Figures
Abstract
This research was designed to explore the variation characteristics of soil C:N:P stoichiometry and enzyme activity in the Qilian Mountains different grassland types. Thus, 7 grassland types (Upland meadow: UM, Alpine meadow: AM, Temperate steppe: ST, Alpine steppe: AS, Temperate Desert Steppe: TDS, Temperate Desert: TD, Alpine desert: AD) of Qilian Natural Reserve were selected to analyze the variation characteristics of soil enzyme activities and stoichiometry of different grassland types and its relationship with environmental factors. The study indicated that the C/N, C/P, and N/P of different grasslands ranged from 5.08 to 17.35, 2.50 to 72.29, and 0.53 to 4.02.The ranking of different types grassland for the C/N was TS ≥ AM ≥ UM ≥ AS ≥ TDS > AD > TD, and the changing pattern of C/P and N/P is similar to that of C/N. The ranking of different types grassland for the urease enzyme activity was UM ≈AS > AD ≈TDS ≈TS ≈AM > TD, and TS ≈AM ≈UM ≈AS ≈AD > TDS > TD for alkaline phosphatase enzyme activity, and AS ≈AM ≈TS ≈TDS≥UM ≥TD ≈AD for catalase enzyme activity. Based on N/P ratio and RDA analysis, nitrogen was the main factor limiting the grassland productivity, and pH, TN, SOC, Richness index and Simpson diversity index were the main environmental factors affecting the soil C:N:P stoichiometry and enzyme activities. Cluster analysis showed that 7 grassland types were clustered into three categories. In conclusion, the stoichiometric characteristics and soil enzyme activities of different grasslands vary with grassland types. Nitrogen was the main factor limiting the grasslands productivity, and pH, TN, SOC, Richness index and Simpson diversity index were the main environmental factors affecting the soil C:N:P stoichiometry and enzyme activities, and the grassland Qilian Mountain can be managed in the ecological district according to the clustering results. The results of this study can provide data support and theoretical guidance for the scientific management and ecological protection of grassland in Qilian Mountains Reserve.
Citation: Li Q, Yang J, He G, Liu X, Zhang D (2022) Characteristics of soil C:N:P stoichiometry and enzyme activities in different grassland types in Qilian Mountain nature reserve-Tibetan Plateau. PLoS ONE 17(7): e0271399. https://doi.org/10.1371/journal.pone.0271399
Editor: Dafeng Hui, Tennessee State University, UNITED STATES
Received: November 20, 2021; Accepted: June 29, 2022; Published: July 14, 2022
Copyright: © 2022 Li 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.
Data Availability: All relevant data are within the article and its Supporting Information files.
Funding: This study was supported by National Natural Science Foundation of China (31160475; 61401439); A new round of grassland Reward and subsidy Benefit evaluation and grassland ecological evaluation in Gansu Province (XZ20191225). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors declare no competing interests.
Introduction
Ecological chemometrics is a theoretical science that explores the regular changes in the ratios of chemical elements (mainly carbon, nitrogen, phosphorus, and potassium) caused by the disturbance of external factors that affect the conservation of energy flow and material cycles in ecosystems, and provides a simpler way to research the mechanism of interexistence between chemical elements and energy cycle of biological substances [1,2]. Carbon (C), nitrogen (N), phosphorus (P) and potassium (K) are the macronutrients of the soil and the main constituent elements of the plant organism. The decomposition of dead branches and leaves returns some of the nutrients to the soil, which continues to provide the necessary nutrients for healthy plant growth [3–5]. Soil, as an indispensable component of grassland ecosystems, is also the place where vegetation communities survive and develop, and the succession process of vegetation communities in turn affects the soil development process, and the two are dependent on each other and mutually constrained [6–8]. Therefore, the influence of soil ecological chemometric characteristics on nutrient cycling and ecosystem balance in grasslands cannot be ignored. Soil enzymes are mainly derived from residues of microorganisms, animals, plants and secretions from their metabolic processes [9,10], actively participating in the biochemical process of the soil system and a key link of "plant-soil enzyme-soil nutrients" [11]. As important indicators of soil fertility evaluation, soil enzyme activity and soil nutrients play an important role in material circulation and energy transformation of soil ecosystems [12], indirectly affecting the circulation of carbon, nitrogen, phosphorus and other elements in the soil. In the context of global climate change, soil enzymes are increasingly critical in the ecologically fragile Qilian Mountain grassland ecosystem [9]. Studies found that [13–15] soil enzymes in various vegetation and grassland have different sensitivity to water and heat, while the sensitivity of the same soil enzyme was also different under vegetation types. Therefore, the influence of soil enzyme characteristics on nutrient cycling and ecosystem balance in grasslands cannot be ignored.
