Geochemical and mineralogical characteristics of weathered ore in the Dalucao REE deposit,Mianning–Dechang REE Belt,western Sichuan Province,southwestern China

The Dalucao deposit in western Sichuan Province, southwest China, is one of the largest and most extensive rare earth element (REE) deposits in the Himalayan Mianning–Dechang REE Belt. Moreover, this is the only deposit identified in the southern part of the belt. The deposit contains the No. 1, 2, and 3 orebodies. The No. 1 and 3 orebodies are hosted in two breccia pipes within syenite–carbonatite rocks that intrude a Proterozoic quartz–diorite pluton. Both breccia pipes have elliptical horizontal cross-sections at the surface, being 200–400 m long, 180–200 m wide, and extending to > 450 m depth. The No. 1 and No. 3 orebodies have total thicknesses of 55–175 m and 14–58 m, respectively. REE mineralization is associated with four brecciation events that are recorded in both pipes. The ore grades in the No. 1 and 3 orebodies are similar, with the rocks containing 1.0–4.5% rare earth oxides (REOs). The No. 1 orebody is characterized by a mineral assemblage comprising fluorite + barite + celestite + bastnäsite (i.e., Type I), whereas the No. 3 orebody is characterized by an assemblage comprising fluorite + celestite + pyrite + muscovite + bastnäsite + strontianite (i.e., Type II). Significant amounts of weathered high-grade REE ore (up to 60 wt.% of the rock mass) is mainly present in the No. 1 orebody. This is the main ore-type targeted for exploration within the Dalucao deposit, but is rarely present in other deposits in the Mianning–Dechang REE Belt.Faulting and cryptoexplosive breccia events, possibly linked to movement on the Panxi Fault, were more common in the No. 1 orebody than in the No. 3 orebody. This facilitated the introduction of ore-forming hydrothermal fluids and provided space for the precipitation of REE minerals. Based on the present results, we infer that the Dalucao deposit was the product of multiple stages of ore formation. REE minerals formed in envelopes around, or fractures within, quartz, fluorite, calcite, barite, and celestite in the brecciated ores. The main REE minerals were deposited from hydrothermal fluids within cryptoexplosive breccia, followed by weathering that increased the ore grade. Petrographic studies and X-ray powder diffraction (XRD) analyses indicate that the weathered ore contains 5–60% REE minerals (including bastnäsite, parisite, and monazite), together with gangue (quartz, barite, celestite, and fluorite), large amount of clay minerals (smectite, illite, kaolinite, and sepiolite), and relict igneous minerals (quartz, albite, and K-feldspar). The weathered samples are strongly enriched in La (up to 92,390 ppm), Ce (up to 103,500 ppm), Pr (up to 8006 ppm), and Nd (up to 16,690 ppm) compared with the unweathered brecciated ores. Conversely, Sr concentrations are significantly more enriched in the brecciated ores (up to 256,500 ppm) than in the weathered ores (generally less than 2671 ppm with one exception of 37,850 ppm) due to less celestite. Calcite is largely absent from the weathered ores (except one sample with up to 30% mode), which contrasts with the brecciated ores that contain up to 75% calcite. The effects of weathering, oxidation, loss of ions, and hydration on the brecciated ores led to the refertilization of the REEs and an increase in the grade of the ore deposit.     

Geology,mineralogy and fluid inclusion data of the Kizilcaören fluorite–barite–REE deposit,Eskisehir, Turkey

