Petrology of Ocellar Lamprophyres in South Delhi Fold Belt,Danva, Sirohi District,Rajasthan, India

Ocellar lamprophyres are reported from Danva, in Sirohi district, Rajasthan which lies in the Pindwara-Watera sector of the South Delhi Fold Belt (SDFB). They intrude mafic metavolcanics and garnetiferous biotite schist of the Ajabgarh Group of the Delhi Supergroup. These lamprophyres are unaltered, show porphyritic and panidiomorphic textures with olivine, clinopyroxene, amphibole, biotite and spinels constituting the phenocryst phase in a ground mass of clinopyroxene, amphibole, mica and analcime. Petrochemically, these lamprophyres can be classified as analcime monchiquite (alkaline lamprophyre), though they have some affinity towards ultramafic lamprophyres and lamproites. Chemistry of the minerals suggests that the clinopyroxenes have a compositional range of diopside and salite, amphiboles are typically kaersutites, biotites are titanium rich and spinels are Al-rich ulvospinels. These minerals plot in discriminant fields of minerals from alkaline and ultramafic lamprophyres.The Danva lamprophyres are characterized by a variety of ocellar features that include (i) porphyritic ocellus with microphenocrysts of kaersutites and biotite in ground mass of analcime, (ii) zoned ocellus with concentric zones of carbonates and analcime and (iii) composite ocellus in which type (i) ocellus enclose the type (ii) ocellus. These ocellar features are interpreted to represent late stage magmatic segregation and magmatic crystallization involving two immiscible magmatic liquids.The Danva lamprophyres are in strike continuity of the Pipela lamprophyres and therefore confirm alkaline magmatism for over 20 kms in SDFB during end-Neoproterozoic tectono-thermal event. The close spatial association of the lamprophyres with Cu-Zn-Au deposits of Danva and Pipela area and the first report of monchiquite with affinity towards ultramafic lamprophyres and lamproites may be significant in gold (and possibly diamond) exploration in the SDFB.     

An occurrence of ardennite in quartz veins in piemontite schist,Western Otago,New Zealand

Summary Ardennite of complex composition: (Mn²⁺ _3.488Ca_0.509Ba_0.002)₌₄(Mg_0.916916 Fe³⁺ _0.165 Mn³⁺ _0.099Cu_0.033Ni_0.009Zn_0.006 Ti_0.008Al_4.764)₌₆(As⁵⁺ _0.823V⁵⁺ _0.022P_0.005B_0.069Al_0.042Si_5.039)₌₆O_21.81(OH)_6.17 occurs in crack-seal quartz veins in quartz-albite-piemontite-spessartine-phengitehematite-chlorite-rutile-tourmaline ± calcite schist of the Haast Schist Group near Arrow Junction, western Otago, New Zealand. The Mn²⁺/Mn³⁺-ratio is sensitive to calculations and to accuracy of analyses. Boron is detected in ardennite for the first time. Other properties include = 1.734(3), = 1.735(3), = 1.751(3), 2V_Z = 30(2)°;a = 8.721(1),b = 5.816(1),c = 18.545(3) Å,V = 940.7(2) ų. Associated mineral phases are spessartine, hematite, piemontite containing 0.7% SrO and 0.06% PbO, and phengite. Later-stage vein minerals comprise chlorite, albite, and manganoan calcite which were deposited under less highly oxidizing conditions. Digenite with minor intergrown covellite occurs in small amount with manganoan calcite and quartz in a cross-cutting late-stage veina chalcopyrite and native copper occur in other late-stage veins. Arsenic and other components of the ardennite and associated minerals are derived from highly oxidized ferromanganese oxide- and hydroxide-bearing siliceous pelagic sediments that formed the protolith for the piemontite schist. The veins formed at a relatively early stage after metamorphism peaked in the chlorite zone of the greenschist facies under conditions that have been estimated at about 4.5 kbar, 390 °C.

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Vorkommen von Ardennit in Quarzgängen aus Piemontit-Schiefern, West-Otago, Neuseeland

