Next Article in Journal
DNA Barcoding of Trichobilharzia (Trematoda: Schistosomatidae) Species and Their Detection in eDNA Water Samples
Previous Article in Journal
Effect of Depth across a Latitudinal Gradient in the Structure of Rhodolith Seabeds and Associated Biota across the Eastern Atlantic Ocean
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Altitudinal Patterns of Native and Invasive Alien Herbs along Roadsides in the Dayao Mountain National Nature Reserve, Guangxi, China

1
School of Ecology and Environment, Zhengzhou University, Zhengzhou 450001, China
2
State Key Laboratory of Environmental Criteria and Risk Assessment, Chinese Research Academy of Environmental Sciences, Beijing 100012, China
*
Author to whom correspondence should be addressed.
Diversity 2023, 15(1), 105; https://doi.org/10.3390/d15010105
Submission received: 15 November 2022 / Revised: 29 December 2022 / Accepted: 6 January 2023 / Published: 12 January 2023
(This article belongs to the Topic Plant Invasion)

Abstract

:
Invasive alien plants have rapidly established and spread in nature reserves via roads and now pose a threat to biodiversity. To understand the mechanism and distribution patterns of invasive alien herbs, we compared the altitude patterns of native and invasive alien herbs based on 105 plots in the Dayao Mountain National Nature Reserve. This study also compared the distribution patterns of new (introduced to China after 1900) and old (introduced to China before 1900) invasive alien herbs. In addition, we examined the effects of climatic factors and human activities on the distribution patterns of species richness. In our study, 151 native herbs species and 18 invasive alien herbs species were observed, of which 12 were new invasive alien herbs. Old invasive alien herbs occurred more frequently and occupied a wider range of altitudes than new invasive alien herbs. The richness of native herbs tended to decrease with increasing altitude, and the altitude patterns of the richness of all invasive herbs and new invasive alien herbs were hump-shaped. Based on an analysis using the linear mixed model, the results indicated that temperature was the main factor limiting the altitude patterns of native herbs, and that temperature and human activities were essential factors in the distribution and spread of all invasive alien herbs and new invasive alien herbs. The intensity of human interference is a crucial driver of the spread of new invasive alien herbs to higher altitudes.

1. Introduction

Invasive alien species are one of the major factors threatening global biodiversity and ecosystem functioning [1]. In recent years, with the rapid development of trade and tourism, the rate of introduction of alien species has gradually increased [2,3,4]. Nature reserves are often considered protected zones for the conservation of biodiversity, ecological landscapes and ecosystems [5,6,7]. The high diversity of native species in nature reserves can help them compete with alien species and resist their invasion [8]. Harsh climatic conditions also prevent the invasion of alien species in nature reserves located in mountainous regions [9,10]. However, a growing number of studies [11,12] have demonstrated that invasive alien species have already invaded nature reserves and pose an even greater threat to biodiversity in nature reserves located in mountainous regions. Alien plants could invade the grassland areas from roadsides in the Glacier National Park in the United States [13]. Alien species have been observed between 2400 and 3570 m a.s.l. in protected areas of the Central Andes in Argentina [14], and 46 alien species were recorded in five protected areas of south-central Chile [15]. In China, 176 invasive alien plants have been reported in 53 national nature reserves [16]. Therefore, understanding their distribution patterns and impact factors is particularly important for the effective management of invasive alien species.
Roads are also often studied as pathways for invasive alien species because roadside habitats are usually susceptible to disturbance and present a beneficial environment for the establishment and spread of invasive alien species [17,18]. One study compared the distribution patterns of alien species at different altitudes in 65 regions worldwide, and revealed that in most areas roadside alien species decreased with increasing altitude, with a few showing a single peak pattern [19]. In addition, at altitude gradients, roads can help species cross different climatic gradients [20]. Human activities also help invasive alien species to reach higher altitude ranges [21,22,23]. However, most studies in nature reserves have focused on invasive alien species at low altitudes and in island regions [24,25]. Few studies have examined higher altitudes, particularly the mountainous areas of mainland regions.
In recent years, the acceleration of the infrastructure construction process has facilitated the spread of invasive alien plants [26,27], firstly because disturbance causes damage to roadside habitats and reduces the resistance of native communities to alien plants, and secondly because human activities are gradually shifting to higher altitudes because of the continuous improvement of transportation facilities [18,28]. This phenomenon has provided an opportunity for alien plants to spread to middle and high altitudes. Therefore, human disturbance appears to be more critical than climatic factors in terms of the impact on the altitudinal patterns of alien species [29]. In addition to roads, the climate is also a key factor influencing the distribution patterns of invasive alien plants [30]. Studies have shown that the richness of invasive alien species is lower in mid- and high-altitude regions than at lower altitudes. In the harsh environment at high altitudes, it is difficult for alien species to survive. However, some studies have suggested that the warming climate may facilitate the invasion of alien species into alpine regions [31,32,33]. Therefore, the climate has been cited as the main factor limiting the invasion of alien species at high altitudes [34]. Compared with invasive alien species, relatively few studies have examined the effects of human disturbances on the altitudinal patterns of native species [18]. In mountainous regions, the distribution patterns of native plants at different altitudes are mainly influenced by climatic conditions and are not related to disturbances [35]. Understanding the factors limiting the distribution patterns of native and invasive alien plants can help to conserve plant diversity in mountain regions.
For invasive alien plants, the time of introduction is also a non-negligible factor [36]. The residence time (time since species introduction) is related to most of the factors that may influence the successful invasion of alien species, including the evolutionary process of the species and the occupation of a more extensive range [37]. The size of the propagule pool and opportunities for dispersal increase as alien species adapt to new environments [38]. Recent studies [39,40] have shown that land use changes caused by human activities have resulted in new alien plants spreading rapidly and shifting their distribution to higher altitudes. However, most studies have only considered the time of introduction as a factor for successful invasion, and few have investigated the differences in the distribution of altitudinal patterns of invasive alien plants in relation to different introduction times.
The Guangxi Dayao Mountain National Nature Reserve, located in central Guangxi, is globally significant for its biodiversity [41]. High mountains and complex topographies in nature reserves provide a variety of microenvironments that promote rich biodiversity [42]. To date, some investigations concerning woodland and fern species have been conducted in the reserve [41,42], but few studies have involved invasive alien species. Our aims were to answer the following questions: (1) Do the altitudinal distributional patterns differ between the native and invasive alien herbs? (2) What are the main factors that determine the distribution patterns of native and invasive herbs at altitude? (3) Are there different factors affecting the distribution patterns of old and new invasive alien herbs at altitude?

