Next Article in Journal
Wheat Blast: A Threat to Wheat Production in Zambia Under Climate Change
Previous Article in Journal
Influence of Vineyard Location on Physicochemical Properties, Phenolic Content, and Antioxidant Capacity of ‘Touriga Nacional’ Grapes Cultivated in Brazil and Portugal
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Review

Hero or Villain: The Importance and Impacts of the Genus Juniperus on Ecosystems

by
Cayetano Navarrete-Molina
1,*,
María A. Sariñana-Navarrete
2,
Cesar A. Meza-Herrera
3,
Ángeles De Santiago-Miramontes
1,
José L. Rodriguez-Alvarez
4,
Raúl A. Cuevas-Jacquez
4,
Luis M. Valenzuela-Núñez
5,
Ricardo I. Ramírez-Gottfried
1,
Edir Torres-Rodriguez
1 and
Rubén I. Marín-Tinoco
6,7,*
1
Laguna Unit, Antonio Narro Agrarian Autonomous University, Torreon 27054, Coahuila, Mexico
2
Department of Chemical and Environmental Technology, Technological University of Rodeo, Rodeo 35760, Durango, Mexico
3
Regional Universitary Unit on Arid Lands, Chapingo Autonomous University, Bermejillo 35230, Durango, Mexico
4
Campus Region of the Llanos, National Technological of Mexico, Guadalupe Victoria 34700, Durango, Mexico
5
Faculty of Biological Sciences, Juarez University of the State of Durango, Gomez Palacio 35010, Durango, Mexico
6
Postdoctoral Stay Program, Secretary of Science, Humanities, Technology and Innovation, Benito Juarez 03940, Ciudad de Mexico, Mexico
7
Rural Hospital No. 162, Mexican Social Security Institute, Rodeo 35760, Durango, Mexico
*
Authors to whom correspondence should be addressed.
Int. J. Plant Biol. 2026, 17(3), 23; https://doi.org/10.3390/ijpb17030023
Submission received: 22 November 2025 / Revised: 12 March 2026 / Accepted: 16 March 2026 / Published: 23 March 2026
(This article belongs to the Section Plant Ecology and Biodiversity)

Abstract

The genus Juniperus species is widely distributed in the Northern Hemisphere of the planet Earth. These species are notable for their ability to adapt to extreme environmental conditions, playing a crucial role in ecosystem structure and function. Currently, their expansion is being driven by anthropogenic activities and climate change, posing significant challenges for both control and conservation. The objective of this review was to synthesize the available evidence regarding the ecological importance and impacts of Juniperus on ecosystems, promoting a holistic perspective that contributes to the achievement of the United Nations 2030 Agenda for Sustainable Development. A systematic literature search was conducted using the Scopus database, and only the documents published between 2001 and 2025 were considered for the investigation. The results showed that these species possess a high ecological versatility, favoring their invasive success in disturbed ecosystems, particularly under the influence of climate change and land-use changes. Conversely, Juniperus species facilitate positive ecological outcomes by providing essential ecosystem services that benefit both the human population and the flora and fauna present in these ecosystems. Nevertheless, their expansion also causes negative effects, such as the suppression of herbaceous shrubs and understory cover, alteration of the hydrological function, and accelerated soil erosion, among others. Consequently, the genus Juniperus exhibits a dual ecological role, acting as a hero to many species within these ecosystems, yet a villain to others. In this sense, given its remarkable adaptive dynamism under scenarios of climate change and continuous anthropogenic alterations, it is imperative to promote comprehensive conservation and restoration strategies. These should include ecological monitoring, invasive species control, genetic management, and habitat restoration. Such efforts must be supported by long-term interdisciplinary research to understand and mitigate the ecological, genetic, and social impacts resulting from its expansion. Furthermore, these investigations and strategies must be flexible and locally contextualized to promote genuine ecosystem resilience in the face of the ongoing environmental transformations.

1. Introduction

The genus Juniperus L. (Cupressaceae Bartl.) represents one of the most diverse and widely distributed groups of conifers in the world, comprising approximately 75 recognized species [1,2,3]. These evergreen trees or shrubs, commonly known as “táscate”, “cypress”, “enebro” or “juniper”, inhabit temperate and arid ecosystems ranging from mountainous regions to coastal zones across the Northern Hemisphere [2,3] where they play a vital role in vegetation cover [4,5]. Juniperus species exhibit an exceptional adaptability to extreme climatic conditions, high salinity, and water stress, allowing them to colonize nutrient-poor soils. This characteristic positions them as a key component for ecological stability and the mitigation of desertification [6,7,8,9,10,11]. Such adaptability enables these species to occupy critical ecological niches, where they fulfill essential structural and functional roles in ecosystem dynamics [12,13,14,15]. Beyond their ecological functions, Juniperus species exhibit a notable ethnobotanic importance. Their use has been documented across multiple cultures and industries, including the pharmaceutical and food sectors. They are particularly noted for their reservoir of bioactive compounds, which have been associated with multiple therapeutic properties [2,16,17,18].
Furthermore, the genus plays a vital role in biodiversity conservation by providing invaluable ecosystem services, such as habitat stabilization and the provision of food and resources for numerous wildlife species [13,16,19,20]. Consequently, Juniperus species function as ecological modulators, influencing the surrounding animal and vegetal biodiversity [21,22,23]. In this context, the Juniperus species also stabilizes and enriches the trophic networks by creating microclimates that buffer extreme temperatures and improve soil fertility through the accumulation of organic matter and nutrients, forming “fertility islands” that support diverse plant communities, especially in disturbed areas [21]. However, negative effects have also been reported, including reductions in plant species richness [24], alterations of hydrological functions, increased water runoff, and the exacerbation of soil erosion [25]. Given this duality, several research groups have reported mixed results regarding biodiversity in areas invaded by Juniperus species, particularly in the United States [26,27,28,29,30,31,32,33,34,35]. Furthermore, these species face significant challenges due to anthropogenic activities, climate change, and habitat loss, emphasizing the urgent need for research about their ethnobotanic importance, their biology, ecology, and their conservation strategies [6,36,37,38].
Considering these growing challenges, it is essential to understand both the positive and negative impacts of Juniperus on biodiversity to develop sustainable management and conservation strategies [6,37]. Analyzing the associated benefits and risks is particularly critical in a global context marked by climate change, anthropogenic expansion, and habitat degradation. In this regard, the objective of this review was to analyze the available evidence concerning the ethnobotanical importance and ecological impact (i.e., positive and negative) of Juniperus on biodiversity. Specifically, the information generated during the first quarter of the 21st century was analyzed and synthesized to improve the understanding of these species as potential modulators of ecosystem biodiversity. Moreover, this work promotes a holistic and sustainable perspective aligned with the productive, economic, social, environmental, and cultural objectives, thus supporting the achievement of the United Nations 2030 Agenda for Sustainable Development [39,40,41,42].

2. Methodological Strategy

To achieve the objective of this review, a bibliometric research design was employed, following the recommendations proposed by Ali and Deryanur [43]. The Scopus database was selected as the primary search engine, considering that it is open access and provides extensive multidisciplinary data coverage, advanced search functionalities, and preliminary analysis tools [44]. Compared with other databases, such as Web of Science, Scopus offers broader journal coverage, making it a superior option for interdisciplinary and international research assessments [45,46].
The following search string was used to compile the information presented in this study:
(TITLE-ABS-KEY (Juniperus) AND TITLE-ABS-KEY (use) AND TITLE-ABS-KEY (impact)) AND PUBYEAR > 2000 AND PUBYEAR < 2026.
The search included a publication-year filter to select only studies published between 2001 and 2025. This search strategy retrieved a total of 737 publications, which constituted the overall sample of the study. For the bibliometric analysis, Scopus built-in tools were employed to analyze publication year, subject areas, citations, sources, authors, and affiliations. For the thematic analysis, the Biblioshiny tool was utilized, which is a web application integrated into the R package: Bibliometrix [47]. The use of Biblioshiny as a bibliometric analysis tool is justified by its effectiveness in quantifying and visualizing scientific production, particularly for users without programming knowledge. Considering that the output information generated in Biblioshiny only includes lowercase words, the images were edited with Photoshop V26.4.1; the above was done with the aim of improving the quality of the information. In this regard, the information was organized according to productivity indicators (annual distribution of publications, institutions, countries, and sources), and the conceptual structure of the data was visualized through a keyword co-occurrence analysis and the density of those occurrences [43].

3. General Characteristics of the Publications

Given that conducting a bibliometric analysis was not the main objective of this review, a brief descriptive summary of the principal publication patterns observed during the study period (2001–2025) is presented. In this context, Figure 1 illustrates the annual publication trend, showing that scientific production on this topic initially progressed at a slow pace, with a noticeable increase becoming evident after 2004. Although some fluctuations were observed, a clear upward trend in annual publication outputs is evident throughout the period analyzed. Additionally, it was determined that 50% of all publications were produced during the last eight years of the study period (i.e., 2018–2025). Regarding the three main types of documents published, 93.08% were research articles (686), 3.12% were review papers (23), and 2.31% were conference papers (17). Figure 2 presents the journals that published ten or more documents on the topic, highlighting Rangeland Ecology and Management and Forest Ecology and Management as the journals that have published the highest number of studies in this research area. As expected, English was the dominant publication language, accounting for 96.74% of all documents (713). Complementarily, Figure 3 presents a three-field plot illustrating the relationships between authors’ countries, authors, and publishing journals, where authors from the United States stand out markedly in comparison to those from other countries.
Regarding author productivity, the most prolific researchers (i.e., more than 10 publications) were led by McDowell, N. G., with 15 documents, followed by Pockman, W. T., Camarero, J. J., and Tinner, W., with 13, 11, and 11 documents, respectively. In line with these findings, an analysis of collaboration networks reveals that these authors constitute the largest collaboration nodes for studies addressing the genus Juniperus (Figure 4). Furthermore, authors’ affiliations with the most relevant universities and/or research institutions in the published literature on this topic were identified as: the USDA Forest Service (USA), USDA Agricultural Research Service (USA), Oklahoma State University (USA), the Spanish National Research Council (Spain), the United States Department of Agriculture (USA), Oregon State University (USA), the Chinese Academy of Sciences (China), Northern Arizona University (USA), and the University of New Mexico (USA), with 34, 31, 30, 29, 29, 26, 25, 24, and 21 publications, respectively (Figure 2, Figure 3 and Figure 4).
An analysis of the countries’ scientific output showed that five nations accounted for 53.26% of the total production: the United States (320, 30.65%), Spain (82, 7.85%), China (66, 6.32%), Germany (49, 4.69%), and Switzerland (39, 3.74%). In this context, Figure 5 presents a global collaboration map for the study period (2001–2025), highlighting strong collaborative relationships among the United States, China, and Europe, with color intensity proportional to each country’s scientific productivity; for instance, the United States is shown in dark blue, indicating its position as the most productive country. Additionally, Figure 6 shows two perspectives on the most frequent terms used in titles and keywords for research published on the genus Juniperus during the analyzed period. This analysis confirms that the word Juniperus (451, 15.21%) was the most prevalent, followed by climate change (140, 4.72%), Juniperus communis (128, 4.32%), coniferous tree (123, 4.15%), and forestry (102, 3.44%).

