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The effect of grazing on plant species richness on the Qinghai Plateau, Tibet 1 2 3 Jianjun Cao1, Nicholas M. Holden2, Guozhen Du1* 4 1. The Key Laboratory of Arid Agro-ecology of the Ministry of Education, Lanzhou University 5 6 2. UCD Bioresources Research Centre / Biosystems Engineering, UCD School of 7 Agriculture, Food Science and Veterinary Medicine, University College Dublin, Belfield, 8 Dublin 4, Ireland 9 10 Abstract 11 In Maqu County in the Gansu Province of China there are two predominant forms of grazing 12 managements. Under multi-household (MH) management, grassland is jointly managed by 13 two or more households without fences between household pastures. Under single-household 14 (SH) management fenced-off parcels of grassland are separately managed by one household. 15 Resource management policy in the area assumed that MH management would subject a 16 parcel of land to more grazing pressure than SH use because no individual was responsible 17 for the resource. However, the consequences of this difference in land ownership are not clear 18 in terms of biodiversity and overall agro-ecology, and differences in plant species richness 19 between MH and SH could have long term implications for the region. Comparable land 20 parcels subject to MH and SH were identified and surveyed by quadrat analysis and the data 21 summarized using the Gleason Index. MH land had a greater index values than SH but the 22 differences were not significant. A further analysis of the plant species richness data indicated 1 1 that the number of households using MH land influenced the species richness. Land used by 3 2 to 7 households had significantly lower index values than land used by 8 to 15 households, 3 which in turn had significantly lower index values than land used by >15 households. There 4 was also evidence to suggest that the quality of the forage available deteriorated under SH 5 management. It was concluded that MH grazing resulted in greater species richness than SH 6 and is perhaps an important contributor to biodiversity conservation and grassland 7 management for the region. 8 9 Keywords 10 Multi-household grazing management; Single-household grazing management; Plant species 11 richness; Gleason Index; Maqu County; Gansu Province 12 13 Introduction 14 Anthropogenic land use, whether converting natural landscapes for human use or changing 15 management practices on human-dominated land has transformed large proportion of the 16 planet’s land surface (Foley et al., 2005). Research has revealed the environmental impacts of 17 anthropogenic land use ranging from changes in atmospheric composition (IPCC, 2000) to 18 extensive modification of Earth’s ecosystems. Although land-use practices vary greatly across 19 the world, the ultimate outcome is generally the same: the acquisition of natural resources for 20 immediate human needs, often at the expense of degrading environmental conditions. (Foley 21 et al., 2005). Land use change and land management has in some cases caused a decline in 22 biodiversity (Maurer et al, 2006) and change in vegetation composition (AO et al., 2008) 2 1 through the loss, modification, and fragmentation of habitats, degradation of soil and water, 2 and overexploitation of native species (Pimm, and Raven, 2000). Land use change is not only 3 the main cause of the soil degradation, but it also generates pressure on local, and perhaps 4 fragile, economies (Wang et al., 2004). At present, land use change is a major threat to 5 species diversity of grasslands throughout the world (Maurer et al, 2006), thus developing an 6 understanding grassland ecosystem response to land use change is required in order to 7 manage and prevent land degradation (Zhou et al., 2002) because maintaining plant diversity 8 is a central goal of global biodiversity management (Olff & Ritchie, 1998). Linking 9 ecological theories of species diversity to land management has become a research and 10 management priority for promoting species diversity and sustainable use of natural systems 11 (Bestelmeyer et al., 2003). 12 13 China encompasses enormous variations in topographical features, with high mountain 14 ranges and extensive plateaus, resulting primarily from the collision of the Indian 15 subcontinent with the Asian continent. The resulting habitat heterogeneity contributes to the 16 maintenance of high biodiversity by providing many niches and opportunities for speciation. 