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1.
We examine hypotheses for the formation of light-toned layered deposits in Juventae Chasma using a combination of data from Mars Global Surveyor's Mars Orbiter Camera (MOC), Mars Orbiter Laser Altimeter (MOLA), and Thermal Emission Spectrometer (TES), as well as Mars Odyssey's Thermal Emission Imaging System (THEMIS). We divide Juventae Chasma into geomorphic units of (i) chasm wall rock, (ii) heavily cratered hummocky terrain, (iii) a mobile and largely crater-free sand sheet on the chasm floor, (iv) light-toned layered outcrop (LLO) material, and (v) chaotic terrain. Using surface temperatures derived from THEMIS infrared data and slopes from MOLA, we derive maps of thermal inertia, which are consistent with the geomorphic units that we identify. LLO thermal inertias range from ∼400 to 850 J m−2 K−1 s−1/2. Light-toned layered outcrops are distributed over a remarkably wide elevation range () from the chasm floor to the adjacent plateau surface. Geomorphic features, the absence of small craters, and high thermal inertia show that the LLOs are composed of sedimentary rock that is eroding relatively rapidly in the present epoch. We also present evidence for exhumation of LLO material from the west wall of the chasm, within chaotic and hummocky terrains, and within a small depression in the adjacent plateau. The data imply that at least some of the LLO material was deposited long before the adjacent Hesperian plateau basalts, and that Juventae Chasma underwent, and may still be undergoing, enlargement along its west wall due to wall rock collapse, chaotic terrain evolution, and exposure and removal of LLO material. The new data allow us to reassess possible origins of the LLOs. Gypsum, one of the minerals reported elsewhere as found in Juventae Chasma LLO material, forms only at low temperatures () and thus excludes a volcanic origin. Instead, the data are consistent with either multiple occurrences of lacustrine or airfall deposition over an extended period of time prior to emplacement of Hesperian lava flows on the plateau above the chasm. 相似文献
2.
Simon Catling 《GeoJournal》2004,60(2):149-158
There have been few studies of trainee teachers' conceptions of the term ‘geography’. Building on these, this study identifies
a number of conceptions of geography held by primary school trainee teachers in England. Their ideas are compared with their
understanding of the reasons for teaching geography to young children. Similar outcomes emerge. While a small number of primary
trainee teachers see geography education as concerned with the study of places, a slightly larger group view teaching geography
as developing children's sense of responsibility for the earth and its people. However, by far the largest groups of students
perceive geography's role to be to develop younger children's awareness and knowledge of the environment. Additionally, a
sizeable group of trainees see geography as providing knowledge about the features and countries of the world. The implications
of these findings are considered for the brief geography study units which primary teacher trainees take as part of their
initial teacher training programme in English higher education. The conclusion is that it is important to widen primary trainee
teachers' perspectives during even the briefest of units, not least to enable them to teach the national curriculum requirements
for geography in primary schools.
This revised version was published online in August 2006 with corrections to the Cover Date. 相似文献
3.
The Thermal Emission Spectrometer (TES) on the Mars Global Surveyor spacecraft has detected deposits of coarse-grained, gray crystalline hematite in Sinus Meridiani, Aram Chaos, and Vallis Marineris. We argue that the key to the origin of gray hematite is that it requires crystallization at temperatures in excess of about 100 °C. We discuss thermal crystallization (1) as diagenesis at a depth of a few kilometers of sediments originally formed in low-temperature waters, or (2) as precipitation from hydrothermal solution. In Aram Chaos, a combination of TES data, Mars Orbiter Camera images, and Mars Orbiter Laser Altimeter (MOLA) topography suggests that high concentrations of hematite were formed in planar strata and have since been exposed by erosion of an overlying light-toned, caprock. Lesser concentrations of hematite are found adjacent to these strata at lower elevations, which we interpret as perhaps due to accumulation from physical weathering. The topography and the collapsed nature of the chaotic terrain favor a hydrothermally charged aquifer as the original setting where the hematite formed. Concentration of iron into such an ore-like body would be chemically favored by saline, Cl-rich hydrothermal fluids. An alternative sedimentary origin requires post-depositional burial to a depth of ∼3-5 km to induce thermally driven recrystallization of fine-grained iron oxides to coarse-grained hematite. This depth of burial and re-exposure is difficult to reconcile with commonly inferred martian geological processes. However, shallow burial accompanied by post-burial hydrothermal activity remains plausible. When the hematite regions originally formed, redox balance requires that much hydrogen must have been evolved to complement the extensive oxidation. Finally, we suggest that the coexistence of several factors required to form the gray hematite deposits would have produced a favorable environment for primitive life on early Mars, if it ever existed. These factors include liquid water, abundant electron donors in the form of H2, and abundant electron acceptors in the form of Fe3+. 相似文献
4.