Zusammenfassung Ardennit mit der Zusammensetzung (Mn²⁺ _3.488Ca_0.509Ba_0.002)₌₄(Mg_0.916Fe³⁺ _0.165Mn³⁺ _0.099Cu_0.033Ni_0.009Zn_0.006 Ti_0.008Al_4.764)₌₆(As⁵⁺ _0.823V⁵⁺ _0.022P_0.005B_0.069Al_0.042Si_5.039)₌₆O_21.81(OH)_6.17 tritt in Crack-seal-Quarzgängen in Quarz-Albit-Piemontit-Spessartin-Phengit-Hämatit-Chlorit-Rutil-Turmalin ± Calcit-Schiefern der Haast Schiefer-Gruppe nahe der Arrow Junction, West-Otago, Neuseeland, auf. Die Proportionen von Mn²⁺/Mn³⁺ hängen von der Kalkulation und der Genauigkeit der Analyse ab. Bor wird zum ersten Mal im Ardennit bestimmt. Andere Eigenschaften sind: = 1.734(3), = 1.735(3), = 1.751(3), 2Vz = 30(2)°; a = 8.721(1), b = 5.816(1), c = 18.545(3) Å, V = 940.7(2) Å3. Assoziierte Mineralphasen sind Spessartin, Hämatit, Piemontit, der 0.7% SrO und 0.06% PbO enthält und Phengit. Spät gebildete Gangmineralien, wie Chlorit, Albit und Mn-Calcit, sind unter geringer oxidierenden Bedingungen entstanden. Digenit mit etwas Covellin tritt in kleinen Mengen zusammen mit Mn-Calcit und Quartz in einem querschlägigen Gang auf, Chalcopyrit und gediegenes Kupfer kommen in anderen späten Gängen vor. Arsen und andere Komponenten des Ardennites and der assoziierten Minerale können von hochoxidierten, Fe-Mn-Oxid- und Hydroxyd-führenden, Sireichen, pelagischen Sedimenten hergeleitet werden, die das Ausgangsgestein für den Piemontit darstellen. Die Gänge wurden in einem relativ frühen Stadium, nach dem Metamorphosehöhepunkt, innerhalb der Chloritzone der Grünschiefer-Fazies, unter ungefähr 4.5 kbar und 390°C, gebildet.

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The protection of groundwater dependent ecosystems in Otago, New Zealand

Surface waters (streams, rivers, and wetlands) are the most important groundwater dependent ecosystems (GDEs) in Otago, New Zealand. Pumping wells in the vicinity can deplete water in the GDE. In Otago, most of the surface water resources are allocated and a method, which would assist in the implementation of water management policy, is needed to acknowledge the strong hydraulic link between surface and shallow groundwater. A simplified method has been developed which derives a numerical relationship between the bore pumping rate and the distance between the bore and surface water body beyond which depletion is considered insignificant. A range of GDE depletion scenarios are examined at various combinations of hydraulic parameters to find a minimum distance for a given pumping rate, at which 90% of the modelled surface water depletion scenarios become less than a threshold GDE depletion after a specified time. A buffer zone, based on the minimum distance is placed around GDEs, and groundwater abstraction rights within the buffer are subject to stricter rules. Applicants wishing to abstract from bores within the buffer zone will need to address the environmental impact of the proposed activity on the GDE.     

The greenschist facies in part of eastern Otago,New Zealand

Rocks of the greenschist facies in eastern Otago, New Zealand, have been investigated in an area some thirteen to sixteen kilometers wide and sixty-five kilometers long extending northeastwards approximately normal to the boundary of the schist with lower grade rocks. Quartzo-feldspathic schists predominate but greenschists and metacherts occur sporadically throughout the area. At the southwestern edge of the area schists are in the chlorite zone, slightly above the high-grade limit of pumpellyite. Metamorphic grade increases toward the northeast into the biotite zone which occupies about half the terrane studied and is believed to be everywhere little advanced in metamorphic grade past that of the biotite isograd. Some 130 mineral specimens have been partially analysed with the electron probe. Results derived from these data as well as other mineralogical investigation are as follows: Albite contains a maximum of 1% anorthite plus orthoclase in epidote-bearing rocks from all parts of the area.Compositions of epidotes range from 12% to 32% Ca₂Fe₃(SiO₄)₃(OH), but most lie between 15% and 20%, a compositional field thought by Strens (1965) and Holdaway (1965) to occupy a miscibility gap in the epidote series. Zoning in some epidotes suggests a history of early growth of small, sparse iron-rich epidotes, and later growth of relatively large amounts of iron-poor epidote probably caused by breakdown of prehnite and/or pumpellyite. Muscovites vary widely in celadonite content; but the composition shows little if any dependence on metamorphic grade within the area studied. Most tend to be celadonite-rich, and in this respect are similar in composition to muscovites from rocks of the glaucophane-schist facies.Chlorites range widely in Mg/Fe; but Al/Mg+Fe is relatively uniform. Chlorites associated with actinolite tend to have higher Mg/Fe than those associated with stilpnomelane. Following the classification of Foster (1962) most chlorites are brunsvigite and some are ripidolite. Textural and chemical relations between biotite and coexisting minerals demonstrate that, contrary to some previous suggestions, biotite is not a relict mineral. An alteration product of chlorite bears strong resemblance to biotite, and previous misidentification of this mineral as biotite has caused much confusion regarding the distribution and metamorphic significance of biotite in Otago schists.An attempt to determine the reaction producing biotite is not successful. Possibly biotitebearing rocks have slightly higher biotite component than rocks of the chlorite zone. All newly formed amphibole found in eastern Otago is pale green, Al- and Na-poor actinolite. One of the chemical conditions necessary for the formation of actinolite in schists of eastern Otago is a relatively high Mg/Fe+Al ratio.Stilpnomelane is an integral part of assemblages in which it occurs, being developed under conditions of relatively low and in rocks with a high Fe/Mg + Al ratio. The present highly oxidized state of all stilpnomelane observed in this study is probably not a primary feature of the mineral but developed after metamorphism.Porphyroblastic garnets are accessory constituents in about half the quartzo-feldspathic schists collected from the biotite zone but are extremely rare in specimens of the same lithology from the chlorite zone. Either a garnet-producing reaction began in quartzo-feldspathic schists at about the biotite isograd, or rocks of biotite zone tend to have slightly higher garnet component than those of the chlorite zone. Composition of the garnets ranges widely, extremes being: 77% spess., 18% gross., 5% alm.; 25% spess., 50% gross., 25% alm.; 15% spess., 30% gross., 55% alm. Most of the variation in composition is controlled by host rock composition, but garnets at higher grade tend to have lower spessartine content. The garnets are zoned; generally Mn decreases and Fe increases from core to rim.For the most part chemical equilibrium among different grains and minerals was closely approached over distances of at least a few millimeters. However, profound disequilibrium exists within some individual grains, such as a zoned garnet which over a distance of only 15 microns ranges in spessartine content from 77% in the core to 35% on the rim.This report is a condensed version of part of the author's Ph.D. thesis (Brown, 1966), University of California, Berkeley.     

