Skip to main content
Log in

Seasonal changes in photosynthesis in the desiccation-tolerant fern Polypodium virginianum

  • Original Papers
  • Published:
Oecologia Aims and scope Submit manuscript

Summary

Seasonal changes in photosynthesis were examined in the desiccation-tolerant fern Polypodium virginianum growing in a forest understory along cliff edges of the Niagara Escarpment in southern Ontario, Canada. For plants growing in situ, the photosynthetic response to irradiance was examined on a seasonal basis, to determine the degree to which the utilization of light changed over the growing season. Experiments were executed on control plants, on previously desiccated then rehydrated plants, and on continuously hydrated plants to determine if prior desiccation influenced the response to light. Soil and xylem water potential and temperature were monitored and used as covariates in analyses. The results showed that carbon gain in the spring greatly exceeded that of any other season. Despite this, there was little change in the photosynthetic response to light on a seasonal basis even though plants were exposed to highly variable and highly limited light most of the time. Prior desiccation had a slight influence on photosynthetic rate but not on other photosynthetic parameters such as the light compensation point and Lhalf. Temperature was a significant seasonal covariate and additional experiments conducted in the laboratory showed that the response of photosynthesis to temperature was broad. Xylem water potential was correlated with seasonal changes in relative humidity. The results suggest that P. virginanum persists in hostile cliff-edge habitats by being able to exploit high-light periods in the spring and by thereafter maintaining a low but relatively constant rate of carbon despite prior exposure to fluctuating supplies of light and water.

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

  • Anderson MC (1964) Studies of the woodland light climate. II. Seasonal variation in the light climate J Ecol 52:643–663

    Google Scholar 

  • Bartlett RM, Matthes-Sears U, Larson DW (1990) Organization of the Niagara Escarpment cliff community. II. Characterization of the physical environment. Can J Bot 68:1931–1941

    Google Scholar 

  • Bewley JD, Krochko JE (1982) Dessication-Tolerance. In: Lange OL, Nobel PS, Osmond CB, Ziegler H (ed), Encyclopedia of Plant Physiology Vol. 12b. Springer-Verlag, Berlin, pp. 325–378

    Google Scholar 

  • Boardman NK (1977) Comparative photosynthesis of sun and shade plants. Ann Rev Plant Physiol. 28:355–377

    Google Scholar 

  • Brown RW, Bartos DL (1982) A Calibration Model for Screencaged Peltier Thermocouple Psychrometers. USDA For Serv Res Rap INT-293 Ogden, Utah

  • Chazdon RL, (1988) Sunflecks and their importance to forest understory plants. Adv Ecol Res 18:1–63

    Google Scholar 

  • Cody WJ and Britton DM (1990) Ferns and fern allies of Canada. Research Branch Agriculture Canada. Publ 1829/E, Ottawa

  • dePhamphilis CW, Neufeld HS (1989) Phenology and ecophysiology of Aesculus sylvatica, a vernal understory tree. Can J Bot 67:2161–2167

    Google Scholar 

  • Eickmeier WH (1979) Photosynthetic recovery of the resurrection plant Selaginella lepidophylla after wetting. Oecologia 39:93–106

    Google Scholar 

  • Eickmeier WG (1986) The correlation between high-temperature and desiccation tolerances in a poikilohydric desert plant. Can J Bot 64:611–617

    Google Scholar 

  • Gildner BS (1990) Photosynthetic response to sunflecks in the understorey pteridophyte Polypodium virginianum L. MSc. thesis, University of Guelph

  • Harten JB, Eickmeier WG (1987) Comparative desiccation tolerance of three desert pteridophytes: Response to long-term desiccation. Am Midland Nat 118:337–347

    Google Scholar 

  • Haufler CH, Windham MD (1991) New species of North American Cystopteris and Polypodium, with comments on their reticulate relationships. Am Fern J 81:7–23

    Google Scholar 

  • Hill RH (1972) Comparative patterns of CO2 exchange of three fern species of southeastern Michigan. Michigan Academ 303–310

  • Hutchison BA, Matt D (1977) The distribution of solar radiation within a deciduous forest. Ecol Mono 47:185–207

    Google Scholar 

  • Kappen L (1964) Untersuchungen uber den jahreslauf der frost-, hitze-, und austocknungsresistenz von sporophyten einheimischer Polypodiaceen (Filicinae). Flora 155:123–166

