ALBERT

All Library Books, journals and Electronic Records Telegrafenberg

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
    Publication Date: 2015-05-09
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Bongers, F -- Chazdon, R -- Poorter, L -- Pena-Claros, M -- New York, N.Y. -- Science. 2015 May 8;348(6235):642-3. doi: 10.1126/science.348.6235.642-c.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Forest Ecology and Management Group, Wageningen University. 6700AH, Wageningen, Netherlands. Frans.Bongers@wur.nl. ; Department of Ecology and Evolutionary Biology, University of Connecticut, Storrs, CT 06269-3043, USA. ; Forest Ecology and Management Group, Wageningen University. 6700AH, Wageningen, Netherlands.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/25953999" target="_blank"〉PubMed〈/a〉
    Keywords: Agriculture/*trends ; Animals ; Brazil ; Carbon Cycle ; Cattle ; *Forests ; Humans
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 2
    Publication Date: 2016-02-04
    Description: Land-use change occurs nowhere more rapidly than in the tropics, where the imbalance between deforestation and forest regrowth has large consequences for the global carbon cycle. However, considerable uncertainty remains about the rate of biomass recovery in secondary forests, and how these rates are influenced by climate, landscape, and prior land use. Here we analyse aboveground biomass recovery during secondary succession in 45 forest sites and about 1,500 forest plots covering the major environmental gradients in the Neotropics. The studied secondary forests are highly productive and resilient. Aboveground biomass recovery after 20 years was on average 122 megagrams per hectare (Mg ha(-1)), corresponding to a net carbon uptake of 3.05 Mg C ha(-1) yr(-1), 11 times the uptake rate of old-growth forests. Aboveground biomass stocks took a median time of 66 years to recover to 90% of old-growth values. Aboveground biomass recovery after 20 years varied 11.3-fold (from 20 to 225 Mg ha(-1)) across sites, and this recovery increased with water availability (higher local rainfall and lower climatic water deficit). We present a biomass recovery map of Latin America, which illustrates geographical and climatic variation in carbon sequestration potential during forest regrowth. The map will support policies to minimize forest loss in areas where biomass resilience is naturally low (such as seasonally dry forest regions) and promote forest regeneration and restoration in humid tropical lowland areas with high biomass resilience.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Poorter, Lourens -- Bongers, Frans -- Aide, T Mitchell -- Almeyda Zambrano, Angelica M -- Balvanera, Patricia -- Becknell, Justin M -- Boukili, Vanessa -- Brancalion, Pedro H S -- Broadbent, Eben N -- Chazdon, Robin L -- Craven, Dylan -- de Almeida-Cortez, Jarcilene S -- Cabral, George A L -- de Jong, Ben H J -- Denslow, Julie S -- Dent, Daisy H -- DeWalt, Saara J -- Dupuy, Juan M -- Duran, Sandra M -- Espirito-Santo, Mario M -- Fandino, Maria C -- Cesar, Ricardo G -- Hall, Jefferson S -- Hernandez-Stefanoni, Jose Luis -- Jakovac, Catarina C -- Junqueira, Andre B -- Kennard, Deborah -- Letcher, Susan G -- Licona, Juan-Carlos -- Lohbeck, Madelon -- Marin-Spiotta, Erika -- Martinez-Ramos, Miguel -- Massoca, Paulo -- Meave, Jorge A -- Mesquita, Rita -- Mora, Francisco -- Munoz, Rodrigo -- Muscarella, Robert -- Nunes, Yule R F -- Ochoa-Gaona, Susana -- de Oliveira, Alexandre A -- Orihuela-Belmonte, Edith -- Pena-Claros, Marielos -- Perez-Garcia, Eduardo A -- Piotto, Daniel -- Powers, Jennifer S -- Rodriguez-Velazquez, Jorge -- Romero-Perez, I Eunice -- Ruiz, Jorge -- Saldarriaga, Juan G -- Sanchez-Azofeifa, Arturo -- Schwartz, Naomi B -- Steininger, Marc K -- Swenson, Nathan G -- Toledo, Marisol -- Uriarte, Maria -- van Breugel, Michiel -- van der Wal, Hans -- Veloso, Maria D M -- Vester, Hans F M -- Vicentini, Alberto -- Vieira, Ima C G -- Bentos, Tony Vizcarra -- Williamson, G Bruce -- Rozendaal, Danae M A -- England -- Nature. 