Adaptability of Indocalamus decorus to climate change based on physiological and biochemical responses to elevated carbon dioxide and ozone

doi:10.3832/ifor1571-008

Adaptability of Indocalamus decorus to climate change based on physiological and biochemical responses to elevated carbon dioxide and ozone

Ziwu Guo⁽¹⁾, Minghao Zhuang⁽²⁾, Yingchun Li⁽¹⁾, Shuanglin Chen⁽¹⁾ , Qingping Yang⁽¹⁾

iForest - Biogeosciences and Forestry, Volume 9, Issue 2, Pages 311-317 (2015)
doi: https://doi.org/10.3832/ifor1571-008
Published: Oct 22, 2015 - Copyright © 2015 SISEF

Research Articles

PDF Version

Full Text

Citation

Geo-mapping

Carbon dioxide (CO₂) and ozone (O₃) are important greenhouse gases that contribute to global climate change. The effects of elevated CO₂ and/or O₃ on plants remain unclear. Plant responses to mixtures of the two gases at high concentrations are likely to be complex. Previous studies have shown that the ability to tolerate elevated levels of the two gases varies among plant species; physiological adaptability in the face of changing atmospheric composition also differs among taxa. However, the effects of mixtures of the two greenhouse gases on the growth and physiology of bamboo are largely unexplored, even though bamboos are important vegetation elements throughout tropical and subtropical regions of the planet. In this study, we used open-topped chambers (OTCs) to double the concentrations of atmospheric CO₂ and O₃, and examined changes in membrane lipid peroxidation, photosynthetic physiology, and antioxidase activities in Indocalamus decorus leaves. After 103 days of treatment, elevated O₃ depressed net photosynthetic rate (Pn) without changing stomatal function, but caused no significant oxidative damage in the leaves. High levels of antioxidase activities were maintained in the leaves, indicating that this species had a strong tolerance to elevated O₃. Decreases in reactive oxygen content and antioxidase activity in the leaves highlighted the significant positive effects of elevated CO₂ on photosynthesis in I. decorus. When a mixture of both gases was supplied at high concentrations, we detected no oxidative damage, although photosynthetic capacity was reduced. Negative effects of O₃ were very marked during the early part of the treatment period, but the effects of CO₂ were positive. CO₂mitigated the oxidative damage caused by O₃ and promoted the growth of I. decorus. Thus, I. decorus tolerated the two greenhouse gases, and was able to adapt to elevated CO₂ and O₃ levels. These findings contribute to the current knowledge base on the response of bamboo to global climate change.

Keywords

Antioxidant Enzyme, Carbon Dioxide, Indocalamus decorus, Membrane Lipid Peroxidation, Ozone, Photosynthetic Physiology

Authors’ address

(1)

Research Institute of Subtropical Forestry, Chinese Academy of Forestry, Hangzhou Zhejiang, 311400 (P.R. China)

(2)

College of Environmental Sciences and Engineering, Peking University, Beijing 100871 (P.R. China)

Corresponding author

Shuanglin Chen
cslbamboo@126.com

Citation

Guo Z, Zhuang M, Li Y, Chen S, Yang Q (2015). Adaptability of Indocalamus decorus to climate change based on physiological and biochemical responses to elevated carbon dioxide and ozone. iForest 9: 311-317. - doi: 10.3832/ifor1571-008

Academic Editor

Silvano Fares

Paper history

Received: Jan 23, 2015
Accepted: Aug 18, 2015

First online: Oct 22, 2015
Publication Date: Apr 26, 2016
Publication Time: 2.17 months

Open Access

This article is distributed under the terms of the Creative Commons Attribution-Non Commercial 4.0 International (https://creativecommons.org/licenses/by-nc/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.

Breakdown by View Type

(Waiting for server response...)

