Pervasive gaps in Amazonian ecological research

Biodiversity loss is one of the main challenges of our time,1,2 and attempts to address it require a clear un derstanding of how ecological communities respond to environmental change across time and space.3,4 While the increasing availability of global databases on ecological communities has advanced our knowledge of biodiversity sensitivity to environmental changes,5–7 vast areas of the tropics remain understudied.8–11 In the American tropics, Amazonia stands out as the world’s most diverse rainforest and the primary source of Neotropical biodiversity,12 but it remains among the least known forests in America and is often underrepre sented in biodiversity databases.13–15 To worsen this situation, human-induced modifications16,17 may elim inate pieces of the Amazon’s biodiversity puzzle before we can use them to understand how ecological com munities are responding. To increase generalization and applicability of biodiversity knowledge,18,19 it is thus crucial to reduce biases in ecological research, particularly in regions projected to face the most pronounced environmental changes. We integrate ecological community metadata of 7,694 sampling sites for multiple or ganism groups in a machine learning model framework to map the research probability across the Brazilian Amazonia, while identifying the region’s vulnerability to environmental change. 15%–18% of the most ne glected areas in ecological research are expected to experience severe climate or land use changes by 2050. This means that unless we take immediate action, we will not be able to establish their current status, much less monitor how it is changing and what is being lostinfo:eu-repo/semantics/publishedVersio

Pervasive gaps in Amazonian ecological research

Biodiversity loss is one of the main challenges of our time,1,2 and attempts to address it require a clear understanding of how ecological communities respond to environmental change across time and space.3,4 While the increasing availability of global databases on ecological communities has advanced our knowledge of biodiversity sensitivity to environmental changes,5,6,7 vast areas of the tropics remain understudied.8,9,10,11 In the American tropics, Amazonia stands out as the world's most diverse rainforest and the primary source of Neotropical biodiversity,12 but it remains among the least known forests in America and is often underrepresented in biodiversity databases.13,14,15 To worsen this situation, human-induced modifications16,17 may eliminate pieces of the Amazon's biodiversity puzzle before we can use them to understand how ecological communities are responding. To increase generalization and applicability of biodiversity knowledge,18,19 it is thus crucial to reduce biases in ecological research, particularly in regions projected to face the most pronounced environmental changes. We integrate ecological community metadata of 7,694 sampling sites for multiple organism groups in a machine learning model framework to map the research probability across the Brazilian Amazonia, while identifying the region's vulnerability to environmental change. 15%–18% of the most neglected areas in ecological research are expected to experience severe climate or land use changes by 2050. This means that unless we take immediate action, we will not be able to establish their current status, much less monitor how it is changing and what is being lost

Solubility of Os and Ir in sulfide melt: Implications for Re/Os fractionation during mantle melting

Although both rhenium (Re) and osmium (Os) are highly siderophile elements (HSE), they show contrasting geochemical behaviors during partial melting of the mantle - Re is mildly incompatible whereas Os appears to be compatible. This fundamental difference, unique among commonly used isotopic chronometers, causes large variations of Re/Os in oceanic basalts. However, which mantle phases control the geochemical behavior of these elements during partial melting is controversial. Sulfide is typically regarded as a major host for these elements, but recent studies have shown that silicate phases and spinel may also play a role. Here we report the results of an experimental study on the solubilities of Os and Ir in sulfide melts (or mattes) over a large range of oxygen (fO 2) and sulfur (fS 2) fugacities at 1300 °C. Our experiments indicate that the solubilities of Os and Ir in mattes increase with increasing fS 2, with both Os and Ir dissolving as trivalent species at high fS 2 and metallic species at low fS 2. The effect of fO 2 on Os and Ir solubilities appears to be related to oxygen being dissolved into the matte at more oxidizing conditions. Our results coupled with solubility data for Os and Ir in silicate melts have enabled matte/silicate melt partition coefficients for these elements (D i matte/sil) to be calculated. Assuming a relative oxygen fugacity equal to the quartz-fayalite-magnetite redox equilibrium (i.e. QFM) and a sulfur fugacity of 10 -0.5 bar, calculated D Os matte/sil is ~10 4 and D Ir matte/sil is ~10 6. The low solubilities of Os and Ir in silicate melts, coupled with their high matte/silicate melt partition coefficients, suggest that Os and Ir in fertile mantle with ~200 ppm S are held in the mantle matte phase. However, we show that the empirical range of Re/Os in mid-ocean ridge basalts (MORB) can only be reproduced when sulfide is exhausted by high degrees of partial melting, leaving Os-Ir-rich metal alloy in the mantle residue