2016 Feb 11;530(7589):211-4. doi: 10.1038/nature16512. Epub 2016 Feb 3.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Forest Ecology and Forest Management Group, Wageningen University, PO Box 47, 6700 AA Wageningen, The Netherlands. ; PO Box 23360, Department of Biology, University of Puerto Rico, San Juan, PR 00931-3360, Puerto Rico. ; Spatial Ecology and Conservation Lab, Department of Geography, University of Alabama, Tuscaloosa, Alabama 35487, USA. ; Instituto de Investigaciones en Ecosistemas y Sustentabilidad, Universidad Nacional Autonoma de Mexico, CP58190, Morelia, Michoacan, Mexico. ; Department of Ecology and Evolutionary Biology, Brown University, Providence, Rhode Island 02912, USA. ; Department of Ecology and Evolutionary Biology, University of Connecticut, Storrs, Connecticut 06269, USA. ; Department of Forest Sciences, Luiz de Queiroz College of Agriculture, University of Sao Paulo, Avenida Padua Dias 11, 13418-900, Piracicaba, Sao Paulo, Brazil. ; SI ForestGEO, Smithsonian Tropical Research Institute, Roosevelt Avenue, Tupper Building - 401, Balboa, Ancon, Panama, Panama ; German Centre for Integrative Biodiversity Research (iDiv) Halle-Jena-Leipzig, Deutscher Platz 5e, 04103 Leipzig, Germany. ; Institute for Biology, Leipzig University, Johannisallee 21, 04103 Leipzig, Germany. ; Departamento de Botanica, Universidade Federal de Pernambuco, Pernambuco, CEP 50670-901, Brazil. ; Department of Sustainability Science, El Colegio de la Frontera Sur, Unidad Campeche, Av. Rancho Poligono 2A, Parque Industrial Lerma, Campeche, Campeche, CP 24500, Mexico. ; Department of Ecology and Evolutionary Biology, Tulane University, New Orleans, Louisiana 70130, USA. ; Smithsonian Tropical Research Institute, Roosevelt Avenue, Tupper Building - 401, Balboa, Ancon, Panama, Panama ; Biological and Environmental Sciences, University of Stirling, Stirling FK9 4LA, UK. ; Department of Biological Sciences, Clemson University, 132 Long Hall, Clemson, South Carolina 29634, USA. ; Centro de Investigacion Cientifica de Yucatan, AC, Unidad de Recursos Naturales, Calle 43 No. 130, Colonia Chuburna de Hidalgo, CP 97200, Merida, Yucatan, Mexico. ; Earth and Atmospheric Sciences Department, University of Alberta, Edmonton, Alberta T6G 2E3, Canada. ; Departamento de Biologia Geral, Universidade Estadual de Montes Claros, Montes Claros, Minas Gerais, CEP 39401-089, Brazil. ; Fondo Patrimonio Natural para la Biodiversidad y Areas Protegidas, Calle 72 No. 12-65 piso 6, Bogota, Colombia. ; Biological Dynamics of Forest Fragments Project, Environmental Dynamics Research Coordination, Instituto Nacional de Pesquisas da Amazonia, Manaus, Amazonas, CEP 69067-375, Brazil. ; Centre for Crop Systems Analysis, Wageningen University, PO Box 430, 6700 AK Wageningen, The Netherlands. ; Knowledge, Technology and Innovation Group, Wageningen University, PO Box 8130, 6700 EW Wageningen, The Netherlands. ; Coordenacao de Tecnologia e Inovacao, Instituto Nacional de Pesquisas da Amazonia, Avenida Andre Araujo, 2936 - Aleixo, 69060-001 Manaus, Brazil. ; Department of Physical and Environmental Sciences, Colorado Mesa University, 1100 North Avenue, Grand Junction, Colorado 81501, USA. ; Department of Environmental Studies, Purchase College (State University of New York), Purchase, New York 10577, USA. ; Instituto Boliviano de Investigacion Forestal (IBIF), FCA-UAGRM, Casilla 6204, Santa Cruz de la Sierra, Bolivia. ; World Agroforestry Centre (ICRAF), PO Box 30677 - 00100, Nairobi, Kenya. ; Department of Geography, University of Wisconsin-Madison, 550 North Park Street, Madison, Wisconsin 53706, USA. ; Departamento de Ecologia y Recursos Naturales, Facultad de Ciencias, Universidad Nacional Autonoma de Mexico, Mexico 04510 DF, Mexico. ; Department of Ecology, Evolution and Environmental Biology, Columbia University, New York, New York 10027, USA. ; Section of