Abstract
This review investigates the utilization of the One Health approach to advance sustainable development and enhance health in the Hainan tropical rainforest, which is a unique ecosystem with significant biodiversity and environmental value. The region is confronted with threats arising from human activities and climate change, impacting both the health of the inhabitants and the ecosystem. The Hainan tropical rainforests create an ideal habitat for the transmission of mosquito-borne diseases, such as dengue fever and malaria, between humans and animals. The hot and humid climate creates favorable conditions for mosquito proliferation, while increased human encroachment into forested areas escalates the risk of contact with wildlife reservoirs of these diseases. Proactive surveillance of emerging infectious diseases in the forests and animal populations of Hainan is crucial for early detection and swift response to potential public health hazards. By embracing the interdisciplinary and collaborative principles of the One Health approach, this review aims to safeguard the ecosystem while fostering development. The introduction offers insights into the significance of the One Health concept, its relevance to environmental conservation, human health, and animal health. Subsequently, the paper delves into the practical application of the One Health approach in the Hainan tropical rainforest, using it as a case study. This application entails raising awareness of ecosystem health through educational initiatives and public outreach, implementing effective ecological conservation measures, promoting wildlife conservation efforts, and monitoring and preventing potential disease outbreaks. Furthermore, the paper highlights the importance of the One Health approach in achieving sustainable development in the Hainan tropical rainforest. It also explores potential research directions and associated challenges. By prioritizing the collective well-being of humans, animals, and the environment, the One Health approach offers a means to balance ecosystem conservation and human welfare.
Similar content being viewed by others
Introduction
The Hainan tropical rainforest, located on Hainan Island in China, represents a globally significant symbol of remarkable biodiversity and ecological importance [1]. However, the convergence of zoonotic diseases and environmental degradation poses significant challenges to both human health and sustainable development in this area [2]. Specifically, the Hainan tropical rainforest is confronted with the prevalence and transmission of diseases such as Dengue Fever, which is propagated by the rapid proliferation of Aedes aegypti mosquitoes, and Malaria, facilitated by favorable breeding conditions for Anopheles mosquitoes in the humid rainforest environment [3,4,5]. There are also concerns regarding the transmission of the COVID-19 virus, as interactions between humans and wildlife, along with unhygienic market conditions, can facilitate zoonotic spillover events [6, 33,34,35].
Plant communities in the Hainan tropical rainforest
The Hainan tropical rainforest harbors a wide range of plant species, including several endemic ones that are exclusive to this region. Cycas hainanensis and Hainan hopea (Hopea hainanensis) are notable examples of such endemics [36, 37]. The rainforest’s dense canopy, formed by towering trees that can exceed 30 m in height, creates a complex vertical structure, providing diverse microhabitats for a variety of organisms. Numerous plant species contribute to the rich biodiversity of the rainforest.
One prominent tree species in the Hainan tropical rainforest is the Hainan hopea. Known for its hard and durable wood, it serves as a keystone species, providing habitat and contributing to the forest’s structural integrity [38]. The Hainan hopea plays a vital ecological role by supporting various wildlife species through habitat provision and resource availability [39]. Due to its slow growth and limited distribution, it is considered a protected species in China. Conservation efforts are in place to ensure the sustainable management of this iconic plant species in Hainan.
Another representative plant species found in the Hainan tropical rainforest and other parts of China is Alsophila spinulosa, commonly known as the Chinese tassel fern [40]. Belonging to the family Cyatheaceae, this large, perennial fern can reach heights of up to 10 m. The delicate and feathery appearance of its fronds, along with their vibrant green color, distinguishes it. Alsophila spinulosa thrives in moist and shady environments, often growing in the understory of tropical rainforests [41]. In the forest ecosystem, it plays a crucial ecological role by providing habitat for various organisms. Additionally, its fronds contribute to leaf litter, enriching the soil and supporting the growth of other plants. Conservation efforts are in place to protect Alsophila spinulosa due to habitat loss and collection for horticultural purposes [42]. The sustainable management of this beautiful fern species and the preservation of its natural habitat are vital for its long-term survival.
Cycas hainanensis, also known as the Hainan cycad or Hainan sago palm, is a species of cycad plant native to the tropical rainforests of China. Belonging to the Cycadaceae family, it exhibits a slow growth rate and retains its evergreen foliage. The plant features a robust trunk and large, pinnate leaves resembling palm fronds. Cycas hainanensis thrives in the tropical climate of Hainan Island, particularly in areas with partial shade and well-drained soil. It is commonly found in lowland forests and rocky hillsides. This cycad species holds the status of a living fossil, having existed for millions of years, thus rendering it a significant subject for scientific research and conservation efforts [43]. However, due to habitat loss and illegal collection for ornamental purposes, Cycas hainanensis is now classified as a protected species in China. To ensure its survival, conservation initiatives such as habitat preservation, captive breeding, and public awareness campaigns are being implemented.
Dacrydium pierrei, a coniferous tree belonging to the Podocarpaceae family, is characterized by its vibrant green leaves, reminiscent of the plumage of a bird known as the “Lujun bird.” This resemblance has led to its common name. Native to the mountainous regions of central and southern Hainan Island in China [44]. Pierre’s podocarp possesses a unique attribute: when wounded, it exudes red resin, earning it nicknames like “Tears-of-balsam” or “Red pine”. This resinous secretion holds both cultural and commercial significance. To address conservation concerns, protected areas have been established in the primary habitats of Dacrydium pierrei, such as Jianfengling and Bawangling [45]. These protected areas employ various measures, including artificial regeneration and facilitation of natural regeneration, to restore and conserve this species.
Animal biodiversity of the Hainan tropical rainforest
The Hainan tropical rainforest harbors a diverse array of remarkable and endangered animal species, including the critically endangered Hainan gibbon (Nomascus hainanus). With an estimated population of fewer than 40 individuals, the Hainan gibbon’s presence is crucial for maintaining the ecological equilibrium of the rainforest [46, 47]. Another endemic subspecies found in this region is the Hainan black crested gibbon (Nomascus sp. cf. nasutus hainanus), known for its distinctive vocalizations and significant role in seed dispersal, which influences forest regeneration [48, 49].