ROBERT O''BRIEN BIMAL K.SINHA WILLIAM P.SMITH Statistical Policy Branch Environmental Protection Agency M St. SW Washington DC U.S.A. 《地理学报(英文版)》1991,(3)
The object of this paper is to develop a suitable statistical procedure to evaluate clean-up standards athazardous waste sites.Under the assumptions that contaminant masses at a site follow a gammadistribution and that the data from the pre-remediation baseline sample as well as from the interim orfinal sample taken after a certain period of operation are both distributed as gamma with the same shapeparameter but different scale parameters,we derive a uniformly most powerful unbiased test of thehypothesis that a specified percentage of contaminant mass has been reduced.A large-sampleapproximation of the exact test procedure and a comparison with the likelihood ratio test are provided. 相似文献
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6.
Many recent studies have implicated hydrothermal systems as the origin of martian minerals across a wide range of martian sites. Particular support for hydrothermal systems include silica (SiO2) deposits, in some cases >90% silica, in the Gusev Crater region, especially in the Columbia Hills and at Home Plate. We have developed a model called CHEMCHAU that can be used up to 100 °C to simulate hot springs associated with hydrothermal systems. The model was partially derived from FREZCHEM, which is a colder temperature model parameterized for broad ranges of temperature (<−70 to 25 °C), pressure (1-1000 bars), and chemical composition. We demonstrate the validity of Pitzer parameters, volumetric parameters, and equilibrium constants in the CHEMCHAU model for the Na-K-Mg-Ca-H-Cl-ClO4-SO4-OH-HCO3-CO3-CO2-O2-CH4-Si-H2O system up to 100 °C and apply the model to hot springs and silica deposits.A theoretical simulation of silica and calcite equilibrium shows how calcite is least soluble with high pH and high temperatures, while silica behaves oppositely. Such influences imply that differences in temperature and pH on Mars could lead to very distinct mineral assemblages. Using measured solution chemistries of Yellowstone hot springs and Icelandic hot springs, we simulate salts formed during the evaporation of two low pH cases (high and low temperatures) and a high temperature, alkaline (high pH) sodic water. Simulation of an acid-sulfate case leads to precipitation of Fe and Al minerals along with silica. Consistency with martian mineral assemblages suggests that hot, acidic sulfate solutions are plausibility progenitors of minerals in the past on Mars. In the alkaline pH (8.45) simulation, formation of silica at high temperatures (355 K) led to precipitation of anhydrous minerals (CaSO4, Na2SO4) that was also the case for the high temperature (353 K) low pH case where anhydrous minerals (NaCl, CaSO4) also precipitated. Thus we predict that secondary minerals associated with massive silica deposits are plausible indicators on Mars of precipitation environments and aqueous chemistry. Theoretical model calculations are in reasonable agreement with independent experimental silica concentrations, which strengthens the validity of the new CHEMCHAU model. 相似文献
7.
Climatic hazards are a key feature of life. It is vital that teachers are knowledgeable about these phenomena in order to develop their students’ understanding of them. This study used a mixed methods approach to examine the accuracy and depth of preservice primary teachers’ (n = 430) knowledge of tropical cyclones. The findings suggest that prospective primary teachers hold alternative conceptions about the causes, spatial distribution, and impacts of these phenomena and that their explanations of processes lack structural complexity and integration. Issues raised by these findings and implications for teachers’ geographical knowledge and their professional standards and preservice teacher education are discussed. 相似文献
8.
NASA’s Phoenix lander identified perchlorate and carbonate salts on Mars. Perchlorates are rare on Earth, and carbonates have largely been ignored on Mars following the discovery by NASA’s Mars Exploration Rovers of acidic precipitated minerals such as jarosite. In light of the Phoenix results, we updated the aqueous thermodynamic model FREZCHEM to include perchlorate chemistry. FREZCHEM models the Na-K-Mg-Ca-Fe(II)-Fe(III)-Al-H-Cl-Br-SO4-NO3-OH-HCO3-CO3-CO2-O2-CH4-Si-H2O system, with 95 solid phases. We added six perchlorate salts: NaClO4·H2O, NaClO4·2H2O, KClO4, Mg(ClO4)2·6H2O, Mg(ClO4)2·8H2O, and Ca(ClO4)2·6H2O. Modeled eutectic temperatures for Na, Mg, and Ca perchlorates ranged from 199 K (−74 °C) to 239 K (−34 °C) in agreement with experimental data.We applied FREZCHEM to the average solution chemistry measured by the Wet Chemistry Laboratory (WCL) experiment at the Phoenix site when soil was added to water. FREZCHEM was used to estimate and alkalinity concentrations that were missing from the WCL data. The amount of is low compared to estimates from elemental abundance made by other studies on Mars. In the charge-balanced solution, the dominant cations were Mg2+ and Na+ and the dominant anions were , and alkalinity. The abundance of calcite measured at the Phoenix site has been used to infer that the soil may have been subject to liquid water in the past, albeit not necessarily locally; so we used FREZCHEM to evaporate (at 280.65 K) and freeze (from 280.65 to 213.15 K) the WCL-measured solution to provide insight into salts that may have been in the soil. Salts that precipitated under both evaporation and freezing were calcite, hydromagnesite, gypsum, KClO4, and Mg(ClO4)2·8H2O. Epsomite (MgSO4·7H2O) and NaClO4·H2O were favored by evaporation at temperatures >0 °C, while meridianite (MgSO4·11H2O), MgCl2·12H2O, and NaClO4·2H2O were favored at subzero temperatures. Incongruent melting of such highly hydrated salts could be responsible for vug formation elsewhere on Mars.All K+ precipitated as insoluble KClO4 during both evaporation and freezing simulations, accounting for 15.8% of the total perchlorates. During evaporation, 35.8% of perchlorates precipitated with Na+ and 48.4% with Mg2+. During freezing, 58.4% precipitated with Na+ and 24.8% with Mg2+. Given its low eutectic temperature, the existence of Mg(ClO4)2 in either case allows for the possibility of liquid brines on Mars today. FREZCHEM also showed that Ca(ClO4)2 would likely not have precipitated at the Phoenix landing site due to the strong competing sinks for Ca as calcite and gypsum. Overall, these results help constrain the salt mineralogy of the soil. Differences between evaporites and cryogenites suggest ways to discriminate between evaporation and freezing during salt formation. Future efforts, such as sample return or in situ X-ray diffraction, may make such a determination possible. 相似文献
9.