Ecoinformatics and Biodiversity, Department of Bioscience, Aarhus University, Aarhus 8000, Denmark. ; Departamento de Ecologia, Instituto de Biociencias, Universidade de Sao Paulo, Rua do Matao, travessa 14, No. 321, Sao Paulo, CEP 05508-090, Brazil. ; Universidade Federal do Sul da Bahia, Centro de Formacao em Ciencias Agroflorestais, Itabuna-BA, 45613-204, Brazil. ; Department of Ecology, Evolution, &Behavior, University of Minnesota, Saint Paul, Minnesota 55108, USA. ; Department of Plant Biology, University of Minnesota, Saint Paul, Minnesota 55108, USA. ; School of Social Sciences, Geography Area, Universidad Pedagogica y Tecnologica de Colombia (UPTC), Tunja, Colombia. ; Department of Geography, 4841 Ellison Hall, University of California, Santa Barbara, California 93106, USA. ; Department of Biology, University of Maryland, College Park, Maryland 20742, USA. ; Yale-NUS College, 12 College Avenue West, Singapore 138610. ; Department of Biological Sciences, National University of Singapore, 14 Science Drive 4, Singapore 11754. ; Departamento de Agricultura, Sociedad y Ambiente, El Colegio de la Frontera Sur - Unidad Villahermosa, 86280 Centro, Tabasco, Mexico. ; Institute for Biodiversity and Ecosystem Dynamics (IBED), University of Amsterdam, PO Box 94248, 1090 GE Amsterdam, The Netherlands. ; Bonhoeffer College, Bruggertstraat 60, 7545 AX Enschede, The Netherlands. ; Museu Paraense Emilio Goeldi, CP 399, CEP 66040-170, Belem, Brazil. ; Department of Biological Sciences, Louisiana State University, Baton Rouge, Louisiana 70803-1705, USA. ; Department of Biology, University of Regina, 3737 Wascana Parkway, Regina, Saskatchewan S4S 0A2, Canada.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/26840632" target="_blank"〉PubMed〈/a〉
    Keywords: *Biomass ; Carbon/metabolism ; Carbon Cycle ; Carbon Sequestration ; Ecology ; *Forests ; Humidity ; Latin America ; Rain ; Time Factors ; Trees/*growth & development/metabolism ; *Tropical Climate
    Print ISSN: 0028-0836
    Electronic ISSN: 1476-4687
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Oecologia 75 (1988), S. 625-632 
    ISSN: 1432-1939
    Keywords: Biomass allocation ; Canopy gaps ; Seedling growth ; Shade tolerance ; Tropical rain forest
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary Growth and morphology of seedlings of ten tropical rain forest species were studied at Los Tuxtlas, Mexico. Seedlings were grown in three environmental conditions: the shaded forest understorey (FU, receiving 0.9–2.3% of the daily photosynthetic photon flux, PF, above the canopy), a small canopy gap of approx. 50 m2 (SG, receiving 2.1–6.1% of daily PF), and a large canopy gap of approx. 500 m2 (LG, receiving 38.6–53.4% of daily PF). The growth of all species was enhanced in gaps, and in LG the effect was stronger than in SG. Plants grown in LG had a sunplant morphology, with a high root-shoot ratio (R/S), a high specific leaf weight (SLW) and a low leaf area ratio (LAR). Plants grown in SG or FU showed a shade-plant morphology, with a low R/S, a low SLW and a high LAR. Growth responses varied from species unable to grow in the shade but with strong growth in the sun, to species with relatively high growth rates in both shade and sun conditions. Shade tolerant species were able to grow in the shade because of a relatively high unit leaf rate. The pioneerCecropia had a high growth rate in LG because of a high LAR. Most species showed a complex growth response in which they resembled the shade intolerant extreme in some aspects of the response, and the shade tolerant extreme in other aspects.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Oecologia 82 (1990), S. 122-127 
    ISSN: 1432-1939
    Keywords: Canopy gaps ; Leaf dynamics ; Seedling growth ; Shade tolerance ; Tropical rain forest