The Hainan tropical rainforest is also home to other notable animal species such as the Hainan Eld’s deer (Rucervus eldii hainanus), a critically endangered subspecies characterized by its light brown or reddish-brown coat with white spots and a distinctive throat mane in males. Habitat loss and poaching have led to its critical endangerment, as recognized by the International Union for Conservation of Nature (IUCN) [50]. Additionally, the Hainan black pig, adapted to the forest environment and displaying a smaller body size, contributes to the rainforest’s unique biodiversity [51].
Among the avian species, the Hainan Partridge (Arborophila ardens) stands out as a unique bird endemic to the high-altitude mountainous regions of the Hainan tropical rainforest [52]. Its dense brown feathers with speckled patterns aid in camouflage within the forest environment. While both males and females share a similar appearance, males possess a patch of red bare skin on their heads, adding vibrancy to their overall appearance [53]. Typically observed in pairs or small groups, the Hainan Partridge faces endangerment due to habitat destruction and human disturbance. Consequently, it is assessed as an endangered species by the International Union for Conservation of Nature [1].
The Hainan Peacock Pheasant (Polyplectron katsumatae) is another endemic bird species found exclusively in the Hainan tropical rainforest [54]. This pheasant species, belonging to the Phasianidae family, is admired for its striking plumage and elaborate courtship displays [55]. However, like many other pheasant species, the Hainan Peacock Pheasant is vulnerable to habitat loss and hunting pressures. Therefore, it is considered a protected species in China, necessitating conservation efforts through protected areas and raising awareness about the importance of preserving this unique bird [34].
The Hainan tropical rainforest encompasses a wealth of significant plant and animal species, many of which are endemic and play vital roles in maintaining the ecological balance of the region. Protecting and conserving these unique species and their habitats is essential for the sustainable development of the Hainan rainforest ecosystem in the long term. Collaborative efforts involving scientific research, community engagement, and policy support are key to preserving and managing this valuable natural resource.
Microbial communities and their ecological roles in tropical rainforests
Microorganisms play a crucial role in tropical rainforest ecosystems, contributing significantly to vital processes such as the decomposition of organic matter, nutrient cycling, and the stability of the ecosystem. Additionally, microbial communities enhance biodiversity and promote species adaptability, highlighting their essential regulatory role within these ecosystems [56].
Recent studies have shed light on the complex interactions between microbial communities and tropical rainforest ecosystems. For instance, Soong et al. demonstrated that microbial communities are key drivers of carbon cycling in tropical rainforests. Specific microbial taxa play significant roles in regulating carbon storage and release [57]. Furthermore, Deng et al. found a positive correlation between microbial biodiversity in the rhizosphere of tropical plants and plant health and productivity. This highlights the importance of plant-microbe interactions in sha** rainforest ecosystems [146].
In conclusion, the One Health approach has proven effective in addressing public health challenges in the Hainan tropical rainforest region. Its interdisciplinary nature and collaborative efforts are essential for understanding and mitigating the complex interactions between human, animal, and environmental health. By expanding the application of the One Health approach to other biodiverse ecosystems, we can enhance global infectious disease surveillance, conservation efforts, and sustainable development practices that prioritize the well-being of both humans and the environment.
In addition to the integrated disciplinary approach for conserving the tropical rainforest biosphere, another study aims to develop a tool based on the One Health concept for government utilization in public health security testing [147]. This tool assesses the potential risks of severe zoonotic diseases associated with wildlife trade, providing valuable information for the formulation of stringent regulation and control policies. Furthermore, several urgent plans are underway to address the changes occurring in the tropical rainforest, including the United Nations Decade on Ecosystem Restoration and the accelerated progress towards the Bonn Challenge [148, 149]. These plans aim to restore 350 million hectares of degraded and deforested land by 2030, thereby mitigating the destructive impact of deforestation-induced climate change on the tropical rainforest. Additionally, community participation, outreach, and capacity-building are vital cross-cutting components of effective One Health programs [150]. These initiatives equip local populations with the necessary knowledge and resources to promote health at both the individual and ecosystem levels. While specific ecological, cultural, and socioeconomic contexts may vary, the fundamental principles of One Health, including interdisciplinary cooperation, scientific research, and proactive risk mitigation, are broadly applicable across diverse settings worldwide. Integrating One Health principles into national and global policy agendas is crucial for addressing existing and emerging public health challenges at the interface of humans, animals, and the environment on a global scale.
The urgency and importance of addressing public health issues in the Hainan tropical rainforest region cannot be overstated. It is crucial to emphasize the need for increased efforts from the government, academia, and society at large to promote and support initiatives aimed at sustainable development and health improvement in this region [151]. Multiple studies and literature reports have highlighted the public health concerns in the Hainan tropical rainforest region. For example, researchers investigated the prevalence of zoonotic diseases in the wildlife of this region, highlighting the potential risks for human health [152, 153]. Additionally, scholars conducted research on the impact of deforestation on vector-borne diseases, demonstrating the close relationship between environmental changes and human health outcomes [154, 155]. In recent years, tropical rainforests have witnessed rapid environmental changes, including deforestation, habitat destruction, and climate change, among others [156]. These changes have had multifaceted impacts on human health [157]. As early as 2000, researchers investigated the correlation between environmental changes in the Amazon rainforest and human health [158]. They found that extensive development and deforestation in the Amazon River basin have led to the emergence of new diseases and the increased difficulty of controlling existing diseases. The excessive exploitation of tropical rainforests can also heighten human contact with wildlife, thereby increasing the risk of zoonotic diseases crossing species barriers and transmitting to humans [159, 160]. Recent outbreaks of new infectious diseases such as Ebola and Zika virus have been closely associated with activities in tropical forest regions [161, 162]. Furthermore, excessive deforestation of rainforests can disrupt the activity of vector organisms like mosquitoes, leading to more frequent occurrences of diseases such as malaria and dengue fever [64]. Additionally, climate change is expanding the geographical distribution range of these diseases. These findings underscore the necessity of adopting a comprehensive One Health approach to address the public health challenges in the Hainan tropical rainforest region. However, it is important to acknowledge that there is still progress to be made in implementing One Health practices in the Hainan tropical rainforest. For example, Wang and Zeng, using the Policy Modeling Consistency (PMC) index model, have pointed out that the policies of the Hainan Tropical Rainforest National Park are not sufficiently effective in terms of social and economic outcomes [126]. In comparison to Hong Kong and Singapore, the policies related to the Hainan Tropical Rainforest National Park lack adequate incentives and strategic guidance, primarily due to the absence of descriptive and predictive macro-strategic design [126]. This observation provides us with valuable recommendations and food for thought. By combining efforts from multiple disciplines, we can develop strategies that promote sustainable development, protect biodiversity, and improve the overall health and well-being of the local population in Hainan.
