Data Table | Table Structure |
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Object Name: | Whalen_SOM_pools.csv | Size: | 4083 byte | Authentication: | 660bf3f54130791f50708c0b3b285c79
Calculated By MD5 | Text Format: |
Number of Header Lines: | 1 |
Record Delimiter: | \r\n |
Orientation: | column |
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Field Delimiter: | , |
Quote Character: | " |
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Table Column Descriptions |
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| | | Sample_ID | Species_ID | Species_name | Phyla | Total_C (%) | MAOM_C (%) | POM_C (%) | ChemStable_C (%) | BioStable_C (%) | WaterStable_Agg (%) | single_agg_stability_% |
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Column Name: | Sample_ID
| Species_ID
| Species_name
| Phyla
| Total_C (%)
| MAOM_C (%)
| POM_C (%)
| ChemStable_C (%)
| BioStable_C (%)
| WaterStable_Agg (%)
| single_agg_stability_%
| Definition: | Unique sample identifier | abbreviation representing individual fungal isolates/species | Full fungal species names | Name of fungal phylum | Total carbon concentrations (%) in whole/bulk soil | Carbon concentration of mineral-associated organic matter (MAOM) fraction | Carbon concentration of particulate organic matter (POM) pool | Percent of soil carbon that was chemically stable (i.e., resisted extraction by water, KCl and sodium pyrophosphate) | Proportion of soil carbon that was biologically stable (i.e., resisted decomposition/respiration by active microbial inoculum during 3-month incubation) | Proportion of soil mass that was aggregated and water-stable (>250 microns) | Additional metric of aggregate stability conducted on single aggregate; proportion of initial aggregate mass that was water-stable | Storage Type: | string
| string
| string
| string
| float
| float
| float
| float
| float
| float
| float
| Measurement Type: | nominal | nominal | nominal | nominal | ratio | ratio | ratio | ratio | ratio | ratio | ratio | Measurement Values Domain: | | | Allowed Values and DefinitionsEnumerated Domain | | Code Definition | Code | Control | Definition | Control samples included only model soils and substrate (no fungal inoculum) | Source | |
| Code Definition | Code | Cylindrium elongatum | Definition | Isolate of Cylindrium elongatum | Source | |
| Code Definition | Code | Gymnopus sp. | Definition | Isolate of Gymnopus sp. (no species-level identification available) | Source | |
| Code Definition | Code | Hypocrea minutispora | Definition | Isolate of H. minutispora | Source | |
| Code Definition | Code | Mucor abundans | Definition | Isolate of M. abundans | Source | |
| Code Definition | Code | Mucor mucedo | Definition | Isolate of M. mucedo | Source | |
| Code Definition | Code | Panellus stipticus | Definition | Isolate of P. stipticus | Source | |
| Code Definition | Code | Phacidium lacerum | Definition | Isolate of P. lacerum | Source | |
| Code Definition | Code | Trichoderma koningii | Definition | Isolate of T. koningii | Source | |
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| Allowed Values and DefinitionsEnumerated Domain | | Code Definition | Code | Ascomycota | Definition | Fungal phylum | Source | |
| Code Definition | Code | Basidiomycota | Definition | Fungal phylum | Source | |
| Code Definition | Code | Control | Definition | Control samples (no fungal inoculum; only model soil + substrate) | Source | |
| Code Definition | Code | Mucoromycotina | Definition | Fungal sub-phylum | Source | |
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| | | | | | | | Missing Value Code: | | | | | | | | | | | | Accuracy Report: | | | | | | | | | | | | Accuracy Assessment: | | | | | | | | | | | | Coverage: | | | | | | | | | | | | Methods: | | | | | | | | | | | |
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Data Table | Data: | https://pasta-s.lternet.edu/package/data/eml/edi/1644/1/d43580e80427f5274d49593107a07450 | Name: | Whalen_fungal_traits | Description: | Trait values for individual fungal isolates; trait label abbreviations are as follows: GR_liquid (Optimum growth rate, measured in liquid culture, log-phase growth), CUE_liquid (Optimum CUE, measured in liquid culture, log-phase growth), GR_soil_mass_specific (Fungal growth rates measured in soils, log-phase growth), CUE_soil (Fungal CUE measured in soils, log-phase growth), CUE_soil_18O (Fungal CUE measured at stationary growth using 18-O water incorporation into DNA method), melanin_mg_mg_biomass (Melanin in fungal biomass, mg melanin/mg biomass), Turnover_days (Biomass turnover length, days), BG (Potential activity of betaglucosidase, μmol substrate h-1 g-1 dry soil), CBH (Potential activity of cellobiohydrolase, μmol substrate h-1 g-1 dry soil), NAG (Potential activity of N-acetylglucosaminadase, μmol substrate h-1 g-1 dry soil), PHOS (Potential activity of acid phosphatase, μmol substrate h-1 g-1 dry soil), LAP (Potential activity of leucine aminopeptidase, μmol substrate h-1 g-1 dry soil), ABTS (Potential activity of phenol peroxidase, μmol substrate h-1 g-1 dry soil), TMB (Potential activity of peroxidase, μmol substrate h-1 g-1 dry soil), biomass_aromatic (Relative abundance of aromatic compounds in fungal biomass, %), biomass_lignin (Relative abundance of "lignin" in fungal biomass, %) [NOTE: described as "lignin" by AMDIS database; likely represents fungal melanin], biomass_lipid (Relative abundance of lipids in fungal biomass, %), biomass_polysacc (Relative abundance of polysaccharides in fungal biomass, %), biomass_Nbearing (Relative abundance of N-bearing compounds in fungal biomass, %), biomass_protein (Relative abundance of proteins in fungal biomass, %), biomass_phenol (Relative abundance of phenolic compounds in fungal biomass, %), hyphal_length_m_per_g_drysoil (Hyphal lengths, m/g dry soil), hyphal_surface_area_m2 (Hyphal surface area, m2) | Number of Records: | 27 | Number of Columns: | 26 |
| Table Structure |
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Object Name: | Whalen_fungal_traits.csv | Size: | 6346 byte | Authentication: | 76aa37c90c986c2774d5534bb262b1ce
Calculated By MD5 | Text Format: |
Number of Header Lines: | 1 |
Record Delimiter: | \r\n |
Orientation: | column |
Simple Delimited: |
Field Delimiter: | , |
Quote Character: | " |
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Table Column Descriptions |