4. Diversity and Taxonomy of the Genus Juniperus

The genus Juniperus represents the second largest genus of conifers and the largest within the Cupressaceae family, comprising approximately 75 species divided into three monophyletic sections [48,49]. The Caryocedrus section includes a single dioecious taxon, J. drupacea, native to Greece, Turkey, Lebanon, and Syria [50]. The Juniperus section consists of 14 species, of which 12 are distributed in the Eastern Hemisphere, along with J. jackii (endemic to North America) and the circumboreal species J. communis [48]. Meanwhile, the Sabina section encompasses approximately 60 species distributed across Asia, Africa, southwestern North America, and the Mediterranean region [51]. Based on the concordance between phylogenetic results and morphological characteristics, the genus Juniperus sensu lato has been divided into three genera: Juniperus sensu stricto (sect. Juniperus), Sabina (sect. Sabina), and Arceuthos (sect. Caryocedrus) [52]. The richness of the species observed in this genus is likely associated with key innovations that provide evolutionary advantages for adapting to new environments or in situ habitat changes. As described for other species, these attributes have facilitated the occupation of new adaptive zones [53,54,55,56,57,58,59]. Notable examples of key innovations include seed dispersal during early divergence [59,60] and the development of fleshy fruits [61]. Furthermore, these traits can contribute to the creation of ecological niches, improved individual fitness, rapid diversification, and the expansion of the species’ geographic distribution [52,62,63].
The extensive distribution of Juniperus has likely been influenced by long-distance dispersal and migration across land bridges [64]. It is believed that the genus originated in Eurasia during the Eocene as part of the Tethyan vegetation [51]. Currently, Juniperus species are prominent components of arid and semi-arid landscapes throughout the Northern Hemisphere, possessing significant ecological and economic importance [49]. Their distribution ranges from sea level to above the tree line [51,65]. Although most species preferentially grow on limestone substrates, several taxa grow on granite, sand dunes, and sandstone, with habitats ranging from deserts to swamps [49]. This broad ecological diversity, in contrast with other genera within the Cupressaceae family, can be attributed to key evolutionary traits such as the development of fleshy and berry-like female cones and the dioecious nature of the plants [66]. Additionally, Juniperus has undergone a relatively high frequency of polyploidization events compared to other conifers, with at least 15% of the taxa being tetraploid [67]. Significant morphological variations between the three sections, including leaf shape, female cone size, texture, and color, further maximize the genus’s adaptability to diverse environments [48,50].

5. Ecology and Functions of the Genus Juniperus in Ecosystems

The genus Juniperus exhibits a wide range of ecological characteristics reflecting its adaptability to diverse environments, primarily driven by morphological diversity and reproductive dynamics [68,69]. For instance, J. sabina shows low variability in the morphology of its vegetative organs, a trait associated with its adaptive capacity to arid conditions [68]. Similarly, J. drupacea thrives in mountainous regions, demonstrating significant resilience to frost and drought [6]. Reproductive dynamics, such as sexual dimorphism, observed in certain species, also play a critical role in the genus’ ecology. These dynamics directly impact seed production and regeneration, with a notable decrease in reproductive trees due to aging, as reported for J. thurifera [70]. In contrast, J. foetidissima faces challenges, including low seed viability and unbalanced male-to-female ratios, which affect its reproductive success [71]. In this context, the literature indicates that the Juniperus species exhibit remarkable ecological versatility, with adaptive traits that enable proliferation under adverse climatic conditions and in nutrient-poor soils [10,11]. These findings highlight adaptive capacities often associated with the success of invasive species [13,72]. Furthermore, the expansion of Juniperus has been linked to the reduction in grassland areas, inevitably affecting fodder resources, avifauna composition, and ecosystem services [19,20,21,34,35].
Climate change and anthropogenic activities, particularly land-use changes, facilitate the expansion of Juniperus. These factors have triggered altitudinal migrations and phenological changes, promoting increased Juniperus cover, particularly in semi-arid ecosystems [68,69,73]. This expansion is further amplified by key innovations, such as fleshy fruits, dioecy, and polyploidy, among others [61,67], which enhance adaptive capacity and colonization potential across diverse environments [48,50]. However, studies consistently agree that this remarkable adaptive capacity presents significant challenges for biodiversity conservation, especially in environmentally disturbed contexts where Juniperus can rapidly establish and expand [7,9,68,69]. Moreover, evidence suggests that climate change could increase the distribution range of Juniperus, intensifying their ecological impacts by facilitating the colonization of new niches and increasing competition with other native species [3,6,11,37,73]. Despite this expansive potential, several Juniperus species are currently considered threatened [36,37,38,70].

6. Ethnobotanical Importance of the Genus Juniperus

Aside from their ecological functions, species of the genus Juniperus also exhibit an important ethnobotanical role around the world, with multiple applications in medicine, food, and essential oils. These species are particularly notable for their reservoir of bioactive compounds [2,18], which are associated with a wide range of therapeutic properties (Table 1).
Furthermore, several Juniperus species are used in home and property decoration, housing construction, and are even considered sacred trees in certain regions [108,109,110,111]. Similarly, their wood is used for fuel, charcoal production, and the crafting of small decorative items [4,112]. In addition to their therapeutic uses, essential oils extracted from leaves and fruits are employed in the formulation of cosmetic products [113]. Species such as J. virginiana are utilized in the creation of windbreaks and fence rows and are also processed to produce furniture, lumber, and pencils [113]. Although these species may lack direct nutritional value for humans, they are of significant importance to wildlife; various species of birds, small mammals, and deer consume their fruits, particularly within grassland ecosystems [114]. However, the stability of these ethnobotanical relationships faces challenges derived from anthropogenic intervention and climate change [6,36,37,38].

7. Impacts on Biodiversity by the Genus Juniperus

Species of the genus Juniperus interact with other organisms within their ecosystems through a complex balance of competition and facilitation, which fluctuates according to environmental conditions and the developmental stage of the Juniperus plants [22]. One example of these interactions, which has undoubtedly influenced their colonization dynamics, involves the combination of seed production and highly efficient endozoochorous dispersal. This dispersal is mediated by a diverse group of birds and mammals, resulting in an exceptionally effective seed dissemination [100,113,114,115]. In this context, birds typically function as primary dispersers in forested areas, whereas mammals assume a more significant role in open habitats [116,117]. Furthermore, Juniperus species exhibit a remarkable tolerance to herbivory [118,119,120,121]. However, these ecological interactions often yield dual outcomes; consequently, it is essential to clearly differentiate between the positive and negative impacts of Juniperus on biodiversity.

7.1. Positive Impacts on Biodiversity

Table 2 summarizes the main positive impacts reported for the genus Juniperus on biodiversity in ecosystems.

7.2. Negative Impacts on Biodiversity

Table 3 summarizes the main negative impacts reported for the genus Juniperus on biodiversity in ecosystems.
Given this ecological duality, it is crucial to emphasize the need for balanced management strategies that mitigate negative impacts while acknowledging the potential ecological roles of Juniperus.

8. Management and Conservation Challenges of the Genus Juniperus

As mentioned above, species of the genus Juniperus play a key ecological role in the ecosystems they dominate globally [10,20,29,51,65]. However, Juniperus dominated landscapes are increasingly threatened by various challenges that compromise their capacity to support biodiversity [11,128,129,132]. A major concern is habitat fragmentation, driven primarily by anthropogenic activities such as agriculture, urbanization, and infrastructure development. This fragmentation reduces connectivity between flora and fauna populations, limiting genetic exchange and increasing the vulnerability of native species [130]. Other human pressures include overgrazing and overexploitation, such as indiscriminate logging, which have resulted in significant soil degradation, hindering the natural regeneration of Juniperus species and altering the structural and functional integrity of ecosystems [6,14,15,37,70,129].
Furthermore, the invasion of exotic species represents a significant threat to Juniperus communities across various regions. These invasive taxa alter ecological dynamics by competing for critical resources such as water, nutrients, and light, displacing native species and reducing biodiversity [13,72]. Similarly, the effects of climate change, particularly variations in temperature and precipitation patterns, exacerbate the challenges faced by Juniperus species. These changes directly influence the distribution and survival of species, including Juniperus itself. For example, water stress and extreme temperatures have been proven to threaten the natural regeneration of Juniperus dominated ecosystems, negatively impacting the associated species [37,70,128,135]. Nevertheless, it is important to consider the dual role of these species as their excessive proliferation can also threaten biodiversity in the ecosystems they inhabit [6,22,36,37]. In specific areas, the dominance of Juniperus has been associated with the suppression of growth and reduced species coexistence [2,11,132]. The ability of this genus to establish in poor-nutrient soils and compete effectively for resources such as water and light makes it highly competitive [6,7,9,11]. This monopolization of resources can lead to landscape homogenization, decreasing the structural diversity of the habitat, and compromising the survival of herbaceous and shrubby species that depend on heterogeneous conditions [24,25,34,124,125,133]. Moreover, Juniperus dominance has been shown to alter soil microorganisms, which are essential for organic matter decomposition and nutrient cycling [21,22,25,70].
Given these findings, several challenges arise for biodiversity conservation in Juniperus dominated areas. A critical challenge lies in the implementation of long-term monitoring programs to assess ecosystem health [37,70,128]. Additionally, ecological restoration programs are also required, prioritizing reforestation with native species and controlling invasive species, to mitigate biodiversity loss in areas invaded by Juniperus [11,37,72]. The preservation of genetic variability within Juniperus populations is equally crucial for ensuring adaptability to fluctuating environmental changes. In this regard, seed banks and specialized nursery gardens can play a key role in these conservation efforts [6,7,9,11,68,69]. Other challenges include establishing policies that regulate the sustainable use of ecosystem resources, the creation of protected areas, and the promotion of agroforestry practices, to help in the mitigation of anthropogenic impacts on natural resources [11,37,38,128]. Achieving these goals also requires improving public awareness about the importance of biodiversity in ecosystems, both before and after the Juniperus invasion [72,128,136,137]. Educational and training programs can further encourage a more harmonious relationship between local communities and these ecosystems [37,72,128,137].