Syn-metamorphic gold mineralisation,Invincible Vein,NW Otago Schist,New Zealand

The Invincible Vein fills a fault zone which strikes northeast and dips steeply southeast in the lower Rees Valley, NW Otago. The vein cuts north striking foliation in lower greenschist facies Otago Schist. Structures associated with the fault zone are both brittle and ductile, and the fault zone has had a complex history of post-mineralisation reactivation. Mineralised vein material filling parts of the fault zone consist of quartz, albite, muscovite, chlorite, calcite, pyrite, arsenopyrite and minor gold. These minerals have been strained and locally recrystallised during ductile deformation. Fluid inclusion homogenisation temperatures (140–175°C) and ice melting temperatures (0 to –1°C) indicate that the mineralising fluid was low salinity, low CO₂ water with a density between 0.88 and 0.93 g/cm₃. Arsenopyrite geothermometry implies a temperature of mineralisation of 370 ± 70°C. Mineralisation pressure lay between 2 and 5 kbar. Mineralisation pressure-temperature conditions and mineralogy are essentially the same as for metamorphism of the host schist. Vein calcite oxygen isotope ratios (+12 to +15 per mil) are similar to host schist values. Carbon isotope ratios of vein calcite (– 3 to –5 per mil) are distinctly different from ratios in host schist (–7 to –10 per mil). Elevated vein Cr contents, and isotopically depleted carbon data, are consistent with some degree of equilibration with metavolcanic rocks. It is inferred that metavolcanic rocks of the underlying Aspiring Terrane were a significant source for mineralising fluid and metals. Invincible mineralisation occurred in the latter stages of metamorphism, and is the earliest recognised gold-bearing vein system in the Otago Schist.     

Mineralogy and petrology of a piemontite-bearing schist, western Otago, New Zealand

Abstract. Pink piemontite-spessartine-bearing and grey-green spessartine-bearing manganiferous quartzose schists derived from siliceous pelagites, and green quartzofeldspathic schists, are described from the greenschist facies of the Haast Schist terrane, near Arrow Junction, western Otago. Electron microprobe data are reported for sphene, spessartine-rich garnet, manganoan epidote, piemontite, tourmaline, phengitic muscovite, chlorite, albite, haematite, rutile, manganoan calcite and chalcopyrite. Metamorphism occurred at about 6.4kbar, 400°C. X_co2 was above the quartz-rutile-calcite-sphene buffer (X_co2± 0.02) throughout the recorded metamorphic history of the piemontite schists. It dropped from above to below this critical buffering value in a spessartine-rich schist and it was close to or below the buffering value in the quartzofeldspathic schists. Production of piemontite required high f_O2, believed to be inherited from MnO_x in the parent pelagite. Substantial loss of O₂ (e.g. minimum of 0.19% by weight in one rock) during diagenesis and/or metamorphism is inferred. In the grey-green schists this inhibited piemontite formation. Slight loss of O₂ and Ca²⁺ accompanied minor late-stage replacement of piemontite by second generation spessartine. Observed zoning and mineral replacements indicate rise of temperature, drop in pressure, or invasion by solutions of lower f_O2 and X_CO2 equilibrated with surrounding schists. The detailed chemistry of the minerals studied correlates with available Mn and with bulk-rock (Fe³⁺ x 100)/(Fe²⁺+ Fe³⁺). The oxidation ratio ranges from 24 in average green quartzofeldspathic schist, through 78 in average grey-green manganiferous quartzose schist, to almost 100 in some piemontite-bearing schists. As Fe²⁺ gives way to Fe³⁺, Mg/Fe ratios tend to rise in chlorite, phengite, tourmaline, spessartine, and calcite, Mn increases and Ti decreases in haematite, Mn increases in spessartine and calcite, and Fe increases in rutile. Available divalent cations are depleted relative to Al; chlorite is more aluminous, and phengite more paragonitic than in typical Haast schists.     

