VOL. 77 JULY 1954
ee oo
TRANSACTIONS OF
THE ROYALE SOCIETY
OF SOUTH AUSTRALIA
INCORPORATED
CENTENARY VOLUME
ADELAIDE
PUBLISHED AND SOLD AT THE SOCIETY’S ROOMS
KINTORE AVENUE, ADELAIDE
Registered at the General Post Office, Adelaide,
for tranmission by post as a periodical
VOL. 77 JULY 1954
TRANSACTIONS OF
THE ROYAL SOCIETY
OF SOUTH AUSTRALIA
INCORPORATED
CENTENARY VOLUME
ADELAIDE
PUBLISHED AND SOLD AT THE SOCIETY’S ROOMS
KINTORE AVENUE, ADELAIDE
Registered at the General Post Office, Adelaide,
for tranmission by post as a periodical
ROYAL SOCIETY OF SOUTH AUSTRALIA
INCORPORATED
OFFICERS FOR 1953-1954
Patron
HIS EXCELLENCY AIR VICE-MARSHAL SIR ROBERT GEORGE
K.B.E., C.B., M.C.
President
J. K. TAYLOR, B.A., M.Sc., B.Ag.Sc.
Vice-Presidents
R. V. SOUTHCOTT, M.B., B.S. S. B. DICKINSON, M.Sc.
Secretary Treasurer
L. W. PARKIN, M.Sc. H. M. HALE
Editor
I. G. SYMONS
Librarian Programme Secretary
N. B. TINDALE, B.Sc. T. D. SCOTT, B.Sc.
Members of Council
D. C. SWAN, M.Sc.
S. J. EDMONDS, B.A., M.Sc.
M. F. GLAESSNER, Ph.D., D.Sc.
C. M. DELAND, M.B., B.S.
C. G. STEPHENS, D.Sc.
Auditors
F. M. ANGEL N.S. ANGEL
CENTENARY MEETING OF THE ROYAL SOCIETY OF
SOUTH AUSTRALIA
The Centenary Meeting was held in the Mawson Theatre in the University of Adelaide,
on 24 September 1953, in the presence of the Society’s Patron, His Excellency the
Governor of South Australia, Air Vice-Marshal Sir Robert George, K.B.E., L.B., M.C.,
and Lady George
> VP,
CENTENARY OF THE SOCIETY
By S. B. Dicx1nson*
President of the Society
On this occasion of the centenary of the foundation of the Royal Society
of South Australia it falls to my lot as President to extend to Your Excel-
lency a cordial and warm welcome. We are honoured to have you as our
patron and we also bear in grateful memory the services which have been
rendered by your predecessors. We are equally delighted and honoured that
Lady George has been able to attend this historic meeting.
We welcome the Hon. R. Rudall, Minister of Education, representing
the Government which has given the Society its support over many years.
I also welcome the representatives of kindred societies and other scien-
tific bodies and the many distinguished scientists who have honoured us with
their presence.
Messages of greeting have been received from:
The Royal Society of London; The Linnean Society of New South Wales;
The Royal Society of Australia; The Royal Society of New South Wales; The
Royal Society of Victoria; The Royal Society of Western Australia; The Royal
Society of Tasmania; The Royal Society of Queensland.
On an occasion such as this, when the Royal Society of South Australia
has completed a century’s honourable service to the community, something
different, it seems, should be said, something in recognition of the special
occasion.
We have great cause to be thankful that our Society has been permitted
to survive the full span of 100 years. We are thankful for the honoured place
' it holds in the community, for its friendly association with its kindred scien-
tific societies, for its achievements. Many of its fellows have gained high
renown.
It is natural on this occasion to let our minds wander back and think of
our beginnings when the Society was originally launched on its voyage on
January 10th, 1853. On that day five prominent Adelaide citizens met
together to organise learned discussions on subjects connected with literature and
art. At this meeting the Adelaide Philosophical Society was formed, which later
became the Royal Society by merely a change of name.
I do not intend to say anything about our early history, as much on that
subject will be found meticulously recorded in past numbers of the Trans-
actions™, except to remind you that our originators, besides pledging them-
~
©) R. S, Rogers—“A History of the Society, particularly in its relation to other
Institutions in the State.” Presidential address, Transactions and Proceedings of the
Royal Society, 46, 1922.
C. T. Madigan —"“The Past, Present, and Future of the Society, and its relation
to the Welfare and Progress of the State.” Presidential address, Transactions and Pro-
ceedings of the Royal Society, 60, 1936.
* S. B. Dickinson, M.Sc., Director of Mines, South Australia.
en ee
il
selves to the promotion of public interest in literature and art, also dedicated
themselves to the pursuit of scientific knowledge. This association of scien-
tific and literary interests was perhaps the most outstanding feature of our
early beginning. A more enlightened objective can scarcely be put forward
today when it is becoming more and more apparent that education and cul-
tural interests need to include something of science as well as of literature.
With these noble aspirations it 1s no wonder the Society grew and
flourished.
In the year 1880 Her Majesty Queen Victoria graciously acknowledged
the Society by becoming its Patron. Her Majesty also approved the Society
being styled the Royal Society of South Australia. This title is one of our
most precious possessions, To us it implies a direct association with the
Royal Society of the United Kingdom, and with it the inheritance of a great
name and great responsibilities. We acknowledge gratefully the continued
patronage accorded to us by your Excellency. Jt preserves this link with
the Mother Country, with the Royal Societies of the British Commonwealth,
and the traditions and work which have won the respect of the scientific
world.
In these brief introductory remarks I have not sufficient time to bring
to your attention the many achievements of the Society. Neither is it pos-
sible for me to pay tribute to the many fellows, both past and present, whose
energy and devotion to the pursuit of truth have built up the Society’s
treastire house of knowledge. From the subsequent addresses, however, I
feel you will gain a clear concept of the debt we owe to our members, who
during the past 100 years have given worthy intellectual and scientific guid-
ance to the people of South Australia,
Tt is difficult for the man of the world to understand the altruistic spirit
which induces men of science to band themselves together in societies having
for their sole aim the advancement of knowledge in particular directions; and
in very many cases sacrifice their leisure, and draw upon their limited
resources, not only that knowledge may be increased, but also that the gain
may be published to the world, which is free to make use of it; yet such is
the case.
The publications of otiginal scientific work by the society have been
continuous for 76 years and are to be found on the shelves of every important
scientific library throughout the world.
In its early years the Society participated much more prominently in
public affairs than it does today. It was not uncommon for the Governor
of the State to occupy the Chair, and for the Chief Justice, the Judges, the
Surveyor-General, the Postmaster-General, and leading educationalists and
newspapes editors to engage in lengthy discussions and present reports on
matters relating to development of the Colony. Actually it was the only body
in the country, at that time, which could speak with any authority on matters
of education and pure and applied sciences. The old Society was thus the
forerunner of many of our public institutions and of nearly all the scientific
bodies which have arisen since. It played a major role in the establishment of
the Public Library, the Museum, and the Art Gallery. Its efforts led to the
establishment of many of the Government departments. It was prominent
in the original movement for the establishment of the University in this State.
It is thus fitting that we should be celebrating this historic occasion within the
University. I desire to express our thanks to the Chancellor, the Vice-
Chancellor and members of the staff of the University for their undiminished
support of our efforts. It has aided us immensely in living up to our professed
objective—the advancement of knowledge.
iil
With the establishment of the educational institutions in the State,
especially the University, the interests of the Society gradually turned to
essentially scientific pursuits. Professor Ralph Tate, the first Professor of
Natural History in the University, became the soul of the Society during
these transition years. Besides encouraging original work, an equally strong
desire prompted him to spread scientific knowledge and promote its general
use by the ordinary citizen. His untiring efforts led to the establishment of
the Field Naturalists’ Section of the Society, which encourages the study of
natural history essentially as a hobby. This Section has become a very active
body. Its efforts in collaboration with those of the Fauna and Flora Pro-
tection Committee have been responsible for much of the legislation relating
to the protection of ainmals and plants and also for the establishment of our
National Parks.
In its career of scientific endeavour, which we may date from the foun-
dation of the University, the Society may properly claim to have done out-
standing service. It makes one award for distinction in scientific work and
that is the Sir Joseph Verco Medal. Sir Joseph Verco was one of the greatest
workers and most outstanding personalities in our later history. The award
is made at such times as the Council considers there is a worthy recipient.
They have been made to Professor Walter Howchin, Mr. J]. M. Black, Sir
Douglas Mawson, Professor J. B. Cleland, Professor T. Harvey Johnston,
Professor J. A. Prescott, Mr. H. Womersley, Professor J. G. Wood, Dr. C. T.
Madigan and Mr, H. M. Hale, whose names are prominently recorded in our
annals of science.
Throughout its career the Society has been materially assisted by the
Government of the State in many ways, and continues to enjoy its support.
The annual Government grant largely provides the means of publishing the
results of investigations. For such Government assistance the Council is
truly grateful.
In conclusion I would like to strike a note of dedication. Every conquest
of science brings the human race nearer the day when it will have complete
control over the forces of nature and be able to use them for its own purposes.
I think it is obvious to us all that we have now moved into an era in
which science can be no longer regarded as something extraneous or additional.
On the other hand, it has become an essential part of our everyday life. There
must therefore be no resting, satisfied with achievements, but persistent
endeavour.
Success in the discovery of new natural facts and relationships, however,
is not enough. Whether good or evil uses are made of these discoveries
depends on the aims and character of the community, rather than upon the
studies themselves.
~ I would therefore urge the Society towards a new outlook of service to
the community as well as to science itself. What is more urgent now is to
integrate scientific work and human needs and to do something to lessen the
gap of ignorance between the scientists and the public—a gap that is widen-
ing as scientific specialisation proceeds, Let us hope that the Society will
have an even greater influence in the future than it has had in the past 100
years in this country of ours.
lv
THE BIOLOGICAL SCIENCES
By Wititam P. Rocers *
The body of knowledge which we call the biological sciences covers a
wide field; it embraces a complex of interrelated disciplines. Until recently
it was convenient to divide these disciplines into two groups. One, descrip-
tive biology, included such subjects as morphology, natural history and
taxonomy. The other was called experimental biology and covered such
subjects as ecology, genetics and physiology. But today this type of distinc-
tion between the different biological sciences is going. ‘There is now, for
instance, a branch of biology known as experimental morphology; at one
time the two words would have been regarded almost as contradictory, The
systematist, once regarded as a completely descriptive biologist, cannot even
grasp the significance of his fundamental unit, the species, if he has not an
understanding of ecology and genetics. And, in turn, both these sciences
are Jargely based on an understanding of physiology.
The modern division of biology is not so much between experimental
and descriptive biology but rather between analytical biology and its opposite.
This distinction is tnportant; the major contributions in modern biology,
however diverse they may be, have certainly been made by the analytical
treatment of biological problems. It is difficult to define non-analytical
biology. In Medawar’s words, its field “is hardly yet coherent enough to
have earned itself a special name, but the distinction is partly co-extensive
with the antithesis between vitalism and mechanism, and yet again with the
antithesis between Lamarckism and selection theory.” Indeed, Medawar
considers that, “the threefold belief in vitalism, holism and the inheritance
of acquired characters, combined with an active detestation of mathematical
analysis is a syndrome which has now acquired an almost clinica] dignity.”
This, I think, is the best way to regard non-analytical biology.
In the history of biology in any country we see first the growth of
descriptive biology and later, its merging with experimental biology which,
in its broader aspects, becomes analytical biology. This is the typical and
proper growth of biological science and we see something of this sort of
development in the papers of the Proceedings and Transactions of the Royal
Society of South Australia. The descriptive phase gives us the anatomy and
classification of the plants and animals of this State. Later, with this know-
ledge as background, the examination of the relationships of the organisms
with one another and the environment began and publications in ecology
appeared. At this stage, interest in physiological and genetical investigations
also developed.
As our knowledge of biology passes through these phases it loses more
and more of its local character and becomes, part of general biological science
without particular geographical significance.
The history of biological science in South Australia was fully discussed
by several speakers on the occasion of the centenary of South Australia in
1936. In particular, the late Professor Harvey Johnston looked back over
our publications in zoology. Professor J. G. Wood chose rather to look
forward and ended his address with a discussion on the role of plant
physiology. I will not attempt to review the matters so ably discussed on
that occasion. Rather I would like to discuss what I think would be the
most fruitful way in which biological sciences should develop here in the
future.
* Professor W. P. Rogers, Ph.D., University of Adelaide.
v
I suggest that problems should be investigated not only for their local
interest, but largely with the view that such investigations can make valuable
contributions to biological science in general. Two examples from investi-
gations in animal biology already carried out here will show what I mean.
In a C.S.I.R.O. laboratory, under the leadership of Mr. H. Marston,
what was first a problem in the biology of ruminants of particular signifi-
cance in South Australia has developed into a study of importance the world
over. Thus a problem arising from the deficiency of cobalt in certain pastures
of South Australia has developed into a problem in the metabolism of
vitamin B,,.
In the University, Dr. W. R. Adey has been studying the anatomy and
physiology of the marsupial brain. The marsupial is an animal which is
almost exclusively Australian and thus this work had initially a particular
local flavour. But the results obtained have a very wide significance and
throw light on the cortical perception of deep-seated sensations in mammals
generally and thus are of importance in the general field of animal biology.
If this sort of pattern of development of biological science is to be fol-
lowed in South Australia, what are the chief investigations which have local
significance and yet would have an important bearing on biological science
in general? In animal biology, I think that these problems are fairly obvious.
The first deals with animal ecology. We have in South Australia
ecological problems which are almost unique and the solving of these prob-
lems will have important repercussions in the general field of ecology, The
climate and terrain, the animals and plants in many parts of South Australia
are such that investigations can lead to clear cut results which could not
be obtained in the more complex ecological conditions which prevail in many
other countries. In fact, 1 believe that the investigation of these problems
js something of an obligation; the problems are ours and we have a particular
responsibility to examine them.
The second field of investigation that I think we should take pains to
encourage is that of biology of the marsupials and monotremes. Here we
have a host of problems which are peculiarly Australian but the solving of
them would be of great importance in gaining a fuller understanding of the
higher mammals. The early biologists in South Australia have recognised
these problems and much fine work on the anatomy and natural history of
the marsupials has already been published. But the study of the physiology
of these animals has hardly been attempted, Admittedly the problems are
difficult but that only serves to make our responsibility the greater.
You may perhaps wonder why I should, at this centenary meeting of
the Royal Society of South Australia, give so much emphasis on the matter
of future development of biological science in this State. It is because I
feel very strongly that the Society should take a more active part in encour-
aging the development of biological research. In the past the Society has
played an important but somewhat passive role; it has provided a meeting
place where people could discuss their work and has provided a journal in
which results could be published. It has initiated many schemes which have
aided the development of science in South Australia. In this way it has
given outstanding service in assisting science, particularly in the early years
of South Australia, but in the future, particularly in relation to academic
biological research, I believe that it has an even more important and active
part to play.
To give you the premises on which I base this suggestion I must
briefly review the changes which have occurred in biological science generally
since the activities of the Society were reviewed in 1936. Since that time
two inter-related factors have had considerable effects on the development
vi
of biology. These factors were the growth, or rather the practice of certain
extreme political philosophies and the war of 1939-1945. Both these factors
have led to an increased pressure on biology, both from the “philosophical”
and technicological points of view.
It has become clear that the distortion of biological science to serve
particular brands of political philosophy can have most unfortunate effects,
and, indeed, can lead to the undermining of fundamental importance of fac-
tual evidence on which science is built. It is of course unlikely that circum-
stances in Australia will change and that science here will have to suffer the
indignities that it has in some countries. Nevertheless, bodies such as the
Royal Society of South Australia, which are devoted entirely to the further-
ance of scholarship and research now have an increased responsibility in
preserving the independence of scientific thought.
Now let me consider the effect of the war on the technicological devel-
opment of biological science. During the war the scope of applied biology
was suddenly expanded into a wide variety of previously unconsidetred fields.
Biologists took part in the development of operational research; air, tank,
and submarine crew physiology became important fields of investigation ;
entomologists worked with the troops in many forward areas, Parasitolo-
gists, particularly from America, moved from their laboratories and applied
their knowledge to practical matters in the field. Biologists became involved
in the researches of biological and chemical warfare. There was a wide
recognition of the part biology can play in practical matters and this has led
to an increased pressure on the application of biology for economic purposes.
In those fields of applied biology such as agriculture and medicine which
have been so important in the development of mankind, the importance of
fundamental research has been recognised and efforts have been made to
maintain a basis of fundamental knowledge on which application depends.
But I fear that the application of biological science to economic problems
generally may soon, if it has not already, outstrip our fund of basal informa-
tion, and become even more empirical than it has been in recent years. If we
are to keep a proper balance between applied and academic biological
research, the increased support for applied biology should be paralleled by an
increased support for academic investigations.
I have in this discussion somewhat exaggerated the division between
applied and fundamental biology. As far as the more able biologists are
concerned, this distinction does not really exist. The biologist studying the
economic problem usually has to return continually to the fundamental
aspects if he is to solve his economic problem. But in many parts of the
world those on whose support biologists are dependent for the wherewithal
to carry out their work frequently make an undue and false distinction
between what is “useful” biological research and what is not.
It is here again that I think events have thrust increased responsibilities
on learned societies as supporters of academic research. The success of the
Royal Society of South Australia during the next century of its history may
well depend upon the vigour with which it upholds the independence of
scientific thought and the value of scholarship in scientific research,
vii
AGRICULTURAL SCIENCES
J. A. Prescott *
In the early years of any organization such as a learned society a great
deal of interest is usually taken in the “Arts” as well as the “Sciences,” and
by the arts we understand all those branches of human activity which demand
some special personal skill whether this be handling the plough, painting a
picture or producing a fire by rubbing two sticks together. It is appropriate
therefore that the early records of the Adelaide Philosophical Society should
have included a number of papers on agriculture which dealt with such mat-
ters, on the traditional level of the art, as the fertility of soils, the drying of
fruits, the preservation of meat, viticulture and the fermentation of grape
juice, all of which subjects had already acquired a skill based on long tradition
and experience in overseas countries. The science of agriculture was to come
later, first in its efforts to explain traditional practice and later, by research,
to enlarge the basis of knowledge on which the art itself could be developed.
In a young country such as Australia, traditional experience sometimes
breaks down or is of no avail and research becomes in fact, as no doubt it has
always been, an art itseli—that of manufacturing experience. C. T, Madigan
in his presidential address in 1936 to celebrate the Centenary of the State
recorded that the word “Arts” was quietly dropped out of the interests of
the Society when the rules were revised in 1902.
In dealing with the development of agricultural science in South Aus-
tralia the Society contributed notably through the awareness of one of its
Presidents, E. H. Rennie. In two presidential addresses, those of 1889 and
1901, Rennie concerned himself with the application of his own science of
chemistry to the agricultural needs of the Colony and State, The land now
occupied hy Roseworthy College had been purchased and established as an
experimental farm in 1881 and the College itself opened in 1884 under J. D.
Custance. It was under W. Lowrie’s direction from 1887 until 1901, and
Rennie was in close touch with Lowrie during this period and subsequently,
It was Rennie who took me to see Lowrie on his farm at Echunga when I
reached Adelaide in 1924.
In his address of 1889, Rennie concerned himself with the reputed decline
in wheat yields in relation to soil exhaustion. He referred to the need for
conserving all materials for manurial purposes, such as wood ash, bones and
farmyard manure and deplored the export of superphosphate and sulphate of
ammonia from the colony which was then actually taking place. He realised,
moreover, that the conservation of all possible materials of manurial value
would still be inadequate. “Is it not desirable,” he said, “that experiments
should be undertaken with a view to discovering what are the best methods
of farming in this colony under varying conditions?” He advocated among
other non-agricultural things the production of salt by solar evaporation.
In 1901, when Rennie gave his second address, the agriculture of the
newly formed State was passing through a critical period. Since his pres-
idential address eleven years before, the average yield of wheat in the Colony
had been rather less than five bushels per acre. He claimed there was a
“crying need for accurate scientific investigation, such investigation being
necessary, not merely to elucidate scientific theories but to improve our
material condition.” He was deeply impressed by the very recent European
work on nitrification and nitrogen fixation and recognised the importance of
* Professor J. A. Prescott, C.B.E., D.Sc, A.LC., F.R.S., Director, Waite Agri-
cultural Research Institute, Adelaide.
vili
using peas as a crop for raising the nitrogen level of the soil. He recalled
that Lowrie was puzzled by the small responses of wheat to nitrogenous
fertilisers and that he had attributed this to something that took place in the
process of barefallowing. To Lowrie, the most likely process appeared to be
the fixation of nitrogen by bacteria in symbiosis with algae. Later scien-
tific work established, however, that the nitrification of the reserves of nit-
rogen already in the soil adequately accounted for this.
Scientific investigations on behalf of agriculture of the kind envisaged by
Renhie had to wait, however, nearly 25 years, with the foundation of the
Waite Institute by the University in 1924, Even the need for such a Federal
body as the Commonwealth Scientific and Industrial Research Organization
was foreseen by Rennie for he referred to the advocacy by Sir John Quick
in the first Federal Parliament for an organisation similar to that of the
United States Department of Agriculture. Referring to the current develop-
ments in America and in New South Wales, Rennie said, “We must have
similar work done here.”
I have no doubt whatever that he had a great influence with the Council
of the University in determining its policy when the splendid gift of Peter
Waite became available for the benefit of agriculture in South Australia.
Some practical problems needing urgent attention according to Rennie
were the losses, failures and distresses in the irrigation settlement at Ren-
mark, the depredations of insect pests, the pathology of plant diseases, dis-
eases of wines and rural engineering, Apart from rural engineering, the need
for which is still being discussed, the others have all been taken up at the
Waite Institute either as activities of the University or of the Commonwealth
Research Organization. The soil survey of Australia began in fact at
Renmark.
In the earlier years there were occasional papers, to the Society on some
of these problems. Diseases of wheat had been discussed by the Philosoph-
ical Society. In 1879, J. G. O. Tepper presented a paper on wheat rust and
in 1880 on potato moth. In 1884 F. S. Crawford dealt with the disease of
apricots. Samuel Dixon (1884-1892) took a special interest in native shrubs
as fodder plants and in the effects of settlement and pastoral occupation on
these plants, an interest later to be reflected in the work of T. G. B. Osborn
and J. G. Wood at the Koonamore Vegetation Reserve and published by the
Society in 1925,
The first meeting of the Society which I had the privilege of attending
was that of October 1924 and I recall the important paper then presented
by T. Harvey Johnston on the relation of climate to the spread of Prickly
Pear in Australia. This proved to be the first of a series of papers in applied
climatology to be presented to the Society during the next twenty five years
or so dealing with climate in relation to insect pests, to agricultural pos-
sibilities and to plant introduction. Most, if not all, of this work has been
contributed by officers of the Waite Institute, including J. Davidson, H. C.
Trumble and J. A. Prescott and has had as its background the search for
better criteria of the efficiency of the rainfall than could be provided by the
crude rainfall figures themselves. This work has emphasized the importance
of the evaporative power of the air in modifying the value of the rainfall and
there has been a constant conscious search for criteria which would have the
widest possible application. An interesting development of this work has
been the study of evaporation by C. W. Bonython (1950) arising out of the
need to measure the efficiency of the production of salt by solar evaporation
which may be recalled was mentioned by Rennie in 1889.
This work in climatology also illustrates one of the functions of a society
such as ours. Climatology is the meeting ground of meteorology and geog-
ix
raphy. Any new principles involved in its study must be tested out against
a geographical background and South Australian agriculture and biology
have provided such a background, with Australia as a whole as an extension
of South Australian experience. The Transactions of the Society provide the
ideal medium of publication for such work and it is only at a later stage when
the concepts have matured and been tested in time and can be applied with a
wider geographical framework that publication overseas becomes appropriate.
The most characteristic contribution of the South Australian school of
climatology as recorded in our Transactions has been the establishment of
criteria whereby the length of the season favourable to agricultural and pas-
toral production can be determined as well as that favourable to certain
aspects of insect activity. New methods of characterising temperatures in
terms of the mathematical analysis of the wave form of the annual curve of
mean monthly temperatures have enabled temperature regimes to be more
conveniently defined and this method has been proved particularly useful in
seeking parallel climatic regimes in other parts of the world, specially in
relation to the introduction of new plants to Australia and in relation to the
understanding of the success or failure of species already introduced. The .
success for example of the Monterey pine (Pinus radiata) in South Australia
is related, as was shown by J. A. Prescott and C. EF. Lane-Poole (1947), to the
close parallels in many respects of the climatic regimes of the coast of Cali-
fornia and of south eastern Australia.
Climate is, however, but one aspect of the South Australian environment
and it is natural that the two other ecological components, namely vege-
tation and soils, important in biology, as in agriculture, should have received
attention.
. The basal information on which all vegetation studies must be based is
the systematic account of all the plant species to be encountered in South
Australia—those that are native and those that have been introduced. The
outstanding contribution is, of course, that of J. M. Black whose 45th
addition to the Flora of South Australia appeared in the volume for 1950,
In another field, that of enumeration of species and in relation to their
geography, J. B. Cleland has made important contributions. The first con-
tribution on ecology proper—that is the relationship of plants to their sur-
roundings—came in 1922 when T. G. B. Osborn published two papets in our
‘Transactions—one relating to the Franklin Islands and the second in collab-
oration with R. S. Adamson, a visitor from South Africa, dealing with Ooldea
on the Transcontinental railway. In 1924 there followed the account by these
same two authors of the ecology of the Mount Lofty Ranges and there was
then established by Osborn’s student and successor J. G. Wood and by
Wood’s own students a series of contributions on the ecology of South
Australia which form the basis of the understanding of the vegetation
associations of the State and have further presented opportunities for testing
out ecological concepts developed overseas in an Australian environment.
The plant associations of many parts of South Australia are now reason-
ably well established and one need mention only the work in more recent
years of R. L. Crocker (1944, 1946) R. W. Jessup (1946, 1948, 1951) R. L.
Specht (1948, 1951) and C. D. Boomsma (1946, 1948) to realise how much of
the State has been covered. To one, like myself, who has watched this
development and made frequent use of the information so obtained there is
a continuous tradition starting with Goyder and his line of rainfall presented
in a Parliamentary paper (1866), through the work of our Land Surveyors
and land Valuers to this modern assessment of the resources of the State.
It is fortunate that we have in Australia such large areas of unspoiled
native vegetation, so closely dependent on soil and climate. The surveyors
of this State, as of the other States, have been able to use the description of
our native vegetation as an aid to land classification and this has been
extended to the modern work in soil surveys. These soil surveys and other
work of a more general character on the soils of South Australia have estab-
lished the existence of a range of fertility levels in our native soils which can
most frequently be defined in terms of phosphate content in the soil. Wood
(1939) was able to demonstrate how closely the vegetation associations then
recognised in the State, could be related to this level of soil fertility, to the
degree of soil acidity and to the rainfall.
In the agricultural development of the State, it is almost always necessary
to replace the native vegetation, particularly where this is heath or scrub,
by new associations of pasture plants needing a very much higher level of
soil fertility. The ecological principles established in the study of our native
vegetation can still be applied by the agronomist to the introduced pastures
and to the crops with their associated weeds. There are still however—and
we tend to overlook this—large areas of native grassland and shrub steppe
where the most important problem at the moment is the management of these
areas so as to maintain for all time what is in itself a yaluable asset to the
State. The work of the University Schools (Botany and Waite Institute)
at Koonamore and Yudnapinna should play an important part in, the devel-
opment of scientific principles of pastoral management and this could be
extended to the nearer pastoral country of our mid-north.
The native and introduced plants provide food for a wide fauna, and the
ecology of this fauna, particularly of the insects, has afforded an opportunity
for a series of studies on insect ecology of which the most typical are perhaps
those relating to the two grasshoppers with which we have been plagued
from time to time. The work of J. Davidson (1936) and H. G, Andrewartha
(1940, 1944) are outstanding examples of this kind of work,
The edaphic element in the environment has been the subject of a series
of papers on soils, starting with the paper by Prescott (1927) on the reaction
of our South Australian soils in which the close dependence of soil acidity
on rainfall was first demonstrated for the State and paved the way for further
studies of soils in relation to the climate in which they were encountered.
This led further to the recognition that some soils, those derived from laterite,
and common in the State, owed many of their properties to conditions in the
Pliocene or Miocene and our transactions include a few papers dealing with
laterite. The two major soil groups, the Mallee and the Red Brown Earths
were described in 1932 and 1938 and many of you may recall the extraordin-
ary interest displayed by our members in a paper by C. S. Piper (1932) on
the soils used in the preparation of turf wickets. Formal soil surveys are
not normally suitable for discussion in our Transactions but they afford
many opportunities for pedological discussion amongst which we may include
the mathematical presentation of C. G. Stephens (1947) on soil forming
factors.
Agriculture, as crop and pasture husbandry and even as animal hus-
bandry is in one sense applied ecology and there will always be a scope for
the Society in dealing with the South Australian environment. In the second
sense of applied physiology the opportunity is experimental rather than des-
criptive and for this reason is rarely presented to or discussed in our meetings
—even some aspects of climatology are now reaching the experimental] stage.
in which the water needs of plants are being determined directly by experi-
ment rather than deduced from observations on natural phenomena.
There is still scope however for much descriptive work; our arid regions
in particular, afford abundant scope for studies of soils and climate in relation
to geo-morphology. In soil chemistry there is in sight the possibility of much
xi
work in defining the geochemical provinces of the State, particularly as the
geology and particularly the petrology of the State is so much better known
than was the case 25 years ago. Such studies will give a sounder chemical
background to the understanding of the nature of our problems in soil fertility
particularly with respect to phosphate, to potassium and to the micro
elements.
On the more purely ecological side I should like to see a greater devel-
opment of interest in the physical properties of the soil profile, particularly
the capacity for retaining useful water.
These two groups of studies linking geology through the soil with the
plant associations could be conveniently defined as edaphics. It is in this
direction, I believe, that descriptive science will have most to offer to
agriculture in the next twenty five years or so.
xt
THE ROLE OF GEOLOGY
IN THE ACTIVITIES OF THE ROYAL SOCIETY OF SOUTH AUSTRALIA
By D. Mawson *
What was later to be known as the Royal Society of South Australia
was initiated on the 10th January, 1853, under the title of The Adelaide Phil-
osophical Society. At that time the membership was small but comprised
the State Governor and most of the leading citizens of the period. Their
deliberations were stated to comprise discussion of “all subjects concerned
with science, literature or art.”
Observations of a geological nature were in a minority in those days,
During the 23 years period prior to the change of status in 1876, when it
became known as the Royal Society of South Australia, geological discussions
amounted to only about 10 per cent of the transactions.
The first geological paper was introduced in the gold rush period, at the
October meeting of 1854, That was: “The Geology of Bendigo Gold Field
with speculations on the origin of the Gold” contributed by W. H. Light, who
had been engaged in gold mining at Bendigo, Referring to the auriferous
quartz reefs he advocated that these have a plutonic origin and “were prob-
ably injected in a liquid state from great depths below into veins and crevices
in the stratified rocks.” An explanation which, you will agree, is correct only
in part unless we interpret his “liquid state” as an aqueous solution,
The most notable contributions of that time so far as geology is con-
cerned were several papers by the Rev. Tennison Woods, who was a really
able geologist of that period. He dealt with fossils in the Marine Tertiary
Limestones of the South East of the State. Also there was delivered by the
same author a general paper on the Geology of that area.
The Chief Justice, Hanson, also contributed a lengthy observation on
the geology of the South East, in part intended to correct what he regarded
as weaknesses in Tennison Woods’ arguments. However the latter showed
the amateur geologist Hanson to be in error,
By the year 1872 the Adelaide Philosophical Society had reached a very
low ebb, in fact meetings were suspended for a time. There then arrived in
Adelaide, in the person of Professor Ralph Tate, a dynamic character who lost
no time in reorganising the Society. From thence onward, as the Royal
Society of South Australia it has flourished: a very active organisation and
valuable recording medium for discoveries and developments of scientific
interest within the State.
This advance in the status of the Society coincided with the establishment
of the University of Adelaide which resulted in an accession to the community
of men of scientific and literary standing. That geology should figure prom-
inently thereafter was to be expected, with Professor Tate in the role of prime
mover and President for some years. However, Tate was absorbed not only
in Geological studies but as Professor of Natural Philosophy was required to
cover Botany as well as Geology, With these two interests at heart he soon
reconnoitred large areas of the State and set the foundations for the Geology
of South Australia.
To the time of Tate’s arrival the known fossiliferous strata were
restricted to the Cainozoic Era, and in that division Tennison Woods had
already pioneered the ground in the South Eastern division. Tate rapidly
advanced knowledge of the nature and fossil contents of the marine Tertiary
strata of South Australia, well illustrated in his series of papers published in
the Royal Society’s volumes.
* Professor Sir Douglas Mawson, O.B.E., D.Sc, B.E., F.R.S., University of
Adelaide.
xiii
Tn 1875 trilobites and coral-like fossils from near Maitland on Yorke Penin-
sula were submitted for identification. The latter were eventually identified as
archaeocyathids, The rock formation in which they were obtained was in
the first instance, referred to the Silurian Period, but was later determined as
Cambrian. That discovery was however an isolated occurrence. It was not
until long afterwards that Cambrian fossils were located, widely distributed
in many parts of South Australia.
For years Tate kept a sharp lookout for fossils in the older rocks of the
Mount Lofty Ranges. He was so far unsuccessful that in 1896 he was so cer-
tain that those formations would not be found to yield fossils that he wagered
he would “eat my hat” if Professor T. W. E. David, then visiting Adelaide,
should succeed in discovering any. A few days later David when in company
with the Reverend Walter Howchin, in a field trip south of Adelaide, found
fossil archaeocyathids in the limestones of Sellick’s Hill.
About the time of Tate’s arrival in South Australia, Mesozoic fossils were
found in the far north and it became apparent that the Great Artesian Basin
extended from New South Wales and Queensland far into North Eastern
South Australia.
Thus it was apparent that Tate and the revitalised Royal Society were
responsible for a marked advance in the study of Geology in this State. But
the Society’s influence did not stop there, for in 1877 they pressed the Govern-
ment to appoint a Government Geologist. It was realised that a territory the
size of South Australia, then the largest section of all Australia, for it
included under its jurisdiction Central Australia and the Northern Territory,
must embrace important ore deposits and geological problems of great
national interest such as underground water supplies. The outcome of this
advice to the Government was the appointment of H.Y.L. Brown as the first
Government Geologist and the initiation of the Department of Mines and
Geological Survey; the latter, in these days of our present President, has
blossomed forth on a grand scale.
Thus it was that Tate, during his 25 years of active association with the
Royal Society greatly advanced knowledge of the geology of South Australia.
During the last decade of that period these advances were stimulated by
another active and enthusiastic geologist who for some 40 years did yeoman
service for the Royal Society as its able honorary editor. This was the Rev.
Walter Howchin who had arrived in ill health in South Australia in 1882.
The salubrious climate soon restored his health and he gradually took an
increasing interest in local geological phenomena until in later years, after
appointment as lecturer in Geology and Palaeontology at the University of
Adelaide, he published “The Geology of South Australia.”
Howchin dedicated himself first and foremost to the self-imposed hon-
orary task of editing the Society’s volumes.
In his official position with the Society and with increasing geological
status, Howchin did much to maintain the geological tradition established by
Tate in matters relating to the Society.
Perusing the records I find that during the past 100 years about 364
papers dealing with definitely geological matters have been read before the
Society. Since Tate’s time, that is in the present series of volumes, the
strictly geological contributions have averaged 22% of the papers presented.
During the past 30 years, scientific activities in South Australia have been
greatly increased both by new developments and by expansion of existing
bodies. The scientific life of our community has become more specialised.
The Society no longer listens to dissertations on sewage. problems, reform-
atories and education. Other bodies specialising in more limited spheres of
xiv
enquiry have been established. The chemists, the physicists, the engineers
and the medical fraternity now all have their own organisations. However,
the parent body still remains in full vitality and should always constitute a
forum for students of general and fundamental science though less so for
those involved in the specialisations of applied science.
Our Society should not only provide a medium for the publication of the
results of local scientific research, but would do well to foster a wider field
of activity. It could well be the local disseminator of the latest developments
in the world of science and guardian of the interests of Science in South
Australia. It was in these latter roles that the Adelaide Philosophical Society
functioned one hundred years ago.
Many far-sighted and beneficial developments in South Australia owed their
origin to the Society’s influence in matters of national importance. Thus
through the representations of our Society the following developments were
effected: the establishment of the State Geological Survey; the establishment
of the South Australian Museum and appointment of the Director; the estab-
lishment of the National Park and Flinders Chase; the gazetting of several
fauna and flora reserves. In fact the Royal Society, pressing for the Govern-
ment to undertake beneficial works, prompted most of the major develop-
ments in the State: amongst these may be mentioned the introduction of
universal Public Instruction and the Sewerage System for Adelaide.
Beginning somewhat more than 50 years ago, fostered by the Royal
Society, there was a period of pressure for soil and agricultural research. This
undoubtedly had an influence on the establishment of the Waite Agricultural
Research Institute.
AUSTRALIAN NEREIDAE INCLUDING DESCRIPTIONS OF THREE NEW
SPECIES AND ONE GENUS, TOGETHER WITH SUMMARIES OF
PREVIOUS RECORDS AND KEYS TO SPECIES
BY OLGA HARTMAN (COMMUNICATED BY S. J. EDMONDS)
Summary
The Australian (and New Zealand) Nereidae are recorded with 47 species in 13 genera. One genus,
Anstralonereis is new; two species, Ceratocephala edmondsi and Micronereis halei, and one
subspecies, Platynereis dumerilii antipoda are newly described. There are many new records of
distribution, particularly for the species occurring in the Flindersian and Peronian provinces. The
recorded data of all the species are summarised in a series of charts.
t
AUSTRALIAN NEREIDAE
Including descriptions of three new species and one genus,
together with summaries of previous récofds and keys to species.
By Guica HartMaAn *
Communicated by S. J. Edmonds
[Read & May 1953]
SUMMARY
The Australian (and New Zealawi) Nereidae are recorded with 47 species in 13 genera.
One genus, Ansiralonereis is ews two species, Ceratocephala edmonds and Micronerets halvi,
and one subspecies, Platyaereis diaverili antipoda ate newly described. There are many new
records, of distribution, particularly for the species occtirring in the Flindersian and Peronian
provinces. The recorded data of all the species are summarised in a series of charts.
INTRODUCTION
The polychaetous annelids of the family Nereidae are among the more con-
spicuous, well represented groups of marine invertebrates in the Commonweaith
of Australia. and the Dominion of New Zealand, As in other known geographic
areas, they are largely littoral. Curiously, however, the present study indicates
that the nereids, at least for the southern half of Australia, are unusually diversi-
hed and modified, probably more so than in any other geographic area of comi-
parable size. Thus, among the 47 species in 13 genera, there are some with very
primitive characters, such as presence of setae in the first segment; others, such
as Australonereis, have functional coelomoducts and papillaled ventrum. These
facts make it particularly desirable to recognize their positions or affinities with
the nerejds of other parts. of the world.
In spite of the fairly large number (47) recorded here, it can haedly be
assutned that the number of species is even nearly complete. Much of the coast-
line remains almost unknown with respect to its polychaetous fauna. The records
ta date are largely those made by incidental collecting. There have been no
extensive surveys of coastal arcas such as was done for the echinoderms (Clark,
1946),
Recent. studies by Knox (1951) on the nereids of New Zealand indicate that
there are conspicuous differences in the fauna of the Dominion and the Com-
monvwealth, at least for its southern halt, Coimparison has been difficult in many
cases for the literature is scattered and sometimes obsctire in essential details.
Type collections, if existing, are often deposited in museums outside of Australia.
Au attempt is here made to correlate and assemble these scattered data.
Charts I to IV summarize the records of the 47 species, including: acceptable
naine, date and source of original publication, place of origin, diagnostic accounts,
synonyms, distributional data and new records, ecologic niche. unique charac-
teristics, method of reproduction in so far as known, and the formulae of the
proboscidial processes,
The materials on which these studies are hased were collected mainly from
littoral zones of South Australia, Victoria and New South Wales, thus are largely
south-eastern Australia, These areas fall within the Peronian and Flindersian
provinces of Iledley. Kased on studies of the echinoderm fauna, H. L, Clark
(1946) finds that these two provinces have the most numerous endemic species
(82% of the Peronian and 89% of the Flindersian echinoderms are endemic in
Australiz), If the annelids are equally unique, as a comparison of the charts
indicates, one may expect a widely diversified polychaetous fauna.
* Allan Hancack Foundation of the University of Southern California.
Contribunon No. 148,
Trans Ruy Sac. S. Aust., 77, July, 1954
?
I am indebted to the following people and institutions for the collections on
which the present study is based: Mr. Herbert M. Hale and associates of the
South Australian Museum, Mr. S. J. Edmonds of the University of Adelaide,
and Miss Barbara Dew of Cronulla, New South Wales. The Administration of
the Allan Hancock Foundation of the University of Southern Californa pro-
vided material aid and support to conduct these studies, Illustrations are by
Anker Petersen of the Allan Hancock Foundation.
Types and complete series of species are deposited in the institutions from
which the collections originate. Duplicate series are in the Allan Hancock
Foundation.
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Key To GENERA AND SPECIES
Parapodia uniramouy i wae ae Nea tarnerets quadraticeps
Parapodia biramous after the second Perdponltnn tee rset gage fh quitin” Seapine (> the
First segment with parapodia (hg: t aT mous wee Mtcromereis halet
Fist segment a smooth ring (fig. 3 Pr | Tes Y Saar) Oe PS
Peristomium prolonged forward ventrally to encompass the prostomium
Cheilanereis peristomiatis
Peristominm not prolonged forward ...
Ventrum of antenor segments with rows of apie ( fig, 2) Australonereis ‘chlersi
Ventrum without rows of papillae... - fa. Was ei pros
Proboseis with fleshy, cirmis-like papillae (fig. 13) . eel uw Ceratocephala edmondss
Probescis with dark horny paragnaths on some or wll areas as «! “ui the
Probescis without processes, its epithelium smooth or at most wrinkled
Nicon uestuariensis
Paragnaths absent from oral tihng of proboscis .... ss00 min a. Ceratonereis
Paragnaths absent from maxillary Ging of proboscis... ane wis Eunereis marrt
Paragnaths typically presetit on hoth oral and maxillary rings of proboscis...
Parsgnaths in the form of pectinated rows on sume or all gress ke sth ina
Paragnaths in the form of conical, separated processes, ..., etal
Maxillary ring with conical, and oral ting with pectinated processes Preudunereis
Thoth Fings af proboscis with pectinated processes, or areas 1, If and V tstally bate
Platynerets
Area VI of proboscis with transverse ridges, or the ridges broken up inta poitits in
a straight transverse row a este Shee tees es Perinereis
Area VI of proboscis. with conical processes day S
Median and posterior notopodia with falcigers (fig. 30) ‘OF r also. ‘sflinigers is » Nereis
Notopodia with spinigers; lacking falcigers ..., se a4 ati Neonthes
Prostomium deeply incised at midfront; dorsal cirri very long Ceralonerets wivabilis
Prostomium hot incised in front; dorsal cirri nat unusually long .
Neuropodia with simple and composite Foleigers ine wu Ceratonereis er wihracensis
Neuropodia without simple falcigers ..
Dorsal and ventral cirri greatly reduced: area J “of proboscis “with 34 or “to 6.9.
Pointed patagnaths .... oft Ceratonereis anquisetis
Dorsal and ventral arri not ‘greatly “reduced; area J of prohoscis bare
Ceratonereis lapinigensis
Notopodia without homogomph falcigers .... 4360 a. Pseudonereis rotinestiana
Notopodia with homogomph falcigers in posterior segments Pseudonereis anomala
Notopodia with simple, heavy falcigers (fig. 38) in median and posterior segments
Platynerets bicanaliculate
Notopodia without simple falcigers. dao ses
Posterior notopodia with composite setae in which the aypetmboes “is strikingly
tidged transversely... dose ond Platynereis polyscalma
Posterior notapodia without setac that are ‘distally ridged Las ang ia dn
Posterior notopodia with homogomph falcigers (fix, 37) Oe EES be “ee
Pasterior notopodia without falcigers or only an occasional ineotispicuous one
Plafynereis nunalhacnyts
Modified natatory parapodia in female present afier segment 2
Peenieots dumenhi antipoda
Modified natatory parapodia in female present after segment 30
Platynercix australts
Area VI of proboscis with a single ridge on each side
(Includes Perinerets amblyodonta, barbara, calmani, helleri, cam
guina, obfuscuta, nigropunctata and pseudocamnguinu. See Chart 1V
for distinguishing characteristics of each.)
Area VI of proboscis with two ridges on each side
(Includes Perinerets camiguinaides, variodentafa and vancaunicit. See
Chart IV for distinguishing characteristics, )
Area VI of proboscis with four ridges on a side ..., we Pevingrcis ponmtensts
Area VI of proboscis with a continuous transverse series of cones that extends
across areas V and VI
(includes Perinerets vallata and brevicirrts. See Chart TV for dis-
tinguishing characteristics.)
Notopodial lobe diminishes in size ( fig. 26) in posterior segments a so vere
Nutopodial lobe does not diminish in size Rosterionly we amas oii
Homogomph falcigers distally boldly bifid (fig. a) vr <n Nereis jacksoni
Homogomph falcigers not hoklly bifid (fg, 30) ... vee wey Neveis cockburnensts
16
Vi
12
19
22 =Prostomium deeply incised at middle front ii; tee we ue Neveis falearia
22 'Prostomium not incised at middle front .. om Wo daily ee g fain Ps ae
23 + Notopodial faleigers boldly bifid -.. 2 ne ee Nereis denhamonsis
23 Notopodial faleigers not boldly Wiftl we Nerets peromiensts
24 Notopodial lobe comes to be very large on both sides of dorsal cirrus in medium
and posterior segments
: sha — a — ee wee Meanthes oxypoda
24 Notopodial lobe does not come to be so large ne ew tee ee e5
25 Areas 1 and V of proboscis nearly or quite hare .... =r tied niet mene aw «20
25. Area I, or also V of proboscis with paragnaths dete Hiee try erst 27
26 Notopodial lobe diminishes in posterior segments —~. we Neanthes kerguelensis
26 Notopodial lobe does not diminish in size in back sass wre Neanthes unrfasciata
27. Area V of proboscis bare; area I with 7 or §& comes in an oval patch
Neanthes anyusticallis
27 Area V with paragnaths; area [otherwise yi ter nsey tens nay none 28
28 Area l was only lor 2. comes... 0 cee ee ree Neanthes vaahi
28 Area 1 with many more cones .... pan any lume leads 7a we vs wa 29
29 Arcas V to VIII with a continuous band of many cones in 8 or 9 rows, to only
3 of 4 rows; area J with aboul 40 comes... ae ane Neanthes cricognatha
29 Areas V to VIII with a continuous band of cones, including @ single row of larger
cohes on the maxillary side of the area; area | with about 9 cones
Neanthes, neat ericugnatha
Australonereis, new genus
Type A, saverss (Augener), 1913
This differs from other nereid geticta most strikingly for having paired
fleshy transverse ridges (fig, 2) on the ventrum of anterior segments. The
armature of the proboscis consists of paired distal jaws and soft papillae on the
maxillary ring only; the oral ting is bare. The first segment ot peristomium is
a smooth, apodous. ring. The first two parapodial segments are uniramous; all
others are biramous. Notopodia have spinigerous, comrpesite setae and single
acicula; neuropodia have spinigers and falcigers. In ovigerous adults the median
and posterior segments have paired, papillar processes, presumably coelomostomes,
located on the dorsal side of notopodia, within the base of the dorsal cirrus.
Australonereis approaches Tylonereis Fauvel (1911, p. 376) in its pharyngeal
strictures, but in the latter all setae are homogomph spinigers. Leonnates Kin-
berg (1866, p. 168) also has membranous processes on the proboscis, but they
are limited to the oral ring, whereas the maxillary ring has horny paragnaths.
A single species, 4. chlersi (Augener) is referable to it,
AUSTRALONEREIS EHLERS! (Augener) 1913
Fig. 1-£1
Nereis (Leonnates) ehlersi Augener, 1913 pp. 142-145, pl, 3, fig. 53, text-ig,
WZ a-c,
Leonnates ehtlersi and Leptonereis ehlersi Monro, 1938, pp. 618-623, fig. 7-13.
Locality—Numerous individuals come from Lakes Entrattce, Victoria, on the
inner side of Ninety-mile Beach, where there 1s a considerable tidal current, and
where the watlet ig marine, [rom a sand spit uncovered at low tide; the worms
form beds and occupy U-shaped tubes in which the ends are uncovered (obserya-
tions by Miss Barbara Dew).
‘Australonereis ehlersi has remained known only through sparse catches from
the Swan River area, Western Ausiralia. The present numerous individuals came
from Lakes Entrance, Victoria. They are conspicuously large, measure to 140 mm.
long and 12 nm, wide with parapodia. The body is greatly depressed, especially
in its median and posterior regions, The following description 1s based on speci-
mens from Victoria,
On the everted proboscis the oral ring is dusky and smooth or irregularly
rugose; it lacks processes. The maxillary ring is pale and has a continuons band
of many, more than 50, short, cirrus-like processes in 3 to 5 irregular rows,
Fig. 1-6. Anstralonercis ehlersi
- Anterior end in dorsal view, including first 3 setigers, x 10+5.
Ventral side of body showing segments 10 to 17, x 5*2,
Anterior parapodium from papillated region, seen from the front, x 10+5
4A pire from the middle region of the body, seen from the front,
x 10-5.
$. A slightly more posterior parapodium seen in posterior view; x 10-5.
& A far posterior parapodium showing the Jarge coelomostome adjacent to
the small dorsal cirrus, x 51.
wh
21
They are fewest at the sides and most numerous midventrally; those on the oral
end are slightly larger than those on the maxillary one. They are limited to 2 band
that separates maxillary and oral parts, giving the impression, especially on the
retracted proboscis, of being oral, not maxillary (hence Augener’s observation
that they are oral). The jaws are translucent, light yellow to horny brown dis-
tally ; they have 7 to 9 short, oblique teeth along the cutting edge.
The first 6 parapodial segments have each a slender ventral cirrus on a
papillar elevation. From the seventh segment the ventriim has an additional eleva-
tion within the hase of the ventral cirrus and on the next 9 or 10 segmenits these
papillations increase to about 6 or 7 on a side (fig. 2). The ventrum in this region
is rugose, After segment 30 the papillations diminish rapidly and are absent from
posterior segments.
Parapodia of the first 17 to 19 segments differ from those farther back in
that their distal lobes (both notopodia and neuropodia) are thick and glandular,
The glands are most conspicuous at anterior sides of parapodia and reach their
maximum thickness and extent in segments 10 to 18, where the uppermost lobe
comes tn be transversely rugose and resembles the furrows of the venermtin in
the same region. After about segment 20 these parapodial areas are abruptly
absent, Dorsal and ventral cirri are slender, short and inconspicuous; they are
simple and tapering throughout the body.
Setae are in thick, yellow fascicles and most numerous in anterior segments.
Those in notopodia are entirely spinigerous (fig. 11). Neuropodia have both
spinigers and falcigers (fig. 7-10). The latter have a cutting edge with a single
series of denticles (fig. 7, 9); they terminate in a curved process that is bounded
hy a series of denticulations continuous from the cutting edge Acicula occur
singly in parapodial rami; each is a slender, distally tapering, straight black rod;
the deeply embedded base is pale,
In postmedian segments, from about segment 50 in shorter, to about segment
68-70 in longer, individuals, there is present, immediately within the base of the
dorsal cirrus, a papillar organ which comes to increase im size to surpass that of
its corresponding dorsal cirrus (fig: 6); its distal end is penetrated by a pore,
By means of microtome sections @* it is possible fo trace ducts which penetrate
these papillae, and to follow their coutse inte the coelomic spaces. Occasionally
ohe can find larger ova in the cut. It can hardly be doubted but that these are
coelomoducts which function at maturity for release of gonadial products.
Whether primitively retained from ancestral stages, or secondarily derived might
be determined from a study of the development of this species, Among the
numerous individuals examined, I have found only ovigerous ones, all showing
the coclomostomes present from an anteromedian region to the posterior end of
the body.
In this connection it is interesting to recall a statement by the late F. 5.
Goodrich (1945, p. 173): “In species of Nercidae, co-existing with metanephridia
are a pait of specialized coclomostomes, the so-called ‘dorsal ciliated) organs.’ .. -
They occur in all species... bul may vary somewhat in size. They appear in the
young, persist throughout life, though in the heteronereid phase they are usually
reduced or absent. That this ‘dorsal ciliated organ’ is indeed the representative
in the Nereidae of the coclomoduct or genital funnel of the Capitellidae and other
Polychaeta, .... there can now be no doubt .. . But it has lost its original genital
function in the Nereidae, no longer requires an opening to the exterior, and has
become converted into a ‘ciliophagocytal organ,’ at all events in the majority of
species in which the genital products are known to escape by dehiscence . - . It
is possible, however, that some species still exist which have no specialized
epitokous stage, and that in them the caelamostomes still function as genital dicts.”
be ey OS ed ne "ee
7) J am indebted to My, Donald J. Reish for the preparation of the sections,
22
It seems probable that Australonereis ehlersi is indeed such a species in
which the dorsal ciliated organ is replaced by the coelomostome, and that it func-
tions as a genital duct, acquiring an opening to the exterior. There is no indication
of epitoky or parapodial transformation in the individuals that have been examined,
The pygidium is a terminal, dark brown collar; a pair of long, cirriform
processes is inserted ventrally; each is about as long as the last 10 segments.
Fig, 7-11
Australonerets ehlerst
Neuropodial falciger seen
from the side, x 521.
. Distal end of a neuro-
podial falciger showing
details of cutting edge
and terminal fang, x 2010.
Neuropodial falciger seen
from the cutting edge,
showing arrangement of
single row of denticula-
tions, x 521.
Distal end of a neuro-
podial falciger seen from
the cutting edge, x 2010.
Portion of a homogomph
spiniger seen from the
side, the tapering pointed
tip not shown, x 521.
Australonerets ehlersi was first assigned to the genus Leonnates (Augener,
1913) and later to Leptonerets (Monro, 1938, p. 618). Augener thought that the
oral ring is papillate; Monro found the maxillary ring to have papillae. Augener
found no falcigers above the neuroaciculum; Monro found them in anterior
segments; Augener called the falcigers heterogomph; Monro said they are nearly
to quite homogomph. These discrepancies can readily be attributed to subjective
interpretations. The species cannot be assigned to Leonnates Kinberg or
23
Leptonereis Kinberg. In the first the maxillary ring of the proboscis has horny
paragnaths ; in the second the proboscidial rings are both bare.
Australonereis. ehlersi is now known from opposite sides of the southern
half of Australia, at Swan River, Western Australia and Lakes Entrance, Victoria.
CreratocepHaLa Malmgren, 1867, emended
Type C. tovenr Malmgren
The generic diagnosis is here expanded to include species in which the
pharyngeal papillar processes are present on both rings of the proboscis instead
of only the oral ring (see Hartman, 1952, pp. 15-18, for detailed account),
Ceratocephala edmondsi, n. sp.
Fig. 12-17
Locality—American River, Kangaroo Island, South Australia; very common
in the sand of a cockle (Katelysia sp.) bank (9 specimens}, coll. S. J. Edmonds.
Length of a larget, posteriorly incomplete, individual is 27-39 mm.; width
at the widest (anterior) part is 3-4 mm.; number of segments is more than 60.
The general colour (preserved) is pale with melanistic spots on dorsal and
yentral sides; it resembles that of species of Platynercis, The prostomiuni has
two pairs of eyes that are large, subequal, in trapezoidal arrangement; the
anterior ones are wider apart. The ptoboscis (everted) shows the following parts:
area I (fig, 12) has one papilla, If and V are bare; TIT and EV together have
5 cirriform papillae in a transverse row; V1 has a single papilla on a side; VIL
and VIII have 9 cirriform papillae in a transverse row (fig. 13). Jaws are thin,
translucent, horny brown; they have 7 to 9 shallow crenulations at the cutting
edge.
The first 2 parapodia on a side are uniramous; each has composite spinigers
and falcigers; succeeding parapodia are biramous. From the third a notopodium
is developed and has a full fascicle of composite spinigers. At the cighth or ninth
notopodium there are 15 to 20 spinigers and single black acicula. Neuropodia have
a supra-acictilar bundle of about 10 spinigers and 9 falcigers, and single black
acicula that taper distally and are turned upward at the tip. The sub-acicular setal
bundle has about 14 falcigers (fig. 16) and 7 spinigers (fig. 17). Dorsal and
ventral cirri are simple throughout. A fiftieth parapodium is shown in hg. 14
and an eighth one in fig, 15-
The habitat is sandy beaches in which cockle shells occur; the nereid accupies
a sandy tube constructed with a thin. gelatinous matrix (observation by Mr. S. J.
Edmonds). .
Ceratocephala edmondsi differs from other species of the genus in that the
maxillary ring of the pharynx has papillae instead of lacking them; ventral citri
are simple throughout, instead of double on sume or all segments, The genus is
4 small one, known for only 5 or 6 other species or subspecies (Hartman, 1952,
p. 19) from widely scattered parts of the world. C. edmondsi is the only one
known from Australia, C. sibogae Horst, off Dutch Fast Indies, is the nearest
in geographic range. It is clearly separable from C, edmondsi in. its pharyngeal
processre in that ihe former has papillae nearly absent, with only 2 present on
area V. |
Tt is a pleasure to dedicate the species to its collector, Mr. 5. J. Edmonds
of the University of Adelaide, South Australia.
C. ediondst is known from only one locality, American River, Kangaroo
Island, South Australia, littoral,
2.
13,
14,
15,
16.
17.
24
Fig. 12-17. Ceratocephala edmondst
Anterior end with everted proboscis and first 6 setigers, in dorsal view,
»% 15.
Anterior end with proboscis everted, in. ventral view, x 15,
Fifticth parapodium seen from the front, x 45,
Eighth parapodium seen from the front, x 45.
Neuropodial falciger from a posterior parapodium, x 700.
Articulating portion of a spiniger, seen from the side, x 700
25
Micronerets Claparéde, 1863
Type M. vartecaTta Chiparéde
Micronereis halei, n. sp.
Fig. 18-21
Locality—Sellick Beach, South Austtalia, at outer edge of reef, 16 Januany
1936, at low tide from stones in rock pools (12 individuals), coll, Mr. HW, M.