9. Research Perspectives and Gaps on the Genus Juniperus

As mentioned above, many species of the genus Juniperus play positive ecological roles; however, some exhibit invasive behavior outside their natural ranges, a phenomenon that has garnered growing interest within the scientific community [24,25,35,130,131]. In this context, the genetic characteristics of this genus are of particular interest, as certain genetic traits, such as specific DNA markers, have been linked to the invasive potential of some Juniperus species. For example, genotyping techniques have revealed that certain populations possess genetic variants that enhance tolerance to water stress, extreme temperatures, and nutrient-poor soils [36,73,126,137,138,139]. Furthermore, molecular genetic studies have elucidated dispersal patterns and gene flow, allowing the identification of propagation sources and factors contributing to invasion success. This knowledge is crucial for understanding the adaptive capacity and evolutionary responses to climate change and anthropogenic pressures [51,53,58,73,140,141,142]. Despite these advances, many Juniperus species remain poorly studied, particularly those with restricted distributions or found in less-explored regions. Therefore, further research using genotyping and molecular-level approaches is urgently needed.
The invasion of ecosystems by Juniperus has been associated with alterations in both biotic and abiotic components, positioning the genus as a key driver of soil–plant–animal interactions in invaded areas [11,13,14,15,22,25,37,72,128]. However, there is still a limited understanding of how variations in disturbance regimes affect plant–animal interactions across different species and regions. Additionally, it is necessary to investigate how these interactions are influenced by climate change and increasing anthropogenic pressures. Significant knowledge gaps also remain regarding the impact of genus Juniperus invasions on biogeochemical cycles, particularly carbon and nitrogen cycles. This includes examining the influence of biomass accumulation and leaf chemistry on soil dynamics and greenhouse gas emissions [143,144,145,146,147,148]. Therefore, assessing the potential of Juniperus species to act as carbon sinks, especially in marginal ecosystems, could provide valuable insights for ecological restoration and conservation strategies. Although plant–animal interactions have been documented in ecosystems invaded by Juniperus, their long-term evolutionary dynamics remain largely unexplored [29,31,32,33,34,35,70]. Future studies should integrate remote sensing data and climate projections to predict potential range expansions and evaluate ecosystem-level impacts.
Consequently, further research is needed to develop management strategies based on landscape ecology, which may include the reintroduction of prescribed fire regimes, hydrological management, and the replanting of competitive native species [7,72,149]. Similarly, investigating how variations in interaction networks influence ecosystem resilience to future disturbances is essential [150,151]. Addressing these knowledge gaps requires an interdisciplinary and collaborative research approach, examining not only the negative impact of juniper invasions on biodiversity but also their potential contributions to ecosystem services, including ethnobotanical services, and the human communities that depend on these systems [136,148,149,150,151,152,153,154]. Achieving meaningful progress will necessitate robust collaborations between disciplines such as ecology, genetics, and the social sciences [6,37]. Only through such coordinated efforts can the long-term sustainability of these ecosystems be guaranteed for future generations [39,40,41,42].

10. Conclusions

The analysis of the available literature demonstrates that species of the genus Juniperus generate a duality of effects on the biotic and abiotic components of ecosystems, and that managing their populations is a highly challenging task. Evidence suggests an increase in their distribution range. Therefore, regional and local research with an interdisciplinary and sustainable approach is required, linking ecological knowledge with social acceptance of the need to control or protect these species. The results of this research should form the basis for designing solutions and outreach efforts. Given that these species are dynamic and hold significant biological, economic, cultural, and ecological importance, making the genus Juniperus a hero to many species in ecosystems, and a villain to others.

Author Contributions

Conceptualization, C.N.-M., M.A.S.-N. and C.A.M.-H.; methodology, C.N.-M., M.A.S.-N. and R.I.M.-T.; formal analysis, C.N.-M., M.A.S.-N. and L.M.V.-N.; investigation, Á.D.S.-M., J.L.R.-A., R.A.C.-J., R.I.R.-G. and E.T.-R.; resources, Á.D.S.-M., J.L.R.-A., R.I.R.-G. and E.T.-R.; writing—original draft preparation, R.I.M.-T., C.A.M.-H., R.A.C.-J. and L.M.V.-N.; writing—review and editing, C.N.-M., M.A.S.-N. and C.A.M.-H.; visualization, R.I.M.-T., C.A.M.-H. and L.M.V.-N.; supervision, Á.D.S.-M., J.L.R.-A., R.A.C.-J., R.I.R.-G. and E.T.-R.; project administration, C.N.-M., R.I.M.-T. and L.M.V.-N.; funding acquisition, Á.D.S.-M., J.L.R.-A. and R.A.C.-J.; supervision, C.N.-M., R.I.R.-G. and E.T.-R. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Data Availability Statement

None of the data were deposited in an official repository, yet information can be made available upon request.

Acknowledgments

The authors acknowledge the Science and Technology Council of the State of Durango for the support provided. Likewise, the authors thank the employees of the Technological University of Rodeo for the facilities provided for the development of this research. Additionally, the authors thank Lic. Francisco Gerardo Véliz-Romero for his support in the translation of the manuscript.

Conflicts of Interest

The authors declare no conflicts of interest.

