Evolutionary status of the pre-protostellar core L1498

L1498 is a classic example of a dense cold pre-protostellar core. To study the evolutionary status, the structure, dynamics, and chemical properties of this core we have obtained high spatial and high spectral resolution observations of molecules tracing densities of 10(3)-10(5) cm-3. We observed CCS, NH3, C3H2, and HC7N with NASA's DSN 70 m antennas. We also present large-scale maps of C18O and 13CO observed with the AT&T 7 m antenna. For the high spatial resolution maps of selected regions within the core we used the VLA for CCS at 22 GHz, and the Owens Valley Radio Observatory (OVRO) MMA for CCS at 94 GHz and CS (2-1). The 22 GHz CCS emission marks a high-density [n(H2) > 10(4) cm -3] core, which is elongated with a major axis along the SE-NW direction. NH3 and C3H2 emissions are located inside the boundary of the CCS emission. C18O emission traces a lower density gas extending beyond the CCS boundary. Along the major axis of the dense core, CCS, NH3 and C3H2 emission show evidence of limb brightening. The observations are consistent with a chemically differentiated onion-shell structure for the L1498 core, with NH3 in the inner and CCS in the outer parts of the core. The high angular resolution (9"-12") spectral line maps obtained by combining NASA Goldstone 70 m and VLA data resolve the CCS 22 GHz emission in the southeast and northwest boundaries into arclike enhancements, supporting the picture that CCS emission originates in a shell outside the NH3 emitting region. Interferometric maps of CCS at 94 GHz and CS at 98 GHz show that their emitting regions contain several small-scale dense condensations. We suggest that the differences between the CCS, CS, C3H2, and NH3 emission are caused by a time-dependent effect as the core evolves slowly. We interpret the chemical and physical properties of L1498 in terms of a quasi-static (or slowly contracting) dense core in which the outer envelope is still growing. The growth rate of the core is determined by the density increase in the CCS shell resulting from the accretion of the outer low-density gas traced by C18O. We conclude that L1498 could become unstable to rapid collapse to form a protostar in less than 5 x 10(6) yr.     

Detection of a new interstellar molecular ion, H2COH+ (protonated formaldehyde)

A new interstellar molecular ion, H2COH+ (protonated formaldehyde), has been detected toward Sgr B2, Orion KL, W51, and possibly in NGC 7538 and DR21(OH). Six transitions were detected in Sgr B2(M). The 1(1,0)-1(0,1) transition was detected in all sources listed above. Searches were also made toward the cold, dark clouds TMC-1 and L134N, Orion (3N, 1E), and a red giant, IRC + 10216, without success. The excitation temperatures of H2COH+ are calculated to be 60-110 K, and the column densities are on the order of 10(12)-10(14) cm-2 in Sgr B2, Orion KL, and W51. The fractional abundance of H2COH+ is on the order of 10(-11) to 10-(9), and the ratio of H2COH+ to H2CO is in the range 0.001-0.5 in these objects. The values in Orion KL seem to be consistent with the "early time" values of recent model calculations by Lee, Bettens, & Herbst, but they appear to be higher than the model values in Sgr B2 and W51 even if we take the large uncertainties of column densities of H2CO into account. We suggest production routes starting from CH3OH may play an important role in the formation of H2COH+.     

Octahedral-site Fe2+ quadrupole splitting distributions from Mössbauer spectroscopy along the (OH, F)-annite join

We have performed a detailed Mössbauer study of synthetic annites on the (OH, F)-join. Recently developed data treatment and spectral analysis methods were used to extract true intrinsic Fe²⁺ quadrupole splitting distributions (QSDs) that represent the most information that can be resolved from the spectra. The overall room temperature (RT) QSDs can be consistently interpreted in terms of four QSD contributions (or populations) centered at: QS_HH2.55 mm/s for Fe²⁺O₄(OH)₂ octahedra (cis and trans not resolved), QS_HF 2.35 mm/s for Fe²⁺O₄(OH)F octahedra (cis and trans not resolved), QS_cFF2.15 mm/s for cis-Fe²⁺O₄F₂ octahedra, and QS_tFF 1.5 mm/s for trans-Fe²⁺O₄F₂ octahedra. Each such contribution has a width ( 0.2 mm/s) caused by distortions of the octahedra. Minor contributions due to Fe²⁺O₅(OH) and Fe²⁺O₅F octahedra probably also contribute to the overall Fe²⁺ QSDs. The ferric iron spectral components were also characterized. Here, two distinct types of octahedral Fe³⁺ contributions are seen and interpreted as being due mainly to Fe³⁺O₅OH and Fe³⁺O₅F octahedra, respectively. Tetrahedral Fe³⁺ is seen only in the OH-annite end-member and the total Fe³⁺ content drops significantly on addition of F. On leave from: Department of Materials Physics, University of Science and Technology Beijing, 100083 Beijing, China     