Conclusion
The tropical rainforests in Hainan are confronted with several critical public health issues that demand immediate attention. These issues include emerging infectious diseases, vector-borne diseases, and the health consequences of environmental degradation. This review discusses the risks posed to human populations in the region by zoonotic diseases such as hantavirus and potential novel coronaviruses originating from wildlife. Furthermore, the favorable climate in Hainan promotes the proliferation of disease-transmitting mosquitoes, which facilitate the transmission of diseases like dengue fever and malaria between humans and wildlife. Deforestation and habitat destruction have also contributed to the increase in disease vectors.
The implementation of the One Health approach offers an effective framework to address these interconnected challenges. As exemplified by the experiences in Hainan, key components such as enhanced disease surveillance, interdepartmental coordination, ecological conservation, and public engagement play vital roles. By adopting a collaborative and multidisciplinary strategy, early identification of public health threats and their mitigation through rapid response can be achieved. However, sustained efforts are necessary to involve local communities more extensively in environmental and public health initiatives.
The public health issues examined in the Hainan tropical rainforest underscore the relevance of One Health approaches in various ecosystems worldwide. Similar human-animal-environment interfaces, as observed in regions like the Amazon rainforests, can facilitate the emergence and transmission of zoonotic diseases. By implementing integrated surveillance, conservation measures, and community engagement within a One Health framework, effective preparedness and response can be ensured, spanning from remote forests to urban areas. While specific ecological and socioeconomic contexts may differ, the core principles of interdisciplinary collaboration, research, education, and communication inherent in One Health are broadly applicable across different settings. At local, national, and global levels, policy initiatives embracing the One Health approach have immense potential to cultivate resilient communities and environments worldwide. Addressing complex health challenges at the intersection of humans, animals, and nature necessitates a sustained commitment to cross-sectoral partnerships and evidence-based interventions.
Overall, this review emphasizes the urgency of prioritizing ecosystem and public health in Hainan’s tropical rainforests. While progress has been made in applying One Health principles, there are opportunities to strengthen long-term policies and frameworks to promote sustainability. Future priorities involve conducting further research on disease ecology, bolstering conservation measures, and improving health infrastructure and education. The One Health approach will continue to serve as a comprehensive model for balancing human welfare, animal health, and ecological well-being in this unique region.
Availability of data and materials
Data sharing is not applicable to this article as no datasets were generated or analysed during the current study.
References
Zong L. The path to effective national park conservation and management: Hainan tropical rainforest National Park System Pilot Area. Int J Geoheritage Parks. 2020;8(4):225–9.
Lu L, Chesters D, Zhang W, Li G, Ma Y, Ma H, et al. Small mammal investigation in spotted fever focus with DNA-barcoding and taxonomic implications on rodents species from Hainan of China. PLoS ONE. 2012;7(8):e43479.
Li Y, Zhou G, Zhong D, Wang X, Hemming‐Schroeder E, David RE, et al. Widespread multiple insecticide resistance in the major dengue vector Aedes albopictus in Hainan Province, China. Pest Manag Sci. 2021;77(4):1945–53.
Li Y, Zhou G, Zhong S, Wang X, Zhong D, Hemming-Schroeder E, et al. Spatial heterogeneity and temporal dynamics of mosquito population density and community structure in Hainan Island, China. Parasit Vectors. 2020;13:1–11.
Drews SJ, Wendel S, Leiby DA, Tonnetti L, Ushiro-Lumb I, O'Brien SF, et al. Climate change and parasitic risk to the blood supply. Transfusion. 2023;63(3):638–45.
Wang Y, Leader-Williams N, Turvey ST. Exploitation histories of pangolins and endemic pheasants on Hainan Island, China: baselines and shifting social norms. Front Ecol Evol. 2021;9:608057.
**e X, Huang L, Li J, Zhu H. Generational differences in perceptions of food health/risk and attitudes toward organic food and game meat: The case of the COVID-19 crisis in China. Int J Environ Res Public Health. 2020;17(9):3148.
Heymann DL, Dixon MJMS. The value of the One Health approach: shifting from emergency response to prevention of zoonotic disease threats at their source. Microbiol Spectr. 2013;1(1):10–128. https://doi.org/10.1128/microbiolspec.oh-0011-2012.
Gibbs EPJ. The evolution of One Health: a decade of progress and challenges for the future. Vet Rec. 2014;174(4):85–91.
Hernando-Amado S, Coque TM, Baquero F, Martínez JL. Defining and combating antibiotic resistance from One Health and Global Health perspectives. Nat Microbiol. 2019;4(9):1432–42.
Kelly TR, Machalaba C, Karesh WB, Crook PZ, Gilardi K, Nziza J, et al. Implementing One Health approaches to confront emerging and re-emerging zoonotic disease threats: lessons from PREDICT. One Health Outlook. 2020;2:1–7.
Mackenzie JS, Jeggo M. The One Health approach—why is it so important? Trop Med Infect Dis. 2019;4:88.
Zinsstag J, Schelling E, Crump L, Whittaker M, Tanner M, Stephen C. One Health: the theory and practice of integrated health approaches. Wallingford: CABI; 2021.
Rousham EK, Unicomb L, Islam MA. Human, animal and environmental contributors to antibiotic resistance in low-resource settings: integrating behavioural, epidemiological and One Health approaches. Proc R Soc B Biol Sci. 1876;2018(285):20180332.
Filter M, Buschhardt T, Dórea F, de Abechuco EL, Günther T, Sundermann EM, et al. One Health surveillance codex: promoting the adoption of One Health solutions within and across European countries. 2021;12:100233.
Water S. Hygiene: reinvent the toilet challenge. Bill and Melinda Gates Foundation; 2013. https://docs.gatesfoundation.org/documents/Fact_Sheet_Reinvent_the_Toilet_Challenge.pdf. Accessed 1 Aug 2023.
Kone D. Water, sanitation and hygiene: reinvent the toilet challenge. ECS Meet Abstr. 2012;MA2012-01:79.
Sikkema R, Koopmans MJIE. One Health training and research activities in Western Europe. Infect Ecol Epidemiology. 2016;6(1):33703.
