- Original Article
- Open Access
Effects of adjacent land-use types on the distribution of soil organic carbon stocks in the montane area of central Taiwan
© The Author(s) 2016
- Received: 18 July 2016
- Accepted: 19 October 2016
- Published: 25 October 2016
Soil organic carbon (SOC) stocks can be altered through reforestation and cropping. We estimated the effects of land use on SOC stocks after natural deciduous forests replaced by crops and coniferous plantations by examining the vertical distribution of SOC stocks at different depth intervals in an adjacent Oolong tea (Camellia sinensis L.) plantation, Moso bamboo (Phyllostachys pubescens) forest, Japanese cedar (Cryptomeria japonica) forest, and Taiwania (Taiwania cryptomerioides) forest in central Taiwan. The main soil characteristics, soil nitrogen (N) content, and soil carbon to nitrogen (C/N) ratio were also determined.
Different land uses resulted in significantly higher bulk density, lower cation exchange capacity, SOC, soil N, soil C/N ratio, and SOC stocks in croplands compared to forestlands. Due to the long-term application of chemical fertilizers, a significantly lower soil pH was found in the tea plantation. Croplands had a lower soil C/N ratio because of less C input into the soil and a higher mineralization rate of organic carbon during cultivation. Similar SOC stocks were found in Taiwania and Japanese cedar forests (148.5 and 151.8 Mg C ha−1, respectively), while the tea plantation had comparable SOC stocks to the bamboo forest (101.8 and 100.5 Mg C ha−1, respectively). Over 40% of SOC stocks was stored in croplands and over 56% was stored in forestland within the upper 10 cm of soil.
Coniferous plantations can contribute to a higher SOC stock than croplands, and a significant difference can be found in the top 0–5 cm of soil.
- Bamboo forest
- Carbon to nitrogen ratio
- Japanese cedar
- Land-use type
- Soil organic carbon stocks
- Tea plantation
Carbon dioxide (CO2) can be released into the atmosphere via fossil fuel combustion and land-use changes to accelerate the greenhouse gas effect, leading to worldwide extreme weather, sea level rise, and habitation and ecological damage caused by global warming. In 2010, forests covered over 31% of land area in the world (FAO 2011) and thus have an important role in the C cycle. Since C is fixed as biomass C and soil organic carbon (SOC) in forest systems and by the end of the 20th century over 70% C was sequestrated in soil and peat deposits (Dixon et al. 1994), the role of forest SOC stocks and the possibilities of SOC loss caused by land use have been research areas of interest.
Land-use changes can accelerate SOC stock loss through erosion or vegetation conversion, and SOC stocks in surface soil and subsoil can change after native forest is converted to agricultural systems (Smith et al. 2002; Chen et al. 2004; Schulp et al. 2008; Fu et al. 2010; Don et al. 2011). Soil carbon content is known to decline once the natural forest has been cleared for croplands and plantations. Smith et al. (2002) suggested that converting large-scale of Amazonian tropical forest in Curuá-Una, Brazil to tree plantations of Pinus caribaea var. hondurensis Barrett and Golfari, Euxylophora paraensis Hub., Carapa guianensis Aubl., and Leguminosae decreased 9–13% C stocks in the 0–20 cm soils. Estimates of SOC stocks decline indicated by various researchers worldwide include an SOC stocks decrease of 13% from native forest to plantation and 42% from native forest to cropland (Guo and Gifford 2002), a decrease of 30% due to the conversion of forests to cultivated lands (Murty et al. 2002), and a 25 and 30% SOC loss for the conversion of primary forest to cropland and perennial crops, respectively (Don et al. 2011). In contrast, C can be restored in the mineral soil after cropland reverts to natural vegetation or is reforested to perennial vegetation (Post and Kwon 2000).
