Effect of plateau pika disturbance and patchiness on ecosystem carbon emissions in alpine meadow in the northeastern part of Qinghai–Tibetan Plateau
Plateau pika (Ochotona curzoniae) disturbance and patchiness intensify the spatial heterogeneous distribution of vegetation productivity and soil physicochemical properties, which may alter the ecosystem carbon emission process. Nevertheless, previous research has mostly focused on the homogeneous vegetation patches rather than heterogeneous land surface. Thus, this study aims to improve our understanding of the difference in ecosystem respiration (Re) over heterogeneous land surface in an alpine meadow grassland. Six different land surface types, namely large bald patches, medium bald patches, small bald patches, intact grassland, above pika tunnel and pika pile, were selected to analyze the response of Re to pika disturbance and patchiness and the key controlling factors. The results showed that (1) Re in intact grassland was 0.22–1.07 times higher than pika pile and bald patches, (2) soil moisture (SM) of intact grassland was 2 %–11 % higher than that of pika pile and bald patches, despite the fact that pika disturbance increased the water infiltration rate while soil temperature (ST) in intact grassland was 1–3∘ less than pika pile and bald patches, (3) soil organic carbon (SOC) and total nitrogen (TN) in intact grassland were approximately 50 % and 60 % less than above pika tunnel, whereas they were 10 %–30 % and 22 %–110 % higher than pika pile and bald patches, and (4) Re was significantly correlated with SM, TN and vegetation biomass (P<0.05). Our results suggested that pika disturbance and patchiness altered the ecosystem carbon emission pattern, which was mainly attributed to the reduction in soil water and supply of substrates. Given the wide distribution of pikas and the large area of bald patches, the varied Re in heterogeneous land surfaces should not be neglected in the estimation of ecosystem carbon emissions at the plot or regional scale.
Ecosystem respiration (Re) is the key process for determining the carbon budget in the terrestrial ecosystem. Thus, even small imbalances between CO2 uptake via photosynthesis and CO2 release by ecosystem respiration can lead to significant interannual variation in atmospheric CO2 (Schimel et al., 2001; Cox et al., 2000; Grogan and Jonasson, 2005; Oberbauer et al., 2007; Warren and Taranto, 2011). Dependent on autotrophic (plant) and heterotrophic (microbe) activity, ecosystem respiration is mainly controlled by abiotic factors (primarily temperature and water availability; Chimner and Welker, 2005; Flanagan and Johnson, 2005; Nakano et al., 2008; von Buttlar et al., 2018) and the supply of carbohydrate fixed by leaves, vegetation litter and soil organic matter (Janssens et al., 2001; Reichstein et al., 2002). Therefore, any external disturbance altering environmental conditions and affecting vegetation growth exerts profound influence on ecosystem carbon emission.
One of the basic functions of terrestrial ecosystem is to regulate the carbon balance between the atmosphere and ecosystem (Canadell et al., 2007; Le Quéré et al., 2014; Ahlström et al., 2015). However, this balance could be broken by widespread land degradation (Post and Kwon, 2000; Dregne, 2002), which accompanied the reduction in photosynthetic fixed carbon dioxide from the atmosphere and carbon sequestration by soils (Defries et al., 1999; Upadhyay et al., 2005). It was estimated that land degradation has resulted in 19–29 Pg C loss worldwide (Lal, 2001). Over the past decades, grasslands have experienced patchiness throughout the world, and this process is still ongoing (Baldi et al., 2006; Wang et al., 2009; Roch and Jaeger, 2014). Patchiness generally refers to a landscape that consists of remnant areas of native vegetation surrounded by a more heterogeneous and patchy situation (Kouki and Löfman, 1998). Other than climate change (Yi et al., 2014), vegetation self-organization (Rietkerk et al., 2004; Venegas et al., 2005; McKey et al., 2010) or anthropogenic disturbances (Kouki and Löfman, 1998; Yi et al., 2016), rodent burrowing activities were also considered to be the origin of the patchiness (Wei et al., 2006; Davidson and Lightfoot, 2008). This patchiness intensified spatial heterogeneity of the land surface and led to the changing of the structure and function of the original ecosystem (Herkert et al., 2003; Bestelmeyer et al., 2006; Lindenmayer and Fischer, 2013). For instance, there is abundant evidence that patchiness not only intensified the spatial heterogeneous distribution of ecosystem organic carbon (C) and vegetation productivity (Yan et al., 2016; Qin et al., 2018) but also altered the pattern of coupled water and heat cycling between the land surface and the atmosphere (Saunders et al., 1991; You et al., 2017; Ma et al., 2018). Consequently, this may alter the ecosystem carbon emission process (Juszczak et al., 2013).
