2200万年来风尘沉积的粒度变化及古气候意义

Three eolian deposit formations, including Quaternary loess (QL, Liu et al.3 1985), Hipparion red earth (HRE, also called red clay, Liu et al., 1985) and Miocene loess (ML, Guo et al., 2002) constitute a set of unique paleoclimatic archives in northern China dated back to at least 22Ma ago. The Miocene loess is a recently discovered loess-soil sequence. Detailed investigation has been made on its origin, chronology and paleoclimatic significance (Guo et al., 2002), but further work is still needed to obtain detailed paleoclimate information, and mechanical links behind paleoclimatic changes. In this study, grain size analysis of QL, HRE and ML has been conducted on two sections: Qinan and Xifeng. The objective is focused on comparison of the grain size distribution characteristics (GSDC) among different eolian deposit formations, and reconstruction of the Asian monsoon circulation in the past 22 Ma. Results show that GDSC of ML resembles that of QL and HRE, and GDSC of ML is especially similar to HRE. Both ML and HRE contain a significant proportion of fine fraction, however, QL has a large amount of coarse sediments. This is mainly due to that the wind system transported aeolian dust was weaker in the late Tertiary than that in the Quaternary. Grain size difference between loess and paleosol in ML is much smaller than that in QL, indicating that the climatic fluctuations during the late Tertiary were much smaller than that happened in the Quaternary The grain size records of the past 22 Ma reveal several evolution phases of the Asia winter monsoon. -2.7 Ma BP is the most important boundary in the process of the winter monsoon evolution: the wind strength have significantly enhanced since 2.7 Ma ago. During a period between -22.0 and -3.6 Ma, three periods with relatively stronger winter monsoon are recorded in the QA-I section, between 21.2 and 19.9, and 16.0 and 13.3, and 8.7 to 6.9 Ma, respectively. From 3.6 to 2.7, the winter monsoon was enhanced gradually. In the Miocene time, the intensified winter monsoon phases (between 21.2 and 19.9, and 16.0 and 13.3, and 8.7 and 6.9 Ma) seemed to have a close relationship with the uplift of the Tibetan Plateau and/or the ongoing global cooling, but the forcing mechanism behind the Asia winter monsoon evolution need to be further investigated. During the Pliocene-Pleistocene time, the Asia winter monsoon strengthened at 3.6 and 2.7Ma ago are in good agreement with the ongoing global cooling and the Arctic ice sheet development. In the mean time, much evidence suggests that an intense uplift of the Tibetan Plateau occurred at ~3.6 Ma, which is synchronous with a major increase in Asia winter monsoon. Therefore, two major factors may be invoked to explain the winter monsoon enhancement: Arctic ice sheet development and Tibetan uplift. We propose that changes in location and intensity of the Siberian-Mongolian high that were caused by the Tibetan uplift and Arctic ice sheet development might be an important factor for Asian winter monsoon evolution in the Pliocene-Pleistocene.

7.0Ma以来中国黄土粉尘源区的化学风化历史研究-Sr同位素比值的证据

To investigate the changes in the chemical weathering intensity of dust source region in Asia continent, ~(87)Sr/~(86)Sr ratios of acid-washed residues from the loess deposits in China and Tajikistan were analyzed, respectively. The results and conclusions are listed as below. 1. The oscillation of ~(87)Sr/~(86)Sr ratios of acid-insoluble residues in the Chinese Loess Plateau was mainly attributed to the chemical weathering intensity of the source region and the grain size. Counteracted the effect of particle size, the calibrated 87Sr/S6Sr ratio can be used as a proxy for the chemical weathering intensity of the source region. 2. The Sr/ Sr ratios of red clay-loess sequence from the Loess Plateau indicate that the chemical weathering intensity of the dust source region between 7.0 and 2.6 Ma is stronger than that in the Quaternary period. This also suggests a general decline in chemical weathering intensity of the source region from 2.6 Ma to the present. Such pattern is more remarkable since 1.0 Ma BP. 3. The ~(87)Sr/~(86)Sr ratios of the Tajik loess during 0.8-1.8 Ma is much more higher than those from 0.8 Ma to the present. This implies that the chemical weathering intensity of the source region in Central Asia is much stronger during 0.8-1.8 Ma than the period since 0.8 Ma. 4. The record of Sr isotope ratios from both sections shows an accelerating course of aridity of the Asian dust source region over the Quaternary period.

