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1.
The main group pallasites and the mesosiderites fall within the oxygen isotope group previously determined for the calcium-rich achondrites (eucrites, howardites and diogenites), consistent with derivation from a common source material, and perhaps a common parent body. The group IIE iron meteorites were derived from the same source material as H-group ordinary chondrites. The chondrite-like silicate inclusions in group IAB iron meteorites are not related to the ordinary chondrites, but may be related to the enstatite chondrites. Several meteorites previously considered “anomalous” fall into these groups: Pontlyfni and Winona with the IAB irons, and Netschaëvo possibly with the H chondrites and IIE irons. The unusual pallasites Eagle Station and Itzawisis have remarkable oxygen isotopic compositions, and have more of the 16O-rich component than any other meteorite. Bencubbin and Weatherford are also unusual in their isotopic compositions, and may bear some relationship to the C2 carbonaceous chondrites. Lodran and Enon are isotopically similar to one another and are close to the achondrite-mesosiderite-pallasite group.  相似文献   

2.
Allan Hills 85085 is a unique chondrite with affinities to the Al Rais-Renazzo clan of carbonaceous chondrites. Its constituents are less than 50 μm in mean size. Chondrules and microchondrules of all textures are present; nonporphyritic chondrules are unusually abundant. The mean compositions of porphyritic, nonporphyritic and barred olivine chondrules resemble those in ordinary chondrites except that they are depleted in volatile elements. Ca-, Al-rich inclusions are abundant and largely free of nebular alteration; they comprise types similar to those in CM and CO chondrites, as well as unique types. Calcium dialuminate occurs in several inclusions. Metal, silicate and sulfide compositions are close to those in CM-CO chondrites and Al Rais and Renazzo. C1-chondrite clasts and metal-rich “reduced” clasts are present, but opaque matrix is absent. Siderophile abundances in ALH85085 are extremely high (e.g., Fe/Si= 1.7 × solar), and volatiles are depleted (e.g., Na/Si= 0.25 × solar, S/Si= 0.03 × solar). Nonvolatile lithophile abundances are similar to those in Al Rais, Renazzo, and CM and CO chondrites.ALH85085 agglomerated when temperatures in the nebula were near 1000 K, in the same region where Renazzo, Al Rais and the CI chondrites formed. Agglomeration of high-temperature material may thus be a mechanism by which the fractionation of refractory lithophiles occurred in the nebula. Chondrule formation must have occurred at high temperatures when clumps of precursors were small. After agglomeration, ALH85085 was annealed and lightly shocked. C1 and other clasts were subsequently incorporated during late-stage brecciation.  相似文献   

3.
We have developed a closed-system combustion technique and utilized it to progressively oxidize a gas-rich, highly carbonaceous acid residue and a fine-grained (<4 μm) matrix sample from the Allende C3V meteorite and analyze the released gases mass spectrometrically. For the residue complete gas mobilization occurs at temperatures below 600°C. The temperature interval over which most of the gases are released coincides with that for combustion of most of the carbon. Release is primarily due to chemical attack rather than thermal activation of the gases. There are somewhat different oxidation thresholds for the heavy gases (Ar, Kr, and Xe) and the light gases (He, Ne), indicating chemically different sites for the two groups. Relative enhancement of isotopically anomalous components near 600°C is as large as in any open-system oxidation method. Differential combustion of the matrix sample reveals three distinct outgassing peaks, the first matching the release from the carbonaceous residue (“combustibles”), the second attributed to sulfides, and the third tentatively assigned to silicates. They comprise about 53%, 7% and 40% of the total heavy gases respectively. While the “sulfides” exhibit a small fission-like component, the Xe in the “silicates” appears isotopically uniform with roughly AVCC composition. The “combustibles” of the matrix contain relatively less excess129Xe than the residue, perhaps indicating that ～10% of the total129Xe in the residue was acquired from “silicates” by redistribution during acid treatment. We cannot rule out the possibility that planetary gases assigned to “sulfides” or “silicates” actually reside in carbonaceous phases somehow sheltered within soluble mineral assemblages, or in acid-soluble carbonaceous phases resistant to oxidation. Integrated releases below and above 600°C during the matrix combustion exhibit virtually identical heavy gas elemental composition, implying similar fractionation during planetary gas entrapment in various materials or in the same material in various environments.  相似文献   

