Literature DB >> 28314006

Water stress, temperature, and light effects on the capacity for isoprene emission and photosynthesis of kudzu leaves.

Thomas D Sharkey1, Francesco Loreto1.   

Abstract

Kudzu (Pueraria lobata (Willd) Ohwi.) is a vine which forms large, monospecific stands in disturbed areas of the southeastern United States. Kudzu also emits isoprene, a hydrocarbon which can significantly affect atmospheric chemistry including reactions leading to tropospheric ozone. We have studied physiological aspects of isoprene emission from kudzu so the ecological consequences of isoprene emission can be better understood. We examined: (a) the development of isoprene emission as leaves developed, (b) the interaction between photon flux density and temperature effects on isoprene emission, (c) isoprene emission during and after water stress, and (d) the induction of isoprene emission from leaves grown at low temperature by water stress or elevated temperature. Isoprene emission under standard conditions of 1000 μmol photons·m-2·s-1 and 30°C developed only after the leaf had reached full expansion, and was not complete until up to two weeks past the point of full expansion of the leaf. The effect of temperature on isoprene emission was much greater than found for other species, with a 10°C increase in temperature causing a eight-fold increase in the rate of isoprene emission. Isoprene emission from kudzu was stimulated by increases in photon flux density up to 3000 μmol photons·m-2·s-1. In contrast, photosynthesis of kudzu was saturated at less than 1000 μmol·m-2·s-1 photon flux density and was reduced at high temperature, so that up to 20% of the carbon fixed in photosynthesis was reemitted as isoprene gas at 1000 μmol photons·m-2·s-1 and 35°C. Withholding water caused photosynthesis to decline nearly to zero after several days but had a much smaller effect on isoprene emission. Following the relief of water stress, photosynthesis recovered to the prestress level but isoprene emission increased to about five times the prestress rate. At 1000 μmol photons·m-2·s-1 and 35°C as much as 67% of the carbon fixed in photosynthesis was reemitted as isoprene eight days after water stress. Leaves grown at less than 20°C did not make isoprene until an inductive treatment was given. Inductive treatments included growth at 24°C, leaf temperature of 30°C for 5 h, or witholding water from plants. With the new information on temperature and water stress effects on isoprene emission, we speculate that isoprene emission may help plants cope with stressful conditions.

Entities:  

Keywords:  Induction (isoprene emission); Isoprene emission; Kudzu (isoprene emission); Pueraria lobata (Willd) Ohwi; Temperature response

Year:  1993        PMID: 28314006     DOI: 10.1007/BF00320984

Source DB:  PubMed          Journal:  Oecologia        ISSN: 0029-8549            Impact factor:   3.225


  12 in total

1.  On the relationship between isoprene emission and photosynthetic metabolites under different environmental conditions.

Authors:  F Loreto; T D Sharkey
Journal:  Planta       Date:  1993-03       Impact factor: 4.116

2.  The role of biogenic hydrocarbons in urban photochemical smog: Atlanta as a case study.

Authors:  W L Chameides; R W Lindsay; J Richardson; C S Kiang
Journal:  Science       Date:  1988-09-16       Impact factor: 47.728

3.  What do the hydrocarbons from trees contribute to air pollution?

Authors:  R A Rasmussen
Journal:  J Air Pollut Control Assoc       Date:  1972-07

4.  Relationships among Isoprene Emission Rate, Photosynthesis, and Isoprene Synthase Activity as Influenced by Temperature.

Authors:  R K Monson; C H Jaeger; W W Adams; E M Driggers; G M Silver; R Fall
Journal:  Plant Physiol       Date:  1992-03       Impact factor: 8.340

5.  Delayed Onset of Isoprene Emission in Developing Velvet Bean (Mucuna sp.) Leaves.

Authors:  J Grinspoon; W D Bowman; R Fall
Journal:  Plant Physiol       Date:  1991-09       Impact factor: 8.340

6.  Enzymatic synthesis of isoprene from dimethylallyl diphosphate in aspen leaf extracts.

Authors:  G M Silver; R Fall
Journal:  Plant Physiol       Date:  1991-12       Impact factor: 8.340

7.  Isoprene emission from aspen leaves : influence of environment and relation to photosynthesis and photorespiration.

Authors:  R K Monson; R Fall
Journal:  Plant Physiol       Date:  1989-05       Impact factor: 8.340

