Several studies have shown that soil microorganisms play a key role in the success of plant invasion. Thus, ecologists have become increasingly interested in understanding the ecological effects of biological invasion on soil microbial communities given continuing increase in the effects of invasive plants on native ecosystems. This paper aims to provide a relatively complete depiction of the characteristics of soil microbial communities under different degrees of plant invasion. Rhizospheric soils of the notorious invasive plant Wedelia trilobata with different degrees of invasion (uninvaded, low-degree, and high-degree using its coverage in the invaded ecosystems) were collected from five discrete areas in Hainan Province, P. R. China. Soil physicochemical properties and community structure of soil microorganisms were assessed. Low degrees of W. trilobata invasion significantly increased soil pH values whereas high degrees of invasion did not significantly affected soil pH values. Moreover, the degree of W. trilobata invasion exerted significant effects on soil Ca concentration but did not significantly change other indices of soil physicochemical properties. Low and high degrees of W. trilobata invasion increased the richness of the soil fungal community but did not pose obvious effects on the soil bacterial community. W. trilobata invasion also exerted obvious effects on the community structure of soil microorganisms that take part in soil nitrogen cycling. These changes in soil physicochemical properties and community structure of soil microbial communities mediated by different degrees of W. trilobata invasion may present significant functions in further facilitating the invasion process.
Citation: Si C, Liu X, Wang C, Wang L, Dai Z, Qi S, et al. (2013) Different Degrees of Plant Invasion Significantly Affect the Richness of the Soil Fungal Community. PLoS ONE 8(12): e85490. https://doi.org/10.1371/journal.pone.0085490
Editor: Fei-Hai Yu, Beijing Forestry University, China
Received: August 8, 2013; Accepted: November 27, 2013; Published: December 31, 2013
Copyright: © 2013 Si et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: This study was partially supported by the National Natural Science Foundation of China (30970556, 31170386), the Doctoral Program of Higher Education of China (20093227110004), the Priority Academic Program Development of Jiangsu Higher Education Institutions (PAPD), and Universities Natural Science Research Project of Jiangsu Province (13KJB610002). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Biological invasion is an important element of global change [1-4]. Invasive species have become a serious problem in the global scope because these invaders exert multiple effects on the structure and/or functions of their surrounding ecosystems [1-5]. In recent decades, ecologists have become increasingly interested in successful mechanisms of plant invasion to determine why some plants are strongly invasive while others are not [6,7]. Numerous studies have found that some plants successfully invade certain environments because these species can accelerate the succession of soil microbial communities in their rhizosphere and then strengthen the metabolic activities and community structure of the soil microorganisms to facilitate their further invasion [5,8-11]. Thus, considering the continuing increase in anthropogenic activities, the effects of plant invasion on soil microbial communities have recently received increased research interest.
Gradual succession occurs after invaders are transported from their natural habitat and progressively establish populations in invaded ecosystems [12-14]. Invasive plants exert different degrees of invasion in affected areas , and the community structure of soil microorganisms may be significantly affected by plant invasion along different stages of succession. Thus, understanding the effects of different degrees of plant invasion on soil microbial communities is important in elucidating the mechanism underlying the success of plant invasion. Unfortunately, existing studies on plant invasion mainly focus on the impacts of invasive plants on native ecosystems; such studies often ignore the invasion degrees of invading species or do not discuss the effects of different degrees of plant invasion on the community structure of soil bacteria and fungi.
The present study was carried out using cross-site comparisons to provide a relatively complete depiction of the responses of soil microbial communities to different invasion degrees mediated by Wedelia trilobata. W. trilobata is a creeping, mat-forming perennial herb native to the tropics of Central America, which has invaded many areas of tropics and subtropics [15,16]. It has been listed as one of the most malignant weeds listed by the International Union for Conservation of Nature and Natural Resources (IUCN) . In the 1970s, W. trilobata was introduced to China as an ornamental and groundcover plant, and rapidly escaped from gardens to roadsides and plantations [15,16]. W. trilobata has become recognized as a notorious weed in southern China [15,16,18]. The characteristic such as high nutrient cycling rates [especially soil nitrogen (N)] is invoked to explain the successful invasion of W. trilobata [19,20]. This study aims (1) to examine the effects of different degrees of W. trilobata invasion on soil physicochemical properties and (2) detect the effects of different degrees of W. trilobata invasion on the community structure of bacteria and fungi in soil subsystems. We hypothesize that (1) increasing degrees of W. trilobata invasion enhance soil nutrient element concentrations (especially soil N) because invasive plants have high nutrient cycling rates, especially for N [6,8,14,19-22], and that (2) low degrees of W. trilobata invasion significantly increases the richness of the soil bacterial community whereas high degrees of W. trilobata invasion significantly increases the richness of the soil fungal community because soil microbial communities are dominated by bacteria in early succession and by fungi in late succession .
Materials and Methods
Samples were obtained from five areas, namely, Haikou (19°32'–20°05'N, 110°10'–110°41'E), Tunchang (19°08'–19°37'N, 109°45'–110°15'E), Sanya (18°09'–18°37'N, 108°56'–109°48'E), Qionghai (18°58'–19°28'N, 110°07'–110°40'E), and Danzhou (19°11'–19°52'N, 108°56'–109°46'E); all areas were located in Hainan Province, P. R. China, with an area of 35 400 km2 and an altitude of 1 811.6 m. The study areas feature a subtropical humid climate, with an annual mean temperature of approximately 24 °C and an annual precipitation of approximately 1 500 mm. The samples were collected from public land. No specific permissions were required to obtain samples from these locations, and details on why this area was chosen need not be provided. Ethical approval to conduct the present study was not required because we did not handle or collect animals considered in any animal welfare regulations, and no endangered or protected species were involved in our sampling or experiments.