4.
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5.
If surface anomalies in the composition of the metallic-line A stars (Am stars) are due to a precipitation of planet-like bodies (planetoids) on them, then one should expect a correlation to exist between the overabundance of heavier-than-iron elements on these stars and their “standard” abundances in the solar system (since chondrites provide the “standard” level for these elements). However, an anticorrelation was revealed.Nevertheless, this fact supports the original suggestion on the origin of the metallicism of A stars, and can easily be explained within the author's hypothesis on the formation of the Sun from matter escaping from the proto-Jupiter. During the terminal stages of mass transfer, the matter was strongly depleted in refractories (forming the rocky core of Jupiter). Therefore the composition of the meteorites formed should not coincide with the primary composition of the matter. Thus the Sun's outer layers may also have a distorted composition. The author concludes that it is desirable to revise the “standard” abundances of elements heavier than iron.From a comparison of the surface composition of Am stars with the composition of lunar anorthosites and that of rocks in the upper zones of the Skaergaard intrusion (Greenland), the Am phenomenon may be seen to result from a precipitation of large geochemically differentiated planetoids onto a star. Such planetoids (including the Moon) condense in the cooled envelope of the primary component of a close binary stellar system.  相似文献   

6.
Chondritic meteorites and their components formed in the protoplanetary disk surrounding the nascent sun. We show here that the two volumetrically dominating components of carbonaceous chondrites, chondrules and matrix did not form independently. They must have been derived from a single, common source. We analyzed Ca and Al in chondrules and matrix of the CV type carbonaceous chondrites Allende and Y-86751. The Ca/Al-ratios of chondrules and matrix of both chondrites are complementary, but in case of Allende chondrules have sub-chondritic and matrix super-chondritic Ca/Al-ratios and in case of Y-86751 chondrules have super-chondritic and matrix sub-chondritic Ca/Al-ratios. This rules out the redistribution of Ca between chondrules and matrix during parent body alteration. Tiny spinel grains in the matrix produce the high Al in the matrix of Y-86751. In Allende these spinels were most probably included in chondrules. The most plausible explanation for this Ca- and Al-distribution in the same type of chondrite is that both chondrules and matrix formed from the same chemical reservoir. Tiny differences in nebular conditions during formation of these two meteorites must have led to the observed differences. These are severe constraints for all models of chondrule formation. Any model involving separate formation of chondrules and matrix, such as the X-wind model can be excluded.  相似文献   

7.
Optically “striated” orthopyroxenes in two ordinary chondrites, Allegan (H5) and Quenggouk (H4), are compared with shock-affected orthopyroxenes in Saint-Sévérin (LL6) and Ambapur Nagla (H5) by high-voltage transmission electron microscopy. The striated orthopyroxenes have very many, thin, evenly distributed lamellae of clinopyroxene. They are undeformed and also lack evidence of partial inversion from clinopyroxene to orthopyroxene. Striated orthopyroxene does not seem to be a reliable indicator of prograde metamorphism. Instead, it is interpreted as inverted protopyroxene, produced during the cooling of chondrules at slower rates than the rapid quenching of Type 3 chondrules. The conclusions are consistent with retrograde models for the evolution of H-group chondrites, in which the higher Petrologic Types are attributed to retarded cooling due to accretionary processes leading to the growth of the parent body. The thermal histories of ordinary chondrites could be greatly clarified by further experimental work on inversions in bronzitic pyroxenes.  相似文献   

8.
The concentration of 10 to 15 siderophile elements was determined in the magnetic and non-magnetic portions of Abee (E4) and Hvittis (E6). The results indicate that, with the exception of Cu, W and Fe, all elements are strongly concentrated in the metal phase. Unlike ordinary chondrites, the metal phase of Abee and Hvittis consists exclusively of kamacite, which is very homogeneous and shows no systematic variation in composition with grain size.Differences in siderophile element content between Abee and Hvittis can be accounted for exclusively by differences in metal content and composition. These differences reflect different degrees of refractory siderophile loss, metal-silicate fractionation and loss of moderately volatile elements. The Ir/Ni ratio is 25% lower in Abee than in Hvittis, indicating that more Ir (Os, Pt, etc.) was lost from Abee during the refractory element fractionation. Abee and the other E4–5 members have also lost no metal and are not depleted in moderately volatile elements. In Abee the non-refractory elements Fe to Ge are present in CI ratios, and this meteorite has also Ir/Re ratios ?CI.These differences, which are recorded in the composition of the metal phase, make a straightforward genetic relationship between the two enstatite chondrite groups difficult to accept. In particular, the different Ir/Ni ratios, which were established very early in the chemical history of these chondrites, at the time of the refractory element fractionation, force us to conclude that E4–5 and E6 chondrites evolved from two different reservoirs, and that exchange of material among them never occurred. However, members of both groups have similar cosmic ray exposure ages suggesting derivation from the same parent body, which poses some interesting problems.  相似文献   

