Open scientific data

The concept of open scientific data has developed in parallel with the concept of scientific data.

Scientific data was not formally defined until the late 20th century. Before the generalization of computational analysis, data has been mostly an informal terms, frequently used interchangeably with knowledge or information.[3] Institutional and epistemological discourses favored alternative concepts and outlooks on scientific activities: "Even histories of science and epistemology comments, mention data only in passing. Other foundational works on the making of meaning in science discuss facts, representations, inscriptions, and publications, with little attention to data per se."[4]

The first influential policy definition of scientific data appeared as late as 1999, when the National Academies of Science described data as "facts, letters, numbers or symbols that describe an object, condition, situation or other factors".[5] Terminologies have continued to evolve: in 2011, the National Academies updated the definition to include a large variety of dataified objects such as "spectrographic, genomic sequencing, and electron microscopy data; observational data, such as remote sensing, geospatial, and socioeconomic data; and other forms of data either generated or compiled, by humans or machines" as well as "digital representation of literature"[5]

While the forms and shapes of data remain expansive and unsettled, standard definitions and policies have recently tended to restrict scientific data to computational or digital data.[6] The open data pilot of Horizon 2020 has been voluntarily restricted to digital research: "'Digital research data' is information in digital form (in particular facts or numbers), collected to be examined and used as a basis for reasoning, discussion or calculation; this includes statistics, results of experiments, measurements, observations resulting from fieldwork, survey results, interview recordings and images"[7]

Overall, the status scientific data remains a flexible point of discussion among individual researchers, communities and policy-makers: "In broader terms, whatever 'data' is of interest to researchers should be treated as 'research data'"[6] Important policy reports, like the 2012 collective synthesis of the National Academies of science on data citation, have intentionally adopted a relative and nominalist definition of data: "we will devote little time to definitional issues (e.g., what are data?), except to acknowledge that data often exist in the eyes of the beholder."[8] For Christine Borgman, the main issue is not to define scientific data ("what are data") but to contextualize the point where data became a focal point of discussion within a discipline, an institution or a national research program ("when are data").[9] In the 2010s, the expansion of available data sources and the sophistication of data analysis method has expanded the range of disciplines primarily affected by data management issues to "computational social science, digital humanities, social media data, citizen science research projects, and political science."[10]

Opening and sharing have both been major topic of discussion in regard to scientific data management, but also a motivation to make data emerge as a relevant issue within an institution, a discipline or a policy framework.

For Paul Edwards, whether or not to share the data, to what extent it should be shared and to whom have been major causes of data friction, that revealed the otherwise hidden infrastructures of science: "Edwards' metaphor of data friction describes what happens at the interfaces between data 'surfaces': the points where data move between people, substrates, organizations, or machines (...) Every movement of data across an interface comes at some cost in time, energy, and human attention. Every interface between groups and organizations, as well as between machines, represents a point of resistance where data can be garbled, misinterpreted, or lost. In social systems, data friction consumes energy and produces turbulence and heat – that is, conflicts, disagreements, and inexact, unruly processes."[11] The opening of scientific data is both a data friction in itself and a way to collectively manage data frictions by weakening complex issues of data ownership. Scientific or epistemic cultures have been acknowledged as primary factors in the adoption of open data policies: "data sharing practices would be expected to be community-bound and largely determined by epistemic culture."[12]

In the 2010s, new concepts have been introduced by scientist and policy-makers to more accurately define what open scientific data. Since its introduction in 2016, FAIR data has become a major focus of open research policies. The acronym describe an ideal-type of Findable, Accessible, Interoperable, and Reusable data. Open scientific data has been categorized as a commons or a public good, which is primarily maintained, enriched and preserved by collective rather than individual action: "What makes collective action useful in understanding scientific data sharing is its focus on how the appropriation of individual gains is determined by adjusting the costs and benefits that accrue with contributions to a common resource"[13]

Punch-card storage in US National Weather Records Center in Asheville (early 1960s). Data holding have expanded so much that the entrance hall has to be used as a storage facility.

The emergence of scientific data is associated with a semantic shift in the way core scientific concepts like data, information and knowledge are commonly understood.[14] Following the development of computing technologies, data and information are increasingly described as "things":[15] "Like computation, data always have a material aspect. Data are things. They are not just numbers but also numerals, with dimensionality, weight, and texture".[16]

After the Second World War large scientific projects have increasingly relied on knowledge infrastructure to collect, process and analyze important amount of data. Punch-cards system were first used experimentally on climate data in the 1920s and were applied on a large scale in the following decade: "In one of the first Depression-era government make-work projects, Civil Works Administration workers punched some 2 million ship log observations for the period 1880–1933."[17] By 1960, the meteorological data collections of the US National Weather Records Center has expanded to 400 millions cards and had a global reach. The physically of scientific data was by then fully apparent and threatened the stability of entire buildings: "By 1966 the cards occupied so much space that the Center began to fill its main entrance hall with card storage cabinets (figure 5.4). Officials became seriously concerned that the building might collapse under their weight".[18]