Qilian Mountain is located on the eastern edge of the Tibet Plateau in China, adjacent to the Mongolian Plateau and the Loess Plateau [16]. It is the birthplace of the inland rivers for Heihe, Shiyang and Shule, the water source of the Hexi Oasis in northwest China [17], and also one of the most sensitive regions for global climate change [17–19]. Due to altitude and region differences, Qilian Mountains boasts many types of grassland and the grasslands was the largest vegetation type in this region [20]. The study found that, changes in grassland types could cause changes in many natural factors and ecological processes [21], such as soil enzyme activity, soil nutrients [22–25], and vegetation characteristics [26,27]. At present, what are the changing patterns of soil ecological chemometric characteristics and soil enzyme activity of different grassland types in Qilian Mountain? And there is no relevant explanation for this scientific question. Scholars had conducted more studies on Qilian Mountain grasslands, but these studies have mainly focused on vegetation characteristics, biodiversity and soil nutrients [6,7,13–15,28], and no studies have been reported on soil ecological chemometrics and soil enzyme activities in different grassland types. This paper selected the Qilian Mountain grassland as the research object, to identified the characteristics changes of soil stoichiometric and enzyme activity in different grassland types. To explore the following questions: 1) Are there nutrient limitations in different grassland types in the Qilian Mountains? 2) What are the environmental factors that affect grassland soil stoichiometric characteristics and soil enzyme activities? 3) Is the Qilian Mountains grassland managed in different zones according to the grassland types? The solution of the above scientific problems will further reveal the relationship between the nutrient cycling mechanism and ecosystem balance in the Qilian Mountains, and provide a basis for the protection and scientific management of the local grassland ecosystem.
Materials and methods
Study area
The study sites were located in the Qilian Mountains Nature Reserve of eastern Qinghai-Tibetan Plateau, China (94°10′-103°04′E, 35°50′-39°19′N) (http://www.qilianshan.com.cn/html/1/271/160/168/index.html). At the horizontal direction, four vegetation zones existed in the order of forest, shrub, grassland and desert from southeast to northwest. At the vertical direction, three vegetation belts are distributed as steppe, forest and alpine meadow from low to high altitude (856–5564 m). The main soil types are aridisols, inceptisols and entisols. The precipitation varies from 100 to 500 mm, from June to September. The average annual temperature is approximately -2.0°C; the average annual relative humidity range is 20%-70%; the annual evaporation is 1200–1400 mm; the frost-free period is 90–120 days [20].
Sample selection
This research area was mainly focused on the Qilian mountain nature reserve in Gansu Province, China. The grassland types and utilization were showed in Table 1. Plant species in the sample field were identified and classified by the grassland College of Gansu Agricultural University. Although the voucher specimen of plant species has not been deposited in a publicly available herbarium, plant species can be investigated in the field. Meanwhile, the plant and soil samples were collected with permission from the Qilian Mountains Nature Reserve Administration, Gansu province, China. All authors committed that all methods were carried out in accordance with relevant guidelines and regulations.
Sample collection
The sampling time was from July to August 2019, when the plants were in full bloom. The central area of the typical distribution area of the above 7 grassland types (Upland meadow: UM, Alpine meadow: AM, Temperate steppe: ST, Alpine steppe: AS, Temperate Desert Steppe: TDS, Temperate Desert: TD, Alpine desert: AD) were selected for the sampling sites (Table 1). A total of 6 random sampling quadrates (1 m × 1 m) were selected in each site. In each quadrate, plant species, coverage, height, the density of the respective species and aboveground biomass were measured and recorded. Aboveground parts of the green plants of the respective species were harvested by clipping to the soil surface. All the aboveground plant samples were placed into envelopes and then tagged, respectively. All the green plant samples were immediately dried at 105°C for 0.5 h, then oven-dried at 60°C for 48 h and weighed [20].
