Abstract
Cultural ecosystem services provide intangible benefits such as recreation and aesthetic enjoyment but are difficult to quantify compared to provisioning or regulating ecosystem services. Recent technologies offer alternative indicators, such as social media data, to identify popular locations and their features. This study demonstrates how large volumes of citizen science and social media data can be analyzed to reveal patterns of human interactions with nature through unconventional, scalable methods. By applying spatial statistical methods, data from the citizen science platform iNaturalist are analyzed and compared with ground-truth visitation data. To minimize data bias, records are grouped by taxonomic information and applied to the metropolitan area of Seoul, South Korea (2005–2022). The taxonomic information included in the iNaturalist data were investigated using a standard global biodiversity database. The results show citizen science data effectively quantify public preferences for scenic locations, offering a novel approach to mapping cultural ecosystem services when traditional data are unavailable. This method highlights the potential of large-scale citizen-generated data for conservation, urban planning, and policy development. However, challenges like bias in user-generated content, uneven ecosystem coverage, and the over- or under-representation of locations remain. Addressing these issues and integrating additional metadata—such as time of visit, demographics, and seasonal trends—could provide deeper insights into human–nature interactions. Overall, the proposed method opens up new possibilities for using non-traditional data sources to assess and map ecosystem services, providing valuable information for conservation efforts, urban planning, and environmental policy development.
1. Introduction
We obtain numerous benefits from nature through various forms of relationships with it [1,2]. These diverse values of nature include instrumental (e.g., health benefits of recreation), intrinsic (e.g., the non-use value of species), and relational values (e.g., sense of place, cultural meaning of activities) [2]. Collectively, these non-material contributions of nature to people are often referred to as cultural ecosystem services (CESs), encompassing physical and mental health benefits, landscape aesthetics, and social relations [3,4,5]. CESs play a significant role in enhancing human well-being, fostering enjoyment, and creating a sense of place imparted by nature [6].
Species, as integral components of ecosystems, are pivotal in sustaining the cultural benefits derived from nature [7]. The growing recognition of the role of species and biodiversity in human–nature relationships highlights their importance [8,9]. For instance, certain species enhance the aesthetic and recreational value of landscapes through activities such as wildlife watching [10,11], hiking [12,13], and photography [14,15]. In many regions, specific species hold cultural significance, forming the basis for traditional cultural practices, rituals, and festivals, thereby symbolizing cultural heritage and collective memory [16].
Despite these benefits, increasing urbanization has led to a growing disconnect between people and nature [17,18]. Urban areas, which host dense human populations, present unique challenges and opportunities for biodiversity conservation and the CESs derived from it [19,20]. Urban environments often support diverse species, making them critical for understanding human–nature interactions [21,22]. Activities such as species observation in urban areas not only raise public awareness but also provide valuable data on wildlife distribution and behavior in rapidly changing environments [23,24]. Additionally, the use of digital tools like citizen science platforms and mobile apps amplifies these efforts by enabling broader participation in biodiversity monitoring [25]. These tools have significant social impacts, fostering inclusivity and community engagement, bridging gaps between urban residents and nature, and promoting environmental stewardship among diverse populations [26]. As urbanization is predicted to expand to 68% of the global population by 2050 [27], understanding how urban residents engage with nature and species is essential for fostering a stronger human–nature connection. By enabling public participation in biodiversity monitoring, these tools can provide valuable data to inform conservation strategies, identify at-risk species, and track ecological changes in urban environments [28,29].
However, compared to other ecosystem services, CESs and biodiversity remain challenging to quantify and map, which hinders effective natural resource management [30,31]. To address this, alternative approaches, such as crowdsourced social media data, have been employed to explore human–species relationships and patterns in nature appreciation [32,33]. In recent years, crowdsourced data have proven invaluable for environmental monitoring and species conservation [34,35,36]. These data not only help analyze how people enjoy nature, e.g., [37], but also aid in data acquisition for biodiversity monitoring [38]. Engaging the public in data collection provides information on species distribution, behavior, and population trends that might otherwise be difficult to gather through traditional scientific methods [36,39]. For example, the use of crowdsourced data in species distribution models has more than doubled since the 2010s [36]. By engaging the public in data collection, this collaborative approach enhances our understanding of human–species connections while empowering communities to actively participate in the preservation of biodiversity and the health of our natural environments [23,40,41]. This is particularly significant in urban areas, where crowdsourced species data contribute to a deeper understanding of urban diversity [42].
South Korea is one of the countries experiencing strong industrialization and urbanization [43]. As a result, it has become one of the most urbanized countries globally, with 18.3% of its population residing in Seoul, the capital of the country. This figure rises to 45% when including the greater Seoul Capital Area [44]. Addressing the well-being of this rapidly growing urban population has driven efforts to better understand species dynamics and ecosystem services in the region [45]. For example, Park and Han [45] analyzed the ecological network functions in Seoul, and Jo et al. [46] highlighted the importance of biodiversity enhancement in urban forests for Seoul citizens. Additionally, Serret et al. [47] investigated pollinator families observed in Seoul from 2016 to 2018 using a citizen science program. Despite these efforts, comprehensive information about the distribution of various species and the specific locations people visit remains limited.
To address this gap, we investigate crowdsourced data to better understand the relationship between species and humans. The objectives of this study are to:
- Identify species distribution patterns in the Seoul Capital Area using crowdsourced data;
- Evaluate the consistency of these data with field observations;
- Determine visitors’ preferences for different types of species.
In addition, we explore methodological advancements to better analyze and interpret crowdsourced data.
2. Methods and Materials
2.1. Study Area
This study focuses on the Seoul Capital Area in South Korea (Figure 1). The Seoul Capital Area, located in northwest South Korea, includes the city of Seoul (the capital), the Incheon metropolis, and Gyeonggi Province (Figure 1). With an area of 12,685 km2, the Seoul Capital Area is home to approximately 26 million people, of which nearly 10 million reside in Seoul. Tourism in this area is substantial as the area serves many domestic and international visitors [44].
Figure 1.
Spatial distribution of visitors (2005–2022) across different tourism site types, reported by the national visitation statistics. Circle colors refer to the different types of visiting sites, while sizes indicate the number of visitors (2005–2022). Korean administrative district boundaries are overlaid for location reference.
2.2. Visitor Statistics
The Korean government publishes the visitor statistics regularly [48], which provide the number of visitors to major tourist destinations across the country. The dataset aims to generate national statistics to estimate tourist demand. Additionally, it evaluates the capacity of tourism facilities and supports planning for resource development. The raw data are collected quarterly by local governments and individual tourist sites, and subsequently reported to the Ministry of Culture, Sports, and Tourism (MCST). The dataset allows for comparisons across different regions and time periods [48].
From 2005 to 2022, the visitor statistics data in the study area covered the number of visitors and locations for the total 694 tourist sites, including natural and cultural attractions (Figure 1). We converted the tourism sites to a set of spatial points using the given coordinates and categorized sites by types of area, namely, ‘sightseeing’, ‘nature’, and ‘culture’, for further analysis following the definition provided by the Korea Culture and Tourism Institute [48]. Generally, indoor facilities such as museums are categorized into the ‘sightseeing’ category, outdoor sightseeing areas such as palaces and temples are categorized into the ‘culture’ category, and natural parks and mountains are categorized into the ‘nature’ category. The information of visitors was categorized into international visitors and domestic visitors depending on their home location. The proportion of domestic visitors was much larger than that of foreigners. Note that the distinction between domestic and foreign visitors is not utilized in this study.
2.3. iNaturalist Database
The iNaturalist platform was utilized to estimate the species distribution patterns by analyzing citizen-science records of biodiversity in the Seoul Capital Area. iNaturalist is a widely used cloud-based platform that enables users to upload photographs of flora, fauna, and insects, which can then be taxonomically identified within the platform. The data from the iNaturalist were acquired via the iNaturalist API and the ‘rinat’ package v0.1.9 [49] for the study period. In the Seoul Capital Area, the acquired data consist of a total of 75,373 records, with 4398 common names and 9049 scientific names. The dataset covers 13 taxonomic groups (kingdom/phylum/class). The breakdown by taxonomic level shows 6 kingdoms, 1 division, and 6 classes: Animalia, Plantae, Insecta, Fungi, Protozoa, and Chromista; Mollusca (phylum), Aves (class), Mammalia (class), Reptilia (class), Amphibia (class), Arachnida (class), and Actinopterygii (class). Most of the downloaded iNaturalist data (99.4%) include scientific names, while 71.6% include common names. We excluded records without scientific names and those labeled as ‘Homo Sapiens’ leaving us with 74,889 records.