By the end of the 1960s, knowledge infrastructure have been embedded in a various set of disciplines and communities. The first initiative to create a database of electronic bibliography of open access data was the Educational Resources Information Center (ERIC) in 1966. In the same year, MEDLINE was created – a free access online database managed by the National Library of Medicine and the National Institute of Health (USA) with bibliographical citations from journals in the biomedical area, which later would be called PubMed, currently with over 14 million complete articles.[19] Knowledge infrastructures were also set up in space engineering (with NASA/RECON), library search (with OCLC Worldcat) or the social sciences: "The 1960s and 1970s saw the establishment of over a dozen services and professional associations to coordinate quantitative data collection".[20]

Early discourses and policy frameworks on open scientific data emerged immediately in the wake of the creation of the first large knowledge infrastructure. The World Data Center system (now the World Data System), aimed to make observation data more readily available in preparation for the International Geophysical Year of 1957–1958.[21] The International Council of Scientific Unions (now the International Council for Science) established several World Data Centers to minimize the risk of data loss and to maximize data accessibility, further recommending in 1955 that data be made available in machine-readable form.[22] In 1966, the International Council for Science created CODATA, an initiative to "promote cooperation in data management and use".[23]

These early forms of open scientific data did not develop much further. There were too many data frictions and technical resistance to the integration of external data to implement a durable ecosystem of data sharing. Data infrastructures were mostly invisible to researchers, as most of the research was done by professional librarians. Not only were the search operating systems complicated to use, but the search has to be performed very efficiently given the prohibitive cost of long-distance telecommunication.[24] While their conceptors have originally anticipated direct uses by researcher, that could not really emerge due to technical and economic impediment:

The designers of the first online systems had presumed that searching would be done by end users; that assumption undergirded system design. MEDLINE was intended to be used by medical researchers and clinicians, NASA/RECON was designed for aerospace engineers and scientists. For many reasons, however, most users through the seventies were librarians and trained intermediaries working on behalf of end users. In fact, some professional searchers worried that even allowing eager end users to get at the terminals was a bad idea.[25]

Christine Borgman does not recall any significant policy debates over the meaning, the production and the circulation of scientific data save for a few specific fields (like climatology) after 1966.[23] The insulated scientific infrastructures could hardly be connected before the advent of the web.[26] Projects, and communities relied on their own unconnected networks at a national or institutional level: "the Internet was nearly invisible in Europe because people there were pursuing a separate set of network protocols".[27] Communication between scientific infrastructures was not only challenging across space, but also across time. Whenever a communication protocol was no longer maintained, the data and knowledge it disseminated was likely to disappear as well: "the relationship between historical research and computing has been durably affected by aborted projects, data loss and unrecoverable formats".[28]

The World Wide Web was originally conceived as an infrastructure for open scientific data. Sharing of data and data documentation was a major focus in the initial communication of the World Wide Web when the project was first unveiled in August 1991 : "The WWW project was started to allow high energy physicists to share data, news, and documentation. We are very interested in spreading the web to other areas, and having gateway servers for other data".[29]

The project stemmed from a close knowledge infrastructure, ENQUIRE. It was an information management software commissioned to Tim Berners-Lee by the CERN for the specific needs of high energy physics. The structure of ENQUIRE was closer to an internal web of data: it connected "nodes" that "could refer to a person, a software module, etc. and that could be interlined with various relations such as made, include, describes and so forth".[30] While it "facilitated some random linkage between information" Enquire was not able to "facilitate the collaboration that was desired for in the international high-energy physics research community".[31] Like any significant computing scientific infrastructure before the 1990s, the development of ENQUIRE was ultimately impeded by the lack of interoperability and the complexity of managing network communications: "although Enquire provided a way to link documents and databases, and hypertext provided a common format in which to display them, there was still the problem of getting different computers with different operating systems to communicate with each other".[27]

The web rapidly superseded pre-existing closed infrastructure for scientific data, even when they included more advanced computing features. From 1991 to 1994, users of the Worm Community System, a major biology database on worms, switched to the Web and Gopher. While the Web did not include many advanced functions for data retrieval and collaboration, it was easily accessible. Conversely, the Worm Community System could only be browsed on specific terminals shared across scientific institutions: "To take on board the custom-designed, powerful WCS (with its convenient interface) is to suffer inconvenience at the intersection of work habits, computer use, and lab resources (…) The World-Wide Web, on the other hand, can be accessed from a broad variety of terminals and connections, and Internet computer support is readily available at most academic institutions and through relatively inexpensive commercial services."[32]

Publication on the web completely changed the economics of data publishing. While in print "the cost of reproducing large datasets is prohibitive", the storage expenses of most datasets is low.[33] In this new editorial environment, the main limiting factors for data sharing becomes no longer technical or economic but social and cultural.

The development and the generalization of the World Wide Web lifted numerous technical barriers and frictions had constrained the free circulation of data. Yet, scientific data had yet to be defined and new research policy had to be implemented to realize the original vision laid out by Tim Berners-Lee of a web of data. At this point, scientific data has been largely defined through the process of opening scientific data, as the implementation of open policies created new incentives for setting up actionable guidelines, principles and terminologies.

