Sylvie Gourlet-Fleury’s research while affiliated with Université de Montpellier and other places

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Publications (210)


Conceptual model of the expected role of the sampling effect (blue paths) and the tree‐packing effect (red paths) on AGB (a) and ΔAGB (b) components. AGB, log transformed above‐ground biomass; AGV, log transformed mean individual above‐ground volume; MPD, mean pairwise distance; Ntrees, log transformed number of trees; P.MaxDBH, potential maximum diameter; rPD, rarefied phylogenetic diversity; WD, log transformed mean wood density weighted by AGV; Δ, Net change.
Effects of disturbance (silvicultural treatments) on tree stand structure and diversity over time. Above‐ground biomass (AGB, a), mean individual tree above‐ground volume (AGV, b), mean wood density (WD, c), number of trees (Ntree, d), potential maximum tree diameter (P.MaxDBH, e), rarefied phylogenetic diversity (rPD, f) and mean pairwise distance (MPD, g) are reported for the four census dates. Error bars represent 95% confidence interval.
Results of the structural equation models for the effect of phylogenetic diversity on above‐ground biomass (AGB) components via the sampling effect (in blue) and the tree‐packing effect (in red) in 1992. AGV, log transformed mean individual above‐ground volume; MPD, mean pairwise distance; Ntrees, log transformed stem density; P.MaxDBH, potential maximum tree diameter; rPD, rarefied phylogenetic diversity; WDv, log transformed mean wood density weighted by AGV. Bold arrows and numbers represent significant effects (p < 0.05) and light‐dotted arrows represent non‐significant effects. Standardized regression coefficients are given for all paths. Model fit statistics are provided in Table S6.
Results of the structural equation models for the effect of phylogenetic diversity on above‐ground biomass productivity (ΔAGB) components via the sampling effect (in blue) and the tree‐packing effect (in red) for the first (1992–1998, a–c) and second monitoring period (2012–2018, d–f). MPD, mean pairwise distance; rPD, rarefied phylogenetic diversity; ΔAGV, change in log transformed mean individual above‐ground volume; ΔP.MaxDBH, change in potential maximum tree diameter; ΔWDv, change in log transformed mean wood density weighted by AGV. Bold arrows and numbers represent significant effects (p < 0.05), and light‐dotted arrows represent non‐significant effects. Standardized regression coefficients are given for all paths. The model fit statistics are presented in Tables S9 and S10.
Model coefficients for the effects of diversity on ΔAGB via the sampling and the tree‐packing effects. ‘All effects’ represents the sum of all effects in the SEM pathways. A standardized slope estimate is considered as significant if the 95% confidence interval does not intersect zero.
Evolutionary diversity impacts tropical forest biomass and productivity through disturbance‐mediated ecological pathways
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August 2024

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Sylvie Gourlet‐Fleury

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Significant research efforts have been made to uncover links between biodiversity and biomass productivity in forest ecosystems. However, the causal link between these two ecosystem components, and the underlying mediation role of disturbance, are yet poorly understood for hyper‐diverse tropical forests, because multiple ecological mechanisms are sequentially or simultaneously in play, leading to contradictory results in observational studies. Here, we introduce a novel framework for inferring the expected effects of evolutionary diversity on biomass stocks and productivity within forest ecosystems using observational field data. This framework involves an analytical decomposition of stand biomass into three key components: the number of trees, the mean size of trees and the mean wood density. Through this approach, we can distinguish structure‐ and compositional‐based diversity effects, which likely have distinct ecological origins. We tested this framework in one of the oldest tropical forest experiments, where different levels of silvicultural disturbances were applied in the 1980s, with regular monitoring since then. Our results revealed that disturbance history mediates the effect of evolutionary diversity on forest biomass dynamics and that several Biodiversity Ecosystem Function (BEF) relationships may be hidden behind the composite biomass variable. We specifically found an overall significant negative relationship between evolutionary diversity and biomass productivity soon after disturbances (~5–8 years), mostly via mean tree size, despite a positive evolutionary diversity effect on mean wood density. This result reflects that the productivity of disturbed forests is driven by a few dominant and disturbance‐prone species with low wood density and large potential stature, and not by niche complementarity among species. However, these effects rapidly vanished with time, with non‐significant overall effect of evolutionary diversity on productivity both ~30 years after disturbance and in the undisturbed plots. Synthesis. By disentangling the effects of evolutionary diversity on the different components of forest biomass, our framework unveiled how evolutionary diversity impacts forest productivity through different ecological mechanisms, and suggests that it plays a major role, albeit mainly negative, only soon after a disturbance.

