This tutorial provides best-practice principles when standardising traits with terms of the Ecological Trait-data Standard (ETS, https://terminologies.gfbio.org/terms/ets/pages/).
We focus this document on the first of the three use-cases for the ETS vocabulary: The publication of project-specific primary data. To comply with the FAIR principles of scientific data management and aim at findability, accessibility, interoperability and reusability (Wilkinson et al. 2016), trait data should apply the following principles when preparing data for publication:
Label your dataset! data should be published with appropriate metadata and provide a descriptive title and keywords to be findable by search engines. Keywords should include the general label “trait-data”, and more specific labels such as “functional traits” or “morphometric traits”, as well as the taxa covered by the dataset.
State terms of use! To enable re-use, the metadata must contain the name of the author or owner of the data, the suggested citation for the data, as well as the license model or terms of use of the data. Recommended are copyright wavers and licenses that permit re-use without seeking authorization from the rights holder, such as Creative Commons (CC) licenses, which also can warrant attribution and citation (CC by) (Kissling et al. 2018). Ideally, these statements are provided by the data-hoster in a machine-readable way, by using standardised fields of metadata or hyperlink references.
Use independent file formats! For reasons of long-term accessibility, data should not be uploaded in proprietary spreadsheet formats but rather in software-independent file formats (like .xlsx or .odt), or comma- or tab-separated text files (‘.csv’ or ‘.tsv’) that are compatible with all computing platforms and internationalisation settings by applying a unified character encoding (e.g., UTF-8 or ASCII). For internationalisation, use points as decimal delimiters and set date-formats to ISO 8601, i.e., “YYYY-MM-DD”.
Use standard terms! Draw column or field names from the ETS vocabulary wherever possible. If co-variates or any ancillary data are not covered by the vocabulary, apply terms of the Darwin Core Standard (DwC).
Use URI references! Wherever possible, the concepts used to describe the dataset should be referenced to globally accessible Uniform Resource Identifiers (URIs). These references allow data users and software tools to relate the dataset to well-defined concepts of taxa or traits, or measurement units, etc. The ETS-terms ‘traitID’ and ‘taxonID’ are defined to label fields with URIs as values.
Provide definitions! Metadata must reference the data standards, taxonomic concepts and trait ontologies applied in the dataset as well as any user-defined terms and trait concepts. To provide own trait-concepts, use the terms provided within the ETS section “Terms for traitlists”.
Publish raw data! When publishing trait-data, priority is on containing measurement values while minimizing the risk of purporting errors through data conversion or aggregation. Thus, data should be published as they have been recorded, i.e., in original units and raw values, along with standardised values that match a unified and compatible scheme of a data standard. This is true for the core terms, i.e., the trait value and the item of observation and its taxon assignment, but also for any co-variates reported along with it.
Keep original values! For the core terms, data providers should provide standardised values conforming to consensus terms of the own research field. The ETS provides terms for maintaining user-defined entries (such as project specific taxon abbreviations) along with the standard terms (using the ‘verbatim*’ duplicates of the terms). For co-variates, the extensions of the vocabulary provide column names for standardised values only, e.g., elevation above sea-level. These should adhere to accepted standards wherever possible. If any conversion was applied to obtain these data, users should keep the original values in user-defined columns, e.g., by appending ‘verbatim*’ to the column name. Also, additional co-variates, e.g., on environmental growth conditions of the specimen, should be provided in user-defined columns. Any user-defined columns must be adequately defined in the accompanying meta-information.
Report Uncertainty! If publishing aggregate data (e.g., averages for multiple measurements), report the \(n\) and dispersion of the aggregate value. This allows to weigh data from multiple sources when producing compilations. Any sources of bias or noise should be reported along with the data (e.g., observer ID, conditions of measurement etc.). Use terms of the ETS extension “Measurement or Fact”.
Use Identifiers! Well-defined identifiers (‘IDs’) are key elements to structure the datasets and relate them to complementing datasets, if necessary (Fig. 2 c & d). For instance, for occurrence level data where multiple trait measurements are reported for each individual specimen, the same user-defined entry for ‘occurrenceID’ would link several measurements across the rows of the dataset. Similarly, multivariate measurements, for instance gas chromatography data or x-y-z data of morphometric coordinates could be linked via a ‘measurementID’. In literature data, summarised traits are usually given at the taxon level instead of the individual organism (e.g., reported as means or factorials) and a ‘taxonID’ is the key identifier. In larger compilations, a ‘datasetID’ allow to trace data origin to the primary source and keep track of authorship and original reference. Beyond being just of structural use for the dataset, identifiers are capable of linking own data to consensus taxonomy and trait terminology via URIs, which point to external terminology services.
If trait data have been collated at the species level from different literature sources or from expert knowledge, or as aggregated measurements collated from raw data, they usually are reported in a observation-level wide-table format, with a column of values for each trait recorded and a row for each species (or taxon) for which data were available. The wide-table format is widely used for the production of lookup-tables at the species level, which may either report qualitative facts (from literature or expert knowledge) or aggregated quantitative traits (averages or ranges of trait values for this taxon).
This wide-table format is straightforward for maintaining and managing new data for the data author. In terms of analysis, it allows to easily correlate traits with each other and analyse trade-offs between traits. However, wide-tables need to clearly differentiate missing data and traits not applicable to a given taxon (often filled in as ‘NA’ or dummy numbers, e.g., ‘999’). Additional information (e.g., on variation of means or literature source) may be stored in secondary columns or accompanying datasheets. When applying the data standard to wide-table data, the columns for taxa or individuals may be labelled using the terms of the ETS. Taxon concepts should be referenced to globally available concepts using URIs, e.g., by referring to GBIF Taxonomy. Taxa authors and fine-grained higher taxonomy must then be consistent with the linked concept, or may be omitted as redundant and to avoid confusion.
Remarks should be provided in a human-readable form within the table and provided with further detail in the metadata, if necessary.
For wide tables, it is essential that the multiple trait columns are labelled in unambiguous ways and be linked to trait concepts provided in the metadata or a secondary spreadsheet.
