Geology, water geochemistry and geothermal potential of the jemez springs area, Canon de San Diego, new Mexico

Studies of the geology, geochemistry of thermal waters, and of one exploratory geothermal well show that two related hot spring systems discharge in Canõn de San Diego at Soda Dam (48°C) and Jemez Springs (72°C). The hot springs discharge from separate strands of the Jemez fault zone which trends northeastward towards the center of Valles Caldera. Exploration drilling to Precambrian basement beneath Jemez Springs encountered a hot aquifer (68°C) at the top of Paleozoic limestone of appropriate temperature and composition to be the local source of the fluids in the surface hot springs at Jemez Springs. Comparisons of the soluble elements Na, Li, Cl, and B, arguments based on isotopic evidence, and chemical geothermometry indicate that the hot spring fluids are derivatives of the deep geothermal fluid within Valles Caldera. No hot aquifer was discovered in or on top of Precambrian basement. It appears that low- to moderate-temperature geothermal reservoirs (< 100°C) of small volume are localized along the Jemez fault zone between Jemez Springs and the margin of Valles Caldera.     

The progressive intensification of northern hemisphere glaciation as seen from the North Pacific

Ocean Drilling Project (ODP) site 882 (50°22′N, 167°36′E) provides the first high-resolution GRAPE density, magnetic susceptibility, carbonate, opal and foraminifera (planktonic and benthic) stable isotopes records between 3.2 and 2.4 Ma in the Northwest Pacific. We observed a dramatic increase in ice rafting debris at site 882 at 2.75 Ma, which is coeval with that found in the Norwegian Sea, suggesting that the Eurasian Arctic and Northeast Asia were significantly glaciated from 2.75 Ma onwards. Prior to 2.75 Ma planktonic foraminifera δ¹⁸O records indicate a warming or freshening trend of 4°C or 2‰ over 80 ka. If this is interpreted as a warm pre-glacial Pliocene North Pacific, it may have provided the additional moisture required to initially build up the northern hemisphere continental ice sheet. The dramatic drop in sea surface temperatures (SST>7.5°C) at 2.75 Ma ended this suggested period of enhanced SST and thus the proposed moisture pump. Moreover, at 2.79 and 2.73 Ma opal mass accumulation rates (MAR) decrease in two steps by five fold and is accompanied by a more gradual long-term decrease in CaCO₃ MARs. Evidence from the Southern Ocean (ODP site 704) indicates that just prior to 2.6 Ma there is a massive increase in opal MARs, the opposite to what is found in the North Pacific. This indicates that the intensification of northern hemisphere glaciation was accompanied by a major reorganisation of global oceanic chemical budget, possibly caused by changes in deep ocean circulation. The initiation of northern hemisphere glaciation occurred in the late Miocene with a significant build up of ice on southern Greenland. However, the progressive intensification did not occur until 3.5–3 Ma when the Greenland ice sheet expanded to include northern Greenland. Following this stage we suggest that the Eurasian Arctic and Northeast Asia glaciated at 2.75 Ma, approximately 100 ka before the glaciation of Alaska (2.65 Ma) and 200 ka before the glaciation of the North East American continent (2.54 Ma).     

Subarctic Pacific evidence for a glacial deepening of the oceanic respired carbon pool

Measurements of benthic foraminiferal cadmium:calcium (Cd/Ca) have indicated that the glacial–interglacial change in deep North Pacific phosphate (PO₄) concentration was minimal, which has been taken by some workers as a sign that the biological pump did not store more carbon in the deep glacial ocean. Here we present sedimentary redox-sensitive trace metal records from Ocean Drilling Program (ODP) Site 882 (NW subarctic Pacific, water depth 3244 m) to make inferences about changes in deep North Pacific oxygenation – and thus respired carbon storage – over the past 150,000 yr. These observations are complemented with biogenic barium and opal measurements as indicators for past organic carbon export to separate the influences of deep-water oxygen concentration and sedimentary organic carbon respiration on the redox state of the sediment. Our results suggest that the deep subarctic Pacific water mass was depleted in oxygen during glacial maxima, though it was not anoxic. We reconcile our results with the existing benthic foraminiferal Cd/Ca by invoking a decrease in the fraction of the deep ocean nutrient inventory that was preformed, rather than remineralized. This change would have corresponded to an increase in the deep Pacific storage of respired carbon, which would have lowered atmospheric carbon dioxide (CO₂) by sequestering CO₂ away from the atmosphere and by increasing ocean alkalinity through a transient dissolution event in the deep sea. The magnitude of change in preformed nutrients suggested by the North Pacific data would have accounted for a majority of the observed decrease in glacial atmospheric pCO₂.