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| | | SampleID | Species_ID | Phyla | GR_liquid | CUE_liquid | GR_soil_mass_specific | CUE_soil | CUE_soil_18O | melanin_mg_mg_biomass | Turnover_days | BG | CBH | NAG | PHOS | LAP | ABTS | TMB | biomass_aromatic | biomass_lignin | biomass_lipid | biomass_polysacc | biomass_Nbearing | biomass_protein | biomass_phenol | hyphal_length_m_per_g_drysoil | hyphal_surface_area_m2 |
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Column Name: | SampleID
| Species_ID
| Phyla
| GR_liquid
| CUE_liquid
| GR_soil_mass_specific
| CUE_soil
| CUE_soil_18O
| melanin_mg_mg_biomass
| Turnover_days
| BG
| CBH
| NAG
| PHOS
| LAP
| ABTS
| TMB
| biomass_aromatic
| biomass_lignin
| biomass_lipid
| biomass_polysacc
| biomass_Nbearing
| biomass_protein
| biomass_phenol
| hyphal_length_m_per_g_drysoil
| hyphal_surface_area_m2
| Definition: | Unique sample identifier | Fungal isolate/species name abbreviation | Fungal phylum name | Optimum growth rate measured in liquid culture during log-phase growth | Optimum carbon use efficiency, measured during log-phase growth | Growth rate measured in soils | Carbon use efficiency measured in soils during log-phase growth | Carbon use efficiency measured during stationary growth using 18O-water incorporation into DNA method | Melanin concentration in fungal biomass | Biomass turnover length | Potential activity of beta-glucosidase enzyme | Potential activity of cellobiohydrolase enzyme | Potential activity of N-acetyl-glucosaminadase enzyme | Potential activity of acid phosphatase enzyme | Potential activity of leucine aminopepsidase enzyme | Potential activity of phenol oxidase | Potential activity of peroxidase | Relative abundance of aromatic compounds in fungal biomass | Relative abundance of "lignin" in fungal biomass (likely melanin; misidentified by AMDIS software) | Relative abundance of lipids in fungal biomass | Relative abundance of polysaccharides in fungal biomass | Relative abundance of N-bearing compounds in fungal biomass | Relative abundance of proteins in fungal biomass | Relative abundance of phenolic compounds in fungal biomass | Fungal hyphal lengths | Fungal hyphal surface areas | Storage Type: | string
| string
| string
| float
| float
| float
| float
| float
| float
| float
| float
| float
| float
| float
| float
| float
| float
| float
| float
| float
| float
| float
| float
| float
| float
| float
| Measurement Type: | nominal | nominal | nominal | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | Measurement Values Domain: | | | Allowed Values and DefinitionsEnumerated Domain | | Code Definition | Code | Ascomycota | Definition | Fungal phylum | Source | |
| Code Definition | Code | Basidiomycota | Definition | Fungal phylum | Source | |
| Code Definition | Code | Mucoromycotina | Definition | Fungal phylum | Source | |
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| Unit | micrograms biomass-C produced/biomass-C/hour | Type | real |
| Unit | Units of carbon (ratio) | Type | real |
| Unit | micrograms biomass-C produced/biomass-C/hour | Type | real |
| Unit | Units of carbon | Type | real |
| Unit | Units of carbon | Type | real |
| Unit | mg melanin/mg biomass | Type | real |
| | Unit | micromoles substrate/hour/gram dry soil | Type | real |
| Unit | micromoles substrate/hour/gram dry soil | Type | real |
| Unit | micromoles substrate/hour/gram dry soil | Type | real |
| Unit | micromoles substrate/hour/gram dry soil | Type | real |
| Unit | micromoles substrate/hour/gram dry soil | Type | real |
| Unit | micromoles substrate/hour/gram dry soil | Type | real |
| Unit | micromoles substrate/hour/gram dry soil | Type | real |
| | | | | | | | Unit | meters hyphae/gram dry soil | Type | real |
| Unit | m^2 hyphae/gram dry soil | Type | real |
| Missing Value Code: | | | | | | | | | | | | | | | | | | | | | | | | | | | Accuracy Report: | | | | | | | | | | | | | | | | | | | | | | | | | | | Accuracy Assessment: | | | | | | | | | | | | | | | | | | | | | | | | | | | Coverage: | | | | | | | | | | | | | | | | | | | | | | | | | | | Methods: | | | | | | | | | | | | | | | | | | | | | | | | | | |
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Data Table | Data: | https://pasta-s.lternet.edu/package/data/eml/edi/1644/1/98e72eb9ce8b60fdebf85f449eceb02d | Name: | Whalen_trait_multifunctionality | Description: | Final calculations of effective trait multifunctionality based on the modified averaging approach using Hill numbers (proposed by Byrnes et al. 2023). Columns C-X include the standardized values for each trait that were used in the averaging calculation. Data are outputs from the ‘multifunc’ package in R. Trait label information is available in/associated with "Whalen_trait_data.csv" file. | Number of Records: | 27 | Number of Columns: | 26 |
| Table Structure |
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Object Name: | Whalen_trait_multifunctionality.csv | Size: | 7714 byte | Authentication: | 76b1e2ac7a3da8ffe015068c85527a56
Calculated By MD5 | Text Format: |
Number of Header Lines: | 1 |
Record Delimiter: | \r\n |
Orientation: | column |
Simple Delimited: |
Field Delimiter: | , |
Quote Character: | " |
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Table Column Descriptions |
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| | | SampleID | Species | GR_liquid.std | CUE_liquid.std | GR_soil_mass_specific.std | CUE_soil.std | CUE_soil_18O.std | melanin_mg_mg_biomass.std | Turnover_days_norm2.std | BG.std | CBH.std | NAG.std | PHOS.std | LAP.std | ABTS.std | TMB.std | biomass_aromatic.std | biomass_lipid.std | biomass_polysacc.std | biomass_Nbearing.std | biomass_protein.std | biomass_phenol.std | hyphal_length_m_per_g_drysoil.std | hyphal_surface_area_m2.std | meanFunction | effective_trait_multifunctionality |
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Column Name: | SampleID
| Species
| GR_liquid.std
| CUE_liquid.std
| GR_soil_mass_specific.std
| CUE_soil.std
| CUE_soil_18O.std
| melanin_mg_mg_biomass.std
| Turnover_days_norm2.std
| BG.std
| CBH.std
| NAG.std
| PHOS.std
| LAP.std
| ABTS.std
| TMB.std
| biomass_aromatic.std
| biomass_lipid.std
| biomass_polysacc.std
| biomass_Nbearing.std
| biomass_protein.std
| biomass_phenol.std
| hyphal_length_m_per_g_drysoil.std
| hyphal_surface_area_m2.std
| meanFunction
| effective_trait_multifunctionality
