550 research outputs found
I.C. Engine Fundamental (I)
This text has been compiled for those trainees taking part in the six months Marine Engineering Course at SEAFDEC/TD, to be used in conjunction with the lectures and practical training on the subject of the Internal Combustion Engines for Fishing Boats. The text deals with fundamentals of the prime mover in the form of heat engines, specifically the internal combustion engine, and has been based on the technical senior-high school level requirements in Japan. Further applications, including small automobile engines, rotary and diesel engines etc. Will be explained in the next edition of this text series (I.C. Engine Fundamentals (II)) by the same author
Emblemata Florentii Schoonhovii I.C. Goudani : partim moralia, partim etiam civilia /
Signatures: *⁶ A-2G⁴ 2H⁶.Title and emblems engraved by Crispijn van de Passe the Younger; see Landwehr. Engraved port. of the author (*6v), signed with initials (MN?).Each of the LXXIV emblems is preceded by a motto and followed by explanatory Latin couplets and a Commentarius in prose.Landwehr, J. Emblem and fable books (3rd ed.),Mode of access: Internet.At head of front pastedown of c. 3 is the signature: Wäterling. Below is the embossed bookplate of G. Delmay, printed black on red, and at the lower left-hand corner is the label of John Landwehr. The facing flyleaf is inscribed in pencil: de la bibliotheque Max Rooses, perhaps the writer on painting who lived 1839-1914. At foot of t.p. are the initials F.K.At head of front pastedown of Getty c. 2 are bibliographical notes in pencil, and at the foot is Ulrich Middeldorf's label. Slip of paper with bibliographical note written in black ink tipped onto verso of front free endpaper. Signature at foot of t.p.: F. Travers. Another signature at head of *2r: John Crumpe. Slip from bookseller's catalog describing this copy has been tipped onto back pastedown.At upper left-hand corner of front pastedown of c. 1 is Theodore Besterman's calligraphic label, signed with the initials P.S. Facing flyleaf signed by Joannes van Zeller Junior and dated 1660.Binding, c. 1: vellum over stiff paper, edges sprinkled red. Copy 2: later polished calf, rebacked. Boards tooled in gilt with 2 frames of double fillets, and fleurons at corners of the inner frame. Edges of boards tooled in gilt, turn-ins tooled in blind. Page edges gilt. Copy 3: later vellum. Edges sprinkled blue.In Getty c. 2, leaf *6 with port. is bound before *1; in its place following *5 is bound 2E4, the section title leaf for Poemata aliquot. Leaf I4 with p. 71-72 is wanting
The provenancing of flint artefacts using palynological techniques
The provenancing of flint artefacts has proved problematic in the past. Acid maceration to extract age-diagnostic organic-walled microplankton from sedimentary materials is a technique routinely employed in both industrial hydrocarbon exploration and Quaternary studies. Here we assess the application of this technique to provenance determination of flint nodules from three locations (two in southern England and one in the Inner Hebrides, Scotland), each of which has abundant local evidence of flint utilization for artefact manufacture in prehistory. We show that, whilst not all flint nodules yield abundant or well preserved organic-walled microfossils assemblages, there is a significant potential for the use of this technique, which deserves further investigation
Evaluating the consistency and discrepancies among biomass datasets in the Cornwall region through a comparative analysis of their methodologies and performance
Biomass data is essential for environmental monitoring and management, but inconsistencies and uncertainties among these datasets hinder accurate estimates. This study comprehensively compares GEDI, ESA CCI, and ICESat-2 biomass datasets for Cornwall, an analysis not previously been conducted, evaluating spatial distribution, statistical properties, uncertainty, and saturation.
GEDI offers high-resolution, precise biomass estimates suitable for ecological studies, despite its coarser resolution compared to the other datasets. ESA CCI provides global coverage and integrates various data sources for climate change mitigation, but early signal saturation is an issue. ICESat-2 combines field measurements with satellite data, offering detailed temporal insights, but uncertainty is higher in Cornwall's complex landscape.
This analysis revealed significant biomass estimate variations due to sensor differences, methodologies, and processing techniques. GEDI and ICESat-2 captured broader biomass ranges compared to ESA CCI's predominantly lower values. Methodological transparency varies, although GEDI’s enhanced clarity is evident through precision categorisation. Lidar-based GEDI outperformed optical and radar methods such as those by ESA CCI, which saturated earlier. Resampling impacts are evident in altered statistical properties, with higher R-squared values indicating stronger large-scale relationships but reduced detail at coarser resolutions.
