A cool Paternoster image:
Image from page 144 of “Journal and proceedings of the Royal Society of New South Wales” (1867)
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Identifier: journalproceedi471913roya
Title: Journal and proceedings of the Royal Society of New South Wales
Year: 1867 (1860s)
Authors: Royal Society of New South Wales Royal Society of New South Wales. Transactions of the Royal Society of New South Wales Royal Society of New South Wales. Transactions and proceedings of the Royal Society of New South Wales
Subjects: Science
Publisher: Sydney, Royal Society of New South Wales
Contributing Library: Smithsonian Libraries
Digitizing Sponsor: Biodiversity Heritage Library
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Text Appearing Before Image:
is in House Sparrows and in Bovines in N.S. W. By J. Burton Cleland, m.d., ch.m. Principal Microbiologist to the Government of N. S. WalesArt. IV.—Note on the Growth of Flowering Stem of Xanthorrhma hastilis, R.Br. By J. Burton Cleland, m.d., ch.m…Art. V.—Note on Agar-agar Seaweed from Western Australia By J. Burton Cleland, m.d., ch.m Art. VI.—Notes on Eucalyptus, (with descriptions of New Species) No. I. ByJ.H. Maiden Art. VII.—Note on the Paraffins of Eucalyptus Oils. By H. G Smith, f.c.s. Art. VIII.—The Seedlings of the Angophoras, and description of a New Species. By Cuthbert Hall, m.d., ch.m. (Communi cated by R. T. Baker). [ With Plates II – IV.] Art. IX.—On the Essential Oils of the Angophoras. By H. G Smith, f.c.s. Page. 59 7072757695 98106 ISSUED FEBRUARY 5th, 1911 Vol. XLVII. Part II. JOURNAL AND PROCEEDINGS ROYAL SOCIETY NEW SOUTH WALES 1913. PART II., (pp. 113-247). Containing Papers read in AUGUST to DECEMBER WITH FIVE PLATES. (Plates v, vi, vii, viii, ix.)
Text Appearing After Image:
SYDNEY: PUBLISHED BY THE SOCIETY, 5 ELIZABETH STREET NORTH, SYDNEY. LONDON AGENTS : GEORGE ROBERTSON & Co., PROPRIETARY LIMITED, 17 Warwick Square, Paternoster Row, London, E.C. • 1913. F, WHITE Typ., 344 Kent Street Sydney. ESSENTIAL OILS OF THE ANGOPHORAS. 113 The average yield of oil was 0*19 per cent. The crudeoil was somewhat darker in colour than that of A, Bakeri,due to the larger amount of ester and free acid in the oil,the latter more readily attacking the iron of the still. Theodour resembled that of A. Bakeri, and the aromaticsecondary odour was also similar. The chief constituents in the oil of this species wereidentical with those in the oil of A. Bakeri, although thegeranyl-valerianate was a little more pronounced, as wasalso the sesquiterpene. Phellandrene and cineol were, ofcourse, both absent. The crude oil had specific gravity at 15° C. = 0.8809 ;rotation aD = + 24°.9; refractive index at 21°.5 = 1*4678 ;and was insoluble in 10 volumes 80 per cent, alcohol.
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