东菲律宾海新型铁锰结壳中元素的赋存状态

为了解东菲律宾海新型铁锰结壳中元素的赋存状态, 采用化学提取方法对3个结壳样品进行了物相分析.不同类型结壳中成矿和稀土元素的赋存状态总体一致, 表明它们形成于相近的地质和海洋环境中.成矿元素中的Fe和Cu绝大部分赋存在残渣态中, Mn、Co和Ni则主要赋存在锰氧化物结合态、有机结合态和残渣态中, 并且埋藏型结壳样品锰氧化物结合态中赋存了相对更高比例的成矿元素.三价稀土元素主要集中在锰氧化物结合态中.两个沉积物表层结壳样品中的Ce主要集中在残渣态中.而埋藏型结壳样品中的Ce则主要赋存在锰氧化物结合态中, 这可能与该样品此相态中赋存了相对较多的Mn有关.呈碳酸盐结合态和有机结合态的稀土元素含量仅各占稀土总量的1%左右, 表明两者对结壳中稀土元素的富集作用很小.      

西太平洋海山富钴结壳稀土元素(REE)组成原位LA-ICPMS测定

利用激光剥蚀电感耦合等离子体质谱(LA-ICPMS)微区原位分析方法,对采自西太平洋海山具完整三层结构的富钴结壳样品进行了稀土元素(REE)含量测定,结果表明, 虽然均产于西太平洋海山且均具有明显的三层结构,富钴结壳化学组成受地理位置和沉积环境影响很大。绝大多数西太平洋富钴结壳具有高ΣREE、高LREE/HREE、δCe正异常和δEu基本无异常或微弱正异常的特点, 显示它们主要由正常海水沉积形成。结壳不同层圈之间REE组成有较大的区别, 其原因主要在于其形成环境和矿物组成不同。样品0327稀土元素总量(∑REE)由亮煤层到疏松层到外层逐渐升高,且亮煤层δCe和Y/Ho变化非常大,最大值分别为38.61和105.5,显示该层生长环境较为氧化且相对动荡,而样品0346中三层结构的∑REE都非常高,且变化趋势与0327正好相反,从亮煤层到致密层∑REE有降低的趋势。 亮煤层形成时海水相对较氧化的环境有利于铁锰氧化物的形成和Ce⁴⁺等稀土元素的吸附,导致其中ΣREE较疏松层和外层为高,而后期磷酸盐化导致REE元素的迁移和亏损。在结壳生长剖面上,由最外层到疏松层和亮煤层,δCe呈明显上升趋势,且变化范围趋大,说明该结壳所处的海水环境在由老至新的生长过程中由相对动荡和氧化变为相对平静和还原。     

Composition and distribution of REE in ferromanganese crusts of the Belyaevsky and Medvedev seamounts in the Sea of Japan

This paper presents the results of the integrated study of ferromanganese crusts from the Belyaevsky (Central Basin) and Medvedev (Honshu Basin) seamounts from the Sea of Japan. The study of the mineral composition using powder diffraction and optical and electron microscopy showed that the crusts are made up of todorokite, birnessite, and pyrolusite minerals typical of hydrothermal ferromanganese deposits of the World Ocean. The composition of the ferromanganese crusts from the Sea of Japan was determined by ICP-MS and ICP-OES. The contents of Mn, Fe, Co, Cu, Ni, and other major and trace elements indicate the hydrothermal genesis of the crusts. The obtained data on the composition of ferromanganese crusts of the Sea of Japan, as well as their comparison with different types of deposits of the World Ocean, suggest the endogenic genesis of the studied crusts. However, the REE and Y distribution patterns testify to a significant admixture of hydrogenic matter, which participated in the growth of ferromanganese crusts from the Belyaevsky and Medvedev seamounts.     

The REE species and their distribution in ferromanganese crusts in the Sea of Japan

Polished sections of ferromanganese crusts on underwater rises in the Sea of Japan were studied with a JXA8100 microprobe analyser. Mineral phases of REE have been detected. They have Ln₂O₃ chemical composition, where Ln is La–Ce–Pr–Nd, La–Ce–Nd, or, much more rarely, La–Ce and La–Ce–Pr. With regard to the same chemical composition of REE grains in the ore crusts and basalts from Medvedev Volcano, it has been concluded that these REE were supplied during postvolcanic gas–hydrothermal processes.     