References

  1. Adams, R.P.; Johnson, S.T.; Anderson, J.; Rushforth, K.; Farhat, P.; Valentin, N.; Siljak-Yakovlev, S. The Origin of Juniperus xpfitzeriana, an Allotetraploid Hybrid of J. chinensis × J. sabina. Phytologia 2019, 101, 164–174. [Google Scholar]
  2. Majid, G.A.; Ali Hijazi, M.; El Lakany, A.; Aboul Ela, M. Review on Chemical Constituents and Biological Activities of Genus Juniper. Int. J. Pharm. Pharm. Sci. 2024, 16, 12–20. [Google Scholar] [CrossRef]
  3. Yermagambetova, M.M.; Abugalieva, S.I.; Turuspekov, Y.K.; Almerekova, S.S. Conspectust of the Genus Juniperus L. Growing in Kazakhstan. Proc. Appl. Bot. Genet. Breed. 2022, 183, 161–170. [Google Scholar] [CrossRef]
  4. Farjon, A. The Kew Review: Conifers of the World. Kew Bull. 2018, 73, 8. [Google Scholar] [CrossRef]
  5. Rahmonov, O.; Szczypek, T.; Niedźwiedź, T.; Myga-Piątek, U.; Rahmonov, M.; Snytko, V.A. The Human Impact on the Transformation of Juniper Forest Landscape in the Western Part of the Pamir Alay Range (Tajikistan). Environ. Earth Sci. 2017, 76, 324. [Google Scholar] [CrossRef]
  6. Boratynski, A.; Donmez, A.A.; Bou Dagher-Kharrat, M.; Romo, Á.; Tan, K.; Ok, T.; Iszkuło, G.; Sobierajska, K.; Marcysiak, K. Biology and Ecology of Juniperus drupacea Labill. Dendrobiology 2023, 90, 1–29. [Google Scholar] [CrossRef]
  7. Dakhil, M.A.; El-Barougy, R.F.; El-Keblawy, A.; Farahat, E.A. Clay and Climatic Variability Explain the Global Potential Distribution of Juniperus phoenicea Toward Restoration Planning. Sci. Rep. 2022, 12, 13199. [Google Scholar] [CrossRef] [PubMed]
  8. Douaihy, B.; Vendramin, G.G.; Boratyński, A.; Machon, N.; Bou Dagher-Kharrat, M. High Genetic Diversity with Moderate Differentiation in Juniperus excelsa from Lebanon and the Eastern Mediterranean Region. AoB Plants 2011, 2011, plr003. [Google Scholar] [CrossRef] [PubMed]
  9. Ilnitsky, O.A.; Plugatar, Y.V.; Pashtetsky, A.V. Water Relation Features of Juniperus excelsa M. Bieb under Progressive Soil Drought Stress of the Soutern Coast of the Crimea. Plant Biol. Hortic. Theory Innov. 2020, 152, 5–14. [Google Scholar] [CrossRef]
  10. Kahveci, G.; Alan, M.; Köse, N. Distribution of Juniper Stands and the Impact of Environmental Parameters on Growth in the Drought-stressed Forest-steppe Zone of Central Anatolia. Dendrobiology 2018, 80, 61–69. [Google Scholar] [CrossRef]
  11. Varsamis, G.; Tsiftsis, S.; Koutseri, I.; Merou, T. Optimising Juniperus excelsa (Cupressaceae) Germination for Sustainable Eco-system Restoration in the Prespa Area (Western Macedonia, Greece). Nat. Conserv. Res. 2024, 9, 21–31. [Google Scholar] [CrossRef]
  12. Herrero, A.; Zamora, R. Plant Responses to Extreme Climatic Events: A Field Test of Resilience Capacity at the Southern Range Edge. PLoS ONE 2014, 9, e87842. [Google Scholar] [CrossRef]
  13. Boogar, A.R.; Salehi, H.; Pourghasemi, H.R.; Blaschke, T. Predicting Habitat Suitability and Conserving Juniperus spp. Habitat Using SVM and Maximum Entropy Machine Learning Techniques. Water 2019, 11, 2049. [Google Scholar] [CrossRef]
  14. Ren, J.W.F.; Coffman, G.C. Integrating the Resilience Concept into Ecosystem Restoration. Restor. Ecol. 2023, 31, e13907. [Google Scholar] [CrossRef]
  15. Török, P.; Bullock, J.M.; Jiménez-Alfaro, B.; Sonkoly, J. The Importance of Dispersal and Species Establishment in Vegetation Dynamics and Resilience. J. Veg. Sci. 2020, 6, 935–942. [Google Scholar] [CrossRef]
  16. Ghasemnezhad, A.; Ghorbanzadeh, A.; Sarmast, M.K.; Ghorbanpour, M.A. Review on Botanical, Phytochemical, and Pharmacological Characteristics of Iranian Junipers (Juniperus spp.). In Plant Derived Bioactive: Production, Properties and Therapeutic Applications; Swamy, M.K., Ed.; Springer: Singapore, 2020; pp. 493–508. [Google Scholar] [CrossRef]
  17. Gonçalves, A.C.; Flores-Félix, J.D.; Coutinho, P.; Alves, G.; Silva, L.R. Zimbro (Juniperus communis L.) as a Promising Source of Bioactive Compounds and Biomedical Activities: A Review on Recent Trends. Int. J. Mol. Sci. 2022, 23, 3197. [Google Scholar] [CrossRef] [PubMed]
  18. Zubi, W.S.; Elamari, A.A.; Buzgaia, N.M. Antimicrobial Activity and Bioactive Compounds of Juniper phoenicea: A Mini Review. EC Microbiol. 2025, 21, 1–11. [Google Scholar]
  19. Rahmonov, O.; Abramowicz, A.; Pukowiec-Kurda, K.; Fagiewicz, K. The Link Between a High-Mountain Community and Ecosystem Services of Juniper Forests in Fann Mountains (Tajikistan). Ecosyst. Serv. 2021, 48, 101255. [Google Scholar] [CrossRef]
  20. Shaheen, H.; Awan, S.N.; Aziz, S. Distribution Pattern, Conservation Status, and Associated Flora of the Genus Juniperus in Subalpine Pastures of the Kashmir Himalayas. Mt. Res. Dev. 2017, 37, 487–493. [Google Scholar] [CrossRef]
  21. Allegrezza, M.; Corti, G.; Cocco, S.; Pesaresi, S.; Chirico, G.B.; Saracino, A.; Bonanomi, G. Microclimate Buffering and Fertility Island Formation During Juniperus communis Ontogenesis Modulate Competition Facilitation Balance. J. Veg. Sci. 2016, 27, 616–627. [Google Scholar] [CrossRef]
  22. García-Cervigón, M.A.I. Facilitation in Mediterranean Mountains Engineering Role of Juniperus sabina L. at Community: Population and Individual Levels. Doctoral Dissertation, University of Valladolid, Valladolid, Spain, 2015. [Google Scholar] [CrossRef]
  23. Linder, H.P.; Bykova, O.; Dyke, J.; Etienne, R.S.; Hickler, T.; Kühn, I.; Marion, G.; Ohlemüller, R.; Schymanski, S.J.; Singer, A. Biotic Modifiers, Environmental Modulation and Species Distribution Models. J. Biogeogr. 2012, 39, 2179–2190. [Google Scholar] [CrossRef]
  24. Monaco, T.A.; Gunnell, K.L. Understory Vegetation Change Following Woodland Reduction Varies by Plant Community Type and Seeding Status: A Region Wide Assessment of Ecological Benefits and Risks. Plants 2020, 9, 1113. [Google Scholar] [CrossRef]
  25. Williams, C.J.; Pierson, F.B.; Kormos, P.R.; Al-Hamdan, O.Z.; Nouwakpo, S.K.; Weltz, M.A. Vegetation, Hydrologic, and Erosion Responses of Sagebrush Steppe 9 Yr Following Mechanical Tree Removal. Rangeland Ecol. Manag. 2019, 72, 47–68. [Google Scholar] [CrossRef]
  26. Atamian, M.T.; Sedinger, J.S.; Heaton, J.S.; Blomberg, E.J. Landscape-level Assessment of Brood Rearing Habitat for Greater Sage-Grouse in Nevada. J. Wildl. Manag. 2010, 74, 1533–1543. [Google Scholar] [CrossRef]
  27. Boone, J.D.; Ammon, E.; Johnson, K. Long-term Declines in the Pinyon Jay and Management Implications for Piñon–Juniper Woodlands. In Trends and Traditions—Avifaunal Change in Western North America, Studies of Western Birds; Shuford, W.D., Gill, R.E., Jr., Handel, C.M., Eds.; Western Field Ornithologists: Long Beach, CA, USA, 2018; Volume 3, pp. 190–197. [Google Scholar] [CrossRef]
  28. Casazza, M.L.; Coates, P.S.; Overton, C.T. Linking Habitat Selection and Brood Success in Greater Sage-Grouse. In Ecology, Conservation, and Management of Grouse; Studies in Avian Biology; Sandercock, B.K., Martin, K., Segelbacher, G., Eds.; University of California Press: Oakland, CA, USA, 2011; Volume 39, pp. 151–167. [Google Scholar]
  29. Morano, S.; Stewart, K.M.; Dilts, T.; Ellsworth, A.; Bleich, V.C. Resource Selection of Mule Deer in a Shrub-Steppe Ecosystem: Influence of Woodland Distribution and Animal Behavior. Ecosphere 2019, 10, e02811. [Google Scholar] [CrossRef]
  30. Prochazka, B.G.; Coates, P.S.; Ricca, M.A.; Casazza, M.L.; Gustafson, K.B.; Hull, J.M. Encounters with Pinyon-Juniper Influence Riskier Movements in Greater Sage-Grouse Across the Great Basin. Rangel. Ecol. Manag. 2017, 70, 39–49. [Google Scholar] [CrossRef]
  31. Remington, T.E.; Deibert, P.A.; Hanser, S.E.; Davis, D.M.; Robb, L.A.; Welty, J.L. Sagebrush Conservation Strategy—Challenges to Sagebrush Conservation; U.S. Geological Survey Open-File Report 2020–1125; U.S. Geological Survey: Reston, VA, USA, 2021; 327p. [CrossRef]
  32. Sauer, J.R.; Niven, D.K.; Hines, J.E.; Ziolkowski, J.D.J.; Pardieck, K.L.; Fallon, J.E.; Link, W.A. The North American Breeding Bird Survey, Results and Analysis 1966—2019, Version 2.07. USGS Patuxent Wildlife Research Center: Laurel, MD, USA, 2019. Available online: https://www.usgs.gov/tools/north-american-breeding-bird-survey-results-and-analysis (accessed on 26 January 2026).
  33. Severson, J.P.; Hagen, C.A.; Maestas, J.D.; Naugle, D.E.; Forbes, J.T.; Reese, K.P. Restoring Sage-Grouse Nesting Habitat Through Removal of Early Successional Conifer. Restor. Ecol. 2017, 25, 1026–1034. [Google Scholar] [CrossRef]
  34. Shinneman, D.J.; McIlroy, S.K.; Poessel, S.A.; Downing, R.L.; Johnson, T.N.; Young, A.C.; Katzner, T.E. Ecological Effects of Pinyon-Juniper Removal in the Western United States—A Synthesis of Scientific Research, January 2014–March 2021; U.S. Geological Survey Open-File Report; U.S. Geological Survey: Reston, VA, USA, 2023; 56p. [CrossRef]
  35. Soliveres, S.; Eldridge, D.J. Do Changes in Grazing Pressure and the Degree of Shrub Encroachment Alter the Effects of In-dividual Shrubs on Understorey Plant Communities and Soil Function? Funct. Ecol. 2014, 28, 530–537. [Google Scholar] [CrossRef]
  36. Kokkoris, I.P.; Kougioumoutzis, K.; Charalampopoulos, I.; Apostolidis, E.; Apostolidis, I.; Strid, A.; Dimopoulos, P. Conservation Responsibility for Priority Habitats Under Future Climate Conditions: A Case Study on Juniperus drupacea Forests in Greece. Land 2023, 12, 1976. [Google Scholar] [CrossRef]
  37. Recio, M.; Díaz-García, M. Trends in the “Flowering” Periods of Juniperus Species (Cupressaceae) in the Province of Malaga (Western Mediterranean) During the Last Six Decades (1971–2023). Agric. For. Meteorol. 2025, 372, 110712. [Google Scholar] [CrossRef]
  38. Shi, Y.-C.; Chen, Q.; Du, M.-R.; Xiao, S.-L.; Li, S.-F.; Wang, X.-F.; Li, Q.; Tang, C.Q. Community and Population Characteristics and Future Potential Habitats Under Climate Change of Juniperus Species in Yunnan, Southwestern China. Plants 2025, 14, 2754. [Google Scholar] [CrossRef]
  39. Marin-Tinoco, R.I.; Ortega-Ramírez, A.T.; Esteban-Mendez, M.; Silva-Marrufo, O.; Barragan-Ledesma, L.E.; Valenzuela-Núñez, L.M.; Briceño-Contreras, E.A.; Sariñana-Navarrete, M.A.; Camacho-Luis, A.; Navarrete-Molina, C. Antioxidant and Antibacterial Activity of Mexican Oregano Essential Oil, Extracted from Plants Occurring Naturally in Semiarid Areas and Cultivated in the Field and Greenhouse in Northern Mexico. Molecules 2023, 28, 6547. [Google Scholar] [CrossRef]
  40. Meza-Herrera, C.A.; Navarrete-Molina, C.; Luna-García, L.A.; Pérez-Marín, C.; Altamirano-Cárdenas, J.R.; Macías-Cruz, U.; García-de la Peña, C.; Abad-Zavaleta, J. Small Ruminants and Sustainability in Latin America & the Caribbean: Regionalization, Main Production Systems, and a Combined Productive, Socio-Economic & Ecological Footprint Quantification. Small Rumin. Res. 2022, 211, 106676. [Google Scholar] [CrossRef]