    Google Scholar 

  • Kershaw KA (1985) Physiological ecology of lichens. Cambridge University Press, Cambridge

    Google Scholar 

  • Kumura M, Ohya M, Tanaka E (1972) Production processes of Ophiopogon planiscapus population grown in a mixed forest stand. JIBP/PP Photosynthesis level III, Rep 1971: 76–79, as cited: Koizumi H (1985) Studies on the life history of an evergreen herb, Pyrola japonica, population on a forest floor in a warm temperate region. 1. Growth, net production and matter economy. Bot Mag Tokyo 98: 383–392

    Google Scholar 

  • Koizumi H, (1989) Studies on the life history of an evergreen herb, Pyrola japonica, population on a forest floor in a warm temperate region. 2. Photosynthesis, respiration and gross production. Bot Mag Tokyo 102:521–532

    Google Scholar 

  • Larson DW, Spring SH, Matthes-Sears U, Bartlett RM (1989) Organization of the Niagara Escarpment cliff community. Can J Bot 67:2731–2742

    Google Scholar 

  • Lellinger DB (1985) A Field Manual of the Ferns and Fern Allies of the United States and Canada. Smithsonian Institution Press, Washington DC. p. 197

    Google Scholar 

  • Lloyd RM, Lang FA (1964) The Polypodium vulgare complex in North America. B. Fern Gazz 9:168–177

    Google Scholar 

  • Ludlow CJ, Wolf FT (1975) Photosynthesis and respiration rates of ferns. Am Fern J 65:43–48

    Google Scholar 

  • Matthes-Sears U, Larson DW (1990) Environmental controls of carbon uptake in two woody species with contrasting distributions at the edge of cliffs. Can J Bot 68:2371–2380

    Google Scholar 

  • Nobel PS, Calkin HW, Gibson AC (1984) Influences of PAR, temperature and water vapor concentration on gas exchange by ferns. Physiol Plant 62:527–534

    Google Scholar 

  • Oppenheimer HR, Halevy AH (1962) Anabiosis of Ceterach officinarum et dc. Bull. Res. Counc. of Israel XI 11D 3: 127–147

    Google Scholar 

  • Pearcy RW (1990) Sunflecks and photosynthesis in plant canopies. Ann. Rev. Plant Physiol. Plant Mol Bio 41:421–453

    Google Scholar 

  • Pitelka LF, Curtis WF (1986) Photosynthetic responses to light in an understory herb, Aster acuminatus. Am J Bot 73:535–540

    Google Scholar 

  • SAS Institute Inc. (1988) SAS/STAT user's guide, Release 6.03 Edition. SAS Institute Inc., Cary, NC

    Google Scholar 

  • Schwab KB, Schreiber U, Heber U (1989) Response of photosynthesis and respiration of resurrection plants to desiccation and rehydration. Planta 177:217–227

    Google Scholar 

  • Smith E (1937) The influence of light and carbon dioxide on photosynthesis. J Gen Physiol 20:807–830

    Google Scholar 

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

    Google Scholar 

  • Stuart TS (1968) Revival of respiration and photosynthesis in dried leaves of Polypodium polypodioides. Planta 83:185–206

    Google Scholar 

  • Taylor RJ, Pearcy RW (1976) Seasonal patterns of the CO2 exchange characteristics of understory plants from a deciduous forest. Can J Bot 54:1094–1103

    Google Scholar 

  • Tenhunen JD, Lange OL, Gebel J, Beyschlag W, Weber JA (1984) Changes in photosynthetic capacity, carboxylation efficiency, and CO2 exchange of leaves of Quercus suber. Planta 162:193–203

    Google Scholar 

  • Tingely DT, Evans RC, Bates EH, Gumpertz ML (1987) Isoprene emissions and photosynthesis in three ferns — the influence of light and temperature. Physiol Plant 69:609–616

    Google Scholar 

  • Woodward FI (1990) From ecosystems to genes: The importance of shade tolerance. TREE 5:111–115

    Google Scholar 

  • Yoshie F, Kawano S (1986) Seasonal changes in photosynthetic characteristics of Pachysandra terminalis (Buxaceae), an evergreen woodland chamaephyte, in the cool temperate regions of Japan. Oecologia 71:6–11

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Gildner, B.S., Larson, D.W. Seasonal changes in photosynthesis in the desiccation-tolerant fern Polypodium virginianum . Oecologia 89, 383–389 (1992). https://doi.org/10.1007/BF00317416

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00317416

Key words

Navigation