The Kizilcaören fluorite–barite–Rare Earth Element (REE) deposit occurs as epithermal veins and breccia fillings in altered Triassic metasandstones and Oligocene–Miocene pyroclastics adjacent to alkaline porphyritic trachyte and phonolite. This deposit is the only commercial source of REE and thorium in Turkey. Most of the fluorite–barite–REE mineralisation at Kizilcaören has been formed by hydrothermal solutions, which are thought to be genetically associated with alkaline volcanism. The occurrence of the ore minerals in vuggy cavities and veins of massive and vuggy silica indicate that the ore stage postdates hydrothermal alteration. The deposit contains evidence of at least three periods of hypogene mineralisation separated by two periods of faulting. The mineral assemblage includes fluorite, barite, quartz, calcite, bastnäsite, phlogopite, pyrolusite and hematite as well as minor amounts of plagioclase feldspar, pyrite, psilomelane, braunite, monazite, fluocerite, brockite, goethite, and rutile. Fluid inclusion microthermometry indicates that the barite formed from low salinity (0.4–9.2 equiv. wt% NaCl) fluids at low temperatures, between 105 and 230 °C, but fluorite formed from slightly higher salinity (<12.4 equiv. wt% NaCl) fluids at low and moderate temperatures, between 135–354 °C. The depositional temperature of bastnäsite is between 143–286 °C. The local coexistence of liquid- and vapour-rich inclusions suggests boiling conditions. Many relatively low-salinity (<10.0 equiv. wt% NaCl), low and moderate temperature (200–300 °C) inclusions might be the result of episodic mixing of deep-saline brines with low-salinity meteoric fluids. The narrow range of δ³⁴S (pyrite and barite) values (2.89–6.92‰ CDT)suggests that the sulphur source of the hydrothermal fluids are the same and compatible with a volcanogenic sulphate field derived from a magmatic sulphur source.     

REE and isotope (Sr,S, and Pb) geochemistry to constrain the genesis and timing of the F–(Ba–Pb–Zn) ores of the Zaghouan District (NE Tunisia)

The F–(Ba–Pb–Zn) ore deposits of the Zaghouan District, located in NE Tunisia, occur as open space fillings or stratabound orebodies, hosted in Jurassic, Cretaceous and Tertiary layers. The chondrite-normalized rare earth element (REE) patterns may be split into three groups: (i) “Normal marine” patterns characterizing the wallrock carbonates; (ii) light REE (LREE) enriched (slide-shaped) patterns with respect to heavy REE (HREE), with small negative Ce and Eu anomalies, characteristic of the early ore stages; (iii) Bell-shaped REE patterns displaying LREE depletion, as well as weak negative Ce and Eu anomalies, characterizing residual fluids of subsequent stages. The ⁸⁷Sr/⁸⁶Sr ratios (0.707654–0.708127 ± 8), show that the Sr of the epigenetic carbonates (dolomite, calcite) and ore minerals (fluorite, celestite) are more radiogenic than those of the country (Triassic, Jurassic, Cretaceous, lower Miocene) sedimentary rocks. The uniformity of this ratio, throughout the District, provides evidence for the isotopic homogeneity and, consequently, the identity of the source of the mineralizing fluids. This signature strongly suggests that the radiogenic Sr is carried by Upper Paleozoic basinal fluids.The δ³⁴S values of barite, associated to mineralizations, are close to those of the Triassic sea water (17‰). The δ³⁴S values of sulfide minerals range from − 13.6‰ to + 11.4‰, suggesting two sulfur-reduced end members (BSR/TSR) with a dominant BSR process.Taking account of the homogeneity in the Pb-isotope composition of galenas (18.833–18.954 ± 0.001, 15.679–15.700 ± 0.001 and 38.690–38.880 ± 0.004, for the ²⁰⁶Pb/²⁰⁴Pb, ²⁰⁷Pb/²⁰⁴Pb and ²⁰⁸Pb/²⁰⁴Pb ratios respectively), a single upper crustal source for base-metals is accepted. The Late Paleozoic basement seems to be the more plausible source for F–Pb–Zn concentrated in the deposits. The genesis of the Zaghouan District ore deposits is considered as the result of the Zaghouan Fault reactivation during the Late Miocene period.     

REE Geochemistry and Mineralogy in Ores of the Talgan Cu–Zn Massive Sulfide Deposit,Southern Urals

Doklady Earth Sciences - The high REE concentrations (57.23–561.2 ppm) in thin-layered sulfide ores of the Talgan Cu–Zn massive sulfide deposit (Southern Urals) are related to the...     