Climate research has been a pioneering field in the conceptual definition of open scientific data, as it has been in the construction of the first large knowledge infrastructure in the 1950s and the 1960s. In 1995 the GCDIS articulated a clear commitment On the Full and Open Exchange of Scientific Data: "International programs for global change research and environmental monitoring crucially depend on the principle of full and open data exchange (i.e., data and information are made available without restriction, on a non-discriminatory basis, for no more than the cost of reproduction and distribution).[34] The expansion of the scope and the management of knowledge infrastructures also created to incentives to share data, as the "allocation of data ownership" between a large number of individual and institutional stakeholders has become increasingly complex.[35] Open data creates a simplified framework to ensure that all contributors and users of the data have access to it.[35]

Open data has been rapidly identified as a key objective of the emerging open science movement. While initially focused on publications and scholarly articles, the international initiatives in favor of open access expanded their scope to all the main scientific productions.[36] In 2003 the Berlin Declaration supported the diffusion of "original scientific research results, raw data and metadata, source materials and digital representations of pictorial and graphical and scholarly multimedia materials"

After 2000, international organizations, like the OECD (Organisation for Economic Co-operation and Development), have played an instrumental role in devising generic and transdisciplinary definitions of scientific data, as open data policies have to be implemented beyond the specific scale of a discipline of a country.[5] One of the first influential definition of scientific data was coined in 1999[5] by a report of the National Academies of Science: "Data are facts, numbers, letters, and symbols that describe an object, idea, condition, situation, or other factors".[37] In 2004, the Science Ministers of all nations of the OECD signed a declaration which essentially states that all publicly funded archive data should be made publicly available.[38] In 2007 the OECD "codified the principles for access to research data from public funding"[39] through the Principles and Guidelines for Access to Research Data from Public Funding which defined scientific data as "factual records (numerical scores, textual records, images and sounds) used as primary sources for scientific research, and that are commonly accepted in the scientific community as necessary to validate research findings."[40] The Principles acted as soft-law recommendation and affirmed that "access to research data increases the returns from public investment in this area; reinforces open scientific inquiry; encourages diversity of studies and opinion; promotes new areas of work and enables the exploration of topics not envisioned by the initial investigators."[41]

After 2010, national and supra-national institutions took a more interventionist stance. New policies have been implemented not only to ensure and incentivize the opening of scientific data, usually in continuation to existing open data program. In Europe, the "European Union Commissioner for Research, Science, and Innovation, Carlos Moedas made open research data one of the EU's priorities in 2015."[10]

First published in 2016, the FAIR Guiding Principles[2] have become an influential framework for opening scientific data.[10] The principles have been originally designed two years earlier during a policy ad research workshop at Lorentz, Jointly Designing a Data FAIRport.[42] During the deliberations of the workshop, "the notion emerged that, through the definition of, and widespread support for, a minimal set of community-agreed guiding principles and practice"[43]

The principles do not attempt to define scientific data, which remains a relatively plastic concept, but strive to describe "what constitutes 'good data management'".[44] They cover four foundational principles, "that serve to guide data producer": Findability, Accessibility, Interoperability, and Reusability.[44] and also aim to provide a step toward machine-actionability by expliciting the underlying semantics of data.[43] As it fully acknowledge the complexity of data management, the principles do not claim to introduce a set of rigid recommendations but rather "degrees of FAIRness", that can be adjusted depending on the organizational costs but also external restrictions in regards to copyright or privacy.[45]

The FAIR principles have immediately been coopted by major international organization: "FAIR experienced rapid development, gaining recognition from the European Union, G7, G20 and US-based Big Data to Knowledge (BD2K)"[46] In August 2016, the European Commission set up an expert group to turn "FAIR Data into reality".[47] As of 2020, the FAIR principles remain "the most advanced technical standards for open scientific data to date"[48]

In 2022, the French Open Science Monitor started to publish an experimental survey of research data publications from text mining tools. Retrospective analysis showed that the rate of publications mentioning sharing of their associated has nearly doubled in 10 years, from 13% (in 2013) to 22% (in 2021).[49]

By the end of the 2010s, open data policy are well supported by scientific communities. Two large surveys commissioned by the European Commission in 2016 and 2018 find a commonly perceived benefit: "74% of researchers say that having access to other data would benefit them"[50] Yet, more qualitative observations gathered in the same investigation also showed that "what scientists proclaim ideally, versus what they actually practice, reveals a more ambiguous situation."[50]

Until the 2010s, the publication of scientific data referred mostly to "the release of datasets associated with an individual journal article"[51] This release is documented by a Data Accessibility Statement or DAS. Several typologies or data accessibility statements have been proposed.[52][53] In 2021, Colavizza et al. identified three categories or levels of access:

• DAS 1: "Data available on request or similar"[54]
• DAS 2: "Data available with the paper and its supplementary files"[54]
• DAS 3: "Data available in a repository"[54]

Supplementary data files have appeared in the early phase of the transition to scientific digital publishing. While the format of publications have largely kept the constraints of the printing format, additional materials could be included in "supplementary information".[33] As a publication supplementary data files have an ambiguous status. In theory they are meant to be raw documents, giving access to the background of research. In practice, the released datasets have often to be specially curated for publication. They will usually focus on the primary data sources, not on the entire range of observations or measurements done for the purpose of the research: "Identifying what are "the data" associated with any individual article, conference paper, book, or other publication is often difficult [as] investigators collect data continually."[55] The selection of the data is also further influenced by the publisher. Editorial policy of the journal largely determines "goes in the main text, what in the supplemental information" and editors are especially weary on including large datasets which may be difficult to maintain in the long run.[55]