A New Fossil Termite(Isoptera,Stolotermitidae,Stolotermes)from the Early Miocene of Otago,New Zealand

<正>The forewing of a termite from Early Miocene lake sediments in Otago,southern New Zealand is figured and described.It exhibits the generic characters of the damp-wood termite Stolotermes Hagen,but differs from forewings of the known species in size and venation pattern and is described as Stolotermes kupe sp.nov.S.kupe represents the first confident record of fossil Stolotermitidae and extends the fossil record of the family back to the Early Miocene.It also is the first direct evidence of fossil Isoptera from New Zealand,though silicified termite faecal pellets,referable to Kalotermes brauni,have been previously described.S.kupe indicates that Stolotermitidae has been present in the Australasian region since at least the Early Miocene.     

Petrology of the Blue Mountain Complex, Marlborough, New Zealand

Blue Mountain is a central-type alkali ultrabasic-gabbro ringcomplex (1?1?5 km) introducing Upper Jurassic sediments, Marlborough,New Zealand. The ultrabasic-gabbroic rocks contain lenses ofkaersutite pegmatite and sodic syenite pegmatite and are intrudedby ring dykes of titanaugite-ilmenite gabbro and lamprophyre.The margin of the intrusion is defined by a ring dyke of alkaligabbro. The plutonic rocks are cut by a swarm of hornblende-biotite-richlamprophyre dykes. Thermal metamorphism has converted the sedimentsto a hornfels ranging in grade from the albite-epidote hornfelsfacies to the upper limit of the hornblende hornfels facies. The rocks are nepheline normative and consist of olivine (Fo_82-74),endiopside (Ca₄₅Mg₄₈Fe₇-Ca₃₆Mg₅₅Fe₉), titanaugite (Ca₄₀Mg₅₀Fe₁₀-Ca₄₄Mg₃₉Fe₁₇),plagioclase (An_73-18), and ilmenitetitaniferous magnetite, withvarious amounts of titaniferous hornblende and titanbiotite.There is a complete gradation between end-iopside and titanaugitewith the coupled substitution R_y^+z+Si(Ti⁺⁴+Fe⁺³)+Al⁺³ and asympathetic increase in CaAl₂SiO₆ (0?2-10?2 percent) and CaTiAl₂O₆(2?1-8?1 per cent) with fractionation. Endiopside shows a small,progressive Mg enrichment along a trend subparallel to the CaMgSi₂O₆-Mg₂Si₂O₆boundary, and titanaugite is enriched in Ca and Fe⁺²+Fe⁺³ withdifferentiation. Oscillatory zoning between endiopside and titanaugiteis common. Exsolved ilmenite needles occur in the most Fe-richtitanaugites. The amphiboles show the trend: titaniferous hornblende(1?0–5?7 per cent TiO₂)kaersutite (6?4 per cent TiO₂)Fe-richhastingsite (18?0–19?1 per cent FeO as total Fe). Biotiteis high in TiO₂ (6?6–7?8 per cent). Ilmenite and titaniferousmagnetite (3?5–10?6 per cent TiO₂) are typically homogeneousgrains; their composition can be expressed in terms of R⁺²RO₃:R⁺²O:R₂⁺³O₄. The intrusion of igneous rocks was probably controlled by subterraneanring fracturing. Subsidence of the country rock within the ringfracture provided space for periodic injections of magma froma lower reservoir up the initial ring fracture to form the BlueMountain rocks at a higher level. Downward movement of the floorof the intrusion during crystallization caused inward slumpingof the cumulates which affected the textural, mineralogical,and chemical evolution of the rocks in different parts of theintrusion. The order of mineral fractionation is reflected by the chemicalvariation in the in situ ultrabasic-gabbroic rocks and the successiveintrusions of titanaugite-ilmenite gabbro and lamprophyre ringdykes, marginal alkali gabbro and lamprophyre dyke swarm. Aninitial decrease, then increase in SiO₂; a steady decrease inMgO, CaO, Ni, and Cr: an initial increase, then decrease inFeO+Fe₂O₃, TiO₂, MnO, and V; almost linear increase in Al₂O₃and late stage increase in alkalis and P₂O₃, implies fractionationof olivine and endiopside, followed by titanaugite and Fe-Tioxides, followed by plagioclase, hornblende, biotite, and apatite.Reversals in the composition of cumulus olivine and endiopsideand Solidification Index, indicate that the ultrabasic-gabbroicsequence is composed of four main injections of magma. The ultrabasic rocks crystallized under conditions of high PH₂Oand fairly high, constant P_O2; P_H2 and P_O2 increased duringthe formation of the gabbroic rocks until fracturing of thechamber roof occurred. The abundance of euhedral amphibole inthe latter injection phases suggests that amphibole accumulatedfrom a hydrous SiO₂ undersaturated magma when an increase inP_O2, stabilized its crystallization. Plutonic complexes similar to Blue Mountain are found withinand beneath the volcanic piles of many oceanic islands, e.g.Canaries, Reunion, and Tahiti, and those intruding thick sedimentarysequences, as at Blue Mountain, e.g. the pipe-like intrusionsof the Monteregian Hills, Quebec.     

