Literature DB >> 28311975

Altitudinal changes in the incidence of crassulacean acid metabolism in vascular epiphytes and related life forms in Papua New Guinea.

M J Earnshaw1, K Winter2, H Ziegler3, W Stichler3, N E G Cruttwell4, K Kerenga5, P J Cribb6, J Wood6, J R Croft5, K A Carver1, T C Gunn7.   

Abstract

The occurrence of Crassulacean acid metabolism (CAM), as judged from δ13C values, was investigated in epiphytes and some related plant species at a series of sites covering the approximate altitudinal range of epiphytes in Papua New Guinea. Comprehensive collections were made at each site and the occurrence of water storage tissue and blade thickness was also determined. Some 26% of epiphytic orchids from a lowland rainforest (2-300 m.a.s.l) showed δ13C values typical of obligate CAM and possessed leaves thicker than 1 mm. A second group of orchids, mostly with succulent leaves, possessed intermediate δ13C values between -23 and -26% and accounted for 25% of the total species number. Some species of this group may exhibit weak CAM or be facultative CAM plants. The remainder of the lowland rainforest species appeared to be C3 plants with δ13C values between -28 and -35%. and generally possessed thin leaves. Obligate CAM species of orchids from a lower montane rainforest (1175 m.a.s.l) comprised 26% of the species total and mostly possessed thick leaves. The remainder of the species were generally thin-leaved with δ13C values between -26 and -35%. largely indicative of C3 photosynthesis. Orchids with intermediate δ13C values were not found in the lower montane rainforest. Obligate CAM appeared to be lacking in highland epiphytes from an upper montane rainforest and subalpine rainforest (2600-3600 m.a.s.l). However the fern, Microsorium cromwellii had a δ13C value of -21.28%. suggesting some measure of CAM activity. Other highland ferns and orchids showed more negative °13C values, up to-33%., typical of C3 photosynthesis. The highland epiphytic orchids possessed a greater mean leaf thickness than their lowland C3 counterparts due to the frequent occurrence of water storage tissue located on the adaxial side of the leaf. It is suggested that low daytime temperatures in the highland microhabitats is a major factor in explaining the absence of CAM. The increased frequency of water storage tissue in highland epiphytes may be an adaptation to periodic water stress events in the dry season and/or an adaptation to increased levels of UV light in the tropicalpine environment.

Entities:  

Keywords:  Altitude; CAM; Epiphytes; Tropical habitat; δ13C

Year:  1987        PMID: 28311975     DOI: 10.1007/BF00379417

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


  15 in total

1.  Response of the Succulent Leaves of Peperomia magnoliaefolia to Dehydration: Water Relations and Solute Movement in Chlorenchyma and Hydrenchyma.

Authors:  J E Schmidt; W M Kaiser
Journal:  Plant Physiol       Date:  1987-01       Impact factor: 8.340

2.  Dependence of CO2 gas exchange and acid metabolism of the alpine CAM plant Sempervivum montanum on temperature and light.

Authors:  Johanna Wagner; Walter Larcher
Journal:  Oecologia       Date:  1981-08       Impact factor: 3.225

3.  Stratification of δ13C values of leaves in Amazonian rain forests.

Authors:  E Medina; P Minchin
Journal:  Oecologia       Date:  1980-01       Impact factor: 3.225

4.  The distribution of C3 and C4 grasses and carbon isotope discrimination along an altitudinal and moisture gradient in Kenya.

Authors:  Larry L Tieszen; Michael M Senyimba; Simeon K Imbamba; John H Troughton
Journal:  Oecologia       Date:  1979-01       Impact factor: 3.225

5.  DARK CO2 FIXATION, HABITAT PREFERENCE AND EVOLUTION WITHIN THE BROMELIACEAE.

Authors:  Ernesto Medina
Journal:  Evolution       Date:  1974-12       Impact factor: 3.694

6.  Crassulacean acid metabolism in the shade. Studies on an epiphytic fern, Pyrrosia longifolia, and other rainforest species from Australia.

Authors:  K Winter; C B Osmond; K T Hubick
Journal:  Oecologia       Date:  1986-01       Impact factor: 3.225

7.  Photosynthetic pathways in the Bromeliaceae of Trinidad: relations between life-forms, habitat preference and the occurrence of CAM.