Geochemical features and genesis of continental cobalt-rich ferromanganese crusts

Mass cobalt-rich ferromanganese microcrusts and nodules similar in morphology and chemical composition to cobalt-rich ferromanganese deep-ocean crusts were found in Cenozoic volcanic rocks in southern Primorye. Research has shown that ore genesis of this type is genetically related to argillization and destruction of siliceous rocks by CO₂-rich fluids, which is confirmed by experimental data on carbon erosion of iron-containing materials. Two types of this fluid ore genesis are recognized: (1) relatively high-temperature (vapor-condensate), related to late volcanic processes and fracture gas infiltration, and (2) low-temperature (vapor-liquid-condensate), controlled by degassing followed by carbon mobilization (gasification). Primarily colloidal ferromanganese segregations have high contents of Co, Ni, Pb, Cu, and Ce, typical of oceanic ore genesis. Regardless of the concentrations of these metals in the protoliths, their contents in microcrusts are similar (n-10n wt.%). This indicates the same ore genesis mechanism and similar sorption properties of the colloidal ferromanganese material formed. Barium- and cerium-rich ferromanganese microcrusts and nodules are abundant. Condensed drops of iron-containing platinum were found in apobasaltic nickel-rich ferromanganese segregations. There is a cerium paradox expressed as a minimum or a total lack of cerium among rare-earth phosphates associated with ferromanganese microcrusts. Fluid destruction and oxide metallization of ocean-floor basalts are assumed to be the main source of metals for oceanic ferromanganese crusts and nodules.     

Exploration and research progress on ion-adsorption type REE deposit in South China

Since 2011, certain advances have been made through the resource investigation, metallogenesis research, mining supervision and environmental protection of ion-adsorption type rare earth element (REE) deposit in South China. Firstly, some progress has been made in REE prospecting in Jiangxi, Guangdong, Guangxi and Yunnan. REE deposits are not only found within the weathering crusts of granites and felsic volcanic rocks, but also within the weathering crusts of epimetamorphic rocks and basic magmatic rocks. Secondly, the methods of exploration, delineating ore bodies and calculation of reserves have been improved, which intuitively reflect the thickness, REE composition and value of weathering crust. Thirdly, the relationship between REEs and weathering degree and the rule of distribution, migration and enrichment of REEs in the weathering profile was summarized through the analysis of big data, which can predict the metallogenetic horizon of REEs. Fourthly, a method for quick, accurate and dynamic investigation of the REE deposit has been established by using high resolution remote sensing technology. Finally, the relation between the production status of REE mines and water pollution has been revealed based on long-term hydrochemical monitoring data of rivers and wells in mines and surrounding areas.     

岩石—土壤—铁芒萁系统中稀土元素的分布、迁移和累积

在赣南非稀土矿区和四处不同稀土矿区内取样,用ICP-MS法测定岩石-土壤-铁芒萁系统中15个稀土元素的含量,并对其分布、迁移、累积特征进行了研究。结果表明:稀土元素在岩石、土壤各层含量由高到低的顺序为C(心土层)>A(表土层)>B(底土层)>D(成土母岩);在铁芒萁植物体内的分布规律是:轻稀土元素含量为叶>根>茎>叶柄;重稀土元素含量为根>叶>茎>叶柄;稀土元素演化、迁移的难易是由稀土元素的重轻所决定的;岩-土-芒萁系统各环节间稀土元素的含量模式基本相似,表征元素在岩石→土壤→植物大系统中存在着向量(非均衡性)关系。     

Effect of Phosphatization on Element Concentration of Cobalt-Rich Ferromanganese Crusts

1 Introduction Co-rich ferromanganese crusts occurring on submarine guyots have received much attention from scientists since the beginning of the 1980’s because they are enriched in Co, Mn, Pt, and rare earth elements (REEs), and have large potential mineral resources, occurring as they do on topographic highs relative to polymetallic nodules in the C-C (Clarion-Clipperton) zone (Halbach et al., 1982, 1989; Hein et al., 1992, 1999; Usui and Someya, 1997; Yamazaki and Sharma, 1998, 2000…     

