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Climate Change and Its Impact on Mountainous Plant Species: A Review

Written By

Patrush Lepcha

Submitted: 30 January 2024 Reviewed: 30 January 2024 Published: 08 April 2024

DOI: 10.5772/intechopen.1004445

Sustainable Forest Management - Surpassing Climate Change and Land Degradation IntechOpen
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Sustainable Forest Management - Surpassing Climate Change and Land Degradation [Working Title]

Dr. Surendra N. Kulshreshtha

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Abstract

Climate change poses unprecedented threats to ecosystems worldwide, and mountainous regions with rare ecosystems, unique landscapes, a large number of endemic species, and enormous plant biodiversity are highly sensitive to the effects of climate change. Early spring and late autumn events are major phenological changes observed in plants in response to climate change, and such changes mainly disturb the interaction between plants and their pollinators, thereby affecting the fitness and survival of both species. Climate warming is causing plant species to shift upward along the elevational gradient in the mountain, resulting in species accumulation at higher elevations and range contraction of several alpine plant species. Further, climate warming is augmenting the plant invasion by removing climatic barriers, thus threatening the diversity of native plant species. Moreover, climate warming is contributing to habitat fragmentation and loss and accelerating the associated impacts. All these impacts of climate change can potentially alter the composition, structure, and function of pristine mountain ecosystems, which leads to irreversible biodiversity losses. Thus, various climate change mitigation strategies, such as conventional mitigation strategies, negative emissions technologies, and radiative forcing or geoengineering technologies, are suggested to stabilize climate warming, thereby conserving irreversible global biodiversity loss.

Keywords

  • climate change
  • habitat fragmentation
  • habitat shift
  • mountain ecosystem
  • phenology
  • plant invasion

1. Introduction

Climate change refers to long-term alterations in local, regional, or global weather patterns (e.g., changes in temperature, precipitation, humidity, and atmospheric pressure) due to natural and anthropogenic activities. An increase in global air and oceanic temperature, the retreating of the global ice sheets, a rise in sea level, extreme weather events such as prolonged drought, frequent heat waves, erratic rainfall, an increase in flooding events, and the frequent occurrence of pests and diseases are the consequences of the climatic change evident at national and international levels. These events are posing unprecedented threats to the agroeconomy, the livelihood of marginal populations, global biodiversity, and the structure, composition, and functions of various ecosystems across the globe. Climate change, therefore, has become a formidable intergovernmental challenge that impacts various domains of the environment, ecology, sociopolitics, and socioeconomy [1].

Mountains are unique ecosystems recognized for their complexity and diversity [2]. They harbor about 23% of the Earth’s forests and 30% of all land, along with high levels of biodiversity and endemism [3]. Approximately 1/4th of the global human population inhabits mountainous regions across the globe, and many of them are poor [3]. Thus, the biodiversity of the mountains is pivotal for the sustainable development and survival of human societies [4]. Mountains possess the most distinct climatic gradients on earth and are one of the key “experimental fields of nature” because of the sharp environmental gradients they cover and the spatial fragmentation they generate at the otherwise global occurrence of habitat types and wilderness [5]. An average temperature decrease of −6°C is observed in mountains with every 1000 meters increase in elevation due to adiabatic lapse rate, and inversely, precipitation increases with increasing elevation because air masses cool and condense if it is elevated to higher elevations [6]. Thus, temperature and soil moisture are the major factors that determine the zonation of ecosystems along mountain gradients [5]. Such a type of zonation is the unique feature that differentiates mountain forests from other forests. The definition of mountain forest is obscure; however, a reasonable definition according to Price et al. [7] is “forests on land with an elevation of 2500 m above sea level or higher, irrespective of slope, or on land with an elevation of 300–2500 m and a slope with sharp changes in elevation within a short distance.” However, mountain environments are highly sensitive to climate change [8, 9] and experience climate warming at a rapid pace compared to the Northern Hemisphere [10] or the lowlands [11]. Also, the future air temperatures of these regions are predicted to be higher than present-day temperatures [10, 12]. The macroclimate warming on mountains has accelerated the rate of species accumulation and potentially jeopardized the primary function of mountains, which is to act as long-term refugia for biodiversity [13].

Climate influences the vegetation patterns (structure, distribution, and ecology) of forests around the world [14]. Global warming of 1–2°C is sufficient to impact most landscapes and ecosystems by altering species composition, productivity, and biodiversity [15]. When environmental conditions alter, living organisms either escape, adapt, or become extinct [5]. In the case of plants, they mostly change their phenology [16] and shift their distributional range to higher latitudes and/or elevations [17, 18] to track climatic niches in response to climate change. Changes in flowering phenology often lead to plant-pollinator mismatches, which impact the reproduction, dispersal, fitness, and survival of the plants and associated pollinators and other species. The latitudinal or elevational shifts of plant species change the native species composition, increase the probability of the spread of alien invasive species (e.g., Eupatorium, Lantana, and Parthenium spp.) in the native ecosystems, and risk biodiversity. These events potentially accelerate competition among native and non-native plant species, which can lead to habitat fragmentation, biodiversity loss, and eventually the extinction of native flora. Therefore, this chapter delves into the influence of climate change on the phenology, habitat shifting, plant invasion, habitat fragmentation, and their consequences on native mountain biodiversity and ecosystems, along with the prospect of the preservation of mountain ecosystems and their unique plant diversity.

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2. Climate change influencing plant phenology

Phenology is the study of the timing of various seasonal events in an organism’s life cycle [19], including the response of organisms to climatic or seasonal changes (such as variation in temperature, precipitation, and duration of sunlight) in the environment in which they live [20]. Plants are adapted to the annual-seasonal cycle of a particular region, and seasonal atmospheric variations regulate the different stages of a plant’s life cycle, such as the appearance of leaves and buds, first bloom or flowering, pollination, fertilization, seed dispersal, leaf senescence, and germination [20]. Temperature and photoperiod are the two major environmental factors that cause and control phenological patterns, especially in higher-latitude ecosystems [11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23]. The global climate warming phenomenon has drastically changed the various biological processes [24, 25, 26], including phenology [27, 28]. Thus, phenological events are sensitive and the most prominent indicators of climate change [29, 30, 31, 32]. However, according to the study on Mediterranean shrubland and Mediterranean mountain forest, rainfall and water availability also affect plant phenology in addition to temperature [33]. Nonetheless, the early arrival of the growing season of vegetation, the early bud break, leaf flush or flowering during spring, and late leaf senescence and fruit maturation during autumn are the most widely studied impacts of climate change on plant phenology [34, 35, 36, 37].