In August 2010, rhizospheric soil samples with different degrees of W. trilobata invasion were collected from the five aforementioned areas. One sample area was divided into three sites according to the degree of W. trilobata invasion, i.e., uninvaded (0%, CK), low degree (<35%, LD), and high degree (>75%, HD) using the coverage of W. trilobata in the invaded ecosystems. Five soil samples within an approximately 5 cm radius of W. trilobata rhizosphere from each invasion degree in each site were collected. A total of fifteen treatment combinations were obtained: 5 sample areas × 3 invasion degrees (the related information is shown in Table 1).
|Invasion situation||No. of sample site||Degree of invasion||Sample area|
All soil samples were stored in sealed sterile bags and immediately transported back to the laboratory. The soil samples were passed through a 2 mm sieve to remove leaves, plant roots, and gravel. All soil samples from one site were homogenized by thorough mixing and then stored in a refrigerator at 4 °C for further processing. Sieving and homogenization steps were carried out to decrease the discrepancies brought about by the inhomogeneity of soil contents and reduce the effects of serendipitous foreign materials on parameter determination.
Determination of soil physicochemical properties
Soil pH values were measured using a glass electrode (1:5 soil–water ratios) after shaking the samples for approximately 30 min to equilibrate . Soil moisture was determined by sampling 5 g of soil and then drying it at 105 °C for 24 h to achieve a constant weight. Soil organic matter was analyzed using the method of K2Cr2O7–H2SO4 oxidation. Soil N concentration was determined by the Semimicro-Kjeldahl method. Soil phosphorus (P) concentration was determined using the Mo-Sb antispetrophotography method. Soil potassium (K) concentration was determined with the NaOH-melt method. The concentrations of iron (Fe), manganese (Mn), calcium (Ca), and magnesium (Mg) were determined through atomic absorption spectrophotometry.
Determination of genetic diversity in soil microbial communities
Genetic diversity in the soil microbial communities in the rhizospheres of W. trilobata was analyzed by denaturing gradient gel electrophoresis (DGGE). 16S rRNA and 18S rRNA genes were amplified with the universal bacterial primers 341F/907R  and the universal fungal primers NS1/Fung [26,27], respectively. A 40-base pair G + C-rich sequence (GC-clamp) was attached to the 5' end of the forward primers to prevent the complete separation of the strands during DGGE. PCR amplification was performed with 25 µL of 2 × Power Taq PCR MasterMix (Invitrogen, USA), 1 μL of each primer (10 μM), 1 µL of DNA extract, and 1 µL of BSA (10 mg mL−1); sterile ultrapure water was used to adjust the mixture to a final volume of 50 µL. PCR amplification was run on a MyCycler thermal cycle (Bio-Rad, USA). PCR amplification of 16S rRNA was performed as follows: initial denaturation at 94 °C for 5 min, followed by 35 cycles of denaturation at 94 °C for 40 s, annealing at 55 °C for 50 s and an extension at 72 °C for 50 s, and a single extension at 72 °C for 7 min; the program was ended at 25 °C. The 18S rRNA PCR program was carried out with an initial denaturation step at 94 °C for 5 min, followed by 35 cycles of denaturation at 94 °C for 30 s, annealing at 55 °C for 30 s and elongation at 72 °C for 40 s; a final elongation step at 72 °C was performed for 7 min and the program was ended at 4 °C.
DGGE was carried out using a Dcode universal mutation detection system (Bio-Rad, USA). PCR samples (30 µL) containing approximately equal amounts of PCR amplicons were loaded onto the 1 mm thick 8% (w/v) polyacrylamide gels in 1 × TAE buffer using a denaturing gradient ranging from 30% to 80% for bacterial PCR samples and 10% to 50% for fungal PCR samples (100% denaturant was defined as 7 M urea and 40% deionized formamide). Electrophoreses were performed at 60 °C and 120 V for 12 h. After staining with SYBR Green I nucleic acid gel stain (Molecular Probes, Carlsbad, CA, USA), the gels were scanned and analyzed with QuantityOne software (version 4.5, Bio-Rad, USA).
All recognized DGGE bands were excised under UV light, and a bead beating method was applied to extract DNA from the gel slices . After purification with a DNA fragment purification Kit (Toyobo, Osaka, Japan), the eluted DNA was used for re-amplification with the original primer set (without the GC clamp). PCR products were sequenced by Sangon Biotech (Shanghai) Co., Ltd. (Shanghai, P. R. China). The sequences were submitted to National Center for Biotechnology Information (NCBI, http://www.ncbi.nlm.nih.gov/) for BLAST to determine their phylogenetic affiliation, and the closest relatives were identified for phylogenetic analysis.