Meanwhile, a 60-meter sample line was set for each sample site. The sample spots were set at a 20-meter interval. Four soil samples were taken around each sample spot using soil drills with a depth of 0–30 cm, respectively. Four soil samples from each layer were mixed as one sample. The samples were put into a sample bag and taken back indoors for air-drying, measured for soil organic matter, Total N, Total P, pH and soil enzyme activity.
Sample determination
Soil samples were air-dried at room temperature, where visible roots and other debris were removed. Each composite soil sample was sieved through a 2-mm sieve. The Walkley-Black method was used to determine soil organic matter [29]. the Kjeldahl acid digestion method was used to determine total N (Foss Kjeltec 8400, FOSS, DK) [29]. The Mo-Sb colorimetry (UV-2102C, UNICO, Shanghai, China) was used to measure the total P [29]. The potential method (water/soil ratio: 2.5: 1) was used to measure soil pH value. the phenol sodium-hypochlorite sodium colorimetric method was used to measure urease enzyme activity [30]. According the amount of glucose (mg) generated in a 1-g soil sample after cultivation at 37°C for 24 h was calculated Sucrase enzyme activity [30]. The disodium phenyl phosphate method was used to measure alkaline phosphatase enzyme activity [30]. The KMnO4 titration was used to measure catalase enzyme activity [30].
Statistical analyses
Data statistics and plotting were carried out by Excel 19.0. All results were presented as mean and standard deviations. One-way ANOVA (P < 0.05), Correlation and cluster analysis were performed with SPSS version 19.0 (SPSS Inc., Chicago, IL, USA). PCA analysis was performed using Canoco 5.0.
The IV (Important Values) of each plant species was calculated by the following formula [14,31]:
(1)
Plant diversity was estimated using the three standard multi-dimensional biodiversity indices, i.e., Pielou Evenness index, Shannon-Weiner (H’). Simpson diversity index was calculated based on the following equations.
(2)
where H’ represents the Shannon-Weiner index; Pi, the total number of individual species proportion of ith species in the community; S, the encountered species number; Pi, the proportion of the total number of individual species belonging to I th species in the community; ln Pi, the natural logarithm of Pi.
(3)
where S represents encountered species number; Pi, the total number of individual species proportion of i th species in the community.
(4)
where H’ represents the Shannon-Weiner index; S, the number of species
(5)
where S means the number of species.
Result
Vegetation characteristics and soil nutrient
Total coverage of different grassland types ranged from 28.33% to 85.00% (Table 2), the ranking of different types grassland for was AM ≈ UM ≈TS ≈ AS> TDS >TD ≈ AD. And grass layer height of different grassland types ranged from 5.63 to 27.20 cm (Table 2), the ranking of different types grassland for was TD ≈ AD > TS ≈ AS ≈ UM > AM >TDS. And AGB of different grassland types ranged from 136 to 486 g·m-2 (Table 2), the ranking of different types grassland for was TS ≈ AS ≈ UM > TD ≈ AM >TDS > AD. The variation pattern of Shannon Weiner diversity index in different grassland types was similar to that of AGB. And Pielou Evenness index of different grassland types ranged from 0.92 to 0.99 (Table 2), the ranking of different types grassland for was TS ≈ AS ≈ UM > TD ≈ AM >TDS > AD. Pielou Evenness index of different grasslands ranged from 0.92 to 0.99, the Pielou Evenness index in AD was higher than that in AS, in AS was higher than that in AD, but no significant differences were found between other treatments. Simpson diversity index of different grasslands ranged from 0.09 to 0.31, the ranking of different types grassland for was TD > TDS ≈ AD > TS ≈ AS ≈ UM ≈AM. Richness index of different grasslands ranged from 3.52 to 9.24, the ranking of different types grassland for was TS ≈ AS > UM ≈AM > TD ≈ TDS ≈ AD. The pH of different grasslands ranges from 7.63 to 8.54(Fig 1A), the pH in TD and TDS was higher than that in UM, AS, and AD, and in UM, AS and AD was higher than that in AM, but no significant differences were found between other treatments. The SOC of different grasslands ranged from 2.87 to 75.93 g kg-1(Fig 1B), The ranking of different types grassland f was TS ≈ AM > AS > AD > TDS ≈TD. The variation pattern of total N in different grassland types was similar to that of SOC (Fig 1C).
