A genetic model for the Biggenden gold-bearing Fe skarn deposit, Queensland, Australia: geology, mineralogy, isotope geochemistry and fluid inclusion studies

Abstract

<p>The Biggenden gold-bearing Fe skarn deposit in southeast Queensland, Australia, is a calcic magnetite skarn that has been mined for Fe and gold (from the upper portion of the deposit). Skarn has replaced volcanic and sedimentary rocks of the Early Permian Gympie Group, which formed in different tectonic settings, including island arc, back arc, and mid-ocean ridge. This group has experienced a hornblende-hornfels grade of contact metamorphism due to the intrusion of the Late Triassic Degilbo Granite. The intrusion is a mildly oxidized I-type monzogranite that has geochemical characteristics intermediate between those of granitoids typically associated with Fe-Cu-Au and Sn-W-Mo skarn deposits. The skarn mineralogy indicates that there was an evolution from prograde to various retrograde assemblages. Prograde garnet (Adr_11-99Grs_1-78Alm_0-8Sps_0-11), clinopyroxene (Di_30-92Hd_7-65Jo_0-9), magnetite, and scapolite formed initially. Epidote and Cl-bearing amphibole (mainly ferropargasite) were the early retrograde minerals, followed by chlorite, calcite, actinolite, quartz, and sulfides. Late-stage retrograde reactions are indicated by the development of nontronite, calcite, and quartz. Gold is mainly associated with sulfide minerals in the retrograde sulfide stage. The fluids in equilibrium with the ore-stage calcites had δ¹³C and δ¹⁸O values that indicate deposition from magmatically derived fluids. The calculated δ¹⁸O values of the fluids in equilibrium with the skarn magnetite also suggest a magmatic origin. However, the fluids in equilibrium with epidote were a mixture of magmatic and meteoric water, and the fluids that deposited chlorite were at least partly meteoric. δD values for the retrograde amphibole and epidote fall within the common range for magmatic water. Late-stage chlorite was deposited from metasomatic fluids depleted in deuterium (D), implying a meteoric water origin. Sulfur isotopic compositions of the Biggenden sulfides are similar to other skarn deposits worldwide and indicate that sulfur was most probably derived from a magmatic source. Based on the strontium (⁸⁷Sr/⁸⁶Sr) and lead (²⁰⁶Pb/²⁰⁴Pb, ²⁰⁷Pb/²⁰⁴Pb and ²⁰⁸Pb/²⁰⁴Pb) isotope ratios, the volcanic and sedimentary rocks of the Gympie Group may have contributed part of the metals to the hydrothermal fluids. Lead isotope data are also consistent with a close age relationship between the mineralization at Biggenden and the crystallization of the Degilbo Granite. Microthermometric analysis indicates that there is an overall decrease in fluid temperature and salinity from the prograde skarn to retrograde alterations. Fluid inclusions in prograde skarn calcite and garnet yield homogenization temperatures of 500 to 600°C and have salinities up to 45 equivalent wt % NaCl. Fluid inclusions in quartz and calcite from the retrograde sulfide-stage homogenized between 280 and 360°C and have lower salinities (5–15 equivalent wt % NaCl). In a favored genetic model, hydrothermal fluids originated from the Degilbo Granite at depth and migrated through the shear zone, intrusive contact, and permeable Gympie Group rocks and leached extra Fe and Ca and deposited magnetite upon reaction with the adjacent marble and basalt.</p>