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Grid DAP Data | Sub- set | Table DAP Data | Make A Graph | W M S | Source Data Files | Acces- sible | Title | Sum- mary | FGDC, ISO, Metadata | Back- ground Info | RSS | E | Institution | Dataset ID |
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data | graph | files | public | [H. longicornis Population Structure] - Haloptilus longicornis population structure (Atlantic Ocean) - Microsatellite data. (Basin-scale genetics of marine zooplankton) | I M | background | BCO-DMO | bcodmo_dataset_699458 |
Row Type | Variable Name | Attribute Name | Data Type | Value |
---|---|---|---|---|
attribute | NC_GLOBAL | access_formats | String | .htmlTable,.csv,.json,.mat,.nc,.tsv |
attribute | NC_GLOBAL | acquisition_description | String | Refer to the following publication for complete methodology details: Goetze, E.,\u00a0Andrews, K., Peijnenburg, K. T. C. A., Portner, E., Norton, E. L. (2015) Temporal Stability of Genetic Structure in a Mesopelagic Copepod.\u00a0\u00a0PLoS One\u00a010(8): e0136087.\u00a0[doi:10.1371/journal.pone.0136087](\\"http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0136087\\") In summary (excerpted from above): For\u00a0H.\u00a0longicornis species 1, deviations from Hardy-Weinberg equilibrium (HWE) and linkage disequilibrium were examined using ARLEQUIN v3.5.1.3 and GENEPOP v4.2 for all microsatellite loci [36\u201338]. We tested for the presence of null alleles in microsatellite data using MICROCHECKER v2.2.3 [39], and estimated null allele frequencies and calculated population pairwise\u00a0FST\u00a0values with correction for null alleles in FreeNA [40]. Microsatellite genetic diversity indices of observed and expected heterozygosity, average alleles per locus, and allele richness were calculated in GENETIX v4.05 and FSTAT [35,41]. Pairwise\u00a0FST\u00a0values were calculated among all sample sites using both microsatellite and mtCOII data, as a measure of population subdivision across samples (ARLEQUIN v3.5.1.3, [38]). Significance was assessed following correction for multiple comparisons using the false discovery rate (FDR, [42,43]). Pairwise \u03a6ST\u00a0values also were calculated for the mtCOII data. We identified the nucleotide substitution model that best fit our mtCOII data using the Akaike Information Criterion, as implemented in jModelTest v2.1.4 [44], and the K81 or three- parameter model was selected as the best model (TPM3uf+G). The Tamura and Nei substitution model, which was the closest available model in Arlequin, was used to calculate pairwise and global \u03a6ST\u00a0values, and to estimate genetic diversity at each site. Hierarchical Analyses of Molecular Variance (AMOVA) based on\u00a0FST\u00a0were carried out to partition the genetic variance across both space (ocean gyres) and time (sampling years), for both marker types. In these analyses, we tested for population structure under the following groupings: with samples stratified by (1) northern and southern subtropical gyres (2 gyres), and (2) across two sampling years (2010, 2012). Global\u00a0FST\u00a0values were estimated using non-hierarchical AMOVAs among all samples, as well as among subsets of the data across ocean gyres and sampling years. Significance was tested with 10,000 permutations of genotypes or haplotypes among populations. Principal coordinate analysis (PCA) plots of linearized pairwise\u00a0FST\u00a0values based on both mtCOII and microsatellite data were used to visualize spatial and temporal genetic differentiation among samples. Population structure was further examined using a Bayesian clustering method implemented in STRUCTURE [45,46] for microsatellite loci. We used admixture and correlated allele frequency models, with a burn-in of 105\u00a0steps followed by 106\u00a0steps, with and without using sampling location as a prior. We ran these analyses for each of the 2010 and 2012 datasets using\u00a0K\u00a0= 1 to\u00a0K\u00a0= 10, and for the dataset of combined years using\u00a0K\u00a0= 1 to\u00a0K\u00a0= 20. We ran three separate replicates for each K to investigate consistency of Pr(X|K). The true\u00a0K\u00a0was evaluated by visual inspection of barplots and comparing Pr(X|K) across\u00a0K\u00a0values. |