DGGE banding profiles of both bacterial community and fungal community were digitized after average background subtraction for the entire gel using QuantityOne (version 4.6.2, Bio-Rad, USA). The relative intensity of a specific band was transformed according to the sum of the intensities of all bands in a pattern . Bands with relative contributions below 1% were discarded from the analysis, and the Shannon–Wiener diversity (H') and Pielou evenness (EH) indices were used to estimate the community structure of the soil microorganisms. H' was determined by the following equation: H'=-ΣPilnPi , where Pi is the importance probability of the bands in a track. Pi was calculated as follows: Pi=ni/N, where ni is the band intensity for individual bands and N is the sum of the intensities of all of the bands in a single lane . EH was calculated as follows: EH=H'/lnS , where S is defined as the band amount present in a single lane [32,33].
A phylogenetic tree of the relationship between the sequences of the predominant DGGE bands and those in GenBank determined by BLAST was created through the Neighbour-joining method using Molecular Evolutionary Genetics Analysis (MEGA, version 5.1).
All data were checked for deviations from normality and homogeneity of variance before analysis. The effects of the degree of W. trilobata invasion on soil microbial communities and Shannon–Wiener diversity (H') and Pielou evenness (EH) indices of soil microorganisms were determined by analysis of variances (ANOVA) with site considered as a block effect using Statistical Product and Service Solutions (SPSS, version 17.0). Statistical significance was set at P <0.05.
Soil physicochemical properties
Low degrees of W. trilobata invasion significantly increased soil pH values (Table 2, P < 0.05) whereas high degrees of W. trilobata invasion did not significantly affect soil pH values (Table 2, P > 0.05). Low and high degrees of W. trilobata invasion increased soil moisture; the difference between the effects of high and low degrees of invasion on soil moisture was not significant (Table 2, P > 0.05).
|Invasion situation||Soil pH||Soil moisture||Organic matter||N||P||K||Fe||Mn||Ca||Mg|
Soil Ca concentration under low degrees of W. trilobata invasion was significantly higher than that under high degrees of W. trilobata invasion (Table 2, P < 0.05). K concentrations decreased significantly with increasing degree of W. trilobata invasion (Table 2, P < 0.05). Both low and high degrees of W. trilobata invasion did not significantly change soil organic matter, N, P, Fe, Mn, and Mg concentrations (Table 2, P > 0.05).
The ANOVA results revealed that the degrees of W. trilobata invasion significantly affected the soil Ca concentration (Table 3, P < 0.05). However, the degrees of W. trilobata invasion did not pose obvious effects on other indices of soil physicochemical properties (Table 3, P > 0.05).
|Soil pH||Soil moisture||Organic matter||N||P||K||Fe||Mn||Ca||Mg||H'-B||H'-F||EH-B||EH-F|
DGGE pattern and soil microbial communities' structure
The community structures of soil microorganisms were compared based on DGGE analysis of 16S rRNA and 18S rRNA gene fragments. The DGGE patterns showed remarkable differences in composition among the five sample areas (Figures 1A and 1B). A significant difference was observed between Shannon–Wiener diversity of soil bacterial community and that of soil fungal community under uninvaded and low degrees of W. trilobata invasion but not under high degree of W. trilobata invasion (Figure 2A). The degrees of W. trilobata invasion significantly effected Shannon–Wiener diversity of soil fungal community (Figure 2A; Table 3, P < 0.05). However, both low and high degrees of W. trilobata invasion did not pose significant effects on Shannon–Wiener diversity of soil bacterial community (Figure 2A; Table 3, P > 0.05) or on Pielou evenness of both soil bacterial community and soil fungal community (Figure 2B; Table 3, P > 0.05).
Straight lines indicate the DGGE bands for which the sequence was determined. Arabic numerals lies above the figure represent sample sites.
Symbols: open bars, soil bacterial community; filled bars, soil fungal community. Error bars indicate standard errors (SE, n = 3).
A total of 51 DGGE bands were sequenced, including 21 predominant 16S rRNA gene-based DGGE bands for soil bacterial community and 30 predominant 18S rRNA gene-based DGGE bands for soil fungal community (Figures 1A and 1B). The relationships of the 21 predominant 16S rRNA gene-based DGGE bands and the 30 predominant 18S rRNA gene-based DGGE bands are shown in the phylogenetic tree in Figures 3A and 3B. Obvious differences in the soil microbial communities (especially for the soil bacterial community) were observed among sites with different degrees of W. trilobata invasion (Figures 3A and 3B). For example, low degrees of W. trilobata invasion significantly increased the abundance of bands 1 and 5 of the soil bacterial community in Haikou as well as the abundance of band 5 of the soil bacterial community in Tunchang (Figures 1A and 3A). Increasing degrees of W. trilobata invasion increased the abundance of bands 1 and 5 of soil bacterial community in Sanya (Figures 1A and 3A). Both low and high degrees of W. trilobata invasion decreased the abundance of band 5 of the soil bacterial community in Qionghai (Figures 1A and 3A). Bands 1 and 5 of the soil bacterial community were respectively identified as Nitrobacter and Nitrosomonadaceae through BLAST (Figure 3A).
Soil physicochemical properties
Previous studies have shown that plant invasion significantly elevates soil pH values [34-37]. This result may be mainly attributed to the fact that invasive plants have high nitrate uptake rates, which elevate soil pH values because the decrease in soil nitrate are known to elevate soil pH values [34,38]. Similar values are only obtained under low degrees of W. trilobata invasion in the present study. High degrees of W. trilobata invasion did not significantly affect soil pH values. In previous studies, the metabolic activities and community structure of soil microorganisms were highly correlated with soil pH values [39-41]. Thus, we believe that changes in soil pH values mediated by low degrees of W. trilobata invasion can enhance the succession of soil microbial communities in the rhizosphere and facilitate further invasion. Changes in soil pH values may play a minor role in the invasion process under high degrees of W. trilobata invasion.
