34 research outputs found
Spatial and temporal fluctuations in bird communities along a forest-farmland gradient in western Kenya
The impacts of human activities, notably the conversion of tropical forests into farmland habitat, has profound impacts on biological diversity and ecosystem functions (Millennium Ecosystem Assessment 2005). It is widely debated to what extent human modified landscapes can maintain tropical biodiversity and their ecosystem functionality (e.g. Waltert et al. 2004, Sekercioglu et al. 2007). In this thesis, I have used a huge and temporarily replicated dataset to assess the value of different habitat types differing in land-use intensities for bird communities in tropical East Africa. I investigated bird abundance and species richness along a forest-farmland habitat gradient and assessed spatial and temporal fluctuations of bird assemblages and their food resources.
I could show that forest and farmland habitats harbor distinct bird communities. Moreover, the protection of natural forests merits the highest priority for conserving the high diversity of forest-dependent bird species. My study, however, also shows that farmland habitats in the proximity of natural forest can support a high bird diversity. High bird diversity in tropical farmlands depends on a high structural complexity, such as in small-scale subsistence farmlands. From my findings, I conclude that the conversion of forest to farmland leads to substantial losses in bird diversity, in particular in specialized feeding guilds such as insectivores, while the conversion of structurally heterogeneous subsistence farmlands to sugarcane plantation causes erosion of bird diversity in agricultural ecosystems. Both findings are important for conservation planning in times when tropical forests and agroecosystems are under constantly high pressure due to increasing human population numbers and global demands for biofuel crops (Gibbs et al. 2008). From an ecosystem function perspective, my study demonstrates the potential of agroecosystems in supporting important ecosystem functions, such as seed dispersal by frugivorous birds and pest control by insectivorous birds. I could show that bird abundances in both frugivorous and insectivorous guilds were strongly predicted by their respective food resources, implying that seasonal shifts in fruit and invertebrate abundance at Kakamega forest and surrounding farmlands affect community dynamics and appear to influence local movement patterns of birds. The most interesting finding of this study was that feeding guilds responded idiosyncratically to resource fluctuations. Frugivore richness fluctuated asynchronously in forest and farmland habitats, suggesting foraging movements and fruit tracking across habitat borders. In contrast, I found that insectivores fluctuated synchronously in the two habitat types, suggesting a lack of inter-habitat movements. I therefore predict that insectivorous bird communities in this forest-farmland landscape may be more susceptible to the combined effects of land-use and climate change, due to their narrow habitat niche and limited capacity to track their resources.
The fact that a number of bird species regularly moved across the landscape mosaic in my study system implies that birds are able to provide long-distance seed dispersal across habitat borders. Thus, birds may enhance forest regeneration in human-modified landscapes, such as those in most parts of tropical Africa, given that forest remnants are protected within an agricultural habitat matrix. In order to effectively conserve tropical biodiversity within forest-farmland mosaics, this study advocates for conservation strategies that go beyond forest protection and explicitly integrate farmlands into forest management plans and policies. This should emphasize the retention of keystone habitat elements within tropical farmland landscapes, such as indigenous trees, forest galleries and hedgerows, whose presence enhance species diversity. Such grassroot-level approaches can be operationalized for instance through providing incentives to farmers to maintain their traditional subsistence land-use practices and through community-based livelihood projects aiming at enhancing local habitat heterogeneity and inter-habitat connectivity