attribute | NC_GLOBAL | awards_0_award_nid | String | 537990 |
attribute | NC_GLOBAL | awards_0_award_number | String | OCE-1338959 |
attribute | NC_GLOBAL | awards_0_data_url | String | http://www.nsf.gov/awardsearch/showAward.do?AwardNumber=1338959 |
attribute | NC_GLOBAL | awards_0_funder_name | String | NSF Division of Ocean Sciences |
attribute | NC_GLOBAL | awards_0_funding_acronym | String | NSF OCE |
attribute | NC_GLOBAL | awards_0_funding_source_nid | String | 355 |
attribute | NC_GLOBAL | awards_0_program_manager | String | David L. Garrison |
attribute | NC_GLOBAL | awards_0_program_manager_nid | String | 50534 |
attribute | NC_GLOBAL | awards_1_award_nid | String | 539716 |
attribute | NC_GLOBAL | awards_1_award_number | String | OCE-1029478 |
attribute | NC_GLOBAL | awards_1_data_url | String | http://www.nsf.gov/awardsearch/showAward.do?AwardNumber=1029478 |
attribute | NC_GLOBAL | awards_1_funder_name | String | NSF Division of Ocean Sciences |
attribute | NC_GLOBAL | awards_1_funding_acronym | String | NSF OCE |
attribute | NC_GLOBAL | awards_1_funding_source_nid | String | 355 |
attribute | NC_GLOBAL | awards_1_program_manager | String | David L. Garrison |
attribute | NC_GLOBAL | awards_1_program_manager_nid | String | 50534 |
attribute | NC_GLOBAL | cdm_data_type | String | Other |
attribute | NC_GLOBAL | comment | String | Haloptilus longicorns population structure Erica Goetze, PI Version 20 March 2017 |
attribute | NC_GLOBAL | Conventions | String | COARDS, CF-1.6, ACDD-1.3 |
attribute | NC_GLOBAL | creator_email | String | info at bco-dmo.org |
attribute | NC_GLOBAL | creator_name | String | BCO-DMO |
attribute | NC_GLOBAL | creator_type | String | institution |
attribute | NC_GLOBAL | creator_url | String | https://www.bco-dmo.org/ |
attribute | NC_GLOBAL | data_source | String | extract_data_as_tsv version 2.3 19 Dec 2019 |
attribute | NC_GLOBAL | date_created | String | 2017-05-04T17:20:16Z |
attribute | NC_GLOBAL | date_modified | String | 2019-03-28T19:36:57Z |
attribute | NC_GLOBAL | defaultDataQuery | String | &time<now |
attribute | NC_GLOBAL | doi | String | 10.1575/1912/bco-dmo.699458.1 |
attribute | NC_GLOBAL | infoUrl | String | https://www.bco-dmo.org/dataset/699458 |
attribute | NC_GLOBAL | institution | String | BCO-DMO |
attribute | NC_GLOBAL | instruments_0_acronym | String | Thermal Cycler |
attribute | NC_GLOBAL | instruments_0_dataset_instrument_description | String | PCR products were genotyped |
attribute | NC_GLOBAL | instruments_0_dataset_instrument_nid | String | 699475 |
attribute | NC_GLOBAL | instruments_0_description | String | General term for a laboratory apparatus commonly used for performing polymerase chain reaction (PCR). The device has a thermal block with holes where tubes with the PCR reaction mixtures can be inserted. The cycler then raises and lowers the temperature of the block in discrete, pre-programmed steps. (adapted from http://serc.carleton.edu/microbelife/research_methods/genomics/pcr.html) |
attribute | NC_GLOBAL | instruments_0_instrument_name | String | PCR Thermal Cycler |
attribute | NC_GLOBAL | instruments_0_instrument_nid | String | 471582 |
attribute | NC_GLOBAL | instruments_0_supplied_name | String | ABI3730 Genetic Analyzer |
