Volume 41 Issue 8
Aug.  2022
Turn off MathJax
Article Contents
Jiahui Chen, Min Gao, Guangcheng Chen, Heng Zhu, Yong Ye. Biomass accumulation and organic carbon stocks of Kandelia obovata mangrove vegetation under different simulated sea levels[J]. Acta Oceanologica Sinica, 2022, 41(8): 78-86. doi: 10.1007/s13131-021-1891-2
Citation: Jiahui Chen, Min Gao, Guangcheng Chen, Heng Zhu, Yong Ye. Biomass accumulation and organic carbon stocks of Kandelia obovata mangrove vegetation under different simulated sea levels[J]. Acta Oceanologica Sinica, 2022, 41(8): 78-86. doi: 10.1007/s13131-021-1891-2

Biomass accumulation and organic carbon stocks of Kandelia obovata mangrove vegetation under different simulated sea levels

doi: 10.1007/s13131-021-1891-2
Funds:  The National Natural Science Foundation of China under contract Nos 41776097 and 42076142; the Scientific Research Foundation of Third Institute of Oceanography, Ministry of Natural Resources under contract No. 2019017; the Fujian Provincial Key Laboratory of Marine Ecological Conservation and Restoration under contract No. EPR2020003.
More Information
  • Corresponding author: E-mail: yeyong@xmu.edu.cn
  • Received Date: 2021-07-01
  • Accepted Date: 2021-08-30
  • Available Online: 2022-06-10
  • Publish Date: 2022-08-15
  • Mangrove forests are vulnerably threatened by sea level rise (SLR). Vegetation organic carbon (OC) stocks are important for mangrove ecosystem carbon cycle. It is critical to understand how SLR affects vegetation OC stocks for evaluating mangrove blue carbon budget and global climate change. In this study, biomass accumulation and OC stocks of mangrove vegetation were compared among three 10 year-old Kandelia obovata (a common species in China) mangrove forests under three intertidal elevations through species-specific allometric equations. This study simulated mangrove forests with SLR values of 0 cm, 40 cm and 80 cm, respectively, representing for the current, future ~100 a and future ~200 a SLR of mangrove forests along the Jiulong River Estuary, China. SLR directly decreased mangrove individual density and inhibited the growth of mangrove vegetation. The total vegetation biomasses were (12.86±0.95) kg/m2, (7.97±0.90) kg/m2 and (3.89±0.63) kg/m2 at Sites SLR 0 cm, SLR 40 cm and SLR 80 cm, respectively. The total vegetation OC stock decreased by approximately 3.85 kg/m2 (in terms of C) from Site SLR 0 cm to Site SLR 80 cm. Significantly lower vegetation biomass and OC stock of various components (stem, branch, leaf and root) were found at Site SLR 80 cm. Annual increments of vegetation biomass and OC stock also decreased with SLR increase. Moreover, significant lower sedimentation rate was found at Site SLR 80 cm. These indicated that SLR will decrease mangrove vegetation biomass and OC stock, which may reduce global blue carbon sink by mangroves, exacerbate global warming and give positive feedback to SLR.
  • loading
  • [1]
    Alongi D M. 2014. Carbon cycling and storage in mangrove forests. Annual Review of Marine Science, 6: 195–219. doi: 10.1146/annurev-marine-010213-135020
    [2]
    Bouillon S, Borges A V, Castañeda-Moya E, et al. 2008. Mangrove production and carbon sinks: a revision of global budget estimates. Global Biogeochemical Cycles, 22(2): GB2013
    [3]
    Breithaupt J L, Smoak J M, Smith III T J, et al. 2012. Organic carbon burial rates in mangrove sediments: Strengthening the global budget. Global Biogeochemical Cycles, 26(3): GB3011
    [4]
    Capooci M, Barba J, Seyfferth A L, et al. 2019. Experimental influence of storm-surge salinity on soil greenhouse gas emissions from a tidal salt marsh. Science of the Total Environment, 686: 1164–1172. doi: 10.1016/j.scitotenv.2019.06.032
    [5]
    Chen Jiahui, Chen Guangcheng, Gu Yantao, et al. 2020a. Fate of leaf litter in restored Kandelia obovata (S. L.) mangrove forests with different ages in Jiulong River Estuary, China. Restoration Ecology, 28(2): 369–377. doi: 10.1111/rec.13079
