I‐Fang Sun

ORCID: 0000-0001-9749-8324
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Research Areas
  • Ecology and Vegetation Dynamics Studies
  • Forest ecology and management
  • Plant and animal studies
  • Animal Ecology and Behavior Studies
  • Species Distribution and Climate Change
  • Wildlife Ecology and Conservation
  • Plant Water Relations and Carbon Dynamics
  • Land Use and Ecosystem Services
  • Forest Management and Policy
  • Forest Ecology and Biodiversity Studies
  • Fire effects on ecosystems
  • Plant Parasitism and Resistance
  • Forest Insect Ecology and Management
  • Tree Root and Stability Studies
  • Ecosystem dynamics and resilience
  • Soil Geostatistics and Mapping
  • Mycorrhizal Fungi and Plant Interactions
  • Aeolian processes and effects
  • Bayesian Methods and Mixture Models
  • Rangeland and Wildlife Management
  • Botany and Plant Ecology Studies
  • Conservation, Biodiversity, and Resource Management
  • Marine and environmental studies
  • Scarabaeidae Beetle Taxonomy and Biogeography
  • Sustainability and Ecological Systems Analysis

National Dong Hwa University
2016-2025

National Museum of Natural History
2020

ForestGEO
2006-2020

Universiti Brunei Darussalam
2020

National Taiwan University
2019

Chinese Academy of Sciences
2013

Tunghai University
1997-2012

University of Georgia
2007

University of California, San Diego
2006

Smithsonian Tropical Research Institute
2006

The classical environmental control model assumes that species distribution is determined by the spatial variation of underlying habitat conditions. This niche-based has recently been challenged neutral theory biodiversity which ecological drift a key process regulating coexistence. Understanding mechanisms maintain in communities critically depends on our ability to decompose diversity into contributions different processes affecting it. Here we investigated effects pure habitat, spatial,...

10.1890/07-1880.1 article EN Ecology 2009-02-26
James A. Lutz Tucker J. Furniss Daniel J. Johnson Stuart J. Davies David Allen and 93 more Alfonso Alonso Kristina J. Anderson‐Teixeira Ana Andrade Jennifer L. Baltzer Kendall M. L. Becker Erika M. Blomdahl Norman A. Bourg Sarayudh Bunyavejchewin David F. R. P. Burslem C. Alina Cansler Ke Cao Min Cao Dairón Cárdenas Li‐Wan Chang Kuo‐Jung Chao Wei‐Chun Chao Jyh‐Min Chiang Chengjin Chu George B. Chuyong Keith Clay Richard Condit Susan Cordell H. S. Dattaraja Álvaro Duque Corneille E. N. Ewango Gunter A. Fischer Christine Fletcher James A. Freund Christian P. Giardina Sara J. Germain Gregory S. Gilbert Zhanqing Hao Térese B. Hart Billy C. H. Hau Fangliang He Andy Hector Robert W. Howe Chang‐Fu Hsieh Yuehua Hu Stephen P. Hubbell Faith Inman‐Narahari Akira Itoh David Janík Abdul Rahman Kassim David Kenfack Lisa Korte Kamil Král Andrew J. Larson Yide Li Yiching Lin Shirong Liu Shawn Lum Keping Ma Jean‐Remy Makana Yadvinder Malhi Sean M. McMahon William J. McShea Hervé Memiaghe Xiangcheng Mi Michael D. Morecroft Paul M. Musili Jonathan A. Myers Vojtěch Novotný Alexandre A. Oliveira Perry S. Ong David A. Orwig Rebecca Ostertag Geoffrey G. Parker Rajit Patankar Richard P. Phillips Glen Reynolds Lawren Sack Guo‐Zhang Michael Song Sheng‐Hsin Su Raman Sukumar I‐Fang Sun H. S. Suresh Mark E. Swanson Sylvester Tan Duncan W. Thomas Jill Thompson María Uriarte Renato Valencia Alberto Vicentini Tomáš Vrška Xugao Wang George D. Weiblen Amy Wolf Shuhui Wu Han Xu Takuo Yamakura Sandra Yap Jess K. Zimmerman

Abstract Aim To examine the contribution of large‐diameter trees to biomass, stand structure, and species richness across forest biomes. Location Global. Time period Early 21st century. Major taxa studied Woody plants. Methods We examined large density, biomass using a global network 48 (from 2 60 ha) plots representing 5,601,473 stems 9,298 210 plant families. This was assessed three metrics: largest 1% ≥ 1 cm diameter at breast height (DBH), all DBH, those rank‐ordered that cumulatively...

10.1111/geb.12747 article EN publisher-specific-oa Global Ecology and Biogeography 2018-05-08

Summary The relationship between species richness and ecosystem function, as measured by productivity or biomass, is of long‐standing theoretical practical interest in ecology. This especially true for forests, which represent a majority global biodiversity. Here, we conduct an analysis relationships tree richness, biomass 25 forest plots area 8–50 ha from across the world. data were collected using standardized protocols, obviating need to correct methodological differences that plague many...

10.1111/1365-2745.12132 article EN Journal of Ecology 2013-08-28

Maintaining tree diversity Negative interaction among plant species is known as conspecific negative density dependence (CNDD). This ecological pattern thought to maintain higher in the tropics. LaManna et al. tested this hypothesis by comparing how changes with intensity of local biotic interactions tropical and temperate latitudes (see Perspective Comita). Stronger specialized seem prevent erosion biodiversity forests, not only limiting populations common species, but also strongly...