AVONET: morphological, ecological and geographical data for all birds
Functional traits offer a rich quantitative framework for developing and testing theories in evolutionary biology, ecology and ecosystem science. However, the potential of functional traits to drive theoretical advances and refine models of global change can only be fully realised when species-level information is complete. Here we present the AVONET dataset containing comprehensive functional trait data for all birds, including six ecological variables, 11 continuous morphological traits, and information on range size and location. Raw morphological measurements are presented from 90,020 individuals of 11,009 extant bird species sampled from 181 countries. These data are also summarised as species averages in three taxonomic formats, allowing integration with a global phylogeny, geographical range maps, IUCN Red List data and the eBird citizen science database. The AVONET dataset provides the most detailed picture of continuous trait variation for any major radiation of organisms, offering a global template for testing hypotheses and exploring the evolutionary origins, structure and functioning of biodiversity.Additional co-authors: Samuel E. I. Jones, Claire Vincent, Anna G. Phillips, Nicola M. Marples, Flavia A. Montaño-Centellas, Victor Leandro-Silva, Santiago Claramunt, Bianca Darski, Benjamin G. Freeman, Tom P. Bregman, Christopher R. Cooney, Emma C. Hughes, Elliot J. R. Capp, Zoë K. Varley, Nicholas R. Friedman, Heiko Korntheuer, Andrea Corrales-Vargas, Christopher H. Trisos, Brian C. Weeks, Dagmar M. Hanz, Till Töpfer, Gustavo A. Bravo, Vladimír Remeš, Larissa Nowak, Lincoln S. Carneiro, Amilkar J. Moncada R., Beata Matysioková, Daniel T. Baldassarre, Alejandra Martínez-Salinas, Jared D. Wolfe, Philip M. Chapman, Benjamin G. Daly, Marjorie C. Sorensen, Alexander Neu, Michael A. Ford, Luis Fabio Silveira, David J. Kelly, Nathaniel N. D. Annorbah, Henry S. Pollock, Ada M. Grabowska-Zhang, Jay P. McEntee, Juan Carlos T. Gonzalez, Camila G. Meneses, Marcia C. Muñoz, Luke L. Powell, Gabriel A. Jamie, Thomas J. Matthews, Oscar Johnson, Guilherme R. R. Brito, Kristof Zyskowski, Ross Crates, Michael G. Harvey, Maura Jurado Zevallos, Peter A. Hosner, James M. Maley, F. Gary Stiles, Hevana S. Lima, Kaiya L. Provost, Moses Chibesa, Mmatjie Mashao, Jeffrey T. Howard, Edson Mlamba, Marcus A. H. Chua, Bicheng Li, M. Isabel Gómez, Natalia C. García, Martin Päckert, Jérôme Fuchs, Jarome R. Ali, Elizabeth P. Derryberry, Monica L. Carlson, Rolly C. Urriza, Kristin E. Brzeski, Dewi M. Prawiradilaga, Matt J. Rayner, Eliot T. Miller, Rauri C. K. Bowie, René-Marie Lafontaine, R. Paul Scofield, Yingqiang Lou, Lankani Somarathna, Denis Lepage, Marshall Illif, Eike Lena Neuschulz, Mathias Templin, D. Matthias Dehling, Jacob C. Cooper, Olivier S. G. Pauwels, Kangkuso Analuddin, Jon Fjeldså, Nathalie Seddon, Paul R. Sweet, Fabrice A. J. DeClerck, Luciano N. Naka, Jeffrey D. Brawn, Alexandre Aleixo, Katrin Böhning-Gaese, Carsten Rahbek, Susanne A. Fritz, Gavin H. Thomas, Matthias Schleunin
Seed-dispersal networks are more specialized in the Neotropics than in the Afrotropics