8.  Leaf Isoprene Emission Rate Is Dependent on Leaf Development and the Level of Isoprene Synthase.

Authors:  J. Kuzma; R. Fall
Journal:  Plant Physiol       Date:  1993-02       Impact factor: 8.340

9.  A gas-exchange study of photosynthesis and isoprene emission inQuercus rubra L.

Authors:  F Loreto; T D Sharkey
Journal:  Planta       Date:  1990-11       Impact factor: 4.116

Review 10.  Multivalent feedback regulation of HMG CoA reductase, a control mechanism coordinating isoprenoid synthesis and cell growth.

Authors:  M S Brown; J L Goldstein
Journal:  J Lipid Res       Date:  1980-07       Impact factor: 5.922

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  31 in total

1.  Differential controls by climate and physiology over the emission rates of biogenic volatile organic compounds from mature trees in a semi-arid pine forest.

Authors:  Allyson S D Eller; Lindsay L Young; Amy M Trowbridge; Russell K Monson
Journal:  Oecologia       Date:  2015-10-29       Impact factor: 3.225

2.  Isoprene Emission Response to Drought and the Impact on Global Atmospheric Chemistry.

Authors:  Xiaoyan Jiang; Alex Guenther; Mark Potosnak; Chris Geron; Roger Seco; Thomas Karl; Saewung Kim; Lianhong Gu; Stephen Pallardy
Journal:  Atmos Environ (1994)       Date:  2018-06       Impact factor: 4.798

3.  Diurnal and seasonal variation of isoprene biosynthesis-related genes in grey poplar leaves.

Authors:  Sabine Mayrhofer; Markus Teuber; Ina Zimmer; Sandrine Louis; Robert J Fischbach; Jörg-Peter Schnitzler
Journal:  Plant Physiol       Date:  2005-08-26       Impact factor: 8.340

4.  Modelling the drought impact on monoterpene fluxes from an evergreen Mediterranean forest canopy.

Authors:  Rüdiger Grote; Anne-Violette Lavoir; Serge Rambal; Michael Staudt; Ina Zimmer; Jörg-Peter Schnitzler
Journal:  Oecologia       Date:  2009-02-14       Impact factor: 3.225

5.  Kudzu (Pueraria montana) invasion doubles emissions of nitric oxide and increases ozone pollution.

Authors:  Jonathan E Hickman; Shiliang Wu; Loretta J Mickley; Manuel T Lerdau
Journal:  Proc Natl Acad Sci U S A       Date:  2010-05-17       Impact factor: 11.205

6.  Environmental and developmental controls over the seasonal pattern of isoprene emission from aspen leaves.

Authors:  R K Monson; P C Harley; M E Litvak; M Wildermuth; A B Guenther; P R Zimmerman; R Fall
Journal:  Oecologia       Date:  1994-09       Impact factor: 3.225

7.  Isoprene Acts as a Signaling Molecule in Gene Networks Important for Stress Responses and Plant Growth.

Authors:  Zhaojiang Zuo; Sarathi M Weraduwage; Alexandra T Lantz; Lydia M Sanchez; Sean E Weise; Jie Wang; Kevin L Childs; Thomas D Sharkey
Journal:  Plant Physiol       Date:  2019-02-13       Impact factor: 8.340

8.  The interacting effects of elevated atmospheric CO2 concentration, drought and leaf-to-air vapour pressure deficit on ecosystem isoprene fluxes.

Authors:  Emiliano Pegoraro; Ana Rey; Greg Barron-Gafford; Russell Monson; Yadvinder Malhi; Ramesh Murthy
Journal:  Oecologia       Date:  2005-10-22       Impact factor: 3.225

9.  Differences in the response sensitivity of stomatal index to atmospheric CO2 among four genera of Cupressaceae conifers.

Authors:  Matthew Haworth; James Heath; Jennifer C McElwain
Journal:  Ann Bot       Date:  2010-01-20       Impact factor: 4.357

10.  Natural abundance carbon isotope composition of isoprene reflects incomplete coupling between isoprene synthesis and photosynthetic carbon flow.

Authors:  Hagit P Affek; Dan Yakir
Journal:  Plant Physiol       Date:  2003-04       Impact factor: 8.340

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