Espinosa-Gongora C, Jessen LR, Dyar OJ, Bousquet-Melou A, González-Zorn B, Pulcini C, et al. Towards a better and harmonized education in antimicrobial stewardship in European veterinary curricula. Antibiotics. 2021;10(4):364.
Pieracci EG, Hall AJ, Gharpure R, Haile A, Walelign E, Deressa A, et al. Prioritizing zoonotic diseases in Ethiopia using a one health approach. One Health. 2016;2:131–5.
Barrett MA, Bouley TA, Stoertz AH, Stoertz RW. Integrating a One Health approach in education to address global health and sustainability challenges. Front Ecol Environ. 2011;9(4):239–45.
Mackenzie JS, McKinnon M, Jeggo M. One Health: from concept to practice. In: Yamada A, Kahn L, Kaplan B, Monath T, Woodall J, Conti L, editors. Confronting emerging zoonoses. Tokyo: Springer; 2014. p. 163–89.
Waltner-Toews D. Zoonoses, One Health and complexity: wicked problems and constructive conflict. Philos Trans R Soc B: Biol Sci. 2017;372(1725):20160171.
Meng H-H, Zhou S-S, Li L, Tan Y-H, Li J-W, Li J. Conflict between biodiversity conservation and economic growth: insight into rare plants in tropical China. Biodivers Conserv. 2019;28:523–37.
Bolt LM, Brandt LSE, Molina RL, Schreier AL. Maderas rainforest conservancy: a One Health approach to conservation. Am J Primatol. 2022;84(4–5):e23293.
Smout FA, Skerratt LF, Butler JRA, Johnson CN, Congdon BC, Thompson RCA. The hookworm Ancylostoma ceylanicum: an emerging public health risk in Australian tropical rainforests and indigenous communities. One Health. 2017;3:66–9.
Lowe R, Lee S, Martins LR, Torres CC, Castro MC, Pascual M. Emerging arboviruses in the urbanized Amazon rainforest. BMJ. 2020;371:m4385.
Ellwanger JH, Kulmann-Leal B, Kaminski VL, Valverde-Villegas JM, Veiga ABGD, Spilki FR, et al. Beyond diversity loss and climate change: impacts of Amazon deforestation on infectious diseases and public health. An Acad Bras Cienc. 2020;01:92.
He J, Lin S, Kong F, Yu J, Zhu H, Jiang H. Determinants of the beta diversity of tree species in tropical forests: implications for biodiversity conservation. Sci Total Environ. 2020;704:135301.
Zhu ZX, Harris A, Nizamani MM, Thornhill AH, Scherson RA, Wang HF. Spatial phylogenetics of the native woody plant species in Hainan, China. Ecol Evol. 2021;11(5):2100–9.
Lan G, Wu Z, Yang C, Sun R, Chen B, Zhang X. Tropical rainforest conversion into rubber plantations results in changes in soil fungal composition, but underling mechanisms of community assembly remain unchanged. Geoderma. 2020;375:114505.
Lan G, Wu Z, Chen B, **e G. Species diversity in a naturally managed rubber plantation in Hainan Island, South China. Trop Conserv Sci. 2017;10:1940082917712427.
Mo J, Li J, Liu F, Li X, Li D. A survey of mammals and birds diversity in Jianfengling district of Hainan Province by using camera-trap**. Sci Silvae Sin. 2019;55(10):203–10.
Chang J, Chen D, Liang W, Li M, Zhang Z. Molecular demographic history of the Hainan peacock pheasant (Polyplectron katsumatae) and its conservation implications. Chin Sci Bull. 2013;58:2185–90.
Bryant JV, Turvey ST, Wong MH, Traylor-Holzer K. Conserving the world's rarest ape: action planning for the Hainan gibbon. Oryx. 2015;49(3):391–2.
Erhuan W, Donghai L, **aobo Y, Yongling Z, Ning Y. Study on distribution characteristics and population dynamics of wild Cycas Hainanensis in Hainan Island. For Ecol Manag. 2021;4:130.
Critchfield WB, Little EL. Geographic distribution of the pines of the world. Washington, D.C.: U.S. Department of Agriculture, Forest Service; 1966.
Zhang L, Zhang H-L, Chen Y, Nizamani MM, Zhou Q, Su X. Analyses of community stability and inter-specific associations between a plant species with extremely small populations (Hopea hainanensis) and its associated species. Front Ecol Evol. 2022;10:922829.
Chen Y, Zhang H-L, Zhang L, Nizamani MM, Zhou T, Zhang H, et al. Genetic diversity assessment of Hopea hainanensis in Hainan Island. Front Plant Sci. 2022;13:1075102.
Ruibai Z, **aobo Y, Donghai L, Chunlin Q, Jianbi L. Study on geographical distribution and distribution characteristics of cyatheaceae in Hainan Island. For Ecol Manag. 2018;2:65.
Yang Q-J, Li R. Predicting the potential suitable habitats of Alsophila spinulosa and their changes. J Appl Ecol. 2021;32(2):538–48.
Song P, Hong W, Wu C, Feng L, Fan H, Zhu H, et al. Population structure and its dynamics of rare and endangered plant Alsophila spinulosa. J Appl Ecol. 2005;16(3):413–8.
Wu E, Li D, Yang X, Zuo Y, Li L, Zhang P, et al. Population structure of Cycas hainanensis and its relationship with forest canopy density. Biodivers Sci. 2021;29(11):1461.
Wu C, Chen Y, Chen Q, Hong X, Han W, Li X. Characteristics of seed rain and soil seed bank of Dacrydium pierrei in Bawangling, Hainan. J Trop Subtrop Bot. 2018;26(1):13–23.
Wu C, Xu Y, Chen Y, Chen Q, Hong X, Han W, et al. Study on soil seed bank of Dacrydium pierrei natural regeneration in Bawangling, Hainan, China. Forest Res Bei**g. 2018;31(2):83–91.
Mootnick A, Chan B, Moisson P, Nadler T. The status of the Hainan gibbon Nomascus hainanus and the eastern black gibbon Nomascus nasutus. Int Zoo Yearb. 2012;46(1):259–64.
Deng H, Zhang M, Zhou J. Recovery of the critically endangered Hainan gibbon Nomascus hainanus. Oryx. 2017;51(1):161–5.
Fan P. The past, present, and future of gibbons in China. Biol Conserv. 2017;210:29–39.