The importance of this research and its results lies in its potential to enhance the accuracy of biomass estimation and improved ecological research, land use planning, carbon accounting and climate change mitigation efforts. By examining the differences and complementarities between these datasets, this study supports more informed decision making in selecting appropriate data sources. Furthermore, the insights gained from this analysis can inform efforts in biomass mapping not only in Cornwall but also in other regions with similar ecological characteristics. To ensure biomass mapping produces comparable, reliable, and consistent results, user-friendly product documentation employing consistent terminology is strongly recommended
Phylogenetic assessment of heterotrophic bacteria from a water distribution system using 16S rDNA sequencing
Determination of a heterotrophic plate count (HPC) for drinking-water samples alone is not enough to assess possible health hazards associated with sudden changes in the bacterial count. Speciation is very crucial to determine whether the population includes pathogens and (or) opportunistic pathogens. Most of the isolates recovered from drinking water samples could not be allocated to a specific phylogenetic branch based on the use of conventional diagnostic methods. The present study had to use phylogenetic analysis, which was simplified by determining and using the first 500-bp sequence of the 16S rDNA, to successfully identify the type and species of bacteria found in the samples. Gram-positive bacteria α-, β-, and γ-Proteobacteria were found to be the major groups representing the heterotrophic bacteria in drinking water. The study also revealed that the presence of sphingomonads in drinking water supplies may be much more common than has been reported so far and thus further studies are merited. The intermittent mode of supply, mainly characterized by water stagnation and flow interruption associated possibly with biofilm detachment, raised the possibility that the studied bacterial populations in such systems represented organisms coming from 2 different niches, the biofilm and the water column. © 2005 NRC Canada.Abraham WR, 1999, INT J SYST BACTERIOL, V49, P1053; AMY PS, 1992, APPL ENVIRON MICROB, V58, P3367; Assanta MA, 1998, J FOOD PROTECT, V61, P1321; BEJ AK, 1991, APPL ENVIRON MICROB, V57, P2429; BOTTGER EC, 1989, FEMS MICROBIOL LETT, V65, P171, DOI 10.1016-0378-1097(89)90386-8; Boye K, 1999, MICROBIOL RES, V154, P23; BRAUNHOWLAND EB, 1993, APPL ENVIRON MICROB, V59, P3219; BURKE V, 1984, APPL ENVIRON MICROB, V48, P367; CARSON LA, 1978, APPL ENVIRON MICROB, V36, P839; Chang CT, 2002, APPL ENVIRON MICROB, V68, P3159, DOI 10.1128-AEM.68.6.3159-3161.2002; CLARK J, 1977, CAN J MICROBIOL, V26, P827; Covert TC, 1999, APPL ENVIRON MICROB, V65, P2492; Dewettinck T, 2001, APPL MICROBIOL BIOT, V57, P412, DOI 10.1007-s002530100797; Domingo JWS, 2003, WATER SCI TECHNOL, V47, P149; Fernandez M, 1997, PEDIATR INFECT DIS J, V16, P1007, DOI 10.1097-00006454-199710000-00023; Francis CA, 2001, WATER RES, V35, P3758, DOI 10.1016-S0043-1354(01)00073-2; Furuhata K, 1993, Nihon Koshu Eisei Zasshi, V40, P1047; GELDREICH EE, 1985, J AM WATER WORKS ASS, V77, P72; GILARDI GL, 1984, J CLIN MICROBIOL, V20, P626; HIRAISHI A, 1995, APPL ENVIRON MICROB, V61, P2099; HOLMBERG SD, 1986, ANN INTERN MED, V105, P683; HOLMES B, 1994, J CLIN MICROBIOL, V32, P1970; Holt J. G., 1994, BERGEYS MANUAL DETER; Joseph SW, 2000, ASM NEWS, V66, P218; Kalmbach S, 1999, INT J SYST BACTERIOL, V49, P769; KAYE KM, 1992, CLIN INFECT DIS, V14, P1010; KIM S, 2000, INT J SYST EVOL