    [6]
    Chen Guangcheng, Chen Bin, Yu Dan, et al. 2016. Soil greenhouse gas emissions reduce the contribution of mangrove plants to the atmospheric cooling effect. Environmental Research Letters, 11(12): 124019. doi: 10.1088/1748-9326/11/12/124019
    [7]
    Chen Guangcheng, Gao Min, Pang Bopeng, et al. 2018. Top-meter soil organic carbon stocks and sources in restored mangrove forests of different ages. Forest Ecology and Management, 422: 87–94. doi: 10.1016/j.foreco.2018.03.044
    [8]
    Chen Jiahui, Huang Yingying, Chen Guangcheng, et al. 2020b. Effects of simulated sea level rise on stocks and sources of soil organic carbon in Kandelia obovata mangrove forests. Forest Ecology and Management, 460: 117898. doi: 10.1016/j.foreco.2020.117898
    [9]
    Chen Luzhen, Wang Wenqing. 2017. Ecophysiological responses of viviparous mangrove Rhizophora stylosa seedlings to simulated sea-level rise. Journal of Coastal Research, 33(6): 1333–1340
    [10]
    Chen Luzhen, Wang Wenqing, Lin Peng. 2004. Influence of water logging time on the growth of Kandelia candel seedlings. Acta Oceanologica Sinica, 23(1): 149–157
    [11]
    Chen Yaping, Ye Yong. 2013. Growth and physiological responses of saplings of two mangrove species to intertidal elevation. Marine Ecology Progress Series, 482: 107–118. doi: 10.3354/meps10274
    [12]
    Chen Yaping, Ye Yong. 2014. Early responses of Avicennia marina (Forsk. ) Vierh. to intertidal elevation and light level. Aquatic Botany, 112: 33–40. doi: 10.1016/j.aquabot.2013.07.006
    [13]
    Donato D C, Kauffman J B, Murdiyarso D, et al. 2011. Mangroves among the most carbon-rich forests in the tropics. Nature Geoscience, 4(5): 293–297. doi: 10.1038/ngeo1123
    [14]
    Duarte C M, Losada I J, Hendriks I E, et al. 2013. The role of coastal plant communities for climate change mitigation and adaptation. Nature Climate Change, 3(11): 961–968. doi: 10.1038/nclimate1970
    [15]
    Ellison A M, Farnsworth E J. 1997. Simulated sea level change alters anatomy, physiology, growth, and reproduction of red mangrove (Rhizophora mangle L.). Oecologia, 112(4): 435–446. doi: 10.1007/s004420050330
    [16]
    Gao Yu, Zhou Jian, Wang Liming, et al. 2019. Distribution patterns and controlling factors for the soil organic carbon in four mangrove forests of China. Global Ecology and Conservation, 17: e00575. doi: 10.1016/j.gecco.2019.e00575
    [17]
    Gilman E L, Ellison J, Duke N C, et al. 2008. Threats to mangroves from climate change and adaptation options: a review. Aquatic Botany, 89(2): 237–250. doi: 10.1016/j.aquabot.2007.12.009
    [18]
    Horton B P, Rahmstorf S, Engelhart S E, et al. 2014. Expert assessment of sea-level rise by AD 2100 and AD 2300. Quaternary Science Reviews, 84: 1–6. doi: 10.1016/j.quascirev.2013.11.002
    [19]
    Hossain D, Inafuku M, Iwasaki H, et al. 2017. Differential enzymatic defense mechanisms in leaves and roots of two true mangrove species under long-term salt stress. Aquatic Botany, 142: 32–40. doi: 10.1016/j.aquabot.2017.06.004
    [20]
    Howard J, Hoyt S, Isensee K, et al. 2014. Coastal Blue Carbon: Methods for Assessing Carbon Stocks and Emissions Factors in Mangroves, Tidal Salt Marshes, and Seagrass Meadows. Arlington, VA, USA: Conservation International, Intergovernmental Oceanographic Commission of UNESCO, International Union for Conservation of Nature
    [21]
    Kauffman J B, Donato D C. 2012. Protocols for the Measurement, Monitoring and Reporting of Structure, Biomass and Carbon Stocks in Mangrove Forests. Bogor, Indonesia: Center for International Forestry Research
    [22]
    Kauffman J B, Trejo H H, del Carmen Jesus Garcia M, et al. 2016. Carbon stocks of mangroves and losses arising from their conversion to cattle pastures in the Pantanos de Centla, Mexico. Wetlands Ecology and Management, 24(2): 203–216. doi: 10.1007/s11273-015-9453-z
    [23]