2. Materials and Methods

2.1. Study Area

The study was conducted in the Dayao Mountain National Nature Reserve, which is located in the central eastern area of Guangxi, China (110°01′–110°22′ E; 23°52′–24°22′ N). The protected area encompasses an area of 256 km2 and is divided into seven zones: Changtan River, Demei Mountain, Hekou, Huaping Mountain, Longjun Mountain, Pingzhu Mountain, and Shengtang Mountain (Figure 1). The center of the nature reserve is at high altitudes, gradually decreasing in all directions, and the geosphere is mainly composed of Cambrian sand, shale, and Devonian clastic rocks [41]. Shengtang Mountain is the central peak, which reaches 1979 m a.s.l. [42]. In this study, several areas of the reserve were surveyed along major roads, and we purposefully selected sites where invasive alien species could be reflected in the reserve. We did not set up sampling sites in areas without major roads and with low human activity levels. The main climatic feature is the significant subtropical mountain climate. The annual hours of sunshine average equal 1268.6 h, the average temperature is 17 °C, the average temperature of the hottest month (July) is 23.9 °C, and the average temperature of the coldest month (January) is 8.3 °C [41]. The annual precipitation range is 1380~2700 mm, with an annual average relative humidity rate of 83%. The forest cover in the reserve is very high, at more than 95% [43]. The main natural vegetation types are deciduous broad-leaved forests and evergreen broad-leaved forests in the low mountainous areas below 1000 m a.s.l. In the higher regions, montane evergreen broad-leaved forests and middle mountain mixed coniferous forests are widely distributed [43].

2.2. Data Collection

The field survey was conducted in July 2021, and the sample sites were distributed across seven parts of the reserve. Thirty-three sampling sites were situated along a road that is intensively used for human activities and by vehicles, covering the altitude range between 200 and 1400 m a.s.l. The sample sites were located in the reserve’s experimental area and buffer zone. The road edges were defined as consisting of distinct areas ranging from 0.5 to 4 m adjacent to the road, which are vulnerable to human activities [3]. For each sampling site, a 2 m-wide sample strip was established parallel to the road. Then, three to six 1 m × 1 m plots were randomly marked out in each sample strip, giving a total of 105 plots to be surveyed. For each plot, we recorded all of the native and invasive alien herbs and the individual numbers of each species. The invasive alien herbs and native herbs were distinguished in accordance with Ma [44]. The invasive alien herbs were identified as herbs with harmful effects in accordance with Ma [44]. The location and altitude of each plot were recorded using the Global Positioning System (GPS). Since the 19th century, the rate of introduction of invasive alien plants in China has increased rapidly, with 266 species of invasive plants having been introduced since 1900 [4]. Therefore, we classified invasive alien herbs as either old invasive alien herbs (introduced to China before 1900) or new invasive alien herbs (introduced to China after 1900) (Table S1). The introduction time of each invasive alien herb was obtained from Ma’s study [44].

2.3. Climatic and Human Disturbance Factors

Three climatic factors were selected, namely the annual precipitation, annual mean temperature, and mean temperature of the warmest quarter, based on previous studies [45,46]. The climate data for each site were obtained from the WorldClim data website (accessed on 23 December 2021) (https://worldclim.org) by extracting a 30-year (1970–2000) national average of meteorological data. Human disturbance was evaluated based on two indexes: (1) the distance from the plot to the nearest human settlement, which was calculated using ArcGIS; (2) the interference intensity, which was evaluated based on the habitat type around the plot (Table S2) and was estimated using a 4-grade scale: 1 = no significant interference; 2 = weak interference; 3 = moderate interference; 4 = heavy interference [47].

2.4. Data Analysis

We examined the potential covariance between the variables using the GGally package (Figure S1). We removed the annual mean temperature because it had strong covariance with other factors (>0.70). The native herbs, all invasive alien herbs, old invasive alien herbs, and new invasive alien herbs were the response variables. The annual precipitation, mean temperature of warmest quarter, interference intensity, and distance from the plot to the nearest human settlement were the explanatory variables. Firstly, four linear models (LM) were built and used to extensively assess the relationship between explanatory and response variables. The normality of the residuals and the homogeneity of the variance were checked using the visual inspection method for the model residuals, and the variables generally conformed to a normal distribution. Secondly, to determine the relative importance of each explanatory variable, four linear mixed models (LMM) were built based on these response variables. Climate and human disturbance factors were treated as fixed effects, and the sampling sites were treated as random effects. These variables in the mixed model were decomposed using the MuMIn and glmm.hp packages, and the contribution of each variable was calculated separately. The model analysis was performed using the lmer function of the lme4 package in R (R Core Team 2022) [48].

3. Results

3.1. Composition and Distribution of Native and Invasive Alien Herbs

In this nature reserve, a total of 151 native herb species have been recorded, belonging to 62 families and 123 genera. These species are mainly classified into Poaceae and Asteraceae, with 16 and 11 genera, respectively.
A total of 18 invasive alien herbs were observed, belonging to 8 families and 15 genera. Half of all invasive alien herbs were classified into Asteraceae. When we classified these species as old or new invasive alien herbs, the number of new invasive alien herb species was twice as large as that of old invasive alien herbs. The frequency of occurrence of old invasive alien herbs was higher than that of new invasive alien herbs. For example, the frequency rates of Bidens pilosa, Erigeron canadensis, and Ageratum conyzoides were 40.95%, 34.29%, and 32.38%, respectively. However, the frequency of most new invasive alien herbs was less than 10%, with the exception of Crassocephalum crepidioides, Praxelis clematidea, and Erechtites valerianifolius (Figure 2a). In addition, 18 invasive alien herbs were classified as 12 annual and 6 perennial invasive alien herbs. Annual invasive alien herbs occurred more frequently than perennial invasive alien herbs. The frequency of occurrence of all perennial invasive alien herbs was less than 10% (Figure 2b).
Old invasive alien herbs were found at higher altitudes and occupied a wider range of altitudes (Figure 3a). For example, Bidens pilosa, Ageratum conyzoides, and Erigeron canadensis were distributed in the range of 250–1300 m a.s.l. Although of the new invasive alien herbs Crassocephalum crepidioides was distributed in the altitude range of 300–1300 m, the other new invasive alien herbs were distributed in a narrow altitude range. Annual invasive alien herbs were distributed in the range of 250–1400 m a.s.l., whereas perennial invasive alien herbs were distributed in a smaller altitude range (Figure 3b).