MICR, V6, P2031; KIROV SM, 1993, INT J FOOD MICROBIOL, V20, P179, DOI 10.1016-0168-1605(93)90164-C; KLINGLER JM, 1992, APPL ENVIRON MICROB, V58, P2089; Kolbert CP, 1999, CURR OPIN MICROBIOL, V2, P299, DOI 10.1016-S1369-5274(99)80052-6; KORVICK JA, 1989, ARCH INTERN MED, V149, P1449, DOI 10.1001-archinte.149.6.1449; Koskinen R, 2000, J APPL MICROBIOL, V89, P687, DOI 10.1046-j.1365-2672.2000.01167.x; Kuhn I, 1997, APPL ENVIRON MICROB, V63, P2708; LANE DJ, 1985, P NATL ACAD SCI USA, V82, P6955, DOI 10.1073-pnas.82.20.6955; Lechevallier M.W., 1980, APPL ENVIRON MICROB, V30, P739; MAKI JS, 1986, APPL ENVIRON MICROB, V51, P1047; Merino S, 1995, INT J FOOD MICROBIOL, V28, P157, DOI 10.1016-0168-1605(95)00054-2; Norton CD, 2000, APPL ENVIRON MICROB, V66, P268; PATT TE, 1976, INT J SYST BACTERIOL, V26, P226; PEARSON WR, 1988, P NATL ACAD SCI USA, V85, P2444, DOI 10.1073-pnas.85.8.2444; Perola O, 2002, J HOSP INFECT, V50, P196, DOI 10.1053-jhin.2001.1163; Pollock TJ, 1999, J IND MICROBIOL BIOT, V23, P436, DOI 10.1038-sj.jim.2900710; REASONER DJ, 1985, APPL ENVIRON MICROB, V49, P1; Rice EW, 2000, J CLIN MICROBIOL, V38, P4296; RUTHERFORD PC, 1988, J CLIN MICROBIOL, V26, P2441; Schubert RHW, 2000, INT J HYG ENVIR HEAL, V203, P83, DOI 10.1078-S1438-4639(04)70012-7; Sekiguchi H, 2002, APPL ENVIRON MICROB, V68, P5142, DOI 10.1128-AEM.68.10.5142-5150.2002; September SM, 2004, APPL ENVIRON MICROB, V70, P7571, DOI 10.1128-AEM.70.12.7571-7573.2004; SPINO DF, 1985, APPL ENVIRON MICROB, V50, P1213; Springer B, 1996, J CLIN MICROBIOL, V34, P296; STACKEBRANDT E, 1988, INT J SYST BACTERIOL, V38, P321; Tang YW, 1998, J CLIN MICROBIOL, V36, P3674; Tokajian S, 2004, WATER QUAL RES J CAN, V39, P64; TOKAJIAN S, 2004, J CHEMOTHERAPY, V16, P104; Tokajian S, 2003, WATER SCI TECHNOL, V47, P229; Tokajian S, 2004, J WATER HEALTH, V2, P115; Ultee A, 2004, J APPL MICROBIOL, V96, P560, DOI 10.1111-j.1365-2672.2004.02174.x; VANDEPEER Y, 1994, COMPUT APPL BIOSCI, V10, P569; Williams MM, 2004, J APPL MICROBIOL, V96, P954, DOI 10.1111-j.1365-2672.2004.02229.x; WINTZINGERODE F, 1999, APPL ENVIRON MICROB, V65, P283; Woo PCY, 2000, J CLIN MICROBIOL, V38, P3515; 1994, MICROBIOLOGICAL EXAM30302
Iohannis de Brunes I.C. Emblemata of zinne-werck : voorghestelt in beelden, ghedichten, en breeder uijt-legginghen, tot uijt-druckinghe en verbeteringhe van verscheijden feijlen onser eeuwe.
Signatures: pi² *⁴ A-2X⁴ 2Y⁴(-2Y4) 2Z-3A⁴ 3B².Emblematic engravings by Christof Le Blon, Johann Gelle, Willem van de Passe, Albert Poel and Jan Gerrits Swelinck, all after Adriaen van de Venne. See Landwehr. Woodcut head-pieces, initials (some historiated).First published 1624. As described by Landwehr, the 1636 ed. is the same as the 1st, except that the imprint on the engraved t.p. was changed to read: Den tweeden druck, Amsterdam, I. E. Kloppenburgh, 1636. The present copy corresponds rather to Praz's description of the 1636 ed., with 378 rather than 360 p., an additional 52nd emblem, and the "zedespreucken" at the end.Praz, M. Studies in 17th-cent. imagery (2nd ed.),Landwehr, J. Emblem books in the Low Countries,Mode of access: Internet.Binding: modern vellum, author & title lettered on spine
Solubilisation of a teichoic acid-synthesising system from the membrane of Bacillus licheniformis by freezing and thawing
Edmonton Exhibition - 02
Photograph - An exhibit by the Athabasca Board of Trade arranged by I.C. Shank at the Edmonton Exhibition, Edmonton, Albert
Isreal C. Shank - 03
Photograph - Portrait of I.C. Shank, Chief Superintendent of the RCMP. New Westminster, British Columbi
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