9.
In order to better constrain the Li isotope composition of the bulk solar system and Li isotope fractionation during accretion and parent body processes, Li isotope compositions and concentrations were determined on a number of meteorite falls and finds. This is the first comprehensive study that systematically investigates a representative set of samples from carbonaceous chondrites (CI, CM2, CO3, CV3, CK4 and one ungrouped member), enstatite chondrites (EH, EL), ordinary chondrites (H, L, LL), and achondrites (one eucrite, diogenites, one pallasite, and a silicate inclusion from a IAB iron).

Carbonaceous chondrites have an average isotope composition of δ7Li = + 3.2‰ ± 1.9 (2σ) which agrees with the average composition of relatively pristine olivines (representative for the bulk composition) from the Earth primitive upper mantle (PUM). This is lighter than the average δ7Li of the basaltic differentiates of the Earth, Moon and Mars and the achondrites. It is an important observation, however, that the lighter end of the isotopic range of the differentiates always coincides with the averages of the mantle olivines and the carbonaceous chondrites. From this we conclude that the bulk of the inner solar system consists mostly of material from carbonaceous chondrites and that the variation seen in the differentiates is due to planetary body processes. Ordinary chondrites are significantly lighter than carbonaceous chondrites. No significant differences in δ7Li exist between enstatite chondrites (n = 3) and carbonaceous or ordinary chondrites. The difference between carbonaceous and ordinary chondrites and the variability within the chondrites could indicate the existence of distinct Li isotope reservoirs in the early solar nebula.  相似文献   


10.
We have analyzed the nickel isotopic composition of meteoritic materials by high-precision mass spectrometry. The samples analyzed include almost all meteorite types for which large isotopic anomalies have been reported for oxygen, silver, magnesium and titanium. These samples are C1, C3, L, LL, H and E chondrites, IVB irons, Eagle Station pallasite and inclusion, matrix and “whole rock” samples of the Allende meteorite. The result is that we have not found any anomaly for nickel isotopic compositions within our accuracy of 0.7‰ for61Ni/60Ni, 0.4-0.08‰ for62Ni/60Ni and 1–1.5‰ for64Ni/60Ni.  相似文献   

11.
Ten whole chondrules separated from the Dhajala (H3, 4), Hallingeberg (L3), and Semarkona (LL3) chondrites were individually analyzed for bulk element composition by instrumental neutron activation with half of each chondrule subsequently sacrificed for oxygen isotopic analysis and half retained for petrographic and electron microprobe analysis. On a three-isotope plot (δ17O vs. δ18O), the chondrules neither cluster near their respective chondrite hosts nor in the vicinities of previously recognized chondrite group averages. Instead, they define a trend resolvable into mixing and fractionation components but dominated by mixing in a manner similar to that previously observed for clasts from the LL3 chondrite ALHA76004. Covariations of chondrule isotopic mixing and fractionation parameters with petrological parameters were sought by two-variable linear least-squares regression analyses. However, the only two isotopic/petrological correlations significant at the 95% confidence level were δ17O vs. total bulk Fe (r = ?0.68) and mixing parameter,m18, vs. bulk weight ratio (CaO + Al2O3)/MgO (r = +0.67). Other correlations of apparent statistical significance were found by treating the chondrules as separate porphyritic (3 porphyritic olivine-pyroxene, 1 porphyritic olivine, 1 barred olivine) and non-porphyritic (4 radial pyroxene, 1 granular pyroxene/cryptocrystalline) textural subgroups. The reliability of the trends, based on so few samples, is not clear but the results at least indicate that possible existence of distinct isotopic/petrological subgroups of chondrules should be further investigated. Absence of certain isotopic/petrological trends expected as condensation effects argues against direct nebular condensation as the dominant process of chondrule formation. Instead, a model involving melting of heterogeneous solids, followed by various degrees of liquid/gas exchange, is favored. In any case, chondrule oxygen isotopic evolution was dominated by two-component mixing; fractional vaporization was, at most, a second-order effect. In addition to chondrules, parent bodies of unequilibrated ordinary chondrites must have also incorporated a16O-rich component which might have been fine-grained “matrix”.  相似文献   

