Catherine Potvin

ORCID: 0000-0002-5640-9329
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About
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Research Areas
  • Ecology and Vegetation Dynamics Studies
  • Conservation, Biodiversity, and Resource Management
  • Forest ecology and management
  • Plant Water Relations and Carbon Dynamics
  • Forest Management and Policy
  • Economic and Environmental Valuation
  • Plant responses to elevated CO2
  • Plant and animal studies
  • Soil Carbon and Nitrogen Dynamics
  • Plant Parasitism and Resistance
  • Species Distribution and Climate Change
  • Land Use and Ecosystem Services
  • Agriculture, Land Use, Rural Development
  • Agroforestry and silvopastoral systems
  • Seedling growth and survival studies
  • Climate Change Policy and Economics
  • Forest Ecology and Biodiversity Studies
  • Atmospheric and Environmental Gas Dynamics
  • Plant nutrient uptake and metabolism
  • Plant Stress Responses and Tolerance
  • Atmospheric chemistry and aerosols
  • Tree Root and Stability Studies
  • Neuroscience of respiration and sleep
  • Weed Control and Herbicide Applications
  • Neonatal Respiratory Health Research

McGill University
2015-2024

Smithsonian Tropical Research Institute
2015-2024

Western University
2018

University of Saskatchewan
2018

University of British Columbia
2018

Ecological Society of America
2017

Theodore Roosevelt High School
2017

Université Laval
2001-2014

Panama Canal Authority
2010

University of Basel
2005

Physiological ecologists often analyze the responses of physiological or biochemical traits to environmental factors such as temperature, irradiance, water potential, concentrations CO2, O2, and inorganic nutrients. The data for a response curve typically are gathered by sequential sampling same plant animal, their analysis should explicitly allow this repeated—measures design. Unfortunately, statistical curves in ecology generally has either been ignored incorrectly done. In an effort...

10.2307/1938276 article EN Ecology 1990-08-01

After making a case for the prevalence of nonnormality, this paper attempts to introduce some distribution—free and robust techniques ecologists offer critical appraisal potential advantages drawbacks these methods. The presented fall into two distinct categories, methods based on ranks "computer—intensive" techniques. Distribution—free rank tests have features that can be recommended. They free practitioner from concern about underlying distribution are very outliers. If observations is...

10.2307/1939920 article EN Ecology 1993-09-01

Abstract As of 2020, the world has an estimated 290 million ha planted forests and this number is continuously increasing. Of these, 131 are monospecific under intensive management. Although important in providing timber, they harbor less biodiversity potentially more susceptible to disturbances than natural or diverse forests. Here, we point out increasing scientific evidence for increased resilience ecosystem service provision functionally species (hereafter referred as forests) compared...

10.1111/conl.12829 article EN cc-by Conservation Letters 2021-07-16

The area of forest plantations is increasing worldwide helping to meet timber demand and protect natural forests. However, with global change, monospecific are increasingly vulnerable abiotic biotic disturbances. As an adaption measure we need move that more diverse in genotypes, species, structure, a design underpinned by science. TreeDivNet, network tree diversity experiments, responds this assessing the advantages disadvantages mixed species plantations. currently consists 18 distributed...

10.1007/s13280-015-0685-1 article EN cc-by AMBIO 2015-08-11

Summary Plant functional traits, in particular specific leaf area ( SLA ), wood density and seed mass, are often good predictors of individual tree growth rates within communities. Individuals species with high , low small seeds tend to have faster rates. If community‐level relationships between traits general predictive value, then similar should also be observed analyses that integrate across taxa, biogeographic regions environments. Such global consistency would imply could serve as...