In Taiwan, only a few researches related to the effects of land-use change on SOC stocks have been published. Tsai et al. (2010) and Jien et al. (2010) estimated SOC stocks of 63 forest soils (excluding Histosols and Spodosols) and 140 cropland soils in the upper 100 cm depth, indicating that converting forestlands to croplands can significantly result in SOC stocks loss. Tsui et al. (2013) also estimated the SOC stocks under bamboo, grass, and secondary forests with the different elevation between 300 and 1000 m for Andisols and Inceptisols in Yangingshan National Park in northern Taiwan and suggested that elevation is a simple and effective predictor of SOC stocks. Lin et al. (2016) investigated SOC stocks in afforested and abandoned fields at different elevation and found that SOC stocks varied with elevation, land use, and soil depth.
Forests cover over 58% of the total land area of Taiwan (Taiwan Forestry Bureau 1994), and this amount of coverage would be expected to contribute to more SOC sequestration. However, crops and plantations have been widely replaced many of the native broad-leaved forests in the montane area in central Taiwan. Cash crops mostly tea tree and bamboo can be commonly found in the montane area at the elevation from 1000 to 1500 m because of their high economic value and the proper climate for their growth; therefore, many of local farmers use the forestlands illegally in an effort to increase economic benefits. Consequently, crops gradually replaced natural broad-leaved forests, and land overuse and abuse have become pervasive. Besides, most of the natural broad-leaved forests in the same area had been logged since the 1950s. To counter this, the Experimental Forest, National Taiwan University (NTU) has been reforesting land after the logging of natural forests and after reclaiming illegally used lands.
Since SOC stocks are likely to be different in these areas due to past tillage, long-term fertilization, afforestation, and reforestation (Guo and Gifford 2002; Smith et al. 2002; Chen et al. 2004; Degryze et al. 2004; Jandl et al. 2007; Jien et al. 2011) and because knowledge about SOC stocks of adjacent land-use types in the montane area in Taiwan is still scarce, obtaining information on the changes to SOC stocks in different land-use types is essential and imperative. The aim of this study was to investigate soil characteristics and the C/N ratio and to estimate the effects of land-use type on the distribution of SOC stocks in adjacent lands in the montane area of central Taiwan.
To estimate the difference in SOC stocks among the local land uses of the selected area, we identified four land-use types as study sites: conventionally tilled cropland with Oolong tea (Camellia sinensis L.), conventionally tilled cropland with Moso bamboo (Phyllostachys pubescens), and two coniferous plantations with Japanese cedar (Cryptomeria japonica) and Taiwania (Taiwania cryptomerioides). Tea tree and bamboo are the predominant cash crops planted by local farmers because of their high economic value. Japanese cedar was first introduced from Japan in 1902, and Taiwania is a native pine species of Taiwan; both are the main coniferous species used for afforestation and reforestation by the Experimental Forest, NTU in Nantou.
Environmental information of the four study sites
Dominant species and understory
Camellia sinensis L.
Japanese cedar forest
Lasianthus fordii Hance, Elatostema lineolatum Forst. var. majus Thwait., Diplazium virescens Kunze, Amischotolype hispida (Less. & Rich.) Hong, Schefflera octophylla (Lour.) Harms, Monachosorum henryi Christ, Lasianthus wallichii Wight, Zingiber kawagoii Hayata
Polygonum chinense Linn., Angiopteris lygodiifolia Rosenst., Diplazium dilatatum Blume, Ardisia cornudentata Mez ssp. morrisonensis (Hayata) Yuen P. Yang var. stenosepala (Hayata) Yuen P. Yang, Monachosorum henryi Christ, Elatostema lineolatum Forst. var. majus Thwait., Selaginella doederleinii Hieron
Soil sampling and analysis
In April 2015, three soil profiles were selected in a 25 × 20 m subplot of each site. Because slope can affect the estimation of SOC stocks, we chose profiles that had slopes between 5° and 10°. Soil carbon stocks within 0–50 cm soil of all land-use types was estimated for comparing soil carbon under the same depths since the depth of soil under bamboo forest was around 50 cm. Therefore, three samples were collected at specific intervals from the surface to 50 cm depth (0–5, 5–10, 10–30 and 30–50 cm) of each soil profile. Collected soil samples were air dried, ground, passed through a sieve (<2 mm), and stored for chemical and physical properties analyses and estimation of SOC stocks. Before soil sample collections, three samples at each depth were collected with volumetric cores for determining bulk density (BD). Core-collected soil samples were oven dried (105 °C) to constant weight prior to calculating their BDs (Blake and Hartge 1986). Particle size was determined by the pipette method (Gee and Bauder 1986). Soil pH was measured in deionized water (water–soil ratio 1:1) by glass electrode (McLean 1982). Soil samples were finely ground using a ball grinder (Oscillating Mill MM400; Retsch, Newtown, PA, USA) before SOC and N analysis. A CHN analyzer (Perkin Elmer 2400 CHN; Perkin Elmer, Norwalk, CT, USA) was used to analyze soil carbon and nitrogen. The CEC of the soil was carried out using NH4-acetate buffer solution (pH 7; Thomas 1982).