Different lower-case letters mean different type grasslands significant differences at 0.05 level. TS, Temperate steppe; AM, Alpine meadow; AS, Alpine steppe; UM, Upland meadow; AD, Alpine desert; TDS, Temperate Desert Steppe; TD, Temperate Desert.
The total P of different grasslands ranges from 1.03 to 1.79 g kg-1(Fig 1D), The ranking of different types grassland was AM ≈ UM > TS ≈ AS > TD ≈ AD ≈ TDS.
Stoichiometric ratio of C, N, and P
The C/N of different grasslands ranged from 5.08 to 17.35 (Fig 2A). C/N in TS was higher than that in UM and AS, and in AM was higher than that in TDS, and in AD, UM, and AS is higher than that in TD, but no significant differences were found between other treatments. The C/P of different grasslands ranged from 2.50 to 72.29 (Fig 2B). The N/P of different grasslands ranges from 0.53 to 4.02 (Fig 2C). The changing pattern of C/P and N/P is similar to that of C/N. N/P ratio can be used as an index for determining the nutrient factors that limit productivity, and N/P<10 and N/P > 20 are used as indicators to evaluate the productivity of vegetation limited by nitrogen or phosphorus (Li et al., 2018). The N/P of different grasslands ranged from 0.53 to 4.04, while the plants’ productivity of different grassland was mainly limited by nitrogen.
Soil enzyme activity
Fig 3A shows that the urease enzyme activity of different grasslands is from 0.03 to 0.62 mg·g-1·24h-1. Urease enzyme activity in UM and AS was higher than that in AM, TS, TDS, and AD, and was higher than that in TD, but no significant differences were found between other treatments. The ranking of different types grassland for the urease enzyme activity was UM ≈ AS > AD ≈ TDS ≈ TS ≈ AM > TD. Alkaline phosphatase enzyme activity of different grasslands ranged from 2.46 to 69.09 mg·g-1·24h-1 (Fig 3B). The enzyme activity of alkaline phosphatase in UM, AM, TS, AD, and AS was higher than that in TDS, and in TDS was higher than that in TD, but no significant differences were found between other treatments. Therefore, the alkaline phosphatase enzyme activity was in a ranking order of TS ≈ AM ≈ UM ≈ AS ≈ AD > TDS > TD. Catalase enzyme activity of different grasslands ranges from 2.46 to 69.09 mg·g-1·24h-1 (Fig 3C). The catalase enzyme activity in AM, TS, and AS was higher than that in AD, but no significant differences were found between other treatments. Therefore, catalase enzyme activity was in a ranking order of AS ≈ AM ≈ TS ≈ TDS≥ UM ≥ TD ≈ AD. Sucrase enzyme activity of different grasslands ranged from 0.03 to 2.29 mg·g-1·24h-1 (Fig 3D). Sucrase enzyme activity in TD was lower than that in UM, AM, TS, AD, TDS, and AS, but no significant differences were found between other treatments.
Relationship between soil stoichiometric, enzyme activity and environmental factors
The correlations between soil stoichiometric, enzyme activity and environmental factors are shown in Table 3. There were significantly correlations between C/N and total coverage, Shannon-Weiner, Simpson diversity, Richness, pH, SOC, TN (P < 0.05). There were significantly correlations between C/P and Shannon-Weiner, Richness, pH, SOC, TN (P < 0.05). There were significantly correlations between N/P and Shannon-Weiner, Richness, pH, SOC, TN (P < 0.05). There were significantly correlations between Alkaline phosphatase and total coverage, Shannon-Weiner, Simpson diversity, Richness, pH, SOC, TN (P < 0.05). There was significantly correlations between Catalase and total coverage (P < 0.05). RDA analysis was carried out on the environmental factors and soil soil stoichiometric, enzyme activity in Fig 4. As shown Fig 4, in the first two axes of environmental factors explained 99.97% (Fig 4A) and 99.87% (Fig 4B) of soil stoichiometric and enzyme activity, which had biological statistical significance. That was, the first two axes can more completely reflect the information of soil stoichiometric and enzyme activity with environmental factors. Based on the Monte Carlo test in the RDA analysis (Table 4), Richness index, SOC and TN significantly affected soil stoichiometric (P < 0.05), while Simpson diversity index and pH significantly affected soil activity (P < 0.05). That was, pH, TN, SOC, Richness index and Simpson diversity index were the main environmental factors affecting the soil C:N:P stoichiometry and enzyme activities in different grassland types in Qilian Mountain nature reserve. Cluster analysis based on vegetation and soil variables shows that 7 grassland types are clustered into three categories (Fig 5). The first category was UM, AS, AM, TS, the second category was TDS and TD, and the third category was AD.