The climate warming in the Himalaya is higher than the average global temperature increase [38], and such warming immensely impacts the biodiversity in mountainous regions [39]. These regions are the “natural laboratory,” which is ideal for studying the influence of climate change on floral phenology [40]. Variation in flowering phenology in response to climate change in mountainous regions has attracted many ecologists [40], and their studies have found that the mean flowering time of the mountain plant species is sensitive to temperature changes [41] as well as to changes in elevation, temperature, and precipitation along the elevation gradient of the mountains [42]. The temperate plant species in the Himalaya showed a mean phenological advancement of 1.9 days in spring events and a mean delay of 1.4 in autumn events per decade, and the average growing season length was extended by 3.3 days per decade [43]. Studies on flowering phenology in temperate mountains (e.g., the Alps) also indicated that spring phenology has preponded over the last few decades [44, 45, 46], and spring flowering times became earlier in the southern subtropical Nanling region of southern China in response to climate warming [47]. Field-based observations in the Himalaya showed that some species of Rhododendron are flowering a month earlier than in the past [48]. A similar result of 15 days early flowering in Rhododendron arboreum Smith compared to previous reports was observed in Kumaun Region of Central Himalaya (India) [49]. These shifts in peak flowering dates in R. arboretum over the past 100 years were due to the elevated seasonal and annual average maximum temperatures [50]. The mean flowering time in Rhododendron spp. advances 2.27 days per 1°C rise in mean annual temperature [41]. Periodic leafing and bud break in trees in the Himalayan forests has also advanced by 0.20 days per year for the past 30 years, and these changes are related to an increase in atmospheric temperature at the rate of 0.038°C per year [51].

The phenological responses of various plant species to climate change can cause asynchronous ecological interactions that threaten the structure and function of the ecosystem [52, 53]. Early and late flowering of the plants impact their ability to adapt to the surrounding environment, which determines the survival and death of the plant species [54]. Plant species can adapt to the changing environment if the changes in their flowering phenology can track the rate of climate change; however, if the flowering phenological changes of the species cannot track the rate of climate change, such species cannot adapt and are eliminated [40]. Thus, the phenological alterations affect the demography, fitness, and survival of the plant species [55, 56]. Further, the survival of plant species depends on the reproductive success of pollinators [40]. Therefore, the risk of plant-pollinator mismatches increases with changing flowering phenology, which threatens the stability of the plant community and impacts ecosystem structure and functions [57]. For example, the changes in the timing of flowering of Corydalis yanhusuo W. T. Wang gave rise to a phenological mismatch with bumblebees (pollinators), which resulted in a low seed setting rate [58]. These observations indicate the inimical impact of climate warming on the phenology of plants [59, 60]. Thus, plant phenology is becoming an instrumental tool to monitor the effects of climate warming on vegetation shifts, which have detrimental impacts on biodiversity and ecosystem functioning [61, 62].

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3. Climate change causing habitat shifts

Climate change is altering the environmental conditions of the habitats of plant and animal species, causing them to shift their habitat range in search of their climatic niche for survival [63]. Plant species either change elevational range or latitudinal range in response to climate change [64]. However, the tolerance level of individual species to environmental change determines the need for a shift and its extent [63]. It has been predicted that climate warming will shift the distributions of plants and animals toward the pole along the latitudinal gradient and toward higher elevation along the elevational gradient in the track of isotherms [65]. For example, a meta-analysis of more than 1700 plant species indicated that climate change is attributing to the advance of spring events by 2.3 days per decade and an average range shift of 6.1 m/decade toward the pole [17]. Several studies in the Alps indicated upslope elevational shifts of species in response to climate change, and they were able to track their ecological niche with rising global temperatures [66, 67, 68, 69]. A study on changes in the optimum elevation of 171 forest plants between 1905–1985 and 1986–2005 indicated the upslope migration of plant species across six mountain ranges in France [66]. A study on Mt. Gongga (China) also depicted an upward shift of 53 plant species in response to climate change [70]. In the Nordic region (Northern Europe), the distribution of cereal and grass is likely to shift by up to 92.8 and 178.7 km, depending on the intensity of climate change [71], and some crop species have already been introduced to new areas [72]. Our study on large cardamom (Amomum subulatum Roxb., a commercially important spice crop of Sikkim, India) also indicated that cultivars previously grown at low elevations (below 975 m asl) are shifted to high elevations (above 975 m), and climate change is augmenting this elevational shift [73].

The plant diversity of the Alpine region in the mountain range is higher than the global average [74, 75]; thus, the Alpine meadows are included under the 200 critical global ecoregions [76]. However, plant species in the GLORIA (Global Observation Research Initiative in Alpine Environments) network of mountains in Europe have shifted their elevational distributions to higher elevations between 2001 and 2008, with an average shift of 2.7 m/year [77]. Telwala et al. [78] suggested that the winter temperature of alpine regions of Sikkim Himalaya (India) has become warmer than the winter temperature of the last two centuries, and the upper elevation limit of the species was shifted to 23–998 m with an average upward displacement rate of 27.5 ± 22.1 m per decade. About 87% of the 124 endemic plant species have shifted their geographic range in the region, which caused an increase in species richness in the upper alpine zone compared to the nineteenth century, and the plant assemblages and community structure of the region were substantially different compared to the last century [78]. The species richness of vascular plants on Mount Schrankogel, which is a major GLORIA site located in the Tyrolean Alps (Austria), increased by 11.8% within a decade [79]. Similarly, Parolo and Rossi [80] also reported that plant species richness in the Italian Alps was higher between the years 2003–2005 compared to 1954–1958. In addition to elevational shifts of mountain species [69], climate change can also cause contraction of the elevational ranges of mountain plants, which accelerates the threat of local extinctions of the endemic alpine species [80, 81, 82, 83, 84]. Such redistribution of plant species to new areas may alter the existing native plant communities and increase competition for space and nutrients for survival, which may disturb the prevalent structure and function of the mountain. Besides competition for resources and space, such exotic species expanding the elevational area and becoming invasive could disturb the functioning of the mountain ecosystem and increase the loss of mountain biodiversity [85, 86].

Along with the redistribution of native plants along mountain slopes, non-native plant species also tend to shift upward and expand their elevational range to colonize new habitats in the mountain ecosystem [87, 88, 89, 90]. This habitat expansion or redistribution of non-native plant species toward the higher elevation of the mountain exerts an additional threat to native plants by increasing competition between them and non-native plant species at higher elevations [91]. Native and non-native species follow distinct patterns of distribution along the elevational gradients of the mountain because they have different ecological backgrounds and evolutionary histories [92, 93]. Thus, the direction and magnitude of elevational range shifts for native and non-native plant species differ significantly under changing macroclimates. However, several controversial results on species redistributions have also been reported in the past few decades, both at regional [66, 94] and global levels [95]. Apart from rising temperatures, changes in precipitation and the functional traits of plant species, such as their ability to disperse and colonize new areas, also contribute to the upward shift of species along an elevational gradient [70]. For example, studies in California [94] and the Mediterranean mountains of southern Europe [77] found that changes in precipitation patterns contributed more than temperature increases to the elevational shifts of plant species. Therefore, it is crucial to determine the major abiotic and biotic factors responsible for species redistribution. Nonetheless, the distinct macroclimatic gradients along the slope from the bottom of the valley to the top of the mountains act as a natural experimental field to investigate the effect of climate change on biodiversity [96, 97].