attribute | NC_GLOBAL | keywords | String | bco, bco-dmo, biological, chemical, data, dataset, diploid, diploidGenotype1_HALOM264, diploidGenotype1_HALOMS175, diploidGenotype1_HALOMS27, diploidGenotype1_HALOMS32, diploidGenotype1_HALOMS86, diploidGenotype1_HALOMS91, diploidGenotype1_HALOMX66, diploidGenotype2_HALOM264, diploidGenotype2_HALOMS175, diploidGenotype2_HALOMS27, diploidGenotype2_HALOMS32, diploidGenotype2_HALOMS86, diploidGenotype2_HALOMS91, diploidGenotype2_HALOMX66, dmo, erddap, genotype1, genotype2, halom264, haloms175, haloms27, haloms32, haloms86, haloms91, halomx66, management, oceanography, office, preliminary, sample, sample_id, station |
attribute | NC_GLOBAL | license | String | https://www.bco-dmo.org/dataset/699458/license |
attribute | NC_GLOBAL | metadata_source | String | https://www.bco-dmo.org/api/dataset/699458 |
attribute | NC_GLOBAL | param_mapping | String | {'699458': {}} |
attribute | NC_GLOBAL | parameter_source | String | https://www.bco-dmo.org/mapserver/dataset/699458/parameters |
attribute | NC_GLOBAL | people_0_affiliation | String | University of Hawaii at Manoa |
attribute | NC_GLOBAL | people_0_affiliation_acronym | String | SOEST |
attribute | NC_GLOBAL | people_0_person_name | String | Erica Goetze |
attribute | NC_GLOBAL | people_0_person_nid | String | 473048 |
attribute | NC_GLOBAL | people_0_role | String | Principal Investigator |
attribute | NC_GLOBAL | people_0_role_type | String | originator |
attribute | NC_GLOBAL | people_1_affiliation | String | Woods Hole Oceanographic Institution |
attribute | NC_GLOBAL | people_1_affiliation_acronym | String | WHOI BCO-DMO |
attribute | NC_GLOBAL | people_1_person_name | String | Hannah Ake |
attribute | NC_GLOBAL | people_1_person_nid | String | 650173 |
attribute | NC_GLOBAL | people_1_role | String | BCO-DMO Data Manager |
attribute | NC_GLOBAL | people_1_role_type | String | related |
attribute | NC_GLOBAL | project | String | Plankton Population Genetics,Plankton_PopStructure |
attribute | NC_GLOBAL | projects_0_acronym | String | Plankton Population Genetics |
attribute | NC_GLOBAL | projects_0_description | String | Description from NSF award abstract: Marine zooplankton show strong ecological responses to climate change, but little is known about their capacity for evolutionary response. Many authors have assumed that the evolutionary potential of zooplankton is limited. However, recent studies provide circumstantial evidence for the idea that selection is a dominant evolutionary force acting on these species, and that genetic isolation can be achieved at regional spatial scales in pelagic habitats. This RAPID project will take advantage of a unique opportunity for basin-scale transect sampling through participation in the Atlantic Meridional Transect (AMT) cruise in 2014. The cruise will traverse more than 90 degrees of latitude in the Atlantic Ocean and include boreal-temperate, subtropical and tropical waters. Zooplankton samples will be collected along the transect, and mitochondrial and microsatellite markers will be used to identify the geographic location of strong genetic breaks within three copepod species. Bayesian and coalescent analytical techniques will test if these regions act as dispersal barriers. The physiological condition of animals collected in distinct ocean habitats will be assessed by measurements of egg production (at sea) as well as body size (condition index), dry weight, and carbon and nitrogen content. The PI will test the prediction that ocean regions that serve as dispersal barriers for marine holoplankton are areas of poor-quality habitat for the target species, and that this is a dominant mechanism driving population genetic structure in oceanic zooplankton. Note: This project is funded by an NSF RAPID award. This RAPID grant supported the shiptime costs, and all the sampling reported in the AMT24 zooplankton ecology cruise report (PDF). Online science outreach blog at: https://atlanticplankton.wordpress.com |