RDA analysis of soil stoichiometric (A) and enzyme activity (B) with environmental factors. Note: Alklphos: Alkaline phosphatase; SimDivIn: Simpson diversity index; Grsslayhe: Grass layer height; PieEvin: Pielou Evenness index; Richindex: Richness index.
Discussion
Soil ecological stoichiometric characteristics (C/N, C/P, and N/P) have a strong regulatory effect on the carbon fixation process in terrestrial ecosystems (Zhang et al., 2016) [32], which is an important parameter to measure soil quality [33], reflecting the ability of soil to release nitrogen and mineralized phosphate nutrients. Due to the influence of climate, landform, soil biology, and human interference, the total amount of soil carbon, nitrogen, and phosphorus varies greatly [34,35]. Among them, C/N is an indicator of the decomposition speed of soil organic matter, which affects the internal circulation of soil C and N elements, and is inversely proportional to the rate of organic matter decomposition [36]. C/P is a reflection of the P release and P sequestration potential of soil decomposing organic matter [37,38]. N/P is an indicator of the abundance and deficiency of soil nutrient supply [39]. In ours research, C/N of different grasslands ranged from 5.08 to 17.35, C/P of different grasslands ranged from 2.50 to 72.29, and N/P of different grasslands ranged from 0.53 to 4.04. That was, the overall organic matter decomposition in Qilian Mountains grasslands was slow and the mineralized decomposition P capacity was limited, and the plants’ productivity of different grassland was mainly limited by nitrogen. In ours research, there were significant differences in C/N, C/P, and N/P among different grassland types, and the water and heat conditions in the distribution areas of different grassland types were different, which was the main reason for the differences in C/N, C/P, and N/P. At the same time, since C and N almost simultaneously respond to environmental changes, this also indirectly reflects the principle of stoichiometry, that is, C and N are structural components, and the organic matter accumulation formation and digestion require relative amounts of N, fixed amount of C and other nutrients.
Soil enzymes can decompose complex organic compounds into smaller organic compounds and inorganic nutrients. Soil enzymes are the most active and sensitive components in soil, promoting the nutrient cycle of soil and the supply of nutrients needed for plant growth [40]. Soil enzymes are an important index for evaluating the soil quality of different grasslands [41,42]. In ours research, there were significant differences in alkaline phosphatase, urease, sucrase, and catalase among different grassland types.Due to differences in the distribution area and plant composition of different grasslands, the characteristics of vegetation community structure (height, coverage) are different, leading to heterogeneity in the absorption of light and heat resources, further causing differences in hydrothermal conditions and aeration conditions in soil [4,43]. Besides, the difference in growth status and litter of different grasslands affects soil microbial biomass and flora composition, thus leading to differences in soil enzyme activity [31].
There are interactions between soil stoichiometric characteristics, soil enzyme activities and environmental factors. And vegetation characteristics, and soil indicators of grassland are the most intuitive forms to characterize the attributes and characteristics of grassland [19,20]. In ours research, there were significantly correlations between C/N and total coverage, Shannon-Weiner, Simpson diversity, Richness, pH, SOC, TN, and significantly correlations between C/P and Shannon-Weiner, Richness, pH, SOC, TN, and significantly correlations between N/P and Shannon-Weiner, Richness, pH, SOC, TN, which was reflecting the coupling relationship between soil stoichiometric characteristics and environmental factors. Meanwhile, RDA analysis found that, Richness index, SOC and TN significantly affected soil stoichiometric, which was similar to the findings of Deng et al [44]. Abiotic factors can indirectly affect soil enzyme activity by altering soil microbial activity or community structure [12], while soil nutrient cycling and carbon turnover depend on soil enzyme activity [45]. The key factors affecting soil enzyme activity (SOM content, N:P, total nitrogen content, number of bacteria, number of fungi, number of actinomycetes) include both biological and abiotic factors. In ours research, there were significantly correlations between Alkaline phosphatase and total coverage, Shannon-Weiner, Simpson diversity, Richness, pH, SOC, TN, and significantly correlations between Catalase and total coverage. Meanwhile, RDA analysis found that, Simpson diversity index and pH significantly affected soil activity, which was similar to the findings of Wang et al. [46]. The seven grassland types were clustered into three categories (AD, TDS and TD, others types grassland). That was, different types of grasslands in the Qilian Mountains can be divided into three groups for ecological management, effectively solving the problems caused by the large differences in uses and functions of different grasslands and the distribution of small patches to the management.