Hale and Mr. K. Sheard.
This is a small, white species, greatest length is about 7 mm. ; width 0°55 mm,
without and 0°85 mm, with parapodia, Number of segments is 20 to 25. The
prostomium is broadly quadrate (fig. 18); its posterior margin is clearly marked
off from the first segment. There are 2 pairs of lenticulaied eyes, with the anterior
pair slightly larger and wider apart than the posterior one; all are similar in that
the basal part is dark red and there is a large, spherical pate lens. The frontal
margin of the prostomium is weakly indented, and the smal] oval paired palpi
can be seen only by viewing the prostomium from below. There are no prostomial
frontal antennae. The four pairs of tentacular cirri are directed forward and
outward; all are similar with slight variation in length; the antero-ventral pair
are shortest and the dorsal posterior pair arc longest. All 8 are on short bases
(not shown in fig. 18). Each has a slight subdistal swelling, diffusely brown in
colour, with a simulted articulation just below the brown pigment.
The first segment has uniramous parapodia in which the setal lobe is long,
compressed, directed laterally ; it has a cirriform ventral cirrus that is attached
near the middle of the parapodial base; it extends distally not as far as the Jobe.
Stumps of 8 to 10 slender setae and single acicula are visible. The second para-
podium is’ similar to the first but a little larger.
The third and successive segments have biramous parapodia. Notopodia
and neuropodia are widely separated from eath other, The dorsal cirrus is a long,
cirriform process at the upper, outer edge; the ventral citrus is similar but
somewhat shorter afd attached near the middle of the lower base of the para-
podium. In addition, both notopodia and neuropodia have a long, digitate lobe
that extends distally, attached one at the inferior outer edge of the notopodium,
the other at the superior outer edge of the neuropodium (fig. 20). These Inbes
resemble dorsal and ventral cirri but they are not so thick and extend laterally
not quite as far as the cirri. Acicular lobes are compressed, broadly triangular and
have an acute tip.
All setae are homogomph spinigers (fig. 2) with the longest appendages
several times as long as the shortest ones. The uppermost have the longest
appendage and the length diminishes gradually ventrally. Notopodia have 15 to
25 spinigers and single yellow acicula, Neuropodia have 15 to 20 spinigers and
single yellow acicula,
The pharyngeal apparatus (seen only by dissection since the proboscis was
not everted on any individual) is a subspherical, muscularized mass. It connects
distally with the mouth and proximally with the thin-walled, alimentary tract.
There are no paragnaths, A pair of large translucent, yellow jaws are inserted,
one on either side of the muscular tissue. Each jaw is broadly oval at the base
and continued distally to end in about 6 triangular teeth along the concave cutting
edge (fig. 19). If the jaws are dimorphic in this species as they have been
described for M. variegata Claparéde ( Racovitza, 1893), it may be presumed that
the description is based on the jaws of a female individual.
‘The only other known species of the genus is Micrunereis viriegata Cla-
paréde, from the Mediterranean Sea, more widely recorded from western Canada
(Berkeley and Berkeley, 1948, p. 60), though with some doubt. M. variegala
Claparéde differs from M. hale? in that digitate lobes are lacking fron: the inner,
26
Fig. 18-21. Micronereis halet
18. Anterior end in dorsal view, proboscis retracted, x 94,
19, An entire jaw plate showing distal toothed edge and embedded part,
x 417,
20. A median parapodium in posterior view, x 62:5,
21. Spinigerous seta from a median parapodium, x 1638,
27
proximal margins in the first; the pharyngeal jaws lack the broad base, and the
first parapodia have conspicuous tufts of setae. Prostomial and peristomial struc-
tures also differ (see Fauvel 1923, pp. 332-333, for illustrated account).
It is a pleasure to name this species for its collector, Mr. Herbert M. Hale,
Director of the South Australian Museum.
Micronereis halet has been found only from littoral zones in South Australia.
Namanerzrs. Chamberlin, 1919
Type N. guapraticers (Blanchard)
NAMANEREIS QUADRATICEPS (Blanchard), 1849
Lycastis quadraticeps Benham, 1909, pp. 242-244, pl. ix, fig. 2-10.
This brackish nereid was fitst described from Chile. Benham (1909, p. 244)
recorded it from Campbell Island, on shore near the exit of a creek from the
flank of Mount Honey; the shore above high-water mark is traversed by numerous
little watercourses oozing through the earth above (Benham); also in sea pools,
Benham's detailed description compares so favourably with individuals I have
examined from southern and central California, from a similar brackish niche,
that specific identity seems probable, The only differences 1 can find are these:
The pygidium shown by Benham (his fig. 5) as a constricted collar with a pair
of divergent lateral processes, is shorter and has a longer venttal lobe with the
anal aperture between the upper and lower parts; the ventral portion has a pair
of small, oval papillae inserted at the distalmost margin. Neuropodial falcigers
are shown by Benham with a single series of subequal crenulations at the cutting
edge; I see a single row of teeth that are longest near the base and diminish in
size to near the distal third. The pharyngeal jaws have teeth that are long, sharp,
obliquely inserted. These differences may haye no specific importance,
Namanereis quadraticeps may be expected to occur in high mtertidal zones
of the southern shores of Australia; it should be sought especially in zones where
there is only a light spray of sea-water,
Neantues Kinberg, 1866
Type N. vaari Kinberg
The collections have made possible an examination of the type species from
the type locality, for a gentis which is widely represented in littoral zones of the
Northern Hemispdere. Both atokal and epitokal individuals of both sexes are
represented, The account below is based om these collections.
NEANTHES VAALIY Kinherg, 1866
; Fig. 22-25
Neanthes vaalii Kinberg, 1866, p, 171.
Nereis albanyensis Augener, 1913, pp. 149-154, pl. ii, fig. 6, text fig. 14,
Neanthes vaalic Augener, 1922, pp. 20-21-
Localities—American River, Kangaroo Island, in mud flats (5 individuals),
call. S. J. Edmonds; Port Adelaide, in tidal river (2 male and 8 female epitokes),
coll. S. J. Edmonds; Rushcutters Bay, Port Jackson, scraped off hull of a yacht,
6 Oct. 1950, (1), coll. B. Dew; Athol Bight, public jetty, off piles, 12 Oct. 1950,
(2), coll. B. Dew; Milsons Point, Port Jackson, off piles and mooring chains,
23 Oct., 1950, (3), coll. B. Dew; Venus Bay Inlet, Eyre Peninsula, South Aus-
tralia, associated with clusters.of Modiolus, (3), coll. S- J. Edmonds; Point
Wynyard, north-west Tasmania, Apr. 1936 (4 tiny individuals), coll. H. M. Hale
and N. B, Tindale,
28
Preserved, the pigment pattern resembles that of Platynercis species in having
dark segmental spots over the dorsum and parapodia. Length of atoke individuals
(preserved) is 70 mm. Notopodia have spinigers only; neuopodia have a supra-
acicular fascicle of homogomph spinigers and heterogomph falcigers, and a sub-
acicular fascicle of heterogomph spinigers and heterogomph falcigers (fig. 25),
There are no notopodial falcigers.
In male epitokes the first 7 sepments have thickened dorsal cirri; the first
18 segments are otherwise unmodified, or the eighteenth is slightly changed with
a jew accessory lobes, Natatory setae are present from segment 19. Natatory
parapodia are present to the end of the body; the pygidium has a rosette of many
similar, slender papillae. Overall size is somewhat less than that for the female
which measures to 50 mm. long.
Typical natatory parapodia (fig. 24) have dorsal cirri that are crenulate,
and accessory lobes, In epitokal females modified natatory setae are present from
segments 21 to 89; parapodia from 90 to 102 (posterior end) differ in having
only single dark acicula in each ramus (setae lacking); the body terminates in a
pygidium with a constricted smooth collar,
In mature individuals the 4 prostomial eyes are enlarged, arranged in a
rectangle; each is a circular convex disk, purplish red at the periphery, fading
centrally ; each has a tiny white circular lens,
In atokal individuals the notopodia lack conspicuous preacicular and post-
acicular lobes such as characterize northetn reptesentatives of the genus Neanthes,
notably N. virens (Sars) and N, brandi (Malmgren). Median (fg. 22) and
posterior (fig, 23.) parapodia are similar to one another.
The pharyngeal processes (based on a female epitokal individual from Port
Adelaide) are arranged thus: I has 2 cones in tandem; If has 10 cones in @
triangular area; III has about 22 cones in a broadly oval patch; IV has a large
crescent of about 30 cones of larger and smaller cones; area V has 3 cones in a
triangle; V1 has 3 cones in a transverse line; VII and VIII (continuous) have
2 or 3 irregular rows of 30 or more cones.
Nerets ulbanyensis Augener, 1913, p. 152. froni Western Australia has been
referred to Neanthes vaalii Kinberg (Augener, 1922, p. 20). Nereis (Neanthes)
albanyensis Kott (1951, p. 106) from Peint Peron, Western Australia, is another
species and belongs to the genus Nereis, s,s, since there are dorsal falcigers in
notopedia.
The distribution of Neanthes vaaltt is indicated in Chart I.
NEANTHES, near CRICOGNATHA {Ehblers) 1905
Nereis cricognatha Ehlers, 1905, p. 29; Augener, 1913, pp. 163-164.
Neanthes cricognatha Knox, 1951, pp. 217-218, pl.45, fig. 6-8; Fauvel, 1947, p, 8.
Nereis arenaceodentata Benham, 1916, p. 134, pl. 46, fig. 1-3.
Lacalities—American River, Kangaroo Island, {2}, coll. S, J. Edmonds;
Port Adelaide, otiter harbour pilings, sublittoral fouling materials, (1), coll, S. J.
Edmonds; Sellick Beach, South Australia, on edge of reef permanently covercd,
(2), coll, H. M. Hale.
[Length attains about 30 mn. Notopodia lack homogomph falcigers, thus this
is regarded as a species of Neanthes. Parapodial lobes are bordered with a dark,
glandular margit. On the proboscis both oral and maxillary rings have complete
circlets of many paragnaths.
The present individuals differ from Neanthes ericognatha previously recorded
(see synonymy above) in that areas V to VIIL of the proboscis have a circlet of
larger cones on the maxillary side, and 4 to 7 rows of uniformly much smaller
cones on the oral side,
The distribution of the stem species js indicated in Chart Il.
Fig. 22-25 Neanthes vaalti
22. A median parapodium in anterior view, showing maximum deyelopment
of acicular lobe, x 35-7.
23. Fifteenth last parapodium in anterior view, x 63°2,
24. Thirtieth parapodium from an epitokous male specimen, x 15-7.
25. Falcigerous neuropodial hook from an unmodified parapodium, x 658.
30
NEANTHES KRRGUELENSIS (McIntash), 1885
Nereis kerguelensis McIntosh, 1885, pp. 225-227, pl. 35, fig. 10-12, pl. 16s, fig. 17,
18; Fauvel, 1916, p, 433: Benham, 1916, p. 122.
Locatities—Port Willunga, S, Aust., 18 Nov,, 1945, (2), coll. 5. J. Edmonds;
and Sellick Beach, S$. Aust., on edge of reef, Jan. 1936, (1), coll, H. M. Hale,
Notopodia have spinigers only, thus this is referred to Neanthes Kinberg. On
the proboscis areas I and V are bare; VI has one cone ona side; VII and VIIT
have a single row of 9 cones; each of areas Il, IT] and IV has a heap of small
paragnaths. In posterior parapodia the notopodial lobe diminishes in size and is tar
surpassed by the acicular lobe of the same segment.
Nereis kerguelensis oligodonte. Augener (1913, pp. 164-166), from Westeru
Australia, also lacks homogomph falcigers and is presumably a species of
Neanthes, It differs frony the stem species in having only 3 cones in a transverse
row on areas VIT and VIIT.
NEANTHES ANGUSTICOLLIS (Augener), 1913
Nereis angusticolis Augener, 1913, pp. 145-149, pl. 2, fig. 14. text fig. 13.
Not Kinberg, 1866, p. 169.
Notopodial falcigers are absent, thus this is referred to Neanthes Kinherg.
On the proboscis area I has 7 or & cones in an oval heap, IT has at feast 20 in
an oblique triangular area; [11 has about 12 in an oblique oval group; IV has
about 25 cones in a triangle; V is bare; VI has 9 or 6 in a rounded group; VIL
and VIII fotm a broad transverse band with 2 ar 3 ta 5 rows, the band widest
midventrally and narrowing toward the ends, Acicula are black and occur singly
in parapodial bases,
Nereis angusticollis Kinberg (1866, p. 160) from Tahiti is a Nereis, sensu
stricto, since there are homogomph falcigers in notapodia.
Nereis Litnaeus, 1758
Type N. Pe_acica Linnaeus
The species of Nereis from the southern half of Australia are peculiar for
having several in which the notopodial lobe diminishes in size going back, and
homogomph falcigers have a large lateral tooth near the apex. These characters
are known for N. falearia, N. jacksoni, N. denhamensis and N. thompsont {see
helow). In others the oral ring is nearly to quite bare, approaching a condition
in species of Ceratonereis Kinberg; such are the species N. jacksom and N. fal-
coria, Others have tentacular (buceal) cirri that are annulate, as in N. cockburn-
ensis. These features are neither generic nor limited to Australian species, but
are more frequently encountered among species from the southern hemisphere
than elsewhere, Thus, the coarsely toothed homogomph falciger is known for
N, sonata-persica Fuuvel from Persia, and for N, fusachalensis Langerhans trom
Madeira, The postericr notopodial lobe diminishes in size in Neanthes kerguelensis
(Melntosh) (see Ehlers, 1897). Annulation of tentacular cirri is encountered in
other species and genera, notably Nereis eugeniae (see Ehlers, 1897), Nereis
angusta Kinberg (1866), Neanthes kerguelensis {see Ehlers, 1897), Neanthes
ruficeps (Ehlers, 1905) and Platynereis australis (see Ehlers, 1905), all from
the Southern Hemisphere.
The several species discussed below ate those which have oceurred in
greatest abundance and for which some details have been obscure-
NeREIS DENHAMENSIS Angencr, 1913
Nerets denhamensis Augener, 1913, pp. 156-159, pl. 3. fig. 51, text fig. 16;
Fauvel, 1922, p. 494; Kott, 1951, pp. 99-101, fig. 3, 4-
3
Homogomph falcigers first. appear alter seginent 20 to 30 and number 3 or 4
in a fascicle; they are thicker than their accompanying spinigers. The falcate
appendage is short, weakly curved and projects from the end of the shaft for
only about hali its length; the cutting edge has 2 or 3 small teeth.
On the proboscis area J has 1 or 2 cones in tandem; I! has about 12 cones
in 2 rows; IIT has about 12 cones in 3 rows; IV has 12 to 15 cones in a triangular
patch; V has none; VI has 8 to 10 in an oval patch of 2 or 3 rows; VIT and VIII
have a single row of 8 to 10 larger cones.
In epitokal male individuals the parapodial change to natatory condition ts
at segment 15. Dorsal cirri of modified segments are sharply geniculate in their
distal extremity and crenulate along the outer margin of the basal pert.
One character named by Augener (1913, p. 158) but not commented on
further, states that: “An den vorderen Rudera mit dorsalen Gratenborsten ist die
Spitze der ventralen Sicheln gedeckt.” If this indicates the presence of a hooded
condition of anterior neurofalcigers, it describes a character unique for this
species.
See Chari 1 for distribution.
Nereis JACKSON] Kinberg, 1866
Fig. 26-29
Nereis jacksoni Kinberg, 1866, p. 169; Augener, 1922, pp. 27-30, fig. 6; Augener,
1927, pp, 130-133; Knox, 1951, pp. 216-217; Kott, 1951, pp. 95-98; fig, 3.
Nereis heirissonensis Augener, 1913, pp. 159-163, pl. 3, fig, 52, text fig. 17.
Localities—Sellick Beach, Sth, Aust,, on edge of recf permanently covered
and at low tide, Jan. 1936, (1), coll. H, M. Hale and K. Sheard; Shell Point,
Botany Bay, N.S.W,, from a 6-month fouling plate, estuarine, Feb, 1947, (4),
coll, B. Dew; Cape Cove, Port Jackson, N.S.W., dredged in 3-4 fms, from a
gritty bottom, Oct, 1950 (4), coll. B. Dew; Hungry Paint, Cronulla, N.S.W.,
under rocks, Sept. 1950, (2), coll. B. Dew,
The proboscis has few paragnaths; areas T and VY have none; EH and IIT
have a few cones and 1V has a few more; V1 has 1 to 4 only; VII and VIII have
a single row of only 2 fo about 7 cones (see also Chart 1V), Jaws are dark
amber in colour, thin, and haye 5 or 6 oblique teeth at the cutting edge.
Prostomial antennae are long; they extend forward to near the distal end
of the palpi. Peristomial cirri are short, the longest reaches back only to about
the second setigerous segment and others are shorter; all are irregularly
annulated. The 4 eyes are embedded and visible through the smooth epithelium;
the 2 of a side are neater together but widely separated from those of the opposile
side; the anterior ones are the larger, Each eye bas a reddish purple iris and a
large pale to white Jens, nearly or over half as large as the diameter of the eye.
The anterior margin of the prostomitim is entire, not incised.
In posterior segments the notopodial, or supra-acicular, lobe diminishes
(fig. 26) conspicuously in size but is visible as a distinct lobe to the end of the
hady. Homogomph falcigers are present in median and posterior segments ; their
earliest presence varies from the fourteenth, or not before segment 17 or 18.
They have an appendage (fig. 27, 28) that is short, distally bifid; those in front
are similar to those behind or the latter may Jack the basal-most teeth (fig. 29),
Some individuals from Shell Point, Botany Bay, taken 2 Feb, 1941, are
ovigerous, with large ova crowding the body cavity from the third setiger more
posteriorly. There are no signs of epitoky, such as the presence of modified lobes
or specialized setae. Indications are that development is direct. This is in contra-
diction to what Kort (1951, p. 97) found for individuals from Western Australia.
Augener (1913, pp. 159-60) examined about 50 specimens taken from May to
September and found them all atokal,
The more extended distribution is indicated in Chart IV.
32
; NeEREIS THOMPSONI Kott, 1951
Nereis (Neanthes) thompsoni Kott, 1951, pp. 103-105, fig. 5.
This is here referred to Nerets since notopodia have homogomph falcigers.
lt bears resemblance to Nerets denhamensis (see above) but differs in its much
higher paragnathal count, See Charts I to IV for diagnostic characteristics.
Fig, 26-29 Nereis jacksoni
26, Twenty-sixth parapodium seen from the front, x 40.
27, A homogomph falciger from twenty-sixth parapodium seen from the
side, x 620. ;
28. A homogomph falciger from twenty-sixth parapodium seen from the
cutting edge, x 620.
29. A homogomph falciger from a far posterior parapodium, x 400.
NEREIS PERONIENSIS Kott, 1951
Neréis callaona peroniensis Kott, 1951, pp. 101-102, fig. 4,
This is here erected to specific category since its affinities are believed to be
more remote from Nerets callaoana Grube than its author thought. In N. per-
oniensis the homogomph. falcigers of posterior notopodia taper distally to a blunt
point and have a coarse tooth at the cutting edge. In N. callaona Grube the
corresponding falciger has a much longer appendage that is distally anchylosed
and there are no coarse teeth along the cutting edge (see N, pseudonereis Hart-
man 1940, pls: 26, 27, a synonym of Nereis callaona Grube, for further charac-
teristics). N. cailaona Grube ts known only from Peru.
) I am indebted to Mr. Donald J. Reish for having made a comparison of type
specimens. 7
33
N. peroniensis Kott comes nearer Nereis sonata persica Fauvel, as described
by Pruvot (1930, pp. 47-50, pl. 3) from New Caledonia, In both the pharyngeal
armature and notopodial falcigers show great resemblance.
NEREIS COCKBURNENSIS Atigener, 1913
Fig, 30-32
Nereis cockburnensis Augener, 1913, pp. 153-156, fig. 15 a-c.
Localities—Sellick Beach, 5. Aust., from stones in rock pools, Apr. 1936
(about 31 individuals meluding some epitokes), coll. H. Hale; Sellick Beach,
St, Vincent Gulf, from limestone reef covered at dead low water, Jan. 1937, (10),
coll. H. M. Hale; Royal Australian Navy torpedo range at Pittwater, Broken Bay,
from piles and under tocks, (5), coll. B. Dew; Pennington Bay, south coast of
Kangaroo Island, (3), coll. S. J, Edmonds,
Tentacular cirri are annulate, resemble those of a eunicid [thus not as shown
by Augener, 1913, pl. 3, fig. 47). The longest cirri when laid back, reach to the
hfth setigerous segment,
A wnique and heretofore undescribed feature is the presence of 2 kinds of
notopodial falcigers. Anterior segments, from the first biramous one, haye homo-
gomph falcigers with a toothed cutting edge (fig. 30) resembling that of the
corresponding neuropodial, heterogomph falciger (31). In median and posterior
segments these notopodial falcigergs are replaced by ohe which has a shorter
appendage and traces of transverse ridges (fig. 32).
On the proboscis area I has a single tooth or 3 small cones in tandem
(Augener described none); II has 10 cones in 2 rows (Augener gave 8 cones
in 2 rows); II] has only 4 to 6 cones (Augener said 2 m tandem) ; 1V has about
18 cones in 3 rows with the largest ones on the side toward the jaws (Augener
gave 5 to 11 cones in 2 or 3 rows). Area V has about 8 smaller cones or varying
to only 1 cone (Augener gave 6 coties in 2 tows); VU has 5 or 4 cones in a
circular area (as Augener stated) ; VIL and VIII have a continuous band of many
paragnaths with a single row of about 9 larger ones on the side toward the jaws
(Atgener described a broad band of many), and 5 to 7 irregular rows of many
closely spaced cones on the side toward the mouth,
In postmedian segments the upper notopodial lobe comes to be small, triangu-
lar and diminishes farther back as an inconspicuous Jobe,
An epitokal ovigerous individual, from Sellick Beach, 11 April 1936, has
homogomph faleigers present from the first biramous parapodium. Accessory
natatory lobes are first present from segment 17, at the upper base of the dorsal
cirrus. Natatory setae are also present, but not yet emergent, from seement 17.
The last 11 segments lack accessory Johes, indicating the presence of a third body
region in epitoky.
Nerets cockhyrnensis was first described from Sharks Bay in 244. meters,
and Cockburn Sound, South Channel in 63-8 metres on a rocky bottom. The
present collections come from South Australia and New South Wiles,
Peeineneis Kinberg, 1866
Type P. ametyoponta (Schmarrda)
The 14 species indicated on Charts I io IV (see above) are largely tropical
or subtropical, thus belonging mainly to the Damperian and Solanderian pro-
vinces or to New Zealand. A few species oceur along southern shores of Aus-
tralia (see below).
PERINEREIS AMBLYODUNTA (Schmarda), 1861
Nereis amblyodonta Schinarda, 1861, p, 106; Ehlers, 1905, p. 28.
Perinereis novae-hallandiaeg Kinberg, 1866, p. 175 and 1910, pl. 20, fig. 9.
Nereis (P arpersis) amblyodonta Augencr, 1913, pp. 174-175; Augener, 1922,
pp. 22-23.
»
4
Localt#ies—American River and lagoons, Kangaroo Island, under rocks and
in mud flats; also in Venus Bay jetty, with colonies of Gealeolaria, (8), coll. S. J.
Edmonds; Port Willunga, S. Aust., in colonies of Hormosira, (4), coll. Miss P.
Mawson; Port Jackson, Sydney Harbour, N.S.W., under rocks and in chimps
of Galeolaria, (7), coll. B. Dew; Milsons Point, Port Jackson, N.S.W., wharf
piles and on mooring chains, (1), coll. B. Dew.
Nerets cockburnensts
Fig. 30-32
30. A notopodial — falciger
from sixth parapodium,
x 650.
31. A nenropodial falciger
from sixth parapodium,
x 650.
32. A notopodial — falciger
from a far posterior seg-
ment, x 650.
as
This species is easily identified for the presence of long dorsal lobes of
posterior notopodia, and for the arrangement of paragnaths on areas V and VI.
See Charts I to IV for further details and more extended distribution.
35
PERINEREIS VARIODENTATA Augener, 1913
Nereis (Perinereis) variodentata Augener, 1913, pp. 179-182, pl. 3, fig. 50, text
fig. 19.
Localities—Sellick Beach, St. Vincent Gulf, S, Aust., from stones in rock
pools at low tide and from limestone reef covered at dead low water, (2), coll.
H. M. Hale; Pt, Wynward, north-west Tasmania, April 1936, (2), coll N, B.
Tindale.
See Charts [ to IV for distinguishing characteristics and distribution.
PERINEREIS VALLATA (Grube) 1857
Nereilepas pacifica Schmarda, 1861, p. 107.
Nereis (Periagress) vailata Augener, 1913, pp. 175-177; Augener, 1923, pp. 26-
9
Perinereis vallata Fauval, 1932, pp. 108-109; Knox, 1951, pp. 218-219, pls, 45-46.
Locelity—Port Willunga, S. Aust., (1), coll. 5. J. Edmonds.
See Charts I ta IV for further details.
PratyNertis Kinberg, 1866
Type P. wacaLHarnsis. Kinberg
Among the 5 species to be encountered in littoral zones in Australia and
New Zealand, 1, P. australis (Schmarda) is perhaps limited to New Zealand;
another, P. polyscalma Chamberlin, is tropical. P. magalhaensis Kinberg, P. dum-
erilii antipoda, new subspecies, and P. bicenaliculata (Baird) occur in the
Peronian and Flindersian proyinces but all are not limited to them. See also
Charts I-IV, above.
PLATYNEREIS DUMERILIT ANTIPODA, new subspecies
Fig, 33-37
Nereis (Platynereis) australis Augener, 1913, pp. 182-184, and Augener, 1923,
pp. 35-39. Not Schmarda, 1861. .
Localities—Pennington Bay, south coast of Kangaroo Island, among algae,
(5), coll. S. J. Edmonds; Pittwater, Broken Bay, N.S5.W., on piles. Sept, 1949,
associated with Nereis cockburnensis and Perinereis calmani, (2, including 1 sub-
epitoke), coll. B. Dew; Hungry Point, Cronulla, N.S.W., Aug. 1950, (2) coll.
B. Dew: Elizabeth Bay, Port Jackson, N,S.W., from mooring buoy, 28 Oct.
1950 (1 subepitoke female), coll. B. Dew; Point Wynward, north-west Tas-
mania, (5), coll. H. M. Hale; Sellick Beach, St. Vincent Gulf, 5. Aust., lime-
stone reef covered at dead low water (8 juveniles), coll. H. M. Hale.
These individuals have been compared with Platynerets dumerii (Audouin
mn M. Edwards) from the Mediterranean Sea. A comparison of diagnostic parts
ollows:
P_d. antipoda P. dumerilit
South Australia Mediterranean Sea
Notopodial spinigers in median and 1-3/40, thus ure shorter- 1/80, ius are longer-
posterior segments have a length/ appendaged appendaged
width ratio of:
Median parapodia, at about seg- 3 spinigers and 10 spinigers only
ment 40, have a supra-acicular 3 falcigers
fascicle oft
First presence of notopodial (fig. Anteromedian segments, Postmedian segments, and
37) faleigers is in: where they are numer- they are incolispicuous
ous and conspicuous and few
Acicula are coloured: light to dark brown black
36
Dorsal lobe of median and posterior subquadrate subtriangular
segments is:
Paragnaths of area VI are: obscure, with 2 weakly 2 well-developed rows. of
developed rows of pectinae —pectitiae
Dorsal cirri of posterior segments very long (fig. 36) not so long
are;
In female epitoke, the upper base a long digitate lobe a short foliaceous lobe
of the ventral cirrus has: (fig. 35)
In female epitoke, the posterior a dipitate process no digitate process
neuroacicular Jobe has: (fig. 36)
In female epitoke, the parapodial segment 22/23 segment 22-23/24 or
change is at: 22/23, or 24/25
In the female epitoke the first 7 pairs of dorsal cirri enlarge (fig. 33) gradually.
The phatyngeal armature (specimen from Pt. Wynyard, Tasmania) shows
areas I, IT and V bare; JIT has 2 rows of obscure pectinae; 1V is the most con-
spicuous area of the pharynx, with about 4 transverse series of pectinae; VI has
2 or 3 short lines of very weak pectinae; VII and VIII is an interrupted band
with about 5 patches of 2 short rows each,
Individuals from Tasmania have simple gregarines in the alimentary tract,
through middle and posterior third regions of the body.
P. dumerilii ocellata Pruyot (1930) from New Caledonia differs from
P. dumerilii antipeda in that area VI of the proboscis is hare; the prostomium is
marked with 3 dark spots, resembling eyes, hence the varietal name.
P, dumerilit antipoda is known only from the Flindersian province,
PLATYNEREIS MAGALIAENSIS Kinberg
Platynercis magalhaensis Kinberg, 1866, p. 177.
Nereis (Perinercis) magalhaensis Augener, 1923, pp, 28-39.
Locality—Sellick Beach, $8. Aust., low tide, 16 Jan., 1936, (2), coll. H. M.
Hale and K. Sheard.
This is hardly separable from P. australis (Schmarda} from New Zealand,
except in its epitokal stages. In this the male epitoke has the first 21 segments
unmodified and natatory setae from segment 22; the female has 25 segments
unmodified and natatory setae from segment 26. In both species the notopodia
nearly or quite lack falcigers; a weakly developed one may be found in posterior
segments, Other characteristics are detailed in Charts I to IV, above.
PLATYNEREIS BICANALICULATA (Baird), 1863
Fig. 38, 39
Nereis bicanaliculata Baird, 1863, p. 109,
Nereis agassizi Ehlers, 1868, pp. 542-546, pl. 23, fiz. 1.
Localities—Hungry Point, Cronulla, N.S.W., on fouling plate, 28 Sept.,
1950 (1 female); Athol Bight, public jetty, 12 Oct. 1950, on kelp root (9);
Camp Coye, Watsons Bay, Port Jackson, in 6-8 fms., 6 Oct. 1950 (6, including
subepitokes) ; Port Jackson, on piles and mooring chains, 23 Oct. 1950 (15);
all collections are from New South Wales, made by Miss Barbara Dew,
This strikingly characterized species is well known from the north-east
Pacific as Platynereis agussizi (Ehlers), It was arresting to find it well repre-
sented in the collections. from New South Wales. This led to a re-examination
of large series from various parts af the Pacific, including some from Hawaii,
33,
34,
35.
36.
de.
37
Fig. 33-37, Platynereis dumerilii antipoda
wan et parapodium from female epitoke, showing enlarged dorsal cirrus,
x 100,
Twenty-second parapodium from female epitoke, in posterior view, x 70,
Twelfth epitokal parapadium from female, in posterior view, x 50. d
ce posterior parapodiym from female epitoke, seen from the front,
x B83, ;
A notopodial falciger from a posterior segment (specimen from Tas-
mania), x 832,
38
Nereis bicanaliculata Baird from Vancouver Island, western Canada, and many
other collections from widely scattered parts of the eastern Pacific. I am unable
to distinguish them morphologically, and am therefore indicating the synonymy
above,
Fig. 38-39
Platynereis bicanaliculata
38. A simple notopodial fal-
ciger from a specimen
from New South Wales,
x 500.
39, A comparable notopodial
falciger from one from
California, x 500,
Most individuals (preserved) from New South Wales are melanistic, have
paired dark patches over the sides of the body and along the parapodial bases.
Large, simple, notopodial falcigers (fig. 38) are present from about segment 10
or 12 to the posterior end of the body; they occur singly or by twos or threes
and have a dark brown to black tip. A corresponding falciger taken from a
specimen from California is shown in fig. 39.
39
Neuropoilial falcigers ate composite, first present from about segment 50
and continue to the end of the body; they are most numerous in a fascicle in front
and diminish in number behind.
On the pharynx the Australian individuals differ slightly from those of Cali-
Fotis a that area IV of the proboscis is less, instead of more, conspicuous than
area UE.
The presence of simple notopodial falcigers is not limited to this genus ofr
species, hence cannot be regarded as generic, Ceratonereis erythraeensis Fauvel
has similar hooks in neuropodia,
The type collection of Nereis bicanaticulata Blaird (1863) deposited in the
British Museum (Natural History) contains 8 pale (faded) specimens in good
condition, The largest one, somewhat over 50 mm. long (thus about 2 inches as
Baird stated) consists of about 96 segments; it is posteriorly incomplete. In some
individuals the parapodia are subepitokous but none has natatory setae. In all,
there are one or 2 dark brown, simple notopodial falcigers, first present in para-
podia from segment 12 or 13 to the postertor end. On the proboscis areas I, Il
and V are bare; LII has a broad, oval patch; [V has a broad crescent of 7 to 10
irregular rows (this is the most conspicuous region) ; VI has 2 or 3 rows of
pectinae; VII and VIII, continuous, have 5 transverse rows of pectinae with faint
indications af 2 other rows at the ends proximal to area VI. Jaws have 7 oblique
tevth and a distal fang. These individuals are inseparable from what has usually
beet cae? Platynereis agassisi (Ehlers), widely known from the north-east
acmec,
Throughout its range, Pletynercis bicanaliculata is apt to occur with (or near)
Plaiynereis dumerilii (Aydouin and M, Edwards) or one of its varieties. They
ate easily separable in that P. bicanaliculuta has large, simple falcigers in noto-
ia whereas P, dumerilii (and its subspecies or varieties) have composite
alcigers in notopodia, P. bicanaliculata remains unknown except in northern and
southern parts of the Pacific; P. dumerilii is cosmopolitan in warm. seas.
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Grune, E. 1869 Beschreibung never von der Nora Expedition mitvebrachter Aymelirter
und einer Tandplanarie, Zool-Bat. Gesells.. Wien, Verh., 16, pp. 173-184
Grune, E, 1878 Annulata Semperiana. Acad. Sci St. Petersburg, Mem., 25, 3M pp. 15 pls.
Hartman, ©. 1940 Polychaetous annelidg, Ft, 2, Chrysopetalidae to Gowiadidae. Hanenck
Pacific Exped, 7, pp. 173-287, 14 pls,
Hartman, ©, 1948 ‘The Marine Annelida erected by Kinbere with notes on some other
types in the Sweilish State Museum. Arlo Zool, Stockholm, 424, pn. 1-137, 18 pls.
Hartman, O, 1952 Iphitime and Ceratocephala (Polychaetous annelids) fram California,
Southern Calif. Acad, Sci., Bull., 51, pp. 9-20, 2 pls.
HaerMax, ©. 1953 Non-pelacic Polychaeta. Swedish Antarctica Exped, (901-1903, Further
Soclosical Results of the Swedish Antarctic Expedition, 4, No, 11, yp, 1-83, 1 chare,
21 figs.
41
Hforsr, R. 1889 Contributions towards the Knowledge of the Avinelida Polychaeta. Notes
Leyden Mus. Jentini, 11, pp. 161-184, 2 pls.
Horst, R. 1924 Polychaeta. errantia of the Sihoga-Expedition. Netreidae and Hesionidae,
Sihoga-Exped. Leyden, 99, (Motiogr, 24, Ic), pp. 145-198, 7 pls.
Kirxeer¢, J, 1866 Annulata nova. Oerv. Vet. Akad, Stockholm, 22, pp. 167-169 and 239-258
KinperG, J. 1910 Annulater. Kongliga Svenska Fregatten Eugenies Resa omkring jorden,
1851-53. Uppsala and Stockholm, Almoauist and Wicksells., 78 pp. 29 pls.
Kwox, G. A. 1951 The Polychaetous Amnelids of Banks Peninsula. Rec, Canterbury Mus.,
5, pp. 213-229, pls: 44-50
Kort, ParrrctA 1951 Nereidae and Ennicidac of South-western Australia; also notes on the
Ecology of Western Australian Limestone Reefs, Roy. Soc. West, Australia, Jour., 33,
pp, 85-130, 7 figs. >
McIstosn, W. C. 1885 Report on the Annelida Polychacta collected by H.M-S. Challenger
during the years 1873-76, Challenger Reports, 12, pp. 1-554, 55 and 39a pls.
MAkENZELLER, FE. vow. 1879 Stidjapanische Anneliden. Akas. Wiss. Wien, Denkschr., 41,
pp. 109-152, 6 pls.
Monro, C. 1926 On the Polvchaecta collected by H-MLS. .4lert, 1881-1882. Fannhes Hesioni-
dae and Nereidae. Linn Soc. London, Jour,, 36, pp, 311-323
Monro, C. 1930 Polychaete Worms, Discovery Reports, 2, pp. 1-222, 91 figs.
Monro, C, 1931 Polychaeta, Oligochaeta, Echiuroidea and Sipunculoidea, Great Barrier
Reef (Qld) Exp. 1928-20. Sci. Rep. Brit. Mus. (Nat. Hist.), 4 (1), pp. 1-37,
15 figs.
Monro, C. 1936 Polychaete Worms. If, Discovery Reports, 12, pp. 59-198, 34 figs,
Monro, C, 1937 The John Murray Expedition 1933-34. Scientific Reports, Polychateia.
8, No. 8 pp. 243-321, 28 figs,
Monro, C. 1938 On a small collection of Polychaeta from Swan River, Western Australia.
Ann. Mag. Nat. Hist. London, ser, 11, 2, pp. 614-624, 13 figs. |
Monro, C. 19399 Polychaeta Antarctic Research Expedition, 1929-1931. Adelaide, Australia.
Reports, Ser. B (Zoology and Botany), 4, pt. 4, pp. 89-156, 28 figs.
Monro, C, 193%) On some Tropical Polychaeta in the British Museum, mostly collected by
Dr. C, rpeslat al Zanzibar, Tahiti and the Marquesas, Novitat. Zool, Landon, 41,
pp. 302-30.
Oxupa, §. 1938 Polychaetous Annelids from the vicinity of the Mitsui Institute of Marine
Biology. Japan, Jour. Zool., 8, pp. 75-105, 15 figs.
Oxuna, S. 1940 Polychactous Annelids of the Ryukyn Islands. Biogeogr. Soc. Japan, Bull.,
10, No. 1, pp. 1-24, 9 figs,
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Arch, zool. exp, gen. Paris, 70, pp. 1-94, & figs. 3 pls. ;
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1, pp, 1-588
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THE MOLLUSCAN FAUNA OF THE PLIOCENE STRATA UNDERLYING
THE ADELAIDE PLAINS
BY N. H. LUDBROOK
Summary
The molluscan fauna of the South Australian Pliocene is best developed and preserved in the Dry
Creek Sands which have been thrown down to the west of the City of Adelaide by the Para Fault.
red
THE MOLLUSCAN FAUNA OF THE PLIOCENE STRATA UNDERLYING
THE ADELAIDE PLAINS
PART I
By. N. H. Luprroox *
[Read 9 April 1953]
SUMMARY
Thé molliscan fauna of the South Australian Pliccene is best deyeloped and pre-
served in the Dry Creek Sands which have been thrown down to the west of the City
of Adelaide by the Para Fault.
Pliocene strata were deposited unconformably on a post-Burdigalian erosion surface,
and are overlain by Pleistocene to Recent sands and clays, mainly of freshwater origin,
and nodular kunkar. In the Adelaide Basin shell heaps concentrated by ctrrents are
frequent im the north-eastern portion, and are of economic importance since they
generally mark the aquifer.
Readily distingttishable lithologically, the light-grey fine sharp quartz sands carry
a well-preserved rich molluscan fauna, mainly of the epineritic environment.
The molltisca cotistitute essentially a tropical marine fauna in which four distinct
elements may be recognized: a dominant Indo-Pacific, a Tethyan Eocene, a Recent
Australasian, and a cosmopolitan, The presence of undoubted Tethyan Eocene subgetiera
js of particular interest. The stage at which these reached Australia ts not at present
determinable, but it is Hkely that they date at least from the Oligocene. Distinct from
the two tropical elements are a large autochthonous Australasian element probably
derived from an endemic stock, and a fourth element coimposed of cosmopolitan of
widespread subgenera.
Since 5790 of the species are restricted to the fauna, the age is detertninable only
by correlation with known Pliocene faunas in Australia. Available evideiice suggests
that the strata may be slightly younger than Pliocette strata (“Kalimian") in Eastern
Victoria, but much work remains to be done before complete correlation is achieved.
I, INTRODUCTION
During the past 70 years the Adelaide Plains, comprising the eastern portion
oi the St. Vincent Gulf—Adelaide Plains graben on which the City of Adelaide is
built, have been at first intermittently and recently intensively drilled in the search
for a supplementary or alternative water supply for the domestic and agricultural
needs of the city and its environs.
For the fiity years following the drilling of the first deep hole at Kent Town,
close to the city area, borings were sunk at sporadic intervals by landowners for
agricultural purposes. With the growth of the city and threatened failure of
normal water supply from storage reservoirs in times of drought, a programme
of drilling was initiated by the South Australian Mines Department in 1934 and
greatly intensified in 1945. The area drilled covers some 250 square miles
from the Gawler River 18 miles north of Adelaide, south to Brighton 9 miles
south-south-west of the city, bounded on the west by Gulf St. Vincent and on
the east by the foothills of the Mount Lofty Range along the line of the Burnside
and Eden Faults.
Practice has heen to seal the Government bores until drought necessitates
opening them to supplement the city water supply.
Material from several of the borings. was submitted to the writer by the
South Australian Mines Department for palaeontological exaniination. Results
of examination of the mollusca are embodied in the present study.
During the past twenty years, Australian molluscan systematics have become
confused by the reluctance of some workers to recognize generic affinitres between
most of the Australian species and their relatives elsewhere. As a result, accurate
* Department of Mines, South Australia.
Trans. Rey Suc. S. Aust., 77, July, 1954
43
and detailed correlation of faunas has not been attempted. An additional problem
arises from the fact that faunas from type areas are imperfectly known, Collect-
ing has been done from easily accessible localities where fossils are numerous,
but little systematic sampling has been carried out.
With the aim of reducing some of the anomalies so created a representative
series of the mollusca contained in the bores submitted to the writer was taken
to London for comparison with type and other material in the British Museum.
The fauna has now been completely revised and the nomenclature brought into
line with that employed by specialists outside Australia,
The stage name “Adelaidean” previously in use for the strata is abandoned
in accordance with the suggestion of Mawson and Sprigg (1950, p. 69), Howchin
(1928. p. 422) proposed the term for the richly fossiliferous marine sub-surface
strata, which he considered to be of Upper Pliocene age, known only from borings
within short distances of Adelaide. Smce confusion is always hkely to arise from
the use of the term Adelaidean for the Pliocene marine sands when there is the
well-established Adelaide System (formerly Series) of Pre-Cambrian age, Glaess-
ner (1951, p. 280) has recommended its replacement by the name Dry Creek
Sands,
‘II. HISTORICAL SURVEY
The Dry Creek Sands were first discovered in 1889 when a deep bore ih
search of water was sunk at Dry Creek, 6 miles due north of Adelaide, by the
Australian Smelting Company. On this classical boring the discovery of marine
deposits younger than beds then considered to be of Miocene age and older than
admitted Pleistocene strata was claimed.
In the following year a bore was sunk at Croydon 34 miles north-west of
Adelaide and reported upon by Tate (1890b), who published a section showing
that the Pliocene strata recognized in the Dry Creek Bore were penetrated at
340 feet; a thickness of 406 fect for the Pliocene was postulated. The boring
was stopped at 800 feet. Subsequently a second bore was sunk at Croydon to
a depth of 2.296 feet, adjacent to the first. The Pliocene and underlying strata
were again reported upon by Tate (1898}, Pliocene being identified from 395
to 715 feet.
No detailed palaeontological work was done to advance the knowledge of
the fauna, although varying and speculative opinions on the age of the strata
and their relative stratigraphical position were published, These may be briefly
summarized as follows:
Tate and Dennant (1896, p. 148) placed them above the beds now known as
Kalimnan in Victoria and in the Pliocene.
Hall and Pritchard (1902, p. 80) named the Kalimnan (p. 78) and con-
sidered the beds described by Tate from Dry Creek to be contemporaneous and
therefore of “Miocene” age.
Howchin (1914, p. 156) differentiated them from the Kalinman (“Second
Marine Series? Miocene”) as “Third Marine Series—Older Pliocene.”
Chapman (1916, p. 156) accepted the view of Hall and Pritchard that the
beds were contemporaneous with the Kalimnan, but supported the tarlier view
of McCoy and the Geological Survey of Victoria that the Kalimnan was Lower
Phiocene in age. -
Howchin (1928, p. 422; 1929, p, 235) mtroduced the name Adelaidean, and
“proposed to distinguish ..., the Adelaidean Upper Pliocene” from the Werri-
kooian Upper Pliocene of Victoria.
In a preliminary note on the stratigraphical position of the beds the writer
expressed the view (Ludbrook, 1938, p. 445) that the beds now known as the
Dry Creek Sands were probably contemporaneous with other beds of accepted
Lower Pliocene age in Southern Australia. This opinion was strongly opposed by
Howchin and Parr (1938, p. 289) and Parr (1939) who continued to maintain
44
an Upper Pliocene age for the fauna, Chapman (in Howchin and Parr, 1938,
p. 290) agreed with Howchin that the Dry Creek Sands were younger than the
Kalimnan, but considered them contemporaneous with the Pliocene beds at Hallett
Cove.
Singleton (1941, p, 22) established and defined the Adelaidean as a Stage.
MAP SHOWING POSITION OF BORES STUDIED
978 e207
BORE al?
SECTION LINE
hye
yb
Fig. 1
Bore 215 is within the boundary of the
City of Adelaide.
On completion of a systematic study and analysis of the gastropod fauna
of Abattoirs Bore, and taking into account the view of Howchin and Parr that
the foraminifera had a more recent aspect than those of the Kalimnan, the writer
(1941, p. 80) placed the Dry Creek Sands in the Lower-Middle Pliocene.
Since the present work was completed the publication of a comprehensive
report on the geology and underground water resources of the Adelaide Plains
area (Miles, 1952) has added greatly to the knowledge of the subsurface geology
of the area. In an appendix to the report Crespin and Cotton (1952) have corre-
lated the Pliocene strata with the Kalimnan of Victoria, the faunal differences
being attributed to facies.
In the present study the molluscan fauna has been increased to 380 species,
78 of which have not been previously described; four new subgenera have been
erected, The composition of the fauna has been determined as accurately as
possible, its relationships with other comparable faunas analysed and its bearing
upon the stratigraphical position of the strata discussed. The establishment beyond
doubt of a faunal link between the European Eocene, Australian Pliocene, and
the Recent Indo-Pacific Region is an important fact to emerge. Some faunal
45
migration, probably by way of Tethys, has almost certainly taken place, and
closer study of faunas linking Australia to the Northern Hemisphere is
warranted. There is at present no evidence of any faunal link with known
American Tertiaries, and the study confirms the opinion that the deep waters of
the Pacific Ocean have always been a barrier between the faunas of its western
shores and those of the east, except in the extreme north and south where move-
ment along the coastline has been possible.
SECTION ALONG LINE 4B FROM BORES7 TO BORE 2i5
5 2 Unfestireaue matted chy
cis [ix] Untmusfereve sands & grovel
Sy Chay
20 ES Ged, wreund
‘ sy clay
| beeniah sendy cley
DET.
EF Masato
PLEISTOCENE TO RECENT
200 Bd Sand gravel 305 be
ES alvishelay 415
330. el Lineatone
HOT SAMPLED IN DETAIL!
NOT SAMPLED 1
Dark send, chy
wy
=
a
8
J
a
Fes} Kegilfaceaur amid
ET Te he
| an pendy mart
aS
fa Blue blac mudiparen,
ma
:
Yeltes dandy mar!
MIOCENE /
HORIZONTAL SCALE
ce]
MILES
Fig. 2
UI. GENERAL AND STRUCTURAL GEOLOGY
Pliocene strata ate exposed as isolated remnants at irregular intervals along
the eastern coast of Gulf St, Vincent from Aldinga Bay in the south 10 the
City of Adelaide in the north (Howchin, 1923; Segnit, 1940). Pliocene lime-
stone formerly outcropped along the banks of the River Torrens (Howchin, 1923,
p- 283) and has been exposed in quarries on the south bank of the River at the
tear of Government House (Tate, 1882, p. 40) and in the University grounds.
ft has been frequently penetrated in shallow well sinkings and in borings in the
City area at about 50 10 70 feet depth, including Kent Town Bore (Tate, 1882),
Black Forest Bore (Howchin, 1935), Bank of the New South Wales Well
(Cotton, 1947), and was noted by the writer in West End Brewery No, 2 Well,
6
Hindley Street, at depth from 69 to 70 feet, Fossils typical of the Dry Creek
Sands were present mainly as moulds. Elsewhere the Pliocene has been penetrated
only by borings into the Dry Creek Sands from Gawler River in the north to
Glenelg in the south. The average depth below datum level at which the beds
are penetrated ig 315 feet. Where the thickness is proved, the beds are generally
from 150 to 180 feet thick, although an exceptional thickness of 320 teet was
passed through in the Croydon Bore (Tate, 1898, p. 195). The average thickness
iu six bores which reached the Miocene is 190 feet.
The greater thickness of the Dry Creek Sands as compared with that of the
sandy limestones in the City area and in exposures south of Adchiide is consequent
upon tectonic movements which disturbed the area in Jate Tertiary and Quaternary
times. The Moimt Lofty Ranges and Adelaide Plains are units in a system of
regional meridional block faulting in which the St. Vincent Gulf-Adelaide Plains
form a graben and the Mount Lofty Ranges a horst to the east. The general
structure of the fault system has been described chiefly by Benson (1911),
Fenner (1930), and Sprigg (1945). The major faults in the Adelaide Plains
and Western Mount Lofty Ranges are shown on fig. | The trend Imes are broadly
N.N.E.- §.5,W.
Fenner (1930, p. 15} has suggested that two periods of block iawlting are
probably involved; while there is at present no direct evidence that this is the
case, it is not improbable that the orogenic movements which elevated the Mount
Lofty Ranges horst antedated the deposition of the Dry Creek Sands and their
subsequent down-faulting to the west of the Para Fault.
To the south and east of the Para Fault in the immediate neighbourhond of
Adelaide only the more resistant caleareaus equivalents of the Dry Creek Sands
have been preserved at shallaw depth. West of the Para Fault, however, the
sediments have been thrown down to a maximum of the order of 350 feet, and
an average thickness of 190 feet of unconsolidated sands has been preserved
beneath a cover of later marine and freshwater sediments. The subsurface rela-
tionship of the Dry Creek Sands to the overlying and underlying sedi-
ments and to the Para Fault is shown in the section (fig. 2) dtawn along the
line AB of fig. 1. The position of the Pliocene remnant underlying the City is
shown hy the narrow band 69 feet below the surface in Bore 215 to the east
of the fault.
IV. SEDIMENTATION AND LITHOLOGY
The Dry Creek Sands and their equivalents in the Phocene were deposites!
in a2 shallow bay or gulf of the Pliocene seas after the depression af the ol:ler
strata which had been reduced to base surface at the end of the Mesozoic ane
submerged during the early Tertiary,
At the close of the Lower Miocene a cycle of erosion occurred in South
Australia, where, unlike Eastern Victoria, no continuous sequence from Lower
Miocene to Pliocene is revealed and a marked unconformity separates the
Pliocene from the underlying strata, the youngest of which sre Lower Miocene,
with the restricted Lower Miocene foraminifer, dustrotrillina howchinit.
On this Tertiaty erosion surface the Dry Creek Sands and the sandy Hme-
stones were deposited. As revealed in the borings, the Dry Creek Sands are
a well-defined lithological and palaeontological unit usually readily distinguishable
from the underlying tarlier Tertiary strata. The Miocene is generally but not
always a yellowish sandy marl or calcareous santstone. The sand grains are
frequently muck encrusted, Overlying the Miocene, the light-grey or sitvery, fine.
sharp Pliocene sands and clays, carry a rich marine fauna. Intercalated bands of
grey and white limestone occur apparently irregularly throughout the strata,
Present knowledge does not permit the correlation of these bands in any way.
They may be the equivalents of the more resistant members of the Phocene which
47
underlie the City to the east of the Para Fault, but the writer’s opinion is that
the sandy limestones to the east of ihe Para Fault represent the shallow littoral
facies.
Bores examined in detail demonstrate that very fossiliferous bands occur
at more than one level in the Pliocene, their position probably being
determined by the operation of currents in the bay in which the sands were
deposited, The indication is that the general direction of such currents was north-
easterly. This would account for the unusually rich bands penetrated in Abattoirs,
Weymouth’s, and Salisbury Bores in the north-eastern portion of the basin.
These highly fossiliferous bands were not deposited evenly on the floor of the
_COMPOSITION OF THE FAUNA
y
eb - boo BO
ih ow
\~wae
J = "Tanjukus’, L © “Lenpferdian”, B} > “Baresferdian y Baiconbien’, By © Baiensdahen’ ce 'Chetlenharnian™
Fig. 3
basin in still water, but were produced by the concentration of shells along the
shore lines by surface currents. Variation in intensity of the currents would
account for the uneven distribution of the load. As the highly fossiliferous shelly
band is most frequently the aquifer, boring generally stops when it is reached.
Where the band has been passed through and the boring continued, less fossilifer-
ous strata are revealed.
48
Overlying the Dry Creek Sands are approximately 300 feet of superficial
clays, sands, and gtavels of Pleistocene to Recent age of alluvial deltaic origin
consequent upon the upliit of the Mount Lofty Ranges horst. They form a helt
af piedmont alluvitim widening northwards and about 10 miles wide in the
immediate vicinity of Adelaide. North of Adelaide remains of extinct marsupials,
including Diprotodon, have been found in the alluvium.
Except for two recent incursions of the sea, cach represented by less than
five feet of sediments (Miles, 1952, p. 32) there was no general submergence
of the Adelaide Plains during the Quaternary.
The downward succession from Recent to Miocene may be exemplified by
Filsell’s Bore (No, 169), examined by the writer and sampled to a depth of
540 [vet when boring ceased in the Miocene;
Surface -302 feet.
302-517 feet.
—- 317-348 feet,
| 343-360 Feet.
360-373 feet.
Clays and gravels of Pleistocene to Recent age.
Greyish-brown fine glauconitic sand with Rotalia beccarii,
Ostrea. sp. and “Mactra” sp,
Greemsh-grey silt with a similar fossil content.
Fine grey sand, highly fossiliferous, with typical assemblage,
mainly imolltsca,
Fine sharp quartz sand, highly fossiliferous with mostly
small mollusca and foraminifera, together with six species
of bryozna.
378-382 feet.
382-396 feet,
396-409 Feet.
ADOPTS Feet.
443-452 feel.
4152-192 feet.
Dark-grey fine fossiliferous sand.
Fine silver-grey sand, very highly fossiliferons, with a
typical molluscan assemblage, mostly pelecypoda.
Fine grey fossiliferous silt, 90% disappearing on washing,
with the pelecypod Cond ylocardia tenuicostae and associated
but not restricted foraminifera and gastropoda,
Fine grey fossiliferous silt.
flard grey fossiliferous limestone.
Grey fossiliferous sands with brynzoa and an admixture of
Pliocene and Miocene fossil species. indicating that the
lowest level of the Pliocene hus been reached and the
Miocene penetrated,
Yellowish sands, much encrusted with calcium carbonate,
with the Miocene foraminifer. Operculina wictoriensis and
bryozoon Mecynoetia proboscidea.
Hard yellow limestone with Operculina victoriensis and an
associated Miocene fauna,
Greyish-brown sands with a similar fossil content.
492-504 feet.
S(i4¥-524 feet.
524-530 feet.
From the manner of collecting the samples only over broad intervals accurate
zoning cannot be achieved, From the surface to 302 feet the typical alluvial clays
and gravels forming the stitface cover of the Adelaide Plains are probably of
Pleistocene to Reeent age. These correspond to the 341 feet of sand and clay
penetrated in Abattoirs Bore (level of collar 170 feet). From 302 feet to 348 feet
the section may be Upper Pliocene in age, No restricted fossils are present; they
are generally few. and Recent in character. The Dry Creek Sands occur from
348 feet to approximately 475 fcet, the highly fossiliferous band being between the
382 and 396-fnot level, Pre-Pliocene beds occur below 492 feet and the lithology
shows a protiounced change at that level, the characteristic yellow colour replacing
the grey sainds of the Pliocene. The Miocene foraminifer Operculina victoricusis
makes its appearance. The change from Dry Creek Sands to the underlying
Miocene may also be indicated by the sudden increase in the number of bryazoa
which are not common in the Pliocene, although they do occur in some nitinbers
representing numerous species in certain borings, such as Hindmarsh.
a
The sandy limestones underlying the City of Adelaide carry Dry Creek
mnolluscs—mainly in the form of moulds of Pwurritelia (Haustator) avricula
adefaidensis, Polinices (Conuber) balteatella, and species of Polinices, 'Mar-
ginella,” Emarginula, Euchelus, and “Venus.” Where they are belter preserved as tn
the unleached block removed in the excavations for the foundations of the Bank
of New South Wales building the determinable fauna is similar to that of the
calcareous sandstones exposed at [Hallett Cove and Ainge Bay, with Chlamys
antiausiralis, Chlamys (Equichlamys) consobrinus, Chlamys (Equichlamys)
sublifrons, Spondylus spondylotdes, OStrea arenicola, Glycymeris (Veletuceta)
subradians, Diastoma provisi, and Polinices (Conuber) batteatella, The lime-
stones are allochthonous, of the fassiliferous-fragmental type commonly found in
association wilh quattzose sandstone (Krumbein and Sloss, 1951, p. 139), Accord-
ig to those authors, such associated rucks are depusited under essentially stable
conditions with mild subsidence ot the depositional area.
V, PALAEOECOLOGY
The environmental and climatic conditions under which the community
preserved in the Dry Creek Sands lived are determinable ouly by the thanato-
coenose or assemblage of fossils so well represented in borings such as Abattnirs
(No. 89), Weymouth’s (No. 207), snd Hindmarsh (No. 6). That it is most
unlikely that the mollusca existed in fife in the position in which they were
deposited has already been suggested in the pteyious section, where the role
played by surface currents in deposition of the sediments is briefly cescribed.
