Paul Ehrlich's Colonial Connections: Scientific Networks and Sleeping Sickness Drug Therapy Research, 1900-1914
In: Social history of medicine, Band 22, Heft 1, S. 61-77
ISSN: 1477-4666
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In: Social history of medicine, Band 22, Heft 1, S. 61-77
ISSN: 1477-4666
Forest inventory plots are widely used to estimate biomass carbon storage and its change over time. While there has been much debate and exploration of the analytical methods for calculating biomass, the methods used to determine rates of wood production have not been evaluated to the same degree. This affects assessment of ecosystem fluxes and may have wider implications if inventory data are used to parameterise biospheric models, or scaled to large areas in assessments of carbon sequestration. Here we use a dataset of 35 long-term Amazonian forest inventory plots to test different methods of calculating wood production rates. These address potential biases associated with three issues that routinely impact the interpretation of tree measurement data: (1) changes in the point of measurement (POM) of stem diameter as trees grow over time; (2) unequal length of time between censuses; and (3) the treatment of trees that pass the minimum diameter threshold ("recruits"). We derive corrections that control for changing POM height, that account for the unobserved growth of trees that die within census intervals, and that explore different assumptions regarding the growth of recruits during the previous census interval. For our dataset we find that annual aboveground coarse wood production (AGWP; in Mg ha−1 year−1 of dry matter) is underestimated on average by 9.2% if corrections are not made to control for changes in POM height. Failure to control for the length of sampling intervals results in a mean underestimation of 2.7% in annual AGWP in our plots for a mean interval length of 3.6 years. Different methods for treating recruits result in mean differences of up to 8.1% in AGWP. In general, the greater the length of time a plot is sampled for and the greater the time elapsed between censuses, the greater the tendency to underestimate wood production. We recommend that POM changes, census interval length, and the contribution of recruits should all be accounted for when estimating productivity rates, and suggest methods for doing this. ; European Union ; UK Natural Environment Research Council ; Gordon and Betty Moore Foundation ; CASE sponsorship from UNEP-WCMC ; Royal Society University Research Fellowship ; ERC Advanced Grant "Tropical Forests in the Changing Earth System" ; Royal Society Wolfson Research Merit Award
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This is the peer reviewed version of the following article: Honorio Coronado, E. N., Dexter, K. G., Pennington, R. T., Chave, J., Lewis, S. L., Alexiades, M. N., Alvarez, E., Alves de Oliveira, A., Amaral, I. L., Araujo-Murakami, A., Arets, E. J. M. M., Aymard, G. A., Baraloto, C., Bonal, D., Brienen, R., Cerón, C., Cornejo Valverde, F., Di Fiore, A., Farfan-Rios, W., Feldpausch, T. R., Higuchi, N., Huamantupa-Chuquimaco, I., Laurance, S. G., Laurance, W. F., López-Gonzalez, G., Marimon, B. S., Marimon-Junior, B. H., Monteagudo Mendoza, A., Neill, D., Palacios Cuenca, W., Peñuela Mora, M. C., Pitman, N. C. A., Prieto, A., Quesada, C. A., Ramirez Angulo, H., Rudas, A., Ruschel, A. R., Salinas Revilla, N., Salomão, R. P., Segalin de Andrade, A., Silman, M. R., Spironello, W., ter Steege, H., Terborgh, J., Toledo, M., Valenzuela Gamarra, L., Vieira, I. C. G., Vilanova Torre, E., Vos, V., Phillips, O. L. (2015), Phylogenetic diversity of Amazonian tree communities. Diversity and Distributions, 21: 1295–1307. doi:10.1111/ddi.12357, which has been published in final form at 10.1111/ddi.12357 ; Aim: To examine variation in the phylogenetic diversity (PD) of tree communities across geographical and environmental gradients in Amazonia. Location: Two hundred and eighty-three c. 1 ha forest inventory plots from across Amazonia. Methods: We evaluated PD as the total phylogenetic branch length across species in each plot (PDss), the mean pairwise phylogenetic distance between species (MPD), the mean nearest taxon distance (MNTD) and their equivalents standardized for species richness (ses.PDss, ses.MPD, ses.MNTD). We compared PD of tree communities growing (1) on substrates of varying geological age; and (2) in environments with varying ecophysiological barriers to growth and survival. Results: PDss is strongly positively correlated with species richness (SR), whereas MNTD has a negative correlation. Communities on geologically young- and intermediate-aged substrates (western and central Amazonia respectively) have the highest SR, and therefore the highest PDss and the lowest MNTD. We find that the youngest and oldest substrates (the latter on the Brazilian and Guiana Shields) have the highest ses.PDss and ses.MNTD. MPD and ses.MPD are strongly correlated with how evenly taxa are distributed among the three principal angiosperm clades and are both highest in western Amazonia. Meanwhile, seasonally dry tropical forest (SDTF) and forests on white sands have low PD, as evaluated by