Robert M. Ewers’s research while affiliated with Imperial College London and other places

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Publications (243)


Groner_et_al_2025_TREE_SI.pdf
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April 2025

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Robert M. Ewers
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Figure I. Dynamic workflow for managing flood risks in tropical ecosystems through 'harmonized' ecosystem modeling. Left: proposed (dashed) and agreed (solid) parameterization of update intervals as a function
Harmonizing nature’s timescales in ecosystem models

Trends in Ecology & Evolution

Modeling complex, nonlinear ecosystem processes across different timescales presents a significant challenge. We identify two key issues: selecting a representative timestep that captures interconnected processes across various timescales, and simulating these processes in an appropriate sequence. By synthesizing existing ecosystem frameworks, we find shared compromises between biological realism and computational performance. For the representative timestep, these include ‘selective elimination of timescales’, ‘biting the bullet’, ‘each in their own time’, and ‘capture the unseen’. For processing order, we identify hierarchical, logical, iterative, and random approaches. Similar challenges exist in other disciplines, and we show how transferring methods from multiple fields, along with smarter computing, can improve timescale integration. Overcoming these challenges requires innovative transdisciplinary solutions, and we outline directions for future research.


Tropical forest clearance impacts biodiversity and function, whereas logging changes structure

January 2025

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1,123 Reads

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5 Citations

Science

The impacts of degradation and deforestation on tropical forests are poorly understood, particularly at landscape scales. We present an extensive ecosystem analysis of the impacts of logging and conversion of tropical forest to oil palm from a large-scale study in Borneo, synthesizing responses from 82 variables categorized into four ecological levels spanning a broad suite of ecosystem properties: (i) structure and environment, (ii) species traits, (iii) biodiversity, and (iv) ecosystem functions. Responses were highly heterogeneous and often complex and nonlinear. Variables that were directly impacted by the physical process of timber extraction, such as soil structure, were sensitive to even moderate amounts of logging, whereas measures of biodiversity and ecosystem functioning were generally resilient to logging but more affected by conversion to oil palm plantation.



Towards using virtual acoustics for evaluating spatial ecoacoustic monitoring technologies

December 2024

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128 Reads

Small microphone arrays and sound‐source localisation algorithms are increasingly prevalent in the passive acoustic monitoring (PAM) of ecosystems. These technologies enable analysis of natural soundscapes' spatial features, yielding additional insights into biodiversity and ecosystem health. While many of these technologies have been evaluated in the field, there is a lack of controlled, repeatable methods to test them. We developed an ambisonic virtual sound environment (VSE) for simulating real natural soundscapes to evaluate spatial PAM technologies. We validated this novel approach using a PAM recorder with a six‐microphone array, from which we extracted a typical suite of ecoacoustic metrics, including acoustic indices and avian species predictions and localisations from the software BirdNET and HARKBird, respectively. We first verified whether the VSE could replicate natural soundscapes well enough to test PAM technologies by comparing these metrics between field and VSE‐based recordings. To pilot the VSE as an environment for testing PAM hardware, we assessed how orientation impacts the six‐microphone array's performance by using the same suite of metrics to compare VSE recordings made with the array at various pitch angles. Finally, we piloted the VSE as a test platform for PAM software by investigating how BirdNET and HARKBird perform on bird calls added to the VSE‐replicated soundscapes. While the VSE and field recordings had similarities in some metrics, including spectral composition and BirdNET predictions, ambisonics' perceptual bias and susceptibility to spatial aliasing limited the spatial analyses that could be undertaken. Our trials nonetheless revealed that device orientation impacts the performance of HARKBird and certain ecoacoustic indices, and that BirdNET and HARKBird perform best on louder, more directional bird calls. Our results demonstrate the potential for this approach, but highlight limitations to using an ambisonics‐based VSE. We thus provide guidelines for the use and refinement of such systems towards more standardised, controlled benchmarking of PAM technologies, empowering practitioners to make more informed decisions on using these vital tools.