SOC stock estimation
The effects of land use and soil depth on soil characteristics and SOC stocks in soil profiles were assessed by analysis of variance (ANOVA) using the generalized linear model (GLM) (SAS Institute Inc. 1985).
The soil characteristics of the four study sites are listed in Additional file 1: Table S1). Soil texture was mostly sandy loam and loam, with sand being the dominant particle (60–84%) at all sites. All soil profiles showed similar trends of BD increasing with increasing depth and decreasing SOC. The BD of the croplands was generally higher than in the forestlands, and the difference was found to be significant in each layer (p < 0.001). Soil pH of the four study sites ranged from 2.8 to 4.2. A vertical gradient was observed for all soil profiles, with the lowest values in the surface soils and the highest in the deepest layers. Soil pH was negatively correlated with SOC in each profile. Japanese cedar and Taiwania forests had very similar soil pH at each depth. Among all study sites, the lowest and highest soil pH values were found at 0–5 cm in the tea plantation and at 30–50 cm in the bamboo forest (p < 0.001). In the four study sites, SOC ranged from 4.83 to 335 g kg−1, with the highest SOC found at 0–5 cm depth in all profiles and SOC decreasing with depth. The similar level of SOC in the forestlands was significantly higher than in the croplands (p < 0.001). Cation exchange capacity showed a positive correlation with SOC and a negative correlation with soil pH.
Vertical distribution of soil N and C/N ratio
Soil N and C/N ratio at different soil depths in different land-use types
Japanese cedar forest
ANOVA for significance of
JC = TW > TP = BM***
JC > TW > TP = BM***
0–5 > 5–10 > 10–30 = 30–50***
0–5 = 5–10 > 10–30 > 30–50***
Vertical distribution of SOC stocks
SOC stocks (Mg C ha−1) in different land-use types
Tea plantation (Mg C ha−1)
Bamboo forest (Mg C ha−1)
Japanese cedar forest (Mg C ha−1)
Taiwania forest (Mg C ha−1)
ANOVA for significance of
JC = TW > TP = BM***
0–5 = 10–30 > 5–10 > 30–50***
Effects of land use on soil characteristics
As shown in Additional file 1: Table S1, BD and soil pH increased with soil depth while SOC and CEC decreased with soil depth in all land-use types. The significantly higher BD found in all soil layers in the croplands compared to the forestlands can be attributed to cultivation activities and less SOC content. Bulk density is directly affected by SOC content and cultivation and increased after the original forests were converted to cultivated land (Lal and Kimble 2001; Murty et al. 2002; Don et al. 2011). More SOC and less soil disturbance in the forestlands likely led to the lower BD at the same depth for these sites compared to the croplands. The lowest pH was found in the surface soil of the tea plantation. The significantly low soil pH at each depth in the tea plantation may be due to the long-term application of a chemical fertilizer since the intensive application of nitrogen fertilizers has been shown to decrease soil pH after an undisturbed forest was converted to a tea plantation (Camellia sinensis) (Bahrami et al. 2010). Low soil pH caused by the long-term application of a chemical fertilizer is commonly found in croplands throughout Taiwan. Bamboo forests received less fertilization and soil disturbance and thus were less affected by cultivation practices compared to the tea plantation.