3.2. Altitude Distribution Patterns of Native and Invasive Alien Herbs

The richness of native herbs tends to slowly decrease with increasing altitude (Figure 4a). The richness of invasive alien herbs was represented by a single hump pattern with a peak at 900 m a.s.l. (Figure 4a). The richness of new invasive alien herbs depicted a single hump pattern with a peak at 1000 m a.s.l. (Figure 4b). The richness of old invasive alien herbs was evenly distributed across altitudes (Figure 4b).

3.3. Factors Determining the Distribution Patterns of Native and Invasive Herbs

Based on the results of the linear model analysis (Table 1), the altitude pattern of native herbs was mainly explained by the temperature (Figure 5a) and could not be correlated with human disturbance (Figure 5e).
The altitude patterns of all invasive alien herbs were significantly correlated with the temperature and interference intensity (Figure 5b,f). The distribution patterns of the new invasive alien herbs were mainly explained by the temperature and interference intensity (Figure 5c,g). The altitude patterns of old invasive alien herbs were correlated with the disturbance intensity only (Figure 5h).
Based on the results of the linear mixed model analysis (Table S3), the temperature explained 70.18% of the variation in richness of native herbs and was positively correlated with it (p < 0.05, Figure 6a).
The distribution pattern of all invasive alien herbs was significantly negatively correlated with the temperature (p < 0.05, Figure 6b) and positively correlated with the interference intensity (p < 0.05, Figure 6b). The temperature explained 34.81% of the variation, but the interference intensity explained 39.71% of the variation. The richness pattern of new invasive alien herbs was mainly explained by the temperature and interference intensity (Table S3). The temperature negatively impacted the richness pattern of new invasive alien herbs and explained 53.49% of the variation (p < 0.05, Figure 6c), whereas the interference intensity had a positive impact and explained 34.15% of the variation (p < 0.05, Figure 6c). None of the environmental factors had a significant effect on the richness of old invasive alien herbs (p > 0.05, Figure 6d).
The annual precipitation had no significant effect on the richness of either native or invasive herbs (p > 0.05, Figure 6).

4. Discussion

4.1. Altitudinal Patterns of Native and Invasive Alien Herbs

This study found that invasive alien herbs in the Dayao Mountain National Nature Reserve showed a hump-shaped distribution pattern according to altitude. In contrast with our research, invasive alien herbs are currently concentrated at lower altitudes in montane areas [47]. First, this may be in response to the arid environment at low altitudes [49] and the cold climate at high altitudes [50]. Second, our study was based on the altitudinal distribution pattern of roadside species. Invasive alien plants can occupy the remaining ecological niches because of the destruction of the original ecosystem, and then can gradually spread from lower to higher altitudes [51]. In addition, our results also suggested that the factors affecting the altitude patterns of native and invasive alien herbs were different. Native herbs have gradually adapted to the local environment through long-term development and evolution [52]. Under the influence of human activities, ecological damage may also lead to changes in the altitude patterns of native herbs [53].
In this study, differences were identified between the two invasive alien groups. Old invasive alien herbs were evenly distributed across the altitudes, whereas new invasive alien herbs showed a hump-shaped distribution pattern. The invasive alien plants with a longer residence time had a wider distribution range [54]. Becker et al. [55] showed that the altitude of invasive species increases with the time since introduction. Over time, under propagule pressure [56] and long-term genetic evolution [57], the old invasive alien plants have gradually adapted to the colder environment in order to survive at higher altitudes. In addition, human disturbance is an essential factor in the movement of species across different climatic zones [20]. Contrary to the old invasive alien herbs, the number of newly introduced aliens is increasing every year [58], even though they are not adapted to the cold environment of high altitudes [3]. Therefore, the hump-shaped distribution pattern of the new invasive alien herbs also indicated that conditions of drought at low altitudes and cold temperatures at high altitudes are unsuitable for plant survival.

4.2. Effects of Environmental Factors on the Richness of Native and Invasive Herbs

In recent years, the influence of environmental factors on species distribution has received extensive attention in studies of species distribution patterns across altitudinal gradients [25,59,60]. Our study revealed a significant difference in the explanatory variables between native and invasive alien herbs. The richness of native herbs was only positively correlated to temperature. This is the response of plants to climatic constraints, suggesting that higher temperatures allow for greater species richness [61]. Native plants have adapted to the local climate over tens of thousands of years of genetic evolution [62].
In contrast to native herbs, anthropogenic disturbance is an important factor affecting the richness of invasive alien plants. This is because human activities can destroy pristine ecosystems and provide more opportunities for invasive alien species [63,64]. The Dayao Mountain National Nature Reserve is a tourist destination, and tourism is a major human disturbance. With the rise of tourism, road construction has increased in reserves. Roads can expand the distribution range of alien species, acting as invasive pathways for alien species in mountainous areas [65]. The destruction of roadside habitats by pedestrians and vehicles also increases the number of suitable ecological niches for alien species [66]. In addition, we found a significant negative correlation between the richness of invasive alien herbs and temperature. This relationship suggested that mountain microenvironments provide suitable climatic conditions for the survival of invasive alien herbs and that plant invasion may be promoted in such environments [39]. Human activities play a stronger role than climatic factors in explaining the altitudinal pattern of invasive alien herbs in the Dayao Mountain National Nature Reserve.