    Kelleway J J, Saintilan N, Macreadie P I, et al. 2016. Seventy years of continuous encroachment substantially increases ‘blue carbon’ capacity as mangroves replace intertidal salt marshes. Global Change Biology, 22(3): 1097–1109. doi: 10.1111/gcb.13158
    [24]
    Kitaya Y, Jintana V, Piriyayotha S, et al. 2002. Early growth of seven mangrove species planted at different elevations in a Thai estuary. Trees, 16(2–3): 150–154. doi: 10.1007/s00468-002-0166-6
    [25]
    Krauss K W, McKee K L, Lovelock C E, et al. 2014. How mangrove forests adjust to rising sea level. New Phytologist, 202(1): 19–34. doi: 10.1111/nph.12605
    [26]
    Krauss K W, Twilley R R, Doyle T W, et al. 2006. Leaf gas exchange characteristics of three neotropical mangrove species in response to varying hydroperiod. Tree Physiology, 26(7): 959–968. doi: 10.1093/treephys/26.7.959
    [27]
    Kristensen E, Bouillon S, Dittmar T, et al. 2008. Organic carbon dynamics in mangrove ecosystems: a review. Aquatic Botany, 89(2): 201–219. doi: 10.1016/j.aquabot.2007.12.005
    [28]
    Leppälammi-Kujansuu J, Salemaa M, Kleja D B, et al. 2014. Fine root turnover and litter production of Norway spruce in a long-term temperature and nutrient manipulation experiment. Plant and Soil, 374(1–2): 73–88. doi: 10.1007/s11104-013-1853-3
    [29]
    Li S W, Chan Benny K K, Tam Nora F Y. 2009. Barnacle fouling impedes the gaseous exchange and food production of the mangroves Kandelia obovata, a dominant mangrove species in Hong Kong and Taiwan. Hydrobiologia, 618(1): 199–203. doi: 10.1007/s10750-008-9576-9
    [30]
    Li Zhengjie, Wang Wenqing, Zhang Yihui. 2014. Recruitment and herbivory affect spread of invasive Spartina alterniflora in China. Ecology, 95(7): 1972–1980. doi: 10.1890/13-2283.1
    [31]
    Liu Xiu, Xiong Yanmei, Liao Baowen. 2017. Relative contributions of leaf litter and fine roots to soil organic matter accumulation in mangrove forests. Plant and Soil, 421(1–2): 493–503. doi: 10.1007/s11104-017-3477-5
    [32]
    Local Chronicles Office of Xiamen Municipal People’s Government. 2014. Yearbook of Xiamen. Beijing: Zhonghua Book Company, 22
    [33]
    Local Chronicles office of Xiamen Municipal People’s Government. 2015. Yearbook of Xiamen. Beijing: Zhonghua Book Company, 33
    [34]
    Lovelock C E, Cahoon D R, Friess D A, et al. 2015. The vulnerability of Indo-Pacific mangrove forests to sea-level rise. Nature, 526(7574): 559–563. doi: 10.1038/nature15538
    [35]
    Lu Weizhi, Chen Luzhen, Wang Wenqing, et al. 2013. Effects of sea level rise on mangrove Avicennia population growth, colonization and establishment: evidence from a field survey and greenhouse manipulation experiment. Acta Oecologica, 49: 83–91. doi: 10.1016/j.actao.2013.03.009
    [36]
    Mafi-Gholami D, Zenner E K, Jaafari A. 2020. Mangrove regional feedback to sea level rise and drought intensity at the end of the 21st century. Ecological Indicator, 110: 105972. doi: 10.1016/j.ecolind.2019.105972
    [37]
    Munns R, Tester M. 2008. Mechanisms of salinity tolerance. Annual Review of Plant Biology, 59: 651–681. doi: 10.1146/annurev.arplant.59.032607.092911
    [38]
    Murdiyarso D, Purbopuspito J, Kauffman J B, et al. 2015. The potential of Indonesian mangrove forests for global climate change mitigation. Nature Climate Change, 5(12): 1089–1092. doi: 10.1038/nclimate2734
    [39]
    National Oceanographic Information Center, Ministry of Natural Resources, China. 2019. Ocean Blue Book on Climate Change in China in 2019. China Environment Supervision, 10: 4.
    [40]
    Otero X L, Méndez A, Nóbrega G N, et al. 2017. High heterogeneity in soil composition and quality in different mangrove forests of Venezuela. Environmental Monitoring and Assessment, 189(10): 511. doi: 10.1007/s10661-017-6228-4
    [41]
    Perera K A R S, De Silva K H W L, Amarasinghe M D. 2018. Potential impact of predicted sea level rise on carbon sink function of mangrove ecosystems with special reference to Negombo estuary, Sri Lanka. Global and Planetary Change, 161: 162–171. doi: 10.1016/j.gloplacha.2017.12.016