Petrology of the Blue Mountain Complex, Marlborough, New Zealand

Blue Mountain is a central-type alkali ultrabasic-gabbro ringcomplex (lxl7middot;5 km) introducing Upper Jurassic sediments,Marlborough, New Zealand. The ultrabasic-gabbroic rocks containlenses of kaersutite pegmatite and sodic syenite pegmatite andare intruded by ring dykes of titanaugite-ilmenite gabbro andlamprophyre. The margin of the intrusion is defined by a ringdyke of alkali gabbro. The plutonic rocks are cut by a swarmof hornblendebiotite-rich lamprophyre dykes. Thermal metamorphismhas converted the sediments to a hornfels ranging in grade fromthe albite-epidote hornfels facies to the upper limit of thehornblende hornfels facies. The rocks are nepheline normative and consist of olivine (Fo_82–74),endiopside (Ca₄₅Mg₄₈Fe₇–Ca₃₆Mg₅₅Fe₉), titanaugite (Ca₄₀Mg₅₀Fe₁₀–Ca₄₄Mg₃₉Fe₁₇),plagioclase (An_73–18), and ilmenitetitaniferous magnetite,with various amounts of titaniferous hornblende and titanbiotite.There is a complete gradation between endiopside and titanaugitewith the coupled substitution R_y⁺²+Si;;(Ti⁺⁴+Fe⁺³+Al⁺³ and asympathetic increase in CaAl₂SiO₆ (0·2–10·2percent) and CaTiAl₂O₆ (2·1–8·1 per cent)with fractionation. Endiopside shows a small, progressive Mgenrichment along a trend subparallel to the CaMgSi₂O₆–Mg₂Si₂O₆boundary, and titanaugite is enriched in Ca and Fe⁺²+Fe⁺³ withdifferentiation. Oscillatory zoning between endiopside and titanaugiteis common. Exsolved ilmenite needles occur in the most Fe-richtitanaugites. The amphiboles show the trend: titaniferous hornblende(1·0–57middot;7 per cent TiO₂) kaersutite (6·4per cent TiO2) Fe-rich hastingsite (18·0–19·1per cent FeO as total Fe). Biotite is high in TiO₂ (6·6–7·8per cent). Ilmenite and titaniferous magnetite (3·5–10·6per cent TiO₂) are typically homogeneous grains; their compositioncan be expressed in terms of R⁺²RO₃:R⁺²O:R₂⁺³O₄. The intrusion of igneous rocks was probably controlled by subterraneanring fracturing. Subsidence of the country rock within the ringfracture provided space for periodic injections of magma froma lower reservoir up the initial ring fracture to form the BlueMountain rocks at a higher level. Downward movement of the floorof the intrusion during crystallization caused inward slumpingof the cumulates which affected the textural, mineralogical,and chemical evolution of the rocks in different parts of theintrusion. The order of mineral fractionation is reflected by the chemicalvariation in the in situ ultrabasic-gabbroic rocks and the successiveintrusions of titanaugite-ilmenite gabbro and lamprophyre ringdykes, marginal alkali gabbro and lamprophyre dyke swarm. Aninitial decrease, then increase in SiO2; a steady decrease inMgO, CaO, Ni, and Cr: an initial increase, then decrease inFeO+Fe₂O₃, TiO₂, MnO, and V; almost linear increase in A1₂O₃and late stage increase in alkalis and P₂O₃, implies fractionationof olivine and endiopside, followed by titanaugite and Fe-Tioxides, followed by plagioclase, hornblende, biotite, and apatite.Reversals in the composition of cumulus olivine and endiopsideand Solidification Index, indicate that the ultrabasic-gabbroicsequence is composed of four main injections of magma. The ultrabasic rocks crystallized under conditions of high P_H2Oand fairly high, constant     