Conclusion
This study has demonstrated that stoichiometric characteristics and soil enzyme activities of different grasslands vary with grassland types. Based on N/P ratio and RDA analysis, nitrogen was the main factor limiting the grassland productivity, and pH, TN, SOC, Richness index and Simpson diversity index were the main environmental factors affecting the soil C:N:P stoichiometry and enzyme activities. Cluster analysis showed that 7 grassland types were clustered into three categories, that was, the grassland Qilian Mountain can be managed in the ecological district basing in three categories of clustering results. The results of this study can provide data support and theoretical guidance for the scientific management and ecological protection of grassland in Qilian Mountains Reserve.
Acknowledgments
The authors are grateful all of the teachers, students and technicians involved in the initial data collection process for providing guidance and assistance.
References
- 1. Shi S W, Peng C H, Wang M, Zhu Q A, Yang G, Yang Y Z, et al. A global meta-analysis of changes in soil carbon, nitrogen, phosphorus and sulfur, and stoichiometric shifts after forestation. Plant and Soil, 2016, 407(1/2): 323–340.
- 2. Nkurunziza L, Watson CA, Öborn I, et al. Socio-ecological factors determine crop performance in agricultural systems[J]. Scientific reports, 2020, 10(1):4232.
- 3. Dong X, Xin Z M, Huang Y R. Soil C:N:P stoichiometry in typical shrub communities in the Ulan Buh Desert. Acta Ecologica Sinica, 2019, 9(17):6247–6256. (in Chinese)
- 4. Liu J, Qiu L P, Cheng J M. Soil Enzymatic Activities of Five Typical Grassland Communities in Water wind Erosion Crisscross Region on the loess Plateau. ACTA AGRRSTIA SINCA, 2017, 25(1): 32–37. (in Chinese)
- 5.
Wang X G. Ecological stoichiometry of carbon, nitrogen and phosphorus in soils and plants in the eastern and western savanna of northern China. Beijing: Chinese Academy of Sciences University, 2015. (in Chinese).
- 6. Fang Y, An S S, Ma R T. Chemometrics characteristics of grassland plants and soil under different restoration methods in Yunwu Mountain. Journal of Applied Ecology, 2017, 28(1): 80–88. (in Chinese)
- 7. Li Y F, Liang S, Zhao Y Y, Li W B, Wang Y J. Machine learning for the prediction of L. chinensis carbon, nitrogen and phosphorus contents and understanding of mechanisms underlying grassland degradation. Journal of Environmental Management, 2017, 192: 116–123.
- 8. Bui E N, Henderson B L. C:N:P stoichiometry in Australian soils with respect to vegetation and environmental factors. Plant and Soil, 2013, 373(1/2): 553–568.
- 9. Steinauer K, Tilman D, Wragg P D. Plant diversity effects on soil microbial functions and enzymes are stronger than warming in a grassland experiment. Ecology, 2015, 96(1): 99–112.
- 10. Veres Z., Kotroczó Z., Fekete I. Soil extracellular enzyme activities are sensitive indicators of detrital inputs and carbon availability. Appl. Soil Ecol. 2015, 92, 18–23.
- 11. Jassey V.E.J., Reczuga M.K., Zielińska M. Tipping point in plant–fungal interactions under severe drought causes abrupt rise in peatland ecosystem respiration. Glob. Chang. Biol. 2018, 24, 972–986.