attribute | NC_GLOBAL | projects_0_end_date | String | 2015-11 |
attribute | NC_GLOBAL | projects_0_geolocation | String | Atlantic Ocean, 46 N - 46 S |
attribute | NC_GLOBAL | projects_0_name | String | Basin-scale genetics of marine zooplankton |
attribute | NC_GLOBAL | projects_0_project_nid | String | 537991 |
attribute | NC_GLOBAL | projects_0_start_date | String | 2013-12 |
attribute | NC_GLOBAL | projects_1_acronym | String | Plankton_PopStructure |
attribute | NC_GLOBAL | projects_1_description | String | Description from NSF award abstract: This research will test whether habitat depth specialization is a primary trait driving large-scale population genetic structure in open ocean zooplankton species. Very little is known about population connectivity in marine zooplankton. Although zooplankton were long thought to be high-gene-flow systems with little genetic differentiation among populations, recent observations have challenged this view. In fact, zooplankton species may be genetically subdivided at macrogeographic, regional, or even smaller spatial scales. Recent studies also indicate that subtle, species-specific ecological factors play an important role in controlling gene flow among plankton populations. The investigator hypothesizes that depth-related habitat, including diel vertical migration (DVM) behavior, plays a critical role in controlling dispersal of plankton among ocean regions, through interactions with ocean circulation and bathymetry. This study will compare the population genetic structures of eight planktonic copepods that utilize different depth-related habitats, in order to test key predictions of genetic structure based on the interaction of organismal depth with the oceanographic environment. The objectives of the research are to: 1) Develop novel nuclear markers that can be used to resolve genetic structure and estimate gene flow among copepod populations, 2) Characterize the spatial patterns of gene flow among populations in distinct ocean regions of the Atlantic, Pacific, and Indian Oceans for eight target species using a multilocus approach, and 3) Test the central hypothesis that depth-related habitat will significantly impact the extent of genetic structure both across and within ocean basins, the magnitude and direction of gene flow among populations, and in the timing of major slitting events within species. Drawing on genomic resources (cDNA libraries) recently developed by the PI, five (or more) polymorphic nuclear markers will be developed for each species. These new markers will be used, in combination with the mitochondrial gene cytochrome oxidase I, to characterize the population genetic structure of each species throughout its global distribution using graph theoretic and coalescent analytical techniques. Gene flow among populations and the timing of major splitting events will be estimated under a coalescent model (IMa), and empirical support for the hypothesis of depth-related trends in population structure will be assessed using graph theoretic congruence tests. Because the depth specialization and diel vertical migration behaviors of the target species are representative of distinct zooplankton species groups, the results of this study will have broad implications for understanding and predicting the genetic structure of these important grazers in pelagic ecosystems. Publications produced with support from this award include: Burridge, A., Goetze, E., Raes, N., Huisman, J., Peijnenburg, K. T. C. A. (in revision) Global biogeography and evolution of Cuvierina pteropods. BMC Evolutionary Biology. Andrews, K. R., Norton, E. L., Fernandez-Silva, I., Portner†, E. Goetze, E. (in