| Definition: | Unique sample identifier | Species label | Standardized value for optimum growth rate, output from R 'multifunc' package | Standardized value for optimum CUE, output from R 'multifunc' package | Standardized values for growth rate measured in soils, output from 'multifunc' package in R | Standardized values for carbon use efficiency measured in soils, output from 'multifunc' package in R | Standardized values for carbon use efficiency, measured in soils at stationary growth | Standardized values for biomass melanin, output from 'multifunc' package in R | Standardized values for turnover, output from multifunc package in R | Standardized values for beta-glucosidase activity | Standardized values for cellobiohydrolase activity | Standardized values for N-acetyl-glucosaminadase activity | Standardized values for acid phosphatase activity | Standardized values for leucine aminopeptidase activity | Standardized values for phenol oxidase activity | Standardized values for peroxidase activity | Standardized values for relative abundance of aromatics in fungal biomass | Standardized values for relative abundance of lipids in fungal biomass | Standardized values for relative abundance of polysaccharides in fungal biomass | Standardized values for relative abundance of N-bearing compounds in fungal biomass | Standardized values for relative abundance of proteins in fungal biomass | Standardized values for relative abundance of phenols in fungal biomass | Standardized values for hyphal lengths in soil | Standardized values for hyphal surface area in soils | Average trait multifunctionality scores, calculated with 'multifunc' package in R | Effective trait multifunctionality scores; calculated using 'multifunc' package in R | Storage Type: | string
| string
| float
| float
| float
| float
| float
| float
| float
| float
| float
| float
| float
| float
| float
| float
| float
| float
| float
| float
| float
| float
| float
| float
| float
| float
| Measurement Type: | nominal | nominal | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | Measurement Values Domain: | | | Unit | micrograms biomass-C produced/biomass-C/hour | Type | real |
| Unit | Units of carbon (ratio) | Type | real |
| Unit | micrograms biomass-C produced biomass-C-1 hr-1 | Type | real |
| Unit | Units of carbon (ratio) | Type | real |
| Unit | Units of carbon (ratio) | Type | real |
| Unit | mg melanin/mg biomass | Type | real |
| | Unit | micromoles substrate h-1 g-1 dry soil | Type | real |
| Unit | micromoles substrate h-1 g-1 dry soil | Type | real |
| Unit | micromoles substrate h-1 g-1 dry soil | Type | real |
| Unit | micromoles substrate h-1 g-1 dry soil | Type | real |
| Unit | micromoles substrate h-1 g-1 dry soil | Type | real |
| Unit | micromoles substrate h-1 g-1 dry soil | Type | real |
| Unit | micromoles substrate h-1 g-1 dry soil | Type | real |
| | | | | | | Unit | meters hyphae/g dry soil | Type | real |
| Unit | m2 hyphae/gram dry soil | Type | real |
| | | Missing Value Code: | | | | | | | | | | | | | | | | | | | | | | | | | | | Accuracy Report: | | | | | | | | | | | | | | | | | | | | | | | | | | | Accuracy Assessment: | | | | | | | | | | | | | | | | | | | | | | | | | | | Coverage: | | | | | | | | | | | | | | | | | | | | | | | | | | | Methods: | | | | | | | | | | | | | | | | | | | | | | | | | | |
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Data Table | Data: | https://pasta-s.lternet.edu/package/data/eml/edi/1644/1/6d3e7212b30ae81dee4172ce7807f84a | Name: | Whalen_SOM_formation_potential | Description: | Final calculations of SOM formation potential (effective multifunctionality calculated based on fungal contributions to multiple SOM pools), based on the modified averaging approach using Hill numbers (proposed by Byrnes et al. 2023). Columns E-J include the standardized values for each SOM pool that were used in the averaging calculation. Data are outputs from the ‘multifunc’ package in R. Input values can be found in the "Whalen_SOM_pools.csv" file. | Number of Records: | 27 | Number of Columns: | 12 |
| Table Structure |
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Object Name: | Whalen_SOM_formation_potential.csv | Size: | 3777 byte | Authentication: | 4bc273508d91a9e970822b34bc8fab80
Calculated By MD5 | Text Format: |
Number of Header Lines: | 1 |
Record Delimiter: | \r\n |
Orientation: | column |
Simple Delimited: |
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Quote Character: | " |
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Table Column Descriptions |
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| | | SampleID | Species2 | Species_name | Phyla | Total_C.std | MAOM_C.std | ChemStable_C.std | BioStable_C.std | WaterStable_Agg.std | POM_C.std | meanFunction | effective_SOM_multifunctionality |
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Column Name: | SampleID
| Species2
| Species_name
| Phyla
| Total_C.std
| MAOM_C.std
| ChemStable_C.std
| BioStable_C.std
| WaterStable_Agg.std
| POM_C.std
| meanFunction
| effective_SOM_multifunctionality
| Definition: | Unique sample identifier | Species label/abbreviation | Full species name | Fungal phylum name | Standardized values for total soil carbon concentrations | Standardized values for carbon concentration of mineral-associated organic matter (MAOM) fraction | Standardized value for proportion of SOM-C that was chemically stable | Standardized value for proportion of SOM-C that was biologically stable (i.e., resisted decomposition by active microbial community during 3 month incubation) | Standardized value for water-stable aggregates; proportion of soil mass that was aggregated and water-stable | Standardized value for carbon concentration of particulate organic matter (POM) fraction | Average SOM multifunctionality score (i.e., SOM formation potential); calculated using multifunc package in R | Effective SOM multifunctionality (i.e., SOM formation potential); calculated using multifunc package in R | Storage Type: | string
| string
| string
| string
| float
| float
| float
| float
| float
| float
| float
| float
| Measurement Type: | nominal | nominal | nominal | nominal | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | Measurement Values Domain: | | | | Allowed Values and DefinitionsEnumerated Domain | | Code Definition | Code | Ascomycota | Definition | Name of fungal phylum | Source | |
| Code Definition | Code | Basidiomycota | Definition | Name of fungal phylum | Source | |
| Code Definition | Code | Mucoromycotina | Definition | Name of fungal phylum | Source | |
