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Pubblicazioni Scientifiche

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Is randomized branch sampling suitable to assess wood volume of temperate broadleaved old-growth forests?
Mostra abstract
Old-growth forests are characterized by the presence of large and very large trees. The estimation of their wood volume and biomass is essential in order to monitor the ecological processes in these stands and their contribution to carbon cycle. However, conventional wood volume estimation techniques based on mensuration of stem diameter at breast height and tree height is most often unfeasible for large and very large trees in old-growth forests because volume models or tables are usually elaborated from trees of smaller size grown up in regularly managed forest stands. Random Branch Sampling (RBS) is often proposed as a possible estimation alternative under such conditions. Starting from the ground level some of the parts of the main trunk and of the branches are sampled and measured to estimate the overall wood volume (or other biophysical variables). The application of RBS in old-growth forests, where tree cutting is usually forbidden or very difficult, requires that the crown of the tree can physically be reached to measure the sampled parts. We argue that under such conditions it is usually preferable to fully measure all the components of the tree crown because RBS estimates are not precise if based on only one sampling path and that, on the other hand, measuring the main trunk and all the branches by tree-climbing consumes the same time as replicating several RBS paths on the same tree. To demonstrate our hypothesis we selected 16 large beech trees located in the old-growth forest of Mount Cimini in Central Italy. Using a modern tree-climbing approach the main trunk and all the branches were measured and recorded in the field. The database was used to simulate RBS paths. Real values from volume census were contrasted with estimates based on RBS. On the whole, RBS estimates based on one single path prove to be highly imprecise. Even for trees characterized by a rather regular form, at least three RBS paths should be repeated on the same tree to maintain the relative standard error under or near 15%. This paper introduces the problem and describes the experimental test. The results are discussed under the perspective of standardized application of the proposed methodology. © 2013 Elsevier B.V.
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.
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.
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.
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.
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.
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.