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Location of the PSPs (in red) nearby the city of M’Baïki in the Central African Republic at the northern edge of the Congo basin as visible on the tree cover map⁷² shown as inset. The same silvicultural treatments (control, logging, and logging + thinning) have been applied to the 4 ha-plots (in red) and to the 50 m-wide buffer zones (hashed) in the three experimental blocks (Boukoko 1, Boukoko 2 and La Lole). Each 4 ha-plot is divided into four 1 ha subplots.
Field work during inventory campaigns in the M’Baïki PSPs. Trees are spatially located in the 4-ha plots (a) and numbered in the 1-ha subplots (b,c), their girth is measured at breast height (d) and 50 cm above deformation, up to 4.50 m high with a ladder for extremely irregularly shaped trees (e). © E. Dubiez for (a) in 2007 and A. Fayolle for (b–e) in 2011. The height of measurement (hom) is painted on the trees, in red for the trees belonging to the 36 valuable timber species or species complexes recognized at installation (Table 2), and in yellow for all other trees (a).
Structure of the general database for the M’Baïki PSPs data, with relationships between the eight data tables (in grey) and the two geojson files (in blue).
Dynamics of forest structural attributes (stem density (a), N in ha⁻¹ and basal area (b), in m² ha⁻¹) and demographic rates (mortality (c) and recruitment (d), both expressed in number of trees %yr⁻¹) and computed at the scale of 4-ha plots with a color code and line type according to the experimental blocks and silviculural treatments, respectively. The 35 inventory campaigns are indicated with dots on (a).
40 years of forest dynamics and tree demography in an intact tropical forest at M’Baïki in central Africa

July 2024

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137 Reads

Scientific Data

A vast silvicultural experiment was set up in 1982 nearby the town of M’Baïki in the Central African Republic to monitor the recovery of tropical forests after disturbance. The M’Baïki experiment consists of ten 4-ha Permanent Sample Plots (PSPs) that were assigned to three silvicultural treatments in 1986 according to a random block design. In each plot, all trees with a girth at breast height greater than 30 cm were spatially located, numbered, measured, and determined botanically. Girth, mortality and newly recruited trees, were monitored almost annually over the 1982–2022 period with inventory campaigns for 35 years. The data were earlier used to fit growth and population models, to study the species composition dynamics, and the effect of silvicultural treatments on tree diversity and aboveground biomass. Here, we present new information on the forest stand structure dynamics and tree demography. The data released from this paper cover the three control plots and constitute a major contribution for further studies about the biodiversity of intact tropical forests.


Local forest structure and host-specificity influence liana community composition in a moist central African forest.

June 2024

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115 Reads

Lianas are important components of tropical forest diversity and dynamics, yet little is known about the drivers of their community structure and composition. Combining extensive field and LiDAR data, we investigated the influence of local topography, forest structure and tree composition on liana community structure and composition in a moist forest in northern Republic of Congo. We inventoried all lianas ≥ 1 cm in diameter in 144 20×20 m quadrats located in four 9-ha permanent plots, where trees and giant herbs were inventoried. We characterized the functional strategies of selected representatives of the main liana taxa using a set of resource-use leaf and wood traits. Finally, we used complementary statistical tests, including multivariate and randomization schemes, to test whether forest structure, topography and tree composition influence the structure, floristic, and functional composition of liana communities. The structure of liana communities was strongly shaped by local forest structure, with higher abundances and total basal areas in relatively open-canopy forests, where lianas competed with giant herbs. Liana floristic composition exhibited a weak spatial structure over the study site, but was marginally influenced by local forest structure and topography. Only forest structure had a weak but significant effect on liana functional composition with more conservative strategies—higher stem tissue density and lower PO4 leaf concentration and SLA values—in tall and dense forests. Finally, we found evidence of host specificity with significant attraction/repulsion for 19% of the tested liana and tree species associations, suggesting that the unexplained floristic variation may be partly attributed to these host species-specific associations, although the underlying mechanisms behind remain elusive. Overall, our findings demonstrate that the structure of liana communities can be much better predicted than their composition, calling for a better understanding of the implication of the large functional diversity observed in liana communities.


