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Carbon and Nitrogen Economy of Diplacus aurantiacus, a Californian Mediterranean-Climate Drought-Deciduous Shrub

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Mediterranean-Type Ecosystems

Part of the book series: Ecological Studies ((ECOLSTUD,volume 43))

Abstract

Accumulating evidence suggests a fairly direct link between leaf nitrogen content and photosynthetic rate per unit leaf mass (Takeda 1961; Natr 1972; Yoshida and Coronel 1976; Brown 1978; Mooney et al. 1978). In addition to specific relationships obtained on individual species (as cited above), Winner (1980) has observed an overall correlation of 0.64 (P < 0.001) between nitrogen content and photosynthetic rate among nine different chaparral species in which the measurements of photosynthesis were not controlled for leaf age or stomatal conductance.

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References

  • Anderson JM (1973) The breakdown and decomposition of sweet chestnut (Castanea sativa Mill.) and beech (Fagus sylvatica L.) leaf litter in two deciduous woodland soils. Oecologia 12: 275–288.

    Google Scholar 

  • Bocock KL (1964) Changes in the amounts of dry matter, nitrogen, carbon, and energy in decomposing woodland leaf litter in relation to the activities of the soil fauna. Journal of Ecology 52: 273–284.

    Article  Google Scholar 

  • Brown KL (1964) Changes in the amounts of dry matter, nitrogen, carbon, and energy in decomposing woodland leaf litter in relation to the activities of the soil fauna. Journal of Ecology 52: 273–284.

    Article  Google Scholar 

  • Brown RH (1978) A difference in N use efficiency in C3 and C4 plants and its implications in adaptation and evolution. Crop Science 18: 93–98.

    Article  CAS  Google Scholar 

  • Chapin FS III, Johnson DA, McKEndrick JD (1980) Seasonal movement of nutrients in plants of differing growth form in an Alaskan tundra ecosystem: implications for herbivory. Journal of Ecology 68: 189–210.

    Article  CAS  Google Scholar 

  • Gosz JR, Likens GE, Bormann FH (1973) Nutrient release from decomposing leaf and branch litter in the Hubbard Brook Forest, New Hampshire. Ecological Monographs 43: 173–191.

    Article  Google Scholar 

  • Grubb PJ (1977) Control of forest growth and distribution on wet tropical mountains with special reference to mineral nutrition. Annual Review of Ecology Systematics 8: 83–107.

    Article  CAS  Google Scholar 

  • Gulmon SL, Chu CC (1981) The effects of light and nitrogen on photosynthesis, leaf characteristics, and dry matter allocation in the chaparral shrub, Diplacus aurantiacus. Oecologia 49: 207–212.

    Article  Google Scholar 

  • Kummerow J, Krause D, Jow W (1977) Root systems of chaparral shrubs. Oecologia 29: 163–177.

    Google Scholar 

  • Kvet J, Ondok JP, Necas J, Jarvis PG (1971) Methods of growth analysis. In: Sestak Z, Catsky J, Jarvis PG (eds) Plant photosynthetic production — a manual of methods. Junk, The Hague, pp. 343–391.

    Google Scholar 

  • Larcher W (1975) Physiological plant ecology. Springer-Verlag, Berlin. 252pp.

    Google Scholar 

  • Lincoln DE (1980) Leaf resin flavonoids of Diplacus aurantiacus. Biochemical Systematics and Ecology 8: 397–400.

    Article  CAS  Google Scholar 

  • Lincoln DE, Newton TS, Ehrlich PR, Williams KS (1982) Coevolution of the checkerspot butterfly Euphydryas chalcedona and its larval food plant Diplacus aurantiacus: larval response to protein and leaf resin. Oecologia. In press.

    Google Scholar 

  • Lousier JD, Parkinson D (1978) Chemical element dynamics in decomposing leaf litter. Canadian Journal of Botany 56: 2795–2812.

    Article  CAS  Google Scholar 

  • Maclean DA, Wein RW (1978) Weight loss and nutrient changes in decomposing litter and forest floor material in New Brunswick forest stands. Canadian Journal of Botany 56: 2730–2749.

    Article  CAS  Google Scholar 

  • Maggs J, Pearson CJ (1977) Litter fall and litter layer decay in coastal scrub at Syndney, Australia. Oecologia 31: 239–250.

    Article  Google Scholar 

  • Miller PC, Stoner WA (1979) Canopy structure and environmental interactions. In: Solbrig OT, Jain S, Johnson GB, Raven PH (eds) Topics in plant population biology. Columbia University Press, New York, pp 428–460.

    Google Scholar 

  • Mooney HA, Ferrar PJ, Slatyer RO (1978) Photosynthetic capacity and carbon allocation patterns in diverse growth forms of Eucalyptus. Oecologia 36: 103–111.