Scientific datasets have been increasingly acknowledged as an autonomous scientific publication. The assimilation of data to academic articles aimed to increase the prestige and recognition of published datasets: "implicit in this argument is that familiarity will encourage data release".[51] This approach has been favored by several publishers and repositories as it made it possible to easily integrate data in existing publishing infrastructure and to extensively reuse editorial concepts initially created around articles[51] Data papers were explicitly introduced as "a mechanism to incentivize data publishing in biodiversity science".[56]

The first digital databases of the 1950s and the 1960s have immediately raised issues of citability and bibliographic descriptions.[57] The mutability of computer memory was especially challenging: in contrast with printed publications, digital data could not be expected to remain stable on the long run. In 1965, Ralph Bisco underlined that this uncertainty affected all the associated documents like code notebooks, which may become increasingly out of date. Data management have to find a middle ground between continuous enhancements and some form of generic stability: "the concept of a fluid, changeable, continually improving data archive means that study cleaning and other processing must be carried to such a point that changes will not significantly affect prior analyses"[58]

Structured bibliographic metadata for database has been a debated topic since the 1960s.[57] In 1977, the American Standard for Bibliographic Reference adopted a definition of "data file" with a strong focus on the materiability and the mutability of the dataset: neither dates nor authors were indicated but the medium or "Packaging Method" had to be specified.[59] Two years later, Sue Dodd introduced an alternative convention, that brought the citation of data closer to the standard of references of other scientific publications:[57] Dodd's recommendation included the use of titles, author, editions and date, as well as alternative mentions for sub-documentations like code notebook.[60]

The indexation of dataset has been radically transformed by the development of the web, as barriers to data sharing were substantially reduced.[57] In this process, data archiving, sustainability and persistence have become critical issues. Permanent digital object identifiers (or DOI) have been introduced for scientific articles to avoid broken links, as website structures continuously evolved. In the early 2000s, pilot programs started to allocate DOIs to dataset as well[61] While it solves concrete issues of link sustainability, the creation of data DOI and norms of data citation is also part of legitimization process, that assimilate dataset to standard scientific publications and can draw from similar sources of motivation (like the bibliometric indexes)[62]

Accessible and findable datasets yield a significant citation advantage. A 2021 study of 531,889 articles published by PLOS estimated that there is a "25.36% relative gain in citation counts in general" for a journal article with "a link to archived data in a public repository".[63] Diffusion of data as a supplementary materials does not yield a significant citation advantage which suggest that "the citation advantage of DAS [Data Availability Statement] is not as much related to their mere presence, but to their contents"[64]

As of 2022, the recognition of open scientific data is still an ongoing process. The leading reference software Zotero does not have yet a specific item for dataset.

Within academic research, storage and redundancy has proven to be a significant benefit of open scientific data. In contrast, non-open scientific data is weakly preserved and can only "be retrieved only with considerable effort by the authors" if not completely lost.[65]

Analysis of the uses of open scientific data run into the same issues as for any open content: while free, universal and indiscriminate access has demonstrably expanded the scope, range and intensity of the reception it has also made it harder to track, due to the lack of transaction process.

These issues are further complicated by the novelty of data as a scientific publication: "In practice, it can be difficult to monitor data reuse, mainly because researchers rarely cite the repository"[66]

In 2018, a report of the European Commission estimated the cost of not opening scientific data in accordance with the FAIR principles: it amounted at 10.2 billion annually in direct impact and 16 billions in indirect impact over the entire innovation economy.[67] Implementing open scientific open data at a global scale "would have a considerable impact on the time we spent manipulating data and the way we store data."[67]

The development of scientific open data is not limited to scientific research. It involves a diverse set of stakeholders: "Arguments for sharing data come from many quarters: funding agencies—both public and private—policy bodies such as national academies and funding councils, journal publishers, educators, the public at large, and from researchers themselves."[69] As such, the movement for scientific open data largely intersects with more global movements for open data.[70] Standards definition of open data used by a wide range of public nd private actors have been partly elaborated by researchers around concrete scientific issues.[71] The concept of transparency has especially contributed to create convergences between open science, open data and open government. In 2015, the OECD describe transparency as a common "rationale for open science and open data".[72]

Christine Borgman has identified four major rationales for sharing data commonly used across the entire regulatory and public debate over scientific open data:[69]

• Research reproducibility: lack of reproducibility is frequently attributed to deficiencies in research transparency and data analysis process. Consequently, as "a rationale for sharing research data, [research reproducibility] is powerful yet problematic".[73] Reproducibility only applies to "certain kinds of research", mostly in regards to experimental sciences.[73]
• Public accessibility: this rationale that "products of public funding should be available to the public" is "found in arguments for open government".[74] While directly inspired by similar arguments made in favor of open access to publications, its range is more limited as scientific open data "has direct benefits to far fewer people, and those benefits vary by stakeholder"[75]
• Research valorization: open scientific data may bring a substantial value to the private sector. This argument is especially used to support "the need for more repositories that can accept and curate research data, for better tools and services to exploit data, and for other investments in knowledge infrastructure".[75]
• Increased research and innovation: open scientific data may significantly enhanced the quality of private and public research. This argument aims for "investing in knowledge infrastructure to sustain research data, curated to high standards of professional practices"[75]