中新世以来中国北方风尘堆积的粘土矿物组成及其古环境意义

In northern China, the loess-soil sequence of the last 2.6 Ma, the Hipparion Red-Earth of eolian origin and recently reported Pliocene-Miocene loess-soil sequence provide a near continuous continental eolian record of climatic history for the past 22.0 Ma. This work aims to investigate the composition and structure of clay minerals contained in deposits, and to explore their implications for environmental evolutions over the last 22.0 Ma. Clay minerals, which were extracted from eolian samples collected at Xifeng (0-6.2 MaBP) and Qinan (6.2-22.0 MaBP) sections, were analyzed qualitatively and semi-quantitatively by using X-ray diffraction (XRD), differential thermal analysis (DTA), thermogravimetric analysis (TG) and chemical analysis. The main conclusions are as follows: Over the last 22.0 Ma, the clay mineral assemblage among Quaternary loess-soils, Hipparion Red-Earth, and Miocene loess-soils shows similar components, mainly consisting of illite (55-80%), kaolinite (7-20%), chlorite (4-13%), smectite (2-23%) as results calculated by comparing major peak areas. There are no obvious differences in both types and amounts of clay minerals between loess and interbedded soils, suggesting that overwhelming part of the clay minerals is derived from the source. According to the components of clay minerals, the whole sequence of eolian deposits in the Loess Plateau can be divided into ten clay mineral assemblage zones over the last 22.0 Ma, whose corresponding ages are: 22.0-21.0 MaBP, 21.0-18.0 MaBP, 18-16.2 MaBP, 16.2-13.0 MaBP, 13.0-10.0 MaBP, 10.0-5.5 MaBP, 5.5-4.4 MaBP, 4.4-2.8 MaBP, 2.8-1.0 MaBP, 1.0-0 MaBP, respectively. This may imply that dust supply changed at least nine times over the past 22.0 Ma. The loess illite has a better crystaliinity, higher value of the FWHM and IC, than the interbedd soils. Previous studies indicated that irregular mixed layer minerals could form under relatively warm and humid conditions (Han, 1982). According to the general distribution of clay minerals of zonal soil (Chamley, 1989), the clay mineral assemblage of eolian deposits in Xifeng and Qinan sections is typical of temperature-humid and warm-subarid environment. Therefore, our results indicate climatic environment in Loess Plateau did not change remarkably since 22.0 Ma, and fluctuated between temperature-humid and warm-subarid climate. 4. The illite generally presents poorer crystaliinity during the period of 22.0 to 2.8 MaBP than in the last 2.8 Ma BP, especially at the intervals of 3.5-4.5 Ma BP, 14.0-17.0 MaBP and 20.0-22.0 Ma BP, which indicates that the weathering intensity was stronger in Neogene than in Quaternary. 5. The relatively low ice volume and high global temperature may be responsible for the strange weathering intensity during the interval of the 3.5-4.5 Ma BP, 14.0-17.0 Ma BP and 20.0-22.0 Ma BP.

西部黄土高原中新世风尘沉积剖面的磁性地层学和沉积学研究

Observation of the Miocene aeolian dust deposits in Qin'an area provide a long-timescale, almost continuous geological record for understanding significant environmental changes, such as the environmental evolution of Asian monsoons and the inland Asian aridification, and make possible new explorations of global and regional environmental evolutions and other relevant studies. However, the QA-I and QA-II sections that are previously investigated are near to each other, and there is a lack in understanding the spatial characteristics of changes in paleoenvironment. Therefore, new sections of Miocene aeolian dust deposits are needed to complete the present spatial framework. Meanwhile, it is necessary to carry out in-depth studies, which are already belated, on the depositional characteristics of these Miocene aeolian dust deposits.This thesis choose the Miziwan section and Shaogou section that are west to Liupan Mountain for magnetostratigraphic studies, results of which are compared with the QA-I section with respect to the lithology, magnetic susceptibility and paleomagnetic polarity stratigraphy. Quartz-fraction grain size of 300 samples from the QA-I section was analyzed. In addition, 30 out of these samples were determined in terms of the quartz morphological characteristics by using scanning electronic microscopy. On the basis of these data and the correlation with the Xifeng sequence of aeolian dust deposits, the following 3 conclusions are drawn as below:The upper and the lower boundary age of the Miziwan section are 11.6 Ma B.Rand 18.5 Ma B.R, respectively. The Shaogou section spans from 15.1 Ma B.P, to20.8 Ma B.R The lower boundary age of both sections is no older than that of theQA-I section. The Miziwan and the Shaogou sections can be well correlated withthe QA-I section in terms of the field lithological features, magnetic susceptibilityand magnetic polarity stratigraphy.Sedimentological evidence of the QA-I quartz grain size and quartz morphologicalcharacteristics further supports the previous conclusion that the QA-Iloess-paleosol sequence is of aeolian origin, and also verifies the accretionalfeatures in paleosols of this sequence in terms of the grain-size composition.Modifications of the grain-size composition of the original dusts due to later-stageweathering and pedogenesis are common characteristic of Miocene and Quaternary aeolian dust depositions. The above-mentioned processes further rework and refine the bulk grain size, which is more evident in paleosol layers. 3, Like the hipparion Red-Earth and the Quaternary aeolian deposits, the Miocene loess deposits are transported by near-ground winter monsoons. However, the average wind intensity evidenced by the quartz median grain size of Miocene loess, together with the maximum wind intensity by the quartz maximum grain size, is weaker than those of the Quaternary.