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| | | | | | | | | Missing Value Code: | | | | | | | | | | | | | Accuracy Report: | | | | | | | | | | | | | Accuracy Assessment: | | | | | | | | | | | | | Coverage: | | | | | | | | | | | | | Methods: | | | | | | | | | | | | |
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Data Table | Data: | https://pasta-s.lternet.edu/package/data/eml/edi/1644/1/d9ae5cef5c71b8edf4a2d80094c0bd70 | Name: | Whalen_PyGCMS_whole soil_classes | Description: | Relative abundances of chemical compound classes (e.g., aromatics, lipids, etc.) within whole soils characterized by ramped pyrolysis gas chromatography-mass spectrometry (ramped Py-GCMS); temperatures correspond to the stepped temperature of combustion, increasing from 330C to 735C. Compounds that combust at higher temperatures have higher thermal stabilities than those that combust at lower temperatures. | Number of Records: | 234 | Number of Columns: | 12 |
| Table Structure |
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Object Name: | Whalen_PyGCMS_whole soil_classes.csv | Size: | 29674 byte | Authentication: | 3e3268914b22eaa0cf3c58c0c5c9e2b8
Calculated By MD5 | Text Format: |
Number of Header Lines: | 1 |
Record Delimiter: | \r\n |
Orientation: | column |
Simple Delimited: |
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Table Column Descriptions |
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| | | SampleID | Species | Phyla | Temp | Aromatic | Lignin | Lipid | Polysaccharide | N-Bearing | Protein | Phenol | Unknown Origin |
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Column Name: | ShortName
| Species
| Phyla
| Temp
| Aromatic
| Lignin
| Lipid
| Polysaccharide
| N-Bearing
| Protein
| Phenol
| Unknown Origin
| Definition: | unique sample identifier | Species name/abbreviation | Fungal phyla (names) | Pyrolysis temperature | Relative abundance of aromatic compounds | Relative abundance of lignin (misclassified; likely fungal melanin) | Relative abundance of lipids | Relative abundance of polysaccharides | Relative abundance of N-bearing compounds | Relative abundance of proteins | Relative abundance of phenols | Relative abundance of unknown origin compounds | Storage Type: | string
| string
| string
| string
| float
| float
| float
| float
| float
| float
| float
| float
| Measurement Type: | nominal | nominal | nominal | nominal | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | Measurement Values Domain: | | Allowed Values and DefinitionsEnumerated Domain | | Code Definition | Code | Ceu | Definition | Phacidium lacerum | Source | |
| Code Definition | Code | Control | Definition | Control (model soils and substrate only; no fungal inoculum) | Source | |
| Code Definition | Code | Csp | Definition | Cylindrium elongatum | Source | |
| Code Definition | Code | Hm_ANA | Definition | Hypocrea minutispora (non-sporulating) | Source | |
| Code Definition | Code | Hm_TEL | Definition | Hypocrea minutispora (sporulating) | Source | |
| Code Definition | Code | Mm | Definition | Mucor mucedo | Source | |
| Code Definition | Code | Mr | Definition | Mucor abundans | Source | |
| Code Definition | Code | Ps | Definition | Panellus stipticus | Source | |
| Code Definition | Code | Rt | Definition | Gymnopus sp. | Source | |
| Code Definition | Code | Tk | Definition | Trichoderma koningii | Source | |
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| Allowed Values and DefinitionsEnumerated Domain | | Code Definition | Code | Ascomycota | Definition | Name of fungal phylum | Source | |
| Code Definition | Code | Basidiomycota | Definition | Name of fungal phylum | Source | |
| Code Definition | Code | Control | Definition | Control samples (no fungal inoculum; only model soil and substrate) | Source | |
| Code Definition | Code | Mucoromycotina | Definition | Name of fungal phylum | Source | |
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| Allowed Values and DefinitionsEnumerated Domain | | Code Definition | Code | 330 | Definition | Pyrolysis thermal fraction, combustion temperature 330C | Source | |
| Code Definition | Code | 396 | Definition | Pyrolysis thermal fraction, combustion temperature 396C | Source | |
| Code Definition | Code | 444 | Definition | Pyrolysis thermal fraction, combustion temperature 444C | Source | |
| Code Definition | Code | 503 | Definition | Pyrolysis thermal fraction, combustion temperature 503C | Source | |
| Code Definition | Code | 600 | Definition | Pyrolysis thermal fraction, combustion temperature 600C | Source | |
| Code Definition | Code | 735 | Definition | Pyrolysis thermal fraction, combustion temperature 735C | Source | |
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Data Table | Data: | https://pasta-s.lternet.edu/package/data/eml/edi/1644/1/28fb79cd345d9c04222c835975f0abf4 | Name: | Whalen_PyGCMS_MAOM_classes | Description: | Relative abundances of chemical compound classes (e.g., aromatics, lipids, etc.) within mineral-associated organic matter (MAOM) fraction, characterized by pyrolysis gas chromatography-mass spectrometry (Py-GCMS). Samples were pyrolyzed at a single temperature (600C). | Number of Records: | 39 | Number of Columns: | 10 |
| Table Structure |
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Object Name: | Whalen_PyGCMS_MAOM_classes.csv | Size: | 4265 byte | Authentication: | a9a085e9f2a31e2559d9dba53a9971f6
Calculated By MD5 | Text Format: |
Number of Header Lines: | 1 |
Record Delimiter: | \r\n |
Orientation: | column |
Simple Delimited: |
Field Delimiter: | , |
Quote Character: | " |
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Table Column Descriptions |
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| | | Sample_ID | Species_ID | Aromatic | Phenol | Lipid | Polysaccharide | N-Bearing | Protein | Lignin | Unknown Origin |
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Column Name: | Sample_ID
| Species_ID
| Aromatic
| Phenol
| Lipid
| Polysaccharide
| N-Bearing
| Protein
| Lignin
| Unknown Origin
| Definition: | Unique sample identifier | Species label/abbreviation | Relative abundance of aromatic compounds | Relative abundance of phenols | Relative abundance of lipids | Relative abundance of polysaccharides | Relative abundance of N-bearing compounds | Relative abundance of proteins | Relative abundance of "lignin" (misclassified; likely fungal melanin) | Relative abundance of compounds with unknown origin | Storage Type: | string
| string
| float
| float
| float