That many of the mollusca were dead before their shells were deposited is
demonstrated by the fact that large numbers of pelecypnds and gastropods, many
of them very small, have been bored by predatory mollusca, perhaps the Hinia
(Reticunassa) which occurs numerously in the Hindmarsh Bore. Shells were
obviously piled in heaps by surface currents operating towards the north-east,
such heaps constituting the shelly band of “oyster bed” which is generally the
aquifer in the Dry Creek Sands and in which the oyster Ostrea arenicole is one
of the conimonest species,
Notwithstanding the mode of deposition, the fauna is sufficiently uniform
for an accurate estimate of the ecology to he made, It has long been recognised
that Australian Pliocene and Miocene mollusca belonged in the main to tropical
genera chiefly inhabiting the Indo-Pacific region today. However, no serious
attempt has been made to correlate them in any detail, The origin and relation-
ships of the Dry Creek Sands fauna will be discussed in detail in the sueceed-
ing séclien and separately, under such species as are concerned, in the taxonomic
study of the species,
The Dry Creek Sands carry essentially a tropical marine fauna, with a large
percentage of its subgenera tepresented in the Indo-Pacific region today. The
subgenus, as a practical indicator of climatic conditions (Chavan, 1949) has been
freely employed throughout this study. The living community now partly pre-
served in the Dry Creel Sands undoubtedly inhabited a sandy bay of the Pliocene
seas with relatively sheltered conditions and little disturbance except from surface
currents, Apart from the evidence of differential deposition of load, the presence
of bryozoa which require circulating waters for their existence indicates that
the sediments were not lai] down in still waters. The environment was epineritic,
with shallow water species and subgenera prevailing, East of the Para Fault the
limestones ate tnore characteristic of the littoral environment and littoral species
af Chlumys and Polinices (Conuber) are more common.
The geaus Terebratia, formerly identified from the Dry Creek Sands and
apparently indicating tropical mangrove swamp conditions (Crespin and Colton,
1952, p. 233) similar to these of the native habitat in Northern Australia, has
E
30
been erroneously identified. The restricted species described as Terebralia ade-
laidensis Howchin and Cotton is not a Terebrafia but a Thericinm belonging to
a lineage represented in the Italian Pliocene, Recent Indo-Pacific, and probably
the Parisian Eocene.
Tropical subgenera of the littoral or epineritic environment which occur in
the Dry Creek Sands include the pelecypoda Arca, Cucullaca, Pinctada, Sportelia,
Belluctna, Prophetilora, Vasticardixm, and the gastropoda Notohaliotis, Laetifur-
tor, Pulehrastele, Calthalotia, Tugali, Gena, Cocculinella, Nina, Pelecydint,
Obtortio, Semibittium, Semivertagus, Amaes, Margineulima, Agatha, Pyrga-
lampros, Cypraeerato, Globularia, Trunculariopsis, Pterochelus, Latiaxis, Fusinis,
Bavyspira, Turrancilla, Mitra, Tudicla, Cymbiola, Aulicina, Cancellaphero,
Gibberula, Closia, Volvarina, Tomopleura, Etrema, Veprecula, Floraconus.
Subgenera inhabiting warm seas but with a greater range of thermal tolerance
than the above are the pelecypoda Barbatia, Tucetona, Tucetilia, Chama, Milthe,
Regozara, and the gastropoda Emarginula, Astele, Phasianotrochus, Euriclaneulus,
Minolia, Spectamen, Phenacolepas, Tenagodus, Ataxacerithium, Hirtoscala, Niso,
Syrnola, Puposyrnola, Turbanilla, Chemnitzia, Pyrgiscus, Cheilea, Sabia, Argo-
buccinnm, Cymatiella, Murexsul, Homolocantha, Phos, Reticunassa, Serrata.
The distribution table (pp, 56-62) attempts to show the horizontal distribution
of cach of the species constituting the molluscat fauna recovered from the
Pliocene of 14 borings. Hores are arranged from north to south from the most
northerly, Tennant's Bore (No. 189), to the most southerly, Brooklyn Park
(No. 17). Numbers of the bores are as follows: Tennant’s (189}, Weymouth’s
(207), Abattoirs (89), Dry Creek (178), Glanville (57), Filsell’s (169),
Holden’s (81), York (14}, Croydon {51}, Hindmarsh (6), Bore 65, Cowandilla
(5), Kooyonga (105), Brooklyn Park (17). The inference to be drawn from
the table is that there is greater concentration of species in the northerly bores.
and that in the southerly bores those that are to the east and nearer the Para Fault
and the presumed shoreline are more fossiliferous, Such concentrations have been
effected apparently on or near the shore line, generally towards the north-east
of the bay.
The associated foraminiferal fauna contains a number of genera living today
in shallow warm waters, including the Peneroplid genera Peneroplis, Sorites,
Amphisorus, and Marginopora, Marginopora vertebralis is extremely common in
some borings, and together with Peneroplis planatus ts exposed on weathered
surfaces of the sandy limestones of the littoral facies. Rotalia beccarit is found
in almost every sample and is perhaps the mast commonly occurring foraminifer
in the Dry Creek Sands. Its presence in large numbers is indicative of a bay-
littoral environment. Associated with the Peneroplidae and Rotaliidae are species
typical of the Recent Flindersian Province such as Flintina triguetra ( Brady) and
Nubecularia luctfuga vat, lapidea Wiesner.
VIL FAUNAL RELATIONSHIPS
Four distinct elements may be recognised in the fauna: a dominant Recent
Indo-Pacific, a Tethyan Eocene, a Recent Australasian, and a cosmopolitan,
A. Tue Recent Inpo-Pacipic ELEMENT
The dominant element in the fauna is Indo-Pacific. Although the
tropical character of Australian Tertiary molluscs has always been recog-
nised, no detailed attempt has hitherto been made to correlate Australian
Tertiary faunas with the living faunas of the Indo-Pacific Region. With the
possible exception of one or two species living today in North Queensland, with
which examples in the Dry Creek Sands appear to be conspecific. the fauna has
nO species in common with the Recent Indo-Pacific, but the resemblance or affinity
in many cases is remarkably close and the species are subgenerically identical.
31
The affinities between species of pelécypoda appear ta be less striking than those
between gastropod species. This is perhaps due to the fact that the gastropoda
are more restricted and generally shorter ranging than pelecypoda, and such
affinities as do occur are more conspicuous.
Species of pelecypoda which may he directly correlated with Indo-Pacific
or Northern Australian specics are: Montlilora (Prophetilora) chavani sp. nov.
with M. (P.) arizelo Iredale; Vasticardtum submaculosum sp, nov, with V.
maculosum Wood, V. transcendens Melvill and Standen, and V. mauritianum
Deshayes ; Antigona {Proxichione) cognata (Pritchard) with A, (P.) listert Gra
and A. (P.) refiexlatum Linné,; Gafroriuns perarnatum N, H. Woods with
G. dispar Dillwyn; Veremolpa protemarica (Cotton) with F. marica (Linne).
The scaphopod species Dentalium (Dentalium) howchini (Cotton and Ludbrook)
is related to D, (D.) elephantinum Linné, Affinities in the gastropoda are to be
found between Calliostoma (Lactifautor) spp, and C. (L,) deceptum Simith;
Astele (Pulchrastele) planiconicum (Ludbrook) and A. (P.) seplenartum Melvill
and Standen; Thalotia (Calthalotia) nitidissima (Ludbrook) and T. (C.)
arruersi¢ Watson; Clanculus (Euriclanculus) quadricingulatus Ludbrook and
C. (E.) cevlonicus G. and H. Nevill; /sanda (Minolia) perglobosa (Ludbrook)
and [, (M.) pulcherrima Angas; Speclamen planicarinatum sp. nov. and
S. hiangulatum Adams; Spectamen preecursor sp, nov, and S. sayademalha Mel-
vill; Trbiola (Partwbiola) depressispira (Ludbrook) and T. (P.) _carinata,
T. (P.) quinguecarinata and T. (P.) novemcdrinata all of Melvill; Therictun
adelaidense (Howchin and Cotton) and 7. opporlumen Bayle; Amaca
(Amaea) triplicata (Tate) and A, (A) kieneri (Canefri); Tranculariopsis pera-
mangus (Ludbrook) and T, érunculits (Linné) ; Hemolocantha antecedetis
sp, nov, and H. secunda (Lamarck) and H. varicose Sowerby ; Latiaxis dissitus
Cotton and L. mawae (Gray); Austromitra angusticostata Ludbrook and
A. capensis (Dunker), 4. turtiger (Reeve), A. kowtensis (Sowerby), 4. capri-
cormia Hedley; Tudicla sinotecta Ludbrook and T, spirillus (Linné) ; Cymbtola
tabulota (Tate) and C. pulchra (Sowerby), Volvaring (7) incommoda sp. nov.
and F’, (2?) sercodes Tomlin, V. (?) serra Bavay-
BR, Tue Tetuvan Eocewe ELEMENT
One of the most interesting faets to emerge {rom the attempt to correct the
generic and subgeneric locations of the mollusca is that several subgenera well
represented in the European Eocene have closely allied representatives in the
Dry Creek Sands. This is perhaps not altogether unexpected in view of the
dominance of the Indo-Pacific element to which the Tethyan Eocene is ancestral
{Martin 1914; Umbgrove, 1930; Davies, 1934, p. 104). It seems somewhat
improbable that the ‘Tethyan element in the South Australian Pliocene was intro-
duced by late migration by way of the East Indies. Molluscan faunas of the
East Indieg and those of the Australian Tertiaries seem to have less in common
than might be expected. The most convincing conclusion to he drawn is that the
Tethyan molluscan elements had already reached Australia during the Eocene
or Qligovene, This is supported by the writer's recent discovery of the subgenus
Bellucina in clays of prohable Eocene age from the South-last of South Aus-
tralia. Tethyan foraminifera Nwmmulites, Discocyclina, and Pellatispira have
been recorded from the Eocene of the North West Cape—Cape Cuvier area in
Western Australia (Chapman ard Crespin, 1945), and additions to the knowledge
of ihe Tertiaries in the North-West of Western Australia may establish the
presence of an allied molluscan fauna,
Present knowledge of the affinities of pre-Pliocene Tertiary mollusca from
southern Australia is too limited to petmit confirmation in more than the one
instance cited af the preservation of the Eocene element within the Australian
faunas, but that this is the case is more than probable. It is supported by the
52
strong Indo-Pacific affinity of the foraminiferal and molluscan faunas of the
Tertiary marine sedimentary rocks exposed at intervals over a wide geographical
range trom Notth West Cape in, Western Australia to north-western Victoria.
The geological record over this area is very imperfect and no gid conclusions
may be drawn, but information is available to suggest that thermal conditions
were very uniform over this and the whole of the Indo-Pacific region during
most of the Tertiary, and no sudden change of temperature ur ecological condi-
tions led to the extinction of faunas between the end of the Eocene and the Middle
Pliocene.
Evidence of the preservation of a Tethyan element in the fauna is
based on the presence of species of the following subgenera, cach having close
relatives int the European or English Eocene and also in the Recent or late-
Tertiary Indo-Pacific fauna: Chlamys s. str. with the C. varia series in the
Parisian Eocene, and also it the Miocene and Pliocene of ‘the Red Sea region
and Zanzibar Protectorate (this series is fairly widely spread and would not
in itself indicate a Tethyan clement, but is regarded as worthy of note in view
of the presence of the other undoubted Tethyan subgenera); Lentipectest, repre-
sented by L. cornens (Sowerby) in the English Eocene and L. borneajus (Cox)
in the Pliocene of the North Borneo. Arcturellina, closely allied to the Parisian
Eocene species aspernla, aigensis, prevosti, pulchra, ambigua, and serricata, all
of Deshayes; Sportellu with S. dubia Defrance in the European Eocene atid
5. jubota living in North Queensland ; Monitilara s, str. represenved in the Parisian
Eocene by M, clegans Detrance and the Australian Recent Peronian by M. ram-
sayi Smith; Gibbolucina with G. ellipsoidalis Cozsmann and Peyrot in the Parisian
Eocene, G. ca/losa (Lamarck) in the Indo-Pacific; Seliveina with B. ligata
(Cossinann and Pissarro) in the Parisian Eocene, B. evcosma Dall in the Indo-
Pacific; Semivertagus with S. unisuleatum Lamarck in the Parisian Eocene;
Coxellaria (created below) related to C. cieve (Lamarck) and C. multispira
(Deshayes); Globularia, very like Globularia sigaretina Lamarck from the Cal-
eaite Grossier. There ate in addition the following subgenera common to the
European Eocene, Adelaide Pliocene, and Recent Indo-Pacific which have not
been studied in detail by the writer who accepts the authority of Wenz (Handb,
der Palaozool, Gastropoda) that they occur in both the Tethyan Eocene and
Recent Inde-Pacific taunas: Semibitiivm, Margineulima, Fusinus, Twdicla,
Auticing and Gibberult.
It is emphasised that, despite resemblances between certain elements in
the fauna and elements in the Recent Indo-Pacific and the Tethyan Eocene
moliuscan faunas, the total composition of the faunas in each case is very distinct
and local ecological conditions tio doubt very rapidly produced divergent
branches from a common stock. One of the most striking features is the general
lack of specific resemblance between the Tertiary mollusea of the East Indies
and Australia, although both appear to be influenced by a Tethyan Eocene
element. As an example, of the mollusea described from the Pliocene of North
Borneo (Cox, 1948) only two species may be regarded as showing any relation-
ship to Australian Pliocene species; Lentipecten. horneanys (Cox), related to
Lentipecten adelaidensis sp.nov., and Timoclea bataviana which from external
features appears to belong to Verenrolpa and to be rejazed ta PY’. protomarica of
the Dry Creek Sands and to . marica of the Recent Indo-Pacific, It is therefore
surprising to: find so close an affinity between the Dry Creek Sands Pliocene and
the Indo-Pacific Recent Furnas.
C. THe AUSTRALASIAN ELEMENT
Distinct from the tropical element which, as shown above, in some species
represents a preservation of Tethyan features, is a large autochthonous element
which has developed since early Yertiary times in Australia and which is not
53
represented elsewhere other than to a limited extent in New Zealand, No work
has been done in Australia to establish the lineages of the subgenera comprising:
this element, and it may at present be assumed to have arisen from a native stock.
At this stage it is not possible to give the vertical stratigraphical ranges of the
subgenera so that the horizons at which they separately first appear may be
indicated, |
The Australasian element, corifined fo Australia with the exception of those
subgenera marked with an asterisk which occur also in New Zealand, is com-
posed mainly of the subgenera Ennucula, Neotrigonia, *Cuna, Condylocardia,
*Myllitd, Pseudarcopagia, *Tawera, Anapella, Horpetopoma, *Phasianotrochus,
Euriclanclus, Starkeyna, Partubiola, *Munditia, Bellastraca, *Linewmera, Cteno-
colpus, *Colpospira, *Zeacumantys, Ddnnevigena, *Evelynella, *Zeacrypta, Tylo-
spira, *Ellatrivia, Notocypraed, : Umbilia, Conuber, Sigaretatrema, *Taniella,
*Tasmatica, Hypocassis Antephalium, *Cymatiella (also in Pacific), *Muresxstel
(also in the Pacific), Litosamia, Enattmene, Bedeva, +Pleia, Cupidoliva, *Austro-
mitra, Tumitra, Axstroharpa, Amorid, Ericusa, Sydaphera, Inquisitor, *Filo
drillia, Pervicucta.
‘The lineages of subgenera commor to Australia and New Zealand are not
definitely established in Australia, although some are known in New Zealand
at least from the Eocene and are not late Tertiary introductions with the Notonec-
tian Immigration during the New Zealand Castlechfhan ( Marwick, 1929). There
was some addition of Indo-Pacific units to the New Zealand fauna during the
early Tertiary (Marwick, 1925), although the Indo-Pacific element is ve much
weaker in the New Zealand than it is in Australian faunas, Australian elements
may have been introduced during the early Tertiary also,
D. CosMorouitaN ELEMENT ;
The rest of the fauna is composed of cosmopolitan subgenera or those which
have not as yet been sufficiently studied for any precise pronouncement upon their
affinitics to be made,
VII. AGE OF THE FAUNA
The problem of dating the faunas of the Australian region and of correlating
therm with the European time-scale has never been an easy one, and although much
has heen added to the knowledge of Australian Tertiary stratigraphy during
recent years by study of the mictofaunas, an accurate or reliable determination
of the Sequence and comparable time relationship has still to be made
In the absence of restricted zone fossils the most reliable method appears
to be to correlate the total faunal assemblages with faunas of established age
elsewhere in the Australian and neighbouring regions,
There is no doubt that the Dry Creek Sands are post-Miocene. They rest with
angular unconformity on beds not younger than Butdigalian and contain 110
restricted Miocene zone fossils, The mollusca, however, are almost totally unlike
the Recent mollusca inhabiting the adjacent coastal waters, and atiy attempt to
apply the method initiated hy Lyell of assessing the percentage of living species’
would give an entirely etroneotis result-
The table (fig. 3) has been constructed to show the composition of the
fauna from the best information available at present. The “stage” names hitherto
employed for Victorian and South Australian pre-Phiocene Tertiaries are here
us¢d only to give some indication of the length of range of the unrestricted
species. They will be abandoned when acturate zoning of the strata is achieved.
- Salient features of the analysis are:
1, The very low percentage (11) of Jemmy's Point (“Kalimnan") species.
2. ‘The very high percentage (57) of restricted spectes.
3. The 10% of Recent species not occurring at Jemmy’s Point,
54
This purely statistical evidence would suggest that the Dry Creek Sands
are younger than the Jemmy’s Point Formation (“Kalimnan”). The latter being
accepted as Lower Pliocene in age, the Dry Creek Sands could then be regarded
as late Lower Pliocene or early Middle Pliocene,
From the non-statistical viewpoint the exact correlation of the Jemmy's
Point Formation and the Dry Creek Sands is limited by factors of distance and
facies. The type section at Jemmy’s Point, Kalimna, Gippsland, is 650 miles
east of Adelaide. The strata in that locality were laid down without stratigraphical
break (Crespin, 1943) in a sedimentary sequence embracing stages frotn at least
Oligocene to Pliocene. The Dry Creek Sands were deposited after a period of
denudation with a break in the Miocene-Pliocene seqiience, There was during
Pliocene times no connection by way of Bass Strait between the two areas. For
this reason the term “Bass Strait Province” introduced by Crespin (1950, p. 423)
is somewhat misleading,‘"’ since it implies the existence of Bass Strait prior to its
foundering. The Jemmy's Point area was separated from the Pliocene seas to the
west by the long peninsula of which Tasmania formed the southerly part, and
diverse influences indubitably prevailed im the two areas.
“Kalimnan” species recorded from the Dry Creek Sands are frequently not
typical. Whether this is due to stratigraphical er environmental facies variation
is 2 question which can only be answered by close study of all Pliocene faunules
over the geographical range between Adelaide and East Gippsland. Were the
personal factor permitted to operate to the extent of separating some of the South
Australian examples from the typical species, the number of restricted moliusca
in the Dry Creck Sands would be even higher and the number of “Kalimaan"”
further reduced. On the other hand, as yet no detailed study similar to the
present one has been made of the Jemmy’s Point mollusca or of mollusca from
Pliocene localities elsewhere in Victoria to enable one to express a confident
opinion that some of the restricted Dry Creek Sands mollusca do not occur in
the Victorian Pliocene. Furthermore, the fauna of the Dry Creek Sands differs
markedly from that of the estuarine Pliocene strata of the Murray River. One
can only emphasise that much detailed work remains to be done before the
Pliocene sequence in Southern Australia is definitely established,
From the microfauna! aspect the only beds which have been correlated
with the Dry Creek Sands ate limestones in north-western Australia and on the
Nullabor Plains from which the foraminiferal assemblage of the Dry Creek Sands
has been reported (Crespmn, 1950, p. 425).,‘?)
The New Zealand Waitotaran is more closely related to the Dry Creek
Sands than is the Nukumaruan, and if any significance may be attached to
trans-Tasman correlation of climatic conditions, the similar conditions prevailing
during the South Australian Pliocene and the Wattotaran, with sudden extitiction
of tropical forms at the end of the period of deposition of the Dry Creek Sands
may be worthy of note. The Nukumartian was marked hy a cold-water faunal
immigration brought about by the advance and later retreat of subantarctic
waters m the Middle Pliocene (Fleming, 1944, p. 209), It is certain that somewhat
similat conditions existed in southern Australia where the Dry Creek Sands and
their equivalents represent the last link with the tropical waters of the Indo-
Pacife. The only suggestion of a gradual infiltration of colder water forms
is provided by the presence in the Dry Creek Sands of the Flindersian fora-
minifera Flintina triguetra (Brady), Crébrobulimina polystoma (Parker and
Jones) and Nubecularia lucifuga var. lapidea Wiesner, and Flindersian
1 Tt is also liable to confusion with the term Basan Province in use for the land
fauna of Tasmania.
) As Miss Crespin has identified the foraminifer Austrotrillina howchini frony what
Fd be the same formation on the Nullarbor Plains, the second correlation requires con-
Fmattan.
55
mollusca not related to tropical forms, including Nucula (Ennucula) beach-
portensis Verco, Nuculana (Scaeoleda) verconis (Tate), Limopsis vixornata
Verco, Lissarca rubricata (Tate) and Lissarca rhomboidalis Verco, Bornia
irigonale (Tate), Mysella ovalis Tate, Hiatella angasi (Angas) Batilloria (Zeacu-
mantus) diemenensis Quoy and Gaimard, B. (Batillariella) estuarina (Tate)
Trophon (Litozamia) goldsteini Tenison-Woods, Mitrella (Dentimitrella) lin-
colnensis Reeve, Retusa (Semiretusa) apiculata (Tate), and Volvulella rostrata
(Adams). These are all species of autochthonous genera which have probably
evolved from endemic Australian elements.
56
DISTRIBUTION. TABLE
SPECIES , \ ; BORE
a < . SSSLRSexae ew Es
' ‘ m= a “ ™ -
a a A a a
Nucula (Ennucula) kalinnae Singleton Hie tee geile ORE rm et Be et ee
Nucula (Ennucula) beachportensis Verco .. seid cet > aati eS pan ae ate at. a
Nucula. (Ennuciula) venusta N. H. Woods ni, wha Le es ber ee ee
Pronucula morundiana (Tate) me ae jase weit Haji hb ee t= Ser.
Nuculana (Scaedleda) woodsi (Tate) an) aes) Se ee ee SS
Nuculana (Scaeoleda) crebrecostata (T. W.) ene. wre ae Roe SX Se ier 5 eo
Nuculana (Scaeoleda) verconis (Tate) toe fae We Sahoo SS ee xl
Arca negata (Cotton) .... Ae sng we tee) foe ae HE SB ea ee fee epee yo =
Barbatia (Barbatia) epitheca Cotton a a i > es ee ee ee
Barbatta (Acar) coma (Cotton) sg chen a Da SN ee dee get eet Se et Se
Cucullaea cortoensis McCoy np ey! Oe tee Coes ee aa eo
Cucullaea praelonga Singleton wi? cine fair bad ole Spe ee xx
Limopsis beaumariensis Chapman wae eas Cs XK KH EH NEE HLH
Limopsts macéoyi Chapman... ease aa OK XK KO
Limopsis eucosmus Verco im O52. Fie las dee beet! oe A te mie
Limapsis vixornata Verco aod wae ‘ste a x SS —
Lissarca- rubricata (Tate) ates ste seve dap a eh ES ee Hh Ke
Lissarca rhomboidalis Verco .... fang ass a we SX a eee eel att
Glycymeris (Tucetona) convera (Tate) ae CXR KH UK XH K_X
Glycmeris (Tucetilla) tenuicostata (Reeve Tn Paes ee Mee eee HE tye
Glycymeris (Veletuceta) subradians Basedow wh gir do SRM Re Sa ee peep
Pinctada crassicardia (Tate) sone tate ath ow O-XXxX--~_-x--—x__
Loapha hyotidoidea Tate a, Te a Se ne St. ee eel Pe a xox
Ostreg urenicolaTate t.. icd aed tute te ae ee Ee SCO ee
Neotrigonia trua Cotton np i | aS shh anh ome bo Le See coh te og LeuSe
Chlamys (Chlamys) polyaktinos sp. nav... ee, we = EOL ee Be
_Chlamys (Chlamys) antiaustralis (Tate)... nue KO KEK AK XK XEKE
Chlamys (Equichlamys) consobrina (Tate) bite wah We = 2 ee Se en Ss Hs
Chlamys (Mesopeplum) incerta (T. W.) ew ao & RE scecteaa lier x--
Lentipecten adelaidensis sp. noy. ti0 is jas <Seistetet: ee SS oe A, Se
Propeamusstum atkinsoni (Johnston)* pn a oe On ROS RS eae Fre TL Rss Sy
Hinwites corioensis McCoy eee KE
Spondylus spondyloides (Tate) wee OC XX KKK KHOR LK
Lima bassi T, W. ee ce ee OY Do eS
Anomia tatet Chap. and Sing. cp «ae tn wet, Mee OOK ae ee lee ee ol
Brachidontes hirsttus Lamarck ead weet Se ate eS = ee ee Se
Myadora ulea Cotton —,.., an ble ny save ee Sods hae eee
Myadora tenuilirata Tate anes Sioa ats ess e56e- ah ae te Sm” ela lees ee
Myadora corrugata Tate vate ttt Least sates 1 Rl Re ee pee
Cleidothaerus adelaidensis Cotton — .... fxs te Selamat te! eo ba ew ee _
Humphreyia strangei Adams nee im ost a Pad 1 ee Pee SBP, Shi
Humphreyia incerta (Chenu) Miike hp he, Biep ten So eee ee Op
Cuspidaria subrosirata Tate 4, 0 sus ieee tats me a ror me ol whe
Eucrassatella camura (Pritchard)... Hagen fests we CX XEX--~3XX-_ KK
Fucrassatella kingicoloides (Pritchard) gy x EX
Cuna polita (Tate) toes oon savy aece otee beh oe Me % Si
Cuna aporema Cottan .,.. se Aen bist ale a ee, ee eee Woe te Sela eS Sod oe
Cardita compia (Tate) wile uty Wp -sea pet SE Shae
Cardsta subdeceptiva sp, nov. 00 eee ee XL LLL
Gluns spinulosa (Tate) oS See Tey ant ope eh Set See Ge mt sal copan! et
Glans dennantt (Chap, and Cres.) __.... ass ite at oe See eee = Se
Pleurameris pecten (Tate)... asad cae cher ak} ee ES eS Bias ce x Ss
Pleuromeris subpecten sp. nov. sap bees ant ie ot Se a ees ae a
Pleurameris trigonalis (Tate) iis Se ae oe eee ee 2 be
Cyelocardia (Scalaricardita) subcompacta (Chapman and
Crespin} «, — x —- = --~2 +H a
37
SPECIES - BORE
ASSESESB eS ARES
mam tT - -_ _
Cyclocardia (Arcturellina) hindmarshensis sp. nov. we = Kobe xX -- KB
Cyclocardia (Arcturellina) peridonea sp. nov. as en or Ke Se xos-+
Condylocardia tenicostae Chap.and Gab. .... sab Wiis, Sy =o ee
Sportetla jubata Hedley hee pees why sp we oO XX - 7 -- +x
Chama lamellifera T. W. ae bis aA St ate eH eee he ee
Myrtea fabuloides (‘Tate) tos ats aonb ede SE Boe ae eS ee ee
Monitilora (Monitilora) idonew sp. nov: r a coe Xo ew ow
Monitilora (Prophetilora) chavani sp_nov. ie by Do @ lee ee eee ee fash -=
Eomiltha (Gibbolitcina) salebrosa (Nr H. Woods) te ea tithe: bh oe 2 — a
Eomiltha confirmans sp. nov. WA Yat pee Se Sel a
Linga (Bellucina) nucifarmis (Tate) dite ay we SX EKEXX-- He XH
Callucina balcombica (Cossmann) 1 eee HERR OR Xe
Gonimyrtea salishuryensts Sp. NOV. a oo sas ah na — He ae a
Ganimyrted. crasstOr SP. TOV. sens senses io sCasvppiiaw “estesate ee de ee SSS a
Gonimyrtea validtor sp. nov... gore inst ies cae : ee a Kno +
Goninvyriea notabilior sp. nov. Aco Sipe ee eS eS HS ee SE ee
Miltha hora (Cotton) bie sais se ae wa Se eee x—-xX xx
Divatucina cumings (Ad. and Ang.) wae ae EE HE SE OR aE RES
Diplodonta solitaria N. H. Woods w+ Sa ee witty Pam ae eee cr ey ots ee
Numellasuborbicularis (Tate) wow =e KS ee
Thyasira sinuata (N.H. Woods) un ee eae SK RR TH ee
Borma.trigonale (Tate) et ee a ae | Kae se
Litigiella adeluidensis sp. nov. peed wa shee ee i ane ee x2 —
Mylkta hindmarshensis sp.nov. as wie Se iy ee x= -e
Pyaperyeina micans (Tate) ae eee EO RRR OOO
Properycina torrensensts syi. nov. ie ty esi ee
Platomysia sp, i. SS cw teh we athe marta ocglet we ee x--
Montocuta sevicea Tate ee, X---
Mysella anomala Angas seh ape aja’ Hess we TOT kKR-- RS KK x--—- +
Mysella ovalis Tate —.... ule as i ewe SKS HE Re Oe
Mysella macer N. 31. Woods 2.00 eee KOO OO =<
Mysella tellinoides NTT, W. wooo we SE KH HR x--+-
Vasticardinm (Regezara) praccygnorum #03 TOV: an ne EE He See ee
Fasticardium (Vasticardium) submaculosum ep. oy. «a. —S eee eee “<<
Fulvia tenticostata (Lamarck) " beg we Fee EOS Hee Hee
Nemocardium (Prattlum) proterothetidis sp. nGv. i a
Dostnia (Kereta) johnstoni Tate... anes a
Notocallista (Striacallista) mollesta Wewk “. So 2exeoloones ~---
Notocallista (Striacallista) pestis Marwick ne EER ee oe SS Se ee
Antigona connata (Pritchard) we wae Se x—--—-xX-—
Antigona (Hina) cainogioca (T. Woods) ae wk EK eH eRe ee
Gafrarium perornatum N, H, Woods sein) pees we TO XS eee eer eee
Tawera pernitida (N, HH. Wonds) ee x—---=
Tawere gallinula Lam. s aren lies ts we - - XN -- HH Hee Kee
Tamera tacurvilamellata sp, noy. — ass nit oe ee es SS ae ee St ep Se SS
Chioneryx dennanit Chan. and Cres. ant ist we SPX RENOR SL HLS x —
Placamen subrobarata (Tate) nde pave het we + -EXKXX-—--—--—--~—~—-— x
Rassitnaallportt (T.Wds.) .. Ni eee SE ee ee Set
Timaclea (Veremolpa) protomarica (Cotton)/ me won eS aee eo Sees
Venerupis baupertina Tate... ass ehins sate wy — 2S eet voscien—
Gari hamiltonensts (Tate) ae a, a, a
Gari aequalis (Tate)... ast me fave peep emt BE RSE eee a ee
Macomaralbhi. (Finlay) ave Pr tsi saab abe tee el XS ss 55 SH SH a S
Tellina masoni Tate... wo se wee) woe SE He Gee aS
Tellina albinelloides Tate. sie wre ete ose sian fem 8 RE eee ec x-——
Psendarcopuata detrita N. A. Woods. abe Hes wih ae a oS ei eid a=
Semele westculosa Tate ack a fave set win toon Eten es po elt 2 — N=
Solecurtus dennanli Tate rt uit stu ots i @eMS ee eee Osos fee
58
SPECIES
BORE
Solecurtus. subrectangularis N. H. W. peor gees
Mactvra (Electromactra) howchiniona Tate aii
Anapella variabilis (Tate) eats
Zenatiopsis angustata Tate au. abo aed nad
Corbula ephanulla Tate sy) “pase anon fasta
Corbula adelaidensts nom. nov. bite chin, ated
Hiatella austraks (Lam.) sear tae
Hiaiella angasi (Angas) oe
Dentalium (Dentolium) howchini Cott. and Lud. mais
Dentatium (Fissidentalium) bifrons Tate sees
Dentalium (Fissidentalium) mawsont sp. nov. ata
Dentalium (Antalis) denotatum sp.nov. ay san
Siphonodentalium (Pulsellum) adelatdense sp. nov,
Cadulus (Dischides) yatalensts sp, nov. sis
Cadulus (Gadila) acuminatus Tate...
Acanthochiton (Eoplax) adelaidae Ash. and Cott. .
Chiton (Anthochiton) relatus Ash. and Cott. Site
Cryptoplax ludbrookae Ashby Pe ont ahd
Hahotts (Notohaliotis) naevosoides MeCoy_ aie
Ewmarginula didactica sp. noy ese.
Emarginula delicatissima Ch. and Gab...
Emarginuladennanti Ch. and Gaby ye seeneee
Emargimula dilatorta sp.nov. 4.0 see utes nee
Tuogali cicatricosa Adams ah Goats a
Tugali inforitunata Lud. rs
Tugali nota Cotton wont wer wage
Amblychilepas acra (Cotton) |
Fiuchelus (Herpetopoma) plocenicus (Lud. >
Calliostoma (Laetifautor) oblsquicancellatum (Lud. )
Calliostoma (Laetfantor) stinicarinatum (Lud,)
Calltastoma (Laetifautor) crebrinodulosum (Lud.)
Calliostoma (Laetifautor) bicarinatun (hn, ) oh
Astele (Astele) fanuticem Lud. a ete
Astele ( Pulchrastele) planiconicum (Lud. > pate
Astele (Pulchrastele) tuberculatum (Lud.) i.
Cantharidus (Phasianotrochus) laxegemmatus (Lud) sabe
Cantharidus (Phasianotrochus) subsimplex (Lud. )
Thalatia (Calthalotia) nitidissima (Lud.) f
Thalotia (Calthalotia) fictitis (Lud, ) ae
Clanculus (Euriclanculus) quadricingulatus Lud.
Clanculus ( Euriclanculus) eucorinatus Lud. ante
Isanda (Minolia) perglobosa (Lud.) ie abt
Npectamen plantcarinatii Sp, NOV, ewer sued
Spectamen praecursor sp. nov, east vo sees
Gena incalia Cotton ss ase epee
Tetnostoma depressultun ( Ch. and Gab. } aioe sore
Starkeyna. pulcherrima (Ch. and Gab.) vis vue
Tubiola (Pariubiola) depressispira (Lud.) 7
Tubiola (Partubiola) varihrata (Lud.) Ty!
Crossea (Dokicrossea) cf. labiata T. Wi or,
Collonia omissa sp, tov. ws ina wats
Astraza (Bellastraea) hesperus Sp: nov. wie tee
Liotina (Mundifia) tarmanica T. Woods... tone
Phasianelladennanti Crespin 0.0 se tee seen
Pellax jeyuma sp.nov... ve
Phenacoletas tela Lud. sage mi Sos
Cocculinella salisburyensis sp, nov... ans
Tectarius (Nina) adelaidensis (Cott.)*
BR FRE
Pbrprdeutrerd sd
we
nwa
ttiti
Plt riwt tr tripe tet
Pibeali ltt
Awl aka | wat li Re lL a
Al
ai
AMA | LAR
ee
mame ee Se ee He ee
SPECIES BORE
SSBERRSSAaSTS* SS
—- oF - - -
Amphithalamas (Pisinna) chrysahdus (Ch. pal Geb) ww ee eee ee
Merelina (Linemera) varisculpta sp. nov. ... phe eM ae ee age ee eh cvs
Turbvella praenovarensis sp.nov. eee KR ee
Turboella elimatiag sp.noy, in, 0 wee sete Sannin ne Meee Paes HE eR ee rhe
Kaurnella denotata Lud. Ted beet tape nif} ey ay SES ee HS SS Xs ee
Pseudohiotia angost Crosse... en eee Soa” eee ee, enone wr ee
Cingula (Pelecydium) eylindracea T: ‘Woods wh wos EOE BO Se oe SH xa--—-
Rissomanivea Adams ... 0 om “i 2p bade ase a A ag a ene ee ed Swe em pces
Rissoina élegantula Angas .... eos wile, dalle Se ee ee hae st
Rissoina tinelo sp. nov. Ha sgt, cele Hue tee ey ee > er
Diastoma provist Tate —XxXXXXxX-XX—XEX
Turrifella (Haustator) acricula adelaidensis Cott. & Wds. — XxX--xXXKxX-xX¥---—-—
Turritella (Haustator) subacricula Cott. and Wds. aii ee et ee ee i So
Turritella (Ctenocolpus) triliz Cott.and Wds. _.... ve SOM oS ee oy OE Pe
Turritella (Colpospira) platyspiroides sp. nov. abe Peg t oe OM ay eth
Turriiella (Peyrotsa) murrayana subrudis ig & Was. ee NS en ee ee
Glyptozaria spectabilss sp. nov. Pe we amet Se
Archilectonica (Discotectomca} qoounonensis UT. Woods) WX Boo See oe tee
Tenagodws australis (Q.& G.) wid dae ha mm oc x foe to eS xx
Obtertio liratus Lud... ~~ te ae eRe Sea eee ew
Batillaria (Zeacumantus) diemenensis., (Q. &G) divde tae na a eS Se tae as ee
Batillaria (Zeacumantus) multilirata (Lud.) ee be SH He SS KEo---
Batillania (Zeacumoanius) bsvaricata (Lud,) wet cre ORK oe US xo-=-
Batillaria (Batillariella) estuarina (Tate) .-. a. fa fins Ee me ep ee ee
Manulona orrugosa Lud. at, <isee ees ie (EK oe Se
Manulona hrasuturalis Lud, .... % sere ath ea Se oe Oe
Ataxocerithtum cf, concatenotum Tate ’ = 2 4S eee x 43
Alaxecerithium bideniiculatum sp.nov. oy. an a eee Ewe >
Adelacerithium meruitun Lud. fot WT petp jee Ghent tae 2g SS es a
Diala (Mereldia) incommoda (Lud.) fee —egh oe thoi ea oe Loo Ha te
Rittium (Semibittium) subgranarium sp. nov. ee ag Se ge Se Be ge os oe Ee
Thenciwm (subg. n. ov.) adelaidense How. and Crit e sauas PSE aban popended ee x-.x-+
Thericium (subg. n. nov.) pritchard: (Harris) oo. 0 wa Ke
Thericiume (subg. n. nov.) fallax (Lud. ) ths weg ee IE Se le ae ee Se
Sentvertagus capillaius Tate .... a Rie eal pee) en IG RE ee ,
Tlypotrochus semiplicaius sp.nov. ,,, we ee Oe ee ee Ke
Cerithiella (subger. nov.) trigemmata Chap. ‘and Cres, im =e oS Se ee
Cervithiella (subgen.noy.) perelongata (Lud.) wed | ee ES Kile ee ee
Cerithiella (subgen. nov.) supérspiralis sp, nov. wu wm eH ee
Triphora (Isotriphora) salishuryensis sp. nov. wm ee KIS eH ee
Amaea (Amaea) triplicata (Tate)... eee ee KE ee
Cirsatrema (Dannevigena) sp. By aed) eds > ote, eg BUR Se ea oe
Scala (Hirtoscala) sp. .... vere ga See eee eee ee eae
Melanella ( Margineulisna) longiconica (Lud. ,) veee eich. Qty Soe ce ee i ee
Melanella (Margineulima} minuticonia (Lud.} we KH He ee
Letosivaca (Leiosfraca) acutissima Sowerby |... wee ae ee ae Se x—-=+-
Niso psilaT. Woods — ... syne Abate ASR ie” 6 PK ES Che lee —
Syrnola (Syrnola) tincta ‘Angas. an leh OO, ER Se eet S ee he ely
Symola (Agatha) praefasciate sp, nov. wi othe ee KH He
Svrnola (Agatha) jonesiana (Tate) sb bet oe HE A ee ee ee -
Syrnola (Agatha) infrasuleata (Tate) nn ant Cte gee es ep te ee x—-—-—a
Syrnola (Pupasynnala) tasmanica T, Woods sk wah tee Sh RE ee, Sy ee en es =
Syrnola (Puposynnola) acrisecta- Lud. nbs vo we ee Ko So eg oS
Symnola (Euelynella) adelaidensis Lud. Mite aati ee I ee eh ee ee Kon -—
Turbonilla ( Turbonslla) mariage T. Woods 0 un ae KH ey
Turbenilla (Chemnttzia) mappingae sp. nov. mm me = X¥X---H------—--
Turbonilla (Chemnitsa) wurongae sp, nov, ap at ee Ee x-+-+--
Turbontile (Chemnitsia) subfuscaLud, — ....
SPECIES
BORE
Turbonilla (Chemnitzia) adelaidensis sp. nov. 3
Turbonilia (Chevsnitsia) ourrongae sp. nov.
Turbonilla (Chemnttzia) widningae sp. nov.
Turbonilla (Chemnitzia) sp. ....
Turbonilla (Pyrgalampros) vixcosiata Lud.
Turbonilla (Pyrgiscus) “liraecostata” T, Woods...
Turbonilla (Pyrgiscus) radtcans Chap. and Cres. ....
Cheilea adelaidensis Lud. PUM ane
Hipponys (Sabta) conica (Schum.)
Cerithioderma cf. accrescens (Tate)
Capulus circinatus Tate 7 ae ost
Calyptraea (Sigapatella) crassa Tate’ ote ley
Crepidula (Zeacrypta) immersa Angas odd ones
Crepidula (Zeacrypta) dubitabilis Tate site ken
Crepidula (Zeacrypta) hainswortht Jakins, _—
Tylospira coronata marwicki (Fin.) fics thee
Proterato (Cypraeerato) subaustralis sp. nov. Aes
Ellatrivia wirrata Lud, tispe isi <aitg siaa
Notocypraeaeryma-Cotton eee
Umlilia cera Cotto anne ates cts) take
Globularia sp.
Polinices (Pottnices) subjugum (Cotton) ans
Polinices (Conuber) sulbwarians (Tate) en
Poknices (Conuber) cunninghamensts Harr.* ant
Polinices (Conuber) balteatelia (Tate) pais isn
Sigaretotrena subinfundibulum (Tate) mee sisi.
Tanew hamiltonensts (T. Woods) — «., we SE
Tanieglla weymouthensts sp, nov. hon’ Pee mee
Prosiuber microsculptum sp.nov. an vive ape
Austrocochlis sabstolida (Tate) os ati,
Tasmatica modestina sp, hoy, ... “ass ent
Cassis (Hypocassis) salisburyensis sp. nov.
Semicassis (Antephalium) muelleri Tate ....
Semicassis (Antepholinm) suffiata (T. Woods)
Semicassis (? Casmaria) radiata Tate de, Ba, She
Argobuccinum basss Angas aa ee auc 1 ops
Cymatiella adeloidensis Lud, .... sons
Charonia (Austrotriton) armata (Tate) tee aHES
Charonia (Austrotrtton) radialts (Tate)... pry
Trunculariopsis peramangns (Lird.) bee a
Hexaples (Murexsul) suboctogonts sp. nov. neck
Hexoplex (Murexsul) bicanicus (Tate)
Pterynotus (Pterorhelas) trinodosus (2) (Tate) |
Homolacontha antecedens sp.nov. .. aac
Trophon (Litosamia) galdsteini T, Woods
Trophon (Enatimene) metungensis eb and Cres.
Bedeva crassiplicata (Lid.) geet ten
Typhis lacintatus Tate ,... ont a: aie aves
Latiaxis dissitus Cotton* ets wang
Mitrella (subgen. nov.) lincolnensis ( Reeve) haa
Mitreila (subgen. nov.) musscula (Lud.) =
Mitrélla (subgen. nov.) sp. dea oes
Mitrella (Adeemtrella) insolentior (Lud. Serer Oo
Phos gregsont Tate “3
Hinia (Reticunossa) spiraliscabra Chap. and Cres.
Hinia (Reticunassa) subcontca sp, fiov. sans ens
Fasciolaria {Pleta) sp. Se ae iter
Fusinus dictyotis(?) Tate)... <a
vies errr) eves
Lop Ra
fir: i
baste
Ye Pop y
mos +t
\
|
|
|
|
i
{
\
|
tal
|
prt tav
\
— ee ae es ee eS
ee |
\
>
{
|
|
I
|
|
*
'
|
{
|
|
*
4
|
fl
SPECIES
BORE
63
Olivella (Cuptdoliva) nymphalis (Tate)
Ancilla (Baryspira) tatei Marwick 10.0 sus
Ancilla (Turrancilla) adelaidensis sp. nov,
Austromitra angusticostata Lud.
lustromitra mawsont sp. nov, <a <p
dustromitra payciplicata sp. nov. goal astg eae
Austromitra multiplicata-sp. nov. save ate wie
Mitraria (Eumitra) coxi sp. tov sy neti
Mitraria (Eumitra) glabra (?) PavaTianee ‘te hie
anny peers
Mitraria (Eumitra) sp, 5 ne sie
Miirarta (Eumitra). fodinalis (Tate) athe ier
Tudicla sinolecta Lud. .... ons awe ssp
Harpa (Austroharpa) tater Finlay vee eke) att
Cymbiola (Cymbiola) tabulata (Tate) git ase
Cymbiola (Aulicina) uncifera c ESE). asp aun
Amoria grayt Lud. a. a) ee
Ericusa elltpsoidea (Tate) aa 1
Abhera (Sydaphera) wannanensis (Tate) *
Cancellaphera confirmans sp. NOV...
Margmella (Eratoidea) glaessnert sp. nov. sass
Marginella (Firatoidea) wentwarthi T. Woods .:.
hee anes
Marginella (Fratoidea) meta Cotton* .... iy
Marginella (Eratoidea) crista eatin er
Gibberula clima (Cotton) * ,... fo seus
Gibberula talla (Cotton) * ase ate sae
Gibberula cassida (Catton) * a. ue a
Closta moana (Lud.) te hai HY,
Closia arena (Cotton) * at caprsh othe
Closia doma (Cotton)
Closia planilabrum sp. nov.
Serrata charma (Cotton)
Serrata metula (Cotton) * , ike
Serrata bicrassiplicata sp. nov. we aig
Serrala weymouthensts sp. nov.
Polvarima (°) incommoda sp. tov. ....
Xenuroturris (Veruturris) tomopleurotides Powell
Xenuroturris (Veraturris) bisculpta Powell wt
FE pidirona-adelaidensis (Lud.) &
[pidirona powelli sp, nov. sates gts
Jiratomina adelaidensts Powell seve
Inquisttor detritus Lud, Sick
Inquisitor sp. ss bh Font Seve aves
Splendrillia trucidata (Lud. ae ae site sees
Splendrillia adelaidae Powell .... — end
Syntomodrillia decemcostata (Lud.) “5 .
Syntomodrillia ludbrookae Powell — .... ae, ee
Tomopleura ludbrookae Powell veal asi inte
Maorttomella nutans Powell. .... Pe hezs le
Guraleus (Guraleus) chapplet Powell _ wat faite
Guraleus (Guraleus) ludbrookae Powell asa ase
erers
Gurulens (Euguraleus) subnitidus Lud, ae sav
Guraleus (Euguraleus) uadeluidensis Powell iF
Guraleus (Euguralens) powellt sp.nov. oy at
Guraleus (81) sp. asi
Guraleus CF vchapusilliady abbreviatus Powell
Guraleus (Paraguraleus) incisus Powell 4.
. Mappingta acukspira Lud. fiteaiem Heit — eile
Mappingia matronalis sp. nov. ats bz nt
—-—- — = —
106
17
~ eee ie ee ee ee ee ee
ee
a eae eae a a i ee
— eee ae ae i ae i ee =
ae ee Ke ee ee
a
ee
— eee ee ee ee ee
itd
bret
AA laAAL IL RR OM
Prrutr rd
~— ee we eae ae i ae i ee
ae ee Se eer See Ee ee
SPECIES
Filodrillia peramoena (Lud.) cas
Filodriliia ludbrookae Powell
Etremopsis contigua Powell
Asperdaphne (Aspertilia) bas ade Powell
Nepotilla powellt sp. nov.
Penestrodaphne pulchra Powell.
Pseudexomilus caelatus Powell
Conus (Floraconus) hamiltonensis Tate
Strioterebrum (Pervicacia) crassum (Tate)
Strioterebrum (Pervicacia) subspectabilis (Tate)
Hastula (Nototerebra) tenisoni (Finlay)
Terebra (s.l.) spp. se
Acteon scrobiculatus T, WwW.
Acteon sp.
anaes
onan aces
Semiactaeon tardior Sp. TOV, ... or
Semiactaeon stratosculpium sp. nov.
Retusa (Semtretusa) canaligradata sp nov,
Retusa (Semiretusa) apiculata (Tate)
Retusa (Semiretusa) coxi sp. nov.
Volvulella rostrata (Adams) ....
Cylichna angustata (Tate and Coss.)
Cylichna anticingulata sp. nov.
Scaphander tenuis Harris *
Damoniella bullaeformis (Coss.)
Damoniella partisculpta sp. nov.
one “
oe
Veprecula (7?) adelatdensis Powell...
wear
oon
sas
62
BORE
SSSetznasaxXxunvrevses
= 4 “ - ~
Eirema weymouthensis sp, nov. x6 wi 2 SP eee ee oA ae A
deve eee nese we — X X—_—-—-—— = Ke ee ee ee
a oo ew — XS ee —- — — = ee Se ee
wre — — X— —H— meee ee SS
Peery oe —XX—---—---—--|--—-=-—s =
wnee seer eee acer wae ee ee eee ee le ~—e
veer we > ee ee
veee Peery a
= aes . a ee
sae etse wes ome MO mes we ee aia i es
ae wee a, _
os: —_—- Be — ee Ke Ke ee ee =
rte otee we |= XS —-— —- — — NM a SS) as ie
Perry peas anes eens — —- F-—-— ee — —- ee ee a
a. nese suse wan = X X —- —- —- —- — — xx
nee see esos = K— — | ee eS ei Se
. ae asee i a rn
eee i
wees oe —~ Xe ee RH Ke —_ Ke ee —
vase euee i x—_-—— =
ny asee woos eaes oe — Xe — i i re ie ee ie Ee
< wees ance oe = XXX -—- -—-— - — = xX—_w_=— =
seep 24 owe =—- Xe — —-— —- — — x—--—--—-
oy sane fore owe — X X —- — —- — — — Xe — = =
a soe oven we — XS — ee eee +
sen tore = =X see ese Se eee ew = =
than those tabulated.
*From borings other
63
ACKNOWLEDGMENTS ©
The writer is very greatly indebted to Dr. L, R. Cox of the British Museurn
(Natural History) for most generous help and advice throughout the work; to
the Director and Trustees and to Mr. W. N. Edwards, Keeper of Geology of
the Museum, for permitting most of the work to be undertaken there; to Dr.
W. J. Rees and Mr. G. L. Wilkins of the mollusca section and te the librarians
in the general, geology, and zoology libraries of the Museum for assistance in
the search for material and literature; to Drs. Thorson and Lemche of the Uni-
versitetets Museum, Copenhagen, for the generous loan of type specimens; to
Monsieur A. Chavan and Dr, Myra Keen for help with the classification of diffi-
cult groups; to the Director of Mines, South Australia, for the loan of the
typescript of portion of a bulletin im the press on the Hydrology of the Adelaide
Basin; and to Dr. M. F-. Glaessner for the loan of additional material from the
Tate Collection.
REFERENCES
Benson, W. N. 1911 Note descriptive of a Stercogram of the Mount Lofty Ranges, South
Australia. Trans. Roy. Soc. S. Aust. 34, 108-111, pls. 20, 21
Cuapman, F, 1916 Cainjozoic Geology of the Mallee and other Victorian Bores: Rec,
Genl, Surv. Viet, 3, (4), 327-430
Crapman, F., and Cresprm, IT, 1935 Foraminiferal Limestones of Eocene Age from North-
West Division, Western Australia, Proc. Roy. Soc. Vict, 48, (1.s.), (1), 55-62
Cravan, A. 1949 Remarques sur la signification climatique des Mollusques marins fossiles.
Bull. Soc. Geol. France, ser. 5, 19, (7-9), 507-512
Cortow, Th, C. 1947 Some Tertiary Molluscs from the Adelaidean Stage (PHocene) of
South Australia. Rec. .S. Aust. Mus., 8, (4), 653-670
Cox, L, R. 1948 Neogene Mollusca from the Dent Peninsula, British North Bornes,
Schweiz. Pal. Abhandl., 66, 1-70, pls, 1-9
Cresvin, J, 1943 Stratigraphy of the Tertiary Marine Rocks in Gippsland, Victoria, Comm.
Aust, Dept. Supply and Shipping, Min, Res. Surv. Bull, 9 ¢ Pal. ser. 4). (Processed)
Crespin, I, 1950 Australian Tertiary Microfaunas and their Relutionships 10 Assemblages
elsewhere in the Pacific region. Journ. Pal., 24, 421-429
Cresprn, I and Corron, B, C. 1952 The Stratigraphy and Palaeontology of the Sub-
surface Deposits of the Adelaide Plains, $, Aust. Dept, Mines Geol. Surv. Bull, 27,
Appendix III, 227-238
Davies, A, M. 1934 Tertiary Faunas, 2
Fenner, C. 1930 The Major Structural and Physiographic Features of South Australia.
Trans. Roy. Soc. S. Aust, 54, 1-36
Freminc, C. A. 1944 Molluscan Evidence of Pliocene Change in New Zealand. Trans, Roy.
Soc. N,Z,, 74, (3), 207-220. Two text figs.
Guagssner, M. F, 1951 Three Foraminiferal Zones in the Tertiary of Australia. Geol,
Mar. 88, (4), 273-283
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ANOTHER NEW SPECIES OF BOYDAIA (SPELEOGNATHIDAE;
ACARINA) FROM AUSTRALIA
BY H. WOMERSLEY
Summary
A second species of Boydaia (Speleognathidae) from Australia is described. It was found freeliving
with cetoparasitic mites on a rat from Mount Glorious, Queensland.
65
ANOTHER NEW SPECIES OF BOYDAIA (SPELEOGNATHIDAE; ACARINA)
FROM AUSTRALIA
By H, Woscersiey *
[Read 9 July 1953]
SUMMARY
A second species of Boyduiw (Speleognathidae) from Australia is described. It was
found Sreeliving with cetoparasitic mites on a rat from Mount Glorious, Queensland.
While my previous paper (A new gets and species of Speleognathidae
(Acarina), from South Australia, Trans. Roy. Soc. S, Aust., 1953, 76, 82), was in
the press, another new species of Boyduia was discovered amongst a lot of Trom-
biculid and Laelaptid mites collected from a rat, Rettas asstmilis, from Mount
Glorious, Queensland, on 6 August 1951 by Dr. F_ H, Derrick.
Unfortunately it was represented only by a single specimen, but while being
closely related to Boydaia striatus (Crossley), it is abundantly distinct in many
characters. While all previously known species of Speleognathidae, except
Speleognathus australis Wom, are parasitic in the nasal secretions of birds and
frogs (S. australis will probably be found to affect birds also), the occurrence
of this new species externally on a tat is probably accidental and not natural.
Boydaia derricki sp. n,
Descriplion—Female. Shape elongate ovoid, widest between coxae II and
I1I. Length of idiosoma 780«, width 520z. Gnathosoma visible from above 104
long. Dorsum with longitudinal and transverse punctate striations as figured,
with 20 short stout ciliated or bush-like setae, arranged one small one 5p tong in
front of each sensilla, then two rows of 4 ta Su long, two rows of 2 and a row of
4 to 8n long. and then 2, 11p long. Sensillae filamentous, but ciliated, appearing
slightly thicker distally, 282 long, On the anterior margin m front of each
sensilla is a small but distinct lens. Palpi 3-segnrented, all segments free from
gnathosoma; the basal segment dorsally on the inside carries a long slender
apparently shortly ciliated seta, on the second and third segment a short bushy
seta; ventrally the third segment carries three short bushy setae, The basal seg-
ment of the chelicerae basally bears two short bushy setae and the apical segment
appears as a lobe-like structure without teeth. Venter: sttiate punctate; coxae
in two groups widely separated; with strong subcuticular reticulations; coxae I
with two short, 5» bushy setae, I[-1V with one such seta, Between coxae II a
pair of short 5, bushy setae and a similar pair between coxae III and between
coxae IV, Genital slit 48» long, forked posteriorly and flanked on each side by
three setae 5u long; on each side of anus a seta 8 long, and posteriorly a pair of
setae 124 long. Legs stout, length including coxae but excluding claws, 1 520,
IT 480n, ITT 430u, LV 455y, furnished with short bushy setae, which on tarsi
reach 14 in length; claws strong and curved to 52 long, with a bushy hair-like
pulvillus in between; segments of legs longitudinally finely striate punctate.
Lecality and Host—One specimen collected on Rattus assimilis, Mount
Glorious, Queensland, 6 Atigust 1951 by Dr. E. H. Derrick.
Remarks—In the presence of distinct eyes and striated cuticle, this species
is tlose to B, striatus (Crossley), It differs, however, in its more elongate shape,
in having only three setae on each side of the genital opening, in lacking the fine
simple setae on the legs as figured by Crossley for striatus and in relatiyely
stonter legs.
“South Australian Musetn
pane Roy Soc, S. Aust,, 77, July, 10354
ry f
CRON oe
D
TAK ys ae,
IS) _«
Boydaia derricki n. sp.
A, dorsal view; B, ventral view; C, left eye and sensilla; D, dorsal view of
gnathosoma and palps; E, ventral view of gnathosoma and palps; F, dorsal
view of tibia and tarsus of leg I; G, ventral view of tibia and tarsus of Jeg I.
REFERENCES
Boyp, Evizaneto M. 1948 <A new Mite from the respiratory tract of the Starl-
ing. Proc. Ent. Soc., Washington, 50, 9-14
Crosstey, D. A,, Jnr. 1952 Two new Nasal Mites from Columbiform Birds.
J. Parasitol, 38, (5), 385
Porter, J. C., and StRanptMann, R. N. 1952 Nasal Mites of the English
Sparrow
Womerstey, H. 1936 On a new Family of Acarina with a description of a
new Genus and Species. A.M.N.H.,, (10), 18, 312-315
Womerstey, H. 1952 (1953) A new Genus and Species of Speleognathidae
(Acarina) from South Australia, Trans, Roy, Soc. S. Aust., 76, 82-84
EIGHT NEW SPECIES OF TROMBICULIDAE (ACARINA) FROM
QUEENSLAND
BY H. WOMERSLEY
Summary
Eight new larval species of Trombiculid Mites (Trombiculidae, Acarina) are described from
Mackay and Brisbane areas of Queensland.
67
EIGHT NEW SPECIES OF TROMBICULIDAE (ACARINA)
FROM QUEENSLAND
By H. Womers-ey *
[Read 9 July 1953}
SUMMARY
Eight new larval species of Trombiculid Mites (Trombiculidae, Acarina) are
described from the Mackay and Brisbane areas of Queensland.