  41. Meza-Herrera, C.A.; Navarrete-Molina, C.; Macias-Cruz, U.; Arellano-Rodriguez, G.; De Santiago-Miramontes, A.; Sariñana-Navarrete, M.A.; Marin-Tinoco, R.I.; Perez-Marin, C.C. Dairy Goat Production Systems: A Comprehensive Analysis to Reframe their Global Diversity. Animals 2024, 14, 3717. [Google Scholar] [CrossRef] [PubMed]
  42. Navarrete-Molina, C.; Meza-Herrera, C.A.; Herrera-Machuca, M.A.; Macias-Cruz, U.; Veliz-Deras, F.G. Not All Ruminants Were Created Equal: Environmental and Socio-Economic Sustainability of Goats Under a Marginal-Extensive Production System. J. Clean. Prod. 2020, 255, 120237. [Google Scholar] [CrossRef]
  43. Ali, R.; Dinçer, D.A. Bibliometric Evaluation of the Use of Biomimicry as a Nature Compatible Design Approach in Landscape Architecture Within the Context of Sustainability and Ecology. Biomimetics 2025, 10, 559. [Google Scholar] [CrossRef]
  44. Burnham, J.F. Scopus Database: A Review. Biomed. Digit. Libr. 2006, 3, 1. [Google Scholar] [CrossRef]
  45. Archambault, É.; Campbell, D.; Gingras, Y.; Larivière, V. Comparing Bibliometric Statistics Obtained from the Web of Science and Scopus. J. Am. Soc. Inf. Sci. Technol. 2009, 60, 1320–1326. [Google Scholar] [CrossRef]
  46. Mongeon, P.; Paul-Hus, A. The Journal Coverage of Web of Science and Scopus: A Comparative Analysis. Scientometrics 2016, 106, 213–228. [Google Scholar] [CrossRef]
  47. Aria, M.; Cuccurullo, C. Bibliometrix: An R-tool for Comprehensive Science Mapping Analysis. J. Informetr. 2017, 11, 959–975. [Google Scholar] [CrossRef]
  48. Adams, R.P.; Schwarzbach, A.E. Phylogeny of Juniperus Using nrDNA and Four cpDNA Regions. Phytologia 2013, 95, 179–187. [Google Scholar]
  49. Adams, R.P. Junipers of the World: The Genus Juniperus, 4th ed.; Trafford Publishing: Bloomington, IN, USA, 2014; 415p, ISBN 1490723250/9781490723259. [Google Scholar]
  50. Jagel, A.; Dörken, V.M. Morphology and Morphogenesis of the Seed Cones of the Cupressaceae-Part II Cupressoideae. Bull. CCP 2015, 4, 51. [Google Scholar]
  51. Liu, K.; Li, E.; Cui, X.; Wang, Y.; Xu, C.; Suo, Z.; Dong, W.; Zhang, Z. Key Innovations and Niche Variation Promoted Rapid Diversification of the Widespread Juniperus (Cupressaceae). Commun. Biol. 2024, 7, 1002. [Google Scholar] [CrossRef]
  52. Yang, Y.; Ferguson, D.K.; Liu, B.; Mao, K.S.; Gao, L.M.; Zhang, S.Z.; Wan, T.; Rushforth, K.; Zhang, Z.X. Recent Advances on Phylogenomics of Gymnosperms and a New Classification. Plant Divers. 2022, 44, 340–350. [Google Scholar] [CrossRef] [PubMed]
  53. Blaimer, B.B.; Santos, B.F.; Cruaud, A.; Gates, M.W.; Kula, R.R.; Mikó, I.; Rasplus, J.-Y.; Smith, D.R.; Talamas, E.J.; Brady, S.G.; et al. Key Innovations and the Diversification of Hymenoptera. Nat. Commun. 2023, 14, 1212. [Google Scholar] [CrossRef] [PubMed]
  54. Ding, W.-N.; Ree, R.H.; Spicer, R.-A.; Xing, Y.-W. Ancient Orogenic and Monsoon-Driven Assembly of the World’s Richest Temperate Alpine Flora. Science 2020, 369, 578–581. [Google Scholar] [CrossRef] [PubMed]
  55. Meier, J.I.; Stelkens, R.B.; Joyce, D.A.; Mwaiko, S.; Phiri, N.; Schliewen, U.K.; Selz, O.M.; Wagner, C.E.; Katongo, C.; Seehausen, O. The Coincidence of Ecological Opportunity with Hybridization Explains Rapid Adaptive Radiation in Lake Mweru Cichlid Fishes. Nat. Commun. 2019, 10, 5391. [Google Scholar] [CrossRef]
  56. Ronco, F.; Matschiner, M.; Böhne, A.; Boila, A.; Büscher, H.H.; El Taher, A.; Indermaur, A.; Malinsky, M.; Ricci, V.; Kahmen, A.; et al. Drivers and Dynamics of a Massive Adaptive Radiation in Cichlid Fishes. Nature 2021, 589, 76–81. [Google Scholar] [CrossRef]
  57. Vamosi, J.C.; Vamosi, S.M. Key Innovations Within a Geographical Context in Flowering Plants: Towards Resolving Darwin’s Abominable Mystery. Ecol. Lett. 2010, 13, 1270–1279. [Google Scholar] [CrossRef]
  58. Wang, Y.; Li, E.; Sun, J.; Zhang, Z.; Dong, W. Phylogenetic Diversity and Interspecies Competition Shaped Species Diversity in Adaptive Radiated Ligustrum (Oleaceae). J. Syst. Evol. 2025, 63, 229–244. [Google Scholar] [CrossRef]
  59. Zhou, B.-F.; Yuan, S.; Crowl, A.A.; Liang, Y.-Y.; Shi, Y.; Chen, X.-Y.; An, Q.-Q.; Kang, M.; Manos, P.S.; Wang, B. Phylogenomic Analyses Highlight Innovation and Introgression in the Continental Radiations of Fagaceae Across the Northern Hemisphere. Nat. Commun. 2022, 13, 1320. [Google Scholar] [CrossRef] [PubMed]
  60. Pinna, M.S.; Canadas, E.M.; Bacchetta, G. Initial Constraints in Seedling Dynamics of Juniperus macrocarpa Sm. Plant Ecol. 2014, 215, 853–861. [Google Scholar] [CrossRef]
  61. Bolmgren, K.; Eriksson, O. Fleshy Fruits Origins, Niche Shifts, and Diversification. Oikos 2005, 109, 255–272. [Google Scholar] [CrossRef]
  62. Matuszak, S.; Favre, A.; Schnitzler, J.; Muellner-Riehl, A.N. Key Innovations and Climatic Niche Divergence as Drivers of Diversification in Subtropical Gentianinae in Southeastern and Eastern Asia. Am. J. Bot. 2016, 103, 899–911. [Google Scholar] [CrossRef]
  63. Yoder, J.B.; Clancey, E.; Des Roches, S.; Eastman, J.M.; Gentry, L.; Godsoe, W.; Hagey, T.J.; Jochimsen, D.; Oswald, B.P.; Robertson, J.; et al. Ecological Opportunity and the Origin of Adaptive Radiations. J. Evol. Biol. 2010, 23, 1581–1596. [Google Scholar] [CrossRef]
  64. Mao, K.; Hao, G.; Liu, J.; Adams, R.P.; Milne, R.I. Diversification and Biogeography of Juniperus (Cupressaceae): Variable Diversification Rates and Multiple Intercontinental Dispersals. New Phytol. 2010, 188, 254–272. [Google Scholar] [CrossRef]
  65. Adams, R.P. Juniperus of Canada and the United States: Taxonomy, Key and Distribution. Lundellia 2019, 21, 1–34. [Google Scholar] [CrossRef]
  66. Leslie, A.B.; Beaulieu, J.M.; Crane, P.R.; Donoghue, M.J. Explaining the Distribution of Breeding and Dispersal Syndromes in Conifers. Proc. R. Soc. B Biol. Sci. 2013, 280, 20131812. [Google Scholar] [CrossRef] [PubMed]
  67. Farhat, P.; Hidalgo, O.; Robert, T.; Siljak-Yakovlev, S.; Leitch, I.J.; Adams, R.P.; Bou Dagher-Kharrat, M. Polyploidy in the Conifer Genus Juniperus: An Unexpectedly High Rate. Front. Plant Sci. 2019, 10, 676. [Google Scholar] [CrossRef]
  68. Abdikarimova, P.U.; Kali, A.; Shorin, S.S.; Beisenova, R.; Rakhymzhan, Z.; Nugmanov, A.; Myrzagaliyeva, A. Bioecological Characteristics of Cossack Juniper (Juniperus sabina) in Kazakhstan. Int. J. Des. Nat. Ecodyn. 2024, 19, 1223–1230. [Google Scholar] [CrossRef]
  69. Bandaruk, R.S.; Butchenkov, I.E.; Gritskevitch, E.R. Variety of Life Forms of Juniperus communis L. As an Indicator of Ecological Plasticity in the Urban Environment. In Environmental Problems of the XXI Century; Sakharov Readings; Belarusian State University: Minsk, Belarus, 2021; pp. 338–341. [Google Scholar] [CrossRef]
  70. Avramidou, E.V.; Korakaki, E.; Malliarou, E.; Boutsios, S. Studying the Genetic and the Epigenetic Diversity of the Endangered Species Juniperus drupacea Labill. Towards Safeguarding its Conservation in Greece. Forests 2023, 14, 1271. [Google Scholar] [CrossRef]
  71. Proutsos, N.; Solomou, A.; Karetsos, G.; Tsagari, K.; Mantakas, G.; Kaoukis, K.; Bourletsikas, A.; Lyrintzis, G. The Ecological Status of Juniperus foetidissima Forest Stands in the Mt. Oiti-Natura 2000 Site in Greece. Sustainability 2021, 13, 3544. [Google Scholar] [CrossRef]
  72. Franzese, J.; Ripa, R.R. Common Juniper, An Overlooked Conifer with High Invasion Potential in Protected Areas of Patagonia. Sci. Rep. 2023, 13, 9818. [Google Scholar] [CrossRef]
  73. Ghorbanzadeh, A.; Ghasemnezhad, A.; Sarmast, M.K.; Ebrahimi, S.N. An Analysis of Variations in Morphological Characteristics, Essential Oil Content, and Genetic Sequencing Among and Within Major Iranian Juniper (Juniperus spp.) Populations. Phytochemistry 2021, 186, 112737. [Google Scholar] [CrossRef]
  74. Bais, S.; Gill, N.S.; Rana, N. Effect of Juniperus communis Extract on Reserpine Induced Catalepsy. Inven. Impact Ethnopharmacol. 2014, 2014, 1–4. [Google Scholar]
  75. Bais, S.; Gill, N.S.; Kumar, N. Neuroprotective Effect of Juniperus communis on Chlorpromazine Induced Parkinson Disease in Animal Model. Chin. J. Biol. 2015, 2015, 542542. [Google Scholar] [CrossRef]
  76. Cioanca, O.; Hancianu, M.; Mihasan, M.; Hritcu, L. Anti-acetylcholinesterase and Antioxidant Activities of Inhaled Juniper Oil on Amyloid Beta (1–42)-Induced Oxidative Stress in the Rat Hippocampus. Neurochem. Res. 2015, 40, 952–960. [Google Scholar] [CrossRef]
  77. Orhan, N.; Orhan, I.E.; Ergun, F. Insights into Cholinesterase Inhibitory and Antioxidant Activities of Five Juniperus Species. Food Chem. Toxicol. 2011, 49, 2305–2312. [Google Scholar] [CrossRef]
  78. Alkhedaide, A.; Nassan, M.A.; Ismail, T.A.; Soliman, M.M.; Mohamed, E.H.; Amer, H.H.; Aldhahrani, A. Hypoglycemic and Antioxidant Effect of Juniperus procera Extract on Rats with Streptozotocin induced Diabetes. Pathophysiology 2019, 26, 361–368. [Google Scholar] [CrossRef]
  79. Amokrane, D.; Mohammedi, A.; Yekhlef, R.; Belfennache, D.; Zerrouki, N.D.; Aly, S.H.; Elanany, M.A.; Ali, M.A. Insecticidal Activity, GC/MS Analysis, and in Silico Studies of Juniperus phoenicea Essential Oil Against Aphis spiraecola. Univers. J. Agric. Res. 2024, 12, 51–64. [Google Scholar] [CrossRef]
  80. El-Sawi, S.A.; Motawae, H.M.; El-Shabrawy, A.O.; Sleem, M.A.; Sleem, A.A.; Maamoun, M.A.N.I. Antihyperglycemic Effect of Juniperus phoenicea L. on Alloxan-induced Diabetic Rats and Diterpenoids Isolated from the Fruits. J. Coast. Life Med. 2015, 3, 906–909. [Google Scholar] [CrossRef]
  81. Manvi, G. Screening and Evaluation of Pharmacognostic, Phytochemical and Hepatoprotective Activity of J. communis L. Stems. Int. J. Pharma Bio Sci. 2010, 1, 17–23. [Google Scholar]
  82. Orhan, N.; Aslan, M.; Pekcan, M.; Orhan, D.D.; Bedir, E.; Ergun, F. Identification of Hypoglycaemic Compounds from Berries of Juniperus oxycedrus subsp. oxycedrus Through Bioactivity Guided Isolation Technique. J. Ethnopharmacol. 2012, 139, 110–118. [Google Scholar] [CrossRef]
  83. Orhan, N.; Hoçbaç, S.; Orhan, D.D.; Asian, M.; Ergun, F. Enzyme Inhibitory and Radical Scavenging Effects of Some Anti-diabetic Plants of Turkey. Iran. J. Basic Med. Sci. 2014, 17, 426. [Google Scholar]
  84. Abdellah, F.; Laid, B.; Hammoudi, S.M.; Benaraba, R. In Vitro Evaluation of the Antimicrobial and Antioxidant Activities of Juniperus oxycedrus Essential Oil (Cade oil). Int. J. Innov. Eng. Sci. Res. 2018, 2, 66–76. [Google Scholar]
  85. Fernandez, A.; Cock, I.E. The Therapeutic Properties of Juniperus communis L.: Antioxidant Capacity, Bacterial Growth Inhibition, Anticancer Activity and Toxicity. Pharmacogn. J. 2016, 8, 273–280. [Google Scholar] [CrossRef]
  86. Gumral, N.; Kumbul, D.D.; Aylak, F.; Saygin, M.; Savik, E. Juniperus communis Linn Oil Decreases Oxidative Stress and Increases Antioxidant Enzymes in the Heart of Rats Administered a Diet Rich in Cholesterol. Toxicol. Ind. Health 2015, 31, 85–91. [Google Scholar] [CrossRef] [PubMed]