2.4. GBIF Database
It is known that the iNaturalist database introduces some uncertainties in its taxonomic classification [28]. To address these uncertainties, we compared the iNaturalist data with the Global Biodiversity Information Facility (GBIF) [50], a global repository that aims to provide a more structured and standardized biodiversity database, incorporating data obscuration where necessary [28,51]. To retrieve standardized taxonomic information for iNaturalist species, we used the scientific names recorded in iNaturalist to query the GBIF database. The data retrieval process was carried out in GNU R, using the ‘rgbif’ package [52,53]. In addition to taxonomic data, we also retrieved the Red List categories from the International Union for Conservation of Nature (IUCN) for species found in iNaturalist. The IUCN Red List provides the conservation status of species, classifying them into nine categories: Extinct (EX), Extinct in the Wild (EW), Critically Endangered (CR), Endangered (EN), Vulnerable (VU), Near Threatened (NT), Least Concern (LC), Data Deficient (DD), and Not Evaluated (NE) [54].
2.5. Point Pattern Analysis
We performed a point pattern analysis using the Cross-K function to assess the spatial relationship between two distinct point patterns: the locations of MCST visitors and the locations of iNaturalist records. Cross-K, an extension of the K function, is utilized to investigate spatial clustering or dispersion between two datasets, primarily for understanding spatial dependencies in tourism and biodiversity data. The Cross-K function computes the expected number of points from one dataset within a specified distance of points from the other, allowing spatial relationships between the two point patterns to be evaluated based on the distribution of one set of points relative to the other [55,56].
Compared to traditional grid-based analyses (e.g., [31,37]), the Cross-K function directly accounts for the spatial configuration of individual points, rather than relying on aggregated gridded data. We adopted this approach to identify underlying spatial patterns that may not be captured by raster-based methods, thereby enabling a more nuanced examination of spatial dependencies.
In this study, the Cross-K function measures how the presence of one set of points (e.g., visitor statistics) is related to the presence of another set (e.g., iNaturalist records). The Cross-K statistic typically measures the difference in spatial patterns between two datasets relative to a Complete Spatial Random (CSR) process, which serves as a null model of spatial randomness [56,57]. Under CSR, points are distributed randomly and independently across the given area. In this study, the CSR model acts as a baseline against which the observed data are compared. The difference between the spatial distribution of the iNaturalist data and CSR represents the deviation of the observed patterns from those expected under CSR. This difference indicates whether the iNaturalist records are clustered, dispersed, or randomly distributed around the locations of visitors compared to a random pattern.
As our study is irregularly shaped, a translation correction was applied in the Cross-K analysis [56]. This correction addresses boundary effects in spatial point pattern analysis by adjusting or shifting the spatial data, thereby mitigating edge bias and ensuring a more accurate representation of spatial relationships [56].
The Cross-K function was evaluated for every 500 m from 0 to 10 km. The 500 m interval was chosen to capture fine-scale spatial relationships while encompassing a 10 km radius to account for broader spatial interactions. To summarize the metrics, we normalized the differences between the estimates of the Visitor–iNaturalist process and the CSR process. These differences were aggregated and normalized on a scale from −1 (representing the largest repulsion) to 1 (representing the largest attraction), across all taxonomic groups. The visitation counts from the MCST visitation statistics and the population size of the iNaturalist records were used as weights in the calculations. In addition to the Cross-K analysis, we visualized the patterns using kernel density estimation, employing a Gaussian kernel with a parameter of , which controls the width of the kernel [58]. All computations and visualizations were performed in GNU R, primarily using the ‘spatstat’ v3.3-0 [59] and ‘stats’ packages in GNU R v4.4.2. [60]
3. Results
3.1. Descriptive Statistics
The spatial distribution of the visitor statistics is shown in Figure 1. For the study period (2005–2022), the number of visitors in each category varies significantly. General sightseeing, such as museums and attractions, received the highest number of visitors (1175 million) compared to other types ‘culture’ (205 million) and ‘nature’(105 million). Visitors at these sightseeing spots are concentrated in central Seoul and the northern Gyeonggi-do area near the DMZ (Demilitarized Zone) (Figure 1). Areas classified as ‘nature’, which include mountains and parks, are distributed across the whole region, while ‘culture’ sites are concentrated in densely populated areas. Figure 2 shows the temporal variations in the number of visitors over the study period. The number of visitors significantly decreased starting in 2020, presumably due to the lockdown in South Korea, which lasted until 2022. The visitor statistics suggest that tourism activities were restricted due to the pandemic, leading to fewer movements.
Figure 2.
Annual trend in the number of visitors during the study period (2005–2022).
Figure 3 shows the distribution of a total of 74,889 records in the study area. The majority of the iNaturalist data are categorized under the taxa Insecta (40.58%), Plantae (24.49%), and Aves (20.65%), followed by Arachnida (4.00%), Amphibia (3.15%), Fungi (2.35%), Animalia (1.4%), Mammalia (1.23%), Mollusca (0.81%), Reptilia (0.75%), Actinopterygii (0.60%), Protozoa (0.02%), and Chromista (0.01%) (Appendix A Table A1). Given the high prevalence of taxonomic information in most records, iNaturalist data in the area primarily contain information on insects, plants, and birds (Figure 1). The iNaturalist taxonomic group information is not perfectly standardized as the taxonomic levels vary across groups. In particular, the Animalia category contains both freshwater fishes and unidentified Arthropods, leading to heterogeneity within the group. Note that we exclude Chromista in the following analysis due to the extremely low number of records (n = 6). Figure 4 shows the temporal variation in the number of iNaturalist records over the study period. In contrast to the visitor statistics, iNaturalist records actually increased over time, primarily driven by a higher number of bird-related data points in 2020. This suggests that more people went outdoors to photograph birds and uploaded the data to the platform.
Figure 3.
iNaturalist data points used for the analysis (2005–2022; n = 74,889). Circle colors represent iNaturalist taxonomic group information included in the metadata. Korean administrative district boundaries are overlaid for location reference.
Figure 4.
Annual trend in the number of iNaturalist records during the study period (2005–2022).
3.2. Spatial Point Patterns
To visualize spatial point patterns, kernel density estimation was performed for the visitor statistics. The density estimates were visualized separately for four categories: (a) all visitors together, (b) visitors to cultural heritage sites, (c) visitors to natural sites, and (d) visitors to general tourist facilities (Figure 5). Kernel density estimation was also performed for iNaturalist records. Among all taxonomic groups, the densities of the groups clustered with natural sites are shown (Figure 6). A visual inspection indicates a potential correlation between the iNaturalist record density and the visitor statistics, which revealed iNaturalist records are somewhat concentrated around natural tourism sites.
Figure 5.
Estimated kernel density of the visitor statistics for (a) all categories together, (b) culture sites, (c) nature sites, and (d) general sightseeing sites.
Figure 6.
Estimated kernel density of the iNaturalist records for the taxonomic groups clustered around the nature-based tourism sites: (a) Animalia, (b) Aves, (c) Mollusca, and (d) Plantae.
3.3. Comparison of iNaturalist and Visitor Statistics
To quantify the relationships more solidly, a Cross-K analysis was conducted to provide a more rigorous statistical comparison between the two datasets. In Figure 7, Cross-K analysis is summarized to illustrate the relationship between the visitor statistics and the iNaturalist records, both in the form of spatial point patterns. When considering all iNaturalist records, no clear association between visitor statistics and the crowdsourced data was observed. However, when analyzed by type of tourism site, certain taxonomic groups showed meaningful associations with visitor statistics. As shown in Appendix A Figure A1, for the selected taxonomic groups, the observed point patterns (solid black line) show higher K values compared to the random process (dotted red line). At nature-based tourism sites, Animalia, Plantae, Amphibia, Mollusca, and Aves exhibited strong clustering. It should be noted that in the dataset, Animalia is somewhat inconsistently categorized, with species including worms and freshwater fishes as well as unidentified species (e.g., scientific name recorded simply ’Animalia’). For Mollusca, the observed associations suggest that snails and slugs are commonly found in nature protection areas that attract visitors, allowing for further interpretation (see species list in Appendix A Table A1).
Figure 7.
Summary of the point pattern analysis using Cross-K between MCST visitor statistics and iNaturalist records. Values represent the normalized differences between iNaturalist observations and a Complete Spatial Random (CSR) process.
In contrast, cultural and sightseeing sites exhibited a negative relationship with all taxonomic groups in relation to visitor statistics. The results of the Cross-K analysis showed that most taxonomic groups exhibited strong negative relationships with the number of visitors to cultural tourism sites. This was especially evident after the application of translation correction. Note that in the preliminary analysis, when the baseline Poisson model was applied, a positive relationship was observed across all site types.
3.4. Supplementing iNaturalist Data with Information from the GBIF Database
The comparisons between the taxonomic group information from iNaturalist and the GBIF database are presented in Figure 8 and Figure 9, illustrating how the iNaturalist taxonomic group data differs from the GBIF database at various taxonomic levels. Note that we queried GBIF data for each of the Top 30 species within each iNaturalist taxa group, leaving us with a total of 342 species. In Figure 8, the diagram on the left represents a kingdom-level comparison, showing that a large portion of iNaturalist records fall into the Animalia kingdom. Some records marked as Animalia and Mammalia in iNaturalist data belong to the Plantae kingdom, suggesting possible misclassification in the iNaturalist data. The Phylum-level comparison (Figure 8 on the right) breaks the iNaturalist taxonomic groups into more specific phyla, such as Arthropoda, Chordata, and Basidiomycota. This reveals that the Animalia group in iNaturalist data is substantially mixed up, for example, Arthropoda should not have been included. Except for species belonging to Arthropoda, most of the iNaturalist Animalia group species are worms and algae.