Order | Suborder | Family | SpeciesID | Author | Body_Size | Dispersal_ability | Feeding_guild | Remark |
---|---|---|---|---|---|---|---|---|
Araneae | Labidognatha | Anyphaenidae | Anyphaena accentuata | (Walckenaer, 1802) | 6.25 | 1.00 | c | |
Araneae | Labidognatha | Araneidae | Aculepeira ceropegia | Walckenaer, 1802 | 11.00 | 1.00 | c | |
Araneae | Labidognatha | Araneidae | Agalenatea redii | (Scopoli, 1763) | 6.93 | 0.50 | c | |
Araneae | Labidognatha | Araneidae | Araneus diadematus | Clerck, 1757 | 11.88 | 1.00 | c | |
Araneae | Labidognatha | Araneidae | Araneus marmoreus | Clerck, 1757 | 10.03 | 0.75 | c | |
Araneae | Labidognatha | Araneidae | Araneus quadratus | Clerck, 1757 | 12.25 | 1.00 | c | |
Araneae | Labidognatha | Araneidae | Araneus sturmi | (Hahn, 1831) | 4.63 | 0.75 | c |
|
Araneae | Labidognatha | Araneidae | Araneus triguttatus | Fabricius, 1775 | 5.25 | 0.50 | c |
|
Araneae | Labidognatha | Araneidae | Araniella alpica | (L. Koch, 1869) | 6.00 | 0.75 | c |
|
Araneae | Labidognatha | Araneidae | Araniella cucurbitina | (Clerck, 1757) | 5.50 | 1.00 | c | |
Araneae | Labidognatha | Araneidae | Araniella opisthographa | (Kulczynski, 1905) | 4.38 | 0.75 | c | |
Araneae | Labidognatha | Araneidae | Argiope bruennichi | (Scopoli, 1772) | 11.78 | 1.00 | c | |
Araneae | Labidognatha | Araneidae | Cercidia prominens | (Westring, 1851) | 5.38 | 0.50 | c | |
Araneae | Labidognatha | Araneidae | Cyclosa conica | (Pallas, 1772) | 5.75 | 0.75 | c | |
Araneae | Labidognatha | Araneidae | Cyclosa oculata | (Walckenaer, 1802) | 5.08 | 0.75 | c | |
Araneae | Labidognatha | Araneidae | Gibbaranea gibbosa | (Walckenaer, 1802) | 6.75 | 0.00 | c | |
Araneae | Labidognatha | Araneidae | Gibbaranea omoeda | (Thorell, 1870) | 9.13 | 0.50 | c |
|
Araneae | Labidognatha | Araneidae | Hypsosinga albovittata | (Westring, 1851) | 4.15 | 0.50 | c | |
Araneae | Labidognatha | Araneidae | Hypsosinga sanguinea | (C.L. Koch, 1844) | 3.75 | 0.75 | c | |
Araneae | Labidognatha | Araneidae | Larinioides cornutus | (Clerck, 1757) | 10.35 | 0.75 | c | |
Araneae | Labidognatha | Araneidae | Mangora acalypha | (Walckenaer, 1802) | 4.50 | 1.00 | c | |
Araneae | Labidognatha | Araneidae | Nuctenea umbratica | (Clerck, 1757) | 11.25 | 1.00 | c |
|
Araneae | Labidognatha | Araneidae | Singa hamata | (Clerck, 1757) | 5.90 | 0.75 | c | |
Araneae | Labidognatha | Clubionidae | Clubiona brevipes | Blackwall, 1841 | 5.50 | 0.50 | c |
|
Araneae | Labidognatha | Clubionidae | Clubiona diversa | O. P.-Cambridge, 1862 | 4.00 | 0.50 | c | |
Araneae | Labidognatha | Clubionidae | Clubiona leucaspis | Simon, 1932 | 4.05 | 0.50 | c |
|
Araneae | Labidognatha | Clubionidae | Clubiona neglecta | O. P.-Cambridge, 1862 | 6.25 | 0.75 | c | |
Araneae | Labidognatha | Clubionidae | Clubiona reclusa | O. P.-Cambridge, 1863 | 5.75 | 0.75 | c | |
Araneae | Labidognatha | Clubionidae | Clubiona stagnatilis | Kulczynski, 1897 | 6.25 | 0.50 | c | |
Araneae | Labidognatha | Dictynidae | Argenna subnigra | (O. P.-Cambridge, 1861) | 2.25 | 0.75 | c | |
Araneae | Labidognatha | Dictynidae | Dictyna pusilla | Thorell, 1856 | 2.45 | 0.50 | c | |
Araneae | Labidognatha | Dictynidae | Lathys humilis | (Blackwall, 1855) | 2.20 | 0.50 | c |
|
Araneae | Labidognatha | Dictynidae | Nigma flavescens | (Walckenaer, 1830) | 3.08 | 0.75 | c |
|
Araneae | Labidognatha | Gnaphosidae | Micaria pulicaria | (Sundevall, 1831) | 3.55 | 1.00 | c | |
Araneae | Labidognatha | Linyphiidae | Araeoncus humilis | (Blackwall, 1841) | 1.60 | 1.00 | c | |
Araneae | Labidognatha | Linyphiidae | Baryphyma pratense | (Blackwall, 1861) | 2.20 | 0.50 | c | |
Araneae | Labidognatha | Linyphiidae | Bathyphantes approximatus | (O. P.-Cambridge, 1871) | 2.63 | 0.50 | c | |
Araneae | Labidognatha | Linyphiidae | Bathyphantes gracilis | (Blackwall, 1841) | 1.98 | 1.00 | c | |
Araneae | Labidognatha | Linyphiidae | Bathyphantes parvulus | (Westring, 1851) | 2.15 | 0.75 | c | |
Araneae | Labidognatha | Linyphiidae | Centromerita bicolor | (Blackwall, 1833) | 3.25 | 1.00 | c | |
Araneae | Labidognatha | Linyphiidae | Centromerus sylvaticus | (Blackwall, 1841) | 3.43 | 1.00 | c | |
Araneae | Labidognatha | Linyphiidae | Ceratinella brevipes | (Westring, 1851) | 1.45 | 0.50 | c | |
Araneae | Labidognatha | Linyphiidae | Ceratinella scabrosa | (O. P.-Cambridge, 1871) | 1.88 | 0.50 | c |
|
Araneae | Labidognatha | Linyphiidae | Cinetata gradata | (Simon, 1881) | 1.45 | 0.50 | c |
|
Araneae | Labidognatha | Linyphiidae | Cnephalocotes obscurus | (Blackwall, 1834) | 1.73 | 0.75 | c |
scientificName | order | family | taxonID | Body_Size | Dispersal_ability | Feeding_guild | measurementRemarks |
---|---|---|---|---|---|---|---|
Anyphaena accentuata | Araneae | Anyphaenidae | http://www.gbif.org/species/2159474 | 6.25 | 1.00 | c | |
Aculepeira ceropegia | Araneae | Araneidae | http://www.gbif.org/species/2160943 | 11.00 | 1.00 | c | |
Agalenatea redii | Araneae | Araneidae | http://www.gbif.org/species/2154595 | 6.93 | 0.50 | c | |
Araneus diadematus | Araneae | Araneidae | http://www.gbif.org/species/2134131 | 11.88 | 1.00 | c | |
Araneus marmoreus | Araneae | Araneidae | http://www.gbif.org/species/2160133 | 10.03 | 0.75 | c | |