Fig. 1. The key processes incorporated into the Virtual Ecosystem. The model replicates the ecosystem dynamics in four ecological domains, each constructed as a separate module generating the dynamics of plants, animals, soil microbes and the abiotic environment respectively. The key metabolic processes that operate at the scale of individual organisms -plants, animals and microbes -are incorporated into the plant, animal and soil modules respectively. Modules will be dynamically connected through the transfer of matter and energy.
New insights to be gained from a Virtual Ecosystem

December 2024

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127 Reads

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3 Citations

Ecological Modelling

The myriad interactions among individual plants, animals, microbes and their abiotic environment generate emergent phenomena that will determine the future of life on Earth. Here, we argue that holistic ecosystem models – incorporating key biological domains and feedbacks between biotic and abiotic processes and capable of predicting emergent phenomena – are required if we are to understand the functioning of complex, terrestrial ecosystems in a rapidly changing planet. We argue that holistic ecosystem models will provide a framework for integrating the many approaches used to study ecosystems, including biodiversity science, population and community ecology, soil science, biogeochemistry, hydrology and climate science. Holistic models will provide new insights into the nature and importance of feedbacks that cut across scales of space and time, and that connect ecosystem domains such as microbes with animals or above with below ground. They will allow us to critically examine the origins and maintenance of ecosystem stability, resilience and sustainability through the lens of systems theory, and provide a much-needed boost for conservation and the management of natural environments. We outline our approach to developing a holistic ecosystem model – the Virtual Ecosystem – and argue that while the construction of such complex models is obviously ambitious, it is both feasible and necessary.


Figure 1. Study sites and study design. (a) Location of the study sites with respect to the 136 Indian subcontinent. Sample images taken from all four habitats are shown. (b) An enlarged 137 view of the scrubland habitat shows the various plots in each land use, along with sample 138 images from all three land uses. Five plots in each land use type were set up to record audio in 139 each habitat. 140 Audio Data Collection and Feature Extraction
Figure 2. GMM Training Workflow in a given fold of cross-validation. We first 178 standardised the columns of the audio feature vector. It was followed by a PCA to reduce the 179 dimensions of the training data. This PCA-reduced data was then segregated based on the land 180 use, and three GMMs were trained for the three land uses in each habitat. 181
Interpretable and Robust Machine Learning for Exploring and Classifying Soundscape Data

November 2024

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80 Reads

The adoption of machine learning in Passive Acoustic Monitoring (PAM) has improved prediction accuracy for tasks like species-specific call detection and habitat quality estimation. However, these models often lack interpretability, and PAM generates vast amounts of non-informative data, as soundscapes are typically information sparse. Here, we developed ecologically interpretable methods that accurately predict land use from audio while filtering unwanted data. Audio from habitats in Southern India (evergreen forests, deciduous forests, scrublands, grasslands) was collected and categorised by land use (reference, disturbed, and agriculture). We used Gaussian Mixture Models (GMMs) on top of a Convolutional Neural Network (CNN)-based feature extractor to predict land use. Thresholding based on likelihood values from GMMs improved model accuracy by excluding uninformative data, enabling our method to outperform models such as Random Forests and Support Vector Machines. By analysing areas of acoustic feature space driving predictions, we identified “keystone” soundscape elements for each land use, including both biotic and anthropogenic sources. Our approach provides a novel method for ecologically meaningful interpretation and exploration of large acoustic datasets independent of specific feature extractors. Our study paves the way for soundscape monitoring to deliver robust and trustworthy habitat assessments on scales that would not otherwise be possible.


Challenges for implementing zero deforestation commitments in a highly forested country: Perspectives from Liberia’s palm oil sector

October 2024

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25 Reads

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3 Citations

World Development

Halting deforestation is essential to address climate change and biodiversity loss. However, in highly forested, low-income countries like Liberia, “zero deforestation” commitments (ZDCs) adopted by companies may restrict agricultural expansion that has been promoted in national strategies to alleviate poverty. In such situations, examining contrasting perspectives among stakeholders is important to inform ZDCs’ implementation. Here, we applied Critical Systems Heuristics in 94 interviews to explore stakeholders’ perspectives on, and thereby develop a systematic understanding of, ZDCs in Liberia’s concession-based palm oil sector. We found that regulatory, institutional, and political factors that were needed to support commitments’ implementation were missing. Concessions had initially been allocated without communities’ consent being adequately obtained, and oil palm expansion had subsequently been stalled by zero deforestation. This produced a situation where communities that lost farmland to oil palm were reluctant to allow further expansion, while communities in forest areas were frustrated by a lack of promised oil palm expansion. Consequently, although limited oil palm expansion suggests ZDCs were effective after they were adopted, this was perceived to have come at the expense of anticipated improvements in community welfare, with community members in highly forested areas feeling deprived of development. We argue that neither the complete development of Liberia’s oil palm concessions nor limited development with zero deforestation will necessarily improve communities’ welfare without reforming the concession system to promote community-led, deforestation-free agricultural development. This requires public governance reforms, novel mechanisms for agricultural investment, and the localisation of international standards to facilitate zero deforestation in smallholder agriculture.


