993 resultados para Niagara on the Lake, Ontario


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Copy imperfect: t.p. wanting. Title page transcription based on NUC entry.

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Submitted to the Minister of Marine and Fisheries of Canada.

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v.31 Ball clays -- v.32 Granites of Scotland -- v.33 Synopsis of the mineral resources of Scotland -- v.34 Rock wool -- v. 35 Limestones of Scotland -- v.36 Cambro-Ordovician limestones and dolomites of the Ord and Torran areas, SKye and the Kishorn area, Ross-Shire -- v.37 Limestones of Scotland : chemical analyses and petrography

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Yellow, black ink on linen; plan, four cross-sections; unsigned; 102 x 83 cm.; Scales vary [from photographic copy by Lance Burgharrdt]

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Yellow, black ink on linen; location, type, amounts of plantings; footpaths, pool; unsigned; 40 x 43 cm.; Scale: 1" = 4' [from photographic copy by Lance Burgharrdt]

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Not in Bitting, K.G. Gastronomic bib.

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On cover: Lakes of western Vermont.

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James Armstrong, chairman 1886 to his death, after which A.T. Freed was chairman.

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Includes bibliographical references (p. viii-ix) and index.

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Report.--Evidence: Ontario; Quebec; New Brunswick; Nova Scota.

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Boron and chlorine were determined in rain water and in atmospheric moisture condensed in a "Saratov" refrigerator. Ocean is the main source of boron on the earth surface. Boron evaporates from the ocean and enriches atmospheric precipitation: B/Cl ratio of ocean water (0.00024) increases by factor of 10-15. Assuming that the average Cl content in global river runoff is 7.8 mg/l and boron content 0.013 mgl, B/Cl ratio in this runoff is 0.0017. The average B/Cl ratio in rain water of the Golubaya (Blue) Bay (Gelendzhik, Black Sea region) is 0.0026 and in condensates of atmospheric moisture during onshore and offshore winds in the same region it averages from 0.0029 to 0.0033. The maximum boron content in the condensates of this region during onshore winds was 0.032 mg/l and the minimum during offshore winds, 0.004 mg/l. /Cl ratio in sea water over the Atlantic Ocean and in the Gelendzhik area of the Black Sea varied within narrow range, mostly from 0.0025 to 0.0035. Similar B/Cl ratio (0.0024) was found for atmospheric precipitation on the slope of the Terskei Ala-Tau near the Issyk-Kul Lake in 1969. Thus, although chemistries of boron and chlorine (in chlorides) are very different, the B/Cl ratio in the atmosphere is fairly constant. This can be taken as a confirmation of an assumption that salt composition of sea water passes into the atmosphere in molecularly dispersed state. Supposing that the ocean-atmosphere system is in equilibrium as regards to the boron budget, it can be assumed that the same amount of boron passes from the ocean into bottom sediments and from lithosphere rocks and soils into the hydrosphere.

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Knowledge on the expected effects of climate change on aquatic ecosystems is defined by three ways. On the one hand, long-term observation in the field serves as a basis for the possible changes; on the other hand, the experimental approach may bring valuable pieces of information to the research field. The expected effects of climate change cannot be studied by empirical approach; rather mathematical models are useful tools for this purpose. Within this study, the main findings of field observations and their implications for future were summarized; moreover, the modelling approaches were discussed in a more detailed way. Some models try to describe the variation of physical parameters in a given aquatic habitat, thus our knowledge on their biota is confined to the findings based on our present observations. Others are destined for answering special issues related to the given water body. Complex ecosystem models are the keys of our better understanding of the possible effects of climate change. Basically, these models were not created for testing the influence of global warming, rather focused on the description of a complex system (e. g. a lake) involving environmental variables, nutrients. However, such models are capable of studying climatic changes as well by taking into consideration a large set of environmental variables. Mostly, the outputs are consistent with the assumptions based on the findings in the field. Since synthetized models are rather difficult to handle and require quite large series of data, the authors proposed a more simple modelling approach, which is capable of examining the effects of global warming. This approach includes weather dependent simulation modelling of the seasonal dynamics of aquatic organisms within a simplified framework.