Yet collaboration between the different actors and stakeholders of the data lifecycle is partial. Even within academic institution, cooperation remains limited: "most researchers are making [data related search] without consulting a data manager or librarian."[76]

The global open data movement has partly lost its cohesiveness and identity during the 2010s, as debates over data availability and licensing have been overcome by domain specific issues: "When the focus shifts from calling for access to data to creating data infrastructure and putting data to work, the divergent goals of those who formed an initial open data movement come clearly into view and managing the tensions that emerge can be complex."[77] The very generic scope of open data definition that aims to embrace a very wide set of preexisting data cultures does not well take into account the higher threshold of accessibility and contextualization necessitated by scientific research: "open data in the sense of being free for reuse is a necessary but not sufficient condition for research purposes."[78]

Since the 2000s, surveys of scientific communities have underlined a consistent discrepancy between the ideals of data sharing and their implementation in practice: "When present-day researchers are asked whether they are willing to share their data, most say yes, they are willing to do so. When the same researchers are asked if they do release their data, they typically acknowledge that they have not done so"[79] Open data culture does not emerge in a vacuum and has to content with preexisting culture of scientific data and a range of systemic factors that can discourage data sharing: "In some fields, scholars are actively discouraged from reusing data. (…) Careers are made by charting territory that was previously uncharted."[80]

In 2011, 67% of 1329 scientist agree that lack of data sharing is a "major impediment to progress in science."[81] and yet "only about a third (36%) of the respondents agree that others can access their data easily"[82] In 2016, a survey of researchers in the environment science find overwhelming support easily accessible open data (99% as at least somewhat important) and institutional mandates for open data (88%).[83] Yet, "even with willingness to share data there are discrepancies with common practices, e.g. willingness to spend time and resources preparing and up-loading data".[83] A 2022 study of 1792 data sharing statements from BioMed Central found that less 7% of the authors (123) actually provided the data upon requests.[84]

The prevalence of accessible and findable data is even lower: "Despite several decades of policy moves toward open access to data, the few statistics available reflect low rates of data release or deposit"[85] In a 2011 poll for Science, only 7.6% of researchers shared their data on community repositories with local websites hosted by universities or laboratories being favored instead.[86] Consequently "many bemoaned the lack of common metadata and archives as a main impediment to using and storing data".[86]

According to Borgmann, the paradox of data sharing is partly due to the limitation of open data policies which tends to focus on "mandating or encouraging investigators to release their data" without meeting the "expected demand for data or the infrastructure necessary to support release and reuse"[87]

In 2022, Pujol Priego, Wareham and Romasanta stressed that incentives for the sharing of scientific data were primarily collective and include reproducibility, scientific efficiency, scientific quality, along with more individual retributions such as personal credit[88] Individual benefits include increased visibility: open dataset yield a significant citation advantage but only when they have been shared on an open repository[63]

Important barriers include the need to publish first, legal constraints and concerns about loss of credit of recognition.[89] For individual researchers, datasets may be major assets to barter for "new jobs or new collaborations"[33] and their publication may be difficult to justify unless they "get something of value in return".[33]

Lack of familiarity with data sharing, rather than a straight rejection of the principles of open science is also ultimately a leading obstacle. Several surveys in the early 2010s have shown that researchers "rarely seek data from other investigators and (…) they rarely are asked for their own data."[80] This creates a negative feedback loop as researchers make little effort to ensure data sharing which in turns discouraged effective use whereas "the heaviest demand for reusing data exists in fields with high mutual dependence."[80] The reality of data reuse may also be underestimated as data is not considered to be a prestigious data publication and the original sources are not quoted.[90]

According to a 2021 empirical study of 531,889 articles published by PLOS show that soft incentives and encouragements have a limited impact on data sharing: "journal policies that encourage rather than require or mandate DAS [Data Availability Statement] have only a small effect".[91]

Copyright has been the primary focus of the legal literature of open scientific data until the 2010s. The legality of data sharing was early on identified a crucial issue. In contrast with the sharing of scientific publication, the main impediment was not copyright but uncertainty: "the concept of 'data' [was] a new concept, created in the computer age, while copyright law emerged at the time of printed publications."[94] In theory, copyright and author rights provisions do not apply to simple collections of facts and figures. In practice, the notion of data is much more expansive and could include protected content or creative arrangement of non-copyrightable contents.