  87. Höferl, M.; Stoilova, I.; Schmidt, E.; Wanner, J.; Jirovetz, L.; Trifonova, D.; Krastev, L.; Krastanov, A. Chemical Composition and Antioxidant Properties of Juniper Berry (Juniperus communis L.) Essential Oil. Action of the Essential Oil on the Antioxidant Protection of Saccharomyces cerevisiae Model Organism. Antioxidants 2014, 3, 81–98. [Google Scholar] [CrossRef] [PubMed]
  88. Ramadan, M.M.; Ali, M.M.; Ghanem, K.Z.; El-Ghorabe, A.H. Essential Oils from Egyptian Aromatic Plants as Antioxidant and Novel Anticancer Agents in Human Cancer Cell Lines. Grasas Aceites 2015, 66, e080. [Google Scholar] [CrossRef]
  89. Reza, M.M.; Soheila, M.; Farkhondeh, M. Study the Relationship Between Antioxidant Potential and Phenolic Contents of Juniperus excelsa Fruit. Int. J. Pharm. Pharm. Sci. 2014, 6, 192–194. [Google Scholar]
  90. Ved, A.; Gupta, A.; Rawat, A.K.S. Antioxidant and Hepatoprotective Potential of Phenol Rich Fraction of Juniperus communis Linn. Leaves. Pharmacogn. Mag. 2017, 13, 108. [Google Scholar] [CrossRef]
  91. Weli, A.M.; Al-Hinai, J.R.; Al-Mjrafi, J.M.; Alnaaimi, J.R.; Hossain, M.A.; Saeed, S.; Aktar, M.S. Effect of Different Polarities Leaves Crude Extracts of Omani Juniperus excels on Antioxidant, Antimicrobial and Cytotoxic Activities and Their Bio-chemical Screening. Asian Pac. J. Reprod. 2014, 3, 218–223. [Google Scholar] [CrossRef]
  92. Zheljazkov, V.D.; Kacaniova, M.; Dincheva, I.; Radoukova, T.; Semerdjieva, I.B.; Astatkie, T.; Schlegel, V. Essential Oil Composition, Antioxidant and Antimicrobial Activity of the Galbuli of Six Juniper Species. Ind. Crops Prod. 2018, 124, 449–458. [Google Scholar] [CrossRef]
  93. Abbassy, M.A.; Marei, G.I. Antifungal and Chemical Composition of Essential Oils of Juniperus communis L. and Thymus vulgaris L. Against Two Phytopathogenic Fungi. J. Appl. Sci. Res. 2013, 9, 4584–4588. [Google Scholar]
  94. Abu-Darwish, M.; Gonçalves, M.; Cabral, C.; Cavaleiro, C.; Salgueiro, L. Chemical Composition and Antifungal Activity of Essential Oil from Juniperus phoenicea subsp. phoenicea Berries from Jordan. Acta Aliment. 2013, 42, 504–511. [Google Scholar] [CrossRef]
  95. Cabral, C.; Francisco, V.; Cavaleiro, C.; Gonçalves, M.J.; Cruz, M.T.; Sales, F.; Batista, M.T.; Salgueiro, L. Essential Oil of Juniperus communis subsp. alpina (Suter) Čelak Needles: Chemical Composition, Antifungal Activity and Cytotoxicity. Phytother. Res. 2012, 26, 1352–1357. [Google Scholar] [CrossRef]
  96. Falasca, A.; Caprari, C.; De Felice, V.; Fortini, P.; Saviano, G.; Zollo, F.; Iorizzi, M. GC-MS Analysis of the Essential Oils of Juniperus communis L. Berries Growing Wild in the Molise Region: Seasonal Variability and In Vitro Antifungal Activity. Bio-chem. Syst. Ecol. 2016, 69, 166–175. [Google Scholar] [CrossRef]
  97. Banerjee, S.; Mukherjee, A.; Chatterjee, T.K. Evaluation of Analgesic Activities of Methanolic Extract of Medicinal Plant Juniperus communis Linn. Int. J. Pharm. Pharm. Sci. 2012, 4, 547–550. [Google Scholar]
  98. Akdogan, M.; Koyu, A.; Ciris, M.; Yildiz, K. Anti-hypercholesterolemic Activity of Juniperus communis Lynn Oil in Rats: A Biochemical and Histopathological Investigation. Biomed. Res. 2012, 23, 321–328. [Google Scholar]
  99. Abdel-Kader, M.S.; Hamad, A.M.; Alanazi, M.T.; Alanazi, A.H.; Ali, R.; Foudah, A.I.; Alqarni, M.H. Characterization and Hepatoprotective Evaluation of Sesquiterpenes and Diterpenes from the Aerial Parts of Juniperus sabina L. Saudi Pharm. J. 2019, 27, 920–929. [Google Scholar] [CrossRef]
  100. Aljaiyash, A.; Ghanmi, M.; Satrani, B.; Labiad, H.; Echchelh, A.; Chaouch, A. Chemical Composition of Essential Oils of Ripe and Unripe Berries and Leaves of Juniperus phoenicea L. and Determination of Their Antimicrobial Activities. Int. J. Innov. Res. Sci. Eng. Technol. 2016, 4, 7–14. [Google Scholar]
  101. Eryiğit, T.; Okut, N.; Ekici, K.; Yildirim, B. Chemical Composition and Antibacterial Activities of Juniperus horizontalis Essential Oil. Can. J. Plant Sci. 2014, 94, 323–327. [Google Scholar] [CrossRef]
  102. Khoury, M.; El Beyrouthy, M.; Ouaini, N.; Iriti, M.; Eparvier, V.; Stien, D. Chemical Composition and Antimicrobial Activity of the Essential Oil of Juniperus excelsa M. Bieb. Growing Wild in Lebanon. Chem Biodivers. 2014, 11, 825–830. [Google Scholar] [CrossRef]
  103. Mazari, K.; Bendimerad, N.; Bekhechi, C.; Fernandez, X. Chemical Composition and Antimicrobial Activity of Essential Oils Isolated from Algerian Juniperus phoenicea L. and Cupressus sempervirens L. J. Med. Plants Res. 2010, 4, 959–964. [Google Scholar] [CrossRef]
  104. Ehsani, E.; Akbari, K.; Teimouri, M.; Khadem, A. Chemical Composition and Antibacterial Activity of Two Juniperus Species Essential Oils. Afr. J. Microbiol. Res. 2012, 6, 6704–6710. [Google Scholar] [CrossRef]
  105. Kalaba, V.; Marjanović-Balaban, Ž.; Kalaba, D.; Lazić, D.; Cvjetković, V.G. Antibacterial Activity of Essential Oil of Juniperus communis L. Qual. Life 2020, 11, 18–24. [Google Scholar] [CrossRef]
  106. Sati, S.C.; Joshi, S. Antibacterial Potential of Leaf Extracts of Juniperus communis L. from Kumaun, Himalaya. Afr. J. Microbiol. Res. 2010, 4, 1291–1294. [Google Scholar]
  107. Ivanova, D.I.; Nedialkov, P.T.; Tashev, A.N.; Olech, M.; Nowak, R.; Ilieva, Y.E.; Kokanova-Nedialkova, Z.K.; Atanasova, T.N.; Angelov, G.; Najdenski, H.M. Junipers of Various Origins as Potential Sources of the Anticancer Drug Precursor Podophyllotoxin. Molecules 2021, 26, 5179. [Google Scholar] [CrossRef]
  108. Emami, S.A.; Asili, J.; Mohagheghi, Z.; Hassanzadeh, M.K. Antioxidant Activity of Leaves and Fruits of Iranian Conifers. Evidence-based Complement. Altern. Med. 2007, 4, 313–319. [Google Scholar] [CrossRef]
  109. Khan, M.; Khan, A.-u.; Najeeb-ur-Rehman; Gilani, A.-H. Pharmacological Explanation for the Medicinal Use of Juniperus excelsa in Hyperactive Gastrointestinal and Respiratory Disorders. J. Nat. Med. 2012, 66, 292–301. [Google Scholar] [CrossRef]
  110. Sela, F.; Karapandzova, M.; Stefkov, G.; Cvetkovikj, I.; Kulevanova, S. Chemical Composition and Antimicrobial Activity of Essential Oils of Juniperus excelsa Bieb. (Cupressaceae) Grown in R. Macedonia. Pharm. Res. 2015, 7, 74–80. [Google Scholar] [CrossRef]
  111. Unlu, M.; Vardar-Unlu, G.; Vural, N.; Donmez, E.; Cakmak, O. Composition and Antimicrobial Activity of Juniperus excelsa Essential Oil. Chem. Nat. Compd. 2008, 44, 129–131. [Google Scholar] [CrossRef]
  112. Farjon, A. World Checklist and Bibliography of Conifers, 2nd ed.; Kew: The Royal Botanic Gardens; The University of Chicago Press: Chicago, IL, USA, 2001; 316p. [Google Scholar]
  113. Kavetsou, E.; Pitterou, I.; Katopodi, A.; Petridou, G.; Adjali, A.; Grigorakis, S.; Detsi, A. Preparation, Characterization, and Acetylcholinesterase Inhibitory Ability of the Inclusion Complex of β-Cyclodextrin–Cedar (Juniperus phoenicea) Essential Oil. Micro 2021, 1, 250–266. [Google Scholar] [CrossRef]
  114. Sahib, N.; Boumediene, M.; Abid, M.; Mihamou, A.; Serghini-Caid, H.; Elamrani, A.; Hano, C.; Addi, M. Phenotypic Comparison of Three Populations of Juniperus turbinata Guss. In North-Eastern Morocco. Forests 2022, 13, 287. [Google Scholar] [CrossRef]
  115. Escribano-Ávila, G.; Sanz-Pérez, V.; Pías, B.; Virgós, E.; Escudero, A.; Valladares, F. Colonization of Abandoned Land by Juniperus thurifera is Mediated by the Interaction of a Diverse Dispersal Assemblage and Environmental Heterogeneity. PLoS ONE 2012, 7, e46993. [Google Scholar] [CrossRef]
  116. Martínez de León, R.; Moreno-Letelier, A. Spatiotemporal Diversification of Global Junipers: Traces of Niche Conservatism and Trait-Dependent Diversification. Ecol. Evol. 2025, 15, e70910. [Google Scholar] [CrossRef]
  117. Escribano-Ávila, G.; Calviño-Cancela, M.; Pías, B.; Virgós, E.; Valladares, F.; Escudero, A. Diverse Guilds Provide Complementary Dispersal Services in a Woodland Expansion Process After Land Abandonment. J. Appl. Ecol. 2014, 51, 1701–1711. [Google Scholar] [CrossRef]
  118. DeSoto, L.; Olano, J.M.; Rozas, V.; De la Cruz, M. Release of Juniperus thurifera Woodlands from Herbivore-Mediated Arrested Succession in Spain. Appl. Veg. Sci. 2010, 13, 15–25. [Google Scholar] [CrossRef]
  119. Ferreira, L.M.M.; Celaya, R.; Benavides, R.; Jáuregui, B.M.; García, U.; Santos, A.S.; García, R.R.; Rodrigues, M.A.M.; Osoro, K. Foraging Behaviour of Domestic Herbivore Species Grazing on Heathlands Associated with Improved Pasture Areas. Livest. Sci. 2013, 155, 373–383. [Google Scholar] [CrossRef]
  120. Olano, J.M.; Zavala, M.A.; Rozas, V. Disruption of Juniperus thurifera Woodland Structure in its Northwestern Geographical Range: Potential Drivers and Limiting Factors. Eur. J. For. Res. 2012, 131, 563–570. [Google Scholar] [CrossRef]
  121. Zweifel-Schielly, B.; Leuenberger, Y.; Kreuzer, M.; Suter, W. A Herbivore’s Food Landscape: Seasonal Dynamics and Nutritional Implications of Diet Selection by a Red Deer Population in Contrasting Alpine Habitats. J. Zool. 2012, 286, 68–80. [Google Scholar] [CrossRef]
  122. Castellanos, M.C.; Donat-Caerols, S.; González-Martínez, S.C.; Verdú, M. Can Facilitation Influence the Spatial Genetics of the Beneficiary Plant Population? J. Ecol. 2014, 102, 1214–1221. [Google Scholar] [CrossRef]
  123. Cavin, L.; Mountford, E.P.; Peterken, G.F.; Jump, A.S. Extreme Drought Alters Competitive Dominance Within and Between Tree Species in a Mixed Forest Stand. Funct. Ecol. 2013, 27, 1424–1435. [Google Scholar] [CrossRef]
  124. García-Cervigón, M.A.I.; Gazol, A.; Sanz, V.; Camarero, J.J.; Olano, J.M. Intraspecific Competition Replaces Interspecific Facilitation as Abiotic Stress Decreases: The Shifting Nature of Plant–Plant Interactions. Perspect. Plant Ecol. 2013, 15, 226–236. [Google Scholar] [CrossRef]
  125. García-Cervigón, M.A.I.; Linares, J.C.; Aibar, P.; Olano, J.M. Facilitation Promotes Changes in Leaf Economics Traits of a Perennial Forb. Oecologia 2015, 179, 103–116. [Google Scholar] [CrossRef]
  126. He, Q.; Bertness, M.D.; Altieri, A.H. Global Shifts Towards Positive Species Interactions with Increasing Environmental Stress. Ecol. Lett. 2013, 16, 695–706. [Google Scholar] [CrossRef] [PubMed]
  127. Van Auken, O.W. (Ed.) Western North American Juniperus Communities: A Dynamic Vegetation Type; Volume 196 Ecological Studies: Analysis and Synthesis; Springer Science & Business Media: New York, NY, USA, 2008; 316p, ISBN 0387340033/9780387340036. [Google Scholar]
  128. Baker, J.P.; Cottrell, J.; Ennos, R.; Perry, A.; Green, S.; Cavers, S. Not Like Other Conifers: Evaluation of Phenotypic Diversity in British Common Juniper, Juniperus communis, Indicates Genetic Isolation and Local Adaptations Among Remnant Populations. bioRxiv 2024. [Google Scholar] [CrossRef]