Plateau pikas (Ochotona curzoniae, hereafter pikas) are small mammals endemic to the alpine grasslands of the Qinghai–Tibetan Plateau (QTP; Smith and Foggin, 1999; Lai and Smith, 2003). Living underground, they excavated deep layers of soil to the surface through foraging and digging activities (Lai and Smith, 2003) and led to substantial bald piles on the ground. The bald pile was considered to gradually become bald patches under soil erosion, gravity, freeze–thaw and other factors (Chen et al., 2017; Ma et al., 2018). As a consequence, natural vegetation patches and adjacent bald patches with different sizes and pika piles represent the most common landscape pattern in the alpine meadow grassland on the QTP. Previous studies have demonstrated that pika disturbance and patchiness weaken the function of alpine meadow as a carbon sink (Liu et al., 2013; Peng et al., 2015; Qin et al., 2018) and accelerated the ecosystem carbon emission rate (Qin et al., 2015a). Nevertheless, most of these studies have mainly focused on ecosystem carbon emission rate under the homogeneous land surface rather than heterogeneous land surfaces. Thus, the specific aims of this study were to (1) investigate the spatial heterogeneity of Re among different surface types (plateau pika pile, above pika tunnel, and different sizes of bald patches and vegetation) of alpine grassland and to (2) illuminate the potential regulating mechanism of pika disturbance and patchiness to ecosystem respiration (Re) in an alpine meadow grassland in the northeastern part of Qinghai–Tibetan Plateau (QTP).
2.1 Site description
This study was conducted at the permanent plots at the Suli Alpine Meadow Ecosystem Observation and Experiment Station (98∘18′33.2′′, 38∘25′13.5′′; 3887 m a.s.l.; Northwest Institute of Eco-Environment and Resources, Chinese Academy of Sciences). The study area is characterized by a continental arid desert climate, with low mean annual air temperature, little rainfall and high evaporation (Wu et al., 2015). The mean annual air temperature was approximately −4 ∘C, and the annual precipitation ranged from 200 to 400 mm (Chang et al., 2016). The permafrost type at our site is transition, and the active layer depth is 2.78±1.03 m (Chen et al., 2012). The dominant plant species in the study area were Kobresia capillifolia and Carex moorcroftii (Qin et al., 2014). Soils was classified as “felty”, with a pH of 8.56, and consisted of 30.96 % silt and fine soils, 57.52 % fine sand, and 10.68 % coarse sand; soil bulk density is 1.41 g cm−3 within 0–40 cm depth of the soil layer (Qin et al., 2015b). The grassland in this area suffered from degradation due to permafrost degradation and external disturbance from grazing livestock and small mammals, i.e., plateau pikas (Yi et al., 2011; Qin et al., 2015a). As a result, a mosaic pattern of vegetation patches, bald patches with different sizes, and pika piles were common.
