What Could Citizens’ Assemblies Do for American Politics?


Essay by Nick Romeo: “Last July, an unusual letter arrived at Kathryn Kundmueller’s mobile home, in central Oregon. It invited her to enter a lottery that would select thirty residents of Deschutes County to deliberate for five days on youth homelessness—a visible and contentious issue in an area where the population and cost of living have spiked in recent years. Those chosen would be paid for their time—almost five hundred dollars—and asked to develop specific policy recommendations.

Kundmueller was being invited to join what is known as a citizens’ assembly. These gatherings do what most democracies only pretend to: trust normal people to make decisions on difficult policy questions. Many citizens’ assemblies follow a basic template. They impanel a random but representative cross-section of a population, give them high-quality information on a topic, and ask them to work together to reach a decision. In Europe, such groups have helped spur reform of the Irish constitution in order to legalize abortion, guided an Austrian pharmaceutical heiress on how to give away her wealth, and become a regular part of government in Paris and Belgium. Though still rare in America, the model reflects the striking idea that fundamental problems of politics—polarization, apathy, manipulation by special interests—can be transformed through radically direct democracy.

Kundmueller, who is generally frustrated by politics, was intrigued by the letter. She liked the prospect of helping to shape local policy, and the topic of housing insecurity had a particular resonance for her. As a teen-ager, following a falling-out with her father, she spent months bouncing between friends’ couches in Vermont. When she moved across the country to San Jose, after college, she lived in her car for a time while she searched for a stable job. She worked in finance but became disillusioned; now in her early forties, she ran a small housecleaning business. She still thought about living in a van and renting out her mobile home to save money…(More)”.

Sortition: Past and Present


Introduction to the Journal of Sortition: “Since ancient times sortition (random selection by lot) has been used both to distribute political office and as a general prophylactic against factionalism and corruption in societies as diverse as classical-era Athens and the Most Serene Republic of Venice. Lotteries have also been employed for the allocation of scarce goods such as social housing and school places to eliminate bias and ensure just distribution, along with drawing lots in circumstances where unpopular tasks or tragic choices are involved (as some situations are beyond rational human decision-making). More recently, developments in public opinion polling using random sampling have led to the proliferation of citizens’ assemblies selected by lot. Some activists have even proposed such bodies as an alternative to elected representatives. The Journal of Sortition benefits from an editorial board with a wide range of expertise and perspectives in this area. In this introduction to the first issue, we have invited our editors to explain why they are interested in sortition, and to outline the benefits (and pitfalls) of the recent explosion of interest in the topic…(More)”.

The Bridging Dictionary


About: “What if generative AI could help us understand people with opposing views better just by showing how they use common words and phrases differently? That’s the deceptively simple-sounding idea behind a new experiment from MIT’s Center for Constructive Communication (CCC). 

It’s called the Bridging Dictionary (BD), a research prototype that’s still very much a work in progress – one we hope your feedback will help us improve.

The Bridging Dictionary identifies words and phrases that both reflect and contribute to sharply divergent views in our fractured public sphere. That’s the “dictionary” part. If that’s all it did, we could just call it the “Frictionary.” But the large language model (LLM) that undergirds the BD also suggests less polarized alternatives – hence “bridging.” 

In this prototype, research scientist Doug Beeferman and a team at CCC led by Maya Detwiller and Dennis Jen used thousands of transcripts and opinion articles from foxnews.com and msnbc.com as proxies for the conversation on the right and the left. You’ll see the most polarized words and phrases when you sample the BD for yourself, but you can also plug any term of your choosing into the search box. (For a more complete explanation of the methodology behind the BD, see https://bridgingdictionary.org/info/ .)…(More)”.

The People Say


About: “The People Say is an online research hub that features first-hand insights from older adults and caregivers on the issues most important to them, as well as feedback from experts on policies affecting older adults. 

This project particularly focuses on the experiences of communities often under-consulted in policymaking, including older adults of color, those who are low income, and/or those who live in rural areas where healthcare isn’t easily accessible. The People Say is funded by The SCAN Foundation and developed by researchers and designers at the Public Policy Lab.

We believe that effective policymaking listens to most-affected communities—but policies and systems that serve older adults are typically formed with little to no input from older adults themselves. We hope The People Say will help policymakers hear the voices of older adults when shaping policy…(More)”

In the hands of a few: Disaster recovery committee networks


Paper by Timothy Fraser, Daniel P. Aldrich, Andrew Small and Andrew Littlejohn: “When disaster strikes, urban planners often rely on feedback and guidance from committees of officials, residents, and interest groups when crafting reconstruction policy. Focusing on recovery planning committees after Japan’s 2011 earthquake, tsunami, and nuclear disasters, we compile and analyze a dataset on committee membership patterns across 39 committees with 657 members. Using descriptive statistics and social network analysis, we examine 1) how community representation through membership varied among committees, and 2) in what ways did committees share members, interlinking members from certain interests groups. This study finds that community representation varies considerably among committees, negatively related to the prevalence of experts, bureaucrats, and business interests. Committee membership overlap occurred heavily along geographic boundaries, bridged by engineers and government officials. Engineers and government bureaucrats also tend to be connected to more members of the committee network than community representatives, giving them prized positions to disseminate ideas about best practices in recovery. This study underscores the importance of diversity and community representation in disaster recovery planning to facilitate equal participation, information access, and policy implementation across communities…(More)”.