REE Geochemistry and Mineralization Characteristics of the Zudong and Gnanxi Granites, Jiangxi Province

The Zudong and Guanxi granites are original rocks of the ion adsorption-type HREE and LREE deposits in weathering crust of granites. The ΣREE value and LREE/HREE ratio of the Zudong granite are 264 ppm and 0.81-0.24 respectively, and the average Y/ΣREE ratio is 35.8-54.5%. This is mainly due to magmatic crystallization and evolution and deuteric metasomatism (albitization, muscovitization and fluorite-doveritization). These alterations resulted in endogenic mineralizations of yttrium-group REE fluorine carbonates, silicates and arsenates. The Guanxi granite is characterized by LREE enrichment (the average LREE/HREE ratio is 2.43).     

Y–REE Mineralization in Biotite–Arfvedsonite Granites of the Katugin Rare-Metal Deposit,Transbaikalia, Russia

Doklady Earth Sciences - This paper reports on the results of studies of the carbonate–fluoride isolations with extremely high Y and REE concentrations from biotite–arfvedsonite granite...     

A review of the genesis of the world class Bayan Obo Fe–REE–Nb deposits,Inner Mongolia,China: Multistage processes and outstanding questions

The Bayan Obo Fe–REE–Nb deposit is the world's largest rare earth element (REE) resource and with the increasing focus on critical metal resources has become a focus of global interest. The deposit is hosted in the Palaeoproterozoic Bayan Obo Group, mainly concentrated in the H8 dolomite marble. The ores consist of light REE enriched monazite and bastnäsite, with a wide array of other REE minerals. Niobium mineralisation is hosted primarily in aeschynite and pyrochlore, although there are a wide range of other Nb-minerals. The origin of the host dolomite and ore bodies has been a subject of intense debate. The host dolomite has been proposed to be both of sedimentary origin and an igneous carbonatite. Carbonatite dykes do occur widely in the area, and consideration of the textural, geochemical and isotopic composition of the dolomite suggests an origin via intrusion of magmatic carbonatite into meta-sedimentary marble, accompanied by metasomatism. The origin of the ore bodies is complex, indicated most strongly by an ~ 1 Ga range in radiometric age determinations. Compilation of available data suggests that the ores were originally formed around 1.3 Ga (Sm–Nd isochron ages; Th–Pb ages of zircon), close in time to the intrusion of the carbonatite dykes. The ores were subsequently subjected to several stages of deformation and hydrothermal overprint, culminating in deformation, metamorphism and fluid flow related to the Caledonian subduction of the Mongolian Plate under the North China Craton from ~ 450 to 420 Ma (Th–Pb ages of monazite). This stage resulted in the formation of the strong foliation (‘banding’) of the ore. The presence of undeformed veins with alkali mineral fills, and the overprinting of the foliation by Nb minerals suggest that secondary fluid flow events may also have contributed to the metal endowment of the deposits, as well as remobilising the original Fe and REE mineralisation. The alteration mineralogy and geochemistry of the ores are comparable to those of many REE mineralised carbonatites. Initial Nd isotope ratios at 450 Ma, however, suggest crustal sources for the metals. These conflicting lines of evidence can be reconciled if a (at least) two stage isotopic evolution is accepted for the deposits, with an original mantle-sourced, carbonatite-related metal accumulation forming around 1.3 Ga with εNd close to 0. The ore was remobilised, with associated re-equilibration of Th–Pb isotope systematics during deformation at ~ 450 Ma. A further stage of alkaline hydrothermal fluid was responsible for Nb mineralisation at this stage. The complex geological history, with multiple stages of alkaline, high field strength element-rich, metasomatic fluid flow, is probably the main reason for the exceptional metal endowment of the Bayan Obo area.     

