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  • 1
    Call number: AWI Bio-22-94888
    In: Ecological studies, 29
    Type of Medium: Monograph available for loan
    Pages: XVII, 686 Seiten , Illustrationen
    ISBN: 0-387-90325-9 , 3-540-90325-9
    Series Statement: Ecological studies 29
    Language: English
    Note: Contents Preface List of Contributors Section I. Floristics, Vegetation, and Primary Production Ia. Vascular Plants Ib. Nonvascular Plants 1. Introduction / LARRY L. TIESZEN Background Research Design and Site Selections Overview of the Barrow Ecological System References 2. Vegetation, Floristics, and Phytogeography of Northern Alaska / D. F. MURRAY Tundra Landscapes and Vegetation Floristics and Phytogeography Acknowledgments References 3. Spatial and Temporal Variation of the Vegetation and its Productivity / P. J. WEBBER Introduction and Site Overview Methods Results Discussion Summary and Conclusions Acknowledgments References 4. Seasonal Dynamics of Above- and Belowground Production of Vascular Plants at Barrow, Alaska / J. G. DENNIS , L. L. TIESZEN and M. A. VETTER Introduction Methods and Materials Results Discussion Acknowledgments References 5. Floristics, Phytogeography and Ecology of Arctic Alaskan Bryophytes / W. C. STEERE The Bryophyte Flora and its Floristic Elements Ecology and Physical Factors of the Environment Acknowledgments References 6. Composition and Bryomass of the Moss Layers of Two Wet-Tundra-Meadow Communities near Barrow, Alaska / J. R. RASTORFER Introduction Materials and Methods Results Discussion Acknowledgments References 7. The Role of Lichens in the Structure, Productivity, and Mineral Cycling of the Wet Coastal Alaskan Tundra / M. E. WILLIAMS , E. D. RUDOLPH , E. A. SCHOFIELD , and D. C. PRASHER Introduction Environmental Setting Lichen Occurrence Methods Results and Discussion Conclusions Acknowledgments References 8. The Role of Algae in Tundra Soil / R. E. CAMERON , A. D. KNOX , and F. A. MORELLI Introduction Methods Results and Discussion Conclusions Acknowledgments References 9. Ecto- and Endomycorrhizae of Arctic Plants at Barrow, Alaska / O. K. MILLER, JR. and G. A. LAURSEN Introduction Distribution of Ectomycorrhizae Distribution of Endomycorrhizae Distribution of Mycorrhizal Fungi Carbon, Nitrogen, and Phosphorus Conclusions and Discussion Acknowledgments References Section II. Photosynthesis, Respiration and Water Relations. IIa. Plant and Community Photosynthesis IIb. Photosynthesis and Water Relations 10. Photosynthesis in the Principal Barrow, Alaska Species: A Summary of Field and Laboratory Responses / L. L. TlESZEN Introduction Methods Results and Discussion Conclusions Acknowledgments References 11. Primary Production Processes in Arctic Bryophytes at Barrow, Alaska / W. C. OECHEL and B. SVEINBJÖRNSSON Introduction Field Research Site Methods Results and Discussion Conclusions Acknowledgments References 12. Meteorological Assessment of CO2 Exchange Over an Alaskan Arctic Tundra / P. I. COYNE and J. J. KELLEY Introduction Theory Experimental Procedure Data Analysis Results Contents Discussion Acknowledgments References 13. Constraints on Tundra Productivity: Photosynthetic Capacity in Relation to Solar Radiation Utilization and Water Stress in Arctic and Alpine Tundras / M. M. CALDWELL, D. A. JOHNSON and M. FAREED Introduction Methods Results and Discussion Acknowledgments References 14. Some Aspects of Water Relations of Arctic and Alpine Regions / P. C. MILLER, W. A. STONER, and J. R. EHLERINGER Introduction Conceptual Framework Methods Results Discussion and Conclusions Acknowledgments References 15. Radio-Tracer Measurement of Transpiration in Tundra Vegetation, Barrow, Alaska / J. J. KORANDA , B. CLEGG, and M. STUART Introduction Methods Results and Discussion Conclusions Acknowledgments References 16. Simulation of the Effect of the Tundra Vascular Plant Canopy on the Productivity of Four Moss Species / W. A. STONER, P. C. MILLER, and W. C. OECHEL Introduction Simulation Models and Methods Results and Discussion Acknowledgments References Section III. Growth and the Allocation and Use of Mineral and Organic Nutrients IIIa. Growth and Organic Nutrient Allocation IIIb. Inorganic Nutrient Utilization, Response to Fertilization, and Nitrogen Fixation IIIc. Growth, Nutrient and Population Modeling 17. Translocation and Allocation of 14C-Photoassimilate by Dupontia fisheri / M. L. ALLESSIO and L. L. TIESZEN Introduction Materials and Methods Results Discussion Acknowledgments References 18. Growth, Turnover, and Respiration Rates of Roots and Tillers in Tundra Graminoids / W. D. BILLINGS, K. M. PETERSON, and G. R. SHAVER Introduction Methods Results Conclusions Acknowledgments References 19. The Interactions of Organic Nutrients, Soil Nitrogen, and Soil Temperature and Plant Growth and Survival in the Arctic Environment / B. H. MCCOWN Introduction Materials and Methods Results Discussion and Conclusions Acknowledgments References 20. Plant Nutrient Limitations of Tundra Plant Growth / A. ULRICH and P. L. GERSPER Introduction Methods Results and Discussion Discussion and Conclusions Acknowledgments References 21. Phosphate Uptake and Nutrient Utilization by Barrow Tundra Vegetation / F. S. CHAPIN, III Introduction Methods Results Discussion Acknowledgments References 22. Effects of Nitrogen and Phosphorus Fertilization on Carbohydrate and Nutrient Levels in Dupontia fisheri and Arctagrostis latifolia / J. D. MCKENDRICK, V. J. OTT , and G. A. MITCHELL Introduction Methods Results and Discussion Conclusions Acknowledgments References 23. Nitrogen Fixation in Arctic and Alpine Tundra / V. ALEXANDER, M. BILLINGTON, and D. M. SCHELL Introduction Methods Results and Discussion Conclusions Acknowledgments References 24. A Model of Plant Growth and Phosphorus Allocation for Dupontia fisheri in Coastal, Wet-Meadow Tundra / W. A. STONER, P. C. MILLER, and L. L. TIESZEN Introduction Description of the Model Results Discussion Acknowledgments References 25. A Model of Carbohydrate, Nitrogen, Phosphorus Allocation and Growth in Tundra Production / P. C. MILLER, W. A. STONER, L. L. TIESZEN , M. ALLESSIO, B. MCCOWN , F. S. CHAPIN, and G. SHAVER Introduction Results and Discussion Acknowledgments References 26. A Simulation Model of Population Processes of Arctic Tundra Graminoids / B. A. LAWRENCE , M. C. LEWIS , and P. C. MILLER Introduction The Model Methods of Simulations Validation Simulation Experiments Summary Acknowledgments References 27. Summary / L. L. TIESZEN Introduction Historical and Floristic Relationships Abiotic Relationships Spatial and Temporal Relationships Summary References Appendix: Checklists of Vascular Plants, Bryophytes, and Lichens for the Alaskan U.S. IBP Tundra Biome Study Areas - Barrow, Prudhoe Bay, Eagle Summit / BARBARA M. MURRAY AND DAVID F. MURRAY Introduction Checklists References Index
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  • 2
    Publication Date: 2022-05-26
    Description: From the Foreward: This book is one of a series of volumes reporting results of research by U. S. scientists participating in the International Biological Program (IBP). As one of the 58 nations taking part in the IBP during the period July 1967 to June 1974 , the United States organized a number of large, multidisciplinary studies pertinent to the central IBP theme of "the biological basis of productivity and human welfare."