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary Leaf dynamics of eight tropical rain forest species seedlings was studied in three environments: the shaded forest understorey, a small gap of ±50 m2, and a large gap of ±500 m2. Leaf production rate and leaf loss rate were enhanced in gaps, and a large gap resulted in larger increases than a small gap. For most species net leaf gain rate was larger in gaps, although this rate was not always largest in the large gap. Leaf loss decreased, and leaf survival percentages increased with increasing shade tolerance of species, indicating a slower leaf turnover for more shade tolerant species. Leaf area growth rate was only partly determined by net leaf gain rate. Ontogenetic effects on leaf size were also important, especially in the large gap. Species which possessed leaves with high specific leaf weight (SLW) showed lower leaf loss rates and higher leaf survival percentages than species with low SLW leaves. Leaf life span seemed to be related to leafcost per unit area. The relation of specific patterns in leaf production and leaf loss to the regeneration mode of the species is briefly discussed.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Plant ecology 126 (1996), S. 167-179 
    ISSN: 1573-5052
    Keywords: Canopy gaps ; Canopy openness ; French Guiana ; Gap closure ; Gap formation ; Hemispherical photographs ; Rain forest ; Shallow soils ; Spatial patterns
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Formation and closure of canopy gaps was monitored for three years in 12 ha of primary rain forest at Nouragues, French Guiana. At the first inventory, in April 1991, 74 openings in the canopy 〉 4 m2 (sensu Brokaw 1982a) were located; 60 of these gaps were formed before January 1990. Between January 1990 and December 1993, 5 to 15 gaps were annually formed, opening 0.64–1.33% of the forest canopy each year. Of all gaps, 41% were created by a falling, snapped tree, 34% by a falling, uprooted tree, 22% by a falling branch, and 3% by a falling dead stem. A refined nearest neighbour analysis showed that gaps formed after January 1990 were clustered: uprooting of trees seemed to be related to shallow soils, and relatively many other trees fell when a tree uprooted, independent of the dbh of the uprooted tree. In 37 gaps, canopy openness in the gap centre (determined by hemispherical photographs) was monitored over three years. In 54% of the gaps, canopy openness increased in two successive years. It is reasoned that edges of especially large gaps may frequently be re-disturbed by falling trees or branches. Results suggest that gaps have closed after around 15 years. More data are needed to verify this.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 6
    ISSN: 1573-5052
    Keywords: Bana ; Leaves ; Phytomass ; Root/shoot ratio ; Spodosol ; Structure ; Tropical forest ; Wetland
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Bana, or Low Amazon Caatinga is an evergreen sclerophyllous woodland. It occurs on bleached quartz sands in the lowlands of SW Venezuela, where it occupies relatively small ‘islands’ amidst Tall Amazon Caatinga which is exclusively developed on tropaquods. There is an outer vegetation belt about 20 m in width in which trees over 10 m in height occur (Tall Bana); its structure and floristic composition resemble Tall Amazon Caatinga. Low Bana (maximum tree height usually below 5 m) follows next. The central part is occupied by Open Bana in which even lower trees are very widely spaced. Destructive phytomass sampling was carried out for chemical analyses in seven plots along a 150 m line across the zonation. The total dry matter of living plants including roots of Tall Bana (30–32 kg/m2) compares rather well with 41 kg/m2 in Tall Amazon Caatinga. This is only 9–14 kg/m2 in Low Bana, and 4–6 kg/m2 in Open Bana. The average root % of total phytomass increases from 41% in Tall Bana to 63% in Low Bana, and is 88% in Open Bana. Average total dry dead above-ground phytomass (including standing trees and stumps) declines from 1 kg/m2 in Tall Bana to 0.2 kg/m2 in Open Bana. An accumulation of