Abstract
The three-dimensional arrangement of plant components, both within and among individual trees, is fundamental for characterizing forest ecosystems. This structure not only influences but also responds to environmental changes, playing a key role in regulating light regimes, forest productivity, as well as physiological and biophysical processes. Over the past few decades, terrestrial laser scanning (TLS, or terrestrial LiDAR) has provided a unique perspective of this 3D structure, offering new insights into ecological processes and forest disturbances, as well as enhancing structural assessments in forest and carbon inventories. Here, we examine recent advancements in TLS and its applications in forest science. We also explore how increasing computational power, alongside the rise of artificial intelligence, is empowering researchers to tackle more complex questions, paving the way for breakthroughs in understanding forest ecosystem dynamics in a changing world.
Similar content being viewed by others
Introduction
Remote sensing has revolutionized our understanding of forests worldwide. Since the first Earth observation missions were launched in the 1970s, remote sensing has contributed to quantifying and monitoring forest extent1,2, as well as forest functioning3. From tropical to boreal forests, these technologies have enabled us to track habitat loss4, ecosystem health5, and carbon storage6 at unprecedented spatial coverage and analytical depth, becoming an essential tool in monitoring key planetary boundaries related to land system change and climate regulation7,8.
Over the past decades, the field of forest remote sensing has made fast advancements in both methodological and computational capabilities. The field has shifted from simply mapping landscapes to actively monitoring dynamic processes at increasingly near real-time9. The ability to analyze the physiological and structural characteristics of forests has rapidly become both technically and operationally feasible. Light Detection and Ranging (LiDAR, also known as laser scanning) sensors mounted on aerial platforms have added a new dimension to these capabilities. By emitting laser pulses to measure distances, LiDAR technology provides precise and accurate, three-dimensional measurements of forest canopies. Although the first applications of airborne laser scanning (ALS) in forest studies began in the 1980s10,11, its widespread adoption did not gain momentum until after the 2000s12. Since then, LiDAR has become the remote sensing gold standard for quantifying forest structural characteristics such as canopy height and cover, and topographical features of the forest floor.
Among the remote sensing tools available to scientists, none provides a more accurate and detailed view of forest structure than terrestrial LiDAR technology, also known as terrestrial laser scanning (TLS). Unlike airborne systems, TLS instruments are positioned at ground level, allowing them to capture detailed measurements of both the forest understory and the upper canopy. Compared to other ground-based methods, such as mobile laser scanning, terrestrial photogrammetry, or traditional inventory techniques, TLS offers superior geometric accuracy and structural completeness, particularly for detailed modeling of individual trees and stand structure.
The adoption of TLS is much more recent in comparison to other remote sensing tools, increasing quickly from around 2010 onwards (Table 1). The first review articles on TLS applications in forests appeared in 2011, offering foundational insights into using TLS to assess forest structure, including tree height, stem diameter, and biomass13. Subsequent reviews highlighted TLS’s ability to improve plot-scale forest measurements and estimate tree metrics14, as well as its broader applications across forest science disciplines15. More recent reviews have summarized key developments and future challenges in TLS, reflecting the growing and diversifying TLS research community16,17. However, with the fast adoption of TLS for studying vegetation, substantial progress has been made beyond these latest assessments.
Although many factors have contributed to the uptake of TLS in forest studies, three aspects stand out: price, speed, and size. While high-end TLS instruments—typically characterized by high ranging accuracy and long effective range—remain prohibitively expensive for many research groups, the availability of more affordable devices has substantially increased in recent years, making the technology more accessible. Recent instruments are not only lighter but also offer significantly faster point acquisition rates. In addition, modern scanning protocols have become more efficient, as many systems no longer require fixed calibration targets for registration, reducing setup time and enabling faster fieldwork workflows18. These improvements allow researchers to cover greater areas more rapidly with multiple scan positions, which helps reduce occlusion and improve the completeness of forest structural data.
While increased accessibility and hardware improvements to TLS instruments have reduced or eliminated major data collection bottlenecks, extracting accurate information from the resulting point clouds remains a significant challenge. Recent algorithmic advances, including co-registration methods19, deep learning approaches for crown delineation20, and automated pipelines for large-scale tree extraction21, are streamlining TLS data processing and enabling more efficient analysis of complex point clouds. Together, these developments are expanding the scope of ecological research and transforming how we study forest structure and dynamics. This review provides a forward-looking assessment of the use of TLS technology in forest studies. We outline advancements made over the past years, explore emerging questions that TLS has the potential to address, and highlight the key challenges and bottlenecks that still limit its broader adoption and application.
TLS and increasing realism in modeling forests
The rapid increase in our ability to use TLS to capture extremely detailed 3D descriptions of tree and forest structure has led to an increasing interest in so-called “digital twin” or virtual forest approaches16,22. But what does this mean in practice: do digital twins represent a useful new conceptual framework, a rebadging of “a model” or somewhere in between? There is no doubt that the concept of digital twins is being used to underpin some very large initiatives in linking climate, observation, and modeling (https://destination-earth.eu/).
According to Batty23 the term digital twin was coined in the early 2000s by Michael Grieves24 and has subsequently been used in a range of contexts. In its original sense, a digital twin represents a digital mirror image of a physical process, designed to match it precisely in both space and time, with a bidirectional flow of data between the physical and digital counterparts. A model, on the other hand, is generally considered as an abstraction of a physical process, keeping the key elements we are interested in, but simplifying or even ignoring those we are not. A model is therefore a simplified representation of a physical system, whereas a digital twin implies a representation with the maximum detail we can provide23.
A good example of where TLS has facilitated this distinction between a model and a digital twin is in the process of representing radiative transfer in vegetation22,25. This is a crucial application for quantifying and understanding the processes affecting canopy photosynthesis, modeling the Earth’s radiation budget, and biophysical feedback between vegetation and climate26. A great deal of work has gone into developing simplified radiative transfer models of vegetation for successful global monitoring of vegetation properties27,28, using a range of approximations to represent, for example, leaf and soil scattering properties, leaf amount, and physical arrangements in space. However, an alternative approach has been to represent the 3D physical canopy as accurately as possible, including every leaf or needle, branch, and soil element in 3D, and then solving the radiative transfer problem using, for example, Monte Carlo ray tracing (MCRT)29,30.
A limitation in this high-detail MCRT approach, however, is that it requires the spectral properties of every canopy element, including leaves, bark, and soil, to be known. In practice, acquiring such detailed measurements for every forest is not feasible, which prevents the use of these models for inversion—that is, retrieving canopy properties from remotely sensed reflectance. Between simplified parametric models and full 3D reconstructions, intermediate approaches like voxel-based representations (used in models, e.g., DART31) offer a balance between structural realism and computational efficiency, and can be parameterized with TLS data. Thus, rather than serving in large-scale monitoring applications, radiative transfer models based on TLS data help create a detailed scientific understanding of how forest structure influences multi-angular scattering processes of forest canopies22. TLS data can also broaden the scope for modeling canopy scattering, such as estimating photon recollision probability within forest canopies32. The progression of canopy realism in radiative transfer is illustrated in Fig. 1.
On the left, parametric radiative transfer models depict forests as simple geometric shapes or approximations. In contrast, TLS-based reconstructions (right) provide high-resolution models of forest stands, including individual tree structures, detailed branching systems through quantitative structure models (QSMs), and foliage elements. TLS instruments capture dense 3D point clouds by scanning forests from multiple ground-based positions. These point clouds can then be processed to reconstruct tree geometry, crown shapes, and canopy surface details, supporting realistic structural inputs for modeling frameworks. The integration of TLS data into advanced modeling frameworks supports full forest reconstructions with applications in radiative transfer simulations, enhancing the realism of digital twins for forest ecosystems.
Another area where TLS is enabling this progression from simplified models to digital twins is in functional structural plant modeling (FSPM). The FSPM approach seeks to model the external structural expression of underlying genetic and phenotypic behavior33,34. FSPMs predict the 3D plant structure that arises from these underlying behaviors. The difficulty is testing and validating these structural predictions for real trees. There have been various attempts to couple 3D tree structure with FSPMs via manual measurements and even procedural models33,35. However, the advancements in TLS have opened the way to a much more effective parameterization of FSPMs, as well as direct tests of their predictions. O’Sullivan et al.34 suggested that TLS will contribute to FSPM development in two key areas: first, by parameterizing static FSPMs to simulate interactions between structure, environment, and physiology; and second, by enabling the testing and calibration of dynamic FSPM predictions to explore ecological and environmental hypotheses. Potapov et al.36, for example, developed a stochastic version of an existing FSPM (LIGNUM) for producing tree structures consistent with detailed TLS data. Sievänen et al.37 used TLS measurements of pine trees of different ages to construct a pseudo-time series of growth of a single tree. They used an FSPM to stochastically simulate crown development to match the TLS-derived crown development and suggested the resulting best-matching FSPM parameters represent the underlying crown development mechanisms. This ability to establish quantitative links between structure and function has enabled the development of a so-called structural economics spectrum, embedding tree size and structural diversity in the wider framework of plant resource use38.
Advances in capturing tree and forest structure via TLS are enabling the transition from simplified structural representations to digital twins, with very high levels of structural detail, using so-called quantitative structure models (QSMs), the algorithmic enclosure of point clouds in topologically-connected, closed volumes39,40. This, in turn, throws up some interesting challenges in terms of how best to use or interpret this detail. In radiative transfer modeling, for example, the challenge is no longer one of representing structure, but how to assign the underlying scattering properties of that structure—the leaves, branches, soil, etc. that make up the resulting scene model. This process will look very different across different wavelength domains, from the shortwave visible to thermal and microwave. In the case of FSPMs, a challenge will be how to feed back the phenotypic information expressed in observed structure to the underlying functional process representation. Challenges of course open further opportunities.
Returning to the question of whether digital twins represent something new and useful for forest monitoring, in the sense used here at least, digital twins are different from models and serve a different purpose. In essence, they allow us to move away from assumptions about tree and forest structure that have been imposed on us simply because of our inability to make the necessary measurements. TLS data are breaking this barrier down, which will benefit a wide range of ecological and environmental applications. The following sections explore these advancements at various levels. We discuss how TLS provides detailed insights into individual tree morphology, supports forest inventories, and aids in quantifying both the structural complexity of forest habitats and the impact of disturbances within these ecosystems.
Understanding the architecture of trees
Tree architecture, also known as tree structure or morphology, refers to the 3D size and arrangement of a tree’s fundamental components (e.g., trunks, twigs, branches, leaves, and needles). The aboveground arrangements determine the efficiency of light capture for photosynthesis, influence competition for resources, and affect ecological processes such as carbon storage, water, and nutrient cycling41. As a result, commonalities exist in the overall structure of different tree species, particularly in the stem and branching patterns, and in their functional roles within the ecosystem.
The architecture of a tree results from the interaction between genetic factors ultimately linked to the plant’s functional strategies (i.e., reproduction) that dictate morphological characteristics unique to each species and both long-term and short-term adaptations to the environment42. These adaptations are influenced by a variety of factors, including biotic pressures like competition for space and increases in liana abundance43, as well as abiotic elements such as light and water availability44,45. Additionally, wind (an abiotic factor) can influence tree architecture both by causing mechanical damage, particularly in structurally unstable trees, and by driving acclimation processes that shape tree form over time46. These effects can extend to neighboring trees and alter overall forest canopy structure46. Therefore, quantifying tree architecture can provide useful information for improving forest management strategies, assessing ecosystem productivity, and modeling carbon dynamics.
Architectural metrics, such as stem diameter, tree height, and crown area, can be easily measured from TLS point clouds47. However, capturing more complex metrics, such as branching patterns and woody volumes, requires more advanced modeling approaches to reconstruct the three-dimensional distribution of tree components16. QSMs of trees can capture the woody branching structure in detail, including the 3D topological branching pattern, as well as the diameters, lengths, surface areas, angles, and volumes of the stems and branches (Fig. 2). Typically, these models consist of a hierarchical collection of geometric primitives, mostly cylinders, which locally approximate the diameter and general geometry of the stem and branches. Collectively, these primitives provide an approximation of the entire woody structure, including the total woody volume48.
The QSM was generated using the TreeQSM algorithm and consists of cylinders approximating the tree’s woody component. Each branch is displayed in a different color. Four panels highlight quantitative structural information computed from the model. A The total branch length per branch order (excluding the stem), highlighting the distribution of smaller, higher-order branches. B Branch volume distribution across orders, indicating that larger branches are concentrated in lower orders. C Branch volume to height, showcasing how woody branch volume is distributed vertically within the tree. D The relationship between branch segment (excluding the stem) diameter and volume, emphasizing the contribution of smaller diameters to overall tree volume.
Several methods exist for generating QSMs from point cloud data, each with different assumptions and outputs. These include TreeQSM40, SimpleForest (formerly known as SimpleTree)48, which is part of the broader Computree platform49, 3D Forest50, and AdQSM51. More recent developments include TreeGraph52 and L1-Tree53. Most methods follow a common workflow: segmenting the point cloud into stems and branches, followed by cylinder fitting to reconstruct geometry. However, some methods, such as Treegraph52 and TreeQSM40, first derive a complete topology before addressing volume. Differences also arise in implementation: TreeQSM, for example, requires MATLAB, while some offer standalone or open-source solutions. These methods were also built for different purposes, such as targeting the volume or branching structure, and have been validated for different metrics. It is noteworthy that there is not a lot of validation data for many of the more complex metrics, such as individual branch diameters and lengths.
The processing of TLS point cloud data presents major challenges that impact the accuracy of QSM methods. The first is the need for a leaf-wood separation pre-processing step. This step is crucial because leaves can both obscure woody components and emulate them in the point cloud, potentially confusing QSM algorithms and leading to the creation of artificial branching structures. Another challenge is occlusion, where parts of the stem or branches may not be captured due to limited visibility from the scanner positions. Furthermore, accurate segmentation of individual trees from dense plot-level point clouds remains a critical bottleneck, especially in structurally complex forests. Recent advances in artificial intelligence are helping to overcome these challenges. Convolutional neural networks and point-based classifiers have achieved high accuracy in distinguishing foliage from woody elements in complex canopies54,55. To address occlusion, generative models and deep completion networks are being used to infer missing structural details and reconstruct plausible tree geometry from incomplete point clouds56. In the case of individual tree segmentation, 3D deep learning segmentation frameworks are now enabling automated, high-precision delineation of individual trees across a range of scanning platforms, reducing the reliance on manual input and improving scalability20,57.
Additionally, the accuracy of total tree volume estimates using QSMs is heavily influenced by the visibility of the tree structure in TLS data, making reliable volume and biomass estimates (assuming wood density is known) highly dependent on data quality. For many species, the total tree volume primarily consists of the stem and large branches, which are the most visible components in TLS data. Due to the centimeter-scale size of LiDAR laser beams upon contact with trees, point clouds often overestimate the diameters of small branches, leading to inflated volume estimates in QSMs58. One approach to address this overestimation is to apply filtering techniques or to incorporate actual twig diameter measurements59 to adjust the cylinder diameters for greater accuracy. More generally, estimates of the size and shape of small or distant branches, particularly those with diameters close to the TLS footprint, are likely to be unreliable without strong validation. These structural uncertainties propagate into biomass estimates, especially when combined with intra-tree and intra-species variability in wood density.
A new asset in forest inventories
Forest inventories have long been employed to assess and monitor the condition, composition, and changes in forests over time. These inventories provide important data for understanding forest resources, informing policy decisions, and assessing carbon stocks and biodiversity. For instance, National Forest Inventories (NFIs) are an essential tool for countries to report on their forest status to international organizations and agreements, such as the Food and Agriculture Organization or the United Nations Framework Convention on Climate Change. ALS has been adopted already for decades in operational and commercial forest inventories, particularly in Nordic countries, to enhance efficiency.
Research studies and reviews commonly agree on the technological readiness of TLS for operational inventories, in particular with respect to accurate geometric measurements at the centimeter to millimeter scales15,16,17. Recent benchmarking studies have shown that TLS can estimate tree attributes such as diameter at breast height (DBH) with errors typically below 2 cm and stem curve profiles with comparable accuracy in boreal forests60. In tropical agroforestry systems, TLS has also produced strong correlations with field-based measurements of canopy openness (r = 0.79) and tree height (r = 0.58)61. These findings confirm that TLS provides structural estimates comparable in accuracy to conventional methods, while also capturing three-dimensional complexity beyond what field inventories typically offer.
TLS therefore delivers not only standard inventory metrics, but also allows estimation of structurally detailed attributes that are typically unmeasured in the field, such as crown area and volume, foliage clumping (relevant for modeling light interception)62, and the space around a tree (for assessing growth potential)63 (Fig. 3). Given that the raw point clouds record rich 3D information, previously collected TLS data can be reprocessed to extract novel metrics as algorithms improve, even years after the original data collection. Moreover, the possibility of increasing sampling plot size with TLS compared to traditional inventories has been discussed to improve the representativity of samples and the link to airborne and satellite remote sensing data17,63.
TLS instruments collect detailed 3D point clouds of forest plots, enabling accurate measurement of both tree- and stand-level structural attributes. At the tree level, TLS enables detailed measurements of tree height, crown dimensions, branching, and stem form, along with temporal monitoring. At the stand level, TLS provides metrics like basal area, competition indices, canopy height, and structural complexity, complementing traditional inventory methods with higher accuracy and expanded measurement capabilities.
Deriving additional information from inventory data, such as stem volume and tree biomass, strongly relies on estimates from allometric models. Ensuring the reliability of these models is therefore critical for accurate assessments. In some recent NFIs, differences in stem volume estimates have been observed when using models with varying predictors, such as two (DBH and height) versus three (DBH, height, and diameter at 6 m) variables. To address such discrepancies, projects utilizing TLS data have been undertaken to develop improved stem volume models64,65. For example, studies have shown that stem form can vary over time64 and across regions65,66, with changes most pronounced in the lower parts of tree stems. These findings highlight the importance of regionally calibrated allometric models and the potential of TLS data to capture variability in stem form across tree species and geographic areas.
Forest management, which includes activities such as thinning, clear-cutting, and selective harvesting, can have significant effects on tree growth, particularly in terms of stem form. For instance, management practices aimed at reducing competition for light and nutrients can influence how trees allocate resources to their trunks, resulting in changes in stem and branch diameters, height, and form. TLS has proven effective in assessing growth changes in trees after forest management interventions, capturing structural changes in tree morphology67,68,69. It has also been employed to generate competition indices using crown information, which improves upon traditional approaches relying solely on DBH or height70,71. Furthermore, point clouds derived from TLS enable a more comprehensive assessment of tree competition by quantifying the occupied space around trees, providing detailed insights into tree interactions and their surroundings72,73.
TLS data has been used in characterizing differences in stem form over both time and space64,74. For instance, bitemporal TLS data were used to capture stem growth dynamics, volumetric changes, and localized deformations, providing useful insights into tree responses to environmental factors and management interventions72,75. Bitemporal TLS data were also applied to assess changes in stem shape and identify relationships between stem deformation and drought stress, highlighting how environmental factors can influence tree morphology over time76. Interannual TLS data have further enhanced the understanding of tree dynamics. Seasonal radial growth has been detected in TLS point clouds collected before and after the growing season, although the study also highlighted important challenges in detecting millimeter-scale changes in stem diameter77. Furthermore, defoliation was assessed from TLS scans conducted during a single growing season and linked to independently measured growth losses69.
High temporal resolution TLS data of individual trees, e.g., once every 30–60 min, are also becoming increasingly accessible78,79. Multi-temporal approaches enable the monitoring of tree structural dynamics, such as movement and responses to environmental factors, at detailed temporal scales, offering deeper insights into plant physiology and interactions with their surroundings. Campos et al.80 presented a measurement station that collects TLS data with high temporal resolution, whereas Wang et al.81 developed a tool quantifying plant movements from point cloud time series. These datasets were used by Yrttimaa et al.82 in assessing height and diameter growth of individual trees.
In the context of forest inventories, determining the tree species is relevant for several applications. Although allometric models based on tree height and stem diameter are not necessarily species-specific, TLS-based allometric models could vary across species, caused by species-specific branching patterns and crown sizes83. Even though classification algorithms have been proposed84,85,86, their performance often falls short of inventory needs due to limited training data, sensitivity to scan conditions, and the difficulty of distinguishing species with similar shapes. Finally, best practices and standardization in field protocols are required for adoption in NFIs15. As technology advances rapidly, time series of TLS data face the challenge of comparability: point clouds acquired with different types of scanners may vary, and there is a need to ensure the reliability of attributes derived from possibly very different datasets.
From trees to forests: dynamics, functioning, and habitat complexity
Moving from trees to forests, stand-level canopy structure represents the spatial occupation and arrangement of individual trees, along with their leaves, branches, and stems87,88, and plays a crucial role in regulating forest ecosystem functions89,90. A fundamental step toward understanding this structure is quantifying how plant components are distributed in three-dimensional space.
Voxel-based approaches are particularly effective in this context, as methods have been developed to account for occlusion and enable the transformation of raw TLS point clouds into spatially explicit, biophysically meaningful estimates, such as plant area density91,92. Similarly, TLS-derived gap fraction metrics are important for describing canopy openness, which not only characterizes structural properties but also influences ecological processes such as light penetration and microclimate regulation93,94. Building on these foundational measurements, the concept of canopy structural complexity integrates multiple dimensions of forest organization, offering a more holistic perspective on how forest structure underpins ecosystem function95,96.
From the perspective of biodiversity measurement, McElhinny et al.96 reviewed stand structural complexity and characterized it by the richness and abundance of structural attributes, where commonly used attributes include DBH, tree height, and leaf area index. However, these metrics alone do not fully capture the spatial occupation and arrangement of canopy elements. TLS provides precise positional data for canopy elements, allowing to directly describe canopy structural complexity based on the three-dimensional spatial distribution of canopy elements95,97.
Recent studies emphasized that a comprehensive quantification of forest canopy structural complexity should include volumetric capacity, spatial arrangement, and the identity or functional traits of canopy elements98. However, current technology for extracting species and functional traits using TLS data remains limited99. Consequently, canopy structural complexity derived from TLS data primarily focuses on volumetric capacity and spatial arrangement. With advancements in the conceptualization of canopy structural complexity, this attribute is increasingly valued for its role in elucidating forest ecosystem functions. For example, Hardiman et al.100 found that increasing canopy structural complexity provides a mechanism for the potential maintenance of productivity in aging forests where the leaf area index cannot increase.
Forest canopy structural complexity is shaped by the spatial filling of individual trees, with species-specific modification strategies in crown architecture serving as key determinants. Species with different ecological functions can occupy distinct vertical canopy layers based on their ecological niches. A typical example is that light-demanding species often dominate in environments with higher light availability in the upper canopy and canopy gaps, while shade-tolerant species can grow and survive in the lower canopy layers of late-successional forests101,102. Genotypic variability allows tree crowns to complement each other, while phenotypic plasticity enables them to adjust their shape and size in response to local competition, thereby optimizing the use of canopy space102,103,104. Precise structural information extracted from TLS data is boosting the study on these phenomena105,106.
On a larger scale, canopy structural complexity and these related biotic determinants would be influenced by abiotic factors such as climate and soil45,87,107. Ehbrecht et al.104, using TLS data from 279 plots, demonstrated that annual precipitation and its seasonality largely explain the variation in forest structural complexity in primary forests across all major forested biomes, with more humid climates supporting greater complexity.
Although canopy structural complexity has become a prominent attribute in forest ecosystem research, the methods for quantifying this complexity vary across studies. Metrics derived from TLS data to assess canopy structural complexity can be categorized into three types: horizontally, vertically, and unified metrics95,108. Horizontally metrics (e.g., canopy cover, canopy occlusion, Fig. 4A) primarily quantify the distribution of canopy elements on the horizontal plane, which cannot account for their vertical arrangement109. In contrast, vertically metrics (e.g., foliage height diversity, effective number of layers, Fig. 4B) capture the vertical heterogeneity of canopy elements while potentially overlooking their horizontal distribution97,110. Unified metrics aim to quantify forest canopy structural complexity by integrating both horizontal and vertical arrangement and distribution, addressing the limitations of metrics that consider only one orientation108. Currently, commonly used unified metrics include canopy entropy (Fig. 4C), canopy rugosity, clumping, and stand structural complexity index62,107,111. These metrics quantify canopy structural complexity from different perspectives and may complement or covary with each other. Further investigation is still needed to identify the appropriate metrics for specific ecological contexts, which will require collaboration between experts in TLS technology and ecological mechanisms.
A Horizontally-focused metrics, such as canopy cover, describe the distribution of canopy elements on the horizontal plane. B Vertically-focused metrics, such as foliage height diversity, capture vertical heterogeneity within the canopy. C Unified metrics, such as canopy entropy, integrate both horizontal and vertical dimensions to provide a comprehensive measure of structural complexity. Together, these metrics offer diverse perspectives for understanding forest ecosystems.
Building on the role of TLS-derived metrics in assessing canopy structural complexity, these metrics have been applied as proxies for habitat characterization, enabling detailed analyses of vegetation vertical density and openness112,113,114,115. These metrics can then be related to biodiversity, including abundance and diversity of birds114, the impact of large herbivores on forest structure116,117, and animal-environment interactions118. The increasing robustness and reliability of algorithms to characterize point clouds into ecologically meaningful components opens the opportunity to use TLS-derived structural metrics as proxies for biodiversity patterns and habitat complexity.
An often-overlooked component influencing forest structural complexity is dead wood, both standing and downed, which plays a crucial role in enhancing biodiversity by providing habitat for various species of fungi, insects, birds, and mammals. Assessing the amount of dead wood and its dynamics is often difficult with traditional field methods. Thus, methods have been developed for estimating the volume of standing dead trees119, as well as for identifying downed dead wood from TLS point clouds120. Similarly, TLS data has been used to develop volume allometry for standing dead trees of varying decay classes121. The development of accurate dead wood mapping and volume allometry is key for assessing the biomass and carbon storage in dead trees, as well as understanding their contribution to habitat complexity. Despite these advances, there remains a significant gap in our understanding of how TLS can effectively be used to assess dead wood across different stages of decay. Dead wood undergoes various changes in structure and composition as it decomposes, and further research is needed to evaluate the potential of TLS data to capture these changes based on structural attributes such as volume, shape irregularities, and surface texture.
Characterizing forest disturbances in the three-dimensional space
Forest disturbances are characterized by changes in the stand composition, structure, or function, and may be triggered by natural factors such as wildfires, insect outbreaks, and storms, or by human-induced factors such as logging and land conversion. Although large-scale disturbances are easily observed from satellite imagery, some are subtle and cannot be detected even by high spatial resolution imagery or ALS data. Even in cases when these disturbances can be detected by platforms over the canopy122,123, these approaches are limited in their capability to quantify structural changes characterized by shifts in the plant distribution along the forest vertical profile.
In recent years, TLS studies have provided unprecedented insights into forest disturbances92 (Fig. 5). The high level of detail in TLS data has enabled analyses of how edge effects alter individual tree morphology, revealing the impact of forest fragmentation on the architecture of Amazonian trees124. While young trees colonizing the edges develop thicker branches, resulting in 50% more woody volume than trees of similar size and height in the interior, large trees near the edges tend to have disproportionately lower heights, leading to a 30% reduction in their woody volume. This shift in tree architecture caused by edge effects contributed to a net loss of 6.0 Mg ha−1 of aboveground biomass in Central Amazonian forests.
TLS enables detailed assessment of vertical structural changes caused by logging (top left), volumetric changes in ground vegetation following fire events (top right), as well as shifts in phenological and structural diversity arising from edge effects in fragmented forests (bottom). These examples illustrate the capability of TLS to quantify changes in forest ecosystems with high precision, offering deeper insights into the impacts of disturbances across different spatial and temporal scales.
TLS has also drawn conclusions into the effects of selective logging on TLS-derived structural traits of tropical forests. Machine learning models of structural traits accurately quantified the effects of varying logging intensities on the forest canopy at multiple scales125. This approach worked across multiple spatial scales: at finer scales (1–5 m), it detected disturbances from individual tree harvesting and canopy changes caused by logging trails, while at coarser scales (>20 m), it provided an overview of the overall structural integrity of forests under different logging intensities. TLS data revealed structural changes persisting for decades after logging, highlighting the long-term impact of these disturbances. For example, in forests on Mount Kenya, TLS detected logging legacies in canopy structural traits even 40–70 years post-harvest94. These persistent impacts were evident in the canopy ratio, which describes the relative distribution of canopy material across vertical layers of the forest and helps quantify how logging alters the vertical balance between upper and lower canopy strata.
Further demonstrating the versatility of TLS in forest disturbance studies, recent research applied TLS to quantify fire-induced changes in ground vegetation structure. Bitemporal TLS data detected reductions in vegetation volume following fire, illustrating how TLS can capture both large-scale disturbances and subtle changes in understory structure when pre- and post-disturbance data are available126. The study quantified substantial reductions in vegetation volume post-fire, with partial regrowth, providing detailed insights into fire-induced structural changes. Variation in these changes was observed between and within sites, highlighting the complexity of surface fire dynamics and underscoring the need for multi-site observations.
Advances in quantifying structural features are now enabling direct links between TLS data and the impacts of disturbances on broader ecosystem processes, such as shifts in phenology, microclimate regulation, and overall forest functioning. Bimonthly TLS data over a period of 8 months have demonstrated that forest edge effects affected the phenology and the synchronized interactions between the upper and lower canopy strata of Amazonian forests127. The study argued that these changes occurred because edge-induced disturbances increased light availability in the understory throughout the year and also changed the airflow, disrupting the natural vertical gradients of temperature and humidity within the forest. As a result, the forest’s capacity to regulate microclimate and sustain synchronized phenological cycles is weakened, further amplifying the impacts of fragmentation on ecosystem stability.
Despite the progress in understanding forest disturbances through 3D structural data, challenges remain in fully utilizing TLS technology to quantify changes in the function of disturbed forests. These environments, particularly in tropical ecosystems, often have denser understory vegetation, which exacerbates occlusion and hinders accurate tree segmentation. Future developments in segmentation algorithms will be critical to overcoming these barriers, enabling more precise extraction of individual trees and improving our understanding of how disturbances influence physiological traits that underpin changes in tree architecture and demographic processes. Additionally, advances in taxonomic classification algorithms will enhance our capacity to assess shifts in species composition arising from disturbances, particularly within the understory, where traditional remote sensing methods have struggled to provide reliable data.
Discussion and perspectives
From the simple measurement of tree trunk circumferences to the construction of realistic digital forest models, characterizing forest structures is essential to understand these ecosystems88,98. This information is critical for monitoring and predicting the effects of human-induced disturbances92,125, which will help us better comprehend the future of the planet’s forests. TLS technology plays a pivotal role in this effort, and its importance is likely to grow. This contribution will emerge from two key fronts: first, the high-definition reconstruction of forest structure and composition, enabled by advanced computational algorithms, and combined with the ability to monitor these factors over time (i.e., 4D monitoring), promises an unprecedented understanding of forest ecology and its role in the Earth system. Second, the unique capability of TLS to foster digital forest representations will enhance large-scale analytical frameworks (e.g., radiative transfer models), boosting the application of Earth Observation data and ecosystem process simulations.
However, TLS approaches do not come without challenges, nor should they be viewed as a complete replacement for established techniques. Traditional methods, such as measuring stem diameters with a metric tape, will remain far more practical and cost-effective. While TLS usage has expanded over the past two decades, access to high-end instruments—typically characterized by millimeter-level ranging accuracy, long effective range, and fast acquisition rates (e.g., 100,000 points per second)—remains challenging for many researchers due to limited availability and high cost. Consequently, selecting TLS equipment often involves a trade-off between the required structural detail, the complexity of the target vegetation, and available resources, though the increasing availability of more affordable devices has greatly improved accessibility18. For instance, in dense, multi-layered tropical forests, entry-level instruments may suffice for measuring basal areas and canopy heights18, but they may fall short for producing accurate QSMs and detailed structural metrics128. Conversely, in sparse forests with simpler structures, high-end instruments may be unnecessary, as more affordable devices can provide sufficiently accurate data, making the cost-benefit of advanced equipment less justifiable. This trade-off is likely to shift in the coming years as technological advancements make better instruments more accessible and affordable for a wider range of applications.
As we move forward, achieving the full potential of TLS will require smoother and more standardized data processing pipelines. Despite its numerous advantages, implementing TLS in operational inventories is hindered by factors such as the speed of data collection, which depends on the protocol and technology used. Earlier protocols and lower-cost instruments required registering individual scan positions using retroreflective or spherical targets, whereas recent high-end systems have enabled targetless scanning. These improvements, along with faster scanning rates, have drastically shortened the time needed for individual scans. Furthermore, similar sensor technologies, such as mobile laser scanning and terrestrial photogrammetry, have matured for faster point cloud acquisition15,17,63. Another bottleneck for effective analysis of acquired point clouds is a lack of appropriate, standardized, and possibly commercialized software15. Although automatic algorithms and pipelines are expected to reduce the time required for analyzing large point cloud datasets129, standardized benchmarks are still lacking63.
While no universally adopted international standards exist, TLS-specific guidelines have been proposed to promote consistent data acquisition protocols18. Interoperability between TLS datasets is challenged by differences in scanner resolution, beam properties, and native data formats. However, most instruments allow export to open formats such as LAS (LASer File Format) via manufacturer software, enabling broader use in community-developed processing tools and libraries47,95,115.
Independent of technology and protocol, environmental conditions, particularly wind and precipitation, often limit the effective field time of TLS. Wind-induced movement in vegetation can introduce noise into point clouds, creating “ghost branches” that lead to errors in QSMs and volume estimates58. Accessing remote areas remains a logistical challenge, often requiring airborne platforms. Drones can be useful in some cases but are limited by operational constraints (often restricted to line-of-sight flying, for example). Weather conditions such as wind and rain affect both TLS and other remote sensing approaches, including drones. Compared to drones, TLS offers greater structural detail and accuracy for generating QSMs, along with safer deployment, as it avoids crash risks and typically requires fewer regulatory approvals—making it a practical tool for detailed field measurements.
Finally, coordinated global TLS initiatives will be essential to transform TLS into a worldwide asset, complementing and underpinning recent and upcoming satellite missions. For such initiatives to succeed, standardized protocols must be developed to harmonize data collected with different instruments and sampling strategies, ensuring consistency and comparability across studies. Open and harmonized TLS data catalogs remain scarce, although many datasets have been published through individual projects, field experiments, or regional monitoring campaigns. Efforts toward global coordination are advancing. The FOR-species20K initiative130, for example, provides TLS-derived structural data for over 20,000 trees across diverse forest biomes, offering a valuable open-access resource for comparative studies. Methodological efforts such as StrucNet131 aim to promote cross-biome consistency in TLS acquisition, but the substantial volume of raw data produced presents additional challenges. Addressing these requires efficient data distribution pipelines to enable access to processed and standardized outputs, such as derived metrics and variables, that can serve as inputs for models or benchmarks in large-scale studies. With that said, as scientists and industry work to narrow these gaps, TLS has already proven to be an essential piece in the intricate puzzle of tools helping society to better understand and coexist with the world’s forests.
Data availability
This review does not include original data. All data discussed are from previously published and publicly available sources.
References
Hansen, M. C. et al. High-resolution global maps of 21st-century forest cover change. Science 342, 850–853 (2013).
Tucker, C. J., Townshend, J. R. G. & Goff, T. E. African land-cover classification using satellite data. Science 227, 369–375 (1985).
Asner, G. P. et al. Airborne laser-guided imaging spectroscopy to map forest trait diversity and guide conservation. Science 355, 385–389 (2017).
Hansen, M. C. et al. The fate of tropical forest fragments. Sci. Adv. 6, eaax8574 (2020).
Grantham, H. S. et al. Anthropogenic modification of forests means only 40% of remaining forests have high ecosystem integrity. Nat. Commun. 11, 5978 (2020).
Mo, L. et al. Integrated global assessment of the natural forest carbon potential. Nature 624, 92–101 (2023).
Lenton, T. M. et al. Remotely sensing potential climate change tipping points across scales. Nat. Commun. 15, 343 (2024).
Richardson, K. et al. Earth beyond six of nine planetary boundaries. Sci. Adv. 9, eadh2458 (2023).
Woodcock, C. E., Loveland, T. R., Herold, M. & Bauer, M. E. Transitioning from change detection to monitoring with remote sensing: a paradigm shift. Remote Sens. Environ. 238, 111558 (2020).
Dubayah, R. O. & Drake, J. B. Lidar remote sensing for forestry. J. For. 98, 44–46 (2000).
Wehr, A. & Lohr, U. Airborne laser scanning—an introduction and overview. ISPRS J. Photogramm. Remote Sens. 54, 68–82 (1999).
Beland, M. et al. On promoting the use of lidar systems in forest ecosystem research. Ecol. Manag. 450, 117484 (2019).
Dassot, M., Constant, T. & Fournier, M. The use of terrestrial LiDAR technology in forest science: application fields, benefits and challenges. Ann. Sci. 68, 959–974 (2011).
Newnham, G. J. et al. Terrestrial laser scanning for plot-scale forest measurement. Curr. For. Rep. 1, 239–251 (2015).
Liang, X. et al. Terrestrial laser scanning in forest inventories. ISPRS J. Photogramm. Remote Sens. 115, 63–77 (2016).
Calders, K. et al. Terrestrial laser scanning in forest ecology: Expanding the horizon. Remote Sens. Environ. 251, 112102 (2020).
Liang, X. et al. Close-range remote sensing of forests: the state of the art, challenges, and opportunities for systems and data acquisitions. IEEE Geosci. Remote Sens. Mag. 10, 32–71 (2022).
Wilkes, P. et al. Data acquisition considerations for terrestrial laser scanning of forest plots. Remote Sens. Environ. 196, 140–153 (2017).
Cai, Z., Chin, T.-J., Bustos, A. P. & Schindler, K. Practical optimal registration of terrestrial LiDAR scan pairs. ISPRS J. Photogramm. Remote Sens. 147, 118–131 (2019).
Wielgosz, M., Puliti, S., Xiang, B., Schindler, K. & Astrup, R. SegmentAnyTree: a sensor and platform agnostic deep learning model for tree segmentation using laser scanning data. Remote Sens. Environ. 313, 114367 (2024).
Wilkes, P. et al. TLS2trees: A scalable tree segmentation pipeline for TLS data. Methods Ecol. Evol. 14, 3083–3099 (2023).
Calders, K. et al. Realistic forest stand reconstruction from terrestrial LiDAR for radiative transfer modelling. Remote Sens.10, 933 (2018).
Batty, M. Digital twins. Environ. Plan B Urban Anal. City Sci. 45, 817–820 (2018).
Grieves, M. & Vickers, J. Digital twin: mitigating unpredictable, undesirable emergent behavior in complex systems. in Transdisciplinary Perspectives on Complex Systems 85–113. https://doi.org/10.1007/978-3-319-38756-7_4 (Springer International Publishing, 2017).
Liu, C. et al. Implications of 3D forest stand reconstruction methods for radiative transfer modeling: a case study in the temperate deciduous forest. J. Geophys. Res. Atmos. 127, e2021JD036175 (2022).
Janoutová, R. et al. Detailed reconstruction of trees from terrestrial laser scans for remote sensing and radiative transfer modelling applications. In Silico Plants 3, diab026 (2021).
Knyazikhin, Y., Martonchik, J. V., Myneni, R. B., Diner, D. J. & Running, S. W. Synergistic algorithm for estimating vegetation canopy leaf area index and fraction of absorbed photosynthetically active radiation from MODIS and MISR data. J. Geophys. Res. Atmos. 103, 32257–32275 (1998).
Yang, B. et al. Estimation of leaf area index and its sunlit portion from DSCOVR EPIC data: theoretical basis. Remote Sens. Environ. 198, 69–84 (2017).
Disney, M. I., Lewis, P. & North, P. R. J. Monte Carlo ray tracing in optical canopy reflectance modelling. Remote Sens. Rev. 18, 163–196 (2000).
Winiwarter, L. et al. Virtual laser scanning with HELIOS++: a novel take on ray tracing-based simulation of topographic full-waveform 3D laser scanning. Remote Sens. Environ. 269, 112772 (2022).
Gastellu-Etchegorry, J. P., Martin, E. & Gascon, F. DART: a 3D model for simulating satellite images and studying surface radiation budget. Int. J. Remote Sens. 25, 73–96 (2004).
Wang, D., Schraik, D., Hovi, A. & Rautiainen, M. Direct estimation of photon recollision probability using terrestrial laser scanning. Remote Sens. Environ. 247, 111932 (2020).
Godin, C. & Sinoquet, H. Functional–structural plant modelling. New Phytol. 166, 705–708 (2005).
O’Sullivan, H., Raumonen, P., Kaitaniemi, P., Perttunen, J. & Sievänen, R. Integrating terrestrial laser scanning with functional–structural plant models to investigate ecological and evolutionary processes of forest communities. Ann. Bot. 128, 663–684 (2021).
Sinoquet, H., Le Roux, X., Adam, B., Ameglio, T. & Daudet, F. A. RATP: a model for simulating the spatial distribution of radiation absorption, transpiration and photosynthesis within canopies: application to an isolated tree crown. Plant Cell Environ. 24, 395–406 (2001).
Potapov, I., Järvenpää, M., Åkerblom, M., Raumonen, P. & Kaasalainen, M. Bayes Forest: a data-intensive generator of morphological tree clones. Gigascience 6, 1–13 (2017).
Sievänen, R., Raumonen, P., Perttunen, J., Nikinmaa, E. & Kaitaniemi, P. A study of crown development mechanisms using a shoot-based tree model and segmented terrestrial laser scanning data. Ann. Bot. 122, 423–434 (2018).
Verbeeck, H. et al. Time for a plant structural economics spectrum. Front. For. Glob. Change 2, 43 (2019).
Raumonen, P. et al. Massive-scale tree modelling from TLS data. ISPRS Ann. Photogramm. Remote Sens. Spat. Inf. Sci. 2, 189–196 (2015).
Raumonen, P. et al. Fast automatic precision tree models from terrestrial laser scanner data. Remote Sens. 5, 491–520 (2013).
Tomlinson, P. B. Tree architecture: new approaches help to define the elusive biological property of tree form. Am. Sci. 71, 141–149 (1983).
Malhi, Y. et al. New perspectives on the ecology of tree structure and tree communities through terrestrial laser scanning. Interface Focus 8, 20170052 (2018).
Moorthy, K. et al. Terrestrial laser scanning to detect liana impact on forest structure. Remote Sens. 10, 810 (2018).
Archibald, S. & Bond, W. J. Growing tall vs growing wide: tree architecture and allometry of Acacia karroo in forest, savanna, and arid environments. Oikos 102, 3–14 (2003).
Su, Y. et al. Large-scale geographical variations and climatic controls on crown architecture traits. J. Geophys Res. Biogeosci. 125, e2019JG005306 (2020).
Jackson, T. D. et al. Wind shapes the growth strategies of trees in a tropical forest. Ecol. Lett. 27, e14527 (2024).
Terryn, L. et al. Analysing individual 3D tree structure using the R package ITSMe. Methods Ecol. Evol. 14, 231–241 (2023).
Hackenberg, J., Spiecker, H., Calders, K., Disney, M. & Raumonen, P. SimpleTree—an efficient open source tool to build tree models from TLS clouds. Forests 6, 4245–4294 (2015).
Computree. Computree: collaborative platform for remote sensing data processing. https://computree.onf.fr/?page_id=589 (2024).
Trochta, J., Krůček, M., Vrška, T. & Král, K. 3D forest: an application for descriptions of three-dimensional forest structures using terrestrial LiDAR. PLoS ONE 12, e0176871 (2017).
Fan, G., Nan, L., Dong, Y., Su, X. & Chen, F. AdQSM: a new method for estimating above-ground biomass from TLS point clouds. Remote Sens. 12, 3089 (2020).
Yang, W. et al. Treegraph: tree architecture from terrestrial laser scanning point clouds. Remote Sens. Ecol. Conserv. https://doi.org/10.1002/rse2.399 (2024).
Feng, Y. et al. L1-Tree: A novel algorithm for constructing 3D tree models and estimating branch architectural traits using terrestrial laser scanning data. Remote Sens. Environ. 314, 114390 (2024).
Li, H. et al. WLC-Net: a robust and fast deep learning wood–leaf classification method. Forests 16, 513 (2025).
Han, T. & Sánchez-Azofeifa, G. A. A deep learning time series approach for leaf and wood classification from terrestrial LiDAR point clouds. Remote Sens. 14, 3157 (2022).
Bornand, A., Abegg, M., Morsdorf, F. & Rehush, N. Completing 3D point clouds of individual trees using deep learning. Methods Ecol. Evol. 15, 2010–2023 (2024).
Henrich, J., van Delden, J., Seidel, D., Kneib, T. & Ecker, A. S. TreeLearn: a deep learning method for segmenting individual trees from ground-based LiDAR forest point clouds. Ecol. Inf. 84, 102888 (2024).
Morhart, C. et al. Limitations of estimating branch volume from terrestrial laser scanning. Eur. J. Res. 143, 687–702 (2024).
Morales, A. & MacFarlane, D. W. Reducing tree volume overestimation in quantitative structure models using modeled branch topology and direct twig measurements. For. Int. J. For. Res. https://doi.org/10.1093/forestry/cpae046 (2024).
Liang, X. et al. International benchmarking of terrestrial laser scanning approaches for forest inventories. ISPRS J. Photogramm. Remote Sens. 144, 137–179 (2018).
Montoya-Sánchez, V. et al. Comparing airborne and terrestrial LiDAR with ground-based inventory metrics of vegetation structural complexity in oil palm agroforests. Ecol. Indic. 166, 112306 (2024).
Schraik, D., Wang, D., Hovi, A. & Rautiainen, M. Quantifying stand-level clumping of boreal, hemiboreal and temperate European forest stands using terrestrial laser scanning. Agric. Meteorol. 339, 109564 (2023).
Kükenbrink, D., Marty, M., Bösch, R. & Ginzler, C. Benchmarking laser scanning and terrestrial photogrammetry to extract forest inventory parameters in a complex temperate forest. Int. J. Appl. Earth Obs. Geoinf. 113, 102999 (2022).
Kangas, A., Henttonen, H., Pitkänen, T., Sarkkola, S. & Heikkinen, J. Re-calibrating stem volume models—Is there change in the tree trunk form from the 1970s to the 2010s in Finland? Silva Fenn. 54,10269 (2020).
Kangas, A., Pitkänen, T. P., Mehtätalo, L. & Heikkinen, J. Mixed linear and non-linear tree volume models with regional parameters to main tree species in Finland. For. Int. J. For. Res. 96, 188–206 (2023).
Hulshof, C. M., Swenson, N. G. & Weiser, M. D. Tree height–diameter allometry across the United States. Ecol. Evol. 5, 1193–1204 (2015).
Saarinen, N. et al. Understanding 3D structural complexity of individual Scots pine trees with different management history. Ecol. Evol. 11, 2561–2572 (2021).
Saarinen, N. et al. Effects of stem density on crown architecture of Scots pine trees. Front. Plant Sci. 13, 817792 (2022).
Jacobs, M. et al. Assessment of defoliation and subsequent growth losses caused by Lymantria dispar using terrestrial laser scanning (TLS). Trees 36, 819–834 (2022).
Metz, J. et al. Crown modeling by terrestrial laser scanning as an approach to assess the effect of aboveground intra- and interspecific competition on tree growth. Ecol. Manag. 310, 275–288 (2013).
Ronoud, G. et al. Terrestrial laser scanning in assessing the effect of different thinning treatments on the competition of Scots pine (Pinus sylvestris L.) forests. Remote Sens.14, 5196 (2022).
Yrttimaa, T. et al. Exploring tree growth allometry using two-date terrestrial laser scanning. Ecol. Manag. 518, 120303 (2022).
Ronoud, G. et al. Characterizing the competitive stress of individual trees using point clouds. Ecol. Manag. 572, 122305 (2024).
Burkardt, K. et al. Influence of heterozygosity and competition on morphological tree characteristics of Quercus rubra L.: a new single-tree based approach. New For. 52, 679–695 (2021).
Luoma, V. et al. Revealing changes in the stem form and volume allocation in diverse boreal forests using two-date terrestrial laser scanning. Forests 12, 835 (2021).
Jacobs, M., Rais, A. & Pretzsch, H. How drought stress becomes visible upon detecting tree shape using terrestrial laser scanning (TLS). Ecol. Manag. 489, 118975 (2021).
Yrttimaa, T. et al. Capturing seasonal radial growth of boreal trees with terrestrial laser scanning. Ecol. Manag. 529, 120733 (2023).
Puttonen, E. et al. Quantification of overnight movement of birch (Betula pendula) branches and foliage with short interval terrestrial laser scanning. Front. Plant Sci. 7, 222 (2016).
Puttonen, E. et al. A clustering framework for monitoring circadian rhythm in structural dynamics in plants from terrestrial laser scanning time series. Front. Plant Sci. 10, 486 (2019).
Campos, M. B. et al. A long-term terrestrial laser scanning measurement station to continuously monitor structural and phenological dynamics of boreal forest canopy. Front. Plant Sci. 11, 606752 (2021).
Wang, D., Puttonen, E. & Casella, E. PlantMove: a tool for quantifying motion fields of plant movements from point cloud time series. Int. J. Appl. Earth Obs. Geoinf. 110, 102781 (2022).
Yrttimaa, T. et al. Tree height and stem growth dynamics in a Scots pine dominated boreal forest. Trees For. People 15, 100468 (2024).
Poorter, L., Bongers, L. & Bongers, F. Architecture of 54 moist-forest tree species: traits, trade-offs, and functional groups. Ecology 87, 1289–1301 (2006).
Åkerblom, M., Raumonen, P., Mäkipää, R. & Kaasalainen, M. Automatic tree species recognition with quantitative structure models. Remote Sens. Environ. 191, 1–12 (2017).
Terryn, L. et al. Tree species classification using structural features derived from terrestrial laser scanning. ISPRS J. Photogramm. Remote Sens. 168, 170–181 (2020).
Chen, J. et al. Tree species recognition from close-range sensing: a review. Remote Sens. Environ. 313, 114337 (2024).
Atkins, J. W. et al. Integrating forest structural diversity measurement into ecological research. Ecosphere 14, e4633 (2023).
LaRue, E. A., Hardiman, B. S., Elliott, J. M. & Fei, S. Structural diversity as a predictor of ecosystem function. Environ. Res. Lett. 14, 114011 (2019).
Ma, Q. et al. Tree mortality during long-term droughts is lower in structurally complex forest stands. Nat. Commun. 14, 7467 (2023).
Nakamura, A. et al. Forests and their canopies: achievements and horizons in canopy science. Trends Ecol. Evol. 32, 438–451 (2017).
Vincent, G. et al. Mapping plant area index of tropical evergreen forest by airborne laser scanning. A cross-validation study using LAI2200 optical sensor. Remote Sens. Environ. 198, 254–266 (2017).
Maeda, E. E. et al. Shifts in structural diversity of Amazonian forest edges detected using terrestrial laser scanning. Remote Sens. Environ. 271, 112895 (2022).
Hancock, S. et al. Characterising forest gap fraction with terrestrial lidar and photography: an examination of relative limitations. Agric. Meteorol. 189–190, 105–114 (2014).
Jia, J. et al. Forest structural and microclimatic patterns along an elevational gradient in Mount Kenya. Agric. Meteorol. 356, 110188 (2024).
Atkins, J. W. et al. Quantifying vegetation and canopy structural complexity from terrestrial LiDAR data using the FORESTR R package. Methods Ecol. Evol. 9, 2057–2066 (2018).
McElhinny, C., Gibbons, P., Brack, C. & Bauhus, J. Forest and woodland stand structural complexity: its definition and measurement. Ecol. Manag. 218, 1–24 (2005).
Ehbrecht, M., Schall, P., Juchheim, J., Ammer, C. & Seidel, D. Effective number of layers: a new measure for quantifying three-dimensional stand structure based on sampling with terrestrial LiDAR. Ecol. Manag. 380, 212–223 (2016).
LaRue, E. A. et al. A theoretical framework for the ecological role of three-dimensional structural diversity. Front. Ecol. Environ. 21, 4–13 (2023).
Alonzo, M., Bookhagen, B. & Roberts, D. A. Urban tree species mapping using hyperspectral and lidar data fusion. Remote Sens. Environ. 148, 70–83 (2014).
Hardiman, B. S., Bohrer, G., Gough, C. M., Vogel, C. S. & Curtis, P. S. The role of canopy structural complexity in wood net primary production of a maturing northern deciduous forest. Ecology 92, 1818–1827 (2011).
Canham, C. D., Finzi, A. C., Pacala, S. W. & Burbank, D. H. Causes and consequences of resource heterogeneity in forests: interspecific variation in light transmission by canopy trees. Can. J. For. Res. 24, 337–349 (1994).
Jucker, T., Bouriaud, O. & Coomes, D. A. Crown plasticity enables trees to optimize canopy packing in mixed-species forests. Funct. Ecol. 29, 1078–1086 (2015).
Chambel, M. R., Climent, J., Alia, R. & Valladares, F. Phenotypic plasticity: a useful framework for understanding adaptation in forest species. For. Syst. 14, 334–344 (2005).
Ehbrecht, M. et al. Global patterns and climatic controls of forest structural complexity. Nat. Commun. 12, 519 (2021).
Barbeito, I. et al. Terrestrial laser scanning reveals differences in crown structure of Fagus sylvatica in mixed vs. pure European forests. Ecol. Manag. 405, 381–390 (2017).
Krůček, M., Trochta, J., Cibulka, M. & Král, K. Beyond the cones: How crown shape plasticity alters aboveground competition for space and light—evidence from terrestrial laser scanning. Agric Meteorol. 264, 188–199 (2019).
Liu, X. et al. Enhancing ecosystem productivity and stability with increasing canopy structural complexity in global forests. Sci. Adv. 10, eadl1947 (2024).
Liu, X. et al. A novel entropy-based method to quantify forest canopy structural complexity from multiplatform lidar point clouds. Remote Sens. Environ. 282, 113280 (2022).
Tang, H. et al. Definition and measurement of tree cover: a comparative analysis of field-, lidar- and landsat-based tree cover estimations in the Sierra National Forests, USA. Agric. Meteorol. 268, 258–268 (2019).
Clawges, R., Vierling, K., Vierling, L. & Rowell, E. The use of airborne lidar to assess avian species diversity, density, and occurrence in a pine/aspen forest. Remote Sens. Environ. 112, 2064–2073 (2008).
de Conto, T., Armston, J. & Dubayah, R. Characterizing the structural complexity of the Earth’s forests with spaceborne lidar. Nat. Commun. 15, 8116 (2024).
Ashcroft, M. B., Gollan, J. R. & Ramp, D. Creating vegetation density profiles for a diverse range of ecological habitats using terrestrial laser scanning. Methods Ecol. Evol. 5, 263–272 (2014).
Puletti, N., Galluzzi, M., Grotti, M. & Ferrara, C. Characterizing subcanopy structure of Mediterranean forests by terrestrial laser scanning data. Remote Sens. Appl. 24, 100620 (2021).
Shokirov, S. et al. Habitat highs and lows: using terrestrial and UAV LiDAR for modelling avian species richness and abundance in a restored woodland. Remote Sens. Environ. 285, 113326 (2023).
Lecigne, B., Eitel, J. U. H. & Rachlow, J. L. viewshed3d: an R package for quantifying 3D visibility using terrestrial lidar data. Methods Ecol. Evol. 11, 733–738 (2020).
Eichhorn, M. P. et al. Effects of deer on woodland structure revealed through terrestrial laser scanning. J. Appl. Ecol. 54, 1615–1626 (2017).
Li, S., Hou, Z., Ge, J. & Wang, T. Assessing the effects of large herbivores on the three-dimensional structure of temperate forests using terrestrial laser scanning. Ecol. Manag. 507, 119985 (2022).
Blakey, R. V., Law, B. S., Kingsford, R. T. & Stoklosa, J. Terrestrial laser scanning reveals below-canopy bat trait relationships with forest structure. Remote Sens. Environ. 198, 40–51 (2017).
Putman, E. B. et al. Detecting and quantifying standing dead tree structural loss with reconstructed tree models using voxelized terrestrial lidar data. Remote Sens. Environ. 209, 52–65 (2018).
Yrttimaa, T. et al. Detecting and characterizing downed dead wood using terrestrial laser scanning. ISPRS J. Photogramm. Remote Sens. 151, 76–90 (2019).
Klockow, P. A. et al. Allometry and structural volume change of standing dead southern pine trees using non-destructive terrestrial LiDAR. Remote Sens. Environ. 241, 111729 (2020).
Aquino, C. et al. Reliably mapping low-intensity forest disturbance using satellite radar data. Front. For. Glob. Change 5, 1018762 (2022).
Reiche, J. et al. Forest disturbance alerts for the Congo Basin using Sentinel-1. Environ. Res. Lett. 16, 024005 (2021).
Nunes, M. H. et al. Edge effects on tree architecture exacerbate biomass loss of fragmented Amazonian forests. Nat. Commun. 14, 8129 (2023).
Ghizoni Santos, E., Henrique Nunes, M., Jackson, T. & Eiji Maeda, E. Quantifying tropical forest disturbances using canopy structural traits derived from terrestrial laser scanning. Ecol. Manag. 524, 120546 (2022).
Tienaho, N., Saarinen, N., Yrttimaa, T., Kankare, V. & Vastaranta, M. Quantifying fire-induced changes in ground vegetation using bitemporal terrestrial laser scanning. Silva Fenn. 58, 23061 (2024).
Nunes, M. H. et al. Forest fragmentation impacts the seasonality of Amazonian evergreen canopies. Nat. Commun. 13, 917 (2022).
Lau, A. et al. Quantifying branch architecture of tropical trees using terrestrial LiDAR and 3D modelling. Trees 32, 1219–1231 (2018).
Murtiyoso, A. et al. A review of software solutions to process ground-based point clouds in forest applications. Curr. For. Rep. 10, 401–419 (2024).
Puliti, S. et al. Benchmarking tree species classification from proximally sensed laser scanning data: introducing the FOR- species20K dataset. Methods Ecol. Evol. 16, 801–818 (2025).
Calders, K. et al. StrucNet: a global network for automated vegetation structure monitoring. Remote Sens. Ecol. Conserv. 9, 587–598 (2023).
Synge, E. H. XCI. A method of investigating the higher atmosphere. Lond. Edinb. Dublin Philos. Mag. J. Sci. 9, 1014–1020 (1930).
Maiman, T. H. Stimulated optical radiation in ruby. Nature 187, 493–494 (1960).
Link, L. E., Krabill, W. B. & Swift, R. N. A prospectus on airborne laser mapping systems. Adv. Space Res. 3, 309–322 (1983).
Spring, A. P. A history of laser scanning, Part 1: space and defense applications. Photogramm. Eng. Remote Sens. 86, 419–429 (2020).
Acknowledgements
E.E.M. acknowledges support from the Research Council of Finland (grant no. 363501). I.S. acknowledges support from the Helsinki Institute of Sustainability Science (HELSUS). L.T. was funded by Ghent University Bijzonder Onderzoeksfonds (Grant No. 01G01923). M.R. acknowledges support from the Research Council of Finland (grant no. 341963). Y.S. acknowledges support from the National Natural Science Foundation of China (grant no. 32422059). M.D. acknowledges support from NCEO, as well as NERC grant reference number NE/X019071/1, “UK EO Climate Information Service”. M.H. acknowledges funding from the European Union to the Open-EarthMonitor Cyberinfrastructure (Grant No. GA101059548) and Open Geospatial Carbon Registry (Grant no. 101218854). E.L. was supported by a UKRI Future Leaders Fellowship (MR/Y033981/1). P.R. acknowledges support from the Research Council of Finland through the Flagship of Advanced Mathematics for Sensing, Imaging and Modelling (grant no. 359185) and the Centre of Excellence of Inverse Modelling and Imaging (grant no. 353090). B.B. acknowledges funding from the NextGenCarbon project funded by the European Union (grant number 101184989). N.S. acknowledges the support from the UNITE Flagship project funded by the Research Council of Finland (grant no. 357906). K.C. was funded by the European Union (ERC-2021-STG Grant agreement No. 101039795). Views and opinions expressed are, however, those of the author(s) only and do not necessarily reflect those of the European Union or the European Research Council Executive Agency. Neither the European Union nor the granting authority can be held responsible for them.
Author information
Authors and Affiliations
Contributions
E.E.M. conceived the idea for the review and coordinated the writing process. B.B., K.C., M.D., E.R.L., M.H.N., P.R., M.R., N.S., I.S., Y.S., L.T., and J.T. contributed to writing specific sections and provided critical revisions throughout the manuscript. J.T. created the figures with input from all authors. M.H. provided feedback during the revision process.
Corresponding author
Ethics declarations
Competing interests
The authors declare no competing interests.
Peer review
Peer review information
Nature Communications thanks Jiapeng Huang and the other, anonymous, reviewer(s) for their contribution to the peer review of this work.
Additional information
Publisher’s note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Rights and permissions
Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
About this article
Cite this article
Maeda, E.E., Brede, B., Calders, K. et al. Expanding forest research with terrestrial LiDAR technology. Nat Commun 16, 8853 (2025). https://doi.org/10.1038/s41467-025-63946-6
Received:
Accepted:
Published:
DOI: https://doi.org/10.1038/s41467-025-63946-6