Unravelling lunar mantle source processes via the Ti isotope composition of lunar basalts

Formation and crystallisation of the Lunar Magma Ocean (LMO) was one of the most incisive events during the early evolution of the Moon. Lunar Magma Ocean solidification concluded with the coeval formation of K-, REE- and P-rich components (KREEP) and an ilmenite-bearing cumulate (IBC) layer. Gravitational overturn of the lunar mantle generated eruptions of basaltic rocks with variable Ti contents, of which their δ49Ti variations may now reflect variable mixtures of ambient lunar mantle and the IBC. To better understand the processes generating the spectrum of lunar low-Ti and high-Ti basalts and the role of Ti-rich phases such as ilmenite, we determined the mass dependent Ti isotope composition of four KREEP-rich samples, 12 low-Ti, and eight high-Ti mare basalts by using a 47Ti-49Ti double spike. Our data reveal significant variations in δ49Ti for KREEP-rich samples (+0.117 to +0.296 %) and intra-group variations in the mare basalts (-0.030 to +0.055 % for low-Ti and +0.009 to +0.115 % for high-Ti basalts). We modelled the δ49Ti of KREEP using previously published HFSE data as well as the δ49Ti evolution during fractional crystallisation of the LMO. Both approaches yield δ49TiKREEP similar to measured values and are in excellent agreement with previous studies. The involvement of ilmenite in the petrogenesis of the lunar mare basalts is further evaluated by combining our results with element ratios of HFSE, U and Th, revealing that partial melting in an overturned lunar mantle and fractional crystallisation of ilmenite must be the main processes accounting for mass dependent Ti isotope variations in lunar basalts. Based on our results we can also exclude formation of high-Ti basalts by simple assimilation of ilmenite by ascending melts from the depleted lunar mantle. Rather, our data are in accord with melting of these basalts from a hybrid mantle source formed in the aftermath of gravitational lunar mantle overturn, which is in good agreement with previous Fe isotope data.SCOPUS: ar.jinfo:eu-repo/semantics/publishe

The redox dependence of titanium isotope fractionation in synthetic Ti-rich lunar melts

Equilibria between Ti oxides and silicate melt lead to Ti isotope fractionation in terrestrial samples, with isotopically light Ti oxides and isotopically heavy coexisting melt. However, while Ti is mostly tetravalent in terrestrial samples, around 10% of the overall Ti is trivalent at fO2 relevant to lunar magmatism (~ IW-1). The different valences of Ti in lunar samples, could additionally influence Ti stable isotope fractionation during petrogenesis of lunar basalts to an unknown extent. We performed an experimental approach using gas mixing furnaces to investigate the effect of Ti oxide formation at different fO2 on Ti stable isotope fractionation during mare basalt petrogenesis. Two identical bulk compositions were equilibrated simultaneously during each experiment to guarantee comparability. One experiment was investigated with the EPMA to characterize the petrology of experimental run products, whereas the second experiment was crushed, and fabricated phases (i.e., oxides, silicates and glass) were handpicked, separated and digested. An aliquot of each sample was mixed with a Ti double-spike, before Ti was separated from matrix and interfering elements using a modified HFSE chemistry. Our study shows fO2-dependent fractionation within seven samples from air to IW-1, especially ∆49Ti-melt and ∆49Tiarmalcolite-orthopyroxene become more fractionated from oxidized to reduced conditions (− 0.092 ± 0.028-  − 0.200 ± 0.033 ‰ and  − 0.089 ± 0.027- − 0.250 ± 0.049 ‰, respectively), whereas ∆49Tiorthopyroxene-melt shows only a minor fractionation (− 0.002 ± 0.017-0.050 ± 0.025 ‰). The results of this study show that Ti isotope fractionation during mare basalt petrogenesis is expected to be redox dependent and mineral-melt fractionation as commonly determined for terrestrial fO2 may not be directly applied to a lunar setting. This is important for the evaluation of Ti isotope fractionation resulting from lunar magmatism, which takes place under more reducing conditions compared to the more oxidized terrestrial magmatism.Deutsche ForschungsgemeinschaftProjekt DEA

