pedobiologia
– start-page: 299
  year: 1988
  end-page: 488
– volume: 31
  start-page: 1021
  year: 1999
  end-page: 1030
  article-title: Seasonal changes in soil microbial communities along a fertility gradient of temperate grasslands
  publication-title: Soil Biology and Biochemistry
– volume: 8
  start-page: 217
  year: 2006
  end-page: 230
  article-title: Two invasive plants alter soil microbial community composition in serpentine grasslands
  publication-title: Biological Invasions
– start-page: 173
  year: 1985
  end-page: 199
– year: 1959
– volume: 35
  start-page: 895
  year: 2003
  end-page: 905
  article-title: Experimental analysis of the effect of exotic and native plant species on the structure and function of soil microbial communities
  publication-title: Soil Biology and Biochemistry
– start-page: 117
  year: 1988
  end-page: 201
– volume: 114
  start-page: 65
  year: 1990
  end-page: 71
  article-title: The role of the external mycelial network in the effect of soil‐disturbance upon the vesicular – arbuscular mycorrhizal colonization of maize
  publication-title: New Phytologist
– volume: 59
  start-page: 176
  year: 2005a
  end-page: 181
  article-title: Soil sterilization and organic carbon, but not microbial inoculants, change microbial communities in replanted peach orchards
  publication-title: California Agriculture
– volume: 36
  start-page: 1793
  year: 2004
  end-page: 1800
  article-title: Comparison of phospholipid fatty acid (PLFA) and total soil fatty acid methyl esters (TSFAME) for characterizing soil microbial communities
  publication-title: Soil Biology and Biochemistry
– volume: 36
  start-page: 1
  year: 1998
  end-page: 12
  article-title: Determinants of soil microbial communities: effects of agricultural management, season, and soil type on phospholipid fatty acid profiles
  publication-title: Microbial Ecology
– volume: 35
  start-page: 489
  year: 2003
  end-page: 500
  article-title: Soil microbial community composition and land use history in cultivated and grassland ecosystems of coastal California
  publication-title: Soil Biology and Biochemistry
– volume: 36
  start-page: 49
  year: 2004
  end-page: 55
  article-title: Pasture and forest soil microbial communities show distinct patterns in their catabolic respiration responses at a landscape scale
  publication-title: Soil Biology and Biochemistry
– year: 1993
– volume: 68
  start-page: 106
  year: 2004
  end-page: 115
  article-title: Microbial community composition across the Great Plains: landscape versus regional variability
  publication-title: Soil Science Society of America Journal
– volume: 23
  start-page: 41
  year: 1956
  end-page: 78
  article-title: Vegetation of the Great Smoky Mountains
  publication-title: Ecological Monographs
– volume: 63
  start-page: 1531
  year: 1997
  end-page: 1542
  article-title: Survival and phospholipid fatty acid profiles of surface and subsurface bacteria in natural sediment microcosms
  publication-title: Applied and Environmental Microbiology
– start-page: 9
  year: 1990
  end-page: 34
– volume: 23
  start-page: 239
  year: 1980
  end-page: 250
  article-title: Nonselective biochemical methods for the determination of fungal mass and community structure in estuarine detrital microflora
  publication-title: Botanica Marina
– volume: 61
  start-page: 475
  year: 1997
  end-page: 481
  article-title: Compositional and functional shifts in microbial communities because of soil warming
  publication-title: Soil Science Society of America Journal
– year: 2003
– volume: 5
  start-page: 441
  year: 2003
  end-page: 452
  article-title: Diversity and dynamics of microbial communities in soils from agro‐ecosystems
  publication-title: Environmental Microbiology
– volume: 132
  start-page: 1815
  year: 1986