    [42]
    Pérez A, Machado W, Gutierrez D, et al. 2017. Changes in organic carbon accumulation driven by mangrove expansion and deforestation in a New Zealand estuary. Estuarine, Coastal and Shelf Science, 192: 108–116
    [43]
    Pupin B, Nahas E. 2015. Phosphorus fractions in soils of the mangrove, restinga and Atlantic forest ecosystems from Cardoso Island, Brazil. Soil Research, 53(3): 253–262. doi: 10.1071/SR14334
    [44]
    Ruan Hailin, Yang Yanming, Li Yanchu, et al. 2010. Study of the variation in sea level around Taiwan Island during the last 16 years. Journal of Oceanography in Taiwan Strait, 29(3): 394–401
    [45]
    Sippo J Z, Lovelock C E, Santos I R, et al. 2018. Mangrove mortality in a changing climate: an overview. Estuarine, Coastal and Shelf Science, 215: 241–249
    [46]
    Tam Nora Fung-Yee, Wong Yushan, Lan C Y, et al. 1995. Community structure and standing crop biomass of a mangrove forest in Futian Nature Reserve, Shenzhen, China. Hydrobiologia, 295(1–3): 193–201. doi: 10.1007/BF00029126
    [47]
    Wang Gang, Guan Dongsheng, Peart M R, et al. 2013. Ecosystem carbon stocks of mangrove forest in Yingluo Bay, Guangdong Province of South China. Forest Ecology and Management, 310: 539–546. doi: 10.1016/j.foreco.2013.08.045
    [48]
    Wang Gang, Guan Dongsheng, Xiao Ling, et al. 2019. Ecosystem carbon storage affected by intertidal locations and climatic factors in three estuarine mangrove forests of South China. Regional Environmental Change, 19(6): 1701–1712. doi: 10.1007/s10113-019-01515-6
    [49]
    Wang Dezhi, Wan Bo, Liu Jing, et al. 2020. Estimating aboveground biomass of the mangrove forests on northeast Hainan Island in China using an upscaling method from field plots, UAV-LiDAR data and Sentinel-2 imagery. International Journal of Applied Earth Observation and Geoinformation, 85: 101986. doi: 10.1016/j.jag.2019.101986
    [50]
    Wu Mengxing, He Ziying, Fung Shingting, et al. 2020. Species choice in mangrove reforestation may influence the quantity and quality of long-term carbon sequestration and storage. Science of the Total Environment, 714: 136742. doi: 10.1016/j.scitotenv.2020.136742
    [51]
    Yáñez-Espinosa L, Terrazas T, López-Mata L. 2001. Effects of flooding on wood and bark anatomy of four species in a mangrove forest community. Trees, 15(2): 91–97. doi: 10.1007/s004680000081
    [52]
    Yang Shengchi, Shih Shangshu, Hwang Gwowen, et al. 2013. The salinity gradient influences on the inundation tolerance thresholds of mangrove forests. Ecological Engineering, 51: 59–65. doi: 10.1016/j.ecoleng.2012.12.049
    [53]
    Ye Yong, Chen Yaping, Chen Guangcheng. 2013. Litter production and litter elemental composition in two rehabilitated Kandelia obovata mangrove forests in Jiulongjiang Estuary, China. Marine Environmental Research, 83: 63–72. doi: 10.1016/j.marenvres.2012.10.011
    [54]
    Ye Yong, Gu Yantao, Gao Haiyan, et al. 2010. Combined effects of simulated tidal sea-level rise and salinity on seedlings of a mangrove species, Kandelia candel (L.) Druce. Hydrobiologia, 641: 287–300. doi: 10.1007/s10750-010-0099-9
    [55]
    Ye Yong, Tam Nora Fung-Yee, Wong Yushan, et al. 2004. Does sea level rise influence propagule establishment, early growth and physiology of Kandelia candel and Bruguiera gymnorrhiza?. Journal of Experimental Marine Biology and Ecology, 306(2): 197–215
    [56]
    Zhang Yihui, Huang Guanmin, Wang Wenqing, et al. 2012. Interactions between mangroves and exotic Spartina in an anthropogenically disturbed estuary in southern China. Ecology, 93(3): 588–597. doi: 10.1890/11-1302.1
  • 加载中

Catalog

    通讯作者: 陈斌, bchen63@163.com
    • 1. 

      沈阳化工大学材料科学与工程学院 沈阳 110142

    1. 本站搜索
    2. 百度学术搜索
    3. 万方数据库搜索
    4. CNKI搜索

    Figures(5)

    Article Metrics

    Article views (301) PDF downloads(16) Cited by()
    Proportional views
    Related

    /

    DownLoad:  Full-Size Img  PowerPoint
    Return
    Return