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Sacred groves: a model of Zagros forests for carbon sequestration and climate change mitigation

Published online by Cambridge University Press:  22 May 2023

Aioub Moradi
Affiliation:
Department of Forestry, The Center for Research and Development of Northern Zagros Forestry, University of Kurdistan, Sanandaj, Iran
Naghi Shabanian*
Affiliation:
Department of Forestry, The Center for Research and Development of Northern Zagros Forestry, University of Kurdistan, Sanandaj, Iran
*
Corresponding author: Dr Naghi Shabanian; Email: n.shabanian@uok.ac.ir
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Summary

Forests are the most important carbon pools among terrestrial ecosystems, and ensuring less disturbance of sacred groves might constitute a form of forest management for carbon sequestration and climate change reduction. The carbon contents in Zagros oak sacred groves and silvopastoral lands were compared to determine the carbon sequestration potential of these forests. Using a nested sampling design, we measured total carbon content (tC ha–1; aboveground tree biomass, aboveground sapling biomass, belowground biomass, soil organic carbon, leaf litter, herbs and grasses and dead wood and fallen stumps) in both forest groves and silvopastoral lands. The mean total biomass and mean total carbon content varied between sacred groves (453.8 t ha–1 and 338.79 tC ha–1, respectively) and silvopastoral lands (89.4 t ha–1 and 113.46 tC ha–1, respectively). Mean soil organic carbon was significantly lower (71.44 tC ha–1) in silvopastoral lands than in sacred groves (125.49 tC ha–1). The mean total sequestered carbon dioxide (CO2) was 1243.36 tCO2 ha–1 in the sacred groves and 416.40 tCO2 ha–1 in silvopastoral lands. We conclude that human activities have reduced the CO2 absorption capacity of the forests. The substantial disparities between the landscapes emphasize the need to restore damaged forests, and sacred groves might be a useful model for increasing carbon storage in these forests.

Type
Research Paper
Copyright
© The Author(s), 2023. Published by Cambridge University Press on behalf of Foundation for Environmental Conservation

Introduction

Increased concerns about global warming have resulted in special attention being paid to forests, soils and their ability to sustain carbon sequestration (Johnsen et al. Reference Johnsen, Wear, Oren, Teskey, Sanchez and Will2001, Pahlavan Yali et al. Reference Pahlavan Yali, Zarrinkafsh and Moeini2016). Forest ecosystems are the most important carbon pools among terrestrial ecosystems and can mitigate climate change (Labrecque et al. Reference Labrecque, Fournier, Luther and Piercey2006, Pan et al. Reference Pan, Birdsey, Fang, Houghton, Kauppi and Kurz2011, Lin & Ge, Reference Lin and Ge2019, Santini et al. Reference Santini, Adame, Nolan, Miquelajauregui, Piñero and Mastretta-Yanes2019, Zhang et al. Reference Zhang, Du, Zhou, Li, Mao and Dong2019). The high capacity of these ecosystems to reduce greenhouse gas emissions makes carbon management a key component of future natural climate solutions (Griscom et al. Reference Griscom, Adams, Ellis, Houghton, Lomax and Miteva2017, Fargione et al. Reference Fargione, Bassett, Boucher, Bridgham, Conant and Cook-Patton2018, Ontl et al. Reference Ontl, Janowiak, Swanston, Daley, Handler and Cornett2020). The Zagros forests span more than 5 million ha and are considered to represent the natural forest ecosystems of Iran, and their economic value in terms of carbon sequestration is substantial (Jazirehi & Ebrahimi Rostaghi Reference Jazirehi and Ebrahimi Rostaghi2013). Despite severe and continuous exploitation of these forests, some parts have been less disturbed, notably sacred groves, which are sacred religious areas and cemeteries (Pungetti et al. Reference Pungetti, Oviedo and Hooke2012, Plieninger et al. Reference Plieninger, Quintas-Soriano, Torralba, Mohammadi Samani and Shakeri2020). In these, a more natural state of the Zagros forests can be found (Shakeri Reference Shakeri2007, Jazirehi & Ebrahimi Rostaghi Reference Jazirehi and Ebrahimi Rostaghi2013).