  end-page: 1826
  article-title: Phospholipid ester‐linked fatty acid biomarkers of acetate‐oxidizing sulfate‐reducers and other sulfide‐forming bacteria
  publication-title: Journal of General Microbiology
– volume: 320
  start-page: 1039
  year: 2008
  end-page: 1043
  article-title: Microbial biogeography: from taxonomy to traits
  publication-title: Science
– volume: 28
  start-page: 292
  year: 1999
  end-page: 300
  article-title: Phospholipid fatty acid profiles as indicators for the microbial community structure in soils along a climatic transect in the Judean Desert
  publication-title: Biology and Fertility of Soils
– volume: 35
  start-page: 1863
  year: 2008
  end-page: 1878
  article-title: Patterns of woody plant species richness in the Iberian Peninsula: environmental range and spatial scale
  publication-title: Journal of Biogeography
– volume: 65
  start-page: 118
  year: 2001
  end-page: 126
  article-title: Short‐term dynamics of nitrogen, microbial activity, and phospholipid fatty acids after tillage
  publication-title: Soil Science Society of America Journal
– volume: 27
  start-page: 229
  year: 1995
  end-page: 240
  article-title: Microbial community structure and pH response in relation to soil organic matter quality in wood‐ash fertilized, clear‐cut or burned coniferous forest soils
  publication-title: Soil Biology and Biochemistry
– start-page: 101
  year: 2002
  end-page: 113
– volume: 9
  start-page: 870
  year: 2006
  end-page: 886
  article-title: The influence of biotic interactions on soil biodiversity
  publication-title: Ecology Letters
– volume: 38
  start-page: 1797
  year: 2006
  end-page: 1811
  article-title: Microbial communities of a native perennial bunchgrass do not respond consistently across a gradient of land‐use intensification
  publication-title: Soil Biology and Biochemistry
– start-page: 39
  year: 2005b
  end-page: 47
– volume: 73
  start-page: 1045
  year: 1992
  end-page: 1055
  article-title: Partialling out the spatial component of ecological variation
  publication-title: Ecology
– year: 2006
– year: 1995
– volume: 70
  start-page: 940
  year: 2006
  end-page: 949
  article-title: Soil quality and water intake in traditional‐till vs. no‐till paired farms in Washington's Palouse region
  publication-title: Soil Science Society of America Journal
– volume: 114
  start-page: 305
  year: 2003
  end-page: 317
  article-title: Responses of soil microbial processes and community structure to tillage events and implications for soil quality
  publication-title: Geoderma
– volume: 35
  start-page: 265
  year: 1998
  end-page: 278
  article-title: Impacts of carbon and flooding on soil microbial communities: phospholipid fatty acid profiles and substrate utilization patterns
  publication-title: Microbial Ecology
– volume: 4
  start-page: 102
  year: 2006
  end-page: 112
  article-title: Microbial biogeography: putting microorganisms on the map
  publication-title: Nature Reviews Microbiology
– volume: 15
  start-page: 440
  year: 2005
  end-page: 447
  article-title: Responses of soil microbial community structure and diversity to agricultural deintensification
  publication-title: Pedosphere
– ident: e_1_2_7_39_1
  doi: 10.1021/jf00104a043
– start-page: 299
  volume-title: Microbial lipids
  year: 1988
  ident: e_1_2_7_57_1
– ident: e_1_2_7_11_1
  doi: 10.1016/S0038-0717(00)00067-5
– ident: e_1_2_7_35_1
  doi: 10.1007/978-3-642-75115-8_2
– ident: e_1_2_7_27_1
  doi: 10.1016/S0016-7061(03)00046-6
– ident: e_1_2_7_44_1
  doi: 10.1016/j.pedobi.2006.03.003
– volume-title: The vegetation of Wisconsin: an ordination of plant communities
  year: 1959
  ident: e_1_2_7_14_1
– ident: e_1_2_7_30_1
  doi: 10.1128/aem.63.4.1531-1542.1997
– ident: e_1_2_7_5_1
  doi: 10.2307/1940179
– ident: e_1_2_7_10_1