中国富钴结壳合同区海水的稀土元素特征及其意义

通过对西太平洋34件海水样品的稀土元素（REY:REE+Y）测试及其与研究区富钴结壳稀土耦合特征分析,揭示了海水稀土特征及其成因.海水的稀土含量随水深呈现逐渐增加的趋势,∑ REY范围为14.0×10-12~65.5×10-12,平均值为31.9×10-12,其中Y的绝对值（均值为6.0×10-12~24.1×10-12）和相对值（（Y/Ho）_N均值为1.98）均较高,La含量次之（均值为1.8×10-12~11.6×10-12）,Ce含量相对较低（均值为2.4×10-12~8.8×10-12）,δCe范围为0.33~1.03（均值为0.66）,（La/Yb）_N平均值为0.71.海水稀土元素北美页岩标准化后显示左倾模式,具有显著的Ce负异常、Y正异常和无明显的Eu异常特征.研究区普遍发育水成成因的富钴结壳,即其稀土元素和其他组分均源自海水.富钴结壳的稀土含量相对海水富集6~7个数量级,其Ce正异常和Y负异常的稀土模式与海水构成良好的耦合关系,指示富钴结壳类组分对海水稀土清扫具有选择性,是造成海水稀土模式的重要因素.海山上发育的磷块岩以及周围盆地深海泥中的磷酸盐组分,它们具有较高的稀土含量和类似于海水的稀土模式,指示海洋磷酸盐消耗稀土时并未分馏而是继承海水模式.海水独特的稀土模式特征是补给与消耗平衡作用的结果,铁锰氧化物和海洋磷酸盐是两种典型的海洋自生组分,它们对海水稀土特征的形成至关重要.      

西太平洋海山富钴结壳的稀土和铂族元素特征及其意义

为了探讨富钴结壳的稀土和铂族元素是否有相似的形成机制,对西太平洋海山富钴结壳稀土和铂族元素进行了类比研究.结果表明:富钴结壳的∑REY范围为1 433.7×10-6~2 888.0×10-6,其中Ce占到近50%,北美页岩标准化后显示较平坦的稀土模式和显著的Ce正异常特征.根据稀土配分模式及已有的Nd同位素结果,富钴结壳具有亲陆壳属性.富钴结壳具有极高的Pt (115.5×10-9~1 132.0×10-9)、(Pt/Pd)_N和 (Pt/Os)_N值,Ir与Pt及Rh与Pt显示良好相关性.经球粒陨石标准化后显示较一致PGE (platinum-group elements) 配分模式,从Os到Pt逐渐富集,Pd元素强烈亏损.已有的Os同位素研究结果显示物源在地质历史时期从幔源属性向陆源属性变化,但富钴结壳PGE元素内部相对含量仍在一定程度上保持稳定.研究认为:富钴结壳对海水中的稀土清扫具有选择性,Ce的正异常恰恰是结壳对海水稀土中Ce的优先选择造成的,从而导致海水亏损Ce.然而海水中Ce的亏损并未改变新形成富钴结壳的稀土模式,原因是在海洋中存在适量的具有亏损Ce特征的磷酸盐等组分,理论上只需要氧化物类稀土与磷酸盐类稀土消耗的稀土与海水中的补给平衡即可.只是在相关过程中,海洋中氧化物类对稀土的选择更具有主动性,而磷酸盐类表现更多的继承关系.尽管Os同位素显示物源供给发生变化,然而富钴结壳PGE模式相对稳定.因此富钴结壳PGE模式同样可以用富钴结壳对PGE的选择性吸收解释,因富钴结壳优先选择Pt与Ir以及相对排斥Pd和Os,形成了现有独特的PGE模式.      

Abnormally high mercury contents in hydrogenic ferromanganese crusts from Seth Guyot (Northwestern Pacific)

Variations in mercury contents in marine sediments have implications for hydrothermal activity, paleoclimate, depositional environments, and primary bioproduction. Mercury contents reach 148 ppb in hydrogenic ferromanganese crusts on flat-topped seamounts. Such crusts, with up to 4120 ppb Hg, were dredged from the slopes of Seth Guyot in the western Marcus-Wake Seamounts in 1982, during the 13th cruise of RV Vulkanolog. The Seth Fe-Mn crusts are of the same origin as hydrogenic Co-rich ferromanganese deposits from seamounts in other oceanic regions. Mercury accumulated in the Cenozoic as Fe-Mn oxyhydroxides in the crusts adsorbed Hg from bottom water. The process was especially rapid during the Pliocene volcano-tectonic rejuvenated stage.     