| float
| float
| float
| float
| float
| Measurement Type: | nominal | nominal | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | Measurement Values Domain: | | | | | | | | | | | Missing Value Code: | | | | | | | | | | | Accuracy Report: | | | | | | | | | | | Accuracy Assessment: | | | | | | | | | | | Coverage: | | | | | | | | | | | Methods: | | | | | | | | | | |
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Data Table | Table Structure |
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Object Name: | Whalen_PyGCMS_MAOM_compounds.csv | Size: | 40485 byte | Authentication: | 9f9a78f2a15c33dbbe7470af54b47aef
Calculated By MD5 | Text Format: |
Number of Header Lines: | 1 |
Record Delimiter: | \r\n |
Orientation: | column |
Simple Delimited: |
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Table Column Descriptions |
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| | | SampleID | Species | Phyla | (E)-1,3-Butadien-1-ol | 1 H-Pyrrole, 2-ethyl- | 1,3,5,7-Cyclooctatetraene | 1,3,5-Cycloheptatriene | 1,3,5-Cyclooctatriene | 1,3-Butadiene | 1-Butyne, 3,3-dimethyl- | 1-Heptene | 1-Hexene, 3-methyl- | 1H-Inden-1-one, 2,3-dihydro- | 1H-Indene, 2,3-dihydro-1,1,3-trimethyl-3-phenyl- | 1H-Pyrrole,1-methyl- | 1H-Pyrrole,2-methyl- | 1H-Pyrrole,3-methyl- | 1H-Pyrrole-2-carboxaldehyde | 1H-Pyrrole-2-carboxaldehyde,1-methyl- | 1-Pentene, 3-ethyl-2-methyl- | 1-Propene, 3-azido- | 1-Undecanol | 2(3H)-Benzofuranone, 3-methyl- | 2(3H)-Furanone, 5-methyl- | 2(5H)-Furanone | 2(5H)-Furanone,5-methyl- | 2,3,5-Trimethylnaphthalene | 2,3,6-Trimethylnaphthalene | 2,5-Furandione, 3-methyl- | 2-Acetylfuran | 2-Cyclopenten-1-one,2,3-dimethyl- | 2-Cyclopenten-1-one,2-hydroxy-3-methyl- | 2-Cyclopenten-1-one,2-methyl- | 2-Cyclopenten-1-one,3-methyl- | 2-Furanmethanol | 2H-1-Benzopyran-2-one | 2H-Pyran-2-one | 2-Methylthiophene | 2-Pentanone | 2-Propen-1-ol | 2-Propenenitrile, 2-methyl- | 2-Propenoic acid,anhydride | 2-Propenoic acid,ethenyl ester | 2-Pyridinealdehyde | 2-Pyridinecarbonitrile | 3-Acetamidofuran | 3-Decene | 3-Methylindole | 3-Methylthiophene | 3-Phenylpyridine | 3-Pyridinecarbonitrile | 4H-Pyran-4-one, 3-hydroxy-2-methyl- | 4-Pyridinamine | 4-Pyridinecarbonitrile | 4-Pyridinecarboxaldehyde | 5-Dimethylaminopyrimidine | 5-Ethyl-2-furaldehyde | 5H-1-Pyrindine | 7-Tetradecene | Acenaphthene | Acenaphthylene | Acetamide, N-(2,4-dihydroxyphenyl)- | Acetic acid, cyano-, ethyl ester | Acetophenone | Aniline | Anthracene | Benzaldehyde | Benzene | Benzene2 | Benzene,(1,3-dimethylbutyl)- | Benzene,(1-methylethyl)- | Benzene,1,2,3,4-tetramethyl- | Benzene,1,2,3-trimethyl- | Benzene,1,2-diethyl- | Benzene,1-ethenyl-3-methyl- | Benzene,1-ethenyl-4-methoxy- | Benzene,1-methoxy-4-methyl- | Benzene,butyl- | Benzene,heptyl- | Benzene,hexyl- | Benzene,pentyl- | Benzene,propyl- | Benzenepropanenitrile | Benzofuran | Benzofuran,2,3-dihydro- | Benzofuran,2-methyl- | Benzoic acid, 4-hydroxy-3-methoxy-Vanillic acid) | Benzonitrile | Benzyl nitrile | Biphenyl | Butanal, 2-methyl- | C14_alkene_3 | C8_H16 | C9_H8 | Cyanamide, dimethyl- | Cyclopent-2-ene-1-one, 2,3,4-trimethyl- | Cyclopentanone | Dimethylbenzofuran | Disulfide, dimethyl | Ethylphenol | Fluoranthene | Fluorene | Furan,2,3,5-trimethyl- | Furan,2,5-dimethyl- | Furan,2-ethyl- | Furan,2-ethyl-5-methyl- | Furan,3-methyl- | Furfural | Hex-2-yn-4-one, 2-methyl- | Hexadecanoic acid, methyl ester (Palmitic acid-C16) | Hexanedinitrile | Hydroquinone | Indane | Indole | Methanesulfonic acid, methyl ester | Monobenzone | m-xylene | Naphthalene | Naphthalene,1,2-dihydro-4-methyl- | n-Heptadecane | n-Hexadecane | Nicotinyl Alcohol | n-Octane | n-Pentadecane | n-Triacontane (C30) | n-Tridecane | n-Undecane | Oxirane, ethenyl- | p-Aminotoluene | Phenanthrene | Phenol,2,4-bis(1,1-dimethylethyl)- | Phenol,2-methoxy- (Guaiacol) | Phenol,3,4-dimethyl- | Phenol,3-methyl- | Phenol,4-methyl- | Phosphonic acid, (p-hydroxyphenyl)- | Piperidine-2,5-dione | Propane, 2-nitro- | Propanenitrile | p-Xylene | Pyrazolo[5,1-c][1,2,4]benzotriazin-8-ol | Pyridine | Pyridine2 | Pyridine 2-methyl | Pyridine 3-methyl | Pyridine, 2-ethyl | Pyridine, 3,5-dimethyl- | Pyrimidine | Pyrrole | Thiophene | Toluene | Trimethylphenol | Vinylfuran |
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Column Name: | SampleID
| Species
| Phyla
| (E)-1,3-Butadien-1-ol
| 1 H-Pyrrole, 2-ethyl-
| 1,3,5,7-Cyclooctatetraene
| 1,3,5-Cycloheptatriene
| 1,3,5-Cyclooctatriene
| 1,3-Butadiene
| 1-Butyne, 3,3-dimethyl-
| 1-Heptene
| 1-Hexene, 3-methyl-
| 1H-Inden-1-one, 2,3-dihydro-
| 1H-Indene, 2,3-dihydro-1,1,3-trimethyl-3-phenyl-
| 1H-Pyrrole,1-methyl-
| 1H-Pyrrole,2-methyl-
| 1H-Pyrrole,3-methyl-
| 1H-Pyrrole-2-carboxaldehyde
| 1H-Pyrrole-2-carboxaldehyde,1-methyl-
| 1-Pentene, 3-ethyl-2-methyl-
| 1-Propene, 3-azido-
| 1-Undecanol
| 2(3H)-Benzofuranone, 3-methyl-
| 2(3H)-Furanone, 5-methyl-
| 2(5H)-Furanone
| 2(5H)-Furanone,5-methyl-
| 2,3,5-Trimethylnaphthalene
| 2,3,6-Trimethylnaphthalene
| 2,5-Furandione, 3-methyl-
| 2-Acetylfuran
| 2-Cyclopenten-1-one,2,3-dimethyl-
| 2-Cyclopenten-1-one,2-hydroxy-3-methyl-
| 2-Cyclopenten-1-one,2-methyl-
| 2-Cyclopenten-1-one,3-methyl-
| 2-Furanmethanol
| 2H-1-Benzopyran-2-one
| 2H-Pyran-2-one
| 2-Methylthiophene
| 2-Pentanone
| 2-Propen-1-ol
| 2-Propenenitrile, 2-methyl-
| 2-Propenoic acid,anhydride
| 2-Propenoic acid,ethenyl ester
| 2-Pyridinealdehyde
| 2-Pyridinecarbonitrile
| 3-Acetamidofuran
| 3-Decene
| 3-Methylindole
| 3-Methylthiophene
| 3-Phenylpyridine
| 3-Pyridinecarbonitrile
| 4H-Pyran-4-one, 3-hydroxy-2-methyl-
| 4-Pyridinamine
| 4-Pyridinecarbonitrile
| 4-Pyridinecarboxaldehyde
| 5-Dimethylaminopyrimidine
| 5-Ethyl-2-furaldehyde
| 5H-1-Pyrindine
| 7-Tetradecene
| Acenaphthene
| Acenaphthylene
| Acetamide, N-(2,4-dihydroxyphenyl)-
| Acetic acid, cyano-, ethyl ester
| Acetophenone
| Aniline
| Anthracene
| Benzaldehyde
| Benzene
| Benzene2
| Benzene,(1,3-dimethylbutyl)-
| Benzene,(1-methylethyl)-
| Benzene,1,2,3,4-tetramethyl-
| Benzene,1,2,3-trimethyl-
| Benzene,1,2-diethyl-
| Benzene,1-ethenyl-3-methyl-
| Benzene,1-ethenyl-4-methoxy-
| Benzene,1-methoxy-4-methyl-
| Benzene,butyl-
| Benzene,heptyl-
| Benzene,hexyl-
| Benzene,pentyl-
| Benzene,propyl-
| Benzenepropanenitrile
| Benzofuran
| Benzofuran,2,3-dihydro-
| Benzofuran,2-methyl-
| Benzoic acid, 4-hydroxy-3-methoxy-Vanillic acid)
| Benzonitrile
| Benzyl nitrile
| Biphenyl
| Butanal, 2-methyl-
| C14_alkene_3
| C8_H16
| C9_H8
| Cyanamide, dimethyl-