REE and Sr isotope characteristics of carbonate within the Cu–Co mineralized sedimentary sequence of the Nchanga Mine,Zambian Copperbelt

Carbonate, largely in the form of dolomite, is found throughout the host rocks and ores of the Nchanga mine of the Zambian Copperbelt. Dolomite samples from the hanging wall of the mineralization show low concentrations of rare-earth elements (REE) and roof-shaped, upward convex, shale-normalized REE patterns, with positive Eu*_SN anomalies (1.54 and 1.39) and marginally negative Ce anomalies (Ce*_SN 0.98,0.93). In contrast, dolomite samples associated with copper and cobalt mineralization show a significant rotation of the REE profile, with HREE enrichment, and La/Lu_SN ratios <1 (0.06–0.42). These samples also tend to show variable but predominantly negative Eu*_SN and positive cerium anomalies and an upwardly concave MREE distribution (Gd-Er). Malachite samples from the Lower Orebody show roof-tile-normalized REE patterns with negative europium anomalies (Eu*_SN 0.65–0.80) and negative cerium anomalies (Ce*_SN 0.86–0.9). The carbonate ⁸⁷Sr/⁸⁶Sr signature correlates with the associated REE values. The uppermost dolomite samples show Neoproterozoic seawater-like ⁸⁷Sr/⁸⁶Sr ratios ranging from 0.7111 to 0.7116, whereas carbonate from Cu–Co mineralized samples show relatively low concentrations of strontium and more radiogenic ⁸⁷Sr/⁸⁶Sr, ranging between 0.7136–0.7469. The malachite samples show low concentrations of strontium, but give a highly radiogenic ⁸⁷Sr/⁸⁶Sr of 0.7735, the most radiogenic ⁸⁷Sr/⁸⁶Sr ratio. These new data suggest that the origin and timing of carbonate precipitation at Nchanga is reflected in the REE and Sr isotope chemistry. The upper dolomite samples show a modified, but essentially seawater-like signature, whereas the rotation of the REE profile, the MREE enrichment, the development of a negative Eu*_SN anomaly and more radiogenic ⁸⁷Sr/⁸⁶Sr suggests the dolomite in the Cu–Co mineralized samples precipitated from basinal brines which had undergone significant fluid–rock interaction. Petrographic, REE, and ⁸⁷Sr/⁸⁶Sr data for malachite are consistent with the original sulfide Lower Orebody being subject to a later oxidizing event.     

Integrated U–Pb and Sm–Nd geochronology for a REE-rich carbonatite dyke at the giant Bayan Obo REE deposit,Northern China

The Bayan Obo deposit in North China contains the largest rare-earth element (REE) resources in the world, but its forming time remains controversial. Nearly one hundred carbonatite dykes occur around the Bayan Obo deposit, including dolomite, calcite and calcite–dolomite carbonatite varieties. Zircons from a REE-rich carbonatite dyke and wallrock quartz conglomerate at Bayan Obo have been analyzed for U–Pb to determine the age of the dyke. Zircon from the carbonatite dyke, analyzed by conventional isotope dilution thermal ionization mass spectrometry (ID-TIMS), yielded an upper intercept age of 1417 ± 19 Ma. This age is confirmed by SHRIMP U–Pb analysis of zircon from the same carbonatite dyke, which gave a ²⁰⁷Pb/²⁰⁶Pb weighted mean age of 1418 ± 29 Ma. In situ Nd isotope measurements of monazite collected from the carbonatite dyke gave an isochron age of 1275 ± 87 Ma. These results demonstrate that the dyke intruded ~ 1400 Ma. In view of predecessor's results, it is clarified that the REE mineralization at Bayan Obo occurred at ca. 1400 Ma, consistent with the timing of carbonatite dyke intrusion in the region. The youngest detrital zircons from the quartz conglomerate yielded a ²⁰⁷Pb/²⁰⁶Pb weighted mean age of 1941 ± 7 Ma using LA ICP-MS U–Pb method. Detrital zircons in the carbonatite dyke also gave a mean apparent age of 1932 ± 3 Ma using ID-TIMS U–Pb method and 1914 ± 14 Ma using SHRIMP U–Pb method. These ages constrain the beginning active time of the Zha'ertai–Bayan Obo rift in the northern margin of the North China Craton after ~ 1900 Ma.     

