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41.
Picophytoplankton and bacterioplankton in the Mississippi River plume and its adjacent waters 总被引:3,自引:0,他引:3
Hongbin?LiuEmail author Michael?Dagg Lisa?Campbell Juanita?Urban-Rich 《Estuaries and Coasts》2004,27(1):147-156
Picoplankton abundance and distribution in the Mississippi River plume and its adjacent waters were studied during two cruises
in April (high discharge) and October (low discharge) 2000 using flow cytometry. Concentrations of photosynthetic picoplankton,Synechococcus and picoeukaryotes were low in the turbid plume water but high in the coastal waters—i.e., the green waters resulting from
mixing of river and oceanic waters. In this region, three types ofSynechococcus, characterized by their phycoerythrin chromophore composition, were found:Synechococcus cells with a low phycourobilin to phycoerythrobilin ratio (PUB:PEB) occurred throughout the region and dominated the totalSymechococcus abundance during both seasons; high PUB:PEB cells, which are the dominant strains in the open or blue ocean, occurred only
at the outer shelf stations; and PEB-onlySynechococcus were abundant in most of the surveyed area during april, but were not observed during October.Prochlorococcus cyanobacteria only occurred at the oceanic stations, but extended farther inshore in October compared to April. This was
a consequence of the reduced discharge and plume size during October. Picophytoplankton were a less important component of
total phytoplankton biomass in the turbid river water and more important in the oligotrophic Gulf water. Seasonally, the contribution
of picophytoplankton to total phytoplankton biomass in the surveyed area was higher during low discharge in October than during
high discharge in April, even though the spring 2000 river discharge was unusually low and might not present a typical high
discharge scenario. The abundance of heterotrophic bacteria was weakly correlated to chlorophylla (chla) concentration, but better correlated to picophytoplankton biomass. A higher proportion of High DNA bacteria occurred in
the river-impacted regions during both seasons, with the ratio of High DNA bacteria to Low DNA bacteria significantly higher
in April. 相似文献
42.
Pablo?SarricoleaEmail authorView authors OrcID profile Oliver?Meseguer-Ruiz Javier?Martín-Vide Luis?Outeiro 《Theoretical and Applied Climatology》2018,134(1-2):193-204
Atmospheric circulation patterns in southern Chile (42° 30′ S) were studied in order to determine and analyse the most characteristic synoptic types and their recent trends, as well as to gain an understanding of how they are associated with low-frequency variability patterns. According to the Jenkinson and Collison (J&C) classification method, a 16-point grid of sea-level pressure data was employed. The findings reveal that some synoptic types show statistically significant trends with a 95% confidence level, positively for anticyclonic westerly hybrids (AW) and advective types for third and fourth quadrant wind flows (W, NW, and N) and negatively for SW and cyclonic hybrids (CS and CSW). A model has been constructed of the linear regression of some weather types with teleconnections that most affect Chile: the undetermined types (U), AW were associated with El Niño or the warm phase of the Pacific Decadal Oscillation (PDO), whereas the cyclonic northerly and cyclonic northeasterly types (CN and CNE) were associated with La Niña or cool phase of the PDO. The weather types associated with Antarctic Oscillation (AAO) in its positive phase are anticyclonic northerly and northeasterly and northerly advection types, while in its negative phase are cyclonic southwesterly and advection types. 相似文献
43.
Matthieu?E.?GalvezEmail author Olivier?Beyssac Karim?Benzerara Nicolas?Menguy Sylvain?Bernard Simon?C.?Cox 《Contributions to Mineralogy and Petrology》2012,164(5):895-914
Understanding the mobility of chemical elements during fluid–rock interactions is critical to assess the geochemical evolution of a rock undergoing burial and metamorphism and, more generally, to constrain the geochemical budget of the subduction factory. In particular, determining the behavior and mobility of Ti in aqueous fluids constitutes a great challenge that is still under scrutiny. Here, we study plant fossils preserved in blueschist metasedimentary rocks from the Marybank Formation (New Zealand). Using scanning and transmission electron microscopies (SEM and TEM), we show that the carbonaceous material (CM) composing the fossils contains abundant nano-inclusions of Ti- and Fe-oxides. These nanocrystals are mainly anatase, rutile, and Fe–Ti oxides. The mineral composition observed within the fossils is significantly different from that detected in the surrounding rock matrix. We propose that Ti and Fe might have been mobilized by the alteration of a detrital Ti–Fe-rich protolith during an early diagenetic event under acidic and reducing conditions. Aqueous fluids rich in organic ligands released by the degradation of organic matter may have been involved. Moreover, using mass balance and petrological observations, we show that the contrasted mineralogy between the rock matrix and the fossil CM might be the consequence of the chemical isolation of fossil CM during the prograde path of the rock. Such an isolation results from the early formation of quartz and Fe-rich phyllosilicate layers enclosing the fossil as characterized by SEM and TEM investigations. Overall, this study shows that investigating minerals associated with CM down to the nanometer scale in metamorphic rocks can provide a precious record of early prograde geochemical conditions. 相似文献
44.
