Manfred Finckh

Dr. Manfred Finckh

orcid

Research Focus & Metrics

Academic Career Length

28Years (1999-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

View All Publications
11 February 2022 in Global Change Biology
Verified
Journal Article
Open access
PDF file
JLJonas Lembrechts
Jonas Lembrechts
JHJohan van Den Hoogen
Johan van Den Hoogen
JAJuha Aalto
Juha Aalto
MAMichael B. Ashcroft
Michael B. Ashcroft
PFPieter De Frenne
Pieter De Frenne
JLJonathan Lenoir
Jonathan Lenoir
Research in global change ecology relies heavily on global climatic grids derived from estimates of air temperature in open areas at around 2 m above the ground. These climatic grids do not reflect conditions below vegetation canopies and near the ground surface, where critical ecosystem functions occur and most terrestrial species reside. Here, we provide global maps of soil temperature and bioclimatic variables at a 1‐km2resolution for 0–5 and 5–15 cm soil depth. These maps were created by calculating the difference (i.e. offset) between in situ soil temperature measurements, based on time series from over 1200 1‐km2pixels (summarized from 8519 unique temperature sensors) across all the world's major terrestrial biomes, and coarse‐grained air temperature estimates from ERA5‐Land (an atmospheric reanalysis by the European Centre for Medium‐Range Weather Forecasts). We show that mean annual soil temperature differs markedly from the corresponding gridded air temperature, by up to 10°C (mean = 3.0 ± 2.1°C), with substantial variation across biomes and seasons. Over the year, soils in cold and/or dry biomes are substantially warmer (+3.6 ± 2.3°C) than gridded air temperature, whereas soils in warm and humid environments are on average slightly cooler (−0.7 ± 2.3°C). The observed substantial and biome‐specific offsets emphasize that the projected impacts of climate and climate change on near‐surface biodiversity and ecosystem functioning are inaccurately assessed when air rather than soil temperature is used, especially in cold environments. The global soil‐related bioclimatic variables provided here are an important step forward for any application in ecology and related disciplines. Nevertheless, we highlight the need to fill remaining geographic gaps by collecting more in situ measurements of microclimate conditions to further enhance the spatiotemporal resolution of global soil temperature products for ecological applications.

6 July 2011 in Journal of Vegetation Science
Verified
Journal Article
Closed access
PDF file
JDJürgen Dengler
Jürgen Dengler
FJFlorian Jansen
Florian Jansen
FGFalko Glöckler
Falko Glöckler
RPRobert K. Peet
Robert K. Peet
MCMiquel De Cáceres
Miquel De Cáceres
NSNick Spencer
Nick Spencer

21 June 2021 in Global Ecology and Biogeography
Verified
Journal Article
Open access
PDF file
FSFrancesco Maria Sabatini
Francesco Maria Sabatini
JLJonathan Lenoir
Jonathan Lenoir
THTarek Hattab
Tarek Hattab
EAElise Aimee Arnst
Elise Aimee Arnst
MCMilan Chytrý
Milan Chytrý
HBHelge Bruelheide
Helge Bruelheide
Motivation: Assessing biodiversity status and trends in plant communities is critical for understanding, quantifying and predicting the effects of global change on ecosystems. Vegetation plots record the occurrence or abundance of all plant species co‐occurring within delimited local areas. This allows species absences to be inferred, information seldom provided by existing global plant datasets. Although many vegetation plots have been recorded, most are not available to the global research community. A recent initiative, called ‘sPlot’, compiled the first global vegetation plot database, and continues to grow and curate it. The sPlot database, however, is extremely unbalanced spatially and environmentally, and is not open‐access. Here, we address both these issues by (a) resampling the vegetation plots using several environmental variables as sampling strata and (b) securing permission from data holders of 105 local‐to‐regional datasets to openly release data. We thus present sPlotOpen, the largest open‐access dataset of vegetation plots ever released. sPlotOpen can be used to explore global diversity at the plant community level, as ground truth data in remote sensing applications, or as a baseline for biodiversity monitoring.Main types of variable contained: Vegetation plots (n = 95,104) recording cover or abundance of naturally co‐occurring vascular plant species within delimited areas. sPlotOpen contains three partially overlapping resampled datasets (c. 50,000 plots each), to be used as replicates in global analyses. Besides geographical location, date, plot size, biome, elevation, slope, aspect, vegetation type, naturalness, coverage of various vegetation layers, and source dataset, plot‐level data also include community‐weighted means and variances of 18 plant functional traits from the TRY Plant Trait Database.Spatial location and grain: Global, 0.01–40,000 m².Time period and grain: 1888–2015, recording dates.Major taxa and level of measurement: 42,677 vascular plant taxa, plot‐level records.Software format: Three main matrices (.csv), relationally linked.