Tropical beetles more sensitive to impacts are less likely to be known to science

August 2024

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230 Reads

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11 Citations

Current Biology

Insects are posited to be declining globally. This is particularly pertinent in tropical forests, which exhibit both the highest levels of biodiversity and the highest rates of biodiversity loss. However, for the hyper-diverse tropical insects there are scant data available to evidence declines. Understanding tropical insect diversity and its response to environmental change has therefore become a challenge, but it is estimated that 80% of tropical insect species remain undescribed 1 . Insect biodiversity predictions are based mostly on well-studied taxa and extrapolated to other groups, but no one knows whether resilience to environmental change varies between undescribed and described species. Here, we collected staphylinid beetles from unlogged and logged tropical forests in Borneo and investigated their responses to environmental change. Out of 252 morphospecies collected, 76% were undescribed. Undescribed species showed higher community turnover, reduced abundance and decreased probability of occurrence in logged forests. Thus the unknown components of tropical insect biodiversity are likely more impacted by human-induced environmental change. If these patterns are widespread, how accurate will assessments of insect declines in the tropics be?


Stand‐level stem CO2 efflux (EA) along the logging gradient from old‐growth (green) to moderately (twice logged; light brown) and heavily logged (four times logged; dark brown), with EA partitioned into maintenance (dotted) and growth (lines) respiration. There was no difference in stand‐level EA between logged and old‐growth plots (T‐test; P = 0.59). Error bars represent propagated SE of stand‐level EA (a). Mean tree‐level EA, with SE, along the logging gradient, whereby tree‐level EA was significantly higher in logged than old‐growth plots (Wilcoxon signed‐rank test; P = < 0.001, b). Stem surface area index (SAI) along the logging gradient with error bars that represent surface area index error, which was assigned as 10% based on the uncertainty in allometry based on Robertson et al. (2010). SAI was significantly higher in old‐growth than logged plots (T‐test; P = 0.03, c). Stand‐level stem carbon use efficiency (CUE), which was calculated as woody stem net primary productivity/(woody stem net primary productivity + stand‐level EA), along the logging gradient. Stem CUE was significantly higher in logged than old‐growth plots (T‐test; P = 0.039). Error bars represent propagated SE of stand‐level CUE (d). For plot codes, see Table 1.
Tree‐level stem CO2 efflux is higher in logged than old‐growth plots (P < 0.001). Tree‐level EA increases with increasing growth rate (P < 0.001); (a) and with tree diameter at 1.3 m height (DBH; P < 0.001); (b), as determined by a generalised linear model. Axes are shown with logarithmic scaling. Brown line represents logged plots (moderately logged–light brown triangles; heavily logged–dark brown squares) and green line represents old‐growth plots (green circles), with ±95% confidence intervals.
Partial least squares regression (PLS‐R) variable importance projection scores (a, c) and coefficients (b, d) for the variables that influence tree‐level stem CO2 efflux (EA) in logged (brown) and old‐growth (green) forest plots. Asterisk (*) indicates variables that were significant within the model as determined by Jack‐knifing (P < 0.05), solid outline represents coefficients from Component 1 (b, d) and dashed outline represents coefficients from Component 2 (b). Trait acronyms and abbreviations are as follows, whereby δ¹⁵N is foliar 15N isotope, Pm is foliar phosphorus content, lumen fraction is vessel lumen fraction, N. Vessels is number of vessels within wedge, DBH is stem diameter at 1.3 m height, δ¹³C is foliar 13C isotope, subplot BA is the basal area of trees in a 20 × 20 m subplot minus the basal area of the target tree (as a proxy for competition) and Npa is foliar nitrogen. Subscripts ‘pa’ and ‘m’ indicate units per leaf area (mg mm⁻²) and per leaf dry mass (mg g⁻¹), respectively. Further variable descriptions can be found in Supporting Information Table S1 and output in Table S2.
Linear model between stand‐level stem CO2 efflux (EA) and basal area (BA) by forest type (old‐growth, green; logged, brown) (R² = 0.51, P = 0.05) (a). Linear model between stand‐level EA and stem surface area index (SAI) by forest type (R² = 0.61, P = 0.026) (b). Stand‐level stem carbon use efficiency declines with increasing BA (c; R² = 0.53, P = 0.02). Stand‐level maintenance respiration increases with increasing stem SAI (d; R² = 0.59, P = 0.009). Error band represent 95% CI and old‐growth plots are represented by green circles, moderately logged plots by light brown triangles, and heavily logged plots by dark brown squares. For plot codes, see Table 1.
Stand‐level stem CO2 efflux declines with increasing soil magnesium and soil phosphorus (a; R² = 0.63, P = 0.02), and maintenance respiration declines with increasing soil calcium (b; R² = 0.73, P = 0.002). Explanatory variables are log‐transformed, x‐axes are shown with logarithmic scaling and error bands represent ±95% confidence interval. Old‐growth plots are represented by circles, moderately logged plots by triangles and heavily logged plots by squares. For plot codes, see Table 1.
From tree to plot: investigating stem CO2 efflux and its drivers along a logging gradient in Sabah, Malaysian Borneo