L.C. and I.G. were supported by the Robert Bosch Foundation. D.M.D. (DE 2754/1‐1), F.S. (HE 3041/20‐1), M.Q., V.S., E.L.N. (Research Unit 823‐825), and K.B.G., M.S. and M.G.R.V. (FOR 1246) thank the German Research Foundation (DFG) for funding. F.A.F.J. ac‐knowledges funding by a CAPES scholarship, N.F. and D.G.S. by the Robert Bosch Foundation, M.G., C.E., A.P. and M.A.P. by Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP 2010/52315‐7; 2015/15172‐7; 2016/18355‐8) and Conselho Nacional de Desenvolvimento Científico (CNPq), M.C.M. by Doctoral Fellowships from COLCIENCIAS and Rufford, M.S.S. by Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET) and FONCyT (PICT2013‐2759 and PICT2016‐0608), P.G.B. by CONICET (PIP 2014‐592) and FONCyT (PICT 2013‐1280), R.A.R. by a Doctoral Fellowship from CONICET, R.H. and S.T. (IF/00441/2013) and M.C. (SFRH/BD/96050/2013) by Fundação para a Ciência e Tecnologia, Portugal, and A.T. (CGL2013‐44386‐P) and D.G. (CGL2015‐68963‐C2‐2‐R) by the Spanish government.Dugger, P.J., Blendinger, P.G., Böhning-Gaese, K., Chama, L., Correia, M., Dehling, D.M., Emer, C., Farwig, N., Fricke, E.C., Galetti, M., García, D., Grass, I., Heleno, R., Jacomassa, F.A.F., Moraes, S., Moran, C., Muñoz, M.C., Neuschulz, E.L., Nowak, L., Piratelli, A., Pizo, M.A., Quitián, M., Rogers, H.S., Ruggera, R.A., Saavedra, F., Sánchez, M.S., Sánchez, R., Santillán, V., Schabo, D.G., da Silva, F.R., Timóteo, S., Traveset, A., Vollstädt, M.G.R., Schleuning, M
Functional connectivity of animal-dispersed plant communities depends on the interacting effects of network specialization and resource diversity
Plant functional connectivity-the dispersal of plant propagules between habitat patches-is often ensured through animal movement. Yet, there is no quantitative framework to analyse how plant-animal interactions and the movement of seed dispersers influence community-level plant functional connectivity. We propose a trait-based framework to quantify plant connectivity with a model integrating plant-frugivore networks, animal-mediated seed-dispersal distances and the selection of target patches by seed dispersers. Using this framework, we estimated how network specialization, between-patch distance and resource diversity in a target patch affect the number and diversity of seeds dispersed to that patch. Specialized networks with a high degree of niche partitioning in plant-frugivore interactions reduced functional connectivity by limiting the diversity of seeds dispersed over long distances. Resource diversity in the target patch increased both seed number and diversity, especially in specialized networks and within short and intermediate distances between patches. Notably, resource diversity was particularly important at intermediate distances, where the number and diversity of seeds reaching a patch increased more strongly with resource diversity than at longer distances. Using a trait-based framework, we show that resource diversity in the target patch is a major driver of connectivity in animal-dispersed plant communities.This work was supported by the Deutsche Forschungsgemeinschaft (DFG) within the framework of the Research Unit REASSEMBLY (FOR 5207; sub-projects SCHL 1934/5-1 and NE 1863/4-1). This research is also supported by María de Maeztu Excellence Unit 2023-2027 ref. CEX2021-001201-M, funded by MCIN/AEI/10.13039/501100011033. ID was supported by a Marie Curie Postdoctoral Fellowship (HORIZON-TMAMSCA-101068643) and an Ikerbasque postdoctoral fellowship.With funding from the Spanish government through the "Maria de Maeztu Centre of Excellence" accreditation (CEX2021-001201-M).Peer reviewe
FIGURE 1 in AVONET: morphological, ecological and geographical data for all birds