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4. Climate change and plant invasion

Invasive plants are non-native plant species that are intentionally or inadvertently introduced into new geographic areas, eventually posing a threat to native plant diversity. Species with a broader physiological niche can tolerate a wide range of environments, and such species have a high potential to become invasive [98]. Biological invasions aided by climate change can exert extremely critical environmental impacts [99] and thus significantly contribute to environmental change across the globe [100]. Climate change intensifies the risks and losses in ecosystems through different mechanisms, including the removal of climatic barriers, thereby augmenting the spread of invasive species [101, 102]. Compared to native plants, invasive plant species tend to shift their niche rapidly and are likely to adapt to new dwelling environments quickly [101, 103]. In addition, a rise in atmospheric carbon dioxide (CO2) concentration and global warming favors the survival of invasive plant species over native plant species [104]. For example, the range of alien evergreen plants in Swiss forests has expanded in response to a decrease in the frequency of frost intervals due to climate warming [105]. Therefore, vegetation communities across the globe are expected to change because of the increases in global temperature [106].

Climate change has already elevated the spread of invasive species [107] and accelerated the expansion of native species [108], transforming them into invasive ones. For example, Yushania maling (Gamble) R.B. Majumdar & Karthik, which is native to the temperate zones of the Eastern Himalaya [109, 110], whose occurrence in Darjeeling district of West Bengal, India, was first recorded during the 1980s [111]. It has spread rapidly in the forest areas, potentially due to climate change causing a threat to the native floral diversity and ecosystems [109, 110, 112, 113]; thus, it is now considered a native invasive species in the region [109, 110, 113]. In mountain ecosystems, non-native invasive species are abundant between low and mid-elevations; however, anthropogenic activities and ongoing climate change are likely to accelerate their spread and dominance at high elevations [114]. Priyanka and Joshi [115] also suggested that most parts of the western and southern regions of the western Himalaya (India) tend to become suitable for the expansion of invasive pant Lantana camara L. in the future due to increased warming. In Kashmir (part of the western Himalaya), the invasive species are already augmenting the homogenization of the terrestrial ecosystems [116]. These invasive species are invading protected areas of the region and disturbing the habitat and food availability of the native wildlife [117, 118]. Such reports indicate that the mountainous regions are vulnerable to plant invasion due to climate change, specifically climate warming.

Invasive plant species are known to alter the diversity and composition of the native flora and form nearly mono-specific stands (homogenization). They also impact a wide range of abiotic and biotic factors that could potentially change the function and services contributed by the invaded ecosystems. Invasive plant species can directly impact the activity, productivity, and survival of native biota [119]. They have superior potential to compete for space and resources and a more efficient capacity to utilize resources than the native species. Thus, they have a major influence on resources (e.g., nutrients) and space in new habitats, as well as modify ecological processes, thereby outcompete native species and degrade the habitats of native biota in the ecosystems [120]. In brief, invasive plant species displace native plant species from their original habitats, degrade ecosystems, have a negative impact on human health [121, 122], homogenize the world’s biological systems, and cause global biodiversity loss. Therefore, climate change-driven biological invasions could potentially disrupt the diversity, composition, structure, function, and services of mountain ecosystems and cause a severe impact on mountain biodiversity.

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5. Habitat fragmentation and biodiversity loss due to climate change

Global biodiversity is under severe threat due to increasing anthropogenic activities (e.g., habitat destruction) and climate change. Habitat fragmentation or habitat loss of plants is generally attributed to human-induced causes such as change in land-use patterns, deforestation, overexploitation, intentional forest fires, and pollution. However, climate change also causes fragmentation of favorable habitats, leading to a decline in the habitat quality of the species [123]. Habitat fragmentation produces small populations with widening spatial isolation, which potentially accelerates the risk of extinction [124, 125, 126]. Mantyka-Pringle [127] suggested that recent climate and climate change are key factors that determine the negative effects of habitat loss, and raising temperatures is the major determinant of habitat loss and fragmentation effects, while change in precipitation over the past 100 years is of secondary importance. Further, habitat loss and fragmentation effects were highest in regions with high maximum temperatures [127], suggesting that climate change is contributing to enhanced habitat fragmentation across the globe. In landscapes undergoing habitat fragmentation, certain species will obviously be affected by habitat loss, and in such a scenario, associated or dependent species may also be lost, causing populations to decline [128, 129, 130]. Nonetheless, there has been massive biodiversity loss over the past few decades that can potentially initiate the sixth mass extinction crisis due to the environmental changes induced by anthropogenic activities [131].

Climate change is considered a major factor in the decline of global biodiversity. At a basic level, climate change is influencing the reduction of genetic diversity in populations due to rapid migration and directional selection, which can further affect the resilience and functioning of the ecosystem [132]. At the community level, the “web of interactions” among different populations is likely to be modified due to the various effects of climate change [133, 134]. As described in the sections above, climate change alters phenological events, thereby disrupting plant-pollinator interactions [57]. This can cause the extinction of both pollinators and plants, with expected impacts on the structure of plant-pollinator networks [135, 136]. Based on the study of 9650 inter-specific systems, which include pollinators and parasites, about 6300 species are expected to disappear along with the extinction of their associated species [137]. Several climatic variables determine the geographical distribution ranges of various species, and therefore, species shift their distribution range depending upon their dispersal capacities and go locally extinct in response to climate change [138, 139]. Such redistribution of species reduces biodiversity at low elevations and latitudes and causes habitat fragmentation and range contraction of several native species in alpine and polar ecosystems, paving the way for their disappearance from the ecosystem. Further, a global rise in temperature favors the survival of invasive alien plant species over native plant species [106]. These invasive plant species are known to alter the environment they invade, have efficient dispersal and reproductive capacity, and thus outcompete the native plant species in terms of space and resource utilization. They homogenize the diversity and composition of the invaded region, resulting in the loss of native biodiversity. Most of the studies at present indicate that habitat loss and fragmentation have a greater impact on species and ecosystems than climate warming [140, 141, 142, 143]. However, in due course, the effect of climate change is expected to increase and contribute more to determining population trends than habitat fragmentation and loss [144]. Based on this chapter, the consequences of climate change on mountainous plant species and the different ways in which climate change leads to biodiversity loss are summarized in Figure 1.

Figure 1.

Impact of climate change on mountainous plant species leading to biodiversity loss.

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6. Climate change mitigation and future prospective

As of now, the discussion in this chapter has strongly indicated that climate warming is the major driver of climate change-related biological consequences like change in plant phenology, upward elevational shift, plant invasion, habitat fragmentation, and biodiversity loss. Therefore, global climate change mitigation strategies should focus primarily on minimizing or stabilizing the global temperature increase in order to regulate the biological issues that arise due to climate change. There is ample literature that provides knowledge about the initiation of global summits and conventions aimed at framing policies to regulate climate change and biodiversity loss. Therefore, this section directly focuses on the three widely discussed climate change mitigation strategies suggested recently by Fawzy et al. [145]:

  1. Conventional mitigation strategies: energy-related emissions of various gases are the major driver for raising the concentration of atmospheric greenhouse gases. Therefore, conventional mitigation strategies prioritize the use of decarbonization technologies and techniques that decrease carbon dioxide (CO2) emissions. Conventional mitigation strategies are deployed in four main sectors: on the supply side (power sector) and on the demand side (industry, buildings, and transportation sectors). Mitigation efforts on the supply side include decarbonization through the utilization of renewable energy, fuel switching to low-carbon fuels such as natural gas and renewable fuels, carbon capture and storage, and nuclear power. On the demand side, mitigation efforts include gaining efficiency through the utilization of sector-specific technologies; energy-efficient methods that reduce the consumption of energy; and the inclusion of renewable power technologies that are within the energy matrix of sectors on the demand side [146, 147]. Most of the conventional mitigation technologies are well established and have an acceptable level of managed risk.