In the northern Zagros forests, livelihoods include animal husbandry and traditional agriculture. Animal husbandry has a long tradition, and the leaves of local oak trees are used to provide livestock fodder. Overgrazing is one of the most significant human disturbances (Zhou et al. Reference Zhou, Li, Chen, Zhang and Li2011, Hu et al. Reference Hu, Li, Guo, Niu, He, Li and Yu2016, Schulz et al. Reference Schulz, Voigt, Beusch, Alemida-Cortez, Kowarik, Walz and Cierjacks2016, Gebregergs et al. Reference Gebregergs, Tessema, Solomon and Birhane2019), and grazing exclusion can help with the recovery of degraded ecosystems and enhance carbon sequestration (Qiu et al. Reference Qiu, Wei, Zhang and Cheng2013, Hu et al. Reference Hu, Li, Guo, Niu, He, Li and Yu2016, Ma et al. Reference Ma, Ding and Li2016, Atsbha et al. Reference Atsbha, Belayneh Desta and Zewdu2019, Gebregergs et al. Reference Gebregergs, Tessema, Solomon and Birhane2019, Liu et al. Reference Liu, Sheng, Wang, Ma, Huang and Li2020). Grazing, cutting down trees, collecting fodder and firewood and harvesting other crops from sacred groves are all forbidden by local community laws (Plieninger et al. Reference Plieninger, Quintas-Soriano, Torralba, Mohammadi Samani and Shakeri2020). The Zagros sacred groves represent an opportunity to see what the Zagros forests might look like in a less disturbed state. Here, we compare the carbon content of the sacred groves and silvopastoral lands to improve understanding of the capacity of Zagros oak forests to sequester carbon.

Methods

Study site description

The study area includes sacred groves and silvopastoral lands in Baneh County (Zagros Mountains, Iran; 35º48′02″–36°11′40″N and 45°32′45″–46°10′25″E; Fig. 1). The climate is semi-humid and cold. The total annual precipitation is 600–800 mm. Dominant tree species are the oaks Quercus brantii Lindel, Quercus libani Olive and Quercus infectoria Olive. This study focused on the villages of Hange Jal, Booien Olya, Nejo, Yaghoub Abad and Gashkese, in each of which cemeteries more than 1 ha in area were selected as sacred groves. Silvopastoral areas were chosen from the forests surrounding these stands that had the same physiographical characteristics as the sacred groves. The land use of the forest is subject to Galazani, which involves gathering the branches and leaves of oak trees to feed livestock in the cold season, livestock grazing and other usages, such as harvesting the wood, by forest residents (Fig. 1).

Figure 1. Examples of a sacred grove and silvopastoral land in Hange Jal village.

Sampling design

We used nested concentric plots (ICIMOD et al. 2010, Karki et al. Reference Karki, Joshi, Udas, Adhikari, Sherpa and Kotru2016), each including a large circular plot (250 m2 with an 8.20m radius) for tree measurements, a larger sub-plot (100 m2 with a 5.65-m radius) for saplings, a smaller sub-plot (3.14 m2 with a 1.00-m radius) to count regeneration (seedlings) and the smallest sub-plot (0.56-m radius) for leaf litter, herbs, grasses and soil samples (Fig. 2). Sampling centres were determined using a systematic random method, and 20 plots were surveyed in each site (10 plots in sacred groves, 10 plots in the silvopastoral lands, study total of 100 plots).

Figure 2. Concentric nested circular plots. DBH = diameter at breast height.

Measurement of forest carbon stock

In both land-use areas, the diameter at breast height (DBH) and height of individual trees (DBH ≥5 cm) were measured. All trees that were measured were documented and identified to the species level. In the laboratory, the wood-specific densities (ρ) of the different tree species in each land use were measured. Above ground tree biomass (AGTB), aboveground sapling biomass (AGSB), mass of leaf litter, herbs and grass (LHG) and mass of dead wood and fallen stumps (DWS) were calculated using the allometric equations of Chave et al. (Reference Chave, Andalo, Brown, Cairns, Chambers and Eamus2005) and ICIMOD et al. (2010). Belowground biomass (BGB) was calculated using the equation of Cairns et al. (Reference Cairns, Brown, Helmer and Baumgardner1997). Soil organic carbon (SOC) was measured in 100 soil samples taken from depths of 0–15 and 15–30 cm. The percentage of SOC was determined using the Walkley and Black (Reference Walkley and Black1934) method (Nosetto et al. Reference Nosetto, Jobbagy and Paruelo2006, Amanuel et al. Reference Amanuel, Yimer and Karltun2018). The SOC stock was then calculated using the formulae of ICIMOD et al. (2010) and Karki et al. (Reference Karki, Joshi, Udas, Adhikari, Sherpa and Kotru2016). The total carbon content (tC ha–1) within each land use was then estimated from the sum of the above variables (ICIMOD et al. 2010, Karki et al. Reference Karki, Joshi, Udas, Adhikari, Sherpa and Kotru2016, Sumarga et al. Reference Sumarga, Nurudin and Suwandhi2020). The total forest carbon stock was converted into a carbon dioxide (CO2) equivalent by multiplying by 3.67 (Pearson et al. Reference Pearson, Brown and Birdsey2007).