Araneus quadratus | Araneae | Araneidae | http://www.gbif.org/species/2159970 | 12.25 | 1.00 | c | |
Araneus sturmi | Araneae | Araneidae | http://www.gbif.org/species/2159735 | 4.63 | 0.75 | c | non-grassland species |
Araneus triguttatus | Araneae | Araneidae | http://www.gbif.org/species/2160067 | 5.25 | 0.50 | c | non-grassland species |
Araniella alpica | Araneae | Araneidae | http://www.gbif.org/species/2159883 | 6.00 | 0.75 | c | non-grassland species |
Araniella cucurbitina | Araneae | Araneidae | http://www.gbif.org/species/2158387 | 5.50 | 1.00 | c | |
Araniella opisthographa | Araneae | Araneidae | http://www.gbif.org/species/2158384 | 4.38 | 0.75 | c | |
Argiope bruennichi | Araneae | Araneidae | http://www.gbif.org/species/2158385 | 11.78 | 1.00 | c | |
Cercidia prominens | Araneae | Araneidae | http://www.gbif.org/species/2144644 | 5.38 | 0.50 | c | |
Cyclosa conica | Araneae | Araneidae | http://www.gbif.org/species/5170994 | 5.75 | 0.75 | c | |
Cyclosa oculata | Araneae | Araneidae | http://www.gbif.org/species/2134203 | 5.08 | 0.75 | c | |
Gibbaranea gibbosa | Araneae | Araneidae | http://www.gbif.org/species/2134053 | 6.75 | 0.00 | c | |
Gibbaranea omoeda | Araneae | Araneidae | http://www.gbif.org/species/2134068 | 9.13 | 0.50 | c | non-grassland species |
Hypsosinga albovittata | Araneae | Araneidae | http://www.gbif.org/species/2134110 | 4.15 | 0.50 | c | |
Hypsosinga sanguinea | Araneae | Araneidae | http://www.gbif.org/species/2138915 | 3.75 | 0.75 | c | |
Larinioides cornutus | Araneae | Araneidae | http://www.gbif.org/species/2138546 | 10.35 | 0.75 | c | |
Mangora acalypha | Araneae | Araneidae | http://www.gbif.org/species/2138356 | 4.50 | 1.00 | c | |
Nuctenea umbratica | Araneae | Araneidae | http://www.gbif.org/species/2138349 | 11.25 | 1.00 | c | non-grassland species |
Singa hamata | Araneae | Araneidae | http://www.gbif.org/species/2158735 | 5.90 | 0.75 | c | |
Clubiona brevipes | Araneae | Clubionidae | http://www.gbif.org/species/2137224 | 5.50 | 0.50 | c | non-grassland species |
Clubiona diversa | Araneae | Clubionidae | http://www.gbif.org/species/2143869 | 4.00 | 0.50 | c | |
Clubiona leucaspis | Araneae | Clubionidae | http://www.gbif.org/species/2144214 | 4.05 | 0.50 | c | non-grassland species |
Clubiona neglecta | Araneae | Clubionidae | http://www.gbif.org/species/2143966 | 6.25 | 0.75 | c | |
Clubiona reclusa | Araneae | Clubionidae | http://www.gbif.org/species/2144189 | 5.75 | 0.75 | c | |
Clubiona stagnatilis | Araneae | Clubionidae | http://www.gbif.org/species/2144246 | 6.25 | 0.50 | c | |
Argenna subnigra | Araneae | Dictynidae | http://www.gbif.org/species/2143910 | 2.25 | 0.75 | c | |
Dictyna pusilla | Araneae | Dictynidae | http://www.gbif.org/species/2137146 | 2.45 | 0.50 | c | |
Lathys humilis | Araneae | Dictynidae | http://www.gbif.org/species/2158202 | 2.20 | 0.50 | c | non-grassland species |
Nigma flavescens | Araneae | Dictynidae | http://www.gbif.org/species/2158180 | 3.08 | 0.75 | c | non-grassland species |
Micaria pulicaria | Araneae | Gnaphosidae | http://www.gbif.org/species/2144854 | 3.55 | 1.00 | c | |
Araeoncus humilis | Araneae | Linyphiidae | http://www.gbif.org/species/2158811 | 1.60 | 1.00 | c | |
Baryphyma pratense | Araneae | Linyphiidae | http://www.gbif.org/species/2158809 | 2.20 | 0.50 | c | |
Bathyphantes approximatus | Araneae | Linyphiidae | http://www.gbif.org/species/2160397 | 2.63 | 0.50 | c | |
Bathyphantes gracilis | Araneae | Linyphiidae | http://www.gbif.org/species/2160408 | 1.98 | 1.00 | c | |
Bathyphantes parvulus | Araneae | Linyphiidae | http://www.gbif.org/species/2159204 | 2.15 | 0.75 | c | |
Centromerita bicolor | Araneae | Linyphiidae | http://www.gbif.org/species/2144779 | 3.25 | 1.00 | c | |
Centromerus sylvaticus | Araneae | Linyphiidae | http://www.gbif.org/species/2159061 | 3.43 | 1.00 | c | |
Ceratinella brevipes | Araneae | Linyphiidae | http://www.gbif.org/species/5168243 | 1.45 | 0.50 | c | |
Ceratinella scabrosa | Araneae | Linyphiidae | http://www.gbif.org/species/2145001 | 1.88 | 0.50 | c | non-grassland species |
Cinetata gradata | Araneae | Linyphiidae | http://www.gbif.org/species/2158999 | 1.45 | 0.50 | c | non-grassland species |
Cnephalocotes obscurus | Araneae | Linyphiidae | http://www.gbif.org/species/2159393 | 1.73 | 0.75 | c |
In observation wide-tables, each row is centered around a single physical occurrence of a species, e.g., phenotypic variation of traits within species would usually be recorded per observation where each replicate taken on a distinct individual specimen would be recorded in a row, with the respective trait values stored in columns (see Table B1). Those data are common in investigations of evolutionary trade-offs and trait correlation, or of intra-specific variation along environmental gradients. Occurrence data would also capture phenotypic variation arising from morphotypes and sexual dimorphism. This format is the most intuitive for recording own empirical measurements and therefore is common for measured quantitative data but rarely found for reported qualitative facts obtained from the literature.
