Skip to main content
Log in

The effects of climatic pattern on lichen productivity: Cetraria cucullata (Bell.) Ach. in the arctic tundra of northern Alaska

  • Published:
Oecologia Aims and scope Submit manuscript

Summary

The climatic control of productivity for two populations of the lichen Cetraria cucullata (Bell.) Ach. growing in the arctic tundra of northern Alaska (70°28′N, 157°23′W) was examined. Respiratory losses of carbon vary with tissue temperature, tissue water content, and time since wetting. Potential net photosynthetic gains of carbon are affected by photon flux density, tissue temperature, and water content. The net CO2 exchange responses of populations growing on ridge tundra and on upland tundra differ and these differences reflect possible adaptation to the normal environmental regimes in the two habitats. Simulation of the lichen's net carbon balance using continuous hourly records of photon flux density, temperature, and water content for the unusually dry period June 28 through July 17, 1977 show that lichen biomass is actually lost during climatic regimes leading to frequent but short periods of lichen metabolic activity. This result is confirmed by the negative relative growth rates measured for C. cucullata over the same monitoring period. This observed loss of biomass may be attributable to depletion of carbon reserves to reactivate dormant metabolism without sufficiently long periods favorable for net photosynthetic activity to replenish the lost reserves. These results illustrate that environmental limits exist on the success of the dormancy strategy characteristic of lichen and moss carbon metabolism.

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

  • Bailey RH (1976) Ecological aspects of dispersal and estabolishment in lichens. In: Brown DH, Hawksworth DL and Bailey RH (eds) Lichenology: progress and problems. Academic Press New York pp 215–247

    Google Scholar 

  • Barr AJ, Goodnight JH, Sall JP, Helwig JT (1976) A user's guide to SAS. SAS Institute, Raleigh, North Carolina

    Google Scholar 

  • Bliss LC (1956) A comparison of plant development in microenvironments of arctic and alpine tundras. Ecol Monogr 26:303–337

    Google Scholar 

  • Britton ME (1966) Vegetation of the arctic tundra. Oregon State University Press Corvallis

    Google Scholar 

  • Carstairs AG, Oechel WC (1978) Effects of several micro-climatic factors and nutrients on net carbon dioxide exchange in Cladonia alpestris (L.) Rabh. in the subarctic. Arctic and Alpine Research 10:81–94

    Google Scholar 

  • Clebsch EEC, Shanks RE (1968) Summer climatic gradients and vegetation near Barrow, Alaska. Arctic 21:162–171

    Google Scholar 

  • Dilks TJK, Proctor MCF (1974) The pattern of recovery of bryophytes after dessication. J Bryol 8:97–115

    Google Scholar 

  • Dilks TJK, Proctor MCF (1976) Effects of intermittent dessication on bryophytes. J Bryol 9:249–264

    Google Scholar 

  • Draper NR, Smith H (1966) Applied regression analysis, Wiley New York pp 407

    Google Scholar 

  • Farrar JF (1976a) Ecological physiology of the lichen Hypogymnia physodes, II. Effects of wetting and drying cycles and the concept of “physiological buffering”. New Phytol 77:105–113

    Google Scholar 

  • Farrar JF (1976b) The lichen as an ecosystem: observation and experiment. In: Brown DH, Hawskworth DL and Bailey RH (eds) Lichenology: progress and problems Academic Press New York pp 385–406

    Google Scholar 

  • Farrar JF (1978) Ecological physiology of the lichen Hypogymnia physodes, IV. Carbon allocation at low temperatures. New Phytologist 81:65–69

    Google Scholar 

  • Farrar JF, Smith DC (1976) Ecological physiology of the lichen Hypogymnia physodes, III. The importance of the rewetting phase. New Phytol 77:115–125

    Google Scholar 

  • Hanson HC (1955) Vegetation types in northwestern Alaska and comparisons with communities in other arctic regions. Ecology 36:111–140

    Google Scholar 

  • Harris GP (1972) The ecology of corticolous lichens, III. A simulation model of productivity as a function of light intensity and water availability. J Ecol 69:19–40