Soil organic carbon showed a decreasing trend with increasing soil depth, in agreement with earlier studies (Yimer et al. 2007; Fu et al. 2010; Guan et al. 2015). The distinctly higher SOC content in the forestlands could be due to the higher C input and more soil organic matter accumulation compared to the croplands. On the other hand, the significantly lower SOC content in the croplands could be due to less C input, more soil disturbance, and a higher C mineralization rate caused by cultivation (Yimer et al. 2007; Sainju et al. 2008; Mancinelli et al. 2010). The negative correlation between soil pH and SOC implied that H+ released from soil organic matter could reduce pH since organic matter is one of the main sources of H+ in soil (Satrio et al. 2009). Nevertheless, compared with SOC, fertilizers were likely to have a greater effect on soil pH, particularly as the SOC content in the tea plantation was not as high as that in the Japanese cedar and Taiwania forests. The positive correlation between CEC and SOC and the negative correlation between CEC and soil pH was also found in all land-use types, in agreement with the results of Martel et al. (1978) and Bahrami et al. (2010). The low soil pH in the tea plantation was expected to contribute to a higher CEC, but this was not the case. Hence, we suggest that the SOC content had a stronger effect on the CEC than on soil pH in this study, and the higher CEC in coniferous plantations can be explained by their higher SOC content.
The results indicate that cultivation of croplands could lead to a lower CEC, less SOC, and a higher BD compared to coniferous plantations and a significant lower soil pH in tea plantation; these findings are in agreement with those of Lugo et al. (1986) and van Straaten et al. (2015) for estimating the effects of land-use change in subtropical soils and tropical forests.
Effects of land use on soil N and C/N ratio
The declining trend in soil N, which was similar to the distribution of SOC in soil profiles, in all land-use types is in agreement with previous studies (Table 2) (Wang et al. 2012; Guan et al. 2015). Soil N and the soil C/N ratio in the croplands were significantly lower than those parameters in forestlands (p < 0.001). The marked effects of land use on soil N and C/N ratio in the upper 10 cm of soils indicated a greater C loss when the surface was disturbed from cultivation activities, such as plowing and harvesting in croplands. Tea leaves and bamboo shoots are usually harvested four times and twice a year, respectively, and a large amount of aboveground biomass is removed during harvesting and weeding. Our results are consistent with those of Saikh et al. (1998) who reported that deforestation and cultivation resulted in lower N and C/N ratio. The lower C/N ratio in croplands could be a consequence of less C input to the soil and a higher mineralization rate of organic carbon caused by more oxygen being introduced and a higher soil temperature during cultivation (Yimer et al. 2007). In contrast, the higher soil C/N ratio in forestlands was due to the distinct SOC accumulation and lower SOC decomposition rate. The C/N ratio can directly affect the SOC decomposition rate by changing the decomposer organisms, and the decomposition rate of SOC pool decreases greatly once the C/N ratio increases (Enríquez et al. 1993; Xu et al. 2016). Our results indicate that cultivation resulted in a lower soil N and C/N ratio in the croplands and that the higher C input and lower SOC decomposition rate in the forestlands led to the higher soil N and C/N ratio.