  doi: 10.1046/j.1462-2920.2003.00404.x
– ident: e_1_2_7_25_1
  doi: 10.1038/nature03073
– ident: e_1_2_7_21_1
  doi: 10.1073/pnas.0507535103
– ident: e_1_2_7_38_1
  doi: 10.1038/nrmicro1341
– volume: 68
  start-page: 106
  year: 2004
  ident: e_1_2_7_37_1
  article-title: Microbial community composition across the Great Plains: landscape versus regional variability
  publication-title: Soil Science Society of America Journal
– volume: 132
  start-page: 1815
  year: 1986
  ident: e_1_2_7_16_1
  article-title: Phospholipid ester‐linked fatty acid biomarkers of acetate‐oxidizing sulfate‐reducers and other sulfide‐forming bacteria
  publication-title: Journal of General Microbiology
– ident: e_1_2_7_17_1
  doi: 10.1016/j.soilbio.2004.05.002
– start-page: 117
  volume-title: Microbial lipids
  year: 1988
  ident: e_1_2_7_41_1
– volume-title: Principles and applications of soil microbiology
  year: 2005
  ident: e_1_2_7_51_1
– ident: e_1_2_7_36_1
  doi: 10.1017/CBO9780511615146
– ident: e_1_2_7_24_1
  doi: 10.1111/j.0021-8901.2004.00938.x
– ident: e_1_2_7_8_1
  doi: 10.1016/j.soilbio.2005.09.027
– ident: e_1_2_7_46_1
– ident: e_1_2_7_49_1
  doi: 10.1007/s003740050496
– ident: e_1_2_7_29_1
  doi: 10.2136/sssaj2005.0160
– ident: e_1_2_7_20_1
  doi: 10.1111/j.1469-8137.1990.tb00374.x
– volume-title: The Jepson manual: higher plants of California
  year: 1993
  ident: e_1_2_7_26_1
– ident: e_1_2_7_59_1
  doi: 10.2136/sssaj1997.03615995006100020015x
– ident: e_1_2_7_40_1
  doi: 10.1046/j.1365-2699.1998.252166.x
– ident: e_1_2_7_47_1
  doi: 10.1016/S0038-0717(03)00028-2
– ident: e_1_2_7_12_1
  doi: 10.2136/sssaj2001.651118x
– start-page: 173
  volume-title: Bacterial systematics
  year: 1985
  ident: e_1_2_7_33_1
– ident: e_1_2_7_31_1
  doi: 10.1016/S0038-0717(03)00120-2
– start-page: 101
  volume-title: Manual of environmental microbiology
  year: 2002
  ident: e_1_2_7_43_1
– volume: 15
  start-page: 440
  year: 2005
  ident: e_1_2_7_58_1
  article-title: Responses of soil microbial community structure and diversity to agricultural deintensification
  publication-title: Pedosphere
– ident: e_1_2_7_45_1
– ident: e_1_2_7_55_1
  doi: 10.2307/1943519
– ident: e_1_2_7_13_1
  doi: 10.1128/AEM.72.5.3357-3366.2006
– ident: e_1_2_7_53_1
  doi: 10.1111/j.1461-0248.2006.00931.x
– ident: e_1_2_7_28_1
– ident: e_1_2_7_2_1
  doi: 10.1016/0038-0717(94)00140-V
– ident: e_1_2_7_42_1
  doi: 10.1016/S0016-7061(97)00032-3
– ident: e_1_2_7_4_1
  doi: 10.1007/s10530-004-3856-8
– ident: e_1_2_7_32_1
  doi: 10.1073/pnas.0608361104
– start-page: 39
  volume-title: Proceedings of the Soil Environment and Vine Mineral Nutrition Symposium
  year: 2005
  ident: e_1_2_7_19_1
– ident: e_1_2_7_23_1
  doi: 10.1126/science.1153475
– ident: e_1_2_7_56_1
  doi: 10.1046/j.1365-2699.2001.00563.x
– ident: e_1_2_7_34_1
  doi: 10.1016/S0269-7491(01)00211-1
– ident: e_1_2_7_7_1
  doi: 10.1007/s002489900087
– ident: e_1_2_7_48_1
  doi: 10.1016/j.soilbio.2005.12.005
– ident: e_1_2_7_52_1
  doi: 10.1111/j.1365-2699.2008.01931.x
– ident: e_1_2_7_22_1
  doi: 10.1128/AEM.01809-07
– ident: e_1_2_7_18_1
  doi: 10.3733/ca.v059n03p176
– ident: e_1_2_7_6_1
  doi: 10.1007/s002489900082
– ident: e_1_2_7_50_1
  doi: 10.1016/j.soilbio.2003.08.018
– ident: e_1_2_7_9_1
– ident: e_1_2_7_15_1
  doi: 10.1038/nature01548
– ident: e_1_2_7_3_1
  doi: 10.1016/S0038-0717(99)00016-4
– volume: 23
  start-page: 239
  year: 1980
  ident: e_1_2_7_54_1
  article-title: Nonselective biochemical methods for the determination of fungal mass and community structure in estuarine detrital microflora
  publication-title: Botanica Marina
SSID ssj0005456
Score 2.4327862
Snippet Although patterns are emerging for macroorganisms, we have limited understanding of the factors determining soil microbial community composition and...