Chernobyl radiocaesium in a karst system,Marble Cave,Crimea

 Surface contamination with radioactive caesium introduced into the environment after the accident at the Chernobyl nuclear plant was high enough in the Crimean Mountains to allow using radiocaesium as an indicator of penetration of radioactive contamination into a karst system. Caesium concentrations have been studied in soils above Marble Cave, Tchatyrdag Plateau, in percolation waters and in sediments transported by percolation waters within the cave. Contamination of the daylight surface with ¹³⁷Cs is about 30 kqB m^–2 which is approximately 13 times higher than the density of global fallouts. Besides ¹³⁷Cs, almost all samples showed presence of ¹³⁴Cs with the ¹³⁷Cs/¹³⁴Cs ratio close to that of Chernobyl contaminations. Concentrations of ¹³⁷Cs range from 9 to 15 mBq l^–1 in the present percolation waters in the cave. In sediments related to percolation waters ¹³⁴Cs is detected in some samples besides ¹³⁷Cs, although the effect of ²²⁸Ac is not ruled out. Surprisingly, the highest concentrations of radiocaesium were measured in "old" sediments in the cave's lower series. These sediments are not associated with modern percolation and are represented by a clay/moonmilk alternating sequence deposited in an old dried cave lake. Moonmilk layers have higher caesium content than clay. It is assumed that Chernobyl caesium was transported into the cave with aerosols which were then deposited mainly in areas where condensation occurs. The sampling site is located just in the boundary between two microclimatic zones with a temperature gradient of 0.5  °C. Active condensation processes occur in this area. Caesium was not detected in another similar sampling site (old lake deposits) located within homogeneous microclimatic conditions. If the above interpretation is correct, these results show the geochemical significance of the aerosol-condensation mechanism of mass transport and localisation. Received: 1 June 1995 · Accepted: 4 December 1995     

Springs of Great Britain

Predictably, in a country such as Britain, with its preponderance of consolidated, sedimentary, mainly fissure-flow aquifers, there is a very large number of springs, many of which are, or have been, used for public supply. Migratory springs are a feature of the British (Ur. Cretaceous) Chalk, the most important British aquifer. The Chalk's low specific yield and high capillary moisture retention together give rise to very considerable fluctuations (more than 33 m in some areas) of the unconfined water table. Along the gentle dip slopes of the Chalk (North and South Downs of southern and southeastern England) springs may migrate laterally for several miles, giving rise to seasonal streams locally known as bournes or lavants. However, springs such as at Duncton, West Sussex, at the base of the much steeper scarp slopes of the Chalk, form point sources, the flows from which tend to be relatively steady; such springs commonly supply and are the original reason for the existence of many of the small towns and villages which nestle along the bases of the chalk scarps of Sussex and Kent.Where the Chalk forms coastal cliffs, a number of springs break out at the base of the cliff between high and low tide levels; there are major chalk coastal springs, for instance, at St. Margaret's Bay (Kent) and at Arish Mells, east of Lulworth Cove, Dorset. Such springs are not used for direct supply (their salinity is usually too high) but are indicators of the presence of local reserves of groundwater for possible future development.     