The puzzling ecology of African Marantaceae forests

April 2024

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132 Reads

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1 Citation

American Journal of Botany

Marantaceae forests are tropical rainforests characterized by a continuous understory layer of perennial giant herbs and a near absence of tree regeneration. Although widespread in West‐Central Africa, Marantaceae forests have rarely been considered in the international literature. Yet, they pose key challenges and opportunities for theoretical ecology that transcend the borders of the continent. Specifically, we ask in this review whether open Marantaceae forests and dense closed‐canopy forests can be considered as one of the few documented examples of alternative stable states in tropical forests. First, we introduce the different ecological factors that have been posited to drive Marantaceae forests (climate, soil, historical and recent anthropogenic pressures, herbivores) and develop the different hypotheses that have been suggested to explain how Marantaceae forests establish in relation with other vegetation types (understory invasion, early succession after disturbance, and intermediate successional stage). Then, we review the underlying ecological mechanisms that can explain the stability of Marantaceae forests in the long term (tree recruitment inhibition, promotion of and resilience to fire, adaptive reproduction, maintenance by megaherbivores). Although some uncertainties remain and call for further empirical and theoretical research, we found converging evidence that Marantaceae forests are associated with an ecological succession that has been deflected or arrested. If verified, Marantaceae forests may provide a useful model to understand critical transitions in forest ecosystems, which is of particular relevance to achieve sustainable forest management and mitigate global climate change.



Competition and site weakly explain tree growth variability in undisturbed Central African moist forests

June 2023

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93 Reads

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4 Citations

Identifying and quantifying factors that influence tree growth are crucial issues to ensure sustainable forest management, particularly in moist tropical forests. Tree growth depends on several factors comprising ontogenic stage, competition by neighbours and environmental conditions. Several studies have focused on one or two of them, but very few have considered all three, especially in Central Africa. We investigated the effects of diameter and competition on tree growth, in four Central African sites characterized by their soil physicochemical properties, at both tree community and population levels. We calibrated growth models using diameter data collected on 29,741 trees between 2015 and 2018, on twelve 4 or 9‐ha plots spread over the four sites. These models included diameter, wood density, competition indices and site effect as explainable variables at the community level and excluded wood density at the population level. At the community level, the best models explained 11% of growth variability with a decreasing effect of species wood density, diameter, site and competition. Our results show that even if low, site effect can result from different soil nutrients depending on both tree size and species wood density. We observed higher tree growth on sites with (i) high exchangeable K, organic C, total N and total P for low wood density species; (ii) high available P and C:N for small trees, high exchangeable Ca and Mg for medium to large trees, all belonging to medium and hard wood density species. At the population level, the best models explained between 0 to 43% of growth variability, with significant competition effect (resp. site effect) for 21 (resp. 9) of the 43 species studied. Site ranking varied greatly between the 9 species concerned, probably reflecting different sensitivities to the scarcity of particular soil nutrients. Synthesis. Our study provides original results on the factors influencing tree growth in Central Africa, showing that the potential effect of soil nutrients depends on tree size and species wood density. Remaining highly unpredictable at the population level, this effect makes it essential to increase the number of dynamics monitoring systems in logging concessions.