Constraining the process of intracontinental subduction in the Austroalpine Nappes: Implications from petrology and Lu‐Hf geochronology of eclogites

AbstractHigh‐ and ultrahigh‐pressure rocks occur in the Austroalpine Nappes in a ~400 km long belt from the Texel Complex in the west to the Sieggraben Unit in the east. Garnet growth during pressure increase was dated using Lu‐Hf chronometry. The results range between c. 100 and 90 Ma, indicating a short‐lived period of subduction. Combined with already published data, our estimates of metamorphic conditions indicate a field gradient with increasing pressure and temperature from the northwest to the southeast, where the rocks experienced ultrahigh‐pressure metamorphism. The P‐T conditions of the eclogites generally lie on the ‘warm’ side of the global range of subduction‐zone metamorphic conditions. The oldest Cretaceous eclogites (c. 100 Ma) are found in the Saualpe‐Koralpe area derived from widespread gabbros formed during Permian to Triassic rifting. In the Texel Complex garnets showing two growth phases yielded a Variscan‐Eoalpine mixed age indicating re‐subduction of Variscan eclogite‐bearing continental crust during the Eoalpine orogeny. Jurassic blueschist‐facies metamorphism at Meliata in the Western Carpathians and Cretaceous eclogite‐facies metamorphism in the Austroalpine are separated by a time gap of c. 50 Ma and therefore do not represent a transition from oceanic to continental subduction but rather separate events. Thus, we propose that subduction initiation was intracontinental at the site of a Permian rift.German Science Foundation (DFG)Slovak Research and Development Agency http://dx.doi.org/10.13039/50110000535

Fractionation of rhenium from osmium during noble metal alloy formation in association with sulfides: Implications for the interpretation of model ages in alloy-bearing magmatic rocks

Although Earth's continental crust is thought to derive from melting of the Earth's mantle, how the crust has formed and the timing of its formation are not well understood. The main difficulty in understanding how the crust was extracted from the Earth's mantle is that most isotope systems recorded in mantle rocks have been disturbed by crustal recycling, metasomatic activity and dilution of the signal by mantle convection. In this regard, important age constraints can be obtained from Re-Os model ages in platinum group minerals (PGM), as Re-poor and Os-rich PGM show evidence of melting events up to 4.1 Ga. To constrain the origin of the Re-Os fractionation and Os isotope systematics of natural PGM, we have investigated the linkage between sulfide and PGM grains of variable composition via a series of high-temperature experiments carried out at 1 bar. We show that with the exception of laurite, all experimentally-produced PGM, in particular Pt3Fe (isoferroplatinum) and Pt-Ir metal grains, are systematically richer in Re than their sulfide precursors and will develop radiogenic 187Os/188Os signatures over time relative to their host base metal sulfides. Cooling of an PGM-saturated sulfide assemblage shows a tendency to amplify the extent of Re-Os fractionation between PGM and the different sulfide phases present during cooling. Conversely, laurite grains (RuS2) are shown to accept little to no Re in them and their Os isotope composition changes little over time as a result. Laurite is therefore the PGM that provides the most robust Re-depletion ages in mantle lithologies. Our results are broadly consistent with observations made on natural PGM, where laurites are systematically less radiogenic than Pt-rich PGM. These experimental results highlight the need for the acquisition of large datasets for both mantle materials and ophiolite-derived detrital grains that include measurements of the Os isotope composition of minerals rich in highly siderophile elements at the grain scale (i.e. PGM and base metal sulfides). Only with such datasets is it possible to identify past episodes of mantle melting.SCOPUS: ar.jinfo:eu-repo/semantics/publishe