Volcanic eruptions dry fogs and the european palaeoenvironmental record: Localised phenomena or Hemispheric impacts?

Grattan, John and Pyatt, J.P 'Volcanic eruptions dry fogs and the european palaeoenvironmental record: Localised phenomena or Hemispheric impacts?' Global and Planetary Change, 21(1999) 173-179

Structure of glasses and melts

Wilding, M. C., Benmore, C. J. (2006). Structure and Glasses and Melts. reviews in Mineralogy and Geochemistry, 63 (1), 275-311 RAE2008

An unrecognized source of PCB contamination in schools and other buildings

An investigation of 24 buildings in the Greater Boston Area revealed that one-third (8 of 24) contained caulking materials with polychlorinated biphenyl (PCB) content exceeding 50 ppm by weight, which is the U.S. Environmental Protection Agency (U.S. EPA) specified limit above which this material is considered to be PCB bulk product waste. These buildings included schools and other public buildings. In a university building where similar levels of PCB were found in caulking material, PCB levels in indoor air ranged from 111 to 393 ng/m3; and in dust taken from the building ventilation system, < 1 ppm to 81 ppm. In this building, the U.S. EPA mandated requirements for the removal and disposal of the PCB bulk product waste as well as for confirmatory sampling to ensure that the interior and exterior of the building were decontaminated. Although U.S. EPA regulations under the Toxic Substances Control Act stipulate procedures by which PCB-contaminated materials must be handled and disposed, the regulations apparently do not require that materials such as caulking be tested to determine its PCB content. This limited investigation strongly suggests that were this testing done, many buildings would be found to contain high levels of PCBs in the building materials and potentially in the building environment. The presence of PCBs in schools is of particular concern given evidence suggesting that PCBs are developmental toxins.

Tropospheric aerosol detection over Southern Ireland using a backscatter Raman lidar

Lidar is an optical remote sensing instrument that can measure atmospheric parameters. A Raman lidar instrument (UCLID) was established at University College Cork to contribute to the European lidar network, EARLINET. System performance tests were carried out to ensure strict data quality assurance for submission to the EARLINET database. Procedures include: overlap correction, telecover test, Rayleigh test and zero bin test. Raman backscatter coefficients, extinction coefficients and lidar ratio were measured from April 2010 to May 2011 and February 2012 to June 2012. Statistical analysis of the profiles over these periods provided new information about the typical atmospheric scenarios over Southern Ireland in terms of aerosol load in the lower troposphere, the planetary boundary layer (PBL) height, aerosol optical density (AOD) at 532 nm and lidar ratio values. The arithmetic average of the PBL height was found to be 608 ± 138 m with a median of 615 m, while average AOD at 532 nm for clean marine air masses was 0.119 ± 0.023 and for polluted air masses was 0.170 ± 0.036. The lidar ratio showed a seasonal dependence with lower values found in winter and autumn (20 ± 5 sr) and higher during spring and winter (30 ± 12 sr). Detection of volcanic particles from the eruption of the volcano Eyjafjallajökull in Iceland was measured between 21 April and 7 May 2010. The backscatter coefficient of the ash layer varied between 2.5 Mm-1sr-1 and 3.5 Mm-1sr-1, and estimation of the AOD at 532 nm was found to be between 0.090 and 0.215. Several aerosol loads due to Saharan dust particles were detected in Spring 2011 and 2012. Lidar ratio of the dust layers were determine to be between 45 and 77 sr and AOD at 532 nm during the dust events range between 0.84 to 0.494.