Authors:  Howard Griffiths; J Andrew C Smith
Journal:  Oecologia       Date:  1983-11       Impact factor: 3.225

8.  Two types of carbon fixation in tropical orchids.

Authors:  T F Neales; C S Hew
Journal:  Planta       Date:  1975-01       Impact factor: 4.116

9.  Light-Stimulated Burst of Carbon Dioxide Uptake following Nocturnal Acidification in the Crassulacean Acid Metabolism Plant Kalanchoë diagremontiana.

Authors:  K Winter; J D Tenhunen
Journal:  Plant Physiol       Date:  1982-12       Impact factor: 8.340

10.  Carbon isotope discrimination in alpine succulent plants supposed to be capable of crassulacean acid metabolism (CAM).

Authors:  C B Osmond; H Ziegler; W Stichler; P Trimborn
Journal:  Oecologia       Date:  1975-09       Impact factor: 3.225

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  10 in total

1.  The effects of salinity, crassulacean acid metabolism and plant age on the carbon isotope composition of Mesembryanthemum crystallinum L., a halophytic C(3)-CAM species.

Authors:  Klaus Winter; Joseph A M Holtum
Journal:  Planta       Date:  2005-06-21       Impact factor: 4.116

2.  Photosynthetic pathway, chilling tolerance and cell sap osmotic potential values of grasses along an altitudinal gradient in Papua New Guinea.

Authors:  M J Earnshaw; K A Carver; T C Gunn; K Kerenga; V Harvey; H Griffiths; M S J Broadmeadow
Journal:  Oecologia       Date:  1990-09       Impact factor: 3.225

3.  Crassulacean acid metabolism in Kalanchoë species collected in various climatic zones of Madagascar: a survey by δ13C analysis.

Authors:  Manfred Kluge; Jeanne Brulfert; Didier Ravelomanana; Joseph Lipp; Hubert Ziegler
Journal:  Oecologia       Date:  1991-11       Impact factor: 3.225

4.  Crassulacean acid metabolism (CAM) in an epiphytic ant-plant, Myrmecodia beccarii Hook.f. (Rubiaceae).

Authors:  Edward W J Tsen; Joseph A M Holtum
Journal:  Photosynth Res       Date:  2012-03-23       Impact factor: 3.573

5.  Are thick leaves, large mesophyll cells and small intercellular air spaces requisites for CAM?

Authors:  Ana Herrera
Journal:  Ann Bot       Date:  2020-05-13       Impact factor: 4.357

6.  How prevalent is crassulacean acid metabolism among vascular epiphytes?

Authors:  Gerhard Zotz
Journal:  Oecologia       Date:  2003-10-31       Impact factor: 3.225

7.  The occurrence of crassulacean acid metabolism in Cymbidium (Orchidaceae) and its ecological and evolutionary implications.

Authors:  H Motomura; T Yukawa; O Ueno; A Kagawa
Journal:  J Plant Res       Date:  2008-02-02       Impact factor: 2.629

8.  Biomonitors of atmospheric nitrogen deposition: potential uses and limitations.

Authors:  Edison A Díaz-Álvarez; Roberto Lindig-Cisneros; Erick de la Barrera
Journal:  Conserv Physiol       Date:  2018-03-13       Impact factor: 3.079

9.  Effects of geographic isolation on the Bulbophyllum chloroplast genomes.

Authors:  Jiapeng Yang; Fuwei Zhang; Yajie Ge; Wenhui Yu; Qiqian Xue; Mengting Wang; Hongman Wang; Qingyun Xue; Wei Liu; Zhitao Niu; Xiaoyu Ding
Journal:  BMC Plant Biol       Date:  2022-04-19       Impact factor: 5.260

10.  Exploring molecular evolution of Rubisco in C3 and CAM Orchidaceae and Bromeliaceae.

Authors:  Carmen Hermida-Carrera; Mario A Fares; Marcel Font-Carrascosa; Maxim V Kapralov; Marcus A Koch; Arnau Mir; Arántzazu Molins; Miquel Ribas-Carbó; Jairo Rocha; Jeroni Galmés
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