Lu–Hf garnet systematics of a polymetamorphic basement unit: new evidence for coherent exhumation of the Adula Nappe (Central Alps) from eclogite-facies conditions

The Adula Nappe in the Central Alps is a mixture of various pre-Mesozoic continental basement rocks, metabasics, ultrabasics, and Mesozoic cover rocks, which were pervasively deformed during Alpine orogeny. Metabasics, ultrabasics, and locally garnet–mica schists preserve eclogite-facies assemblages while the bulk of the nappe lacks such evidence. We provide garnet major-element data, Lu profiles, and Lu–Hf garnet geochronology from eclogites sampled along a north–south traverse. A southward increasing Alpine overprint over pre-Alpine garnets is observed throughout the nappe. Garnets in a sample from the northern Adula Nappe display a single growth cycle and yield a Variscan age of 323.8 ± 6.9 Ma. In contrast, a sample from Alpe Arami in the southernmost part contains unzoned garnets that fully equilibrated to Alpine high-pressure (HP) metamorphic conditions with temperatures exceeding 800 °C. We suggest that the respective Eocene Lu–Hf age of 34.1 ± 2.8 Ma is affected by partial re-equilibration after the Alpine pressure peak. A third sample from the central part of the nappe contains separable Alpine and Variscan garnet populations. The Alpine population yields a maximum age of 38.8 ± 4.3 Ma in line with a previously published garnet maximum age from the central nappe of 37.1 ± 0.9 Ma. The Adula Nappe represents a coherent basement unit, which preserves a continuous Alpine high-pressure metamorphic gradient. It was subducted as a whole in a single, short-lived event in the upper Eocene. Controversial HP ages and conditions in the Adula Nappe may result from partly preserved Variscan assemblages in Alpine metamorphic rocks

Redox controls on tungsten and uranium crystal/silicate melt partitioning and implications for the U/W and Th/W ratio of the lunar mantle

The timing of core formation is essential for understanding the early differentiation history of the Earth and the Moon. Because Hf is lithophile and W is siderophile during metal-silicate segregation, the decay of 182Hf to 182W (half-life of 9 Ma) has proven to be a useful chronometer of core-mantle differentiation events. A key parameter for the interpretation of 182Hf/182W data is the Hf/W ratio of the primitive (i.e. undepleted) mantle. Since W is incompatible during mantle melting, its ratio relative to U and other similarly incompatible elements in basalts (e.g. Th, La) may be used as proxies for their mantle sources. However, the assumption that W and U are equally incompatible may be flawed for petrological systems that equilibrated over a large range of oxygen fugacity (fO2). Although W is typically perceived as being homovalent, evidence suggests that U is heterovalent over the range of fO2 inferred for the silicate mantles of the Earth and the Moon.Here we report new partitioning data for W, U, high-field-strength elements (HFSE), and Th between clinopyroxene, orthopyroxene, olivine, plagioclase and silicate melt. In agreement with previous studies, we show that these elements behave as homovalent elements at fO2 characteristic of Earth's upper mantle. However, both W and U become more compatible at low fO2, indicating a change in their redox state, with W becoming more compatible at progressively lower fO2. This result for W is particularly unexpected, because this element was thought to be hexavalent even at very low fO2. The much higher compatibility of W4+ (the species inferred here at low fO2) relative to W6+ means that even a small fraction of W4+ will have a significant effect on the overall compatibility of W. Our results imply that over the range of reducing conditions in which lunar differentiation is thought to have taken place (i.e. ~IW-2 to IW-0.5), W is likely to become fractionated from U. When our partitioning data are applied to model the fractional crystallization of a lunar magma ocean, lunar trends for U/W, Hf/W and Th/W are well reproduced. The result of this model carries with it the implication that the Hf/W of the bulk silicate fractions that comprise the Earth and the Moon are virtually identical