10.1111/1365-2745.12401 article EN Journal of Ecology 2015-03-24
Daniel S. Falster Remko A. Duursma Masae I. Ishihara Diego R. Barneche Richard G. FitzJohn and 91 more Angelica Vårhammar Masahiro Aiba Makoto Ando Niels P. R. Anten Michael J. Aspinwall Jennifer L. Baltzer Christopher Baraloto Michael Battaglia John J. Battles Ben Bond‐Lamberty Michiel van Breugel James Camac Yves Claveau Lluís Coll Masako Dannoura Sylvain Delagrange Jean‐Christophe Domec Farrah R. Fatemi Feng Wang Veronica Gargaglione Yoshiaki Gotō Akio Hagihara Jefferson S. Hall Steve Hamilton Degi Harja Tsutom Hiura Robert J. Holdaway Lindsay B. Hutley Tomoaki Ichie Eric J. Jokela Anu Kantola Jeff W. G. Kelly Tanaka Kenzo David A. King Brian D. Kloeppel Takashi Kohyama Akira Komiyama Jean‐Paul Laclau Christopher H. Lusk Douglas A. Maguire Guerric Le Maire Annikki Mäkelä Lars Markesteijn John D. Marshall Katherine A. McCulloh Itsuo Miyata Karel Mokany Shigeta Mori Randall W. Myster Masahiro Nagano Shawna L. Naidu Yann Nouvellon Anthony P. O’Grady Kevin L. O’Hara Toshiyuki Ohtsuka Noriyuki Osada Olusegun O. Osunkoya Pablo Luís Peri Any Mary Petriţan Lourens Poorter Angelika Portsmuth Catherine Potvin Johannes Ransijn Douglas E.B. Reid Sabina Cerruto Ribeiro Scott D. Roberts Rolando Rodrı́guez Angela Saldaña-Acosta I. Santa Regina Kaichiro Sasa N. Galia Selaya Stephen C. Sillett Frank J. Sterck Kentaro Takagi Takeshi Tange Hiroyuki Tanouchi David T. Tissue Toru Umehara Hajime Utsugi Matthew A. Vadeboncoeur Fernando Valladares Petteri Vanninen Jian R. Wang Elizabeth Wenk Richard Williams Fabiano de Aquino Ximenes Atsushi Yamaba Toshihiro Yamada Takuo Yamakura Ruth D. Yanai R.A. York

Understanding how plants are constructed—i.e., key size dimensions and the amount of mass invested in different tissues varies among individuals—is essential for modeling plant growth, carbon stocks, energy fluxes terrestrial biosphere. Allocation patterns can differ through ontogeny, but also coexisting species adapted to environments. While a variety models dealing with biomass allocation exist, we lack synthetic understanding underlying processes. This is partly due suitable data sets...

10.1890/14-1889.1 article EN Ecology 2015-05-01

Abstract Plant diversity effects on community productivity often increase over time. Whether the strengthening of is caused by temporal shifts in species-level overyielding (i.e., higher diverse communities compared with monocultures) remains unclear. Here, using data from 65 grassland and forest biodiversity experiments, we show that strength at scale underpinned changes species yield. These trends are shaped plant ecological strategies, which can be quantitatively delimited functional...

10.1038/s41467-024-46355-z article EN cc-by Nature Communications 2024-03-07

Changes in land use, habitat fragmentation, nutrient enrichment, and environmental stress often lead to reduced plant diversity ecosystems. However, it remains controversial whether these reductions will affect energy flow cycling. Diversity has two components: species richness, or the number of a given area, evenness, how well distributed abundance biomass is among within community. We experimentally varied evenness identity dominant an old field Quebec test productivity would increase with...

10.1890/0012-9658(2000)081[0887:baefio]2.0.co;2 article EN Ecology 2000-04-01

We report data on leaf litter production and decomposition from a manipulative biodiversity experiment with trees in tropical Panama, which has been designed to explore the relationship between tree diversity ecosystem functioning. A total of 24 plots (2025 m 2 ) were established 2001 using six native species, 1‐, 3‐, 6‐species mixtures. estimated during dry season 2005 traps; was assessed bag approach following wet season. Litter course highly variable among species. Tree significantly...

10.1111/j.2007.0030-1299.16065.x article EN Oikos 2007-09-27

Abstract We developed an analytical method that quantifies the relative contributions of mortality and individual growth to ecosystem function analysed results from first biodiversity experiment conducted in a tropical tree plantation. In Sardinilla, central Panama, over 5000 seedlings were planted monoculture mixed‐species plots. After 5 years growth, plots yielded, on average, 30–58% higher summed basal area than did monocultures. Simulation models revealed increased yield was due mostly...