Effects of land use on SOC stocks
We showed that coniferous plantations tended to accumulate more SOC and contribute to higher SOC stocks through the entire 0–50 cm soil profile (Table 3). The approximately 126 Mg C ha−1 of SOC stocks at 0–30 cm depth for Japanese cedar was in accordance with a previous study indicating SOC stocks for a 51-year-old Japanese cedar (Cryptomeria japonica) plantation ranged from 97.2 to 166 Mg C ha−1 in subtropical zone of northeastern Taiwan (Chang et al. 2006). Soil organic carbon stocks within the upper 50 cm of soils in forestlands were also significantly higher than in croplands, although tea plantation and bamboo forest had a higher BD, which contributed to higher SOC stocks. Guan et al. (2015) also estimated SOC stocks in coniferous and bamboo plantations in mid-subtropical area, southeastern China and found that a Chinese fir (Cunninghamia lanceolata [Lamb.] Hook) plantation had higher SOC stocks than a Moso bamboo (Phyllostachys heterocycla [Carr] Mitford cv. Pubescens) plantation after natural forest conversion. However, the difference was not significant since the time span after forest conversion was 17 and 18 years, respectively. The longer land-use history (over 40 years) of our study sites could have led to the greater difference between the coniferous plantations and the bamboo forest. The variation of SOC stocks at each depth in the four land-use types, especially in the upper 5 cm, indicated that land use affected the SOC stocks and that forestlands accumulated much more SOC than croplands in the surface soils.
The removal of the understory vegetation in the croplands from cultivation and weeding and the harvesting of tea and bamboo each year likely removed a significant amount of biomass and reduced C and litter input to the soil (Guan et al. 2015). Aside from cultivation and harvesting, allelopathic compounds released from bamboo during leaf decomposition could also reduce C input. Allelopathic compounds released from bamboo (Phyllostachys edulis (Carr.)) leaves can reduce the seedling abundance and species richness and then to prevent the growth of understory plants, thus reducing litter; this would also reduce the input of SOC in the bamboo forest (Chou and Yang 1982; Chang and Chiu 2015). Meanwhile, the diversity and composition of soil bacterial communities could be different in coniferous plantations and croplands, which could affect the SOC decomposition rate and then the SOC stocks. Lin et al. (2014a) indicated that Japanese cedar (Cryptomeria japonica) and Moso bamboo (Phyllostachys eduis) forests in central Taiwan showed the different diversity and composition of soil bacterial communities because of the intensive management to increase soil disturbances in the bamboo forest. Lin et al. (2014b) also suggested that the diversities of bacterial communities of the replanted Calocedrus formosana and Cryptomeria japonica forests increased compared to natural hardwood forest in a perhumid area in northern Taiwan.
Furthermore, intensive agricultural practices in tea plantation and bamboo forest could also lead to lower SOC. Intensive practices, such as annual applications of inorganic fertilizers and deep tillage, would improve aeration in the soil profile and thus increase the rate of decomposition of soil organic matter, reducing SOC stocks (Sainju et al. 2008; Mancinelli et al. 2010). Chang and Chiu (2015) indicated that frequent human disturbances such as bamboo shoot harvesting could accelerate the degradation of soil organic matter in a Moso bamboo (Phyllostachy edulis) forest in central Taiwan. Li et al. (2013) also indicated that long-term intensive practices reduced SOC stocks in Moso bamboo (Phyllostachys pubescens) forests in southeastern China. Removal of understory vegetation in croplands not only reduced C input but also increased soil temperature, which enhanced mineralization of soil organic matter and led to a decrease in SOC and SOC stocks (Wang et al. 2011). In contrast, less soil disturbance and a slower SOC decomposition rate in forestlands may result in a greater accumulation of SOC and thus contribute to greater SOC stocks. The finding of different SOC stocks in croplands compared to forestlands is consistent with the results of previous studies. After natural forests were converted to different land-use types, SOC stocks in croplands decreased more than in plantations (Guo and Gifford 2002; Don et al. 2011). Thus, cultivation in this area by local farmers resulted in a decrease in SOC stocks, whereas coniferous reforestation can store more SOC and somehow alleviate SOC losses.
