Petrography and Mineral Chemistry of Monte Epomeo Green Tuff, Ischia Island, South Italy: Constraints for Identification of the Y-7 Tephrostratigraphic Marker in Distal Sequences of the Central Mediterranean

The 56 ka Monte Epomeo Green Tuff (MEGT) resulted from the largest volume explosive eruption from Ischia island (south Italy). Its tephra is one of the main stratigraphic markers of the central Mediterranean area. Despite its importance, a detailed characterisation of the petrography and mineral chemistry of MEGT is lacking. To fill this gap, we present detailed petrographic description and electron microprobe mineral chemistry data on samples collected on-land from the MEGT. Juvenile clasts include pumice, scoria, and obsidian fragments with porphyritic/glomeroporphyritic, vitrophyric, and fragmental textures. The porphyritic index is 13–40 vol.%, and phenocryst phases include alkali-feldspar, plagioclase, clinopyroxene, ferrian phlogopite, and titano-magnetite, in order of decreasing abundance; accessory phases include sphene, hydroxy-fluor-apatite, and rare edenite. Plagioclase varies from predominant andesine to subordinate oligoclase, whereas alkali-feldspar is more variable from sanidine to anorthoclase; quasi-pure sanidine commonly occurs as either rim or recrystallisation overgrowth of large phenocrysts due to hydrothermal alteration. Secondary minerals include veins and patches of carbonate minerals, Fe-Mn oxyhydroxides, clay minerals, and zeolites. Clinopyroxene is ferroan diopside (En45–29Fs7–27) and never reaches Na-rich compositions. This feature allows the discrimination of MEGT from aegirine-bearing, distal tephra layers erroneously attributed to MEGT, with implications for the areal distribution of Ischia explosive deposits.

High-Resolution Analysis of Critical Minerals and Elements in Fe–Mn Crusts from the Canary Island Seamount Province (Atlantic Ocean)

Two Fe–Mn crusts among 35 samples, from six seamounts in the Canary Island Seamount Province, were selected as representatives of the endpoint members of two distinct types of genetic processes, i.e., mixed diagenetic/hydrogenetic and purely hydrogenetic. High-resolution analyses pursued the main aim of distinguishing the critical elements and their association with mineral phases and genetic processes forming a long-lived Fe–Mn crust. The Fe–Mn crust collected on the Tropic Seamount is composed of dense laminations of Fe-vernadite (>90%) and goethite group minerals, reflecting the predominance of the hydrogenetic process during their formation. Based on high-resolution age calculation, this purely hydrogenetic crust yielded an age of 99 Ma. The Fe–Mn crust collected on the Paps Seamount shows a typical botryoidal surface yielding an age of 30 Ma. electron probe microanalyzer (EPMA) spot analyses show two main types of manganese oxides, indicating their origin: (i) hydrogenetic Fe-vernadite, the main Mn oxide, and (ii) laminations of interlayered buserite and asbolane. Additionally, the occurrence of calcite, authigenic carbonate fluor-apatite (CFA) and palygorskite suggests early diagenesis and pervasive phosphatization events. Sequential leaching analysis indicated that Co, Ni, Cu, Ba and Ce are linked to Mn minerals. Therefore, Mn-oxides are enriched in Ni and Cu by diagenetic processes or in Co and Ce by hydrogenetic processes. On the other hand, Fe-oxides concentrate V, Zn, As and Pb. Moreover, the evidence of HREE enrichment related to Fe-hydroxides is confirmed in the mixed hydrogenetic/diagenetic crust.

STATUS KARIES DAN KADAR FLUOR YANG DIKONSUMSI PENDUDUK USIA 12 – 14 TAHUN DI DESA WIAU LAPI BARAT

Dental caries is microbiological disease on dental hard tissue which caused localized demineralization from inorganic structure and destruction of organic substantive part of dental. Fluor protects teeth from caries, by deliberating metabolism of plaque bacteria which could make carbohydrate fermentation through hydroxide-apatite transform into fluor-apatite which more stabilize and acid resistant. The aim of this research is to identify the rate of caries grade among adolescent aged 12 – 14 years and the amount of fluor proportion by consumed in the daily consumed West Wiau Lapi village. This research is descriptive cross-sectional research. Respondent amount is 59 and this research using total sampling method. The result of caries degree is calculated by DMF-T index and fluor analyzing using Spectrofotometer and the length of wave is 525 nm. This research concluded that the caries grade arrange in intermediate degree, and the fluor amount posture is very low. Keyword: caries grade, fluor amount Abstrak: Karies gigi adalah penyakit mikrobiologis struktur keras gigi yang menyebabkan demineralisasi terlokalisasi dari bagian inorganik dan kerusakan dari substansi organik yang berawal dari permukaan eksternal dari gigi. Fluor berfungsi melindungi gigi dari karies, dengan cara menghambat metabolisme bakteri plak yang dapat memfermentasi karbohidrat melalui perubahan hidroksi-apatit pada enamel menjadi flour-apatit yang lebih stabil dan lebih tahan terhadap pelarutan asam. Tujuan penelitian ini untuk mengetahui gambaran derajat karies anak-anak usia 12-14 tahun dan kadar fluor dalam air minum yang dikonsumsi di desa Wiau Lapi Barat. Penelitian ini merupakan penelitian deskriptif potong lintang. Penelitian ini menggunakan metode total sampling dan mempunyai responden penelitian berjumlah 59 orang. Hasil perhitungan derajat karies dihitung dengan indeks DMF-T dan uji fluor digunakan alat spektrofotometer dengan panjang gelombang 525 nm, dari hasil penelitian disimpulkan bahwa derajat karies di desa Wiau Lapi Barat dalam status menengah dan kandungan fluor sangat rendah. Kata kunci: status karies, kadar fluor