Aim Although patterns are emerging for macroorganisms, we have limited understanding of the factors determining soil microbial community composition and...
ABSTRACT Aim  Although patterns are emerging for macroorganisms, we have limited understanding of the factors determining soil microbial community composition...
Aim  Although patterns are emerging for macroorganisms, we have limited understanding of the factors determining soil microbial community composition and...
SourceID pubmedcentral
proquest
pubmed
crossref
wiley
jstor
istex
fao
SourceType Open Access Repository
Aggregation Database
Index Database
Enrichment Source
Publisher
StartPage 27
SubjectTerms Acid soils
Agricultural ecosystems
agricultural management
Agricultural soils
agroecosystems
altitude
anaerobes
atmospheric precipitation
basins
Biomass
California
climatic factors
community structure
Desert soils
deserts
disturbance
disturbed soils
environmental impact
Fatty acids
floods
Forest soils
Gram-negative bacteria
Gram-positive bacteria
Grassland soils
irrigated soils
irrigation
land use
microbial biomass
microbial communities
Microbiology
phospholipids
PLFA
soil bacteria
Soil ecology
soil fungi
soil microbial community
Soil microorganisms
soil pH
soil water content
Soils
sulfate-reducing bacteria
Tillage
water
Wetland soils
xerophytes
Title Land use and climatic factors structure regional patterns in soil microbial communities
URI https://api.istex.fr/ark:/67375/WNG-9HD73HKS-1/fulltext.pdf
https://www.jstor.org/stable/40405783
https://onlinelibrary.wiley.com/doi/abs/10.1111%2Fj.1466-8238.2009.00486.x
https://www.ncbi.nlm.nih.gov/pubmed/24443643
https://www.proquest.com/docview/1242432186
https://www.proquest.com/docview/1272713678
https://www.proquest.com/docview/1826585236
https://www.proquest.com/docview/1999970612
https://www.proquest.com/docview/46454934
https://pubmed.ncbi.nlm.nih.gov/PMC3891896
Volume 19
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwrV1LbxMxEB5BJSQuPAqhCwWMhLhtlF17Hz7ySBvx6IESNTfL9nohSthU3UYq_HpmvI-SUqoKccpKO7aytmfmG3vmM8BLoY0oRlaHOpZlKJzMQoN-IuSFE0ZbE6eGaoc_HaSTqXg_S2Zt_hPVwjT8EP2GG2mGt9ek4NrUF5U8DXP0OR3tpMjTIeFJSt0ifPT5nEmKgEJTaERN4tlmUs-lHW14qpulXiF-paE_61IXLwOlf-ZW_o55vdPauwuL7nObXJXFcH1qhvbnBSbI_zMe9-BOi23Z62Yx3ocbrtqGW2PPi_1jGwbj86I6FGutSv0Ajj7qqmDr2jH6tcu5p5Fl7VVArKG4XZ84RrdIUOTAjj0raFWzecXq1XzJvs89oRS-sk3FC_HEPoTp3vjL20nYXvgQ2hTDnDAu88JydNtpkpUFlxrRkxFW60gWkRa6yGxqeGKKEnGLHDkrnTV5UmY8QZ-LYHIAW9WqcjvAysRhZCqpNyFs4aSI8hLRcZG6TJhcB5B1k6tsy4ZOl3Is1UZUlCoaT7qrUyo_nuosgKhvedwwglyjzQ6uH6W_ouFW08OYjosj2h6IkgBe-UXV96VPFpRslyXq6GBfycm7jE8-HKoogIFfdb2gGBHYznkAu90yVK0BqlVEZT-cLhwL4EX_Gk0HnQfpyq3WJIPglSj78itkcF4wooz5Vf1gkCEzwsoBPP-LjGeOk1wE8KjRj_4zEF8KjrgYZ2RDc3oBIkDffFPNv3kidDpjzyX-s8QrxrWnQ-2P3-DD439s9wRuNzkktBG3C1uoBe4pQtNT88wbnV-Hq36M