Wei W, Wang X, Claro F, Ding Y, Souris A-C, Wang C, et al. The current status of the Hainan black-crested gibbon Nomascus sp. cf. nasutus hainanus in Bawangling National Nature Reserve, Hainan, China. Oryx. 2004;38(4):452–6.
Wong MH, Mo Y, Chan BPL. Past, present and future of the globally endangered Eld’s deer (Rucervus eldii) on Hainan Island, China. Glob Ecol Conserv. 2021;26:e01505.
Rattanaronchart S. Present situation of Thai native pigs [dissertation]. Chiangmai: Chiangmai University; 1994.
Yang C, Chen X, Zhang Z, Liang W. First report of home range size of Hainan partridge Arborophila ardens, a vulnerable species endemic to Hainan Island. Ornithol Sci. 2023;22(1):87–92.
Rao X, Yang C, Liang W. Breeding biology and novel reproductive behaviour in the Hainan partridge (Arborophila ardens). Avian Res. 2017;8(1):1–6.
Liang W, Zhang Z. Hainan peacock-pheasant (Polyplectron katsumatae): an endangered and rare tropical forest bird. Chinese Birds. 2011;2(2):111–6.
Turvey ST, Ma H, Zhou T, Teng T, Yu C, Archer LJ, et al. Local ecological knowledge and regional sighting histories of Hainan peacock-pheasant Polyplectron katsumatae: pessimism or optimism for a threatened island endemic? Bird Conserv Int. 2023;33:e25.
Warren SD. Microorganisms of the Phyllosphere: origin, transport, and ecological functions. Front Glob Change. 2022;5:843168.
Soong JL, Fuchslueger L, Marañon-Jimenez S, Torn MS, Janssens IA, Penuelas J, et al. Microbial carbon limitation: the need for integrating microorganisms into our understanding of ecosystem carbon cycling. Glob Chang Biol. 2020;26(4):1953–61.
Deng Z, Wang Y, **ao C, Zhang D, Feng G, Long W. Effects of plant fine root functional traits and soil nutrients on the diversity of rhizosphere microbial communities in tropical cloud forests in a dry season. Forests. 2022;13(3):421.
Adeniyi AS. Effects of slash and burning on soil microbial diversity and abundance in the tropical rainforest ecosystem, Ondo state, Nigeria. African J Plant Sci. 2010;4(9):322–9.
Ammitzboll H, Jordan GJ, Baker SC, Freeman J, Bissett A. Diversity and abundance of soil microbial communities decline, and community compositions change with severity of post-logging fire. Mol Ecol. 2021;30(10):2434–48.
Sánchez-Galindo LM, Sandmann D, Marian F, Lauermann T, Maraun M, Scheu S. Differences in leaf and root litter decomposition in tropical montane rainforests are mediated by soil microorganisms not by decomposer microarthropods. PeerJ. 2022;10:e14264.
Wang Q-W, Tao L, Lu S-Y, Zhu C-Q, Ai L-L, Luo Y, et al. Genetic and hosts characterization of hantaviruses in port areas in Hainan Province, PR China. PLoS One. 2022;17(3):e0264859.
Yue Y, Liu Q, Liu X, Zhao N, Yin W. Dengue fever in mainland China, 2005–2020: a descriptive analysis of dengue cases and Aedes data. Int J Environ Res Public Health. 2022;19(7):3910.
Gan SJ, Leong YQ, bin Barhanuddin MF, Wong ST, Wong SF, Mak JW, et al. Dengue fever and insecticide resistance in Aedes mosquitoes in Southeast Asia: a review. Parasit Vectors. 2021;14(1):1–19.
Hasan MJ, Tabassum T, Sharif M, Khan MA, Bipasha AR, Basher A, et al. Comparison of clinical manifestation of dengue fever in Bangladesh: an observation over a decade. BMC Infect Dis. 2021;21:1–10.
Imad HA, Phumratanaprapin W, Phonrat B, Chotivanich K, Charunwatthana P, Muangnoicharoen S, et al. Cytokine expression in dengue fever and dengue hemorrhagic fever patients with bleeding and severe hepatitis. Am J Trop Med Hyg. 2020;102(5):943.
Guan Q, Upadhyay A, Han Q. History of dengue fever prevalence and Management in a One Health perspective in Hainan Island, China. In: Sperança M, editor. Dengue fever in a One Health perspective - latest research and recent advances. London: IntechOpen; 2023.
Wang C, Zhang B, Chen W, Chen Y. A comprehensive report on three epidemics of dengue fever and dengue hemorrhagic fever in Hainan Island. Disease Surveillance. 1992;7(6):4. https://doi.org/10.3784/j.issn.1003-9961.1992.6.151.
Zhao Z, Lin H. Control measures of dengue fever and dengue hemorrhagic fever were analyzed by preventive medicine in South China. South China J Prev Med. 1989;3:77–80.
Du J, Zhang L, Hu X, Peng R, Wang G, Huang Y, et al. Phylogenetic analysis of the dengue virus strains causing the 2019 dengue fever outbreak in Hainan, China. Virol Sin. 2021;36:636–43.
Vasconcelos MPA, Sánchez-Arcila JC, Peres L, de Sousa PSF, dos Santos Alvarenga MA, Castro-Alves J, et al. Malarial and intestinal parasitic co-infections in indigenous populations of the Brazilian Amazon rainforest. J Infect Public Health. 2023;16(4):603–10.
Salim M, Masroor MS, Parween S. An overview on human helminthic parasitology I. Nematodes, the roundworms. Int J Med Res. 2021;7(5):161–6.
Rahantamalala A, Rakotoarison RL, Rakotomalala E, Rakotondrazaka M, Kiernan J, Castle PM, et al. Prevalence and factors associated with human Taenia solium taeniosis and cysticercosis in twelve remote villages of Ranomafana rainforest, Madagascar. PLoS Negl Trop Dis. 2022;16(4):e0010265.
Liu Q, **g W, Kang L, Liu J, Liu M. Trends of the global, regional and national incidence of malaria in 204 countries from 1990 to 2019 and implications for malaria prevention. J Travel Med. 2021;28(5):taab046.
Zawawi A, Alghanmi M, Alsaady I, Gattan H, Zakai H, Couper K. The impact of COVID-19 pandemic on malaria elimination. Parasite Epidemiol Control. 2020;11:e00187.
Amimo F, Lambert B, Magit A. What does the COVID-19 pandemic mean for HIV, tuberculosis, and malaria control? Trop Med Health. 2020;48:1–4.