Soil moisture is an important driver of plant invasion [42,43]. Many studies have revealed a positive correlation between soil moisture and the degrees of plant invasion [44,45]. Other researchers have found that invasive plants positively affect soil moisture in the invaded ecosystem [37,46] and that soil moisture is a major factor that influences the metabolic activities and community structure of soil microorganisms [47-49]. Therefore, changes in soil moisture induced by invasive plants can affect the changes in soil microbial communities in the rhizosphere and enhance plant invasiveness. However, in the present study, both low and high degrees of W. trilobata invasion did not significantly affect soil moisture. This result indicates that W. trilobata invades ecosystems via pathways other than through soil moisture changes.
Accumulated evidence suggests that invasive plants have high rates of nutrient cycling, especially for N [6,8,14,19-22], and higher soil P availability is often correlated with the invasion degrees of plants [50,51]. Thus, we hypothesize that W. trilobata invasion can enhance soil nutrient element concentrations (especially soil N and P) with increasing invasion degree. Differing from our initial hypothesis, however, the results of the present study showed that both low and high degrees of W. trilobata invasion did not exert significant effects on soil N, soil P, and soil organic matter concentrations. This result is consistent with a previous study  that found neutral effects of plant invasion on soil N or P. Other study  found no difference in soil N concentrations with and without the invasion by Phalaris arundinacea in wet prairie vegetation. The neutral effect of plant invasion on soil N may be because of the compensation of increased N demand with increased N supply . As such, we believe that W. trilobata invades ecosystems via pathways other than through high rates of nutrient cycling.
Structure of soil microbial communities
Several studies have shown that plants successfully invade some environments because these species can accelerate the succession of soil microbial communities in their rhizosphere and promote microbial functions, which facilitate invasion process [5,8-11]. Thus, with continuous increases in anthropogenic activities causing accelerated rates of biological invasion, considerable interest in understanding the ecological effects of plant invasion on soil microbial communities has grown [5,9,55-57]. Some investigators have suggested that invasive plants trigger the changes in the structure of biological communities in invaded ecosystems [1,13,14,58,59], especially soil microbial communities [5,9,55-57], in a way that results in positive feedback for the invading plants and negative feedback for the native plant communities [5,60-62]. Recent studies have confirmed that bacteria dominate soil microbial communities in early succession and that fungi dominate these communities in late succession . Based on this finding, we hypothesized that low degrees of W. trilobata invasion increased the richness of soil bacterial community whereas high degrees of W. trilobata invasion increased the richness of soil fungal community. Results obtained in the present study are only partly consistent with our hypothesis. Both low and high degrees of W. trilobata invasion significantly increased the richness of soil fungal community. However, the richness of soil fungal community showed no significant difference between low and high degrees of W. trilobata invasion. Moreover, both low and high degrees of W. trilobata invasion did not exert significant effects on the richness of soil bacterial community. Thus, the results of the present study show that different degrees of plant invasion can trigger changes in the richness of soil fungal community but not in soil bacterial community. This finding indicates that soil fungal community play an important role in the invasion process of invasive plants. Changes in the soil fungal community mediated by W. trilobata invasion may be attributed to changes in the soil physicochemical properties after plant invasion [1,13,59]. Differences in soil characteristic may also contribute to differences in the invasion degrees of invasive plants as well as the community structure of soil microorganisms. The results of the present study are partly inconsistent with those presented in a previous study , which found that Acacia dealbata invasion can lead to significant increases in the richness of soil bacterial community and significant reductions in the richness of soil fungal community in grassland ecosystems. Differences in results may be attributed to differences in the soil physicochemical properties studied, plant species used, time span of plant invasion, and the time scale of the studies.
Invasive plants often feature faster growth rates and respond more opportunistically to nutrients (especially N) . Several studies [65,66] show that the invasion degree induced by plants is positively correlated with soil nutrients (especially N). Thus, invasive plants may maximize their invasiveness by accelerating soil nutrient cycling (especially N cycling) [67-70], particularly through the changes in the community structure of functional microorganism, such as soil microorganisms that take part in N cycling (i.e., N-fixing bacteria, nitrifying bacteria, nitrosifying bacteria, ammonia oxidizing bacteria, and denitrifying bacteria) [68,69,71-74]. Low degrees of W. trilobata invasion significantly increased the abundance of Nitrobacter and Nitrosomonadaceae in Haikou as well as the abundance of Nitrosomonadaceae in Tunchang. W. trilobata invasion also increased the abundance of Nitrobacter and Nitrosomonadaceae in Sanya but decreased the abundance of these bacteria in Qionghai. This finding indicates that invasive plants show altered invasiveness through changes in community structure of soil microorganisms that take part in N cycling.
The present study sought to determine the effects of different degrees of plant invasion on soil microbial communities to better understand the mechanism of plant invasion. Different degrees of W. trilobata invasion can trigger changes in soil physicochemical properties. Both low and high degrees of W. trilobata invasion significantly increased the richness of soil fungal community but not that of soil bacterial community. Invasive plants can induce changes in the community structure of soil microorganisms that take part in N cycling. Changes in the soil physicochemical properties and community structure of soil microbial communities mediated by W. trilobata invasion may play an important role in facilitating further invasion.