A more effective method that allows for high flexibility and easier data merging is the storage of traitdata in long-table formats (Wickham 2014; Parr et al. 2016). This data format corresponds has a row-based structure: each row contains a single measurement or fact of a specific trait, referenced to a single specimen (or one occurrence of an individual organism at a particular space and time) which is assigned to a specific taxon (see Table B2). Identifiers can provide structure and link measurements that are correlated by assigning a unique ID for each single individual. Also, multivariate trait measurements can be recorded in this format by linking multiple rows via a unique measurement identifier. Long-table datasets purport multiple advantages for data handling (e.g., filtering, sub-setting and aggregating data), visualization (e.g., plot measured values by factor variable or taxon) and statistical modelling (e.g., ANOVA for testing difference of trait value by sex) (Wickham 2014). As long-table data share a larger set of columns, merging of datasets is in most cases easier for the end-user.
However, a disadvantage of the long-table data structure is the mixing of units or even factor levels in the ‘traitValue’ column. The mixed content of this column prohibits filtering data based on their values. Data-splitting techniques or a database system are tools to disentangle the data. Note also, how the datasets become bulkier, as many information and labels are now repeated on all measurements as instances of the same individual organism (i.e., one occurrence).
label | species | plot | weight | wing_length | wing_width | wing_area | wing_loading |
---|---|---|---|---|---|---|---|
F1 | Chiasmia_clathrata | HEG9 | 5.174 | 12.59 | 8.34 | 141.9974 | 0.0364 |
F2 | Xanthorhoe_spadicearia | HEG9 | 8.058 | 11.38 | 7.63 | 99.4278 | 0.0810 |
F3 | Chiasmia_clathrata | HEG4 | 5.586 | 15.01 | 11.40 | 231.4057 | 0.0241 |
F4 | Chiasmia_clathrata | HEG6 | 4.797 | 14.90 | 12.39 | 249.6584 | 0.0192 |
F6 | Chiasmia_clathrata | HEG9 | 14.263 | 11.47 | 13.60 | 210.9555 | 0.0676 |
F7 | Chiasmia_clathrata | HEG9 | 4.731 | 12.82 | 11.61 | 201.2838 | 0.0235 |
F8 | Chiasmia_clathrata | HEG9 | 9.200 | 12.85 | 13.85 | 240.6808 | 0.0382 |
F11 | Chiasmia_clathrata | HEG9 | 4.611 | 9.83 | 13.85 | 184.1161 | 0.0250 |
F12 | Xanthorhoe_spadicearia | HEG9 | 5.173 | 10.59 | 6.63 | 80.3989 | 0.0643 |
F14 | Chiasmia_clathrata | HEG9 | 5.181 | 12.50 | 11.63 | 196.5976 | 0.0264 |
F15 | Chiasmia_clathrata | HEG9 | 14.159 | 13.50 | 8.33 | 152.0783 | 0.0931 |
F16 | Chiasmia_clathrata | HEG9 | 8.745 | 12.44 | 12.06 | 202.8879 | 0.0431 |
scientificName | traitName | traitValue | traitUnit | traitID | verbatimTraitName | taxonID | occurrenceID | measurementID | locationID |
---|---|---|---|---|---|---|---|---|---|
Chiasmia clathrata | wing_length | 12.5900 | mm | wing_length | http://www.gbif.org/species/4525078 | F1 | 2557 | HEG9 | |
Chiasmia clathrata | body_weight | 5.1740 | mg | http://t-sita.cesab.org/BETSI_vizInfo.jsp?trait=Body_weight | weight | http://www.gbif.org/species/4525078 | F1 | 1 | HEG9 |
Chiasmia clathrata | wing_area | 141.9974 | mm2 | http://t-sita.cesab.org/BETSI_vizInfo.jsp?trait=Wing_surface | wing_area | http://www.gbif.org/species/4525078 | F1 | 7669 | HEG9 |
Xanthorhoe spadicearia | wing_length | 11.3800 | mm | wing_length | http://www.gbif.org/species/1986166 | F2 | 2558 | HEG9 | |
Xanthorhoe spadicearia | body_weight | 8.0580 | mg | http://t-sita.cesab.org/BETSI_vizInfo.jsp?trait=Body_weight | weight | http://www.gbif.org/species/1986166 | F2 | 2 | HEG9 |
Xanthorhoe spadicearia | wing_area | 99.4278 | mm2 | http://t-sita.cesab.org/BETSI_vizInfo.jsp?trait=Wing_surface | wing_area | http://www.gbif.org/species/1986166 | F2 | 7670 | HEG9 |
Chiasmia clathrata | wing_length | 15.0100 | mm | wing_length | http://www.gbif.org/species/4525078 | F3 | 2559 | HEG4 | |
Chiasmia clathrata | body_weight | 5.5860 | mg | http://t-sita.cesab.org/BETSI_vizInfo.jsp?trait=Body_weight | weight | http://www.gbif.org/species/4525078 | F3 | 3 | HEG4 |
Chiasmia clathrata | wing_area | 231.4057 | mm2 | http://t-sita.cesab.org/BETSI_vizInfo.jsp?trait=Wing_surface | wing_area | http://www.gbif.org/species/4525078 | F3 | 7671 | HEG4 |
Chiasmia clathrata | wing_length | 14.9000 | mm | wing_length | http://www.gbif.org/species/4525078 | F4 | 2560 | HEG6 | |