    Description: Direct financial support of the Biome-wide program was derived from three major sources: the National Science Foundation, the State of Alaska and the petroleum industry through the University of Alaska. The NSF funding was under the joint sponsorship of the U. S. Arctic Research Program (Division of Polar Programs) and the U. S. International Biological Program (Ecosystem Analysis). The Army Research Office and the Department of Energy (previously AEC and ERDA) both contributed funded projects to the Program. Industry support was provided through unrestricted grants from: Atlantic Richfield Company, Alyeska Pipeline Service Company, BP Alaska, Inc. Cities Service Company, Exxon Company, USA (Humble Oil and Refining Company), Gulf Oil Corporation , Marathon Oil Company, Mobil Oil Company, Prudhoe Bay Environmental Subcommittee of the Alaska Oil and Gas Association, Shell Oil Company, Standard Oil Company of California, Standard Oil (Indiana) Foundation Inc., and Sun Oil Company.
    Keywords: Tundra ecology ; Coastal ecology ; Ecology ; Barrow, Alaska
    Repository Name: Woods Hole Open Access Server
    Type: Book
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  • 3
    Electronic Resource
    Electronic Resource
    Cambridge, MA, USA : Blackwell Science Inc
    Restoration ecology 6 (1998), S. 0 
    ISSN: 1526-100X
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: We studied two tallgrass prairies and adjacent restoration areas in northeast Kansas to analyze (1) the invasion of native tallgrass prairie species from native prairie source populations into replanted areas; (2) the establishment of planted prairie species five and 35 years after being sown; and (3) the effects of native prairie species on soil organic matter. For the majority of dominant species, composition differed statistically between sampled areas even though seed rain was available from the native tallgrass prairie remnants. Plant community differences were statistically different between each native prairie area and all respective restoration sites according to the Multiple Response Permutation Procedure. In addition, species richness was greatly reduced in replanted areas compared to adjacent native prairie remnants. Soil carbon isotope ratios indicated that the planting of warm-season grasses resulted in substantial replacement of old soil organic matter by the newly replanted grasses but that it did not create substantial increases of soil organic matter beyond replacement. The lack of accumulation reflects a nutrient-poor system (nitrogen-poor in particular), and the relative absence of native or introduced nitrogen-fixing plant species on the replanted areas may be a significant factor. It appears that restoration of the original highly diverse vegetation component of the tallgrass prairie ecosystem, even when aided by seeding and an adjacent prairie seed source, will occur on carbon- and nitrogen-depleted soils only over very long periods of time (perhaps centuries), if at all.
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  • 4
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 276 (1978), S. 97-98 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] STABLE, rather than radioactive, tracers are being used in metabolic studies, and Lyon and Baxter1 have reported "natural baseline" carbon isotope ratios from human tissue samples. The use of natural isotope ratios is also an area of active research interest because of the ecological and ...
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  • 5
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Physiologia plantarum 39 (1977), S. 0 
    ISSN: 1399-3054
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: Potted vegetable plants of Amaranthus lividus, Gynandropsis gynandra and Crotalaria brevidens were grown outside under normal tropical conditions and rate of photosynthesis and transpiration were determined simultaneously in attached leaves under a range of leaf temperatures and irradiances. Photosynthetic rates were consistently higher in G. gynandra than in A. lividus and C. brevidens. However, in C. brevidens and G. gynandra the leaf resistances were lower and transpiration rates were higher than those in A. lividus.The results on optimum temperature requirements for maximum rates of CO2 fixation, coupled with data on CO2 compensation points and leaf anatomy provided clear evidence that G. gynandra and A. lividus are C4 species, while C. brevidens is a C3 species. The differential effects of light intensity and temperature on stomata and mesophyll resistances in C3 and C4 species are discussed in relation to rates of photosynthesis and transpiration.
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  • 6
    ISSN: 1432-1939
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary Tundra plant growth forms can generally be characterized as consisting predominantly of low-growing perennial grasses and sedges, perennial herbaceous forbs, dwarf deciduous shrubs, and dwarf evergreen shrubs. Gross aboveground carbon allocation, leaf growth, and photosynthesis pattern studies were initiated to develop a quantitative understanding of the functional importance of these particular tundra growth forms. Photosynthetic capacities of 13 species were determined under standardized exposure conditions using a14CO2 field system and ranged between 5 and 47 mg CO2·g dry wt-1·h-1. These results, in conjunction with detailed leaf growth determinations, support the generalization that species with an evergreen growth form have lower photosynthetic capacities than species with a perennial graminoid, forb, or deciduous shrub growth form. However, these low photosynthetic capacities in evergreen shrubs are associated with relatively extended leaf longevities. Conversely, deciduous shrub forms exhibited high photosynthetic capacities, but were offset by relatively short leaf longevity periods. The perennial grasses, sedges, and forbs showed patterns intermediate to these. As a result, it appears that among tundra species of different growth form, photosynthetic capacity is inversely related to leaf longevity.