We wish to acknowledge Analysis and Testing Center of Jiangsu University for the analysis of soil nutrient element concentrations. We also greatly appreciate to Sangon Biotech (Shanghai) Co., Ltd. (Shanghai, P. R. China) for the sequencing of PCR products. We are grateful to the two anonymous referees and the academic editor for their constructive comments that improved this manuscript.
Conceived and designed the experiments: DD CW. Performed the experiments: CS XL. Analyzed the data: LW. Contributed reagents/materials/analysis tools: ZD SQ. Wrote the manuscript: CW.
- 1. Hulme PE, Pysek P, Nentwig W, Vilà M (2009) Will threat of biological invasions unite the European Union? Science 324: 40–41. doi:https://doi.org/10.1126/science.1171111. PubMed: 19342572.
- 2. Hickman JE, Wu SL, Mickley LJ, Lerdau MT (2010) Kudzu. (Pueraria montana) invasion doubles emissions of nitric oxide and increases ozone pollution. Proc Natl Acad Sci U_S_A 107: 10115–10119. doi:https://doi.org/10.1073/pnas.0912279107.
- 3. Gurevitch J, Fox GA, Wardle GM, Inderjit , Taub D (2011) Emergent insights from the synthesis of conceptual frameworks for biological invasions. Ecol Lett 14: 407–418. doi:https://doi.org/10.1111/j.1461-0248.2011.01594.x. PubMed: 21513009.
- 4. Powell KI, Chase JM, Knight TM (2013) Invasive plants have scale-dependent effects on diversity by altering species-area relationships. Science 339: 316–318. doi:https://doi.org/10.1126/science.1226817. PubMed: 23329045.
- 5. Kulmatiski A, Beard KH, Stevens JR, Cobbold SM (2008) Plant-soil feedbacks: a meta-analytical review. Ecol Lett 11: 980–992. doi:https://doi.org/10.1111/j.1461-0248.2008.01209.x. PubMed: 18522641.
- 6. van Kleunen M, Weber E, Fischer M (2010) A meta-analysis of trait differences between invasive and non-invasive plant species. Ecol Lett 13: 235–245. doi:https://doi.org/10.1111/j.1461-0248.2009.01418.x. PubMed: 20002494.
- 7. Schmidt JP, Drake JM (2011) Why are some plant genera more invasive than others? PLOS ONE 6: e18654. doi:https://doi.org/10.1371/journal.pone.0018654. PubMed: 21494563.
- 8. Laungani R, Knops JMH (2009) Species-driven changes in nitrogen cycling can provide a mechanism for plant invasions. Proc Natl Acad Sci U S A 106: 12400–12405. doi:https://doi.org/10.1073/pnas.0900921106. PubMed: 19592506.
- 9. Kiers ET, Duhamel M, Beesetty Y, Mensah JA, Franken O et al. (2011) Reciprocal rewards stabilize cooperation in the mycorrhizal symbiosis. Science 333: 880–882. doi:https://doi.org/10.1126/science.1208473. PubMed: 21836016.
- 10. Suding KN, Harpole WS, Fukami T, Kulmatiski A, MacDougall AS et al. (2013) Consequences of plant-soil feedbacks in invasion. J Ecol 101: 298–308. doi:https://doi.org/10.1111/1365-2745.12057.
- 11. Svensson JR, Nylund GM, Cervin G, Toth GB, Pavia H (2013) Novel chemical weapon of an exotic macroalga inhibits recruitment of native competitors in the invaded range. J Ecol 101: 140–148. doi:https://doi.org/10.1111/1365-2745.12028.
- 12. Catford JA, Daehler CC, Murphy HT, Sheppard AW, Hardesty BD et al. (2012) The intermediate disturbance hypothesis and plant invasions: Implications for species richness and management. Perspect - Plant Ecol 14: 231–241. doi:https://doi.org/10.1016/j.ppees.2011.12.002.
- 13. Wilson SD, Pinno BD (2013) Environmentally-contingent behaviour of invasive plants as drivers or passengers. Oikos 122: 129–135. doi:https://doi.org/10.1111/j.1600-0706.2012.20673.x.
- 14. Theoharides KA, Dukes JS (2007) Plant invasion across space and time, factors affecting nonindigenous species success during four stages of invasion. New Phytol 176: 256–273. doi:https://doi.org/10.1111/j.1469-8137.2007.02207.x. PubMed: 17822399.
- 15. Song LY, Li CH, Peng SL (2010) Elevated CO2 increases energy-use efficiency of invasive Wedelia trilobata over its indigenous congener. Biol Invasions 12: 1221–1230. doi:https://doi.org/10.1007/s10530-009-9541-1.
- 16. Wu W, Zhou RC, Huang HR, Ge XJ (2010) Development of microsatellite loci for the invasive weed Wedelia trilobata (Asteraceae). Am J Bot 97: e114-e116. doi:https://doi.org/10.3732/ajb.1000327. PubMed: 21616811.
- 17. Lowe S, Browne M, Boudjelas S, De Poorter M (2000). p. 100. of the World's Worst Invasive Alien Species A selection from the Global Invasive Species Database. The Invasive Species Specialist Group (ISSG) a specialist group of the Species Survival Commission (SSC) of the World Conservation Union. IUCN. 12 pp.