Chiasmia clathrata | body_weight | 4.7970 | mg | http://t-sita.cesab.org/BETSI_vizInfo.jsp?trait=Body_weight | weight | http://www.gbif.org/species/4525078 | F4 | 4 | HEG6 |
Chiasmia clathrata | wing_area | 249.6584 | mm2 | http://t-sita.cesab.org/BETSI_vizInfo.jsp?trait=Wing_surface | wing_area | http://www.gbif.org/species/4525078 | F4 | 7672 | HEG6 |
Chiasmia clathrata | wing_length | 11.4700 | mm | wing_length | http://www.gbif.org/species/4525078 | F6 | 2561 | HEG9 | |
Chiasmia clathrata | body_weight | 14.2630 | mg | http://t-sita.cesab.org/BETSI_vizInfo.jsp?trait=Body_weight | weight | http://www.gbif.org/species/4525078 | F6 | 5 | HEG9 |
Chiasmia clathrata | wing_area | 210.9555 | mm2 | http://t-sita.cesab.org/BETSI_vizInfo.jsp?trait=Wing_surface | wing_area | http://www.gbif.org/species/4525078 | F6 | 7673 | HEG9 |
Chiasmia clathrata | wing_length | 12.8200 | mm | wing_length | http://www.gbif.org/species/4525078 | F7 | 2562 | HEG9 | |
Chiasmia clathrata | body_weight | 4.7310 | mg | http://t-sita.cesab.org/BETSI_vizInfo.jsp?trait=Body_weight | weight | http://www.gbif.org/species/4525078 | F7 | 6 | HEG9 |
Chiasmia clathrata | wing_area | 201.2838 | mm2 | http://t-sita.cesab.org/BETSI_vizInfo.jsp?trait=Wing_surface | wing_area | http://www.gbif.org/species/4525078 | F7 | 7674 | HEG9 |
Chiasmia clathrata | wing_length | 12.8500 | mm | wing_length | http://www.gbif.org/species/4525078 | F8 | 2563 | HEG9 | |
Chiasmia clathrata | body_weight | 9.2000 | mg | http://t-sita.cesab.org/BETSI_vizInfo.jsp?trait=Body_weight | weight | http://www.gbif.org/species/4525078 | F8 | 7 | HEG9 |
Chiasmia clathrata | wing_area | 240.6808 | mm2 | http://t-sita.cesab.org/BETSI_vizInfo.jsp?trait=Wing_surface | wing_area | http://www.gbif.org/species/4525078 | F8 | 7675 | HEG9 |
Chiasmia clathrata | wing_length | 9.8300 | mm | wing_length | http://www.gbif.org/species/4525078 | F11 | 2564 | HEG9 | |
Chiasmia clathrata | body_weight | 4.6110 | mg | http://t-sita.cesab.org/BETSI_vizInfo.jsp?trait=Body_weight | weight | http://www.gbif.org/species/4525078 | F11 | 8 | HEG9 |
Chiasmia clathrata | wing_area | 184.1161 | mm2 | http://t-sita.cesab.org/BETSI_vizInfo.jsp?trait=Wing_surface | wing_area | http://www.gbif.org/species/4525078 | F11 | 7676 | HEG9 |
Xanthorhoe spadicearia | wing_length | 10.5900 | mm | wing_length | http://www.gbif.org/species/1986166 | F12 | 2565 | HEG9 | |
Xanthorhoe spadicearia | body_weight | 5.1730 | mg | http://t-sita.cesab.org/BETSI_vizInfo.jsp?trait=Body_weight | weight | http://www.gbif.org/species/1986166 | F12 | 9 | HEG9 |
Xanthorhoe spadicearia | wing_area | 80.3989 | mm2 | http://t-sita.cesab.org/BETSI_vizInfo.jsp?trait=Wing_surface | wing_area | http://www.gbif.org/species/1986166 | F12 | 7677 | HEG9 |
Chiasmia clathrata | wing_length | 12.5000 | mm | wing_length | http://www.gbif.org/species/4525078 | F14 | 2566 | HEG9 |
If data contain covariate information, the two-dimensional data table can cover these by adding more columns. The three extensions of the ETS complement the core terms according to different layers of metadata information: 1) the “taxon” extension includes terms to describe more details on the taxon concept applied, 2) the “Measurement or Fact” extension adds information on the methodology or context of the measurement of the trait value, and 3) the “occurrence” extension provides terms to describe the individual specimen and its observation context.
A data table for instance should report on the taxonomic resolution of the trait observation, especially if it is reported on something else than the species level (by setting taxonRank
: genus). The additional terms for taxon hierarchies (kingdom
to genus
) would allow the data user to extract information on genera or families, but this would be redundant with an unambiguous taxon concept has being provided within taxonID
. Further columns would provide detail on the measurement accuracy (measurementResolution
) or the number of individuals on which an aggregated measure has been determined (by reporting individualCount
: n and aggregateMeasure
: ‘TRUE’). Data providers can easily contain information on sex or life stage of the specimen (using terms sex
or lifeStage
), or on the location of sampling (e.g., verbatimLocality
, all ‘occurrence’ terms).