| Cyclopent-2-ene-1-one, 2,3,4-trimethyl-
| Cyclopentanone
| Dimethylbenzofuran
| Disulfide, dimethyl
| Ethylphenol
| Fluoranthene
| Fluorene
| Furan,2,3,5-trimethyl-
| Furan,2,5-dimethyl-
| Furan,2-ethyl-
| Furan,2-ethyl-5-methyl-
| Furan,3-methyl-
| Furfural
| Hex-2-yn-4-one, 2-methyl-
| Hexadecanoic acid, methyl ester (Palmitic acid-C16)
| Hexanedinitrile
| Hydroquinone
| Indane
| Indole
| Methanesulfonic acid, methyl ester
| Monobenzone
| m-xylene
| Naphthalene
| Naphthalene,1,2-dihydro-4-methyl-
| n-Heptadecane
| n-Hexadecane
| Nicotinyl Alcohol
| n-Octane
| n-Pentadecane
| n-Triacontane (C30)
| n-Tridecane
| n-Undecane
| Oxirane, ethenyl-
| p-Aminotoluene
| Phenanthrene
| Phenol,2,4-bis(1,1-dimethylethyl)-
| Phenol,2-methoxy- (Guaiacol)
| Phenol,3,4-dimethyl-
| Phenol,3-methyl-
| Phenol,4-methyl-
| Phosphonic acid, (p-hydroxyphenyl)-
| Piperidine-2,5-dione
| Propane, 2-nitro-
| Propanenitrile
| p-Xylene
| Pyrazolo[5,1-c][1,2,4]benzotriazin-8-ol
| Pyridine
| Pyridine2
| Pyridine 2-methyl
| Pyridine 3-methyl
| Pyridine, 2-ethyl
| Pyridine, 3,5-dimethyl-
| Pyrimidine
| Pyrrole
| Thiophene
| Toluene
| Trimethylphenol
| Vinylfuran
| Definition: | Unique sample identifier | Species name | Fungal phylum (name) | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Storage Type: | string
| string
| string
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| Measurement Type: | nominal | nominal | nominal | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | Measurement Values Domain: | | | Allowed Values and DefinitionsEnumerated Domain | | Code Definition | Code | Ascomycota | Definition | Fungal phylum (name) | Source | |
| Code Definition | Code | Basidiomycota | Definition | Fungal phylum (name) | Source | |
| Code Definition | Code | Control | Definition | Control (no fungal inoculum; model soil and substrate only) | Source | |
| Code Definition | Code | Mucoromycotina | Definition | Fungal phylum (name) | Source | |
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Data Table | Data: | https://pasta-s.lternet.edu/package/data/eml/edi/1644/1/4b262a6bdc2e2537e384a9149d96af18 | Name: | Whalen_PyGCMS_whole soil_compounds | Description: | Relative abundances of individual compounds within whole soils, characterized by ramped pyrolysis gas chromatography-mass spectrometry (ramped Py-GCMS). "Temp" column corresponds with the temperature at which samples were pyrolyzed, ranging from 330C to 735C. Compounds that combust at higher temperatures have greater thermal stabilities than those that combust at lower temperatures. | Number of Records: | 234 | Number of Columns: | 202 |
| Table Structure |
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Object Name: | Whalen_PyGCMS_whole soil_compounds.csv | Size: | 213739 byte | Authentication: | dcd89fb29239cb2a90037dc4ee2485a3
Calculated By MD5 | Text Format: |
Number of Header Lines: | 1 |
Record Delimiter: | \r\n |
Orientation: | column |
Simple Delimited: |
Field Delimiter: | , |
Quote Character: | " |
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Table Column Descriptions |
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| | | SampleID | Species | Phyla | Temp | (E)-1,3-Butadien-1-ol | 1 H-Pyrrole, 2-ethyl- | 1,2,3-Benzenetriol | 1,2-Benzenediol, 3-methoxy- | 1,3,5,7-Cyclooctatetraene | 1,3,5-Cycloheptatriene | 1,3,5-Cyclooctatriene | 1,3-Butadiene | 1,3-Octadiene | 1-Heptene | 1-Hexadecene | 1-Hexene, 3-methyl- | 1H-Inden-1-one, 2,3-dihydro- | 1H-Indene, 2,3-dihydro-1,1,3-trimethyl-3-phenyl- | 1H-Pyrrole, 1-methyl- | 1H-Pyrrole, 2-methyl- | 1H-Pyrrole, 3-methyl- | 1H-Pyrrole-2-carboxaldehyde | 1H-Pyrrole-2-carboxaldehyde, 1-methyl- | 1H-Tetrazole, 1-methyl- | 1-Propene, 3-azido- | 1-Undecanol | 2(3H)-Benzofuranone, 3-methyl- | 2(3H)-Furanone, 5-methyl- | 2(5H)-Furanone | 2(5H)-Furanone, 5-methyl- | 2,3,5-Trimethylnaphthalene | 2,3,6-Trimethylnaphthalene | 2,5-Furandione, 3-methyl- | 2,6-Di-tert-butylbenzoquinone | 2-Acetylfuran | 2-Amino-4-methylpyrimidine | 2-Butanone, 3,3-dimethyl- | 2-Butenedioic acid, 2-methyl-, (E)- | 2-Cyclohexen-1-one | 2-Cyclopenten-1-one, 2,3-dimethyl- | 2-Cyclopenten-1-one, 2-hydroxy-3-methyl- | 2-Cyclopenten-1-one, 2-methyl- | 2-Cyclopenten-1-one, 3-methyl- | 2-Furanmethanol | 2H-1-Benzopyran-2-one | 2H-Pyran-2-one | 2-Methylthiophene | 2-Naphthalenol, 3-methoxy- | 2-Propen-1-ol | 2-Propenenitrile, 2-methyl- | 2-Propenoic acid, anhydride | 2-Propyn-1-amine | 2-Pyridinealdehyde | 2-Pyridinecarbonitrile | 2-Pyrimidinamine | 3-Acetamidofuran | 3-Decene | 3-Furaldehyde | 3-Methylindole | 3-Methylpyridazine | 3-Methylthiophene | 3-Methylthiophene-2-carbonitrile | 3-Penten-2-one, (E)- | 3-Phenylpyridine | 3-Pyridinecarbonitrile | 3-Pyridinol | 4(1H)-Pyridinone, 2,3-dihydro-1-methyl- | 4H-Pyran-4-one, 3-hydroxy-2-methyl- | 4-Hydroxy-2-methylacetophenone | 4-Pyridinamine | 4-Pyridinecarbonitrile | 4-Pyridinecarboxaldehyde | 5-Dimethylaminopyrimidine | 5-Ethyl-2-furaldehyde | 5H-1-Pyrindine | 6-Methyl-1,2,3,4-tetrahydroquinoline | 7-Methylindan-1-one | 7-Tetradecene | Acenaphthene | Acenaphthylene | Acetamide, N-(2,4-dihydroxyphenyl)- | Acetophenone | Aniline | Anthracene | Benzaldehyde | Benzaldehyde, 4-methoxy- | Benzene | Benzene2 | Benzene, (1,3-dimethylbutyl)- | Benzene, (1-methylethyl)- | Benzene, 1,2,3,4-tetramethyl- | Benzene, 1,2,3-trimethyl- | Benzene, 1,2-diethyl- | Benzene, 1,3-bis(1,1-dimethylethyl)- | Benzene, 1-ethenyl-3-methyl- | Benzene, 1-ethenyl-4-methoxy- | Benzene, 1-ethyl-4-methoxy- | Benzene, 1-methoxy-4-methyl- | Benzene, 2,4-diisocyanato-1-methyl- | Benzene, butyl- | Benzene, heptyl- | Benzene, hexyl- | Benzene, pentyl- | Benzene, propyl- | Benzenepropanenitrile | Benzo[a]anthracene | Benzofuran | Benzofuran, 2,3-dihydro- | Benzofuran, 2-methyl- | Benzoic acid, 4-hydroxy-3-methoxy-Vanillic acid) | Benzonitrile | Benzyl nitrile | Biphenyl | Butanal, 2-methyl- | C11_H12 | C14_alkene_3 | C8_H16 | C9_H8 | Cyanamide, dimethyl- | Cyclopent-2-ene-1-one, 2,3,4-trimethyl- | Cyclopentanone | Diethyltoluamide (DEET) | Dimethyl trisulfide | Dimethylbenzofuran | Dimethylpyrrole (2,5 or 2,4) | D-Limonene | Ethanone, 1-(1-methyl-1H-pyrrol-2-yl)- | Ethylbenzene | Ethylphenol | Fluoranthene | Fluorene | Furan, 2,3,5-trimethyl- | Furan, 2,4-dimethyl- | Furan, 2,5-dimethyl- | Furan, 2-ethyl- | Furan, 2-ethyl-5-methyl- | Furan, 3-methyl- | Furfural | Furfural, 5-methyl- | Hex-2-yn-4-one, 2-methyl- | Hydroquinone | Indane | Indole | Levoglucosan | Levoglucosenone | Mequinol | Methanesulfonic