press) Multilocus evidence for globally-distributed cryptic species and distinct populations across ocean gyres in a mesopelagic copepod. Molecular Ecology. Halbert , K. M. K., Goetze, E., Carlon, D. B. (2013) High cryptic diversity across the global range of the migratory planktonic copepods Pleuromamma piseki and P. gracilis. PLOS One 8(10): e77011. doi:10.1371/journal.pone.0077011 Norton , E. L., Goetze, E. (2013) Equatorial dispersal barriers and limited connectivity among oceans in a planktonic copepod. Limnology and Oceanography 58: 1581-1596. Peijnenburg, K. T. C. A., Goetze, E. (2013) High evolutionary potential of marine zooplankton. Ecology & Evolution 3(8): 2765-2781. doi: 10.1002/ece3.644 (both authors contributed equally). Fernandez-Silva, I., Whitney, J., Wainwright, B., Andrews, K. R., Ylitalo-Ward, H., Bowen, B. W., Toonen, R. J., Goetze, E., Karl, S. A. (2013) Microsatellites for Next-Generation Ecologists: A Post-Sequencing Bioinformatics Pipeline. PLOS One 8(2): e55990. doi:10.1371/journal.pone.0055990 Bron, J. E., Frisch, D., Goetze, E., Johnson, S. C., Lee, C. E., Wyngaard, G. A. (2011) Observing Copepods through a Genomic Lens. Frontiers in Zoology 8: 22. Goetze, E. (2011) Population differentiation in the open sea: Insights from the pelagic copepod Pleuromamma xiphias. Integrative and Comparative Biology 51: 580-597. Master’s theses supported under this award include: Emily L. Norton. Empirical and biophysical modeling studies of dispersal barriers for marine plankton. (2013). University of Hawaii at Manoa. K. M. K. Halbert. Genetic isolation in the open sea: Cryptic diversity in the Pleuromamma piseki - P. gracilis species complex. (2013). University of Hawaii at Manoa. |
attribute | NC_GLOBAL | projects_1_end_date | String | 2014-07 |
attribute | NC_GLOBAL | projects_1_geolocation | String | Global Ocean |
attribute | NC_GLOBAL | projects_1_name | String | Does habitat specialization drive population genetic structure of oceanic zooplankton? |
attribute | NC_GLOBAL | projects_1_project_nid | String | 539717 |
attribute | NC_GLOBAL | projects_1_start_date | String | 2010-08 |
attribute | NC_GLOBAL | publisher_name | String | Biological and Chemical Oceanographic Data Management Office (BCO-DMO) |
attribute | NC_GLOBAL | publisher_type | String | institution |
attribute | NC_GLOBAL | sourceUrl | String | (local files) |
attribute | NC_GLOBAL | standard_name_vocabulary | String | CF Standard Name Table v55 |
attribute | NC_GLOBAL | summary | String | Haloptilus longicornis population structure (Atlantic Ocean) - Microsatellite data. |
attribute | NC_GLOBAL | title | String | [H. longicornis Population Structure] - Haloptilus longicornis population structure (Atlantic Ocean) - Microsatellite data. (Basin-scale genetics of marine zooplankton) |
attribute | NC_GLOBAL | version | String | 1 |
attribute | NC_GLOBAL | xml_source | String | osprey2erddap.update_xml() v1.3 |
variable | station | String | ||
attribute | station | bcodmo_name | String | station |
attribute | station | description | String | Station number where sampling occurred |
attribute | station | long_name | String | Station |
attribute | station | units | String | unitless |
variable | sample_id | String | ||
attribute | sample_id | bcodmo_name | String | sample |
attribute | sample_id | description | String | PI issued sample ID number |
attribute | sample_id | long_name | String | Sample Id |
attribute | sample_id | nerc_identifier | String | https://vocab.nerc.ac.uk/collection/P02/current/ACYC/ |
attribute | sample_id | units | String | unitless |
variable | diploidGenotype1_HALOMS175 | byte | ||
attribute | diploidGenotype1_HALOMS175 | _FillValue | byte | 127 |
attribute | diploidGenotype1_HALOMS175 | actual_range | byte | 93, 113 |
