Skip to main content
Log in

Microhabitat, water relations, and photosynthesis of a desert fern, Notholaena parryi

  • Published:
Oecologia Aims and scope Submit manuscript

Summary

Interrelationships between morphology, microhabitat, water relations, and photosynthesis of a xeric fern, Notholaena parryi D.C. Eat. (Pteridaceae), were examined in the western Colorado desert. In its typical microhabitat rock outcroppings protected N. parryi from direct sunlight and moderated the diurnal variations in air temperature. For example, frond temperature at noon in late winter was 15.3° C, which was 7.3° C cooler than an energy budget simulation predicting frond temperature at an exposed site. The lowest soil water potential leading to daytime stomatal opening was about-1.5 MPa (-15 bars). Rainfall runoff that was channeled to the periphery of the rocks caused Ψsoil near the fern roots to rise above-1.5 MPa even after light rainfalls, and it remained above-1.5 MPa longer after rainfall than in non-rocky sites.

The water potential gradient along the stipe necessary to support the observed rates of transpiration was about-10 MPa m-1; such a large gradient reflected the small conducting area in the xylem. The water vapor conductance decreased as the frond temperature was raised, an effect that became proportionally greater as the soil dried out. The daytime water-use efficiency (mass CO2 fixed/mass water transpired) was 0.0058 for a spring day. Individual fronds reached 90% of light saturation for photosynthesis at only 100 μEinsteins m-2 s-1, a photosynthetically active radiation similar to that from the diffuse sunlight incident on the generally north-facing microhabitat of the fern. Below 50 μE m-2 s-1 the quantum requirement was 13 Einsteins absorbed/mole CO2 fixed. The ratio of chlorophyll to P700 was 552, indicating a fairly large photosynthetic unit that is characteristic of plants adapted to shaded habitats. The temperature optimum for net photosynthesis shifted from 13° C in midwinter (mean daily air temperature of 11° C) to 19° C in early fall (air temperature of 23° C).

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  • Alberte, R.S., McClure, P.R., Thornber, J.P.: Photosynthesis in trees. Organization of chlorophyll and photosynthetic unit size in isolated gymnosperm chloroplasts. Plant Physiol. 58, 341–344 (1976)

    Google Scholar 

  • Arnon, D.I.: Copper enzymes in isolated chloroplasts. Polyphenoloxidase in Beta vulgaris. Plant Physiol. 24, 1–15 (1949)

    Google Scholar 

  • Billings, W.D., Morris, R.J.: Reflection of visible and infrared radiation from leaves of different ecological groups. Amer. J. Bot. 38, 327–331 (1951)

    Google Scholar 

  • Caldwell, M.M., Moore, R.T.: A portable small stage photoelectric planimeter for leaf area measurements. J. Range Management 24, 394–395 (1971)

    Google Scholar 

  • Danin, A.: Mediterranean elements in rocks of the Negev and Sinai deserts. Roy. Bot. Garden, Edinburgh, Notes 31, 437–440 (1972)

    Google Scholar 

  • Ehleringer, J., Björkman, O.: Quantum yields for CO2 uptake in C3 and C4 plants. Dependence on temperature, CO2, and O2 concentrations. Plant Physiol. 59, 86–90 (1977)

    Google Scholar 

  • Grillos, S.J.: Ferns and fern allies of California, 104 pp. Berkeley: Univ. California Press 1966

    Google Scholar 

  • Hall, A.E., Schulze, E.-D., Lange, O.L.: Current perspectives of steady-state stomatal responses to environment. In: Water and plant life — problems and modern approaches. Ecological studies series, Vol. 19 (O.L. Lange, L. Kappen, E.-D. Schulze, eds.), pp. 169–188. Berlin-Heidelberg-New York: Springer 1976

    Google Scholar 

  • Hellkvist, J., Richards, G.P., Jarvis, P.G.: Vertical gradients of water potential and tissue water relations in Sitka spruce trees measured with the pressure chamber. J. Appl. Ecol. 11, 637–667 (1974)

    Google Scholar 

  • Hevly, R.H.: Adaptations of cheilanthoid ferns to desert environments. J. Arizona Acad. Sci. 2, 164–175 (1963)

    Google Scholar 

  • Hill, R.H.: Comparative patterns of CO2 exchange of three fern species of southeastern Michigan. Mich. Acad. 4, 303–310 (1972)

    Google Scholar 

  • Hillel, D., Tadmor, N.: Water regime and vegetation in the central Negev highlands of Israel. Ecology 43, 33–41 (1962)

    Google Scholar 

  • Knoblock, I.W., Volz, P.A.: Studies in the fern genus Cheilanthes Swartz — I. The leaf blade anatomy of some species of the genus. Phytomorphology 14, 508–527 (1964)

    Google Scholar 

  • Lange, O.L., Schulze, E.-D., Evenari, M., Kappen, L., Buschbom, U.: The temperature-related photosynthetic capacity of plants under desert conditions. I. Seasonal changes of the photosynthetic response to temperature. Oecologia (Berl.) 17, 97–110 (1974)