The eight species of Trombiculidae described in the present paper were all
collected in the Mackay and Brisbane areas of Queensland by Dr. E, H, Derrick
and his colleagues during a survey of those areas.
Mast of them were collected by the card method, the others being from
animal hosts.
The types and some paratypes are in the South Australian Museum. Other
paratypes in the Queensland Institute for Medical Research, Brisbane.
Trombicula derricki sp. n.
Fig. 1 A-G
Description of Larvae—Length (unengorged) 2084, width 169%. Scutum as
figured, almost as deep as wide with deep evenly rounded posterior margin;
anterior margin only lightly sinuous; SB a little im front of line of PL; scutal
setae fairly long, tapering and ciliated, AM the shortest, PL the longest; sensillae
filamentous with ciliations on distal half; surface with only moderately numerous
punctae. Eyes 2-} 2, on ocular shields, posterior the smaller. Palpi moderately
stout, setae on femur, genu and tibia all ciliated or branched, tibial claw trifurcate.
Chelicerae simple with only the apical tricuspid cap. Dorsal setae 34 arranged
2,.6.8,8.6.4, to 454 long, except the humerals which are 50, long. Ventrally, a
pair of branched setae on maxillae, one on each coxa, a pair between coxae I and
between coxae III, and thereafter 84/6.64 to 34n long. Legs 7-segmented, I 260
long, II 234», III 273p; specialised setae on leg 1, 2 genualae, 1 microgenuala,
2 tibialae, 1 microtibiala, on tarsi 1 sensory rod, 1 microspur, 1 terminala; on
leg II 1 genuala, 2 tibialae, on tarsi 1 sensory rod, 1 microspur; and on leg IIL
1 mastitibiala; 2 mastitarsalae.
The Standard Data derived from 17 species collected on cards are:—
Standard Theoretical Observed Coeff, of
Mean Deviation Range Range Variationx
AW - 62-4+0-45 1°86 + 0°32 56-8 —68-0 58*5— 64-4 2-9
PW - 78-140-49 2-01 + 0-34 72-1 —B4-L 72+8-— 81-2 2-6
SB ~ 24554021 0-87 + 0-15 21-9 — 27-1 22-4 —25-2 36
ASB - 26:8+0-35 1-42 + 0-24 22*5—31'1 25-2 — 28-0 5*3
PSB - 27-62 0°23 0-93 + 0-16 24-8 —30-4 25-2 —28-0 2:3
sD ~ 545-049 2:00 + 0-34 48°5 —60°5 50-4— 56:0 3:7
A-P - 28-0 No variation recorded :
AM - 33-4+0-30 1-20 + 0-21 29°8— 37-0 30-8 — 56+4 33.
AL - 39+5+ (32 1-32 + 0°22 35-6 — 43-4 36°4— 42-0 3-3
PL - 45-34 0°35 1-43 + 0-25 41-0— 49-6 42-0 —47-6 3:2
Sens - 62:5 +032 1-24 40-23 58:6— 66-0 61-6— 64-4 Z-0
Loc. and Host—Seventeen specimens collected on cards. Mt. Jukes, Queens-
land, 6 September 1951 (E. H. Derrick),
* South Australian Museum.
Trans. Roy Soc. S. Aust., 77, July, 1954
68
Remarks—This species is closely related to novae-hollandiae Hitst and its
allies, in having a long nude outstanding mastitibiala and two such mastitarsalae
on leg III. In the shape of the scutum it is similar to novae-hollandiae, but the
posterior margin is evenly round whereas in novae-hollandiae it is slightly but
perceptibly flattened medially.
From all the novae-hollandiae group, however, derricki has a long outstanding
but ciliated seta on telofemur III.
Fig. 1 Trombicula derricki sp. n.
A, dorsal view; B, ventral view; C, scutum (x 500); D, tip of chelicera;
E, palp; F, tibia and tarsus of Jeg IIL; G, maxillary seta.
6
The species is named in honour of the finder, and the holotype and para-
types are in the South Australian Museum.
This and the following two species will come into caption 23 of Womersley
1952 on p. 36 forming a group with novue-hollandiae, this portion of the key
being emended as follows :—
23. Leg III with 2 mastitibialae and 1 mastitarsala = - - - - - «@
a. With ‘a long outstanding ciliated seta on telofemur III. Setae-on palpal
femur, genu and tibia all ciliated. Posterior scutal margin evenly rounded.
scutal punctae moderate in number, Sensillac ciliated distally with SB
slightly in front of PL_ DS 34, arranged 2,6.8.8.6.4. to 45y long.
AW 62-4+5:6, PW 78:1+6:0, SB 24-542-6, ASH 20-5442,
PSB 27-642°8, SD 54-5+6-0, A-P 28:0, AM 33-4+ 5-6,
AL 39543-9, PL 45-344-3, Sens. 62-34 3-7.
Trombicula. desricki sp. n.
Without any such long outstandifg seta on telofemur III, - - - $
-b. Posterior sewtal margin not so deep behind PL and medially very lightly
concave. Setae on palpal femur, genu and tibia sparsely branche. Scutal
punctae fairly numerous. Sensillae nude or with very indistinct barbs basally.
SE ahout in line with PL. DS 30, arranged 2.6:6.6.4.4.2, to 45y,
AW 63-84 5°3, PW. 86-45 47°65, SB 29-7+4-2, ASB 52-2451,
PSB 17:5 +3:6, SD 49-144-0, A-P 31-142-7, AM 45:7+ 6:3,
AL 42-35 + 3-95, PL 49-5+3:9, Sens. tu 89-6,
Trombicula antechinus sp. 1.
Posterior scutal margin decper hehind PL and not shaped as aboye - c
c. Scutal posterior margin evenly rounded and with sparser punctae. Seta on
palpal femur 2-branched and on genu 1-branched, on tibia dorsal 2-branched,
lateral 1-branched, and ventral 3-4 branched. Sensillae nude or with indistinct
barbs basally, SB slightly behind PL. DS 30, arranged 2.6,.6.6.4.4.2. to 45.
AW 63°34+5°2, PW 80:4+6-3, SB 27-2+3-6, ASB 32+-4274-2,
PSB 21-24+4-2, SD 53-55+5-05; A-P 24-843-5, AM 36:0+4:3,
AL 38-446°7, PL 45:0+6°3, Sens. to 89-6,
Trombicula thylogale sp. n-
Scutal posterior margin deep behind PL and rather flattened medially.
Scttal punctae numerous. Setae on palpal femur, geny and tibia all ciliated.
Sensillac barbed or shortly ciliated distally and SB slightly behind PL.
DS 32, arranged 2.6.6.6.6.4.2 to 80),
‘Trombicula novue-hollandiae Hirst
(Standard Data as in 1952 key.}
Trombicula antechinus sp. #.-
Fig. 2 A-F
Description of Larvae—Length of idiosoma (engorged) 377», width 2806p.
Scutum as figured, ASB about twice the length of PSB, posterior margin rather
shallow and lightly concave medially; anterior margin only lightly sinuous; SB
a little in front of PT.; scutal sctae fairly long, tapering and ciliated; AL slightly
shorter than AM, Pl. the longest; sensillae nude or indistinctly barbed basally;
punctae fairly numerous. Eyes 2+ 2, on ocular shields, posterior the smaller.
Palpi moderately stout, setae on femur, genau and tibia all btanched or ciliated,
tibial claw trifurcate. Chelicerae simple with only the tricuspid cap, Dorsal
setae 30, arranged 2.6.6.6.4.4.2., to 45y long, except the humerals which are 50
long. Ventrally, a pair of branched setae on maxillae, one on each coxa, a pair
between coxae I and between coxae TIE, and therafter 4.4.4/2.4.64, to 42~ long.
Legs 7-segmented, I 234 long, IT 208 long, III 247. long; specialised setae on
leg 1, 1 genuala, 1 microgentiala, 2 tibialae, 1 microtibiala, on tarsi 1 sensory rod,
1 microspur, 1 terminala; on Jeg IT, 1 genuala, 2 tibialae, on tarsi 1 sensory rod,
1 microspur; and on leg III, 1 genuala, 1 tibiala, 1 mastitibiala, 2 mastitarsalae,
76
Fig. 2 Trombicula antechinus sp. n.
A, dorsal view; B, ventral view; C, scutum (x 500); D, tip of chelicera;
E, palp; F, tibia and tarsus of leg III.
71
The Standard Data derived from 16 of 23 specimens collected on Antechinus
flavipes are:—
Standard Theoretical Obsetved Coeff. of
Mean Deviation Range Range Variation
AW - 63-8 +0-44 1-78 + 0-32 58:5 — 69-1 61-6— 67-2 2:3
PW - 86-45+ 0-64 2°55 + 0-45 78-8 — 94-1 84-0 — 92-4 29
SB - 29-7 +0-35 1-42 + 0-25 25-5 — 33-9 28-0 — 32:2 4-8
ASB - 32:2 +0-43 1-71 +0-25 2741 — 37-3 28-6 — 33-6 5°46
PSB - 17-5 «0-30 1:21 + 0-21 13-9— 211 16-8 — 19-6 7-6
sD ~ 49-1 +0-34 1-35 + 0-24 45-1— 53-1 47*6—50°4 27
A-P - 31:1 40°22 0-89 + 0-16 28:4— 33-8 29-4 — 35-6 2:8
AM - 45°7 +0660 2°09 + 0-3 39-4 — 52-0 42-0 — 47-6 4:5
AL - 43-35 + 0°33 1°32 + 0-23 38-4 — 46-3 39-2 — 44-8 31
PL - 49-5 +0-32 1+30 + 0-23 45-6— 53-4 47-6 -— 50-4 2-6
Sens. - to 89-6
Loc. and Host—Twenty-three specimens from a marsupial mouse, Antechinus
fievipes from Mt. Glorious, Queensland, 6 August 1951 (coll. E. H. Derrick).
Remarks—In the mastitibiala and mastitarsalae on leg III, this species comes
near to novae-hollondiae, as in the amended key.
Trombicula thylogale sp. n.
Fig, 3 A-G
Description of Larvae—Length of idiosoma (slightly engorged) 312y, width
231. Scutum as figured, ASB nearly twice the length of PSB, posterior margin
evenly rounded, and anterior margin lightly convex; SB slightly behind line of
PL, scutal setae fairly long, tapering and ciliated; AM slightly shorter than AL,
PL the longest; sensillae nude or with indistinct barbs basally; surface with
sparse punctae, Eyes 2-4-2, on ocular shields, posterior the smaller, Palpi
moderately stout, setae on femur 2-branched, genu 1-branched, on tibia, dorsal
2-branched, lateral 1-branched, and ventral 3-4 branched; tibial claw trifurcate.
Chelicerae simple with only the apical tricuspid cap. Dorsal setae 30, arranged
2.6.6.6.4.4.2, to 45p long, except the humerals which are 48p long. Ventrally, a
pair of branched setae on maxillae, one on each coxa, a pair between coxae I and
between coxae III, and thereafter 6.2.4,6.6, to 34 long. Legs 7-segmented, I 2735p
long, II 234 long, Lil 273. long; specialised setae on leg I, 1 genuala, 1 micto-
genuala, 2 tibialae, 1 microtibiala, on tarsi 1 sensory rod, 1 microspur, 1 terminala;
on leg II, 1 genuala, 2 tibialae, on tarsi 1 sensory rod, 1 microspur ; and on leg IIT,
1 genuala, } tibiala, 1 microtibiala, 2 mastitarsalae.
The Standard Data derived from 16 of 29 specimens collected on Thylagale
auilcaxt are —
Standard Theoretical Observed Coeff, of
Mean Davistion Range Range Variation
AW - 63-39 +0°43 1°73 + 0-31 58+1— 68+5 61-6 — 67-2 2:7
PW - 80-4 +052 2-09 + 0°37 74+1— 86+7 75-6 — 84-0 2°6
SB = 27-2 +0-30 1-21 + 0-21 23°6— 30-8 25-2— 29-4 4x4
ASB - 32-4 +0-35 1°39 + 0-25 28-2 — 36-6 30-8 —33°6 433
PSB - 21:2 +0355 1-39 + 0-25 17-0 — 25-4 19-6 — 22-4 6:5
SD — 53°55+0-42 1-68 + 0:30 48-5 — 58-6 50-4 — 56-0 31
A-P += 243 +0-30 1-18 + 0-21 21-3— 28-3 22-4— 26°6 4B
AM - 36°0 +0-38 1-44 + 0:27 31-7 —4053 33-6 — 39-2 4-0
AL - 384 +059 2-23 + 0:42 31-7 —45*1 33-6 — 42-0 5°83
PL. - 45-0 +052 2:09 © 0°37 38-7 —51+3 42-0 —Al-6 4-6
Sens. = to 89-6
v2
Loc, and Host—Twenty-nine speciméns, frotn a wallaby, Thylogale. wilcoxt
from Mt. Tamborine, 28 June 1951 (coll. E. H. Derrick), me
Remarks—Belongs to the novae-hollandiae group and separated from the
other allied species as in the emended key.
Fig. 3 Trombicula thylogale sp. n,
A, dorsal view; B, ventral view; C, scttum (x 500); D, tip of chelicera;
E, palp, F, tibia and tarsus of leg III; G, maxillary seta.
Trombicula mackayensis sp. n.
Fig. 4 A-G
Description of Larvae—Length of idiosoma (unengorged) 208, width 182.
Scutum as figured; pentagonal, posterior margin with straight sides and rounded
apex; anterior margin only lightly sinuous and highest in front of AM; SB
slightly in front of line of PL; scutal setae fairly long, tapering and ciliated,
AM the shortest, PL the longest; sensillae filamentous with ciliations on distal
73
half; ‘punctae fairly numerous. Eyes 2-+ 2, on ocular shields, posterior the
smallet, Palpi moderately stout, setae on femur and genu branched or ciliated,
Fig. 4 Trombicula mackayensis sp n.
A, dorsal view; B, ventral view; C, scutum (x 500); D, tip of chelicera;
E, palp; F, tibia and tarsus of leg III; G, maxillary seta.
long, except the humerals which are 50p long. Ventrally, a pair of branched setae
on maxillae, one on each coxa, a pair between coxae I and between coxae III and
thereafter 8.2/6.4.6, to 34y long. Legs, 7-segmented, I 247» long, II 234 long,
I]i 260p long; specialised setae on leg I, 1 genuala, 1 microgenuala, 2 tibiala,
74
1 microtibiala, on tarsi i sensory rod, 1 microspur, and 1 terminala; on leg II,
1 genuala, 2 tibialae, on tarsi 1 sensory rod and 1 microspur; and on leg III,
i genuala and 1 tibiala.
The Standard Data derived from 4 specimens, the type population, collected
on card are:—
Standard Theoretical Observed Coeff, of
Mean Deviation Range Range Variation
AW - 72:45+0:35 +70 + 0°25 70°35 — 74-55 7174—72+8 0-9
PW - 89:9 +0-88 1°76 + 0-62 84-6 +- 95-2 88-2—92+4 2-0
SB - 29-7 + 0°35 0:70 + O25 27°6 —31°8 29+4— 308 2-4
ASB - 30:1 +0°70 1-4 + 0-50 25°9 —34-3 28-0— Ws 4-7
PSB - 30-8 No variation
sD - 60°59 +0°70 1-4 +050 5657 — 65-1 58-8 — 61°6 2.3
A-P - 25-2 No variation recorded
AM - 37-1 +0-70 1-4 + 0-50 32-9 —41-3 36+4— 39-2 $3
AL - 40-6 +0-81 1°62 + 0:57 35:8 — 45-2 39-2— 42-0 4-0
PL - 49-0 +0-81 1-62 + 0-57 44-2 —53-8 47-6 — 50-4 3d
Sens. - 61-6 No variation recorded
Loc. and Host—Four specimens from card at Mt. Jukes, Queensland, 6 Sep-
tember 1951, and a second population of approximately 50 specimens from
Mt. Glorious, Queensland, 5 September 1952 (coll, E, H, Derrick).
Remarks—In the pentagonal scutum and differential characters, this species
is very closely related to kashmirensis Wom. 1952 from India; and from which it
differs in the smaller scutum and in the nature of the palpal setae,
The Standard Data derived from 16 of the specimens from Mt. Glorious
only differ in the slightly but insignificantly lower values of AW and PW, SB,
and a longer PL and are as follows:—
Standard Theoretical Observed Coeff. of
Mean Deviation Range Range Variation
AW - 66:6 +0-46 1-85 +0°33 61-1— 72-1 63-0 — 70-0 2-8
PW 84:3 +0-41 1-66 + 0°30 79°3—89°3 81-2— 86-8 1-96
SE 27-8 +0-19 0°68 + 12 25-B— 29-8 26:6—29-4 2-5
ASB 27°85 + 0-24 6-95 + 0:17 25-0 — 30°7 25-2 — 28-0 34
PSB 31°3 40°37 1-47. + 0-27 26:9 — 35+7 28-0— 33-4 1-7
sD 59-0 + 0:52 2-09 + (37 52-7 — 65*3 53+2— 61-6 355
A-P 25-6 +£0-32 1-28 + 0-23 21+8 -—29+2 22-4 — 280 5-0
AM 34-0 + 6-23 0-93 + 0-16 3142 36-8 33°6-—— 36-4 27
AL 38-0 +0-35 1-39 + 0-24 33-8 — 42-2 36-4 — 39-2 3-6
PL 45-0 +0-30 1-20 + 0°21 41°4— 48-6 42-0 — 47-6 2-6
Sens. 62-3 +0-30 1-21 +0-21 58-7 — 65-9 61-6 — 64-4 1-9
Euschongastia parva sp. n.
Fig. 5 A-D
Description of Larvae—Shape oval. Length of idiosoma (unengorged) 234,
width 169, Scutum as figured, almost twice as broad as deep; posterior margin
not very deep behind PL and distinctly concave medially ; SB behind line of PL;
A-P almost twice the length of PSB; AM shortest, AL the longest; sensillae
globose with setules, Eyes 24-2, on ocular shields, posterior the smaller, Palpi
moderately stout, seta on femur and genu ciliated or branched; on tibia, dorsal
and lateral nude, ventral branched; tibial claw trifurcate, Chelicerae simple with
only the apical trictispid cap. Galeal setae nude. Dorsal setae 34 arranged
2.6.6.6.8.4.2, to 354 long, except humerals which are 40g long. Ventrally; a pair
of branched setae on maxillae, one on each coxa, and a pair between coxae I
and between coxae If] and thereafter 6.4.6/4.6.4.2, to 30n long. Legs 7-seg-
Fig. 5
A, dorsal view; B, ventral view; C, scutum (x 500); D, palp.
Euschongastia parva sp. n.
mented, 1 260, long, II 234» long, III 260y long; specialised setae on leg I,
2 genualae, 1 microgenuala, 2 tibialae, 1 microtibiala, and on tarsi 1 sensory rod,
1 microspur ; on leg II, 2 tibialae, and on tarsi, 1 sensory rod, 1 microspur; and
on leg IIT, 1 genuala and 1 tibiala.
The Standard Data derived from the type and 3 paratypes are:—
Mean
AW - 61:6 +1-14
PW - 78:4
S.B, - 22°75 + 0-67
ASB - 22-4
PSB - 91 +0-70
SD - 31°5 40-70
A-P - 22-4
AM - 30:8
AL - 60:2 40°81
PL - 56°0
Sens.
- 30-8 with head 19+6x 19-6.
76
Standard Theoretical
Deviation Range
2-29 + 0°80 54°38. — 68-4
No variation recorded
1:34 + 0:47 18*75— 26°75
No variation recorded
1-40 + 0-47 4-9 —13-3
1-4 + 0-47 27-3 — 35-7
No variation recorded
No variation recorded
1:62 + 0-57 55-4 —65-0
No variation recorded
Observed Coeff. of
ange Variation
58-8 — 64-4 3-7
21:0— 23-8 5:9
8-4— 11-2 15-5
30-8— 33-6 4-4
58-8— 61-6 27
No variation recorded
Loc. and Host—Four specimens collected on card at Mt. Jukes, Queensland,
6 September 1951 (coll. E. H. Derrick).
Remarks—In Womersley’s 1952 key to t
he species of Euschongastia (sic
Ascoschongastia) this species runs down to couplet 40, but differs from both
echymipera Wom. and Kohls, and innisfailensis Wom, and Heasp. in the shape of
the scutum and the Standard Data,
Fig. 6
Euschongastia popei sp. n.
A, dorsal view; B, ventral view; C, scutum (x 500); D, tip of chelicera;
E, palp; F, maxillary seta.
Euschongastia popei sp. n.
Fig. 6 A-F
Description of Larvae—Length of idiosoma (engorged) 390p, width 338p.
Scutum as figured, posterior margin fairly deep behind line of PL and distinctly
concave medially; in two of the specimens the margin of the scutum runs just
77
inside of the base of the PL, setae, which thus lie out from the scutum proper.
Anterior margin sinuous; SB in front of line of PL; scutal setae ciliated and
tapering; AL the shortest, PL the longest; sensillae globose with setules. Eyes ?,
not observable. Palpi moderately stout; setae all nude except the one on femur;
tibial claw trifurcate. Chelicerae simple with only the apical tricuspid cap, Galeal
setae nude, Dorsal setae 32 arranged 2.6.6.6.6.4,2, to 34m long, except the humerals
which are 39, long. Ventrally; a pair of ciliated setae on maxillae, one on each
coxa, a pair between coxae I and between coxae ITI and thereafter 6.84/10.84,
to 25p long. Legs, 7-segmented, I 195 long, I 169, long, I11 208, long; specia-
lised setae on leg I, 2 genualae, 1 microgenuala, 2 tibialae, 1 microtibiala, and on
tarsi 1 sensory rod, 1 microspur, 1 terminala; on Icg II, 1 genuala, 2 tibialae,
and on tarsi 1 sensory rod, 1 microspur; and on leg III, 1 genuala, 1 tibiala.
The Standard Data derived from the type and 4 paratypes are:—
Standard Theoretical Observed 4
Mean Deviation Ra Range Variation
AW - 48721+12 2-50 + 0-80 41-2 — 56-2 47-6 — 53-2 5-1
PW - 70:0+1-25 2°80 + 0-89 61-6 —78-4 67-2 —72-9 4-0
SB - 28:0+0-77 1-7) +& 0°54 22°9 —J331 26°6— 30-8 61
ASB 23-45> 0-68 1-53 + 0-49 18-2 —28-1 22-4 — 25°2 65
PSB » 20-70-48 1*53- 0-49 16-1 —25-2 19-6 22-4 7+4
SD - 44-241-37 3+D7 + 0:97 35° —53-2 42-0 — 47-6 69
A-P - 28-0 No variation recorded
AM - 27:4+0-56 1-25+ 0-40 23°65 — 31-15 28-0 —25-2 4-6
AL -~ 21°820-56 1-25 0-40 18-05 — 25-55 19-6— 22-4 5+8
PL - 40-34 0-68 1-53= 0-49 35:7 —449 39-2— 42-0 3-8
Sens. - 430-8 with head 16-8x 19-6, Only 1 determination
Loc. and Host—Five specimens collected on Rattus assimilis at Mt. Glorious,
Queensland, 6 August 1951 (coll. E. H. Derriclr).
Remarks—Like precana sp.n., the above new species will also run down (0
couplet 39 containing cocrongense Hirst from which it differs in the differently
shaped and very much smaller scutum, as well as having the seta on the palpal
genu nude. From procana sp.n. it differs in the smaller number and different
structute of the dorsal setae as well as having only the femoral seta of the palpi
branched.
In two of the four specimens the scutal margin runs inside of the PL seta
base, which can ‘thus be said to be “off” the scutum. This incipient development
again stresses the view that the off-scutal position of PL within the genus
Euschéngastia should not be used to create other genera as has been done by some
workers,
Euschongastia procana sp. n.
Fig. 7 A-E
Description of Larvae—Shape oval. Length of idiosoma (unengorged) 273u,
width 195y. Scutum as figured; posterior margin deep behind line of PL, and
slightly concave medially; anterior margin sinuous; scutal setac long, tapering
with slender denticles; AL the shortest, PL the longest; sensillae globose with
setules. Eyes 2+ 2, on ocular shields, posterior the smaller, Palpi moderately
stout; setae on femur and genu ciliated or branched; on tibia, dorsal and lateral
nude, ventral branched; tibial claw trifurcate, Chelicerae simple with only the
apical tricuspid cap. Galeal setae nude. Dorsal setae with slender denticules, 68. in
nunber and arranged 2.10.14.18.12.6.4.2, to 53u long, except humerals which are
78
Fig. 7 Euschongastia procana sp. n.
A, dorsal view; B, ventral view; C, scutum (x 500); D, palp; E, dorsal seta
62p long. Ventrally, a pair of ciliated setae on maxillae, one on each coxa, a pair
between coxae I and between coxae III, and thereafter 12.8.6/8.6.4.2, to 28p long.
Legs 7-segmented, I 299p, Il 247m, III 286 long; specialised setae on leg I,
2 genualae, 1 microgenuala, 2 tibialae, 1 microtibiala and on tarsi, 1 sensory tod,
1 microspur, 1 subterminala, 1 terminala; on leg IT, 1 genuala, 2 tibialae, and on
tarsi 1 sensory rod, 1 microspur; and on leg III, 1 genuala, 1 tibiala.
79
Fig. 8 Euschongastia andromeda sp.n,
A, dorsal view; B, ventral yiew; C, scutum (x 500) of type of specimen;
D, scutum (x 500) of paratype specimen; E, tip of chelicera; F, palp;
G, tibia and tarsus of leg IIL.
50
The Standard Data for the type and 1 paratype collected on card are :—
Standard Theoretical Observed Coeff, of
Mean Deviation Range Range Variation
AW - 56:0 No variation recorded
PW - 81-2 No variation recorded
SB - - BO+0-99 1+4+0-7 23+8 — 322 26-6 — 29-4 5D
ASB ~ 26:620-99 1-407 2274 —~30°8 25:52 — 28-0 53
PSB - 22-4 No variation recorded
SD - - 46-0+0-99 1-4+0°7 44-8— §3-2 47-6 — 50-4 2-9
AP- - 280 No variation recorded
AM - - 47-6 No variation recorded
Al, - - 39-2 No variation recorded
PI. - - 61-6 No variation recorded
Sens. - 37-8+0-99 1-4+0-7 33*6 —A2+1) 4G+4 — 39-2 3-7
with head 22-4 5 19-6
Loc. and Host—Two specimens collected on card at Mt. Jukes, Queenstand,
6 September 1951 (coll, E. H. Derrick).
Femarks—In Womersley’s key (1952, p. 236) this species runs down to
couplet 39, along with coorongense Lrst, from which it differs markedly in the
more denticulate scutal and dorsal setae, the much greater number of dorsal setae,
and in having the ventral seta of the palpal tibia branched, as well as in the smaller
scutum.
Euschongastia andromeda sp.n.
Pig. 8 A-G
Descripiton of Larvae—Shape oval. Length of idiosoma (unengotged) 274p,
width 182», Scutum as figured; nearly twice as wide as deep; posterior margin
very shallow behind line of PL, and slightly concave medially; anterior margin
sinuous; SB in front of PL; scutal setae long, tapering and ciliated; AL the
shortest, PL the longest; sensillae globose with setules, Eyes 2+ 2, on ocular
shields; posterior the smaller. Palpi moderately stout; setae on femur and genu
branched or ciliated; on tarsi dorsal and lateral nude, ventral branched; tibial
¢law trifurcate. Cheliccrae simple with apical tricuspid cap, Galeal setae nude.
Dorsal setae 44 arranged 2.8.8.8.10.4.2.2, to 36 long, except humerals which are
42, long, Ventrally, a pair of ciliated setae on maxillae, one on each of coxae I
and JI, two on coxae [1I, a pair between coxae I and between coxae III, and
thereafter 6.64/2.6.6.2.2, to 31 long. Legs 7-segmented; specialised setae on
leg 1, 2 genualae, 1 microgenuala, 2 tibialae, 1 microtibiala, and on tarsi, 1 sensory
rod, 1 microspur, 1 terminala; on leg II, 1 genuala, 2 tibialae, and on tarst
i sensory rod, 1 micruspur; and on leg III, 1 genuala, 1 tibiala, also on tibia 2
very long but basally ciliated setae and two similar ones on tarsi.
The Standard Data derived from the type and 1 paratype are:-— AW 74-2,
67:2; PW &86°8, 81:2; SB 29-4, 28:0; ASB 28-0, 28:0; PSB 11-2, 14-0; SD
39°2, 42-0; A-P 36°4, 36°4; AM 42-0, 42:0; AL 33:6, 33°6, PL 56-0, 56-0} Sens.
39-2, 39-2 with head 22-4 x 19-6.
Loc. and Host—Two specimens collected on card at Mt. Tamborine, Queens-
land, 14 May 1952 (coll. E, H. Derrick).
Remarks—tIn having 2 setae on coxae [II this species is closely related to
petrogae Wom., in couplet 29 of Womersley’s key 1952 on p. 234. It differs,
however, in the fewer and different dorsal setae as well as the Standard Data,
and the shape of the scutum. The setae on the palpal femur, genu and tibia ventral
are only sparsely branched. However, more characteristic are the long but basally
ciliated setae on tibia and tarsi of lee IEL The Standard Data of the paratype
are somewhat higher in AW and PW than in the type, probably due to undue
compression.
THE ECOLOGICAL SURROUNDINGS OF THE NGALIA NATIVES IN
CENTRAL AUSTRALIA AND NATIVE NAMES AND USES OF PLANTS
BY J. B. CLELAND AND N. B. TINDALE
Summary
This paper describes the physical features and the vegetation of the region occupied by the Ngalia
aboriginal people, some 200 miles north-west of Alice Springs. The native names and uses of
various plants are recorded.
81
THE ECOLOGICAL SURROUNDINGS OF THE NGALIA NATIVES IN
CENTRAL AUSTRALIA AND NATIVE NAMES AND USES OF PLANTS
By J, B. Creranp and N, B. Tinpace
{Read 9 July 1953]
SUMMARY
Tats paper describes the physical features and the vegetation of the region occupied
by the Ngatia aboriginal people, some 200 miles north-west of Alice Springs. The native
hames and uses of various plants are recorded.
The Sixteenth Anthropological Expedition, organised by the University of
Adelaide to study the natives, left Adelaide for Alice Springs on 10 August 1952.
The Expedition was financed by a liberal grant from the Wenner-Gren Corpora-
tion for Anthropological Research Incorporated (previously the Viking Fund)
of New York, supplemented by substantial assistarice from the University of
Adelaide and its Board for Anthropological Research and from the South Aus-
tralian Museum, and by transport facilities granted by the Commonwealth and
State Governments.
On arrival at Alice Springs the Expedition proceeded by motor yehicle to
Yuendumu, on the track to the Granites and situated 192 miles to the north-west
of Alice Springs. During its stay at this Government Station for Natives, inten-
sive work was carried out on many aspects of native life, including a study of
theit sutroundings and the uses made of plant substances. This paper contains
a general account of the country and is followed by a record of the native names
for various plants and the uses made of ther.
DESCRIPTLON OF THE COUNTRY NOW OCCUPIED BY THE
NGALIA PEOPLE CENTRED ON YUENDUMU
These people are still within their tribal limits and occupy the area where
their mythical ancestors lived and were transformed into natural features.
The country consists of extensive plains, traversed at intetvals by occasional
water courses, now dry, which after heavy rain in Jantiary and February must
be torrents almost deserving of the name of rivers. Such a one is Cockatoo Creek.
These are fed by smaller subsidiary channels taking an irregular cotirse from
the rocky hills and even rugged mountains which form irregular ranges breaking
up the plains, sometimes into narrow stretches but often into areas of many
miles in extent. The soil is a sandy loam, very boggy in places alter rains, some-
times more sandy so that trucks dig in deeply, and covered with small pebbles
as one approaches the hills. At the base of these hills the stones become larger
and on their lower slopes become small or large boulders strewn irregularly up
the sides and making climbing laborious.
The flat countty known as. Ngalia plain, forming the southern portion of
the tribal area, is a shallow synclinal basin filled with sand and loam, underlying
which are quartzite beds containing rounded waterworn pebbles and other evi-
dences of a shallow water origin. They outcrop along the northern edge of Butt
Plain and at Central Mount Wedge with a northerly dip and appear again at
Ngama near Mount Eclipse and at Cockatoo Creek with a southerly dip. These
littoral beds are underlain by granites and metamorphosed old rocks. The granites
form great domes at Mount Doreen and Mount Hardy, and associated igneous
rocks form the many jagged hills around that area.
The grain of the country is east and west but the streams tend to run across
it. They are thus consequential, some passing through the grapite areas from
ers Rey Soc. S, Aust,, 77, July, 1954
&2
south to north, including the Lander and Cockatoo Creeks, while others, includ-
ing Gidgea Creek, which liey near the eastern boundary of the tribal area, cut
across from north to seuth to fill a long series of salt Jagoons and salt marshes,
which together form att ancient river valley on the Burt Plait: and trending away
west towards Lake Eaton. These salt marshes form the southern boundary of
the Ngalia tribe between Tilmouth Well and Mount Cockburn,
On the plains occur the red kangaroo {Macropus rufus) whose young “fying
does” are blue, the emu, and the bustard (“native turkey”); on the hills the
euro (M. rebustus) and a wallaby.
The yegetation on the plains consists essentially of mulga (Acacia ancura
and A. spp.) in dense thickets in places, making progress between these small
trees in a car a difficult matter, but usually in a more open arrangement inter-
spersed with shrubs and small trees, and sometimes quite scattered, diversified hy
grassy patches a few acres or a mile or so im extent, with or almost without
scattered shrubs. The grassy patches often constst of Triodia, so-called “spinifex,”
probahly m the poorer sol, or of various other species such as colonies of kan-
garoo grass (Themeda eustralis) and the taller and more robust tussocky
Th. evenacea (often in boggy places), and elsewhere smaller grasses such as
species of Enneapogon, Aristida, Triraphis mollis and Eragrostis.
The rocky hills show a wealth of species, commencing as the ground begins
to mse near their bases and is covered with the tessellated smaller fragments of
disruption, Native pines (Callifris) present a picturesque appeatance amongsi
the rocks, native figs (Ficus platypoda) may scramble over many boulders, a hill
type of mulga occurs, there are several Eremophilas, species of Aracia peculiar
to the slopes or the rising ground at the base, one of which has phyllodes like
a Lycopodium, a few small, often strongly scented and sticky composites, some
with yellow flowers, and several species of Goodeniaceae, some quite handsome
with blue or mauve or yellow flowers. Prickly Yriodia tussocks sparsely
oveupy the intervals and may reach formidable proportions in the better soil
round the base of the hill. The picturesque white boles of the ghost gum (Ewe.
papwana) and the tessellated trunks of bloodwoods( Ettc, ternrinalis?) are scattered
on the slopes or adjacent plains.
The waters in this country consist of rockholes in the bills, or oecasional
soaks on the plains, or waterholes left in the creeks and rivers after floods, Their
presence is often indicated by flocks of chestnut-eared finches (a sure indication
of their proximity) and by the relative abundance of other small birds. As rain
may not fall for many months, as for instance between May and November, the
smaller rockholes, and those unshaded and shallow, and the soaks tend to dry
up and the natives become dependent on the larger more permanent supplies.
This, of course, means that much of the larger game is also restricted to the neigh-
hourhood of these remaining waters and so may be decimated, and that any
vegetable and insect foods still available (such as roots and “witchetty’ grubs)
tend to be eaten ont,
The vegetable food supplies consist of fruits, of grains and seeds which are
winnowed, pounded, and made into dampers, of roots and tubers, of occastomal
leaves and pods (such as those of Marsdenia australis), of honey-bearing flowers
as, for example, those af the corkwoods (Hakee spp.) of which there are four
species, and of galls on Acacias. ;
Of the fruits the most important are the native peach (Eucarya ceumeinala)
which occurs in the area, the native plum (the pltim-coloured smaller fruit of
Santalum lonceolatum), the currant-like Emits of Carissa Brownit {Apocytia-
ceac) growing in little colonies near the banks of water courses, the currants of
the broad-leafed Plectronta latifolia which occurs as scattered tall shrubs amongst
the wulga, of the fruits of several species of Solatwm, native figs (Ficus ploty-
foda) growing amongst rocky hills and having fruits like small Moreton Bay
83
figs, the fruits ef Capparis Mitchellii (native pomegranate} which species is
widely distributed but not abundant, and the little cucumbers of Cicumis Melo
var. agrestis (which we did not see), The little “tomatoes” of the various
Solanums are much relished, We met with several species af which one,
S. petrophitim, with Jarge blue flowers and upright detsely prickly stems which
bear small yellowish to whitish tather dry fruits, is not eaten, Another spectes,
S. ellipticum, rather like this in upright habit but with fewer prickles and with
fruits becoming greyish-green is eaten, Near Mount Eclipse another very prickly
species (S. phlomoides) with large fruits whose stalks become recurved has
edible fruits and on rocky hills still another has its pale green tomatoes on the
underside of the spreading almost prostrate stems, A common edible species on
the plains with very few prickles may be a new species and another prickly species
with prostrate stems and quite small flowers has sweet-tasting somewhat yellowish
fruits. There are thus in this region five species at least of Solantin whose fruits
are sought after as feod. Summed up, as regards the fruits available to these
people, it may be said that some such us the native peach may yield a con-
siderable amount of fruit capriciously and for a short time; that the two
currants in season may supply a certain amount of food that requires time for
gathering; that the fruits of Samtelwm are not numerous and the shrubs not in
great quantity; and that the Solanums yield in their season a moderate amount
of fresh fruit, The fruits in fact do not constitute an important source of food
but are valuable adjuncts.
The grains and sceds available are mostly small but in such abundance that
enough can he collected to form a valuable addition to the diet. The grains seem
to be derived from panic grasses, and as with other small seeds are winnowed
by rocking to and fro in a wooden or bark dish. The common purslane (Portulaca
oleracea) is a prolific yielder of minute seeds and so are some of the “mouse-tail”
Chenopodiums of which we found one species. Various Acacia seeds are gathered
and even the small seeds of the Coolabah (Eucalyptus microtheca) and of
E, gamophylla may be utilized where these trees are available.
The seedling shoots of the coral tree (Erythrina vespertilio), winch occurs
in the district, are also eaten.
Nearly 250 species of plants were collected and the following notes deal with
about 60 of these of anthropological interest.
GRAMINEAE
Grasses Stich as Andropogon exaltatus (a lemon-scented grass) and Aristida sp.,
both tall species of similar habit, also Panicum decompasitum, native name
‘kalbal’bi. Seeds of the latter are termed wan:a wan:a-tatba = dish-gathered
grain and are gathered, husked and ground between stone mills to make a
damper bread. Nzgalia.
Aristida, browniana (= stipoides), a small tussocky grass, ’jepere. No use.
Enneapogon nigricans, "jepere. No use.
Triodia pungens (porcupine grass, often called “spinifex”). from which “gun”
was obtained, mana. 7. pungens is also catled ’mananknara, Ngalia.
CYPERACEAE
Bulb of Cyperits bulbosus, ‘jalka. Is eaten, Ngalia,
CASUARINACEAE
Casuarina decaisneana (desert oak). ’kurukara, jirkali (see Eucalyptus termina-
lis), Grows in the desert sandhill country; yields a “honey,” wama jurukara
(in hot weather), probably a species of lerp. Ngalia.
PROTEACRKAR
Hakea lewcaptera (neediebush), maro-okullba. Not used.
Grevillea striata. (beefwood), ‘ildi:lba. Not of use to the aborigines,
84
Santalum lanceolatum (native plum), ‘marukiri, mokaki, me:kari, ‘merkari, The
fruit is considered to be good food, Negalia,
LORANTHACEAE
Loranthus Exocarpi on Eremophila sp. and on Grevillea striata (beefwood),
flowers red or yellow, the fruits which ate eaten red or black are called
jamilbiri,
L. maidenii probably, a hoary grey mistletoe on Acacia spp,, narankiri. The grape-
like fruits are eaten. This is the food plant of the butterfly Ogyris hewitsoni
parsonst, Angel,
CHENOPODIACEAE
Kochia sp., ’kaiparu. No use is made of it. Ngalia.
AMARANTHACEAE
Philotus (Trichinium) obovatum, wanaparnaba. Used to line a wooden dish when
carrying a child. Ngalia,
Pt. alopecuroides (or Pt, nobile), ’walpa’ralpuri. No use. Ngalia.
Gomphrena brownn. The petianth segments, which are densely woolly outside,
are used as “down” for ceremonial purposes. This downy material was identi-
fied for us by Mr. R. V. Smith of the National Herbarium, Melbourne,
PorTULACACEAE
Portulaca oleracea, wakadi, also ’manjaru. The women gather the fine seed,
’wakadi ‘nula, for food and grind it between stones. Negalia,
NycTAGINACEAE
Boerhavia diffusa, ’waibi. The natives eat the root which may be large; it is a good
food.
LEGUMINOSAE
Acacia notabilis, "mandala. A lerp scale on the leaves and stems is eaten. Ngalia.
A, ligulata, ‘wardaruka. Not used. Ngalia.
A. aneura, s. lat. (mulga), ‘mandja. Negalia.
A, anewra, (mulga), ‘mandja, The seed ‘nuluparu. Ngalia; ‘wanari. The seed,
‘kaijura, Pintubi.
A. kempeana (witchetty bush), ‘erepili, also ‘nalkiri, ‘nalkidi, ‘yalkiti. The seeds
are eater and also grubs in the roots.
A, cambagei (gidya), ’sidji.
Al, cuthbertsoni, pi:li, pirlt. The seeds are sometimes eaten.
A, sp., with long linear phyllodes, ’paykuna, also called jirkili and wakalberi.
The ash from the burnt branchlets is mixed with the leaves of the native
tobacco in forming the quid. Ngalia. The alkaline ash probably helps in liberat-
ing the alkaloid,
Cassia pleurocarpa, ‘ya:na. Children eat a small borer grub in the roots called
"nalkiti ‘na:na. Ngalia.
C. eremophila, ‘pundi, ’pundi ‘wari. No use. Negalia.
A yam, the taproot probably of the pea Vigna lanceolata, is eaten. "Wapiti a
rant species of yam, ?Vigna or an Jpomoea; galatji is also a yam and “jala.
Negalia.
Erythrina australis (bean tree), jinindi. The young shoot is steamed and eaten,
Negalia.
HKUPISORBIACEAE
Euphorbia eremophila and Phyllanthus sp. have no native names,
ManvackaE
yam:uramjuri is a species of mallow with stellate hairs, No use made of it.
Negalia. .
85
Sida sp., ‘maykur’maykurupa. Not used by the natives. Ngalia.
Sida inclusa, java ‘man ja ‘man ja. Not used by the natives, Ngalia.
MyrTACEAE
Eucalyptus papuana (ghost gum), ‘wapinunga. The thick bark, yapiri, is stripped
off and tsed in the process of making “spinifex” gum, as a yapiri pindi
(bark dish).
E. terminalis ? (bloodwood), tjambali, jirkala. Bark used for dishes. Negalia.
E. pachyphylla, tjitilbara. The honey in the flowers is eaten. Ngalia.
E. gamophylla, ’waralju, ’warilji ‘warilji. The flowers yield sweet honey, ‘qul:u
‘waralju. Ngalia.
APOCYNACEAE
Carissa browmii, mayari.'A prickly shrub up to six feet high, with a currant-like
fruit which is eaten. Nealia, "Maninidji (manigidji) has also been noted for
Carissa brownii but the description of its “plum-like brown fruits’ being
good food suggests some mistake. Ngalia.
ASCLEPIADACEAE
Sarcostemma australis, kitjikitji. Not used. Ngalia,
Pentatropis kempeana? ‘manilba, The long bean-like follicles are eaten.
Marsdenia australis, 'jupali. The leaves and pods (follicles) are eaten and con-
sidered good. Ngalia.
CONVOLVULACEAE
Evolvulus alsinoides, ‘marna. Not used, Ngalia.
SOLANACEAE
Solanum sp? nova (5 petals, few prickles), kararupa (Walpiri tribe), jakadjeri
(Ngalia tribe). The tomatoes are good food.
S. quadriloculatum (very prickly), warukalukalu. Kangaroo food, not tised by
natives, Ngalia.
S. sp. identified as S. ellipticum but probably a new species, eight miles west of
Yuendumu, japindiri, has a pale sweet edible fruit.
S. ellipticum, prostrate, with large fruits, grows amongst frocks, near Mt. Eclipse,
naliljiriki, nalijiriki. Cooked, ripe or green, and eaten, also eaten by euros and
wallabies.
The Solanums and tobaccos were identified for us by Mr. R. T. Smith, of the
National Herbarium, Melbourne. It will be seen that two Solanums which differed
in habit and were given different native names were both referred to S. ellipticum.,
Later research will doubtless be able to separate these.
S. phlomoides A, Cunn., fruits reflexed, near Mt. Eclipse, wanakitji. Tomatoes
eaten. Negalia.
S. phlomoides (referred to), upright about 2 feet tall, at foot of Wolfram Hill
near Mt. Doreen, with big edible fruit, yandjawali. Ngalia.
. Nicotiena ingulba (native tobacco), in sandy loam under Erythrina trees south
of Mt. Eclipse. Used by the natives for chewing after wiltmg over a fire
and mixing with the ash of paykima (Acacia sp-).
N. occidentalis, near Mt. Doreen, ? yungarai. Not used.
Duboisia myoporoides, a poison bush, growing on the sandhills, warkalba, Negalia,
BIGNONIACEAE
Tecoma doratoxylon, wenbiri or wanbiri. Wood used for spears.
MyYororRAcEAE
Eremophila longifolia (emu bush), galurupu. Not eaten by the matives but good
emu food. Ngalia,
86
RvUBIACEAE
Plectronia latifolia, tawaljurv. Fruits eaten,
CAM PANULACEAE
Tsotoma petraee, ’muldu. The plant may be used for chewing with ashes in the
imatiner of native tobacco; is a substitute for tobacto; is a “strotig chew.”
Negalia. This Jsotoma evidently contains some strong alkaloid(?), as it is
spoken of by the hatives in the Musgrave Ranges about 500 miles south as
“cheeky b--r". The Department of Chemistry, University of Adelaide, has
been trying to obtain sufficient quantities for analysis, Tt is widely distributed
in the dry interior,
GooDENTACKAE
Seaevold sp. and Goodenia ? sp., pala. Not used by the natives. Negalia,
Geodenit ? sp., wadia, Not used. Negalia.
LU nipentiFiep
"Maruko. The fluffy pods (?) are used for decoration, Ngalia. Perhaps the hairy
perianth segments of Gompirene brownii (see Amaranthaceae}.
Kende, a large type of tree, one seen by an ancestral being iti a desert place.
"Wadia, a tree. Ngalia (see Goodente sp, above, which has the same name but is
a smalf undershrub).
Though the localities mentioned in the following notes are widely separated
from Ytiendumu and each other, this opportunity is taken of recording informa-
tion about three other plants used by Australian natives,
Pterocaulon (Compositae) as a substitute for native tobacco
In 1940 the late Rev. J. R. BR. Love fotwatded ftom Kunmunya Mission,
north of Derby, Western Australia, to the late Professor T, Harvey Johnston the
leavés of a plant “used by the Worora tribe of aborigines as a substitute for
chewing tobacco.” The plant has been identified as Pierocaulon glandulosum var.
velutinum. (Compositae). Mr. Love goes on to say: “It is not a tobaced at all, nor
is it regarded very highly by the people. It has a pungent smell, something like
‘penny royal,’ and is chewed, they tell me, when tobacco is not available.
“The name of it is ‘njuni-uni. The wild tobacco, which the men tell me
is to be procured in the sandstone ranges, I have never secured. It tiust be
scarce there, not like the mingulba, which is so plentiful in the Musgrave Ranges.
“My attention was drawn fo this yuni-yjuni by the unwillingness of ‘the
women to root out a plant of it that appeared in a bed of pumpkins—seed cartied
by the wind, J suppose.”
“Tubers’ on the Roots of the Grass Poa drummondii
In September 1952 Pastor Hoff, who was then looking after the natives
recently transferred from Ooldea to Yalata, 50 miles west of Colona near the
Great Australian Bight, forwarded us specitnens of grass, identified ‘as Poa
Drummondi by Mrs. E. Robertson of the Waite Institute. The grass was grow-
ing in a flat between sandhills and the native children dig out the “tibers”
attached to the roots and eat them. These “tubers” are whitish swellings, 5 to
20 mm. long and about 3 mm. in diameter, along the course of the roots or
attached to them (probably on rootlets), single or two or three separated by
constrictions. The swellings are friable in textiite and have little taste but perhaps
a slightly mealy one.
Seeds of Stenapetalum lineare (Cruciferae) eaten
Pastor Hoff also fotwarded from Yalata for (detitification specimens of
Stenopetalum lneare, the seeds of which were eaten by the natives.
A CARVED HUMAN FIGURE FROM THE DURACK RANGES, NORTH-
WESTERN AUSTRALIA
BY CHARLES P. MOUNTFORD
Summary
This paper records a carved human figure from an aboriginal ceremonial cave in the Durack Ranges
of north-western Australia.
A CARVED HUMAN FIGURE FROM THE DURACK RANGES,
NORTH-WESTERN AUSTRALIA
By Cuartes P, Mounrrorp *
[Read 9 July 1953]
SUMMARY
This paper records a carved human figure from an aboriginal ceremonial cave in
the Durack Ranges of north-western Australia.
The fact that the Australian aborigines carve human figures in wood has been
known for many years. Warner (1929) saw mortuary posts erected over the
graves of the dead at Milingimbi on which “a series of incisions . . . . give it the
appearance of a carved head with one or more necks.” Worms (1942) recorded
carved human figures used in the Goranada ceremony of the Kimberley region
of north-western Australia, Berndt (1948 and 1949) described wooden figures
from Yitrkalla, north-eastern Arnhem Land, and Mountford (1953) a number
of similar figures from the same locality,
In 1938 the Rev. F. W. Chaseling presented a mortuary post, made by the
aborigines of Yirrkalla, to the Australian Museum, Sydney. Mountford (1953)
and three years later Mr. Roy Vyse presented another carved figure, from the
Durack Ranges of north-western Australia (the subject of this paper), to the
South Australian Museum.
THE Carved FIcure
Early in 1941 a drover gave Mr. Roy Vyse a carved wooden human figure
which he had taken from an aboriginal ceremonial cave in the Durack Ranges,
south-west of Wyndham, north-western Australia. He stated that the aborigines
were rriost angry over the theft. In the same year Mr. Vyse presented this figure
(A.31105) to the South Australian Museum.
Plate I, B, C, and D, show the wooden figure of a woman. Her arms are
part of the body, and her head turned sideways. There is a belt round her waist,
and engraved body decorations across her chest, abdomen and back. These body
decorations, although crudely executed and somewhat ott of position, are similar
to those seen by the author on performers in the Central Australian ceremonies
and those on a dancing aboriginal engraved on a baobab nut from Derby, north-
western Australia (pl. i, fig. A),
As there is little direct evidence associated with this specimen, the sole object
of this paper is to record its existence, in the hope that it will stimulate inquiries
for other examples of the carved human figure.
REFERENCES
Bernpt, Ronatp and CaTHertne 1948 Oceania, 18, No. 4, pl. 1, 2
Bernot, 1949 American Anthropologist, 51, No. 2, pl. 1-3
Mounrrorn 1953 “Myth, Art and Symbolism of Arnhem Land” (in press)
Warner, Litoyp 1937 “A Black Civilisation,” 504
Worms, Ernest 1942 Annali Lateranensi. Vatican City. Pl. 4, 7
ne
*Plonorary Associate in Ethnology, South Australian Museum.
‘Trans, Roy Soc. S. Aust., 77, July, 1954
88
rage Does
I carvings. from north-western Australia.
Aborigina
Plate [,
THE GENUS NEOTROMBIDIUM (ACARINA : LEEUWENHOEKIIDAE) I.
DESCRIPTION OF THE OVUM AND LARVA OF NEOTROMBIDIUM
BARRINGUNENSE HIRST 1928, WITH AN ACCOUNT OF THE BIOLOGY
OF THE GENUS
BY R. V. SOUTHCOTT
Summary
The genus Neotrombidium Leonardi 1901 has been known hitherto from only the adult and
nymphal forms. This paper records the experimental rearing of the larva of the Australian
Neotrombidium barringunense Hirst 1928 from eggs laid by adults. The ovum and larva of this
species are described. From this larval description it is shown that the monotypic larval genus
Monunguis Wharton 1938, with M. streblida Wharton 1938 as type, found parasitic on a Streblid
(Diptera) ectoparasite on a bat in a cave in Yucatan, Mexico, belongs to Leonard’s genus, which has
taxonomic priority. This correlation shows that the range of Neotrombidium includes Central
America as well as the previously recorded South America and Australia.
9
THE GENUS NEOTROMBIDIUM (ACARINA ;: LEEUWENHOEKIIDAE)
I. DESCRIPTION OF THE OVUM AND LARVA OF NEOTROMBIDIUM
BARRINGUNENSE HIRST 1928, WITH AN ACCOUNT OF THE BIOLOGY
OF THE GENUS
By R, V. Sowtneorr
[Read 9 July 1953]
SUMMARY
The genus Neatrombidiuin Leonardi 1901 has been known hitherto from only the adult
and nymphal forms. This paper records the experimental rearing of the larva of the Aus-
tralian. Neotrombidium barringunense First 1928 from eggs laid by adults. The ovum and
larva of this species are deseribed. From this larval description it 1s shown that the mano-
typic larval genus Monungeis Wharton 1938, with M. streblida Wharton 1938. as type, found
patasitic on a Streblid (Diptera) ectoparasite on a bat ina cave in Yucatan, Mexico, helongs
to Leonardi's genus, which has taxonomic priority, This correlation shows that the range
of Neatrombidinn includes Central America as. well as the previously recorded South America
and Australia,
Further Australian records of the distribution of N, barringunense are given, the species
being known from the eastern half of Australia. In the Adelaide region the adults and nymphs
are found most commonly under the fresh bark of the bluegum, Eucalyplur leucorylon. Adult
females lay 30-'50 eggs, average 40, at a time, and there appears to be orily one oviposition,
Adult temales survive oviposition by 7-30 days. About three to four weeks is passed in the
egg stage. Other aspects of the biology of the species are discussed.
In 1901 Leonardi erected the genus Neotrombidium for N. furcigerum from
Argentina. In 1912 Berlese added a second species to the genus, NV. ophtalmicum
(sic), originally described as Trombidium ophtalmicum Berlese 1888 from Para-
puay, Hirst added NV, barringunense in 1928, giving as locality iniormation, “Bar-
rmgun, New South Wales, on the Queensland border, a single specimen
Found by the author under the bark of a living Eucalypt.” In 1929 Hirst
recorded the specics again, noting that “this species is very abundant under
the bark of gum-trees on the banks of the River Darling at Menindie,
New South Wales, July 1928.” In 1936 Womersley recorded this species
from Long Gully, Mount Lofty Ranges, South Australia, 12 May
1934, and from Bathurst, N.S.W., 31 May 1934. In 1945 Womersley erected
the family Leenwenhoekiidae for Leeuwenhoekia Oudemans 1911 and related
genera, separating these trom the Trombiculidae Ewing 1944, and also from the
old family Trombidiidae Leach 1815. G, M. Kohls and C. B. Philip, of the United
States Typhus Commission, had succeeded in rearing three species of the genus
Acomatacarus Ewing 1942 from New Guinea from larvae to nymphs, and this
reared material was serit to Mr. Womersley for description. This showed that
the genus Neotrombidiwm, whose larval form was unknown, had malare Fonns
similar to those of Leeuwenhockia, Acomatacayus, cte., and should he placed in
this family.
For some years the present writer has attempted to correlate larval and
adult Trombidiids (s,1,) as well as other mites, by rearing experiments, In the
family Trombidiidae (s.1.) a number of genera have heen so correlated. In 1939
Womersley was permitted to describe the larvae of Chyseria and Caenothrombinm
which the writer had thus reared during 1938. In 1946 the writer recorded
that the ege of Microtrombidinm hirsulum Wom. 1945 hatches direct to the
nymph, the larval stage being suppressed. Several other genera have been reared,
these correlations at present awaiting description. From 1938 onwards the writer
attempted to rear the larva of Nedtrombidium barringunense, which species is not
Trans. Roy Soc. S. Aust, 77, July, 1954
0
uncommon in the Adelaide region, Technical difficulties however prevented success,
and the studies were interrupted by the war. In 1948 these experiments were
resumed with N. borningunense, and the larva was reared from eggs laid by
adults in captivity (see later).
Description of Egg. Fig. 1 A-C. Colour reddish-orange. Length 240,, width
145u. The eggs are in the deutovum stage when first laid, in fact in mounted
gravid females the eggs show considerable development. When first laid the eggs
are smooth and ovoid, but within a few days become very irregular from a
number of protuberances, and it is this stage that is figured. This stage is more
irregular than for most of the Trombidiidse (s.J.). Some of the protuberances can
be identified as containing various parts of the larva. On the under-surface the
projecting legs can he seen; protuberances I, II and II in fig. 1C correspond
to legs I, Il and IIL.
Fig. 1, A-C Neotrombidium barringunense Hirst, ovum. A,B: dorsal views;
C; Sateral view. 1, I and III indicate developing legs I, If and TfL.