Tungsten Mineralization and Mica REE Geochemistry,Huangsha,Jiangxi

The Huangsha Ag-rich tungsten deposit is genetically related to a buried granite which shows apparent vertical zoning in alteration.Greisen-type W(Mo) ores coccur at the top or the intrusive and sulfide-wolframite-quartz veins developed at the major stage of mineralization are present in low-grade metamorphic rocks in the outer-contacts.The veins exhibit a reversed zonation in the vertical section with silver concentrated in the lower part in association with sulfides.Micas,characterized by high Si and low Al.are extensively developed both in the granite and in the veins.They have similar cell parameters.belonging to 2M1 type,but those in the veins are understanding of the petrogenesis, evolution and mineralization of the granite.     

Zircon U–Pb ages of the Mianning–Dechang syenites,Sichuan Province,southwestern China: Constraints on the giant REE mineralization belt and its regional geological setting

The Himalayan Mianning–Dechang (MD) rare earth element (REE) belt in western Sichuan Province, southwestern China, is approximately 270 km long and 15 km wide, and contains total reserves of more than 3 Mt of light REEs (LREEs), comprising one giant (Maoniuping), one large (Dalucao), two small–medium-sized (Muluozhai and Lizhuang), and numerous smaller REE deposits. The belt occurs within the eastern Indo-Asian collision zone (EIACZ), where its location is controlled by large-scale strike-slip faults and tensional fissure zones. Himalayan carbonatite–syenite complexes consist predominantly of alkaline syenite stocks and carbonatite sills or dikes that host REE mineralization. Previous studies have reported inconsistent ages for alkaline magmatism syenite formation and REE mineralization. Here, we present new results of sensitive high-resolution ion micro-probe U–Pb dating of zircons from syenites from the Dalucao, Maoniuping, Lizhuang and Diaoloushan areas, the first systematic and precise age determinations for these rocks in the MD belt. The new data give concordant ages of 12.13 ± 0.19 and 11.32 ± 0.23 Ma for the Dalucao deposit, 22.81 ± 0.31 and 21.3 ± 0.4 Ma for Maoniuping, 26.77 ± 0.32 Ma for Muluozhai, and 27.41 ± 0.35 Ma for Lizhuang. These ages, which should be regarded as maximum ages for the REE mineralization in the study area, can be split into two groups, i.e. 11–12 Ma in the southern part of the MD belt and 12–27 Ma in the northern part, suggesting a progression of magmatism from north to south. These data suggest that the majority of carbonatite–syenite magmatism within the EIACZ occurred during the main stage of Himalayan metallogenesis. The ages presented in this study suggest that strike-slip shear along the MD belt was initiated at ca. 27 Ma and ended ca. 12 Ma. This timing is consistent with movements along the adjacent Ailaoshan–Red River strike-slip fault in southeastern Tibet (to the south of the MD belt) and one of the three Cenozoic strike-slip faults in eastern Tibet. Ascent of an asthenospheric mantle diapir beneath the EIACZ in the Cenozoic may have provided a thermal mechanism for the generation of magmas that formed the carbonatite–syenite complexes in the study area. Alternatitvely, the magmas may have been generated by decompression melting associated with the transition from a transpressional to a transtensional regime at 38–40 Ma. The precise age results for syenite magmatism in the study area indicate that this transition occurred prior to carbonatite–syenite magmatism and the formation of the MD REE belt, which is consistent with the regional tectonic model.     

REE Characteristics and Petrogenesis of Amphibolites in the Dabie Complex

Based on their REE features, stratoid or lenticular amphibolites in the Dabie Complex are di-vided into two types:one is characterized by flat REE distribution patterns and the other by LREE-enrichment. Results of the REE quantitative modeling suggest that the amphibolites were formed from 20% partial melting of garnet lherzolite and 35-56% fractional crystallization of olivine(type TH1) or 14-20% fractional crystallization of olivine and clinopyroxene(type TH2).     