FIGURE 1 The sampling of avian morphological traits over time. The number of species (above x axis) and the number of specimens (below x axis) measured for landmark studies along with their year of publication is indicated by the vertical bars. Each bar indicates the maximum number of species and specimens measured for any trait. The number of traits in each study is represented by circle sizes (continuous from 1 to 15, with examples shown in the legend). Studies openly providing raw trait data are indicated in black. AVONET contains the raw specimen-level data for Pigot et al. (2020), along with substantial expansion in coverage of both species and specimens-per-species. To provide historical context, coloured time periods correspond roughly to interest in 'ecomorphology' (blue) and 'functional traits' (red). Citations for studies not used in the main text are provided in the Supplementary MaterialPublished as part of Tobias, Joseph A., Sheard, Catherine, Pigot, Alex L., Devenish, Adam J. M., Yang, Jingyi, Sayol, Ferran, Neate‐Clegg, Montague H. C., Alioravainen, Nico, Weeks, Thomas L., Barber, Robert A., Walkden, Patrick A., MacGregor, Hannah E. A., Jones, Samuel E. I., Vincent, Claire, Phillips, Anna G., Marples, Nicola M., Montaño‐Centellas, Flavia A., Leandro‐Silva, Victor, Claramunt, Santiago, Darski, Bianca, Freeman, Benjamin G., Bregman, Tom P., Cooney, Christopher R., Hughes, Emma C., Capp, Elliot J. R., Varley, Zoë K., Friedman, Nicholas R., Korntheuer, Heiko, Corrales‐Vargas, Andrea, Trisos, Christopher H., Weeks, Brian C., Hanz, Dagmar M., Töpfer, Till, Bravo, Gustavo A., Remeš, Vladimír, Nowak, Larissa, Carneiro, Lincoln S., Moncada R., Amilkar J., Matysioková, Beata, Baldassarre, Daniel T., Martínez‐Salinas, Alejandra, Wolfe, Jared D., Chapman, Philip M., Daly, Benjamin G., Sorensen, Marjorie C., Neu, Alexander, Ford, Michael A., Mayhew, Rebekah J., Fabio Silveira, Luis, Kelly, David J., Annorbah, Nathaniel N. D., Pollock, Henry S., Grabowska‐Zhang, Ada M., McEntee, Jay P., Carlos T. Gonzalez, Juan, Meneses, Camila G., Muñoz, Marcia C., Powell, Luke L., Jamie, Gabriel A., Matthews, Thomas J., Johnson, Oscar, Brito, Guilherme R. R., Zyskowski, Kristof, Crates, Ross, Harvey, Michael G., Jurado Zevallos, Maura, Hosner, Peter A., Bradfer‐Lawrence, Tom, Maley, James M., Stiles, F. Gary, Lima, Hevana S., Provost, Kaiya L., Chibesa, Moses, Mashao, Mmatjie, Howard, Jeffrey T., Mlamba, Edson, Chua, Marcus A. H., Li, Bicheng, Gómez, M. Isabel, García, Natalia C., Päckert, Martin, Fuchs, Jérôme, Ali, Jarome R., Derryberry, Elizabeth P., Carlson, Monica L., Urriza, Rolly C., Brzeski, Kristin E., Prawiradilaga, Dewi M., Rayner, Matt J., Miller, Eliot T., Bowie, Rauri C. K., Lafontaine, René‐Marie, Scofield, R. Paul, Lou, Yingqiang, Somarathna, Lankani, Lepage, Denis, Illif, Marshall, Neuschulz, Eike Lena, Templin, Mathias, Dehling, D. Matthias, Cooper, Jacob C., Pauwels, Olivier S. G., Analuddin, Kangkuso, Fjeldså, Jon, Seddon, Nathalie, Sweet, Paul R., DeClerck, Fabrice A. J., Naka, Luciano N., Brawn, Jeffrey D., Aleixo, Alexandre, Böhning‐Gaese, Katrin, Rahbek, Carsten, Fritz, Susanne A., Thomas, Gavin H. & Schleuning, Matthias, 2022, AVONET: morphological, ecological and geographical data for all birds, pp. 581-597 in Ecology Letters 25 (3) on page 585, DOI: 10.1111/ele.13898, http://zenodo.org/record/630898
FIGURE 3 Morphological trait sampling for all bird families. AVONET contains 718,662 in AVONET: morphological, ecological and geographical data for all birds
