ALBERT

Notes: Abstract Petrographic, mineral chemical and whole-rock major oxide data are presented for the lavas of the Main Volcanic Series of Patmos, Dodecanesos, Greece. These lavas were erupted about 7 m.y. ago and range in composition from ne-trachybasalts through hy-trachybasalts and trachyandesites to Q-trachytes. To some extent, the ne-trachybasalts are intermediate in composition to the alkaline lavas found on oceanic islands and the calc-alkaline lavas of destructive plate margins. Major oxide variation is largely explicable in terms of fractional crystallization involving removal of the observed phenocryst and microphenocryst phases viz. olivine, plagioclase, clinopyroxene and Ti-magnetite in the mafic lavas, plagioclase, clinopyroxene, mica and Ti-magnetite in the evolved lavas. Apatite, which occurs as an inclusion in other phenocrysts or as microphenocrysts must also have been removed. However, mass balance calculations indicate that the chemistry of the hy-trachybasalts is inconsistent with an origin via fractional crystallization alone and the complex zoning patterns and resorbtion phenomena shown by phenocrysts in these lavas show that they are hybrids formed by the mixing of 80-77% ne-trachybasalt with 20–23% trachyandesite. It is estimated that the mixing event preceded eruption by a period of 12 h-2 weeks suggesting that mixing triggered eruption. Combined fractionation and mixing cannot explain the relatively low MgO contents of the hy-trachybasalts and it is concluded that assimilation also occurred. Assimilation, and especially addition of volatiles to the magmas, may be responsible for the evolutionary trend from ne-normative to hy-normative magmas and was probably facilitated by intensified convection resulting from mixing. A model is presented whereby primitive magma undergoes fractionation in an intracrustal magma chamber to yield more evolved liquids. Influx of hot primitive magma into the base of the chamber facilitates assimilation, but eventually mixing yields the hy-trachybasalts and finally the ne-trachybasalts are erupted.

Notes: Abstract The post-caldera Kameni islands of the Santorini volcanic complex, Aegean Sea, Greece are entirely volcanic and were formed by eleven eruptions between 197 B.C. and 1950. Petrographic, mineral chemical and whole-rock major and trace element data are presented for samples of lava collected from the products of seven eruptive cycles which span the entire period of activity. The main phenocryst phases are plagioclase, clinopyroxene, orthopyroxene and titaniferous magnetite, which are weakly zoned (e.g. plagioclase — An55 to An42). The lavas are typical calc-alkaline dacites and show a restricted range of composition (from 64.1 to 68.4 wt. % SiO2). The phenocrysts were in equilibrium with the melts at temperatures of 960–1012 °C, pressures of 800–1500 bars and oxygen fugacities of 10−9.6-10−9.9 bars. The pre-eruptive water content of the magmas was 3–4 wt. % but since the lavas contain only 0.1–0.4 wt. % H2O, a considerable amount (about 0.01–0.015 km3) of water was lost prior to or during eruption. This indicates that the magmas rose to the surface gradually allowing the (largely) non-explosive loss of volatiles. The lavas were probably extruded initially from more or less cylindrical conduits which developed into fissures as the eruptions proceeded. The post-caldera lavas evolved from more mafic parental magmas (basalt-andesite) via fractional crystallization. The small range of compositional variation shown by these lavas can be explained in terms of near-equilibrium crystallization. Analyses of samples of lavas belonging to single eruption cycles and to individual flows indicate that the underlying magma chamber is compositionally zoned. The average composition of erupted magma has remained approximately constant since 1570 A.D. but that fact that the 197 B.C. magma was sligthly richer in SiO2 provides additional evidence that the magma chamber is compositionally zoned. Crystal settling has not affected the composition of the magma over a 2,200 year period of time which indicates that the melts do not behave as Newtonian fluids. Zonation was thus probably established prior to the 197 B.C. eruption though it is possible that it is developed and maintained by crystal-liquid differentiation processes other than crystal settling (e.g. boundary layer crystallization). The data indicate that there has been no significant cooling during 2,200 years; the maximum amount of cooling is 〈50 °C and is probably less than ∼30 °C. Two hypotheses are considered to explain the thermal and chemical buffering of the post-caldera magma chamber: (i) The magma chamber is large and heat losses due to conduction are largely compensated by latent heat supplied by thick, partially crystalline cumulate sequences. (ii) Periodic influx of hot mafic magma, which does not mix with the dacitic magma, inhibits cooling. The second alternative is favored because the post-caldera lavas differ geochemically from the pre-caldera lavas which signifies that a new batch of magma was formed and/or emplaced after the catastrophic eruption of 1390 B.C., and hence that mafic magmas may still be reaching upper crustal levels.