10.1126/science.aam5678 article EN Science 2017-06-30

Abstract Numerous studies have shown reduced performance in plants that are surrounded by neighbours of the same species 1,2 , a phenomenon known as conspecific negative density dependence (CNDD) 3 . A long-held ecological hypothesis posits CNDD is more pronounced tropical than temperate forests 4,5 which increases community stabilization, coexistence and diversity local tree 6,7 Previous analyses supporting such latitudinal gradient 8,9 suffered from methodological limitations related to...

10.1038/s41586-024-07118-4 article EN cc-by Nature 2024-02-28

Abstract All species must partition resources among the processes that underly growth, survival, and reproduction. The resulting demographic trade‐offs constrain range of viable life‐history strategies are hypothesized to promote local coexistence. Tropical forests pose ideal systems study as they have a high diversity coexisting tree whose tend align along two orthogonal axes variation: growth–survival trade‐off separates with fast growth from survival stature–recruitment achieve large...

10.1002/ecy.4527 article EN cc-by Ecology 2025-01-01

The search for simple principles that underlie the spatial structure and dynamics of plant communities is a long-standing challenge in ecology1–6. In particular, relationship between species coexistence distribution plants challenging to resolve species-rich communities7–9. Here we present comprehensive analysis patterns 720 tree 21 large forest plots their consequences coexistence. We show with low abundance tend be more spatially aggregated than abundant species. Moreover, there...

10.1038/s41586-025-08604-z article EN cc-by-nc-nd Nature 2025-02-26

An ecological community's species diversity tends to erode through time as a result of stochastic extinction, competitive exclusion, and unstable host-enemy dynamics. This erosion can be prevented over the short term if recruits are highly diverse preferential recruitment rare or, alternatively, survive preferentially, which increases ages individuals increase. Here, we present census data from seven New Old World tropical forest dynamics plots that all show latter pattern. Within local...

10.1126/science.1117715 article EN Science 2006-01-26

Species–area relationships (SARs) characterize the spatial distribution of species diversity in community ecology, but biological mechanisms underlying SARs have not been fully explored. Here, we examined roles dispersal limitation and habitat heterogeneity shaping two large‐scale forest plots. One is a 24‐ha subtropical Gutianshan National Nature Reserve, China. The other 50‐ha tropical rain Barro Colorado Island, Panama. Spatial point pattern models were applied to investigate...

10.1890/08-1646.1 article EN Ecology 2009-11-01

ABSTRACT Aims With the aim of understanding why some world's forests exhibit higher tree beta diversity values than others, we asked: (1) what is contribution environmentally related variation versus pure spatial and local stochastic to assessed at forest plot scale; (2) resolution are these beta‐diversity components more apparent; (3) determines in observed across regions/continents? Location World‐wide. Methods We compiled an unprecedented data set 10 large‐scale stem‐mapping plots...

10.1111/j.1466-8238.2012.00770.x article EN Global Ecology and Biogeography 2012-05-15

Long-term surveys of entire communities species are needed to measure fluctuations in natural populations and elucidate the mechanisms driving population dynamics community assembly. We analysed changes abundance over 4000 tree 12 forests across world periods 6-28 years. Abundance all large consistent with models which temporal environmental variance plays a central role. At some sites we identify clear drivers, such as fire drought, that could underlie these patterns, but at other there is...

10.1111/ele.12296 article EN Ecology Letters 2014-05-07

The spatial dispersion of individuals in a species is an important pattern that controlled by many mechanisms. In this study we analyzed distributions tree large‐scale (20 ha) stem‐mapping plot species‐rich subtropical forest China. O‐ring statistic was used to measure patterns with abundance >10. Ω 0–10 , the mean conspecific density within 10 m tree, as intensity aggregation species. Our results showed: (1) aggregated distribution dominant plot. percentage decreased increased scale. (2)...

10.1111/j.1600-0706.2009.16753.x article EN Oikos 2009-03-31

Summary An important goal in plant community ecology is to understand how species traits determine demographic performance. Several functional have been shown correlate with growth and mortality rates trees, but less known about the relationships between change tree size. We examined associations of across 43 Fushan 25‐ha subtropical rain forest plot northern Taiwan. estimated 95th percentile maximum stem diameter, wood density six leaf (leaf area, specific thickness, succulence, mass‐based...

10.1111/1365-2745.12221 article EN Journal of Ecology 2014-02-25

Abstract Based on the framework of attribute diversity (a generalization Hill numbers order q ), we develop a class functional measures sensitive not only to species abundances but also trait‐based species‐pairwise distances. The new method refines and improves conventional species‐equivalent approach in three areas: (1) often gives similar values (close unity) assemblages with contrasting levels diversity; (2) when distance metric is unbounded, depends presence/absence other study; (3)...

10.1002/ecm.1343 article EN Ecological Monographs 2018-11-21

Neutral and niche theories give contrasting explanations for the maintenance of tropical tree species diversity. Both have some empirical support, but methods to disentangle their effects not yet been developed. We applied a statistical measure spatial structure data from 14 large forest plots test prediction theory that is incompatible with neutral theory: in heterogeneous environments should separate out space according preferences. chose across range topographic heterogeneity, tested...

10.1098/rspb.2013.0502 article EN Proceedings of the Royal Society B Biological Sciences 2013-06-19

Summary Tree size shapes forest carbon dynamics and determines how trees interact with their environment, including a changing climate. Here, we conduct the first global analysis of among‐site differences in aboveground biomass stocks fluxes are distributed tree size. We analyzed repeat censuses from 25 large‐scale (4–52 ha) plots spanning broad climatic range over five continents to characterize biomass, woody productivity, mortality vary diameter. examined median, dispersion, skewness...

10.1111/nph.17995 article EN New Phytologist 2022-02-24
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