Distribution of rare earths in uranium oxides of the main types of uranium deposits: Causes and genetic meaning

Three groups of industrial uranium deposits that differ in the distribution of lanthanides in U oxides have been recognized. A dependence of the REE distribution type on the Yttrium content and Yttrium index YI = (La + Ce)/Y that controls the formation of REE phases capable of selective accumulation of lanthanides has been discovered. This indicates the important role of crystal–chemical fractionation in the distribution of lanthanides. Preferable accumulation of Sm–Gd by U oxides has been found to occur at relatively low contents of Y. In Proterozoic uranium deposits, the yttrium specialization of oxides predominates, while in most Phanerozoic deposits the lanthanum–cerium specialization is typical. These results extend the possibilities of using REEs in ores for purposes of study of the genesis of various uranium deposits.     

Rare Earth Elements Composition and Constraint on the Genesis of the Polymetallic Crusts and Nodules in the South China Sea

The rare earth elements(REE) composition of the polymetallic crusts and nodules obtained from the South China Sea(SCS) were analyzed through inductively coupled plasma mass spectrometry.Results revealed great differences in the REE abundances(∑REE) of the SCS polymetallic crusts and nodules; the crusts show the highest ∑REE, whereas the nodules exhibit the lowest ∑REE. The similarity in their NASC-normalized patterns, the enriched light REE(LREE), the markedly positive Ce anomaly(δCe), and the non-or weakly positive Eu anomaly(δEu), suggest that the polymetallic crusts and nodules are of hydrogenetic origin. Moreover, the REE contents and their relevant parameters are quite different among the various layers of the crusts and nodules, which probably results from the different marginal sea environments and mineral assemblages of the samples. The growth profiles of the SCS polymetallic crusts and nodules reveal the tendency ∑REE and δCe to slightly increase from the outer to the inner layers, suggesting that the growth environments of these samples changed smoothly from an oxidizing to a relatively reducing environment; in addition, the crust ST1 may have experienced a regressive event(sea-level change) during its growth, although the REE composition of the seawater remained relatively stable. On the basis of the regional ∑REE distribution in the SCS crusts and nodules,the samples collected near the northern margin were influenced by terrigenous material more strongly compared with the other samples, and the REE contents are relatively low. Therefore, the special geotectonic environment is a significant factor influencing the abundance of elements, including REE and other trace elements. Compared with the oceanic seamount crusts and deep-sea nodules from other oceans,the SCS polymetallic crusts and nodules exhibit special REE compositions and shale-normalized patterns, implying that the samples are of marginal sea-type Fe-Mn sedimentary deposits, which are strongly affected by the epicontinental environment, and that they grew in a more oxidative seawater environment. This analysis indicates that the oxidized seawater environment and the special nano property of their Fe-Mn minerals enrich the REE adsorption.     

Rare earth element variations resulting from inversion of pigeonite and subsolidus reequilibration in lunar ferroan anorthosites

We present results of a secondary ion mass spectrometry study of the rare earth elements (REEs) in the minerals of two samples of lunar ferroan anorthosite, and the results are applicable to studies of REEs in all igneous rocks, no matter what their planet of origin. Our pyroxene analyses are used to determine solid-solid REE distribution coefficients (D = C_REE in low-Ca pyroxene/C_REE in augite) in orthopyroxene-augite pairs derived by inversion of pigeonite. Our data and predictions from crystal-chemical considerations indicate that as primary pigeonite inverts to orthopyroxene plus augite and subsolidus reequilibration proceeds, the solid-solid Ds for orthopyroxene-augite pairs progressively decrease for all REEs; the decrease is greatest for the LREEs. The REE pattern of solid-solid Ds for inversion-derived pyroxene pairs is close to a straight line for Sm-Lu and turns upward for REEs lighter than Sm; the shape of this pattern is predicted by the shapes of the REE patterns for the individual minerals.Equilibrium liquids calculated for one sample from the compositions of primary phases, using measured or experimentally determined solid-liquid Ds, have chondrite-normalized REE patterns that are very slightly enriched in LREEs. The plagioclase equilibrium liquid is overall less rich in REEs than pyroxene equilibrium liquids, and the discrepancy probably arises because the calculated plagioclase equilibrium liquid represents a liquid earlier in the fractionation sequence than the pyroxene equilibrium liquids. “Equilibrium” liquids calculated from the compositions of inversion-derived pyroxenes or orthopyroxene derived by reaction of olivine are LREE depleted (in some cases substantially) in comparison with equilibrium liquids calculated from the compositions of primary phases. These discrepancies arise because the inversion-derived and reaction-derived pyroxenes did not crystallize directly from liquid, and the use of solid-liquid Ds is inappropriate. The LREE depletion of the calculated liquids is a relic of formation of these phases from primary LREE-depleted minerals. Thus, if one attempts to calculate the compositions of equilibrium liquids from pyroxene compositions, it is important to establish that the pyroxenes are primary. In addition, our data suggest that experimental studies have underestimated solid-liquid Ds for REEs in pigeonite and that REE contents of liquids calculated using these Ds are overestimates.Our results have implications for Sm-Nd age studies. Our work shows that if pigeonite inversion and/or subsolidus reequilibration between augite and orthopyroxene occurred significantly after crystallization, and if pyroxene separates isolated for Sm-Nd studies do not have the bulk composition of the primary pyroxenes, then the Sm-Nd isochron age and ε_Nd will be in error.     