12.
A fragment found in soil from the Apollo 12 site (12037, from the rim of Bench Crater) appears to be a unique type of chondrite, petrologically and chemically distinct from other chondrites and lunar rocks. Inclusions consisting of shocked pyroxene rimmed by euhedral troilite crystals are set in a black aphanitic matrix. Abundant magnetite in the matrix exhibits microscopic morphologies (framboids and plaquets) characteristic of C1 chondrites. The bulk composition of this sample has high Mg/Si and low Fe/Si relative to other chondrites, and P and S are strongly enriched. Most compositional differences between this meteorite and other chondrites may be explained by fractionation of Fe phases, such as magnetite and troilite. Low refractory element contents preclude mixing with lunar materials. This sample may be a surviving fragment of the meteoritic component present in the lunar regolith. Its characteristics suggest that ancient meteoritic debris sampled by the moon may be significantly different from that captured by the present-day earth.  相似文献   

13.
Major, minor and trace element abundances were determined in seven Angra dos Reis samples including whole rocks, fassaite (clinopyroxene), olivine and whitlockite separates via sequential instrumental neutron activation analysis. The chondritic normalized rare earth element (REE) abundance pattern for the Angra dos Reis clinopyroxene separates shows a concave downward shape with a small negative Eu anomaly. The strong fractionation between the light and the heavy REE in olivine separates could be attributed to the presence of islands of kirschsteinite in the olivines. The large-ion lithophile trace elements were highly enriched in the whitlockite separate as expected (e.g. La ≈ 370 ppm). The lower Hf and Sc abundances in whitlockite compared to that in the equilibrium “magma” could be the result of favorable partitioning of Hf and Sc in baddeleyite, which may have crystallized prior to or with whitlockite in the interstitial liquid. Comparison of whole rock with mineral separate data shows the presence of ～3% olivine, ～2.6% spinel and small amounts of metallic Ni-Fe and troilite in the whole rock.The trace element abundances in the derivative magma from which the Angra dos Reis clinopyroxene crystallized were estimated from the clinopyroxene data and the clinopyroxene mineral-liquid partition coefficients. From the derivative magma, the trace element abundances in the possible parent magmas were calculated by assuming that these parent magmas have undergone different degrees of clinopyroxene fractional crystallization to yield the Angra dos Reis derivative magma. Using the trace element abundances in these possible parent magmas, a two-stage crystal-liquid fractionation model with source material containing olivine, orthopyroxene and clinopyroxene is presented for the genesis of Angra dos Reis. Possible combinations of the degree of equilibrium non-modal partial melting, the source mineral composition and the initial element abundances required to generate possible Angra dos Reis parent magmas are calculated by the multilinear regression analysis method. Favorable solutions for this two-stage crystal-liquid fractionation model could be that Angra dos Reis crystallized at ～70% fractional crystallization of clinopyroxene from magmas generated by reasonable degrees of equilibrium partial melting (～7–10%) of deep-seated primitive source materials (olivine ～54–30%, orthopyroxene ～33–53%, and clinopyroxene ～13–17%) with trace element (Ba, Sr, REE and Sc) abundances ～3.5–4.7 × chondrites. These calculated REE abundances in the Angra dos Reis parent body are very similar to those suggested for the primordial moon (～3–5 × chondrites).Possible genetic relationships between Angra dos Reis and other achondrites, especially cumulate eucrites and nakhlites, are studied. Apparently, the unique Angra dos Reis could not be related to those achondrites by crystal-liquid fractionation of the same parent body.  相似文献   