2.2 Field observation
In early June 2016, three 100 m × 100 m plots were established as replicates. Each 100×100 m plot had a distance of less than 50 m which had similar plants and terrain. In each plot, six representative land surface types were selected: (1) large bald patch with a size larger than 9.0 m2 (LP), (2) medium bald patch with a size of 1.0–9.0 m2 (MP), (3) small bald patch with a size of less than 1.0 m2 (SP), (4) intact grassland patch (IG), (5) above pika tunnel (PT) and (6) old pika pile (PP; Fig. 1; Yi et al., 2016; Qin et al., 2018). There were no other mammals, e.g., marmot and zokor, in our study plots. All of the piles in each plot were created by plateau pikas. They were distinguished easily in aerial photographs. Large bald patches had less vegetation cover, and the smallest side was larger than 3 m. Medium patches also covered less vegetation cover, and the largest side was in a range of 1 to 3 m; small bald patches were characterized by less vegetation cover, and the largest side was less than 1 m. Intact grassland was characterized by high vegetation cover, and no large and medium bare land was found. Pika tunnel and pika pile usually coexisted. Pika tunnel is approximately 6 cm in diameter, and pika pile is in the front of pika tunnel and is 60 cm in diameter or less in vegetation cover. We calculated the threshold area of large, medium and small patches by aerial photographs. Each aerial photograph has 12 million pixels. At a height of 20 m, the resolution of each pixel is ∼1 cm, and each photograph covers ∼26 m × 35 m of ground. Pixels in each aerial image were first classified into two groups, i.e., vegetated or bare patches (Yi, 2017). Then patches with different sizes were created using the OpenCv Library. Finally, fractions of vegetation and bare patches (large, medium and small patches) were calculated. For each surface type in each plot, six 1 m × 1 m quadrats were set up, of which three were used for soil-saturated hydraulic conductivity measurement and three were used for soil compactness measurement and soil and vegetation sampling. We also set up another three 1 m × 1 m quadrats and three 2 m × 2 m quadrats in each surface type in a 100 m × 100 m plot for measuring soil temperature, soil moisture and ecosystem respiration.
A meteorological tower was established at our observation station in 2008. Air temperature (∘C) at 2.0 m was measured by HMP45C (Vaisala; Helsinki, Finland), and precipitation was measured using an all-weather precipitation gauge (Geonor T-200B, Norway; Wu et al., 2015). Soil temperature and moisture at 10 cm were measured by using an auto-measurement system (Decagon Inc., USA) from early June to late August. The system consisted of an EM50 logger and five 5TM sensors. The data were logged automatically every 30 min. Soil-saturated hydraulic conductivity and compactness were measured once each month between June and August. Soil-saturated hydraulic conductivity was measured by a DualHead Infiltrometer (Decagon Inc., USA). The measurement process included a soak time of 15 min and a hold time of 20 min at the low pressure head (5 cm) and high pressure head (15 cm) with two cycles. Each measurement took 95 min altogether. Soil compactness was measured with the TJSD-750 (Hangzhou Top Instrument Co., LTD, Hangzhou, China) from the soil surface to 10 cm depth. Ecosystem respiration rates were measured using the LICOR-8150 Automated Soil CO2 Flux System, which was an accessory for the LI-8100A that could connect 16 individual chambers at one time and was sampled and controlled by the LI-8100A Analyzer Control Unit. The air temperature inside of the chamber was measured using the internal thermistor of the chamber. The ecosystem CO2 fluxes were calculated by the equation as follows:
where Fc is the soil CO2 efflux rate (µmol m−2 s−1), V is volume (cm3), P0 is the initial pressure (kPa), W0 is the initial water vapor mole fraction (mmol mol−1), R is the ideal gas constant (J K−1 mol−1), S is soil surface area (cm2), T0 is initial air temperature (∘C) and is the initial rate of change in the water-corrected CO2 mole fraction (µmol−1 s−1).
Six LICOR-8100-104 long-term opaque chambers (20 cm in diameter; LICOR, Inc., Lincoln, NE, USA) were used to measure alternately between three replicates for six land surface types. Therefore, at least 3 days were required to complete one rotation of measurements of ecosystem respiration. To measure ecosystem respiration, 18 polyvinyl chloride collars with a 20 cm inner diameter and 12 cm height were inserted into the soil, with 3–4 cm exposed to the air (Qin and Yi, 2013). All of the collars were installed at least 24 h before the first measurement to reduce disturbance-induced ecosystem CO2 effluxes. Ecosystem respiration rates were measured every 7–10 days from 16 June to 20 August 2016, depending on weather conditions. A round-the-clock measurement protocol was carried out, and ecosystem respiration rates were measured every 30 min. Each measurement took 1 min and 45 s, including the pre-purge (10 s), dead band (15 s), observation length (1 min) and post-purge 20 s.