Participatory seascape mapping: A community-based approach to ocean governance and marine conservation


Paper by Isabel James: “Despite the global proliferation of ocean governance frameworks that feature socioeconomic variables, the inclusion of community needs and local ecological knowledge remains underrepresented. Participatory mapping or Participatory GIS (PGIS) has emerged as a vital method to address this gap by engaging communities that are conventionally excluded from ocean planning and marine conservation. Originally developed for forest management and Indigenous land reclamation, the scholarship on PGIS remains predominantly focused on terrestrial landscapes. This review explores recent research that employs the method in the marine realm, detailing common methodologies, data types and applications in governance and conservation. A typology of ocean-centered PGIS studies was identified, comprising three main categories: fisheries, habitat classification and blue economy activities. Marine Protected Area (MPA) design and conflict management are the most prevalent conservation applications of PGIS. Case studies also demonstrate the method’s effectiveness in identifying critical marine habitats such as fish spawning grounds and monitoring endangered megafauna. Participatory mapping shows particular promise in resource and data limited contexts due to its ability to generate large quantities of relatively reliable, quick and low-cost data. Validation steps, including satellite imagery and ground-truthing, suggest encouraging accuracy of PGIS data, despite potential limitations related to human error and spatial resolution. This review concludes that participatory mapping not only enriches scientific research but also fosters trust and cooperation among stakeholders, ultimately contributing to more resilient and equitable ocean governance…(More)”.

Citizen science as an instrument for women’s health research


Paper by Sarah Ahannach et al: “Women’s health research is receiving increasing attention globally, but considerable knowledge gaps remain. Across many fields of research, active involvement of citizens in science has emerged as a promising strategy to help align scientific research with societal needs. Citizen science offers researchers the opportunity for large-scale sampling and data acquisition while engaging the public in a co-creative approach that solicits their input on study aims, research design, data gathering and analysis. Here, we argue that citizen science has the potential to generate new data and insights that advance women’s health. Based on our experience with the international Isala project, which used a citizen-science approach to study the female microbiome and its influence on health, we address key challenges and lessons for generating a holistic, community-centered approach to women’s health research. We advocate for interdisciplinary collaborations to fully leverage citizen science in women’s health toward a more inclusive research landscape that amplifies underrepresented voices, challenges taboos around intimate health topics and prioritizes women’s involvement in shaping health research agendas…(More)”.

My Voice, Your Voice, Our Voice: Attitudes Towards Collective Governance of a Choral AI Dataset


Paper by Jennifer Ding, Eva Jäger, Victoria Ivanova, and Mercedes Bunz: “Data grows in value when joined and combined; likewise the power of voice grows in ensemble. With 15 UK choirs, we explore opportunities for bottom-up data governance of a jointly created Choral AI Dataset. Guided by a survey of chorister attitudes towards generative AI models trained using their data, we explore opportunities to create empowering governance structures that go beyond opt in and opt out. We test the development of novel mechanisms such as a Trusted Data Intermediary (TDI) to enable governance of the dataset amongst the choirs and AI developers. We hope our findings can contribute to growing efforts to advance collective data governance practices and shape a more creative, empowering future for arts communities in the generative AI ecosystem…(More)”.

Towards Civic Digital Twins: Co-Design the Citizen-Centric Future of Bologna


Paper by Massimiliano Luca et al: “We introduce Civic Digital Twin (CDT), an evolution of Urban Digital Twins designed to support a citizen-centric transformative approach to urban planning and governance. CDT is being developed in the scope of the Bologna Digital Twin initiative, launched one year ago by the city of Bologna, to fulfill the city’s political and strategic goal of adopting innovative digital tools to support decision-making and civic engagement. The CDT, in addition to its capability of sensing the city through spatial, temporal, and social data, must be able to model and simulate social dynamics in a city: the behavior, attitude, and preference of citizens and collectives and how they impact city life and transform transformation processes. Another distinctive feature of CDT is that it must be able to engage citizens (individuals, collectives, and organized civil society) and other civic stakeholders (utilities, economic actors, third sector) interested in co-designing the future of the city. In this paper, we discuss the motivations that led to the definition of the CDT, define its modeling aspects and key research challenges, and illustrate its intended use with two use cases in urban mobility and urban development…(More)”.

Social licence for health data


Evidence Brief by NSW Government: “Social licence, otherwise referred to as social licence to operate, refers to an approval or consensus from the society members or the community for the users, either as a public or private enterprise or individual, to use their health data as desired or accepted under certain conditions. Social licence is a dynamic and fluid concept and is subject to change over time often influenced by societal and contextual factors.
The social licence is usually indicated through ongoing engagement and negotiations with the public and is not a contract with strict terms and conditions. It is, rather, a moral and ethical responsibility assumed by the data users based on trust and legitimacy, It supplements the techno-legal mechanisms to regulate the use of data.
For example, through public engagement, certain values and principles can emerge as pertinent to public support for using their data. Similarly, the public may view certain activities relating to their data use as acceptable and beneficial, implying their permission for certain activities or usecase scenarios. Internationally, although not always explicitly referred to as a social licence, the most common approach to establishing public trust and support and identifying common grounds or agreements on acceptable practices for use of data is through public engagement. Engagement methods and mechanisms for gaining public perspectives vary across countries (Table 1).
− Canada – Health Data Research Network Canada reports on social licence for uses of health data, based on deliberative discussions with 20 experienced public and patient advisors. The output is a list of agreements and disagreements on what uses and users of health data have social licence.
− New Zealand – In 2022, the Ministry of Health commissioned a survey on public perceptions on use of personal health information. This report identified conditions under which the public supports the re-use of their data…(More)”.