  2. Negative emissions technologies or carbon dioxide removal methods: include the techniques deployed to capture and sequester atmospheric CO2 [148]. For example, wetland construction and restoration, afforestation and reforestation, direct air carbon capture and storage, bioenergy carbon capture and storage, enhanced weathering, ocean alkalinity enhancement, soil carbon sequestration, etc. To date, afforestation and reforestation, as well as bioenergy carbon capture and storage, are included in the IPCC assessments [149]. However, a study suggested that negative emissions technologies are still in their infancy; therefore, climate policy should remain focused on conventional mitigation technologies, while further financial resources should be invested to accelerate the progress of negative emissions technologies [150].

  3. Radiative forcing geoengineering technologies: focus on the reduction or stabilization of atmospheric temperature by altering the radiation balance of the earth through managing solar and terrestrial radiation. Unlike the above two strategies, this technique suggests stabilizing temperature without changing the concentration of greenhouse gases. For example: cirrus cloud thinning, marine sky brightening, stratospheric aerosol injection, space-based mirrors, surface-based brightening, etc. However, these strategies are still theoretical, in the early stages of trial, and uncertain and risky in terms of large-scale practical utilization. Therefore, radiative forcing geoengineering techniques are still not included in climate policy frameworks [151, 152].

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7. Conclusion

Climate change is one of the major issues facing our planet in the anthropocene. Mountainous regions of the world harbor unique ecosystems and high biodiversity and are considered the refugia of biodiversity. However, these regions of the world are highly sensitive to climate change; therefore, the impact of climate change is highly visible on mountains as compared to lowlands. Climate warming, or an increase in the global earth’s temperature, is the major climatic change that is impacting the entire world and the mountains in particular. The phenological changes, such as early spring events and late autumn events, are evidently disturbing the various plant-animal interactions, such as plant-pollinator interactions. Raising temperatures are compelling various plant species to shift their geographic ranges in search of suitable climatic niches. Climate warming is further removing climatic barriers for invasive alien plant species and increasing the possibilities of their invasions in new areas. Climate change, along with other anthropogenic activities, is contributing to major habitat fragmentation or loss for several plant species. All these responses of mountainous plants to climate change would alter the species composition, structure, and functioning of the mountain ecosystems, eventually leading to the extinction and biodiversity loss of native plant species. Therefore, it is pivotal to mitigate climate change in order to conserve the sixth biodiversity extinction because the economy and livelihood of people living on mountains directly or indirectly depend on the biodiversity and services provided by mountain ecosystems. The major focus of climate change mitigation should be reducing or stabilizing the global temperature because global warming is the major driver of most of the biological changes caused by climate change. Conventional mitigation strategies, negative emissions technologies, carbon dioxide removal methods, and radiative forcing geoengineering technologies are the major strategies that can be explored further for climate change mitigation.

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Acknowledgments

The author would like to extend gratitude to the editor Dr. Surendra N. Kulshrestha from the University of Saskatchewan, Canada; Ms. Ivana Barac (Publishing Process Manager, IntechOpen); and the entire team of IntechOpen for proving an opportunity to contribute a chapter to this book.

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Conflict of interest

The author has no conflict of interest in the publication.