- 12. Kivlin S N, Treseder K K. Soil extracellular enzyme activities correspond with abiotic factors more than fungal community composition. Biogeochemistry, 2014, 117(1):23–37. (2014).
- 13. Schindlbacher A, Schnecker J, Takriti M. Microbial physiology and soil CO2 efflux after 9 years of soil warming in a temperate forest no indications for thermal adaptations. Global Change Biology, 2015, 21:4265–4277.
- 14. Kreyling J, Beierkuhnlein C, Elmer M. Soil biotic processes remain remarkably stable after 100-year extreme weather events in experimental grassland and heath. Plant & Soil, 2008, 308(1–2):175–188.
- 15. Cao D, Shi F, Koike T. Halophyte Plant Communities Affecting Enzyme Activity and Microbes in Saline Soils of the Yellow River Delta in China. Clean Soil Air Water, 2014, 42(10):1433–1440.
- 16. Gao Y.F., Zhao C.Y., Rong Z.L. Energy exchange between the atmosphere and a subalpine meadow in the Qilian Mountains, northwest China. Journal of Hydrology, 2019.
- 17. Yao X X, Bai G, Wu J P. Study of Grassland Vegetation Characteristics and Soil Nutrient and Their Correlation between Different Grassland Types in Alpine Pastoral Area of Qilian Mountains. ACTA AGRESTIA SINCA, 2018, 26(02):108–116. (in Chinese) CNKI: SUN:CDXU.0.2018-02-014.
- 18. Wang G H, Ren J Z, Zhang Z H. A Study on the population diversity of plant community, in Hexi mountain-oasis-desert area: General features. ACT A PRATACULTURAE SINICA, 2001, 10(1): 1–12. 1004–5759 (2001) 01-0001-12.
- 19. Gao X, Huang X X, Kevin Lo. Vegetation responses to climate change in the Qilian Mountain Nature Reserve, Northwest China. Global Ecology and Conservation, 2021, 28.
- 20. Li Q, Liu X N, Zhang D G. Characteristics of AGB and Soil Trace Elements of Different Grassland Types in Qilian Mountain Reserve. Grassland and Turf, 2021, 41(03):48–56. (in Chinese)
- 21. Bai X J, Zeng Q C, Fakher A, Dong Y H & An S S. Characteristics of soil enzyme activities and microbial biomass carbon and nitrogen under different vegetation zones on the Loess Plateau, China, Arid Land Research and Management, 2018.
- 22. Li Y H, Chu X Z. Effect of Different Land Use Types on Soil Enzyme Activity on the Edge of Ganjiahu Wetland in Xinjiang. Key Engineering Materials, 2012, 500:238–242.
- 23. Fu C F, Bian Z H, Xi J J. Spatial distribution characteristics of soil moisture in different types of sand dune in the Mu Us Sandy Land, adjacent to north of Chinese Loess Plateau. Environmental Earth Sciences, 2019, 77(4):151.1–151.12.
- 24. Niu X Y., Sun X M., Chen D S. Soil microorganisms, nutrients and enzyme activity of Larix kaempferi plantation under different ages in mountainous region of eastern Liaoning Province, China. Journal of Applied Ecology, 2015, 26(9):2663–2672.
- 25. Schrama Maarten J. J., V C, Eric J. W. Visser Grassland cutting regimes affect soil properties, and consequently vegetation composition and belowground plant traits. Plant & Soil, 2015, 366(1–2):401–413.
- 26. Gu Z K, Du G Z, Zhu W X. Distribution pattern of soil nutrients in different grassland types and soil depths in the eastern Tibetan Plateau. PRATACULTURAL SCIENCE, 2012,29(04):507–512. (in Chinese).
- 27. Zhang D G. Studies on the characteristics of soil fertility and relationship among nutritive factors in alpine grassland soil of Qilian mountains. Acta Prataculturae Sinica, 2002, 11(3):76–79. (in Chinese)
- 28. Liu M, Li Z P, Zhang T L. Changes of soil ecological stoichiometric ratios under different land uses in a small catchment of subtropical China, Acta Agriculturae Scandinavica, Section B-Soil & Plant Science, 2016, 66:1, 67–74,
- 29.