Article Usage

Total Article Views: 27324
(from publication date up to now)

Breakdown by View Type
HTML Page Views: 22328
Abstract Page Views: 1123
PDF Downloads: 2822
Citation/Reference Downloads: 13
XML Downloads: 1038

Web Metrics
Days since publication: 2657
Overall contacts: 27324
Avg. contacts per week: 71.99

Article Citations

Article citations are based on data periodically collected from the Clarivate Web of Science web site
(last update: Jul 2021)

Total number of cites (since 2016): 1
Average cites per year: 0.17

(no Plumx Metrics available for this paper)

Publication Metrics

by Dimensions ^©

Articles citing this article

List of the papers citing this article based on CrossRef Cited-by.

(1)

Asada K (1992)
Ascorbate peroxidase: a hydrogen peroxide-scavenging enzyme in plant. Physiologia Plantarum 85: 235-241.
CrossRef | Gscholar

(2)

Bai YM, Wang CY, Wen M (2005)
Responses of soybean to O₃, CO₂ and their combination. Chinese Journal of Applied Ecology 16 (2): 545-549. [in Chinese with English abstract]
Online | Gscholar

(3)

Booker FL, Fiscus EL (2005)
The role of ozone flux and antioxidants in the suppression of ozone injury by elevated CO₂ in soybean. Journal of Experimental Botany 56 (418): 2139-2151.
CrossRef | Gscholar

(4)

Chen JX, Wang XF (2006)
Experiment instruction of plant physiology. South China University Technology Press, Guangzhou, China, pp. 54-124. [in Chinese]
Gscholar

(5)

Darbah JNT, Kubiske ME, Nelson N, Oksanen E, Vapaavuori E, Karosky DF (2008)
Effects of decadal exposure to interacting elevated CO₂ and/or O₃ on paper birch (Betula papyrifera) reproduction. Environmental Pollution 155: 446-452.
CrossRef | Gscholar

(6)

Donnelly A, Craigon J, Black CR, Colls J, Landon G (2001)
Does elevated CO₂ ameliorate the impact of O₃ on chlorophyll content and photosynthesis in potato (Solanum tuberosum)? Physiologia Plantarum 111: 501-511.
CrossRef | Gscholar

(7)

Ellsworth DS, Reich PB, Naumburg ES, Koch GW, Kubiske ME, Smith SD (2004)
Photosynthesis, carboxylation and leaf nitrogen responses of 16 species to elevated CO₂ across four free-air CO₂ enrichment experiments in forest, grassland and desert. Global Change Biology 10: 2121-2138.
CrossRef | Gscholar

(8)

Farquhar GD, Sharkey TD (1982)
Stomatal conductance and photosynthesis. Annual Review of Plant Physiology 33: 317-345.
CrossRef | Gscholar

(9)

Gaucher C, Costanzo N, Afif D, Mauffette Y, Chevrier N, Dizengremel P (2003)
The impact of elevated ozone and carbon dioxide on young Acer saccharum seedlings. Physiologia Plantarum 117: 392-402.
CrossRef | Gscholar

(10)

Gaucher C, Costanzo N, Widden P, Renaud JP, Dizengremel P, Mauffette Y, Chevrier N (2006)
Response to an ozone gradient of growth and enzymes implicated in tolerance to oxidative stress in Acer saccharum (Marsh). Annals of Forest Science 63 (4): 387-397.
CrossRef | Gscholar

(11)

Guidi L, Cagno RD, Soldatini GF (2000)
Screening of bean cultivars for their response to ozone as evaluated by visible symptoms and leaf chlorophyll fluorescence. Environmental Pollution 107: 349-355.
CrossRef | Gscholar

(12)

Guidi L, Nali C, Lorenzini G, Filippi F, Soldatini GF (2001)
Effects of chronic ozone fumigation on the photosynthetic process of poplar clones showing different sensitivity. Environmental Pollution 113: 245-254.
CrossRef | Gscholar

(13)

Handa IT, Körner C, Hättenschwiler S (2005)
A test of the tree-line carbon limitation hypothesis by in situ O₂ enrichment and defoliation. Ecology 86 (5): 1288-1300.
CrossRef | Gscholar