The Paleoproterozoic Montviel carbonatite-hosted REE–Nb deposit,Abitibi, Canada: Geology,mineralogy, geochemistry and genesis

The Montviel 250 Mt carbonatite-hosted REE–Nb deposit is hosted in a Paleoproterozoic alkaline suite located in the Sub-Province of Abitibi, in the Archean Province of the Superior. The alkaline intrusion consists of biotite clinopyroxenites, melano- to leucosyenites, a melteigite–ijolite–urtite series, riebeckite granite, a series of carbonatites and a carbonatite polygenic breccia. The carbonatite series includes silicocarbonatites, calciocarbonatites, rare magnesiocarbonatites, ferrocarbonatites and mixed carbonatites and are cut by a late, high-energy carbonatite polygenic breccia. Diamond drill hole assays and microscope observations indicate that Nb is hosted in pyrochlore from silicocarbonatite whereas the REE mineralization is mainly hosted in ferrocarbonatite, late mixed carbonatites and polygenic breccia, in REE-bearing carbonates and fluorocarbonate minerals. Diamond drill hole underground mapping and systematic assays have shed light on zones enriched in Nd and LREE with preferential Ba and Sr hydrothermal precipitation and zones enriched in Dy, Y and HREE displaying preferential F and P bearing hydrothermal precipitation. Petrographic observations, electron microprobe analyses, LA-ICPMS and X-ray diffraction were used to study the mineralization processes and to identify and quantify the REE-bearing burbankite–(Ce), carbocernaite–(Ce), ewaldite–(Y), huanghoite–(Nd), cordylite–(Ce), cordylite–(Nd), kukharenkoite–(Ce) and synchysite–(Ce). Most minerals are enriched in total LREE with values around 19.3 wt.%, have total MREE values around 2.2 wt.% and extremely variable total HREE values, with very high contents of Dy and Y averaging around 0.3 wt.% and 1.0 wt.%, respectively, and with total HREE reaching up to 10.0 wt.%. A paragenetic sequence is proposed that consists of: (1) a silicocarbonatite Nb stage, and (2) a calciocarbonatite stage, dominated by magmatism but accompanied by hydrothermal fluids, (3) a main ferrocarbonatite stage, dominated by episodes of Ba- and Sr-hydrothermalism and LREE mineralization, F- and P-hydrothermalism and HREE mineralization and evolved ferrocarbonatitic magmatism, (4) a renewed, mixed carbonatite magmatic stage with minor but increasing hydrothermalism, and (5) a terminal stage of fluid pressure buildup and explosion, leading to the creation of a HREE-enriched polygenic breccia. Globular melt inclusions of Ba–Cl–F (± Si–O) may indicate the presence and contribution of barium-bearing chlorofluoride melts during hydrothermal activity and mineralization of the carbonatite.     

Sources of Magmatic Rocks from the Deep-Sea Floor of the Arctic Ocean and the Central Atlantic: Evidence from Data on the U–Pb Age,Hf Isotopes,and REE Geochemistry of Zircons

The results of geochronological (U–Pb), isotope–geochemical (Lu–Hf), and geochemical (REEs) studies of young (MZ, KZ) and xenogenic (AR, PR) zircons from magmatic rocks of the Central Arctic rises of the Arctic Ocean (AO) and the crest zone of the Mid-Atlantic Ridge (MAR) are presented. The data obtained show that the depleted mantle could be a source of young (KZ) zircons of the MAR, whereas young (MZ) zircons of the MAR and all xenogenic (AR, PR) zircons of the AO and MAR are from crustal rocks of the continental lithosphere.     

REE Characteristics of the Lala IOCG Deposit, Sichuan, China

Please?refer?to?the?attachment(s)?for?more?details.     

Structural and Morphological Features of the Participation of Microorganisms in the Formation of Nb–REE–Rich Ores of the Tomtor Field (Russia)

Doklady Earth Sciences - Data indicating the important role of microorganisms in the redistribution of REEs in the weathering crust and the decisive role in the concentration of REEs during the...     

