Growing citizen science for conservation to support diverse project objectives and the motivations of volunteers

2019 ◽  
Vol 25 (4) ◽  
pp. 342
Author(s):  
Shane Orchard

Interest in citizen science has been increasing worldwide, accompanied by research oriented at identifying needs and recommending options for supporting the field. In this context, synthesising research on citizen science is becoming increasingly important. This short communication reviews recent findings in the New Zealand literature with a focus on community-based monitoring, and identifies considerations for supporting further growth of the citizen science field. The perspective offered here is that reducing barriers to participation is the surest way to maintain citizen science momentum, and that this will be assisted by a comprehensive understanding of diversity in the motivations for citizen science activities on the ground. Participant-focussed considerations are useful in both the research design stage and in the context of identifying methods for longer term support.

2019 ◽  
Author(s):  
Marcelino Jr Lunag ◽  
Jessie C. Elauria ◽  
Juanito D. Burguillos

This study confirms that lack of space due to high population density restricts household members and the barangay to comply with the existing law regarding composting. With these, community involvement in the design stage of compost bin as initial stage was done accordingly. The participants were voluntarily interviewed and were given questionnaires, which was endorsed and approved by barangay committee.


2020 ◽  
Vol 1 (4) ◽  
pp. 5-10
Author(s):  
V. Barysheva ◽  
O. Druzhinina

The article is devoted to the analysis of the system object from the point of view of design from design, sociocultural and philosophical positions. The authors systematize the definitions of a system object of design proposed in the 1960–1980s by theorists and practitioners, art historians, cultural experts and philosophers from different countries, including Russia, which allows a comprehensive understanding of the phenomenon of design culture. This article is devoted to the characteristic properties of the system object in design. They were considered and analyzed on the example of the «Absheron» design-program when designing of agricultural village). This concept was developed at the All-Union Scientific Research Institute of Technical Aesthetics (VNIITE) in 1983. Using the same example, the features of the approach to designing a system object in design was observed not only as a separate product, but as a sociocultural situation that constantly changes at each design stage.


2021 ◽  
Vol 10 (4) ◽  
pp. 207
Author(s):  
Annie Gray ◽  
Colin Robertson ◽  
Rob Feick

Citizen science initiatives span a wide range of topics, designs, and research needs. Despite this heterogeneity, there are several common barriers to the uptake and sustainability of citizen science projects and the information they generate. One key barrier often cited in the citizen science literature is data quality. Open-source tools for the analysis, visualization, and reporting of citizen science data hold promise for addressing the challenge of data quality, while providing other benefits such as technical capacity-building, increased user engagement, and reinforcing data sovereignty. We developed an operational citizen science tool called the Community Water Data Analysis Tool (CWDAT)—a R/Shiny-based web application designed for community-based water quality monitoring. Surveys and facilitated user-engagement were conducted among stakeholders during the development of CWDAT. Targeted recruitment was used to gather feedback on the initial CWDAT prototype’s interface, features, and potential to support capacity building in the context of community-based water quality monitoring. Fourteen of thirty-two invited individuals (response rate 44%) contributed feedback via a survey or through facilitated interaction with CWDAT, with eight individuals interacting directly with CWDAT. Overall, CWDAT was received favourably. Participants requested updates and modifications such as water quality thresholds and indices that reflected well-known barriers to citizen science initiatives related to data quality assurance and the generation of actionable information. Our findings support calls to engage end-users directly in citizen science tool design and highlight how design can contribute to users’ understanding of data quality. Enhanced citizen participation in water resource stewardship facilitated by tools such as CWDAT may provide greater community engagement and acceptance of water resource management and policy-making.