References

  1. 1. Feliciano D, Recha J, Ambaw G, MacSween K, Solomon D, Wollenberg E. Assessment of agricultural emissions, climate change mitigation and adaptation practices in Ethiopia. Climate Policy. 2022;22(4):427-444
  2. 2. Messerli B, Ives J, editors. Mountains of the Word. A Global Priority. New-York: Parthenon Publishing; 1997. p. 496
  3. 3. Zhang L, Wang J. Mountain biodiversity, species distribution and ecosystem functioning in a changing world. Diversity. 2023;15(7):799
  4. 4. Perrigo A, Hoorn C, Antonelli A. Why mountains matter for biodiversity. Journal of Biogeography. 2019;47(10):1-11
  5. 5. Spehn E, Rudmann-Maurer K. Impacts of climate change on mountain biodiversity in Europe. In: Discussion Paper of Convention on the Conservation of European Wildlife and Natural Habitats, 6-9 December 2010. Starsbourg, France: Council of Europe; 2010
  6. 6. Berlyn GP. Some thoughts on mountain forests: Their benefits and sustainability. Journal of Sustainable Forestry. 2023;42(10):961-966
  7. 7. Price MF, Gratzer G, Duguma LA, Kohler T, Maselli D, Romeo R. Mountain Forests in a Changing World - Realizing Values, Addressing Challenges. Rome: FAO/MPS and SDC; 2011
  8. 8. Beniston M. Climatic change in mountain regions: A review of possible impacts. In: Diaz HF, editor. Climate Variability and Change in High Elevation Regions: Past, Present & Future. Advances in Global Change Research. Vol. 15. Dordrecht: Springer; 2003. pp. 5-31
  9. 9. Beniston M. The risks associated with climatic change in mountain regions. In: Huber U, Bugmann H, Reasoner M, editors. Global Change and Mountain Regions: An Overview of Current Knowledge. Dordrecht, Netherlands: Springer; 2005. pp. 511-520
  10. 10. Rebetez M, Reinhard M. Monthly air temperature trends in Switzerland 1901-2000 and 1975-2004. Theoretical and Applied Climatology. 2008;91:27-34
  11. 11. Mountain Research Initiative EDW Working Group. Elevation-dependent warming in mountain regions of the world. Nature Climate Change. 2015;5:424-430
  12. 12. Nogués-Bravo D, Araújo MB, Errea MP, Martínez-Rica JP. Exposure of global mountain systems to climate warming during the 21st century. Global Environmental Change. 2007;17(3-4):420-428
  13. 13. Steinbauer MJ, Grytnes JA, Jurasinski G, Kulonen A, Lenoir J, Pauli H, et al. Accelerated increase in plant species richness on mountain summits is linked to warming. Nature. 2018;556(7700):231-234
  14. 14. Negi GCS, Samal PK, Kuniyal JC, Kothyari BP, Sharma RK, Dhyani PP. Impact of climate change on the Western Himalayan Mountain ecosystems: An overview. Tropical Ecology. 2012;53(3):345-356
  15. 15. Leemans R, Eickhout B. Another reason for concern: Regional and global impacts on ecosystems for different levels of climate change. Global Environment Change. 2004;14(30):219-228
  16. 16. Cleland EE, Chuine I, Menzel A, Mooney HA, Schwartz MD. Shifting plant phenology in response to global change. Trends in Ecology and Evolution. 2007;22(7):357-365
  17. 17. Parmesan C, Yohe G. A globally coherent fingerprint of climate change impacts across natural systems. Nature. 2003;421(6918):37-42
  18. 18. Chen IC, Hill JK, Ohlemuller R, Roy DB, Thomas CD. Rapid range shifts of species associated with high levels of climate warming. Science. 2011;333(6045):1024-1026
  19. 19. Visser ME, Caro SP, Van Oers K, Schaper SV, Helm B. Phenology, seasonal timing and circannual rhythms: Towards a unified framework. Philosophical Transactions of the Royal Society B: Biological Sciences. 2010;365(1555):3113-3127
  20. 20. Moza MK, Bhatnagar AK. Phenology and climate change. Current Science. 2005;89(2):243-244
  21. 21. Ferrera TS, Pelissaro TM, Eisinger SM, Righi EZ, Buriol GA. Phenology of native tree species in the central region of the state of Rio Grandedo Sul/Brazil. Ciência Florestal. 2017;27(3):753-766
  22. 22. Souza IM, Funch LS. Synchronization of leafing and reproductive phenological events in Hymenaea L. species (Leguminosae, Caesalpinioideae): The role of photoperiod as the trigger. Brazilian Journal of Botany. 2017;40:125-136
  23. 23. Singh P, Negi GCS. Impact of climate change on phenological responses of major Forest trees of Kumaun Himalaya. ENVIS Bulletin Himalayan Ecology. 2019;24:112-116
  24. 24. Hughes L. Biological consequences of global warming: Is the signal already apparent? Trends in Ecology and Evolution. 2000;15(2):56-61
  25. 25. Intergovernmental Panel on Climate Change (IPCC). Summary for policymakers. In: Metz B, Davidson OR, Bosch PR, editors. Climate Change 2007: Mitigation. Contribution of Working Group III to the Fourth Assessment Report of the IPCC. UK and USA: Cambridge University Press; 2007
  26. 26. Chapin FS, Randerson JT, McGuire AD, Foley JA, Field CB. Changing feedbacks in the climate–biosphere system. Frontiers in Ecology and the Environment. 2008;6(6):313-320
  27. 27. Lesica P, Kittelson PM. Precipitation and temperature are associated with advanced flowering phenology in a semi-arid grassland. Journal of Arid Environments. 2010;74(9):1013-1017
  28. 28. Woods T, Kaz A, Giam X. Phenology in freshwaters: A review and recommendations for future research. Ecography. 2022;2022(6):e05564
  29. 29. Schwartz MD. Green-wave phenology. Nature. 1998;394(6696):839-840
  30. 30. Menzel A, Fabian P. Growing season extended in Europe. Nature. 1999;397(6721):659
  31. 31. Beaubien EC, Freeland HJ. Spring phenology trends in Alberta, Canada: Links to ocean temperature. International Journal of Biometeorology. 2000;44(2):53-59
  32. 32. Sparks T, Menzel A, Stenseth N. European cooperation in plant phenology. Climate Research. 2009;39:175-177
  33. 33. Peñuelas J, Filella I, Zhang XY, Llorens L, Ogaya R, Lloret F, et al. Complex spatiotemporal phenological shifts as a response to rainfall changes. New Phytologist. 2004;161(3):837-846
  34. 34. Garonna I, de Jong R, Schaepman ME. Variability and evolution of global land surface phenology over the past three decades (1982-2012). Global Change Biology. 2016;22(4):1456-1468
  35. 35. Iler AM, CaraDonna PJ, Forrest JR, Post E. Demographic consequences of phenological shifts in response to climate change. Annual Review of Ecology, Evolution, and Systematics. 2021;52:221-245
  36. 36. Liu Q , Piao S, Campioli M, Gao M, Fu YH, Wang K, et al. Modeling leaf senescence of deciduous tree species in Europe. Global Change Biology. 2020;26(7):4104-4118
  37. 37. Xie Y, Thammavong HT, Park DS. The ecological implications of intra- and inter-species variation in phenological sensitivity. New Phytologist. 2022;236(2):760-773
  38. 38. Singh SP, Singh V, Skutsch M. Rapid warming in the Himalayas: Ecosystem responses and development options. Climate and Development. 2010;2(3):221-232
  39. 39. Dedieu JP, Lessard-Fontaine A, Ravazzani G, Cremonese E, Shalpykova G, Beniston M. Shifting mountain snow patterns in a changing climate from remote sensing retrieval. Science of the Total Environment. 2014;493:1267-1279
  40. 40. Zu K, Chen F, Li Y, Shrestha N, Fang X, Ahmad S, et al. Climate change impacts flowering phenology in Gongga Mountains, Southwest China. Plant Diversity. 2023. DOI: 10.1016/j.pld.2023.07.007