Within Gusev Crater and Meridiani Planum on Mars, the Mars exploration rovers have found Br concentrations in soils and rocks in the hundreds of ppm range. Relative to Earth compositions, these are high Br concentrations. Because of low Br concentrations on Earth, Br largely precipitates from seawater as a minor constituent in halite crystals rather than as a separate phase mineral. This is also likely to be the case for Mars. But given that the surface chemistries on Mars are significantly different than on Earth, minerals other than halite could serve as sinks for Br. The specific objectives of this paper were to (1) incorporate Br solution phase chemistries into the FREZCHEM model, (2) integrate the Siemann–Schramm Br/Cl mineral model into FREZCHEM, and (3) apply this mineral model to Br/Cl partitioning in Burns formation rocks as an indicator of past environments in the Meridiani Planum region of Mars. We showed that: (1) a molar-based model for Br substitution into halite and bischofite provided a better fit to experimental data than the standard mass-based model; (2) the concentrations of all of the soluble salts (mainly of Na, Mg, Ca, Cl, Br, and SO4) in the Burns formation, except for Ca, were significantly related to stratigraphic depth; (3) the likely precipitation of Ca as gypsum on Mars precluded Ca precipitating as a CaCl2 salt and thus impacts the possible minimum eutectic brine temperatures relevant to the Burns formation; (4) bischofite (MgCl2⋅6H2O) was a much more important sink for Br than halite; (5) Br/Cl patterns in the Burns formation, and within the three formation layers, argued in support of salt upwelling through groundwater evaporation; and (6) the high concentrations of Br in the surface layers of the Burns formation suggested that there was little water leaching and removal of soluble phases from the upper part of the stratigraphic succession. 相似文献
10.
Major uncertainties exist with respect to the aqueous geochemical evolution of the Martian surface. Considering the prevailing cryogenic climates and the abundance of salts and iron minerals on Mars, any attempt at comprehensive modeling of Martian aqueous chemistry should include iron chemistry and be valid at low temperatures and high solution concentrations. The objectives of this paper were to (1) estimate ferrous iron Pitzer-equation parameters and iron mineral solubility products at low temperatures (from < 0 °C to 25 °C), (2) incorporate these parameters and solubility products into the FREZCHEM model, and (3) use the model to simulate the surficial aqueous geochemical evolution of Mars.Ferrous iron Pitzer-equation parameters were derived in this work or taken from the literature. Six new iron minerals [FeCl2·4H2O, FeCl2·6H2O, FeSO4·H2O, FeSO4·7H2O, FeCO3, and Fe(OH)3] were added to the FREZCHEM model bringing the total solid phases to 56. Agreement between model predictions and experimental data are fair to excellent for the ferrous systems: Fe-Cl, Fe-SO4, Fe-HCO3, H-Fe-Cl, and H-Fe-SO4.We quantified a conceptual model for the aqueous geochemical evolution of the Martian surface. The five stages of the conceptual model are: (1) carbonic acid weathering of primary ferromagnesian minerals to form an initial magnesium-iron-bicarbonate-rich solution; (2) evaporation and precipitation of carbonates, including siderite (FeCO3), with evolution of the brine to a concentrated NaCl solution; (3) ferrous/ferric iron oxidation; (4) either evaporation or freezing of the brine to dryness; and (5) surface acidification.What began as a dilute Mg-Fe-HCO3 dominated leachate representing ferromagnesian weathering evolved into an Earth-like seawater composition dominated by NaCl, and finally into a hypersaline Mg-Na-SO4-Cl brine. Weathering appears to have taken place initially under conditions that allowed solution of ferrous iron [low O2(g)], but later caused oxidation of iron [high O2(g)]. Surface acidification and/or sediment burial can account for the minor amounts of Martian surface carbonates. This model rests on a large number of assumptions and is therefore speculative. Nevertheless, the model is consistent with current understanding concerning surficial salts and minerals based on Martian meteorites, Mars lander data, and remotely-sensed spectral analyses. 相似文献