Long-term cultivation in croplands significantly led to lower soil pH, CEC, SOC, soil N, soil C/N ratio, and SOC stocks but higher BD compared to coniferous plantations. We suggest that the variation in SOC stocks in different land-use types is mainly affected by less soil disturbance and higher SOC content in the forestlands and less C input and higher C mineralization in the croplands because of less understory vegetation, more harvesting, allelopathy, and intensive agricultural practices. Taiwania forest stored the highest SOC stocks similar to Japanese cedar forests, while the bamboo forest and tea plantation had the lowest SOC stocks. Soil organic carbon stocks at 0–50 cm depth in coniferous plantations were significantly higher than in croplands, with a significant difference found in the upper 5 cm. Our data indicate that cropping will result in less SOC stocks compared to reforestation and that Taiwania and Japanese cedar forests have the potential to sequester more SOC than tea plantation and bamboo forest, particularly in the montane area of central Taiwan.
CCP and CWP conducted the field study, data analyses and wrote the manuscript with inputs from other authors. CKW and CCH performed sample analyses. All authors read and approved the final manuscript.
This study was funded by the Experimental Forest, NTU (Project no. 104-B-19). The authors thank Dr. Yan-Jen Lai, Experimental Forest, NTU, for providing the high-resolution map of the Experimental Forest.
The authors declare that they have no competing interests.
Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
- Bahrami A, Emadodin I, Ranjbor Atashi M, Rudolf Bork H (2010) Land-use change and soil degradation: a case study, North of Iran. Agric Biol J North Am 1:600–605Google Scholar
- Batjes NH (1996) Total carbon and nitrogen in the soils of the world. Eur J Soil Sci 47:151–163View ArticleGoogle Scholar
- Blake GR, Hartge KH (1986) Bulk density. In: Klute A (ed) Agronomy monograph 9, 2nd edn. ASA and SSSA, Madison, pp 365–375Google Scholar
- Chang EH, Chiu CY (2015) Changes in soil microbial community structure and activity in a cedar plantation invaded by moso bamboo. Appl Soil Ecol 91:1–7View ArticleGoogle Scholar
- Chang YF, Lin ST, Tsai CC (2006) Estimation of soil organic carbon storage in a Cryptomeria plantation forest of northeastern Taiwan. Taiwan J For Sci 21:383–393 (in Chinese) Google Scholar
- Chen CR, Xu ZH, Mathers NJ (2004) Soil carbon pools in adjacent national and plantation forests of subtropical Australia. Soil Sci Soc Am J 68:282–291View ArticleGoogle Scholar
- Cheng CH, Hung CY, Chen CP, Pai CW (2013) Biomass carbon accumulation in aging Japanese cedar plantations in Xitou, central Taiwan. Bot Stud 54:60–68View ArticleGoogle Scholar
- Chou CH, Yang CM (1982) Allelopathic research of subtropical vegetation in Taiwan. II. Comparative exclusion of under story by Phyllostachys edulis and Cryptomeria japonica. J Chem Ecol 8:1489–1508View ArticlePubMedGoogle Scholar
- Degryze S, Six J, Paustian K, Morris SJ, Paul EA, Merckx R (2004) Soil organic carbon pool changes following land-use conversions. Glob Change Biol 10:1120–1132View ArticleGoogle Scholar
- Dixon RK, Brown S, Houghton RA, Solomon AM, Trexler MC, Wisniewski J (1994) Carbon pools and flux of global forest ecosystems. Science 263:185–190View ArticlePubMedGoogle Scholar
- Don A, Schumacher J, Freibauer A (2011) Impact of tropical land-use change on soil carbon stocks- a meta-analysis. Glob Change Biol 17:1658–1670View ArticleGoogle Scholar
- Enríquez S, Duarte CM, Sand-Jensen K (1993) Patterns in decomposition rates among photosynthetic organisms: the importance of detritus C:N: P content. Oecologia 94:457–471View ArticleGoogle Scholar