dead matter in Low and Open Bana, relative to the above-ground phytomass of living plants, is noted and this contrasts with the general absence of raw humus in the soil. Eighty-two species of woody plants (dbh≥1 cm) were recorded on the total plot area (640 m2); 90% of the species are also known to occur in Tall Amazon Caatinga. The species number declines from 59 in Tall Bana to 18 in Open Bana. Mesophylls sensu strictu dominate in Tall Bana, while notophylls are dominant in Low and Open Bana. Herbaceous species are less numerous: most of them belong to the Araceae, Bromeliaceae, Orchidaceae, Droseraceae, Eriocaulaceae and Xyridaceae.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 7
    ISSN: 1573-5052
    Keywords: Diversity ; Floristics ; Physiognomy ; Scale problem ; Stratification ; Vertical vegetation structure
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The vertical structure of one hectare of tropical rain forest was studied at Los Tuxtlas, State of Veracruz, Mexico. The structure was analysed at various scales of analysis, using different methodologies e.g. profile diagrams (0.1 ha) and vertical structure diagrams (1 ha). All profile diagrams suggested presence of stratification to some extent. However, simultaneous evaluation of several adjacent profile diagrams showed that the use of one profile diagram only can be very misleading: gaps or layers apparent in a diagram did usually not reflect gaps or layers that could be recognized in the field. Structure diagrams of abundance, basal area and crown cover showed that this forest community is not stratified, with the exception of an understorey layer below 7.5 m dominated by palms. The vertical structure was described using arbitrarily chosen height intervals. From the forest floor to the canopy top basal area, percentage of deciduous species (and individuals), and percentage of compound-leaved species (and individuals), increased, but total number of individuals and number of species decreased. Leaf sizes tended to decrease in the same direction, and crown cover was approximately evenly distributed. Species from different families dominated different parts along the vertical plane. It is concluded that the vertical structure of tropical rain forest can best be described as a complex gradient, involving many community features. Stratification can best be emphasized as a special case of such a gradient.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 8
    ISSN: 1573-5052
    Keywords: Allometry ; Diversity ; Dynamics ; Physiognomy ; Population structure ; Tropical rain forest ; Vegetation structure
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Physiognomy, structure and floristic composition of one hectare of lowland tropical rain forest was studied in detail at Los Tuxtlas, Mexico. Physiognomically, the Los Tuxtlas forest should be classified as ‘lowland tropical high evergreen rain forest’. The forest showed a closed canopy at 30–35 m. Of all woody, non-climbing species with a DBH≥1.0 cm 89.4% (94.5% of all individuals) were evergreen, 25.4% (59.5% of the individuals) had compound leaves, and over 80% of species (and individuals) had leaves in the notophyll and mesophyll size classes. The forest structure was characterized by a low density (2976 individuals with a DBH≥1.0 cm, 346 individuals with a DBH≥10.0 cm, per ha, excluding vines) with an average basal area (38.1 m2, DBH≥1.0 cm, 34.9 m2, DBH≥10.0 cm, per ha, excluding vines). This was attributed to the relative maturity of the forest on the study plot. The study plot contained 234 species (11 208 individuals with a height ≥0.5 m), of which 55.1% (34.8% of individuals) were trees, 9.4% (6.8%) shrubs, 3.4% (44.3%) palms, 20.1% (5.2%) vines, 6.8% (8.7%) herbs and 5.1% (0.3%) of unknown lifeform. Furthermore, 58 species of epiphytes and hemi-epiphytes were found. Diversity of trees, shrubs and palms with a DBH≥1.0 cm was calculated as Shannon-Wiener index (4.65), Equitability