August 2024

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203 Reads

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2 Citations

Stem respiration constitutes a substantial proportion of autotrophic respiration in forested ecosystems, but its drivers across different spatial scales and land‐use gradients remain poorly understood. This study quantifies and examines the impact of logging disturbance on stem CO2 efflux (EA) in Malaysian Borneo. EA was quantified at tree‐ and stand‐level in nine 1‐ha plots over a logging gradient from heavily logged to old‐growth using the static chamber method. Tree‐level results showed higher EA per unit stem area in logged vs old‐growth plots (37.0 ± 1.1 vs 26.92 ± 1.14 g C m⁻² month⁻¹). However, at stand‐level, there was no difference in EA between logged and old‐growth plots (6.7 ± 1.1 vs 6.0 ± 0.7 Mg C ha⁻¹ yr⁻¹) due to greater stem surface area in old‐growth plots. Allocation to growth respiration and carbon use efficiency was significantly higher in logged plots. Variation in EA at both tree‐ and stand‐level was driven by tree size, growth and differences in investment strategies between the forest types. These results reflect different resource allocation strategies and priorities, with a priority for growth in response to increased light availability in logged plots, while old‐growth plots prioritise maintenance and cell structure.


Citations (76)


... High microclimate heterogeneity of intact forests provides thermal refugia for diverse groups of forest dwellers (Senior et al., 2018;Woods et al., 2015), particularly in the tropics where ectotherms are under greater thermal stress under climate change (Giam, 2017;Hoang & Kanemoto, 2021;Scheffers et al., 2014;Zellweger et al., 2020). However, this buffering effect may diminish with habitat disturbance caused by human activity and extreme climatic events (Marsh et al., 2025;Senior et al., 2017; but see Senior et al., 2018), which can reduce canopy cover and vegetation complexity, thereby simplifying the biotic and abiotic environments within forests (Santos et al., 2024;Senior et al., 2017). ...

Reference:

Butterflies respond to habitat disturbance in tropical forests through activity shifts
Tropical forest clearance impacts biodiversity and function, whereas logging changes structure

Science

... For systemic transformation to occur and last, both institutions and behaviour have to change (Lyons-White et al., 2025;Sterman, 2008;Tengberg & Valencia, 2018). Acknowledging the distinction between formal and informal institutions (North, 1990;Pejovich, 2006), change is thus required in three dimensions: informal norms, formal regulations, and behaviour. ...

Challenges for implementing zero deforestation commitments in a highly forested country: Perspectives from Liberia’s palm oil sector
  • Citing Article
  • October 2024

World Development

... While these models have made notable progress in balancing biological realism with computational performance, they rely on compromises to address the challenges of multiple timesteps. Such compromises are typically guided by the model's intended purposewhether to enhance understanding of ecosystem dynamics [15], predict ecosystem responses under alternative scenarios [13], or inform management decisions [16] and the sensitivity of the system to timescale choices, which can vary depending on the processes being modeled [17,18]. Here we discuss the trade-offs and implications of four commonly used approaches to dealing with multiple timescales. ...