    Google Scholar 

  • Haugen RK, Brown J (1980) Coastal-inland distributions of summer air temperature and precipitation in northern Alaska. Arctic and Alpine Res 12:403–412

    Google Scholar 

  • Hoffman GR, Gates DM (1970) An energy budget approach to the study of water loss in cryptogams. Bull. Torrey Bot Club 97:361–366

    Google Scholar 

  • Kappen L (1973) Response to extreme environments. In: Ahmadjian V, and Hale ME (eds) The Lichens. Academic Press, New York pp 311–380

    Google Scholar 

  • Kappen L, Lange OL, Schulze E-D, Evenari M, Buschbom U (1979) Ecophysiological investigations on lichens of the Negev Desert. VI. Annual course of the photosynthetic production of Ramalina maciformis (Del) Bory Flora 168:85–108

    Google Scholar 

  • Kärenlampi L (1971) Studies on the relative growth rate of some fruticose lichens. Rep Kevo Subarctic Res Stat 7:33–39

    Google Scholar 

  • Kershaw KA (1975) Studies on lichen-dominated systems, XIV. The comparative ecology of Alectoria nitidula and Cladina alpestris. Can J Bot 53:2608–2613

    Google Scholar 

  • Kershaw KA, Harris GP (1971) Simulation studies and ecology: use of the model. In: Statistical Ecology, Volume 3, Patil GP, Pielou EC, and Waters WE (eds), Pennsylvania State University Press University Park pp 23–42

    Google Scholar 

  • Komarkova V, Webber PJ (1980) Two low arctic vegetation maps near Atkasook, Alaska. Arctic and Alpine Res 12:447–472

    Google Scholar 

  • Lange OL (1969) Ecophysiological investigations on lichens of the Negev Desert. I CO2 gas exchange of Ramalina maciformis (Del) Bory under controlled conditions in the laboratory. Flora 158 B:324–359 Translated from German as Natl Res Coun Can Tech Transl 1654

    Google Scholar 

  • Lange OL, Schulze E-D, Koch W (1970) Ecophysiological investigations on lichens of the Negev Desert, II CO2 gas exchange and water conservation of Ramalina maciformis (Del) Bory in its natural habitat during the summer dry period. Flora 159 B:38–62 Translated from German as Natl Res Coun Can Tech Transl 1655

    Google Scholar 

  • Lange OL, Kappen L (1972) Photosynthesis of lichens from Antarctica. In: Llano GA (ed) Antarctic terrestrial biology American Geophysical Union, Washington pp 83–95

    Google Scholar 

  • Lange OL, Geiger IL, Schulze E-D (1977) Ecophysiological investigations on lichens of the Negev Desert. V. A model to simulate net photosynthesis and respiration of Ramalina maciformis. Oecologia (Berl) 28:247–259

    Google Scholar 

  • Larson DW (1978) Patterns of lichen photosynthesis and respiration following prolonged frozen storage. Can J Bot 56:2119–2123

    Google Scholar 

  • Larson DW (1979) Preliminary studies of the physiological ecology of Umbilicaria lichens. Can J Bot 57:1398–1406

    Google Scholar 

  • Larson DW, Kershaw KA (1975a) Studies on lichen-dominated systems, XIII. Seasonal and geographical variation of net CO2 exchange of Alectoria ochroleuca. Can J Bot 53:2598–2607

    Google Scholar 

  • Larson DW, Kershaw KA (1975b) Studies on lichen-dominated systems, XVI. Comparative patterns of net CO2 exchange in Cetraria nivalis and Alectoria ochroleuca collected from a raised-bench ridge. Can J Bot 53:2884–2982

    Google Scholar 

  • Larson DW, Kershaw KA (1975c) Acclimation in arctic lichens. Nature 254:421–423

    Google Scholar 

  • Lechowicz MJ (1976) Environmental response structure of Cladonia lichens from contrasting climates. PhD thesis, at University of Wisconsin-Madison (University Microfilms, Ann Arbor, Dissertation Abstract 77-3409)