Figure 8.
Sankey diagrams comparing iNaturalist taxonomic group data with the GBIF database: the kingdom-level comparison (left) and the Phylum (division)-level comparison (right).
Figure 9.
Sankey diagrams comparing iNaturalist taxonomic group data with the GBIF database: the class-level comparison (left) and the order-level comparison (right).
The class-level comparison (Figure 9 on the left) indicates that iNaturalist taxonomic groups are primarily classified at this level, with many groups closely matching their respective classes, except for Plantae and Chromista, aside from Animalia. The order-level comparison (Figure 9 on the right) provides evidence that iNaturalist groups are beyond this level.
We calculated the frequency and distribution of IUCN Red List categories for species found in the iNaturalist data (Figure 10 and Appendix A Table A2). Among the total 342 species from the top 30 species within each iNaturalist taxa group, we retrieved an IUCN class code from the GBIF database for 332 species. Of these, 216 species are categorized as Not Evaluated (NE), followed by Least Concern (LC) (n = 94). The Extinct (EX) and Extinct in the Wild (EW) categories were not identified (Figure 10). Smaller proportions are seen in the Near Threatened (NT) category (four species, 1.20%), Vulnerable (VU) category (six species, 1.81%), and Endangered (EN) category (seven species, 1.79%). The IUCN classification suggests that the study area may not host a large number of threatened species; however, this is insufficient evidence since 65.8% of the species remain unevaluated (NE), and their conservation status is therefore unknown.
Figure 10.
Species frequency in the iNaturalist data for each of the Top 30 species per taxa group across IUCN Red List categories. Note that the x-axis is log scaled.
4. Discussions
This study clustered visitor statistics in the Seoul Capital Area using data from a crowdsourced social media database, where users upload species observations. The iNaturalist data were found to be heavily concentrated in tourist hotspots within Seoul’s urban areas and northern Gyeonggi Province. However, categorizing the data by taxonomic groups revealed significantly different patterns. Notably, while the overall correlation between visitor statistics and iNaturalist data is weak, specific taxonomic groups showed strong clustering with ecotourism sites compared to cultural sites, whereas others exhibited negative patterns. These findings suggest that motivations for visiting cultural sites are less related to species observation, whereas natural sites show higher correlations with certain taxonomic groups. For instance, specific groups demonstrated strong positive cross-K relationships with natural sites, though preferences varied among species [61].
Animalia, Aves, Mollusca, and Plantae, in particular, demonstrated a positive cross-K relationship with visitor numbers in natural areas (Figure 7). Charismatic species appear to attract more visitors and foster pro-conservation behaviors [62]. Among the iNaturalist observations, Insecta, Plantae, and Aves were the most frequently recorded groups. Birdwatching, which accounted for the highest number of animal-related records, is especially popular in urban areas due to its psychological benefits and positive effects on human well-being [63]. However, iNaturalist user preferences often exhibit biases toward visually striking or culturally significant species. This leads to the over-representation of charismatic fauna and flora, such as large mammals and colorful birds, while less conspicuous organisms, like fungi and invertebrates, are under-represented [64,65]. Geographical factors, such as road density and accessibility, also influence observation patterns [66].
Given these biases, interpreting the causality of observed relationships requires caution. For example, while people may prefer freshwater environments where Mollusca and fish species are found [67], it remains unclear whether visitors specifically sought these areas for species observation. Over-reliance on simple correlations or iNaturalist data alone may lead to misleading conclusions, as demonstrated in Potsikas et al. [68], Cao and Hochmair [69]. The platform is more suited to exploring the discovery of plant and animal species in relation to the CES of ‘non-use values’ [61]. Complementing social media data with field observations and interviews could provide a deeper understanding of visitor motivations, particularly for cultural and natural sites. While crowdsourced data are rich, they may over- or under-represent specific activities or species depending on location [31,70]. Moreover, incorporating ground data at the national level [71] and enhancing global datasets could align local and global biodiversity records [72]. Such integrated approaches can prioritize conservation planning for endangered species and mitigate biodiversity loss.
Social media data have been widely used to analyze CES, often through aggregated methods like photo-user days (PUDs) using platforms such as Flickr [73]. While these methods offer insights into CES distribution, they risk obscuring finer-scale patterns. This study addresses these limitations by employing point pattern analysis, which preserves the granularity of data. This approach improves the accuracy of spatial analyses and helps identify localized patterns essential for biodiversity conservation and ecosystem management [74].
While the use of social media data for species distribution and CES analysis is cost-effective and captures spatiotemporal patterns of ecosystems [70,71,75], these findings must be contextualized within broader social–environmental frameworks. For instance, how can such patterns inform global discussions on sustainable tourism, biodiversity conservation, and equitable access to natural spaces? This study demonstrates the potential of social media platforms to engage broader audiences in biodiversity awareness but highlights the need for critical evaluations of biases and uneven ecosystem representations [71].
These comparisons reveal how social media-based observations may over-represent certain taxonomic groups, particularly those that are more visible or commonly observed, while GBIF’s more standardized records might show a more even distribution across different groups. The differences between these two datasets underscore the strengths and limitations of each, suggesting the complementary nature of combining both sources for a more holistic understanding of global biodiversity.
Despite its value, the iNaturalist database has limitations, including inconsistent taxonomic classifications and biases in species representation. Many species remain Not Evaluated (NE) under the IUCN Red List within the Seoul Capital Area, limiting biodiversity assessments. Moreover, geographical factors like road connectivity and accessibility may further influence data collection and observation patterns [61]. Future studies should prioritize integrating multiple databases to enhance reliability and reduce biases in conservation planning [31,76].
This research not only advances understanding within the Seoul Capital Area but also contributes to global knowledge on the intersections of visitor behavior, species observation, and ecosystem services. By integrating diverse data sources and considering local socio-ecological contexts, future studies can offer more comprehensive assessments. Ultimately, this study underscores the dual potential of social media data: as a research tool and as a means to inspire inclusive global dialogues on human–nature relationships.
5. Conclusions
This study highlights the potential of crowdsourced data, such as iNaturalist, to provide valuable insights into biodiversity and CESs while addressing its limitations. Patterns of species observations strongly align with ‘nature’ areas, reflecting ecotourism motivations, whereas cultural sites show weaker correlations. Charismatic species attract more visitors and promote conservation awareness, but biases in user preferences and geographic accessibility lead to under-representation of less conspicuous taxa. While social media data are cost-effective and capture spatial and temporal trends, their biases necessitate integration with field observations and alternative datasets for comprehensive assessments. Beyond the Seoul Capital Area, this research underscores the role of citizen science in advancing biodiversity conservation and sustainable tourism, advocating for inclusive approaches that bridge public engagement and equitable access to natural spaces. Moreover, the findings can inform governmental decision-making processes, supporting the development of evidence-based policies for biodiversity conservation and sustainable land use planning.
Author Contributions
H.K.: conceptualization, writing—original draft preparation, writing—review and editing, and funding acquisition; B.S.: conceptualization, methodology, data curation, formal analysis, writing—original draft preparation, and visualization; J.K.: data curation and writing—review and editing; and H.L.: conceptualization, methodology, writing—original draft preparation, and writing—review and editing. All authors have read and agreed to the published version of the manuscript.
Funding
This paper was supported by Konkuk University in 2023. Bumsuk Seo was partially supported by the Brain Pool program (RS–2023–00261884) by the National Research Foundation of Korea. This research was conducted as part of the National Institution of Ecology’s research project, “Development of Policy Decision Support System Base on Ecosystem Services Assessment (Project No. NIE–B–2025–03)”.
Data Availability Statement
The raw data supporting the conclusions of this article will be made available by the authors on request.
Conflicts of Interest
The authors declare no conflicts of interest.
Appendix A
Figure A1.
Cross-K analysis between the MCST visitation statistics and the iNaturalist data in the study area (2005–2022) for the iNaturalist taxonomic groups clustered around the nature-based tourism sites. The observed point patterns are solid black lines and the random processes are dotted red lines for (a) Animalia, (b) Aves, (c) Mollusca, and (d) Plantae.
Table A1.
List of the top 30 species from iNaturalist data in the study area and their frequencies. Some taxonomic groups contain fewer than 30 species (e.g., Chromista). Note that missing common names in the original data are left intentionally to illustrate how the data are presented.
Table A1.