Location and characteristics of the three study sites in the southwestern Democratic Republic of the Congo (Atlantic highland evergreen forest [Atla‐F]) and in the northern Republic of Congo (semideciduous forest [Semi‐F] and evergreen‐semideciduous forest on sandstone [Sand‐F]) in central Africa on a background map of tree cover (Hansen et al., 2013). The mean annual temperature (MAT; in degrees Celsius), mean annual rainfall (MAR; in millimeters), number of species and trees sampled, and sampling effort in terms of diameter (D, in centimeters) range are provided for the three sites.
Tree‐level determinants of liana load: (a) standardized coefficients of liana load with error bars showing confidence intervals (***p < 0.001) and all coefficients from fixed effects and random effects are shown in Appendix S1: Table S2; (b, c) bivariate relationships between the liana load categories and the significant variables with box plots showing tree height and crown depth for each of liana load categories (0: 0%; 1: 1%–25%; 2: 25%–50%; and 3: >50% of the crown covered by lianas) where the significant differences (nonparametric Kruskal–Wallis test) are shown by different letters using post hoc Kruskal–Wallis multiple comparisons between medians.
Species‐level determinants of liana prevalence: (a) standardized coefficients with error bars showing confidence intervals (***p < 0.001) and all coefficients from fixed effects and random effects shown in Appendix S1: Table S2; (b, c) bivariate relationships between the liana prevalence and light requirement with the Pearson correlation coefficient (r) and the dispersal mode where the significant differences (nonparametric Kruskal–Wallis test) are shown by different letters using post hoc Kruskal–Wallis multiple comparisons between medians. Deciduous leaf habit (evergreen vs. deciduous), regeneration guild (SB, shade‐bearer and P, pioneer), and dispersal mode (Un, unassisted; An, animal dispersal; and Wi, wind).
Height–diameter allometric relationships between liana‐loaded trees and liana‐free trees in three forests sites (Atlantic highland evergreen forest [Atla‐F]; semideciduous forest [Semi‐F]; and evergreen‐semideciduous forest on sandstone [Sand‐F]).
Intensity, determinants, and impacts of liana load on tropical trees in central Africa

December 2022

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1 Citation

Lianas can create dense foliage that reduces the light available for the host trees on which they grow and can directly damage the host trees during their development. A better estimation of liana load and understanding of the determinants and impacts of liana load in tropical forests are both important in community ecology and ecosystem science. This has, however, never been studied to date in central Africa. Here, we evaluated the intensity, determinants, and impacts of liana load in three forest sites in central Africa. We determined the liana load categories for all trees belonging to 78 of the most dominant tree species (2683 trees in total), with tree diameters ranging from 10 to 250 cm. The liana load was visually estimated as the liana cover on host tree using simple scale indices, and the proportion of trees covered by lianas defined as the liana prevalence was estimated for each species. Overall, 42% of the 2683 trees were liana‐loaded and the number of liana‐loaded trees was higher for smaller diameter classes in the three forest sites. Within each forest site, there was a significant difference in liana prevalence among coexisting species. Taller trees with shallow crowns were less covered by liana at the tree level, whereas trees belonging to light‐demanding and wind‐dispersed species showed a lower liana prevalence rate at the species level. In each forest site, the liana load significantly affected tree height–diameter allometry, with liana‐loaded trees being shorter for the same diameter. Lianas promote the structural complexity and influence tree diversity and ecosystem functioning of tropical forests.



Figure 9.1 : Carte des tourbières de la cuvette centrale (zones violettes et rouges) qui s'étendent sur le territoire de la République du Congo et celui de la République démocra-tique du Congo Source : OFAC 2020 ; Dargie et al. 2017
Figure 9.2 : Carte des tourbières de la cuvette centrale du bassin du Congo, vérifiée sur le terrain, la tourbe se trouvant sous deux types de végétation, une forêt marécageuse de palmiers et une forêt marécageuse de feuillus Source : Dargie et al. 2017
Figure 9.3 : Cartographie des types de forêts marécageuses en Afrique Centrale sur base d'images satellites MODIS, PALSAR et données LiDAR Source : Betbeder et al. 2013
Figure 9.4 : Évolution récente de la température (1981-2019, données TerraClimate à 2 m et ERA5) mesurée dans trois types d'occupation des sols (tourbière, eau libre et savane, situés en bas à droite sur la carte, et calculs faits à partir des données écologiques de Dargie et al. 2017) dans le Centre du bassin du Congo : la tendance linéaire concernant les tourbières est représentée par une ligne de tirets longs ; les projections pour 2050 selon les scénarios RCP 6.0 et 8.5 de l'exercice CMIP5 sont figurées par des tirets courts et des pointillés.
Les tourbières de la cuvette centrale du bassin du Congo Réalités et perspectives