Osei SA, Biney RP, Anning AS, Nortey LN, Ghartey-Kwansah G. Low incidence of COVID-19 case severity and mortality in Africa; Could malaria co-infection provide the missing link? BMC Infect Dis. 2022;22(1):78.
Gavi S, Tapera O, Mberikunashe J, Kanyangarara M. Malaria incidence and mortality in Zimbabwe during the COVID-19 pandemic: analysis of routine surveillance data. Malar J. 2021;20(1):233.
Li Y, Huang Y, Chen R, Huang W, Xu H, Ye R, et al. An innovative three-layer strategy in response to a quartan malaria outbreak among forest goers in Hainan Island, China: a retrospective study. Infect Dis Poverty. 2022;11(1):1–10.
Carrasco-Escobar G, Qquellon J, Villa D, Cava R, Llanos-Cuentas A, Benmarhnia T. Time-varying effects of meteorological variables on malaria epidemiology in the context of interrupted control efforts in the amazon rainforest, 2000–2017. Front Med. 2021;8:721515.
Chaves LSM, Bergo ES, Conn JE, Laporta GZ, Prist PR, Sallum MAM. Anthropogenic landscape decreases mosquito biodiversity and drives malaria vector proliferation in the Amazon rainforest. PLoS One. 2021;16(1):e0245087.
Morgan CE, Topazian HM, Brandt K, Mitchell C, Kashamuka MM, Muwonga J, et al. Association between domesticated animal ownership and Plasmodium falciparum parasite prevalence in the Democratic Republic of the Congo: a national cross-sectional study. Lancet Microbe. 2023;4(7):E516–23.
Ma H. Local perceptions of biodiversity loss and conservation: insights from rural communities around a key protected area in Hainan, China [dissertation]. London: Royal Holloway, University of London; 2021.
Garry RF. The evidence remains clear: SARS-CoV-2 emerged via the wildlife trade. Proc Natl Acad Sci. 2022;119(47):e2214427119.
**ao K, Zhai J, Feng Y, Zhou N, Zhang X, Zou J-J, et al. Isolation of SARS-CoV-2-related coronavirus from Malayan pangolins. Nature. 2020;583(7815):286–9.
Hassanin A, Tu VT, Curaudeau M, Csorba G. The ecological niche of SARS-CoV-2-like viruses in bats, as inferred from phylogeographic analyses of Rhinolophus species [Preprint]. 2021. Available from: https://www.preprints.org/manuscript/202103.0409/v1.
Cho CT, Wenner HA. Monkeypox virus. Bacteriol Rev. 1973;37(1):1–18.
Arita I, Henderson D. Smallpox and monkeypox in non-human primates. Bull World Health Organ. 1968;39(2):277.
Gould DJ, Cadigan FC, Ward RA. Falciparum malaria: transmission to the gibbon by Anopheles balabacensis. Science. 1966;153(3742):1384–4.
Cadigan F Jr, Ward R, Puhomchareon S. Transient infection of the gibbon with Plasmodium vivax malaria. Trans R Soc Trop Med Hyg. 1968;62(2):295–6.
Halpin K, Young PL, Field H, Mackenzie J. Isolation of Hendra virus from pteropid bats: a natural reservoir of Hendra virus. J Gen Virol. 2000;81(8):1927–32.
Zhang H, Yang X, Li G. Detection of dengue virus genome RNA in some kinds of animals caught from dengue fever endemic areas in Hainan Island with reverse transcription-polymerase chain reaction. Chin J Exp Clin Virol. 1998;12(3):226–8.
Jiang L, Chen S, Zheng X, Ma S, Zhou J, Zhang Q, et al. Detection of serum antibodies against Japanese encephalitis virus in bats in Hainan and Guangdong provinces of China. J Southern Med Univ. 2015;35(5):720–3.
Epstein JH, Anthony SJ, Islam A, Kilpatrick AM, Ali Khan S, Balkey MD, et al. Nipah virus dynamics in bats and implications for spillover to humans. Proc Natl Acad Sci. 2020;117(46):29190–201.
Giangaspero M. Nipah virus. Trop Med Surg. 2013;1(129):2.
Si D, Marquess J, Donnan E, Harrower B, McCall B, Bennett S, et al. Potential exposures to Australian bat lyssavirus notified in Queensland, Australia, 2009–2014. PLoS Negl Trop Dis. 2016;10(12):e0005227.
Barrett JL. Australian bat lyssavirus [dissertation]. Brisbane: The University of Queensland; 2004.
Leroy EM, Kumulungui B, Pourrut X, Rouquet P, Hassanin A, Yaba P, et al. Fruit bats as reservoirs of Ebola virus. Nature. 2005;438(7068):575–6.
Leendertz SAJ, Gogarten JF, Düx A, Calvignac-Spencer S, Leendertz FH. Assessing the evidence supporting fruit bats as the primary reservoirs for Ebola viruses. EcoHealth. 2016;13:18–25.
Morens DM, Breman JG, Calisher CH, Doherty PC, Hahn BH, Keusch GT, et al. The origin of COVID-19 and why it matters. Am J Trop Med Hyg. 2020;103(3):955.
Rothan HA, Byrareddy SN. The epidemiology and pathogenesis of coronavirus disease (COVID-19) outbreak. J Autoimmun. 2020;109:102433.
Shereen MA, Khan S, Kazmi A, Bashir N, Siddique R. COVID-19 infection: emergence, transmission, and characteristics of human coronaviruses. J Adv Res. 2020;24:91–8.
Field HE. Hendra virus ecology and transmission. Curr Opin Virol. 2016;16:120–5.
Han G-Z. Pangolins harbor SARS-CoV-2-related coronaviruses. Trends Microbiol. 2020;28(7):515–7.
Zhang T, Wu Q, Zhang Z. Probable pangolin origin of SARS-CoV-2 associated with the COVID-19 outbreak. Curr Biol. 2020;30(7):1346–51.
Liu P, Jiang J-Z, Wan X-F, Hua Y, Li L, Zhou J, et al. Are pangolins the intermediate host of the 2019 novel coronavirus (SARS-CoV-2)? PLoS Pathog. 2020;16(5):e1008421.
He Q, Yan S, Garber PA, Ren B, Qi X, Zhou J. Habitat restoration is the greatest challenge for population recovery of Hainan gibbons (Nomascus hainanus). Integr Zool. 2023;18(4):630–46.