FIGURE 3 Morphological trait sampling for all bird families. AVONET contains 718,662 individual trait measurements, all of which are used to calculate species averages. However, sampling per species varies across families depending on taxonomy. Upper phylogram shows sampling under BirdLife International (11,009 species in 243 families). Families where sampling completeness is below 75% indicated by lighter shading. Most families with lower sampling are species poor (numbers in black circles show species richness). Lower panels show that sampling improves under more conservative taxonomic treatments of eBird (10,661 species in 249 families) and BirdTree (9993 species in 194 families). Coloured bars indicate the proportion of species in each family measured to different levels of completeness. 'Complete set' means a full set of all 9 core morphological traits (not necessarily from the same individual). 'Individuals' means any individual bird with one or more traits measuredPublished as part of Tobias, Joseph A., Sheard, Catherine, Pigot, Alex L., Devenish, Adam J. M., Yang, Jingyi, Sayol, Ferran, Neate‐Clegg, Montague H. C., Alioravainen, Nico, Weeks, Thomas L., Barber, Robert A., Walkden, Patrick A., MacGregor, Hannah E. A., Jones, Samuel E. I., Vincent, Claire, Phillips, Anna G., Marples, Nicola M., Montaño‐Centellas, Flavia A., Leandro‐Silva, Victor, Claramunt, Santiago, Darski, Bianca, Freeman, Benjamin G., Bregman, Tom P., Cooney, Christopher R., Hughes, Emma C., Capp, Elliot J. R., Varley, Zoë K., Friedman, Nicholas R., Korntheuer, Heiko, Corrales‐Vargas, Andrea, Trisos, Christopher H., Weeks, Brian C., Hanz, Dagmar M., Töpfer, Till, Bravo, Gustavo A., Remeš, Vladimír, Nowak, Larissa, Carneiro, Lincoln S., Moncada R., Amilkar J., Matysioková, Beata, Baldassarre, Daniel T., Martínez‐Salinas, Alejandra, Wolfe, Jared D., Chapman, Philip M., Daly, Benjamin G., Sorensen, Marjorie C., Neu, Alexander, Ford, Michael A., Mayhew, Rebekah J., Fabio Silveira, Luis, Kelly, David J., Annorbah, Nathaniel N. D., Pollock, Henry S., Grabowska‐Zhang, Ada M., McEntee, Jay P., Carlos T. Gonzalez, Juan, Meneses, Camila G., Muñoz, Marcia C., Powell, Luke L., Jamie, Gabriel A., Matthews, Thomas J., Johnson, Oscar, Brito, Guilherme R. R., Zyskowski, Kristof, Crates, Ross, Harvey, Michael G., Jurado Zevallos, Maura, Hosner, Peter A., Bradfer‐Lawrence, Tom, Maley, James M., Stiles, F. Gary, Lima, Hevana S., Provost, Kaiya L., Chibesa, Moses, Mashao, Mmatjie, Howard, Jeffrey T., Mlamba, Edson, Chua, Marcus A. H., Li, Bicheng, Gómez, M. Isabel, García, Natalia C., Päckert, Martin, Fuchs, Jérôme, Ali, Jarome R., Derryberry, Elizabeth P., Carlson, Monica L., Urriza, Rolly C., Brzeski, Kristin E., Prawiradilaga, Dewi M., Rayner, Matt J., Miller, Eliot T., Bowie, Rauri C. K., Lafontaine, René‐Marie, Scofield, R. Paul, Lou, Yingqiang, Somarathna, Lankani, Lepage, Denis, Illif, Marshall, Neuschulz, Eike Lena, Templin, Mathias, Dehling, D. Matthias, Cooper, Jacob C., Pauwels, Olivier S. G., Analuddin, Kangkuso, Fjeldså, Jon, Seddon, Nathalie, Sweet, Paul R., DeClerck, Fabrice A. J., Naka, Luciano N., Brawn, Jeffrey D., Aleixo, Alexandre, Böhning‐Gaese, Katrin, Rahbek, Carsten, Fritz, Susanne A., Thomas, Gavin H. & Schleuning, Matthias, 2022, AVONET: morphological, ecological and geographical data for all birds, pp. 581-597 in Ecology Letters 25 (3) on page 589, DOI: 10.1111/ele.13898, http://zenodo.org/record/630898
FIGURE 5 AVONET presents raw morphological data for 90,020 in AVONET: morphological, ecological and geographical data for all birds
FIGURE 5 AVONET presents raw morphological data for 90,020 individual birds at an average of 8.1–9.0 individuals per species (varying by taxonomy), providing a foundation for a new generation of studies investigating or accounting for intraspecific variance. This figure illustrates how variance is partitioned for a key morphological trait (beak length). Left-hand panels show that most variance is explained at higher taxonomic levels (orders, family and species), whereas intraspecific (individual) variation is contrastingly low, supporting the use of species averages in comparative studies. Curves are normal distributions based on SD; percentages (%) show proportion of variance at each level. Right-hand panels show beak length variance within families and within species (restricting