SPSS version 23 was used for all analyses. The data and residuals were tested for normality. After assessing the homogeneity of variance, t-tests were used to compare the mean values of the variables between the two land uses.

Results

The studied variables were significantly different between the sacred groves and silvopastoral lands (Table 1). Aboveground and belowground tree biomass values in the sacred groves were c. five times greater than in the silvopastoral areas. In the silvopastoral areas, the values of herbs and grass, leaf litter and dead and fallen wood were much lower than in the sacred groves (Table 1). Total forest biomass and total carbon in the sacred groves were five- and three-fold greater, respectively, than in the silvopastoral lands (Table 2).

Table 1. Mean biomass values under the two land uses. The same superscript letters beside the means of any variable indicate no difference at the 1% level between attributes.

The same Roman letters beside means of any parameter indicate no difference at the 5% level between two land uses.

AGSB = aboveground sapling biomass; AGTB = aboveground tree biomass; BGB = belowground biomass; DWS = dead wood and fallen stumps; LHG = leaf litter, herbs and grass; TFBI = total forest biomass.

Table 2. Mean total carbon content and composition percentages by type under the two land uses.

AGSB = aboveground sapling biomass; AGTB = aboveground tree biomass; BGB = belowground biomass; DWS = dead wood and fallen stumps; LHG = leaf litter, herbs and grass; SOC = soil organic carbon; TBC = total biomass carbon; TC = total carbon.

Biomass

The mean total biomass values of the sacred groves and silvopastoral lands were 453.8 and 89.4 t ha–1, respectively (Table 1). However, the proportions of the biomass in each of the pools were similar between the land uses; most of the biomass was in AGTB and the least was in AGSB (Table 1). The DWS biomass was substantially greater in the sacred groves (Table 1). Although the LHG biomass was also much greater in sacred groves than in the silvopastoral areas, the percentage of LHG in the total biomass was greater in the latter.

Carbon content

The mean total carbon contents were 338.79 and 113.46 tC ha–1, respectively, in the sacred groves and silvopastoral lands, and the carbon distributions among the carbon pools also differed (Table 2). AGTB and soil contributed most to the total forest carbon stock, while ABSB contributed the least in both land uses. The mean SOC was significantly lower (71.44 tC ha–1) in the silvopastoral lands than in the sacred groves (125.49 tC ha–1). Importantly, in silvopastoral lands the soil carbon (62.96% of total carbon) was greater than the total biomass carbon (37.04% of total carbon). The mean total sequestered carbon dioxide (CO2) was 1243.36 tCO2 ha–1 in sacred groves and 416.40 tCO2 ha–1 in silvopastoral lands.

Discussion

We compared for the first time the biomass and carbon storage capacity of sacred groves in the Zagros forests with those of adjacent heavily used silvopastoral lands. Aboveground biomass and the total quantity of carbon in all carbon pools were substantially greater in sacred groves than in silvopastoral fields. In the sacred groves there were multi-storey tree cover, trees of greater height and diameter, denser canopy, more abundant leaf litter, greater deadwood, richer grass cover under the canopy and greater species diversity. These findings agree with earlier studies (Dibaba et al. Reference Dibaba, Soromessa and Workineh2019, Baul et al. Reference Baul, Chakraborty, Nandi, Mohiuddin, Kilpeläinen and Sultana2021), suggesting that forest stands with high species diversity and trees with large diameters and heights may in themselves store more carbon. For example, in homestead forests in Bangladesh, Baul et al. (Reference Baul, Chakraborty, Nandi, Mohiuddin, Kilpeläinen and Sultana2021) inferred that when tree height and DBH increased by one unit each, the biomass carbon stock increased by 11 and 3 Mg C ha−1, respectively. Dibaba et al. (Reference Dibaba, Soromessa and Workineh2019) observed that larger trees with greater diameters have the greatest carbon stores in terms of biomass. Wegiel and Polowy (Reference Wegiel and Polowy2020) demonstrated that the amount of carbon stored in plants is strongly related to their biomass. The greater the potential of aboveground and belowground biomass to produce carbon in diverse species and ecosystems, the more carbon is stored in tree trunks, leaf litter and soil.