2.3 Soil and vegetation sampling
Soil samples were collected during the period of late July to early August 2016. In each surface type of each plot, five soil cores were collected using a stainless-steel auger (5 cm in diameter) at depths of 0–10, 10–20, 20–30 and 30–40 cm and were combined into one composite sample for each depth in each quadrat. Another five soil cores were sampled by a cylindrical cutting ring (7 cm in diameter and 5.2 cm in depth) to determine soil bulk density from each land surface type. Pika tunnels were approximately 6 cm in diameter and 40 cm in depth. Therefore, soil samples were available to collect at the depth of 40 cm. In total, 512 soil samples were collected. Soil samples were firstly air dried; then gravel and stone were removed from the samples with manual sieving, and they were finally weighed. The remaining soil samples with a diameter of less than 2 mm were ground to pass through a 0.25 mm sieve for analysis of soil organic carbon (SOC) and soil total nitrogen (TN) concentration. SOC was measured by dichromate oxidation using the Walkley–Black acid digestion method (Nelson and Sommers, 1982). TN was determined by digestion and then tested using a flow injection analysis system (FIAstar 5000, Foss Inc., Sweden). Aboveground and belowground biomasses were determined within a 1 m × 1 m quadrat on 4 August 2016 during peak biomass and species diversity. There were a total of 108 aboveground and belowground vegetation samples (3 plots × 6 land surface types × 3 replicates) from the study area. Aboveground biomass was determined by clipping all aboveground living plants at the ground level, drying them (oven-dried at 65 ∘C for 48 h) and weighing them. Belowground biomass was sampled by collecting five soil columns, and each soil column was 5 cm in diameter and 40 cm in depth. Soil cores were washed with a gentle spray of water over a fine mesh screen until soil separated from the roots, and then they were dried (oven-dried at 65 ∘C for 48 h) and weighed.
2.4 Statistical analysis
The soil organic C and total N densities in different land surface were calculated using Eqs. (2) and (3):
where SOC is soil organic C density (kg m−2), TN is soil total N density (kg m−2), ρ is the soil bulk density (g cm−3), σgarvel is the relative volume of gravel (% w∕w), CSOC is soil organic C content (g kg−1), CTN is soil total N content (g kg−1) and Di is soil thickness (cm) at layer i (i=1, 2, 3 and 4).
The data were presented as mean ± standard deviation. Statistical analyses were performed using the SPSS 17.0 statistical software package (SPSS Inc., Chicago, IL, USA). One-way analysis of variance (ANOVA) and a multi-comparison of the least significant difference (LSD) test were used to determine differences at the p=0.05 level. The relationships of ecosystem respiration with biotic and abiotic factors were analyzed by Pearson correlation analysis using R.
3.1 Ecosystem respiration
Ecosystem respiration showed significant difference among varied land surface types during the growing season (Table 1; P<0.001). Except for pika pile, ecosystem respiration was at a maximum in August and at a minimum in June (Fig. 2). In June, ecosystem respiration in intact grassland, above pika tunnel, small patch and pika pile had no significant difference, and the lowest ecosystem respiration was found in large and medium patches (Fig. 2). Average ecosystem respiration in intact grassland was 4.01 µmol m−2 s−1 in July, which was 24.35 % to 137.39 % higher than other surface types (Fig. 2). In August, average ecosystem respiration was 4.07 and 4.85 µmol m−2 s−1 for intact grassland and above pika tunnel, respectively, 2.59–3.81 µmol m−2 s−1 for bald patches, and 1.18 µmol m−2 s−1 for pika pile (Fig. 2).
3.2 Microclimate and soil hydrothermal characteristics
Mean temperature and total rainfall during the growing season from 1 May to 30 September 2016 were 6.18 ∘C and 343.4 mm, respectively (Fig. 3). Soil temperature and moisture were significantly different among various land surface types (Table 1, P<0.05). The monthly average soil temperature was in a range of 8.20–13.72 ∘C from June to August, which was approximately 1–3∘ higher in pika pile and bald patches than the intact grassland (Fig. 4a; P<0.05). The monthly mean soil moisture from June to August was approximately 30 % for intact grassland and above pika tunnel, 25 % for small patch and pika pile, and 20 % for larger and medium patch (Fig. 4b). Soil-saturated hydraulic conductivity also showed significant variation in different land surface types (P=0.027, Table 2). For example, soil-saturated hydraulic conductivity in large bald patch, medium bald patch, small bald patch, intact grassland patch, above pika tunnel and old pika pile was 1.54, 1.53, 2.14, 2.13, 2.12 and 2.58 cm h−1, respectively (Fig. 5). Soil-saturated hydraulic conductivity in intact grassland patch was approximately 40 % higher than medium and large patches and 17 % lower than pika pile, while there was no significant difference between intact grassland patch, small patch and above pika tunnel (P>0.05).