  41. 41. Hart R, Salick J, Ranjitkar S, Xu J. Herbarium specimens show contrasting phenological responses to Himalayan climate. Proceedings of the National Academy of Sciences of the United States of America. 2014;111(29):10615-10619
  42. 42. Rafferty NE, Diez JM, Bertelsen CD. Changing climate drives divergent and nonlinear shifts in flowering phenology across elevations. Current Biology. 2020;30(3):432-441
  43. 43. Khanduri VP, Sharma CM, Singh SP. The effects of climate change on plant phenology. The Environmentalist. 2008;28:143-147
  44. 44. Ovaskainen O, Skorokhodova S, Yakovleva M, Sukhov A, Kutenkov A, Kutenkova N, et al. Community-level phenological response to climate change. Proceedings of the National Academy of Sciences of the United States of America. 2013;110(33):13434-13439
  45. 45. CaraDonna PJ, Iler AM, Inouye DW. Shifts in flowering phenology reshape a subalpine plant community. Proceedings of the National Academy of Sciences of the United States of America. 2014;111(13):4916-4921
  46. 46. Vitasse Y, Ursenbacher S, Klein G, Bohnenstengel T, Chittaro Y, Delestrade A, et al. Phenological and elevational shifts of plants, animals and fungi under climate change in the European Alps. Biological Reviews of the Cambridge Philosophical Society. 2021;96(5):1816-1835
  47. 47. Song Z, Du Y, Primack RB, Miller-Rushing AJ, Ye W, Huang Z. Surprising roles of climate in regulating flowering phenology in a subtropical ecosystem. Ecography. 2021;44(9):1379-1390
  48. 48. Shrestha UB, Gautam S, Bawa KS. Widespread climate change in the Himalayas and associated changes in local ecosystems. PLoS One. 2012;7(5):e36741
  49. 49. Shah S, Verma A, Tewari A. Timing of shifts in phenological events in Rhododendron arboreum Smith. Influenced by climatic irregularities in Kumaun regions of central Himalaya. Global Journal of Scientific Researches. 2014;2(2):56-59
  50. 50. Gaira KS, Rawal RS, Rawat B, Bhatt D. Impact of climate change on the flowering of Rhododendron arboreum in central Himalaya, India. Current Science. 2014;106(12):1735-1738
  51. 51. Negi GCS, Singh P, Singh SP. Atmospheric warming-associated phenology earliness does not increase the length of growing season in Himalayan trees. Forest Science. 2021;67(6):694-700. DOI: 10.1093/forsci/fxab040
  52. 52. Thackeray SJ, Henrys PA, Hemming D, Bell JR, Botham MS, Burthe S, et al. Phenological sensitivity to climate across taxa and trophic levels. Nature. 2016;535(7611):241-245
  53. 53. Pelayo RC, Llambí LD, Gámez LE, Barrios YC, Ramirez LA, Torres JE, et al. Plant phenology dynamics and pollination networks in summits of the high tropical Andes: A baseline for monitoring climate change impacts. Frontier in Ecology and Evolution. 2021;9:679045
  54. 54. CaraDonna PJ, Cunningham JL, Iler AM. Experimental warming in the field delays phenology and reduces body mass, fat content and survival: Implications for the persistence of a pollinator under climate change. Functional Ecology. 2018;32:2345-2356
  55. 55. Kharouba HM, Ehrlén J, Gelman A, Bolmgren K, Allen JM, Travers SE, et al. Global shifts in the phenological synchrony of species interactions over recent decades. Proceedings of the National Academy of Sciences of the United States of America. 2018;115(20):5211-5216
  56. 56. Portalier SM, Candau JN, Lutscher F. A temperature-driven model of phenological mismatch provides insights into the potential impacts of climate change on consumer–resource interactions. Ecography. 2022;2022(8):e06259
  57. 57. Franco-Cisterna M, Ramos-Jiliberto R, de Espanés PM, Vazquez DP. Phenological shifts drive biodiversity loss in plant-pollinator networks. bioRxiv Preprint. 2020. DOI: 10.1101/2020.04.03.023457
  58. 58. Kudo K, Ida TY. Early onset of spring increases the phenological mismatch between plants and pollinators. Ecology. 2013;94(10):2311-2320
  59. 59. Menzel A, Sparks TH, Estrella N, Koch E, Aasa A, Ahas R, et al. European phenological response to climate change matches the warming pattern. Global Change Biology. 2006;12(10):1969-1976
  60. 60. Piao S, Liu Q , Chen A, Janssens IA, Fu Y, Dai J, et al. Plant phenology and global climate change: Current progresses and challenges. Global Change Biology. 2019;25(6):1922-1940
  61. 61. Menzel A. Phenology: Its importance to the global change community. An editorial comment. Climate Change. 2002;54(4):379-385
  62. 62. Inouye DW. Climate change and phenology. WIREs Climate Change. 2022;13(3):e764
  63. 63. Shifting habitats. Nature Climate Change. 30 Apr 2020;10:377
  64. 64. Davis MB, Shaw RG. Range shifts and adaptive responses to quaternary climate change. Science. 2001;292(5517):673-679
  65. 65. Lenoir J, Svenning JC. Latitudinal and elevational range shifts under contemporary climate change. Encyclopedia Biodiversity. 2013;4:599-611
  66. 66. Lenoir J, Gégout JC, Marquet PA, de Ruffray P, Brisse H. A significant upward shift in plant species optimum elevation during the 20th century. Science. 2008;320(5884):1768-1771
  67. 67. Gaston KJ. The Structure and Dynamics of Geographic Ranges. UK: Oxford University Press; 2003
  68. 68. Menéndez R, González-Megías A, Jay-Robert P, Marquéz-Ferrando R. Climate change and elevational range shifts: Evidence from dung beetles in two European Mountain ranges. Global Ecology and Biogeography. 2014;23(6):646-657
  69. 69. Rowe KC, Rowe KMC, Tingley MW, Koo MS, Moritz C. Spatially heterogeneous impact of climate change on small mammals of montane California. Proceedings of the Royal Society B: Biological Sciences. 2015;282(1799):20141857
  70. 70. Zu K, Wang Z, Zhu X, Lenoir J, Shrestha N, Lyu T, et al. Upward shift and elevational range contractions of Subtropical Mountain plants in response to climate change. Science of the Total Environment. 2021;783:146896
  71. 71. Nainggolan D, Abay AT, Christensen JH, Termasen M. The impact of climate change on crop mix shift in the Nordic region. Scientific Reports. 2023;13:2962
  72. 72. Odgaard MV, Bøcher PK, Dalgaard T, Svenning JC. Climate and non-climatic drivers of spatiotemporal maize-area dynamics across the northern limit for maize production—A case study from Denmark. Agriculture, Ecosystems & Environment. 2011;142(3-4):291-302
  73. 73. Lepcha P, Gaira KS, Pandey A, Chettri SK, Lepcha J, Lepcha J, et al. Elevation determines the productivity of large cardamom (Amomum subulatum Roxb.) cultivars in Sikkim Himalaya. Scientific Reports. 2023;13:21673
  74. 74. Körner C. Alpine Plant Life: Functional Plant Ecology of High Mountain Ecosystems. Berlin: Springer; 1999
  75. 75. Salick J, Zhendong F, Byg A. Eastern Himalayan alpine plant ecology, Tibetan ethnobotany, and climate change. Global Environmental Change. 2009;19(2):147-155
  76. 76. Olson DM, Dinerstein E. The global 200: A representation approach to conserving the Earth’s Most biologically valuable ecoregions. Conservation Biology. 1998;12(3):502-515
  77. 77. Pauli H, Gottfried M, Dullinger S, Abdaladze O, Grabherr G. Recent plant diversity changes on Europe's mountain summits. Science. 2012;336(6079):353-355
  78. 78. Telwala Y, Brook BW, Manish K, Pandit MK. Climate-induced elevational range shifts and increase in plant species richness in a Himalayan biodiversity epicentre. PLoS One. 2013;8(2):e57103
