Literature DB >> 28309897

CO2 gas exchange and transpiration of Welwitschia mirabilis Hook. fil. in the central Namib desert.

D J von Willert1, B M Eller2, E Brinckmann1, R Baasch1.   

Abstract

The diurnal course of CO2 gas exchange, 14CO2 incorporation, malate and citrate content, and traspiration of Welwitschia mirabilis were measured in one of its natural habitats, the Welwitschia-Vlakte in the central Namib desert (Namibia), in order to decide which CO2 fixation pathway is used by this gymnosperm.The CO2 gas exchange of Welwitschia is that of a C3 plant under arid conditions. Younger leaf parts show a two-peaked pattern of photosynthetic CO2 uptake whereas in older parts the morning peak is followed by net CO2 release during the rest of the day. The maximum rates of net photosynthesis decrease from 3.4 μmol m-2 s-1 in 1-year-old parts to 1 μmol m-2 s-1 in 7-year-old parts. No net CO2 uptake was detected during the night. The diurnal CO2 balance indicates that the old leaf parts live at the expense of the younger ones. Irrigation of Welwitschia plants resulted in an increased CO2 uptake throughout the light period with maximum rate of 4.1 μmol m-2 s-1. 14CO2 was only incorporated during the day.The water loss of Welwitschia by transpiration is considerable, reaching a peak value of 1.9 mmol m-2 s-1 around noon. Leaf conductance corresponds with the twopeaked pattern of CO2 uptake.Although there is no sign of a crassulacean acid metabolism in Welwitschia the leaf contains rather high amounts of malate (up to 200 μmol g-1 dry matter) and citrate (up to 250 μmol g-1 dry matter), which depend on leaf age but do not show any significant day-night oscillation.In spite of all this the δ13C values are in the range of-17.77 to-19.64‰. Possible reasons for such a high 13C content in a C3 plant are discussed.

Entities:  

Year:  1982        PMID: 28309897     DOI: 10.1007/BF00386713

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


  7 in total

1.  Leaf temperatures and energy balance ofWelwitschia mirabilis in its natural habitat.

Authors:  E -D Schulze; B M Eller; D A Thomas; D J V Willert; E Brinckmann
Journal:  Oecologia       Date:  1980-01       Impact factor: 3.225

2.  Effect of salinity and humidity on δ13C value of halophytes-Evidence for diffusional isotope fractionation determined by the ratio of intercellular/atmospheric partial pressure of CO2 under different environmental conditions.

Authors:  G D Farquhar; M C Ball; S von Caemmerer; Z Roksandic
Journal:  Oecologia       Date:  1982-01       Impact factor: 3.225

3.  The activity and malate inhibition/stimulation of phosphoenolpyruvate-carboxylase in crassulacean-acid-metabolism plants in their natural environment.

Authors:  D J von Willert; E Brinckmann; B Scheitler; D A Thomas; S Treichel
Journal:  Planta       Date:  1979-10       Impact factor: 4.116

4.  Environmental control of crassulacean acid metabolism in Welwitschia mirabilis Hook. Fil. in its range of natural distribution in the Namib desert.

Authors:  E D Schulze; H Ziegler; W Stichler
Journal:  Oecologia       Date:  1976-12       Impact factor: 3.225

5.  Irrigation magnifies CAM-photosynthesis in Opuntia basilaris (Cactaceae).

Authors:  Zac Hanscom; Irwin P Ting
Journal:  Oecologia       Date:  1978-01       Impact factor: 3.225

6.  Seasonal Patterns of Acid Metabolism and Gas Exchange in Opuntia basilaris.

Authors:  S R Szarek; I P Ting
Journal:  Plant Physiol       Date:  1974-07       Impact factor: 8.340

7.  The effect of leaf age on leaf resistance and CO2 exchange of the CAM plant Bryophyllum fedtschenkoi.

Authors:  M B Jones
Journal:  Planta       Date:  1975-01       Impact factor: 4.116

  7 in total
  1 in total

1.  Water loss and malate fluctuations during the day for plants in the southern Namib desert.

Authors:  D J V Willert; E Brinckmann; B M Eller; B Scheitler
Journal:  Oecologia       Date:  1984-03       Impact factor: 3.225

  1 in total

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