3.3 Soil and vegetation properties
Soil and vegetation properties showed significant variation in different land surface types (Table 2; P<0.001). Soil compactness was over 0.30 Pa in intact grassland and above pika tunnel, approximately 0.20 Pa for bald patches, and less than 0.10 Pa for pika pile (Fig. 6). Mean SOC and TN density in intact grassland were 52.45 % and 59.14 % less than above pika tunnel, whereas they were 9.69 %–30.12 % and 22.47 %–109.62 % higher than pika pile and bald patches (Fig. 7). Aboveground and belowground biomasses in intact grassland were approximately 30 % higher than above pika tunnel, 90 % higher than pika pile, and 123 %–252 % and 134 %–289 % higher than bald patches (Fig. 8a, b).
3.4 Factors regulating ecosystem respiration
We analyzed the relationships of ecosystem respiration with biotic and abiotic factors for six land surface types (Fig. 9). Correlation analysis showed that ecosystem respiration had no significant correlation with soil temperature (P>0.05; Fig. 9). However, ecosystem respiration was significantly and positively related to soil moisture (P<0.01), soil total nitrogen (P<0.05), and aboveground (P<0.05) and belowground biomasses (P<0.05; Fig. 9).
4.1 Effect of pika disturbance on ecosystem respiration
Pika burrowing activities increased oxygen content in deep soil, which contributed to the decomposition of soil organic matter (Martin, 2003). The deposition of urine and feces by small herbivorous mammals could also promote ecosystem nutrition circulation (Clark et al., 2005). It was suggested that excreta deposited by pikas and frequently found in or near their burrows supplied organic C available to microbial decomposition with an increase in ecosystem CO2 emission (Cao et al., 2004). Indeed, SOC and TN densities reached up to 14.54 and 0.98 kg m−2 in above pika tunnel, which was 2.45 and 2.10 times higher, respectively, than that in intact grassland (Fig. 7). The consistent results reported that the contents of available soil nutrients around the pika burrow were higher than those in control sites on an alpine meadow (Zhang et al., 2016). We also found that SOC and TN densities in pika pile decreased 13.35 % and 42.93 % when compared to intact grassland. This was because pika burrowing activity transferred deeper, nutrient-poor soil to the soil surface, improved soil aeration, increased the rate of organic carbon mineralization and soil erosion, and took away soil nutrition (Wei et al., 2006; Qin et al., 2015a; Chen et al., 2017). However, except in July, no significant difference in Re was found between intact grassland and above pika tunnel, while Re in pika pile was 42.08 % less than intact grassland (Fig. 2). A similar result was also found in an alpine meadow on the QTP (Peng et al., 2015), which indicated that ecosystem respiration decreased with increasing of pika holes because of grassland biomass regulating soil C and N, with an increasing number of pika holes. These results confirmed that pika disturbance did not increase ecosystem carbon emission directly but facilitated CO2 emission into the atmosphere through pika holes (Qin et al., 2015a). The difference in ecosystem respiration between intact grassland and pika piles was mainly related to changes in vegetation biomass and soil moisture. For example, both aboveground and belowground biomasses decreased 244.62 % and 279.89 % in pika piles compared with intact grassland (Fig. 8). The reduction in vegetation biomass production decreased aboveground plant respiration and root respiration by decreasing carbon allocation (e.g., root exudates, litter and available SOC; Raich and Potter, 1995; Högberg et al., 2002; Yang et al., 2018). Consistent with previous studies which demonstrated that pika burrowing activity increased the water infiltration rate (Hogan, 2010; Wilson and Smith, 2015), our results also showed that soil-saturated hydraulic conductivity in pika pile was significantly higher than bald and vegetation patches (Fig. 5). Nevertheless, the increased water infiltration was unable to increase soil moisture in pika piles. For example, soil moisture in pika piles was approximately 5 % lower than intact grassland (Fig. 4). Our result was inconsistent with previous studies, which reported that old pika mound had the highest soil moisture during the summer (Ma et al., 2018) and that moderate pika burrowing activities increased surface soil moisture (Li and Zhang, 2006). This difference may have contributed to the high pika density in alpine meadow (Guo et al., 2017). Moreover, pika piles were loose (Fig. 6) with less vegetation cover (Fig. 8), which was not beneficial for soil moisture storage.