Real time analysis of atmospheric single particles in urban environments using aerosol time of flight mass spectrometry

In order to determine the size-resolved chemical composition of single particles in real-time an ATOFMS was deployed at urban background sites in Paris and Barcelona during the MEGAPOLI and SAPUSS monitoring campaigns respectively. The particle types detected during MEGAPOLI included several carbonaceous species, metal-containing types and sea-salt. Elemental carbon particle types were highly abundant, with 86% due to fossil fuel combustion and 14% attributed to biomass burning. Furthermore, 79% of the EC was apportioned to local emissions and 21% to continental transport. The carbonaceous particle types were compared with quantitative measurements from other instruments, and while direct correlations using particle counts were poor, scaling of the ATOFMS counts greatly improved the relationship. During SAPUSS carbonaceous species, sea-salt, dust, vegetative debris and various metal-containing particle types were identified. Throughout the campaign the site was influenced by air masses altering the composition of particles detected. During North African air masses the city was heavily influenced by Saharan dust. A regional stagnation was also observed leading to a large increase in carbonaceous particle counts. While the ATOFMS provides a list of particle types present during the measurement campaigns, the data presented is not directly quantitative. The quantitative response of the ATOFMS to metals was examined by comparing the ion signals within particle mass spectra and to hourly mass concentrations of; Na, K, Ca, Ti, V, Cr, Mn, Fe, Zn and Pb. The ATOFMS was found to have varying correlations with these metals depending on sampling issues such as matrix effects. The strongest correlations were observed for Al, Fe, Zn, Mn and Pb. Overall the results of this work highlight the excellent ability of the ATOFMS in providing composition and mixing state information on atmospheric particles at high time resolution. However they also show its limitations in delivering quantitative information directly.

Solid phase velocity measurements utilising electrostatic sensors and cross correlation signal processing

Gas-solids two phase systems are widely employed within process plant in the form of pneumatic conveyors, dust extraction systems and solid fuel injection systems. The measurement of solids phase velocity therefore has wide potential application in flow monitoring and, in conjunction with density measurement instrumentation, solids mass flow rate measurement. Historically, a number of authors have detailed possible measurement techniques, and some have published limited test results. It is, however, apparent that none of these technologies have found wide application in industry. Solids phase velocity measurements were undertaken using real time cross correlation of signals from two electrostatic sensors spaced axially along a pipeline conveying pulverised coal (PF). Details of the measurement equipment, the pilot scale test rig and the test results are presented.

Columnar aerosol properties in a northeastern atlantic site (plymouth united kingdom) by means of ground based skyradiometer data during years 2000-2008.

Between 2000 and 2008, columnar optical and radiative properties were measured at the Plymouth Marine Laboratory (PML), UK (50° 21.95′N, 4° 8.85′W) using an automatic Prede POM01L sun–sky photometer. The database was analyzed for aerosol optical properties using the SKYRAD radiative inversion algorithm and calibrated using the in situ SKYIL calibration method. Retrievals include aerosol optical depth, Ångström wavelength exponent, aerosol volume distribution, refractive index and single scattering albedo. The results show that the Plymouth site is characterized by low values of aerosol optical depth with low variability (0.18 ± 0.08 at 500 nm) and a mean annual Ångström exponent of 1.03 ± 0.21. The annual mean of the single scattering albedo is 0.97, indicative of non-absorbing aerosols. The aerosol properties were classified in terms of air mass back trajectories: the area is mainly affected by Atlantic air masses and the dominant aerosol type is a mixture of maritime particles, present in low burdens with variable size. The maritime air masses were defined by annual mean values for the AOD (at 500 nm) of 0.13–0.14 and a wavelength exponent of 0.96–1.03. Episodic anthropogenic and mineral dust intrusions occasionally occur, but they are sporadic and dilute (AOD at 500 nm about 0.20). Tropical continental air masses were characterized by the highest AOD at 500 nm (0.34) and the lowest wavelength exponent (0.83), although they were the least represented in the analysis.