any metric. Main conclusions: High ses.PDss and ses.MNTD reflect greater lineage diversity in communities. We suggest that high ses.PDss and ses.MNTD in western Amazonia results from its favourable, easy-to-colonize environment, whereas high values in the Brazilian and Guianan Shields may be due to accumulation of lineages over a longer period of time. White-sand forests and SDTF are dominated by close relatives from fewer lineages, perhaps reflecting ecophysiological barriers that are difficult to surmount evolutionarily. Because MPD and ses.MPD do not reflect lineage diversity per se, we suggest that PDss, ses.PDss and ses.MNTD may be the most useful diversity metrics for setting large-scale conservation priorities. ; FINCyT - PhD studentship ; School of Geography of the University of Leeds ; Royal Botanic Garden Edinburgh ; Natural Environment Research Council (NERC) ; Gordon and Betty Moore Foundation ; European Union's Seventh Framework Programme ; ERC ; CNPq/PELD ; NSF - Fellowship
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Aim: The accurate mapping of forest carbon stocks is essential for understanding the global carbon cycle, for assessing emissions from deforestation, and for rational land-use planning. Remote sensing (RS) is currently the key tool for this purpose, but RS does not estimate vegetation biomass directly, and thus may miss significant spatial variations in forest structure. We test the stated accuracy of pantropical carbon maps using a large independent field dataset. Location: Tropical forests of the Amazon basin. The permanent archive of the field plot data can be accessed at: http://dx.doi.org/10.5521/FORESTPLOTS.NET/2014_1 Methods: Two recent pantropical RS maps of vegetation carbon are compared to a unique ground-plot dataset, involving tree measurements in 413 large inventory plots located in nine countries. The RS maps were compared directly to field plots, and kriging of the field data was used to allow area-based comparisons. Results: The two RS carbon maps fail to capture the main gradient in Amazon forest carbon detected using 413 ground plots, from the densely wooded tall forests of the north-east, to the light-wooded, shorter forests of the south-west. The differences between plots and RS maps far exceed the uncertainties given in these studies, with whole regions over- or under-estimated by >???25%, whereas regional uncertainties for the maps were reported to be ??5%. Main conclusions: Pantropical biomass maps are widely used by governments and by projects aiming to reduce deforestation using carbon offsets, but may have significant regional biases. Carbon-mapping techniques must be revised to account for the known ecological variation in tree wood density and allometry to create maps suitable for carbon accounting. The use of single relationships between tree canopy height and above-ground biomass inevitably yields large, spatially correlated errors. This presents a significant challenge to both the forest conservation and remote sensing communities, because neither wood density nor species assemblages can be reliably mapped from space.
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Understanding the processes that determine aboveground biomass (AGB) in Amazonian forests is important for predicting the sensitivity of these ecosystems to environmental change and for designing and evaluating dynamic global vegetation models (DGVMs). AGB is determined by inputs from woody productivity (woody NPP) and the rate at which carbon is lost through tree mortality. Here, we test whether two direct metrics of tree mortality (the absolute rate of woody biomass loss and the rate of stem mortality) and/or woody NPP, control variation in AGB among 167 plots in intact forest across Amazonia. We then compare these relationships and the observed variation in AGB and woody NPP with the predictions of four DGVMs. The observations show that stem mortality rates, rather than absolute rates of woody biomass loss, are the most important predictor of AGB, which is consistent with the importance of stand size-structure for determining spatial variation in AGB. The relationship between stem mortality rates and AGB varies among different regions of Amazonia, indicating that variation in wood density and height/diameter relationships also influence AGB. In contrast to previous findings, we find that woody NPP is not correlated with stem mortality rates, and is weakly positively correlated with AGB. Across the four models, basin-wide average AGB is similar to the mean of the observations. However, the models consistently overestimate woody NPP, and poorly represent the spatial patterns of both AGB and woody NPP estimated using plot data. In marked contrast to the observations, DGVMs typically show strong positive relationships between woody NPP and AGB. Resolving these differences will require incorporating forest size structure, mechanistic models of stem mortality and variation in functional composition in DGVMs. This article is protected by copyright. All rights reserved. ; This paper is a product of the European Union's Seventh Frame-work Programme AMAZALERT project (282664). The field dataused in this study have