Anteriorly the protuberances for the palpi and chelicerae are identifiable
(see fig. 1. A,B), Further back on the dorsum is a large nasus, which appears to
correspond to the tiastts of the dorsal scutum of the larva. Ranged around the
Jateral sides and postetior pole are several blunt or pointed protuberances, of
anknown function,
Description of Larva, Fig. 2, 3 A-C. Colour orange. Body ovoid, as figured;
length from tip of nasits of dorsal scutum to posterior end of abdomen 150,
width 140, Dorsal scutum 92, long by 784 wide, roughly triangular, the apex of
the triangle forwards, where the shield narrows to a blunt nasus which partly
overlies the gnathosoma (capitulam), The anterolateral borders of the shield
ate concave, the other borders are convex except that the posterior border is
considerably flattened, Scutum with a pair of sensillary setae, long, fine, very
faintly ciliated, 46. long, arising from large sensillary areolae in the posterior
half of the shield; with three pairs of non-sensillary setae, the anterior (antero-
median) arising on the nasus as shown, fine, pointed, ciliated, 224 long; the
antero-lateral arising very close to the edge of the antero-lateral shoulders of
the shield, comparatively slender, but thicker than the antero-median, with
adpressed ciliations, and slightly tapering, blunted at the tip, 224 long; the postero-
lateral setae similar to the aritero-lateral, arising at the postero-lateral angle of
the shicld, 18y Jong. The scutum is porose over its posterior half, Eyes two an
each side, sessile, situated alongside the lateral borders of the shield, the anterior
eye the larger. Dorsum of abdomen with about 20 setae, similar to scutal non-
|
sensillary setae, only longer, 24-26« long, arranged in rows of 6,4,4,2,4, Ventral
surface: attached to the posteromedial angle of coxa I is a long pointed sparsely
ciliated seta 35a long; between coxae III is a pair of similar setae, 30p long;
behind coxae II are three rows of setae, long, pointed, sparsely ciliated, 40+
\ ee ae SOUTHCOTT
Fig. 2 Neéotrombidium barringunense Hirst, larva. Dorsal view, entire.
long, artanged in rows of 2, 4, 2; in addition there is a shorter poitited seta,
with a few similar pointed ciliations, 164 long on each side of the anus. Coxae I
and II are contiguous on each side, with the usual stigmal opening (utstigma)
betweén them. Goxaé I and III show a recticular porose patterning in their lateral
halves, net present on coxa II. Toward the anterolateral angle of coxa I arises
a long pointed strongly ciliated seta 40» long; on coxa II is @ similar seta 5a
long; on coxa III similar, 424 long. Legs of norinal length, leg I 245p long,
92
TI 245,, III 265, (all lengths include coxa and claw). Each tarstis of the legs
with a single strong falciform claw. Setae and spines of legs as figured. Tarsus I
and II are provided on their dorsal surface with a solenoidal spine. Tarsi with-
out Haller’s type organ. Tarsus I stout, 54p long by 23n high. Metatarsus I stout,
sinuotis, 38. long. Gnathosoma (capitulum) compact. Basal segment of chelicera
loop
SOUTHCOTT
Fig. 3, A-C Neotrombidium barringunense Hirst, larva. A: ventral view,
entire; B: tarsus and tibia of palp, ventral; C: tips of cheliceral digits.
elongated, ovoid, 40» long by 14 wide, cheliceral digit curved, with a minute
external tooth. Galeal seta short, curved, pointed, ciliated, 14» long. No hypo-
stomal lip present. Setae on basis capituli long, tapering, ciliated, pointed, 404 long.
Palpi as figured. Palpal femur, genu, tibia, tarsus with 1,1,3,8 setae respectively.
Claw of palpal tibia strongly bifurcate, as shown.
93
GEOGRAPHICAL DISTRIBUTION OF N. BARRINGUNENSE
The follawing additional localities are recorded: —(Queensland: Dead Man's
Gully, north of Cairns, 29 November 1943, 4 specimens under bark of Lucalyp-
tus sp.; 31 December 1943, 1 specimen from similar habitat; 2 January 1944,
1 specimen {no further field notes). Irvinebank, 28 September 1944, | specimen
from under hark Eucalyptus sp. South Australia: Adelaide region (see next
section). {All specimens collected by writer.)
BIOLOGY IN THE ADELAIDE REGION
Around Adelaide, Sotith Australia (Glen Osmond and Heywood Park),
adults or nymphs have been taken by the writer from May onwards to February,
over 1938-1941 and 1948-1951. An occasional specimen has heen found in soil,
or under the bark of Encalyptus camaldylensis, but practically all the specimens
from the Adelaide region have been taken under the bark of the trunks of
Excalyptus leucoxylon, in the splits between fresh layers of damp bark, and I
have no doubt that in the Adelaide region at least there is a very strong associa-
tion between this mite and Eucalyptus leucoxylon, By August or September the
adult females ate seen to he, in mounted specimens, gravid with eggs which show
a good deal of development, About 30-50. (average 40) eggs can be counted filling
(he body in these mounts, Oviposition has occurred on six occasions with captive
females, Only one oviposition has been observed with each female, up to 40 or
perhaps more eggs being iaid. After oviposition mounted femules contain no eggs,
On three cecasions I have succeeded in rearing larvae from eggs laid in captivity.
Details of Successful Rearings
{1} Experiment ACB 398, Two adults were taken from under bark of
Eucalyptus lencoxylon at Heywood Park, South Australia 26 September 1948,
and these were placed in a glass tube with some bark from the tree. On 14 No-
vember 1948 the mites were healthy and no eggs were present in the tube. On
7 Decetnber the tube was re-examined. One adult mite was rather shrunken.
Nine active larvae were running around the tube. No attempt at feeding these was
made, and by 28 December all the larvae were dead. The adult was shrunken,
hut otherwise appeared healthy,
It appears from this experiment that the period from oviposition ta hatching
of the larvae is less than 23 days. The eggs were fiot seen, except as egg skins
present along with the larvae.
(2) Experiment ACB 399, Two specimens of N. barringwrense, one adult,
one nymphal, were captured in the same situation us ACB 398 on 26 September
1948, and confined in a damp atmosphere in a glass tube. Water was added
periodically as droplets to maintain humidity. Eggs, of the same colour as the
adult, were laid between 10-17 October 1948, a total of 19 being laid. On 17 Gcto-
tober the eggs were recorded as “almost smonth," having heen laid in a little
pit formed between the cork and the glass wall of the tube, ur else scatlered
around over the surface of the cork or the glass. By J9 October the eggs were
irregular, with the typical deutovum outline. The eggs hatched out initially on
12 November 1948, and continued to hatch ot:t on subsequent days.
Hence the period between oviposition and hatching ranged from
29-5 + 3-5 days upwards.
(3) Experiment ACB 400. Eight specimens of N. barringunense were cap-
tured in the same situation as the preceding on 26 September 1948. These were
Placed in a damp tube with some bark from the tree. The tube was kept humid
hy the periodical addition of droplets of water, Some of the specimens were
o
damaged in capture, and by 14 Noverher it was recorded that five adults were
alive but some were a little shrunken and that ten living healthy larvae were
running around in the tube. The tube was then allowed to dry aut, but one adult
survived until 2 February 1949 when it was extremely shrunken, ity ghdomen
scaphoid across the dorsum.
Hence the period from oviposition to hatching wag tess than 43 days,
From these and other experiments one may conclude that in the Adelaide
region eggs are laid in November or early December, and that three to four weeks
is passed in the egg stage. Some of the larvae were placed on human skin to see
if any attempt at parasitization would be made, but none was observed, I recorded
with one batch of larvae that they appeared to be positively, though weakly,
phototropic. Adults of this species can withstand extreme desiccation for weeks,
and it is sometimes a cause for wonder how they can survive when so extremely
shrunken. Usually Trombidiids (s1.) do not withstand desiccation well, The
habitat of N. basringunense—under damp bark of Eucalyptus—is a yery unusual
one, the majority of Trombidiids (sJ.} dwelling in damp soil, and presimably
the power of this species to withstand dry conditions is necessary for survival
with their choice of habitat.
DISCUSSION ON THE AFFINITIES OF THE LARVA
Wharton (1938) described as new Monunguis streblida, a remarkable larval
Trombidiid mite parasitic on the batfies Plereliipsis araneae Coquillett and
Trichobius dugesii Townsend (Diptera:Streblidae) from the Cinquo de Mayas
Cave, Tekax, Yucatan, Mexico, This larval mite has a strong resemblance to the
larva of Neotrombidium barringunense. Tt has one large claw to each tarsus, and
the dorsal secutym is similar, except for a bizarre appearance or structure between
the scutal genailla, sketched by Wharton, which has na comparable structure in
N. barringunenss, and may be an artefact. In the two forms the dorsal scutum
shows a strong resemblance in shape and chaetotaxy, Wharton states that the
coxa J and coxa II of Monunguis ave separated, but unfortunately he does not
figure this feature. In this latter feature Wharton compares Monunguis with the
European larval mite Rohaxltia biungulem Oudemans 1911. Oudemans (1912)
says of this latter species “coxae Il und II getrennt,” and comments on its
“Hydrachnid,” especially Limnocharid, affinities. Vitzthum (1913) appears to
have been responsible for considering Rohaultia biunguium as the larva of the
previously described adult species Johnstonianu errans (Johnston 1852), although
I can find no grounds stated by him anywhere for this correlation. It would
appear from Willmann (1947) that the only grounds used by Vitxthum were
that the adults and farvac were associated im the field. Similar considerations
have led other students of the Acarina into error. Thus Womersley (1934)
accepted the species now known as Sphaerotarsus womersteys Southcott 1946 as
the nymph of Cagculisoma ripicola Womersley 1934 on what appeared to be a
stroug association in the field. Oudemans (1912) classified the larvae now
grouped under Trombicula and related genera under the genus Microtrombsdium,
quite erroneously.
Unfortunately Wharton does not, in his very brief description, comment or
the presence or otherwise of the “urstigma.” but as he places the larval
Monunguis in the Trombidiidae as against the Erythraeidae one may assume that
it is present. The only serious point of difference in the descriptions of Monunguts
and larval Neotrombidianm lies in the contiguity or otherwise of coxae I and H,
in which possibly Wharton was mistaken. There are so many resemblances
between these larvae that there appears little doubt that Monunguts and Neo-
trombidium are congeneric, and as the latter genus has priority it must take
55
precedence over Monunguis. NeStrombidinm streblidwa {Wharton 1938) is
undoubtedly specifically distinct from the only other known Jarval species of this
genus, Neotrombidiwm barringunense Hirst 1928. These species differ in the
stricture of the non-sensillary setae of the dorsal scutum, the number and arrange
ment of the dorsal setae of the abdomen, and in various other characters.
DISCUSSION ON THE BIOLOGY OF NEOTROMBIDIUM
Previously the genus Neotrombidivm has been known as the adult forms
from Australia and South America. The correlation recorded in this paper extends
the known range to Central America.
Wharton states that the farvae (NV. streblidum) “were found to be parasitic
on the streblid flies which imfest the bats” in the Yucatan caves. The species
ef hats concerned are not mentioned by Wharton, but from other articles in the
accourit of the fatina of the Yucatan caves (Pearse 1938 a and b, Pearse and
Kellogg 1938) it appears these flies were obtained from two specimens (male
and female) of the fruit-eating bat Artbeus jamaicensis yucetamcys (Allen) on
29 July 1936,
It is reasonable to assume that the larvae of the Australian A’, barringunense
have the same type of host as does the American species, aud we may expect to
find the larvae in Australia parasitic on the Streblid flies parasitic on Australian
bats. The genus Artibexs is not represented in Australia (Troughton 1943),
hence any further stiggestions as to what bais may be concerned must remain
conjectural. In fact, only a few fruit hats have been recorded from South Aus-
tralia, and these appear to have heeti stragglers (Wood Jones. 1925). Of the
dipterous family Streblidae no species appears to have been described from
Australia, and they certainly appear to be far from common. Tillyard (1926)
states that one undescribed Streblid has “been taken by Dr. Illingworth in north
Queensland.” A few other dipterous bat parasites (Nycteribiidae) appear to occur
in Australia, and one species has been described (Tillyard 1926, Rainbow 1904,
Speiser 1905),
The larvae of the Trombiculidae and Leeuwenhoekiidae are parasitic on
vertebrates, only a few exceptions to this rule having been recorded. On one
occasion the writer captured a larva of Tragardhula pentagoxa Womersley 1952
running freely over the black fur on the thorax of a female Troides priemus
(butterfly) in rain forest eight miles east of Wondecla, north Queensland, on
20 October 1943 (not August, as recorded by Womersley). Audy (reported in
Womersley 1952 and tm fit.) has found the larval Trombicula rara Walch 1923
parasitic on the pill-millipede Sphaegropacus globus-magicus Jeekel 1951, as well
as Trombicula frittst Wharton 1945 parasitic on the scorpion Heterometrus longi-
manus in Malaya. André (1943) recorded Leenwenhoekia paradoxa André 1943
parasitic on the scorpion Ruthus gibbosus Brulé on the island of Gavdos (south
oi Crete). These findings arc exceptional, hut demonstrate that such larvae may
utilize an arthropod host.
It is difficult to imagine how in the open forest situations in which Nea-
irombidium borringunense is found in Australia the numbers of adults of this
species are maintained if only the apparently rare Streblid flies may be used as
hosts by the larvae. In the cases observed in captivity the adult female lays a
number of eggs, either in a Ivose cluster, or scattered singly, the batches observed
in the tubes numbering between 20-40 eggs, Only one oviposition has been
observed in each female, Gravid females contain 30-50 eggs (average 40), which
frequently show considerable differentiation of the contained embryo, although
the egg is inittally smooth on being laid, After oviposition the females are devoid
of eggs in mounted specimens, which is confirmatory of the suggestion that there
96
is only one ayiposition. Oviposition ig not immediately lethal to the female; in
Neotrombidium barringunmense 1 have observed the female ta survive 7 - 30 days
after oviposition, which usually leaves it very shrunken, (With other Trombidiid
mites I have.on occasions. obseryed the female to survive months after oviposition,
under suitable conditions, which aré easier to maintain than those required for
Neotrombidium). The slight disparity between the numbers of eggs observed
after oviposition and the number within the ovaries of the gravid female may be
due to experimental errors—e.g., the mites tend to lay their eggs in any minute
crack in the bark provided, or in the corks sealing the tubes, etc.
Presumably the larva of Neotrombidium barringunense hatches out under
the bark of Eucalyptus leucovylon or some similar habitat, runs up the tree to
find a suitable host, either free in the tree or parasitic on a bat, and after feeding
pupates, presumably after falling to the forest floor, and finally reaches its
Eucalypt habitat asa nymph, and remains there to complete the remainder of its
life cycle, It is worthy of investigation whether the flies of the related Dipterotis
family Hippoboscidae, which occur on birds in small numbers, might serve as 2
host for the larval mites.
Although such 2 life history as outlined may appear fantastic, it is not more
so than for example Fabre has recorded in his classic researches on the life of
the anthrax fly.
REFERENCES
Anprt, M. 1943 Une Espéce Nouvelle de Lecuwenhoekia (Acarien), Parasite
de Scorpions. Bull. Mus. Hist. Nat. (Paris), 2e Série, 15, (5), 294
Beeresz, A. 1888. Bull. Soc. Ent. Ital., 20, 179
Bertese, A 1912 Redia, 8, 50
Hirst, §. 1928 On some new Australian Mites of the Families Trombidiidae
and Erythraeidae. Ann, Mag. Nat. Hist., Ser. 10, 1, 563
IDest, S. 1929 Additional Notes on Australian Mites of the Family Trom-
bidiidae, with Descriptions of New Forms, Proc, Zool, Soc., London,
2, 165
Jones, F. Woon 1925 Mammals of South Australia, Pt. 111. The Monodelphia,
Adelaide
Leonarpr, G. 1901 Zool. Anz., 25, 17
Ovpemans, A.C. 1912 Die bis jetzt bekannten Larven von Thrombidiidae und
Erythraeidae. Zool. Jahrb., Suppl. 14, 1-230
Pearss, A. S. 19383 Fauna of the Caves of Yucatan, Carnegie Inst., Wash.,
Publn. 491
Pearse, A, S. 1938b Insects from Yucatan Caves, Article XVIII, page 237,
in Fauna of the Caves of Yucatan. Edited by A, S. Pearse (see Pearse
19382}
Pearse, A. S., and Kentoce, R. 1938 Mammalia from Yucatan Caves, Article
XXIV, page 301, in Fauna of the Caves of Yucatan, Edited by A, Ss.
Pearse (see Pearse 19382)
Rainnow, W. J. 1904 A New “Bat Tick.” Rec. Aust. Mus., 5, (2), 78
Sourxeorr, R- V. 1946 Studies on Trombidiidae (Acarina). Some Observa-
tions on the Biology of the Microtrombidiinae. Proc, Linn. Soc, N.S.W.,
70, (5-6), 312
Seemser, P. 1905 Literatur-Referate. Z. f. Wiss, Ins.-biol., I, 349
Trtyarn, R. J. 1926 The Insects of Australia and New Zealand, Sydney,
page 378
TsovgHton, E, 1943 Furred Animals of Australia, Sydney
Wauarton, G, W. 1938 Acarina of Yucatan Caves, Article X in Fatina of the
Caves of Yucatan, Edited by A. S. Pearse (see Pearse 19384), p. 137
97
Wittmann, C. 1947 Trombidiidae. Lfg. 71 b. Das Tierreich, Berlin
WomersLey, H: 1934 A Revision of the Trombid (sic) and Erythraeid Mites
of Australia with Descriptions of New Genera and Species. Rec. S. Aust.
Mus., 5, (2), 179
Wowmerstey, H. 1936 Additions to the Trombidiid and Erythraeid Acaritie
Fauna of Australia and New Zealand. J. Linn. Soc. London (Zool.),
40, (269), 107
Womerstey, H. 1939 Further Notes on the Australian Trombidiidae with
Description of New Species. Trans. Roy. Soc. S. Aust., 63, (2), 149
Womersitey, H. 1945 Acarina of Australia and New Guinea. The Family
Lecuwenhoekiidae. Trans. Roy. Soc. S. Aust., 69, (1), 96
Womersiey, H.. 1952 The Scrub-Typhus and Scrub-Itch Mites (Trombicul-
idae, Acarina) of the Asiatic-Pacific Region. Rec. S. Aust. Mus., 10,
pts. i and ii, 1-673
DESCRIPTION OF A NEW GENUS AND SPECIES OF LARVAL
TROMBICULID MITE FROM NEW GUINEA
BY R. V. SOUTHCOTT
Summary
A new genus and species of Trombiculid mite, Babiangia bulbifera n. gen., n. sp., is described from
New Guinea. One specimen was captured free on the forest floor, but 11 specimens were taken
froma single small skink, Lygosoma (Homolepida) forbessii? The engorged specimens parasitic on
the lizard were parasitic beneath the body scales, an unusual form of parasitization for a
Trombiculid mite on a lizard. The engorged larvae showed a general convergence in body shape
towards that of the Pterygosomid mites, which are obligatory parasites of lizards. The
morphological affinities and biology of Babiangia bulbifera are discussed.
98
DESCRIPTION OF A NEW GENUS AND SPECIES OF
LARVAL TROMBICULID MITE FROM NEW GUINEA
By R. V. Soorrcorr
[Read 9 July 1953]
SUMMARY
A new genus and species of Trombiculid mite, Babiangia bulbtfera un. gen, nm sp. is
described from New Guinea. One specimen was captured free on the forest floor, but I1
specimens were taken from a2 single small skink, Lygosoma (Homolepida) forkesuf The
engorged specimens parasitic on the lizard were parasitic beneath the body scales, an unusual
form of parasitization for a Trombiculid mite on a lizard. The engorged larvae showed a
general convergence in body shape towards that of the Pterygosomid mites, which are
obligatory peraiies of lizards. The morphological affinities and biology of Babsangta bulbifera
are discussed.
In this paper a new genus and species of larval Trombiculid mite from
New Guinea is described,
Babiangia n. gen.
Definition—Dorsal scutum quadrangular, broader than long with two sen-
sillary setae placed anteriorly; with five non-sensillary setae, an anterior median
seta, two anterolateral and two posterolateral setae. Dorsal scutum extends
posteriorly beyond the posterolateral setae. Palpal claw bifurcate. Cheliceral fang
(digit) simple, without accessory teeth, Galeal seta simple. Eyes two on cach
side, the posterior eye the larger. Posterior ventral setae of abdomen with
expanded bulbous bases, All legs with seven segments (including coxa, basi- and
telo-femur. Empodium of tarsi thickened, equal to the tarsal claws. No whip-like
setae on legs. When engorged the larva is of Pterygosomid facies.
Babiangia bulbifera n. sp.
Fig. 1-3
Description of Larva—Colour light pink. Length (including mouthparts) of
unengorged type specimen 255,, width 175» (engorged specimens measure 300),
Jong by 350% wide). Shape roughly globular when unengorged. Engorged speci-
mens are flattened dorsoventrally, and then of Pterygosomid facies, with a distinct
posterior notch (fig. 3 shows a specimen in which the posterior notch is not a
marked feature). Dorsal scutum quadrangular, wider than long, 72« long by
97 wide, widest anteriorly, with sides almost straight. Anterior edge slightly
concave, anterolatera! corners flattened, lateral sides straight except for a slight
conyexity in the region of the posterolateral non-sensillary seta. Shield with two
sensillary setae, ciliated in their distal halves, 69 long, arising toward the antero-
lateral corners of the shield. Inter-sensillary distance 72». Scutal non-sensillary
setae slender, pointed, faintly ciliated distally, the anterolateral arising as shown
at the junction of the short anterolateral border with the lateral border of the
shield, 37 long. Anterior median seta similar, 54» long, arising a short distance
(9x) behind the middle of the anterior border. Posterolateral non-sensillary setae
similar but very slightly swollen at proximal end, 2% long, arising a little behind
the middle of the lateral border of the shield, close to the edge, which is there
a little convex. The shield shows the normal slight porosity.
99
Standard seutal data for the type specimen are {in micra) :
AW PW SB ASB PSB SD A-P AM AL PL Sens.
95 72 72 18 60 78 34 54 37 29 69
Eyes two on each side, mounted on a distinct shield. In unengorged specimens
the eye-shield is close to the lateral border of the scutum. The posterior eye is
considerably larger than the anterior.
a
Aik
we"\ N=.
\ vi \ ’, a | f
" \ Be
oh
SOUTHCOTT
Fig. 1 Babiangia bulltfera n.gen., n. Sp. Dorsal view, entire, unengorged,
Dorsum of abdomen with 20 setae, long, pointed, slightly thickened in their
proximal halves, ciliated, 33 - 63» long, arranged as figured.
Ventral abdominal surface: a pair of pointed ciliated setae, 26m long, between
the fused coxae 1 and IJ; a similar pair 21h long between coxae III. Behind
coxae IIT and anterior to the anus is a group of pointed ciliated setae with bulbous
bases, 25-27 long. Lateral to the anus are four long strong ciliated setae,
thickened proximally, medial pair 47 long, lateral pair 60 long.
Legs of normal length, leg I 295 long, IT 245, III 295p (all lengths includ-
ing coxae and claws). Coxae normal, as figured. Each coxa with a single long
curved pointed ciliated seta; that on I arises towards the posterolateral angle, is
46p long; on LI arises close to the posterolateral angle, 35, long; on IH arises
160
near the anterolateral angle, 63» long. Chaetotaxy of legs as figured. Setaé of legs
mostly strong and heavily ciliated, No long whip-like setae on legs. Metatarsus
I 48u long, On metatarsus III, neat its distal end, is a long strong tapering pointed
ciliated seta, 53 long, with a bulbous proximal part. Tarsus I and I] with the
normal solenoidal spine, not present on IJI. On tarsus III the claws are reinforced
by a strong curved ciliated seta arising distally on its posterior aspect. On all
tarsi the empodium is thickened and is as strong as the claws, Tarsus I 76p
long by 24y high,.
SOUTHCOTT
200; ff
Fig. 2 Babiangia bulbifera n, gen, n.sp. Ventral view, entire, unengorged.
Chelicerae and palpi stout and compact, Cheliceral digit strong, curved,
simple, without apical cap. Galeal seta short simple curved pointed, 15y long,
Seta on basis capituli long, strongly and unilaterally ciliated, 40 long. Palpi as
figured. Palpal femur, genu, tibia, tarsus, with 1,1,3,8 setae respectively. Femoral
seta ciliated, genual seta simple, tibial setae simple. Claw of palpal tibia bifurcate,
the axial prong being internal.
Locality—Babiang, Aitape region of New Guinea. (1) a single specimen,
Type, free, unengorged, from the rain forest floor, 22 December 1944 (R.V.S.)
(ACB 582). (2) 11 specimens parasitic under the body scales of a lizard (Lygo-
101
soma (Homolepida) forbesii?) (identified by J. R. Kinghorn, Australian
Museum), same situation, 24 December 1944 (R.V.S.) (ACB 258 A-K). (All
specimens in author’s collection.)
Fig. 3 Babiangia bulbifera, n. gen., n.sp. Dorsal view of an engorged specimen,
DISCUSSION ON GENERIC CLASSIFICATION
In keys offered in standard classifications of the family Trombiculidae, ¢.g.,
those of Wharton e¢ al, (1951) and Womersley (1952) this form would be
classified as Trombicula. Structurally Babiangia differs from Trombicula in the
shape and chaetotaxy of the dorsal scutum, and in having the posterior eye larger
than the anterior, Babiangia has a resemblance to the genus Novotrombicula
Womersley and Kohls 1947, having the dorsal scutum similarly produced
posteriorly, but in the latter genus the shield so extended takes in two of the
dorsal abdominal setae. Babiangia differs also in having the empodium thickened
and similar to the claws; in Novotrombicula and normally in Trombicula the
empodium is long and slender.
DISCUSSION ON BIOLOGY
The specimens of Babiangia bulbifera taken parasitic on the lizard appeared
to show a good deal of adaptation to their host, The specimens were completely
hidden under the scales, and were only found because it was noticed that some
of the scales of the trunk and tail showed a little tenting, and that there was a
slight gap under their free edge. The flattening of the body of the mite, and
102
general resemblance to the shape of the Pterygosomid mites, in the engorged
specimens is remarkable, showing a strong convergence. Parasitization of lizards
and other reptiles by Trombiculid mites is well known, but mostly the reptile is
merely one of a number of possible hosts, no particular adaptation being shown,
and the Trombiculids are not found under scales but clustered as is normal in
mammals and birds on some suitable soft patch of skin, e.g., in the axillae, groins
and external auditory meati, with the bodies of the mites projecting free above the
surface (Michener 19464 and b, Southcott 1947, Hyland 1951),
REFERENCES
Hyianp, K, E. 1951 Observations on the Chigger Mite Trombicula (Eutrom-
bicula) splendens Ewing (Acarina:Trombiculidae). Ann. Ent. Soc.
America, 44, (3), 297
MicHeEner, C. D. 19462 Observations on the Habits and Life History of a
Chigger Mite, Eutrombicula batatas (Acarina:Trombiculinae), ibid.,
39, (1), 101
MicHener, C. D. 1946b Taxonomic and Bionomic Notes on Some Panamanian
Chiggers (Acarina, Trombiculinae), ibid., 44, 411
SoutHcotr, R. V. 1947 Observations on the Epidemiology of Tsutsugamushi
Disease in North Queensland, Med. J. Aust., 2, 441
Wuanzton, G, W., Jenkins, D. W., BRENNAN, J. M., Fuuver, H. S., Kouts,
G. M., and Pup, C. B. 1951 The Terminology and Classification of
Trombiculid Mites (Acarina:Trombiculidae). J. Parasit., 37, (1), 13
Womerstry, H. 1952 The Scrub-Typhus and Scrub-Itch Mites (Trombiculi-
dae, Acarina) of the Asiatic-Pacific Region. Rec. S. Aust. Mus., 10,
Pts. 1 and 2, 1-673
Womerstey, H., and Kouts, G. M. 1947 New Genera and Species of Trom-
biculidae from the Pacific Islands. Trans, Roy. Soc. S. Aust., 71, (1), 3
STRATIGRAPHY AND STRUCTURE OF THE NORTHERN TERRITORY
OF AUSTRALIA
BY PAUL S. HOSSFELD
Summary
The Northern Territory of Australia covers an area exceeding 520,000 square miles. Very large
areas have not been examined geologically. The existence of formations of most of the major
geological divisions has been recognised. Those not recorded, or doubtfully so, are formations of
the Silurian, Triassic and marine phases of the Tertiary Period.
103
STRATIGRAPHY AND STRUCTURE OF THE NORTHERN TERRITORY
OF AUSTRALIA
By Paut 5. Hossretp *
[Read 10 September 1953]
CONTENTS
Page
Sum MARY - - - - - 3 - “
TL. Inprropucrion - - - - - “ - = - 104
II. Georocy - - - - - - - = « - 104
A. GENERAL - - - = - “i = ~ - 105
B. ArcHAgOzOIC - - - - - - - - - 105
The Musgrave Block - - - * e £ -~ 106
The Arunta Block - - - - - - - ~ 107
C. Prorerozoic - - - - . - : " - 110
Lower Proterozoic - - - - - = é - 112
Middle Proterozoic - - - - m > 7 - 115
(a) The Hatches Creek Group - = . - - - 115
(b) The Carpentaria Group - - - - - - We
The Newer Granites and Metallogenesis - - - - - 120
Upper Proterozoic - “ ~ “ 7 - 3 - 124
Ages and Correlation of the Lower to Middle Precambrian Rocks ~ 126
Correlation with Queensland and Western Australia - - - 127
Structures and Trend Lines of the Precambrian Rocks - - 128
D. Late Prorerozoic AND CAMDRIAN - - - - * - 131
The Buldivan Series ~ - - - - 4 - - 431
(a) The Buldiva Quartzite - - : 2 E ~ 433
(b) The Daly River Group or Upper Buldivan Series - - 134
(c) Volcanics - - - - - ~ - - 136
The Amadeus Geosyncline - - - - - - - 137
Age and Correlation - - - - = - - - 140
E. Orvovictan - - - - a - = - - 142
F, Sicuaian ~ - - - - - - - - 144
G. Devonran - - - - ~ = is ri ~ 145
The Collia Series - - - - - - - - 145
H. Carsonrrerous - - - & « « = - 146
I. Permian - - - - - - - - - 147
The Port Keats District - - e - “ + - 147
The Burt Range Basin - . - = = - 147
Other Areas in North Australia - - - - ~ - 147
The Finke Series - - - - 4 = - 148
The Elliott Creek Formation - - - = = - 148
J. Trtassic ~ = - “ - = = 4 - 149
K. Jurassic - - - - - - - - - 149
L. Creracrous - - - - re = = s ~ 149
The Great Australian Artesian Basin - - - - - 152
The Burt Trough = - - - - - - - - 152
M, Carnozorc - - - - - - we « - 155
TI. ReFerences AND Braviocrarny - - - - - - - 156
IV. IeLustrations - rs =
SUMMARY
The Notthern Territory of Australia covers an area exceeding 520,000 square
aniles. Very large areas have not been examined geologically. The existence of formations
of most of the major geological divisions has been recognised. Those not recorded, or
eoubthiily so, are formations of the Silurian, Triassic and marine phases of the Tertiary
eriod.
The rocks, structures and succession of events are discussed from the oldest,
the Archaeozoic, ta the close of the Mesozoic Era. The incompleteness of geological
mapping and great extent of recent surface accumulations, have necessitated the use
of inferred occurrences and boundaries to a large extent in the compilation of the
* School of Geology, University of Adelaide.
‘Trans. Roy Soc. S. Aust., 77, July, 1954
04
geological map and discussion of the history of the region. The use of all published
works, together with the extensive observations made by the author, have made it
possible to arrive at a number of conclusions, even though some be tentative, regarding
the structure and geological evolution of the Northern Territory,
Where practicable, correlations have been attempted with formations in Oteens-
land, Western and South Australia.
I. INTRODUCTION
The Northern Territory of Australia has an area in excess of 520,000
square miles and occupies therefore more than one-sixth of the total area of the
continent. Reference will be made to its two divisions, Central and North
Australia, which had short-lived separate administrations from 1927-31 (Sec
General Map). ;
It is a frontier province to this day. Except for mining camps, mission
centres and pastoral holdings, the few settlements are confined to the Over-
land Telegraph Line and to the two unconnected lines of railway. There
are ¢normous areas tin which roads and eyen tracks do not exist, and water
supply is temporary and precarious. Wide expanses of sand-plain, the large
areas of closely spaced sand dunes as well as the rugged topography af
many sectors make access difficult and hazardous. It is not surprising there-
fore that much of the Territory is not mapped and considerable areas have
nat been explored.
Geological examinations have been made of numerous areas, but the
greater portion of the region has Leen traversed by very widely spaced
reconnaissance suryeys and many areas have not been examined at all by
gtologists.
From 1935-41, the Aerial, Geological and Geophysical Survey of North-
ern Australia (A.G.G.S.N.A.). sponsored jointly hy the Governments of the
Commonwealth, Queensland and Western Australia, conducted investigations
in the above two States and the Territory. The writer was the Senior Geolo-
gist in charge of the Northern Territory Geological Party of that Survey,
which will be referred to generally in the text by its abbreviated title of
Northern Australia Survey or as N.A.S., but bibliographic references will
be given as A-G.G.5.N.A, During the course of this survey, the writer con-
ducted extensive ground and air reconnaissance surveys over large parts of
the Territory, and selected areas for aerial photography. Of the numerous
Jarge areas selected and photographed, many were examined and mapped
subsequently with the aid of the aerial photographs. A number of reports
were written by the present writer and his assistant geologists; the majority
have been printed and are listed in the attached Bibliography. The titles of
others, not printed, will be found in the A.G,G,S.N.A. reports. Where ‘possible
the rocks and minerals characteristic of each area examined were collected int
triplicate; the chief collection was forwarded to the Bureau of Mineral
Resources at Canberra, the others were sent to the Mines Branch at Alice
Springs and to the Department of Geolugy at the University of Adelaide.
The termination of field activities by the N.A.S. in 1941 ended systematic
geological examimation in the Territory during the remaining war years
Since then geological work has been carried out chiefly by officers: of the
Commonwealth Bureau of Mineral Resources, Canberra, and the contribution
of aerial photography of large sectors of the Territory is rapidly advancing
our knowledge of largely unknown areas.
The writer gratefully acknowledges the assistance by the Council of
the University of Adelaide in making research grants during 1949 and 1950,
and to the Professor of Geology, Sir Dauglas Mawsou, for the use of facilities
in the investigation and compilation of the material presented herein.
105
Through the courtesy and co-operation of the Commonwealth Survey
Tiirectorate. the writer was able to examine Jarge numbers of aerial photo-
graphs of areas not covered by the N.A,S. photography.
Reference must be made also to the great value of the pioneering work
of early explorers and geologists, especially H. Y. L. Brown, Davidson,
Maurice, Streich, Tate, Tictkens and Winnecke, and to numerous more
recent contributors.
. The writer desires to place on record his appreciation of the work done
in the Territory by the Assistant Geologists of the N.A.S., notably that of
A. H, Voisey, A. W. Kleeman, C. J. Sullivan, V. M, Cottle and T. V. Lewis.
Il. GEOLOGY
A. GENERAL
The geological record includes formations of nearly all the maio:
divisions, the Silurian and Triassic being the only ones whose presence has
not been proved. (See General Map.) Some formations have received no
definite age determinations as yet, but a tentative classification has been made
where this appeared reasonable. Such formations include the Collia Series
and Elliott Creek Formation of North Australia, the Post-Ordovician Can-
glomerate and the Finke Series of Central Australia,
Despite the large amount of detailed mapping that has been carried out
in the last thirty years, little except highly generalized information is avyail-
able of the greater part of the Territory. Large areas are unexploréd
geologically and many of those traversed at very wide intetvals by carly
explorers have not been visited since,
Enormous areas are deyoid of solid outcrops and the subjacent rocks
have been classifed on indirect evidence stich as vegetation and soils.
topography, scattered wells and bores and isolated outcrops. The absence of
solid outcrops over large areas is the result of various factors such as:
1. Extensive duricrust with or without sand-cover.
2. Large areas of parallel sand-dunes.
3. Large planed areas produced, some by marine, some by aeolian action,
4, Large areas of alluvium and lacustrine deposits.
5. Horizontal or sub-horizontal sediments, many in areas of graded
internal drainage.
A very large proportion of the otiteropping rocks are Precambrian in
age and their correlation depends on structural and lithological features,
lt is possible therefore, except in limited sectors, to deal only with the
broader features of geological structure and succession, All available publi-
cations and observations were examined and considered, but specific refer-
ence in the text to cach one was impracticable. The interpretation, and tn
a number of instances, modification of widely divergent views were facilitated
by the writer’s extensive knowledge of the Territory obtained during the
N.A. Survey and on other occasions. As a result, the writer found it possible
to extend considerably, boundaries of formations from areas examined on
the ground te others examined from the air or on aerial photographs.
B. ARCHAEOZOIC
The oldest formations known in the Territory occur within the areas
accupied by the Arunta Complex (Mawson and Madigan, 1930, p. 417).
Descriptions of the rock types, their location and mineralization are to be
found in many reports of the early explorers, but predominantly in those
of H, Y. L. Brown, to whose pioneering investigations we vwe much of our
106
earlier knowledge of the geology. Of the more recent investigators, the
more important contributions are those of Chewings, Hodge-Smith, Hossfeld,
Mawson and Madigan, Voisey, Wilson, and Ward.
The investigations of the N.A. Survey showed that determination of
the stratigraphical sequence and chronological succession, while laborious
and difficult, is possible; but as is to be expected, will require much detailed
field and laboratory work,
The formations of the Arunta Complex outcrop in two distinct areas
separated by a great thickness of younger sediments. The two areas are
known as the Musgrave and Arunta Blocks (Pitjentara and Arunta Shields,
respectively, of Chewings, 1935). The intervening area occupied by younger
sediments was named the Amadeus Geosyneline. (Amadeus Sunkiand of
Chewings, 1935.)
Although formations of the Artinta Complex outcrop over Jarge continu-
ous areas in some sectors such as for example in the Harts Ranges, the
Arltunga District and other areas east, north-east and west of Alice Springs,
there exist on these blocks numerous outcrops of younger sediments of
several periods. Many of these indicate by their attitudes and location that
they represent the eroded remnants of deposits which formerly covered
large portions of the old blocks.
Over very large areas also, no solid outcrops exist and the surface
consists of recent aeolian deposits as a veneer over the older rocks. In many
instances information obtained from bores and wells has proved the existence
at shallow depths of Archaeozoic rocks. There are a number of areas,
however, in which the presence of the basement rocks at shallow depths is
inferred. For the purpose of the general map deposits of alluvial or aeolian
origin where they serve merely to obscure the ancient rocks, have been
ignored. Some areas such as the Burt, Hale, and Plenty Plains, are down-
faulted blocks on which sediments ranging from Mesozoic (?) upwards, have
been deposited. It is possible teat other downfaulted basins exist within the
Arunta and Musgrave Blocks,
THE Muscrave Bleck
This black occupies the extreme south-western part of the Territory.
It extends westwards into Western Australia to the Warburton Ranges,
and southwards into South Australia where it forms a large area in the
north-western corner of that State and outcrops as a number of Inselberge
such as the Musgrave, Everard, Mann, Tomkinson and other Ranges.
The greater part of the Musgrave Block in the Northern Territory,
Western and South Australia, is included in a native reservation in which
non-aboriginal settlement is prohibited and access illegal, except by an
official permit. Ft can be understood, therefore, that tracks and water supplies
are scarce and access in general is possible only for well-equipped and
organized parties. The importance of the search for radio-active minerals
is expected to stimulate exploration of these areas of ancient rocks.
A considerable amount of information its available of the Western
Australian sector (Streich, Talbot, Clarke, et. a!.), and of the South Austra-
lian portion (Streich, Brown, Basedow. Jack and Wilson). The Territory
sector has been explored geographicalty but ihe rocks and structures of the
Archaeoseic formations are not well known. More attention has been given
in the past to the more prominent topographical features most of which
are residuats of rocks considered to be of Proterozoic age. Such information
as ts available both from the literature and the writer's limited observations,
indicates that the Territory sector contains a continuation of the rock types
107
and structures noted in the South Australian portion, The extensive develop-
jient of metamorphosed basic igneous rocks—greenstones—recorded in the
western part of the Western Australian sector of the Musgrave Block (Tal-
bot and Clarke, 1917), is not repeated either in South Australia or the
Northerm Territory. Similar altered basic rocks (dolerites and gabbros
chiefly) do occur but are of less importance.
The adjacent parts of Western Australia (Talbot and Clarke, 1917) and
of South Australia (Wilson, 1947) contain large areas of acid rocks, many
of which appear to be of rgneous origin. The oldest rocks recognised in these
areas and of the Northern Territory sector of the Musgrave Block are in-
tensely altered sediments now consisting chiefly of gneisses in which garnet,
cordierite, spinel, biotite and sillimanite are developed. Some outcrops of
schists, conglomerates and guartzites, mylonitized in part, are recorded, but
are scarce. It is probable that the vast aeclian deposits which obscure the
outcrops over so much of the area, cover to a large extent the more easily
eroded rocks. The known tock types as recorded, probably do not give a
true picture of the types and relative amounts of the Archaeozoic rocks of
the region.
In the ancient metasediments there are numerous, predominantly con~
cordant, masses of granite gneisses; many of them of great size. The
recognition, both in Western and South Australia, that these acid “ortho-
gneisses” include many hypersthene-bearing rocks similar to the Charnockite
Series of India, suggests that such may exist also in the Northern Territory,
both in the Musgrave and Arunta Blocks, Subsequently to the intrusion of
these acid rocks or their formation by granitization, there appears to have
occurred a period of igneous activity marked by intermediate to basic in-
trusions, (Wilson, 1947), As these are non-gneissic except in localities of
marked dynamic metamorphism, they appear to be separated by a consid-
erable time interval from the gneissic rocks, and are correlated tentatively
herein with the basic intrusives of later Precambrian age—Lower to Middle
Praterozoic—of Central and North Australia.
Subsequently, acid intrusions took place on a grand scale, producing
very large bathyliths of granitic rocks of which the Everard Ranges Granite
may be regarded as typical. These granites are predominantly non-gneissic,
but exhibit gneissic structure in parts near their margins. These “Newer
Granites,” too, include Charnockitic types. (Wilson, 1947), The gneissic
structure exhibited by these granites near their margins in some localities
and the apparent transition from granite to invaded rock noted in some out-
crops, suggests that some granitizaltion accompanied or was produced by
the intrusion of the acid magma. Finally, there appears ta have come the
introduction of basic rocks, dolerites, gabbros, norites, etc., which exhihit
little alteration and which have been assigned to various ages by different
observers.
To the Archaeozoic Era are referred those igneous rocks which exhibit
predominantly concordant gneissic structure on a regional scale and those
metasediments and igneous rocks into which they are intrusive. Subsequent
sediments and igneous intrusions, though they may have been subjected to
severe deformation, do not show the degree of stress and metamorphism so
characteristic of the older rocks, and are referred to the Proterozoic Era.
Tur AsuntTa Biockn
This block extends from the vicinity of Alice Springs (lat. 23° 45’ 5.
approximately), northwards to a short distance beyond Barrow Creek (lat.
21° 15’ S. approximately). Its greatest east-west extent is approxmmately
108
450 tiles, and it approaches both the Queensland and Western Australian
borders, Further explorations may extend the known outcrops to the east
and west, hut are not expected to result in material changes of the outline
as presented herein.
As in the Musgrave Block, the Precambrian formations of the Arunta
Block consist predominantly of rocks assigned to the Archaeszoic Era, but
include also a considerable proportion of younger rocks of sedimentary and
igneous origin, An enormous time-interval appears to separate the two age-
divisions, and the younger is therefore assigned to the Proterozotc Era.
The oldest known rocks of the Arunta Complex consist of intensely
metamorphosed sediments and igneous rocks. No evidence is available of
the basement on which they rest or of the terrain from which the sediments
were derived. These very ancient rocks have been affected by regional,
dynamic, thermal and contact metamorphism, injection of igneaus materials.
metasomatism and granitization, with regional metamorphism the dominant
feature. Some formations have experienced more than one type of meta-
morphism and in numerous instances variations in type or intensity can lie
observed in a formation or in a bed along its strike.
In many instances it is impossible either to determine the nature of
the material from which the present rock is derived or even to decide whether
its origin was sedimentary or igneous, Detailed observations show, however,
that included in the criginal rocks were conglomerates, arkoses, grits, sand-
stones, mudstones, limestones and volcanics (tuffs and flows), as well as
transgressive igneous rocks such as aplites, pegmatites, basic dykes and
probably sills. The rocks consist of gneisses and schists in great vanety and
include large formations of augen-gneisses and schists. Gneisses range from
acid to basic in composition, including a lustre-motiled hornblende-gneiss,
and represent both ortho- and para-gneisses. Schists have been produced by
the metamorphism and recrystailization of all types of sediments and vol-
canics and have developed a great variety of minerals, including sillimanite.
cyanite, micas, chlorite, talc, garnets, sphene, spinel, hornblende, diopside,
scapolite, epidote and many others. (
Garnets occur in gneisses and schists over very large areas and in
immense numbers, Most of them are small, but their numbers so great that
for miles the sand and soil are red. and consist predominantly of that mineral.
However, crystals over an inch in diameter are plentiful. The largest seen
by the writer had a diameter exceeding 3 inches. Hadge-Smith (1932) records
one of nearly 11 inches diameter. The garnetiferous rocks and some gurnet
reck occur in many parts of the Arunta Block but mainly in the area to
the cast and north of the River Hale, where gem quality stones occur in
large numbers.
Mylonitization was intense in some areas. Conglomerates were trans-
formed ta gneisses and in some instances the original pebbles stretched to
thin. Alms. Calc- and quartz-schists, sheared basic rocks and other recards of
dynamic metamorphism occur plentifully, but tn restricted areas. Injection
of igneous materials, both acid and basic and the granitization and contact
metamorphism of these ancient rocks add to the immense variety of rock
types, developed as stated earlier, in some instances at intervals along the
strike of a bed or a formation.
In addition, subsequent silicification, either selective or general, has
increased the difficulties of determining the original material.
The recognition of originally igneous material depended in many fn-
stances on observations in the field rather than on microscopic determination.
There were instances, however, where the latter confirmed the field evidence-
109
Acid igneous material invaded or was formed in the ancient sediments
and igneous recks which form the basement rocks of the Arunta Complex,
Geth in the Arunta and Musegraye Blocks, enormows areas shaw outcrops
of granite gneisses and related rocks (Pl, IJ, 1). In most instances the gneissic
structure 1s parallel to er concordant with thal of the invaded gneisses and
schists. These “older granites” occur on a vast scale not only in the Northern
‘Territory, but also in South and Western Australia. They were invaded
by basic rucks, priginally dolerites or gabbros and probably some ultra-
hasic types. which rocks haye been metamorphosed and recrystallized to
umphibalite gnetsses and schists.
These anciet( acid and basic igneous rocks have been subjected gener-
illy to the regional and specific types of metamorphism which were experj-
enced by the invaded rocks, The concordance uf many of the granite
gneisses and approach to concordance of others, suggesis that the
original rocks had been subjected to diastrophism, some of a severe character
and therefare, chat some metamorphic activivy, chichy of a regional type.
had occurred before the formation of the granite-gneisses. It is probable
that the acid igneous activity follawed closely upon and was partly synchron-
ous with w period of seyere orogeny and that the final phases were marked
by the introduction of basic igneous material. The severe folding and Taulting
which are such marked features of the Archaeozoic formations of the
Arunta Complex have affected the ancient formations, the “older granites”
and “older basie intrusions” and it is impossible at this stage ta determine
the amount of deformation prior to the period of igneous activily.
Modge-Smith (1932, pp. 423-431) proposed a tentative age classification
wf the formations of the Arunta Complex. The present writer agrees with
the reference to the Froterozoic Era of the Everard Range Granite and the
Molgarna Acid Intrusives. Hodge-Smith, however, went Further and sug
gested a division of those rocks which are predominantly of sedimentary
origin into the Huckitta and Ambalindum Series, the farmer being the
older. In view of the marked lithological differences between his “Huckitta
Series” and racks cuteropping in the Arltunga District, a division af these
-\rehaenzoic rocks is tempting. It 1s difficult, however, to decide whether
Hodge-Smith regarded the rocks of the Arltimga District as members of
his “Ambalindum Series.” Voisey (1938) appears ta take this view but
includes with them the White Range heds, which Hodge-Smith, following
Chewings (1928), defimitely though mistakenly, correlates with the Perta-
knusra or Upper Proterozoic beds. The present writer disagrees with both
the above views, and considers the White Range Quartzite and associated
beds as Post-Archaeozuic and pre-Pertaknurra, and probably of Middle
Proterozoic age. It is possible that detailed structural mapping will «lemon-
strate the existence in the Arltunga District of unconformuble groups of
metasediments within the Archaeozoic rocks, but sit present this must be
merely an interesting speculation and they will he referred te collectively
us the Aruntan Series. Examination of the Harts Ranges shows that these
ranges consist chiefly of a group of highly metamorphosed rocks apparently
of sedimentary origin, which are folded against and dip away from the
gneisses, schists and granite gneisses of the Aritunga Distecit, and appear
ta be ancomformable to them. Some fault boundaries were observed, but the
greater portion of the contacts appear to be unconformable. The northern
continuations of these rocks are cut aff sharply by the fault boundaries wf
the Plenty Trough which contains sediments probably of Mesozoiw and
Cainozoic ages (Fig. 2).
The Harts Range rocks consist of schists and gneisses intruded by very
110
rumerous, muscavite-hearing pegmatites of probably Middle Proterozoic
age. The metamorphism of the original sediments was intense, but in those
sectors examined by the writer, the range of original material appears 10
have been much less than that of the adjacent and presumably older racks
of the Arunta Block, and they do not appear to comtain the granite gneisses
so plentiful elsewhere. It is suggested that the Harts Range metamorphics
may represent a younger division of the Archaeozaic Era. They are classifiee!
tentatively as Upper Archavozoic and will be referred tu as the Riddock
Series.
The Archacozoic rocks ag defined in this paper are those referred to as
the Lower Precambrian by David and Browne (1950).
The metasediments of the Arunta Complex with their sheared ton
glomerates, sheared and reerystallized busic tutis, flows and possibly sills,
as well as the great thickness of other associated rocks. of clastic origin, are
referred to the Warrawoona Series of Western Australia and the Argylla
Series of Queensland,
‘There appears to be little doubt of the correlation of the granite-gneisses
with those of other parts of Australia at or near the top of the older Arch-
aeozoic. (Kalkadoon Series of North-Western Queensland.)
The effect of Archacozoic igneous activity on the introduction of metallic
minerals in the Musgrave or Arunta Blocks has not been determined, The
intense metamorphism and deformation of the rocks as well as the wide
spreaul mineralization during the Proterozoic Era, but especially the enor-
mous depth of material removed by erosion, make such a determination
dificult, There are a few octeurrences including gold, copper and tungsten
which have no apparent connection wilh Proterozoic mineralization, and are
regarded tentatively as of Archacozaie age. All these occurrences, however,
are sinall and of little economic value.
As 15 to be expected in a region of intense deformation, the Archacoavic
rocks exhibit structures which may vary widely in direction within very
short distances, Despite these expected irregularities, however, there 15 a
remarkable tendency, as noted by previous observers, for westerly to north-
westerly strikes ta persist or recur over long distances in the central portians
of the Arunta Block. Towards the western extremity, however, as for
example at Mount Doreen, the strikes change to a north-north-westerly
trend (Hossfeld in A.G.G.S.N_A., 1940b), (Hills, 1946), In the eastern half
of the block, westerly to north-westerly strikes persist, except for loc!
variations, as far as the Jervois Ranges Mineral Field. The writer, while
surveying this field (Hossfeld, 1931), noted a marked change of strike at the
southern end of the field; the swing from east-west to north-north-west
exceeds nitiety degrees, This northerly strike may represent merely a local
departure from the general trend or it may coilinue, as suggested by Hills
(1946), lo the Cloncurry Region in North-Western Queensland. The exten-
sive jitervening cover by the Trldivan Series of Cambrian age. made +)
determination impossible,
Cc. PROTEROZOIC
Trom Darwin in the north to the vienity of Alice Springs in the south,
and froma the Western Australian to the Queensland border there outerop
at intervals, groups of sediments which have been metamorphosed, inteudesd!
by acid and basic igneous rocks, and in most areas contain metallic anineral
deposits. Their metamorphism varies considerably in severity, but except
in a few restricted localives, does not approach in intensity or completeness
the metamorphism exhibited by the Archaeozoie formations, Farther, where-
111
as the Archaeozic rocks include acid and basie igneous rocks which are
regionally gneissic, as well as predominantly non-gneissic intrusions, it is
the latter only which invade the younger, and less metamorphosed rocks.
With the exception of stich areas as the White Range, Jervois Ranges,
McArthur River District, etc, to which some observers have assigned mare
recent ages, these newer metamorphic rocks and their associated igneous
intrusions. have been and are regarded generally as being comparable in
age with the Mosquito Creek Series of Western Australia (David, 1932),
(Hossfeld, 1936-40), ((Matheson and Teichert, 1945), (Noakes, 1949). This
series is regarded by some as Upper Archaeoznic, hy others as lower
Proterozoic. For reasons which will be given below, the latter is adopted
by the present writer. The detailed mapping of the Brock’s Creek District
carried aut by the N_A-S. during 1939 and preceded during 1935-38 by
detailed surveys of many smaller areas in North Australia, indicates that
all the mineral-bearing rocks of the Darwin-Katherine region and beyond
(which includes the Brock’s Creek District), belong tao one confarmalile
Series and represent continuous deposition to a thickness of at least 17,000
to 18,000 feet. These sediments exhibit marked variations in intensity wf
metamorphism in different Jocalities but cannot be separated into age-groups
on that score. The views expressed by some observers, and hased apparently
on the variable degrees of metamorphism exhibited by the sediments, that
unconformable age-groups exist in the mineral-bearing sediments of the
Darwin-Katherine region, have not been confirmed.
Further to the south-west, south and sotith-east, however, there is
evidence of the existence of at Jeast two unconformable divisions af miner-
alized sediments of Precambrian but Post-Archaeozoic age (Fig. 1).
LOWER PROTEROZOIC MIDDLE PROTEROZOIC
(ACICOND) SERIES) (BAVEN PORT SERIES)
Lx =e ~ . 2
RN (A
RP 1 QUARTZITES VDLCANICS AMPHIBOUITES ACID
TuTES © SUATES € SANDSTONES ESHWALES INTRUSIVES
Woe 2 %& ‘ the & WILE
H~2
Piz. 1
Sketch Section at Hatcbes Creek.
As far as is known, the only recorded straligraphical break in the con-
tinuity of these formations is that revealed by the detailed mapping during
the examination hy the N.A. Survey of the latches Creek area, in the
eastern portion of the Davenport Ranges of Central Australia. Near the
southern limits of the mapped area, schistose and sheared porphyries, tuffs,
and related rocks with some slates, are overlain unconformably by the
group of sediments of the Hatches Creek Wolfram Field, In the report,
(A.G.G.S.N.A., 1941), the lower group was referred to by the present writer
as the “Bottom Series.” It is not proposed here to give these rocks a formal
name, as they are being correlated tentatively with similar rocks at Tennant
Creek, The Granites, Tanami, ete., which are being correlated with the meta-
forphosed sediments of the Darwin-Katherine Region. As the survey which
112
located these rocks in the Davenport Ratiges was primarily an economic one
it was impossible tu carry the stratigraphical investigations further at that
lime.
The group which lies unconformahly alve the "Bottom Series” was
Wamed the “Llatehes Creek Series.” Together with the former “Top
Series” it will be referred to as the Hatches Creek Group which is being
included in a division being named the Davenport Series.
Still higher in the sequence, lying unconfarmably an ali of the Pre-
cambrian formations so far discussed, there occurs at intervals oyer a large
part of North Australia a formation of massive arenaceous sediments pre-
dominantly quartzites, but including sandstones, grits and couglumerates.
The age of this formation, which was named the Buldiva Quartzite, has
heen given variously as Upper or Late Proterozoic or Lower Cambrian. Most
observers, including the present writer, correlated it with similar furmations
of the Nullagine of Western Australia. However, the writer cansidered it
to he the basal formation of the Buldiva(n) Series (Hossleld 1937 ¢ et al),
a series which it was stated continues without interruption into the Cambrian
Period and includes the Cambrian sediments of the Daly River area, Barkly
Tableland, etc, To this opinion the present writer adheres, but now regards
the Buldiva Quartzite as considerably younger than the Nullagifie Series
with which it was correlated previously (Fig. 3)-
While it is possible that deposition of the basal members of the Buldiva
Quartzite tay have begun at the close of the Proterozvic Era, the whole
ef the remainder of the Buldivya(n) Series is of Cambrian age. That Series
will be discussed therefore, in the section dealing with the Cambrian Period.
In the Atnadeus Geosyncline, situated between the Arunta and Mus-
grave Blocks, deposition appears to have begun in the Upper Proterozoic
and to have continued throughout the Cambrian and Ordavician Periods
and probably inte the Silurian, These divisions will be referred la in the
sections dealing with the respective Periods.
The area between Borroloola and Wollogorang af which little ts known,
appears to be covered largely by quartzite outcrops which in the western
sector exhibit enormous, long sub-parallel gashes resulting possibly from
the erosion of dyke formations. On the evidence of limrted investigations
along the margins and apparent relationships ta the Cambrian formations
above, and to the Carpentaria Group of adjacent areas, these rocks are being
regarded provisionally as of Upper I’roterozoic age.
Lower Proterozoic
The formations assigned to this age division were correlated with the
Mos¢jtiita Creek Series of Western Australia (David, 1932), (TLossfeld,
1936h), (Voisey, 19392), (Noakes, 1949). As will be shawn later, it is
suggested herein that the formations which have been mapped as Mosquito
Creek Series in Western Australia, may belong to twe uncantormable Fre-
cambrian divisions. It is probable that those formations of North Australia
previously correlated with the Mosquito Creek Series, will be found to be
the equivalent of the older formations of that Series in Western Australia.
A definite correlation is impossible at present. They will be referred to here-
under as the Agiconili Series, after the native tribal name of the district
(Cummanwealth of Australia Bulletin No. 191, in which the Pine Creek and
Union Groups outerop (Hossfeld. 1936 and c),
The Agicondi Series outernjis over a large part af North Australia. It
includes the greater partion uf the rocks outcropping in the triangle formed
bby Darwin, Oenpelli and Maranbuy, and extends southwards to Callia (Wty,
143
3), In this region the sediments have been given the formal name Brack’s
Creck Group (Noakes, 1949), Members of the Series outcrop at intervals
in the valleys and along the dissected edges of the western part of the
Arnhem Jand Plateau.
Same at least of the formations traced into the western part of North
Australia [ram the Ord River in Western Australia (Mattheson and Teichert
1945), appear to belong to the Agicondi Series.