List of the top 30 species from iNaturalist data in the study area and their frequencies. Some taxonomic groups contain fewer than 30 species (e.g., Chromista). Note that missing common names in the original data are left intentionally to illustrate how the data are presented.
| Taxa | Scientific Name | Common Name | Freq |
|---|---|---|---|
| Actinopterygii | Cyprinus rubrofuscus | Amur Carp | 69 |
| Actinopterygii | Cyprinus | Typical Carps | 35 |
| Actinopterygii | Actinopterygii | Ray-finned Fishes | 20 |
| Actinopterygii | Zacco platypus | Pale Chub | 16 |
| Actinopterygii | Oxudercinae | Mudskippers | 13 |
| Actinopterygii | Rhynchocypris oxycephalus | Chinese Minnow | 13 |
| Actinopterygii | Carassius auratus | Goldfish | 12 |
| Actinopterygii | Gobiidae | Gobies | 10 |
| Actinopterygii | Channa argus | Northern Snakehead | 9 |
| Actinopterygii | Micropterus salmoides | Largemouth Bass | 9 |
| Actinopterygii | Monopterus albus | Asian swamp eel | 8 |
| Actinopterygii | Misgurnus anguillicaudatus | Oriental Weatherfish | 7 |
| Actinopterygii | Misgurnus mizolepis | Chinese Weatherfish | 7 |
| Actinopterygii | Mugil cephalus | Sea Mullet | 7 |
| Actinopterygii | Periophthalmus modestus | Shuttles hoppfish | 7 |
| Actinopterygii | Silurus asotus | Amur Catfish | 7 |
| Actinopterygii | Odontobutis interruptus | 6 | |
| Actinopterygii | Pseudogobio esocinus | Pike Gudgeon | 6 |
| Actinopterygii | Pungtungia herzi | Black Stripe Gudgeon | 6 |
| Actinopterygii | Acanthogobius hasta | Javelin Goby | 5 |
| Actinopterygii | Misgurnus | weatherfishes | 5 |
| Actinopterygii | Pseudorasbora parva | Topmouth Gudgeon | 5 |
| Actinopterygii | Carassius | Crucian Carps | 4 |
| Actinopterygii | Chanodichthys erythropterus | predatory carp | 4 |
| Actinopterygii | Coreoperca herzi | 4 | |
| Actinopterygii | Cyprinidae | Cyprinids | 4 |
| Actinopterygii | Cyprinus carpio carpio | Mirror Carp | 4 |
| Actinopterygii | Koreocobitis rotundicaudata | White Nose Loach | 4 |
| Actinopterygii | Rhinogobius | Rhinogobies | 4 |
| Actinopterygii | Rhodeus suigensis | 4 | |
| Amphibia | Hyla japonica | Japanese Tree Frog | 615 |
| Amphibia | Pelophylax nigromaculatus | Black-spotted Frog | 289 |
| Amphibia | Hyla suweonensis | Suweon Tree Frog | 206 |
| Amphibia | Pelophylax chosenicus | Golden Pond Frog | 148 |
| Amphibia | Bufo sachalinensis | Sakhalin toad | 142 |
| Amphibia | Kaloula borealis | Boreal Digging Frog | 130 |
| Amphibia | Hynobius leechii | Gensan Salamander | 123 |
| Amphibia | Rana uenoi | Ueno’s Brown Frog | 123 |
| Amphibia | Bombina orientalis | Oriental Fire-bellied Toad | 98 |
| Amphibia | Onychodactylus koreanus | Korean Clawed Salamander | 79 |
| Amphibia | Glandirana emeljanovi | Imienpo Station frog | 77 |
| Amphibia | Rana huanrensis | Huanren Frog | 66 |
| Amphibia | Rana | Pond Frogs | 60 |
| Amphibia | Rana coreana | Korean Brown Frog | 52 |
| Amphibia | Lithobates catesbeianus | American Bullfrog | 50 |
| Amphibia | Anura | Frogs and Toads | 21 |
| Amphibia | Ranidae | Typical Frogs | 21 |
| Amphibia | Bufo stejnegeri | Water Toad | 19 |
| Amphibia | Hyla | Holarctic Treefrogs | 16 |
| Amphibia | Amphibia | Amphibians | 6 |
| Amphibia | Pelophylax | Water Frogs | 6 |
| Amphibia | Ambystoma mexicanum | Axolotl | 4 |
| Amphibia | Ambystomatidae | Mole Salamanders | 1 |
| Amphibia | Caudata | Salamanders | 1 |
| Amphibia | Duttaphrynus melanostictus | Asian Common Toad | 1 |
| Amphibia | Leptodactylus fallax | Mountain Chicken | 1 |
| Amphibia | Rana latastei | Italian Agile Frog | 1 |
| Amphibia | Ranoidea caerulea | Australian Green Tree Frog | 1 |
| Animalia | Orthomorphella pekuensis | 61 | |
| Animalia | Arthropoda | Arthropods | 49 |
| Animalia | Thereuonema tuberculata | Japanese House Centipede | 40 |
| Animalia | Chiromantes haematocheir | Red-clawed crab | 33 |
| Animalia | Armadillidium vulgare | Common Pill Woodlouse | 31 |
| Animalia | Scolopendra mutilans | Chinese Red-headed Centipede | 31 |
| Animalia | Oxidus gracilis | Greenhouse Millipede | 28 |
| Animalia | Brachyura | True Crabs | 25 |
| Animalia | Polydesmida | Flat-backed Millipedes | 21 |
| Animalia | Bipaliinae | Hammerhead Worms | 19 |
| Animalia | Orisarma dehaani | 19 | |
| Animalia | Tubuca arcuata | Bowed Fiddler Crab | 18 |
| Animalia | Animalia | Animals | 16 |
| Animalia | Diversibipalium | 15 | |
| Animalia | Eriocheir sinensis | Chinese Mitten Crab | 15 |
| Animalia | Oligochaeta | Earthworms and Allies | 15 |
| Animalia | Oxidus | 15 | |
| Animalia | Paradoxosomatidae | 15 | |
| Animalia | Cambaroides similis | Korean Crayfish | 14 |
| Animalia | Eriocheir | 14 | |
| Animalia | Armadillidium | Pillbugs | 13 |
| Animalia | Scutigeridae | Typical House Centipedes | 13 |
| Animalia | Ligia | Sea Slaters | 12 |
| Animalia | Macrophthalmus japonicus | 12 | |
| Animalia | Whitmania edentula | 12 | |
| Animalia | Collembola | Springtails | 11 |
| Animalia | Megascolecidae | Giant Earthworms | 11 |
| Animalia | Pagurus minutus | 11 | |
| Animalia | Armadillidium nasatum | Nosy Pill Woodlouse | 10 |
| Animalia | Ligia exotica | Wharf Louse | 10 |
| Arachnida | Trichonephila clavata | Joro Spider | 421 |
| Arachnida | Araneae | Spiders | 100 |
| Arachnida | Argiope bruennichi | Wasp Spider | 93 |
| Arachnida | Lycosidae | Wolf Spiders | 84 |
| Arachnida | Thomisidae | Crab Spiders | 82 |
| Arachnida | Araneidae | Orbweavers | 79 |
| Arachnida | Salticidae | Jumping Spiders | 79 |
| Arachnida | Orienticius vulpes | 66 | |
| Arachnida | Araneus ventricosus | 64 | |
| Arachnida | Araneomorphae | Typical Spiders | 63 |
| Arachnida | Carrhotus xanthogramma | 61 | |
| Arachnida | Telamonia vlijmi | 51 | |
| Arachnida | Philodromidae | Running Crab Spiders | 47 |
| Arachnida | Myrmarachne | Ant mimic Spiders | 40 |
| Arachnida | Agelenidae | Funnel Weavers | 37 |
| Arachnida | Lycosoidea | Wolf Spiders and Allies | 37 |
| Arachnida | Pisaura | 34 | |
| Arachnida | Araneinae | Typical Orbweavers | 33 |
| Arachnida | Ebrechtella tricuspidata | Triangle Crab Spider | 32 |
| Arachnida | Parasteatoda tepidariorum | Common House Spider | 32 |
| Arachnida | Tetragnatha | Long-jawed Orbweavers | 32 |
| Arachnida | Pardosa | Thin-legged Wolf Spiders | 31 |
| Arachnida | Evarcha albaria | White-eyebrowed Jumping Spider | 30 |
| Arachnida | Neoscona scylloides | 30 | |
| Arachnida | Araneoidea | Araneoid Spiders | 27 |
| Arachnida | Asianellus festivus | 27 | |
| Arachnida | Linyphiidae | Sheetweb and Dwarf Weavers | 27 |
| Arachnida | Plexippoides regius | 26 | |
| Arachnida | Agelena | Grass Funnel-web Spiders | 25 |
| Arachnida | Dolomedes sulfureus | 25 | |
| Aves | Pica serica | Oriental Magpie | 896 |
| Aves | Ardea cinerea | Grey Heron | 551 |
| Aves | Anas zonorhyncha | Eastern Spot-billed Duck | 525 |
| Aves | Passer montanus | Eurasian Tree Sparrow | 478 |
| Aves | Streptopelia orientalis | Oriental Turtle dove | 476 |
| Aves | Columba livia domestica | Feral Pigeon | 459 |
| Aves | Hypsipetes amaurotis | Brown-eared Bulbul | 452 |
| Aves | Anas platyrhynchos | Mallard | 388 |
| Aves | Phalacrocorax carbo | Great Cormorant | 329 |
