Loading...
Pubblicazioni Scientifiche
Filtri di ricerca 5 risultati
Pubblicazioni per anno
Managed forests are a stronghold of non-native beetles in Europe
Basile
,
Marco
,
Lachat
,
Thibault
,
Balducci
,
Lorenzo
,
Chianucci
,
Francesco
,
Chojnacki
,
Lucas
,
Archaux
,
Frédéric
,
N Avtzis
,
Dimitrios N.
,
Bouget
,
Christophe
,
de Smedt
,
Pallieter
,
Doerfler
,
Inken
,
Dumas
,
Yann
,
Elek
,
Zoltán
,
Gosselin
,
Marion
,
Goßner
,
Martin M.
,
Heilmann-Clausen
,
Jacob
,
Hofmeister
,
Jeňýk
,
Hošek
,
Jan
,
Janssen
,
Philippe
,
Justesen
,
Mathias Just
,
Hansen
,
Aslak Kappel
,
Schmidt
,
Inger Kappel
,
Kepfer-Rojas
,
Sebastian
,
Mårell
,
Anders
,
Matula
,
Radim
,
Müller
,
Jörg C. C.
,
Nordén
,
Björn
,
Ódor
,
Péter
,
Paillet
,
Yoan
,
Ravera
,
Sonia
,
Sitzia
,
Tommaso
,
Tinya
,
Flóra
,
Burrascano
,
Sabina
,
Brockerhoff
,
Eckehard G.
Mostra abstract
The species richness of vascular plants in forests can have contrasting effects on the occurrence of non-native insects. The establishment of non-native insect populations may be facilitated by low plant species richness, which reflects the availability of few but easily accessible resources, or hampered by high plant species richness due to spatial dilution of resources or biotic resistance (i.e., resistance against biological invasions). The relationship between the species richness of plants and non-native insects is likely influenced by disturbance regimes, which, in European forests, mostly consists of timber harvesting. We investigated this relationship considering two major forest attributes: (i) species richness of non-native vascular plants and (ii) forest management. From 1101 forest plots in Europe, we gathered occurrences of 1212 vascular plant species, including 160 non-native species, and of 2404 beetle species, including 29 non-native species. We tested the relationship between the species richness of non-native beetles and plants using non-linear quantile regressions. We disentangled the effect of non-native plant species richness from that of management on the species richness of non-native beetles, while accounting for forest structural variables, using structural equation models. We found clear evidence of a hump-shaped relationship between non-native beetle and plant species richness. The general shape of the relationship persisted when considering only woody or non-woody plants, as well as only non-native plants. The relationship was also similar between managed and unmanaged forests. However, the proportion of non-native beetles in managed forests was higher than in unmanaged forests at the same plant species richness. Management had a direct negative effect on non-native beetle species richness, whereas non-native plant species richness had a direct positive effect. When considering all direct and indirect effects, management facilitated the occurrence of non-native beetles indirectly via non-native plants rather than directly. Synthesis and applications. Species richness of native and non-native vascular plants modulates the species richness of non-native beetles through relationships with opposite signs. The interplay with management regimes and forest structures determines whether non-native beetles are promoted. Forest management aimed at reducing the intensity of disturbance while encouraging native plant species richness could promote the dominance of dilution effects and biotic resistance and could moderate the establishment of non-native insects. © 2025 The Author(s). Journal of Applied Ecology © 2025 British Ecological Society.
Silvicultural regime shapes understory functional structure in European forests
Chianucci
,
Francesco
,
Napoleone
,
Francesca
,
Ricotta
,
Carlo
,
Ferrara
,
Carlotta
,
Fusaro
,
Lina
,
Balducci
,
Lorenzo
,
Trentanovi
,
Giovanni
,
Bradley
,
Owen
,
Kovács
,
Bence
,
Mina
,
Marco
,
Cerabolini
,
Bruno Enrico Leone
,
Vandekerkhove
,
Kris
,
de Smedt
,
Pallieter
,
Lens
,
Luc
,
Hertzog
,
Lionel R.
,
Verheyen
,
Kris
,
Hofmeister
,
Jeňýk
,
Hošek
,
Jan
,
Matula
,
Radim
,
Doerfler
,
Inken
,
Müller
,
Jörg C. C.
,
Weisser
,
Wolfgang W.
,
Helback
,
Jan
,
Schall
,
Peter
,
Fischer
,
Markus
,
Heilmann-Clausen
,
Jacob
,
Riis-Hansen
,
Rasmus
,
Goldberg
,
Irina
,
Aude
,
Erik
,
Kepfer-Rojas
,
Sebastian
,
Kappel Schmidt
,
Inger
,
Riis-Nielsen
,
Torben
,
Mårell
,
Anders
,
Dumas
,
Yann
,
Janssen
,
Philippe
,
Paillet
,
Yoan
,
Archaux
,
Frédéric
,
Xystrakis
,
Fotios
,
Tinya
,
Flóra
,
Ódor
,
Péter
,
Aszalós
,
Réka
,
Bölöni
,
János
,
Cutini
,
Andrea
,
Bagella
,
Simonetta
,
Sitzia
,
Tommaso
,
Brazaitis
,
Gediminas
,
Marozas
,
Vitas
,
Ujházyová
,
Mariana
,
Ujházy
,
Karol
,
Máliš
,
František
,
Nordén
,
Björn
,
Burrascano
,
Sabina
functional diversity
functional redundancy
forest understory
sustainable forest management
unmanaged forests
ecosystem resilience
silvicultural regime
Mostra abstract
Managing forests to sustain their diversity and functioning is a major challenge in a changing world. Despite the key role of understory vegetation in driving forest biodiversity, regeneration and functioning, few studies address the functional dimensions of understory vegetation response to silvicultural management. We assessed the influence of the silvicultural regimes on the functional diversity and redundancy of European forest understory. We gathered vascular plant abundance data from more than 2000 plots in European forests, each associated with one out of the five most widespread silvicultural regimes. We used generalized linear mixed models to assess the effect of different silvicultural regimes on understory functional diversity (Rao's quadratic entropy) and functional redundancy, while accounting for climate and soil conditions, and explored the reciprocal relationship between three diversity components (functional diversity, redundancy and dominance) across silvicultural regimes through a ternary diversity diagram. Intensive silvicultural regimes are associated with a decrease in functional diversity and an increase in functional redundancy, compared with unmanaged conditions. This means that although intensive management may buffer communities' functions against species or functional losses, it also limits the range of understory response to environmental changes. Policy implications. Different silvicultural regimes influence different facets of understory functional features. While unmanaged forests can be used as a reference to design silvicultural practices in compliance with biodiversity conservation targets, different silvicultural options should be balanced at landscape scale to sustain the multiple forest functions that human societies are increasingly demanding. © 2024 The Author(s). Journal of Applied Ecology published by John Wiley & Sons Ltd on behalf of British Ecological Society.
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.