    Google Scholar 

  • Lechowicz MJ (1978) Carbon dioxide exchange in Cladina lichens from subarctic and temperate habitats. Oecologia (Berl) 32:225–237

    Google Scholar 

  • Lechowicz MJ (1981) Adaptation and the fundamental niche: evidence from lichens. In: Wicklow DT, and Carroll G (eds) The Fungal Community: Its Organization and Role in the Ecosystem Marcel Dekker New York (in press)

    Google Scholar 

  • Lewis DH, Smith DC (1967) Sugar alcohols (polyols) in fungi and green plants, I Distribution, physiology, and metabolism. New Phytol 66:143–184

    Google Scholar 

  • Mead R, Pike DJ (1975) A review of response surface methodology from a biometric viewpoint. Biometrics 31:803–851

    Google Scholar 

  • Moser TJ, Nash TH III (1978) Photosynthetic patterns of Cetraria cucullata (Bell) Ach. at Anaktuvuk Pass, Alaska. Oecologia (Berl) 34:37–43

    Google Scholar 

  • Moser TJ, Nash TH III, Thomson JW (1979) Lichens of Anaktuvuk Pass, Alaska, with emphasis on the impact of caribou grazing. Bryologist 82:393–408

    Google Scholar 

  • Person SJ, Pegau RE, White RG, Luick JR (1980) In vitro and nylonbag digestabilities of reindeer and caribou forages. J Wildlife Management 44:613–622

    Google Scholar 

  • Richardson DHS (1973) Photosynthesis and carbohydrate movement. In: The Lichens Ahmadjian V and Hale ME (eds), Academic Press New York pp 249–288

    Google Scholar 

  • Ried A (1960) Secondary effects of syneresis on the gas metabolism of crustaceous lichens. Biol Zentralblatt 79:657–678 Transl from German as Nat Res Council Canada TT

    Google Scholar 

  • Rogers RW (1971) Distribution of the lichen Chondropsis semiviridis in relation to its heat and drought resistance. New Phytol 70:1069–1077

    Google Scholar 

  • Sestak Z, Catsky J, Jarvis PG (1971) Plant photosynthetic production, manual of methods, Junk The Hague 818 pp

    Google Scholar 

  • Slavik B (1974) Methods of studying plant water relations. Springer Berlin Heidelberg New York

    Google Scholar 

  • Smith DC, Molesworth S (1973) Lichen physiology, XIII. Effects of rewetting dry lichens. New Phytol 72:525–533

    Google Scholar 

  • Webber PJ, Walker DA (1975) Vegetation and landscape analysis at Prodhoe Bay, Alaska: a vegetation map of the Tundra Biome study area. In: Brown J (ed) Ecological Investigations of the Tundra Biome in the Prudhoe Bay Region, Alaska. Biological Papers of the University of Alaska, Fairbanks, Alaska, Special Report 2 pp 81–91

  • Webber PJ, Komárková V, Hansell H, Seabert K (1977) Soil moisture and soil thaw data and their partial analysis from sixty vegetation plots at Atkasook, Alaska for the summers of 1975 and 1976, pp 32 Internal report, Research on Arctic Tundra Environments (RATE)

  • White RG, Thomson BR, Skogland T, Person S, Russell DE, Holleman DF, Luick JR (1975) Ecology of caribou at Prudhoe Bay, Alaska. In: Ecological Investigations of the Tundra Biome in the Prudhoe Bay Region, Alaska Brown, J (ed), Biological Papers of the University of Alaska, Fairbanks, Alaska, Special Report Number 2 pp 151–201

  • Yarranton GA (1975) Population growth in Cladonia stellaris (Opiz) Pouz, and Vezda. New Phytol 75:99–110

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Lechowicz, M.J. The effects of climatic pattern on lichen productivity: Cetraria cucullata (Bell.) Ach. in the arctic tundra of northern Alaska. Oecologia 50, 210–216 (1981). https://doi.org/10.1007/BF00348040

Download citation

  • Received:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00348040

Keywords

Navigation