attribute | diploidGenotype1_HALOMS175 | bcodmo_name | String | count |
attribute | diploidGenotype1_HALOMS175 | description | String | Diploid genotypes reported for each locus and individual |
attribute | diploidGenotype1_HALOMS175 | long_name | String | Diploid Genotype1 HALOMS175 |
attribute | diploidGenotype1_HALOMS175 | units | String | count |
variable | diploidGenotype2_HALOMS175 | byte | ||
attribute | diploidGenotype2_HALOMS175 | _FillValue | byte | 127 |
attribute | diploidGenotype2_HALOMS175 | actual_range | byte | 93, 119 |
attribute | diploidGenotype2_HALOMS175 | bcodmo_name | String | count |
attribute | diploidGenotype2_HALOMS175 | description | String | Diploid genotypes reported for each locus and individual |
attribute | diploidGenotype2_HALOMS175 | long_name | String | Diploid Genotype2 HALOMS175 |
attribute | diploidGenotype2_HALOMS175 | units | String | count |
variable | diploidGenotype1_HALOMS27 | short | ||
attribute | diploidGenotype1_HALOMS27 | _FillValue | short | 32767 |
attribute | diploidGenotype1_HALOMS27 | actual_range | short | 214, 258 |
attribute | diploidGenotype1_HALOMS27 | bcodmo_name | String | count |
attribute | diploidGenotype1_HALOMS27 | description | String | Diploid genotypes reported for each locus and individual |
attribute | diploidGenotype1_HALOMS27 | long_name | String | Diploid Genotype1 HALOMS27 |
attribute | diploidGenotype1_HALOMS27 | units | String | count |
variable | diploidGenotype2_HALOMS27 | short | ||
attribute | diploidGenotype2_HALOMS27 | _FillValue | short | 32767 |
attribute | diploidGenotype2_HALOMS27 | actual_range | short | 220, 258 |
attribute | diploidGenotype2_HALOMS27 | bcodmo_name | String | count |
attribute | diploidGenotype2_HALOMS27 | description | String | Diploid genotypes reported for each locus and individual |
attribute | diploidGenotype2_HALOMS27 | long_name | String | Diploid Genotype2 HALOMS27 |
attribute | diploidGenotype2_HALOMS27 | units | String | count |
variable | diploidGenotype1_HALOMS32 | short | ||
attribute | diploidGenotype1_HALOMS32 | _FillValue | short | 32767 |
attribute | diploidGenotype1_HALOMS32 | actual_range | short | 126, 150 |
attribute | diploidGenotype1_HALOMS32 | bcodmo_name | String | count |
attribute | diploidGenotype1_HALOMS32 | description | String | Diploid genotypes reported for each locus and individual |
attribute | diploidGenotype1_HALOMS32 | long_name | String | Diploid Genotype1 HALOMS32 |
attribute | diploidGenotype1_HALOMS32 | units | String | count |
variable | diploidGenotype2_HALOMS32 | short | ||
attribute | diploidGenotype2_HALOMS32 | _FillValue | short | 32767 |
attribute | diploidGenotype2_HALOMS32 | actual_range | short | 126, 159 |
attribute | diploidGenotype2_HALOMS32 | bcodmo_name | String | count |
attribute | diploidGenotype2_HALOMS32 | description | String | Diploid genotypes reported for each locus and individual |
attribute | diploidGenotype2_HALOMS32 | long_name | String | Diploid Genotype2 HALOMS32 |
attribute | diploidGenotype2_HALOMS32 | units | String | count |
variable | diploidGenotype1_HALOMS86 | short | ||
attribute | diploidGenotype1_HALOMS86 | _FillValue | short | 32767 |
attribute | diploidGenotype1_HALOMS86 | actual_range | short | 136, 181 |
attribute | diploidGenotype1_HALOMS86 | bcodmo_name | String | count |
attribute | diploidGenotype1_HALOMS86 | description | String | Diploid genotypes reported for each locus and individual |
attribute | diploidGenotype1_HALOMS86 | long_name | String | Diploid Genotype1 HALOMS86 |
attribute | diploidGenotype1_HALOMS86 | units | String | count |
variable | diploidGenotype2_HALOMS86 | short | ||
attribute | diploidGenotype2_HALOMS86 | _FillValue | short | 32767 |
attribute | diploidGenotype2_HALOMS86 | actual_range | short | 136, 181 |