| Aves | Phoenicurus auroreus | Daurian Redstart | 326 |
| Aves | Larus crassirostris | Black-tailed Gull | 307 |
| Aves | Parus minor | Japanese Tit | 301 |
| Aves | Ardea alba | Great Egret | 238 |
| Aves | Egretta garzetta | Little Egret | 216 |
| Aves | Fulica atra | Eurasian Coot | 188 |
| Aves | Tachybaptus ruficollis | Little Grebe | 186 |
| Aves | Sinosuthora webbiana | Vinous-throated Parrotbill | 182 |
| Aves | Corvus macrorhynchos | Large-billed Crow | 177 |
| Aves | Sittiparus varius | Varied Tit | 169 |
| Aves | Poecile palustris | Marsh Tit | 167 |
| Aves | Cyanopica cyanus | Azure-winged Magpie | 150 |
| Aves | Emberiza elegans | Yellow-throated Bunting | 150 |
| Aves | Aix galericulata | Mandarin Duck | 149 |
| Aves | Mergus merganser | Common Merganser | 149 |
| Aves | Anas crecca crecca | Eurasian Green-winged Teal | 140 |
| Aves | Aythya ferina | Common Pochard | 140 |
| Aves | Anser albifrons | Greater White-fronted Goose | 137 |
| Aves | Falco tinnunculus | Eurasian Kestrel | 137 |
| Aves | Fringilla montifringilla | Brambling | 135 |
| Aves | Turdus naumanni | Naumann’s Thrush | 135 |
| Chromista | Botrydium | 1 | |
| Chromista | Chromista | kelp, diatoms, and allies | 1 |
| Chromista | Noctiluca scintillans | sea sparkle | 1 |
| Chromista | Ochrophyta | 1 | |
| Chromista | Phaeophyceae | brown algae | 1 |
| Chromista | Saprolegnia | Cotton Moulds | 1 |
| Fungi | Fungi | Fungi Including Lichens | 298 |
| Fungi | Polyporales | shelf fungi | 87 |
| Fungi | Agaricales | Common Gilled Mushrooms and Allies | 73 |
| Fungi | Trametes | 55 | |
| Fungi | Trametes versicolor | turkey-tail | 48 |
| Fungi | Schizophyllum commune | splitgill mushroom | 40 |
| Fungi | Russula | brittlegills | 38 |
| Fungi | Amanita | amanita mushrooms | 37 |
| Fungi | Agaricomycetes | 33 | |
| Fungi | Basidiomycota | Basidiomycete Fungi | 27 |
| Fungi | Coprinus comatus | Shaggy Mane | 19 |
| Fungi | Polyporaceae | bracket fungi | 17 |
| Fungi | Boletaceae | boletes | 16 |
| Fungi | Dacrymyces spathularia | Fan-shaped Jelly Fungus | 16 |
| Fungi | Ganoderma | Artist’s Brackets, Reishi, and Allies | 16 |
| Fungi | Lecanoromycetes | common lichens | 15 |
| Fungi | Trametes sanguinea | Cinnabar Bracket | 15 |
| Fungi | Boletales | boletes and allies | 13 |
| Fungi | Macrolepiota procera | Parasol | 12 |
| Fungi | Parmelioideae | typical shield lichens | 12 |
| Fungi | Pholiota | Scalycaps | 12 |
| Fungi | Russulaceae | Milkcaps, Brittlegills and Allies | 12 |
| Fungi | Amidella | Amanita Sect. Amidella | 10 |
| Fungi | Phallus luteus | 10 | |
| Fungi | Cladonia | Pixie Cup Lichens | 9 |
| Fungi | Coprinellus micaceus | mica cap | 9 |
| Fungi | Ganoderma lucidum | lacquered bracket | 9 |
| Fungi | Lactarius | Common Milkcaps | 9 |
| Fungi | Lycoperdon | 9 | |
| Fungi | Lycoperdon perlatum | common puffball | 9 |
| Insecta | Lepidoptera | Butterflies and Moths | 678 |
| Insecta | Harmonia axyridis | Asian Lady Beetle | 246 |
| Insecta | Polygonia c-aureum | Asian Comma | 212 |
| Insecta | Lycorma delicatula | Spotted Lanternfly | 198 |
| Insecta | Tenodera sinensis | Chinese Mantis | 198 |
| Insecta | Apis mellifera | Western Honey Bee | 176 |
| Insecta | Lymantria dispar | Spongy Moth | 175 |
| Insecta | Hyalessa maculaticollis | Robust Cicada | 165 |
| Insecta | Hierodula patellifera | Giant Asian Mantis | 162 |
| Insecta | Statilia maculata | Asian Jumping Mantis | 150 |
| Insecta | Halyomorpha halys | Brown Marmorated Stink Bug | 138 |
| Insecta | Geometridae | Geometer Moths | 133 |
| Insecta | Pseudozizeeria maha | Pale Grass Blue | 132 |
| Insecta | Oedaleus infernalis | 131 | |
| Insecta | Exomala orientalis | Oriental Beetle | 128 |
| Insecta | Riptortus pedestris | 128 | |
| Insecta | Ricania sublimata | 109 | |
| Insecta | Tenodera angustipennis | Narrow-winged Mantis | 108 |
| Insecta | Camponotus japonicus | Japanese Carpenter Ant | 106 |
| Insecta | Timomenus komarowi | 106 | |
| Insecta | Pieris rapae | Small White | 103 |
| Insecta | Acrida cinerea | Oriental Longheaded Locust | 100 |
| Insecta | Chironomidae | Non-biting Midges | 100 |
| Insecta | Coccinella septempunctata | Seven-spotted Lady Beetle | 99 |
| Insecta | Formica japonica | Japanese Wood Ant | 99 |
| Insecta | Insecta | Insects | 98 |
| Insecta | Atractomorpha lata | 94 | |
| Insecta | Ichneumonidae | Ichneumonid Wasps | 94 |
| Insecta | Sinochlora longifissa | 93 | |
| Insecta | Papilio xuthus | Chinese Yellow Swallowtail | 92 |
| Mammalia | Sciurus vulgaris | Eurasian Red Squirrel | 134 |
| Mammalia | Felis catus | Domestic Cat | 133 |
| Mammalia | Hydropotes inermis | Water Deer | 93 |
| Mammalia | Eutamias sibiricus | Siberian Chipmunk | 72 |
| Mammalia | Hydropotes inermis argyropus | Korean Water Deer | 36 |
| Mammalia | Nyctereutes procyonoides | Mainland Raccoon Dog | 31 |
| Mammalia | Canis familiaris | Domestic Dog | 30 |
| Mammalia | Sus scrofa | Wild Boar | 19 |
| Mammalia | Mammalia | Mammals | 15 |
| Mammalia | Mustela sibirica | Siberian Weasel | 14 |
| Mammalia | Lutra lutra | Eurasian Otter | 12 |
| Mammalia | Oryctolagus cuniculus | European Rabbit | 11 |
| Mammalia | Meles leucurus | Asian Badger | 9 |
| Mammalia | Mogera robusta | Large Mole | 9 |
| Mammalia | Rattus norvegicus | Brown Rat | 9 |
| Mammalia | Prionailurus bengalensis | Mainland Leopard Cat | 8 |
| Mammalia | Rattus | Old World Rats | 7 |
| Mammalia | Capreolus pygargus | Eastern Roe Deer | 6 |
| Mammalia | Cervus nippon | Sika Deer | 6 |
| Mammalia | Martes flavigula | Yellow-throated Marten | 6 |
| Mammalia | Muroidea | Muroids | 6 |
| Mammalia | Soricidae | Shrews | 6 |
| Mammalia | Ailuropoda melanoleuca | Giant Panda | 5 |
| Mammalia | Ailurus | 5 | |
| Mammalia | Apodemus agrarius | Striped Field Mouse | 5 |
| Mammalia | Lepus coreanus | Korean Hare | 5 |
| Mammalia | Muridae | Old World Mice and Rats | 5 |
| Mammalia | Nyctereutes procyonoides koreensis | Korean Raccoon Dog | 5 |
| Mammalia | Panthera tigris | Tiger | 5 |
| Mammalia | Cervidae | Deer | 4 |
| Mollusca | Karaftohelix kurodana | 67 | |
| Mollusca | Meghimatium | 46 | |
| Mollusca | Gastropoda | Gastropods | 35 |
| Mollusca | Acusta redfieldi | 31 | |
| Mollusca | Sinanodonta lauta | 28 | |
| Mollusca | Acusta | 20 | |
| Mollusca | Nesiohelix samarangae | 18 | |
| Mollusca | Anemina arcaeformis | 16 | |
| Mollusca | Pomacea canaliculata | Channeled Apple Snail | 15 |
| Mollusca | Ambigolimax | Threeband Slugs | 14 |
| Mollusca | Stylommatophora | Common Land Snails and Slugs | 14 |
| Mollusca | Nodularia douglasiae | 13 | |
| Mollusca | Meghimatium fruhstorferi | 12 | |
| Mollusca | Rapana venosa | Veined Rapa Whelk | 12 |
| Mollusca | Helicoidea | 11 | |
| Mollusca | Littorina brevicula | 11 | |
| Mollusca | Meghimatium bilineatum | Chinese Slug | 8 |
| Mollusca | Reishia clavigera | 7 | |
| Mollusca | Aegista | 6 | |
| Mollusca | Umbonium thomasi | Sand Snail | 6 |
| Mollusca | Bullacta caurina | 5 | |
| Mollusca | Karaftohelix | 5 | |
| Mollusca | Magallana gigas | Pacific Oyster | 5 |
| Mollusca | Pomacea | Common Apple Snails | 5 |
| Mollusca | Bekkochlamys subrejecta | 4 | |
| Mollusca | Helicina | 4 | |
| Mollusca | Ostreidae | True Oysters | 4 |