John?W.?Faithfull Tim?J.?DempsterEmail author John?M.?MacDonald Monica?Reilly EIMF 《Contributions to Mineralogy and Petrology》2018,173(12):99
Zircon megacrysts are locally abundant in 1–40 cm-thick orthopyroxenite veins within peridotite host rocks in the Archaean Lewisian gneiss complex from NW Scotland. The veins formed by metasomatic interaction between the ultramafic host and Si-rich melts are derived from partial melting of the adjacent granulite-facies orthogneisses. The interaction produced abundant orthopyroxene and, within the thicker veins, phlogopite, pargasite and feldspathic bearing assemblages. Two generations of zircon are present with up to 1 cm megacrystic zircon and a later smaller equant population located around the megacryst margins. Patterns of zoning, rare earth element abundance and oxygen isotopic compositions indicate that the megacrysts crystallized from crustal melts, whereas the equant zircon represents new neocryst growth and partial replacement of the megacryst zircon within the ultramafic host. Both zircon types have U–Pb ages of ca. 2464 Ma, broadly contemporaneous with granulite-facies events in the adjacent gneisses. Zircon megacrysts locally form?>?10% of the assemblage and may be associated to zones of localized nucleation or physically concentrated during movement of the siliceous melts. Their unusual size is linked to the suppression of zircon nucleation and increased Zr solubility in the Si-undersaturated melts. The metasomatism between crustal melts and peridotite may represent an analog for processes in the mantle wedge above subducting slabs. As such, the crystallization of abundant zircon in ultramafic host rocks has implications for geochemistry of melts generated in the mantle and the widely reported depletion of high field strength elements in arc magmas. 相似文献
45.
近年来,银额盆地哈日凹陷的油气勘探呈现出良好的态势,但对于哈日凹陷油气成藏条件相关研究甚少,已不能满足目前油气勘探开发的需求。本研究基于钻录井、地球物理、分析化验等资料,系统分析哈日凹陷油气成藏的烃源岩、储层、圈闭等条件,总结油气成藏条件配置关系,以期为哈日凹陷的后续油气勘探及地质研究提供依据。哈日凹陷主要发育三套烃源岩,其中银根组烃源岩有机质丰度极高,成熟度较低,有机质类型为Ⅰ-Ⅱ1型;巴二段烃源岩有机质丰度较高,成熟-高成熟,有机质类型为Ⅱ1-Ⅱ2型;巴一段烃源岩有机质丰度中等,成熟-高成熟,有机质类型为Ⅱ1-Ⅱ2型。储层类型为砂(砾)岩常规储层、碳酸质泥岩非常规储层和火山岩储层,且均属于特低孔超低渗储层,其中砂、砾岩储层和灰质泥岩储层物性最好,白云岩储层和火成岩储层次之,目前主力油藏主要集中在砂、砾岩储层和灰质泥岩储层这两种类型中。哈日凹陷主要发育两套岩性圈闭,即巴一段砂岩岩性圈闭和巴二段泥岩岩性圈闭,形成了源内(准)连续成藏模式和近源不连续成藏模式。 相似文献
46.
