3 Collaboration and Thinking Preferences
3.1 Thinking preferences
3.1.1 Learning Objectives
An activity and discussion that will provide:
- Opportunity to get to know fellow participants and trainers
- An introduction to variation in thinking preferences
3.1.3 About the Whole Brain Thinking System
Everyone thinks differently. The way individuals think guides the way they work, and the way groups of individuals think guides how teams work. Understanding thinking preferences facilitates effective collaboration and team work.
The Whole Brain Model, developed by Ned Herrmann, builds upon early conceptualizations of brain functioning. For example, the left and right hemispheres were thought to be associated with different types of information processing while our neocortex and limbic system would regulate different functions and behaviours.
The Herrmann Brain Dominance Instrument (HBDI) provides insight into dominant characteristics based on thinking preferences. There are four major thinking styles that reflect the left cerebral, left limbic, right cerebral and right limbic.
- Analytical (Blue)
- Practical (Green)
- Relational (Red)
- Experimental (Yellow)
These four thinking styles are characterized by different traits. Those in the BLUE quadrant have a strong logical and rational side. They analyze information and may be technical in their approach to problems. They are interested in the ‘what’ of a situation. Those in the GREEN quadrant have a strong organizational and sequential side. They like to plan details and are methodical in their approach. They are interested in the ‘when’ of a situation. The RED quadrant includes those that are feelings-based in their apporach. They have strong interpersonal skills and are good communicators. They are interested in the ‘who’ of a situation. Those in the YELLOW quadrant are ideas people. They are imaginative, conceptual thinkers that explore outside the box. Yellows are interested in the ‘why’ of a situation.
Undertsanding how people think and process information helps us understand not only our own approach to problem solving, but also how individuals within a team can contribute. There is great value in diversity of thinking styles within collaborative teams, each type bringing stengths to different aspects of project development.
Of course, most of us identify with thinking styles in more than one quadrant and these different thinking preferences reflect a complex self made up of our rational, theoretical self; our ordered, safekeeping self; our emotional, interpersonal self; and our imaginitive, experimental self.
3.1.3.1 Bonus Activity: Your Complex Self
Using the statements contrained within this document, plot the quadrilateral representing your complex self.
3.2 Developing a Code of Conduct
Whether you are joining a lab group or establishing a new collaboration, articulating a set of shared agreements about how people in the group will treat each other will help create the conditions for successful collaboration. If agreements or a code of conduct do not yet exist, invite a conversation among all members to create them. Co-creation of a code of conduct will foster collaboration and engagement as a process in and of itself, and is important to ensure all voices heard such that your code of conduct represents the perspectives of your community. If a code of conduct already exists, and your community will be a long-acting collaboration, you might consider revising the code of conduct. Having your group ‘sign off’ on the code of conduct, whether revised or not, supports adoption of the principles.
When creating a code of conduct, consider both the behaviors you want to encourage and those that will not be tolerated. For example, the Openscapes code of conduct includes Be respectful, honest, inclusive, accommodating, appreciative, and open to learning from everyone else. Do not attack, demean, disrupt, harass, or threaten others or encourage such behavior.
Below are other example codes of conduct:
3.4 Data Sharing and Reuse Policies
As with authorship agreements, it is valuable to establish a shared agreement around handling of data when embarking on collaborative projects. Data collected as part of a funded research activity will typically have been managed as part of the Data Management Plan (DMP) associated with that project. However, collaborative research brings together data from across research projects with different data management plans and can include publicly accessible data from repositories where no management plan is available. For these reasons, a discussion and agreement around the handling of data brought into and resulting from the collaboration is warranted and management of this new data may benefit from going through a data management planning process. Below we discuss example data agreements.
The example data policy template provided by the Arctic Data Center addresses three categories of data.
- Individual data not in the public domain
- Individual data with public access
- Derived data resulting from the project
For the first category, the agreement considers conditions under which those data may be used and permissions associated with use. It also addresses access and sharing. In the case of individual, publicly accessible data, the agreement stipulates that the team will abide by the attribution and usage policies that the data were published under, noting how those requirements we met. In the case of derived data, the agreement reads similar to a DMP with consideration of making the data public; management, documentation and archiving; pre-publication sharing; and public sharing and attribution. As research data objects receive a persistent identifier (PID), often a DOI, there are citable objects and consideration should be given to authorship of data, as with articles.
The following example lab policy from the Wolkovich Lab combines data management practices with authorship guidelines and data sharing agreements. It provides a lot of detail about how this lab approaches data use, attribution and authorship. For example:
3.4.0.1 Policy Preview
This policy is communicated with all incoming lab members, from undergraduate to postdocs and visiting scholars, and is shared here with permission from Dr Elizabeth Wolkovich.
3.4.1 Community Principles: CARE and FAIR
The CARE and FAIR Principles were introduced previously in the context of introducing the Arctic Data Center and our data submission and documentation process. In this section we will dive a little deeper.
To recap, the Arctic Data Center is an openly-accessible data repository and the data published through the repository is open for anyone to reuse, subject to conditions of the license (at the Arctic Data Center, data is released under one of two licenses: CC-0 Public Domain and CC-By Attribution 4.0). In facilitating use of data resources, the data stewardship community have converged on principles surrounding best practices for open data management One set of these principles is the FAIR principles. FAIR stands for Findable, Accessible, Interoperable, and Reproducible.
The “Fostering FAIR Data Practices in Europe” project found that it is more monetarily and timely expensive when FAIR principles are not used, and it was estimated that 10.2 billion dollars per years are spent through “storage and license costs to more qualitative costs related to the time spent by researchers on creation, collection and management of data, and the risks of research duplication.” FAIR principles and open science are overlapping concepts, but are distinctive concepts. Open science supports a culture of sharing research outputs and data, and FAIR focuses on how to prepare the data.