Notes: Abstract Green, salitic pyroxenes occur as megacrysts and as cores in diopsidic pyroxene phenocrysts and microphenocrysts in a wyomingite lava from Hatcher Mesa, Leucite Hills, Wyoming. Al-rich phlogopite (16–21% Al2O3), apatite, Fe-Ti-oxide, Mg-rich olivine (Fo93) and orthopyroxene (En61) also occur as megacrysts or as inclusions in diopside phenocrysts. All of these phases are found in ultramafic xenoliths in the host lava, and petrographic and chemical evidence is presented that the megacrysts originate by the disaggregation of the xenoliths. It is concluded that the latter are accidental fragments of the wall rocks traversed by the wyomingite magma and it is suggested that the clinopyroxene-rich xenoliths, from which the green pyroxenes are derived, formed in the upper mantle as a result of local metasomatism or by crystallization from magmas of unknown composition during an earlier igneous event. The precise role of the clinopyroxene-rich xenoliths (which also contain apatite, Fe-Ti-oxide and amphibole) in the genesis of the Leucite Hills magmas cannot be elucidated on the basis of the available data, but it is unlikely that they represent the source material from which these magmas are derived.

Notes: Abstract Trace-element and preliminary Sr- and O-isotopic data are reported for a transitional alkaline-sub-alkaline lava series (MVS) from Patmos, Greece. The lava types belonging to this series are ne-trachybasalt, hy-trachybasalt, hy-trachyandesite and Q-trachyte. Rb, Sr and Ba contents, as well as K/Rb ratios, of the ne-trachybasalts differ from those of alkali basalts of oceanic islands and those of K-rich alkaline lavas of continental regions and are consistent with the occurrence of these volcanics in a destructive plate margin environment. Qualitatively, the variations shown by many trace elements throughout the MVS are explicable in terms of magma evolution via fractional crystallization involving removal of the observed phenocryst phases. Cross-cutting REE patterns can be explained by removal of small amounts of apatite. However, certain features of the data cannot be reconciled with the operation of fractional crystallization alone. These are: a) the compatible behavior of Ba throughout the MVS; b) the moderately (as opposed to highly) incompatible behavior of Zr, Rb and Nb relative to Th; and c) the significant decrease of K/Th, Rb/Th, Zr/Th, Zr/Nb, Nb/Th, Yb/Th, Ta/Th, U/Th and Zr/Ta ratios especially (but not exclusively) in the mafic part of the series. Quantitative modeling indicates that the hy-trachybasalts are anomalously enriched in both highly incompatible and highly compatible elements and these lavas are shown to be hybrids formed by mixing of ne-trachybasalt and hy-trachyandesite. Mixing proportions of the end members calculated from incompatible element abundances (∼19% ne-trachybasalt) differ from those calculated from compatible element abundances (∼62% ne-trachybasalt) and are inconsistent with proportions calculated from published mineral chemical data. In addition, mixing cannot account for the observed variations in incompatible element ratios and this is taken as evidence for the simultaneous operation of assimilation. Isotopic variations (87Sr/ 86Sr from 0.7049 to 0.7076 and 18O/16O from 4.7 to 8.6‰) and the positive correlation of isotope ratios with SiO2 and Th contents provide conclusive proof that assimilation occurred. Calculations show that the isotopic characteristics and the concentrations of many trace elements in the Q-trachytes can be explained by fractional crystallization of ne-trachybasalt combined with assimilation of average continental crust (87Sr/86Sr-0.710), and that large amounts of assimilation are not necessary (Ma/Mc=0.55). REE data are not well explained by this model and suggest a crustal end-member enriched in LREE relative to the average crust. Zr and Hf data are also not well explained and indicate that the assimilant was depleted in HFSE relative to average crust or that HFSE are held back in relatively insoluble phases such as zircon in the restite during assimilation. Nevertheless, the results of the modeling demonstrate that Ba concentrations may decrease during AFC processes and that high Sr contents (∼1500 ppm in the MVS ne-trachybasalts) do not render mafic, parental magmas immune to the effects of assimilation in terms of their 87Sr/86Sr ratios. The results of this study confirm conclusions based upon major-oxide and mineral chemical data for the MVS lavas but, more importantly, show that careful analysis of trace element data allows the various processes involved in magma evolution to be identified and quantified, even in the absence of major oxide and isotopic data. Finally, it is reiterated that magma mixing and assimilation may be coupled processes in the magma chambers beneath many volcanic centers, and recognition of this fact has profound implications for studies of magmas erupted at continental margins and through continental crust.