4.2 Effect of patchiness on ecosystem respiration
Our results clearly showed that patchiness resulted in significant reduction in ecosystem carbon emissions. Compared with intact grassland, ecosystem respiration decreased approximately 17 %–48 % for bald patches (Fig. 2). Two possible mechanisms could account for the effects of patchiness on ecosystem respiration. On the one hand, the reduction in SOC and TN decreased microbial respiration by decreasing substrate supply to microbes in the rhizosphere (Nobili et al., 2001; Scott-Denton et al., 2010). Our results indicated that patchiness caused evident loss of SOC and TN (Fig. 7) due to reduction in C input from vegetation and increased C output from soil erosion (Qin et al., 2018). Previous studies have shown that the spatial heterogeneity of soil respiration was attributed to uneven soil organic carbon and total nitrogen content (Xu and Qi, 2010). Soil organic carbon was considered to be the basic substrate of CO2 emission by microbial decomposition (Sikora and Mccoy, 1990), and soil total N enhanced ecosystem CO2 emissions by providing a source of protein for microbial growth (Tewary et al., 1982). On the other hand, low moisture availability limits microbial respiration by restricting access to C substrates, reducing the diffusion of C substrates and extracellular enzymes, and limiting microbial mobility (Yuste et al., 2003; Wang et al., 2014). Our results showed that soil moisture in large and medium patches decreased by 10 % compared to intact grassland (Fig. 4). Previous studies reported that the soil compaction of bald patches decreased the rate of water infiltration (Wuest et al., 2006; Wilson and Smith, 2015); this was similar to our results, which showed that bald patches had less saturated soil hydraulic conductivity (Fig. 5). Low vegetation cover in bald patches was not beneficial for water retention and utilization, where most of soil water was mainly lost by means of evaporation (Yi et al., 2014). We measured evaporation of the intact grassland, isolated grassland, large patches, medium patches and small patches, starting in early June 2016. Results after 3 years indicated that evaporation in bald patches was higher than intact grassland (data were not shown here).
4.3 Factors that affected ecosystem respiration
Most previous studies showed that soil temperature explained most of the temporal variation in ecosystem respiration in the alpine grassland on the QTP (Lin et al., 2011; Qin et al., 2015c; Zhang et al., 2017). Our results indicated that soil temperature in pika piles and bald patches was approximately 1 to 3 ∘C higher than intact grassland (Fig. 4), which mainly resulted from the heterogeneity of the surface albedo, surface soil water retention, heat conduction properties and radiation (Beringer et al., 2005; Pielke, 2005; Yi et al., 2013; You et al., 2017). It was suggested that pika disturbance creates a better soil temperature buffer for them to avoid the extreme cold in winter (Ma et al., 2018), whereas the high soil temperature in bald patch was a disadvantage for the recovery of vegetation because the patch surface had the smallest soil moisture content (Fig. 4) and the largest daily range of soil temperatures (Ma et al., 2018). It was well known that the rising soil temperature under natural conditions enhanced ecosystem respiration by stimulating decomposition of soil organic matter (Conant et al., 2008), increasing plant biomass (Yi et al., 2014) and activity of microbial enzymes (Bond-Lamberty and Thomson, 2010). However, an obvious relationship between Re and soil temperature was not found in the present study (Fig. 9), which suggested that other factors involved in controlling Re were induced by pika disturbance and patchiness. Our results showed that Re was positively correlated with soil moisture, soil total nitrogen, and aboveground and belowground biomasses (Fig. 9). Pika disturbance and patchiness led to the drying and loosening of soil (Figs. 4 and 6). It was considered that loose, dry surface sediments and strong winds were the primary factors responsible for soil erosion (Dong et al., 2010), and wind erosion was especially common in arid and semi-arid regions (Zhang and Dong, 2014). This resulted in the reduction in soil organic carbon, total nitrogen and vegetation biomass (Figs. 7 and 8). The alteration of these biotic and abiotic factors induced by pika disturbance and patchiness led to the decline in ecosystem respiration. Nevertheless, the decline in ecosystem respiration did not completely offset the sequestration of C fixed by photosynthesis because of the lower vegetation cover in bald patches and pika piles. Given the large area covered by bald patches in alpine grasslands, patchiness was more susceptible to erosion and exerted greater influence on ecosystem respiration than pika disturbance. A recent study also reported that bald patches of various sizes in the grasslands played a much more important role than pika direct disturbance in reducing vegetation cover, aboveground biomass, soil carbon and nitrogen (Yi et al., 2016).
