Appendix A: FAIRS(S) Data Sharing Principles
FAIR Principles, as described in https://www.go-fair.org/fair-principles/.
The first step in (re)using data is to find them. Metadata and data should be easy to find for both humans and computers. Machine-readable metadata are essential for automatic discovery of datasets and services, so this is an essential component of the FAIRification process.
F1. (Meta)data are assigned a globally unique and persistent identifier
F2. Data are described with rich metadata (defined by R1 below)
F3. Metadata clearly and explicitly include the identifier of the data they describe
F4. (Meta)data are registered or indexed in a searchable resource
Once the user finds the required data, she/he needs to know how can they be accessed, possibly including authentication and authorisation.
A1. (Meta)data are retrievable by their identifier using a standardised communications protocol
A1.1 The protocol is open, free, and universally implementable
A1.2 The protocol allows for an authentication and authorisation procedure, where necessary
A2. Metadata are accessible, even when the data are no longer available
The data usually need to be integrated with other data. In addition, the data need to interoperate with applications or workflows for analysis, storage, and processing.
I1. (Meta)data use a formal, accessible, shared, and broadly applicable language for knowledge representation.
I2. (Meta)data use vocabularies that follow FAIR principles
I3. (Meta)data include qualified references to other (meta)data
The ultimate goal of FAIR is to optimise the reuse of data. To achieve this, metadata and data should be well-described so that they can be replicated and/or combined in different settings.
R1. (Meta)data are richly described with a plurality of accurate and relevant attributes
R1.1. (Meta)data are released with a clear and accessible data usage license
R1.2. (Meta)data are associated with detailed provenance
R1.3. (Meta)data meet domain-relevant community standards
Appendix B: CARE Data Sharing Principles
CARE principles are grounded in “people and purpose” while FAIR principles are “data focused”. This means that CARE principles address the gaps in FAIR principles in terms of the rights and interest of Indigenous peoples and their world views.
The CARE principles by GIDA are as follows (ref):
Data ecosystems should be designed and function in ways that enable Indigenous Peoples to derive benefit from the data.
C1: For inclusive development and innovation
Governments and institutions must actively support the use and reuse of data by Indigenous
nations and communities by facilitating the establishment of the foundations for Indigenous
innovation, value generation, and the promotion of local self-determined development processes.
C2: For improved governance and citizen engagement
Data enrich the planning, implementation, and evaluation processes that support the service and
policy needs of Indigenous communities. Data also enable better engagement between citizens,
institutions, and governments to improve decision-making. Ethical use of open data has the
capacity to improve transparency and decision-making by providing Indigenous nations and
communities with a better understanding of their peoples, territories, and resources. It
similarly can provide greater insight into third-party policies and programs affecting
C3: For improved governance and citizen engagement
Indigenous data are grounded in community values, which extend to society at large. Any value
created from Indigenous data should benefit Indigenous communities in an equitable manner and
contribute to Indigenous aspirations for wellbeing.
Authority to Control
Indigenous Peoples’ rights and interests in Indigenous data must be recognised and their authority to control such data be empowered. Indigenous data governance enables Indigenous Peoples and governing bodies to determine how Indigenous Peoples, as well as Indigenous lands, territories, resources, knowledges and geographical indicators, are represented and identified within data.
A1: Recognizing rights and interests
Indigenous Peoples have rights and interests in both Indigenous Knowledge and Indigenous data.
Indigenous Peoples have collective and individual rights to free, prior, and informed consent
in the collection and use of such data, including the development of data policies and protocols
A2: Data for governance
Indigenous Peoples have the right to data that are relevant to their world views and empower
self-determination and effective self-governance. Indigenous data must be made available and
accessible to Indigenous nations and communities in order to support Indigenous governance.
A3: Governance of data
Indigenous Peoples have the right to develop cultural governance protocols for Indigenous data
and be active leaders in the stewardship of, and access to, Indigenous data especially in the
context of Indigenous Knowledge.
Those working with Indigenous data have a responsibility to share how data is used to support Indigenous Peoples’ self-determination and collective benefit.
R1: For positive relationships
Indigenous data use is unviable unless linked to relationships built on respect, reciprocity,
trust, and mutual understanding, as defined by the Indigenous Peoples to whom those data
relate. Those working with Indigenous data are responsible for ensuring that the creation,
interpretation, and use of those data uphold, or are respectful of, the dignity of Indigenous
nations and communities.
R2: For expanding capability and capacity
Use of Indigenous data invokes a reciprocal responsibility to enhance data literacy within
Indigenous communities and to support the development of an Indigenous data workforce and
digital infrastructure to enable the creation, collection, management, security, governance,
and application of data.
R3: For Indigenous languages and worldviews
Resources must be provided to generate data grounded in the languages, worldviews, and
lived experiences (including values and principles) of Indigenous Peoples.
Indigenous Peoples’ rights and well-being should be the primary concern at all stages of the data life cycle and across the data ecosystem.
E1: For minimizing harm and maximizing benefit
Ethical data are data that do not stigmatize or portray Indigenous Peoples, cultures,
or knowledges in terms of deficit. Ethical data are collected and used in ways that
align with Indigenous ethical frameworks and with rights affirmed in UNDRIP. Assessing
ethical benefits and harms should be done from the perspective of the Indigenous Peoples,
nations, or communities to whom the data relate.