(14)

He XY, Fu SL, Chen W, Zhao TH, Xu S, Tuba Z (2007)
Changes in effects of ozone exposure on growth, photosynthesis, and respiration of Ginkgo biloba in Shenyang urban area. Photosynthetica 45 (4): 555-561.
CrossRef | Gscholar

(15)

IPCC (2007)
Climate change 2007: the physical science basis. Contribution of Working Group I to the 4th Assessment Report of the IPCC (Solomon S, Qin D, Manning M, Chen Z, Marquis M, Averyt KB, Tignor M, Miller HL eds). Cambridge University Press, Cambridge, UK, pp. 18.
Gscholar

(16)

Karnosky DF, Zak DR, Kubiske ME, Hendrey GR, Weinstein D, Nosal M, Percy KE (2005)
Scaling ozone responses of forest trees to the ecosystem level in a changing climate. Plant, Cell and Environment 28: 965-981.
CrossRef | Gscholar

(17)

Ke DS, Wang AG, Sun GC, Dong LF (2002)
The effect of active oxygen on the activity of ACC synthase induced by exogenous IAA. Acta Botantic Sinica 44 (5): 551-556.
Gscholar

(18)

Kimball BA, Kobayashi K, Bindi M (2002)
Responses of agricultural crops to free-air CO₂ enrichment. Advances in Agronomy 77: 293-368.
CrossRef | Gscholar

(19)

Knorzer OC, Durner J, Boger P (1996)
Alterations in the antioxidative system of suspension-cultured soybean cells (Glycine max) induced by oxidative stress. Physiologia Plantarum 97: 388-396.
CrossRef | Gscholar

(20)

Li Y, Chen SL, Xie SX, Li YC, Zhuang MH, Guo ZW, Yang QP (2012)
Effects of atmospheric ozone stress on photosynthetic physio- response of three dwarf bamboos. Journal of Tropical and Subtropical Botany 20 (3): 263-269. [in Chinese with English abstract]
Gscholar

(21)

Lin JS, Wang GX (2000)
Effects of doubled CO₂ concentration on antioxidant enzymes and programmed cell death of wheat leaves under osmotic stress. Acta Phytophysiologica Sinica 26 (5): 453-457.
Online | Gscholar

(22)

Meyer U, Kollner B, Willenbrink J, Krause GHM (2000)
Effects of different ozone exposure regimes on photosynthesis, assimilates and thousand grain weight in spring wheat. Agriculture, Ecosystems and Environment 78: 49-45.
CrossRef | Gscholar

(23)

Mediavilla S, Santiago H, Escudero A (2002)
Stomatal and mesophyll limitations to photosynthesis in one evergreen and one deciduous Mediterranean oak species. Photosynthetica 40 (4): 553-559.
CrossRef | Gscholar

(24)

Noormets A, Sôber A, Pell EJ, Dickson RE, Podila GK, Sôber J, Isebrands JG, Karnosky DF (2001)
Stomatal and non-stomatal limitation to photosynthesis in two trembling aspen (Populus tremuloides Michx) clones exposed to elevated CO₂ and/or O₃. Plant, Cell and Environment 24: 327-336.
CrossRef | Gscholar

(25)

Noormets A, Kull O, Sôber A, Kubiske ME, Karnosky DF (2010)
Elevated CO₂ responses of photosynthesis depends on ozone concentration in aspen. Environmental Pollution 158: 992-999.
CrossRef | Gscholar

(26)

Nowak RS, Ellsworth DS, Smith SD (2004)
Functional responses of plant to elevated atmospheric CO₂ - do photosynthetic and productivity data from FACE experiments support early predictions? New Phytologist 162: 253-280.
CrossRef | Gscholar

(27)