4.4 Effect of pika disturbance on patchiness
Natural vegetation patches, bald patches with different sizes and pika piles coexisted on the alpine meadow (Fig. 1), which supported the fact that alpine grassland also experienced fragmentation (Qin et al., 2018). Several proposed mechanisms may be accounted for in the formation and development of patchiness in alpine grassland. As one of the dominant forms of land utilization, alpine grasslands are widely used for grazing. Previous studies suggested that overgrazing destroyed the original vegetation and led to a decrease in the coverage and looseness of soil (Dong et al., 2014), which was prone to forming bald patch due to soil erosion (Fécan et al., 1999; Zhang and Dong, 2014). Other than livestock, alpine grassland is also a habitat for many small mammals, such as the plateau pika, zokor (Eospalax fontanierii), marmot (Marmota himalayana) and fox (Vulpes ferrilata). Pikas were considered to be creating a patchy matrix by changing soil properties (Chen et al., 2017), by digging tunnels and through burying activities (Dong et al., 2013). On the one hand, pikas bury vegetation in freshly excavated soil; then small bare soil patches and further large soil patches are formed by linking small bare soil patches by wind and/or water (Wei et al., 2006; Ma et al., 2018). On the other hand, pikas dig tunnels underground. Although pika-made burrows are the primary homes for a wide variety of small birds and lizards (Smith and Foggin, 1999), the collapse of pika tunnels results in the emergence of bald soil patches (Zhou et al., 2003; Cao et al., 2010). Moreover, alpine grassland is underlain by extensive permafrost (Cheng and Wu, 2007). The repeated freeze–thaw causes the cracking of the sod around the barren area (Yang et al., 2003) and creates preconditions for the forming bald patch. However, to date, there is no direct evidence to demonstrate the potential mechanism for forming and developing patchiness for alpine grassland on the QTP. It is, therefore, critical to perform long-term repeated monitoring studies to determine whether bald patches are developed from pika piles or burrow tunnels and to determine the major factors affecting bald patch expansion (Yi et al., 2016).
In this study, we investigated soil physicochemical properties, vegetation biomass and ecosystem respiration (Re) in six land surface types originating from pika disturbance and patchiness. We also analyzed the dominant factors regulating the Re. Our results showed that pika disturbance and patchiness decreased soil moisture but increased soil temperature, which may be conducive to pikas surviving in cold season but disadvantageous for vegetation growth. Patchiness caused an evident decrease in SOC and TN density, while both SOC and TN density showed a different response in pika piles and burrows. Both pika disturbance and patchiness decreased ecosystem carbon emission, and ecosystem respiration strongly correlated with soil moisture, TN and vegetation biomass. Our results indicated that pika disturbance and patchiness led to the changing of ecosystem respiration process, owing to the drying of soil and the reduction in substrate supply. However, the decline in ecosystem respiration may not be able to offset the sequestration of C fixed by photosynthesis.
Data used in this study are archived by the authors and are available on request.
SY and YD designed the study. YQ, WZ, YQ, JC and ZW performed field observation and sampling. All authors contributed to the discussion of the results. YQ led the writing of the paper, and all co-authors contributed to it.
The authors declare that they have no conflict of interest.
The authors would like to thank Jun Zhang and Bingbing Bai for their help in field sampling. This study was jointly supported by grants from the National Natural Science Foundation (41601064), the National Key Research and Development Program of China (2018YFC0406601), the National Natural Science Foundation of China (41690142), the independent grants from the State Key Laboratory of Cryosphere Sciences (SKLCS-ZZ-2018), and the science and technology support program of the Guizhou Science and Technology Agency, “The Key technology and engineering demonstration of farmland system control and restoration in Tongren mercury polluted area” (Qiankehezhicheng2967).
This paper was edited by Michael Weintraub and reviewed by three anonymous referees.
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