  129. Bennion, L.D.; Ward, D. Plant–Soil Feedback from Eastern Redcedar (Juniperus virginiana) Inhibits the Growth of Grasses in Encroaching Range. Ecol. Evol. 2022, 12, e9400. [Google Scholar] [CrossRef] [PubMed]
  130. McKinley, D.C.; Norris, M.D.; Blair, J.M.; Johnson, L.C. Altered Ecosystem Processes as a Consequence of Juniperus virginiana L. Encroachment into North American Tallgrass Prairie. In Western North American Juniperus Communities; Ecological Studies; Van Auken, O.W., Ed.; Springer: New York, NY, USA, 2008; Volume 196, pp. 170–187. [Google Scholar] [CrossRef]
  131. Rodríguez-García, E.; Mezquida, E.T.; Olano, J.M. You’d Better Walk Alone: Changes in Forest Composition Affect Pollination Efficiency and Pre-Dispersal Cone Damage in Iberian Juniperus thurifera Forests. Plant Biol. 2017, 19, 934–941. [Google Scholar] [CrossRef]
  132. Fotiadou, E.; Panou, E.; Graikou, K.; Sakellarakis, F.N.; Chinou, I. Volatiles of all Native Juniperus Species Growing in Greece—Antimicrobial Properties. Foods 2023, 12, 3506. [Google Scholar] [CrossRef]
  133. Donovan, V.M.; Fogarty, D.T.; Twidwell, D. Spot-fire Distance Increases Disproportionately for Wildfires Compared to Pre-scribed Fires as Grasslands Transition to Juniperus Woodlands. PLoS ONE 2023, 18, e0283816. [Google Scholar] [CrossRef]
  134. Kyriazopoulos, A.P.; Abraham, E.M.; Parissi, Z.M.; Korakis, G.; Manousidis, T.; Chrisovelidou, K.; Papanaretou, K. Effects of Juniper Encroachment on Herbage Production and Biodiversity in a Natural Grassland: Preliminary Results. In New Approaches for Grassland Research in a Context of Climate and Socio-Economic Changes; Options Méditerranéennes, Series A; Acar, Z., López-Francos, A., Porqueddu, C., Eds.; CIHEAM: Zaragoza, Spain, 2012; Volume 102, pp. 299–302. Available online: https://om.ciheam.org/om/pdf/a102/00006931.pdf (accessed on 30 January 2026).
  135. Korakaki, E.; Avramidou, E.V.; Solomou, A.D.; Boutsios, S.; Daskalakou, E.N. Sap Flow Responses of the Endangered Species Juniperus drupacea Labill. to Environmental Variables in Parnon Mountain, Greece. Forests 2024, 15, 431. [Google Scholar] [CrossRef]
  136. Dakhil, M.A.; Halmy, M.W.A.; Hassan, W.A.; El-Keblawy, A.; Pan, K.; Abdelaal, M. Endemic Juniperus Montane Species Facing Extinction Risk Under Climate Change in Southwest China: Integrative Approach for Conservation Assessment and Prioritization. Biology 2021, 10, 63. [Google Scholar] [CrossRef]
  137. Jacquemart, A.L.; Buyens, C.; Delescaille, L.M.; Van Rossum, F. Using Genetic Evaluation to Guide Conservation of Remnant Juniperus communis (Cupressaceae) Populations. Plant Biol. 2020, 23, 193–204. [Google Scholar] [CrossRef]
  138. Al-Yasi, H.M.; Al-Qthanin, R. Comparing Genetic Differentiation and Variation Using ISSR and Scot Among Juniper Plant Markers in Saudi Arabia. Front. Plant Sci. 2024, 15, 1356917. [Google Scholar] [CrossRef]
  139. Yang, Y.; Bian, Z.; Ren, G.; Liu, J.; Shrestha, N. Niche Conservatism Limits the Distribution of Medicago in the Tropics. Ecography 2022, 2022, e06085. [Google Scholar] [CrossRef]
  140. Khoshhal, S.M.; Mosavizadeh, S.J.; Sharifani, M. Evaluation of Junipers spp. Genetic Diversity in Northern Iran Using ISSR Markers. Ecol. Iran. For. 2018, 6, 14–20. [Google Scholar] [CrossRef]
  141. Liu, J.; Wang, J.; Morreale, S.J.; Schneider, R.L.; Li, Z.; Wu, G.L. Contributions of Plant Litter to Soil Microbial Activity Improvement and Soil Nutrient Enhancement Along with Herb and Shrub Colonization Expansions in an Arid Sandy Land. Catena 2023, 227, 107098. [Google Scholar] [CrossRef]
  142. Galgóci, M.; Kormuťák, A.; Klobučník, M.; Gömöry, D.; Boleček, P. Pollen Viability in Three Juniperus Taxa. Biologia 2025, 80, 511–517. [Google Scholar] [CrossRef]
  143. Men, X.; Bao, Y.; Wu, M.; Liao, C.; Cheng, X. Soil Enzyme Activities Responded Differently to Short-Term Litter Input Manipulation Under Coniferous and Broad-Leaved Forests in the Subalpine Area of Southwest China. For. Ecol. Manag. 2023, 546, 121360. [Google Scholar] [CrossRef]
  144. Rostamikia, Y.; Matinizadeh, M.; Anbaran, S.M. Influence of Scattered Greek Juniper Trees on Soil Properties in Semi-Arid Woodlands in the Northwest of Iran. J. For. Sci. Prague 2024, 70, 560–573. [Google Scholar] [CrossRef]
  145. Veldhuis, E.R. Surviving the Nitrogen Crisis: The Case of Juniperus Communis and its Mycorrhizal Fungi; Philosophy of Doctor, University of Groningen: Groningen, The Netherlands, 2023. [Google Scholar] [CrossRef]
  146. Boratyński, A.; Salvà-Catarineu, M.; Marcysiak, K.; Mazur, M.; Romo, Á.; Minissale, P.; Tan, K.; Iszkuło, G.; Witkowski, R.; Mazur, A.; et al. Biology and Ecology of Complex Juniperus phoenicea—J. turbinata—J. canariensis. III. Reproduction, Herbivory, Utilization, Conservation. Dendrobiology 2025, 94, 1–21. [Google Scholar] [CrossRef]
  147. Xu, H.; Ding, M.; Zhang, H.; Zhang, Y.; Huang, P.; Wu, Y.P.; Zou, T.E.; Wang, N.; Zeng, H. Interaction Effects of Vegetation and Soil Factors on Microbial Communities in Alpine Steppe Under Degradation. Environ. Sci. 2024, 45, 4251–4265. [Google Scholar] [CrossRef]
  148. Ahmed, N.; Atzberger, C.; Zewdie, W. Integration of Remote Sensing and Bioclimatic Data for Prediction of Invasive Species Distribution in Data-Poor Regions: A Review on Challenges and Opportunities. Environ. Syst. Res. 2020, 9, 32. [Google Scholar] [CrossRef]
  149. Ninot, J.M.; Anadon-Rosell, A.; Molino, A.; Grau, O.; Caminal, M.; Casanovas, A.; Carrillo, E. Similar Functional Structure and Encroaching Dynamics in Two Juniperus Species with Contrasting Distribution Patterns. Folia Geobot. 2025, 59, 129–146. [Google Scholar] [CrossRef]
  150. Schriver, R.; Sessions, J.; Strimbu, B.M. Landscape Restoration Using Individual Tree Harvest Strategies. Sustainability 2024, 16, 5124. [Google Scholar] [CrossRef]
  151. Adiga, A.; Palmer, N.; Baek, Y.Y.; Mortveit, H.; Ravi, S.S. Network Models and Simulation Analytics for Multi-Scale Dynamics of Biological Invasions. Front. Big Data 2022, 5, 796897. [Google Scholar] [CrossRef]
  152. Naghipour, A.A.; Ashrafzadeh, M.R.; Haidarian, M. Assessing the Potential Distribution of Juniperus excelsa M. Bieb. Under Current and Future Climate Scenarios in the Chaharmahal va Bakhtiari Province, Iran. Sci. Rep. Life Sci. 2021, 2, 8–17. [Google Scholar] [CrossRef]
  153. Özdemir, S.; Gülsoy, S.; Mert, A. Predicting the Effect of Climate Change on the Potential Distribution of Crimean Juniper. Kastamonu Univ. J. For. Fac. 2020, 20, 133–142. [Google Scholar] [CrossRef]
  154. Zaka, M.M.; Samat, A. Advances in Remote Sensing and Machine Learning Methods for Invasive Plants Study: A Comprehensive Review. Remote Sens. 2024, 16, 3781. [Google Scholar] [CrossRef]
Figure 1. Annual number of scientific publications on the genus Juniperus from 2001 to 2025.
Figure 1. Annual number of scientific publications on the genus Juniperus from 2001 to 2025.
Ijpb 17 00023 g001
Figure 2. Main journals and number of documents published on the genus Juniperus from 2001 to 2025.
Figure 2. Main journals and number of documents published on the genus Juniperus from 2001 to 2025.
Ijpb 17 00023 g002
Figure 3. Three-field plot considering the documents published on the genus Juniperus from 2001 to 2025.
Figure 3. Three-field plot considering the documents published on the genus Juniperus from 2001 to 2025.
Ijpb 17 00023 g003
Figure 4. Principal collaboration networks among authors publishing on the genus Juniperus from 2001 to 2025.
Figure 4. Principal collaboration networks among authors publishing on the genus Juniperus from 2001 to 2025.
Ijpb 17 00023 g004
Figure 5. Global country collaboration map for publications related to the genus Juniperus from 2001 to 2025.
Figure 5. Global country collaboration map for publications related to the genus Juniperus from 2001 to 2025.
Ijpb 17 00023 g005
Figure 6. (a) Co-occurrence network and (b) word cloud of the most frequently used terms by the authors in the title and keywords of the documents published on the genus Juniperus from 2001 to 2025.
Figure 6. (a) Co-occurrence network and (b) word cloud of the most frequently used terms by the authors in the title and keywords of the documents published on the genus Juniperus from 2001 to 2025.
Ijpb 17 00023 g006
Table 1. Therapeutic properties of bioactive compounds present in species of the genus Juniperus.
Table 1. Therapeutic properties of bioactive compounds present in species of the genus Juniperus.
Therapeutic PropertiesReference(s)
Neuroprotective and anticataleptic effects in Parkinson’s disease[74,75,76,77]
Antidiabetic and antihyperlipidemic[78,79,80,81,82,83]
Diuretic and anti-inflammatory[17]
Antioxidant[76,77,78,84,85,86,87,88,89,90,91,92]
Antifungal[93,94,95,96]
Analgesic[97]
Antihypercholesterolemic[86,98]
Hepatoprotective[81,90,99]
Antimicrobial[84,91,92,100,101,102,103]
Antiviral[2,85]
Antibacterial[101,104,105,106]
Anticancer[85,88,107]
Asthma and dysmenorrhea[17]
Table 2. Positive impacts of genus Juniperus on ecosystem biodiversity.
Table 2. Positive impacts of genus Juniperus on ecosystem biodiversity.
ImpactReference(s)
Enhancement of habitat ecological stability[6,7]
Mitigation of desertification processes[8,9,10,11]
Provision of resources for wildlife species[13,16,19,20]
Improvement of trophic networks[7]
Creation of microclimates[10]
Improvement of soil quality and fertility[22,70]
Creation of “fertility islands”[21]
Improvement of hydrology[21]
Nurse-plant effects in some ecosystems[122,123,124,125,126]
Provision of diverse ecosystem services[13,34,35]
Table 3. Negative impacts of genus Juniperus on ecosystem biodiversity.
Table 3. Negative impacts of genus Juniperus on ecosystem biodiversity.
ImpactReference(s)
Reduction in plant species richness[24]
Alteration of hydrological functions[25]
Habitat fragmentation[6,34,37]
Exacerbation of soil erosion[25]
Reduction in grassland areas[34]
Negative alteration of ecosystem characteristics[12,13,14,15,35,127]
Modification of plant composition[2,6,7,9,11,37,128,129]
Inhibition of the growth of other species[11,37]
Alteration of fire regimes[2,11,37,128,129]
Reduce the diversity of native plant species[12,13,14,15]
Decrease in floristic richness and genetic variability[6,7,9,11,68,69,130]
Impediment of the movement of flora and fauna[6,34,37]
Disruption of natural regeneration processes[21,22,70]
Interference with critical ecological interactions (i.e., pollination)[27,28,29,30,31,32,33,37]
Population decline of specialized herbivores and pollinators[34,35,130,131]
Modification of the hydrological cycle[13,22,25,35,70,72]
Hindered the survival of fauna[13,16,19,20]
Perturbation of ecosystem processes[21,22,25,70]
Alteration of woody species population dynamics[22]
Monopolization of available resources[2,11,35,129,132]
Preferential establishment of woody over herbaceous species[24,25,133,134]
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.