Pleijel H, Eriksen AB, Danielsson H, Bondesson N, Sellden G (2006)
Different ozone sensitivity in an old and modern Swedish wheat cultivar-grain yield and quality, leaf chlorophyll and stomatal conductance. Environmental and Experimental Botany 56: 63-71.
CrossRef | Gscholar

(28)

Paoletti E, Seufert G, Rocca DG, Thomsen H (2007)
Photosynthetic responses to elevated CO₂ and O₃ in Quercus ilex leaves at a natural CO₂ spring. Environmental Pollution 147: 516-524.
CrossRef | Gscholar

(29)

Ruan YN, He XY, Chen W, Xu S, Xu WD (2007)
Effects of elevated CO₂ on lipid peroxidation and activities of antioxidant enzymes in Ginkgo biloba. Chinese Journal of Acta Ecological Sinica 27 (3): 1106-1112. [in Chinese with English abstract]
Gscholar

(30)

Schwanz P, Polle A (1998)
Antioxidative systems, pigment and protein contents in leaves of adult Mediterranean oak species (Quercus pubescens and Quercus ilex) with lifetime exposure to elevated CO₂. New phytologist 140: 411-423.
CrossRef | Gscholar

(31)

Tausz M, Grulke NE, Wieser G (2007)
Defense and avoidance of ozone under global change. Environmental Pollution 147: 525-531.
CrossRef | Gscholar

(32)

Vurro E, Bruni R, Bianchi A, Di Toppi LS (2009)
Elevated atmospheric CO₂ decreases oxidative stress and increases essential oil yield in leaves of Thymus vulgaris grown in a mini-FACE system. Environmental and Experimental Botany 65: 99-106.
CrossRef | Gscholar

(33)

Wang MY, Zhao TH, Zhang WW, Guo D, He XY, Fu SL (2007)
Effects of elevated CO₂ concentration on photosynthetic characteristics of two urban forest species in Shenyang city. Chinese Bulletin of Botany 24 (4): 470-476. [in Chinese with English abstract]
Gscholar

(34)

Wustman BA, Oksanen E, Kammosky DF, Noormets A, Isebrands JG, Pregitzer KS, Hendrey GR, Sober J, Podila GK (2001)
Effects of elevated CO₂ and O₃ on aspen clones varying in O₃ sensitivity: can CO₂ ameliorate the harmful effects of O₃? Environmental Pollution 115: 473-481.
CrossRef | Gscholar

(35)

Yan K, Chen W, He XY, Zhang GY, Xu S, Wang LL (2010)
Responses of photosynthesis, lipid peroxidation and antioxidant system in leaves of Quercus mongolica to elevated O₃. Environmental and Experimental Botany 69: 198-204.
CrossRef | Gscholar

(36)

Zhang XZ, Chen YF (1994)
Experimental techniques of plant physiology. Liaoning Technology Press, Shenyang, China, pp. 164-165. [in Chinese]
Gscholar

(37)

Zhang WW, Niu JF, Feng ZZ, Wang XK, Tian Y, Yao FF (2011)
Responses of Ilex integra Thunb. seeding to elevated air ozone concentration. Environmental Science 32 (8): 2414-2421. [in Chinese with English abstract]
Online | Gscholar

(38)

Zheng FY, Peng SL (2001)
Meta-analysis of the response of plant ecophysiological variables to doubled atmospheric CO₂ concentrations. Chinese Bulletin of Botany 43 (11): 1101-1109. [In Chinese with English abstract]
Online | Gscholar

(39)

Zhuang MH, Li YC, Guo ZW, Yang QP, Gu LJ, Chen SL (2012)
Physiological response of Indocalamus decorus to simulated atmospheric ozone stress with multiply-increasing concentrations. Journal of Plant Resources and Environment 21 (2): 68-72, 88. [in Chinese with English abstract]
Gscholar

iForest - Biogeosciences and Forestry

Contents

Search

Journal Info

Journal Subjects and Fields

For Authors

For Reviewers

For Readers

SISEF Publishing

Search iForest Contents