Karagoz A, Tombuloglu H, Alsaeed M, Tombuloglu G, AlRubaish AA, Mahmoud A, et al. Monkeypox (mpox) virus: classification, origin, transmission, genome organization, antiviral drugs, and molecular diagnosis. J Infect Public Health. 2023;16(4):531–41.
Patel M, Adnan M, Aldarhami A, Bazaid AS, Saeedi NH, Alkayyal AA, et al. Current insights into diagnosis, prevention strategies, treatment, therapeutic targets, and challenges of monkeypox (mpox) infections in human populations. Life. 2023;13(1):249.
Aden D, Zaheer S, Kumar R, Ranga S. Monkeypox (Mpox) outbreak during COVID-19 pandemic—Past and the future. J Med Virol. 2023;95(4):e28701.
Denner J. Transspecies transmission of gammaretroviruses and the origin of the gibbon ape leukaemia virus (GALV) and the koala retrovirus (KoRV). Viruses. 2016;8(12):336.
Yang X, Zhang Y, Ge X, Yuan J, Shi Z. A novel totivirus-like virus isolated from bat guano. Arch Virol. 2012;157:1093–9.
Jacob ST, Crozier I, Fischer WA II, Hewlett A, Kraft CS, Vega MA, et al. Ebola virus disease. Nat Rev Dis Primers. 2020;6(1):13.
Tomori O, Kolawole MO. Ebola virus disease: current vaccine solutions. Curr Opin Immunol. 2021;71:27–33.
Hoenen T, Groseth A, Feldmann H. Therapeutic strategies to target the Ebola virus life cycle. Nat Rev Microbiol. 2019;17(10):593–606.
Baseler L, Chertow DS, Johnson KM, Feldmann H, Morens DM. The pathogenesis of Ebola virus disease. Annu Rev Pathol. 2017;12:387–418.
Haider N, Rothman-Ostrow P, Osman AY, Arruda LB, Macfarlane-Berry L, Elton L, et al. COVID-19—zoonosis or emerging infectious disease? Front Public Health. 2020;8:763.
Yang L, Liu S, Liu J, Zhang Z, Wan X, Huang B, et al. COVID-19: immunopathogenesis and immunotherapeutics. Signal Transduct Target Ther. 2020;5(1):128.
Nile SH, Nile A, Qiu J, Li L, Jia X, Kai G. COVID-19: pathogenesis, cytokine storm and therapeutic potential of interferons. Cytokine Growth Factor Rev. 2020;53:66–70.
Gusev E, Sarapultsev A, Solomatina L, Chereshnev V. SARS-CoV-2-specific immune response and the pathogenesis of COVID-19. Int J Mol Sci. 2022;23(3):1716.
Hu B, Guo H, Zhou P, Shi Z-L. Characteristics of SARS-CoV-2 and COVID-19. Nat Rev Microbiol. 2021;19(3):141–54.
Cui X, Fan K, Liang X, Gong W, Chen W, He B, et al. Virus diversity, wildlife-domestic animal circulation and potential zoonotic viruses of small mammals, pangolins and zoo animals. Nat Commun. 2023;14(1):2488.
Liu P, Chen W, Chen J-P. Viral metagenomics revealed Sendai virus and coronavirus infection of Malayan pangolins (Manis javanica). Viruses. 2019;11(11):979.
Barton DP, Martelli P, Worthington BM, Lam TT-Y, Zhu X, Shamsi S. Nematode and acanthocephalan parasites of confiscated Sunda pangolins, Manis javanica Desmarest, 1822 (Mammalia: Pholidota: Manidae), with an updated list of the parasites of pangolins. Diversity. 2022;14(12):1039.
Liang T, Tan H, Qi Y. One Health practice in Hainan, China. Asian Pac J Trop Med. 2023;16(6):241–2.
Wang H, Zeng Y. Policy optimization for Hainan tropical rainforest National Park Based on quantitative comparison of regional policies of free trade port areas. Front Environ Sci. 2022;10:891432.
Zhao Z, Li Z, Wang N, Xu J, Wang C, Chen Y, et al. Environment and community prevention of dengue fever in Hainan Island. Chin J Vector Biol Control. 1993;4(5):6.
Zeng XP, Chen Q, Wang MC, Li YW, Zeng XY, Lin CY. Comparison of epidemiological characteristics of local and imported cases of dengue fever in Haikou, 2019. China Trop Med. 2021;8:779–83.
Zhang X, Yan M, Zhang L, Chen B. A study to assess the conservation effectiveness of nature reserves in Hainan, China, from 2000 to 2021. Forests. 2023;14(7):1293.
Yu B, Chao X, Zhang J, Xu W, Ouyang Z. Effectiveness of nature reserves for natural forests protection in tropical Hainan: a 20 year analysis. Chin Geogr Sci. 2016;26:208–15.
Chan BP, Lo YF, Hong XJ, Mak CF, Ma Z. First use of artificial canopy bridge by the world’s most critically endangered primate the Hainan gibbon Nomascus hainanus. Sci Rep. 2020;10(1):15176.
Xue Q, Zeng X, Du Y, Long WJF. Reproductive phenology and climatic drivers of plant species used as food by the Hainan Gibbon, Nomascus hainanus (Primates: Hylobatidae). Forests. 2023;14(9):1732.
Zhang M, Fellowes JR, Jiang X, Wang W, Chan BP, Ren G, et al. Degradation of tropical forest in Hainan, China, 1991–2008: conservation implications for Hainan Gibbon (Nomascus hainanus). Biol Conserv. 2010;143(6):1397–404.
Liu G, Lu X, Liu Z, **e Z, Qi X, Zhou J, et al. The critically endangered Hainan gibbon (Nomascus hainanus) population increases but not at the maximum possible rate. Int J Primatol. 2022;43(5):932–45.
Zeng Z, Song Y, Li J, Teng L, Zhang Q, Guo F. Distribution, status and conservation of Hainan Eld's deer (Cervus eldi hainanus) in China. Folia Zool-Praha. 2005;54(3):249.
Wong MH, Mo Y, Chan BP. Conservation, past, present and future of the globally endangered Eld’s deer (Rucervus eldii) on Hainan Island. China Glob Ecol Conserv. 2021;26:e01505.
Zhang J, Fedder B, Wang D, Jennerjahn TC. A knowledge exchange framework to connect research, policy, and practice, developed through the example of the Chinese island of Hainan. Environ Sci Pol. 2022;136:530–41.