to families with>5 species and species with>5 individuals measured; note different axis scales in upper and lower panel). Sequential ranks show a 'hockey-stick' distribution with examples of the most extreme outlier family (Scolopacidae) illustrated. Extreme within-species values for beak variance may reflect polymorphism or, in some cases, measurement errorPublished as part of Tobias, Joseph A., Sheard, Catherine, Pigot, Alex L., Devenish, Adam J. M., Yang, Jingyi, Sayol, Ferran, Neate‐Clegg, Montague H. C., Alioravainen, Nico, Weeks, Thomas L., Barber, Robert A., Walkden, Patrick A., MacGregor, Hannah E. A., Jones, Samuel E. I., Vincent, Claire, Phillips, Anna G., Marples, Nicola M., Montaño‐Centellas, Flavia A., Leandro‐Silva, Victor, Claramunt, Santiago, Darski, Bianca, Freeman, Benjamin G., Bregman, Tom P., Cooney, Christopher R., Hughes, Emma C., Capp, Elliot J. R., Varley, Zoë K., Friedman, Nicholas R., Korntheuer, Heiko, Corrales‐Vargas, Andrea, Trisos, Christopher H., Weeks, Brian C., Hanz, Dagmar M., Töpfer, Till, Bravo, Gustavo A., Remeš, Vladimír, Nowak, Larissa, Carneiro, Lincoln S., Moncada R., Amilkar J., Matysioková, Beata, Baldassarre, Daniel T., Martínez‐Salinas, Alejandra, Wolfe, Jared D., Chapman, Philip M., Daly, Benjamin G., Sorensen, Marjorie C., Neu, Alexander, Ford, Michael A., Mayhew, Rebekah J., Fabio Silveira, Luis, Kelly, David J., Annorbah, Nathaniel N. D., Pollock, Henry S., Grabowska‐Zhang, Ada M., McEntee, Jay P., Carlos T. Gonzalez, Juan, Meneses, Camila G., Muñoz, Marcia C., Powell, Luke L., Jamie, Gabriel A., Matthews, Thomas J., Johnson, Oscar, Brito, Guilherme R. R., Zyskowski, Kristof, Crates, Ross, Harvey, Michael G., Jurado Zevallos, Maura, Hosner, Peter A., Bradfer‐Lawrence, Tom, Maley, James M., Stiles, F. Gary, Lima, Hevana S., Provost, Kaiya L., Chibesa, Moses, Mashao, Mmatjie, Howard, Jeffrey T., Mlamba, Edson, Chua, Marcus A. H., Li, Bicheng, Gómez, M. Isabel, García, Natalia C., Päckert, Martin, Fuchs, Jérôme, Ali, Jarome R., Derryberry, Elizabeth P., Carlson, Monica L., Urriza, Rolly C., Brzeski, Kristin E., Prawiradilaga, Dewi M., Rayner, Matt J., Miller, Eliot T., Bowie, Rauri C. K., Lafontaine, René‐Marie, Scofield, R. Paul, Lou, Yingqiang, Somarathna, Lankani, Lepage, Denis, Illif, Marshall, Neuschulz, Eike Lena, Templin, Mathias, Dehling, D. Matthias, Cooper, Jacob C., Pauwels, Olivier S. G., Analuddin, Kangkuso, Fjeldså, Jon, Seddon, Nathalie, Sweet, Paul R., DeClerck, Fabrice A. J., Naka, Luciano N., Brawn, Jeffrey D., Aleixo, Alexandre, Böhning‐Gaese, Katrin, Rahbek, Carsten, Fritz, Susanne A., Thomas, Gavin H. & Schleuning, Matthias, 2022, AVONET: morphological, ecological and geographical data for all birds, pp. 581-597 in Ecology Letters 25 (3) on page 591, DOI: 10.1111/ele.13898, http://zenodo.org/record/630898
Cross-realm assessment of climate change impacts on species' abundance trends
Climate change, land-use change, pollution and exploitation are among the main drivers of species' population trends; however, their relative importance is much debated. We used a unique collection of over 1,000 local population time series in 22 communities across terrestrial, freshwater and marine realms within central Europe to compare the impacts of long-term temperature change and other environmental drivers from 1980 onwards. To disentangle different drivers, we related species' population trends to species- and driver-specific attributes, such as temperature and habitat preference or pollution tolerance. We found a consistent impact of temperature change on the local abundances of terrestrial species. Populations of warm-dwelling species increased more than those of cold-dwelling species. In contrast, impacts of temperature change on aquatic species' abundances were variable. Effects of temperature preference were more consistent in terrestrial communities than effects of habitat preference, suggesting that the impacts of temperature change have become widespread for recent changes in abundance within many terrestrial communities of central Europe.Additionally, we appreciate the open access marine data provided by the International Council for the Exploration of the Sea. We thank the following scientists for taxonomic or technical advice: C. Brendel, T. Caprano, R. Claus, K. Desender, A. Flakus, P. R. Flakus, S. Fritz, E.