- 18. Xie LJ, Zeng RS, Bi HH, Song YY, Wang RL et al. (2010) Allelochemical mediated invasion of exotic plants in China. Allelopathy J 25: 31−50.
- 19. Li WH, Zhang CB, Lin JY, Yang CJ (2008) Characteristics of nitrogen metabolism and soil nitrogen of invasive plants. J Trop Subtrop Bot 16: 321–327.
- 20. Ke ZH, Qiu PX, Hu DX, Zhu H, Song LY (2013) Effects of Wedelia trilobata invasion on soil enzyme activities and physical-chemical properties. Ecol - Journal of Environ Sci 22: 432–436. (in Chinese).
- 21. Feng YL, Lei YB, Wang RF, Callaway RM, Valiente-Banuet A et al. (2009) Evolutionary tradeoffs for nitrogen allocation to photosynthesis versus cell walls in an invasive plant. Proc Natl Acad Sci U_S_A 106: 1853–1856. doi:https://doi.org/10.1073/pnas.0808434106.
- 22. Jones RO, Chapman SK (2011) The roles of biotic resistance and nitrogen deposition in regulating non-native understory plant diversity. Plant Soil 345: 257–269. doi:https://doi.org/10.1007/s11104-011-0778-y.
- 23. Jiang JP, Xiong YC, Jiang HM, Ye DY, Song YJ et al. (2009) Soil microbial activity during secondary vegetation succession in semiarid abandoned lands of Loess Plateau. Pedosphere 19: 735–747. doi:https://doi.org/10.1016/S1002-0160(09)60169-7.
- 24. Fu QL, Liu C, Ding NF, Lin YC, Guo B et al. (2012) Soil microbial communities and enzyme activities in a reclaimed coastal soil chronosequence under rice-barley cropping. J Soils Sed 12: 1134–1144. doi:https://doi.org/10.1007/s11368-012-0544-7.
- 25. Muyzer G, Brinkhoff T, Ulrich N, Santegoeds C, Schafer H, et al. (1998) Denaturing gradient gel electrophoresis (DGGE) in microbial ecology. Mol Microb Ecol Manual 3.4.4: 1–27.
- 26. May LA, Smiley B, Schmidt MG (2001) Comparative denaturing gradient gel electrophoresis analysis of fungal communities associated with whole plant corn silage. Can J Microbiol 47: 829–841. doi:https://doi.org/10.1139/w01-086. PubMed: 11683465.
- 27. Hoshino YT, Morimoto S (2008) Comparison of 18S rDNA primers for estimating fungal diversity in agricultural soils using polymerase chain reaction-denaturing gradient gel electrophoresis. Soil Sci Plant Nutr 54: 701–710. doi:https://doi.org/10.1111/j.1747-0765.2008.00289.x.
- 28. Roesti D, Gaur R, Johri BN, Imfeld G, Sharma S et al. (2006) Plant growth stage, fertiliser management and bio-inoculation of arbuscular mycorrhizal fungi and plant growth promoting rhizobacteria affect the rhizobacterial community structure in rain-fed wheat fields. Soil Biol Biochem 38: 1111–1120. doi:https://doi.org/10.1016/j.soilbio.2005.09.010.
- 29. Shannon CE, Weaver W (1949) The Mathematical Theory of Communication. University of Illinois Press, Urbana, IL. pp. 1–117.
- 30. Ikenaga M, Guevara R, Dean AL, Pisani C, Boyer JN (2010) Changes in community structure of sediment bacteria along the Florida Coastal Everglades Marsh-Mangrove-Seagrass salinity gradient. Microb Ecol 59: 284–295. doi:https://doi.org/10.1007/s00248-009-9572-2. PubMed: 19705193.
- 31. Pielou EC (1966) The measurement of diversity in different types of biological collections. J Theor Biol 13: 131–144. doi:https://doi.org/10.1016/0022-5193(66)90013-0.
- 32. Vivas A, Moreno B, del Val C, Macci C, Masciandaro G et al. (2008) Metabolic and bacterial diversity in soils historically contaminated by heavy metals and hydrocarbons. J Environ Monit 10: 1287–1296. doi:https://doi.org/10.1039/b808567f. PubMed: 18974897.
- 33. Vivas A, Moreno B, García-Rodriguez S, Benítez E (2009) As assessing the impact of composting and vermicomposting on structural diversity of bacterial communities and enzyme activities of an olive-mill waste. Bioresource Technol 100: 1319–1326. doi:https://doi.org/10.1016/j.biortech.2008.08.014.
- 34. Ehrenfeld JG, Kourtev P, Huang W (2001) Changes in soil functions following invasions of exotic understory plants in deciduous forests. Ecol Appl 11: 1287–1300. Available online at: doi:10.1890/1051-0761(2001)011[1287:CISFFI]2.0.CO;2.
- 35. Sharma GP, Raghubanshi A (2007) Effect of Lantana camara L. cover on local depletion of tree population in the Vindhyan tropical dry deciduous forest of India. Appl Ecol Environ Res 5: 109–121.
- 36. Fan L, Chen Y, Yuan JG, Yang ZY (2010) The effect of Lantana camara Linn. invasion on soil chemical and microbiological properties and plant biomass accumulation in southern China. Geoderma 154: 370–378. doi:https://doi.org/10.1016/j.geoderma.2009.11.010.