Oxidation and microprobe-induced potassium mobility in iron-bearing phyllosilicates from the Otago schists,New Zealand

Biotite, chlorite and stilpnomelane have undergone post-metamorphic oxidation in situ in the Otago schist, due to surficial weathering. The oxidation results in changes in the chemistry of these minerals. Oxidation of biotite and stilpnomelane is accompanied by loss of potassium, and stilpnomelane with its full metamorphic potassium content is probably rare. analytical work such as KAr dating which depends critically on K₂O contents of biotite and stilpnomelane should therefore proceed with due caution. Potassium in stilpnomelane is very mobile under the microprobe beam, and only approximate K₂O analyses may be obtained.     

Trench-slope channels from the New Zealand Jurassic: the Otekura Formation, Sandy Bay, South Otago

The Otekura Formation (Early Jurassic, Pseudaucella zone) at Sandy Bay comprises part of a 10+ km thick, regressive, forearc shelf and slope sequence, the Hokonui facies belt of the Rangitata Geosyncline. The Otekura Formation is dominantly fine grained, being mostly mudstone, silty mudstone and siltstone. The sediments are volcanogenic throughout. The upper 150 m of the formation contains two 20 m thick, channelized bodies of medium-thick bedded sandy flysch, each associated with thin bedded muddy flysch interpreted as overbank turbidites. Directional indicators within the channel sequence indicate emplacement from the south-southwest. In contrast, rare turbidites that occur below the channel sequence, within the background mudstone sediment, were emplaced from the east, i.e. at right angles to the channelized flows. The immediately overlying Omaru Formation contains more abundant macrofossils, intraclastic conglomerates, and appreciable amounts of traction-emplaced cross-bedded sand. Bioturbated calcareous siltstones with an in situ molluscan fauna follow (Boatlanding Formation), and are of shelf origin. The Omaru Formation is therefore interpreted as a shelf-slope break deposit, and the Otekura Formation as an upper slope facies. Reconnaissance studies indicate that the Otekura Formation is underlain by several kilometres of dominantly fine grained, deep water slope sediments, containing occasional sand and conglomerate filled channels similar to those here described in detail from the Otekura Formation. Such channels are inferred to form when a mass-transported sand, derived from failure higher on the slope, ploughs erosively into the sea floor. After their incision, the channels served for a short time as conduits for downslope transport of sediment, the redeposited deposits of which are found filling each channel. Both channel fills at Sandy Bay are capped by thin-bedded turbidites inferred to have overspilled from similar channels nearby on the slope.     

Petrology of Calc-alkaline Lavas from Ruapehu Volcano and Related Vents, Taupo Volcanic Zone, New Zealand

Most Ruapehu lavas and those of related vents (Taupo VolcanicZone, New Zealand) are calc-alkaline, medium-K basic and acidandesites, though minor volumes of basalt and dacite occur.Nearly all are porphyritic with phenocrysts of plagioclase,augite, olivine (mainly in basalts and basic andesites), orthopyroxene(mainly in acid andesites and dacites), and titanomagnetite(chrome spinel in basic lavas). The lavas have been subdividedinto six groups, each petrographically, geochemically and isotopicallydistinct: Type 1 plagioclase-pyroxene phyric lavas dominate,and range from basalt to dacite. Least squares mass balancecalculations indicate that these lavas were probably generatedfrom low-alumina basalt by combined crystal fractionation (15–55per cent) and crustal assimilation (1–30 per cent). Xenolithstudies indicate that the assimilant is most likely to be apartial melt of gneiss, originally Torlesse terrane greywacke.Crystal accumulation occurs to a minor extent in Type 1 lavasand becomes important in Type 2 (plagioclase-phyric) and Type3 (pyroxene-phyric) lavas. Type 4 lavas are rare and of unknownorigin, though they may be similar to rare hornblende-bearingandesites from nearby Maungakatote volcano. Type 5 lavas areclinopyroxene-olivine-phyric andesites which were probably generatedfrom a primitive basalt by crystal fractionation without crustalassimilation. Type 6 lavas show strong evidence of disequilibriumand were probably generated by mixing Type 5 basalt with Type1 dacite in proportions of between 60:40 and 50:50. The assertion that the assimilant involved in contaminationof most Ruapehu andesites is a partial melt of basement greywackeis a significant departure from previously published theoriesand has important implications for trace element and isotopicmodelling.     