10.1111/j.1461-0248.2007.01148.x article EN Ecology Letters 2008-01-31

• Linking tree diversity to carbon storage can provide further motivation conserve tropical forests and design carbon-enriched plantations. Here, we examine the role of functional traits in determining a mixed-species plantation natural forest Panama. We used species richness, trait diversity, dominance predict across these two forests. Then compared ranking based on wood density, maximum diameter, height, leaf mass per area (LMA) between sites reveal how values changed different Increased...

10.1111/j.1469-8137.2010.03501.x article EN New Phytologist 2010-10-19

High fidelity carbon mapping has the potential to greatly advance national resource management and encourage international action toward climate change mitigation. However, inventories based on field plots alone cannot capture heterogeneity of stocks, thus remote sensing-assisted approaches are critically important at regional global scales. We advanced a high-resolution, national-scale approach applied Republic Panama – one first UN REDD + partner countries. Integrating measurements...

10.1186/1750-0680-8-7 article EN cc-by Carbon Balance and Management 2013-07-16

A plantation of native trees was established in Panama 2001 to study the relationship between biodiversity and ecosystem functioning. Five years later, mixed‐species plots had experienced enhanced tree growth compared with monocultures. Searching for underlying mechanisms, we developed a neighborhood model isolating size identity effects. We found that neighbors is, by far, largest source variation individual‐tree diameter height. Size‐asymmetric competition appears as structuring factor...

10.1890/08-0353.1 article EN Ecology 2009-02-01

Abstract There is increasing evidence that mixed‐species forests can provide multiple ecosystem services at a higher level than their monospecific counterparts. However, most studies concerning tree diversity and functioning relationships use data from forest inventories (under noncontrolled conditions) or very young plantation experiments. Here, we investigated temporal dynamics of diversity–productivity diversity–stability in the oldest tropical experiment. Sardinilla was established...

10.1111/gcb.14792 article EN cc-by Global Change Biology 2019-09-05

Summary 1. Tree plantations play an important role in meeting the growing demand for wood, but there is concern about their high rates of water use. Recent approaches to reforestation tropics involve establishment multispecies plantations, few studies have compared use mixed vs. monospecific stands. 2. We hypothesized that tree species diversity enhances stand transpiration. were estimated monocultures ( n = 5), two‐species mixtures 3), three‐species 3) and five‐species 4). Sap flux...

10.1111/j.1365-2664.2011.02065.x article EN Journal of Applied Ecology 2011-11-08

Although decades of research suggest that higher species richness improves ecosystem functioning and stability, planted forests are predominantly monocultures. To determine whether diversification plantations would enhance aboveground carbon storage, we systematically reviewed over 11,360 publications, acquired data from a global network tree diversity experiments. We compiled maximum dataset 79 monoculture to mixed comparisons 21 sites with all variables needed for meta-analysis. assessed...

10.3389/ffgc.2023.1226514 article EN cc-by Frontiers in Forests and Global Change 2023-11-09

Abstract Enhancing tree diversity may be important to fostering resilience drought‐related climate extremes. So far, little attention has been given whether can increase the survival of trees and reduce its variability in young forest plantations. We conducted an analysis seedling sapling from 34 globally distributed experiments (363,167 trees, 168 species, 3744 plots, 7 biomes) answer two questions: (1) Do drought alter mean plot‐level survival, with higher less variable as increases? (2)...

10.1111/1365-2745.14294 article EN Journal of Ecology 2024-04-08

Trunk carbon (C) concentrations were assessed for 32 species of tropical trees to understand sources variation. The main effect accounted 38% the total variance in C concentration (p < 0.0001). Tectona grandis demonstrated greatest (49.4%), while Ormosia macrocalyx displayed lowest (44.4%). We also observed significant differences among sampling sites (F = 2.2, p 0.02). For three sampled both plantations and natural forests, forest individuals had significantly higher (Dipteryx...

10.1139/x03-018 article EN Canadian Journal of Forest Research 2003-05-30

Summary Over 5000 trees were grown in plots of differing diversity levels (1, 3 and 6 species) a plantation established Panama. Four five years after establishment, we analysed parameters related to the productivity this tropical (tree survival, height biomass as well plot basal area) test for presence biodiversity effects. The relative importance environmental heterogeneity (such soil, topography, drainage) on tree growth mortality was determined using partial redundancy analysis....

10.1111/j.1365-2745.2008.01419.x article EN Journal of Ecology 2008-08-12
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