Vladica Cvetkovi? Suzana Eri? Ma?a Radivojevi? Kristina ?ari? 《Mineralogy and Petrology》2012,106(3-4):131-150
The study focuses on clinopyroxene from mantle xenolith-bearing East Serbian basanites and suggests that dissolution of mantle orthopyroxene played an important role in at least some stages of the crystallization of these alkaline magmas. Five compositional types of clinopyroxene are distinguished, some of them having different textural forms: megacrysts (Type-A), green/colourless-cored phenocrysts (Type-B), overgrowths and sieve-textured cores (Type-C), rims and matrix clinopyroxene (Type-D), and clinopyroxene from the reaction rims around orthopyroxene xenocrysts (Type-E). Type-A is high-Al diopside that probably crystallized at near-liquidus conditions either directly from the host basanite or from compositionally similar magmas in previous magmatic episodes. Type-B cores show high VIAl/IVAl≥1 and low Mg# of mostly <75 and are interpreted as typical xenocrysts. Type-C, D and E are interpreted as typical cognate clinopyroxene. Type-D has Mg#<78, Al2O3?=?6–13?wt.%, TiO2?=?1.5–4.5?wt.%, and Na2O?=?0.4–0.8?wt.% and compositionally similar clinopyroxene is calculated by MELTS as a phase in equilibrium with the last 30?% of melt starting from the average host lava composition. Type-C has Mg#?=?72–89, Al2O3?=?4.5–9.5?wt.%, TiO2?=?1–2.5?wt.%, Na2O?=?0.35–1?wt.% and Cr2O3?=?0.1–1.5?wt.%. This clinopyroxene has some compositional similarities to Type-E occurring exclusively around mantle orthopyroxene. Cr/Al vs Al/Ti and Cr/Al vs Na/Ti plots revealed that Type-C clinopyroxene can crystallize from a mixture of the host basanite magma and 2–20?wt.% mantle orthopyroxene. Sieve-textured Type-C crystals show characteristics of experimentally produced skeletal clinopyroxene formed by orthopyroxene dissolution suggesting that crystallization of Type-C was both texturally and compositionally controlled by orthopyroxene breakdown. According to FeO/MgOcpx/melt modelling the first clinopyroxene precipitating from the host basanite was Type-A (T?~?1250?°C, p?~?1.5?GPa). Dissolution of orthopyroxene produced decreasing FeO/MgOmelt and crystallization of Type-E and sieve-textured Type-C clinopyroxene (0.3–0.8?GPa and 1200–1050?°C). The melt composition gradually shifted towards higher FeO/MgOmelt ratios precipitating more evolved Type-C and Type-D approaching near-solidus conditions (<0.3?GPa; ~950?°C). 相似文献
47.
Dauphiné twinning and texture memory in polycrystalline quartz. Part 3: texture memory during phase transformation 总被引:1,自引:0,他引:1
Hans-Rudolf?WenkEmail author N.?Barton M.?Bortolotti S.?C.?Vogel M.?Voltolini G.?E.?Lloyd G.?B.?Gonzalez 《Physics and Chemistry of Minerals》2009,36(10):567-583
Samples of quartz-bearing rocks were heated above the α (trigonal)–β (hexagonal) phase transformation of quartz (625–950°C)
to explore changes in preferred orientation patterns. Textures were measured both in situ and ex situ with neutron, synchrotron
X-ray and electron backscatter diffraction. The trigonal–hexagonal phase transformation does not change the orientation of
c- and a-axes, but positive and negative rhombs become equal in the hexagonal β-phase. In naturally deformed quartzites measured by
neutron diffraction a perfect texture memory was observed, i.e. crystals returned to the same trigonal orientation they started
from, with no evidence of twin boundaries. Samples measured by electron back-scattered diffraction on surfaces show considerable
twinning and memory loss after the phase transformation. In experimentally deformed quartz rocks, where twinning was induced
mechanically before heating, the orientation memory is lost. A mechanical model can explain the memory loss but so far it
does not account for the persistence of the memory in quartzites. Stresses imposed by neighboring grains remain a likely cause
of texture memory in this mineral with a very high elastic anisotropy. If stresses are imposed experimentally the internal
stresses are released during the phase transformation and the material returns to its original state prior to deformation.
Similarly, on surfaces there are no tractions and thus texture memory is partially lost. 相似文献
48.