Grazing exclusion work has shown that overgrazing is among the most significant of human disturbances impacting the performance of ecosystems and SOC stocks (Liu et al. Reference Liu, Sheng, Wang, Ma, Huang and Li2020), reducing plant cover, biomass and ecosystem productivity (Atsbha et al. Reference Atsbha, Belayneh Desta and Zewdu2019). Grazing exclusion can help recover degraded ecosystems (Hu et al. Reference Hu, Li, Guo, Niu, He, Li and Yu2016) and promote carbon deposition (Hu et al. Reference Hu, Li, Guo, Niu, He, Li and Yu2016, Gebregergs et al. Reference Gebregergs, Tessema, Solomon and Birhane2019). In the Zagros silvopastoral lands, animal husbandry is carried out using traditional methods; exacerbating the loss of grass cover on the forest floor, the branches and leaves of the trees in these forests are also used as fodder for the grazing of livestock through the pollarding system. Pollarding lowers tree production and growth capabilities within this land use (Soltani et al. Reference Soltani, Sadeghi Kaji and Kahyani2020). Low foliage production, little leaf litter on forest floors, sparse grass cover, high soil erosion and compaction of the soil surface result in low biomass and carbon inputs and storage levels that are much lower than predicted in the silvopastoral areas. Under local community rules, grazing is prohibited in sacred groves, and this is evidently one of the main contributors to the increased carbon observed in the sacred groves. Tsegay and Meng (Reference Tsegay and Meng2021) also found that exclosure of forests plays a fundamental role in sustaining sinks of carbon, and Speed et al. (Reference Speed, Martinsen, Mysterud, Mulder, Holand and Austrheim2014) concluded that grazing exclusion can increase aboveground carbon stocks, albeit at a low rate. Dong et al. (Reference Dong, Martinsen, Wu, Zheng, Liang, Liu and Mulder2021) suggested that grazing exclusion increased aboveground and belowground biomass in semi-arid grasslands and that this contributed to increased SOC concentration. In the Zagros forests, the mean carbon pools in sacred groves were significantly greater than in the silvopastoral lands. These sacred groves give an idea of what the biomass and carbon storage levels and distributions might be in restored Zagros forests. Tsegay and Meng (Reference Tsegay and Meng2021) and Gebregergs et al. (Reference Gebregergs, Tessema, Solomon and Birhane2019) demonstrated that aboveground and belowground carbon stocks were significantly greater under grazing exclusion. Sacred groves also have much greater aboveground and belowground carbon stocks. Grazing and tree cutting are prohibited in the Zagros sacred forests, resulting in much greater biomass and carbon storage in trees and soil than within silvopastoral fields.

The present results indicate that Zagros forests are currently far from their natural state; grazing and overexploitation are prominent drivers of this devastation. In the northern Loess Plateau of China, overgrazing has had a detrimental impact on plant development and soil carbon supply, plant cover, height, lead litter, aboveground and belowground productivity and soil carbon stock, all of which declined with increased grazing intensity (Zhu et al. Reference Zhu, Tang, Chen, Shangguan and Deng2018). Other studies, such as that of Limpert et al. (Reference Limpert, Carnell and Macreadie2021), have indicated that grazing exclusion increases the concentration of carbon in the soil and lowers carbon emissions.

Renhui et al. (Reference Renhui, Yinzhan, Liqi, Dong, Yanchun and Yuan2022) demonstrated that plant density, SOC and total nitrogen significantly increase with grazing exclusion; this grazing exclusion also strengthen the relationships between plant variables and SOC. The present results and those from other grazing exclusion studies (Nosetto et al. Reference Nosetto, Jobbagy and Paruelo2006, Qiu et al. Reference Qiu, Wei, Zhang and Cheng2013, Speed et al. Reference Speed, Martinsen, Mysterud, Mulder, Holand and Austrheim2014, Conant et al. Reference Conant, Cerri, Osborne and Paustian2017, Liu et al. Reference Liu, Sheng, Wang, Ma, Huang and Li2020) point to the necessity of restoring silvopastoral lands, balancing grazing and preventing the degradation and overexploitation of these forests. However, grazing has variable effects on SOC depending on the soil type, geography and climate (Wade et al. Reference Wade, Sonnier and Boughton2022), and in different areas livestock grazing may require different management strategies to ensure optimal carbon sequestration.