Integrated chronostratigraphy of Proterozoic-Cambrian boundary beds in the western Anabar region, northern Siberia

Carbonate-rich sedimentary rocks of the western Anabar region, northern Siberia, preserve an exceptional record of evolutionary and biogeochemical events near the Proterozoic/Cambrian boundary. Sedimentologically, the boundary succession can be divided into three sequences representing successive episodes of late transgressive to early highstand deposition; four parasequences are recognized in the sequence corresponding lithostratigraphically to the Manykal Formation. Small shelly fossils are abundant and include many taxa that also occur in standard sections of southeastern Siberia. Despite this coincidence of faunal elements, biostratigraphic correlations between the two regions have been controversial because numerous species that first appear at or immediately above the basal Tommotian boundary in southeastern sections have first appearances scattered through more than thirty metres of section in the western Anabar. Carbon- and Sr-isotopic data on petrographically and geochemically screened samples collected at one- to two-metre intervals in a section along the Kotuikan River, favour correlation of the Staraya Reckha Formation and most of the overlying Manykai Formation with sub-Tommotian carbonates in southeastern Siberia. In contrast, isotopic data suggest that the uppermost Manykai Formation and the basal 26 m of the unconformably overlying Medvezhya Formation may have no equivalent in the southeast; they appear to provide a sedimentary and palaeontological record of an evolutionarily significant time interval represented in southeastern Siberia only by the sub-Tommotian unconformity. Correlations with radiometrically dated horizons in the Olenek and Kharaulakh regions of northern Siberia suggest that this interval lasted approximately three to six million years, during which essentially all 'basal Tommotian' small shelly fossils evolved.     

Derivation of A-type Granites from a Dehydrated Charnockitic Lower Crust: Evidence from the Chaelundi Complex, Eastern Australia

Triassic I- and A-type granites of the Chaelundi Complex, NewEngland Fold Belt, eastern Australia, were generated in a subduction-relatedtectonic setting. Although isotopic ages of the suites are indistinguishable,field relations indicate that the A-type is younger. The mostmafic granitoids from each suite have similar silica contents(66–68% SiO₂), slightly LREE enriched patterns withoutEu anomalies, low Rb/Sr and K/Ba ratios, and high K/Rb ratios,suggesting that both represent parental magmas. The A-type isdistinguished mineralogically by abundant orthoclase and sodicplagioclase (total >60%), ferro-hornblende, annite and allanite.In contrast, the I-type has more hornblende and biotite, whichare more magnesian in composition, and less feldspar. The parentalmagmas of both suites have many similar geochemical characteristics,although the A-type has slightly higher alkalis, Zr, Hf, Znand LREE, and lower CaO, MgO, Sr, V, Cr, Ni and Fe³⁺/Fe. Thegeochemical properties characteristic of leucocratic A-typegranites, such as high Ga/Al, Nb, , HREE and F contents, areonly manifest in the more felsic members of the A-type suite.These features were produced by 70% fractional crystallizationof feldspar, hornblende, quartz and biotite. Both granite suites were generated by water-undersaturated partialmelting of a similar source, but the A-type parent magma resultedfrom lower aH₂O conditions during partial melting. Generationand rapid ascent of the earlier 1-type magma during disequilibriumpartial melting produced a relatively anhydrous, but not refractory,charnockitic lower crust. Continued thermal input from mantle-derivedmagmas, during continuing subduction, partially melted the ‘charnockitized’lower crust at temperatures in excess of 900C, to produce A-typemagmas. Charnockitic magmas (C-type) form in a similar way toA-type magmas, although their different composition reflectsvariations in the anhydrous lower-crustal mineral assemblagesthat remain after the previous (1-type) granite-forming event. The New England Fold Belt was a subduction—accretion complexuntil the late Carboniferous, when the deeper parts underwentpartial melting to produce S-type granites. As the I-and A-typegranites intruded penecontemporaneously, a tonalitic sourcemodel for genesis of the Chaelundi A-type is untenable. KEY WORDS: A-type; charnockitization; eastern Australia ^*Corresponding author.     

Objective measures of the information density of satellite data

Summary We propose and objective method whereby the density of Shannon's information associated with the retrieval of a profile of atmospheric variables from satellite-derived infrared radiance measurements may be estimated. The technique is a natural extension of one we previously proposed to estimate the effective data density in a profile. We test the method in a comparison of simulated satellite instruments to show that the method does indeed provide an objective summary of the spatial distribution of each instrument's information content. We propose that further extensions of the method be developed to include other more traditional data sources in a fully three-dimensional scheme. We also note that analogous and compatible methods may be used to diagnose the information content of meteorological analysis and forecast fields relative to the information contained in the covariance, at the appropriate season, of the corresponding climate fields.With 8 Figures     