  79. 79. Pauli H, Gottfried M, Reiter K, Klettner C, Grabherr G. Signals of range expansions and contractions of vascular plants in the high Alps: Observations (1994-2004) at the GLORIA*master site Schrankogel, Tyrol, Austria. Global Change Biology. 2007;13(1):147-156
  80. 80. Parolo G, Rossi G. Upward migration of vascular plants following a climate warming trend in the Alps. Basic and Applied Ecology. 2008;9(2):100-107
  81. 81. Manne LL, Brooks TM, Pimm SL. Relative risk of extinction of passerine birds on continents and islands. Nature. 1999;399(6733):258-261
  82. 82. Pounds AJ, Martín BR, Coloma LA, Consuegra JA, Fogden MPL, Foster PN, et al. Widespread amphibian extinctions from epidemic disease driven by global warming. Nature. 2006;439(7073):161-167
  83. 83. La Sorte FA, Jetz W. Projected range contractions of montane biodiversity under global warming. Proceedings of the Royal Society B: Biological Sciences. 2010;277(1699):3401-3410
  84. 84. Freeman BG, Scholer MN, Ruiz-Gutierrez V, Fitzpatrick JW. Climate change causes upslope shifts and mountaintop extirpations in a tropical bird community. Proceedings of the National Academy of Sciences of the United States of America. 2018;115(47):11982-11987
  85. 85. Hejda M, Pyšek P, Jarošík V. Impact of invasive plants on the species richness, diversity and composition of invaded communities. Journal of Ecology. 2009;97(3):393-403
  86. 86. Pauchard A, Milbau A, Albihn A, Alexander J, Burgess T, Daehler C, et al. Non-native and native organisms moving into high elevation and high latitude ecosystems in an era of climate change: New challenges for ecology and conservation. Biological Invasion. 2015;18(2):345-353
  87. 87. Dainese M, Aikio S, Hulme PE, Bertolli A, Prosser F, Marini L. Human disturbance and upward expansion of plants in a warming climate. Nature Climate Change. 2017;7(8):577-580
  88. 88. Koide D, Yoshida K, Daehler CC, Mueller-Dombois D, Wildi O. An upward elevation shift of native and non-native vascular plants over 40 years on the island of Hawai'i. Journal of Vegetation Science. 2017;28(5):939-950
  89. 89. Lembrechts JJ, Alexander JM, Cavieres LA, Haider S, Lenoir J, Kueffer C, et al. Mountain roads shift native and non-native plant species' ranges. Ecography. 2017;40(3):353-364
  90. 90. Rew LJ, McDougall KL, Alexander JM, Daehler CC, Essl F, Haider S, et al. Moving up and over: Redistribution of plants in alpine, Arctic, and Antarctic ecosystems under global change. Arctic, Antarctic, and Alpine Research. 2020;52(1):651-665
  91. 91. Bezeng BS, Morales-Castilla I, Van D, Yessoufou K, Daru BH, Davies TJ. Climate change may reduce the spread of non-native species. Ecosphere. 2017;8(3):e01694
  92. 92. Sandoya V, Pauchard A, Cavieres LA. Natives and non-natives plants show different responses to elevation and disturbance on the tropical high Andes of Ecuador. Ecology and Evolution. 2017;7(2):7909-7919
  93. 93. Guo Q , Fei S, Shen Z, Iannone BV, Knott J, Chown SL. A global analysis of elevational distribution of non-native versus native plants. Journal of Biogeography. 2018;45(4):793-803
  94. 94. Crimmins SM, Dobrowski SZ, Greenberg JA, Abatzoglou JT, Mynsberge AR. Changes in climatic water balance drive downhill shifts in plant species’ optimum elevations. Science. 2011;331(6015):324-327
  95. 95. Guo F, Lenoir J, Bonebrake TC. Land-use change interacts with climate to determine elevational species redistribution. Nature Communications. 2018;9(1):1315
  96. 96. Körner C. Why are there global gradients in species richness? Mountains might hold the answer. Trends in Ecology and Evolution. 2000;15(12):513-514
  97. 97. Myers N, Mittermeier RA, Mittermeier CG, da Fonseca GAB, Kent J. Biodiversity hotspots for conservation priorities. Science. 2000;403(6772):853-858
  98. 98. Higgins SI, Richardson DM. Invasive plants have broader physiological niches. Proceeding of the National Academy of Sciences of the United States of America. 2014;111(29):10610-10614
  99. 99. Crowl TA, Crist TO, Parmenter RR, Belovsky G, Lugo AE. The spread of invasive species and infectious disease as drivers of ecosystem change. Frontier in Ecology and the Environment. 2008;6(5):238-246
  100. 100. Dawson W, Schrama M. Identifying the role of soil microbes in plant invasions. Journal of Ecology. 2016;104(5):1211-1218
  101. 101. Hellmann JJ, Byers JE, Bierwagen BG, Dukes JS. Five potential consequences of climate change for invasive species. Conservation Biology. 2008;22(3):534-543
  102. 102. Bradley BA, Wilcove DS, Oppenheimer M. Climate change increases risk of plant invasion in the eastern United States. Biological Invasions. 2010;12(6):1855-1872
  103. 103. Shrestha UB, Shrestha BB. Climate change amplifies plant invasion hotspots in Nepal. Diversity and Distribution. 2019;25(10):1599-1612
  104. 104. Liu Y, Oduor AM, Zhang Z, Manea A, Tooth IM, Leishman MR, et al. Do invasive alien plants benefit more from global environmental change than native plants? Global Change Biology. 2017;23(8):3363-3370
  105. 105. Walther GR. Weakening of climatic constraints with global warming and its consequences for evergreen broad-leaved species. Folia Geobotanica. 2002;37:129-139
  106. 106. Lu X, Siemann E, Shao X, Wei H, Ding J. Climate warming affects biological invasions by shifting interactions of plants and herbivores. Global Change Biology. 2023;19(8):2339-2347
  107. 107. Demertzis K, Iliadis L. The impact of climate change on biodiversity: The ecological consequences of invasive species in Greece. In: Leal Filho W, Manolas E, Azul A, Azeiteiro U, McGhie H, editors. Handbook of Climate Change Communication: Vol. 1. Climate Change Management. Cham: Springer; 2018. DOI: 10.1007/978-3-319-69838-0_2
  108. 108. Kurz WA, Dymond CC, Stinson G, Rampley GJ, Neilson ET, Carroll AL, et al. Mountain pine beetle and forest carbon feedback to climate change. Nature. 2008;452(7910):987-990
  109. 109. Roy A, Bhattacharya S, Ramprakash M, Kumar AS. Modelling critical patches of connectivity for invasive Maling bamboo (Yushania maling) in Darjeeling Himalayas using graph theoretic approach. Ecological Modelling. 2016;329:77-85
  110. 110. Srivastava V, Griess VC, Padalia H. Mapping invasion potential using ensemble modelling. A case study on Yushania maling in the Darjeeling Himalayas. Ecological Modelling. 2018;385:35-44
  111. 111. Chi-Son C, Renvoize SA. A revision of the species described under Arundinaria (Gramineae) in Southeast Asia and Africa. Kew Bulletin. 1989;44(2):349-367
  112. 112. Stapleton CMA. The morphology of woody bamboos. In: Chapman GP, editor. The Bamboo. London, UK: Academic Press; 1997. pp. 251-268
  113. 113. Gaira KS, Pandey A, Sinha S, Badola HK, Lepcha J, Dhyani PP, et al. Maling bamboo (Yushania maling) overdominance alters Forest structure and composition in Khangchendzonga landscape, Eastern Himalaya. Scientific Reports. 2022;12:4468
  114. 114. Alexander JM, Lembrechts JJ, Cavieres LA, Daehler C, Haider S, Kueffer C, et al. Plant invasion into mountains and alpine ecosystems: Current status and future challenges. Alpine Botany. 2016;126:89-103