been generated by the RAINFOR net-work, which has been supported by a Gordon and Betty MooreFoundation grant, the European Union's Seventh FrameworkProgramme projects 283080, 'GEOCARBON'; and 282664,'AMAZALERT'; ERC grant 'Tropical Forests in the ChangingEarth System'), and Natural Environment Research Council(NERC) Urgency, Consortium and Standard Grants 'AMAZO-NICA' (NE/F005806/1), 'TROBIT' (NE/D005590/1) and 'NicheEvolution of South American Trees' (NE/I028122/1). Additionaldata were included from the Tropical Ecology Assessment andMonitoring (TEAM) Network – a collaboration between Conser-vation International, the Missouri Botanical Garden, the Smith-sonian Institution and the Wildlife Conservation Society, andpartly funded by these institutions, the Gordon and Betty MooreFoundation, and other donors. Fieldwork was also partially sup-ported by Conselho Nacional de Desenvolvimento Cientı´fico eTecnolo´gico of Brazil (CNPq), project Programa de PesquisasEcolo´gicas de Longa Duracßa˜o (PELD-403725/2012-7). A.R.acknowledges funding from the Helmholtz Alliance 'RemoteSensing and Earth System Dynamics'; L.P., M.P.C. E.A. andM.T. are partially funded by the EU FP7 project 'ROBIN'(283093), with co-funding for E.A. from the Dutch Ministry ofEconomic Affairs (KB-14-003-030); B.C. [was supported in partby the US DOE (BER) NGEE-Tropics project (subcontract toLANL). O.L.P. is supported by an ERC Advanced Grant and is aRoyal Society-Wolfson Research Merit Award holder. P.M.acknowledges support from ARC grant FT110100457 and NERCgrants NE/J011002/1, and T.R.B. acknowledges support from aLeverhulme Trust Research Fellowship.
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© 2014 The Authors. Global Ecology and Biogeography published by John Wiley & Sons Ltd. ; The accurate mapping of forest carbon stocks is essential for understanding the global carbon cycle, for assessing emissions from deforestation, and for rational land-use planning. Remote sensing (RS) is currently the key tool for this purpose, but RS does not estimate vegetation biomass directly, and thus may miss significant spatial variations in forest structure. We test the stated accuracy of pantropical carbon maps using a large independent field dataset. ; Gordon and Betty Moore Foundation ; European Union's Seventh Framework Programme ; ERC ; NERC ; PRONEX -FAPEAM/CNPq. ; Hidroveg FAPESP/FAPEAM ; Universal/CNPq. ; INCT-CENBAM ; Investissement d'Avenir grants of the French ANR. ; Royal Society Fellowship ; Royal Society Wolfson Research Merit Award
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This is the final version. Available on open access from Wiley via the DOI in this record ; Most of the planet's diversity is concentrated in the tropics, which includes many regions undergoing rapid climate change. Yet, while climate-induced biodiversity changes are widely documented elsewhere, few studies have addressed this issue for lowland tropical ecosystems. Here we investigate whether the floristic and functional composition of intact lowland Amazonian forests have been changing by evaluating records from 106 long-term inventory plots spanning 30 years. We analyse three traits that have been hypothesized to respond to different environmental drivers (increase in moisture stress and atmospheric CO2 concentrations): maximum tree size, biogeographic water-deficit affiliation and wood density. Tree communities have become increasingly dominated by large-statured taxa, but to date there has been no detectable change in mean wood density or water deficit affiliation at the community level, despite most forest plots having experienced an intensification of the dry season. However, among newly recruited trees, dry-affiliated genera have become more abundant, while the mortality of wet-affiliated genera has increased in those plots where the dry season has intensified most. Thus, a slow shift to a more dry-affiliated Amazonia is underway, with changes in compositional dynamics (recruits and mortality) consistent with climate-change drivers, but yet to significantly impact whole-community composition. The Amazon observational record suggests that the increase in atmospheric CO2 is driving a shift within tree communities to large-statured species and that climate changes to date will impact forest composition, but long generation times of tropical trees mean that biodiversity change is lagging behind climate change. ; Support for RAINFOR has come from the Natural Environment Research Council (NERC) Urgency Grants and NERC Consortium Grants "AMAZONICA" (NE/F005806/1), "TROBIT" (NE/D005590/1) and "BIO‐RED" (NE/N012542/1), a European Research Council (ERC) grant (T‐FORCES, "Tropical Forests in the Changing Earth System"), the Gordon and Betty Moore Foundation, the European Union's Seventh Framework Programme (282664, "AMAZALERT") and the Royal Society (CH160091). OLP was supported by an ERC Advanced Grant and a Royal Society Wolfson Research Merit Award. KGD was supported by a Leverhulme Trust International Academic Fellowship. This paper is part of the PhD of AE‐M, which was funded by the ERC T‐FORCES grant. AE‐M is currently supported by T‐FORCES and the NERC project "TREMOR" (NE/N004655/1).
