Middle Bronze Age humidity and temperature variations, and societal changes in East-Central Europe

Archaeological evidence points to substantial changes in Bronze Age societies in the European-Mediterranean region. Isotope geochemical proxies have been compiled to provide independent ancillary data to improve the paleoenvironmental history for the period of interest and support the interpretation of the archaeological observations. In addition to published compositions, in this study we gathered new H isotope data from fluid inclusion hosted water from a stalagmite of the Trió Cave, Southern Hungary, and compared the H isotope data with existing stable isotope and trace element compositions reported for the stalagmite. Additionally, animal bones and freshwater bivalve shells (Unio sp.) were collected from Bronze Age archaeological excavations around Lake Balaton and their stable C and O isotope compositions were measured in order to investigate climate changes and lake evolution processes during this period. The data indicate warm and humid conditions with elevated summer precipitation around 3.7 cal ka BP (Before Present, where present is 1950 CE), followed by a short-term deterioration in environmental conditions at about 3.5 cal ka BP. The environment became humid and cold with winter precipitation dominance around 3.5 to 3.4 cal ka BP, then gradually changed to drier conditions at ∼3.2 cal ka BP. Significant cultural changes have been inferred for this period on the basis of observations during archaeological excavations. The most straightforward consequences of environmental variations have been found in changes of settlement structure. The paleoclimatological picture is well in line with other East-Central European climate records, indicating that the climate fluctuations took place on a regional scale

Tracing the Source of Hydrothermal Fluid in Ophiolite-Related Volcanogenic Massive Sulfide Deposits: A Case Study from the Italian Northern Apennines

The Italian Northern Apennines contain several Fe-Cu-Zn-bearing, Cyprus-type volcanogenic massive sulfide (VMS) deposits, which significantly contribute to the Cu resources of Italy. The massive sulfide lenses and related stockwork mineralizations are hosted by several levels (from basalt to serpentinite) of the unmetamorphosed ophiolitic series; therefore, this region offers perfect locations to study the ore-forming hydrothermal system in detail. A combination of fluid inclusion microthermometry, Raman spectroscopy, electron probe analyses (chlorite thermometry) and stable and noble gas isotope geochemistry was used to determine the fluid source of the VMS system at Bargone, Boccassuolo, Campegli, Casali–Monte Loreto, Corchia, Reppia and Vigonzano. This question of the fluid source is the focus of modern VMS research worldwide, as it has a direct influence on the metal content of the deposit. The obtained temperature and compositional data are both in the typical range of VMS systems and basically suggest evolved seawater origin for the mineralizing fluid. Modification of seawater was most commonly due to fluid–rock interaction processes, which happened during long-lasting circulation in the crust. The role of a small amount of magmatic fluid input was traced only at the lower block of Boccassuolo, which may be responsible for its higher ore grade. This fluid origin model is evidenced by O, H and C stable isotopic as well as He, Ne and Ar noble gas isotopic values

Stable (H, O, C) and noble-gas (He and Ar) isotopic compositions from calcite and fluorite in the Speewah Dome, Kimberley Region, Western Australia: implications for the conditions of crystallization and evidence for the influence of crustal-mantle fluid mixing

In this study, the C-O-isotopic data from calcite at Yungul and Wilmott (Speewah. Western-Australia) are integrated with microthermometry, H2O-, CO2-content and H-He-Ar-isotopic data from fluid inclusions in genetically related calcite and fluorite to map the origin and crystallization paths of the fluids. In addition to the hydrogen isotopic compositions of fluid inclusions in fluorite, oxygen isotopic compositions were also determined by cavity ring-down spectroscopy. The geochemical data suggest mixing of a CO2-dominated mantle fluid and a H2O-domintated crustal brine. The fluid produced by this mixing is characterized by radiogenic (crustal-like) He-3/He-4 ratios, crustal-like dD values, relatively high salinity (19-24wt.% NaCl eq.), moderate homogenization temperatures (150-450 degrees C) and mantle-like CO2/He-3 ratios. Moreover, the large isotopic and elemental variations found in calcite indicate that its formation was accompanied by an extensive degassing (open system) leading to a decrease in dD and an increase in the CO2/He-3 values relative to the starting fluid composition. This degassing is consistent with the fluidal- and breccia-like texture of calcite observed in the field. In contrast, the fluorite which has coarse-grained banded to vughy textures formed in a passive aqueous system. Apparently the fluid that formed the fluorite has the same origin as the calcite, but the higher water content and the more radiogenic He-3/He-4 ratios reflect a greater involvement of crustal fluids. The historical description of the calcite-fluorite system in the Speewah area as "carbonatite" is now considered inappropriate because there is no evidence that crystallization is dominated by magmatic processes