The status of data in international conventions on intellectual property is ambiguous. According to the Article 2 of the Berne Convention "every production in the literary, scientific and artistic domain" are protected.[95] Yet, research data is often not an original creation entirely produced by one or several authors, but rather a "collection of facts, typically collated using automated or semiautomated instruments or scientific equipment."[95] Consequently, there are no universal convention on data copyright and debates over "the extent to which copyright applies" are still prevalent, with different outcomes depending on the jurisdiction or the specifics of the dataset.[95] This lack of harmonization stems logically from the novelty of "research data" as a key concept of scientific research: "the concept of 'data' is a new concept, created in the computer age, while copyright law emerged at the time of printed publications."[95]

In the United States, the European Union and several other jurisdictions, copyright laws have acknowledged a distinction between data itself (which can be an unprotected "fact") and the compilation of the data (which can be a creative arrangement).[95] This principle largely predates the contemporary policy debate over scientific data, as the earliest court cases ruled in favor of compilation rights go back to the 19th century.

In the United States compilation rights have been defined in the Copyright Act of 1976 with an explicit mention of datasets: "a work formed by the collection and assembling of pre-existing materials or of data" (Par 101).[96] In its 1991 decision, Feist Publications, Inc., v. Rural Telephone Service Co., the Supreme Court has clarified the extents and the limitations on database copyrights, as the "assembling" should be demonstrably original and the "raw facts" contained in the compilation are still unprotected.[96]

Even in the jurisdiction where the application of the copyright to data outputs remains unsettled and partly theoretical, it has nevertheless created significant legal uncertainties. The frontier between a set of raw facts and an original compilation is not clearly delineated.[97] Although scientific organizations are usually well aware of copyright laws, the complexity of data rights create unprecedented challenges.[98] After 2010, national and supra-national jurisdiction have partly changed their stance in regard to the copyright protection of research data. As the sharing is encouraged, scientific data has been also acknowledged as an informal public good: "policymakers, funders, and academic institutions are working to increase awareness that, while the publications and knowledge derived from research data pertain to the authors, research data needs to be considered a public good so that its potential social and scientific value can be realised"[12]

The European Union provides one of the strongest intellectual property framework for data, with a double layer of rights: copyrights for original compilations (similarly to the United States) and sui generis database rights.[97] Criteria for the originality of compilations have been harmonized across the membership states, by the 1996 Database Directive and by several major case laws settled by the European court of justice such as Infopaq International A/S v Danske Dagblades Forening c or Football Dataco Ltd et al. v Yahoo! UK Ltd. Overall, it has been acknowledged that significant efforts in the making of the dataset are not sufficient to claim compilation rights, as the structure has to "express his creativity in an original manner"[99] The Database Directive has also introduced an original framework of protection for dataset, the sui generis rights that are conferred to any dataset that required a "substantial investment".[100] While they last 15 year, sui generis rights have the potential to become permanent, as they can be renewed for every update of the dataset.

Due to their large scope in length and protection, sui generis rights have initially not been largely acknowledged by the European jurisprudence, which has raised a high bar its enforcement. This cautious approach has been reversed in the 2010s, as the 2013 decision Innoweb BV v Wegener ICT Media BV and Wegener Mediaventions strengthened the positions of database owners and condemned the reuse of non-protected data in web search engines.[101] The consolidation and expansion of database rights remain a controversial topic in European regulations, as it is partly at odds with the commitment of the European Union in favor of data-driven economy and open science.[101] While a few exceptions exists for scientific and pedagogic uses, they are limited in scope (no rights for further reutilization) and they have not been activated in all member states.[101]

Copyright issues with scientific datasets have been further complicated by uncertainties regarding ownership. Research is largely a collaborative activity that involves a wide range of contributions. Initiatives like CRediT (Contributor Roles Taxonomy) have identified 14 different roles, of which 4 are explicitly related to data management (Formal Analysis, Investigation, Data curation and Visualization).[102]

In the United States, ownership of research data is usually "determined by the employer of the researcher", with the principal investigator acting as the caretaker of the data rather than the owner.[103] Until the development of research open data, US institutions have been usually more reluctant to waive copyrights on data than on publications, as they are considered strategic assets.[104] In the European Union, there is no largely agreed framework on the ownership of data.[105]

The additional rights of external stakeholders has also been raised, especially in the context of medical research. Since the 1970s, patients have claimed some form of ownership of the data produced in the context of clinical trials, notably with important controversies concerning 'whether research subjects and patients actually own their own tissue or DNA."[104]

Numerous scientific projects rely on data collection of persons, notably in medical research and the social sciences. In such cases, any policy of data sharing has to be necessarily balanced with the preservation and protection of personal data.[106]

Researchers and, most specifically, principal investigators have been subjected to obligations of confidentiality in several jurisdictions.[106] Health data has been increasingly regulated since the late 20th century, either by law or by sectorial agreements. In 2014, the European Medicines Agency have introduced important changes to the sharing of clinical trial data, in order to prevent the release of all personal details and all commercially relevant information. Such evolution of the European regulation "are likely to influence the global practice of sharing clinical trial data as open data".[107]

Research management plans and practices have to be open, transparent and confidential by design.