- 37. Kuebbing SE, Classen AT, Simberloff D (2013) Two co-occurring invasive woody shrubs alter soil properties and promote subdominant invasive species. J Appl Ecol. doi:https://doi.org/10.1111/1365-2664.12161.
- 38. Chen T, Liu WL, Zhang CB, Wang J (2012) Effects of Solidago canadensis invadation on dynamics of native plant communities and their mechanisms. Chin J Plant Ecol 36: 253–261. (in Chinese). doi:https://doi.org/10.3724/SP.J.1258.2012.00253.
- 39. Hackl E, Pfeffer M, Donat C, Bachmann G, Zechmeister-Boltenstern S (2005) Composition of the microbial communities in the mineral soil under different types of natural forest. Soil Biol Biochem 37: 661–671. doi:https://doi.org/10.1016/j.soilbio.2004.08.023.
- 40. Högberg MN, Högberg P, Myrold DD (2007) Is microbial community composition in boreal forest soils determined by pH, C-to-N ratio, the trees, or all three? Oecologia 150: 590–601. PubMed: 17033802.
- 41. Li WH, Zhang CB, Jiang HB, Xin GR, Yang ZY (2006) Changes in soil microbial community associated with invasion of the exotic weed, Mikania micrantha H.B.K. Plant Soil 281: 309–324. doi:https://doi.org/10.1007/s11104-005-9641-3.
- 42. Booth MS, Caldwell MM, Stark JM (2003) Overlapping resource use in three Great Basin species: implications for community invasibility and vegetation dynamics. J Ecol 91: 36–48. doi:https://doi.org/10.1046/j.1365-2745.2003.00739.x.
- 43. Wood YA, Meixner T, Shouse PJ, Allen EB (2006) Altered ecohydrologic response drives native shrub loss under conditions of elevated nitrogen deposition. J Environ Qual 35: 76–92. doi:https://doi.org/10.2134/jeq2004.0465. PubMed: 16391279.
- 44. Huebner CD, Tobin PC (2006) Invasibility of mature and 15-year-old deciduous forests by exotic plants. Plant Ecol 186: 57–68. doi:https://doi.org/10.1007/s11258-006-9112-9.
- 45. Chytry M, Maskell LC, Pino J, Pysek P, Vila M et al. (2008) Habitat invasions by alien plants: a quantitative comparison among Mediterranean, subcontinental and oceanic regions of Europe. J Appl Ecol 45: 448–458. doi:https://doi.org/10.1111/j.1365-2664.2007.01398.x.
- 46. Yelenik SG, Stock WD, Richardson DM (2004) Ecosystem level impacts of invasive Acacia saligna in the South African Fynbos. Restor Ecol 12: 44–51. doi:https://doi.org/10.1111/j.1061-2971.2004.00289.x.
- 47. McLean MA, Huhta V (2000) Temporal and spatial fluctuations in moisture affect humus microfungal community structure in microcosms. Biol Fertil Soils 32: 114–119. doi:https://doi.org/10.1007/s003740000225.
- 48. Papatheodorou EM, Argyropoulou MD, Stamou GP (2004) The effects of large- and small-scale differences in soil temperature and moisture on bacterial functional diversity and the community of bacterivorous nematodes. Appl Soil Ecol 25: 37–49. doi:https://doi.org/10.1016/S0929-1393(03)00100-8.
- 49. Dijkstra FA, Cheng W (2007) Moisture modulates rhizosphere effects on C decomposition in two different soil types. Soil Biol Biochem 39: 2264–2274. doi:https://doi.org/10.1016/j.soilbio.2007.03.026.
- 50. Thorpe AS, Archer V, Deluca TH (2006) The invasive forb Centaurea maculosa increases phosphorus availability in Montana grasslands. Appl Soil Ecol 32: 118–122. doi:https://doi.org/10.1016/j.apsoil.2005.02.018.
- 51. Weidenhamer JD, Callaway RM (2010) Direct and indirect effects of invasive plants on soil chemistry and ecosystem function. J Chem Ecol 36: 59–69. doi:https://doi.org/10.1007/s10886-009-9735-0. PubMed: 20077127.
- 52. Scharfy D, Güsewell S, Gessner MO, Venterink HO (2010) Invasion of Solidago gigantea in contrasting experimental plant communities: effects on soil microbes, nutrients and plant-soil feedbacks. J Ecol 98: 1379–1388. doi:https://doi.org/10.1111/j.1365-2745.2010.01722.x.
- 53. Herr-Turoff A, Zedler JB (2005) Does wet prairie vegetation retain more nitrogen with or without Phalaris arundinacea invasion? Plant Soil 277: 19−34. doi:https://doi.org/10.1007/s11104-004-5980-8.
- 54. Windham L, Ehrenfeld JG (2003) Net impact of a plant invasion on nitrogen-cycling processes within a brackish tidal marsh. Ecol Appl 13: 883–896. doi:https://doi.org/10.1890/02-5005.
- 55. Reinhart KO, Callaway RM (2006) Soil biota and invasive plants. New Phytol 170: 445–457. doi:https://doi.org/10.1111/j.1469-8137.2006.01715.x. PubMed: 16626467.
- 56. te Beest M, Stevens N, Olff H, van der Putten WH (2009) Plant-soil feedback induces shifts in biomass allocation in the invasive plant Chromolaena odorata. J Ecol 6: 1281–1290.
