GLORIA

GEOMAR Library Ocean Research Information Access

feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
  • 1
    Online Resource
    Online Resource
    Cham :Springer International Publishing AG,
    Keywords: Endangered ecosystems. ; Electronic books.
    Type of Medium: Online Resource
    Pages: 1 online resource (292 pages)
    Edition: 1st ed.
    ISBN: 9783319392370
    Series Statement: Fascinating Life Sciences Series
    DDC: 571.2
    Language: English
    Note: Intro -- Preface -- Acknowledgments -- A Comment on Plant Names -- List of Abbreviations -- Contents -- 1: Introduction -- 1.1 What Is an Epiphyte? -- 1.2 Other Forms of Structurally Dependent Plants -- 1.3 Other Classification Schemes -- Box 1.1 Different classification schemes for epiphytes (after Benzing 1990, modified) -- 1.4 Epiphytes: A Life Form? -- 1.5 Why Conquer Trees? -- References -- 2: Epiphyte Taxonomy and Evolutionary Trends -- 2.1 Taxonomic Participation -- 2.1.1 Plant Families with a Substantial Number of Vascular Epiphytes -- Box 2.1 Epiphytes and Lithophytes -- 2.1.2 Future Changes in the Proportion of Epiphytic Taxa -- Box 2.2 Canopy Access -- 2.2 The Conquest of Tree Canopies: ``Up´´ and Sometimes ``Down´´ -- 2.3 How Biased Is Our Current View on Epiphytes? -- References -- 3: Biogeography: Latitudinal and Elevational Trends -- 3.1 Latitudinal Trends -- Box 3.1 Comparing Species Richness Patterns of Epiphytic and Terrestrial Ferns Along Elevational and Latitudinal Gradients (Di... -- 3.2 Elevational Trends -- 3.3 Diversity Patterns Within the Tropics -- References -- 4: Functional Anatomy and Morphology -- 4.1 Plant Size -- Box 4.1 Life form and Plant Size (Gerhard Zotz, Niklas Buhk, and Christoph Hahn) -- 4.2 Shoot Architecture -- 4.3 Gametophytes of Epiphytic Ferns -- 4.4 Leaves -- 4.5 A Special Case: Heteroblasty -- 4.6 Roots -- 4.7 Seed Size and Seed Morphology -- References -- 5: Physiological Ecology -- Box 5.1 Size-Related Changes in Foliar delta13C Values of Vascular Epiphytes (Gerold Schmidt and Gerhard Zotz) -- 5.1 The Physical Setting -- 5.2 Plant Water Relations -- 5.3 Temperature and Plant Function -- 5.4 Mineral Nutrition -- 5.4.1 Nutrients in the Forest Canopy -- 5.4.2 Nutrient Uptake -- 5.4.3 Nutrient Concentrations in Tissue of Vascular Epiphytes. , Box 5.2 Luxury Consumption in Epiphytic Bromeliads (Uwe Winkler and Gerhard Zotz) -- 5.4.4 Reproductive Investment -- 5.4.5 Associations with Fungi and Cyanobacteria -- 5.4.6 Special Nutritional Modes Related to Animals -- 5.4.7 Intraspecific Variation in Hemiepiphytes and Facultative Epiphytes -- 5.5 Photosynthesis, Carbon Gain, and Growth -- Box 5.3 CAM Biomass in Epiphytes and Terrestrial Plants -- 5.5.1 Foliar Carbon Gain -- 5.5.2 Carbon Gain by Non-foliar Organs -- 5.5.3 Whole Plant Carbon Budgets -- 5.5.4 Light Flecks and Carbon Gain -- 5.5.5 Photoinhibition -- 5.5.6 Growth -- Box 5.4 Growth Analysis in Vriesea sanguinolenta (Stefan Wester, Cord Mikona, and Gerhard Zotz) -- 5.5.7 Atmospheric CO2, Net CO2 Uptake, and Growth -- References -- 6: Population Biology -- 6.1 Diaspores -- 6.2 Germination and Establishment -- Box 6.1 Light Quality and Germination in Epiphytic Bromeliads (Eva-Maria Voßmann, Stefan Wester, and Gerhard Zotz) -- 6.3 Growth and Survival -- 6.4 Reproduction -- 6.5 Survival on the Ground -- 6.6 Comparative Plant Demography -- Box 6.2 Population Matrix Analysis of an Epiphytic Orchid -- 6.7 Metapopulations -- References -- 7: Epiphyte Communities -- Box 7.1. Sampling Epiphyte Communities -- 7.1 The Host Tree -- 7.1.1 Host Tree Identity -- 7.1.2 Host Tree Size -- 7.1.3 Host Tree Phenology -- 7.2 Community Composition and Structure -- Box 7.2. The San Lorenzo Crane Plot -- 7.2.1 Vertical Structure -- 7.2.2 Horizontal Structure -- 7.3 Community Dynamics -- 7.3.1 Succession -- 7.3.2 Disturbance -- References -- 8: Interactions with Other Organisms -- 8.1 Interactions with the Host Tree -- 8.2 Interactions Among Epiphytes and With Other Structurally Dependent Plants -- 8.3 Interactions with Animals -- 8.3.1 Herbivory -- 8.3.2 Pollination -- 8.3.3 Dispersal -- 8.3.4 Diffuse Interactions. , Box 8.1. Epiphytes and Spider Assemblages (Sabine Armsen and Gerhard Zotz) -- 8.3.5 Ant Gardens and Ant-House Plants -- 8.3.6 Phytotelmata and Biotic Diversity in the Forest Canopy -- 8.4 Interactions with Fungi -- References -- 9: The Role of Vascular Epiphytes in the Ecosystem -- 9.1 Carbon Stores and Carbon fluxes -- 9.2 Forest Hydrology -- 9.3 Nutrient Stores and Fluxes -- References -- 10: Epiphytes and Humans -- 10.1 Land-Use Change -- 10.2 Human Health Issues -- 10.3 Epiphytes as Ornamentals and Non-Timber Forest Products -- 10.4 Invasiveness -- 10.5 Epiphyte Conservation in Times of Global Change -- References -- 11: Epilogue: The Epiphyte Syndrome -- References -- Glossary -- Index.