Nelson D. W., & Sommers L. E. Total carbon, organic carbon, and organic matter. In Sparks D. L., Page A. L., Helmke P. A., Loeppert R. H., Soltanpour P. N., Tabatabai M. A., Johnston C. T., & Sumner M. E.(Eds.), Methods of soil analysis. Part 3: Chemical methods (pp. 961–1010). Madison: Soil Science Society of America, Inc., American Society of Agronomy, Inc, 1996.
- 30.
Soil Physics institute, Nanjing institute of Soil Science, Chinese Academy of Sciences. Soil physical properties determination method. Beijing; Science Press, 1978.
- 31. Li X, Ma R P, An S S. Characteristics of soil organic carbon and enzyme activities in soil aggregates under different vegetation zones on the Loess Plateau. Chinese Journal of Applied Ecology, 2015, 26(8): 2282–2290. (in Chinese)
- 32. Zhang H D, Ru H L, Jiao F. C, N, P, K Stoichiometric Characteristic of Leaves, Root and Soil in Different Abandoned Years in Loess Plateau. Huanjing Kexue, 2016, 37(3):1128–1138.
- 33. Fan H, Wu J, Liu W. Linkages of plant and soil C:N:P stoichiometry and their relationships to forest growth in subtropical plantations. Plant and Soil, 2015, 392(1–2): 127–138.
- 34.
Ao Y M. Study on Sail Ecological Stvichivmetey of Enclosing Life in Typical Steppe, Inner Mongolia Teaching University, 2012. (in Chinese).
- 35. Cleveland C C, Liptzin D. C: N: P stoichiometry in soil: is there a “Redfield ratio” for the microbial biomass?. Biogeochemistry, 2007, 85(3): 235–252.
- 36. Xue L, Kuang L G, Chen H Y. Soil nutrients, microorganisms and enzyme activities of different stands. ACTA PEDOLOGICA SINICA,2003, (02): 280–285.
- 37. Zhang P, Zhang G Q, Zhao Y P. Ecological stoichiometry characteristics of leaf-litter-soil interactions in different forest typesin the Loess hilly-gully region of China. Acta Ecologica Sinica, 2018, 38(14):5087–5098. (in Chinese)
- 38. Jiang Z H, Zhang D G, Li X N. Soil nutrient and stoichiometry of alpine steppe under different altitudes in the three river headwaters region. ACTA AGRESTIA SINICA, 2019, 27(4): 26–34. (in Chinese)
- 39. Li H Y, Zhang J G, Yao T. Soil Nutrients. Enzyme Activities and Ecological Stoichiometric Characteristics in Degraded Alpine Grasslands. Journal of Soil and Water Conservation, 2018, 32(05):287–295. (in Chinese)
- 40. Jiao T. Chang G Z. Zhou X H. Study on relationship between soil enzyme and soil fertility of alpine meadow in different carrying capacities. Acta Prataculturae Sinica, 2009, 18(6): 98–104. (in Chinese).
- 41. Nan L L, Guo Q E, Xiang H. Soil Enzyme Activities Under Main Plant Communities of Saline alkalied Badlands in Gansu Province. Journal of soil and water conservation, 2015, 29(4):311–315. (in Chinese) CNKI:SUN:TRQS.0.2015-04-056.
- 42. Verónica A M, Cruz L, David S R. Enzyme activities as affected by soil properties and land use in a tropical watershed. Applied Soil Ecology, 2007, 35(1):0–45.
- 43. D’Odorico P, He Y, Collins S. Vegetation–microclimate feedbacks in woodland–grassland acetones. Global Ecology & Biogeography, 2013, 22(4):364–379.
- 44. Deng X J, Zhu L F, Song X C, et al. Soil Ecological Stoichiometry Characteristics of Different Stand Types in Maoershan Nature Reserve[J]. Chinese Journal of Soil Science, 2022, 53(2): 366–373. (in Chinese).
- 45. Weintraub S R, Wieder W R, Cleveland C C, et al. Organic matter inputs shift soil enzyme activity and allocation patterns in a wet tropical forest. Biogeochemistry, 2013, 114, 313–326.
- 46. Wang Z W, Wan S Z, Jiang H M, et al. Soil enzyme activities and their influencing factors among different alpine grasslands on the Qingzang Plateau. Chinese Journal of Plant Ecology, 2021, 45, 528–538.