- FAO (2011) State of the world’s forests. Food and Agricultural Organization of the United Nations, RomeGoogle Scholar
- Fu X, Shao M, Wei X, Horton R (2010) Soil organic carbon and total nitrogen as affected by vegetation types in Northern Loess Plateau of China. Geoderma 155:31–35View ArticleGoogle Scholar
- Gee JW, Bauder JW (1986) Particle-size analysis. In: Klute A (ed) Agronomy Monograph 9, 2nd edn. ASA and SSSA, Madison, pp 383–411Google Scholar
- Guan F, Tang X, Fan S, Zhou J, Peng C (2015) Changes in soil carbon and nitrogen stocks followed the conversion from secondary forest to Chinese fir and Moso bamboo plantations. Catena 133:455–460View ArticleGoogle Scholar
- Guo LB, Gifford RM (2002) Soil carbon stocks and land use change: a meta analysis. Glob Change Biol 8:345–360View ArticleGoogle Scholar
- Jandl R, Lindner M, Vesterdal L, Bauwens B, Baritz R, Hagedorn F, Johnson DW, Mikkinen K, Byrne KA (2007) How strongly can forest management influence soil carbon sequestration? Geoderma 13:253–268View ArticleGoogle Scholar
- Jien SH, Hseu ZY, Guo HY, Tsai CC, Chen ZS (2010) Organic carbon storage and management strategies of the rural soils on the basis of soil information system in Taiwan. In: Chen ZS, Agus F (eds) Proceedings of international workshop on evaluation and sustainable management of soil carbon sequestration in Asian countries, IPB International Conference Center, BogerGoogle Scholar
- Jien SH, Chen TH, Chiu CY (2011) Effects of afforestation on soil organic matter characteristics under subtropical forests with low elevation. J For Res 16:275–283View ArticleGoogle Scholar
- Lal R, Kimble JM (2001) Importance of soil bulk density and methods of its importance. In: Lal R, Kimble JM, Follett RF, Stewart BA (eds) Assessment methods for soil carbon. Lewis Publishers, London, pp 31–44Google Scholar
- Li Y, Zhang J, Chang SX, Jiang P, Zhou G, Fu S, Yan E, Wu J, Lin L (2013) Long-term intensive management effects on soil organic carbon pools and chemical composition in Moso bamboo (Phyllostachys pubescens) forests in subtropical China. For Ecol Manag 303:121–130View ArticleGoogle Scholar
- Lin YT, Tang SL, Pai CW, Whitman WB, Coleman DC, Chiu CY (2014a) Changes in the soil bacterial communities in a cedar plantation invaded by moso bamboo. Microb Ecol 67:421–429View ArticlePubMedGoogle Scholar
- Lin YT, Hu HW, Whitman WB, Coleman DC, Chiu CY (2014b) Comparison of soil bacterial communities in a natural hardwood forest and coniferous plantations in perhumid subtropical low mountains. Bot Stud 55:50–58View ArticleGoogle Scholar
- Lin YH, Cheng CH, Huang YH (2016) Soil organic carbon accumulation in afforested/abandoned arable fields in Taiwan. In: Geophysical research abstracts, European Geosciences Union (EGU) General Assembly, Vienna, pp 17–22Google Scholar
- Lugo AE, Sanchez MJ, Brown S (1986) Land use and organic carbon content of some subtropical soils. Plant Soil 96:185–196View ArticleGoogle Scholar
- Mancinelli R, Campiglia E, Di Tizio A, Marinari S (2010) Soil carbon dioxide emission and carbon content as affected by conventional and organic cropping systems in Mediterranean environment. Appl Soil Ecol 46:64–72View ArticleGoogle Scholar
- Martel YA, Kimpe CRD, Laverdiere MR (1978) Cation-exchange capacity of clay-rich soils in relation to organic matter, mineral composition and surface area. Soil Sci Soc Am J 42:764–767View ArticleGoogle Scholar
- McLean EO (1982) Soil pH and lime requirement. In: Page AL, Miller RH, Keeney (eds) Agronomy monograph 9, 2nd edn. ASA and SSSA, Madison, pp 199–224Google Scholar