linkProvider Wiley-Blackwell
linkToHtml http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwrV3db9MwED_BEIIXPgZlgcGMhHjL1MTOhx_56FZY1we2an2zbMeBaiWd1lUa_PXcOWlGx5gmxFMj5Ww1tu_8O_vudwBvhDai6Fod6liWoXAyCw3uEyEvnDDamjg1lDu8P0z7I_F5nIybckCUC1PzQ7QHbqQZ3l6TgtOB9GUtT8McN50l76TI020ElHeowLf3r75ccEkRVKhTjahNPF4N67myp5W96napZ4hgafDPl8GLV8HSP6Mrf0e9ftvaeQjT5QfX0SrH24szs21_XuKC_E8j8ggeNPCWvavX42O45ap1uNvz1Ng_1qHTu8irQ7HGsMyfwNFAVwVbzB2jXzudeCZZ1lQDYjXL7eLUMSokQc4DO_HEoNWcTSo2n02m7PvEc0rhK1snvRBV7FMY7fQOP_TDpuZDaFP0dMK4zAvLcedOk6wsuNQIoIywWkeyiLTQRWZTwxNTlAhdZNdZ6azJkzLjCW67iCc7sFbNKrcBrEwcOqeSehPCFk6KKC8RIBepy4TJdQDZcnaVbQjRqS7HVK04Rqmi8aRynVL58VTnAURty5OaFOQGbTZwASn9FW23Gh3EdGMc0QlBlATw1q-qti99ekzxdlmijoa7SvY_Zry_d6CiADp-2bWCokt4O-cBbC7XoWps0FxFlPnDqeZYAK_b12g96EpIV262IBnEr8Tal18jg_OCTmXMr-sH_QyZEVwOYOsvMp48TnIRwLNaQdrPQIgpOEJjnJEV1WkFiAN99U01-ea50OmaPZf4zxKvGTeeDrXbe48Pz_-x3Rbc6x_uD9Tg03DvBdyvQ0roXG4T1lAj3EtEqmfmlbdAvwBKhoKn
linkToPdf http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwrV3db9MwELdgCMQLH4OywGBGQrylamLnw49A2xU2KsSo1jfLX4GqJa3WVRr89dw5aUbHmCbEUyPlbDX23fl39t3PhLziSnPbMSpUsShC7kQWalgnQmYd18roONVYO_xxmA5G_MM4Gdf5T1gLU_FDNBtuaBneX6OBL2xx0cjTMIc1Z007yfO0DXjyFk87OWp49_M5lRQiharSCNvE482snkt72liqbhZqDgAWx_5snbt4GSr9M7nyd9DrV63-fTJdf2-VrDJtr0512_y8QAX5fwbkAblXg1v6ptLGh-SGK7fJ7Z4nxv6xTVq986o6EKvdyvIROT5UpaWrpaP4a2YTzyNL67uAaMVxuzpxFK-RwNCBLjwtaLmkk5Iu55MZ_T7xjFLwylQlL0gU-5iM-r0v7wZhfeNDaFKIc8K4yK1hsG6nSVZYJhTAJ82NUpGwkeLKZibVLNG2AOAiOs4IZ3SeFBlLYNEFNNkiW-W8dDuEFomD0FRgb5wb6wSP8gLgsU1dxnWuApKtJ1eamg4db-WYyY2wKJU4nnhZp5B-POVZQKKm5aKiBLlGmx3QH6m-gueWo6MYz4sj3B-IkoC89krV9KVOpphtlyXyeLgvxaCbscHBkYwC0vJa1wjyDqLtnAVkd62GsvZASxlh3Q_DG8cC8rJ5Db4DD4RU6eYrlAH0ipx9-RUyMC8QUsbsqn4gyhAZguWA7P1FxlPHCcYD8qSyj-YzAGByBsAYZmTDchoBZEDffFNOvnkmdDxkzwX8s8QbxrWnQ-733sLD039st0fufOr25eH74cEzcrfKJ8FNuV2yBQbhngNMPdUvvP_5BWxJgV8
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Land+use+and+climatic+factors+structure+regional+patterns+in+soil+microbial+communities&rft.jtitle=Global+ecology+and+biogeography&rft.au=Drenovsky%2C+Rebecca+E&rft.au=Steenwerth%2C+Kerri+L&rft.au=Jackson%2C+Louise+E&rft.au=Scow%2C+Kate+M&rft.date=2010&rft.pub=Oxford%2C+UK+%3A+Blackwell+Publishing+Ltd&rft.issn=1466-822X&rft.volume=19&rft.issue=1&rft.spage=27&rft.epage=39&rft_id=info:doi/10.1111%2Fj.1466-8238.2009.00486.x&rft.externalDocID=US201301713315
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1466-822X&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1466-822X&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1466-822X&client=summon