4.3. Effects of Environmental Factors on the Richness of Invasive Alien Herbs at Different Introduction Times

The responses of old and new invasive alien herbs to temperature were different. The richness of old invasive alien herbs was not related to temperature, and new invasive alien herbs negatively correlated with temperature. Gasso et al. [67] showed that it took about 150 years for invasive alien plants to adapt to the local environment or to reach their maximum range. The old invasive alien herbs were all introduced to the Dayao Mountain National Nature Reserve more than 150 years ago and have gradually adapted to the local climate conditions. Thus, they were observed at higher altitudes. Most of the new invasive alien herbs were introduced to China less than 100 years ago. For example, Crassocephalum crepidioides was introduced to China about 90 years ago and Praxelis clematidea was introduced about 40 years ago. Therefore, new invasive alien herbs were significantly correlated with temperature. Polce et al. [39] identified a negative correlation between altitudinal distribution patterns and temperature for new alien plants (>1500 years) in Europe. This is consistent with the results of our study. The mesic hypothesis stated that the microclimate is vital for new alien plants and may increase the likelihood of invasion [39,68]. This means that alien species may form a larger pool of potential species in a suitable microclimate.
Studies [69,70] have shown that the impact of human activities on the altitude pattern of invasive alien plants is more critical than climatic factors. Seebens et al. [71] showed that the global invasion of alien species has not slowed in the past few centuries because of rapid economic development and population growth. The development of commercial imports to China was accelerated by war and the ecological damage caused by the prolonged war in the 20th century, causing the introduction rate of new alien plants to peak in this period [4]. Kalwij et al. [3] showed that the movements of both vehicles and livestock are the means by which the propagules of alien species spread along roads, and have led to an annual increase in the upper altitude limit of roadside alien species, as well as in the rate of introduction of new species. Human disturbances along roadsides destroy the local vegetation composition and soil environment, reducing the biological resistance of native plant communities, creating more available resources and empty ecological niches [55], and creating opportunities for the introduction and establishment of new invasive alien species [3]. Lososova et al. [72] also confirmed that habitat changes can affect the distribution of new invasive alien plants. Thus, changes in roadside habitat can increase the establishment of new alien plants and hiking or other human activities can help them to reach higher altitude ranges [15]. Polce et al. [39] found that in Europe, old invasive alien plants were less affected by human activities than newer ones. This is consistent with the results of our study. Old invasive alien herbs generally reach the limit of their potential range after a long period of adaptation in the invaded regions [55]. New invasive alien plants, when introduced into non-native habitats, spread rapidly under the influence of human disturbance and propagule pressure, but their distribution is not uniform [40]. As a result, the number of new alien plants on the roadside has increased significantly. Unlike the new invasive alien herbs, we found that the richness of the old invasive alien herbs responded to human activities similarly to the native herbs. This phenomenon suggested that the old invasive alien herbs have been adapted over a long period and have been distributed in a wide range of altitudes after a long time of adaptation.

5. Conclusions

This study found that the temperature limited the altitudinal distribution patterns of native herbs, human activities facilitated the introduction and spread of alien plants, and suitable temperatures provided the conditions for alien plants to survive. Although the old invasive alien herbs occurred more frequently and occupied a more extensive altitude range than new invasive alien herbs, we found that human activities appeared to be the main driver of new invasive alien herbs in the reserve. The old invasive alien herbs gradually adapted to the local environmental conditions with increasing residence times. The new invasive alien herbs are currently distributed at low and middle altitudes because their distribution has been restricted by climatic conditions. However, new invasive alien herbs have a higher potential spreading risk under the influence of human activities. Therefore, the monitoring and prevention of newly introduced invasive alien herbs should be strengthened to reduce the proliferation risk.

Supplementary Materials

The following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/d15010105/s1, Figure S1: Results of correlation analysis of explanatory variables. Values above 0.7 are considered to have a strong covariance between variables; Table S1: The checklist of the alien invasive plants in Dayao Mountain National Nature Reserve, Table S2: Plots investigation of herbs in Dayao Mountain National Nature Reserve, Table S3: Linear mixed models constructed for native herbs, all invasive alien herbs, new and old invasive alien herbs richness and various environmental factors at the altitude gradient of the reserve, Table S4: Information on herbs species in plots of Dayao Mountain National Nature Reserve.

Author Contributions

Conceptualization, B.L. and C.Z.; methodology, B.L.; software, B.L. and X.N.; investigation, B.L. and X.N.; data curation, B.L.; writing—original draft preparation, B.L.; writing—review and editing, C.Z.; supervision, C.Z. All authors have read and agreed to the published version of the manuscript.

Funding

This research was supported by grants from the National Key Research and Development Program of China (2020YFC1806300) and the Central Public-Interest Scientific Institution Basal Research Fund (2022YSKY-08).

Institutional Review Board Statement

Not applicable.

Data Availability Statement

The data presented in this study are available on request from the corresponding author.

Conflicts of Interest

The authors declare no conflict of interest. The funders had no role in the design of the study; in the collection, analyses, or interpretation of data; in the writing of the manuscript; or in the decision to publish the results.