2019 ◽  
Vol 102 (10) ◽  
pp. 9382-9388 ◽  
Author(s):  
C.G. Todd ◽  
B. Bruce ◽  
L. Deeming ◽  
G. Zobel

Author(s):  
Tarun Reddy Katapally

UNSTRUCTURED Citizen science enables citizens to actively contribute to all aspects of the research process, from conceptualization and data collection, to knowledge translation and evaluation. Citizen science is gradually emerging as a pertinent approach in population health research. Given that citizen science has intrinsic links with community-based research, where participatory action drives the research agenda, these two approaches could be integrated to address complex population health issues. Community-based participatory research has a strong record of application across multiple disciplines and sectors to address health inequities. Citizen science can use the structure of community-based participatory research to take local approaches of problem solving to a global scale, because citizen science emerged through individual environmental activism that is not limited by geography. This synergy has significant implications for population health research if combined with systems science, which can offer theoretical and methodological strength to citizen science and community-based participatory research. Systems science applies a holistic perspective to understand the complex mechanisms underlying causal relationships within and between systems, as it goes beyond linear relationships by utilizing big data–driven advanced computational models. However, to truly integrate citizen science, community-based participatory research, and systems science, it is time to realize the power of ubiquitous digital tools, such as smartphones, for connecting us all and providing big data. Smartphones have the potential to not only create equity by providing a voice to disenfranchised citizens but smartphone-based apps also have the reach and power to source big data to inform policies. An imminent challenge in legitimizing citizen science is minimizing bias, which can be achieved by standardizing methods and enhancing data quality—a rigorous process that requires researchers to collaborate with citizen scientists utilizing the principles of community-based participatory research action. This study advances SMART, an evidence-based framework that integrates citizen science, community-based participatory research, and systems science through ubiquitous tools by addressing core challenges such as citizen engagement, data management, and internet inequity to legitimize this integration.


2021 ◽  
Author(s):  
◽  
Gloria Fraser

<p>While we know that rainbow people in Aotearoa New Zealand (that is, people of diverse sexualities, genders, and sex characteristics) experience high rates of adverse mental health outcomes, we know much less about the extent to which Aotearoa’s rainbow community members are receiving the mental health support they need. To address this gap I used mixed methods and a reflexive community-based approach to extend current understandings of rainbow mental health support experiences, and to explore how the provision of mental health care can be improved for rainbow people in New Zealand.  I first conducted interviews with 34 rainbow community young adults about their experiences of accessing mental health support. My thematic analysis showed that rainbow people across New Zealand faced significant structural barriers to accessing mental health support. Participants understood mental health settings as embedded within a heteronormative and cisnormative societal context, rather than as a safe place outside this context. This, together with a widespread silence from mental health professionals around rainbow identity, meant that participants actively negotiated coming out in mental health settings. Participants shared a variety of perspectives as to whether it should be standard practice for mental health professionals to ask about rainbow identities, but agreed on a number of subtle acts that could communicate a professional or service is rainbow-friendly. Knowledge about sexuality, gender, and sex characteristic diversity, together with clinical skills of empathy, validation, and affirmation, were described as key components for the provision of effective mental health support.  I conducted a second thematic analysis of data from a subset of the initial interviews, in which 13 participants discussed their experiences of accessing gender-affirming healthcare. Participants reported a lack of funding for gender-affirming healthcare in New Zealand, and described its provision a “postcode lottery”; the care available was largely dependent on the region participants were living in. Mental health assessments for accessing gender-affirming care were often described as tests of whether participants were “really” transgender, and participants discussed the need to express their gender in a particular way in order to access the healthcare they needed.  Thematic analyses of interview data informed the development of an online survey about rainbow peoples’ experiences of accessing mental health support and gender-affirming healthcare in New Zealand (n = 1575). Survey results closely reflected interview findings, indicating that rainbow people have mixed experiences in New Zealand’s mental health settings, and that accessing gender-affirming healthcare is a lengthy and convoluted process.   Finally, interview and survey data were used to develop a resource for mental health professionals, to guide their work with rainbow clients. I sought and incorporated feedback from key stakeholders (n = 108) during resource development. I then distributed the resource to mental health professionals around New Zealand, both in print and online.  Overall, my research shows that widespread knowledge gaps compromise the ability of New Zealand’s mental health professionals to provide culturally competent support to rainbow clients. Knowledge from this thesis can be used to increase awareness of rainbow community members’ mental health support needs, and to inform mental health professionals’ training and self-reflection around sexuality, gender, and sex characteristic diversity.</p>


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