If data are provided in a single two-dimensional data table that applies standard terms of the ETS, this may increase readability and facilitate re-use by synthesis researchers as they do not need to process information stored elsewhere. Data tables conforming to the same data standard can be merged with ease.
ID | Order | Suborder | Family | SpeciesID | Author | Sex | Source | Center_Sampling_region | Body_length | Body_width | Body_height | Thorax_length |
---|---|---|---|---|---|---|---|---|---|---|---|---|
8 | Hemiptera | Heteroptera | Tingidae | Acalypta parvula | (Fallen, 1807) | m | Biodiversity Exploratories | 48 43’ N 09 37’ E | 1.65 | 0.49 | 0.51 | 0.68 |
9 | Hemiptera | Heteroptera | Tingidae | Acalypta platycheila | (Fieber, 1844) | f | Zoological State Collection Munich | 48 11’ N 10 45’ E | 2.39 | 1.13 | 0.73 | 0.59 |
10 | Hemiptera | Heteroptera | Tingidae | Acalypta platycheila | (Fieber, 1844) | f | Zoological State Collection Munich | 48 48’ N 11 06’ E | 2.42 | 1.30 | 0.77 | 0.60 |
11 | Hemiptera | Heteroptera | Tingidae | Acalypta platycheila | (Fieber, 1844) | m | Zoological State Collection Munich | 49 29’ N 10 59’ E | 2.44 | 1.19 | 0.71 | 0.63 |
12 | Hemiptera | Heteroptera | Tingidae | Acalypta platycheila | (Fieber, 1844) | m | Biodiversity Exploratories | 51 20’ N 10 41’ E | 1.63 | 0.81 | 0.56 | 0.50 |
13 | Hemiptera | Heteroptera | Miridae | Acetropis carinata | (Herrich-Schäffer, 1841) | f | Biodiversity Exploratories | 51 20’ N 10 41’ E | 6.45 | 1.79 | 1.05 | 0.74 |
14 | Hemiptera | Heteroptera | Miridae | Acetropis carinata | (Herrich-Schäffer, 1841) | f | Zoological State Collection Munich | NA | 6.28 | 1.82 | 1.23 | 0.72 |
15 | Hemiptera | Heteroptera | Miridae | Acetropis carinata | (Herrich-Schäffer, 1841) | m | Biodiversity Exploratories | 53 02’ N 13 83’ E | 4.46 | 0.98 | 1.49 | 0.57 |
scientificName | traitName | traitValue | traitUnit | occurrenceID | taxonID | family | sex | basisOfRecord | basisOfRecordDescription | decimalLatitude | decimalLongitute |
---|---|---|---|---|---|---|---|---|---|---|---|
Acalypta parvula | Body_height | 0.51 | mm | 8 | http://www.gbif.org/species/2020740 | Tingidae | m | PreservedSpecimen | Biodiversity Exploratories | 48.71667 | 9.61667 |
Acalypta parvula | Body_width | 0.49 | mm | 8 | http://www.gbif.org/species/2020740 | Tingidae | m | PreservedSpecimen | Biodiversity Exploratories | 48.71667 | 9.61667 |
Acalypta parvula | Body_length | 1.65 | mm | 8 | http://www.gbif.org/species/2020740 | Tingidae | m | PreservedSpecimen | Biodiversity Exploratories | 48.71667 | 9.61667 |
Acalypta platycheila | Body_height | 0.73 | mm | 9 | http://www.gbif.org/species/4489001 | Tingidae | f | PreservedSpecimen | Zoological State Collection Munich | 48.18333 | 10.75000 |
Acalypta platycheila | Body_length | 2.39 | mm | 9 | http://www.gbif.org/species/4489001 | Tingidae | f | PreservedSpecimen | Zoological State Collection Munich | 48.18333 | 10.75000 |
Acalypta platycheila | Body_width | 1.13 | mm | 9 | http://www.gbif.org/species/4489001 | Tingidae | f | PreservedSpecimen | Zoological State Collection Munich | 48.18333 | 10.75000 |
Acalypta platycheila | Thorax_width | 1.13 | mm | 9 | http://www.gbif.org/species/4489001 | Tingidae | f | PreservedSpecimen | Zoological State Collection Munich | 48.18333 | 10.75000 |
Acalypta platycheila | Body_height | 0.77 | mm | 10 | http://www.gbif.org/species/4489001 | Tingidae | f | PreservedSpecimen | Zoological State Collection Munich | 48.80000 | 11.10000 |
Acalypta platycheila | Thorax_width | 1.17 | mm | 10 | http://www.gbif.org/species/4489001 | Tingidae | f | PreservedSpecimen | Zoological State Collection Munich | 48.80000 | 11.10000 |
Acalypta platycheila | Body_length | 2.42 | mm | 10 | http://www.gbif.org/species/4489001 | Tingidae | f | PreservedSpecimen | Zoological State Collection Munich | 48.80000 | 11.10000 |
Acalypta platycheila | Body_width | 1.30 | mm | 10 | http://www.gbif.org/species/4489001 | Tingidae | f | PreservedSpecimen | Zoological State Collection Munich | 48.80000 | 11.10000 |
Acalypta platycheila | Thorax_width | 1.09 | mm | 11 | http://www.gbif.org/species/4489001 | Tingidae | m | PreservedSpecimen | Zoological State Collection Munich | 49.48333 | 10.98333 |
Acalypta platycheila | Body_height | 0.71 | mm | 11 | http://www.gbif.org/species/4489001 | Tingidae | m | PreservedSpecimen | Zoological State Collection Munich | 49.48333 | 10.98333 |