REE Geochemistry of Fluorite from the Maoniuping REE Deposit, Sichuan Province, China： Implications for the Source of Ore-forming Fluids

Fluorite is one of the main gangue minerals in the Maoniuping REE deposit,Sichuan Province,China.Fluorite with different colors occurs not only within various orebodies,but also in wallrocks of the orefield.Based on REE geochemistry,fluorite in the orefield can be classified as the LREE-rich,LREE-flat and LREE-depleted types.The three types of fluorite formed at different stages from the same hydrothermal fluid source,with the LREE-rich fluorite forming at the relatively early stage,the LREE-flat fluorite in the middle,and the LREE-depleted fluorite at the latest stage.Various lines of evidence demonstrate that the variation of the REE contents of fluorite shows no relation to the color.The mineralization of the Maoniuping REE deposit is associated spatially and temporally with carbonatite-syenite magmatism and the ore-forming fluids are mainly derived from carbonatite and syenite melts.     

Scale,causality, and the new organism–environment interaction

The fallout from environmental determinism of the early 20th century steered geography away from biological and evolutionary thought. Yet it also set in motion the diversification of how geographers conceive environment, how these environments shape and are shaped by humans, and how scaling negotiates the interpretation of this causality. I illustrate how this plurality of scalar perspectives and practices in geography is embedded in the organism–environment interaction recently articulated in the life sciences. I describe the new fields of epigenetics and niche construction to communicate how ideas about scale from human and physical geography come together in the life sciences. I argue that the two subdisciplinary modes or ‘moments’ of scalar thinking in geography are compatible, even necessary, through their embodiment in organisms. To procure predictability, organisms practice an epistemological scaling to rework the mental and material boundaries and scales in their environment. Yet organisms are also embedded in ontological flux. Boundaries and scales do not remain static because of the agency of other organisms to shape their own predictability. I formally define biological scaling as arising from the interplay of epistemological and ontological moments of scale. This third moment of scale creates local assemblages or topologies with a propensity for persistence. These ‘lumpy’ material outcomes of the new organism–environment interaction have analogues in posthuman and new materialist geographies. They also give formerly discredited Lamarckian modes of inheritance a renewed, but revised acceptance. This article argues for a biological view of scale and causality in geography.     

REE geochemistry of Chaohu and Longgan lakes, eastern China

The rare-earth elements （REEs） are a series of elements including lanthanides with atomic numbers from 57 to 71, as well as Y with an atomic number of 39. The REEs are commonly used as geochemical tracers in the study of many geologic processes because of their unique and chemically coherent behavior. The main purpose of this research is to understand the effect of water-particle interaction on trace metal transport, the distribution and chemical species of the REEs in water through case studies on geochemical behavior of the REEs in the Chaohu and Longgan lakes, eastern China. Concentrations of the dissolved REEs were detected by ICP-MS （Inductively Coupled Plasma-Mass Spectrometry）. Before ICP-MS measurement, REEs were concentrated from water samples by using solvent extraction and back extraction with a mixture 65% HDEHP （2-etheylhexyl hydrogen phosphate） and 35% H2MEHP （2-ehtylhexyl dihydrogen phosphate）. The results showed that the average concentrations of dissolved REEs in summer are higher than in winter for Chaohu Lake： they were 162.6 ng/kg and 86.5 ng/kg, respectively. On the country, the REE contents of winter samples were higher than those of summer water samples for Longganhu Lake： they were 111.1 ng/kg and 44.0 ng/kg, respectively. The contents of suspended particulate matter and pH are the two important factors controlling the concentrations of dissolved REE in the lakes. The contents of the REEs decrease with increasing pH in the Longgan and Chaohu lakes. The suspended particulate matter shows different sorption/desorption toward the dissolved REEs in the two water bodies. Most lake water samples have a fiat NASC-normalized REE pattern, and the others have heavy REE-enrichment patterns relative to NASC, which may imply that the dissolved REEs were mainly present in the form of fine colloids in the Chaohu and Longgan lakes.