14.
《国际泥沙研究》2016,(2):97-109
The determination of grain size distribution in alluvial channels plays a crucial role in understanding fluvial dynamics and processes (e.g., hydraulic resistance, sediment transport and erosion, and habitat suitability). However, to determine an accurate distribution, tremendous field efforts are often required. Traditionally, the grain size distribution of channel beds have been obtained by manually counting a set of randomly selected stones (the“pebble count”). Based on this elementary principle, many authors have proposed different adaptations to overcome weaknesses and problems with the original method; with the development of digital technology, photographic methods have been developed in order to sig-nificantly reduce the time spent in the field. Two of these“image-assisted”methods include Automated Grain Sizing, AGS, and Manual Photo Sieving, MPS. In this study, AGS and MPS were applied under ideal laboratory conditions, to be used as reference, and in two field conditions with different degrees of difficulty in terms of visual determination of the grain size distribution; these included an artificial unlined channel and two natural mountainous streams. The results were compared with those obtained with the pebble-count method. In general, strong agreement between the methods was found when they were applied under favorable conditions (”the laboratory”), and the differences between the image-assisted and pebble count methods were similar to those found in previous studies. Despite being more time consuming, MPS was deemed preferable to AGS when conditions are not optimal;in these cases, the time spent on image elaboration significantly increased in the AGS method (approximately three-fold), but the estimation error of the median grain size decreased by approximately 37%. The use of image-assisted analysis has proven to be robust for characterizing sediment in watercourse beds and reducing fieldwork time, but because field conditions can significantly affect the accuracy of results, the method choice must be carefully considered.  相似文献   

15.
Desertification is a change in soil properties, vegetation or climate, which results in a persistent loss of ecosystem services that are fundamental to sustaining life. Desertification affects large dryland areas around the world and is a major cause of stress in human societies. Here we review recent research on the drivers, feedbacks, and impacts of desertification. A multidisciplinary approach to understanding the drivers and feedbacks of global desertification is motivated by our increasing need to improve global food production and to sustainably manage ecosystems in the context of climate change. Classic desertification theories look at this process as a transition between stable states in bistable ecosystem dynamics. Climate change (i.e., aridification) and land use dynamics are the major drivers of an ecosystem shift to a “desertified” (or “degraded”) state. This shift is typically sustained by positive feedbacks, which stabilize the system in the new state. Desertification feedbacks may involve land degradation processes (e.g., nutrient loss or salinization), changes in rainfall regime resulting from land-atmosphere interactions (e.g., precipitation recycling, dust emissions), or changes in plant community composition (e.g., shrub encroachment, decrease in vegetation cover). We analyze each of these feedback mechanisms and discuss their possible enhancement by interactions with socio-economic drivers. Large scale effects of desertification include the emigration of “environmental refugees” displaced from degraded areas, climatic changes, and the alteration of global biogeochemical cycles resulting from the emission and long-range transport of fine mineral dust. Recent research has identified some possible early warning signs of desertification, which can be used as indicators of resilience loss and imminent shift to desert-like conditions. We conclude with a brief discussion on some desertification control strategies implemented in different regions around the world.  相似文献   

16.
SEM, optical and chemical observations have been performed on 12 H3-6 chondrites, 9 of them being also studied by other groups. Morphological features of chondrules and crystals (growth steps) are shown; the significance of the finely crystallised troilite in Menow and Ambapur Nagla is discussed in the light of the discovery that the NiFe blebs associated with it are Ni-rich (50–60% Ni). Sulphur should have been mobilized without shock evidence possibly as a result of solar heating. Pre-chondritic relict material is recognized by anomalous or variable mineral compositions, and in some cases, by the presence of overgrowths on relict cores. After short notes on individual chondrites, a tentative history of H chondrites is proposed. The chondrule-forming episode is considered as a remelting of pre-existing material. The accretion would immediately follow this event for type 6 (around 1000°C), and would occur at progressively lower temperature for types 5 and 4. Type 3 would represent material coming from an extended source region, an hypothesis consistent with the broader range composition of the particles and with their cooling before accretion to much lower temperatures (below 350°C).  相似文献   

17.
The geochemical study of the Earth's mantle provides important constraints on our understanding of the formation and evolution of Earth, its internal structure, and the mantle dynamics. The bulk Earth composition is inferred by comparing terrestrial mantle rocks with chondrites, which leads to the chondritic Earth model. That is, Earth has the same relative proportions of refractory elements as that in chondrites, but it is depleted in volatiles. Ocean island basalts(OIB) may be produced by mantle plumes with possible deep origins; consequently, they provide unique opportunity to study the deep Earth. Isotopic variations within OIB can be described using a limited number of mantle endmembers, such as EM1, EM2 and HIMU, and they have been used to decipher important mantle processes. Introduction of crustal material into the deep mantle via subduction and delamination is important in generating mantle heterogeneity; however, there is active debate on how they were sampled by mantle melting, i.e.,the role of olivine-poor lithologies in the OIB petrogenesis. The origin and location of high 3He/4He mantle remain controversial,ranging from unprocessed(or less processed) primitive material in the lower mantle to highly processed materials with shallow origins, including ancient melting residues, mafic cumulates under arcs, and recycled hydrous minerals. Possible core-mantle interaction was hypothesized to introduce distinctive geochemical signatures such as radiogenic 186 Os and Fe and Ni enrichment in the OIB. Small but important variations in some short-lived nuclides, including 142 Nd, 182 W and several Xe isotopes, have been reported in ancient and modern terrestrial rocks, implying that the Earth's mantle must have been differentiated within the first 100 Myr of its formation, and the mantle is not efficiently homogenized by mantle convection.  相似文献   