References

  1. Perrings, C.; Naeem, S.; Ahrestani, F.; Bunker, D.E.; Burkill, P.; Canziani, G.; Elmqvist, T.; Ferrati, R.; Fuhrman, J.A.; Jaksic, F.; et al. Ecosystem Services for 2020. Science 2010, 330, 323–324. [Google Scholar] [CrossRef] [PubMed]
  2. Hulme, P.E. Trade, transport and trouble: Managing invasive species pathways in an era of globalization. J. Appl. Ecol. 2009, 46, 10–18. [Google Scholar] [CrossRef]
  3. Kalwij, J.M.; Robertson, M.P.; van Rensburg, B.J. Annual monitoring reveals rapid upward movement of exotic plants in a montane ecosystem. Biol. Invasions 2015, 17, 3517–3529. [Google Scholar] [CrossRef] [Green Version]
  4. Li, Y.; Shen, Z. Roles of Dispersal Limit and Environmental Filtering in Shaping the Spatiotemporal Patterns of Invasive Alien Plant Diversity in China. Front. Ecol. Evol. 2020, 8, 544670. [Google Scholar] [CrossRef]
  5. Tittensor, D.P.; Walpole, M.; Hill, S.L.L.; Boyce, D.G.; Britten, G.L.; Burgess, N.D.; Butchart, S.H.M.; Leadley, P.W.; Regan, E.C.; Alkemade, R.; et al. A mid-term analysis of progress toward international biodiversity targets. Science 2014, 346, 241–244. [Google Scholar] [CrossRef] [PubMed]
  6. Braun, M.; Schindler, S.; Essl, F. Distribution and management of invasive alien plant species in protected areas in Central Europe. J. Nat. Conserv. 2016, 33, 48–57. [Google Scholar] [CrossRef]
  7. Bhatta, S.; Joshi, L.R.; Shrestha, B.B. Distribution and impact of invasive alien plant species in Bardia National Park, western Nepal. Environ. Conserv. 2020, 47, 197–205. [Google Scholar] [CrossRef]
  8. Byers, J.E. Impact of non-indigenous species on natives enhanced by anthropogenic alteration of selection regimes. Oikos 2002, 97, 449–458. [Google Scholar] [CrossRef]
  9. Foxcroft, L.C.; Jarosik, V.; Pysek, P.; Richardson, D.M.; Rouget, M. Protected-Area Boundaries as Filters of Plant Invasions. Conserv. Biol. 2011, 25, 400–405. [Google Scholar] [CrossRef] [Green Version]
  10. Gonzalez-Moreno, P.; Diez, J.M.; Ibanez, I.; Font, X.; Vila, M. Plant invasions are context-dependent: Multiscale effects of climate, human activity and habitat. Divers. Distrib. 2014, 20, 720–731. [Google Scholar] [CrossRef]
  11. Thalmann, D.J.K.; Kikodze, D.; Khutsishvili, M.; Kharazishvili, D.; Guisan, A.; Broennimann, O.; Mueller-Schaerer, H. Areas of high conservation value in Georgia: Present and future threats by invasive alien plants. Biol. Invasions 2015, 17, 1041–1054. [Google Scholar] [CrossRef] [Green Version]
  12. Shackleton, R.T.; Foxcroft, L.C.; Pysek, P.; Wood, L.E.; Richardson, D.M. Assessing biological invasions in protected areas after 30 years: Revisiting nature reserves targeted by the 1980s SCOPE programme. Biol. Conserv. 2020, 243, 108424. [Google Scholar] [CrossRef]
  13. Tyser, R.W.; Worley, C.A. Alien flora in grasslands adjacent to road and trail corridors in Glacier National-park, Montana (USA). Conserv. Biol. 1992, 6, 253–262. [Google Scholar] [CrossRef]
  14. McDougall, K.L.; Lembrechts, J.; Rew, L.J.; Haider, S.; Cavieres, L.A.; Kueffer, C.; Milbau, A.; Naylor, B.J.; Nunez, M.A.; Pauchard, A.; et al. Running off the road: Roadside non-native plants invading mountain vegetation. Biol. Invasions 2018, 20, 3461–3473. [Google Scholar] [CrossRef] [Green Version]
  15. Liedtke, R.; Barros, A.; Essl, F.; Lembrechts, J.J.; Wedegartner, R.E.M.; Pauchard, A.; Dullinger, S. Hiking trails as conduits for the spread of non-native species in mountain areas. Biol. Invasions 2020, 22, 1121–1134. [Google Scholar] [CrossRef] [Green Version]
  16. Gong, L.; Li, J.; Liu, X.; Zhao, X.; Zhao, C. Analysis of invasive alien species in Chinese national nature reserves. Ecol. Sci. 2017, 36, 210–216. [Google Scholar] [CrossRef]
  17. Pollnac, F.; Seipel, T.; Repath, C.; Rew, L.J. Plant invasion at landscape and local scales along roadways in the mountainous region of the Greater Yellowstone Ecosystem. Biol. Invasions 2012, 14, 1753–1763. [Google Scholar] [CrossRef]
  18. Lembrechts, J.J.; Alexander, J.M.; Cavieres, L.A.; Haider, S.; Lenoir, J.; Kueffer, C.; McDougall, K.; Naylor, B.J.; Nunez, M.A.; Pauchard, A.; et al. Mountain roads shift native and non-native plant species’ ranges. Ecography 2017, 40, 353–364. [Google Scholar] [CrossRef]
  19. Guo, Q.; Fei, S.; Shen, Z.; Iannone, B.V., III; Knott, J.; Chown, S.L. A global analysis of elevational distribution of non-native versus native plants. J. Biogeogr. 2018, 45, 793–803. [Google Scholar] [CrossRef]
  20. Pauchard, A.; Kueffer, C.; Dietz, H.; Daehler, C.C.; Alexander, J.; Edwards, P.J.; Arevalo, J.R.; Cavieres, L.A.; Guisan, A.; Haider, S.; et al. Ain’t no mountain high enough: Plant invasions reaching new elevations. Front. Ecol. Environ. 2009, 7, 479–486. [Google Scholar] [CrossRef]
  21. Barros, A.; Pickering, C.M. Non-native Plant Invasion in Relation to Tourism Use of Aconcagua Park, Argentina, the Highest Protected Area in the Southern Hemisphere. Mt. Res. Dev. 2014, 34, 13–26. [Google Scholar] [CrossRef] [Green Version]
  22. Yang, M.; Lu, Z.; Fan, Z.; Liu, X.; Hens, L.; De Wulf, R.; Ou, X. Distribution of non-native plant species along elevation gradients in a protected area in the eastern Himalayas, China. Alp. Bot. 2018, 128, 169–178. [Google Scholar] [CrossRef]
  23. Ibanez, T.; Hart, P.; Ainsworth, A.; Gross, J.; Monello, R. Factors associated with alien plant richness, cover and composition differ in tropical island forests. Divers. Distrib. 2019, 25, 1910–1923. [Google Scholar] [CrossRef] [Green Version]
  24. Landi, S.; Tordoni, E.; Amici, V.; Bacaro, G.; Carboni, M.; Filibeck, G.; Scoppola, A.; Bagella, S. Contrasting patterns of native and non-native plants in a network of protected areas across spatial scales. Biodivers. Conserv. 2020, 29, 2035–2053. [Google Scholar] [CrossRef]
  25. Rojas-Sandoval, J.; Ackerman, J.D.; Tremblay, R.L. Island biogeography of native and alien plant species: Contrasting drivers of diversity across the Lesser Antilles. Divers. Distrib. 2020, 26, 1539–1550. [Google Scholar] [CrossRef]