June 2022

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2,613 Reads

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12 Citations

Au niveau mondial, ce sont les écosystèmes des tourbières, ces zones humides dont le sol présente une accumulation de matière organique partiellement décomposée, qui stockent le volume le plus important de carbone terrestre par unité de surface (Rydin and Jeglum 2006 ; Leifeld and Menichetti 2018). Elles couvrent près de 3 % de la surface terrestre du globe (Yu et al. 2010 ; Page et al. 2011 ; Dargie et al. 2017), ce qui représente plus du carbone total stocké dans la végétation de la Terre et près de deux fois le volume de carbone présent dans ses forêts (Crump 2017). Les tourbières drainées et dégradées émettent énormément de gaz à effet de serre, c’est-à-dire 5 % des émissions mondiales d’origine anthropique (IPCC 2014), qui sont censées augmenter. Par conséquent, la protection et la gestion durable de ces milieux naturels, tout comme des mesures de restauration à prendre d’urgence (notamment par la réhumidification) peuvent éviter des émissions et conserver le carbone stocké dans ces écosystèmes (Leifeld and Menichetti 2018 ; FAO 2020b).


Tallo: A global tree allometry and crown architecture database

June 2022

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2,202 Reads

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45 Citations

Global Change Biology

Data capturing multiple axes of tree size and shape, such as a tree's stem diameter, height and crown size, underpin a wide range of ecological research - from developing and testing theory on forest structure and dynamics, to estimating forest carbon stocks and their uncertainties, and integrating remote sensing imagery into forest monitoring programs. However, these data can be surprisingly hard to come by, particularly for certain regions of the world and for specific taxonomic groups, posing a real barrier to progress in these fields. To overcome this challenge, we developed the Tallo database, a collection of 498,838 georeferenced and taxonomically standardized records of individual trees for which stem diameter, height and/or crown radius have been measured. These data were collected at 61,856 globally distributed sites, spanning all major forested and non-forested biomes. The majority of trees in the database are identified to species (88%), and collectively Tallo includes data for 5,163 species distributed across 1,453 genera and 187 plant families. The database is publicly archived under a CC-BY 4.0 licence and can be access from: https://doi.org/10.5281/zenodo.6637599. To demonstrate its value, here we present three case studies that highlight how the Tallo database can be used to address a range of theoretical and applied questions in ecology - from testing the predictions of metabolic scaling theory, to exploring the limits of tree allometric plasticity along environmental gradients and modelling global variation in maximum attainable tree height. In doing so, we provide a key resource for field ecologists, remote sensing researchers and the modelling community working together to better understand the role that trees play in regulating the terrestrial carbon cycle.


Citations (59)


... As with any other large tropical forest block, several forest types, with specific structure and functional and faunistic compositions, occur or co-occur along environmental gradients, from for example, permanently flooded to terra firme forests, semi-deciduous to evergreen forests or open to dense canopy forests Fonteyn et al., 2023;R ejou-M echain et al., 2014;R ejou-M echain et al., 2021). Besides, central Africa is home to peculiar but widespread forest types which origins still remain debated, such as the monodominant Gilbertiodendron dewevrei forests (Hart et al., 1989;Katembo et al., 2020) and the so-called Marantaceae forests, a forest type with an understory dominated by giant herbs and hypothesized to correspond to an arrested succession (Pouteau et al., 2024). Central African forests and their fauna are, however, heavily threatened by both increasing human pressure (Lhoest et al., 2020;Vancutsem et al., 2021) and climate change (Bush et al., 2020;Kasongo Yakusu et al., 2023;Wimberly et al., 2023), highlighting the urgent need for characterizing and understanding the distribution of forest composition and structure at scales compatible with ecosystem management strategies. ...

Reference:

Combining satellite and field data reveals Congo's forest types structure, functioning and composition
The puzzling ecology of African Marantaceae forests

American Journal of Botany

... Forest growth dynamics function as a vital indicator of variability within forest architecture and functionality, encompassing phenomena such as ecological succession, disturbances, anthropogenic activities, and evolving climatic patterns (Coops 2015). The precise analysis and elucidation of arboreal transformations and their determinants, coupled with the adoption of appropriate stewardship approaches, are indispensable for augmenting tree vitality and informing effective silvicultural practices (Ndamiyehe Ncutirakiza et al. 2024). ...