In Central Austrahia similar formations have been recorded at widely
separated Iwealities and are being correlated with it. These include the head-
wuters area of the Winnecke Creek, Tanami and adjacent area, The Granites
Goldfield and vicinity, the Tennant Creek Goldfield and surrounding areas.
the “Boltom Series” of the Hatches Creek Woliram Field and a number of
other areas indicated on the General Map. All of these are regarded as
members of the one series and because of the above correlation, will be
referred to herein as the Agicondi Series.
aRTG
aes
BYAREL SAVEN POAT
PEESPNEL EL No
; Sas +5
SS S
CROOVICLAN TEATIARY
am G te MESOZOIC e
[a]
te
=
a * 45 Se MILES
@ACHAEDZOIC PROTEROZOIC
tae Uppar lower’ Midulte
Fig. 2
Siretch Section across the Hart’s and Davenpart Ranges,
As stilted aliaye, outerops correlated with this Series are well distribwied
in the Territory. Many are relatively small inliers and do not provide good
outcrops. The lirgest and most ¢emtinuons area and exhibiting the best
outcrops as well as being exposed in many mine workings, is that occurring
within the Darwin-Oenpelli-Maranboy triangle. In the Rrock’s Creeley Dis-
trict, and supplemented by detailed mapping of numerous additional areas,
the N.A. Survey was able to determine the existence of a thickness of 17,000
to 18,000 feet of sediments. This figure is a minimum as neither the top nor
hase af the Series was determined. The present writer believes, however,
thal the Galden Dyke Group as described in the official report (Hossfeld,
19364) contains the oldest known sediments of the Agicondi Series (Voigey,
1939a, per contra vide). The shallow water facies af some of the lower mem-
liers of the Golden Dyke Group, chiefly conglomerates and sandstones,
suggests that the hase of the Series may be at a shallow depth in this area.
As a result of surveys during 1935, the present writer divided the sedi-
ments In the vicmity of Pine Creek, into the Pine Creek and Union Groups
with somewhat ill-defined transition beds. (Hossfeld, 1936b and c)}. The
former consists predominantly of greywackes and other sandstones with
some grit and slates. Many of the beds are tufts or partly tuffaceous.
The Union Group consists chiefly of slates with subordinate sreywackes
and grits. The slates weather to a distinctive red colour, which has Leen
used in 4 tentative correlation of slates of other areas as for example those
north of the Daly River (Ilossfeld, 1937c¢),
Voisey (1939a) divided the Mosquita Creek sediments of that region
inta three series, tle Golden Dyke, Pine Creck and Muldiva Series, While
there was some justification for the initial division of the sediments by the
present writer in 14933 and 1936 into the Pine Creel, Union, Golden Dyke
Groups and the Daly River and Muldiva stages, at a time when little was
known vf the suceessign, their division at a later date by Voisey inte three
series appedirs to have been quite Uinevessary.
T
114
The original field terms Pine Creek, Union and Golden Dyke Groups
ete,, have last their importance and are being retained here merely for
convenience of reference and description.
The Agicondi Series of the Northern Territory consisted originally of
arcnaceous and argillaceous sediments with a considerable amount of tufface-
ous mitterial and very few calcareous deposits, Subsequent metamorphism
has transformed the shales to slates, phyllites and schists. the greywackes aril
other sandstones to schists and quartzites, and the few limestones to marbles.
Tatts and prophyriecs have become schistose, grits and conglomerates have
heen sheared and their components fattened in some localities, and a
auceole of hornfels surrounds wholly or in purt many of the granite intri-
sions. The degree of metamurphism varies in ditferemt localities and this
induced some of the earlier observers to suggest the existence of different
age-groups, and the possible occurrence of rocks of Archaeozuic age in North
Australia.
No break in cantinuity has been diseevered there, and the metamorphisin
dues not approach in severity in any of the «reas examined, that which 1s
sa vhuracteristic of the Archaeozoic formations of the Arunta Complex.
The writer regards his “Bottom Series” of the Hatches Creek Wolfram
Field as belonging te the Agicondi Series (Fig. 1). Tt 1s possible, of course,
that these rocks which exhibit marked metamorphism, and consist as fur
us examined of sheared amphibolites, porphyries and tufts, chloritic and quartz
mic sthists, slates and amygdaloidal rocks, probably tufts, represent a group
intermediate in age between the Archaeozoic rocks of the Arunta Complex
and the Agicondi Series. However, similar formations outerop at intervals
to the north-west in the cores of eroded anticlines until the Tennant Creek
Goldheld is reached, Here they outcrop over a large area, forming the country
rock of that poldfiell, and have been correlated by other workers with the
Mosquite Creek Series. There is a close resemblance between the rock types
of the scattered Central Australian areas such as Tennant Creek, The Gran-
ites, Tanami and adjacent areas, Winnecke Creek and many other smaller
outcrops, and those occurring in the Darwin-OQenpelli-Maranboy triangle of
North Australia. This resemblance includes not only their dominant
arenaccous-argillaceous character, but also the large proportion of tuffaceous
materials, the paucity of limestones and the degree of metamurphism. The
predominantly shallow-water facies sugyests that they were laid dewn in
slowly subsiding basins, These appew ta have formed in a large mobile
region extending aver most of, and beyond the Territory, Offshore and
marginal volcanocs appear to have been numeruus, The composition of those
tuffs in the Pine Creek District whith were examined microscopically stg-
gests original lavas of intermediate composition, dacites or andesites, but
probably the latter,
Subsequently to the deposition of the sediments, a period of igneous
activity resulted in the introduction wf basic material. This appears to have
been chiefly doleritic or gabbroie and was introduced largely in the form of
sill. Dykes and bosses have been mapped but are rare. In some areas such
as the Golden Dyke, some thermal metamorphism resulted, particularly
where relatively thin sediments were lacated hetween two sills.
Asa result of subsequent uralitization and similar processes, these racks
have been altered to amphibolites, The occurrence of similar amphibolites
is not confined to rucks assigned to the Agicondé Series. Phey uccur im racks
of Archaeozoie age in many parts cf the Arunta Block but are of DPost-
Archaegavic age, They occur also in the Hatches Creek Group in the Daven-
port Ranges, and are reported from similar formations in the adjacent Mar
115
chison Ranges. These amphibolites therefore, aceur at intervals throughout
the Northern Territory, intruding formations considered as ranging from
Archaeozoic to Middle Proterozoic (Figs. 1, 2 and 3), and prabably helong
la two distinct periods.
Subsequently to the basic intrusions but possibly contemporaneous in
part, the regian experienced severe deformation. Folding af the sediments
ant basic sills, resulted eventually in the development of structures of great
variety. In many areas as, for example, in the Brock’s Creek District, but
by no means confined to that area, dome and basin folds were developed.
Tightly folded and overfolded structures occur in many localities and shear-
ing, some of it of severe character. is recorded from numerous areas,
Dynamic metamorphism of the sediments resulted in the formation af
schists, cherts, quartzites and sheared rock types and the development of
metamorphic minerals.
This was followed by the introduction on a grand scale of acid igneaus
racks chiefly granitic in composition but including some more calcic types
The writer considers that the available evidence indieates that this 1tneous
activity took place during the closing stages of orogeny of a later, anil
uncunlormable series, the Davenport Series, and chranologically therefure
helongs to a later section of this paper.
Mippie Prorerozuic
All formations believed to be of this age are being included in a division
which is being named the Davenport Series. The name is derived from the
Davenport Ranges which consist predominantly of these formations. Further,
they were studied in detail in this area at Hatches and Wauchope Creek,
and in the former locality were shown to lie unconformably on rocks
correlated with the Agicondi Series which is regarded as of Lower Protero-
zole age.
The formations included in the Davenport Series are referred to two
groups:
(a) The Hatches Creck Group,
(b) The Carpentaria Group.
(a) Tue Tlarcues CREEK Grover
Representatives of this group were mapped and examined in detail in
the Hatches Creek Wolfram Field near the eastern extremity of the Daven-
port Ranges of Central Australia. As a result the writer divided the forma-
tions Into two and possibly three proups which were named the ‘“Rottom,"
“Watches Creek" and “Top Series,” with some doubts of the validity of
separation of the last two. The “Bottom Series'’ has been correlated with
the Agicondi Series, The “Tlatches Creek’’ and "Top Series” are now con-
sidered to belong to one conformable sequence and are now named the
Hatches Creek Group. In the area where they were first examined, these
two divisions are lithologically dissimilar and separated by a major fauli.
Extension of the examination to other areas of the Davenport Ranyes has
shawn that they belong to one conmformalile sequence. The decision that the
beds previously designated the “Hatches Creek Series” and the “Top Series”
farm a small part only of the total conformable succession, as well as the
occurrence of other groups regarded as of similar age, necessitates the
restriction of “Hatches Creck’’ to a group, and the use of the wider geographi-
cal term “Dayenport Series” for the whole successiuti.
The basal members of the Hatches Creek Group consist of massive
qtiartzites with some coarser beds, lying unconformably on the schistase
formations. of the “Bottom Series.” At and near the unconfermable junction
116
they are sub-horizontal, but dips steepen markedly within a short distance
to the northward and exhibit steep felding and overfolding to the north
(Fig. 1). The repetitian by folding of the lowest formation, the quartzites,
unt their resistance to eresion, have produced the characteristic landscape
of the area which is dominated by sub-parallel ridges of quurtzites with less
resistant! rocks outcropping tn the valleys. As a result access parallel to
the strike ig easy, but difficult across tt. As one proceeds northwards across
the strike, the repetition of hard and soft formations continues until an
outerop of armphibolite 1s reached, This term ts used in a general sense to
include tacks originally of various basic types bul predominantly doleritic,
which have been altered to amphibolites. Once the amphibolites are reached
the aspect of the country changes suddenly and becomes one of “islands"
of sediments, sandstones and seméquartzites, outcropping as inliers in a
“sea"’ of arnphibolite. The seilimenis ate folded, but do not exhibit the same
intensity mor the same degree of metamorphism as do the arenacceus rocks
to the south which have been transformed to dense quartzites, many of them
glassy in appearance.
The sequence appears te consist of a thick arenaccous formation af
the base. originally mainly sandstones with some grits and conglomerate,
succeeded by shales, tuffs and lava flaws, some of which may be sills, and
containing thin beds of sandstone in their upper portions. The explanation
submitted is that, since both are folded, the inlers of the north portion
must have undergone this deformation befare the amphibolite bathohth was
inuiwiled, The partial conformity of the margins of the amphibolite, and
the somewhat less severe folding of the sediments now embedded in it,
suggests that the intrusion occurred during the folding and probably during
the later stages. The existence of this mass of basic material protected the
inliers of sediments from further diastrophic effects and fram the dynamic
metamarphism the results of which are evident in the southern half of the
field and elsewhere in the region,
(ligher mernbers of the Watches Creele Growp are exposed in a synclinal
structure separated from the formations just described, by a major fault,
The ares is in the north-western part of the Hateles Creel Wolfram Viele
and the formations were previously referred to as the “Top Series.” The
rocks <onsist of conglomerates, grits, sanilstanes, quartzite and shales, inter-
calated with quarlz-felspar porphyries, which may have been intrusive or
extrusive but probably the latter. The small outcrop of microsyenite mapped,
appears ta be intrusive into the sandstones.
The mineral deposits of Hatches Creel include walfram, the chici
mineral, some scheelilte, copper-wolfram ore, some bisrauth. a lille molybden
ite and gold. Probably due to stractural control the known deposits are
confitied to the Hatches Creek Group.
The wolfram deposits of the Wauchope Creel Field at the western end of
the Davenport Ranges are contained likewise in sediments of the Hatches
Creeic Group. This group torms the main outerops of the Davenpurt Ranges
as it does of the adjacent Murchison Ranges.
The granite mass known as the “Devils Marbles” near the Wauchope
Creek Wield 1s intrusive inta the Matches Creel Group and believed to have
been responsible for the introduction of the wolfram deposits, No granitic
intrusions were discovered in the vicinity of the IJlutches Creek Field, the
otly acid tocks observed being quartz-porphyries and microsyenite. (Quartz-
porpheries and amphibolite were observed in the vicinity of the Wauchope
Field, and granite outcrops, some of them extensive, oceyr in several localities
band adjacent to the Murchison Raves.
7
The extension of the Hatches Creek Group from the type area and
through the Davenport and Murchison Ranges raises the question of 3s
exisience elsewhere in the Northern Territory. In the absence of fossils and
definite geological horizons, the general lithology, low degree of meta-
merphism and relations to the rocks uf other periods, must be the chief
means of correlation. There are many isolated outcrops in Central Austraha
of predominantly arenaceous formations, quarlzites, sandstones, grits and
canglomeraies with some slaty members, which in the writer’s tpitiean,
occupy a stratigraphical position intermediate between the Lower Protero-
zoic, Agicendi Series and sediments of Jate Proterozoic-Cambrian age. Thev
have been correlated variously in the past by diferent obseryers, Included
are the rocks of the White Range, Winnecke Range, Jervois Ranges, Giles-
Reynoids Ranges. St. Johns Range, Osborne Range and others. It is
proposed to correlate some of these with the Hatches Creek Group of the
Davenport Series, others must remain indeterminate at present. An aren
of gently folded, lightly metamorphosed sediments along the Lower Victoria
and Fitzmaurice Rivers of North Australia will be referred tentatively to
the Hatches Creek Group.
The White Kuxge. The low elevation bearing this name is siliated
about sixty miles in an easterly direction from Alice Springs. Tt contains
a qumber of small gold deposits in the dense, hard, light-coloured quartzite
which forms the low range (Hossfeld, 1937j), Published opinions of the
age of the quartzite differ widely. Madigan (1932b, 1933) definitely correlated
the White Range and similar quactzites of the district with his Pertaknurra
Series, the age of which he considered to be Lower Hraterozaic.
The present writer was in charge of the party which surveyed in detail
net only the White Range bul much of the surrounding areas and carried
out personally aerial and ground reconnaissince aver a large part of the
Eastern Macdonnell Ranges. In the repert on the White Range Goldfield
(Ttossfeld, 19377), the opinion was expressed and reasons were given that
Madigan's correlation should be rejected. Voisey (t939b) agrees with this,
but appears to accept its inclusion in the Ambalindum Series (llodge-Smith.
1932) which, however, by inference he regards as of Archaeozoic age.
The only obvious reason for correlating the White Range Quartzite with
the quartzite of the Pertaknurra Series, is that both are quartzites, Litho-
fogically atl Structurally they are completely different. The former is
mineralized, whereas the latter, which outereps in the vicimty, ig nut. The
former, tow, is silicified to an extent not even approached by the latter,
Outerops of the former can be seen tv strike at sharp angles to ihe direction
maintained by the latter where the two formations meet, south-east of the
White Range. The mistaken correlation of the White Range Quartzite with
the Pertaknurra Quartzite has led ty serious misconceptions not only ain
the identification of other euartzites such as, for example, the Bald J1ill-
Winnecke Quartzites which ure regarded generally as the equivalents uf
the White Range Quartzite, but also with regard to the age of mineralization
of the region, and its stratigraphy and tectonic history. Jensen (1944), in
particular draws far reaching but unfortunately erroneous conclusions fram
this mistaken correlation. It is possible that the White Range Quartzite
can be correlated with the Agicondi Series, The present writer, however,
is of the opinion that its correlation with the Hatehes Creek Group (Daven-
port Series) is more reasanable. The known formations of the Agicondi
Series maintain their chracteristics over such a wide region from the Darwin
area to Central Australia, that it is logical to expect similar characteristics
from beds of that age, if they oceur, on the Arunta Block, No sediments
118
of which this can be said have been recognized on that block as yet, The
maliy similar features, however, of the White Range, Bald Hill-Winnecke
Quartzites ta the rocks of the Davenport and Murchison Ranges and of
seattered outcrops elsewhere, makes (heir correlation, even though it be
tentative at present, a reasonable deduction.
The previous references of the writer (Hossfeld, 1937), and 1940b), of
the quartzites to the Arunta Complex, were made at 2 time when all those
formations of the Arunta Block, older than the Pertaknurra Series, were
referred to the Arunta Complex without age differentiation.
The Jervois Ranges which consist of quartzites, slates and sandstones, are
a synelinal outlier of moderately metamorphosed sediments, lie tncontorm-
ably om Archaeozoic rocks, and according to Madigan (1933) were invaded
by granite. The Jervois Range Mineral Field (Hossfeld, 1931), lies just te
the east of the Jervois Ranges, owing its exposure ta the removal of the
averlying, unconformable formations. The Jervois Ranges were regarded as
Pertaknurra by Madigan (1933), as was the Mopunja (Mopunga) Range
tlearby,
The Pertaknurra Quuartzite (Pl. 1, 1), wherever it has been identified
with certainty, either by following it along the strike or by the fussilifercus
beds above it, preserves its special characteristics with remarkable persist-
evice, Tt is only the isolated outcrops of arenaceous sediments and their
argillaceaus associates outcropping on various parts of the Arunta Block,
which differ so markedly both litholegically and stricturally from the typical
Pertalnurra beds. It is difficult ta understand why these remnants shyuld
ever have been correlated with the Pertaknurra. It ts true that they contain
predominantly arenaceous sediments and lie uncanformably on the Archaeo-
zoi¢ rocks, but there the resemblance ends. Some of them may be correlated
eventually with the Agieondi Series of Central and North Australia. One
such group is the “Amunurunga Series” of Tindale (1933), However, any
definite classtfication of the various outliers is impracticable at present. They
are wlilee than the Pertalenurra and younger than the Archaeozoic formations.
‘The present writer classifies them tentatively as equivalents of the Latches
Creek Group because of their similar lithology, slight mineralization absent
in tnany localities, small numbers of igneous intrusious, moderate diastra-
phism and relatively Jow degree of metamorphism.
In the extreme north-west of the Territory, in the coastal region of the
Victoria and Fitemaurice Rivers, a group of rocks outcrops which appears ta
le older than the Buldivan Series (Cambrian) and is, therefore, regarded
as of Precambrian age, Tt exhibits many similarities to the Hatches Creck
Grou), consisting predaminantly of quartzites and sandstones with inter-
hedded slates and shales. These exhibit litthe metamorphism, and although
cross folding is evident, their structures are predominantly gentle and low
dips are general, a5 compared with the highly folded and strangly meta-
murphosed sediments to the cast and north of Collia, Buldiva and beyond,
which are regarded as members of the Agicondi Series, These Victoria River-
Fitzmaurice beds strike south-westerly towards the Ord River area in which
Mattheson and Teichert (1945) mapped Precambnan formations of similar
types. It is suggested that these beds and a number of scattered inliers with
northsyesterly trends in the Victoria River Downs district, are members
of the Davenport Series atid probably of the Hatches Creek Group. and that
they are the equivalents, in part at least, of the Nullagine Series of Western
Australia. Further reference lo this suggested correlation will be made later,
(b) Tie Carrentasra Grove
Between the dissected margios of the Barkly Tableland {spelt Barkley
119
and Barclay by some authors) and the coast of the Gulf of Carpentaria, a
group of rocks outerops which has been regarded hitherto as probably of
Cambrian age. They were observed and reported by Brown (19082), who
regarded them tentatively as Cambrian. Woolnough (Cwlth. Aust. 1912c)
considered them to be Cambrian, Jensen (Cwlth. Aust. 1914a) regarded them
as Cambrian, but as the result of subsequent work as Senior Geologist of
the Queensland party of the N.A.S., appears to feel less certain of their age
and has referred them tentatively to the Cambrian Period (Jensen, 1940),
Practically all the observations made of this group have been due to and
in the vicinity of mineral deposits, and are therefore somewhat disconnected.
No attempt appears to have been made to carry out a systematic examination
of the group in order to determine its position in the gevlogical record, its
overall structures and constituent members. The work done by Jensen and
his assistant peologists in the N.A.5., supplies the most detailed knowledge
of the group, According to Jensen (1940, the topmost formation is a white
quartzite forming caps cf mesas and tablelands, This appears to be the domin-
ant outcrop in the area between Borrvloola and Wollogorang and is con-
sidered by the present wriler provisionally as Upper Proterozoic,
Below this quartzite there follows a succession consisting chiefly of
4juartzites and volcanics.
These are underlain to the south-east of Redbank by flagey quartzites
and tassive white quartzites,
In the Barney's Creek area, where Brown (1908a) first examined this
group, he found it to consist mainly of quartzite and quartzose sandstene
and a dense blue limestone. All these racks exhibit alteration by silicification,
and contain chert, finty and jasperoid masses. Only a small areca of the total
outcrops of the group has been examined,
Folding and faulting vary considerably, ranging from dips of 45°-65°
in the McArthur River area (Jensen in Cwlth. of Aust, 1912c) and severe
faulting in that sector, to areas where the beds are honzontal or dip at very
low angles and no faulting was observed. A considerable amount of cross-
folding is evident in the more disturbed areas, but directional trends are
very vanable, Ground and aerial reconnaissance as well as examination of
the resulting photographs by the present writer, show very clearly the severe
folding and faulting in the McArthur River area with a gradual decrease to
the Jess disturbed adjacent sectors.
As no formal name appears to have been applied to this sequerice, these
Pre-Buldivan rocks are being named the Carpentaria Group.
The Barkly Tableland formations, which as will be shown later, are
included by the writer in his Buldivan Series, are folded into minor undula-
tions only, As a result, one travels over a monotonous almost level landscape,
eastwards from the Overland Telegraph \.ine in Central Australia, until
one reaches the vicinity of Vop Spring, situated between Anthony's Lagoon
and McArthur River Station. Here a relatively sharp descent down the
dissected margin of the Barkly Tableland brings une below the basal beds
of the Buldivan Series. -
The rocks below that basal formation consist of a group of partly
silicified limestones, quartzites and sandstones referred to earlier, and include
also some argillaceous members. Here and elsewhere along the eastern
margins of the Barkly Tableland, the sudden transition from the gently
dipping Cambrian formations to highly folded and faulted formations is
very striking. Further, fram a region in which metalliferous deposits are
unknown, cne arrives in an area where deposits of copper and silyer-lead
have been mined, Even though must of the deposits were of little economic
120
importance their presence indicates the difference in the history of the Barkly
Yableland formations (The Buldivan Series) and Lhe Carpentaria Gravy ty
which the folded mineralized rocks belong,
It is quite clear that the Buldivam Series are the cover rocks upon the
removal of which the folded, metamorphosed, mineralized members of the
Carpentaria Group were exposed.
The writer considers, therefore, that the Carpentaria Group is of Pre-
cambrian age. It is being included in the Davenport Series, but regarded as
possibly higher in the sequence than the Hatches Creek Group. It is being
correlated with the Luwn Hill and Mt, Isa Series of North-Western Queens-
fand, and assigned to the Middle Proterozoic,
Tur Newer GRANITES AND METALLOGENESIS
The predominantly non-stressed acid igneous rocks which outcrop in
numerous localities in the Archaeozoic, Lower and Midule Proterozoic rocks,
have been growped as the Newer Granites. They consist chiefly of granilés
arul related types, but include also syenites, diorites, etc.. greisen, pegmatities,
aplites and porphyries, They have been recorded from many areas in the
Darwin-Oenpelli-Maranboy triangle, from the eastern and western borders
of Arnhem Land, from Tennant Creek, The Granites (Pl. IIIb), the Daven-
port and Murchison Ranges and from many areas on the Arunta and Mus-
grave Blocks. The “Newer Granites,” although exhibiting some evidence
of stress, possess oriented textures in certain localitics only, and in most
instances these are marginal or confined to restricted areas, All of them are
intrusive into the highly metamorphosed Aruntan and Riddock Series and
therefore by present definition, are Post-Archaeozaic. None have been proved
to invade sediments of undoubted Cambrian age (Madigan. 1933, per contra
vide). They are regarded therefore as of Proterozoic age. The two Protero-
zoic series invaded were the Agicondi and the Davenport Series. These
igneaus intrusions may belong to several epochs or may ‘be co-epochal or
nearly So. The latter view is being put forward by the writer,
Attempts have been made to divide the granitic outcrops of the Brock’s
Creek Disrict into synchronous and subsequent bathyliths (Sullivan, 1948)
and inte granitized and mobile material (Noakes, 1949). Too little detailed
nmuipping and petrological work has been done to establish such distinctions,
It was recognized by the present writer, as the publications of the
A.G.G.5.N.A. listed in the Bibliography show, that a number of granite
outcrops conform reasonably elosely, although never perfectly, to the strikes
of the invaded sediments. However, all stages can be observed in the region.
from the closely conformable outcrops of the Brock’s Creek intrusion, to
the transgressive margins of the adjacent Gulden Dyke outcrops. The writer
considers that too much importance has been assigned by some observers to
such differences in this. region, and the deductions made from the occurrence
of relatively concordant and of discordant granite outcrops, which as obser-
vations show, represent the extremes merely of the types of boundaries of
the intrusions. Similar comments apply to the question of the origin of. any
une of these granite masses by granitization or the invasion of a mobile
magma. It is possible that such will be determined by future investigations,
but the task will be difficult as all gradations appear to exist, and the features
supposedly characteristic of the two types are exhibited by adjacent granite
areas, and in some instances by the one mass.
The granite masses haye produced variable metamorphic effects in the
bnvaded rocks, As the writer has studied these effects in more detail in the
Darwin-Oenpelli-Maranboy triangle than elsewhere, the following observa-
121
tions on the metamorphism due to the granitic invasions will deal chiefly
with that region. .
Metamorphism resulting in the development of andalusite (chiastolite)
schists is a feature obseryed in numerous areas, The andalusite-graphite
schists of the Golden Dyke area (Hossleld, 1936a), are goad examples of
this type. Here as elsewhere 1t appears that certain beds or parts of beds
were more favourable to the development of andalusite and one finds the
crystals developed in larger or smaller numbers or even completely absent
from certain parts of the graphite schists, the boundaries between zones
of varying numbers being formed by the bedding planes. In the Golden
Dyke area and elsewhere in this region, this type of metamorphism does not
appear to have any relation to the visible and determinable vicinity of the
acid igneous rocks (chiefly the Pine Creek Granite) but to be controlled,
as stated above, by the nature of the sediments, and related directly 'to the
structtires, It is Suggested therefore that the dolerite sills (now altered to
amphibolites) which were folded with the sediments and are in close proxim-
ity above and below the andalusite schists, were responsible for the thermal]
metamorphism. In the areas examined by the writer, Lhe dominant metamor-
phic effect of the granitic intrusions has been the formation of aureales af
hornfels surrounding the igneous outcrops. The Pine Creek Granite (Hoss-
GRANITE AMPHIBOLITE
y CRETACEOUS
= SS — ++
AGICON DS SERIES SULDIVAN SERIES COLLIA SERIES AEGELAMAN GROYP SOLDIERS EREER
4-22 ° 4 6 s {0 MILES
LOWER CAMBAIAN DEVONIAN LOWE
PAGTEROZOIC
! es
Fig, 3 -
Section across the Buldiva Area (Adapted from A.G.G.S.N.A. Report N, Terr. No. 18)
feld, 1937 and A.G.G.S.N.A., 1936), (Cullen Granite of Noakes, 1949), which
includes practically all the granitic rocks of the Darwin-Oenpelli-Maranhboy
triangle, possesses partial or complete hornfels aureoles at many of tts aut-
crops. Such were observed also adjacent to the Mt, Litchfield Granite, the
Soldiers Creek Granite, near The Granites Goldfield in Central Australia,
and numerous other areas. The probable effect of the formation of hornfels
on the existence of, and extensions from, known mineral deposits made it
necessary to investigate the hornfcls aureole in detail in several localities.
(Ilossfeld, 1936b, ct. al.). [t was noted that even where the development of
hornfels was a characteristic of some granite mass, such development
depended to a Jarge extent on the type of sediment adjacent to the granite
and therefore, hornfels was not developed everywhere along the contact
zone, It may well be that the absence of bornfels from the margins of some
granite masses in North and Central Australia or even its rarity may be due
not so much to differences in composition, temperature. emplacement, or
genesis of the granite, as to differences in the invaded rocks, and hence the
far-reaching conclusions arrived at by some observers may be based on false
premises, (Sullivan, 1948).
At the Enterprise and associated mines near Pine Creek, (Hossfeld,
1936b) it was possible to study the occurrence of the hornfels and its relation
122
tu the granite, both by surface and sub-surface examination. The Pine Creek
Grauite outcrops near the line of mining leases which lie in the hornfels
zone, It was noted that the harnfels is continuous for some distance from
the granite margin, but as distances increase, a transition zone exists in
which belts of hornfels alternate with belts of rock which macroscopically
at least appear to be unaltered sediments. Both the width and number of
unaltered belts increase, though irregularly, as distance from the granite
contact increase. until the wholly unaltered sediments are reached. The
Enterprise and adjacent mines were situated favourably for a study of the
hornfels zone since the sediments which are almost all tuffaceous grits and
sandstones of the Pine Creek Group, are in this locality tightly folded and
faulted, with predominantly vertical or sub-vertical dips. It is obvious from
the foregoing that, as distance from the granite contact increases, only the
heds most favourable to the formation of harnfels were affected, and with
the increasing distance such effects became more and more difficult to pro-
duce until the limit of such granitic influence was reached (Hossfeld, 1936b}.
The chief controls probably were variations in composition and texture
of the rocks adjacent to the granite margins. The tuffaceous greywackes,
plentiful in some parts of the Agicondi sequence, appear to haye been
particularly favourable to such metamorphisnt. It is not surprising therefore
to find that both the Pine Creek and the Mt. Litchfield Granites and others
possess hornfels aureoles in some localities but lack this feature in others.
In every instance examined, the hornfels was formed alter the granite
emplacement and after the folding of the invaded sediments had heen com-
pleted. An examination of the geological map and a study of the literature
shows that bathyliths of granitic rocks are plentiful in the Agicondi Series
and scarce in the Davenport Series. Mineralization toa is much more
developed in the former. [t could be argued, therefore, that there were two
epochs of igneous activity, which introduced similar acid racks and the same
minerals, the Davenport igneous epoch being merely a minor and final phase
of the main igneous activity of the Agicondi Epoch.
The evidence supplied by many of the granitic outcrops in the Agicondi
Series suggests that the present surfaces are not far below their former crests
or summits. This would indicate that the majority of the cupolas were
emplaced at levels too low to reach the overlying Davenport Series if it ever
existed in those places. There is, however, no evidence available which would
decide whether the Davenport Series existed over a large part of the Arnhem
Block which contains the greater number and larger exposures of granitic
rocks. lt is true that the deposition of the Agicondi Scries was followed
by an orogenic epoch of great severity with penecontemporaneous basic sills
and dykes, and resulting metamorphism. That the granitic intrusions were
synchronous is not accepted, It is known that there are many approximate
concordances in the strikes of the sediments and the invaded granite, but
transverse contacts are plentiful. In a number of instances concordant and
transverse contacts occur im the same intrusion. The strongest evidence
against synchronous intrusions is to be found in a study of the hornfels
iureoles.
It was demonstrated in several areas where outcrops are adequate, that
the metamorphosed sediments can be traced inta the hornfels aureoles
adjacent to granite intrusions, and that the formation of the hornfels and
therefore the emplacement of the granite occurred after the orogeny and
dynamic metamorphism had ceased, For example, chiastolite slates and
achists were traced into the hernfels zone in several localities along the
stcikes of the beds. In the hornfels zone the beds were traced by the
123
recognition of chiastolite crystals delineated on weathered surfaces of the
hornfels, Evidence that mineralization was effected after folding and meta-
morphism had been completed, will be given below.
All of the above features suggest as a possibility that a long time inter-
val scparates the orogeny and regional metamorphism of the Agicondi
Series from the succeeding igneous epoch, The similarity of rock types and
minerals introduced suggests a common ofigin. There seems to be no valid
reason for suggesting the occutrence of a major igneous epoch during the
period of quiescence after the Agicondi orogeny. It is held, therefore, that
the succeeding diastrophic epoch, during which the Davenport Series was
folded, saw the commencement of this major igneous epoch, which was also
the principal metallogenetic epoch of the Northern Territory, Its age is
considered to be Post-Davenport and Late Middle Proterszoic. It is being
correlated with the Cloncurry Epoch (Jones, 1947) which has been referred
to a Late Precambrian age.
These “Middle Proterozoic” granitic intrusions were responsible for the
intraduction of almost all of the known metalliferous and other commercial
mineral deposits of the Northern Territory. The metals introduced include
gold, silver-lead, copper, tungsten, tin, tantalum, a little modybdenum and
bismuth, as well as arsenic, lithium, zirconium and the radio-active metals
thonum, uranium, etc, Muscovite, biotite, beryl and apatite occur in some
localities, introduced largely by the Oolgarna acid pegmatites which probably
were co-epochal with the “Newer Granites,” or nearly so. The tin-bearing
greisen dykes and greisenized pranites of North and Central Australia are
probably of the same age. Many of the above minerals occur within the
Arunta Block, but the great majority are of Post-Archacozoic age and are
correlated with similar deposits in the Proterozeic rocks of other parts of
the Territory.
Jasper-haematite reefs occur at two such widely separated localities as
Tanami near the Western Australian border and Yeuralba near the western
margin of the Arnhem Land Native Reserve. In both localities these reefs
appear to be connected with the mineralization of the locality, and probably
represent alteration products, aboye water level, of pyritic lodes.
Various statements have been made and conclusions drawn from the
proximity in the Brock’s Creek District of granite intrusions, graphite schists
and amphibolites to deposits of gold and copper. In discussing gold-
arsenopyrite-pyrite replacement deposits of that district, Sullivan (1948,
p. 491) writes: “The deposits, however, are associated with graphitic schists,
haematite-rich rocks and amphibolites, and it seems a valid inference that they
lie in the metasomatic aureole of granite cupolas occurring at depth.”
As the detailed examinations of the N.A. Survey demonstrated (Hoss-
feld, 1936a), and subsequent microscopic determinations confirmed, the
amphibolite sills of the district are altered dolerite sills which were intruded
before or at an early stage of the folding of the sediments. These amphibolites
are similar io and apparently contemporaneous with the dykes and bosses,
a few of which have been mapped. The Golden Dyke Area was studied in
detail, and as it is regarded as a type area, the following remarks will be
concerned chiefly with that locality. Metamorphism which produced the
andalusite (chiastolite)-graphite schists preceded the emplacemeiit of the
granite and may owe its formation to the intrusions of basic sills. The grantte
cut across the folded sediments and truncated alike the sediments and am-
phibolite sills, and the hornfels aureole obviously is transgressive also, The
variously metamorphosed sediments and basic rocks can be traced into the
harnfels zone and specimens were collected which show the outlines of formee
124
andalnsite crystals on weathered surfaces of the hornfels. Further, the
mineralization produced by the granite at the Golden Dyke was in the form
af auriferots pyrite. Microscopic examination of the andalusite schist near
the mineral lodes, but beyond the horntcis aurcole shows that pyrite was
deposited in cracks in shattered andalusite crystals, Pyrite was observed alse
in minute quartz veins in the amphibolite, lt is obvious therefore, that neither
the graphite schists nor the amphibolites can have had any genetic connection
with the formation of the gold deposils, nor belong to the metasomattc
aureole of the cranite, It is not surprising, however, to find that positive tests
for gold have been recorded from an amphibolite in the vicinity.
Tn this area, ore depositions due to the granite intrusions affected favour-
able sediments latgely by replacement. The porous sediments affected,
consisted of grits and similar types. The known lenticularity of some of these
beds, a not unusual feature in beds of shallow water facies, accounts for the
Jenticularly of many of the “lodes” and their occurrence in recognizable zanes.
It is not surprising ta find such mineralized zones continuing along the flanks
of an anticline or around a dome shaped fold. because of the continuation
of the Favourable horizons. To postulate on that evidence the existence below,
of a conformable granite cupola, appears to the present writer, unwartranteil
The statement that copper is associated with the occurrence of amphibo-
lite, appears to be just as questionable but as the present writer has hot
investigated the matter adequately, it is sufficicnt here to register a doubl
of the validity of Sullivan’s conclusions.
Upper PRorerozoic
The Amadeus Geosyncline contains an apparently unbroken succession
which includes fossiliferous beds of Cambrian and of Ordovician ages. On
the evidence available (Mawson and Madigan, 1930; Madigan, 1932a) it
appears reasonable to assign the oldest series, the Pertaknurra, and the
succeeding series, the Pertatataka, to the Upper Proterozoic. Aggregates of
oxidized copper minerals oceur in the vicinity of some major faults in the
western part of the area. These are regarded as probably due to direct or
indirect accummulalion of copper from the sediments af the geosycline, and
not as an epoch of mineralization, Nowhere in this region have igneous
activity or metallogenesis been recorded in these beds. Such activity was
postulated (Madigan, 1933, 1937) for outliers on the Arunta Block, and on
the Musgrave Block (Ellis, 1936). Except for the debatable copper minerals
referred to above no such activity has been recognized in any strata which
have been proved definitely to be of Pertaknurra or later age. Tt is only in the
outliers, the ages of which cannot be determined stratigraphically but which
were correlated by various observers with the Pertalknurra Series, that igneous
activity and resulting mineralization have occurred, As stated earlier, the
present writer considers that unless or until it is demonstrated that such
activities did affect the Amadeus Geosyncline deposits, all rocks showing
definite igneous activity or metallogenesis in that region, mist be regarded
as older and therefore, Middle Proterozoic or earlier.
The localities in which quartzites outcrop in the Northern Territory are
large and numerous. In the past, too little account has been taken of the
possibility of quartzites occurring in several unconformable series. The
labelling of quartzites of various ages as equivalents in time, and also the
separation of contemporaneous beds, have resulted in erroneous conceptions
of the stratigraphy, In many areas it has been possible by examination of
lithology and structure of the quartzites and associated beds to arrive at
definite conclusions. In some areas tentative conclusions only could be
reached,
125
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126
Acts AND CORRELATION oF THE Lower To Mippce PRECAMBRIAN Rocks
In the absence of fossil evidence, the division of these rocks is based
pn Jithology, structures, types and intensity mf metamorphism, relaliuns to
later fossiliferous formations, to igneous activity and mineralization,
The formations of the Arunta Complex, with their intense and varied
metamorphism, wide-spread and repeated igneous and diastrophic epochs,
differ so markedly from other Precambrian formations of the Northern
Territory, that they must be separated from them by a very long time
interval. The differences between subsequent formations, while considered
sufficient for their separation from each other in most instances, are pro-
gressive and do not present the sharp and sudden contrasts that exist between
the Arunta Complex and oldest known subsequent formations.
Published opinions in Australia have referred the oldest Post-Arunta Complex
formations variously to the Upper Archaeozoic and Lower Proterozoic. For
the reasons given above, the Arunta Complex (the Aruntan and Riddovck
Series) ‘are being referred herein to the Archaeuzoic, and all recorded sub-
sequent Precambrian formations to the Proterozoic Era, In North and Cen-
tral Australia the existence of predominantly concordant granite gneisses
on a regional scale, is considered as evidence of Archaeozoic age. Whether
the Riddock Series which is being referred tentatively to the Upper Archaeo-
zoic, contains such concordant granite gneisses is not certain. It 1s maintained
however, that although absence of such granitic gneisses does mot imply
necessarily that the rocks are of Post-Archaeozoic age, their presence on a
tegional scale does imply that the containing rocks belong to the Archaeozoic
Fra, Correlation with the adjacent States of Western Australia and Queens-
land is based on the metamorphism, the presence of the ahave concordant
granite gneisses, and on the recorded existence higher in the sequence, af
other, uncomformable Precambrian formations,
The Lower Archaeozoic of Central Australia ts being correlated there-
fore, with the Warrawoona Series of Western Australia and the Kalkadoon-
Argylla Series of North-Western Queensland.
The oldest Past-Ariinta Complex formations recorded in the Northern
Territory are those which have been grouped in this paper as the Agicondi
Series. Tt will be difficult ta identify any formations intermediate in age
hetween the Arunta Complex and the Agicondi Series, Further, if such
existed, they may have been removed completely during the enormous time
interval, or their remnants covered by more recent deposits. For reasons
stated earlier, the Agicondi Series is regarded as Proterozoic rather than
Archaeozoic age, It is characterized’ hy a large proportion of sediments of
volcanic urigin and in parts of the sequence by a marked greywacke facies,
Its metamorphism varies considerably but is severe in restricted areas only.
Regionally considered, however, this metamorphism is much more developed
than that of the inconformable Precambrian deposits which overlie it. The
latter exhibit little metamorphism in most instances. Similarly, deformation
of the Agicondi Series was generally of a severe character, whereas the
succeeding deposits exhibit on the whole, gentler structures,
The occurrence, untunformably above the Agicondi Series, of other
Precambrian deposics, indicate that the series should be referred to the
Lower Proterozoic. Mattheson and Teichert (1945) and Noakes (1949)
appear to share this view, The succession in North Australia, now named
the Agicondi Series, was correlated with the Mosquita Creek Series uf
Western Australia (David, 1932, Hossfeld, 1935, etc,), and thiy appears to
be the opinion of tore recent authors. However, in view of the uncertainty
expressed by Matthesom and Teichert (1945) of the possible divisian of
127
rocks mapped as Mosquito Creek Series in the East Kimberley Region of
Western Australia and on the border of North Australia, and in view alsa,
of the doubts of the present author of the correctness of determination of
some of the formations in that region, it is proposed to correlate the Agicondi
Series in part unly with the Mosquito Creek Series as mapped in the East
Kimberley Region.
Lying unconformably on the Agicondi Series, a sequence of sedimentary
rocks of Precambrian age, which have been natned the Davenport Series,
outcrop over large areas of Central and North Australia, The lawer members
have been described as the Hatches Creek Group with which the Victoria
River quartzites and associated beds are included tentatively, The Carpen-
taria Group may be equivalent in time, bul is being regarded as possibly
higher in the sequence.
Both the Agicondi and Davenport Series contain large proportions of
sediments of tuffaceous origin, both have been intruded by basic and acid
igneous rocks, both series have been folded and metamorphosed and contain
economic mineral deposits. A general review. however, shows that all of
these activities, and apparently also the contemporaneous volcanism, were
very much less severe in the Davenport Series. In the latter, greywackes are
notably scarce, metamorphism slight in most areas, and practically non-
existent in others. Folding was severe in some Incalities, but has not affected
large areas in which the sediments are horizontal or inclined at low angles.
Known igneous intrusions are relatively few in number, but this may have
been more apparent than real. Mineralization is well developed in a few
areas only. In many localities it is restricted to guartz veins and even these
are absent from many areas. The inference is reasonable that the Davenport
Series was deposited on the folded, metamorphosed, and eroded Agicondi
Series during the succeeding period of sedimentation, It is placed therefore,
tn the Middle Proterozoic.
As stated earlier, in the Eastern MacDonnell! Ranges, quartzites anu
associated beds correlated with the Davenport Series outcrop adjacent to
the lowest sediments of the Amadeus Geosyncline. The latter are regarded
as of Upper Proterozoic age and thus strengthen the reference to the Middle
Proterozoic of the older sediments.
CORRELATION WITH QUEENSLAND AND WESTERN AUSTRALIA
The continuation of the Carpentaria Group into Queensland, and the
similarity both lithologically and structurally of this group to the Lawn
Hill Series indicate their correlation. Both are Precambrian in age. A further
correlation, suggested by several authors, of the Lawn Hill and the Mount
Isa Series is accepted by the present writer. Both of these are placed tenta-
tively, therefore, in the Middle Proterozoic.
In Western Australia the Nullagine Series which, in the type area, lies
uncomformably on the Mosquito Creek Series, has been regarded generally
as of Upper Proterozoic age. In its lithology, structure, slight degree or
absence of metamorphism, scarcity or absence of acid igneous intrusions or
mineralization, it bears a strong resemblance to the Davenport Series and
its correlation is suggested here. Absence of folding, metamorphism and
mineralization over large areas is characteristic. but this applies also to some
areas of the Northern Territory.
It is interesting to note the existence at Braeside in the Pilbara District
of silver-lead deposits in rocks which are regarded as members of the Nulla-
gine Series (Finucane, 1938a), and considered to be of Upper Proterozoic
age, The rocks of that area consist of basic lava flows “overlain conformably
128
by a considerable thickness of sedimentary rocks comprising shales, sand-
stones, grits and fine conglomerates,”
It is considered probable that in some areas such as East Kimberley
remote from the type area, the distinctions between the Mosquito Creek
and Nullagine Series have not always been recognized and some areas which
have been mapped as the former, may prove to belong to the Nullagine
Series. Such a possbiility appears to be considered by Mattheson and Teich-
ert (1945, pp. 31 and 32). The present writer believes that much, if not all.
wf the Nullagine Series of Western Australia may be equivalent tm the
Davenport Series, and that some of the areas mapped as_ Mosquito Creek
Series in East Kimberley, may be of the above later age. Should the above
correlation be confirmed, the Nullagine Series would be of Middle Protero-
zoe Age,
STRUCTURES AND TREND Lines or tire LowEr To MIDDLE PRECAMBRIAN Rocks
Tue ARUNTA COMPLEX
Strikes of metasediments, foliation planes and gpneissic structures
exhibit extreme variations of direction even within short distances in many
localities. There is a general tendency, however, as noted by previous
workers, for a cecurrence of westerly strikes which include increasing
amounts of a northerly component as these rocks are traced westwards, The
marked change in strike from a westerly to a nearly meridional direction. in
the Jervois Range area (Hossfeld, 1931), may indicate as suggested by Hills
(1946), a permanent change to that direction which may continue tu the
Cloncurry region, On the other hand, the area examined is too small to
decide whether this is merely one of the numerous erratic changes of strike
recorded in so many parts of the Arunta Block. This block is separated from
other areas of Archaeozoic rocks by such wide expanses, that nothing can
be added to the picture drawn by Hills (op. cit.).
Tar Aciconpr SERIES
Tn the past all Precambrian trends of Post-Archaeozoic age, were com-
bined in attempts to reconstruct the trend lines of the Proterozoic rocles ai
the Territory. The evidence submitted herewith for the occurrence of at
least two orogenic epochs during that era, has resulted in markedly different
interpretation and reconstruction. The large amount of cross-folding in the
Agicondi and Davenport Series has made it necessary to reject the greate.
part of the recorded strikes, and only those which represent the average
trends of the folded structures have been used in such localities. There are
a few areas in which information is insufficient to decide whether the obser-
vations made represent the general direction.
Unfortunately the known outcrops of the Agicondi Series are separated
by very large areas in which they are obscured by later deposits. Extrapola-
(ious were made by examining the formations of other ages but the total
information available is so scattered, that any interpretations must he re-
garded as tentative only. If the reconstruction approaches the true picture,
it would appear that the Agicondi Series was deposited not in a geosyncline,
but rather in a large mobile area, probably subsiding irregularly, and later
folded as a region, and forming a large stable area, the Arnhem Block or
Craton (Fig. 4),
Tue Davenport Series
The reconstructed trends suggest the existence in the Territory of at
least two geosynclines, the Kimberley and Carpentaria Basins. Litercom-
129
munication probably existed and their former extent may have been much
greater than depicted. There is a strong suggestion, however, that a relatively
large craton named the Arnhem Block, a result of the Agicondi orogeny,
existed as a landmass during the Davenport sedimentation. (Fig. 5).
Mean Observed Trends
Suggested Trend Lines _-___
tele) BOG MILES
S352
Fig. 4
Observed and inferred trends of the Agicondi Series (Lower
Proterozoic) of the Northern Territory.
130
In dealing with the tectonics of Australia, Hills (1946) was handicapped
by the paucity of reliable information available from the Northern Territory.
In view of this the following remarks should not be regarded as criticism
of his work, for such is not intended. Because of the references that have
been and will be made by other workers to the paper by Hills (ap. cit.),
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Observed and inferred trends of the Davenport Series (Middle
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131
it is essential to refer to differences of opinion held by the present writer as
a result of additional evidence collected by himself.
No evidence was obtained which would indicate the existence of a
¥ pattern in the Pine Creek-Darwin area. Although there are very numerous
divergences due to deme and basin folding, the general trends range frotn
west-northwest to north-northwest as far ta the south-east as Maranboy and
the Yeuralba District in the western part of Arnhem Land, but exhibit a
ponerse change ta the north and north-north-east towards and beyond
enpelli,
The generally concordant structure lines around the Brock’s Creek
granite intrusion are due to a dome-shaped fold, of which there are a number,
the Golden Dyke (Hossfeld, 1936a). being a good example. It can be stated
definitely that the Brock’s Creek intrusion does not mark the location of a
permanent change in strike of the sediments.
It was demonstrated in the preceding section that the present writer
disagrees with Jensen in the latter's reference of the McArthur River lime-
stones and the Redbank deposits (Jensen, 1940) to the Cambrian and Post-
Nullagine mineralization respectively as quoted by Hills (op. cit.), Madigan’s
reference (1937) to post-Cambrian unstressed granites also is contrary to
the observations ta date of the present writer and consequently so are the
conclusions derived from that correlation by Hills (op. cit.}.
The present writer's observations and all other available evidence indi-
cates that the Agicondi Series continues throughout the western part of
the Arnheim Land region and that the Davenport Series constitutes the
eastern sector. The Buldivan Series, capped by residues of the Lower
Cretaceous Mullaman Group, forms a relatively thin cover, but of sufficient
thickness to give the Arnhem Land Plateau its comparatively high elevation.
This interpretation supports the previously supposed existence of festoons of
ancient rocks which Wade (1924) found difficult to explain.
D. LATE PROTEROZOIC AND CAMBRIAN
Deposits previously referred to this age-grouping are widespread in
the Northern Territory. Differences of opinion have been expressed regard-
ing the ages of the oldest deposits of the sequence, but there is general agree-
ment that the formations occur in two distinct geographical divisions. One,
outcrops to the north of the Arunta Block, the other occurs in the Amadeus
Geosyncline to the south of the above block,
THE BULDIVAN SERIES
Although the deposits of this series had been recorded previously by'
several observers, they had received no formal name until 1946 when they
were named the Buldiva Series by the N.A. Survey (Hossfeld, 1937g). The
term was derived from the Buldiva Area, the first locality where they were
mapped and examined by the above organization. The name is being changed
herein to Buldivan, as suggested by the Australian Code of Stratigraphic
Nomenclature (Raggatt, 1950).
Attention was directed to the deposits of this series during the economic.
survey of the Buldiva Area, because they and younger rocks were found
to act as blankets, obscuring in many areas the mineral-bearing Proterozoic
formations.
The deposits to which the term Buldivan Series was applied, rest with
4 violent unconformity on the métamorphosed, highly folded sediments of
the Agicondi Series and on the intrusive granites and basic igngous rocks.
(Fig. 3.) In most instances where the contacts were examined in the type
132
area, they were found to be faulted against the older rocks. However, good
contacts showing the unconformable junction, were observed subsequently
outside the type locality. The existence of the unconformity was confirmed
by the regional mapping and the consistent differences in lithology, structure
and degree of metamorphism between the Buldivan Series and the underlying
SY a
190 200 309 MILES
Es a |
__p-—n__ Approximate N's S™ Limits of Ordovican Transgression N'™
of Avunta Block
Fig. 4
Approximate limits of Cambrian, Ordovician and Lower Cretaceous
Submergences of the Northern Territory.
143
rocks. In general, the members of the Buldivan Series exhibit gentle dips and
minor folding only, except near fault contacts where dips of up to 30° and
several local crumplings were abserved. The region occupied by this series
is divided partly hy a narrow, elevated area of older rocks, many of them
quartzites, which belong to the Davenport Series, This feature extends from
the vicinity of Newcastle Waters in a southerly direction to a short distance
north of Tennant Creek. The resulting geographical divisions of the Buldivan
Series are being named the Buldiva-Wiso and the Barkly Basins, (Fig. 6),
and the dividing area the Asburton Peninsula. The Buldiva-Wiso Basin
extends from the Douglas River in a southerly direction probably as far as
the sector west of Tennant Creek. The Barkly Basin extends in a south-
easterly direction into Queensland,
The occurrence of inliers of older rocks in the Victoria River region
suggests the existence of other smaller basins such as were mapped in the
Western Austrlian border areas, (Mattheson and ‘Teichert, 1945),
As the map will show, the boundaries, many of them necessarily inferred.
are irregular and there are some outlying areas. Some of these irregularities
are believed to be due to differential uplift by folding or faulting, and the
subsequent removal of the less resistant deposits.
The vast continuous region over which these sediments exist, the out-
liers as well as sttuctural considerations, suggest the former continuation
of these sediments over almost the whole of the Northern Territory, north
of the Arunta Block (Fig. 6).
(a) Tue Burpiva QuartziTR
In the northern sector of the Buldiva Basin, the Buldiva Quartzite is
the basal formation of the series, (Hossfeld, 1937g), (Voisey, 1939a),
(Noakes, 194%), It consists predominantly of massive arenaceous sediments
which have been altered in most localities to a dense, hard quartzite, but
consists chiefly of quartzose sandstones in others. The sequence includes
some grits, thin conglomerate bands and some shale. The original report of
the type area of Buldiva (Hossfeld, 1937p) states: “The quartzites exhibit
well developed ripple marks, worm-iracks, rain prints, sun cracks and bands
of weathered inclusions which may have been either fossils or mud galls.
These features are evidence of the shallow water deposition of the quartzite,
These features are not restricted to any one sectian of the sequence, but
have been found through a thickness of several hundred fect of quartzite,
and over a length of forty miles northwards from Buldiva,"
The Buldiva Quartzile Formation is strongly jointed and the dominant
trends are north-westerly and north-easterly. Actual averages of numbers
of joint directions measured gave bearings of 320° and 57° for the Buldiva
area, and 315° and 63° respectively for the Arnhem Land area. A third trend
in the Buldiva area is approximately east-west; in the Arnhem Land area.
the third joint direction is variable, the observed bearings being between
27° and 42°.
The jomting is predominantly vertical and together with the prevalent
low dips, is responsible for the rugged topography, much of it inaccessible.
No accurate measurements of the thickness of the Buldiva Quartzite in the
Ruldiva area or the possible variations in that thickness elsewhere, as for
instance, in the Arnhem Land Region, are available. In the type area it
appears to be of the order of several hundred feet, and the present writer has
seen no evidence to suggest any marked departure from that estimate in
other parts of the Territory. The estimate of more than a thousand feet
(Noakes, 1949) in folded areas (apparently the Arnhem Lind area) appears
lo the present writer excessive.
134
Outcrops of massive quartzite are well distributed in the north-western
sector of North Australia. They are responsible for the formation of trémen-
dous cliff faces along the dissected western edges of the Arnhem Land Plateau
and along the western sector of the southerly margin. Though some may be
older, they are correlated provisionally with the Buldiva Quartzite. The
quartzite outcraps which occur at intervals along the north aad east coast of
Arnhem land and on Groote Eylandt may represent beds of the Davenport
Series. Where observed, the Buldiva Quartzite and other formations of the
Buldivan Series together with members of the “Lower Cretaceous” Plateau
sandstones, form the cover rocks on the Agicondi and Davenport Series over
a large part of the Arnhem Land Plateau, The former are continuous with
the Agiconili Series of the Darwin-Oenpelli triangle and the latter continue
across the Roper River to the Carpentaria Group of the McArthur River
Area. It is largely due to the presence of the later cover rocks that the
plateau owes its relatively high elevation, There is no evidence to suggest
that the easterly dips of the Buldiva Quartzite at the western margin indicate
the existence of a synclinal structure over the plateau. All of the observations
made, indicate rather a number of gentle flexures and suggest the existence
of some cross-folding with resultant dome and basin folds. Wherever the
valleys and dissected margins of the plateau have been examined, members
of the Buldivan Series or of the Mullaman Group, or both, occupy the upper
sections and form cliff-faces, exposing in the lower sections and on the Aoors
of the valleys rocks of the Agicondi or Davenport Series or igneous rocks
intrusive into them, The Buldiva Quartzite outcrops extensively between the
Finniss River and Collia, and extends southwards. Outcrops at Tanami, in
the Gardiner Range and at intervals to Winnecke Creek may be its equiva-
lents. The absence over large areas of metamorphism, mineralization and
imarked deformation from same quartzites belonging to an older series, makes
correlation of widely separated outcrops difficult and in many instances
impossible. It may well be that some outcrops labelled Buldiva Quartzite
belong in fact to the older, the Davenport Series.
As the Buldiva Quartzite is the basal sedimentary formation of the
Buldivan Series in the type area, the northern sector of the Buldiva-Wiso
Rasin, its age and correlation will be discussed with the rest of the Series.
At intervals between 16 and 18 degrees South Latitude, along the border
area of Western and North Australia, Mattheson and Teichert (1945) have
mapped a great thickness of basic fows with agglomerates. They consider
that these volcanics form the basal portion of the Cambrian sequence in that
region, The volcanics are succeeded by calcareous and argillaceous sediments
the oldest of which is regarded as Late Lower Cambrian, and is probably
the equivalent of the base of the Daly River Group.
The volcanics extend eastwards ito North Australia into the Wave
Hill District, Their extent and positions in the sequence have not been
determined in that region. The existence of volcanics at the base of the
Buldivan Series has been suggested byt not proved so far in other parts of
the Territory.
Ta the southern portion of the Buldiva-Wiso Basin, and in the Barkly
Basin, the lowest members in most localities are relatively thin arenaceous
beds or limestones of variable types,
(b) Tue Daty River Grove ox Upper Bucpivan Series
The deposits aboye the Buldiva Quartzite were described in the NLA.
Survey Report (Hossfeld, 1937g) as follows: “overlying the quartzites .. .
are limestones, argillaceous limestones, slates and fine-grained sandstones.
135
On a hill to the north-west of Collia, and near the western edge of the area,
well preserved stromatoliths and cryptozoa were found in limestones ittter-
bedded with purple slates. The rocks are considered tm be near the base of
the beds overlying the quartzites. Similar structures were found near North-
ern Creek alongside the new road to Daly River, On what is probably a
higher horizon Girvanella was located between the Fish River and Collia
on the Buldiva-Collia track.”
No formal name was given fo these sediments as all of them were
included in the Buldiva(n) Series. They were divided merely into the Lower
Buldiva Series (Buldiva Quartzites) and the Upper Buldiva Series. Votsey
(19392) used the term “Daly River Limestones,” which Noakes (1949)
suggests be named the Daly River Group, The adoption of the latter tert
by the present writer does not imply agreement with Noakes (op. cit.) that
the name “Buldiva Series” should be eliminated. .
Lying conformably above the Buldiva Quartzite in the type area, and
forming a continuous series without an erosional break (Noakes, 1949, per
contra vide), there follows a transition zone of irregularly alternating,
relatively thin beds of limestones (some of them cherty) and quartzites.
These pass upwards into fossiliferous limestones of the Daly River area,
and are succeeded by the other members of the group,
Some fossil localities have been referred ta above. Others are given in
the description of various areas by several authors. The additional localities
examined by the present writer are on the Douglas River where pteropod
limestones (Biconulites “Salterella" hardmani) and Girvanella limestones
outcrop, and near Chinaman Creek south-west of Katherine, where Girvan-
ella-like remains weather from the sediments in immense numbers. There is
general agreement in regarding the lower members of the Daly River Group
as Upper Lower Cambrian.