Sources of rare earth elements in Appin Group limestones,Dalradian, north-east Scotland

Summary Rare earth elements (REE) have been determined in 15 samples from three metamorphosed limestone units of the Appin Group of the Dalradian of north-east Scotland. Total REE contents range from about 7 to about 50 ppm and the light REEs are slightly enriched compared with REE in the North American Shale Composite (NASC). In the more impure limestones, the dominant control on REE content was the clay mineral content in siliciclastic impurities derived from terrestrial sources. In the purer limestones, the correlation between REEs and iron is consistent with the well-documented relationship between iron and REEs in the aqueous environment. REE associated with terrestrial, iron-rich, flocculated organic colloids or marine, authigenic iron-manganese coats may well have contributed significantly to the REE contents. Weak Ce anomalies on NASC-normalised, REE variation diagrams in two samples with very low REE contents suggest a marine influence on the REE distribution.

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Die Quelle von Seltenen Erden in Kalken der Appin Gruppe, Dalradians, NE Schottland

Zusammenfassung An 15 Proben aus metamorphen Kalken der Appin Gruppe der Dalradians NE Schottlands wurde die Zusammensetzung der Seltenen Erden (REE) bestimmt. Der Gesamtgehalt an REE variiert von 7 bis 50 ppm, wobei die leichten REE im Vergleich zum North American Shale Composite (NASC) leicht angereichert sind. In unreinen Kalken wird der REE-Gehalt vom Tonmineralanteil der silikatisch-klastischen Verunreinigungen, die einer terrestrischen Quelle entstammen, kontrolliert. In reinen Karbonatgesteinen besteht eine Korrelation zwischen den REE und Fe, eine Beziehung, die für ein wässriges Milieu bereits bereits gut dokumentiert ist. REEs, die mit terrrestrischen, Fe-reichen, ausgeflockten organischen Kolloiden oder marinen, authigen gebildeten Fe-Mn Überzügen assoziiert sind, könnten beträchtlich zu den REE Gehalten beitragen. Schwache, in auf NASC normalisierten REE-Diagrammen erkennbare Ce-Anomalien von zwei Proben, lassen einen marinen Einfluß vermuten.

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With 5 Figures     

Mobility of rare earth elements in the system soils–plants–groundwaters: a case study of an arid area (Oman)

Groundwater samples from six wells and various species of plants from soils developed on ophiolites were collected from an arid area (AlKhod area, Oman) and analyzed for trace elements including rare earth elements (REEs). The distribution patterns of REEs in plants indicated an enrichment in middle REEs (MREEs?=?Sm to Dy) and heavy REEs (HREEs?=?Ho to Lu), when they are normalized to the REE composition of the Post Archean Australian Shale (PAAS), with a significant negative anomaly in Ce and a positive anomaly in Eu. Compared to Oman ophiolites, the REEs in different species of plants are depleted in Ce and enriched in MREEs and slightly enriched in light REE (LREE?=?from La to Nd). Relative to PAAS, the distribution of REEs in groundwaters revealed similar patterns to the REE distribution in plants. The distribution patterns of REEs in plants relative to those in waters are nearly flat. These patterns suggest that the transfer of REEs from soil solutions to the groundwaters in Oman occurs without any significant fractionation.     