31 March 2021 in Global Ecology and Biogeography
Verified
Journal Article
Open access
PDF file
RTRiccardo Testolin
Riccardo Testolin
FAFabio Attorre
Fabio Attorre
PBPeter Borchardt
Peter Borchardt
RBRobert F. Brand
Robert F. Brand
HBHelge Bruelheide
Helge Bruelheide
BJBorja Jiménez‐Alfaro
Borja Jiménez‐Alfaro
Aim: Alpine ecosystems differ in area, macroenvironment and biogeographical history across the Earth, but the relationship between these factors and plant species richness is still unexplored. Here, we assess the global patterns of plant species richness in alpine ecosystems and their association with environmental, geographical and historical factors at regional and community scales.Location: Global.Time period: Data collected between 1923 and 2019.Major taxa studied: Vascular plants.Methods: We used a dataset representative of global alpine vegetation, consisting of 8,928 plots sampled within 26 ecoregions and six biogeographical realms, to estimate regional richness using sample‐based rarefaction and extrapolation. Then, we evaluated latitudinal patterns of regional and community richness with generalized additive models. Using environmental, geographical and historical predictors from global raster layers, we modelled regional and community richness in a mixed‐effect modelling framework.Results: The latitudinal pattern of regional richness peaked around the equator and at mid‐latitudes, in response to current and past alpine area, isolation and the variation in soil pH among regions. At the community level, species richness peaked at mid‐latitudes of the Northern Hemisphere, despite a considerable within‐region variation. Community richness was related to macroclimate and historical predictors, with strong effects of other spatially structured factors.Main conclusions: In contrast to the well‐known latitudinal diversity gradient, the alpine plant species richness of some temperate regions in Eurasia was comparable to that of hyperdiverse tropical ecosystems, such as the páramo. The species richness of these putative hotspot regions is explained mainly by the extent of alpine area and their glacial history, whereas community richness depends on local environmental factors. Our results highlight hotspots of species richness at mid‐latitudes, indicating that the diversity of alpine plants is linked to regional idiosyncrasies and to the historical prevalence of alpine ecosystems, rather than current macroclimatic gradients.

22 June 2021 in Journal of Vegetation Science
Verified
Journal Article
Open access
PDF file
IBIdoia Biurrun
Idoia Biurrun
Remigiusz PielechRemigiusz Pielech
Remigiusz Pielech
IDIwona Dembicz
Iwona Dembicz
FGFrançois Gillet
François Gillet
ŁKŁukasz Kozub
Łukasz Kozub
JDJürgen Dengler
Jürgen Dengler
Aims: Understanding fine‐grain diversity patterns across large spatial extents is fundamental for macroecological research and biodiversity conservation. Using the GrassPlot database, we provide benchmarks of fine‐grain richness values of Palaearctic open habitats for vascular plants, bryophytes, lichens and complete vegetation (i.e., the sum of the former three groups).Location: Palaearctic biogeographic realm.Methods: We used 126,524 plots of eight standard grain sizes from the GrassPlot database: 0.0001, 0.001, 0.01, 0.1, 1, 10, 100 and 1,000 m2 and calculated the mean richness and standard deviations, as well as maximum, minimum, median, and first and third quartiles for each combination of grain size, taxonomic group, biome, region, vegetation type and phytosociological class.Results: Patterns of plant diversity in vegetation types and biomes differ across grain sizes and taxonomic groups. Overall, secondary (mostly semi‐natural) grasslands and natural grasslands are the richest vegetation type. The open‐access file ”GrassPlot Diversity Benchmarks” and the web tool “GrassPlot Diversity Explorer” are now available online (https://edgg.org/databases/GrasslandDiversityExplorer) and provide more insights into species richness patterns in the Palaearctic open habitats.Conclusions: The GrassPlot Diversity Benchmarks provide high‐quality data on species richness in open habitat types across the Palaearctic. These benchmark data can be used in vegetation ecology, macroecology, biodiversity conservation and data quality checking. While the amount of data in the underlying GrassPlot database and their spatial coverage are smaller than in other extensive vegetation‐plot databases, species recordings in GrassPlot are on average more complete, making it a valuable complementary data source in macroecology.

27 October 2020 in Proceedings of the National Academy of Sciences
Verified
Journal Article
Closed access
PDF file
JAJulie Aleman
Julie Aleman
AFAdeline Fayolle
Adeline Fayolle
CFC. Favier
C. Favier
ASA. C. Staver
A. C. Staver
KDKyle Dexter
Kyle Dexter
MSM. D. Swaine
M. D. Swaine
Significance: We develop a biogeographic approach to analyzing the presence of alternative stable states in tropical biomes. Whilst forest–savanna bistability has been widely hypothesized and modeled, empirical evidence has remained scarce and controversial, and here, applying our method to Africa, we provide large-scale evidence that there are alternative states in tree species composition of tropical vegetation. Furthermore, our results have produced more accurate maps of the forest and savanna distributions in Africa, which take into account differences in tree species composition, and a complex suite of determinants. This result is not only important for understanding the biogeography of the continent but also, to guide large-scaled tree planting and restoration efforts planned for the region.