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 2
    Publication Date: 2023-06-20
    Description: Plant litter decomposition is a key ecological process that is mostly studied at the forest floor. However, decomposition generally starts in the canopy. In this study, we evaluated the effect of litter composition and climate on the initial phase of decomposition in the soil and two contrasting types of canopy microsites along an elevational gradient (0–2200 m a.s.l.). To this end, we incubated standard material composed by green (fast decomposing) and rooibos (slow decomposing) tea bags for three months. Tea bags were placed in soil (buried at 5 cm) and in the canopy at ca. 5 m above the ground in “micro-wetlands” (tank bromeliads) and dry crown microsites (branches). Along the elevational gradient, green tea decomposed faster than rooibos tea in all microsites and forests. Mass loss for both tea types was lowest on branches at all sites, except for green tea in a wet forest where decomposition did not significantly differ among microsites. In wet forests, decomposition did not differ between bromeliads and soil, while in a dry forest, decomposition was faster in bromeliads. We found that the effects of climatic variables [monthly average temperature (TEMP) and total precipitation (PREC) for the incubation months] on decomposition differed between microsites. Along the elevational gradient, the mass loss in soil was positively correlated with TEMP but not with PREC, whereas on branches, mass loss was negatively correlated with TEMP and positively correlated with PREC. Unlike on branches, mass loss in bromeliads slightly decreased with PREC and increased with TEMP. Our study shows that microsite conditions interact with climate (TEMP and PREC) leading to differences in the general decomposition patterns in the forest canopy.
    Description: CONACYT
    Description: Deutscher Akademischer Austauschdienst http://dx.doi.org/10.13039/501100001655
    Description: Heinz Neumüller Stiftung
    Description: Carl von Ossietzky Universität Oldenburg (3092)
    Keywords: ddc:631.4 ; Arboreal soil ; Elevational gradient ; Tea bag index ; Epiphytes ; Bromeliads
    Language: English
    Type: doc-type:article
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 3
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Science Ltd
    Plant, cell & environment 24 (2001), S. 0 
    ISSN: 1365-3040
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: This field study with the C3 bromeliad Vriesea sanguinolenta (Cogn. & Marchal 1874) was initiated to explore the importance of size-related ecophysiological changes in vascular epiphytes in a natural tropical setting. In this species, a step change from atmospheric to tank-forming life form occurs during early ontogeny, followed by a continuous size increase of individuals with water-impounding tanks. Although our study focused on the water-impounding phase, this growth pattern also allowed us to compare ecophysiological consequences of a step change in life form with those associated with size increments among plants of identical life form. The shift in life form was accompanied by relatively minor changes, for example in leaf morphology (decrease in leaf thickness and trichome density) and leaf physiology (decrease in photosynthetic capacity), while there were more substantial changes during the tank-forming phase. A major trend was a decreasing dependence of larger plants on internally stored water due to a more efficient tank. We suggest that the resulting, more reliable water supply in larger plants may be the proximate cause for the observed size-related differences in leaf anatomy (relative reduction of water storage tissue, and relative and absolute increase in chlorenchyma thickness), leaf morphology (increase in stomatal density, decrease in trichome density), and leaf physiology (increase in net rates of CO2 uptake, more conservative stomatal behaviour, higher residual transpiration). The results are compared with previous studies on heteroblasty in bromeliads, but are also discussed in the context of a gradual shift from a drought-tolerance to a drought-avoidance strategy.