晋北中高硫煤中稀土元素的地球化学特征

应用中子活化分析方法，测定了晋北两层中高硫煤中稀土元素的含量。通过对稀土元素的分布模式，相关分析和聚类分析的研究，得出如下认识；成煤环境对稀土元素的含量具有控制作用。但中高硫煤中稀土元素总量会受到沉积期后酸性溶液下渗淋滤作用的影响；同一煤层中各分层的稀土元素应具有基本相同的分布模式，异常的稀土元素分布模式指示了沉积期后地质作用的影响；煤中稀土元素的主要赋存状态为无机相，主要来源为陆源碎屑矿物；煤中与稀土伴生的有害元素有V，P，Mo,Cr,Cu,Mo,Th和Cd等，在加工洗选过程中有洁净潜势。     

Rare earth element distributions among coexisting granulite facies minerals,Scourian complex,NW Scotland

The major rock-forming mineral phases (pyroxenes, plagioclase, garnet, hornblende) of a suite of granulite-facies gneisses from the Scourian complex, NW Scotland, have been analyzed for their rare earth element (REE) content. Although host rock compositions range from felsic to ultramafic, REE abundances and patterns for each mineral group show only limited variation. The REEs exhibit regular and consistent distribution patterns for each mineral which suggest, together with major element and textural considerations, that the observed distribution coefficients approach equilibrium. Total REE content follows the sequence hornblende>clinopyroxene>garnet>plagioclase >orthopyroxene and mass balance calculations show that even in the felsic gneisses>60% of the REEs reside in the major rock-forming minerals. Comparisons of both relative REE abundances and distribution coefficients with those in other rock types reveal a striking resemblance with patterns observed in mineral-liquid pairs of dacitic rocks. These similarities may have arisen during a partial melting episode in which granite-granodiorite melts were generated and removed from the Scourian complex; leaving a residuum which is severely depleted in the incompatible elements, including the REEs.     

Rare earth element geochemistry of oceanic ferromanganese nodules and associated sediments

Analyses have been made of REE contents of a well-characterized suite of deep-sea (> 4000 m.) principally todorokite-bearing ferromanganese nodules and associated sediments from the Pacific Ocean. REE in nodules and their sediments are closely related: nodules with the largest positive Ce anomalies are found on sediments with the smallest negative Ce anomalies; in contrast, nodules with the highest contents of other rare earths (3 + REE) are found on sediments with the lowest 3 + REE contents and vice versa. ${}^{143}\text{Nd}{}^{144}\text{Nd}$ ratios in the nodules (～0.51244) point to an original seawater source but an identical ratio for sediments in combination with the REE patterns suggests that diagenetic reactions may transfer elements into the nodules. Analysis of biogenic phases shows that the direct contribution of plankton and carbonate and siliceous skeletal materials to REE contents of nodules and sediments is negligible. Inter-element relationships and leaching tests suggest that REE contents are controlled by a P-rich phase with a REE pattern similar to that for biogenous apatite and an Fe-rich phase with a pattern the mirror image of that for sea water. It is proposed that 3 + REE concentrations are controlled by the surface chemistry of these phases during diagenetic reactions which vary with sediment accumulation rate. Processes which favour the enrichment of transition metals in equatorial Pacific nodules favour the depletion of 3 + REE in nodules and enrichment of 3 + REE in associated sediments. In contrast, Ce appears to be added both to nodules and sediments directly from seawater and is not involved in diagenetic reactions.     

离子吸附型稀土矿床形成的矿物表/界面反应机制

华南离子吸附型稀土矿床提供了全球超过90%的重稀土,是我国优势的战略性关键金属矿产资源。掌握这类矿床的成矿机制和禀赋特征,可为增加稀土资源储量和高效利用稀土资源提供理论支撑。离子吸附型稀土矿床主要发育在富稀土花岗岩、浅变质岩及火山岩的风化壳中。基岩中的(含)稀土矿物是风化壳中离子态稀土的主要来源,其矿物组合很大程度上决定了稀土矿床的禀赋和分异特征。在物理-化学风化和微生物作用下,造岩矿物、含稀土矿物和稀土独立矿物逐渐溶解,使稀土元素活化和再富集。一方面,母岩风化形成的黏土矿物和铁锰氧化物具有较大的比表面积和一定的表面电荷密度,是稀土离子的主要载体;另一方面,稀土离子通过离子交换、表面吸附与络合、共沉淀,以及形成次生稀土矿物等途径富集在次生矿物表面,其富集-分异特征和赋存状态受矿物类型、pH、微生物活动等因素所控制。利用高分辨透射电镜结合选区电子衍射和电子能量损失谱,以及同步辐射X射线吸收精细结构谱,有望在原子级尺度查明稀土的微观赋存状态。未来研究需更多关注基岩中(含)稀土矿物组合及其演化路径的制约因素、微生物风化对离子吸附型稀土矿床成矿作用的约束,以及稀土元素的微观赋存状态等问题。