  115. 115. Priyanka N, Joshi PK. Effects of climate change on invasion potential distribution of Lantana camara. Journal of Earth Science and Climate Change. 2013;4(6):164
  116. 116. Dhar PA, Reshi ZA. Do alien plant invasions cause biotic homogenization of terrestrial ecosystems in the Kashmir Valley, India? Tropical Ecology. 2015;56(1):111-123
  117. 117. Murphy ST, Subedi N, Jnawali SR, Lamichane BR. Invasive Mikania in Chitwan National Park, Nepal: The threat to the greater one-horned Rhinoceros (Rhinoceros unicornis) and factors driving the invasion. Oryx. 2013;47(3):361-368
  118. 118. Aryal A, Acharya KP, Shrestha UB, Dhakal M, Raubenhiemer D, Wright W. Global lessons from successful Rhinoceros conservation in Nepal. Conservation Biology. 2017;31(6):1494-1497
  119. 119. Pysek P, Jarosik V, Hulme PE, Pergl J, Hejda M, Schaffner U, et al. A global assessment of invasive plant impacts on resident species, communities and ecosystems: The interaction of impact measures, invading species’ traits and environment. Global Change Biology. 2012;18(5):1725-1737
  120. 120. Grice AC. The impacts of invasive plant species on the biodiversity of Australian rangelands. The Rangeland Journal. 2006;28(1):27-35
  121. 121. Zhu B, Ottaviani CC, Naddafi R, Dai ZC, Du DL. Invasive European frogbit (Hydrocharis morsus-ranae L.) in North America: An updated review 2003-2016. Journal of Plant Ecology. 2018;11(1):17-25
  122. 122. Xie W, Zhong C, Li X, Guo Z, Shi S. Hybridization with natives augments the threats of introduced species in Sonneratia mangroves. Aquatic Botany. 2020;160:103166
  123. 123. Li R, Xu M, Wong MHG, Qiu S, Li X, Ehrenfeld DL, et al. Climate change threatens Giant panda protection in the 21st century. Biological Conservation. 2015;182:93-101
  124. 124. Opdam P. Metapopulation theory and habitat fragmentation: A review of holarctic breeding bird studies. Landscape Ecology. 1991;5:93-106
  125. 125. Ellstrand NC, Elam DR. Population genetic consequences of small populationsize: Implications for plant conservation. Annual Review of Ecology and Systematics. 1993;24:217-242
  126. 126. Young A, Boyle T, Brown T. The population genetic consequences of habitat fragmentation for plants. Trends in Ecology and Evolution. 1996;11:413-418
  127. 127. Mantyka-pringle CS, Martin TG, Rhodes JR. Interactions between climate and habitat loss effects on biodiversity: A systematic review and meta-analysis. Global Biology Change. 2011;18(4):1239-1252
  128. 128. Fahrig L. Relative effects of habitat loss and fragmentation on population extinction. The Journal of Wildlife Management. 1997;61(3):603-610
  129. 129. Bender DJ, Contreras TA, Fahrig L. Habitat loss and population decline: A meta-analysis of the patch size effect. Ecology. 1998;79(2):517-533
  130. 130. Fahrig L. How much habitat is enough? Biological Conservation. 2001;100(1):65-74
  131. 131. Shivanna KR. Climate change and its impact on biodiversity and human welfare. Proceedings of the Indian National Science Academy. 2022;88(2):160-171
  132. 132. Botkin DB, Saxe H, Araujo MB, Betts R, Bradshaw RHW, Cedhagen T, et al. Forecasting the effects of global warming on biodiversity. Bioscience. 2007;57(3):227-236
  133. 133. Gilman SE, Urban MC, Tewksbury J, Gilchrist GW, Holt RD. A framework for community interactions under climate change. Trends in Ecology and Evolution. 2010;25(6):325-331
  134. 134. Walther GR. Community and ecosystem responses to recent climate change. Philosophical Transactions of the Royal Society B-Biological Sciences. 2010;365:2019-2024
  135. 135. Kiers ET, Palmer TM, Ives AR, Bruno JF, Bronstein JL. Mutualisms in a changing world: An evolutionary perspective. Ecology Letters. 2010;13(1459):2019-2024
  136. 136. Rafferty NE, Ives AR. Effects of experimental shifts in flowering phenology on plant – Pollinator interactions. Ecology Letters. 2010;14(1):69-74
  137. 137. Koh LP, Dunn RR, Sodhi NS, Colwell RK, Proctor HC, Smith VS. Species coextinctions and the biodiversity crisis. Science. 2004;305(5690):1632-1634
  138. 138. Guisan A, Zimmermann NE. Predictive habitat distribution models in ecology. Ecological Modelling. 2000;135:147-186
  139. 139. Bellard C, Bertelsmeier C, Leadley P, Thuiller W, Courchamp F. Impacts of climate change on the future of biodiversity. Ecology Letters. 2012;15(4):365-377
  140. 140. Sala OE, Chapin FS, Armesto JJ, Berlow E, Bloomfield J, Dirzo R, et al. Biodiversity – Global biodiversity scenarios for the year 2100. Science. 2000;287(5459):1770-1774
  141. 141. Warren MS, Hill JK, Thomas JA, Asher J, Fox R, Huntley B, et al. Rapid responses of British butterflies to opposing forces of climate and habitat change. Nature. 2001;414(6859):65-69
  142. 142. Franco AMA, Hill JK, Kitschke C, Collingham YC, Roy DB, Fox R, et al. Impacts of climate warming and habitat loss on extinctions at species’ low-latitude range boundaries. Global Change Biology. 2006;12(8):1545-1553
  143. 143. Jetz W, Wilcove DS, Dobson AP. Projected impacts of climate and land-use change on the global diversity of birds. Plos Biology. 2007;5(6):e157
  144. 144. Lemoine N, Bauer HG, Peintinger M, Bohning-Gaese K. Effects of climate and land-use change on species abundance in a central European bird community. Conservation Biology. 2007;21(2):495-503
  145. 145. Fawzy S, Osman AI, Doran J, Rooney DW. Strategies for mitigation of climate change: A review. Environmental Chemistry Letters. 2020;18(5):2069-2094
  146. 146. Mathy S, Menanteau P, Criqui P. After the Paris agreement: Measuring the global decarbonization Wedges from National energy scenarios. Ecological Economics. 2018;150:273-289
  147. 147. Hache EN, Nathalie AT, Criqui P, Lavergne JG, Chevallet L, Gentier S, et al. Decarbonization Wedges. French National Alliance for Energy Research Coordination (ANCRE); 2015. DOI: 10.13140/RG.2.1.3040.1360
  148. 148. Ricke KL, Millar RJ, MacMartin DG. Constraints on global temperature target overshoot. Scientific Reports. 2017;7(1):14743
  149. 149. Intergovernmental Panel on Climate Change (IPCC). Global warming of 1.5°C. In: Masson-Delmotte V, Zhai P, Pörtner H-O, Roberts D, Skea J, et al., editors. An IPCC Special Report on the Impacts of Global Warming of 1.5°C above Pre-Industrial Levels and Related Global Greenhouse Gas Emission Pathways, in the Context of Strengthening the Global Response to the Threat of Climate Change, Sustainable Development, and Efforts to Eradicate Poverty. Switzerland: IPCC; 2018
  150. 150. Gasser T, Guivarch C, Tachiiri K, Jones CD, Ciais P. Negative emissions physically needed to keep global warming below 2°C. Nature Communications. 2015;6:7958
  151. 151. Lawrence MG, Schäfer S, Muri H, Scott V, Oschlies A, Vaughan NE, et al. Evaluating climate geoengineering proposals in the context of the Paris agreement temperature goals. Nature Communications. 2018;9:3734
  152. 152. Lockley A, Mi Z, Coffman D. Geoengineering and the block chain: Coordinating carbon dioxide removal and solar radiation management to tackle future emissions. Frontiers of Engineering Management. 2019;6:38-51

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Patrush Lepcha

Submitted: 30 January 2024 Reviewed: 30 January 2024 Published: 08 April 2024