about
(15)N in tree rings as a bio-indicator of changing nitrogen cycling in tropical forests: an evaluation at three sites using two sampling methodsLong-term trends in nitrogen isotope composition and nitrogen concentration in brazilian rainforest trees suggest changes in nitrogen cycleAn improved method and data analysis for ultrasound acoustic emissions and xylem vulnerability in conifer wood.Oxygen isotopes in tree rings record variation in precipitation δ (18)O and amount effects in the south of Mexico.Population dynamics of epiphytic orchids in a metapopulation context.High-resolution densitometry and elemental analysis of tropical wood.Long-term change in the nitrogen cycle of tropical forests.Nitrogen-15 natural abundance in a montane cloud forest canopy as an indicator of nitrogen cycling and epiphyte nutrition.Correlation between water relations and within-canopy distribution of epiphytic ferns in a Mexican cloud forest.Wood density and its radial variation in six canopy tree species differing in shade-tolerance in western Thailand.High gene flow in epiphytic ferns despite habitat loss and fragmentation.A simple program to measure and analyse tree rings using Excel, R and SigmaScan.Effect of canopy position on germination and seedling survival of epiphytic bromeliads in a Mexican humid montane forest.Power games cause sparks in physics, but biologists have learnt from evolution.Global warming, elevational ranges and the vulnerability of tropical biotaGermination of Epiphytic Bromeliads in Forests and Coffee Plantations: Microclimate and Substrate EffectsSurvival and Growth of Juvenile Bromeliads in Coffee Plantations and Forests in Central Veracruz, MexicoSeedling establishment of epiphytic orchids in forests and coffee plantations in Central Veracruz, MexicoPopulation dynamics of epiphytic bromeliads: Life strategies and the role of host branchesHerbivory in epiphytic bromeliads, orchids and ferns in a Mexican montane forestLong-term increases in intrinsic water-use efficiency do not lead to increased stem growth in a tropical monsoon forest in western ThailandStrong radial variation in wood density follows a uniform pattern in two neotropical rain forestsRadial Gradients in Wood Specific Gravity, Water and Gas Content in Trees of a Mexican Tropical Rain ForestStable carbon isotopes in tree rings indicate improved water use efficiency and drought responses of a tropical dry forest tree speciesSize-Dependent Variation of Carbon and Nitrogen Isotope Abundances in Epiphytic BromeliadsNatural 15N abundance of epiphytes depends on the position within the forest canopy: source signals and isotope fractionationStable isotopic composition of carbon and nitrogen and nitrogen content in vascular epiphytes along an altitudinal transect*Vulnerability curves from conifer sapwood sections exposed over solutions with known water potentialsClimatic and edaphic controls over tropical forest diversity and vegetation carbon storageReply to: Data do not support large-scale oligotrophication of terrestrial ecosystemsTRY plant trait database - enhanced coverage and open access
P50
Q28649960-5EEE8554-3F6E-4500-A7DB-93BAEB88FA06Q28748896-93A68688-9B46-4811-BB6E-0D5AEF2F3EA1Q34180362-C3A94746-EBBC-422F-8EBC-28BD6459286FQ35715296-4B8FB397-E4BE-4750-911C-34E790636442Q37358949-914C5902-EA9B-4B8E-BE7C-925098CD93E5Q39067109-2680C7CB-BCBF-4845-8B77-556F91034F69Q39067113-AD55116C-3083-4C7C-9E69-8041B376144AQ39067123-75BB657C-9160-49AC-A1B9-9C91D68CDD2AQ39067127-FD4092D1-BF6A-4695-A7D6-6329FA6C6EBBQ39307477-27728656-19B3-432D-9C51-FB3B9FC928C2Q39597932-F7D37F7E-D7E0-42F4-B217-14BCFC511B00Q40798864-C3677410-1453-4EE0-98A5-24EB92043714Q43042622-45D6D0D8-B275-40E3-93F5-A3299EEDFED3Q48461662-30305AF1-1A76-4B3D-BBE4-9053193E7951Q57036655-F49959AA-4F4B-4789-B18B-5EEF1F216E51Q59825925-D598490B-1868-4339-ABA8-2D5EED66A93DQ59825933-DEF1CF0D-58FA-44A5-802D-C0B8A4F713AEQ59826008-76DC6BEC-B45F-4940-A4F6-191790152245Q59826260-390493F9-0239-4F46-9FF6-74A4DBEC7E30Q59826404-09B68AB7-6E73-4713-B854-190ED6850246Q62547170-A3D66704-D028-428F-B4A7-51B5022B7820Q62550730-57DA4A74-6D0C-424E-80BF-1492E100FF92Q63564244-63370621-F5C1-487A-934B-C83D5C60CE91Q63849763-796784A1-39E3-4C4A-96E5-65507A0ABE2AQ63849791-B6EE7171-F798-4791-86F0-E17CA8346BA8Q63849795-17E215C1-EAA7-4BC1-BAC9-72638132A16EQ63849802-76F775A6-8BCE-4E29-A300-FBD72A5ADB67Q73683013-A071AFCA-7706-41E1-8C6F-D27ECC1CD48BQ90471682-74955D18-D345-48C2-B55D-65D7E3FEE3ADQ92093506-EFA95AB1-BEC2-4AF0-8C64-1D9B4F0B5AABQ92348862-76F41CD6-22FB-4225-AF00-DAD17B3FF874
P50
description
hulumtues
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Peter Hietz
@ast
Peter Hietz
@en
Peter Hietz
@es
Peter Hietz
@nl
Peter Hietz
@sl
type
label
Peter Hietz
@ast
Peter Hietz
@en
Peter Hietz
@es
Peter Hietz
@nl
Peter Hietz
@sl
prefLabel
Peter Hietz
@ast
Peter Hietz
@en
Peter Hietz
@es
Peter Hietz
@nl
Peter Hietz
@sl
P106
P1153
6603724288
P21
P2798
P31
P496
0000-0002-0458-6593
P569
2000-01-01T00:00:00Z