A multi-method analysis of Si-, S- and REE-rich apatite from a new find of kalsilite-bearing leucitite (Abruzzi, Italy)

The crystal chemistry characteristics of a hydroxyl-fluor apatite from a recently discovered kalsilite-bearing leucitite from Abruzzi, Italy, were investigated by electron microprobe, single crystal X-ray diffraction, IR, Raman and micro-Raman spectroscopy. The apatite has exceptionally high S and relatively high Si, Sr and LREE, whereas the HREE content is negligible. The IR spectra confirm the presence of OH calculated from formula difference. A high positive correlation between Ca-site Substitution Index (CSI = 100(10-Ca)/Ca) and Tetrahedral Substitution Index (TSI = 100 (Si+C+S)/P atom/a.p.f.u.) and a systematic parallel increase in REE, S and Si indicate two substitution mechanisms, i.e. REE3+ + Si4+ = Ca2+ + P5+ and Si4+ + S6+ = 2 P5+. Site occupancy data and bond lengths, determined from structural refinements on selected samples, demonstrate that LREE and Sr show a marked preference for the Ca2 site, even though in the LREE-rich samples a partial substitution of LREE for Ca in the Cal site was observed.Tetrahedral distances (from 1.535 to 1.541 Å.) reflect the substitution of Si4+ and S6+ for P5+, which is also confirmed by vibrational spectra. As (SiO4)4− and (SO4)2− substitute for (PO4)3−, the relative intensity of v1 Raman bands of (SO4)2− (at 1007 cm−1) and (SiO4)4− (at 865 cm−1) increase systematically, while that of phosphate decreases and the five components of phosphate v3 modes disappear. Moreover, the (PO4)3− Raman peak broadening is linearly correlated with the Si and S concentrations.Apatite crystals are sometimes zoned with compositions varying from SiO2 = 1.15–2.07 wt.%, Σ(LREE2O3) = 0.56–1.08 wt.% and SrO = 0.58–1.02 wt.% in the core to 3.98–5.03, 4.14–6.73 and 1.97–2.17, respectively, in the rim. A sharp, strong enrichment in Sr and LREE in the rim indicate that the apatite suddenly became an acceptor of these elements in the late stages of crystallization.

Exceptional REE-enrichment in apatite during the low pressure fractional crystallisation of alkali olivine basalt; an example from the British Tertiary Igneous Province

The Cnoc Rhaonastil dolerite boss on Islay, NW Scotland represents a body of alkali-olivine basalt magma which differentiated at low pressure and in situ, from dolerite through teschenite to minor nepheline-syenite. The syenites occur as isolated pods and pegmatitic schlieren within the leucodolerite, and have an exotic mineralogy including Zr-aegirine, Zr-arfvedsonite, Ca-catapleiite, zirconolite and aenigmatite. Fluor-apatite occurs as an accessory phase in the dolerite, but becomes more abundant within the teschenite and syenites. Total REE contents within apatites in the dolerites are typically low (σREE = 0·57–3·21 wt.% oxide), the highest REE contents occurring in irregular, deuterically altered rims and internal patches. The REE-enriched rims also have slightly elevated SiO2 contents at 0·81–0·95 wt.%, suggesting that the substitution scheme Ca2++P5+ ⇔ REE3++Si4+ was operating. These apatites have up to 0·08 wt.% Cl and 3·7 wt.% F, with most being almost pure end-member fluor-apatite. The majority of the teschenite apatites show the least REE-enrichment (σREE = 0·27–0·45 wt.%), coupled with low Na (<0·12 wt.%) and low SiO2 (<0·39 wt.%) contents. However, within the syenites two distinct populations of apatite exist. The first, most common, variety consists of unzoned, low-REE apatites (max. 3·1 wt.% σREE, again in irregular rims and patches), whereas the second variety is often complexly zoned, and has variably enriched zones up to a maximum σREE content of 42 wt.%; this is by far the most REE-enriched natural fluor-apatite so far reported from the British Isles. The REE-enriched zones are often less than 3 μm wide, and have Na content up to 5·4 wt.% Na2O, implying that the substitution scheme Na+ + REE3+⇔2Ca2+ dominated over the more typical scheme involving Si4+ which operated in the dolerites and teschenite. Other zones are either variably enriched in Y (up 2·1 wt.% Y2O3) or Th (up to 0·85 wt.% ThO2). However, there is no correlation between Y and REE contents, suggesting that crystallographic factors were involved in apatite Y and REE partitioning. The REE-rich apatites have very low Cl content (<0·04 wt.%), but high F concentrations (<2·8 wt.%). It is believed that these strongly enriched apatites crystallised under disequilibrium conditions from isolated, variably REE-enriched domains, within the fluid-rich residual syenitic magma. These domains may have been generated by the prior crystallisation of monazite, Ca-catapleiite or zirconolite, which can be found as small inclusions within albite and interstitial analcime. The dynamic process of slumping of the denser teschenite back into the leucodolerite crystal mush is believed to have played an important role in the release of deuteric fluids and the concentration of residual magmas.