- 57. Wardle DA, Bardgett RD, Callaway RM, van der Putten WH (2011) Terrestrial ecosystem responses to species gains and losses. Science 332: 1273–1277. doi:https://doi.org/10.1126/science.1197479. PubMed: 21659595.
- 58. van der Wal R, Truscott AM, Pearce ISK, Cole L, Harris MP et al. (2008) Multiple anthropogenic changes cause biodiversity loss through plant invasion. Global Change Biol 14: 1428–1436. doi:https://doi.org/10.1111/j.1365-2486.2008.01576.x.
- 59. Butchart SHM, Walpole M, Collen B, Strien A, van Scharlemann JPW et al. (2010) Global biodiversity: indicators of recent declines. Science 328: 1164‒1168. doi:https://doi.org/10.1126/science.1187512. PubMed: 20430971.
- 60. Callaway RM, Cipollini D, Barto K, Thelen GC, Hallett SG et al. (2008) Novel weapons: invasive plant suppresses fungal mutualists in America but not in its native Europe. Ecology 89: 1043–1055. doi:https://doi.org/10.1890/07-0370.1. PubMed: 18481529.
- 61. Callaway RM, Thelen GC, Rodriguez A, Holben WE (2004) Soil biota and exotic plant invasion. Nature 427: 731–733. doi:https://doi.org/10.1038/nature02322. PubMed: 14973484.
- 62. Sanon A, Beguiristain T, Cébron A, Berthelin J, Sylla SN et al. (2012) Differences in nutrient availability and mycorrhizal infectivity in soils invaded by an exotic plant negatively influence the development of indigenous Acacia species. J Environ Manage 95: S275–S279. doi:https://doi.org/10.1016/j.jenvman.2011.01.025. PubMed: 21342746.
- 63. Lorenzo P, Rodrĺguez-Echeverrĺa S, González L, Freitas H (2010) Effect of invasive Acacia dealbata Link on soil microorganisms as determined by PCR-DGGE. Appl Soil Ecol 44: 245–251. doi:https://doi.org/10.1016/j.apsoil.2010.01.001.
- 64. Davidson AM, Jennions M, Nicotra AB (2011) Do invasive species show higher phenotypic plasticity than native species and, if so, is it adaptive? A meta-analysis. Ecol Lett 14: 419–431. doi:https://doi.org/10.1111/j.1461-0248.2011.01596.x. PubMed: 21314880.
- 65. Ehrenfeld JG (2003) Effects of exotic plant invasions on soil nutrient cycling processes. Ecosystems 6: 503–523. doi:https://doi.org/10.1007/s10021-002-0151-3.
- 66. Howard TG, Gurevitch J, Hyatt L, Carreiro M, Lerdau M (2004) Forest invasibility in communities in southeastern New York. Biol Invasions 6: 393–410. doi:https://doi.org/10.1023/B:BINV.0000041559.67560.7e.
- 67. Asner GP, Vitousek PM (2005) Remote analysis of biological invasion and biogeochemical change. Proc Natl Acad Sci U S A 102: 4383–4386. doi:https://doi.org/10.1073/pnas.0500823102. PubMed: 15761055.
- 68. Hawkes CV, Wren IF, Herman DJ, Firestone MK (2005) Plant invasion alters nitrogen cycling by modifying the soil nitrifying community. Ecol Lett 8: 976–985. doi:https://doi.org/10.1111/j.1461-0248.2005.00802.x.
- 69. Liao CZ, Peng RH, Luo YQ, Zhou XH, Wu XW et al. (2008) Altered ecosystem carbon and nitrogen cycles by plant invasion: a meta analysis. New Phytol 177: 706–714. doi:https://doi.org/10.1111/j.1469-8137.2007.02290.x. PubMed: 18042198.
- 70. Elgersma KJ, Ehrenfeld JG, Yu S, Vor T (2011) Legacy effects overwhelm the short-term effects of exotic plant invasion and restoration on soil microbial community structure, enzyme activities, and nitrogen cycling. Oecologia 167: 733–745. doi:https://doi.org/10.1007/s00442-011-2022-0. PubMed: 21618010.
- 71. Zou JW, Rogers WE, DeWalt SJ, Siemann E (2006) The effect of Chinese tallow tree (Sapium sebiferum) ecotype on soil-plant system carbon and nitrogen processes. Oecologia 150: 272–281. doi:https://doi.org/10.1007/s00442-006-0512-2. PubMed: 16917777.
- 72. Niu HB, Liu WX, Wan FH, Liu B (2007) An invasive aster (Ageratina adenophora) invades and dominates forest understories in China: altered soil microbial communities facilitate the invader and inhibit natives. Plant Soil 294: 73–85. doi:https://doi.org/10.1007/s11104-007-9230-8.
- 73. Cui QG, He WM (2009) Soil biota, but not soil nutrients, facilitate the invasion of Bidens pilosa relative to a native species Saussurea deltoidea. Weed Res 49: 201–206. doi:https://doi.org/10.1111/j.1365-3180.2008.00679.x.
- 74. Dassonville N, Guillaumaud N, Piola F, Meerts P, Poly F (2011) Niche construction by the invasive Asian knotweeds (species complex Fallopia): impact on activity, abundance and community structure of denitrifiers and nitrifiers. Biol Invasions 13: 1115–1133. doi:https://doi.org/10.1007/s10530-011-9954-5.