Acalypta platycheila | Body_length | 2.44 | mm | 11 | http://www.gbif.org/species/4489001 | Tingidae | m | PreservedSpecimen | Zoological State Collection Munich | 49.48333 | 10.98333 |
Acalypta platycheila | Body_width | 1.19 | mm | 11 | http://www.gbif.org/species/4489001 | Tingidae | m | PreservedSpecimen | Zoological State Collection Munich | 49.48333 | 10.98333 |
Acalypta platycheila | Thorax_width | 0.60 | mm | 12 | http://www.gbif.org/species/4489001 | Tingidae | m | PreservedSpecimen | Biodiversity Exploratories | 51.33333 | 10.68333 |
Acalypta platycheila | Body_height | 0.56 | mm | 12 | http://www.gbif.org/species/4489001 | Tingidae | m | PreservedSpecimen | Biodiversity Exploratories | 51.33333 | 10.68333 |
Acalypta platycheila | Body_length | 1.63 | mm | 12 | http://www.gbif.org/species/4489001 | Tingidae | m | PreservedSpecimen | Biodiversity Exploratories | 51.33333 | 10.68333 |
Acalypta platycheila | Body_width | 0.81 | mm | 12 | http://www.gbif.org/species/4489001 | Tingidae | m | PreservedSpecimen | Biodiversity Exploratories | 51.33333 | 10.68333 |
Acetropis carinata | Body_height | 1.05 | mm | 13 | http://www.gbif.org/species/8426653 | Miridae | f | PreservedSpecimen | Biodiversity Exploratories | 51.33333 | 10.68333 |
Acetropis carinata | Body_length | 6.45 | mm | 13 | http://www.gbif.org/species/8426653 | Miridae | f | PreservedSpecimen | Biodiversity Exploratories | 51.33333 | 10.68333 |
Acetropis carinata | Body_width | 1.79 | mm | 13 | http://www.gbif.org/species/8426653 | Miridae | f | PreservedSpecimen | Biodiversity Exploratories | 51.33333 | 10.68333 |
Acetropis carinata | Thorax_width | 1.45 | mm | 13 | http://www.gbif.org/species/8426653 | Miridae | f | PreservedSpecimen | Biodiversity Exploratories | 51.33333 | 10.68333 |
Acetropis carinata | Body_height | 1.23 | mm | 14 | http://www.gbif.org/species/8426653 | Miridae | f | PreservedSpecimen | Zoological State Collection Munich | NA | NA |
Acetropis carinata | Body_length | 6.28 | mm | 14 | http://www.gbif.org/species/8426653 | Miridae | f | PreservedSpecimen | Zoological State Collection Munich | NA | NA |
Acetropis carinata | Thorax_width | 1.52 | mm | 14 | http://www.gbif.org/species/8426653 | Miridae | f | PreservedSpecimen | Zoological State Collection Munich | NA | NA |
Acetropis carinata | Body_width | 1.82 | mm | 14 | http://www.gbif.org/species/8426653 | Miridae | f | PreservedSpecimen | Zoological State Collection Munich | NA | NA |
Acetropis carinata | Body_height | 1.49 | mm | 15 | http://www.gbif.org/species/8426653 | Miridae | m | PreservedSpecimen | Biodiversity Exploratories | 53.03333 | 14.38333 |
Acetropis carinata | Body_length | 4.46 | mm | 15 | http://www.gbif.org/species/8426653 | Miridae | m | PreservedSpecimen | Biodiversity Exploratories | 53.03333 | 14.38333 |
Two-dimensional spreadsheets are however limited in the number and complexity of co-variates they can contain. As such, for datasets containing multi-layered information on observations, traits, taxa and environmental context, the use of relational database structures may be indicated. Relational databases help to avoid content duplication, as the core table will only maintain identifiers, that relate to secondary data tables containing multiple specifications on the identifier level. For instance, the core table may specify ‘occurrenceID’ for which specific information can be found in a lookup table. The ETS may be applied to describe columns within the individual data tables of relational databases. Compatibility with other database structures is warranted, as ETS terms map to terms of the Darwin Core Standard used in other suggested database structures for trait data, like the generic structure for plant trait databases (Kattge et al. 2011) or the TraitBank structure (Parr et al. 2016).
For publishing relational databases, it is however important to provide sufficient information on how the individual data tables are related, e.g., in a machine readable metadata specification (e.g., in EML language). Further, it must be ensured that data tables are always contained in a single data publication and are not distributed independently of each other, as this would cause issues of broken links if data are updated or lost. Both requirements are met if data are released as a packaged archive, for instance following the Darwin Core Archive specification (Robertson et al. 2009).