17 The estimated number of vascular plant species is nearly 33,000, with 30,000 angiosperms, 18 250 gymnosperms and 2600 pteridophytes, ranking third in plant biodiversity in the world 19 (Lopez-Pujol et al. 2006; Shimono et al., 2010). The Qinghai–Xizang (Tibetan) plateau 20 occupies 2.5 million km2, approximately 25% of the area of the People’s Republic of China. 21 An estimated 70% of the plateau is high altitude grasslands, considered as cold alpine 22 rangelands extend from the moist sub-humid grasslands of the eastern plateau to the 3 1 semi-arid alpine desert steppe in the west, and display a diverse array of plant and wildlife 2 species (Smith & Foggin, 1999; Richard et al., 2006). According to Lopez-Pujol et al. (2006) 3 more than 12,000 species in 1,500 genera of vascular plants have been identified on the 4 plateau, including 3,500 species that are endemic to the plateau. Therefore, maintenance of 5 plant richness on the Tibet Plateau is of both national and global importance. However, these 6 distinctive flora and fauna – many of which are endangered (Smith & Foggin, 1999) – are 7 declining due to many causes of degradation (Richard et al., 2006) including climate change 8 (drying), human population increase, increase in burrowing mammal populations due to 9 ineffective control and hunting of predators, increasing concentration of livestock near winter 10 settlements, reduced mobility due to restrictive pasture tenure, breakdown of traditional 11 regulatory mechanisms, and lack of government investment in rangeland and livestock 12 infrastructure. Some researchers (Gimenez, 2002; Richard et al., 2006; Yang, 2007; Zhang 13 and Li, 2008) have suggested that changes in land use have caused degradation and reduced 14 plant biodiversity, but no field experiments have been conducted to demonstrate these effects. 15 In this paper the effect of changing land management (i.e. a land use change) on plant 16 richness on the Qinghai Tibet plateau will be examined. 17 18 Grassland use change on Qinghai Tibet plateau 19 For thousands of years cold-tolerant livestock grazing by nomadic Tibetan herders on the 20 Qinghai plateau was the dominant and apparently environmentally sustainable land use (Yan 21 et al., 2005). However, in the late 1970s, policy reform led to settling of nomadic farmers, 22 livestock being divided among then and individual family leasing of state owned pasture 4 1 (Manderscheid, 2001). The rationale for privatizing rangeland in China was the belief that 2 open access of privately owned livestock to common rangeland had led to rangeland 3 degradation and that elimination of open-access property rights could solve the problem 4 (Gadgil et al., 1993; Yan et al., 2005), known more generally as the “Tragedy of the 5 Commons” (Hardin, 1968; Ashenafi & Williams, 2005; Wang, 2009). In Hardin’s (1968) 6 theory, the individual will maximize utilization of common land even if this results in 7 degradation because the individual achieves short-term benefits and the longer-term burdens 8 are distributed amongst all with right of access. The suggested solution is private land 9 ownership, which theoretically encourages the owner to utilize the resource sustainably. 10 There is evidence however that suggests the theory is not universal (Crépin and Lindahl, 11 2009) and that common ownership, in the right social setting might be environmentally 12 beneficial. In China, Grassland Supervisor Stations assign rangeland use rights to individual 13 households, establish boundaries by fencing, and set, monitored and enforced stocking rates 14 for individual household pastures (Ranks, 2004). About 70 per cent of usable rangeland was 15 leased through long-term contracts by 2003, of which 68 per cent was contracted to 16 individual households and the rest to groups of households or to villages (Yao, 2003). 17 18 There are predominantly two land use types since the implementation of this system 19 single-household (SH) use and multi-household (MH) use. For MH, grassland is jointly 20 managed by two or more households without boundaries between household pastures, while 21 for SH, grassland is fenced-off and managed by one household. If the number of households 22 is larger enough, MH grassland management is similar to historical nomadic land use while 5 1 SH represents the ideal for the theory of individual ownership to drive sustainable 2 management. 