Non-ideal Mg-Fe binary mixing in cordierite: Constraints from experimental data on Mg-Fe partitioning in garnet and cordierite and a reformulation of garnet-cordierite geothermometer

The non-ideal regular Mg-Fe binary in cordierite has been derived through multivariate linear regression of the expressionRT InK_D +(P- 1)ΔVK ₁ ⁰ , 298 along with updated subfegular mixing parameter of almandine-pyrope solution (Hackler and Wood 1989; Berman 1990). The data base used for multivariate analyses consists of published experimental data (n = 177) on Mg-Fe partitioning between garnet and cordierite in theP-T range 650–1050°C and 4–12 K bar. The non-ideality can be approximated by temperature-dependent Margules parameters. The retrieved values of ΔH_<T> ^o and ΔH_<T> ^o of exchange reaction between garnet and cordierite and enthalpy and entropy of mixing of Mg-Fe cordierite were combined with recent quaternary (Fe-Mg-Ca-Mn) mixing data in garnet to obtain the geothermometric expressions to determine temperature (T Kelvin): $$\begin{gathered} T(WH) = 6832 + 0.031(P - 1) - \{ 166(X_{Mg}^{Gt} )^2 - 506(X_{Fe}^{Gt} )^2 + 680X_{Fe}^{Gt} X_{Mg}^{Gt} + 336(X_{Ca} + X_{Mn} ) \hfill \\ (X_{Mg} - X_{Fe} )^{Gt} - 3300X_{Ca}^{Gt} - 358X_{Mn}^{Gt} \} + 954(X_{Fe} - X_{Mg} )^{Crd} /1.987\ln K_D + 3.41 + 1.5X_{Ca}^{Gt} \hfill \\ + 1.23(X_{Fe} - X_{Mg} )^{Crd} \hfill \\ \end{gathered} $$ $$\begin{gathered} T(Br) = 6920 + 0.031(p - 1) - \{ 18(X_{Mg}^{Gt} )^2 - 296(X_{Fe}^{Gt} )^2 + 556X_{Fe}^{Gt} X_{Mg}^{Gt} - 6339X_{Ca}^{Gt} X_{Mg}^{Gt} \hfill \\ - 99(X_{Ca}^{Gt} )^2 + 4687X_{Ca}^{Gt} (X_{Mg} - X_{Fe}^{Gt} ) - 4269X_{Ca}^{Gt} X_{Fe}^{Gt} - 358X_{Mn}^{Gt} \} + 640(X_{Fe} - X_{Mg} )^{Crd} \hfill \\ + 1.90X_{Ca}^{Gt} (X_{Mg} - X_{Ca} )^{Gt} . \hfill \\ \end{gathered} $$      

Trace metals in suspended particulate matter and in sediment trap material from a permanently anoxic fjord — Framvaren, South Norway

Geochemical studies of the trace metal concentrations in suspended particulate matter (SPM) and sediment trap material from a permanently anoxic fjord, Framvaren, South Norway in 1989 and 1993 indicate that extremely high concentrations of zinc (max = 183920 mg/kg), copper (max = 4130 mg/kg), lead (max = 2752 mg/kg), and cadmium (max= 8.1 mg/kg) sometimes (1993) occur in the SPM collected in the anoxic water layer. The highest concentrations of Zn occur just below the redoxcline at 22 m water depth (in 1993), and copper, lead and cadmium have maximum concentrations between 30 and 80 m depth, where the amount of total SPM is at a minimum (about 0.3 mg/L). On a mass per volume (g/L) basis, the maximum concentrations of Cd, Cu and Fe occur at the interface (21m) and those of Zn occur just below the redoxcline (22 m depth). The SPM and sediment trap data suggest that the metals are precipitated as sulfide minerals in the anoxic water. The presence of particulate sulfides was confirmed by SEM studies that show the occurrence of discrete metal (Cu, Fe, Pb, and Zn) sulfide particles in size from 10–20 m as well as framboidal pyrites (1–5 m in size). Higher levels of metal sulfides at intermediate depths rather than in the deep water of Framvaren (> 100 m), may be due to input of trace metals by water exchange over the sill in the upper part of the water column. In the deep water, less metal sulfide precipitation takes place due to depletion of trace metals, and the dilution of particulate metal concentrations by organic matter and by the chemogenic formation of calcite.