Open licenses have been the preferred legal framework to clear the restrictions and ambiguities in the legal definition of scientific data. In 2003, the Berlin Declaration called for a universal waiver of reuse rights on scientific contributions that explicitly included "raw data and metadata".[108]

In contrast with the development of open licenses for publications which occurred on short time frame, the creation of licenses for open scientific data has been a complicated process. Specific rights, like the sui generis database rights in the European Union or specific legal principles, like the distinction between simple facts and original compilation have not been initially anticipated. Until the 2010s, free licenses could paradoxically add more restrictions to the reuse of datasets, especially in regard with attributions (which is not required for non-copyrighted objects like raw facts): "in such cases, when no rights are attached to research data, then there is no ground for licencing the data"[109]

To circumvent the issue several institutions like the Harvard-MIT Data Center started to share the data in the Public Domain.[110] This approach ensures that no right is applied on non-copyrighted items. Yet, the public domain and some associated tools like the Public Domain Mark are not a properly defined legal contract and varies significantly from one jurisdiction to another.[110] First introduced in 2009, the Creative Commons Zero (or CC0) license has been immediately contemplated for data licensing.[111] It has since become "the recommended tool for releasing research data into the public domain".[112] In accordance with the principles of the Berlin Declaration it is not a license but a waiver, as the producer of the data "overtly, fully, permanently, irrevocably and unconditionally waives, abandons, and surrenders all of Affirmer's Copyright and Related Rights".

Alternative approaches have included the design of new free license to disentangle the attribution stacking specific to database rights. In 2009, the Open Knowledge Foundation published the Open Database License which has been adopted by major online projects like OpenStreetMap. Since 2015, all the different Creative Commons licenses have been updated to become fully effective on dataset, as database rights have been explicitly anticipated in the 4.0 version.[109]

In contrast with the broad incitations for data sharing included in the early policies in favor of open scientific data, the complexity and the underlying costs and requirements of scientific data management are increasingly acknowledged: "Data sharing is difficult to do and to justify by the return on investment."[114] Open data is not simply a supplementary task but has to envisioned throughout the entire research process as it "requires changes in methods and practices of research."[114]

The opening of research data creates a new settlement of costs and benefits. Public data sharing introduces a new communication setting that largely contrasts with private exchange of data with research collaborators or partners. The collection, the purpose and the limitation of data has to be explicited as it is not possible to rely on pre-existing informal knowledge: "the documentation and representations are the only means of communicating between data creator and user."[115] Lack of proper documentation means that the burden of recontextualization fall on the potential users and may render the dataset ultimately useless.[116]

Publication requires additionally further verification in regards to the ownership of the data and the potential legal liability if the data is potentially misused. This clarification phase becomes even more complex in international research projects that may overlap several jurisdictions.[117] Data sharing and the application of open science principles also bring significant long term advantages that may not be immediately visible. Documentation of dataset helps to clarify their chain of provenance and ensure that the original data has not been significantly altered or, if this is the case, that all the further treaments are fully documented.[118] Publication under a free license also makes it possible to delegate some tasks such as long term preservation to external actors.

By the end of the 2010s, a new specialized literature on data management for research has emerged to codify the existing practices and regulatory principles.[119][120][121]

The availability of non-open scientific data decays rapidly: in 2014 a retrospective study of biological datasets showed that "the odds of a data set being reported as extant fell by 17% per year"[122] Consequently, the "proportion of data sets that still existed dropped from 100% in 2011 to 33% in 1991".[65] Data loss has also been singled out as a significant issue in major journals like Nature or Science[123]

Surveys of research practices have consistently shown that storage norms, infrastructures and workflow remain insastifying in most disciplines. Storage and preservation of scientific data have been early on identified as critical issues, especially in relation to observational data which are considered essential to preserve, because they are the most difficult to replicate.[35] A 2017-2018 survey of 1372 researchers contacted through the American Geophysical Union shows that only "a quarter and a fifth of the respondents" report good data storage practices.[124] Short term and unsustainable storage remains widespread with 61% of the respondents storing most or all of their data on personal computers.[124] Due to their ease of use at an individual scale, unsustainable storage solution are viewed favorably in most disciplines: "This mismatch between good practices and satisfaction may show that data storage is less important to them than data collection and analysis".[124]

First published in 2012, the reference model of Open Archival Information System state that scientific infrastructure should seek for long term preservation, that is "long enough to be concerned with the impacts of changing technologies, including support for new media and data formats, or with a changing user community".[125] Consequently, good practices of data management imply both on storage (to materially preserve the data) and, even more crucially on curation, "to preserve knowledge about the data to facilitate reuse".[126]

Data sharing on public repository has contributed to mitigate preservation risks due to the long-term commitment of data infrastructures and the potential redundancy of open data. A 2021 study of 50,000 data availability statement published in PLOS One showed that 80% of the dataset could be retrieved automatically and 98% of dataset with a data DOI could be retrieved either automatically or manually. Moreover, accessibility did not decay significantly for older publications: "URLs and DOIs make the data and code associated with papers more likely to be available over time".[127] Significant benefits have not been found when the open data was not properly linked or documented: "Simply requiring that data be shared in some form may not have the desired impact of making scientific data FAIR, as studies have repeatedly demonstrated that many datasets that are ostensibly shared may not actually be accessible."[128]

Research data management can be laid out in a data management plan or DMP.