3 4 The objective of this paper is to examine the effect on plant richness of grazing management 5 under single household ownership (less likely to cause degradation according to theory) and 6 under multiple household ownership that closely resembles historical nomadism (more likely 7 to cause degradation according to theory). The work addresses the question of whether SH 8 management results in greater or lesser plant species richness, used as an indicator of 9 biodiversity (Ma & Liu, 1994; Fang et al., 2004) compared to MH management. 10 11 12 Materials and Methods 13 The Maqu grassland ecosystem, located Maqu County in the Gansu Province of China is on 14 the eastern Qinghai-Tibet plateau, (101°E; 34°N). The altitude ranges from 2900 m to 4000 m 15 with an annual rainfall of 450 to 780 mm, an annual average temperature of 1.8 oC (ranging 16 from minima of -10.7 oC in January to 11.7 oC in July, and a growing season maxima of 23.6 17 oC 18 59 % is highly productive alpine meadow. The grassland types include mainly alpine meadow 19 (59%), brushy meadow (33%), woodland meadow <1%), saline meadow (<1%), swampy 20 meadow (6%) and upland grass (1%)(Bu et al., 2006). The estimated number of vascular 21 plant species is over 530, with 57 families and 204 genera. 22 6 to 28.9 oC) and 270 frost days annually. The grassland area is about 870,000 ha of which 1 Historically, nomadic grazing with common ownership was the dominant livestock 2 management system in the Maqu. Since 1995 grassland has been progressively allocated to 3 individual households with the intention of maintaining rangeland health and promoting 4 livestock production (Yan et al., 2005). The original nomadic grazing system was replaced by 5 SH and MH grazing systems. In Maqu, the development of MH reflects a long social history 6 of collective living, family relationships, limitation of water resources and a lack of 7 infrastructure (Cao et al., 2009) that represents a compromise between people and 8 government that allow both to progress. A typical household grazes sheep and Yak, with 9 stocking rates of around 2 animals per hectare. When nomadic grazing stopped, herders 10 usually choose winter grasslands as their home place because these grasslands are productive 11 under natural conditions and trafficable at most times of the year. Summer grasslands are 12 difficult to access so less desirable for permanent residence. Generally livestock are 13 transferred in June from winter grasslands to summer grasslands, back to winter grasslands in 14 August, to summer grasslands in September and returned winter grasslands in October. 15 16 All experiments were conducted on winter grassland after herders had transferred to summer 17 grasslands at the beginning of July. Only land managed by farmers who had transferred their 18 livestock at the same time, had similar stocking rates (2 sheep per Ha as overseen by 19 Government) and had the same grassland type was selected. All sampling was conducted over 20 1 week in dry weather on 30 SH and 30 MH plots. Within each plot sampled, 3 sub-plots 21 were identified and three 50cm2×50cm2 quadrats were laid out at randomly selected locations 22 and orientations. The species richness based on species count per quadrat was expressed 7 1 using the Gleason Index (G) calculated as (Ma, 1994): G = S/lnA 2 (1) 3 where S = number of species in the quadrat and A = area of quadrat,. The coverage of 4 individual species was also visually estimated by the same observer for each plot. Land 5 management was classified by the number of households with right of access and an analysis 6 by household pressure (number of households with access to the land parcel) was conducted 7 using SPSS 15.0 statistical software. ANOVA was used to determine the significance of any 8 differences. 9 10 Results 11 The ten most common plant species found on the observation plots (Table 1) vary by land 12 management. Under SH management quality forage typified by Poaprafensis is no longer 13 common. Ligularia virgaurea, Anemone rivularia and Herba Taraxaci have become more 14 common species and are regarded as an indicator as degradation because they are poisonous 15 weeds that exploit bare soil surface exposed by intensive grazing pressure (Zhang et al., 2003; 16 Xie et al., 2010). When summarized by Gleason Index, the species richness of MH (24.4 ± 17 4.2) was marginally higher than that of SH (22.2 ± 3.9), but the difference in species richness 18 was not significant. The results do indicate however that since 1998 two species seem to have 19 been lost with the change to SH management. It is not possible to establish whether this is a 20 progressive tend that might indicate further species decline. 