Colloidal stability of nanoparticles derived from simulated cloud-processed mineral dusts

Laboratory simulation of cloud processing of three model dust types with distinct Fe-content (Moroccan dust, Libyan dust and Etna ash) and reference goethite and ferrihydrite were conducted in order to gain a better understanding of natural nanomaterial inputs and their environmental fate and bioavailability. The resulting nanoparticles (NPs) were characterised for Fe dissolution kinetics, aggregation/size distribution, micromorphology and colloidal stability of particle suspensions using a multi-method approach. We demonstrated that the: (i) acid-leachable Fe concentration was highest in volcanic ash (1 m Mg(-1) dust) and was followed by Libyan and Moroccan dust with an order of magnitude lower levels; (ii) acid leached Fe concentration in the<20 nm fraction was similar in samples processed in the dark with those under artificial sunlight, but average hydrodynamic diameter of NPs after cloud-processing (pH~6) was larger in the former; iii) NPs formed at pH~6 were smaller and less poly-disperse than those at low pH, whilst unaltered zeta potentials indicated colloidal instability; iv) relative Fe percentage in the finer particles derived from cloud processing does not reflect Fe content of unprocessed dusts (e.g. volcanic ash>Libyan dust). The common occurrence of Fe-rich "natural nanoparticles" in atmospheric dust derived materials may indicate their more ubiquitous presence in the marine environment than previously thought.

Volcanic ash supply to the surface ocean – remote sensing of biological responses and their wider biogeochemical significance

Transient micronutrient enrichment of the surface ocean can enhance phytoplankton growth rates and alter microbial community structure with an ensuing spectrum of biogeochemical feedbacks. Strong phytoplankton responses to micronutrients supplied by volcanic ash have been reported recently. Here we: (i) synthesize findings from these recent studies; (ii) report the results of a new remote sensing study of ash fertilization; and (iii) calculate theoretical bounds of ash-fertilized carbon export. Our synthesis highlights that phytoplankton responses to ash do not always simply mimic that of iron amendment; the exact mechanisms for this are likely biogeochemically important but are not yet well understood. Inherent optical properties of ash-loaded seawater suggest rhyolitic ash biases routine satellite chlorophyll-a estimation upwards by more than an order of magnitude for waters with <0.1 mg chlorophyll-a m-3, and less than a factor of 2 for systems with >0.5 mg chlorophyll-a m-3. For this reason post-ash-deposition chlorophyll-a changes in oligotrophic waters detected via standard Case 1 (open ocean) algorithms should be interpreted with caution. Remote sensing analysis of historic events with a bias less than a factor of 2 provided limited stand-alone evidence for ash-fertilization. Confounding factors were poor coverage, incoherent ash dispersal, and ambiguity ascribing biomass changes to ash supply over other potential drivers. Using current estimates of iron release and carbon export efficiencies, uncertainty bounds of ash-fertilized carbon export for 3 events are presented. Patagonian iron supply to the Southern Ocean from volcanic eruptions is less than that of windblown dust on thousand year timescales but can dominate supply at shorter timescales. Reducing uncertainties in remote sensing of phytoplankton response and nutrient release from ash are avenues for enabling assessment of the oceanic response to large-scale transient nutrient enrichment.

Regional ocean-colour chlorophyll algorithms for the Red Sea

The Red Sea is a semi-enclosed tropical marine ecosystem that stretches from the Gulf of Suez and Gulf of Aqaba in the north, to the Gulf of Aden in the south. Despite its ecological and economic importance, its biological environment is relatively unexplored. Satellite ocean-colour estimates of chlorophyll concentration (an index of phytoplankton biomass) offer an observational platform to monitor the health of the Red Sea. However, little is known about the optical properties of the region. In this paper, we investigate the optical properties of the Red Sea in the context of satellite ocean-colour estimates of chlorophyll concentration. Making use of a new merged ocean-colour product, from the European Space Agency (ESA) Climate Change Initiative, and in situ data in the region, we test the performance of a series of ocean-colour chlorophyll algorithms. We find that standard algorithms systematically overestimate chlorophyll when compared with the in situ data. To investigate this bias we develop an ocean-colour model for the Red Sea, parameterised to data collected during the Tara Oceans expedition, that estimates remote-sensing reflectance as a function of chlorophyll concentration. We used the Red Sea model to tune the standard chlorophyll algorithms and the overestimation in chlorophyll originally observed was corrected. Results suggest that the overestimation was likely due to an excess of CDOM absorption per unit chlorophyll in the Red Sea when compared with average global conditions. However, we recognise that additional information is required to test the influence of other potential sources of the overestimation, such as aeolian dust, and we discuss uncertainties in the datasets used. We present a series of regional chlorophyll algorithms for the Red Sea, designed for a suite of ocean-colour sensors, that may be used for further testing.