Data management plans were incepted in 1966 for the specific needs of aeronautic and engineering research, which already faced increasingly complex data frictions.[129] These first examples were focused on material issues associated with the access, transfert and storage of the data: "Until the early 2000s, DMPs were utilised in this manner: in limited fields, for projects of great technical complexity, and for limited mid-study data collection and processing purposes"[130]

After 2000, the implementation of large research infrastructure and the development of open science have changed the scope and the purpose of data management plans. Policy-makers, rather than scientists, have been instrumental in this development: "The first publications to provide general advice and guidance to researchers around the creation of DMPs were published from 2009 following the publications from JISC and the OECD (…) DMP use, we infer, has been imposed onto the research community through external forces"[131]

Empirical studies of data practices in research have "highlighted the need for organizations to offer more formal training and assistance in data management to scientists"[132] In a 2017-2018 international survey of 1372 scientist, most requests for help and formalization were associated with data management plan: "creating data management plans (33.3%); training on best practices in data management (31.3%); assistance on creating metadata to describe data or datasets (27.6%)"[132] The expansion of data collection and data analysis processes have increasingly strained a large range of unformal and non-codified data practices.

The implication of external shareholders in research projects create significant potential tensions with the principles of sharing open data. Contributions from commercial actors can especially rely on some form of exclusivity and appropriation of the final research results. In 2022, Pujol Priego, Wareham and Romasanta created several accommodation strategies to overcome these issues, such as data modularity (with sharing limited to some part of the data) and time delay (with year-long embargoes before the final release of the data).[133]

The Unesco recommendation of Open Science approved in November 2021 define open science infrastructures as "shared research infrastructures that are needed to support open science and serve the needs of different communities"[134] Open science infrastructures have been recognized has major factor in the implementation and the development of data sharing policies.[135]

Leading forms of infrastructures for open scientific data include data repositories, data analysis platform, indexes, digitized library or digitized archives.[136][137] Infrastructures ensure that the costs of publishing, maintaining, and indexing datasets is not entirely supported by individual researchers and institutions. They are additionally key stakeholders in the definition and adoption of open data standards, especially in regards to licensing or documentation.

By the end of the 1990s, the creation of public scientific computing infrastructure became a major policy issue:[138] "The lack of infrastructure to support release and reuse was acknowledged in some of the earliest policy reports on data sharing."[135] The first wave of web-based scientific projects in the 1990s and the early 2000s revealed critical issues of sustainability. As funding was allocated on a specific time period, critical databases, online tools or publishing platforms could hardly be maintained[28] and project managers were faced with a valley of death "between grant funding and ongoing operational funding".[139] After 2010, the consolidation and expansion of commercial scientific infrastructure such as the acquisition of the open repositories Digital Commons and SSRN by Elsevie had further entailed calls to secure "community-controlled infrastructure".[140] In 2015, Cameron Neylon, Geoffrey Bilder and Jenifer Lin defined an influential series of Principles for Open Scholarly Infrastructure[141] that has been endorsed by leading infrastructures such as Crossref,[142] OpenCitations[143] or Data Dryad[144] By 2021, public services and infrastructures for research have largely endorsed open science as an integral part of their activity and identity: "open science is the dominant discourse to which new online services for research refer."[145] According to the 2021 Roadmap of the European Strategy Forum on Research Infrastructures (ESFRI), major legacy infrastructures in Europe have embraced open science principles. "Most of the Research Infrastructures on the ESFRI Roadmap are at the forefront of Open Science movement and make important contributions to the digital transformation by transforming the whole research process according to the Open Science paradigm."[146]

Open science infrastructure represents a higher level of commitment on data sharing. They rely on significant and recurrent investments to ensure that data is effectively maintained and documented and "add value to data through metadata, provenance, classification, standards for data structures, and migration".[147] Furthermore, infrastructures need to be integrated to the norms and expected uses of the scientific communities they mean to serve: "The most successful become reference collections that attract longer-term funding and can set standards for their communities"[137] Maintaining open standards is one of the main challenge identified by leading European open infrastructures, as it implies choosing among competing standards in some case, as well as ensuring that the standards are correctly updated and accessible through APIs or other endpoints.[148]

The conceptual definition of open science infrastructures has been largely influenced by the analysis of Elinor Ostrom on the commons and more specifically on the knowledge commons. In accordance with Ostrom, Cameron Neylon understates that open infrastructures are not only characterized by the management of a pool of common resources but also by the elaboration of common governance and norms.[149] The diffusion of open scientific data also raise stringent issues of governance. In regards to the determination of the ownership of the data, the adoption of free license and the enforcement of regulations in regard to privacy, "continual negotiation is necessary" and involve a wide range of stakeholders.[150]

Beyond their integration in specific scientific communities, open science infrastructure have strong ties with the open source and the open data movements. 82% of the European infrastructures surveyed by SPARC claim to have partially built open source software and 53% have their entire technological infrastructure in open source.[151] Open science infrastructures preferably integrate standards from other open science infrastructures. Among European infrastructures: "The most commonly cited systems – and thus essential infrastructure for many – are ORCID, Crossref, DOAJ, BASE, OpenAIRE, Altmetric, and Datacite, most of which are not-for-profit".[152] Open science infrastructure are then part of an emerging "truly interoperable Open Science commons" that hold the premise of "researcher-centric, low-cost, innovative, and interoperable tools for research, superior to the present, largely closed system."[153]