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  • 7
    ISSN: 1432-1939
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary More than 500 species of the Poaceae are found in Kenya, East Africa. Eighteen of twenty-seven tribes are exclusively (except the Paniceae and Danthonieae) of the C3 photosynthetic type. A floristic analysis of low altitude grasslands suggests that nearly all species at these low altitudes are of the C4 photosynthetic type. At high altitudes, however, nearly all grasses are of the C3 photosynthetic type. Open grassland vegetation was sampled along a transect from arid low altitude sites to the top of Mt. Kenya in an attempt to document the general distributions of the photosynthetic types. The major tribes illustrated three general patterns of distribution. The C4 tribes Chlorideae, Eragrosteae, Sporoboleae, and Aristideae were abundant at low altitudes (or low indices of available soil moisture). The Paniceae and Andropogoneae were also exclusively C4 but were more common at intermediate altitudes. The C3 tribes Aveneae, Festuceae, and Agrostideae were found only at high altitudes. In these open grasslands there were no C3 species below 2,000 m and no C4 species above 3,000 m. The variation in δ13C of the live grass vegetation with altitude confirms these distributional patterns and suggests a sharp transition zone between these two photosynthetic types. The photosynthetic type accounts for broad distributions within the Poaceae but these distributions are further modified by characteristics which may be inherent in the tribal groups. Ecological and paleoecological significance of these patterns of distribution are discussed.
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  • 8
    ISSN: 1432-1939
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary The quantitative plant species composition of the rumen contents of a large number of individuals from eight East African herbivores was determined by direct visual analysis. All plant species were classified as either C3 or C4, and an estimated δ13C for the rumen sample was calculated. This estimated value was compared to a measured value determined directly from rumen subsample. The two methods of determining quantitative C3 and C4 composition differed by less than 1%, and the isotopic analysis has the advantage of being rapid and totally objective. The isotopic analysis allowed us to differentiate between grazers and browsers and to determine the quantitative dependence of each animal on C3 and C4 photosynthetic types. Kongoni, wildebeest, cattle, and sheep were nearly pure grazers on the Athi Kapiti Plains; and the Grant's gazelle were predominantly browsers. Thompson's gazelle, goast and impala were intermediate. The species most dependent upon browse showed a marked and rapid shift to grass within a few days following rain. This isotopic method may have general utility in the study of East African ecology.
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Oecologia 68 (1986), S. 279-284 
    ISSN: 1432-1939
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary The impact of the xylem-tapping mistletoe Phoradendron juniperinum on the nitrogen and water relations of its host Juniperus osteosperma was investigated under natural field conditions. Leaf conductance, leaf water potential, and leaf Kjeldahl nitrogen contents were followed through the growing season on mistletoes, infected junipers (separating infected from uninfected stems) and uninfected junipers. Infected trees experienced lower leaf water potentials than uninfected trees and also had lower leaf conductances and lower leaf nitrogen contents. Infected juniper stems had higher conductances than uninfected stems. Mistletoes had higher leaf nitrogen contents than their hosts and much of this nitrogen appeared as arginine, a potential nitrogen storage compound. Photosynthetic rates (per unit leaf area) were significantly higher in junipers than in the mistletoe, and higher in the uninfected than infected junipers. Water use efficiencies as estimated by carbon isotope ratios were significantly lower in mistletoes than in their hosts. Increased mistletoe infestation appeared to increase absolute water use efficiency of both host and mistletoe.
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  • 10
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 219 (1968), S. 1066-1067 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] This is a preliminary report of a project designed to elucidate the mechanisms of photosynthetic adaptations. We examined the temperature responses of the Hill reaction in two populations (one arctic and one alpine) of Deschampsia caespitosa (L.) Beauv. We present evidence for genetic ...
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