| Mollusca | Semisulcospira libertina | 4 | |
| Mollusca | Acanthochitona achates | 3 | |
| Mollusca | Batillariidae | Mud creeper Snails | 3 |
| Plantae | Plantae | plants | 557 |
| Plantae | Magnoliopsida | dicots | 456 |
| Plantae | Angiospermae | flowering plants | 336 |
| Plantae | Erigeron annuus | annual fleabane | 202 |
| Plantae | Tracheophyta | vascular plants | 157 |
| Plantae | Pinus | pines | 138 |
| Plantae | Bryophyta | mosses | 134 |
| Plantae | Setaria viridis | Green Bristle Grass | 133 |
| Plantae | Chelidonium asiaticum | 124 | |
| Plantae | Asteraceae | sunflowers, daisies, asters, and allies | 122 |
| Plantae | Trifolium repens | white clover | 112 |
| Plantae | Commelina communis | Asiatic dayflower | 110 |
| Plantae | Pinus densiflora | Japanese red pine | 110 |
| Plantae | Taraxacum officinale | common dandelion | 107 |
| Plantae | Prunus | plums, cherries, and allies | 103 |
| Plantae | Rosa | roses | 96 |
| Plantae | Parthenocissus tricuspidata | Japanese creeper | 91 |
| Plantae | Rhododendron | rhododendrons and azaleas | 89 |
| Plantae | Acer palmatum | Japanese maple | 86 |
| Plantae | Rhododendron mucronulatum | Korean rhododendron | 86 |
| Plantae | Hibiscus syriacus | common hibiscus | 80 |
| Plantae | Prunus serrulata | Japanese Cherry | 79 |
| Plantae | Capsella bursa-pastoris | shepherd’s-purse | 76 |
| Plantae | Acer | maples | 74 |
| Plantae | Ginkgo biloba | ginkgo | 72 |
| Plantae | Cornus officinalis | Korean cornel dogwood | 70 |
| Plantae | Poaceae | grasses | 69 |
| Plantae | Coreopsis lanceolata | Lance-leaved Coreopsis | 65 |
| Plantae | Phytolacca americana | American pokeweed | 65 |
| Plantae | Quercus | oaks | 62 |
| Protozoa | Stemonitis | Chocolate Tube Slimes | 3 |
| Protozoa | Ceratiomyxa | Coral Slimes | 2 |
| Protozoa | Hemitrichia serpula | Pretzel slime mold | 2 |
| Protozoa | Mycetozoa | slime molds | 2 |
| Protozoa | Arcyria denudata | carnival candy slime mold | 1 |
| Protozoa | Lycogala | 1 | |
| Protozoa | Myxomycetes | true slime molds | 1 |
| Protozoa | Physarum melleum | 1 | |
| Reptilia | Elaphe dione | Steppe Ratsnake | 65 |
| Reptilia | Rhabdophis tigrinus | Tiger Keelback | 52 |
| Reptilia | Gloydius ussuriensis | Ussuri Mamushi | 51 |
| Reptilia | Oocatochus rufodorsatus | Frog-eating Rat Snake | 37 |
| Reptilia | Pelodiscus maackii | Amur Softshell Turtle | 36 |
| Reptilia | Hebius vibakari | Japanese Keelback | 27 |
| Reptilia | Takydromus wolteri | Mountain Grass Lizard | 27 |
| Reptilia | Gloydius brevicauda | Short-tailed Mamushi | 25 |
| Reptilia | Trachemys scripta | Pond Slider | 23 |
| Reptilia | Pseudemys concinna | River Cooter | 21 |
| Reptilia | Takydromus amurensis | Amur Grass Lizard | 19 |
| Reptilia | Elaphe schrenckii | Manchurian Black Ratsnake | 18 |
| Reptilia | Scincella vandenburghi | Tsushima Ground Skink | 18 |
| Reptilia | Lycodon rufozonatus | Red-banded Snake | 16 |
| Reptilia | Trachemys scripta elegans | Red-eared Slider | 10 |
| Reptilia | Eremias argus | Mongolia Racerunner | 9 |
| Reptilia | Takydromus | Grass Lizards | 9 |
| Reptilia | Mauremys reevesii | Chinese Pond Turtle | 8 |
| Reptilia | Gloydius intermedius | Central Asian Pitviper | 5 |
| Reptilia | Mauremys sinensis | Common thread turtle | 5 |
| Reptilia | Pseudemys nelsoni | Florida Redbelly Turtle | 5 |
| Reptilia | Pseudemys peninsularis | Peninsular Cooter | 5 |
| Reptilia | Trachemys scripta scripta | Yellow-bellied Slider | 5 |
| Reptilia | Colubridae | Colubrid Snakes | 4 |
| Reptilia | Deirochelyinae | Deirochelyine Turtles | 4 |
| Reptilia | Scincella | Ground Skinks | 4 |
| Reptilia | Pseudemys | Cooters | 3 |
| Reptilia | Rhabdophis tigrinus tigrinus | 3 | |
| Reptilia | Aldabrachelys gigantea | Aldabra Giant Tortoise | 2 |
| Reptilia | Centrochelys sulcata | African Spurred Tortoise | 2 |
Table A2.
IUCN Red List categories for the top 30 species in each iNaturalist taxa group from the study area. Note that the IUCN code could not be retrieved from the GBIF database for 10 species.
Table A2.
IUCN Red List categories for the top 30 species in each iNaturalist taxa group from the study area. Note that the IUCN code could not be retrieved from the GBIF database for 10 species.
| IUCN Red List Category | Code | Number of Species | % |
|---|---|---|---|
| Not Evaluated | NE | 216 | 65.06% |
| Data Deficient | DD | 2 | 0.60% |
| Least Concern | LC | 94 | 28.31% |
| Near Threatened | NT | 4 | 1.20% |
| Vulnerable | VU | 6 | 1.81% |
| Endangered | EN | 7 | 2.11% |
| Critically Endangered | CR | 3 | 0.90% |
| Extinct in the Wild | EW | 0 | 0.00% |
| Extinct | EX | 0 | 0.00% |
| (No Data) | - | 10 | 0.03% |
| Total | - | 342 | 100.00% |
References
- Russell, R.; Guerry, A.D.; Balvanera, P.; Gould, R.K.; Basurto, X.; Chan, K.M.; Klain, S.; Levine, J.; Tam, J. Humans and nature: How knowing and experiencing nature affect well-being. Annu. Rev. Environ. Resour. 2013, 38, 473–502. [Google Scholar] [CrossRef]
- Pascual, U.; Balvanera, P.; Anderson, C.B.; Chaplin-Kramer, R.; Christie, M.; González-Jiménez, D.; Martin, A.; Raymond, C.M.; Termansen, M.; Vatn, A.; et al. Diverse values of nature for sustainability. Nature 2023, 620, 813–823. [Google Scholar] [CrossRef]
- Millennium Ecosystem Assessment. Ecosystems and Human Well-Being: Synthesis; Island Press: Washington, DC, USA, 2005. [Google Scholar]
- Fish, R.; Church, A.; Winter, M. Conceptualising cultural ecosystem services: A novel framework for research and critical engagement. Ecosyst. Serv. 2016, 21, 208–217. [Google Scholar] [CrossRef]
- Haines-Young, R.; Potschin, M. Common International Classification of Ecosystem Services (CICES) V5.1 and Guidance on the Application of the Revised Structure; Technical Report; Fabis Consulting Ltd.: Nottingham, UK, 2018. [Google Scholar]
- Bitoun, R.E.; Trégarot, E.; Devillers, R. Bridging theory and practice in ecosystem services mapping: A systematic review. Environ. Syst. Decis. 2022, 42, 103–116. [Google Scholar] [CrossRef]
- Tribot, A.S.; Deter, J.; Mouquet, N. Integrating the aesthetic value of landscapes and biological diversity. Proc. R. Soc. Biol. Sci. 2018, 285, 20180971. [Google Scholar] [CrossRef] [PubMed]
- Beery, T.; Stahl Olafsson, A.; Gentin, S.; Maurer, M.; Stålhammar, S.; Albert, C.; Bieling, C.; Buijs, A.; Fagerholm, N.; Garcia-Martin, M.; et al. Disconnection from nature: Expanding our understanding of human—Nature relations. People Nat. 2023, 5, 470–488. [Google Scholar] [CrossRef]
- Havinga, I.; Marcos, D.; Bogaart, P.; Massimino, D.; Hein, L.; Tuia, D. Social media and deep learning reveal specific cultural preferences for biodiversity. People Nat. 2023, 5, 981–998. [Google Scholar] [CrossRef]
- Curtin, S. Wildlife tourism: The intangible, psychological benefits of human—Wildlife encounters. Curr. Issues Tour. 2009, 12, 451–474. [Google Scholar] [CrossRef]
- Gomez, J.; van Vliet, N.; Canales, N. The values of wildlife revisited. Ecol. Soc. 2022, 27, 23. [Google Scholar] [CrossRef]
- Chhetri, P.; Arrowsmith, C.; Jackson, M. Determining hiking experiences in nature-based tourist destinations. Tour. Manag. 2004, 25, 31–43. [Google Scholar] [CrossRef]