attribute | diploidGenotype2_HALOMS86 | bcodmo_name | String | count |
attribute | diploidGenotype2_HALOMS86 | description | String | Diploid genotypes reported for each locus and individual |
attribute | diploidGenotype2_HALOMS86 | long_name | String | Diploid Genotype2 HALOMS86 |
attribute | diploidGenotype2_HALOMS86 | units | String | count |
variable | diploidGenotype1_HALOM264 | short | ||
attribute | diploidGenotype1_HALOM264 | _FillValue | short | 32767 |
attribute | diploidGenotype1_HALOM264 | actual_range | short | 151, 172 |
attribute | diploidGenotype1_HALOM264 | bcodmo_name | String | count |
attribute | diploidGenotype1_HALOM264 | description | String | Diploid genotypes reported for each locus and individual |
attribute | diploidGenotype1_HALOM264 | long_name | String | Diploid Genotype1 HALOM264 |
attribute | diploidGenotype1_HALOM264 | units | String | count |
variable | diploidGenotype2_HALOM264 | short | ||
attribute | diploidGenotype2_HALOM264 | _FillValue | short | 32767 |
attribute | diploidGenotype2_HALOM264 | actual_range | short | 163, 177 |
attribute | diploidGenotype2_HALOM264 | bcodmo_name | String | count |
attribute | diploidGenotype2_HALOM264 | description | String | Diploid genotypes reported for each locus and individual |
attribute | diploidGenotype2_HALOM264 | long_name | String | Diploid Genotype2 HALOM264 |
attribute | diploidGenotype2_HALOM264 | units | String | count |
variable | diploidGenotype1_HALOMS91 | short | ||
attribute | diploidGenotype1_HALOMS91 | _FillValue | short | 32767 |
attribute | diploidGenotype1_HALOMS91 | actual_range | short | 190, 212 |
attribute | diploidGenotype1_HALOMS91 | bcodmo_name | String | count |
attribute | diploidGenotype1_HALOMS91 | description | String | Diploid genotypes reported for each locus and individual |
attribute | diploidGenotype1_HALOMS91 | long_name | String | Diploid Genotype1 HALOMS91 |
attribute | diploidGenotype1_HALOMS91 | units | String | count |
variable | diploidGenotype2_HALOMS91 | short | ||
attribute | diploidGenotype2_HALOMS91 | _FillValue | short | 32767 |
attribute | diploidGenotype2_HALOMS91 | actual_range | short | 194, 218 |
attribute | diploidGenotype2_HALOMS91 | bcodmo_name | String | count |
attribute | diploidGenotype2_HALOMS91 | description | String | Diploid genotypes reported for each locus and individual |
attribute | diploidGenotype2_HALOMS91 | long_name | String | Diploid Genotype2 HALOMS91 |
attribute | diploidGenotype2_HALOMS91 | units | String | count |
variable | diploidGenotype1_HALOMX66 | short | ||
attribute | diploidGenotype1_HALOMX66 | _FillValue | short | 32767 |
attribute | diploidGenotype1_HALOMX66 | actual_range | short | 178, 193 |
attribute | diploidGenotype1_HALOMX66 | bcodmo_name | String | count |
attribute | diploidGenotype1_HALOMX66 | description | String | Diploid genotypes reported for each locus and individual |
attribute | diploidGenotype1_HALOMX66 | long_name | String | Diploid Genotype1 HALOMX66 |
attribute | diploidGenotype1_HALOMX66 | units | String | count |
variable | diploidGenotype2_HALOMX66 | short | ||
attribute | diploidGenotype2_HALOMX66 | _FillValue | short | 32767 |
attribute | diploidGenotype2_HALOMX66 | actual_range | short | 181, 196 |
attribute | diploidGenotype2_HALOMX66 | bcodmo_name | String | count |
attribute | diploidGenotype2_HALOMX66 | description | String | Diploid genotypes reported for each locus and individual |
attribute | diploidGenotype2_HALOMX66 | long_name | String | Diploid Genotype2 HALOMX66 |
attribute | diploidGenotype2_HALOMX66 | units | String | count |
The information in the table above is also available in other file formats (.csv, .htmlTable, .itx, .json, .jsonlCSV1, .jsonlCSV, .jsonlKVP, .mat, .nc, .nccsv, .tsv, .xhtml) via a RESTful web service.