Another set of community developed principles surrounding open data are the CARE Principles. The CARE principles for Indigenous Data Governance complement the more data-centric approach of the FAIR principles, introducing social responsibility to open data management practices. The CARE Principles stand for:
- Collective Benefit - Data ecosystems shall be designed and function in ways that enable Indigenous Peoples to derive benefit from the data
- 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.
- Responsibility - Those working with Indigenous data have a responsibility to share how those data are used to support Indigenous Peoples’ self-determination and collective benefit. Accountability requires meaningful and openly available evidence of these efforts and the benefits accruing to Indigenous Peoples.
- Ethics - Indigenous Peoples’ rights and wellbeing should be the primary concern at all stages of the data life cycle and across the data ecosystem.
The CARE principles align with the FAIR principles by outlining guidelines for publishing data that is findable, accessible, interoperable, and reproducible while at the same time, accounts for Indigenous’ Peoples rights and interests. Initially designed to support Indigenous data sovereignty, CARE principles are now being adopted across domains, and many researchers argue they are relevant for both Indigenous Knowledge and data, as well as data from all disciplines (Carroll et al., 2021). These principles introduce a “game changing perspective” that encourages transparency in data ethics, and encourages data reuse that is purposeful and intentional that aligns with human well-being aligns with human well-being (Carroll et al., 2021).
3.5 Research Data Publishing Ethics
For over 20 years, the Committee on Publication Ethics (COPE) has provided trusted guidance on ethical practices for scholarly publishing. The COPE guidelines have been broadly adopted by academic publishers across disciplines, and represent a common approach to identify, classify, and adjudicate potential breaches of ethics in publication such as authorship conflicts, peer review manipulation, and falsified findings, among many other areas. Despite these guidelines, there has been a lack of ethics standards, guidelines, or recommendations for data publications, even while some groups have begun to evaluate and act upon reported issues in data publication ethics.
To address this gap, the Force 11 Working Group on Research Data Publishing Ethics was formed as a collaboration among research data professionals and the Committee on Publication Ethics (COPE) “to develop industry-leading guidance and recommended best practices to support repositories, journal publishers, and institutions in handling the ethical responsibilities associated with publishing research data.” The group released the “Joint FORCE11 & COPE Research Data Publishing Ethics Working Group Recommendations” (Puebla, Lowenberg, and WG 2021), which outlines recommendations for four categories of potential data ethics issues:
- Authorship and Contribution Conflicts
- Authorship omissions
- Authorship ordering changes / conflicts
- Institutional investigation of author finds misconduct
- Legal/regulatory restrictions
- Copyright violation
- Insufficient rights for deposit
- Breaches of national privacy laws (GPDR, CCPA)
- Breaches of biosafety and biosecurity protocols
- Breaches of contract law governing data redistribution
- Risks of publication or release
- Risks to human subjects
- Lack of consent
- Breaches of himan rights
- Release of personally identifiable information (PII)
- Risks to species, ecosystems, historical sites
- Locations of endangered species or historical sites
- Risks to communities or societies
- Data harvested for profit or surveillance
- Breaches of data sovereignty
- Risks to human subjects
- Rigor of published data
- Unintentional errors in collection, calculation, display
- Un-interpretable data due to lack of adequate documentation
- Errors of of study design and inference
- Data manipulation or fabrication
Guidelines cover what actions need to be taken, depending on whether the data are already published or not, as well as who should be involved in decisions, who should be notified of actions, and when the public should be notified. The group has also published templates for use by publishers and repositories to announce the extent to which they plan to conform to the data ethics guidelines.
Discussion: Data publishing policies
At the Arctic Data Center, we need to develop policies and procedures governing how we react to potential breaches of data publication ethics. In this exercise, break into groups to provide advice on how the Arctic Data Center should respond to reports of data ethics issues, and whether we should adopt the Joint FORCE11 & COPE Research Data Publishing Ethics Working Group Policy Templates for repositories. In your discussion, consider:
- Should the repository adopt the repository policy templates from Force11?
- Who should be involved in evaluation of the merits of ethical cases reported to ADC?
- Who should be involved in deciding the actions to take?
- What are the range of responses that the repository should consider for ethical breaches?
- Who should be notified when a determination has been made that a breach has occurred?
You might consider a hypothetical scenario such as the following in considering your response.
The data coordinator at the Arctic Data Center receives an email in 2022 from a prior postdoctoral fellow who was employed as part of an NSF-funded project on microbial diversity in Alaskan tundra ecosystems. The email states that a dataset from 2014 in the Arctic Data Center was published with the project PI as author, but omits two people, the postdoc and an undergraduate student, as co-authors on the dataset. The PI retired in 2019, and the postdoc asks that they be added to the author list of the dataset to correct the historical record and provide credit.
3.6 Extra Reading
- Cheruvelil, K. S., Soranno, P. A., Weathers, K. C., Hanson, P. C., Goring, S. J., Filstrup, C. T., & Read, E. K. (2014). Creating and maintaining high-performing collaborative research teams: The importance of diversity and interpersonal skills. Frontiers in Ecology and the Environment, 12(1), 31-38. DOI: 10.1890/130001
- Carroll, S. R., Garba, I., Figueroa-Rodríguez, O. L., Holbrook, J., Lovett, R., Materechera, S., … Hudson, M. (2020). The CARE Principles for Indigenous Data Governance. Data Science Journal, 19(1), 43. DOI: http://doi.org/10.5334/dsj-2020-043