  26. Pretto, F.; Celesti-Grapow, L.; Carli, E.; Brundu, G.; Blasi, C. Determinants of non-native plant species richness and composition across small Mediterranean islands. Biol. Invasions 2012, 14, 2559–2572. [Google Scholar] [CrossRef]
  27. Paudel, S.; Benavides, J.C.; MacDonald, B.; Longcore, T.; Wilson, G.W.T.; Loss, S.R. Determinants of native and non-native plant community structure on an oceanic island. Ecosphere 2017, 8, e01927. [Google Scholar] [CrossRef] [Green Version]
  28. Haider, S.; Kueffer, C.; Bruelheide, H.; Seipel, T.; Alexander, J.M.; Rew, L.J.; Ramon Arevalo, J.; Cavieres, L.A.; McDougall, K.L.; Milbau, A.; et al. Mountain roads and non-native species modify elevational patterns of plant diversity. Glob. Ecol. Biogeogr. 2018, 27, 667–678. [Google Scholar] [CrossRef] [Green Version]
  29. Marini, L.; Battisti, A.; Bona, E.; Federici, G.; Martini, F.; Pautasso, M.; Hulme, P.E. Alien and native plant life-forms respond differently to human and climate pressures. Glob. Ecol. Biogeogr. 2012, 21, 534–544. [Google Scholar] [CrossRef]
  30. Sullivan, J.J.; Williams, P.A.; Timmins, S.M.; Smale, M.C. Distribution and spread of environmental weeds along New Zealand roadsides. N. Z. J. Ecol. 2009, 33, 190–204. [Google Scholar]
  31. Pauchard, A.; Milbau, A.; Albihn, A.; Alexander, J.; Burgess, T.; Daehler, C.; Englund, G.; Essl, F.; Evengard, B.; Greenwood, G.B.; 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. Biol. Invasions 2016, 18, 345–353. [Google Scholar] [CrossRef]
  32. Dainese, M.; Aikio, S.; Hulme, P.E.; Bertolli, A.; Prosser, F.; Marini, L. Human disturbance and upward expansion of plants in a warming climate. Nat. Clim. Change 2017, 7, 577–580. [Google Scholar] [CrossRef]
  33. Carboni, M.; Gueguen, M.; Barros, C.; Georges, D.; Boulangeat, I.; Douzet, R.; Dullinger, S.; Klonner, G.; van Kleunen, M.; Essl, F.; et al. Simulating plant invasion dynamics in mountain ecosystems under global change scenarios. Glob. Change Biol. 2018, 24, E289–E302. [Google Scholar] [CrossRef] [Green Version]
  34. Steyn, C.; Greve, M.; Robertson, M.P.; Kalwij, J.M.; le Roux, P.C. Alien plant species that invade high elevations are generalists: Support for the directional ecological filtering hypothesis. J. Veg. Sci. 2017, 28, 337–346. [Google Scholar] [CrossRef] [Green Version]
  35. Felde, V.A.; Kapfer, J.; Grytnes, J.-A. Upward shift in elevational plant species ranges in Sikkilsdalen, central Norway. Ecography 2012, 35, 922–932. [Google Scholar] [CrossRef]
  36. Pysek, P.; Manceur, A.M.; Alba, C.; McGregor, K.F.; Pergl, J.; Stajerova, K.; Chytry, M.; Danihelka, J.; Kartesz, J.; Klimesova, J.; et al. Naturalization of central European plants in North America: Species traits, habitats, propagule pressure, residence time. Ecology 2015, 96, 762–774. [Google Scholar] [CrossRef]
  37. Richardson, D.M.; Pysek, P. Plant invasions: Merging the concepts of species invasiveness and community invasibility. Prog. Phys. Geogr. -Earth Environ. 2006, 30, 409–431. [Google Scholar] [CrossRef] [Green Version]
  38. Richardson, D.M.; Pysek, P. Naturalization of introduced plants: Ecological drivers of biogeographical patterns. New Phytol. 2012, 196, 383–396. [Google Scholar] [CrossRef]
  39. Polce, C.; Kunin, W.E.; Biesmeijer, J.C.; Dauber, J.; Phillips, O.L.; Network, A.F.S. Alien and native plants show contrasting responses to climate and land use in Europe. Glob. Ecol. Biogeogr. 2011, 20, 367–379. [Google Scholar] [CrossRef]
  40. Eichenberg, D.; Bowler, D.E.; Bonn, A.; Bruelheide, H.; Grescho, V.; Harter, D.; Jandt, U.; May, R.; Winter, M.; Jansen, F. Widespread decline in Central European plant diversity across six decades. Glob. Change Biol. 2021, 27, 1097–1110. [Google Scholar] [CrossRef]
  41. Chen, B.; Wang, L. Investigation and application of wild ornamental ferns in Dayao Mountain National Nature Reserve, Guangxi. Contemp. Hortic. 2021, 44, 83–86. [Google Scholar] [CrossRef]
  42. Chen, B.; Wang, L.; Sun, C. Investigation of wild woody ornamental plant resources in Dayao Mountain National Nature Reserve. Chin. Wild Plant Resour. 2021, 40, 61–67. [Google Scholar] [CrossRef]
  43. Wang, L.; Luo, B.; Tan, M.; Chen, B. Study on Flora of Dayao Mountain Nature Reserve in Guangxi. In Proceedings of the Second China Forestry Academic Conference—S8 Wildlife, Wetland and Nature Reserve, Nanning, China, 7 November 2009; pp. 132–136. [Google Scholar]
  44. Ma, J. Flora of Invasive Aliens in China, 1st ed.; Shanghai Jiao Tong University Press: Shanghai, China, 2021; pp. 39–378. [Google Scholar]
  45. Xu, Z.; Feng, Z.; Yang, J.; Zheng, J.; Zhang, F. Nowhere to Invade: Rumex crispus and Typha latifolia Projected to Disappear under Future Climate Scenarios. PLoS ONE 2013, 8, e70728. [Google Scholar] [CrossRef] [PubMed]
  46. Zhang, X.; Wei, H.; Zhao, Z.; Liu, J.; Zhang, Q.; Zhang, X.; Gu, W. The Global Potential Distribution of Invasive Plants: Anredera cordifolia under Climate Change and Human Activity Based on Random Forest Models. Sustainability 2020, 12, 1491. [Google Scholar] [CrossRef] [Green Version]
  47. Zhang, W.; Yin, D.; Huang, D.; Du, N.; Liu, J.; Guo, W.; Wang, R. Altitudinal patterns illustrate the invasion mechanisms of alien plants in temperate mountain forests of northern China. For. Ecol. Manag. 2015, 351, 1–8. [Google Scholar] [CrossRef]
  48. R Core Team. R: A Language and Environment for Statistical Computing; R Foundation for Statistical Computing: Vienna, Austria, 2022; Available online: https://www.R-project.org/ (accessed on 12 January 2022).
  49. Koerner, C. The use of ‘altitude’ in ecological research. Trends Ecol. Evol. 2007, 22, 569–574. [Google Scholar] [CrossRef]
  50. Haider, S.; Alexander, J.; Dietz, H.; Trepl, L.; Edwards, P.J.; Kueffer, C. The role of bioclimatic origin, residence time and habitat context in shaping non-native plant distributions along an altitudinal gradient. Biol. Invasions 2010, 12, 4003–4018. [Google Scholar] [CrossRef]