Notes: Abstract Pyroxene-Fe−Ti oxide symplectites in a norite from the leuconoritic phase of the Bjerkreim-Sokndal lopolith, SW Norway, have been studied using EMPA (electron microprobe analysis) and TEM (transmission electron microscopy) techniques. Textural and mineralchemical data indicate that the symplectites formed under subsolidus conditions at T=720–736°C and fo 2=10-17 bars. Solidus temperatures are estimated as 981–1060° C. Two models of formation are proposed: non-isochemical replacement of olivine, and growth at boundaries between exsolving grains of orthomagmatic high-Ca pyroxene and Fe−Ti oxide. TEM reveals the presence of low-Ca clinopyroxene and this formed in response to strain and/or shear stress. Comparison with published experimental data indicates that strain rates of up to 10-12 s-1 are necessary to explain the occurrence of low-Ca clinopyroxene. The transition from orthopyroxene to low-Ca clinopyroxene may be related to deformation which accompanied intrusion of the leuconoritic phase of the Bjerkreim-Sokndal lopolith or to local post-intrusive faulting and/or shearing. Selected-area diffraction shows that the Fe−Ti oxide lamellae are oriented with respect to the pyroxene such that (111)oxide/(100)pyroxene. the planes of closest oxygen packing in the constituent phases are thus adjacent to one another which leads to minimal misfit between the structures and to low interfacial strain energy. The same topotactic relationship exists in both lamellar and vermicular parts of symplectites (but is not continuous along the total length of the interface), indicating that the form of the intergrowths is a primary growth feature that to some extent can be explained in terms of growth models for duplex cells. Deformation during growth is probably necessary to account for the lattice distortion observed in the symplectites. Supercooling is necessary for nucleation and growth of the symplectites. A period of cooling under static, fluid-absent conditions allows substantial overstepping of equilibrium reaction boundaries. Nucleation and growth is triggered by local deformation accompanied by influx of fluid or, possibly, melt. Under these conditions growth can be rapid (≈1 year), and low-Ca clinopyroxene forms during or after growth. The proportions of pyroxene and Fe−Ti oxide in symplectites from a variety of rocks fall in a narrow range (70.5:29.5–74.8:25.3) which suggests a common growth mechanism. The interlamellar spacing is related to the amount of supercooling prior to growth, but the effects of fluid on growth rate must be studied before this relationship can be quqntified. Symplectites provide evidence for the development of retrograde mineral assemblages in relatively short time intervals under transitory fluid-present conditions. The models for symplectite formation in the intrusives of southwestern Norway may be applicable to pyroxene-Fe−Ti oxide intergrowths in other slowly cooled basic igneous rocks.