New insights to be gained from a Virtual Ecosystem

Ecological Modelling

... This process of biodiversity loss, through which unique organisms, many of which have yet to be described, are disappearing (Cardoso et al., 2020), threatens essential ecosystem services (Costanza et al., 2014). It has been described as the Earth's sixth mass extinction event (Ceballos et al., 2017;Cowie et al., 2022) and is disproportionally affecting invertebrates, the least understood animal group from taxonomic and biogeographical perspectives (Boyle et al., 2024), and which also represents the largest proportion of known Earth's biodiversity (Schuldt and Assmann, 2010). Invertebrates in general, and insects in particular, inhabit all types of environments, both terrestrial and aquatic (Leandro et al., 2017), playing key roles in numerous ecological processes (Schuldt and Assmann, 2010), such as decomposing organic matter and pollinating more than 75 % of flowering plants (Ollerton et al., 2011). ...

Tropical beetles more sensitive to impacts are less likely to be known to science
  • Citing Article
  • August 2024

Current Biology

... In tropical rainforests, EA is a substantial contributor to the carbon budget, accounting for 23-42% of autotrophic respiration (Mills et al., 2023) and c. 13-25% of total ecosystem respiration (Chambers et al., 2004;Cavaleri et al., 2006;Malhi et al., 2009;Mills et al., 2023). EA is highly reflective of tree metabolism and can provide vital information about forest allocation and investment strategies (Mills et al., 2024), and response to environmental pressures such as drought (Rowland et al., 2018) and elevational gradients (Zach et al., 2008(Zach et al., , 2010Robertson et al., 2010). Yet, current methods of estimating EA allow for a large potential for bias and uncertainty. ...

From tree to plot: investigating stem CO2 efflux and its drivers along a logging gradient in Sabah, Malaysian Borneo

... However, this information is critical for accurately attributing detected animals to a specific site or field in the context of RBP, especially when field parcels are small. Acoustic localisation techniques, which can pinpoint the precise location of animals as sound sources in space, are under development (Buchmann and Schurr, 2024;Rhinehart et al., 2020), with recent technological advances further facilitating this process (Heath et al., 2024). These methods, however, can be costly and are currently too complex for application in RBP. ...

Spatial ecosystem monitoring with a Multichannel Acoustic Autonomous Recording Unit (MAARU)

... pnas.org from logging is too low to have zero impact on biodiversity, recent work in Southeast Asia suggests low intensity logging (<29% biomass removal) is associated with largely intact functional composition ( 32 ). Given logged structurally degraded forests under high human pressures can still harbor considerable biodiversity and maintain ecosystem functioning ( 33 -35 ), it would be worth restoring logged forests of lower integrity wherever feasible as opposed to converting them into agricultural lands or monoculture plantations. ...

Thresholds for adding degraded tropical forest to the conservation estate

Nature

... We summarized taxon responses from 8,130 combinations of surveys and taxa. We compiled biodiversity data from 55 published data sources (Supplementary Table 1), from which we extracted presence-absence data following the methods of ref. 123. Previous analyses of multi-taxa biodiversity data have demonstrated that comparisons of presence-absence data among taxa are more robust than analyses of abundance data 23,124 . ...

Variable responses of individual species to tropical forest degradation

... By necessity, a large focus has been placed on detection as the first step in any analysis pipeline [6]; this corresponds to identifying the presence of animals in soundscapes, often passively acquired by sensors placed in fixed positions and recording continuously. Moreover, this is linked to a key promise of bioacoustics: the automatic, continuous monitoring of biodiversity. ...

Propagating variational model uncertainty for bioacoustic call label smoothing

Patterns

... Regarding software, soundsource localisation algorithms continue to improve, partly thanks to deep learning methods (Grumiaux et al., 2022) and the development of localisation applications for animal vocalisations, such as the avian call localisation tool HARKBird (Sumitani et al., 2019;Suzuki et al., 2017). Together these spatial PAM hardware and software developments are providing superior metrics of ecosystem health and biodiversity (Wijers et al., 2019), including species abundance estimates (Blumstein et al., 2011;Heath, 2022). ...

The Assessment and Development of Methods in (Spatial) Sound Ecology