    Article  Google Scholar 

  • Mooney HA, Harrison AT, Morrow PA (1975) Environmental limitations of photosynthesis on a California evergreen shrub. Oecologia 19: 293–301.

    Google Scholar 

  • Mooney HA, Ehrlich PR, Lincoln D, Williams K (1980) Environmental controls on the seasonality of a drought-deciduous shrub, Diplacus aurantiacus and its predator, the checkerspot butterfly Euphydryas chalcedona. Oecologia 45: 143–146.

    Article  Google Scholar 

  • Moore P (1980) The advantages of being evergreen. Nature 285: 535.

    Google Scholar 

  • Natr L (1972) Influence of mineral nutrients on photosynthesis of higher plants. Photosynthetica 6: 80–99.

    CAS  Google Scholar 

  • Oechel WC, Lawrence W (1981) Carbon allocation and utilization. In: Miller PC (ed) Resource use by chaparral and matorral: a comparison of vegetation function in two mediterranean-type ecosystems. Springer-Verlag, Berlin, pp 185–236.

    Google Scholar 

  • Oechel WC, Lawrence W, Mustafa J, Martinez J (1981) Energy and carbon acquisition. In: Miller PC (ed) Resource use by chaparral and matorral: a comparison of vegetation function in two Mediterrranean type ecosystems. Springer-Verlag, Berlin, pp 151–184.

    Google Scholar 

  • Radin JW, Parker LL (1979a) Water relations of cotton plants under nitrogen deficiency. I. Dependence on leaf structure. Plant Physiology 64: 495–498.

    Article  PubMed  CAS  Google Scholar 

  • Radin JW, Parker LL (1979b) Water relations of cotton plants under nitrogen deficiency. II. Environmental interactions on stomata. Plant Physiology 64: 499–501.

    Article  PubMed  CAS  Google Scholar 

  • Rapp M (1969) Production de litière et apport au sol d’éléments minéraux dans deux écosystèmes Méditerranéens: le fôret de Quercus ilex L. et la garigue de Quercus coccifera L. Oecologia Plantarum 4: 377–410.

    Google Scholar 

  • Schlesinger WH, Chabot BF (1977) The use of water and minerals by evergreen and deciduous shrubs in Okefenokee Swamp. Botanical Gazette 138: 490–497.

    Article  CAS  Google Scholar 

  • Oechel WC, Lawrence W, Mustafa J, Martinez J (1981) Energy and carbon acquisition. In: Miller PC (ed) Resource use by chaparral and matorral: a comparison of vegetation function in two mediterranean-type ecosystems. Springer-Verlag, Berlin, pp 151–184.

    Google Scholar 

  • Schlesinger WH, Hasey MM (1981) Decomposition of chaparral shrub foliage: Losses of organic and inorganic constituents from deciduous and evergreen leaves. Ecology 62: 762–774.

    Article  CAS  Google Scholar 

  • Small E (1972) Photosynthetic rates in relation to nitrogen recycling as an adaptation to nutrient deficiency in peat bog plants. Canadian Journal of Botany 50: 2227–2233.

    Article  CAS  Google Scholar 

  • Takeda T (1961) Studies on the photosynthesis and production of dry matter in the community of rice plants. Japanese Journal of Botany 17: 403–437.

    Google Scholar 

  • Winner WE (1981) The effect of SO2 on photosynthesis and stomatal behaviour of mediterranean-climate shrubs and trees. In: Margaris NS, Mooney HA (eds) Components of productivity of mediterranean-climate regions. Basic and applied aspects. Junk, The Hague.

    Google Scholar 

  • Winner WE, Mooney HA (1980) Ecology of SO2 resistance: I. Effects of fumigations on gas exchange of deciduous and evergreen shrubs. Oecologia 44: 290–295.

    Article  Google Scholar 

  • Yoshida S, Coronel V (1976) Nitrogen nutrition, leaf resistance and leaf photosynthetic rate of the rice plant. Soil Science and Plant Nutrition 22: 207–211.

    CAS  Google Scholar 

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© 1983 Springer-Verlag Berlin · Heidelberg

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Gulmon, S.L. (1983). Carbon and Nitrogen Economy of Diplacus aurantiacus, a Californian Mediterranean-Climate Drought-Deciduous Shrub. In: Kruger, F.J., Mitchell, D.T., Jarvis, J.U.M. (eds) Mediterranean-Type Ecosystems. Ecological Studies, vol 43. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-68935-2_9

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  • DOI: https://doi.org/10.1007/978-3-642-68935-2_9

  • Publisher Name: Springer, Berlin, Heidelberg

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