Share and Cite

MDPI and ACS Style

Navarrete-Molina, C.; Sariñana-Navarrete, M.A.; Meza-Herrera, C.A.; De Santiago-Miramontes, Á.; Rodriguez-Alvarez, J.L.; Cuevas-Jacquez, R.A.; Valenzuela-Núñez, L.M.; Ramírez-Gottfried, R.I.; Torres-Rodriguez, E.; Marín-Tinoco, R.I. Hero or Villain: The Importance and Impacts of the Genus Juniperus on Ecosystems. Int. J. Plant Biol. 2026, 17, 23. https://doi.org/10.3390/ijpb17030023

AMA Style

Navarrete-Molina C, Sariñana-Navarrete MA, Meza-Herrera CA, De Santiago-Miramontes Á, Rodriguez-Alvarez JL, Cuevas-Jacquez RA, Valenzuela-Núñez LM, Ramírez-Gottfried RI, Torres-Rodriguez E, Marín-Tinoco RI. Hero or Villain: The Importance and Impacts of the Genus Juniperus on Ecosystems. International Journal of Plant Biology. 2026; 17(3):23. https://doi.org/10.3390/ijpb17030023

Chicago/Turabian Style

Navarrete-Molina, Cayetano, María A. Sariñana-Navarrete, Cesar A. Meza-Herrera, Ángeles De Santiago-Miramontes, José L. Rodriguez-Alvarez, Raúl A. Cuevas-Jacquez, Luis M. Valenzuela-Núñez, Ricardo I. Ramírez-Gottfried, Edir Torres-Rodriguez, and Rubén I. Marín-Tinoco. 2026. "Hero or Villain: The Importance and Impacts of the Genus Juniperus on Ecosystems" International Journal of Plant Biology 17, no. 3: 23. https://doi.org/10.3390/ijpb17030023

APA Style

Navarrete-Molina, C., Sariñana-Navarrete, M. A., Meza-Herrera, C. A., De Santiago-Miramontes, Á., Rodriguez-Alvarez, J. L., Cuevas-Jacquez, R. A., Valenzuela-Núñez, L. M., Ramírez-Gottfried, R. I., Torres-Rodriguez, E., & Marín-Tinoco, R. I. (2026). Hero or Villain: The Importance and Impacts of the Genus Juniperus on Ecosystems. International Journal of Plant Biology, 17(3), 23. https://doi.org/10.3390/ijpb17030023

Article Metrics

Back to TopTop