- Santarém, F.; Silva, R.; Santos, P. Assessing ecotourism potential of hiking trails: A framework to incorporate ecological and cultural features and seasonality. Tour. Manag. Perspect. 2015, 16, 190–206. [Google Scholar] [CrossRef]
- Basnet, D.; Jianmei, Y.; Dorji, T.; Qianli, X.; Lama, A.K.; Maowei, Y.; Ning, W.; Yantao, W.; Gurung, K.; Rujun, L.; et al. Bird photography tourism, sustainable livelihoods, and biodiversity conservation: A case study from China. Mt. Res. Dev. 2021, 41, D1. [Google Scholar] [CrossRef]
- Davis, R.A.; Greenwell, C.; Davis, B.J.; Bateman, P.W. Liked to death: The impacts of social media and photography on biodiversity. Sci. Total. Environ. 2024, 949, 175106. [Google Scholar] [CrossRef] [PubMed]
- Geng, Y.; Hu, G.; Ranjitkar, S.; Shi, Y.; Zhang, Y.; Wang, Y. The implications of ritual practices and ritual plant uses on nature conservation: A case study among the Naxi in Yunnan Province, Southwest China. J. Ethnobiol. Ethnomed. 2017, 13, 58. [Google Scholar] [CrossRef]
- Turner, W.R.; Nakamura, T.; Dinetti, M. Global urbanization and the separation of humans from nature. Bioscience 2004, 54, 585–590. [Google Scholar] [CrossRef]
- Stanley, M.C.; Galbraith, J.A. Connecting people with place-specific nature in cities reduces unintentional harm. Environ. Res. Ecol. 2024, 3, 023001. [Google Scholar] [CrossRef]
- Bashan, D.; Colléony, A.; Shwartz, A. Urban versus rural? The effects of residential status on species identification skills and connection to nature. People Nat. 2021, 3, 347–358. [Google Scholar] [CrossRef]
- Nguyen, M.H.; Nguyen, M.H.T.; Jin, R.; Nguyen, Q.L.; La, V.P.; Le, T.T.; Vuong, Q.H. Preventing the separation of urban humans from nature: The impact of pet and plant diversity on biodiversity loss belief. Urban Sci. 2023, 7, 46. [Google Scholar] [CrossRef]
- Elmqvist, T.; Fragkias, M.; Goodness, J.; Güneralp, B.; Marcotullio, P.J.; McDonald, R.I.; Parnell, S.; Schewenius, M.; Sendstad, M.; Seto, K.C.; et al. Urbanization, Biodiversity and Ecosystem Services: Challenges and Opportunities: A Global Assessment; Springer Nature: Berlin/Heidelberg, Germany, 2013. [Google Scholar]
- Kageyama, S.; Saito, T.; Tajima, Y.; Hashimoto, S. Human—Nature connectedness is positively correlated with the perceived value of nature regardless of urbanization levels. In Sustainability Science; Springer: Berlin/Heidelberg, Germany, 2024; pp. 1–18. [Google Scholar]
- Tiago, P.; Leal, A.; Rosário, I.; Chozas, S. Discovering urban nature: Citizen science and biodiversity on a university campus. Urban Ecosyst. 2024, 27, 1609–1621. [Google Scholar] [CrossRef]
- Stanford, H.R.; Hurley, J.; Garrard, G.E.; Kirk, H. The contribution of informal green space to urban biodiversity: A city-scale assessment using crowdsourced survey data. Urban Ecosyst. 2025, 28, 1–16. [Google Scholar] [CrossRef]
- Pocock, M.J.; Chandler, M.; Bonney, R.; Thornhill, I.; Albin, A.; August, T.; Bachman, S.; Brown, P.M.; Cunha, D.G.F.; Grez, A.; et al. A vision for global biodiversity monitoring with citizen science. In Advances in Ecological Research; Elsevier: Amsterdam, The Netherlands, 2018; Volume 59, pp. 169–223. [Google Scholar]
- Obracht-Prondzyńska, H.; Radziszewski, K.; Anacka, H.; Duda, E.; Walnik, M.; Wereszko, K.; Geirbo, H.C. Codesigned Digital Tools for Social Engagement in Climate Change Mitigation. Sustainability 2023, 15, 16760. [Google Scholar] [CrossRef]
- World Health Organization. Local Action for Health; WHO: Geneva, Switzerland, 2024. [Google Scholar]
- Contreras-Díaz, R.G.; Nori, J.; Chiappa-Carrara, X.; Peterson, A.T.; Soberón, J.; Osorio-Olvera, L. Well-intentioned initiatives hinder understanding biodiversity conservation: Cloaked iNaturalist information for threatened species. Biol. Conserv. 2023, 282, 110042. [Google Scholar] [CrossRef]
- Bührs, M.; Zepp, H.; Schmitt, T. Evaluating Urban Biodiversity. Erdkunde 2024, 78, 195–224. [Google Scholar] [CrossRef]
- Gould, R.K.; Morse, J.W.; Adams, A.B. Cultural ecosystem services and decision-making: How researchers describe the applications of their work. People Nat. 2019, 1, 457–475. [Google Scholar] [CrossRef]
- Winder, S.G.; Lee, H.; Seo, B.; Lia, E.H.; Wood, S.A. An open-source image classifier for characterizing recreational activities across landscapes. People Nat. 2022, 4, 1249–1262. [Google Scholar] [CrossRef]
- Malinga, R.; Gordon, L.J.; Jewitt, G.; Lindborg, R. Mapping ecosystem services across scales and continents—A review. Ecosyst. Serv. 2015, 13, 57–63. [Google Scholar] [CrossRef]
- La Rosa, D.; Spyra, M.; Inostroza, L. Indicators of Cultural Ecosystem Services for urban planning: A review. Ecol. Indic. 2016, 61, 74–89. [Google Scholar] [CrossRef]
- Haklay, M.; Antoniou, V.; Basiouka, S.; Soden, R.; Mooney, P. Crowdsourced Geographic Information Use in Government; World Bank Publications: Washington, DC, USA, 2014. [Google Scholar]
- Silvertown, J.; Buesching, C.D.; Jacobson, S.K.; Rebelo, T. Citizen science and nature conservation. In Key Topics in Conservation Biology 2; Wiley: Hoboken, NJ, USA, 2013; pp. 127–142. [Google Scholar]
- Feldman, M.J.; Imbeau, L.; Marchand, P.; Mazerolle, M.J.; Darveau, M.; Fenton, N.J. Trends and gaps in the use of citizen science derived data as input for species distribution models: A quantitative review. PLoS ONE 2021, 16, e0234587. [Google Scholar] [CrossRef]
- Lee, H.; Seo, B.; Koellner, T.; Lautenbach, S. Mapping cultural ecosystem services 2.0—Potential and shortcomings from unlabeled crowd sourced images. Ecol. Indic. 2019, 96, 505–515. [Google Scholar] [CrossRef]
- Whitehorn, P.R.; Seo, B.; Comont, R.F.; Rounsevell, M.; Brown, C. The effects of climate and land use on British bumblebees: Findings from a decade of citizen-science observations. J. Appl. Ecol. 2022, 59, 1837–1851. [Google Scholar] [CrossRef]
- Adler, F.R.; Green, A.M.; Şekercioğlu, Ç.H. Citizen science in ecology: A place for humans in nature. Ann. N. Y. Acad. Sci. 2020, 1469, 52–64. [Google Scholar] [CrossRef] [PubMed]
- Allf, B.C.; Cooper, C.B.; Larson, L.R.; Dunn, R.R.; Futch, S.E.; Sharova, M.; Cavalier, D. Citizen science as an ecosystem of engagement: Implications for learning and broadening participation. BioScience 2022, 72, 651–663. [Google Scholar] [CrossRef]
- Chowdhury, S.; Aich, U.; Rokonuzzaman, M.; Alam, S.; Das, P.; Siddika, A.; Ahmed, S.; Labi, M.M.; Marco, M.D.; Fuller, R.A.; et al. Increasing biodiversity knowledge through social media: A case study from tropical Bangladesh. BioScience 2023, 73, 453–459. [Google Scholar] [CrossRef]
- Ziliaskopoulos, K.; Laspidou, C. Using remote-sensing and citizen-science data to assess urban biodiversity for sustainable cityscapes: The case study of Athens, Greece. Landsc. Ecol. 2024, 39, 9. [Google Scholar] [CrossRef]
- Kim, K.; Križnik, B.; Kamvasinou, K. Between the state and citizens: Changing governance of intermediary organisations for inclusive and sustainable urban regeneration in Seoul. Land Use Policy 2021, 105, 105433. [Google Scholar] [CrossRef]
- Korea Statistics. Korea Statistical Information Service (KOSIS), 2024. Available online: http://kosis.kr (accessed on 10 October 2024).