Negative anthropogenic impacts on carbon storage have been reported. For example, Zhu et al. (Reference Zhu, Ciais, Bastos, Ballantyne, Chevallier and Gasser2021) showed that emissions from the land could increase with deforestation. Shaw et al. (Reference Shaw, Rodrigue, Voicu, Latifovic, Pouliot and Hayne2021) demonstrated that anthropogenic and natural disturbances changed a study area from a net carbon sink into a net carbon source, and Hoover et al. (Reference Hoover and Smith2021) suggested that mean aboveground live tree carbon accumulation rates could increase considerably when anthropogenic disturbances are excluded. Our findings are consistent with those from these previous investigations, suggesting that the major differences between biomass and carbon in the two analysed applications were attributable to anthropogenic disturbances.

The proportions of each carbon pool in the overall amount of carbon stored were also substantial. In the sacred groves, two-thirds of the carbon were in aboveground and belowground pools, while one-third was in the soil. In contrast, in silvopastoral lands, the soil accounted for c. two-thirds of the total carbon, the remainder being in belowground and aboveground pools. This indicates a decrease in tree density and seedlings and a reduction in regeneration in the silvopastoral lands. The amount of soil carbon in sacred groves was c. 1.8 times that of silvopastoral lands. The change in the amount of soil carbon sequestration depends on the amount of carbon entering the soil through plant debris and the amount of carbon lost through decomposition (Rice Reference Rice2004). Singh et al. (Reference Singh, Bala, Chaudhuri and Meena2003), Rice (Reference Rice2004), Varamesh (Reference Varamesh2009), Salehi and Noormohammadi (Reference Salehi and Noormohammadi2012) and Pahlavan Yali et al. (Reference Pahlavan Yali, Zarrinkafsh and Moeini2016), amongst others, have pointed to the relationship between SOC sequestration and vegetation percentage, leaf litter, crop residues, land use and management. The significant difference of soil carbon in the present two land-use areas was also attributable to the difference in the return of organic matter to the soil; this was reduced in the silvopastoral lands because, in such lands, in addition to livestock grazing, the production capacity of the main element – trees – is removed due to pruning, reducing the production of foliage and leaving the forest floor bare of leaf litter and grass (Moradi & Shabanian Reference Moradi and Shabanian2022).

Sacred groves with high carbon reserves are part of the Zagros forests. In fact, if the Zagros forests were less degraded, they would be in a similar situation to the sacred groves today, and these forests could have a greater impact on carbon sequestration. Although preventing deforestation is necessary for the mitigation of climate change, it is not sufficient to achieve such mitigation (Erb et al. Reference Erb, Kastner, Plutzar, Bais, Carvalhais and Fetzel2018). Sacred groves can protect forest ecosystems and might help reduce climate change through carbon sequestration (Shrestha et al. Reference Shrestha, Devkota and Sharma2016). The Zagros sacred groves currently store 827 000 kg CO2 ha–1 more than the silvopastoral lands, and this is a sign of the high level of degradation in the forests of the study area.

Conclusions

The Zagros forests offer a useful model of what happens when forests are seriously damaged. The significant differences in biomass and carbon stocks between the sacred groves and silvopastoral lands indicate the potentially great value of restoring these forests. Here, the sacred groves are the most significant sites for biodiversity conservation and for carbon storage, as more formal types of protected areas have frequently failed in these areas (e.g., forest genetic resources under the management of the Department of Natural Resources and Watershed Management of Kurdistan Province in the study area or protected areas under the management of the Department of Environment Protection in the Zagros forests). The number of sacred groves in the forests of the northern Zagros forests is significant; these forests contain essential carbon reserves and high levels of biodiversity that are of great environmental importance. The Zagros forests of western Iran occupy a vast and important area, and the potential role of this natural and valuable ecosystem in storing carbon and perhaps helping to reduce climate change is becoming more apparent.

Acknowledgements

We express our sincere gratitude to the Vice Chancellorship of Research and Technology, University of Kurdistan, for supporting this research.

Financial support

None.

Competing interests

The authors declare none.

Ethical standards

None.