- Murty D, Kirschbaum MK, Mcmurtrie RE, Mcgilvray H (2002) Does conversion of forest to agricultural land change soil carbon and nitrogen? a review of the literature. Glob Change Biol 8:105–123View ArticleGoogle Scholar
- Post WM, Kwon KC (2000) Soil carbon sequestration and land-use change: processes and potential. Glob Change Boil 6:317–328View ArticleGoogle Scholar
- Saikh H, Varadachari C, Ghosh K (1998) Changes in carbon, nitrogen and phosphorus levels due to deforestation and cultivation: a case study in Simlipal National Park, India. Plant Soil 198:137–145View ArticleGoogle Scholar
- Sainju UM, Jabro JD, Stevens WB (2008) Soil carbon dioxide emission and carbon content as affected by irrigation tillage cropping systems, and nitrogen fertilization. J Environ Qual 37:98–106View ArticlePubMedGoogle Scholar
- SAS institute Inc (1985) SAS/STAT user’s guide, version 5. SAS Institute, CaryGoogle Scholar
- Satrio AE, Gandaseca S, Ahmed OH, Majid NMA (2009) The influence of chemical properties on soil carbon storage of a tropical peat swamp forest. Am J Appl Sci 6:1969–1972View ArticleGoogle Scholar
- Schulp CJE, Nabuurs GJ, Verburg PH, de Waal RW (2008) Effects of tree species on carbon stocks in forest floor and mineral soil and implications for soil carbon inventories. For Ecol Manag 256:482–490View ArticleGoogle Scholar
- Smith CK, de Assis Oliverira F, Gholz HL, Baima A (2002) Soil carbon stocks after forest conversion to tree plantations in lowland Amazonia, Brazil. For Ecol Manag 164:257–263View ArticleGoogle Scholar
- Taiwan Forestry Bureau (1994) The third forest resources and land use inventory in Taiwan. Taipei, Taiwan Forest Bureau, p 257 (In Chinese) Google Scholar
- Thomas GW (1982) Cation exchange capacity. In: Page AL, Miller RH, Keeney DR (eds) Agronomy monograph 9, 2nd edn. ASA and SSSA, Madison, pp 149–157Google Scholar
- Tsai CC, Chen ZS, Hseu ZY, Duh CT, Gou HY (2010) Organic carbon storage and management strategies of the forest soils based on the forest soil survey database in Taiwan. In: Chen ZS, Agus F (eds) Proceedings of international workshop on evaluation and sustainable management of soil carbon sequestration in Asian countries, IPB International Conference Center, BogerGoogle Scholar
- Tsui CC, Guo HY, Chen ZS (2013) Estimation of soil carbon stock in Taiwan arable soils by using legacy database and digital soil mapping. In: Soriano MCH (ed) Soil processes and current trends in quality assessment. Intech, Croatia, p 311Google Scholar
- van Straaten O, Corre MD, Wolf K, Tchienkoua M, Cuellar E, Matthews RB, Veldkamp E (2015) Conversion of lowland tropical forests to tree cash crops plantations loses up to one-half of stored soil organic carbon. Proc Natl Acad Sci USA 112:9956–9960View ArticlePubMedPubMed CentralGoogle Scholar
- Wang XL, Zhou J, Wu JP, Chen H, Lin YB, Zhou LX, Fu SL (2011) Impacts of understory species removal and/or addition on soil respiration in a mixed forest plantation with native species in southern China. For Ecol Manag 261:1053–1060View ArticleGoogle Scholar
- Wang S, Wang X, Ouyang Z (2012) Effects of land use, climate, topography and soil properties on regional soil organic carbon and total nitrogen in the Upstream Watershed of Miyun Reservoir, North China. J Environ Sci 24:387–395View ArticleGoogle Scholar
- Xu X, Shi Z, Li D, Rey A, Ruan H, Craine JM, Liang J, Zhou J, Lou Y (2016) Soil properties control decomposition of soil organic carbon: results from data-assimilation analysis. Geoderma 262:235–242View ArticleGoogle Scholar
- Yimer F, Ledin S, Abdelkadir A (2007) Change in soil organic carbon and total nitrogen contents in three adjacent land-use types in the Bale Mountains, southeastern highlands of Ethiopia. For Ecol Manag 242:337–342View ArticleGoogle Scholar