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Lake Annie is a small (37 ha), relatively deep (21 m) sinkhole lake on the Lake Wales Ridge (LWR) of central Florida with a long history of study, including monthly limnological monitoring since June, 1983. The record shows high variability in Secchi disc transparency, which ranged from < 1 to 15 m with a trend toward decreasing values over the latter decade of record. We examined available regional meteorological, groundwater and limnological data to determine the drivers and thermal consequences of variability in water transparency. While total nutrient concentrations and chlorophyll-a were highest during years of low transparency, stepwise regression showed that none of these had a signifi cant effect on transparency after water color was taken into account. Repeated years of high precipitation between 1993–2005 caused an increase in water table height, increasing the transport of dissolved substances from the vegetated watershed into the lake. Groundwater stage explained 73 % of the interannual variability in water transparency. Transparency, in turn, explained 85 % of the interannual variability in the heat budget for the lake, which ranged from 1.8 × 108 to 4.1 × 108 Joules m–2 yr–1, encompassing the range reported across Florida lakes. While surface water temperature was not affected by transparency, depths below 5 m warmed faster during the stratifi ed period during years having a lower rate of light extinction. We show that an increase in precipitation of 20 cm per year reduces the depth of the summer euphotic zone and thermocline by 1.9 and 1.6 m, respectively, and causes a 1-month reduction in the duration of winter mixing in this monomictic lake. Because biota have been shown to respond to shifts in light and heat distribution of much smaller magnitude than exhibited here, our work suggests that subtle changes in precipitation linked to climate fl uctuations may have signifi cant physical as well as biotic consequences.

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The rapid development of nanotechnology and wider applications of engineered nanomaterials (ENMs) in the last few decades have generated concerns regarding their environmental and health risks. After release into the environment, ENMs undergo aggregation, transformation, and, for metal-based nanomaterials, dissolution processes, which together determine their fate, bioavailability and toxicity to living organisms in the ecosystems. The rates of these processes are dependent on nanomaterial characteristics as well as complex environmental factors, including natural organic matter (NOM). As a ubiquitous component of aquatic systems, NOM plays a key role in the aggregation, dissolution and transformation of metal-based nanomaterials and colloids in aquatic environments.

The goal of this dissertation work is to investigate how NOM fractions with different chemical and molecular properties affect the dissolution kinetics of metal oxide ENMs, such as zinc oxide (ZnO) and copper oxide (CuO) nanoparticles (NPs), and consequently their bioavailability to aquatic vertebrate, with Gulf killifish (Fundulus grandis) embryos as model organisms.

ZnO NPs are known to dissolve at relatively fast rates, and the rate of dissolution is influenced by water chemistry, including the presence of Zn-chelating ligands. A challenge, however, remains in quantifying the dissolution of ZnO NPs, particularly for time scales that are short enough to determine rates. This dissertation assessed the application of anodic stripping voltammetry (ASV) with a hanging mercury drop electrode to directly measure the concentration of dissolved Zn in ZnO NP suspensions, without separation of the ZnO NPs from the aqueous phase. Dissolved zinc concentration measured by ASV ([Zn]ASV) was compared with that measured by inductively coupled plasma mass spectrometry (ICP-MS) after ultracentrifugation ([Zn]ICP-MS), for four types of ZnO NPs with different coatings and primary particle diameters. For small ZnO NPs (4-5 nm), [Zn]ASV was 20% higher than [Zn]ICP-MS, suggesting that these small NPs contributed to the voltammetric measurement. For larger ZnO NPs (approximately 20 nm), [Zn]ASV was (79±19)% of [Zn]ICP-MS, despite the high concentrations of ZnO NPs in suspension, suggesting that ASV can be used to accurately measure the dissolution kinetics of ZnO NPs of this primary particle size.