- Park, S.C.; Han, B.H. Using the City Biodiversity Index as a Method to Protect Biodiversity in Korean Cities. Sustainability 2021, 13, 11284. [Google Scholar] [CrossRef]
- Jo, J.H.; Park, S.H.; Koo, J.; Roh, T.; Lim, E.M.; Youn, Y.C. Preferences for ecosystem services provided by urban forests in South Korea. For. Sci. Technol. 2020, 16, 86–103. [Google Scholar]
- Serret, H.; Andersen, D.; Deguines, N.; Clauzel, C.; Park, W.H.; Jang, Y. Towards ecological management and sustainable urban planning in Seoul, South Korea: Mapping wild pollinator habitat preferences and corridors using citizen science data. Animals 2022, 12, 1469. [Google Scholar] [CrossRef]
- Korea Culture and Tourism Institute. Korean Tourism Statistics. Ministry of Culture, Sports, and Tourism. 2024. Available online: https://know.tour.go.kr/stat/visitStatDis/main.do (accessed on 10 October 2024).
- Barve, V.; Hart, E. rinat: Access ‘iNaturalist’ Data Through APIs, 2022. R Package Version 0.1.9. Available online: https://cran.r-project.org/web/packages/rinat/rinat (accessed on 10 October 2024).
- Global Biodiversity Information Facility (GBIF). GBIF: The Global Biodiversity Information Facility, 2025. Available online: https://www.gbif.org (accessed on 5 January 2025).
- Alfeus, M.; Irish, J.; Birkhofer, K. Recognition and completeness metrics from iNaturalist and GBIF can inform future citizen science and research projects: A case study on arthropods in Namibia. In Biodiversity and Conservation; Springer: Berlin/Heidelberg, Germany, 2024; pp. 1–14. [Google Scholar]
- Chamberlain, S.; Boettiger, C. R Python, and Ruby Clients for GBIF Species Occurrence Data. PeerJ 2017. Available online: https://peerj.com/preprints/3304v1/ (accessed on 5 January 2025).
- Chamberlain, S.; Barve, V.; Mcglinn, D.; Oldoni, D.; Desmet, P.; Geffert, L.; Ram, K. rgbif: Interface to the Global Biodiversity Information Facility API, 2025. R Package Version 3.8.1. Available online: https://cran.r-project.org/web/packages/rgbif (accessed on 5 January 2025).
- International Union for Conservation of Nature (IUCN). The Red List Index (RLI): A Tool for Measuring Trends in Biodiversity Status. 2025. Available online: https://www.iucnredlist.org/assessment/red-list-index (accessed on 5 January 2025).
- Baddeley, A.; Rubak, E.; Turner, R. Spatial Point Patterns: Methodology and Applications with R; Chapman and Hall/CRC Press: London, UK, 2015. [Google Scholar]
- Dixon, P. Ripley’s K-function. In Encyclopedia of Environmetrics; El-Shaarawi, A.H., Piegorsch, W.W., Eds.; John Wiley & Sons: Hoboken, NJ, USA, 2002; Volume 3, pp. 1803–1976. [Google Scholar]
- Ripley, B.D. Statistical Inference for Spatial Processes; Cambridge University Press: Cambridge, UK, 1988. [Google Scholar]
- Scott, D.W. Multivariate Density Estimation: Theory, Practice, and Visualization; John Wiley & Sons: Hoboken, NJ, USA, 2015. [Google Scholar]
- Baddeley, A.; Turner, R. spatstat: An R Package for Analyzing Spatial Point Patterns. J. Stat. Softw. 2005, 12, 1–42. [Google Scholar] [CrossRef]
- R Core Team. R: A Language and Environment for Statistical Computing. 2024. Available online: https://www.R-project.org (accessed on 10 October 2024).
- Lee, H.; Seo, B.; Cord, A.F.; Volk, M.; Lautenbach, S. Using crowdsourced images to study selected cultural ecosystem services and their relationships with species richness and carbon sequestration. Ecosyst. Serv. 2022, 54, 101411. [Google Scholar] [CrossRef]
- Skibins, J.C.; Powell, R.B.; Hallo, J.C. Charisma and conservation: Charismatic megafauna’s influence on safari and zoo tourists’ pro-conservation behaviors. Biodivers. Conserv. 2013, 22, 959–982. [Google Scholar] [CrossRef]
- White, M.E.; Hamlin, I.; Butler, C.W.; Richardson, M. The Joy of birds: The effect of rating for joy or counting garden bird species on wellbeing, anxiety, and nature connection. Urban Ecosyst. 2023, 26, 755–765. [Google Scholar] [CrossRef]
- Barbato, D.; Benocci, A.; Guasconi, M.; Manganelli, G. Light and shade of citizen science for less charismatic invertebrate groups: Quality assessment of iNaturalist nonmarine mollusc observations in central Italy. J. Molluscan Stud. 2021, 87, eyab033. [Google Scholar] [CrossRef]
- Di Cecco, G.J.; Barve, V.; Belitz, M.W.; Stucky, B.J.; Guralnick, R.P.; Hurlbert, A.H. Observing the observers: How participants contribute data to iNaturalist and implications for biodiversity science. BioScience 2021, 71, 1179–1188. [Google Scholar] [CrossRef]
- Geurts, E.M.; Reynolds, J.D.; Starzomski, B.M. Turning observations into biodiversity data: Broadscale spatial biases in community science. Ecosphere 2023, 14, e4582. [Google Scholar] [CrossRef]
- Ghimire, R.; Green, G.T.; Paudel, K.P.; Poudyal, N.C.; Cordell, H.K. Visitors’ preferences for freshwater amenity characteristics: Implications from the US household survey. J. Agric. Resour. Econ. 2017, 42, 90–113. [Google Scholar]
- Potsikas, M.; Prouska, K.; Efthimiou, G.; Plakitsi, K.; Kornelaki, A.C. Citizen science practice around Lake Pamvotis and the Ioannina Castle: Using iNaturalist to foster connectedness to nature in citizens and university students. Int. J. Geoheritage Park. 2023, 11, 450–463. [Google Scholar] [CrossRef]
- Cao, J.; Hochmair, H.H. Use of iNaturalist Biodiversity Contribution Data for Modelling Travel Distances to Parks Across the United States. AGILE Gisci. Ser. 2024, 5, 18. [Google Scholar] [CrossRef]
- Egarter Vigl, L.; Marsoner, T.; Giombini, V.; Pecher, C.; Simion, H.; Stemle, E.; Tasser, E.; Depellegrin, D. Harnessing artificial intelligence technology and social media data to support Cultural Ecosystem Service assessments. People Nat. 2021, 3, 673–685. [Google Scholar] [CrossRef]
- Chowdhury, S.; Fuller, R.A.; Ahmed, S.; Alam, S.; Callaghan, C.T.; Das, P.; Correia, R.A.; Di Marco, M.; Di Minin, E.; Jarić, I.; et al. Using social media records to inform conservation planning. Conserv. Biol. 2024, 38, e14161. [Google Scholar] [CrossRef]
- Kim, J.Y.; Do, Y.; Im, R.Y.; Kim, G.Y.; Joo, G.J. Use of large web-based data to identify public interest and trends related to endangered species. Biodivers. Conserv. 2014, 23, 2961–2984. [Google Scholar] [CrossRef]
- Sharp, R.; Tallis, H.; Ricketts, T.; Guerry, A.; Wood, S.; Chaplin-Kramer, R.; Nelson, E.; Ennaanay, D.; Wolny, S.; Olwero, N.; et al. InVEST User’s Guide; Technical Report, The Natural Capital Project; Stanford University: Stanford, CA, USA; University of Minnesota: Minneapolis, MN, USA; The Nature Conservancy: Arlington County, VA, USA; World Wildlife Fund: Gland, Switzerland, 2016. [Google Scholar]
- Qiu, J.; Mitchell, M. Understanding biodiversity–ecosystem service linkages in real landscapes. Landsc. Ecol. 2024, 39, 188. [Google Scholar] [CrossRef]
- Keleş Özgenç, E.; Dönmez, A.H.; Özgenç, E. Evaluating Cultural Ecosystem Services Through Geospatial Social Media Data: A Study of Edirne City. J. Geovis. Spat. Anal. 2024, 8, 30. [Google Scholar] [CrossRef]
- Wood, S.A.; Winder, S.G.; Lia, E.H.; White, E.M.; Crowley, C.S.; Milnor, A.A. Next-generation visitation models using social media to estimate recreation on public lands. Sci. Rep. 2020, 10, 15419. [Google Scholar] [CrossRef]
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content. |
© 2025 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).