Stable (H, O, C) and noble-gas (He and Ar) isotopic compositions from calcite and fluorite in the Speewah Dome, Kimberley Region, Western Australia: implications for the conditions of crystallization and evidence for the influence of crustal-mantle fluid mixing

In this study, the C-O-isotopic data from calcite at Yungul and Wilmott (Speewah. Western-Australia) are integrated with microthermometry, H2O-, CO2-content and H-He-Ar-isotopic data from fluid inclusions in genetically related calcite and fluorite to map the origin and crystallization paths of the fluids. In addition to the hydrogen isotopic compositions of fluid inclusions in fluorite, oxygen isotopic compositions were also determined by cavity ring-down spectroscopy. The geochemical data suggest mixing of a CO2-dominated mantle fluid and a H2O-domintated crustal brine. The fluid produced by this mixing is characterized by radiogenic (crustal-like) He-3/He-4 ratios, crustal-like dD values, relatively high salinity (19-24wt.% NaCl eq.), moderate homogenization temperatures (150-450 degrees C) and mantle-like CO2/He-3 ratios. Moreover, the large isotopic and elemental variations found in calcite indicate that its formation was accompanied by an extensive degassing (open system) leading to a decrease in dD and an increase in the CO2/He-3 values relative to the starting fluid composition. This degassing is consistent with the fluidal- and breccia-like texture of calcite observed in the field. In contrast, the fluorite which has coarse-grained banded to vughy textures formed in a passive aqueous system. Apparently the fluid that formed the fluorite has the same origin as the calcite, but the higher water content and the more radiogenic He-3/He-4 ratios reflect a greater involvement of crustal fluids. The historical description of the calcite-fluorite system in the Speewah area as "carbonatite" is now considered inappropriate because there is no evidence that crystallization is dominated by magmatic processes

Zircon geochronology and geochemistry to constrain the youngest eruption events and magma evolution of the Mid-Miocene ignimbrite flare-up in the Pannonian Basin, eastern central Europe

A silicic ignimbrite flare-up episode occurred in the Pannonian Basin during the Miocene, coeval with the syn-extensional period in the region. It produced important correlation horizons in the regional stratigraphy; however, they lacked precise and accurate geochronology. Here, we used U–Pb (LA-ICP-MS and ID-TIMS) and (U–Th)/He dating of zircons to determine the eruption ages of the youngest stage of this volcanic activity and constrain the longevity of the magma storage in crustal reservoirs. Reliability of the U–Pb data is supported by (U–Th)/He zircon dating and magnetostratigraphic constraints. We distinguish four eruptive phases from 15.9 ± 0.3 to 14.1 ± 0.3 Ma, each of which possibly includes multiple eruptive events. Among these, at least two large volume eruptions (>10 km3) occurred at 14.8 ± 0.3 Ma (Demjén ignimbrite) and 14.1 ± 0.3 Ma (Harsány ignimbrite). The in situ U–Pb zircon dating shows wide age ranges (up to 700 kyr) in most of the crystal-poor pyroclastic units, containing few to no xenocrysts, which implies efficient recycling of antecrysts. We propose that long-lived silicic magma reservoirs, mostly kept as high-crystallinity mushes, have existed in the Pannonian Basin during the 16–14 Ma period. Small but significant differences in zircon, bulk rock and glass shard composition among units suggest the presence of spatially separated reservoirs, sometimes existing contemporaneously. Our results also better constrain the time frame of the main tectonic events that occurred in the Northern Pannonian Basin: We refined the upper temporal boundary (15 Ma) of the youngest counterclockwise block rotation and the beginning of a new deformation phase, which structurally characterized the onset of the youngest volcanic and sedimentary phase