Using the ASV technique to directly measure dissolved zinc concentration, we examined the effects of 16 different NOM isolates on the dissolution kinetics of ZnO NPs in buffered potassium chloride solution. The observed dissolution rate constants (kobs) and dissolved zinc concentrations at equilibrium increased linearly with NOM concentration (from 0 to 40 mg-C L-1) for Suwannee River humic acid (SRHA), Suwannee River fulvic acid and Pony Lake fulvic acid. When dissolution rates were compared for the 16 NOM isolates, kobs was positively correlated with certain properties of NOM, including specific ultraviolet absorbance (SUVA), aromatic and carbonyl carbon contents, and molecular weight. Dissolution rate constants were negatively correlated to hydrogen/carbon ratio and aliphatic carbon content. The observed correlations indicate that aromatic carbon content is a key factor in determining the rate of NOM-promoted dissolution of ZnO NPs. NOM isolates with higher SUVA were also more effective at enhancing the colloidal stability of the NPs; however, the NOM-promoted dissolution was likely due to enhanced interactions between surface metal ions and NOM rather than smaller aggregate size.

Based on the above results, we designed experiments to quantitatively link the dissolution kinetics and bioavailability of CuO NPs to Gulf killifish embryos under the influence of NOM. The CuO NPs dissolved to varying degrees and at different rates in diluted 5‰ artificial seawater buffered to different pH (6.3-7.5), with or without selected NOM isolates at various concentrations (0.1-10 mg-C L-1). NOM isolates with higher SUVA and aromatic carbon content (such as SRHA) were more effective at promoting the dissolution of CuO NPs, as with ZnO NPs, especially at higher NOM concentrations. On the other hand, the presence of NOM decreased the bioavailability of dissolved Cu ions, with the uptake rate constant negatively correlated to dissolved organic carbon concentration ([DOC]) multiplied by SUVA, a combined parameter indicative of aromatic carbon concentration in the media. When the embryos were exposed to CuO NP suspension, changes in their Cu content were due to the uptake of both dissolved Cu ions and nanoparticulate CuO. The uptake rate constant of nanoparticulate CuO was also negatively correlated to [DOC]×SUVA, in a fashion roughly proportional to changes in dissolved Cu uptake rate constant. Thus, the ratio of uptake rate constants from dissolved Cu and nanoparticulate CuO (ranging from 12 to 22, on average 17±4) were insensitive to NOM type or concentration. Instead, the relative contributions of these two Cu forms were largely determined by the percentage of CuO NP that was dissolved.

Overall, this dissertation elucidated the important role that dissolved NOM plays in affecting the environmental fate and bioavailability of soluble metal-based nanomaterials. This dissertation work identified aromatic carbon content and its indicator SUVA as key NOM properties that influence the dissolution, aggregation and biouptake kinetics of metal oxide NPs and highlighted dissolution rate as a useful functional assay for assessing the relative contributions of dissolved and nanoparticulate forms to metal bioavailability. Findings of this dissertation work will be helpful for predicting the environmental risks of engineered nanomaterials.

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Lake Meerfelder Maar (Germany) provides a varved record from the Last Glacial/Interglacial transition back to ca 1500 years BP. This study shows results for the Holocene sequence from new cores collected in 2009 based on varve counting, microfacies and micro-XRF analyses. The main goal of combining those analyses is to provide a new approach for interpreting long-term palaeolimnological proxy data and testing the climate-proxy stationarity throughout the current interglacial period. Varve counting provides a new independent Holocene chronology (MFM2012) with an estimated counting error of 1-0.5% and supported by 14C dating. Varve structure and thickness and geochemical composition of the varves give information about the main environmental processes that affect the lake and its catchment as well as the possible climate variability behind. Varves are couplets of i) a spring/summer laminae composed of monospecific diatom blooms and ii) an autumn/winter sub-layer made of minerogenic material and re-worked sediments. Thickness of the varves and sub-layers reflect lake variability and allow seasons to be distinguished as well as seasonal proxies. Changes in the winter minerogenic influx into the lake are reflected by Ti intensities and the Si/Ti ratio as a indicator for diatom concentration, which can be used as a proxy for water circulation during the early spring. Long-term variability of geochemical composition shows a reduction of the detrital material input (Ti) at 5,000 varve yrs BP and a visible sensitivity to water mixing (Si/Ti) during the Late Holocene. Variations of Ti intensities during the early and mid-Holocene do not show a clear relationship with climate. In contrast, higher values of the Si/Ti ratio together with thicker varves have been interpreted as wind-stress phases, which coincide with centennial variability of European cold/wet episodes during the Late Holocene. Our findings show that a long-term change in the lake and/or variability of the climate system can influence proxy sensitivity of a lacustrine record.