Clinopyroxenes in the tawhiroko tholeiitic dolerite at Moeraki,north-eastern Otago,New Zealand

Clinopyroxenes from various lithologic units in a single tholeiitic dolerite intrusion 50 m thick were analysed with the electron microprobe. Microphenocrysts of augite in the chilled marginal rock have the least scattered CaMgFe ratios, around Ca₃₈Mg₅₀Fe₁₂, and lowest Ti/Al ratios, less than 1/4, of the augites examined; they crystallized prior to emplacement. The augites which crystallized in situ are more Fe-rich and have higher Ti/Al ratios, close to 1/2. Pigeonite started crystallizing later than augite and formed rims to augite crystals. Continuous zoning from augite to subcalcic augite as was previously reported by Benson (1944) for the same dolerite is not observed. Subcaloic ferroaugites, however, link augite and ferropigeonite in the outermost margins of pyroxenes in the later segregations. The small scale differentiation in situ gave rise to globules, veins, and pegmatoids, in which sector-zoning of augite is well developed. The {100} sectors are enriched in MgSiO₃, FeSiO₃, and MnSiO₃ components relative to the {010} and the {110} sectors, and are accordingly depleted in other components. The protosite theory of sector-zoning formation proposed by Nakamura (1973) is further developed and the environment which favours the development of sector-zoning is discussed. The formation of augite rims around quartz-rich xenoliths and the compositional characteristics of the augites concerned are due to local high silica activities. Comments are made concerning some lunar pyroxenes in the light of the present study.     

Tourism and resource development conflicts on the Kawarau and Shotover Rivers,Otago, New Zealand

The Kawarau and Shotover Rivers are in the heart of Southern New Zealand's premier tourist region, focused upon Queenstown in Central Otago. Over the last fifteen years they have become important as the venue for a variety of adventure activities, principally jet boating and white water rafting. These have grown rapidly to become a major part of the regional tourism product. During the same time period, proposals for hydro electric power development on the Kawarau threatened to eliminate white water rafting and severely modify jet boating; during the last five years a revival of the region's gold mining industry, which was founded in the 1860s, has threatened rafting on the Shotover River. This paper examines the ways in which these conflicts were assessed and managed, and points to a new threat, namely that of overcrowding.     

Petrology and geochemistry of the Banks Peninsula volcanoes,South Island,New Zealand

Within the volcanic sequence of the twin volcanoes of Lyttelton and Akaroa, Banks Peninsula, New Zealand a number of different magma series have been distinguished.An early series of hawaiites (McQueens Valley Formation) was erupted about 32 m.y. ago and is of transitional or mildly tholeiitic chemistry. Stratigraphically above the McQueens Valley Formation, but unconformably overlain by the main volcanic dome sequence, is a unit of rhyolite (Gebbies Pass Rhyolites) which is not directly related to the earlier or later basaltic volcanism. The rhyolite was probably formed during intracrustal melting which was related to the rise of basaltic magma into the crust.Between 12 and 9.7 m.y. a large volcanic dome, composed mainly of hawaiite, was built at Lyttelton. Dykes, which intrude the Lyttelton volcanic sequence, range in composition from basalt to trachyte. Late, mildly alkalic, basaltic flank flows (7.5–5.8 m.y.) occur in several areas and they, and the differentiated rocks of the dyke swarm can be related by a crystal fractionation model which has been quantitatively tested.Following construction of the Lyttelton dome a second larger dome was built at Akaroa between 9 and 7.5 m.y. The rocks of the Akaroa Volcano are principally hawaiites but rocks ranging in composition through to trachyte also occur. The differentiated rocks of the Akaroa volcano have derived from the basaltic rocks by a crystal fractionation controlled process, operating during ascent through the crust.None of the Banks Peninsula basalts appear to have derived from primitive (pyrolitic) mantle material, but progressive changes in the chemistry of the basalts with time implies that the mantle source regions were evolving geochemically as partial melting proceeded. Later lavas tend to be more alkalic and to have lower MgO/FeO ratios than earlier lavas. The volcanic rocks of the Banks Peninsula volcanoes were derived by fractional removal of olivine, plagioclase, clinopyroxene, magnetite and apatite from ascending basaltic magma batches. Variations between the suites reflect differences between the parental magma batches.     