References

Amanuel, W, Yimer, F, Karltun, E (2018) Soil organic carbon variation in relation to land use changes: the case of Birr watershed, upper Blue Nile River Basin, Ethiopia. Journal of Ecology and Environment 42: 16.CrossRefGoogle Scholar
Atsbha, T, Belayneh Desta, A, Zewdu, T (2019) Carbon sequestration potential of natural vegetation under grazing influence in Southern Tigray, Ethiopia: implication for climate change mitigation. Heliyon 5: e02329.CrossRefGoogle ScholarPubMed
Baul, TK, Chakraborty, A, Nandi, R, Mohiuddin, M, Kilpeläinen, A, Sultana, T (2021) Effects of tree species diversity and stand structure on carbon stocks of homestead forests in Maheshkhali Island, southern Bangladesh. Carbon Balance and Management 16: 11.CrossRefGoogle ScholarPubMed
Cairns, MA, Brown, S, Helmer, EH, Baumgardner, GA (1997) Root biomass allocation in the world’s upland forests. Oecologia 111: 111.CrossRefGoogle ScholarPubMed
Chave, J, Andalo, C, Brown, S, Cairns, MA, Chambers, JQ, Eamus, D (2005) Tree allometry and improved estimation of carbon stocks. Oecologia 147: 8799.CrossRefGoogle Scholar
Conant, RT, Cerri, CEP, Osborne, BB, Paustian, K (2017) Grassland management impacts on soil carbon stocks: a new synthesis. Ecological Application 27: 662668.CrossRefGoogle Scholar
Dibaba, A, Soromessa, T, Workineh, B (2019) Carbon stock of the various carbon pools in Gerba-Dima moist Afromontane forest, south-western Ethiopia. Carbon Balance and Management 14: 1.CrossRefGoogle ScholarPubMed
Dong, L, Martinsen, V, Wu, Y, Zheng, Y, Liang, C, Liu, Z, Mulder, J (2021) Effect of grazing exclusion and rotational grazing on labile soil organic carbon in north China. European Journal of Soil Science 72: 372384.CrossRefGoogle Scholar
Erb, KH, Kastner, T, Plutzar, C, Bais, ALS, Carvalhais, N, Fetzel, T et al. (2018) Unexpectedly large impact of forest management and grazing on global vegetation biomass. Nature 553: 7376.CrossRefGoogle ScholarPubMed
Fargione, JE, Bassett, S, Boucher, T, Bridgham, SD, Conant, RT, Cook-Patton, SC et al. (2018) Natural climate solutions for the United States. Science Advances 4: 115.CrossRefGoogle ScholarPubMed
Gebregergs, T, Tessema, ZK, Solomon, N, Birhane, E (2019) Carbon sequestration and soil restoration potential of grazing lands under exclosure management in a semi-arid environment of northern Ethiopia. Ecology and Evolution 9: 64686479.CrossRefGoogle Scholar
Griscom, BW, Adams, J, Ellis, PW, Houghton, RA, Lomax, G, Miteva, DA et al. (2017) Natural climate solutions. Proceeding of the National Academy of Sciences of the United States of America 114: 1164511650.CrossRefGoogle ScholarPubMed
Hoover, CM, Smith, JE (2021) Current aboveground live tree carbon stocks and annual net change in forests of conterminous United States. Carbon Balance and Management 16: 17.CrossRefGoogle ScholarPubMed
Hu, Z, Li, S, Guo, Q, Niu, S, He, N, Li, L, Yu, G (2016) A synthesis of the effect of grazing exclusion on carbon dynamics in grasslands in China. Global Change Biololgy 22:13851393.CrossRefGoogle ScholarPubMed
ICIMOD, ANSAB, FECOFUN (2010) Forest Carbon Measurement Guidelines. Kathmandu, Nepal: ICIMOD, 67 pp.Google Scholar
Jazirehi, MH, Ebrahimi Rostaghi, M (2013) Silviculture in Zagros. Tehran, Iran: University of Tehran Press, 560 pp.Google Scholar
Johnsen, KH, Wear, D, Oren, R, Teskey, RO, Sanchez, F, Will, R et al. (2001) Meeting globalpolicy commitments: carbon sequestration and southern pine forests. Journal of Forestry 99: 1421.Google Scholar
Karki, S, Joshi, NR, Udas, E, Adhikari, MD, Sherpa, S, Kotru, R et al. (2016) Assessment of Forest Carbon Stock and Carbon Sequestration Rates at the ICIMOD Knowledge Park in Godavari. Kathmandu, Nepal: ICIMOD, 41 pp.Google Scholar
Labrecque, S, Fournier, R, Luther, J, Piercey, D (2006) A comparison of four methods to map biomass from Landsat-TM and inventory data in western Newfoundland. Journal of Forest Ecology and Management 226:129144.CrossRefGoogle Scholar