index (0.65), and Simpson index (0.10). The dominance-diversity curve showed a lognormal form, characteristic for tropical rain forest. The community structure was characterized by a relative dominance of Astrocaryum mexicanum in the understorey, Pseudolmedia oxyphyllaria in the middle storeys, and Nectandra ambigens in the canopy. Species population structures of 31 species showed three characteristic patterns, differentiated by recruitment: continuously high, discontinuously high, and continuously low recruitment. Height/diameter and crown cover/diameter diagrams suggested a very gradual shift from height growth to crown growth during tree development. Forest turnover was calculated as 138 years. Compared to other tropical rain forests the Los Tuxtlas forest had 1. similar leaf physiognomical characteristics, 2. a lower diversity, 3. a lower density, 4. an average basal area, and 5. a slow canopy turnover.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 9
    Publication Date: 2019
    Description: 〈p〉Old-growth tropical forests harbor an immense diversity of tree species but are rapidly being cleared, while secondary forests that regrow on abandoned agricultural lands increase in extent. We assess how tree species richness and composition recover during secondary succession across gradients in environmental conditions and anthropogenic disturbance in an unprecedented multisite analysis for the Neotropics. Secondary forests recover remarkably fast in species richness but slowly in species composition. Secondary forests take a median time of five decades to recover the species richness of old-growth forest (80% recovery after 20 years) based on rarefaction analysis. Full recovery of species composition takes centuries (only 34% recovery after 20 years). A dual strategy that maintains both old-growth forests and species-rich secondary forests is therefore crucial for biodiversity conservation in human-modified tropical landscapes.〈/p〉
    Electronic ISSN: 2375-2548
    Topics: Natural Sciences in General
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 10
    Publication Date: 2016-06-17
    Description: Water storage in the stems of woody plants contributes to their responses to short-term water shortages. To estimate the contribution of water storage to the daily water budget of trees, time lags of sap flow between different positions of trunk are used as a proxy of stem water storage. In lianas, another large group of woody species, it has rarely been studied whether stored water functions in their daily water use, despite their increasing roles in the carbon and water dynamics of tropical forests caused by their increasing abundance. We hypothesized that lianas would exhibit large time lags due to their extremely long stems, wide vessels and large volume of parenchyma in the stem. We examined time lags in sap flow, diel changes of stem volumetric water content (VWC) and biophysical properties of sapwood of 19 lianas and 26 co-occurring trees from 27 species in 4 forests (karst, tropical seasonal, flood plain and savanna) during a wet season. The plants varied in height/length from 〈5 to 〉60 m. The results showed that lianas had significantly higher saturated water content (SWC) and much lower wood density than trees. Seven of 19 liana individuals had no time lags; in contrast, only 3 of 26 tree individuals had no time lags. In general, lianas had shorter time lags than trees in our data set, but this difference was not significant for our most conservative analyses. Across trees and lianas, time lag duration increased with diurnal maximum changeable VWC but was independent of the body size, path length, wood density and SWC. The results suggest that in most lianas, internal stem water storage contributes little to daily water budget, while trees may rely more on stored water in the stem.
    Print ISSN: 0829-318X
    Electronic ISSN: 1758-4469
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...