Sediments of Cambrian age outcrop, or are obscured by a thin veneer
only of younger rocks, over very large areas in the Northern Territory. They
extend from Western Australia into the Territory on the Ord River Region
and continue apparently without a break, but ohscured in many places by
younger rocks, ta the Daly River Region. They continue eastwards across
the Overland Telegraph Line, forming the Barkly Tableland, and thence into
Queensland. The large, unmapped area bounded approximately by Newcastle
Waters, Wave Hill, The Granites and Barrow Creek, is believed to be urnder-
lain at shallow depths by Cambrian sediments. The eastern portion, west of
Tennant Creek was named by the writer the “Wiso Area” in 1937.
(A.G.G.S.N.A. 1938a) and the natie Wiso Tableland is proposed herein for
the whole region.
The Buldivan Series was defined in the publication referred to earlier
{Hossfeld, 1937g). The writer, in this and subsequent references, included in
that term not only the basal formation, the Puldiva Quartzite, but also the
remaining beds of the sequence, the limestones, shales and associated sedi-
ments of recognized Cambrian age. (Hig. 3). Since then, Noakes (1949) has
eliminated the term, and “Buldivan Series” has been used for the Buldiva
Quartzite alone (David and Browne, 1950). The present writer is convinced
from his field observations in the area to the east of Collia-Buldiva where
good sections exist, that in this area at least, the sequence represents can-
tinuous deposition from the base of the Buldiva Quartzite into the Daly
River Group. Statements to the contrary by Noakes (1949) notwithstanding,
the present writer adheres to his previously published opinion that the
Bulvida(tt) Series includes the whole of the above sediments.
13
Noakes (1949) cites as his main argument the observation that in many
parts of the Brock’s Creek District the Cambrian limestones rest directly
on the Agicondi Series. In this connection Noakes did not refer to the known
existence of fault boundaries in this region, an area in which dislocation by
faulting is recognized as severe and extensive. The prevalence of such fault
junctions and the apparent stratigraphical anomalies which they have pro-
duced along the western and eastern margins of the Cambrian basin, make
it highly probable that they are responsible wholly as they are known in
part to be, for the apparent anomalies quoted by Noakes.
The discovery by the présent writer of a continuous section above the
Ruldiva Quartzite into the Daly River Group, and the juxtaposition and
upparent conformity of the two units over such a large portion of the
Northern Territory, make it improbable that the erosion interval, postulated
by Noakes, exists except perhaps as a local feature, which may have occurred
as a fesult of transgressive deposition in such a large area as the Buldiva
Basin, The twa units then, constitute the Buldivan Series. As stated earlier.
it is generally agreed that deposition of the Daly River Group commenced in
the upper portion of the Lower Cambrian and it follows that the formatian
which is now the Buldiva Quartzite. was deposited during the earlier part uf
that epoch. Deposition may be wholly Cambrian or it may have commenced
during the last stage of the Upper Proterozoic and continued into the Lower
Cambrian,
{c} Votcanics
Numerous exposures of extrusive rocks of great variety are known to
occur in North Australia.
Jensen (Cwlth. Aust. 1915c) records dolerites, diabases, basalts, ande-
sites, rhyolites, phonolites, trachytes and calci-trachytes as weil as tuffs of
the above, and porphyries. In view of the wide tange of composition it is
suggested that they may belong to more than one epoch. However, Noakes
(1949) while acknowledging the incompleteness of field evidence, Suggests
that the volcanics are of Lower Cambrian age, overlie the Buldiva Quartzites
and underlie the Daly River Group, and correlates them apparently with
the Lower Cambrian voleanics of the Kimberley Tegion of Western Aus-
trlaia,
Opinions expressed by previous observers show wide divergences. There
are several areas to which special reference is required at this stage. These
are the Edith River, Maude Creek, Collia, Tipperary-Daly River Road, and
Victoria River.
THE EDITH RIVER VOLCANICS
The observations (Noakes, 194%) of fault boundaries and the resultingr
juxtaposition of the volcanics to the Agicondi Series, to the Buldiva Quariz.-
ite, and the Daly River Group, make a defininte determination impossible
at this stage, The present writer considers, however, that in view of the
recorded occurrence of numerous tuffs and tuffaceous sandstones. in the
Agicondi Series in that locality, the recorded folding of the deposits, and
metamorphism of some of the racks, their reference to the Agicondi Series
appears logical. They ate regarded therefore, by the writer as tentatively
of Lower Proterozoic age,
THE MAUDE CREEK VOLCANICS
The examination of the goldfield of that name (Cattle, 1937b) showed
that the tuffs and porphyries of this area can he correlated with reasonable
certainty with other deposits of the Agicondi Series. A section by Gray
(Cwlth. Aust., 19154) and the accompanying text indicates, hawever, nov
only his recognition of the existence of Precambrian tuffs, but also the
137
occurrence of small deposits of volcanics in the Cambrian sequence. If sub-
sequent work confirms the existence of volcanics of two ages in this locality,
it will explain to sotme extent the differences of opinion expressed in the
past, and will indicate the extension eastward even though perhaps inter-
mittent, of the volcanic accumulations at or mear the base of the Buldivan
Series near the Western Australian border.
Other volcanics such as the Collia and East Victoria River areas and
possilly the Tipperary-Daly River road occurrence are regarded by the
writer as Post-Cambrian and, as will be shown later, tentatively as Devonian,
The work of Mattheson and Tetchert in the border areas resulted in a
threefold division of the Cambrian succession, at the base a great thickness
of basaltic rocks including agglomerates, followed by the Negri and Mt, Elder
Series of Cambrian sediments. Their extension fnto North Australia was
demonstrated but until detailed mapping is done in the extensive Victoria
Riyer drainage basin, these divisians cannot he carried through. The whole
area in which these three groups are believed to outcrop, is shown on the
geological map herein, as Cambrian without any attempt at differentiation.
An exception is made of the volcanics mapped by earlier workers in the
eastern marginal areas of the Victoria River drainage basin. On the evidence
of other observers together with the writer's own obseryations, it is
sugpested that these could be Post-Cambrian and correlated provisionally
with the Collia Series, which is being regarded tentatively as Devonian,
Tue AmMaDEUS GEOSYNCLINE
The Archaeozoic rocks of the Musgrave and Arunta blacks are separated
by the geosynclinal sediments of the Amadeus Geosynicline.
The maximum width of this feature how ranges from 100 to 160 miles.
(Fig. 6), 1t is known to extend for more than 300 miles in a general east-west
direction, but is stated to continue for at least another 150 miles towards and
into Western Australia, (Ellis, 1936). Its northern margin probably lies
near the southern end of Lake Mackay. Hf the postulated continuity of the
Amadeus with the Flinders-Mt. Lofty Geosynecline is accepted, there exists
a known length of at least 1,000 miles with unknown extensions to the west.
The sédiments which rest with violent unconformity on the Arunta Complex
(PL. 11, 1) have been investigated by a number of workers, especially Brown,
Tate and Watt, Chewings, Ward, Mawson and Madigan,
Reference must be made here to the remarkable opinion expressed by
Ellis (1936), that there is no unconformity at the base of the Pertaknurra
Quarttzite and that this formation is part of the Arunta Complex, The exist-
ence of the nonconformity has been established by regional mapping, in-
dividual sections, as well as by the discovery of exposed contacts, One of
these 1s visible in a small quarry south of Alice Springs in Heavitree Gap.
Here, soft argillaeeous beds rest unconformably on massive porphyritic
pranite and are overlain by the Heavitree Quartzite dipping to the south
away from the contact.
In a paper by Mawson and Madigan (1930), the Pre-Ordovician racks
above the Arunta complex were divided in ascending order into the Pata-
knurra and Pataoorrta Series. Madigan (1932a) subsequently changed the
prefix Pata to Terta as being the cotrect spelling of the native word used,
In the above paper Madigan subdivided the former Pertalknurra into Perta-
knurra A and B and an unconformable series above, which he named the
Pertatataka Series. Above this follow the Pertaoorcta (Cambrian), the Lara-
pintine (Ordovician), and finally the Pertnjara {Post-Ordovician) Series, a
total thickness of sediments as measured along Ellery's Creek in the West-
138
ern MacDonnell Ranges of nearly 25,000 feet, In the detailed description
and measurements of the Post-Archaeozoic and Pre-Ordovician sediments
of Ellery’s Creek, Madigan gives the total thicknesses of the series from
above downwards as follows:
Pertaoorrta Series - - - 3,151 feet
Pertatataka Series - - - 3,24 feet
Pertaknurra Series B - - 1,909 feet
{Heavitree Quartzite) A - 1,440 feet
However, in the area fram Alice Springs westwards to the vicinity of
Finniss Gap, tt can be seen that Madigan's Pertaknurra A or Heavitree
Quartzite does not rest directly on the Arunta Complex but is underlain
hy soft argillaceous beds ranging in thickness probably from 12 to 20 feet.
During his examination of these sediments in the Eastern Macdonnell
Ranges, Madigan (1932b). discovered a bed of limestane three feet thick,
vontaining numerous well-preserved Archaeocyathinae, Biconulites (Salter-
ella) were found in this formation, and thus the tentative determination of
the Pertaoorrta Series in the western Macdonnell Ranges as Cambrian, was
confirmed. The division by Madigan (1932a) of the Pre-Ordovician rocks into
three series, the Pertaknurra, Pertatataka and Pertavorrta, ts based chielly
ett lithological and palaeontological evidence. No stratigraphical nor struc-
tural break has been discovered from the base of the sequence to the highest
members of the Larapintine Series, The sole evidence of any break in deposi-
tion appears to be supplied by the conglomerates near the buse of the Perta-
tataka Series. “The boulders included granite and granite-gneiss, bioctite-
gneiss, biotite schist, quartzite and many stromatolith fragments, chiefly
silicified nodules from the limestones, all recognizable at once as from the
immediately underlying Arunta Complex and Pertaknurra Series.” (Madigan,
19322}, The possibility that the assuciated breccia bands were of the nature
of crush lines connected with overthrusting was suggested but discounted
by the long continuation (at least thirty miles) of the quartzite formation
of which they form a part (Mawson and Madigan, 1930), The severe deforma-
tion of the sediments in this and other areas marginal to the southern borders
of the Arunta Block, and especially in the type areas of the Jay and Ellery’s
Creeks, indicates the necessity for a re-examination of the evidence for
Madigan’s sequence and thicknesses.
The sediments of the Amadeus Geosynctine have been folded and faulted
extensively. Many closed structures have been recognized. Some appear in
the various published papers referred to, but the majority were delineated by
the present writer. A generalized representation of the structura! features
appears on the attached gevlogical map.
It is to be noted that the average trend of the folding axes approximates
to a sigmoidal curve bearing in a north-westerly south-easterly direction at
the two observed limits of the geosyncline, Severe deformation is exhibited by
the sediments marginal tu the southern borders of the Arunta Block over a
distance from east to west of approximately 250 miles. In the southern
portion, marginal to the northern borders of the Musgrave Black, outcrops
are widely separated and little is known of the structure. Sufficient outcrops
are available to indicate the existence of a highly disturbed area to the east
and south-east of Lake Amadeus, in which area the faulted Kernot Range,
the basin fold of Mt, Connor, and the subvertical sediments of the Ayers
Rock Horst, form prominent outcrops. The most disturbed area, however,
is that to the east and south-east of Alice Springs. Intense folding and
fracturing exists in this sector, where the trends appear to change their
direction to the north-west south-east in a relatively sharp curve (Fig, 6).
13
Here overfolding, overthrusts and faulting generally are so severe that, even
with the aid of aerial photographs, the structures are difficult of imterpreta-
tion, ‘The greatest horizontal displacements cbseryed, and measured approxi-
mately, appear to have been produced by a relative lateral movement along
a shear plane, of about 7,000 feet.
This highly disturbed sector of the basin is in the area where the
generally east-west trends swing to the south-east. Such a change of direction
ig. ta be expected if the Amadeus Geosyncline is a virtual continuation of the
Fiinders-Mount Lofty Geosynciine and forms a part of the former deposi-
tional basin marginal to the ancient landmass of Yilgarnia, (Andrews, 1937;
Mawson, 1947}, Towards the border of Western Australia the folding appears
to decrease pradually in severity. The geosynclinal structures may continue
to the north-west into Western Australia, but to the north the beds occur
as large residuals over a wide zone and appear to pass gradually into the
less disturbed sediments of the southern continuation of the Buldiva trans-
gression,
In the northern marginal areas ol the geosyncline, the Pertaknurra
(Quartzites have suffered severe deformation and dislocation, Reversed dips
are common along the unconformable junction with the Arunta Complex,
overriding of the older racks on a large scale, fault displacements and block
faulting have produced very complex structures. An anticlinal structure was
formed on part of the southern segment of the Arunta Block. The northern
limb can be recognized by the existence of beds identified with the hasal
formation, the Fertaknurra Quartzite, in elevations such as Simpsan’s Gap
(Hossfeld, 1937¢), Chewings Range, etc., to the west of Alice Springs, Block
faulting has broken the continuity and resulted in the occurrence of numerous
isolated outcrops of this quartzite. In the mest distorted sector, the area
east of Alice Springs, the resulting structures are exceedingly complex. Out-
liers of the Pertnaknurra Quattzite occur in close proximity to much older
(juartzites, and such contiguity has misled some observers inte correlation of
beds, of different ages. The conclusions drawn from such erroneous correla-
tions have been far-reaching, and, quoted by subsequent workers, have pro-
duced considerable confusion, It will be necessary, therefore, to discuss at
length the correlation of the Pertaknurra Series and deductions drawn from
such correlations. The incompetent beds, chiefly limestones und shales
immediately above the Pertaknurta Quartzite, have been distorted so
thoroughly in many areas including Ellery's Creek, that measurement of this
part of Madigan’s type section (1932a) appears impracticable. Nevertheless,
sections were observed in the region where the local thicknesses and sequence
can be determined,
The quartzite (Mt. Blatherskite}, Madigan’s No. 2 Quartzite and re-
garded by him as the base of his Pertatataka Series, which outcrops to the
suuth of Heavitree Gap, is considered by the present writer, on the basis of
its outcrops, overlying sequence and lithology, to be a repetition of the
Tertaknurra Quartzite of Heavitree Gap, Madigan’s No. 2 Quartzite in the
Ellery’s Creek Area which contains the conglomerate and breccia bands
referred to earlier and which was regarded by Madigan {1932a) as the basal
member of his Pertatataka Series, appears toa be very localized in its occur-
tence in the Western Macdonnell Ranges, and has not been recognized in
the Eastern Macdonnell Ranges, (Madigan. 1932b). It is true that the con-
wzlomerate bands could indicate discontinuity of deposition, but this could
have resulted from local uplift by folding or faulting and not of the sequence
as a whole, Deposition except for positive ar negative movements of the
land, resulting in non-deposition or in overlap in some localities, is con-
shiered unbroken from the base int the Ordovician and Post-Ordovician
eds.
140
Madigan himself admits that no unconformity or break in deposition has
been discovered, Nevertheless, he states (Madigan, 1932b, p. 106) “The
Pertaknurra has definitely been intruded by granite, and is aunferous, None
of the later series have been so intruded and no remains of them have been
found inside the berders of the ranges. The orogenic movements which dis-
rupted the Pertaknurra and engulfed part of it in ihe Arunta Complex.
preceded the deposition of all younger formations . . ." “the Pertaknurra
is placed amongst the oldest of Australian sediments and assigned to the
Older Proterozoic, and correlated with the Mosquito Series of Western
Australia . . .” “Pertaknurra time closed with the greatest revolution which
has ever affected the Macdonnells . . .” “This was a time of great granite
intrusion in Central and Western Australia, and a most important metallo-
genetic epoch,”
The above premises and conclusions are not in accordance with Madigan's
statement that na unconformity had been discovered, and is completely
at variance with the opinions held and expressed by the present writer
(Hossfeld, 1937), and subsequently by Voisey (1939b). Reference tu
granitic intrusions and metallogenesis earlier in the present paper indicate
the writer's views on those aspects.
Madigan's conclusions appear to have been based on several features.
1. The observed overthrust faulting of the Pertaknurra Quartzite and
the severe crumpling and folding of the overlying sediments, which as Voisey
(1939b) has shown is of Post-Ordovician age.
2. The assumption following Chewings (1928) that the White Range
and the Bald Hill-Winhecke Quartzites are down-faulted metamorphosed
remnants of Pertaknurra Quartzite, and the conclusion therefrom of a
tremendous orogenic upheaval, with subsequent granitic intrusions ant
mineralization.
3. ‘lhe existence of limestones in close proximity ta some of the older
quartzite outcrops, thus affording a correlation with the lower portion of
the Pertaknurra sequence.
As pointed aut by Voisey (op. cit.) once these errors of correlation by
Matigan are realized, there is no need to postulate a marked time break
above the Pertaknurra Series. It is no longer necessary to ignore the over-
whelming evidence not only of regional continuity of deposition, but alse
of Post Ordovician orogeny. The present writer agrees with Voisey that the
term Pertatataka Series is superfuous, and the original division pf the
sequence by Mawson and Madigan into two series, the Pertaknurra and
Pertaoorrta should be retained.
AGE AND CORRELATION
The Pertaoorrta Series has been determined on palaeontological evidence
as of Cambrian age. Browne (David and Browne. 1950) regards the upper-
most members of Madigan’s Pertatataka Series and consisting of 930 feet
of purple fissile slate with green bands, calcareous slates and reddish sand-
stones, as equivalent to the Purple Slate Stage (Adelaide System) and placed
in the Lower Cambrian, This sequence has been named the Marinoan Series
by Mawson and Sprigg (1950), who regard it as the uppermost division of
the Proterozoic. In view of this published opinion, the age-grouping by
Mawson and Madigan of the Amadeus Geosyncline sediments is being
retained at present. This implies that the Pertaoorrta Series is of Cambrian
age, and that the earlier deposits (Pertaknurra and Pertatataka Series) are
Proterozoic,
141
The main divisions of the Adelaide System are the Para, Narcnota
(Hossfeld, 1935a, pp. 46, 61-63) and the Marinoan Series (Mawson and
Sprigg, 1950), The Para and Narcoota Series were subsequently called the
Torrensian and Sturlian respectively by Mawson and Sprigg in 1950 (op.
cit.)-
Attempts have been made by some authors to correlate the Precambrian
sequence of the Amadeus Geosyncline with the Adelaide System. Such
correlations are tentative at present, partly because the Sturt Tillite which
is such a marked feature of the Narcoota Series of the Adelaide System, has
not been recognized so far, in the Amadeus Geosyncline.
At what stage during the Proterozoic Era deposition commenced cannot
be decided at present. The writer can see no grounds except the mistaken
correlations of Madigan discussed abaye, for regarding the Pertaknurra
Series as Older Proterozoic and equivalent in age to the Mosquito Creek
Series (Agicondi Series), or even to the Middle Proterozoic {Davenport
Series), The Pertaknurra A and B and the former Pertatataka Series will
be referred to collectively as the Pertaknurra Series and are regarded as of
late Middle to Upper Proterezoic age.
No contemporary volcanic activity has heen recorded from the sediments
oj the Amadeus Geosyneline which is classified as a miogeosyncline.
The available evidence indicates that the orogeny of the Amadeus Geo-
syncline took place after the deposition of the TPertnjara Series (Post-
Ordovician). No igneous intrusions nor mineralization due to igneous activity
have been observed by the writer. The only references to igneous intrusions
are those of Madigan, most of whith deal with beds older than the Perta-
knurra and mistakingly correlated with it. In the Jervois Range area Madi-
gan refers to granite intrusive into Cambrian beds, but does not show this
in his sections. Wherever in that sector the present writer observed outcrops
of Cambrian age in close proximity to granite, they were separated by major
faults. Until some definite evidence of Cambrian intrusions in that area is
produced, the present writer maintains that the sediments of the Amadens
Geosyncline and adjacent areas were, in that district as elsewhere, completely
free of igneous activity.
The earliest known deposits of the Buldivan Series, the transgressive
deposition of which probably began from the north-west, are believed to
belong to the base of the Cambrian. Deposition in parts of the basin apparently
conlinued into the Upper Cambrian and with a possible time-hbreak, into
the Ordovician. Since depositian apparently began carlier and continued
longer in the Amadeus Geosyncline, and communication probably was
established with the Cambrian basins to the north, transitional areas should
exist to the north-east and north-west of the Geosyncline. Those to the east
are buried beneath the Mesozoic sediments of the Great Artesian Basin. In
the west where such transitional deposits may exist. gealogical outcrops
are scarce in the large region covered almos{ completely hy recent sand dunes
(Hossfeld, 19404), Such outcrops as do exist are covered to a large extent by
durterust, which in those peneplaned areas has not been removed by denuda-
tion and hence renders identification difficult. However, the dissected regians
of the Kimberley District af the north-west of Western Australia, and the
Victoria River Downs and Wave Hill Districts offer considerable prospects
of adding io our knowledge of the Late Proterozoic—Lower Palaevzvic
succession.
The classification, as Pertaknurra remnants, of numereus gutliers of
arenaceous. sediments on the Arunta Block by previous. observers, has not
been established beyond reasonable doubt, That such do occur is shown
by the recognition of such a remnant at Simpsen’s Gap (Hossfeld, 1937)
142
and by the correlation of part at least of the Chewings Ranges and others,
However, the quartzites of those areas are lithologically and in other respects
so similar to those of definite Pertaknurra age in the vicinity, that there is
littie doubt of their correlation, Although some of these quartzites have been
faulted into the Archaeozoic rocks of the Arunta Complex, they exhibit
none of the metamorphism nor mineralization observed in the White Range
or other similar quartzites. They have not “been absorbed into the Complex,”
but retain their original characteristics.
The Amunurunga Series (Tindale, 1933} and numerous other outliers
on the Arunta Block Have been discussed earlier. These beds which are
lightly metamorphosed are violently unconformable on the Archa¢ozoic rocks
and are overlain unconformably by beds (predominantly quartzite) corre-
lated with the Pertaknurra Series,
At the eastern extremity of the Arunta Block, notably in the Jervois
Ranges, the arenaceous and argillaceous sediments lying unconformably on
the Arunta Complex have been correlated by Madigan (1932b, 1933, 1937)
with the Pertaknurra Series. As stated earlier, the present writer regards
this as improbable, and has correlated them provisionally with the Daven-
port Series,
E. ORDOVICIAN
Rocks of Ordovician age outcrop at intervals over large areas tn Central
Australia, They have not heen recognized so far, from North Australia,
but such sediments may exist in the largely un-mapped region of the narth-
west, between Barrow Creek and the Lower Victoria River.
Ordovician sediments form a portion of the deposits of the Amadeus
Geosyncline between the Musgrave and Arunta Blocks, Extension of these
beds into Western Australia in the Robert Range, Walter James Range
and others is suggested by Ellis (1936).
Eastwards, their outcrops have been recognized as far as the Todd
River, and again, in the vicinity of the Queensland border, where they out-
crap in the Toko Ranges which are practically unexplored, [t is believed that
the Archeaozoic rocks of the Aranta Complex and sediments of the Amadeus
Geosyncline outcrop in that region and ta the suuth-east, until they are
obscured by the Mesozoic sediments of the Great Artesian Basin, and ly
recent atolian deposits.
From the Toku Range, deposits of Ordovician age have been recordril
westwards at intervals, on and near the northern margin of the Arunta
Riock probably to a short distance west of Barrow Creek (Pl. III, 1). Definite
fossil evidence has been obtained from the Toko, Tarlton and Dulcie Ranges
and their continuity further to the west is based on lithological and strati-
graphical features, In the region on the northern flank of the Arunta Block
they do not form part of the thick range of sediments developed in the
Amadeus Basin. They appear to form part of the Barkly Basin succession,
but may be separated by an unconformity from the Cambrian sediments.
In the Barrow Creek District and adjacent areas they overlap the Cambrian
beds and rest unconformably on the Arunta Complex. Such an overlap
is suggested also for a part at least of the Tarlton Ranges.
Deposits of Ordovician age in the western part of the Amadeus Geo-
syncline were inyestigated in 1894 by Tate and Watt during the Horn
expedition and the results published in 1896. Fossils collected at that time
and those collected earlier hy H. Y. L. Brown, were identified as of Ordovi-
cian age, and the series received the name Larapintine ,
It was demonstrated later (Mawson and Madigan, 1930), that the stratr
graphy of the region as described by Tate and Watt (1896) and Ward (1925)
143
required correction, but this did not alter the recognition of the Larapintine
Series as Ordovician.
Subsequent investigations by Madigan (1932a) added considerably to
our knowledge of the stratigraphy, lithology and fossil contents of the
series, The Larapintine portion of the Ellery’s Creek type section (Madigan
op. cit.) shows a total thickness of 5,986 feet, chiefly arenaceous beds with
thin bands of highly fossiliferous limestones and some shales, nearly midway
in the sequence.
Variations in thickness of some of the recognized beds have been
recorded in other areas of the Amadeus Geosyncline. Thus the thickness
of the lower quartzites was found by Tate and Watt to be approximately
6,000 feet in the Levi Range with a decrease of and absence of some beds,
making the total thickness in that area approximately 7,000 feet,
South of the Eastern Macdonnell Ranges the Larapintine deposits,
where examined, appear to be relatively thin. Too little is known of this
region, however, for definite statements of the original thickness of the
series.
North of the Eastern Macdonnell Ranges, the existence of sediments
of Ordovician age was reported first from the Dulcie Range (ITossfeld, 1931;
Tindale, 1931; Madigan, 1932h). Extensions to the eastward towards thé
Queensland border were investigated by Madigan in the Tarlton and Toko
Ranges (Madigan, 1937).
Sub-horizontal sandstones, grits and conglomerates ta the east of
Barrow Creek were correlated tentatively with the Ordovician (Hossfeld,
1937i).
The limited vertical exposures of the sub-horizontal sediments to the
north and east of the Arunta Block make an estimate of their total thickness
impossible at present. The maximum observed appears to be about 800 feet,
recorded from Mt. Ultim in the Dulcie Ranges by Tindale (1931), They will
be referred to as the Dulcie Series.
In the Amadeus Geosyncline the Larapintine Series exhibits predominantly
a littoral or shallow water facies, indicating that throughout the deposition
of about 7,000 feet of sediments, sinking of the floor of the basin kept pace
approximately with the rate of deposition. Calcareous beds are few and thin
in the greater part of the region, but become increasingly numerous to the
east and towards the Queensland border (Madigan, 1937} indicating greater
depths in that direction. The recorded occurrence in the central part of the
area of pscudomorphs after sodium chloride crystals, suggests the existence
of temporarily land-locked arms of the sea and their evaporation.
Within the great thickness examined, recognizable fossils exist in a zone
of less than one hundred feet thick, in the western part of the region. Further
to the east, however, indications are that fossil remains are distributed through
a wider zone of deposition.
The sediments of the Larapintine Series to the south of the Macdonnell
Ranges form many large, continuous oulcreps, but occur also as numerous,
scattered residuals, or as long, continuous beds along the strike. Such dis-
continuity of outcrop is due, not only to folding and faulting, but also tea
removal by erosion and to their burial by later deposits.
The Dulcte Series sediments to the east and north, which are sub-
horizontal or gently flexured, form mesas, some of very large extent, resull-
ing from the dissection of a former continuous elevated region. Whereas
in the Amadeus Basin the Larapintine sediments represent portion of an
apparently uninterrupted sequence from Late Proterazoic or Early Cambrian
times, the corresponding Ordovician deposits on the east and north of the
Arunta Block are of the transgressive type,
144
The geosynclinal deposits of the Amadeus Basin have undergone com-
pression and now exhibit many closed folds, and numerous faults with
resulting repetition of beds, whereas the transgressive beds exhibit little
deformation (Fig, 2). The gentle folding north of the Amadeus Geosyneline
is exhibited both by the Cambrian and Ordovician sediments. The two
periols may be separated by an unconformity, but none has been proved as
yet. Even if such were established, it probably would disclose discontinuity
of deposition without deformation. On present evidence, the folding of the
Buldivan Series appears to have taken place in Late- or Post-Ordovician
times, both in the Barkly and the Buldiva-Wiso Basins, increasing probably
ii severity to the north-east, in the Arnhem Land Region. The general sub-
horizontal attitude could result, as the writer believes it did resuli, in the
removal by erosion of the Ordovician, and much of the Cambrian sediments
It is suggested therefore, that remnants of Ordovician age may exist in
the largely unknown terrain to the north-west of Barrow Creek, which the
writer named the Wiso Region or Tableland. There may be remnants also
of such deposits in the Victoria River Region and even further to the north-
west. The great extent of the Buldivan transgression and the transgressive
nature of the Ordovician sediments, suggests a former much greater extent
of the fatter than that of the scattered dissected remnants of today.
F. SILURIAN
No formations of this pertod have been identified in the Northern
Territory, The possibility exists that such may be found among the sedi-
ments of the unmapped Wiso Region, or im the terrain still further to the
north-west towards the East Kimberley Region.
In the Western Macdunnell Ranges a remarkable conglomerate overlaps
the Ordovician Larapintine Series without an angular unconformity, Macli-
gan (1932a) named this conglomerate the Pertnjara Series, and estimated
a minimum thickness of 9,000 feet. As far as is known at present, this forma-
tian referred to elsewhere as the Post-Ordavician conglomerate, ts restricted
to the western segment of the Amadeus Geosyncline where much of it is
obscured by Cainozoic sands and gravels.
Near the base, the boulders include fossiliferous Larapintine rocks,
Pertaknurra limestones and Archaeozoic rocks up to three feet in diameter,
Higher up in the sequence the percentage of boulders derived from Archaev-
zoic rocks increases. Although examined [for such features, no evidence of
facetting or glacial striation was discovered, and it appears that the con-
glomerate was formed of water-worn material.
No contemporaneous fossils were observed in the conglomerate, the
only fossils recorded being those derived from older sediments. No definite
évidence is available of the age of the Pertnjara conglomerate. Madigan
(19324) suggests its correlation with the Finke River Series, good exposures
of which exist between Horseshoe Bend and Yellow Cliff along the Finke
River, and regards the conglomerate as of Permo-Carboniferous (Permian)
age. This tentative correlation by Madigan must be rejected since the Finke
Series are not folded and rest tinconformably on the eroded surfaces of the
folded Amadeus geosyncline sediments.
The absence of an angular unconformity suggests continuity of deposi-
tiun in the Amadeus Basin after the Ordovician Larapintine Series. Wherever
examined by the writer, the Pertnjara Series participated in the oregeny of
the Amadeus Geosyncline and exhibits severe ditatrophistn, closed folds
und reversed dips in some areas. There appears to be no reason at present
to postulate a long time interval such as the currelation by Madigan would
145
require between the deposition of the Larapintine and the Pertnjara Series.
Local uplift of part of the western portion of the Arunta Block and a part.
of the geosynclinal basin, could have produced the features described by
Madigan. The present writer agrees therefore with the tentative correlation
by Andrews (1937) of the Pertnjara Conglomerate with the Silurian.
G DEVONIAN
The only area in which rocks of definite Devonian age have been
recognized in the Northern Territory is the continuation eastwards from
the Wesiern Australian border of the Burt Range Basin in the Ord River
District, where they have been mapped and described. (Mattheson and
Teichert, 1945; Teichert, 1947). The deposits uf this synclinal basin were
found to contain Upper Devonian, Carboniferous and Permian (?} sediments.
The Devonian succession as determined by Teichcrt is a follows:
Upper Sandstones - - ~ - - - ~ 14,000 feet
Limestones with interbedded shales and
Caleareous Sandstunes - - - - - 4000 _,,
Cockatoo Sandstones and Conglumerates - 4,800 _,,
Total 9,800 ,,
The Cockatoo Sandstones and Conglomerates rest on basalt which has
a thickness ef at least 100 feet, and lies unconformably on Precambrian
quartzites, The age of the basalt has nat been determined, but Teichert
suggests that despite its similarity to the Lower Cambrian basalt of the
Argyle Basin, etc., it may well be of Devonian age.
The lower sandstones are strongly current-bedded.
From fossiliferous horizons in the middle group, Camarotocchia-
Productella assemblages were found identical with those of the Productella .
limestone (Stage IV) of the West Kimberley District.
Teichert considers that deposition commenced early in the Upper
Devonian and continued to the close of that epoch.
Tue CoLiia SERIES
Asa result of the examination by the N.A. Survey in 1936 of the Buldiva-
Collia Area, south of the Lower Daly River, a group of lavas and tuffs with
some sediments was described and named the Collia Series. A description
and map of the area was published (A.G.G.S.N.A., 1937a, and Hossfeld,
19372). (Fig, 3).
The basal beds in some places, notably just west of Collia, are quartzites
containing beds of arleose. Grits are present also, The arkose appears io have
heen derived from the Soldier's Creek Granite which forms large outcrops
in this area. The Collia Series consists mainly of lavas and tufs. Gencrally
these rest unconformably directly on the sediments and intrusives of the
Agicondi Series or on the tilted sediments of the Buldivan Series. The lavas
and tufls range from basic to intermediate types, and some of them contain
appreciable amounts of copper minerals.
Despite the sceplicism expressed by Noakes (1949) and the difference
of opinion indicated by Browne (David and Browne, 1950, p. 23) in amend-
ing the section in the published report (Hossfeld, 1937g) the opinion ex-
pressed in that report by the present writer is being adhered to. This is
supported by Voisey (1939a) who as Assistant Geologist of the N.A. Survey
was responsible for a large proportion of the geological mapping of the
Buldiya-Collia Area. There is no douwht that the Colfia Series which is
horizontal or nearly so, rests unconformably on the eroded, upturned edges
of the sediments of the Buldivan Series. It is, therefore, of Post-Cambrian
K
146
age, It is overlain by sediments which Were named the Plateau Sandstune
Series (Hossfeld, 1937g) and on the evidence of the discovery of Otozamites
bengalensis, were regarded as of Jurassic age. Later, the age determination
was allered ta Lower Cretaceous, and the formal name changed to Mullaman
Group by Noakes (1949). The Cullia Series, therefore, is Post-Cambrian and
TPre-Cretuceous, No other evidence of its age was discovered. The report,
however, by Teichert (op. cit.) of the existence at the base of the
Cockatoo Sandstones of basalt with an observed thickness of 100 feet, which
is being regarded as possibly of Devonian age, and perhaps at the base of
the Upper Devonian, suggests a possible currelation between the Burt Range
drea of Teichert and the Buldiva-Collia area about 150 miles to the
north-east.
Voleanics have been recorded from many localities in North Australia.
Some of these were listed by H. Y. L. Brown, Woolnough and Jensen.
As was to be expected in a region of which so little was known, interpreta-
‘tions of the ages and correlation of these deposits varied very widely. A
region in which the ancient sediments of the Agicondi Series contain Jarge
amounts of tuffs and tuffaceous material and probably lava flows, a region
jn which volcanics occur in some localities in the Cambrian sequence, and
which experienced Post-Cambrian vulcanism, regional reconnaissance did
nut supply in many instances the information necessary for the age deter-
inination and correlation of widely scattered outcrops:
The evidence accumulated over many decades has shown, however, that
there are a very large number of discontinuous outcrops, some widely
scattered, occupying both large and small areas, which are volcanics that
appear to occupy a stratigraphical position above the knowa Cambrian
sediments, Their mode of occurrence varies widely. In many instances they
form: the higher sectors of the landscape as in the Willeroo-Victoria River
Downs-Wave Hill region, in the Nutwood Downs area and others. Accord-
ing to Brown and Jensen in sotrie areas they appear to occupy “erasion
hollows” in the Cambrian limestones. There are large ureas where they
outcrop along the escarpments only of mesas and tablelands, the scarps
being due to the younger “Lower Cretaceous sediments.” Even today when
they have been denuded from very large areas, they outcrop and probably
occur beneath younger sediments over a large part of North Australia. I
is improbable that they were ever continuous over the major part of North
Australia, but they covered apparently a very large terrain. Some of the
occurrences may be identified eventually with the Cambrian deposits, but
many are regarded tentatively as of Post-Cambrian age.
The intense volcanic activity in Eastern Australia during the
Devonian Period may well have extended to a less degree into North
Australia. The classification of the Collia Series and its equivalents in North
Australia as Middle to Upper Devonian is a tentative onc, but at present
no evidence ts available for an earlier or later time.
H. CARBONIFEROUS
Recks of this period are known only from the Burt Range Basin
where they cross from Western Australia into the Northern Territory.
Nothing is known of their further extension eastward, but the total area
within which they outcrop is likely to be small, unless other basins are
discovered. The Carboniferous sediments of the Burt Range Basin in West-
ern Australia have not been examined in detail and at present only 350 feet
of Bryozoan limestone is known. As this limestané eaverlics the sandstones
believed to be the highest members of the Devonian, and by inference, the
Carboniferous sediments are conformable, the latter probably are of Lower
Carboniferous age.
147
I. PERMIAN
Permian rocks are known from the north-western part of ihe Northern
Territory and in other areas some sediments are assigned tentatively to
that period.
Tue Porr Keats Districr
Fossils were found first at Fossil Head, on the northern shore of a
creek estuary north of the mouth of the Fitzmaurice River, by Commander
Stokes in 1839. The outcrops of this and adjacent areas were examined and
described later by H. Y. L. Brown (1906), According to Brown, the Fossil
Head outcrop ‘exhibits the most typical section of Permo-Carboniferous
beds to be seen along the north-western coast of the Northern Territory.”
The beds consist of sandstone, shale and sandrock. Current bedding and
ripplemarks were observed in some of the heds, and the fossiliferous portions
are lenticular, The lower beds are richly fFossiliferous and the fossils
are pseudomorphs of limonite. The beds are practically horizontal with a
very low dip to the westward. The area was tested for coal by several bores.
One bore penetrated 1,500 feet of sediments, and was presumed to be in
Permo-Carboniferous (Permian) beds at that depth. The obesrvation by
Brown that some of the beds in the lower part of the sequence were cal-
careous or limestones, suggests the possibility of the bore having entered
pembtisg beds of the Buldivan Series or the still older beds of the Davenport
eries.
The fossil assemblage indicates affinity with Permian heds in the Desert
and North-west Basins of Western Australia.
The Permian beds of the Port Keats District were given the formal
name of Port Keats Group by Noakes (1949).
The bores did not succeed in proving the existence of workable coal
seams, but in view of the penetration in one bore of a little coal, such a
discovery is not impossible.
The recent work of Mattheson and Teichert (1945) along the Western
Australian border towards the Keep River in the vicinity of latitude 16° S.,
strongly suggests the extension of beds of this age towards. the mouth of
the Victoria River. The areas where they may occur have been indicated bv
the present writer on the geological map, Much of this region consists of
swampy alluvium beneath which the Permian sediments probably continue.
The presence in the Victoria River region of rocks believed to belong
ta the Collia Series, and also of sediments of the Lower Cretaceous Epoch,
and the absence of marked deformation in any Post-Cambrian rocks, will
necessitate detailed field and palaeontological work to separate and map
the different groups.
Tur Burt RANGE BaAsIn
Mattheson and Teichert (1945) discovered in this area a sequence
separated from the Carboniferous Bryozoan limestone by a very slight un-
conformity. The beds consist of conglomerate at the base, succeeded by
coarse-grained sandstone and several hundred feet of higher beds which
could not be examined on that occasion, They are being regarded tentatively
as of Permian age.
OrHer Areas tn Nortu AUSTRALIA
A. wide-spread group of sediments occurring in North Australia from
the virinity of the Western Australian to the Queensland border which hail
been named by the writer “The Plateau Sandstone Series,” have been given
the formal name of Mullaman Group (Noakes, 1949), They were regarded
hy H. ¥, L. Brown (1908) in part at least as Lower Cretaceous. Jensen and
148
others considered them.as probable Permo-Carboniicrous beds, but Brown’s
original age classification was confirmed by later palacontological evidence,
and they will be discussed therefore, in a later section.
The oceurrence in North Australia, within the Proterezvic Kimberley
Basin, of very gently inclined sediments of Permian age, the Port Keats
Group, suggests that possibility also in the similar Proterazoic basin, the
Carpentaria Basin, This suggestion receives some support from the existence
in the coastal region of the Gulf of Carpentaria, of horizontal or gently in-
clined sediments which differ from the “Lower Cretaceous beds” of the
adjacent tablelands. Brown (19084) reports the discovery in a shaft of black
carbonaceous shale similar to that obtained from a bore in Permian beds
at Port Keats. Jensen (Cwlth, Atst. 1914a, Bull, No, 10) reports fossil wood
resembling Calamites and some specimens resembling Lepidodendron. The
present writer Suggests therefore, the strong possibility that Permian
deposits exist in the coastal region of the Gulf of Carpentaria and continue
eastwards into Queensland beneath rocks of Lower Cretaceuus age,
THe FInKe SERIES
Near the central portion of the southern border of the Northern Territory
in approximately Lat. 254 S., terrestrial deposits containing glacial sediments
exist in the vicinity of and along the River Finke. They have been described
by yarious authors including Brown (1905), David and Howchin (1923),
Ward (1925) and Chewings (1935), They outcrop along the slopes of many
buttes and mesas, some of the Jattcr of very large dimensions. Their occur-
rence ig that of residuals of a former continuous formation, now reduced
by dissection and lying unconformably on the folded sediments of the
Amadeus Geesyncline, Their outcrops extend probably from the southern
flanks of the James Range south to the South Australian border and beyond,
They dip gently in a south-easterly direction beneath the Mesozoic sediments
of the Great Artesian Basin, and are generally believed to act as intake
beds of that basin, The area in which they may occur, has a length
from north-west to south-east of about 15 miles. Their knawn lateral
extent is very variable, but may be estimated at an average of 50 miles.
Continuation much further to the west than is indicated on the accom-
panying map is unlikely. The observation, however. of the gradual merging
eastwards of these mesas with the sands of the Simpson Desert, indicates
that the Finke Series may continue to the east much further than is generally
believed.
The lower members consist of glacial tills and sands with thin lenticular
beds of conglomerate and argillaceous sandstone, a total thickness of at least
100 feet. and are overlain by at least 2,000 feet of porous sandstones. The
terrestrial glacial origin of the lower beds is undoubted, but in the absence
of fossil evidence there exist differences of opinion as to their age. Browne
(David and Browne, 1950) considers them to be Carboniferous or Permian,
Talbot and Clarke (1917) considered a possible correlation with the Wilkin-
son Range Series of Western Australia and of the supposed Lower Cretace-
ous glaciation of Northern South Australia, However, it is generally believed
that they are of Palaeozoic age, and tu be carretated, even though tentatively,
with glacial depositis of Lower Permian age in Southern Australia.
THE Evuiotr Creek Formation
In the Elliott Creek area, north of the Daly River, Noakes (1949)
mapped sediments to which he gave the above formal name. The beds con-
sist of thin beds of sandstones, shale and limestone, which lie horizontally
149
in most of the few available outcrops examined, No fossils were found, and
a minimum thickness of 500 feet is suggested. On general grounds these
heds are regarded as of late Palaeozaic age,
J. TRIASSIC
No rocks of this period have been recognized in the Northern Territory:
Browne (David and Browne, 1950) suggests that the porous sandstones
which aggregate the total of at least 2,000 feet above the glacial beds of
the Finke Series may be Triassic (?) and Jurassic. In several localities to
the west of the railway line, especially in the area west of Charlotte Waters,
a number of buttes and small mesas consist of horizontal or nearly horizontal
sediments lying on the Finke Series. They are almost certainly Mesozoic
and may perhaps be regarded, in part at least, as of Triassic age, with
possibly Jurassic beds above.
K. JURASSIC
Outcrops of Jurassic Age have not been recognized definitely anywhere
within the Northern Territory. Their existence, however, is known in the
south-western sector, as aquifers of the Great Artesian Basin.
Outecrops of Jurassic rocks of the Great Artesian Basin are known lo
the south of the Territory border in South Australia, but haye not been
identified with certainty to the north of that border.
Sands‘ overlying the glacial beds of the Finke Series at Yellow Cliff
may be Jurassic in part, and some of the sandy beds to the west of Charlotte
Water may be of that age.
The existence of Jurassic sediments has been proved at depth by water-
bores deilled in the Artesian basin. j
The greatest thickness recorded from a water-bore which, however, did
fot penetrate the complete sequence, is 860 feet (Ward.1925). The sands
are of lacustrine origin and contain lignitic material. The total thickness
in the Territory sector of the basin is not known, but on the evidence of
the few bores, chiefly near the margin of the basin, appears to be somewhat
variable as would be expected of marginal deposits.
Although surface outcrops have not been recognized, the available
evidence suggests that the limits of the Jurassic sediments, at or near the
surface are marked approximately by the north-western margins of the
extensive aeolian sands and sand-dunes of the Simpson Desert (Madigan,
1938) which may, however, cover also large expanses of the Finke Series.
On Paddy’s Hole Plain, south of Arltunga in the Eastern Macdonnell
Ranges, the silicified stems of osmundaceous plants have been recorded as
weathered out from isolated flat-topped hills (Madigan, 1933, 1937). These
are regarded generally as belonging to the Mesozoic Era, and may belong to,
or he derived from Jurassic or Cretaceous outliers of the Artesian Basin.
IL, CRETACEOUS
The existence of marine sediments of Mesozoic age at Point Charles
near Darwin, was recorded as early as 1895 and further work was done in
that and adjacent paris of the coast in subsequent years. (Brown, 1895 and
1906). The occurrence of rocks of similar age was recorded also from the
southern parts of Bathurst and Melville Islands north of Darwin, To these
sediments, Noakes (1949) has given the name Darwin Formation,
At some distance inland, sediments forming mesas and bultes and very
extensive tablelands occur at intervals over a large portion of North Aus-
tralia, They have been recognized as far south at Lat, 18 5., and extend
150
almost from the Western Australian border across the Northern Territory
to the Queensland border. These sediments were referred to in the past by
various writers as the Plateau Sandstones and were assigned a Permo-
Carboniferous age (Jensen and Woolnough) and a Lower Cretaceous age
(Brown), They were given the formal name of Plateau Sandstone Series
(Hossfeld, 1937), This name has been changed to Mallaman Group by
Noakes (op, cit.) who included in it the Point Charles beds and related
sediments of the coastal region (Darwin Formation), The terms and correla-
tion adopted by Noakes are used in the present paper for the sake of con-
venience, but such use does not imply compicte acceptance of his conclusions.
Far too little work has been done on the group, and the few localities from
which fossiis have been collected are too widely spaced for the formation
of general conclusions of what is admittedly a difficult group.
The maxtmum recorded thickness of this group appears to be about
200 feet, but a total of 100 feet is probably nearer the average. The proun
appears to vary considerably in thickness, and within short distances in
some localities; in others it appears to be very uniform. Much of this varia-
tion in thickness appears ta have been due to deposition on a slightly
irregular landscape. That the land surface on which the group was deposited
was one of predominantly low relicf is unquestionable. However, that some
rejief existed in restricted areas at feast is shown by various features which
will be referred to in the discussion which follows. The sediments of the
group were examined in detail in the Buldiva-Collia area and extracts from
the report on that area (Hossfeld, 1937g) are quoted herewith:
“In the Buldiva-Collia area the Plateau Sandstone Series consists of
sedimentary rocks lying almost horizontally on an uneven surface af the
older rocks. Erosion has exposed the older rocks in many places, the Plateau
Sandstones standing above the getieral level as mesas and buttes in the
intérvening area. The characteristic topography of the mesas and buttes
is due ta the horizontal bedding and vertical jointing of the sandstones. The
level surfaces of the mesas and buttes may indicate a former continuous
peneplain,
The basal beds of the Plateau Sandstone Series vary considerably in
texture, composition and thickness according to the nature of the underlying
rock and the former surface relief heneath and adjacent to the area. of
deposition.”
“The plant remains referred to above, and on the evidence of which a
Jurassic age is assigned to the Plateau Sandstone Series, were collected in
a fine-grained white sandstone or siltstone immediately overlying the tin-
bearing conglomerate, These white sandstones and siltstones have been
transformed in places to porcelianites and ribbon stones. They form a per-
sistent horizon and supply good marker beds, The underlying beds cannot
be used for this purpose as they vary in thickness, owing to the irregular
surface on which they were deposited, and in composition which is dependent
on that of the underlying rocks.”
At Buldiva, plant remains were collected by the N.A. Survey and identi-
fied as Otozamites bengalensis by Dr. A. B. Walkom, who suggested a
Jurassic age for the sediments. The determination of radiolaria from the
Darwin Formation and the examination of the macro-fossils collected, has
resulted in the classification of that Formation as probably of Albian age,
Since, according tc Noakes (op. cit.) the Darwin Formation overlies con-
formably the other members of the Mullaman Group and in which the’plant
remains were found, the age of the latter suggested by him is Lower Cretace-
ous and not Jurassic, Duting 1938 and again in 1939, marine fossils were
181
collected by A. W. Kleeman and the writer in the Mullaman Group from
Yeuraiba, a locality within the Arnhem Land Region. The fossils were too
pnorly preserved for delermination.
It is possible that future investigations will support the division by
Noakes of the Mullaman Group into a lower, lacustrine facies and an upper
marine facies. Within the present writer's knowledge, hawever, plant remains
have been collected from only three pr four localities and from horizons
which cannot be correlated stratigraphically. Marine fossils have been
recognized at a few places only. Obviously no such generalizations as are
put forward by Noakes can be supported on a few isolated occurrences over
such a wide area. The examination of the sequence in the Buldiva-Collia
area, at Yeuralba, Pine Creek and south of Birdum by the present writer
suggests that the whole of the group may well be of marine origin, and that
sma!l estuarine and fluviatile deposits were responsible for the few remains
of Otezamites, the only plant identified from these beds.
Because of overlap, terrestrial deposits. and a few durable plant remains
would be preserved near the base of the group, but in successively younger
beds. Conditions at Buldiva where high level cassiterite-bearing gravels
occur near, but fot at the base of the sequence, indicate fluviatile deposits,
possibly resorted by wave action. The plant remains were discovered just
ahove this horizon,
It is suggested here that the group was deposited as a result of a
gradually transgressive epeiric sea which finally extended over the whole
of North Australia at least as far south at lat. 18. S. Deposition probably
commenced in late Jurassic times and continued inta the Lower Cretaceous.
It was continuous apparently with the Lower Cretaceous sea of Queensland
and the adjoining States, in the region which was to become the Great
Australian Artesian Basin. Emergence of North Australia from the Lower
Cretaceous sea probably by negative moverient of sea-level, left the sedi-
ments in a horizontal to sub-horizontal position, in which they are today
over very large areas. The region therewpon became a plain, old at birth
and without experiencing the very long continuous erosion which was
necessary ta produce the peneplanation of diverse rock types and structures
over the greater part of Australia during the Mesozoic Era. The region
formed then a part of the Great Australian Peneplain, The porosity of the
sediments ensured the absorption of the greater portion of the rainfall then
as it does today, and the gradua) loss by evaporation of the greater part
during the long dry seasons, The porosity of the sediments is shown by
the existence of the exceedingly numerous springs which issue from the
beds of the group wherever they and the basement rocks have been exposed
by dissection. .
One very marked feature observed concerns the vegetation developed
on the sedimeuts of the Plateau Sandstones, It js sbvious that the poor and
very porous soil and sediments would develop a flora specially adapted to
such an environment. It is rematkable, however, that over a very large
proportion of the region the only tree which will grow on these rocks is
Lancewood. This occurs as @ thick forest cover and in pure plant communi-
ties. There are many areas it is true, where the existence of the Mullaman
Group is regarded as certain beneath the surface soil, but where Lancewood
does not exist, These are areas where for various reasons soi] cover is ton
deep or unsuitable for the growth of Lancewood, No areas were observed,
however, where Lancewood does exist, which could not with reastnable
certainty be regarded as underlain by the Mullaman Group, The above
remarks apply to the region south of approximately the laticude of Maranboy.
132
Further north, the average rainfall apparently is too high for the ascetic
Lancewood, To the north of Maranboy and other areas of similar rainfall,
Lancewood is still associated with these beds but instead of growing on the
level summits of the mesas and tablelands as it does further south in the
drier region, it grows only on the scree slopes beneath the sandstone escarp-
ments.
The observation and confirmation of this predilection of Lancewood
for the sediments of the Plateau Sandstones facilitated greatly the ground
and aerial reconnaissance of the region. The dark foliage and general density
of the forest cover, made it easy to recognize the timber at great distances
and enabled the writer to map many areas of these sediments. It was possible
to confirm by actual inspection so many of these occurrences, that no doubt
remains of its general applicability.
Tse Great AUSTRALIAN ARTESIAN BASIN
Lower Cretaceous sediments of marine origin underlie the extreme
south-eastern corner of the Territory, Outcrops have been examined and
described from the vicinity of Charlotte Waters and aa far north as Mount
Daniel. Owing to the prevalence of recent aeolian sands, little is known of
the greater part of the boundaries of the basin in this region. The sediments
consist predominantly of dense, blue shales with some thin calcareous bands,
and are fossiliferous in some localities. They have been studied, largely from
bore samples, in the adjacent areas of South Australia and Queensland, and
have been assigned to the Tambo Series, They are believed to underlic
the region known as the Simpson Desert.
Tt is possible that Paddy’s Hole Plain, south of Arltunga, may be under-
lain, in part at least, by Cretaceous sediments, forming a northern outlier
of the Great Basin.
Lying above the Lower Cretaceous sediments of the basin, there are
dissected remnants of sediments correlated with the Winton Series, of Upper
Cretaceous age. These form mesas and buttes and consist of horizontal beds,
capped by duricrust, and indicate the stage to which dissection has reduced
the level of the former peneplain.
Tue Burt Trouce
The continuity of the surface outcrops of the Archaeozoic rocks of the
Arunta Complex is interrupted by a number of plains, covered by recent
soils and sands, The largest of these is the Burt Plain (Birt Plain of Jensen,
1944). (Pls. IIT, 2 and TV, 1), The severe topography exhibited by the Archae-
ozoic rocks north of Alice Springs terminates. abruptly at about 12 miles at
the southern margin of the Burt Plain, which in this sector has a north-south
width of about 50 miles. It terminates a few miles tu the east, but extends
westwards for at least 200 miles. Its furthest western limits have not beetr
efined,
Ground teconnaissance, and observations from the air by the writer.
for a distance of about 100 miles along the northern and southern margins
of the plain, as well as the study of aerial photographs, indicate that the
Sh akees part and perhaps the whole of the Burt Plain is bordered by faults,
(PI. ITT, 2.)
The examination of samples from the 16 mile bore (Hossfeld, 1933},
showed that in this locality, which is close to the southern margin of the
plain there exists a considerable thickness of sediments, which are immensely
younger than the Archaeozojc rocks which form the northern, eastern and
southern boundaries of the plain,
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The total thickness of the sediments penctrated by the bore is 639 feet
with a small possible extension, The sediments consist predominantly of
shale with some beds of grit,
The shales vary from gritty types to very fine material, They include
black carbonaceous shales al several horizons but especially between 515
and 569 feet. Below GI7 feet the sediments contain large amounts of mica
and below 639 the samples consists of fragments of mica schist indicating
either thal Archaeozoic bedrock had been reached, or that this was not
far below.
No fossils were obtained from the bore samples, but the materials from
322 to 639 feet indicate a lacustrine origin and suggest affinities with the
Winton Series.
The thickness penetrated and the nature of the sediments suggest the
strong probability of considerable fateral extent of this formation. The
probability that there exists here a sub-artesian basin of considerable area,
is increased by the amount of water under pressure which has been shown
to exist in the more porous beds.
The existence of carbonaceous shales indicates the possibility of the
discovery of economically important coal deposits.
Little is known of the attitude of the beds, which on general evidence
appear to be sub-horizontal and inclined ta the westwards. Indications are
that some at least of the sediments will prove to be lentictilar in shape. The
discovery of, or failure to discover coal in any one locality must not be
regarded, therefore, as typical of the whole of the Burt Plain. Water supplies
also may be found to occur at various. depths in different bores, and at more
than one horizon in one bore. It is an area which in its water contents and
potential coal deposits, deserves systematic sub-surface exploration. ,
The potability of the water from the 16-mile Bore may be ascribed
possibly to the existence of a western outlet. Ata distance of about 70 miles
to the west of the eastern margin of the Burt Plain, there commences a
series of salt lakes and swamps which continue in a narrow belt for more
than q hundred miles further west. (Plate TV, 1.) Aerial examitation of these
shallow depressions indicates that many are fed by springs issuing from their
higher marginal areas. The writer believes that this zone of salt lakes
and swamps which occupy an area of considerably lower altitude than that
further east, is supplied to a large extent by water discharged from the
basin underlying the Burt Plain and that it is this discharge which has
permitted the existence of potable water in the basin, The gradual but con-
sistent decrease in altitude of the surface of the Burt Plain from east to
west, estimated at an ayerage fall of 35 inches per mile, is believed to
represent fairly closely the inclination of the underlying sediments, That
being so, it follows that there would be a slow, but constant movement of
subterrancan water in that direction. It is true that the run off from the
ridges of older rocks, which form the northern and seuthern margins of the
plain will supply some water to the belt of lakes and swamps, but this is
considered to be a minor contribution,
The most suitable name for the structural feature, the filling of which
has produced the Burt Plain, is the Burt Trough. The existence, on the
border of Western Australia, in the extreme north-west of North Australia,
of the Burt Range, resulted in the structural name of Burt Range Basin
given to the sediments of that area (Mattheson and Teichert, 1945). How-
ever, in view-of the occurrence of the Burt Trough in Central Australia,
the tame proposed should not be confusing. Should it be so regarded, the
135
alternative name “Stuart Trough” is being suggested for obvious historical
and geographical reasons.
Two similar basins, the Plenty atid the Hale Plains, appear to be
connected structurally with the Burt Plain. Both exhibit faulted boundaries,
in part at least, and appear to be continuations of the fracture system
responsible for the Burt Trough.
No evidence is available to the writer of the material underlying the
Vlenty Plain, which is believed, however, to be merely an extension of the
Burt Plain and to have had a similar histery. (Fig. 2).
The occurrence on the Hale and Plenty Plains, and elsewhere in Central
Australia, of lacustrine sediments of Tertiary age, the Arltunga Series (Madi-
gan, 1933), indicates that the underlying sediments were at least of older
Tertiary and probably of Mesozotc age. .
The penetration by a bore of a seam of lignite 12 fect thick in the Hale
Trough, suggests that the sediments of that basin are of Tertiary age and
depésits of Cretaceous age may occur. The osmundaceous plant remains
fram the nearby Paddy's Hale Plain recorded by Madigan (1932b) suggest
such a possibility. Other basins probably exist in Central Australia, and
the Bundey, Sandover and Hanson Rivers are suggested as possibilities. No
evidence is available and the writer does not contend, that the Burt, Plenty
and Hale Troughs referred to and others which may be discovered were
completely co-épochal in their formation. It is believed, however, that the
basins ate not older than Upper Mesozoic.