Limpert, KE, Carnell, PE, Macreadie, PI (2021) Managing agricultural grazing to enhance the carbon sequestration capacity of freshwater wetlands. Wetlands Ecology and Management 29: 231244.CrossRefGoogle Scholar
Lin, B, Ge, J (2019) Valued forest carbon sinks: how much emissions abatement costs could be reduced in China. Journal of Cleaner Prodoction 224: 455464.CrossRefGoogle Scholar
Liu, X, Sheng, H, Wang, Z, Ma, Z, Huang, X, Li, L (2020) Does grazing exclusion improve soil carbon and nitrogen stocks in alpine grasslands on the Qinghai–Tibetan Plateau? A meta-analysis. Sustainability 12: 977.CrossRefGoogle Scholar
Ma, W, Ding, K, Li, Z (2016) Comparison of soil carbon and nitrogen stocks at grazing-excluded and yak grazed alpine meadow sites in Qinghai–Tibetan Plateau, China. Ecological Engineering 87:203211.CrossRefGoogle Scholar
Moradi, A, Shabanian, N (2022) Land-use change in the Zagros forests and its impact on soil carbon sequestration. Environmental, Development and Sustainability. Epub ahead of print. https://doi.org/10.1007/s10668-022-02272-z.CrossRefGoogle Scholar
Nosetto, MD, Jobbagy, EG, Paruelo, JM (2006) Carbon sequestration in semi-arid rangelands: comparison of Pinus ponderosa plantations and grazing exclusion in NW Patagonia. Journal of Arid Environment 67:142156.CrossRefGoogle Scholar
Ontl, TA, Janowiak, MK, Swanston, CW, Daley, J, Handler, S, Cornett, M et al. (2020) Forest management for carbon sequestration and climate adaptation. Journal of Forestry 118: 86101.CrossRefGoogle Scholar
Pahlavan Yali, Z, Zarrinkafsh, M, Moeini, A (2016) Quantitative estimation of soil carbon sequestration in three land use types (orchard, paddy rice and forest) in a part of Ramsar lands, northern Iran. Journal of Water and Soil 30: 758768.Google Scholar
Pan, Y, Birdsey, RA, Fang, J, Houghton, R, Kauppi, PE, Kurz, WA et al. (2011) A large and persistent carbon sink in the world’s forests. Science 333: 988993.CrossRefGoogle ScholarPubMed
Pearson, TR, Brown, SL, Birdsey, RA (2007) Measurement Guidelines for the Sequestration of Forest Carbon. Gen. Tech. Rep. NRS-18. Newtown Square, PA, USA: US Department of Agriculture, Forest Service, Northern Research Station.Google Scholar
Plieninger, T, Quintas-Soriano, C, Torralba, M, Mohammadi Samani, K, Shakeri, Z (2020) Social dynamics of values, taboos and perceived threats around sacred groves in Kurdistan, Iran. People and Nature 2: 12371250.CrossRefGoogle Scholar
Pungetti, G, Oviedo, G, Hooke, D (2012) Sacred Species and Sites: Advances in Biocultural Conservation. Cambridge, UK: Cambridge University Press, 472 pp.CrossRefGoogle Scholar
Qiu, LP, Wei, XR, Zhang, XC, Cheng, JM (2013) Ecosystem carbon and nitrogen accumulation after grazing exclusion in semiarid grassland. PLoS ONE 8: e10371.CrossRefGoogle ScholarPubMed
Renhui, M, Yinzhan, L, Liqi, W, Dong, W, Yanchun, L, Yuan, M et al. (2022) Effects of long-term grazing exclusion on plant and soil properties vary with position in dune systems in the Horqin Sandy Land. CATENA 209: 105860.Google Scholar
Rice, CW (2004) Carbon cycle in soils – dynamics and management. Encyclopedia of Soils in the Environment 4:164170.Google Scholar
Salehi, A, Noormohammadi, E (2012) Effect of grazed and surface scrafication on soil properties and regeneration in centeral Zagros forests (case study: Aleshtar city forests). Journal of Forest and Wood Products 65: 315325.Google Scholar
Santini, NS, Adame, MF, Nolan, RH, Miquelajauregui, Y, Piñero, D, Mastretta-Yanes, A et al. (2019) Storage of organic carbon in the soils of Mexican temperate forests. Journal of Forest Ecology and Management 446: 115125.CrossRefGoogle Scholar
Schulz, K, Voigt, K, Beusch, C, Alemida-Cortez, JA, Kowarik, I, Walz, A, Cierjacks, A (2016) Grazing deteriorates the soil carbon stocks of Caatinga forest ecosystems in Brazil. Journal of Forest Ecology and Management 367: 6270.CrossRefGoogle Scholar