Notes: Abstract The water-undersaturated melting relationships of a mafic, peralkaline, potassic madupite (with about 3% H2O as shown by chemical analysis) from the Leucite Hills, Wyoming, have been studied at pressures up to 30 kb. At low pressures (〈5 kb) leucite is the dominant liquidus phase, but it is replaced at higher pressures by clinopyroxene plus olivine (〈5–7 kb), clinopyroxene (7–12.5 kb), clinopyroxene plus minor spinel (12.5–17.5 kb), and clinopyroxene alone (17.5–〉 30 kb). At all pressures there is a reaction relationship with falling temperature between melt, olivine and probably clinopyroxene to yield phlogopite. Apatite is stable within the melting interval to pressures above 25 kb. Electron microprobe analyses demonstrate that the clinopyroxene is diopsidic, with low aluminium and titanium contents. Pressure has relatively little effect on the composition of the pyroxene. Phlogopite is also aluminium-poor and has only a moderate titanium content. The experimental results indicate that madupite is not the partial melting product of hydrous lherzolite or garnet lherzolite in the upper mantle and it seems improbable that it is derived by melting of mantle peridotite with a mixed H2O-CO2 volatile component. Madupite could, however, be the partial melting product of mica-pyroxenite or mica-olivine-pyroxenite in the upper mantle. It is pointed out that the chemistry of some potassium-rich volcanics may have been affected by volatile transfer and other such processes during eruption and that experimental studies of material affected in this way have little bearing upon the genesis of potassic magmas. Finally, the experimental results enable constraints to be placed upon the P-T conditions of the formation of richterite-bearing mica nodules found in kimberlites and associated rocks. Maximum conditions are 25 kb and 1,100 ° C.

Notes: Abstract Aluminous, silica-deficient metasedimentary xenoliths in siliceous lavas of Mt. Amiata have preserved composite zoning-patterns indicative for complex processes of magma-rock interaction. Petrographic observations and small-scale mineralogical and chemical differences between up to five distinct zones (including the core and envelope of lava) provide evidence that: 1. Partial melt formed in and extracted from the xenoliths was more mafic than the host magma and had a Mg/Fe ratio higher than that of the restite, at least during the peak of thermometamorphism. 2. Liquid-state interdiffusion occurred at the interface between partial melt and the enclosing magma. 3. Certain mineral phases in the restite (notably, hercynitic spinel) became unstable in the presence of a siliceous liquid. Quartz-poor muscovite-biotite schists are considered to be the most likely parent rocks and it is believed that release of volatiles from decomposing micas played a significant role in the high-temperature metamorphic evolution of the xenoliths and their interaction with the magma. The conditions favourable for assimilation were enhanced by injection of mafic magma into the magma chamber. Although this concurrent operation of magma-mixing precludes a quantitative estimate of contamination from the wall-rocks (which was probably of minor importance) the present example indicates that dry acid magma may potentially become more mafic by interaction with partially melted hydrous rocks.

Notes: Abstract A dye process in a textile plant in southern Kentucky (USA) produces large quantities of saline waste-water which eventually enter Lake Cumberland via a municipal sewage treatment plant on Lily Creek. The impact of hypersaline conditions on two fish species native to the Cumberland River drainage system, redbelly dace (Phoxinus erythrogaster) and northern studfish (Fundulus catenatus), was assessed. These species were subjected to salinities of 0, 4, and 10‰ after which routine oxygen consumtpion values were determined. Significant correlations of salinity with oxygen consumption were demonstrated for both species with P. erythrogaster showing greater overall impact of salinity on metabolic rate.

Notes: Abstract The temperature regime of the intertidal microhabitat of two species of co-existing amphibious stichaeoid fishes, Anoplarchus purpurescens and Pholis ornata, were compared with experimentally determined tolerances to elevated temperatures. Studies of the critical thermal maxima of the two species revealed only slight differences in temperature tolerance but exposure to a cycled pattern of high temperatures sharply differentiated the resistance times of the two species with P. ornata capable of tolerating greater cumulative exposure to thermal stress when administered in a cycled program of temperature fluctuations with peak temperature at 27 °C. While the experimentally determined temperature tolerances exceeded those measured in the field, the greater tolerance of P. ornata may facilitate habitation of intertidal mudflats during summer months.