The significance of corona textured inclusions from a high pressure fractionated alkalic lava: North Otago, New Zealand

Rare gabbroic inclusions within a lherzolite-nodule bearing, fractionated, alkalic lava are of two types: olivine-two pyroxene-spinel-metagabbro and amphibole-two pryoxene-spinel-metagabbro. The metagabbros represent cumulates which have crystallized from alkalic basalt magma at high temperature. Metamorphic aggregates and coronas consisting of clinopyroxene-orthopyroxene and spinel with or without amphibole are attributed to complex subsolidus reactions between olivine and plagioclase; olivine, clinopyroxene and plagioclase; olivine and clinopyroxene; olivine, clinopyroxene, plagioclase and ilmenite in response to decreasing temperature as the rocks cooled at pressures of around 11 Kb (35–40 km) and temperatures in the range 1000–1150°C. The lower crust and upper mantle below East Otago must contain bodies of fractionated alkalic basalt showing granulitic mineralogy.     

The geochemistry of the Dunedin Volcano,East Otago,New Zealand: Rare earth elements

A variety of alkaline lavas from the Dunedin Volcano have been analyzed for the rare earth elements (REE) La-Yb. The compositions analyzed were: basalt-hawaiite-mugearite-benmoreite; basanite, nepheline hawaiite, nepheline trachyandesite and nepheline benmoreite; trachyte; phonolite. The series from basalt to mugearite shows continuous enrichment in the REE, consistent with a crystal fractionation model involving removal of olivine and clinopyroxene. From mugearite to benmoreite there is a depletion in the REE which is explained by the appearance of apatite as a liquidus phase. The chondrite normalized REE patterns for the phonolites are characterized by strong enrichment and fractionation coupled with a sharp depletion in Eu. Removal of plagioclase from benmoreite magma is suggested for the derivation of the phonolites. The series basanite-nepheline hawaiite, and basanite-nepheline hawaiite-nepheline benmoreite appear to be high pH₂O analogues of the series basalt-ben-moreite, with enrichment of the REE being achieved by removal of clinopyroxene, kaersutite and olivine. Compared with other lavas the trachyte has low REE abundances and is characterized by a striking positive Eu anomaly.     

Fluid evolution during metamorphism of the Otago Schist, New Zealand: (I) Evidence from fluid inclusions

Fluid inclusion salinities from quartz veins in the Otago Schist, New Zealand, range from 1.0 to 7.3 wt% NaCl eq. in the Torlesse terrane, and from 0.4 to 3.1 wt% NaCl eq. in the Caples terrane. Homogenization temperatures from these inclusions range from 124 to 350  °C, with modal values for individual samples ranging from 163 to 229  °C, but coexisting, low-salinity inclusions exhibiting metastable ice melting show a narrower range of T  _h from 86 to 170  °C with modes from 116 to 141  °C. These data have been used in conjunction with chlorite chemistry to suggest trapping conditions of ≈350–400  °C and 4.1–6.0  kbar for inclusions showing metastable melting from lower greenschist facies rocks, with the densities of many other inclusions reset at lower pressures during exhumation of the schist. The fluid inclusion salinities and Br/Cl ratios from veins from the Torlesse terrane are comparable to those of modern sea-water, and this suggests direct derivation of the vein fluid from the original sedimentary pore fluid. Some modification of the fluid may have taken place as a result of interaction with halogen-bearing minerals and dehydration and hydration reactions. The salinity of fluids in the Caples terrane is uniformly lower than that of modern sea-water, and this is interpreted as a result of the dilution of the pore fluid by dehydration of clays and zeolites. The contrast between the two terranes may be a result of the original sedimentary provenance, as the Torlesse terrane consists mainly of quartzofeldspathic sediments, whilst the Caples terrane consists of andesitic volcanogenic sediments and metabasites which are more prone to hydration during diagenesis, and hence may provide more fluid via dehydration at higher grades.     

Origin and deposition of a graphitic schist-hosted metamorphogenic Au-W deposit,Macraes, East Otago,New Zealand

The Macraes gold-tungsten deposit occurs in a low-angle thrust system in biotite grade Otago Schist. Native gold, scheelite, pyrite and arsenopyrite are found in and adjacent to quartz veins and silicified schist of lenticular reef zones, where the thrust system cuts through graphitic pelitic schist. Mineralization is confined to a shear zone, up to 80 m thick, which is closely sub-parallel to the regional schistosity. Chemical alteration is dominated by silicification, with some addition of Cr and depletion of Sr and Ba. Alteration extends only about 5 m from major veins. Oxygen becomes isotopically heavier away from veins due to temperature decrease as hot fluids penetrated into cooler (250°C?) rock. Graphite within the shear zone rocks has reflectance of 6–7% (in oil), similar to graphite in medium-high grade Otago Schist, and is presumed to be metamorphic in origin. This graphite has acted as a reducing agent to cause precipitation of gold where the thrust system, acting as a conduit for metamorphic fluids, intersects the graphitic schist. The metals were derived from the underlying schist pile which may include an over-thrust oceanic assemblage containing metal-enriched horizons.