    Type of Medium: Electronic Resource
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Naturwissenschaften 86 (1999), S. 39-40 
    ISSN: 1432-1904
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology , Natural Sciences in General
    Type of Medium: Electronic Resource
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Oecologia 107 (1996), S. 151-159 
    ISSN: 1432-1939
    Keywords: Epiphytes ; Orchids ; Water balance ; Crassulacean acid metabolism ; Photoinhibition
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The epiphytic orchid, Dimerandra emarginata, occurs in habitats characterized by high light intensities and very variable water supply. Long-term observations of the water status indicate that this species experienced at least moderate water stress over most of the year. Well-watered, it showed high rates of net CO2 uptake (A, 7 μmol m−2 s−1), high transpiration rates (E, 1.4 mmol m−2 s−1), and little nocturnal acidification. Drought induced crassulacean acid metabolism activity and resulted in a strong decline of both A and E. The same conditions also led to chronic photoinhibition as indicated by a predawn ratio of variable to maximum fluorescence (Fv/Fm) of 0.6 after 9 days of drought. Diurnal changes in fluorescence characteristics were much more pronounced. Midday ratios of dark adapted Fv/Fm were as low as 0.35, but recovered in the afternoon and were probably mostly due to non-photochemical quenching of photosynthesis. Measured water losses of leaves and stems were compared to plant water content (PWC). In large plants, about 32% of PWC was transpired on a single day under well-watered conditions. Model calculations indicate that transpiration per unit leaf area should be strongly dependent upon plant size in this species. Comparisons of calculated daily water loss, PWC and the length of drought periods suggest that D. emarginata can only survive a dry season by drawing on the water reserves of older stems and by an efficient uptake of the occasional rain.
    Type of Medium: Electronic Resource
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 6
    ISSN: 1432-1939
    Keywords: Chlorophyll fluorescence ; Clusia ; Crassulacean acid metabolism ; Phosphoenolpyruvate carboxylase
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary In well-watered plants of Clusia uvitana, a species capable of carbon fixation by crassulacean acid metabolism (CAM), recently expanded leaves gained 5 to 13-fold more carbon during 12 h light than during 12 h dark periods. When water was withheld from the plants, daytime net CO2 uptake strongly decreased over a period of several days, whereas there was a marked increase in nocturnal carbon gain. Photosynthetic rates in the chloroplasts were hardly affected by the water stress treatment, as demonstrated by measurements of chlorophyll a fluorescence of intact leaves, indicating efficient decarboxylation of organic acids and refixation of carbon in the light. Within a few days after rewatering, plants reverted to the original gas exchange pattern with net CO2 uptake predominantly occurring during daytime. The reversible increase in dark CO2 fixation was paralleled by a reversible increase in the content of phosphoenolpyruvate (PEP) carboxylase protein. In wellwatered plants, short-term changes in the degree of dark CO2 fixation were induced by alterations in CO2 partial pressure during light periods: a decrease from 350 to 170 μbar CO2 caused nocturnal carbon gain, measured in normal air (350 μbar), to increase, whereas an increase to 700 μbar CO2, during the day, caused net dark CO2 fixation to cease. The increased CAM activity in response to water shortage may, at least to some extent, be directly related to the reduced carbon gain during daytime.
    Type of Medium: Electronic Resource
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 7
    ISSN: 1432-2048
    Keywords: Carbon dioxide assimilation ; Photosynthesis (canopy) ; Tropical rain forest
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Diel (24 h) courses of net CO2 exchange of leaves were determined in eight species of tropical rainforest plants on Barro Colorado Island, Panama, during 1990 and 1991. The species included three canopy trees, one liana, two epiphytes and one hemiepiphyte. One of the species studied was growing in a rain-forest gap. Daily carbon gain varied considerably across species, leaf age, and season. The analysis of data for all plants from 64 complete day/night cycles revealed a linear relationship between the diurnal carbon gain and the maximum rate of net CO2 uptake, Amax. Nocturnal net carbon loss was about 10% of diurnal carbon gain and was positively related to Amax. We conclude that short-term measurements of light-saturated photosynthesis, performed at periodic intervals throughout the season, allow the annual leaf carbon balance in these rain-forest plants to be predicted.
    Type of Medium: Electronic Resource
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 8
    Publication Date: 2021-10-14
    Repository Name: EPIC Alfred Wegener Institut
    Type: Article , isiRev
    Format: application/pdf
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 9
    Publication Date: 2023-06-21
    Description: The number of available sites for establishment is a key determinant of species richness on habitat islands. While most theoretical studies assume habitat size or capacity to be constant, many natural habitats are characterized by dynamic growth in capacity over ecological timescales. A case in point is provided by trees that serve as habitat for vascular and non-vascular epiphytes. Here, we develop a modeling framework, based on neutral theory, to address the effects of habitat growth on community development, i.e., species richness and abundance. The model is parameterized to the situation of vascular epiphyte communities in tropical lowland forests and includes stochastic reproduction, death, and immigration events from a larger metacommunity. Using numerical simulations, we explore the proportion of growing sites occupied by individuals, the number of empty unoccupied sites, as well as changes in species abundances, species richness, colonization and extinction rates, and the dependence on the abundance in the metacommunity throughout the growth of the habitat. Our analysis suggests two characteristic phases of community development in a growing habitat: (i) an initial phase, characterized by a rapid buildup of empty sites, a slow increase in species abundance, and a fast increase in species richness, and (ii) a second phase, in which the number of empty sites reaches an equilibrium, species richness is accumulating very slowly, while the number of individuals increases unabatedly with habitat capacity.
    Repository Name: EPIC Alfred Wegener Institut
    Type: Article , isiRev
    Format: application/pdf
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...