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Open Acess journal ; While Amazonian forests are extraordinarily diverse, the abundance of trees is skewed strongly towards relatively few 'hyperdominant' species. In addition to their diversity, Amazonian trees are a key component of the global carbon cycle, assimilating and storing more carbon than any other ecosystem on Earth. Here we ask, using a unique data set of 530 forest plots, if the functions of storing and producing woody carbon are concentrated in a small number of tree species, whether the most abundant species also dominate carbon cycling, and whether dominant species are characterized by specific functional traits. We find that dominance of forest function is even more concentrated in a few species than is dominance of tree abundance, with only ≈1% of Amazon tree species responsible for 50% of carbon storage and productivity. Although those species that contribute most to biomass and productivity are often abundant, species maximum size is also influential, while the identity and ranking of dominant species varies by function and by region. ; Gordon and Betty Moore Foundation ; European Union Seventh Framework Programme ; ERC ; Natural Environment Research Council ; PRONEX—FAPEAM/CNPq ; Hidroveg FAPESP/FAPEAM ; Universal/CNPq ; INCT-CENBAM ; Fitogeografia da Transição Amazônia/Cerrado CNPq ; Transição Amazônia/Cerrado ; French ANR - Investissement d'Avenir grants ; CNPq ; Royal Society - Wolfson Research Merit Award ; Dutch Ministry of Economic Affairs
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Estimates of extinction risk for Amazonian plant and animal species are rare and not often incorporated into land-use policy and conservation planning. We overlay spatial distribution models with historical and projected deforestation to show that at least 36% and up to 57% of all Amazonian tree species are likely to qualify as globally threatened under International Union for Conservation of Nature (IUCN) Red List criteria. If confirmed, these results would increase the number of threatened plant species on Earth by 22%. We show that the trends observed in Amazonia apply to trees throughout the tropics, and we predict that most of the world's >40,000 tropical tree species now qualify as globally threatened. A gap analysis suggests that existing Amazonian protected areas and indigenous territories will protect viable populations of most threatened species if these areas suffer no further degradation, highlighting the key roles that protected areas, indigenous peoples, and improved governance can play in preventing large-scale extinctions in the tropics in this century. ; Alberta Mennega Stichting ; ALCOA Suriname ; Amazon Conservation Association ; Banco de la República ; CELOS Suriname ; CAPES (PNPG) ; Conselho Nacional de Desenvovimento Científico e Tecnológico of Brazil (CNPq) Projects CENBAM, PELD (558069/2009-6), PRONEX-FAPEAM (1600/2006), Áreas Úmidas, MAUA; PELD (403792/2012-6), PPBio, PVE 004/2012, Universal (479599/2008-4), and Universal 307807- 2009-6 ; FAPEAM projects DCR/2006, Hidroveg with FAPESP, and PRONEX with CNPq ; FAPESP ; Colciencias ; CONICIT ; Duke University ; Ecopetrol ; FEPIM 044/2003 ; The Field Museum ; Conservation International/DC (TEAM/Instituto Nacional de Pesquisas da Amazônia Manaus ; Gordon and Betty Moore Foundation ; Guyana Forestry Commission ; Investissement d'Avenir grant of the French ANR (CEBA: ANR-10-LABX-0025 ; IVIC ; Margaret Mee Amazon Trust ; Miquel fonds ; MCTI–Museu Paraense Emílio Goeldi–Proc. 407232/2013-3–PVE-MEC/MCTI/CAPES/CNPq; National Geographic Society (7754-04 and 8047-06 to P.M.J.; 6679-99, 7435-03, and 8481-08 to T.W.H.); NSF-0726797 to K.R.Y ; NSF Dissertation Improvement ; Netherlands Foundation for the Advancement of Tropical Research WOTRO (grants WB85-335 and W84-581) ; Primate Conservation Inc. ; Programme Ecosystèmes Tropicaux (French Ministry of Ecology and Sustainable Development) ; Shell Prospecting and Development Peru ; Smithsonian Institution's Biological Diversity of the Guiana Shield Program ; Stichting het van Eeden-fonds ; The Body Shop ; The Ministry of the Environment of Ecuador ; TROBIT ; Tropenbos International ; U.S. National Science Foundation (NSF-0743457 and NSF-0101775 to P.M.J.; NSF-0918591 to T.W.H.) ; USAID ; Variety Woods Guyana ; Wenner-Gren Foundation ; WWF-Brazi ; WWF-Guianas ; XIIéme Contrat de Plan Etat Région-Guyane (French Government and European Union) ; European Union ; UK Natural Environment Research Counci ; European Research Council ; Royal Society Wolfson Research Merit Award
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