scientificName | traitName | traitValue | traitUnit | taxonID | occurrenceID |
---|---|---|---|---|---|
Acalypta parvula | Body_height | 0.51 | mm | http://www.gbif.org/species/2020740 | 8 |
Acalypta parvula | Body_width | 0.49 | mm | http://www.gbif.org/species/2020740 | 8 |
Acalypta parvula | Body_length | 1.65 | mm | http://www.gbif.org/species/2020740 | 8 |
Acalypta platycheila | Body_height | 0.73 | mm | http://www.gbif.org/species/4489001 | 9 |
Acalypta platycheila | Body_length | 2.39 | mm | http://www.gbif.org/species/4489001 | 9 |
Acalypta platycheila | Body_width | 1.13 | mm | http://www.gbif.org/species/4489001 | 9 |
Acalypta platycheila | Thorax_width | 1.13 | mm | http://www.gbif.org/species/4489001 | 9 |
Acalypta platycheila | Body_height | 0.77 | mm | http://www.gbif.org/species/4489001 | 10 |
Acalypta platycheila | Thorax_width | 1.17 | mm | http://www.gbif.org/species/4489001 | 10 |
Acalypta platycheila | Body_length | 2.42 | mm | http://www.gbif.org/species/4489001 | 10 |
Acalypta platycheila | Body_width | 1.30 | mm | http://www.gbif.org/species/4489001 | 10 |
Acalypta platycheila | Thorax_width | 1.09 | mm | http://www.gbif.org/species/4489001 | 11 |
Acalypta platycheila | Body_height | 0.71 | mm | http://www.gbif.org/species/4489001 | 11 |
Acalypta platycheila | Body_length | 2.44 | mm | http://www.gbif.org/species/4489001 | 11 |
Acalypta platycheila | Body_width | 1.19 | mm | http://www.gbif.org/species/4489001 | 11 |
Acalypta platycheila | Thorax_width | 0.60 | mm | http://www.gbif.org/species/4489001 | 12 |
Acalypta platycheila | Body_height | 0.56 | mm | http://www.gbif.org/species/4489001 | 12 |
Acalypta platycheila | Body_length | 1.63 | mm | http://www.gbif.org/species/4489001 | 12 |
Acalypta platycheila | Body_width | 0.81 | mm | http://www.gbif.org/species/4489001 | 12 |
Acetropis carinata | Body_height | 1.05 | mm | http://www.gbif.org/species/8426653 | 13 |
Acetropis carinata | Body_length | 6.45 | mm | http://www.gbif.org/species/8426653 | 13 |
Acetropis carinata | Body_width | 1.79 | mm | http://www.gbif.org/species/8426653 | 13 |
Acetropis carinata | Thorax_width | 1.45 | mm | http://www.gbif.org/species/8426653 | 13 |
Acetropis carinata | Body_height | 1.23 | mm | http://www.gbif.org/species/8426653 | 14 |
Acetropis carinata | Body_length | 6.28 | mm | http://www.gbif.org/species/8426653 | 14 |
Acetropis carinata | Thorax_width | 1.52 | mm | http://www.gbif.org/species/8426653 | 14 |
Acetropis carinata | Body_width | 1.82 | mm | http://www.gbif.org/species/8426653 | 14 |
Acetropis carinata | Body_height | 1.49 | mm | http://www.gbif.org/species/8426653 | 15 |
Acetropis carinata | Body_length | 4.46 | mm | http://www.gbif.org/species/8426653 | 15 |
Acetropis carinata | Body_width | 0.98 | mm | http://www.gbif.org/species/8426653 | 15 |
Acetropis carinata | Thorax_width | 1.45 | mm | http://www.gbif.org/species/8426653 | 15 |
taxonID | scientificName | scientificNameAuthorship | taxonRank | kingdom | phylum | class | order | family | genus | taxonomy |
---|---|---|---|---|---|---|---|---|---|---|
http://www.gbif.org/species/2020740 | Acalypta parvula | (Fallén, 1807) | species | Animalia | Arthropoda | Insecta | Hemiptera | Tingidae | Acalypta | GBIF Backbone Taxonomy |
http://www.gbif.org/species/4489001 | Acalypta platycheila | (Fieber, 1844) | species | Animalia | Arthropoda | Insecta | Hemiptera | Tingidae | Acalypta | GBIF Backbone Taxonomy |
http://www.gbif.org/species/8426653 | Acetropis carinata | (Herrich-Schaeffer, 1841) | species | Animalia | Arthropoda | Insecta | Hemiptera | Miridae | Acetropis | GBIF Backbone Taxonomy |
occurrenceID | sex | basisOfRecord | basisOfRecordDescription | references | decimalLatitude | decimalLongitute |
---|---|---|---|---|---|---|
8 | m | PreservedSpecimen | Biodiversity Exploratories | AEG_26_KEF_august2008 | 48.71667 | 9.61667 |
9 | f | PreservedSpecimen | Zoological State Collection Munich | Schwabmünchen_Schwaben_27.5.1965_leg.G.Schuster | 48.18333 | 10.75000 |
10 | f | PreservedSpecimen | Zoological State Collection Munich | Altmühltal_Wellheim_18.7.34_K.Schmidt | 48.80000 | 11.10000 |
11 | m | PreservedSpecimen | Zoological State Collection Munich | Fürth.i.B._Vach_25.5.32_K.Schmidt | 49.48333 | 10.98333 |
12 | m | PreservedSpecimen | Biodiversity Exploratories | HEG_42_NO_BF_juni2008 | 51.33333 | 10.68333 |
13 | f | PreservedSpecimen | Biodiversity Exploratories | HEG_46_KEF_juni2008 | 51.33333 | 10.68333 |
14 | f | PreservedSpecimen | Zoological State Collection Munich | Ungarn_Sammlung.Hüter | NA | NA |
15 | m | PreservedSpecimen | Biodiversity Exploratories | SEG_13_KEF_juni2008 | 53.03333 | 14.38333 |
Gossner, M. M., N. K. Simons, R. Achtziger, T. Blick, W. H. Dorow, F. Dziock, F. Köhler, et al. 2015a. A summary of eight traits of Coleoptera, Hemiptera, Orthoptera and Araneae, occurring in grasslands in Germany. Scientific Data 2:150013.
Gossner, M. M., N. K. Simons, L. Höck, and W. W. Weisser. 2015b. Morphometric measures of Heteroptera sampled in grasslands across three regions of Germany. Ecology 96:1154–1154.
Kattge, J., K. Ogle, G. Bönisch, S. Díaz, S. Lavorel, J. Madin, K. Nadrowski, et al. 2011. A generic structure for plant trait databases. Methods in Ecology and Evolution 2:202–213.
Kissling, W. D., R. Walls, A. Bowser, M. O. Jones, J. Kattge, D. Agosti, J. Amengual, et al. 2018. Towards global data products of Essential Biodiversity Variables on species traits. Nature Ecology & Evolution 2:1531–1540.
Parr, C. S., K. S. Schulz, J. Hammock, N. Wilson, P. Leary, J. Rice, C. Jr, et al. 2016. TraitBank: Practical semantics for organism attribute data. Semantic Web 7:577–588.
Robertson, T., M. Döring, J. Wieczorek, R. De Giovanni, and D. Vieglais. 2009. Darwin Core Text Guide. http://rs.tdwg.org/dwc/terms/guides/text/index.htm.
Wickham, H. 2014. Tidy data. Journal of Statistical Software 59:1–23.
Wilkinson, M. D., M. Dumontier, I. J. Aalbersberg, G. Appleton, M. Axton, A. Baak, N. Blomberg, et al. 2016. The FAIR Guiding Principles for scientific data management and stewardship. Scientific Data 3:160018.