acid, methyl ester | Monobenzone | m-xylene | Naphthalene | Naphthalene, 1,2-dihydro-4-methyl- | N-Butyl-tert-butylamine | n-Decane | n-Hentriacontane (C31) | n-Heptacosane (C27) | n-Heptadecane | n-Heptane | n-Hexacosane (C26) | n-Hexadecane | Nicotinyl Alcohol | n-Nonacosane (C29) | n-Nonane | n-Octane | n-Pentacosane (C25) | n-Pentadecane | n-Tetracosane | n-Triacontane (C30) | n-Tricosane (C23) | n-Tridecane | Oxirane, ethenyl- | p-Aminotoluene | Pentadecane, 7-methyl | Pentadecanoic acid, 14-methyl-, methyl ester | Phenol | Phenol, 2,4-bis(1,1-dimethylethyl)- | Phenol, 2-methoxy- (Guaiacol) | Phenol, 2-methoxy-4-methyl- (4-Methylguaiacol) | Phenol, 2-Methoxy-4-vinyl- (Vinylguaiacol) | Phenol, 3,4-dimethyl- | Phenol, 3-methyl- | Phenol, 4-ethyl-2,6-dimethoxy- (Ethylsyringol) | Phenol, 4-ethyl-2-methoxy- (Ethylguaiacol) | Phenol, 4-methyl- | Phosphonic acid, (p-hydroxyphenyl)- | Piperidine-2,5-dione | Propanenitrile | p-Xylene | Pyrazolo[5,1-c][1,2,4]benzotriazin-8-ol | Pyridine | Pyridine2 | Pyridine 3-methyl | Pyridine, 2-ethyl | Pyridine, 3,5-dimethyl- | Pyrimidine | Pyrrole | Pyrrolidine, 1-nitroso | Resorcinol (Dihydroxybenzene) | Styrene | Thiophene | Toluene | Trimethylphenol | Vinylfuran |
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Column Name: | SampleID
| Species
| Phyla
| Temp
| (E)-1,3-Butadien-1-ol
| 1 H-Pyrrole, 2-ethyl-
| 1,2,3-Benzenetriol
| 1,2-Benzenediol, 3-methoxy-
| 1,3,5,7-Cyclooctatetraene
| 1,3,5-Cycloheptatriene
| 1,3,5-Cyclooctatriene
| 1,3-Butadiene
| 1,3-Octadiene
| 1-Heptene
| 1-Hexadecene
| 1-Hexene, 3-methyl-
| 1H-Inden-1-one, 2,3-dihydro-
| 1H-Indene, 2,3-dihydro-1,1,3-trimethyl-3-phenyl-
| 1H-Pyrrole, 1-methyl-
| 1H-Pyrrole, 2-methyl-
| 1H-Pyrrole, 3-methyl-
| 1H-Pyrrole-2-carboxaldehyde
| 1H-Pyrrole-2-carboxaldehyde, 1-methyl-
| 1H-Tetrazole, 1-methyl-
| 1-Propene, 3-azido-
| 1-Undecanol
| 2(3H)-Benzofuranone, 3-methyl-
| 2(3H)-Furanone, 5-methyl-
| 2(5H)-Furanone
| 2(5H)-Furanone, 5-methyl-
| 2,3,5-Trimethylnaphthalene
| 2,3,6-Trimethylnaphthalene
| 2,5-Furandione, 3-methyl-
| 2,6-Di-tert-butylbenzoquinone
| 2-Acetylfuran
| 2-Amino-4-methylpyrimidine
| 2-Butanone, 3,3-dimethyl-
| 2-Butenedioic acid, 2-methyl-, (E)-
| 2-Cyclohexen-1-one
| 2-Cyclopenten-1-one, 2,3-dimethyl-
| 2-Cyclopenten-1-one, 2-hydroxy-3-methyl-
| 2-Cyclopenten-1-one, 2-methyl-
| 2-Cyclopenten-1-one, 3-methyl-
| 2-Furanmethanol
| 2H-1-Benzopyran-2-one
| 2H-Pyran-2-one
| 2-Methylthiophene
| 2-Naphthalenol, 3-methoxy-
| 2-Propen-1-ol
| 2-Propenenitrile, 2-methyl-
| 2-Propenoic acid, anhydride
| 2-Propyn-1-amine
| 2-Pyridinealdehyde
| 2-Pyridinecarbonitrile
| 2-Pyrimidinamine
| 3-Acetamidofuran
| 3-Decene
| 3-Furaldehyde
| 3-Methylindole
| 3-Methylpyridazine
| 3-Methylthiophene
| 3-Methylthiophene-2-carbonitrile
| 3-Penten-2-one, (E)-
| 3-Phenylpyridine
| 3-Pyridinecarbonitrile
| 3-Pyridinol
| 4(1H)-Pyridinone, 2,3-dihydro-1-methyl-
| 4H-Pyran-4-one, 3-hydroxy-2-methyl-
| 4-Hydroxy-2-methylacetophenone
| 4-Pyridinamine
| 4-Pyridinecarbonitrile
| 4-Pyridinecarboxaldehyde
| 5-Dimethylaminopyrimidine
| 5-Ethyl-2-furaldehyde
| 5H-1-Pyrindine
| 6-Methyl-1,2,3,4-tetrahydroquinoline
| 7-Methylindan-1-one
| 7-Tetradecene
| Acenaphthene
| Acenaphthylene
| Acetamide, N-(2,4-dihydroxyphenyl)-
| Acetophenone
| Aniline
| Anthracene
| Benzaldehyde
| Benzaldehyde, 4-methoxy-
| Benzene
| Benzene2
| Benzene, (1,3-dimethylbutyl)-
| Benzene, (1-methylethyl)-
| Benzene, 1,2,3,4-tetramethyl-
| Benzene, 1,2,3-trimethyl-
| Benzene, 1,2-diethyl-
| Benzene, 1,3-bis(1,1-dimethylethyl)-
| Benzene, 1-ethenyl-3-methyl-
| Benzene, 1-ethenyl-4-methoxy-
| Benzene, 1-ethyl-4-methoxy-
| Benzene, 1-methoxy-4-methyl-
| Benzene, 2,4-diisocyanato-1-methyl-
| Benzene, butyl-
| Benzene, heptyl-
| Benzene, hexyl-
| Benzene, pentyl-
| Benzene, propyl-
| Benzenepropanenitrile
| Benzo[a]anthracene
| Benzofuran
| Benzofuran, 2,3-dihydro-
| Benzofuran, 2-methyl-
| Benzoic acid, 4-hydroxy-3-methoxy-Vanillic acid)
| Benzonitrile
| Benzyl nitrile
| Biphenyl
| Butanal, 2-methyl-
| C11_H12
| C14_alkene_3
| C8_H16
| C9_H8
| Cyanamide, dimethyl-
| Cyclopent-2-ene-1-one, 2,3,4-trimethyl-
| Cyclopentanone
| Diethyltoluamide (DEET)
| Dimethyl trisulfide
| Dimethylbenzofuran
| Dimethylpyrrole (2,5 or 2,4)
| D-Limonene
| Ethanone, 1-(1-methyl-1H-pyrrol-2-yl)-
| Ethylbenzene
| Ethylphenol
| Fluoranthene
| Fluorene
| Furan, 2,3,5-trimethyl-
| Furan, 2,4-dimethyl-
| Furan, 2,5-dimethyl-
| Furan, 2-ethyl-
| Furan, 2-ethyl-5-methyl-
| Furan, 3-methyl-
| Furfural
| Furfural, 5-methyl-
| Hex-2-yn-4-one, 2-methyl-
| Hydroquinone
| Indane
| Indole
| Levoglucosan
| Levoglucosenone
| Mequinol
| Methanesulfonic acid, methyl ester
| Monobenzone
| m-xylene
| Naphthalene
| Naphthalene, 1,2-dihydro-4-methyl-
| N-Butyl-tert-butylamine
| n-Decane
| n-Hentriacontane (C31)
| n-Heptacosane (C27)
| n-Heptadecane
| n-Heptane
| n-Hexacosane (C26)
| n-Hexadecane
| Nicotinyl Alcohol
| n-Nonacosane (C29)
| n-Nonane
| n-Octane
| n-Pentacosane (C25)
| n-Pentadecane
| n-Tetracosane
| n-Triacontane (C30)
| n-Tricosane (C23)
| n-Tridecane
| Oxirane, ethenyl-
| p-Aminotoluene
| Pentadecane, 7-methyl
| Pentadecanoic acid, 14-methyl-, methyl ester
| Phenol
| Phenol, 2,4-bis(1,1-dimethylethyl)-
| Phenol, 2-methoxy- (Guaiacol)
| Phenol, 2-methoxy-4-methyl- (4-Methylguaiacol)
| Phenol, 2-Methoxy-4-vinyl- (Vinylguaiacol)
| Phenol, 3,4-dimethyl-
| Phenol, 3-methyl-
| Phenol, 4-ethyl-2,6-dimethoxy- (Ethylsyringol)
| Phenol, 4-ethyl-2-methoxy- (Ethylguaiacol)
| Phenol, 4-methyl-
| Phosphonic acid, (p-hydroxyphenyl)-
| Piperidine-2,5-dione
| Propanenitrile
| p-Xylene
| Pyrazolo[5,1-c][1,2,4]benzotriazin-8-ol
| Pyridine
| Pyridine2
| Pyridine 3-methyl
| Pyridine, 2-ethyl
| Pyridine, 3,5-dimethyl-
| Pyrimidine
| Pyrrole
| Pyrrolidine, 1-nitroso
| Resorcinol (Dihydroxybenzene)
| Styrene
| Thiophene
| Toluene
| Trimethylphenol
| Vinylfuran
| Definition: | Unique sample identifier | Species label | Fungal phylum name | Pyrolysis temperature | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Chemical compound name | Storage Type: | string
| string
| string
| string
| float
| float
| float
| float
| float
| float
| float
| float
| float
| float
| float
| float
| float
| float
| float
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| float
| float
| float
| float
| float
| float
| float
| float
| float
| float
| float
| float
| float
| float
| float
| float
| float
| float
| float
| float
| float
| float
| float
| float
| float
| float
| float