Irina?ZhukovaEmail author Hugh?O’Neill Ian?H.?Campbell 《Contributions to Mineralogy and Petrology》2017,172(7):53
Diffusion of Al in synthetic forsterite was studied at atmospheric pressure from 1100 to 1500 °C in air along [100] with activities of SiO2, MgO and Al2O3 (aSiO2, aMgO and aAl2O3) buffered. At low aSiO2, the buffer was forsterite + spinel + periclase (fo + sp + per) at all temperatures, while at high aSiO2 and subsolidus conditions a variety of three-phase assemblages containing forsterite and two other phases from spinel, cordierite, protoenstatite or sapphirine were used at 1100–1350 °C. Experiments at high aSiO2 and 1400 °C used forsterite + protoenstatite + melt (fo + en + melt), and at 1500 °C, fo + melt. The resulting diffusion profiles were analysed by LA–ICP–MS in scanning mode. Diffusion profiles in the high aSiO2 experiments were generally several hundred microns in length, but diffusion at low aSiO2 was three orders of magnitude slower than in high aSiO2 experiments carried out at the same temperature, producing short profiles only a few microns in length and close to the spatial resolution of the analytical method. Interface concentrations of Al in the forsterite, obtained by extrapolating the diffusion profiles to the crystal/buffer interface, were only a fraction of those expected at equilibrium, and varied among the differing buffer assemblages according to (aAl2O3)1/2 and (aSiO2)3/4, pointing to the substitution of Al in forsterite by an octahedral-site, vacancy-coupled (OSVC) component with the stoichiometry Al 4/3 3+ vac2/3SiO4, whereas the main substitution expected from previous equilibrium studies would be the coupled substitution of 2 Al for Mg + Si, giving the stoichiometry MgAl2O4. It is proposed that this latter substitution is not seen on the length scales of the present experiments because it requires replacement of Si by Al on tetrahedral sites, and is accordingly rate-limited by the slow diffusivity of Si. Instead, diffusion of Al by the OSVC mechanism is relatively fast, and at high aSiO2, even faster than Fe–Mg interdiffusion. 相似文献
49.
In Europe, the Wide Wheel abrasion (WWA) test and the B?hme abrasion (BA) test are among the most widely used standard test
methods for determining abrasion resistance of natural stones, the former being the reference test method in EN 14157 Standard.
However, it is stated in the Annex-A (Informative) of EN 14157 Standard that very limited data are available to provide correlations
between these two test methods. To be able to fill this gap, in this study, 25 different natural stones belonging to sedimentary,
metamorphic and igneous groups were tested for their abrasion resistance as well as physico-mechanical properties. Also, for
a better interpretation of abrasion resistance characteristics of the tested stone materials, relationships between abrasion
resistance and physico-mechanical properties were statistically examined. A statistically significant linear correlation (R
2 = 0.85; P value = 0.000) was established between the WWA test and the BA test, which could be used in practice for converting the measured
abrasion resistance values from one testing method to another. It was also found that the correlation between these two test
methods improved significantly (R
2 = 0.93; P value = 0.001) when relatively high-porosity stone materials (porosity ≥1%) were separately evaluated. Both methods of abrasion
resistance employed in the present study showed statistically significant linear correlations with uniaxial compressive strength
and Brazilian tensile strength, the former proving to be a more influencing parameter on resistance to abrasion. Also, from
the point view of representing actual abrasion mechanism of stone materials in practice, the necessity of simulating multi-directional
foot traffic in abrasion testing methods was discussed. In this respect, the reference test method in the EN 14157 Standard
was criticized for not fully meeting this requirement. It was also pointed out that the reference method could have some drawbacks
when applied to coarse-grained granitic rocks having cleavable minerals such as plagioclase and orthoclase feldspars. 相似文献
50.
该种方法利用离子色谱仪的电导检测器与电化学检测器串联 ,十几分钟即可连续完成水中S2 - 、SO2 - 3 、SO2 - 4、S2 O2 - 3 的测定 ,方法具有快速、高效、方便、灵敏、选择性好等特点。方法的检出限分别为 :S2 - 12 5 μg/L ;SO2 - 3 2 2 4 μg/L ;SO2 - 45 0 μg/L ;S2 O2 - 35 0 μg/L。相对标准偏差在 1 5 %~ 6 9%之间 ,能够满足水中S2 - 、SO2 - 3 、SO2 - 4、S2 O2 - 3四种阴离子分析测试的需要。 相似文献