Dong Z, Yuan Z, Long F, Wang C, Zhang C, Yang F, et al. A pilot study on green economy policy assessment of the United Nations—taking the assessment of ecological compensation policy in Hainan Province of China as an example. Environ Strat Plann China. 2022:225–51.
Benis A, Tamburis O, Chronaki C, Moen A. One digital health: a unified framework for future health ecosystems. J Med Internet Res. 2021;23(2):e22189.
McClymont H, Bambrick H, Si X, Vardoulakis S, Hu W. Future perspectives of emerging infectious diseases control: a One Health approach. One Health. 2022;14:100371.
Rabozzi G, Bonizzi L, Crespi E, Somaruga C, Sokooti M, Tabibi R, et al. Emerging zoonoses: the “one health approach”. Saf Health Work. 2012;3(1):77–83.
Chen K-T. Emerging infectious diseases and One Health: implication for public health. Int J Environ Res Public Health. 2022;19:9081.
Dente MG, Riccardo F, Bolici F, Colella NA, Jovanovic V, Drakulovic M, et al. Implementation of the One Health approach to fight arbovirus infections in the Mediterranean and Black Sea region: assessing integrated surveillance in Serbia, Tunisia and Georgia. Zoonoses Public Health. 2019;66(3):276–87.
Guo F, Bonebrake TC, Gibson L. Land-use change alters host and vector communities and May elevate disease risk. EcoHealth. 2019;16(4):647–58.
Johnson CK, Hitchens PL, Pandit PS, Rushmore J, Evans TS, Young CCW, et al. Global shifts in mammalian population trends reveal key predictors of virus spillover risk. Proc Biol Sci. 1924;2020(287):20192736.
Taylor E, Aguilar-Ancori EG, Banyard AC, Abel I, Mantini-Briggs C, Briggs CL, et al. The Amazonian tropical bites research initiative, a hope for resolving zoonotic neglected tropical diseases in the One Health era. Int Health. 2023;15(2):216–23.
Wikramanayake E, Pfeiffer DU, Magouras I, Conan A, Ziegler S, Bonebrake TC, et al. A tool for rapid assessment of wildlife markets in the Asia-Pacific region for risk of future zoonotic disease outbreaks. One Health. 2021;13:100279.
Cooke S, Bennett J, Jones H. We have a long way to go if we want to realize the promise of the “decade on ecosystem restoration”. Conserv Sci Pract. 2019;1(12):e129.
Verdone M, Seidl A. Time, space, place, and the Bonn challenge global forest restoration target. Restor Ecol. 2017;25(6):903–11.
Daszak P, das Neves C, Amuasi J, Haymen D, Kuiken T, Roche B, et al. Workshop report on biodiversity and pandemics of the intergovernmental platform on biodiversity and ecosystem services. Bonn: IPBES; 2020. Available from: https://doi.org/10.5281/zenodo.4147317.
Wang W, Pechacek P, Zhang M, **ao N, Zhu J, Li J. Effectiveness of nature reserve system for conserving tropical forests: a statistical evaluation of Hainan Island, China. PLoS One. 2013;8(2):e57561.
Li Y, Tang C, Zhang Y, Li Z, Wang G, Peng R, et al. Diversity and independent evolutionary profiling of rodent-borne viruses in Hainan, a tropical island of China. Virol Sin. 2023;38(5):651–62.
**a Z-G, Zhang L, Feng J, Li M, Feng X-Y, Tang L-H, et al. Lessons from malaria control to elimination: case study in Hainan and Yunnan provinces. Adv Parasitol. 2014;86:47–79.
Molyneux D. Patterns of change in vector-borne diseases. Ann Trop Med Parasitol. 1997;91(7):827–39.
Ku GW, Seto E, Hai WX, Environment and climate change with vector-born diseases. Proceedings of the 5th international academic conference on environmental and occupational medicine. Dujiangyan; 2010.
Lawler OK, Allan HL, Baxter PW, Castagnino R, Tor MC, Dann LE, et al. The COVID-19 pandemic is intricately linked to biodiversity loss and ecosystem health. Lancet Planet Health. 2021;5(11):e840–50.
Ellwanger JH, Chies JA. Candida auris emergence as a consequence of climate change: impacts on Americas and the need to contain greenhouse gas emissions. Lancet Reg Health. 2022;11:100250.
Confalonieri U. Environmental change and human health in the Brazilian Amazon. Glob Change Human Health. 2000;1:174–83.
Codeço CT, Dal’Asta AP, Rorato AC, Lana RM, Neves TC, Andreazzi CS, et al. Epidemiology, biodiversity, and technological trajectories in the Brazilian Amazon: from malaria to COVID-19. Front Public Health. 2021;9:647754.
Gebara MF, May PH, Platais G. Pandemics, conservation, and human-nature relations. Clim Change Ecol. 2021;2:100029.
Ali S, Gugliemini O, Harber S, Harrison A, Houle L, Ivory J, et al. Environmental and social change drive the explosive emergence of Zika virus in the Americas. PLoS Negl Trop Dis. 2017;11(2):e0005135.
Leroy EM, Rouquet P, Formenty P, Souquière S, Kilbourne A, Froment JM, et al. Multiple Ebola virus transmission events and rapid decline of central African wildlife. Science. 2004;303(5656):387–90.
Acknowledgements
We greatly appreciate the assistance of Dr. **aodong Rao from Hainan University, and we would like to thank all those who have advised and helped us, especially those who have studied together in Hainan.
Funding
This research did not receive any specific grant from funding agencies in the public, commercial, or not-for-profit sectors.
Author information
Authors and Affiliations
Contributions
L.Z.: Conceptualization, On-site research and Writing—original draft preparation, Methodology; S.L.: On-site research and revision suggestions; W.G., C.L. and X.L.: revision suggestions. All authors have read and agreed to publish this version of the manuscript.
Corresponding author
Ethics declarations
Conflict of interest
The authors declare no conflict of interest.
Additional information
Publisher’s Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Rights and permissions
Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
About this article
Cite this article
Zhang, L., Liu, S., Guo, W. et al. Addressing biodiversity conservation, disease surveillance, and public health interventions through One Health approach in Hainan’s tropical rainforest. One Health Adv. 2, 8 (2024). https://doi.org/10.1186/s44280-023-00035-7
Received:
Revised:
Accepted:
Published:
DOI: https://doi.org/10.1186/s44280-023-00035-7