    Google Scholar 

  • Maeda, O.: On the dry matter productivity of two ferns, Osmunda cinnamomea and Dryopteris crassirhizoma, in relation to their geographical distribution in Japan. Jap. J. Bot. 20, 237–267 (1970)

    Google Scholar 

  • Marsh, A.S.: The anatomy of some xerophilous species of Cheilanthes and Pellaea. Ann. Bot. 28, 671–684 (1914)

    Google Scholar 

  • Mooney, H.A., Björkman, O., Berry, J.: Photosynthetic adaptations to high temperature. In: Environmental physiology of desert organisms (N.F. Hadley, ed.), pp. 138–151. Stroudsburg, Pa.: Dowden, Hutchinson, & Ross 1975

    Google Scholar 

  • Nayar, B.K.: The morphology of some species of Cheilanthes. J. Linn. Soc. (Lond.), Bot., 58, 449–460 (1962)

    Google Scholar 

  • Nisbet, R.A., Patten, D.T.: Seasonal temperature acclimation of a prickly-pear cactus in south-central Arizona. Oecologia (Berl.) 15, 345–352 (1974)

    Google Scholar 

  • Nobel, P.S.: An introduction to biophysical plant physiology, 488 pp. San Francisco: Freeman 1974

    Google Scholar 

  • Nobel, P.S.: Water relations and photosynthesis of a desert CAM plant, Agave deserti. Plant Physiol. 58, 576–582 (1976a)

    Google Scholar 

  • Nobel, P.S.: Photosynthetic rates of sun versus shade leaves of Hyptis emoryi Torr. Plant Physiol. 58, 218–223 (1976b)

    Google Scholar 

  • Nobel, P.S.: Internal leaf area and cellular CO2 resistance: Photosynthetic implications of variations with growth conditions and plant species. Physiol. Plant. 40, 137–144 (1977)

    Google Scholar 

  • Nobel, P.S., Zaragoza, L.J., Smith, W.K.: Relation between mesophyll surface area, photosynthetic rate, and illumination level during development for leaves of Plectranthus parviflorus Henckel. Plant Physiol. 55, 1067–1070 (1975)

    Google Scholar 

  • Noy-Meir, I., Orshan, G., Tadmor, N.H.: Multivariate analysis of desert vegetation. III. The relation of vegetation units to habitat classes. Israel J. Bot. 22, 239–257 (1973)

    Google Scholar 

  • Oppenheimer, H.R.: Adaptation to drought: Xerophytism. In: Plant-water relationships in arid and semi-arid conditions, pp. 105–138. Paris: UNESCO 1960

    Google Scholar 

  • Oppenheimer, H.R., Halevy, A.H.: Anabiosis of Ceterach officinarum Lam. et Dc. Bull. Res. Counc. Israel, Bot. 11D, 127–147 (1962)

    Google Scholar 

  • Rabinowitch, E.: Photosynthesis and related processes, Vol. II, Part 1, 1208 pp. New York: Interscience 1951

    Google Scholar 

  • Rejmánek, M.: Ecological meaning of the thermal behaviour of rocks. Flora 160, 527–561 (1971)

    Google Scholar 

  • Schulze, E.-D.: Die Wirkung von Licht und Temperatur auf den CO2-Gaswechsel verschiedener Lebensformen aus der Krautschicht eines montanen Buchenwaldes. Oecologia (Berl.) 9, 235–258 (1972)

    Google Scholar 

  • Schulze, E.-D., Lange, O.L., Kappen, L., Buschbom, U., Evenari, M.: Stomatal responses to changes in temperature at increasing water stress. Planta (Berl.) 110, 29–42 (1973)

    Google Scholar 

  • Shiozawa, J.A., Alberte, R.S., Thornber, J.P.: The P700-chlorophyll a-protein. Isolation and some characteristics of the complex in higher plants. Arch. Biochem. Biophys. 165, 388–397 (1974)

    Google Scholar 

  • Smith, W.K., Nobel, P.S.: Influences of seasonal changes in leaf morphology on water-use efficiency for three desert broadleaf shrubs. Ecology 58 (in press, 1977)

  • Sparling, J.H.: Assimilation rates of some woodland herbs in Ontario. Bot. Gaz. 128, 160–168 (1967)

    Google Scholar 

  • Szarek, S.R., Ting, I.P.: Photosynthetic efficiency of CAM plants in relation to C3 and C4 plants. In: Environmental and biological control of photosynthesis (R. Marcelle, ed.), pp. 289–297. The Hague: Junk 1975

    Google Scholar 

  • Walter, H., Stadelmann, E.: A new approach to the water relations of desert plants. In: Desert biology, Vol. II (G.W. Brown, Jr., ed.), pp. 213–310. New York: Academic Press 1974

    Google Scholar 

  • Witham, H.V.: Ferns of the Colorado desert. California Native Plant Soc. Newsletter 8, 10–13 (1972)

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Nobel, P.S. Microhabitat, water relations, and photosynthesis of a desert fern, Notholaena parryi . Oecologia 31, 293–309 (1978). https://doi.org/10.1007/BF00346249

Download citation

  • Received:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00346249

Keywords

Navigation