Shakeri, Z (2007) Silvicultural and Ecological Effect of Galazani on Oak Trees in Baneh Forest (Kurdistan Province NW Iran). MSc thesis. Tehran, Iran: Tehran University, 65 pp.Google Scholar
Shaw, CH, Rodrigue, S, Voicu, MF, Latifovic, R, Pouliot, D, Hayne, S et al. (2021) Cumulative effects of natural and anthropogenic disturbances on the forest carbon balance in the oil sands region of Alberta, Canada; a pilot study (1985–2012). Carbon Balance and Management 16: 3.CrossRefGoogle Scholar
Shrestha, LJ, Devkota, MP, Sharma, BK (2016) Are sacred groves of Kathmandu Valley efficient in sequestering carbon? Journal of Botany 2016: 7695154.CrossRefGoogle Scholar
Singh, G, Bala, N, Chaudhuri, K, Meena, R (2003) Carbon sequestration potential of common access resources in arid and semi-arid regions of northwestern India. Indian Forest 129: 859864.Google Scholar
Soltani, A, Sadeghi Kaji, H, Kahyani, S (2020) Effects of different land-use systems (grazing and understory cultivation) on growth and yield of semi-arid oak coppices. Journal of Forestry Research 31: 22352244.CrossRefGoogle Scholar
Speed, JDM, Martinsen, V, Mysterud, A, Mulder, J, Holand, O, Austrheim, G (2014) Long-term increase in aboveground carbon stocks following exclusion of grazers and forest establishment in an alpine ecosystem. Ecosystems 17: 11381150.CrossRefGoogle Scholar
Sumarga, E, Nurudin, N, Suwandhi, I (2020) Land-cover and elevation-based mapping of aboveground carbon in a tropical mixed-shrub forest area in west Java, Indonesia. Forests 11: 636.CrossRefGoogle Scholar
Tsegay, G, Meng, XZ (2021) Impact of ex-closure in above and below ground carbon stock biomass. Forests 12: 130.CrossRefGoogle Scholar
Varamesh, S (2009) Comparison of Carbon Sequestration in Broad Leaved and Needle Leaved Species in Urban Forest (Case Study: Chitgar Park of Tehran). MSc thesis. Tehran, Iran: Tarbiat Modares University, 130 pp.Google Scholar
Wade, C, Sonnier, G, Boughton, EH (2022) Does grazing affect soil carbon in subtropical humid seminatural grasslands? Rangeland Ecology & Management 80: 1017.CrossRefGoogle Scholar
Walkley, A, Black, IA (1934) An examination of the Degtjareff method for determining soil organic matter and a proposed modification of the chromic acid titration method. Soil Science 37: 2938.CrossRefGoogle Scholar
Wegiel, A, Polowy, K (2020) Aboveground carbon content and storage in mature scots pine stands of different densities. Forests 11: 240.CrossRefGoogle Scholar
Zhang, M, Du, H, Zhou, G, Li, X, Mao, F, Dong, L et al. (2019) Estimating forest aboveground carbon storage in Hang-Jia-Hu using Landsat TM/OLI data and random forest model. Forests 10: 1004.CrossRefGoogle Scholar
Zhou, Z-Y, Li, F-R, Chen, S-K, Zhang, H-R, Li, G (2011) Dynamics of vegetation and soil carbon and nitrogen accumulation over 26 years under controlled grazing in a desert shrubland. Plant and Soil 341: 257268.CrossRefGoogle Scholar
Zhu, G, Tang, Z, Chen, L, Shangguan, Z, Deng, L (2018) Overgrazing depresses soil carbon stock through changing plant diversity in temperate grassland of the Loess Plateau. Plant, Soil and Environment 64: 16.CrossRefGoogle Scholar
Zhu, L, Ciais, P, Bastos, A, Ballantyne, AP, Chevallier, F, Gasser, T et al. (2021) Decadal variability in land carbon sink efficiency. Carbon Balance and Managemen 16: 15.CrossRefGoogle ScholarPubMed
Figure 0

Figure 1. Examples of a sacred grove and silvopastoral land in Hange Jal village.

Figure 1

Figure 2. Concentric nested circular plots. DBH = diameter at breast height.

Figure 2

Table 1. Mean biomass values under the two land uses. The same superscript letters beside the means of any variable indicate no difference at the 1% level between attributes.

Figure 3

Table 2. Mean total carbon content and composition percentages by type under the two land uses.