E2: For justice
Ethical processes address imbalances in power, resources, and how these affect the
expression of Indigenous rights and human rights. Ethical processes must include
representation from relevant Indigenous communities.
E3: For future use
Data governance should take into account the potential future use and future harm
based on ethical frameworks grounded in the values and principles of the relevant
Indigenous community. Metadata should acknowledge the provenance and purpose and
any limitations or obligations in secondary use inclusive of issues of consent.
Appendix C: GATHER
Appendix D: Metadata Terms
Metadata terms are adapted from AGRIS AP, AgMES and DCMI (See Technical Data Standards). Terms are presented in Table #FIXME. The terms can also be downloaded in JSON format.
Appendix E: JSON Metadata Template
This section contains a JSON metadata template, with all metadata terms (Table #FIXME). Note that some metadata terms are ... to be continued.
Appendix F: Common Licensing Agreements
Creative Commons (CC)
CC offers 6 different types of licenses: CC-BY, CC BY-SA, CC BY-NC, CC BY-NC,SA, CC BY-ND, CC BY-NC-ND
Each license as defined by CC:
|CC BY||This license allows reusers to distribute, remix, adapt, and build upon the material in any medium or format, so long as attribution is given to the creator. The license allows for commercial use.|
|CC BY-SA||This license allows reusers to distribute, remix, adapt, and build upon the material in any medium or format, so long as attribution is given to the creator. The license allows for commercial use. If you remix, adapt, or build upon the material, you must license the modified material under identical terms.|
|CC BY-NC||This license allows reusers to distribute, remix, adapt, and build upon the material in any medium or format for noncommercial purposes only, and only so long as attribution is given to the creator.|
|CC BY-NC-SA||This license allows reusers to distribute, remix, adapt, and build upon the material in any medium or format for noncommercial purposes only, and only so long as attribution is given to the creator. If you remix, adapt, or build upon the material, you must license the modified material under identical terms.|
|CC BY-ND||This license allows reusers to copy and distribute the material in any medium or format in unadapted form only, and only so long as attribution is given to the creator. The license allows for commercial use.|
|CC BY-NC-ND||This license allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator.|
Including the aforementioned licenses, creative commons offers a public domain dedication tool, CC0. In this, a creator forfeits their rights to their work and allows “reusers to distribute, remix, adapt, and build upon the material in any medium or format, with no conditions.”
Any individual with original content can use CC licenses simply by including copyright text and licensing information, with a link to the license that the work is protected by.
Open Data Commons Open Database Licenses (ODbL)
The full ODbL 1.0 here, and a summary here.
In general, it is very similar to the CC BY-SA license, but it requires that you ‘Keep open’ meaning: “If you redistribute the database, or an adapted version of it, then you may use technological measures that restrict the work (such as DRM) as long as you also redistribute a version without such measures.”
FAO data licensing information is included in the “Open Data Licensing for Statistical Databases Policy” document [reference to be added: FAO Data Licensing Information], which builds upon the CC BY-NC-SA 3.0 IGO.
The following corporate databases are under this license:
- Agricultural Market Information Systems
- Global Information System on Water and Agriculture
- Gender and lands rights database
- Food Price Monitoring and Analysis Tool
- Global Individual Food Consumption
- SDG Data Portal.
World Bank Licensing
Similar to the FAO, the World Bank is licensed under a CC license (CC BY 4.0) with additional terms and conditions, which can be found here [reference to be added].
Open Government License
Appendix G: Data Standards
Including known data sources, all definitions, data standards surveyed, explanation of technical standards and mechanisms,
vocabularies identified or constructed (probably just links to these since they maybe large), licenses and site that
explain more about these licenses, types of users and how we will identify, authenticate, and authorize them, meta-data
adopted or developed by GBADs.
|subject, subjectClassification, subjectThesaurus||AGROVOC Agroportal|
|accrualMethod||DCMI Type Vocabulary - Accrual Method|
|accrualPeriodicity||DCMI Type Vocabulary - Accrual Periodicity|
Appendix H: Organizations
Appendix I: GATHER checklist
|GATHER Checklist Item||GBADs Comments and Refinements|
|Objectives and Funding|
|1. Define the indicator(s), populations (including age, sex, and geographic entities), and time period(s) for which estimates were made.||GBADs is concerned with animal, not human, disease estimates. Therefore, the indicator populations are still important but also pertaining to species, disease type, and potentially other indicators such as economic models or estimates and climate and weather information. Definitions of geographic entities (spatialCoverage) and time period(s) (temporalCoverage) remain consistent with the original GATHER checklist.|
|2. List the funding sources for the work.|
|Data Inputs For all data inputs from multiple sources that are synthesized as part of the study:|
|3. Describe how the data were identified and how the data were accessed.|
|4. Specify the inclusion and exclusion criteria. Identify all ad-hoc exclusions.|
|5. Provide information on all included data sources and their main characteristics. For each data source used, report reference information or contact name/institution, population represented, data collection method, year(s) of data collection, sex and age range, diagnostic criteria or measurement method, and sample size, as relevant.||GBADs metadata will have a unique identifier. This should provide a simple method to access all of this information, which will be provided in the metadata of each data attribute.|