21 22 Household access within MH management was clustered into three classes: 3-7 households; 8 1 8-15 households; and >15 households. Species richness was positively correlated (r=0.51, 2 p<0.001) with increase in household access and there were significant differences by 3 household access and management type (Figure 1). The SH and 3-7 household MH plots had 4 lower species richness compared to the MH with >8 households. 5 6 Discussion 7 The results indicate that grassland species richness is linked to household access and the 8 intensity with which animals graze the grassland resource on a year round basis. SH 9 landholdings have little access to a range of pastures so the land has to be used at times when 10 it would traditionally be vacated (e.g. the shift from winter to summer grazing grounds and 11 vice versa) while MH landholdings can be managed in a more traditional manner with land 12 allocated to the most suitable grazing season. Therefore there is more sustained grazing 13 pressure on the plant assemblage in SH plots than in MH plots due to trampling (Ao et al., 14 2008) and non-selective grazing (Milchunas et al., 1998). The MH plots permit animals to be 15 more selective in their grazing choices as they have greater areas to forage over and the 16 owners have more management options for optimizing grazing (Richard et al., 2006; 17 Gimenez, 2002). It would also appear that the social pressure assumed by the theory of the 18 “tragedy of the commons” has not applied. Individuals seem not to have taken personal 19 short-term benefits at the expense of those neighbors they share with. This presumeably 20 reflects a tradition of nomadic cooperation. At the smaller management scale associated with 21 SH, decreased resource heterogeneity may have contributed to decreased niche dimensions 22 leading to the loss of grassland species richness (Olff and Ritchie, 1998; Spiegelberger et al., 9 1 2006; Harpole & Tilman, 2008) and to introduction of new species due to bare soil being 2 exposed. 3 4 Conclusion 5 The results of this study indicate that having a choice of grazing land associated with natural 6 seasonality, and sufficient area to permit selective grazing will protect plant diversity on 7 Qinghai-Tibet Plateau. Under MH (or even nomadic management), livestock can use 8 abundant low-quality food and while creating frequent but small disturbances across the 9 landscape, which is efficient for seed dispersion, provides niche openings for plant 10 development and facilitates spatially heterogeneous urine and dung deposition thus increasing 11 regeneration and soil heterogeneity (Olff & Ritchie, 1998). To achieve sustainable rangeland 12 management, lessons from traditional management (Yan et al., 2005) can be adapted to 13 permit controlled development of the resource without unwanted side-effects. The results of 14 this study indicate that Single household grassland management will probably cause a 15 decrease in plant diversity by focusing grazing pressure on small areas of grassland rather 16 than permiting a more sustainable dispersion over a wider area as can occur under multiple 17 household management. 18 19 Acknowledgements 20 Our work is funded by Ford Foundation (grant 1085-0629) “Grassland management research 21 based on livelihood of herders: A case study from the key water supplement area (Maqu) to 22 Yellow river”. 10 1 2 References 3 Adriansen H K., Nielsen T. 2002. Going Where the Grass is Greener: On the Study of 4 Pastoral Mobility in Ferlo. - Human Ecology. 30(2): 215-226. 5 Ao M, Ito M, Ito K. 2008. 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Responses of grassland ecosystems to precipitation and land 4 use along the Northeast China Transect. - Journal of Vegetation Science 13: 361-368. 15 Table 1: The 10 most common species found in winter grassland of SH and MH in the Maqu County survey 1 2 Rank order 1 2 3 4 5 6 7 8 9 10 3 4 5 6 7 16 Species Kobresia capillifolia Scirpus pumilus Potentiual Festucaovina Kobresia Wild Elymusnutans Ligularia virgaurea Anemone rivularia Herba Taraxaci Kobresia humilis SH 22(+/- 21) 19(+/- 17) 15.6(+/-11) 14(+/-8) 13(+/-8.1) 13(+/-16) 11.9(+/-13.7) 5.9(+/-3.6) 5.3(+/-3.4) 4.1(+/-1.7) Species Scirpus pumilus Festucaovina Kobresia capillifolia Tibeta himalaica(Bakerer) Tsui Poaprafensis Lancea tibetica Hook.F.Et Thomas Elymusnutans Potentiual Kobresia Wild Ranun Culus MH 26(+/- 15) 25(+/-11) 24 (+/- 20) 22(+/-14) 20(+/- 12) 19.3(+/-10.7) 19(+/-15) 16.1(+/-11.5) 15 (+/-12.2) 12(+/-9) 1 17