Using high-resolution images to analyze the importance of crown size and competition for the growth of tropical trees
  • Citing Article
  • January 2024

Forest Ecology and Management

... Pastore et al. 2022). However, it's also important to note that specific tree species, their genetic makeup, local climate, age, competition, and other environmental factors can also influence tree growth, leading to exceptions or variations within these general patterns (Baker et al. 2003;Büntgen et al. 2007;Zielonka and Malcher 2009;Bowman et al. 2013;Filotas et al. 2014;Gourlet-Fleury et al. 2023). ...

Competition and site weakly explain tree growth variability in undisturbed Central African moist forests

... Les entreprises doivent garantir un risque nul ou négligeable de déforestation en assurant la traçabilité des produits et de la chaîne de valeur. Dans ce contexte, la définition des forêts est un enjeu crucial (Chazdon et al., 2016), car l'applicabilité du RDUE en dépend (Lescuyer et al., 2022). En particulier, l'inclusion ou non des parcelles agroforestières dans le périmètre d'application du règlement est un enjeu central. ...

Revue des enjeux liés à l'application du règlement européen de lutte contre la déforestation importée sur les politiques et les réformes de gouvernance relatives aux forêts dans les pays d'Afrique centrale

... They are home to 80% of the Earth's biological diversity and numerous endemic plant and animal species [2]. As a result, they play an important role in the sequestration of atmospheric carbon and contribute to the survival of both rural and urban populations through the ecosystem services they provide, such as dendroenergy and various non-timber forest products [3]. ...

Les tourbières de la cuvette centrale du bassin du Congo Réalités et perspectives

... Vertical and horizontal crown growth are rarely recorded in field data, as they are much more complex and time-consuming to measure than stem diameters. However, they are arguably much more ecologically meaningful when it comes to capturing whole-plant growth strategies and how these vary with tree size, such as hypothesised shifts in biomass allocation away from height growth and towards crown expansion as trees approach maturity (Antin et al., 2016;Marziliano et al., 2019;Jucker et al., 2022;Laurans et al., 2024). Similarly, they are much more informative when it comes to understanding competitive interactions for light and space among neighbouring trees (Jucker et al., 2015;Taubert et al., 2015), as well as providing a way to quantify crown damage and dieback, which are strong predictors of tree mortality (Needham et al., 2022a;Zuleta et al., 2022). ...

Tallo: A global tree allometry and crown architecture database

Global Change Biology

... They are eusocial insects and live in colonies comprising between a few hundred and several million individuals, composed of sterile castes (large and small workers and soldiers) and reproductive castes [2]. Termites are classified into 12 families and 330 genera [3], compromising 3015 species [4]. ...

Macrotermes termite mounds influence the spatial pattern of tree species in two African rainforest sites, in northern Congo. But were they really forests in the past?

Journal of Tropical Ecology

... In our study, we simply removed crowns that were known to have any liana coverage. The development of methods to map liana crowns in drone images (Kaçamak et al., 2022) would allow attributing flower correctly to host or liana, providing more precise information for individual tree crowns. ...

Linking Drone and Ground-Based Liana Measurements in a Congolese Forest

Frontiers in Forests and Global Change

... Journal of Tropical Forest Science 36(2): 150-164 (2024) population dynamics and has revealed many significant deviations (Table 3) from ONADEF values (Forni et al. 2019). Similarly, recent findings for tree mortality rates exhibited significant deviations from the usual value of 1% per year used throughout the Congo Basin (Ligot et al. 2022). Globally, it turns out that the values of the demographic parameters used in the calculation of the rate of reconstitution in Cameroon are potentially biased. ...

Tree growth and mortality of 42 timber species in central Africa
  • Citing Article
  • February 2022

Forest Ecology and Management

... Plot-level biomass data were generated using the collection of tree biomass measurements and a null model for the diameter structure of the forest. This null model had two entries: the stand density N and its basal area G. Following the hypothesis of demographic equilibrium, the null model assumed that the forest had a reverse-J shaped diameter distribution that could be 110 modeled by an exponential distribution (Muller-Landau et al., 2006;Picard et al., 2021). The parameter µ of this exponential distribution can be computed from N and G as: ...

Using Model Analysis to Unveil Hidden Patterns in Tropical Forest Structures