  51. Applestein, C.; Germino, M.J. Patterns of post-fire invasion of semiarid shrub-steppe reveals a diversity of invasion niches within an exotic annual grass community. Biol. Invasions 2022, 24, 741–759. [Google Scholar] [CrossRef]
  52. Roy, K.; Goldberg, E.E. Origination, extinction, and dispersal: Integrative models for understanding present-day diversity gradients. Am. Nat. 2007, 170, S71–S85. [Google Scholar] [CrossRef]
  53. Clark-Tapia, R.; Gonzalez-Adame, G.; Campos, J.E.; Aguirre-Hidalgo, V.; Pacheco-Cruz, N.; Ugalde, J.J.V.T.; Campista-Leon, S.; Peinado-Guevara, L.I.; Alfonso-Corrado, C. Effects of Habitat Loss on the Ecology of Pachyphytum caesium (Crassulaceae), a Specialized Cliff-Dwelling Endemic Species in Central Mexico. Diversity 2021, 13, 421. [Google Scholar] [CrossRef]
  54. Sheppard, C.S.; Brendel, M.R. Competitive ability of native and alien plants: Effects of residence time and invasion status. Neobiota 2021, 65, 47–69. [Google Scholar] [CrossRef]
  55. Becker, T.; Dietz, H.; Billeter, R.; Buschmann, H.; Edwards, P.J. Altitudinal distribution of alien plant species in the Swiss Alps. Perspect. Plant Ecol. Evol. Syst. 2005, 7, 173–183. [Google Scholar] [CrossRef]
  56. Ross, L.C.; Lambdon, P.W.; Hulme, P.E. Disentangling the roles of climate, propagule pressure and land use on the current and potential elevational distribution of the invasive weed Oxalis pes-caprae L. on Crete. Perspect. Plant Ecol. Evol. Syst. 2008, 10, 251–258. [Google Scholar] [CrossRef]
  57. Roy, S.; Simon, J.P.; Lapointe, F.J. Determination of the origin of the cold-adapted populations of barnyard grass (Echinochloa crus-galli) in eastern North America: A total-evidence approach using RAPD DNA and DNA sequences. Can. J. Bot. -Rev. Can. De Bot. 2000, 78, 1505–1513. [Google Scholar] [CrossRef]
  58. Essl, F.; Glaser, M.; Schertler, A. New and old invaders in forests in eastern Austria: The role of species attributes and invasion history. Flora 2021, 283, 151922. [Google Scholar] [CrossRef]
  59. Padalia, H.; Bushra, A.; Singh, G.; Nandy, S.; Rai, I.D.; Rawat, G.S. Spatial patterns of plant functional types and environmental proxies of plant richness in alpine region of Western Himalaya, India. Biodivers. Conserv. 2019, 28, 2221–2244. [Google Scholar] [CrossRef]
  60. Gao, D.; Fu, L.; Sun, J.; Li, Y.; Cao, Z.; Liu, Y.; Xu, P.; Zhao, J. The mid-domain effect and habitat complexity applied to elevational gradients: Moss species richness in a temperate semihumid monsoon climate mountain of China. Ecol. Evol. 2021, 11, 7448–7460. [Google Scholar] [CrossRef]
  61. Alexander, J.M.; Kueffer, C.; Daehler, C.C.; Edwards, P.J.; Pauchard, A.; Seipel, T.; Consortium, M. Assembly of nonnative floras along elevational gradients explained by directional ecological filtering. Proc. Natl. Acad. Sci. USA 2011, 108, 656–661. [Google Scholar] [CrossRef] [Green Version]
  62. Khuroo, A.A.; Weber, E.; Malik, A.H.; Reshi, Z.A.; Dar, G.H. Altitudinal distribution patterns of the native and alien woody flora in Kashmir Himalaya, India. Environ. Res. 2011, 111, 967–977. [Google Scholar] [CrossRef]
  63. Davis, M.A.; Grime, J.P.; Thompson, K. Fluctuating resources in plant communities: A general theory of invasibility. J. Ecol. 2000, 88, 528–534. [Google Scholar] [CrossRef] [Green Version]
  64. Rose, M.; Hermanutz, L. Are boreal ecosystems susceptible to alien plant invasion? Evidence from protected areas. Oecologia 2004, 139, 467–477. [Google Scholar] [CrossRef] [PubMed]
  65. Paiaro, V.; Cabido, M.; Pucheta, E. Altitudinal distribution of native and alien plant species in roadside communities from central Argentina. Austral Ecol. 2011, 36, 176–184. [Google Scholar] [CrossRef]
  66. Woitke, M.; Dietz, H. Shifts in dominance of native and invasive plants in experimental patches of vegetation. Perspect. Plant Ecol. Evol. Syst. 2002, 5, 165–184. [Google Scholar] [CrossRef]
  67. Gasso, N.; Pysek, P.; Vila, M.; Williamson, M. Spreading to a limit: The time required for a neophyte to reach its maximum range. Divers. Distrib. 2010, 16, 310–311. [Google Scholar] [CrossRef]
  68. Huebner, C.D.; Tobin, P.C. Invasibility of mature and 15-year-old deciduous forests by exotic plants. Plant Ecol. 2006, 186, 57–68. [Google Scholar] [CrossRef]
  69. Tanaka, T.; Sato, T. Contemporary patterns and temporal changes in alien plant species richness along an elevational gradient in central Japan. Plant Ecol. Evol. 2016, 149, 177–188. [Google Scholar] [CrossRef]
  70. Irl, S.D.H.; Schweiger, A.H.; Steinbauer, M.J.; Ah-Peng, C.; Arevalo, J.R.; Beierkuhnlein, C.; Chiarucci, A.; Daehler, C.C.; Fernandez-Palacios, J.M.; Flores, O.; et al. Human impact, climate and dispersal strategies determine plant invasion on islands. J. Biogeogr. 2021, 48, 1889–1903. [Google Scholar] [CrossRef]
  71. Seebens, H.; Blackburn, T.M.; Dyer, E.E.; Genovesi, P.; Hulme, P.E.; Jeschke, J.M.; Pagad, S.; Pysek, P.; Winter, M.; Arianoutsou, M.; et al. No saturation in the accumulation of alien species worldwide. Nat. Commun. 2017, 8, 14435. [Google Scholar] [CrossRef]
  72. Lososova, Z.; Chytry, M.; Tichy, L.; Danihelka, J.; Fajmon, K.; Hajek, O.; Kintrova, K.; Kuehn, I.; Lanikova, D.; Otypkova, Z.; et al. Native and alien floras in urban habitats: A comparison across 32 cities of central Europe. Glob. Ecol. Biogeogr. 2012, 21, 545–555. [Google Scholar] [CrossRef]
Figure 1. Location of the Dayao Mountain National Nature Reserve and plant survey sample sites.
Figure 1. Location of the Dayao Mountain National Nature Reserve and plant survey sample sites.
Diversity 15 00105 g001
Figure 2. Occurrence frequency rates of (a) new and old invasive alien herbs and (b) annual and perennial invasive alien herbs in Dayao Mountain Reserve. The y-axis indicates the proportion of samples in which each species was present. Black, white, dark gray, and light gray represent old, new, annual, and perennial invasive alien herbs, respectively.