| float
| float
| float
| float
| float
| float
| float
| float
| float
| float
| float
| float
| float
| float
| float
| float
| float
| float
| float
| float
| float
| float
| float
| float
| float
| float
| float
| float
| float
| float
| float
| float
| float
| float
| float
| float
| float
| float
| float
| float
| float
| float
| float
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| float
| Measurement Type: | nominal | nominal | nominal | nominal | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | ratio | Measurement Values Domain: | | Allowed Values and DefinitionsEnumerated Domain | | Code Definition | Code | Ceu | Definition | Phacidium lacerum | Source | |
| Code Definition | Code | Control | Definition | Control (no fungal inoculum) | Source | |
| Code Definition | Code | Csp | Definition | Cylindrium elongatum | Source | |
| Code Definition | Code | Hm_ANA | Definition | Hypocrea minutispora (non-sporulating) | Source | |
| Code Definition | Code | Hm_TEL | Definition | Hypocrea minutispora (sporulating) | Source | |
| Code Definition | Code | Mm | Definition | Mucor mucedo | Source | |
| Code Definition | Code | Mr | Definition | Mucor abundans | Source | |
| Code Definition | Code | Ps | Definition | Panellus stipticus | Source | |
| Code Definition | Code | Rt | Definition | Gymnopus sp. | Source | |
| Code Definition | Code | Tk | Definition | Trichoderma koningii | Source | |
|
|
| Allowed Values and DefinitionsEnumerated Domain | | Code Definition | Code | Ascomycota | Definition | Fungal phylum (name) | Source | |
| Code Definition | Code | Basidiomycota | Definition | Fungal phylum (name) | Source | |
| Code Definition | Code | Control | Definition | Control (no fungal inoculum) | Source | |
| Code Definition | Code | Mucoromycotina | Definition | Fungal phylum (name) | Source | |
|
|
| Allowed Values and DefinitionsEnumerated Domain | | Code Definition | Code | 330 | Definition | Pyrolysis thermal fraction; combustion temperature 330C | Source | |
| Code Definition | Code | 396 | Definition | Pyrolysis thermal fraction; combustion temperature 396C | Source | |
| Code Definition | Code | 444 | Definition | Pyrolysis thermal fraction; combustion temperature 444C | Source | |
| Code Definition | Code | 503 | Definition | Pyrolysis thermal fraction; combustion temperature 503C | Source | |
| Code Definition | Code | 600 | Definition | Pyrolysis thermal fraction; combustion temperature 600C | Source | |
| Code Definition | Code | 735 | Definition | Pyrolysis thermal fraction; combustion temperature 735C | Source | |
|
|
| | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | Missing Value Code: | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | Accuracy Report: | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | Accuracy Assessment: | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | Coverage: | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | Methods: | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | |
|
Data Table | Data: | https://pasta-s.lternet.edu/package/data/eml/edi/1644/1/0d361415bfdfe662d3f605b3f128a4fc | Name: | Whalen_sequential_extraction_data | Description: | Total organic carbon concentrations and total dissolved nitrogen concentrations in water, KCl and sodium pyrophosphate extracts. Soils with SOM formed by different fungal isolates were subjected to a sequential extraction with water first, then KCl and finally sodium pyrophosphate. | Number of Records: | 112 | Number of Columns: | 6 |
| Table Structure |
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Object Name: | Whalen_sequential_extraction_data.csv | Size: | 6729 byte | Authentication: | f0f8df54d1d032ddee65a065b10005b3
Calculated By MD5 | Text Format: |
Number of Header Lines: | 1 |
Record Delimiter: | \r\n |
Orientation: | column |
Simple Delimited: |
Field Delimiter: | , |
Quote Character: | " |
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Table Column Descriptions |
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| | | SampleID | Extract | Species | Phylum | TOC_mg_L | TDN |
---|
Column Name: | SampleID
| Extract
| Species
| Phylum
| TOC_mg_L
| TDN
| Definition: | Unique sample identifier | Extractant type (water, KCl or sodium pyrophosphate) | Species label/abbreviation | Fungal phyla (names) | Total organic carbon in extract | Total dissolved nitrogen in extract | Storage Type: | string
| string
| string
| string
| float
| float
| Measurement Type: | nominal | nominal | nominal | nominal | ratio | ratio | Measurement Values Domain: | | Allowed Values and DefinitionsEnumerated Domain | | Code Definition | Code | KCl | Definition | Extractant, sodium chloride | Source | |
| Code Definition | Code | Sodium pyrophosphate | Definition | Extractant | Source | |
| Code Definition | Code | water | Definition | Extractant | Source | |
|
|
| Allowed Values and DefinitionsEnumerated Domain | | Code Definition | Code | Ceu | Definition | Phacidium lacerum | Source | |
| Code Definition | Code | Control | Definition | Control sample (no fungal inoculum; model soil and substrate only) | Source | |
| Code Definition | Code | Csp | Definition | Cylindrium elongatum | Source | |
| Code Definition | Code | Hm_anamorph | Definition | Hypocrea minutispora (non-sporulating) | Source | |
| Code Definition | Code | Hm_teleomorph | Definition | Hypocrea minutispora (sporulating) | Source | |
| Code Definition | Code | Mm | Definition | Mucor mucedo | Source | |
| Code Definition | Code | Mr | Definition | Mucor abundans | Source | |
| Code Definition | Code | Ps | Definition | Panellus stipticus | Source | |
| Code Definition | Code | Rt | Definition | Gymnopus sp. | Source | |
| Code Definition | Code | Tk | Definition | Trichoderma koningii | Source | |
|
|
| Allowed Values and DefinitionsEnumerated Domain | | Code Definition | Code | Ascomycota | Definition | Fungal phylum | Source | |
| Code Definition | Code | Basidiomycota | Definition | Fungal phylum | Source | |
| Code Definition | Code | Control | Definition | Control samples (no fungal inoculum; model soil and substrate only) | Source | |
| Code Definition | Code | Mucoromycotina | Definition | Fungal phylum | Source | |
|
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| | | Missing Value Code: | | | | | | | Accuracy Report: | | | | | | | Accuracy Assessment: | | | | | | | Coverage: | | | | | | | Methods: | | | | | | |
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