18.
Microscopic investigations have been done on the chondrites Sena and Nadiabondi (H5, not shocked), Ste. Marguerite en Comines (H4, very slightly shocked), Allegan (H5, slightly shocked). Only in such cases can the matrix be easily observed and compared to those of type 3 chondrites. The <100 μm debris found in types 4 and 5 that we have observed are not the result of the metamorphism of type 3 fines.The abundance of tiny debris is in direct relation with the intensity of the shock though this shock was insufficient to provoke either the induration of the stones or a significant loss of rare gases. The bulk of the fines are the result of local disaggregation of the most brittle parts from chondrules and fragments.A low-temperature matrix has not been observed in these meteorites but only in H3 chondrites, as a coating around the chondrules. The accretion modelists should take into account the absence or the scarcity of fine particles in their calculations.  相似文献   

19.
In many practical cases, it is necessary to characterize the explored area with a regular set of geodata. Regular matrix data (e.g., ordinary maps) are calculated via existing data interpolation and extrapolation. For low frequency (oversampled) data acquired within a dense profile net (e.g., seismic three‐dimensional structural or gravity mapping), this procedure is mathematically more or less stable and, to a certain extent, unique since we might neglect discrepancies resulting from different interpolations. The situation is quite different for high‐resolution and high‐frequency contaminated data (e.g., raw seismic attributes or geochemistry measurements) represented by sparse profiling. Considering the variety of exploration cases, the investigation of different interpolation algorithm efficiency seems very important. Since it is impossible to compare all algorithms by means of formal mathematics, we have designed a test program. A representative set of seismic attribute maps has been artificially destroyed by introducing blank values (from 20% up to 95%) and then restored by different interpolation algorithms— bicubic, bilinear, nearest neighbor, and “smart averaging.” Smart averaging interpolation is done in a “live” window. The position, form, and size of the window are determined by some mathematical criterion on a trial‐and‐error basis. Discrepancies between restored and initial (true) data have been assessed and analysed. It is shown that the total (absolute) efficiency and comparative (relative) efficiency of the algorithms depend mostly upon the initial interpolant data characteristics. Identifying the best interpolation algorithm for all interpretive cases seems impossible. Some aspects of data processing are discussed in connection with interpolation accuracy.  相似文献   

20.
《国际泥沙研究》2020,35(3):287-294
The Suquia River,the largest urban river in Cordoba(Argentina),has been severely polluted for decades.Actions must be taken to restore its environmental quality by managing riparian zones for increased water-self purification.The current study aimed to characterize organic matter(OM) dynamics and humic substances(HS) spectrochemical properties along the lower-middle basin of the Suquia River.Riparian soil(0-20 cm) and sediment(0-10 cm) samples were collected from a reference location(S1)and four polluted sites(S2-S5) during a low-flow period.The contents of soil and sedimentary OM and HS fractions were analyzed by wet oxidation,as well as HS Fourier transform infrared(FT-IR) and ultraviolet-visible(UV-Vis) spectrochemical properties.The OM and HS fractions from riparian soil were high upstream of Cordoba City(S1 and S2,50.2-50.4 g/kg OM) and within a 50 km downstream location(S5,30.9 g/kg OM) owing to a surplus of fresh plant biomass-carbon(C) inputs.Highly heterogeneous sediment samples did not show any significant differences among sites(P 0.05).The lowest values of the ratio of absorbances at 465 and 665 nm(E4/E6)(1.78) and the Δ log K(0.15) coefficient(a measure of HS maturity degree) were obtained downstream of Cordoba City,for both riparian soil and sediment,indicating that HS were enriched by more condensed aromatic structures within highly degraded portions of the river.All samples exhibited similar IR spectra,implying overlapping recalcitrant-C structures at the functional group level,but with different absorbance intensity.Data from the current study constitute a baseline for understanding the chemical nature of HS from sediment and riparian soil along the Suquia River and can be used as a reference for future studies tracking OM compositional changes over time.  相似文献   

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