Figure 2. Occurrence frequency rates of (a) new and old invasive alien herbs and (b) annual and perennial invasive alien herbs in Dayao Mountain Reserve. The y-axis indicates the proportion of samples in which each species was present. Black, white, dark gray, and light gray represent old, new, annual, and perennial invasive alien herbs, respectively.
Diversity 15 00105 g002
Figure 3. The altitudinal distribution range of (a) new and old invasive alien herbs and (b) annual and perennial invasive alien herbs. Old and new invasive alien herbs are indicated by dashed and solid lines, respectively. Annual and perennial invasive alien herbs are indicated by dotted lines and dot-dash lines, respectively. The positions of the symbols show the average altitudes at which the species occurs. Solid and hollow circles denote old and new invasive alien herbs, respectively. Solid and hollow triangles indicate annual and perennial invasive alien herbs, respectively.
Figure 3. The altitudinal distribution range of (a) new and old invasive alien herbs and (b) annual and perennial invasive alien herbs. Old and new invasive alien herbs are indicated by dashed and solid lines, respectively. Annual and perennial invasive alien herbs are indicated by dotted lines and dot-dash lines, respectively. The positions of the symbols show the average altitudes at which the species occurs. Solid and hollow circles denote old and new invasive alien herbs, respectively. Solid and hollow triangles indicate annual and perennial invasive alien herbs, respectively.
Diversity 15 00105 g003
Figure 4. Altitudinal patterns of the richness of (a) native and all invasive alien herbs and (b) new and old invasive alien herbs in the Dayao Mountain Reserve. Hollow triangles and solid circles represent native herbs and all invasive alien herbs, respectively. Solid and open diamonds represent new and old invasive alien herbs, respectively.
Figure 4. Altitudinal patterns of the richness of (a) native and all invasive alien herbs and (b) new and old invasive alien herbs in the Dayao Mountain Reserve. Hollow triangles and solid circles represent native herbs and all invasive alien herbs, respectively. Solid and open diamonds represent new and old invasive alien herbs, respectively.
Diversity 15 00105 g004
Figure 5. Distribution of richness for (a,e) native herbs, (b,f) all invasive alien herbs, and (c,g) new and (d,h) old invasive alien herbs with the mean temperature of the warmest quarter and interference intensity in the Dayao Mountain Reserve.
Figure 5. Distribution of richness for (a,e) native herbs, (b,f) all invasive alien herbs, and (c,g) new and (d,h) old invasive alien herbs with the mean temperature of the warmest quarter and interference intensity in the Dayao Mountain Reserve.
Diversity 15 00105 g005
Figure 6. Effect values of human activities and climatic factors on (a) native herbs, (b) all invasive alien herbs, and (c) new and (d) old invasive alien herbs. Hollow circles represent species richness significantly correlated with environmental factors, solid circles represent species richness not significantly correlated with environmental factors, and dashed lines indicate an effect value of 0.
Figure 6. Effect values of human activities and climatic factors on (a) native herbs, (b) all invasive alien herbs, and (c) new and (d) old invasive alien herbs. Hollow circles represent species richness significantly correlated with environmental factors, solid circles represent species richness not significantly correlated with environmental factors, and dashed lines indicate an effect value of 0.
Diversity 15 00105 g006
Table 1. Linear models were constructed for native herbs, all invasive alien herbs, the richness levels of new and old invasive alien herbs, and various environmental factors at the altitude gradient of the reserve.
Table 1. Linear models were constructed for native herbs, all invasive alien herbs, the richness levels of new and old invasive alien herbs, and various environmental factors at the altitude gradient of the reserve.
Species CategoryEnvironment Variablestp
Native herbsMean temperature of warmest quarter3.0080.003
Annual precipitation0.4150.679
Interference intensity−1.0380.302
Dis. human settlement−1.0600.292
All invasive alien herbsMean temperature of warmest quarter−2.4690.015
Annual precipitation0.1910.848
Interference intensity3.913<0.001
Dis. human settlement−0.3710.712
New invasive alien herbsMean temperature of warmest quarter−4.723<0.001
Annual precipitation−1.7330.086
Interference intensity3.2330.002
Dis. human settlement0.4290.668
Old invasive alien herbsMean temperature of warmest quarter1.1940.235
Annual precipitation1.7670.08
Interference intensity1.8750.05
Dis. human settlement−0.8300.408
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

Li, B.; Ni, X.; Zhao, C. Altitudinal Patterns of Native and Invasive Alien Herbs along Roadsides in the Dayao Mountain National Nature Reserve, Guangxi, China. Diversity 2023, 15, 105. https://doi.org/10.3390/d15010105

AMA Style

Li B, Ni X, Zhao C. Altitudinal Patterns of Native and Invasive Alien Herbs along Roadsides in the Dayao Mountain National Nature Reserve, Guangxi, China. Diversity. 2023; 15(1):105. https://doi.org/10.3390/d15010105

Chicago/Turabian Style

Li, Bai, Xinying Ni, and Caiyun Zhao. 2023. "Altitudinal Patterns of Native and Invasive Alien Herbs along Roadsides in the Dayao Mountain National Nature Reserve, Guangxi, China" Diversity 15, no. 1: 105. https://doi.org/10.3390/d15010105

APA Style

Li, B., Ni, X., & Zhao, C. (2023). Altitudinal Patterns of Native and Invasive Alien Herbs along Roadsides in the Dayao Mountain National Nature Reserve, Guangxi, China. Diversity, 15(1), 105. https://doi.org/10.3390/d15010105

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop