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Benchmarking tree species classification from proximally sensed laser scanning data: Introducing the FOR-species20K dataset
Puliti , Stefano , Lines , Emily R. , Müllerová , Jana , Frey , Julian , Schindler , Zoe , Straker , Adrian , Allen , Matthew J. , Winiwarter , Lukas , Rehush , Nataliia , Hristova , Hristina S. , Murray , Brent A. , Calders , Kim , Coops , Nicholas C. , Höfle , Bernhard , Irwin , Liam A.K. , Junttila , Samuli , Kruček , Martin , Krok , G. , Král , Kamil , Levick , Shaun R. , Lück , Linda , Missarov , Azim , Mokroš , M. , Owen , Harry Jon Foord , Stereńczak , Krzysztof Jan , Pitkänen , Timo P. , Puletti , Nicola , Saarinen , Ninni , Hopkinson , Chris Dennis , Terryn , Louise , Torresan , C. , Tomelleri , Enrico , Weiser , Hannah , Astrup , Rasmus
lidar remote sensing biodiversity deep learning point cloud classification single-tree inventory
Mostra abstract
Proximally sensed laser scanning presents new opportunities for automated forest ecosystem data capture. However, a gap remains in deriving ecologically pertinent information, such as tree species, without additional ground data. Artificial intelligence approaches, particularly deep learning (DL), have shown promise towards automation. Progress has been limited by the lack of large, diverse, and, most importantly, openly available labelled single-tree point cloud datasets. This has hindered both (1) the robustness of the DL models across varying data types (platforms and sensors) and (2) the ability to effectively track progress, thereby slowing the convergence towards best practice for species classification. To address the above limitations, we compiled the FOR-species20K benchmark dataset, consisting of individual tree point clouds captured using proximally sensed laser scanning data from terrestrial (TLS), mobile (MLS) and drone laser scanning (ULS). Compiled collaboratively, the dataset includes data collected in forests mainly across Europe, covering Mediterranean, temperate and boreal biogeographic regions. It includes scattered tree data from other continents, totaling over 20,000 trees of 33 species and covering a wide range of tree sizes and forms. Alongside the release of FOR-species20K, we benchmarked seven leading DL models for individual tree species classification, including both point cloud (PointNet++, MinkNet, MLP-Mixer, DGCNNs) and multi-view 2D-based methods (SimpleView, DetailView, YOLOv5). 2D Image-based models had, on average, higher overall accuracy (0.77) than 3D point cloud-based models (0.72). Notably, the performance was consistently >0.8 across scanning platforms and sensors, offering versatility in deployment. The top-scoring model, DetailView, demonstrated robustness to training data imbalances and effectively generalized across tree sizes. The FOR-species20K dataset represents an important asset for developing and benchmarking DL models for individual tree species classification using proximally sensed laser scanning data. As such, it serves as a crucial foundation for future efforts to classify accurately and map tree species at various scales using laser scanning technology, as it provides the complete code base, dataset, and an initial baseline representative of the current state-of-the-art of point cloud tree species classification methods. © 2025 The Author(s). Methods in Ecology and Evolution published by John Wiley & Sons Ltd on behalf of British Ecological Society.
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2025
Rivista
Methods in Ecology and Evolution
Dettagli
Vol. 16 (4) pp. 801 - 818
DOI
TRY plant trait database – enhanced coverage and open access
Kattge , Jens , Bönisch , Gerhard , Díaz , Sandra M. , Lavorel , Sandra , Prentice , Iain Colin , Leadley , Paul W. , Tautenhahn , Susanne , Werner , Gijsbert , Aakala , Tuomas , Abedi , Mehdi , Acosta , Alicia Teresa Rosario , Adamidis , George C. , Adamson , Kairi , Aiba , Masahiro , Albert , Cécile Hélène , Alcántara , Julio M. , Alcázar C , Carolina , Aleixo , Izabela , Ali , Hamada E. , Amiaud , Bernard , Ammer , Christian , Amoroso , Mariano Martín , Anand , Madhur , Anderson , Carolyn G. , Anten , Niels P.R. , Antos , Joseph A. , Apgaua , Deborah Mattos Guimarães , Ashman , Tia Lynn , Asmara , Degi Harja , Asner , Gregory P. , Aspinwall , Michael J. , Atkin , Owen K. , Aubin , Isabelle , Baastrup-Spohr , Lars , Bahalkeh , Khadijeh , Bahn , Michael , Baker , Timothy R. , Baker , William J. , Bakker , Jan P. , Baldocchi , Dennis D. , Baltzer , Jennifer L. , Banerjee , Arindam , Baranger , Anne , Barlow , Jos B. , Barneche , Diego R. , Baruch , Zdravko , Bastianelli , Denis , Battles , John J. , Bauerle , William L. , Bauters , Marijn , Bazzato , Erika , Beckmann , Michael , Beeckman , Hans , Beierkuhnlein , Carl , Bekker , Renée M. , Belfry , Gavin , Belluau , Michaël , Beloiu Schwenke , Mirela , Benavides , Raquel , Benomar , Lahcen , Berdugo-Lattke , Mary Lee , Berenguer , Erika , Bergamin , Rodrigo Scarton , Bergmann , Joana , Carlucci , Marcos B. , Berner , Logan T. , Bernhardt-Römermann , Markus , Bigler , Christof , Bjorkman , Anne D. , Blackman , Chris J. , Blanco , Carolina Casagrande , Blonder , Benjamin Wong , Blumenthal , Dana M. , Bocanegra-González , Kelly Tatiana , Boeckx , Pascal , Bohlman , Stephanie Ann , Böhning-Gaese , Katrin , Boisvert-Marsh , Laura , Bond , William J. , Bond-Lamberty , Ben P. , Boom , Arnoud , Boonman , Coline C.F. , Bordin , Kauane Maiara , Boughton , Elizabeth H. , Boukili , Vanessa K.S. , Bowman , David M.J.S. , Bravo , Sandra Josefina , Brendel , Marco R. , Broadley , Martin R. , Brown , Kerry A. , Bruelheide , Helge , Brumnich , Federico , Bruun , Hans Henrik , Bruy , David , Buchanan , Serra Willow , Bucher , Solveig Franziska , Buchmann , Nina , Buitenwerf , Robert , Bunker , Daniel E. , Bürger , Jana
functional diversity data coverage data integration data representativeness plant traits try plant trait database
Mostra abstract
Plant traits—the morphological, anatomical, physiological, biochemical and phenological characteristics of plants—determine how plants respond to environmental factors, affect other trophic levels, and influence ecosystem properties and their benefits and detriments to people. Plant trait data thus represent the basis for a vast area of research spanning from evolutionary biology, community and functional ecology, to biodiversity conservation, ecosystem and landscape management, restoration, biogeography and earth system modelling. Since its foundation in 2007, the TRY database of plant traits has grown continuously. It now provides unprecedented data coverage under an open access data policy and is the main plant trait database used by the research community worldwide. Increasingly, the TRY database also supports new frontiers of trait-based plant research, including the identification of data gaps and the subsequent mobilization or measurement of new data. To support this development, in this article we evaluate the extent of the trait data compiled in TRY and analyse emerging patterns of data coverage and representativeness. Best species coverage is achieved for categorical traits—almost complete coverage for ‘plant growth form’. However, most traits relevant for ecology and vegetation modelling are characterized by continuous intraspecific variation and trait–environmental relationships. These traits have to be measured on individual plants in their respective environment. Despite unprecedented data coverage, we observe a humbling lack of completeness and representativeness of these continuous traits in many aspects. We, therefore, conclude that reducing data gaps and biases in the TRY database remains a key challenge and requires a coordinated approach to data mobilization and trait measurements. This can only be achieved in collaboration with other initiatives. © 2019 The Authors. Global Change Biology published by John Wiley & Sons Ltd
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2020
Rivista
Global Change Biology
Dettagli
Vol. 26 (1) pp. 119 - 188
DOI
Continental Contrasts in Climate Extremes That Control Tree Fecundity
Clark , James S. , Andrus , Robert A. , Arianoutsou , Margarita , Ascoli , Davide , Bergeron , Yves , Bogdziewicz , Michał , Boivin , Thomas , Bonal , Raúl , Caignard , Thomas , Cailleret , Maxime , Calama , Rafael A. , Camarero , Jesús Julio , Chianucci , Francesco , Cienciala , Emil , Courbaud , Benoít , Delzon , Sylvain , Dietze , Michael C. , Espelta , Josep Maria , Fady , Bruno , Fyllas , Nikolaos M. , Gilbert , Gregory S. , Gratzer , Georg , Guignabert , Arthur , Hacket-Pain , Andrew J. , Hampe , Arndt , Hanley , Mick E. , Hille Ris Lambers , Janneke , Holik , Jan , Hoshizaki , K. , Hu , Miao , Ibáñez , Inés , Işık , Fatih , Jenkins , Lauren , Johnstone , Jill F. , Journé , Valentin , Kadioglu , Alper Kaan , Kızılaslan , İrem Sena , Knops , Johannes Michael Hubertus , Kobe , Richard K. , Köse , Nesibe , Külah , Eylül U. , Kunstler , Georges , LaMontagne , Jalene M. , Ledwoń , Mateusz , Lehtonen , Aleksi , Loewe-Muñoz , Verónica F. , Lutz , James A. , Mårell , Anders , Meyer , Kira , Moran , Emily V. , Motta , Renzo , Myers , Jonathan A. , Nagel , Thomas A. , Pérez-Ramos , Ignacio M. , Piechnik , Łukasz , Podgórski , Tomasz , Poulton-Kamakura , Renata , Qiu , Tong , Redmond , Miranda D. , Reid , Chantal D. , Rodman , Kyle C. , Rodríguez-Sánchez , Francisco , Šamonil , Pavel , Šebeň , Vladimír , Seget , Barbara , Sharma , Shubhi , Socha , Jarosław Ł. , Steele , Michael A. , Straub , Jacob N. , Sutton , Samantha , Thomas , Peter A. , Vacchiano , Giorgio , Venner , Marie Claude , Venner , Samuel , Zavala , Miguel A. , Zheng , Shiqi , Żywiec , Magdalena
drought climate extremes forest recovery late freeze
Mostra abstract
In 2023, more than half of olive harvests (Olea europaea) across Spain, Greece, and Türkiye were lost to drought. The same year late freeze destroyed 90% of the peach crop (Prunus persica) on the Georgia Piedmont and the apple crop (Malus domestica) in central New York, Vermont, and southern Quebec. Climate extremes now rank with the costliest threats to agriculture, but their role in forest recovery from diebacks that are happening globally is unknown for lack of tree fecundity estimates in forests. Tolerance of climate extremes could depend on past exposure but constrained by phylogenetic conservatism. We report a continental scale analysis of climate extremes and forest fecundity across North America and Europe showing that responses to late freeze and drought are happening now. Species differences are not explained by the traits typically included in ecological studies and they are weakly associated with phylogeny. Late freeze, that is, freezing temperatures that follow the onset of flower development in spring, is shown to be “normal” in North America, but not Europe, potentially explaining failed seed production due to delayed onset and the resultant shorter growing period by North American transplants dating back at least to the 18th century. Drought has thus far had the greatest impacts in dry forested regions, but here too, species differences are not explained by traditional trait values. If responses have been buffered from drought and late freeze by past exposure, acclimation and local adaptation prove inadequate as extremes intensify. © 2026 John Wiley & Sons Ltd.
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2026
Rivista
Global Change Biology
Dettagli
Vol. 32 (2)
DOI
The Relationship Between Maturation Size and Maximum Tree Size From Tropical to Boreal Climates
Journé , Valentin , Bogdziewicz , Michał , Courbaud , Benoít , Kunstler , Georges , Qiu , Tong , Aravena Acuña , Marie Claire , Ascoli , Davide , Bergeron , Yves , Berveiller , Daniel , Boivin , Thomas , Bonal , Raúl , Caignard , Thomas , Cailleret , Maxime , Calama , Rafael A. , Camarero , Jesús Julio , Chang-Yang , Chia Hao , Chave , Jérôme , Chianucci , Francesco , Curt , Thomas , Cutini , Andrea , Das , Adrian J. , Daskalakou , Evangelia N. , Davi , Hendrik , Delpierre , Nicolas , Delzon , Sylvain , Dietze , Michael C. , Calderon , Sergio Donoso , Dormont , Laurent , Espelta , Josep Maria , Farfan-Rios , William R. , Fenner , Michael , Franklin , Jerry F. , Gehring , Catherine A. , Gilbert , Gregory S. , Gratzer , Georg , Greenberg , Cathryn H. , Guignabert , Arthur , Guo , Qinfeng , Hacket-Pain , Andrew J. , Hampe , Arndt , Han , Qingmin , Hanley , Mick E. , Hille Ris Lambers , Janneke , Holik , Jan , Hoshizaki , K. , Ibáñez , Inés , Johnstone , Jill F. , Knops , Johannes Michael Hubertus , Kobe , Richard K. , Kurokawa , Hiroko , Lageard , Jonathan G.A. , LaMontagne , Jalene M. , Ledwoń , Mateusz , Lefèvre , François , Leininger , Theodor D. , Limousin , Jean Marc , Lutz , James A. , Macias , Diana S. , Mårell , Anders , McIntire , Eliot J.B. , Moran , Emily V. , Motta , Renzo , Myers , Jonathan A. , Nagel , Thomas A. , Naoe , Shoji , Noguchi , Mahoko , Norghauer , Julian M. , Oguro , Michio , Ourcival , Jean Marc , Parmenter , Robert R. , Pearse , Ian S. , Pérez-Ramos , Ignacio M. , Piechnik , Łukasz , Podgórski , Tomasz , Poulsen , John R. , Redmond , Miranda D. , Reid , Chantal D. , Šamonil , Pavel , Scher , C. Lane , Schlesinger , William H. , Seget , Barbara , Sharma , Shubhi , Shibata , Mitsue , Silman , Miles R. , Steele , Michael A. , Stephenson , Nathan L. , Straub , Jacob N. , Sutton , Samantha , Swenson , Jennifer J. , Swift , Margaret , Thomas , Peter A. , Uríarte , María , Vacchiano , Giorgio , Whipple , Amy Vaughn , Whitham , Thomas G. , Wright , Stuart Joseph , Zhu , Kai , Zimmerman , Jess K. , Żywiec , Magdalena , Clark , James S.
seed production allometry life history size tree fecundity tree maturation
Mostra abstract
The fundamental trade-off between current and future reproduction has long been considered to result in a tendency for species that can grow large to begin reproduction at a larger size. Due to the prolonged time required to reach maturity, estimates of tree maturation size remain very rare and we lack a global view on the generality and the shape of this trade-off. Using seed production from five continents, we estimate tree maturation sizes for 486 tree species spanning tropical to boreal climates. Results show that a species' maturation size increases with maximum size, but in a non-proportional way: the largest species begin reproduction at smaller sizes than would be expected if maturation were simply proportional to maximum size. Furthermore, the decrease in relative maturation size is steepest in cold climates. These findings on maturation size drivers are key to accurately represent forests' responses to disturbance and climate change. © 2024 John Wiley & Sons Ltd.
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2024
Rivista
Ecology Letters
Dettagli
Vol. 27 (9)
DOI
Masting is uncommon in trees that depend on mutualist dispersers in the context of global climate and fertility gradients
Qiu , Tong , Aravena Acuña , Marie Claire , Ascoli , Davide , Bergeron , Yves , Bogdziewicz , Michał , Boivin , Thomas , Bonal , Raúl , Caignard , Thomas , Cailleret , Maxime , Calama , Rafael A. , Calderon , Sergio Donoso , Camarero , Jesús Julio , Chang-Yang , Chia Hao , Chave , Jérôme , Chianucci , Francesco , Courbaud , Benoít , Cutini , Andrea , Das , Adrian J. , Delpierre , Nicolas , Delzon , Sylvain , Dietze , Michael C. , Dormont , Laurent , Espelta , Josep Maria , Fahey , Timothy J. , Farfan-Rios , William R. , Franklin , Jerry F. , Gehring , Catherine A. , Gilbert , Gregory S. , Gratzer , Georg , Greenberg , Cathryn H. , Guignabert , Arthur , Guo , Qinfeng , Hacket-Pain , Andrew J. , Hampe , Arndt , Han , Qingmin , Holik , Jan , Hoshizaki , K. , Ibáñez , Inés , Johnstone , Jill F. , Journé , Valentin , Kitzberger , Thomas A. , Knops , Johannes Michael Hubertus , Kunstler , Georges , Kurokawa , Hiroko , Lageard , Jonathan G.A. , LaMontagne , Jalene M. , Lefèvre , François , Leininger , Theodor D. , Limousin , Jean Marc , Lutz , James A. , Macias , Diana S. , Mårell , Anders , McIntire , Eliot J.B. , Moore , Christopher M. , Moran , Emily V. , Motta , Renzo , Myers , Jonathan A. , Nagel , Thomas A. , Naoe , Shoji , Noguchi , Mahoko , Oguro , Michio , Parmenter , Robert R. , Pearse , Ian S. , Pérez-Ramos , Ignacio M. , Piechnik , Łukasz , Podgórski , Tomasz , Poulsen , John R. , Redmond , Miranda D. , Reid , Chantal D. , Rodman , Kyle C. , Rodríguez-Sánchez , Francisco , Šamonil , Pavel , Sanguinetti , Javier D. , Scher , C. Lane , Seget , Barbara , Sharma , Shubhi , Shibata , Mitsue , Silman , Miles R. , Steele , Michael A. , Stephenson , Nathan L. , Straub , Jacob N. , Sutton , Samantha , Swenson , Jennifer J. , Swift , Margaret , Thomas , Peter A. , Uríarte , María , Vacchiano , Giorgio , Whipple , Amy Vaughn , Whitham , Thomas G. , Wion , Andreas P. , Wright , Stuart Joseph , Zhu , Kai , Zimmerman , Jess K. , Żywiec , Magdalena , Clark , James S.
plant seed seeds tree trees reproduction fertility satiety satiation
Mostra abstract
The benefits of masting (volatile, quasi-synchronous seed production at lagged intervals) include satiation of seed predators, but these benefits come with a cost to mutualist pollen and seed dispersers. If the evolution of masting represents a balance between these benefits and costs, we expect mast avoidance in species that are heavily reliant on mutualist dispersers. These effects play out in the context of variable climate and site fertility among species that vary widely in nutrient demand. Meta-analyses of published data have focused on variation at the population scale, thus omitting periodicity within trees and synchronicity between trees. From raw data on 12 million tree-years worldwide, we quantified three components of masting that have not previously been analysed together: (i) volatility, defined as the frequency-weighted year-to-year variation; (ii) periodicity, representing the lag between high-seed years; and (iii) synchronicity, indicating the tree-to-tree correlation. Results show that mast avoidance (low volatility and low synchronicity) by species dependent on mutualist dispersers explains more variation than any other effect. Nutrient-demanding species have low volatility, and species that are most common on nutrient-rich and warm/wet sites exhibit short periods. The prevalence of masting in cold/dry sites coincides with climatic conditions where dependence on vertebrate dispersers is less common than in the wet tropics. Mutualist dispersers neutralize the benefits of masting for predator satiation, further balancing the effects of climate, site fertility and nutrient demands. © 2023, The Author(s), under exclusive licence to Springer Nature Limited.
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2023
Rivista
Nature Plants
Dettagli
Vol. 9 (7) pp. 1044 - 1056
DOI
Linking seed size and number to trait syndromes in trees
Bogdziewicz , Michał , Aravena Acuña , Marie Claire , Andrus , Robert A. , Ascoli , Davide , Bergeron , Yves , Brveiller , Daniel , Boivin , Thomas , Bonal , Raúl , Caignard , Thomas , Cailleret , Maxime , Calama , Rafael A. , Calderon , Sergio Donoso , Camarero , Jesús Julio , Chang-Yang , Chia Hao , Chave , Jérôme , Chianucci , Francesco , Cleavitt , Natalie L. , Courbaud , Benoít , Cutini , Andrea , Curt , Thomas , Das , Adrian J. , Davi , Hendrik , Delpierre , Nicolas , Delzon , Sylvain , Dietze , Michael C. , Dormont , Laurent , Farfan-Rios , William R. , Gehring , Catherine A. , Gilbert , Gregory S. , Gratzer , Georg , Greenberg , Cathryn H. , Guignabert , Arthur , Guo , Qinfeng , Hacket-Pain , Andrew J. , Hampe , Arndt , Han , Qingmin , Hoshizaki , K. , Ibáñez , Inés , Johnstone , Jill F. , Journé , Valentin , Kitzberger , Thomas A. , Knops , Johannes Michael Hubertus , Kunstler , Georges , Kobe , Richard K. , Lageard , Jonathan G.A. , LaMontagne , Jalene M. , Ledwoń , Mateusz , Leininger , Theodor D. , Limousin , Jean Marc , Lutz , James A. , Macias , Diana S. , Mårell , Anders , McIntire , Eliot J.B. , Moran , Emily V. , Motta , Renzo , Myers , Jonathan A. , Nagel , Thomas A. , Naoe , Shoji , Noguchi , Mahoko , Oguro , Michio , Kurokawa , Hiroko , Ourcival , Jean Marc , Parmenter , Robert R. , Pérez-Ramos , Ignacio M. , Piechnik , Łukasz , Podgórski , Tomasz , Poulsen , John R. , Qiu , Tong , Redmond , Miranda D. , Reid , Chantal D. , Rodman , Kyle C. , Šamonil , Pavel , Holik , Jan , Scher , C. Lane , van Marle , Harald Schmidt , Seget , Barbara , Shibata , Mitsue , Sharma , Shubhi , Silman , Miles R. , Steele , Michael A. , Straub , Jacob N. , Sun , I. Fang , Sutton , Samantha , Swenson , Jennifer J. , Thomas , Peter A. , Uríarte , María , Vacchiano , Giorgio , Veblen , Thomas Thorstein , Wright , Boyd R. , Wright , Stuart Joseph , Whitham , Thomas G. , Zhu , Kai , Zimmerman , Jess K. , Żywiec , Magdalena , Clark , James S.
fecundity functional traits leaf economics life history strategies size syndrome tree recruitment
Mostra abstract
Aim: Our understanding of the mechanisms that maintain forest diversity under changing climate can benefit from knowledge about traits that are closely linked to fitness. We tested whether the link between traits and seed number and seed size is consistent with two hypotheses, termed the leaf economics spectrum and the plant size syndrome, or whether reproduction represents an independent dimension related to a seed size–seed number trade-off. Location: Most of the data come from Europe, North and Central America and East Asia. A minority of the data come from South America, Africa and Australia. Time period: 1960–2022. Major taxa studied: Trees. Methods: We gathered 12 million observations of the number of seeds produced in 784 tree species. We estimated the number of seeds produced by individual trees and scaled it up to the species level. Next, we used principal components analysis and generalized joint attribute modelling (GJAM) to map seed number and size on the tree traits spectrum. Results: Incorporating seed size and number into trait analysis while controlling for environment and phylogeny with GJAM exposes relationships in trees that might otherwise remain hidden. Production of the large total biomass of seeds [product of seed number and seed size; hereafter, species seed productivity (SSP)] is associated with high leaf area, low foliar nitrogen, low specific leaf area (SLA) and dense wood. Production of high seed numbers is associated with small seeds produced by nutrient-demanding species with softwood, small leaves and high SLA. Trait covariation is consistent with opposing strategies: one fast-growing, early successional, with high dispersal, and the other slow-growing, stress-tolerant, that recruit in shaded conditions. Main conclusions: Earth system models currently assume that reproductive allocation is indifferent among plant functional types. Easily measurable seed size is a strong predictor of the seed number and species seed productivity. The connection of SSP with the functional traits can form the first basis of improved fecundity prediction across global forests. © 2023 John Wiley & Sons Ltd.
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2023
Rivista
Global Ecology and Biogeography
Dettagli
Vol. 32 (5) pp. 683 - 694
DOI
Estimation of foliage clumping from the LAI-2000 Plant Canopy Analyzer: effect of view caps
Chianucci , Francesco , MacFarlane , Craig K. , Písek , Jan , Cutini , Andrea , Casa , Raffaele
leaf area index hemispherical photography apparent clumping index effective leaf area logarithm averaging
Mostra abstract
Key message: Foliage clumping can be estimated from logarithm averaging method in LAI-2000. The spatial scaling of clumping effects considered by the instrument is dependent on the sensor’s azimuthal view. Accurate estimates of foliage clumping index (Ω) are required to improve the retrieval of leaf area index (L) from optical instruments like LAI-2000/2200 Plant Canopy Analyzer (PCA) and digital hemispherical photography (DHP). The logarithm averaging method is often used to approximate L because clumping effects are considered at scales larger than the sensor’s field of view. However, the spatial scaling considered for logarithm averaging typically differs between PCA and DHP, resulting in different estimates of foliage clumping. Based on simulation, we demonstrated that applying restricting azimuth view caps (e.g., 45° or 10°) allows reliable estimation of Ω and more accurate estimation of L from PCA. Simulated Ω and L values were comparable to those measured using the PCA, DHP and litter traps. Linear averaging of the gap fractions across readings at a plot or site yields a concurrent estimate of effective leaf area index (L<inf>e</inf>), thus enabling the calculation of L<inf>e</inf>, L, and Ω from a single instrument fitted with view caps. Users need to be aware that the method they use for averaging gap fractions determines whether they are measuring L<inf>e</inf> or L, and PCA users need to be aware that they are applying increasingly large corrections for foliage clumping as they use more restrictive view caps, a fact that they can use to their advantage to improve estimates of L. © 2014, Springer-Verlag Berlin Heidelberg.
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2015
Rivista
Trees - Structure and Function
Dettagli
Vol. 29 (2) pp. 355 - 366
DOI