-M. Gerstner, J.-P. Maelfait, E.-L. Neuschulz, S. Pauls, C. Printzen, I. Schmitt and H. Turin, and I. Bartomeus for comments on a previous version of the manuscript. R.A. was supported by the EUproject LIMNOTIP funded under the seventh European Commission Framework Programme (FP7) ERA-Net Scheme (Biodiversa, 01LC1207A) and the long-term ecological research program at the Leibniz-Institute of Freshwater Ecology and Inland Fisheries (IGB). R.W.B. was supported by the Scottish Government Rural and Environment Science and Analytical Services Division (RESAS) through Theme 3 of their Strategic Research Programme. S.D. acknowledges support of the German Research Foundation DFG (grant DO 1880/1-1). S.S. acknowledges the support from the FP7 project EU BON (grant no. 308454). S.K., I.Kü. and O.S. acknowledge funding thorough the Helmholtz Association’s Programme Oriented Funding, Topic ‘Land use, biodiversity, and ecosystem services: Sustaining human livelihoods’. O.S. also acknowledges the support from FP7 via the Integrated Project STEP (grant no. 244090). D.E.B. was funded by a Landes–Offensive zur Entwicklung Wissenschaftlich–ökonomischer Exzellenz (LOEWE) excellence initiative of the Hessian Ministry for Science and the Arts and the German Research Foundation (DFG: Grant no. BO 1221/23-1).Peer Reviewe
Serum proteome profiling identifies novel and powerful markers of cystic fibrosis liver disease.
Cystic Fibrosis associated liver disease (CFLD) develops in approximately 30% of CF patients. However, routine sensitive diagnostic tools for CFLD are lacking. Within this study, we aimed to identify new experimental biomarkers for the detection of CFLD.
45 CF patients were included in the study and received transient elastography. Differential regulation of 220 different serum proteins was assessed in a subgroup of patients with and without CFLD. Most interesting candidate proteins were further quantified and validated by ELISA in the whole patient cohort. To assess a potential relation of biomarker expression to the degree of hepatic fibrosis, serum biomarkers were further determined in 18 HCV patients where liver histology was available.
43 serum proteins differed at least 2-fold in patients with CFLD compared to those without liver disease as identified in proteome profiling. In ELISA quantifications, TIMP-4 and Endoglin were significantly up-regulated in patients with CFLD as diagnosed by clinical guidelines or increased liver stiffness. Pentraxin-3 was significantly decreased in patients with CFLD. Serum TIMP-4 and Endoglin showed highest values in HCV patients with liver cirrhosis compared to those with fibrosis but without cirrhosis. At a cut-off value of 6.3 kPa, transient elastography compassed a very high diagnostic accuracy and specificity for the detection of CFLD. Among the biomarkers, TIMP-4 and Endoglin exhibited a high diagnostic accuracy for CFLD. Diagnostic sensitivities and negative predictive values were increased when elastography and TIMP-4 and Endoglin were combined for the detection of CFLD.
Serum TIMP-4 and Endoglin are increased in CFLD and their expression correlates with hepatic staging. Determination of TIMP-4 and Endoglin together with transient elastography can increase the sensitivity for the non-invasive diagnosis of CFLD