The subsidiary basins of the Plenty and Hale Plains are being drained,
though imperfectly, by the rivers of the same names. The Burt Plain itself,
however, despite its relatively high altitude, stated to approximate 2400 feet
near its eastern limits, is still a basin of internal drainage which has been
protected from dissection by the higher ridges of ancient rocks forming
its borders,
The reference by Jensen (1944), to this plain as the “Birt Plain pene-
plain” is cpposed to the geological and topographical evidence. King (1950)
has linked, the Burt Plain and the Missionary Plain with the “Australian”
pediplam. The Missionary Plain may be such a continuation, as may the
extensive peneplaned areas north and north-west of the Arunta Block, The
Burt Plain, however, represents the filling by sediments of a high-level lake
and its formation was considerably above the pediplain and had no con-
nection with its formation.
M. CAINOZOIC
Detailed studies of the Cainozoic deposits uf the Northern Territory
have been published for a few small areas only. The deposits are pre-
dominantly of terrestrial origin and age determinations will be difficult to
establish. Division into Tertiary and Quaternary Periods is impossible at
present in many instances.
No marine deposits of ‘Tertiary age +have been recorded from the
Territory, Such deposits, however, may underlie some of the extensive
coastal plains of the north and west, but if such exist, they would belong,
probably, to Upper Tertiary Times.
Pleistocene to Recent marine deposits have beer observed on the north
and west coast (Noakes, 1949). They appear to he connected chiefly with
world-wide eustatic strandline movements due to glaciations and de-
gilaciations.
Deposits of lacustrine and fluviatile origin exist in mary areas and
indicate extensive lake development during one or more pluvial periods,
156
Deeply eroded stream channels now filled with alluvitim and aeolian deposits
are another indication of former greater rainfall.
Other climatic changes are indicated by the extensive development
af evenly spaced sand dunes, enormous areas of sand plain and large tracts
covered with loessia] material. The present fixation by vegetation of these
aeolian deposits indicates subsequent changes as do the occurrences of
various plant communities, separated from each other by long distances,
The description, discussion, development of the terrestrial deposits of
the Northern Territory and the information which they supply of diastro-
phism and climatic changes are being reserved for a subsequent paper.
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Fig. 1
Looking south from Alice Springs. Archaeozoic Granite Gneisses in foreground,
Unconformable junction of base of Heavitree (Pertaknurra) Quartzite
marked in black,
Fig. 2
Native Gap, north of Alice Springs, showing faulted northerly dipping sand-
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east-north-east.
Trans. Roy. Soc. S. Aust., 1954 ‘ Vol. 77, Plate If
ete
Fig. 1
Horizontal Ordovician sandstones lying uuconformably on the Arunta Complex
at Barrow Creek. Looking east.
Fig. 2
Faulted margin of the southern edge of the Burt Plain, showing massive outcrops
of the Arunta Complex in the background. Looking south,
Trans. Roy. Soe. S. Aust., 1954
Fig, 1
View of part of Burt Plain about 100 miles w
showing some of the numerous salinas of
Vol, 77, Plate
est of the Overland Telegraph Line,
that district. Looking easterly.
~~
F
eet
goo
The Granites, showing the occurrence of an adamellite monadnock in the sandplain,
Vertical.
All photographs are reproduced by permission of Adastra Airways.
GEOLOGICAL MAP OF THE NORTHERN TERR
ITORY OF AUSTRALIA
ri
ut 9 Ve
°
Marine , Estuarine,
Fluviatile, Lacustrine,
Aeolian and Duricrust
(MAPPED IN A FEW
AREAS DISREGARDED
WHERE SHALLOW!
BATHURST Id
MESOZOIC
F<. => UPPER CRETACEOUS
} TO JURASSIC of the
Great Artesian Basin
Darwin
PT CHARLES =
TERTIARY
TO CRETACEOUS ?
of Burt Trough, etc
LOWER CRETACEOUS
Mullaman Grcup,
Plateau Sandstones
TRIASSIC ?
PALAEOZOIC
PERMIAN q : : .
Port Keats Group, - 4 c ees ae.
Borroloola Area, ? r ‘ s . 4 4 ae
Finke River Series?
Port Keats
2 14°
DEVONIAN
Burt Range Basin
Collia Series?
ORDOVICIAN
North of Amadeus
Geosyncline.
0
0
GULF OF CARPENTARIA
CAMBRIAN | Aa = j a4 ee? q ies Z r = pers ? ‘ Z 4 a Pa)
Buldivan Series H ay . i :
SILURIAN ?-CAMBRIAN
Amadeus Geosyncline.
PROTEROZOIC
UPPER PROTEROZOIC
Pertatataka and
Pertaknurra Series.
Borroloola
Wollogorang Area?
MIDDLE PROTEROZOIC
Davenport Series
Hatches Creek Group
Carpentaria Group
Victoria River Beds ? etc.
LOWER PROTEROZOIC
Agicondi Series
ARCHAEOZOIC
UPPER ARCHAEOZOIC
Hart's Ranges etc?
Riddock Series
LOWER ARCHAEOZOIC
Arunta and Musgrave
| Blocks. Aruntan Series
Acid Igneous Intrusions
Strike Trends
“a Generalized
ARUNTA
Xs
? AUSTRALIA.
win
Alice Springs Ms i
SS hal P ™ “ss
ib ; avs
‘ =" *y
GREAT \,
ARTESIAN es
= oo
“>
=
oo.
aw .
f BASIN
MUSGRAVE we f
40 60 ‘ foul £ Kosafeld. =
. ——=———$ —__—_-——— ns Ss (5p Gi ae
161
Tarnor, H. W. B. 1918 The Geological Results of an Expedition to South Australian
Border, ete. Journ. and Proc, Roy. Soc. W. Aust., 3
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85 .
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TIETKENS, phe 1889. Jourtal of Central Australian Exploring Expedition. 5. Aust, Parl
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Vorsey, A. H, 1939b A Contribution to the Geology of the Eastern Macdonnell Ranges,
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Govt. Printer, Canberra
ICHTHYOSTRONGYLUS CLELANDI n.g., n.sp., FROM AN AUSTRALIAN
SHARK
BY PATRICIA M. MAWSON
Summary
Ichthyostrongylus clelandi n.g., n.sp., a Trichostrongyle worm, is described from the spiral valve of
Emissola antarctica from South Australia. This genus is distinguished from others by the shape of
the head.
162
ICHTHYOSTRONGYLUS CLELANDI ng. nap, FROM AN AUSTRALIAN
SHARK
By Patricia M. Mawson *
[Read 10 September 1953]
SUMMARY
Tehthyosirongylus clelandt wg, msp., a Trichostrongyle worm, is described from the
spiral valve of Emissola axtorctica from South Australia. The genus is distinguished from
others by the shape of the head.
A numberof Trichostrongyle worms were found in a tube labelled:
“(1) Flukes from liver of salmon, (2) Cestodes from spiral valve of Sweet
William Shark, Encounter Bay, 1/1922." There is an clement of doubt as to
whether the nematodes, which were very much smaller than the flukes or the
cestodes, came from the salmon, Arripis trutta, or the shark, mtssola antarctica.
Because of the way in which the nematodes were lying intertwined with the
cestodes in thick masses of intestinal material, while the flukes were separate
from these, it has been assumed that they were from the elasmobranch,
The males are up to 4-2 mm. in length, the females to 6-0 mm.; the maximum
body diameter is 0°l mm. in the male and 0-13 mm. in the female. The cuticle
is very markedly striated throughout the body, even on the bursa. The head end
is slightly enlarged, forming a distinctive bulb, not by cuticular inflation but by
thickening of hypodermal tissues and of the anterior oesophageal muscles, The
mouth is surrounded by three strongly cuticularised shallow lips, which give the
appearance of a cap at the anterior end. Each lip bears two rather elongate
papillae. A buccal capsule is absent. The oesophagus is straight and cylindrical
and measures about a tenth of the body length. The nerve ring is very small anc
hard to discern; in those specimens in which it is seen it lies at the midlength of
the oesophagus. The excretory pore, lying shortly behind the nerve ring, is very
distinct, as its duct is strongly cuticularised.
The ovaries are opposed, The vulva lies one-fifth to one-seventh of the body
from the posterior end, The ripest eggs, containing morulae, are 70 by 40 p.
The cuticle aroutid the vulva is slightly inflated, forming a folded belt in this
region.
The male bursa is tightly folded in all specimens; to examine the rays, shown
in fig. 2, it was necessary to tear part of the bursa. The exact form of the dorsal
ray varies slightly, the third bifurcation in some cases taking place nearer to the
second than shown in fig. 2. The spicules are relatively simple for a Tricho-
strongyle worm; the head is provided with a ventral knob; there is a slight swell-
ing at the midlength, and from this projects a dorsal spite. The main body of
the spicule ends in two small points. The overall length of the spicule is 0-13 -
0-14 mm., and that of the simple plate-like gubernaculum 40-48, There is a
pair of rather elongate subventral prebursal papillae.
This, as far as can be ascertained, is only the second record of a Tricho-
strongyle worm from a fish. The first is Agamonema scorpaenae cirrhosae Mac-
Callum 1921, renamed by Travassos (1937, 410) Trichostrongylus (s.1.) ses.
Of this species, Travassos (loc. cit.) states that it was possibly an accidental
occurrence. In the present case, this seems a most unlikely hypothesis. The worms
are present in considerable numbers, and in a perfect state of preservation, and
as they were taken from the spiral yalve of the host, it is not conceivable that
they were ingested with bait. The life history of this Trichostrongyle is, pre-
* University of Adelaide,
Traua. Roy Soc. 5. Alist., 77, July, 1954
163
sumably, similar to that of related genera in ruminants. The infective larvae might
be expected to inhabit the top layer of mud or sand on the sea floor, or to be on
sea weeds growing there. Emissola antarctica is largely a browsing shark.
_ I. clelandi differs from T. maci (s.1.) in the shape of the head, the position
of the vulva, and in the disposition of the lateral and ventral bursal rays; it is
not possible to compare the dorsal ray as this was not figured by MacCallum,
The shape of the head is different from that of any Trichostrongyle of which
the description is available to the author. In the form of the bursa and spicule
it is perhaps closest to Oswaldocruzia Trav., differing from this genus in the
shape of the head. A new genus is proposed, with the following diagnosis :
Ichthyostrongylus n-g.
Trichostrongylidae: head bulbous with three distinct and strongly cuticular-
ised lips; buccal capsule absent. Ovaries opposite; vulva posterior but not close
to anus. Spicule simple, with dorsal spine; gubernaculum present. Bursa symmetri-
cal, dorsal lobe developed; externodorsal rays arising separately from dorsal, and
lying in lateral lobes; dorsal ray dividing three times, forming six branches,
Type species. I. clelandi n.sp. from Emtissola antarctica, Encounter Bay, South
Australia.
The specific name is for the collector of the worms, Dr. J. B. Cleland, in
gratitude for his help.
OQ.) mm.
Fig. 1, head; Fig. 2, spicules and part of bursa; Fig. 3, ventral view of spicules;;
Fig. 4, tail of female; Fig. 5, region of vulva. Fig. 2 and 3 to same scale.
LITERATURE
MAGNE m4 A, 1921 Studies in Helminthology. Zoopathologica, 1, (6),
Travassos, L. 1937 Rivisao da familia Trichostrongylidae Leiper 1912, Monogr.
Inst. Oswaldo Cruz., No, 1, 1-512
—_
PARORCHIS ACANTHUS VAR. AUSTRALITS, N. VAR., WITH AN
ACCOUNT OF THE LIFE CYCLE IN SOUTH AUSTRALIA
BY L. MADELINE ANGEL
Summary
. A review of the history of Parorchis acanthus Nicoll and its synonymy is given.
Stage in the life cycle of P. acanthus var. australis n. var. are described.
. The variety differs from the type species mainly in the absence of an excretory tube in the
tail of the cercaria. Other relatively minor differences are noted.
. The cercaria has been found as a natural infection in South Australia in Bembicium auratum
(Quoy and Gaimard), B. melanostoma (Gmelin), B. nanum (Lamarck), and Emozamia
flindersi (Adams and Angas). It encysts on the surface of hard objects, including a number
of invertebrate animals, which are probably only accidental hosts.
. Cysts were fed to seagulls, Larus novae-hollandiae Stephens, and adult trematodes were
recovered. The adult was found as a natural infection in 1 of 25 seagulls examined by the
late Professor Harvey Johnston.
. The incidence of infection in the different snail hosts is given. This was highest in
Bembicium auratum (up to 66%). The percentage of infection as determined from those
snails which gave off cercariae when isolated, is much less than the true percentage,
determined by crushing the snails.
164
PARORCHIS ACANTHUS VAR, AUSTRALIS, N, VAR., WITH
AN ACCOUNT OF THE LIFE CYCLE IN SOUTH AUSTRALIA
By L. Mavetine Ancet. *
[Read 10 September 1953]
SUMMARY
A review of the history of Parorchis acanthus Nicoll and its synonymy is given,
Stages in the life cycle of P. acanthus var, australis 1. var. are described,
The variety differs from the type species mainly in the absence of an excrétory tube in
the tail of the cercaria, Other relatively minor differences are noted,
The cercaria has been found as a natural infection in South Australia in Bembiciuim
auraitum (Quoy and Gaimard), B. melaonostoma (Gmelin), B. nanum (Lamarck), and
Emasomia findersi (Adams and Angas). It encysts on the surface of hard objects, incluid-
ing a number of invertebrate animals, which are probably only accidental hosts.
Cysts. were fed to seagulls, Larus novae-hollandiae Stephens, and adult trematodes were
recovered. The adult was found as a natural infection in 1 of 25 seagulls examined
by the fate Professor Harvey Johnston. ,
6, The incidence of infection in the different snail hosts is given, ‘This was highest in
Bembicium auratum (up to 669%). The percentage of infection as determined from those
snails which gaye off cercariae when isolated, is much less than the true percentage,
determined by crushing the snails. :
= NS
te
The type as well as other representatives of the adult and larval stages have
been deposited in the South Australian Museum,
This work was commenced with the late Professor Harvey Johnston, to
whom I am greatly indebted for his unfailing help. I wish to acknowledge with
gratitude the help given by Mrs. H. Anderson, who supplied the figures of the
infection of snails trom the Patawalonga Creek determined by crushing, as well
as other details. Acknowledgment is also made of help given by the staff of the
South Australian Musetim in identifying intermediate hosts, and by members of
this department in collecting material, as well as in other ways,
INTRODUCTION
In 1907 and 1912. Lebour described Cercaria purpura sp. ing. from Purpura
lopiius in Great Britain, Later (1914) she identified it, on the grounds of mor-
phological similarity, as FParorchis acanthus Nicoll 1907. P. acanthus was
originally described as Zeugorchts acanthus (Nicoll 1906) and later rehamned and
redescribed (Nicoll 1907 a, 1907 b), Zeugorchis heing pre-occupied.
Stunkard and Shaw (1931) described Cercaria sensifera from Urosalpinx
cinereus from Waood’s Hole, Massachusetts, stating that it might be identical
with Cercaria purpurae, They also suggested that C. sensifera might be the larval
stage of Parorchis avitus Linton 1914. (Linton’s type material, from the herring
gull, Larus argentatus, was from the same region.) Linton (1928) had discussed
the possibility of synonymy of Parorchis avitus with P. acanthus, but did not
change his classification. In 1932 Stunkard and Cable recorded Thais (Purpura)
lapillus as another host of Cercaria sensifera. They had fed cysts of this form
to guinea pigs, white rats, mice and two species of tern, and obtained immature
flukes, which they identified as Parorchis avitus, only from the terns, Sterna
hiryndo and S. dougalli, The diagnosis was confirmed by Linton-
Cable and Martin (1935), who obtained mature adults after feeding meta-
* Department of Zoology, University of Adelaide, South Australia.
Trans. Roy Soc. S. Aust. 77, July, 1954
165
cercariae of Cércaria sensifera to herring gulls, concluded that Parorchis avitus
was invalid, and was a synonym of P. acanthus. Cercaria sensifera was thus
synonymous with C, purpurae.
Rees (1937) from other evidence, independently suggested that C. sensifera
and C. purpurae were identical and that the names of the adults were synonymous.
This suggestion was supported by a later examination of the adult parasites
(Rees 1939). Dawes (1946) listed Parorchis avitus as a synonym of P. acanthus.
j UB
o-1mm
Fig. 1
Parorchis acanthus var. ausjralis. The cercaria.
Fig. 1, stained and mounted; excretory bladder and pore from living specimen.
Position of dorsal collar spies indicated. 2, anterior end of body to show narrow-
ing of cuticle. 3, 4, tail; 3, living, contracted; 4, fixed, elongated.
Fig, 1, 4 to same scale; 2, sketch; 3, sketch. ep, excretory pore,
Maxon and Pequegnat (1949) described a cercaria (Echinostome IT) from
Upper Newport Bay, California, which was probably identical with that described
by Hunter (1943) as the cercaria of P, avitus (Cercaria sensifera Stunkard and
Shaw 1931). Reish (1950) recorded Parorchis acanthus from Larus occidentalis
from Newport, Oregon. Rediae and cercariae which agreed with the descriptions
given by Stunkard and Cable (1932) for those of Parorchis avitus
(= P, acanthus) were found in Thais emarginata from this vicinity. Encysted
cercariae were fed to one golden hamster and one mallard duck, but did not
develop in either animal.
166
The present investigation was’ initiated when megalurous cercariae were found
in a marine tank containing Bembicium auratum (Quoy and Gaimard)} (Anderson,
personal communication). These cercariae, which were similar to Cercoria pur-
furne Lebour as described by Rees (1937), were later found to be a common
parasite of the snails, The cercariae encysted on any hard surface. Cysts, collected
from glass dishes in which the host snails were isolated, were fed to seagulls,
from which adults of a species of Parorchis were recovered later, In al] stages
of the life cycle the only significant difference between the Australian form and
P, aganthus Nicoll was in the absence of an excretory tube in the cercarial tail,
but it is thought that this difference is sufficient to warrant placing the Australian
specimens in a distinct sub-species, for which the name Parorchis acanthus var.
australis is proposed. A description of the life history of this form follows.
THE EGG AND MIRACIDIUM
Eggs were dissected from the adult, fixed in formalin and cleared in glycer-
ine; the range of the larger ones was from 94 by 56y to 98 hy 64, (Rees
(1940) found that ripe eggs were considerably larger than those in which the
tnitacidium was freely formed; her measurements were made in sea-water, the
ripe eggs being 130 by 68, and the young ones 90 by 35). The eggs did not
appear to hatch freely, but those examined had been obtained from a specimen
kept in the refrigerator for two or three days in normal saline, and ynder these
samewhat unnatural conditions the eggs may have been extruded before they
were fully mature. One miracidium hatched quickly when it was placed in sea-
water under a coverslip, and this was the only one which remained alive under
a coverslip for any length of time; it died immediately when neutral red was
added. In this one specimen all the main features described by Rees (1940)
could be seen, te, the rostrum, penetration glands and gland pores, the united
kidney-shaped eyes, the brain region, the apical gland, the lateral processes (which
help the miracidiumi in its escape from the shell}, and the contained redia lying
at the posterior end of the résting miracidium. The artangement of the epithelial
cells was not exantined, but the subepithelial layer of cells was apparent, and
the arrangement of the cilia also corresponded to Rees’ description, No flame cells
were seen, but parts of the excretory tubes were visible in the same positions as
figured by Rees.
THE REDIAE
The rediae were white and opaque. The small (first generation) rediae varied
from 0-34 by 0°052 mm, to 0-63 by 0-060 mm, in ten formalinised specimens,
the average being 0465 by 0-060 mm. They agreed with the description givert
by Stunkard and Shaw (1931) in having a muscular, lip-like snout in front of
the “oral sucker”; also the posterior tip of the body was protruded in a tail-like
or foot-like protuberance, used, like the foot processes, in locomotion. The birth-
pore, as in Rees’ material (1937, p, 66) was thick-lipped, conspicuous and pro-
trusible, Rees (1937, 1940) recorded that first generation rediae did not produce
cercariae, but gave rise to twenty or more daughter rediae. Stunkard and Shaw
(1931) stated that small rediae may contain one or more fully formed cereariae.
No cercariae were observed in the small rediae of the South Australian material.
The large (second generation) tediae varied from 1:39 by 0'255 mm. to
1:92 by 0:345 mm, in ten formaiinised specimens; the average size was 1°67 by
0295 mm. Stunkard and Shaw (1931) stated that rediae increased toa length of
2-1 mm. and a width of 0°4 mm. (presumably in living material), Rees (1937),
for living material, gave the measurement of a fully grown redia as 3°5 mm. by
147
0:46 mm. and of a young redia a§ 0-58 by 0-08 mm. It will be noticed that the
size Is great than that of the Australian form. (Fixation of the rediae in forma-
lin probably does not produce a very great change in size.)
THE CERCARIA
The cercaria was vety similar (anatomically, in habit, and in reaction to
intra-vitam stains) to that described by Stuttkard and Shaw (1931) and Rees
(1937), with the exception that an excretory system could not be demonstrated in
the tail. Lebour (1912) recorded that the excretory system was not continued
into the tail of Cercaria purpurae, but Stunkard and Shaw (1931) found this
feature in Cercaria sensifera, and this supposed difference was one of the
characters by which Stunkard and Cable (1932) separated Parorchis acanthus
and P. azitus. However, in 1937 Rees noted the excretory tube in the tail of
Cercaria purpurae. In 1953 (personal communication) Dr. Rees stated that the
excretory tube in the tail was difficult to find in Parerchis aconthus; that other
workers at Aberystwyth had experienced the same difficulty, but that its presence
had been confirmed on several occasions.
No sign of an excretory tube in the tail was seen in several hundred cer-
cariae examined over a period of eighteen months, Basic fuchsin did not make
the details uf the excretory system any clearer, as it does with most fresh-water
ecercariae; and horse serum, which is also very useful with most forms, caused
the cercariae to encyst immediately, even in very dilute solution, However, the
excretory system, with an excretory pore opening from the bladder to the ventral
body surface, was clearly seen, This latter feature has not been mentioned by
other authors, It would tot be surprising, perhaps, if an excretory pore in the
body should be present at the same time as the two pores in the tail, but failure
to demonstrate the latter over such a long period cannot be ignored.
The number of collar spines was difficult to deterntine. It was at least 60,
and in one specimen possibly 66; there were 10-11 on each side ventrally.
Stunkard and Shaw (1931) recorded 44-48 spines on the dorsal surface and 10
on each side ventrally. Rees (1937) gave the total number as 64.
The ratio of oral sucker to acetabulum varied from 2:3 to 3:4 in living
specimens.
Immediately anterior to the first row of body spines the cuticle was thinner
for a short distance, after which it widened again in the region of the anterior
papillae (fig: 1, 2). This thinning of the cuticle has not been described for
Pararchis acanthus, 1 was noticeable in greatly compressed specimens, as well
as in specimens stained with neutral red which were still elongating and contract-
ing. The region of thinner cuticle was very much paler than the rest of the cuticle.
The cuticular layer, which probably consists of cuticle plus cystogenous material,
is 8-9 wide in living, flattened specimens; it stains a uniform, carmine colour
with neutral red.
The primordia of the reproductive system are obvious in stained specimens,
The only feature in which the tail differed from the descriptions given by
Stunkard and Shaw (1931, p. 265) and Rees (1937, p, 67), apart from the
absence of an excretory tube, was that it was marked with very fine annuli on
which were arranged minute spots, which might have been granules or tiny spines
(fig. 3). These were variable in size, but even the largest were extremely small.
The annuli were seen well after treatment with orange G; there were about six
across the diameter of one of the large vacuolated cells of which the proximal
part of the tail is composed. Stunkard and Shaw ( 1931) and Rees (1937)
described the cuticle of the tail as being thin and smooth,
The following measurements were made on twenty specimens fixed by add-
168
ing an equal volume of boiling 10% formalin to the water containing the cer-
cariae ‘body length 370-670 2 (average 450 4); greatest width 130-225» (average
170 «); width at “waist” (constriction of body immediately postefior to acetabu-
Jum) 105-180 p (average 130») ; tail length 265-595 » (average 450 ») ; tail width
45-60 (average 52»).
Rees (1937) found the body length to be 1:00 mm, expanded and 0-36 mm.
cantracted ; breadth 0-09 mm, expanded, 0°35 mm. contracted, The number of
specimens measured was not mentioned, nor was the method of fixation, but
elsewhere in the paper it was stated that rediae and cercariae were examined
in the living state. Presumably the measurements represent the upper and lower
range for living cercariac examined under a coverslip, and are thus not to be
compared with measurements of specimens fixed in formalin.
Stunkard and Shaw (1931) stated that fixed and stained specimens measured
0°21-0°47 mm. in length and 0°14-0:26 mm. in width; the jails varied from
0:12 to 0°26 mm. in length. The average body size of seven stained and mounted
careabige of Perorciis acanthus yar, australis was 520 by 160», and for the tail,
615 by 504.
Too much importance should not be attached to differences in measurements
of cercariae, especially when the state of preservation of the matertal is variable-
THE CYST
Stunkard and Cable (1932) concluded that the cercariae would encyst on
almost anything with which they came in contact. P. acanthus var. australis
encysts readily on glassware, Animals which were placed in contact with cercariae
and on which cysts were formed were :—the cirripede Alminius modestus (mainly
on the appendages); the isopods H.xosphacroma gigas and Trichoniscus sp.
(mostly on the joints of the legs); insect larvae of the Acalyptrate group (the
body surface of these became so thickly encrusted with cysts that the insects,
though still alive, could barely move); the crab Helice haswellianus (the shell of
the body and legs was heavily encrusted); and the lamellibranch Amphidesma
angusta (on the shell, more concentrated on the free edges, and scattered on the
free edge of the mantle). The lamellibranch Anapella pinguis did not become
infected ; this was buried in the sand, but the siphons were, of course, protruding.
Rees (1948, p. 234) noted that cercariae of P. acanthus normally encyst round the
aperture of the shell and on exposed parts of the body of the host, Nucella
(Purpura) lapiilus. Cysts of the Australian form were sometimes found on the
operculum of Bembiciwn axratum (im one case thirty cysts were present on
the outer surface and the same number near the edge of the inner surface of the
operculum); and occasionally om the inner surface of the shell, but they were
never observed round the aperture, and rarely on the outer sarface of the shell,
Cyst formation follows the same course as that reported by Rees (1937).
Stunkard and Cable (1932) found that most of the cercariae encysted within
48 hours of leaving the snail. The Australian cercatiae encyst within a few hours.
The cercariae encyst immediately when exposed to unfavowtrable conditions
(such as too strong solutions of intra-vital stains), as was observed by Stunkard
and Shaw (1931).
The average measurement of 20 cysts from which the rough outer coat had
been removed was 200 by 1804. Rees gave the cyst diameter as 0-295 mm., of
which the outer layer was 0-045 mm. thick; the cyst enclosed only by the inner
coat would thus be 0-205 mm. in diameter. Lebour and Elmhirst ( 1922), how-
ever, described the cyst as “roundish oval,” which is consistent with the shape oi
the Australian forni.
169
THE METACERCARIA ,
Metacereariae were recovered by breaking the cyst wall with needles. This
often resulted in damage to the metacercaria, but some were recovered intact.
The following measurements apply to specimens mounted in canada balsam.
The length of four specimens averaged 405 (range 300-470). The average
diameter of oral sucker was 65 p, and of ventral sucker 82% (in three specimens),
The metacercaria most favourably mounted for measuring was 400 by 255», with
the oral sucker 68 w (long axis) by 75», and the ventral sucker 87 » in diameter-
Lebour and Elmhirst (1922) gave the measurements (apparently in living speci-
mens) of the oral sucker as 0-08 mm. and of the ventral sucker 0°10-0'14 mm,
The primordia of the genital system were slightly more obvious than in the
cercaria; they consisted of two, small, darkly-staining masses of tissue. One,
circular, or oval in the transverse plane, and situated immediately anterior to the
acetabulum and posterior to the intestinal bifurcation, marked the position of the
genital atrium and its associated structures. The other, slightly larger, circular
or elongated in the longitudinal axis, and situated midway between the acetabulum
and the posterior border of the body, was no doubt the primordium af the gonads
and thete docts.
The excretory formula was the same as for the cercaria, that is
2[(3-+3+3) + (3+3+ 3) I].
THE ADULT
An accurate assessment of the number of collar spines was not possible in
living specimens, and many of them disappeared in the preparation of permanent
mounts. Nicol! (1907 b, p. 346) recorded the number as “about 60.” He men-
tioned that immersion in a weak acid solution for even a short time caused the
spines to disappear wholly or in great part, and suggested this as the reason for
their absence in Distomuy pittactum Brawn, which he transferred to the genus
Parorchis, Stunkard and Cable (1932, p. 333) gave the number of collar spines
a “sbout 68."" Other authors have not recorded the number of spines for the
adult.
Table I gives measurements of adult and juvenile forms, with the measure-
ments given by Nicoli (1907 b) and Linton (1914) for comparison.
Ovaries and testes were measured in three specimens mounted in balsam,
in which all measurements were slightly less than when the flukes were meashred
in cedarwood oil.
The ovary was rotinded or oval in outline; measurements were:—(1) 2404,
(2) 290, in diameter, (3) 240 (long axis) by 255. (Rees (1939) described
the ovary as transversely oval, measuring 0-29 by 0°33 mm.) The margin of the
testes was lobed; they were sometimes elongated in the longitudinal axis, and
sometimes one was situated slightly in advance of the other. In a specimen
5-2 mm. long the right testis was 525 by 450 and the left 560 hy 490 In the
other specimens the testes were larger, but had the appearance of being more
compressed.
EXPERIMENTAL INFECTIONS
Four seagulls (Larus notae-hollandiac) and a white mouse were fed with
cysts. The mouse did not become infected, but adult Parorchis were obtained from
two of the seagulls.
Two seaguils caught at Tailem Bend“) on the River Murray were kept in
re WO SESE NSO ee ee ee ee ee ee ES eee
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ported by the fact that certain birds which can be identified by some deformity have been seen
im the same place for several weeks at a time. Thus birds caught at Tailem Bend, although
they probably return to a roosting ground near Lake Alexandrina (an inlet of the sea) each
hight, are, in all probability, frequenters of the river and its shores, and are eoisidered unhikely
to feed in places where Pembicitin spp, occur.
170
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captivity for several weeks before the experiment was commenced_ The first was
given two insect (Aecalyptrate) larvae which were heavily encrusted with cysts;
it was killed 32 days later. No Parorchis were found, though four heterophyids
and a blood fluke were recovered from the intestine. The second gull was fed
with a large number of cysts scraped from the sides of the tank in which the
snails were kept; they were given 46, 38, 31 and 17 days before the bird was
killed, when five mature and nineteen immature specimens of Parerchis were
recovered. Of these, four adults and twelve juveniles were in the cloaca, and
the remainder in the rectum. When the bird was killed, a period of 10-11 weeks
had elapsed since it could have acquired infection under natural conditions; it
therefore seems almost certain thar the juvenile, if mot the adult, trematodes
had developed from the cysts fed to the birds. Faeces from the birds obtained
1, 7, 22 and 29 days after commencement of the experiment were free of eggs.
Of four seagulls captured at St. Kilda beach (a few miles north of
Adelaide), two were killed immediately; no Parorchis were recovered, The other
two were given meat in which cysts had been packed; neither of the birds was
interested in food, and it is doubtful how many of the cysts were ingested, The
first gull died’ in two days; it was negative for Parorchis, The second died eight
days after exposure to infection, and one medium-sized, egg~bearing specimen of
Pororchis was found in the duodenum (length 4°7 mm.). If this specimen had
developed as a result of the experimental feeding (its Iocation in the duodenum
and the fact that the three other birds from the same locality had not harboured
the infection suggesting this) the trematode must have become egg-bearing in
eight days, whereas nineteen specimens from the other experimental host (from
Tailem Bend) were still immature at least seventeen days after they had been
ingested as cysts. Stunkard and Cable (1932) found that specimens recovered
fifteen days after infestation were not sexually mature.
Two attempts to infect Bembicium spp. with miracidia failed. Ta the first
about 25 Parerchis eggs were put in a small tank with three Bembictum nanwm ;
and in the second, seagull faeces collected from the Patawalonga mud-
flats were used, with eight B, auratum.
The experiments were not repeated, because of the shortage of adult trema-
todes from which to obtain eggs, |
INCIDENCE OF INFECTION IN SNAILS
The cercaria of Parorchis acanthus var. australis was first identified from
Bembicium auratim (Quoy and Gainmvard) collected from a tidal mud-flat at the
mouth of the Patawalonga Creek, Glenelg, South Australia; a high percentage of
the snails was found to be infected,‘?)? The number of infections detected by isolat-
ing each snail in a 3” x 1” tube over a twenty-four hour period was considerably
less than the true number as determined by crushing the snails, For instance, from
April to September 1951 (inclusive}, of 582 B. auratwm isolated, 64 (11%)
gave off cercariae, while in the same period, of 1,072 snails crushed, 633 (59% )
were infected. The true percentage of infections must have beer even higher,
since at least some of the snails crushed were from groups which had been
isolated, and from which those snails actually giving off cercariae had been
removed. In collections made in October-November 1951, and in May-September
1952, infections identified by crushing snails which had not been isolated pre-
viously were 1,159 of 1,758 (66%).
@) Several other types of cercarial infection were found in Rembicium spp. but
Parorchis infections were readily distinguished by the large, characteristic rediac.
172
The high percentage of infection of the snail host seems somewhat surprising,
in view of the fact that in 1939, only one of eight seagulls from this region was
infected with Parorchis acanthus. However, silting up of the stream, which has
occurred rapidly since 1937, has no daubt had a strong influence on the ecology
of the region, and it may well be that in 1939 Bembicium auratum was not
a common member of the fauna as it is today.
These cercariae have also been found in B, nanum (Lamarck) and
B. selanostoma (Gmelin), but the percentage of infection is much less in
both species than in B. awratum. It is, however, impossible to draw any conclusions
as to any host. preference shown by the parasite, because of the different habitats
favoured by the three species of host, In the Patawalonga mud flats B, anratun
is to be found at low tide in small pools where the chances of infection are
high; at low tide B. melunostoma occupies more exposed positions on small rocks,
mangroves, etc.; B. nanum lives on rocks which are exposed at low tide
and subjected to strong wave action at high tide.
Parorchis cercariae wete found by isolation in 1 of 360, and by crushing
in 10 of 431 Bembicivm nonum collected along the coast from Marino
Rocks to Encounter Bay, South Australia, and im two of three B. nemum
from the Patawalonga Creck (where infections were so common in B. auratum).
The infection was not found by isolating over a hundred 8. nonum
collected in February 1952 along the coast of Yorke Peninsula; nor by
crushing 50 of the snails collected south of Corny Point (Yorke Peninsula) and
15 from Salt Creek (Yorke Peninsula) in February 1953.
In October 1952, 11 of 434 B, melonestoma from Port River and Outer
Harbour were found to be infected by crushing, In February 1953, of 450
B. melanostoma collected on Yorke Peninsula, five were infected. These five
infected snails were from a collection of 50 taken at Port Wakefield, where con-
ditions for infection must have been favourable; the remaining 400 were collected
from Pine Point, Stansbury, Salt Creek, Edithburgh and Corny Point.
Infected snails will remain alive and continue to give off cetcariae for some
time under laboratory conditions. Eighteen B. auretum kept under observation
survived 14, 30, 39, 49 (seven snails), 55 (three snails), 61, 88, 91 and 95.days
respectively, Anderson (1953) kept 20 snails out of water for three months; of
the six which survived, five contained rediae.
Other gastropods which were examined during this investigation were:
98 Melaraphe unifasciata and 42 Austrocochlea concamerata from Hallett’s Cove;
22 A. torrt trom Marino Rocks, and a ntimber of Salinatar fragtlis and S. solida
from the Patawalonga. None of these gave off cercariae when isolated. Snails
from Yorke Peninsula were examined after crushing: 50 Neothats texttliose
Thaididae) from an ocean beach south of Corny Point were uninfected, but
two of 13 Emazamte flindersi (Murtcidae) from Port Vincent, and two of 7l
of a same host irom Pine Point were infected with Perorckis acanthus var.
australis,
DISTRIBUTION AND HOSTS OF PARORCHIS ACANTHUS
ADULT
P. acanthus has been recorded from the herring gull (Larus argentatus)
from Great Britain and from the east coast of North America; the common
gull (L. canus) from Scotland; the western guli (ZL, occtdentelis) from the west
coast of North America: the flamingo (Phoeniropterus ruber) from Cuba
(Vigueras, 1941}; and, as a restilt of experimental feeding, from terns (Sterna
hirundo and S, dowgalit) from Massachusetts.
Parorchis acanthus var, australis is now recorded from Soyth Australia.
The adult was found by the late Professor Harvey Johnston in only one of 25
173
seagulls (Larus novae-hollandiae) examined between 1937 and 1951. This positive
host was one of eight gulls caught at Glenelg in 1939; it contained two adults
and one immature specimen of the Auke. The remaining negative birds were from
other parts of St. Vincent’s Gulf (5), American River, Kangaroo Island (1), and
River Murray (11).
CERCARIA ;
The cetcaria has been recorded from Nucella lapillus and Urosalpinx cinereus
irom Great Britain and Massachusetts, U,S.A., and from Thais emarginata from
Oregon. Cerithidea californica trom California also harbours tediae and cer-
cariae which are very probably the larval stages of Pororchis acanthus.
The known South Australian molluscan hosts of P. acanthus var. australis
are Bembicium curatum, B. melanostoma, B. narum and Emozamia flindersi.
LITERATURE
Anperson, H. 1953 Studies on the biology of three species of Bembicium and
their trematode parasites. (M.Sc. thesis; not yet published ).
Cante, R, M., and Martin, W. E. 1935 Parorchis avitus (Linton, 1914), a
synonym of P. acanthus (Nicoll, 1906), Jour. Parasit., 21, (6), 436-437
Dawes, B. 1946 The Trematoda. University Press, Cambridge. 644 pp.
Hunter, W. S. 1943 Studies on cercariae of the common mud-flat snail,
Cerithidea californica, Unptiblished doctor's dissertation. U.C.L.A..
129 pp. (not seen)
Lesour, M. V. 1907 On three mollusk-infesting trematodes. Ann. and Mag.
Nat. Hist., 19, (7), 102-106
Lenour, M. V. 1912 A review of the British marine cercariae, Parasitol,
4, (4), 416-456
Lenour, M. V. 1914 Some larval trematodes from Millport. Parasitol., 7,
(1), 1-11
Lepour, M. V., and Ermurrest, R. 1922 A contribution towards the life his-
tory of Parorchis acanthus Nicoll, a trematode in the herring gull, Jour.
Mar. Biol. Ass. U-K., N.S., 12, 829-832
Linton, E. i Notes ona viviparous distome, Proc. U.S, Nat, Mus., 46,
551-
Lixtox, E. 1928 Notes on trematode parasites of birds, Proc. U.S, Nat. Mus.,
73, 1-36
Maxon, M. G., and Peourcnat, W. E. 1949 Cercariae from Upper Newport
Bay. Jour, Ent. and Zool., 41, (1), 30-55
Nicoun, W. 1906 Zeugorchis ecanthus, gen. and sp, n. Ann. and Mag. Nat.
Hist., 17, (7), 519-522
Nreont., W. 1907a Parerchis, n, nom. for Zeugorchis, Nicoll, 1906. Ann. and
Mag. Nat. Hist., 19, (7), 128
Nicout, W. 1907b Parorchis acanthus, the type of a new genus of trematodes.
Quart, Jour. Mier. Sci., N.S., 51, 345-355
Rees, G. 1937 The anatomy and encysttnent of Cercaria purpurae Lebour,
1911. Proce, Zool., Lond. 107, Series B, Pt. 1, 65-73
Rees, G, 1939 Studies on the germ cell cycle of the digenetic trematade,
Parorchis acanthus Nicoll, Pt. 1, Parasito!., 31, (4), 417-433
Rees, G. 1940 Studies on the germ cell cycle of the digenetic trematode,
Parorchis acanthus Nicoll, Pt. 1, Parasitol., 32, (4), 372-391
Rees, G. 1948 <A study on the effect of light, temperature and salinity on the
emergence of Cercaria purpurae Lebour from Nucella tapillus (L-)
Reis, D. J. 1950 New host and distribution records for two trematodes from
the western gull. Jour, Parasit., 36, (1), 84
174
SrunxKarp, H. W., and SHaw, C, R. 1931 The effect of dilution of sea water
on the activity and longevity of certain marine cercariae, with descrip-
tions of two new species. Biol. Bull., 61, 242-271
StunKarp, H. W., and Casrz, R. M. 1932 The life history of Parorchis avitus
(Linton), a trematode from the cloaca of the gull. Biol. Bull., 62, 328-338
Vicurras, I. P. 1941 Nota sobre varios vermes encontrados en el “flamenco”
(Phoenicopterus ruber),
AN ACCOUNT OF THE NGALIA INITIATION CEREMONIES AT
YUENDUMU, CENTRAL AUSTRALIA, JANUARY 1953
BY IAN V. HANSENL
Summary
This paper records the ceremonial dances and other rites associated with the initiation of young
men of the aboriginal Ngalia tribe of the desert country north-west of Alice Springs, Central
Australia. Illustrations include a plan of the corroboree-ground, details of body markings, and of
native totems.
175
AN ACCOUNT OF THE NGALIA INITIATION CEREMONIES AT
YUENDUMU, CENTRAL AUSTRALIA, JANUARY 1953
By lan V. Hansen
[Read 12 November 1953]
SUMMARY
This paper records the ceremonial dances atid other sites associated with the
initiation of young imen of the aboriginal Ngalia tribe of the desert country forth-
west of Alice Springs, Central Australia. Illustrations include a plan of the corroboret-
ground, details of body markings, and of native totems.
At dusk, Saturday 24 January 1953, a party of 114 aborigines from the
Ilaast Bluff area ptanced into the camp of the Ngalia tribe on the Yuendumu
Native Settlement (in the western part of the Northern Territory, lat. 22° S.,
long. 130° E,) to receive a welcome from the local tribesmen. The visitors were
principally Pintubi and Kukatja people, with some Aranda and Pitjandjara, and
the occasion was the initiation of two Ngalia boys. Both visitors and hosts were
similarly decorated with paint; a black band around the chest, edged with white
bird-down, and the same marking on the upper arms. Thrust into the hair-binding
were wooden “feathers,” made from mulga twigs with long, fine shavings giving
the decoration a bottle-brush effect. Two short “feathers” were worn on the
forehead, and two longer ones (12 to 14 inches) fanned out behind the head.
After receiving damper and water from the Ngalia, the visitors bunched them-
selves closely together, and with spears aloft moved through the scrab to their
camp-site. They walked at an easy pace, at interyals uttering a high-pitched cry
of three notes, the second nearly an octave above the fitst and third. Frequently
this call was broken by a series of loud huffs from the group, which were speeded
up, causing the men to quicken their pace to a trot to keep in time; another
triplet of whoops, and the party dropped back to a_wille.
I had made contact previously with the Haast Bluff natives, and after some
discussion with the Ngalia. “corraboree-boss” they invited me to their camp for
the duration of the ceremonies.
Next morning, at about 5.30 a.m., the men began adorning themselves. The
black and white markings of the welcome were retained, and supplemented with
rather clumsy finger-painted lines of red-ochre. When all were ready the men
left the women, and with the whooping and puffing that was to accompany all
their comings and goings, made for the ceremonial ground (the dancing area),
situated in a mulga patch some half-mile from the camp (fig. 6}. (Baldwin
Spencer 1914, 137.)
Seated in four circles were the singers, beating the ground with sticks, and
chanting. The rhythm was intricately counter-pointed from group to group, and
the chant itself syncopated from time to time with whoops from the song-leader.
During the chanting, groups ef men punctured their old sub-incision wounds
with mulga twigs, and squeezed the blood down the inside of their legs. The
singing ceased, and the first group shuffled across the ground in front of the
novices, who had been seated in front of the singers, So as to display their flow
of blood, the participants bent their knees out, and held their hands at shoulder
level, meanwhile making a buzzing noise through their teeth. (The blood from
the penises of the old men seemed to come more readily than from the younger
members of the party.) This letting of blood continued until every man had
176
played his part: it was accompanied by what appeared to be considerable flippant
talk fromthe others.
During this ceremony the novices were taken by a group of a dozen or
so men, and thrown several times high into the air (cp. Spencer and Gillen 1904,
337). They were then returned to their places, to watch the continued blood-
letting.
Fig. 1 and 2, body decorations; Fig, 3, leafed-pole dancer;
Fig. 4, painted tjurunga; Fig. 5, sacred wanigi.
After nearly fiye hours of watching, the natives returned to camp, and “sat
down” for the remainder of the day. The Haast Bluff people had had an
unpleasant dry journey to Yuendumu, and rested until nightfall, when they sang,
in their camp, till the small hours of the morning.
177
Monday morning saw no activity, but by four in the afternoon the men
were back at the corroboree ground and. preparing for their dances. The per-
formers dressed themselves in two groups, one on each side of the runway.
The blood used in decoration was taken, in the one case from the penis, and, in
the other from the forearm, and sprinkled onto the shoulders of the dancers.
The painting on the bodies was still black and white, with red ochre,
The first dance consisted of a snake ceremony. Twelve young men, hands
on hips of the man in front, formed a serpentine line, and twisted violently from
side to side in time with the chanting of the others. The “head” of the serpent
wore a head-dress of blood-stained kangaroo grass, and held a boomerang behind
his neck; after twisting the line oi men around to face the novices, he gaye a
whoop, and the actors dispersed.
More chanting prefaced the “Kangatoo and Euro” {the latter a small variety
ot kangaroo, living in rocky areas) dance. The “kangaroo,” with a magnificent
“tail” of bond grass, spluttered (a noise made with the tongue and lips) his way
onto the ground, where twenty young men lay spluttering. The “kangaroo” hopped
in) among them, and drew them with him up the runway. He turned to face the
audience, and each of the actors crawled between his legs, hopping to a point just
in front of the novices, where they began to pile one on top of another. With
much noise, this “stacks-on-the-mill” continued until the mound was complete,
and the “kangaroo,” with a leap and a shout, landed on the top. More shouling
and hilarity, and the bodies collapsed in a cloud of dust,
When the runway had been cleared, two holes were dug, about twelve inches
deep, and into these holes a solitary actor placed his legs. He was decorated with
the Black and white band, but wore a bloodstained kangaroo grass head-dress.
In his mouth was a clump of grass similarly stained, and in each hand he held
a bunch of long grass, Ile fixed his eves steadfastly on one of the novices and
began to sway to the rhythm of the chant, swinging his hands together from
side to side. Suddenly the singing stopped, and the actor drew himself up [rom
his crouching position, and quivered, to the accompaniment of two clicking
boomerangs. Then the chant recommenced, Slowly the actor stepped fram the
holes, and, hopping mysteriously, swaying with the music, moved slowly toward
the boy, still with fixed eye, and stopping only to quiver. When he was all but
upon him, his novice took a stick and threw it on the ground in front of him.
Without a sound the actor broke off. This was repeated by another solo dancer
for the other boy, and then two actors went through the same performance, only
that they approached the novices throtigh each other’s legs.
Further chanting followed, and the men made their way back to camp
for food.
After “tea-time” (ie., about 6-7 p.m.) the women were allowed on the
corroboree ground, to dance to the men’s music. Their movements were primi-
tive in the extreme, consisting solely in a jigging up and down in time to the
chant. When they had danced for an hour and a half, the women were herded
from the ground, and the novices were taken, under avuncular guard, to the slight
depression at the side of the runway (see fig. 6), Fifteen minutes after midnight
I was awakened by a renewal of the chant and thump of the sticks, I could see,
in the firelight, that the women had returned and were preparing to dance again,
Behind the men's backs, the women danced the same chorus over and over again,
at at average of sixty choruses per hour. I fell asleep, but was disturbed again at
4.30 by a sudden change in the chant The dancing continued until 6.00 a.tn.
All the women were then herded into the wind-break, save six feinale rela-
tives of the novices, who continued to jig to the chanting. When all the women’s
heads were covered (with rag scarves or open hands) a dozen warriors pranced
M
178
down the runway, knee-raising high, each carrying a wooden tjurunga upright
in front of him. The tjurunga were painted white (see fig. 4), and topped with
turkey-bustard feathers. After one circuit of the fan-area of the ground, the
men stuffed the tjurunga into the mulga wind-break, and broke off. All this time
a watch was kept that all the women’s faces were hidden.
Once again the women and children were herded off the ground, with the
wailing mothers cartying the be-feathered novices off on their shoulders, and
great oral confusion reigned. The men continued to sing, while the whole of the
clearing was cleansed with a bull-roarer. Then, when the novices were soon
returned, they were taken by their male relatives up to the far end of the runway.
PLAN. of — fe;
CORROROREE- GROUND .
A tribesman came forward, and with his back to the small fire in the apex
of the “fan,” scratched dust and dirt onto it with his feet. The audience was
convulsed with laughter. Then the actor worked his way up the runway towards
the novices in a most comical manner, wobbling his knees, and screwing up his
arms, yet all the while preserving a serious expression on his face, On reaching
the fire at the other end, he again scratched dirt upon it, thereby redoubling the
appreciative laughter of the onlookers. Five other men performed in the same
way, some, certainly, more amusing than others.
7g
When the novices had been returned to their usual place, a shield was placed
in the centre of the runway, and in it a quantity of white powder, Two men
pranced in, arms folded, and the first knelt at the shield, and with his finger,
wiped a white streak onto his nose. Much laughter. Then the two pranced down
towards the novices, and, just as they were reached, the hand of the second came
over the shoulder of the other and wiped off the powder, This diversion was
enacted three times, to the immense delight of the audience. Some more chanting
followed, and the men returned to camp at about 7 a.m.
It was now Tuesday. All activities were suspended during the earlier part
of the day, but in the late afternoon the final preparations were begun.
The fathers and other relatives had remained on the corroboree-ground with
the novices, of course, and it was here that the wanigi were made, In the scrub
at the side of the runway, out of sight of ihe boys, the two fathers carefully
cleared a space of twigs and pebbles, and spread muiga branches on the ground.
Into a hole was thrust a wooden tjutunga, and a secotid was laid crosswise upon
it, with a pad of cloth to prevent scratching. The two were then bound together
by a diamond-shaped pattern of hair-string. While this winding continued, a
constant stream of blood from relatives’ forearms played on the string, and was
reverently wiped into the pattern with charcoal. Intermittently the fathers
would begin a chant, joined by the relatives; this chant was the most moving
of all those sung at the ceremonies, starting at almost a falsetto pitch, and sud-
denly plunging to a deep growl. When the binding of the wanigi was completed,
the totems were decorated with white down and bunches of blood-stained turkey
bustard feathers (see fig. 5).
They were then placed gently one on top of another on the swept ground,
with two blood-splashed bull-roarers arranged parallel, and on these, the cireum-
cision knife, Over the whole the relatives let more blood.
On hands and knees, four “uncles” shouted over the totems, with their
lips almost touching (hem, The shout began lustily, and then gradually died away.
‘An answer came from the novices’ depression through the scrub, where their
guardians had snatched up spears and boomerangs, and were brandishing them
and shouting threats. Each time the wanigi patty shouted, there was this flying
to arms. Then stiddenly, without ceremony, the totems had gone, taken off into
the bush.
While the fathers had been engaged, the novices were being painted on chest
and back in white, figured with great care and deliberation (see fig. 1 and 2).
Their hair was bound for the first time, and decorated with turkey-bustard
feathers, surmounted by white down, and when their adornment was complete,
they knelt with chin in hand in their shallow depression. Side by side, they waited,
From the scrub, in single file, came the wanigi party, and. passed by the
kneeling bays. Each man carried a sprig of mulga or witjuti (both species of
Acacia}, and with it stroked the hair of the novices, and threw the sprig onto
their backs. Last in the line carne the fathers, The semi-circle of singers was Te-
formed, and the chant made over the incomplete wamgi was resumed.
Soon the women and children arrived, led by the female relatives of the
boys. The novices were now crouched in their depression, on the backs of
‘“oncles,” and facing inwards. With nmulga and witjuti sprigs as before, the two
mothers slapped the soles of their sons’ feet, causing them to hop on all fours
from their “uncles’” backs, and over towards the seated line of relatives in the
centre of the “fan? When they reached these men, the boys were seized and
pulied hack, to lic on their backs on the now supine line. The female relatives
followed and brushed the bodies of the novices with their sprigs, chattering loudly
the while; then, suddenly, broke off and made for the far end of the runway,
where they sat down.
18)
The rest of the women and children had been arranged (see fig. 6) and the
men resumed their chanting. The novices were now sitting up.
Night had fallen, and the fires were lit. Aiter a period of song the women
and children were all bustled into the wind-break, behind the men, for the entry
of twelve dancers. These men were highly decorated, comparatively. Besides
chalk totemic marks on their backs, they each wore a design of bird-down on
the chest and arms, of brown and white, with some circles and oval shapes on
forehead and cheeks, Each dancer had, attached to his legs at ankle and thigh,
a straight pole of ten to twelve feet in length, bound with drying gum leaves,
surmounted by a gum-leaf crown (see fig, 3),
These men paraded in front of the novices, and, standing before them
singly and in a group, shook the poles with leg movements, causing the leaves
to rattle together. The women, who all this time were crouching with their faces
covered, were then herded quickly from the ceremonial ground. When they were
gone, a sudden Aare in the fire at the far end of the runway revealed the two
wang, stuck in the ground, and seeming to glow dully in the flicker of the
ames.
The pole-dancers formed a line in front of each boy in turn, and his own
wanigi was passed down through the leafed poles towards him. Each novice
was lifted up, and passed his hands over the diamond design of the string; this
done, the wanigi wag returned to its place behind the fre.
In a Iull in the chanting, the wail of the women could be heard, coming from
' the camp.
Several groups burst onta the runway from the “fan” end, each man hold-
ing, with both hands, # boomerang behind his neck. With violent shaking of
the body, and shuffling, they moved backwards into the semi-darkness. This was
repeated several times.
A number of the younger men then snatched up large branches of mulga
from the wind-break, and with a whoop, ran down the runway, dragging them
behind, They piled them on the furthest fire, and when the tinder-dry branches
burst into a brilliant flare, the human table was revealed, kneeling in position in
front of the blaze, Each “uncle” carried his boy down to the fire, and laid him
on the table. One of the leaf-poles of the earlier dance was lit, and held as a torch
above the table. Two runners bolted down to the body of the men, clapped their
hands, shouted, and raced back. At the moment when the foreskin was cut, the
flaring pole was swept down.
After the operation, the boys were seated for several nioments m front of
the fre, and then walled down among their relatives, to the accompaniment of
the triplet of processional whoops, to be formally presented to the old men.
Standing there together, each bay was confronted in tum by two pole-dancers,
who quivered, and were pushed in the chest by the boys, Thereupon these dancers
fell back with a clatter of drying leaves and lay on the ground before the newly-
inttiated.
The boys were seated, and the two bull-roarers, prepared earlier by the
fathers, were brought twirling down the runway, to be presented to the boys,
and explained, Two relatives. limped down from beyond the circumcision fire,
carrying the wanigi on one foot, made a circlé in front of the boys, and waited
while they were hoisted onto their “uncles’” shoulders. Then, clutching bull-
sparer and wanigi, the now young men were borne off into the blackness of the
scrub.
Their adult education and discipline had begun. For several months iow
they would have to five apart from the tribe
181
ACKNOWLEDGMENTS
- I should like to express sincere thanks to Rev. T. J. Fleming, Baptist Mission,
Yuendumu, without whose understanding and encouragement it would not have
been possible to witness the ceremonies. Help is also acknowledged from the
Native Affairs Branch at Alice Springs, Officers B. Greenfield and L. Wilson,
and Mr. N. B. Tindale, Ethnologist, South Australian Museum.
REFERENCES
Spencer, BALDwIn 1914 Native Tribes of the Northern Territory of Aus-
tralia, 88-176
Spencer and Giten 1904 The Northern Tribes of Central Australia, 528-374
Passim Eixin, Basepow (inter al.) .
THE METAMORPHIC AND IGNEOUS HISTORY OF ROSETTA HEAD,
SOUTH AUSTRALIA
BY D. R. BOWES
Summary
This paper gives an account of the metamorphic and igneous history of the Rosetta Head area.
Regional metamorphism of folded greywacke and subgreywacke types of ? Early Palaeozoic
age produced quartz biotite schists which were later intruded by granite. The conditions required
for metamorphic differentiation were provided by the presence of the granite magma and
andalusite, cordierite, albite and chlorite schists were formed at the expense of some quartz
biotite schists. The material not wanted in these transformations formed andalusite chlorite and
andalusite cordierite chlorite “sweats” and numerous quartz and quartz felspar veins. The final
intrusion of the granite rechrystallized and partially mobilized some of the albite chlorite schists.
A mush consisting of coarse albites and chlorites in a mobile base, which was capable of
intrusion, was produced. This mush was pushed up along the granite-country rock contact by the
intruding magma and in cooling gave rise to coarse albite chlorite rocks of igneous aspect. The
formation of the porphyritic granite of Rosetta Head and its unusual features are explained by
the assimilation of albite- and chlorite-rich rocks in a potash-rich magma.
182
THE METAMORPHIC AND IGNEOUS HISTORY OF ROSETTA HEAD,
SOUTH AUSTRALIA
By D. R. Bowes*
[Read 12th Nov., 1953]
SUM MARY - Se oO wee eee FO Seo 122
L Isrropuction - - - « ~ ¥. —s 3 je ry 182
II Recrowan SeTtixe any Structure - - += - - = 184
Til Tae Country Rocks - = + = = = = = + 187
IV Tse Anpatustre, Corprertte, Carorire, ALBITE Scwists - - 19]
V Tse Coarse Avsite Cuore Rocses or Ienrous AsPecT - - 200
VI Tue Granitic Rocks - - - = 2 + = . « 208
VII Tue Perrotocy oF THE SERIES - -~ - - = - 212
VIII Extent Anp AGE of THE INTRUSION - - - = - 213
ACKNOWLEDGMENTS i 213
BIBLIOGRAPHY - - = - > “ ~ A 2 2 213
SUMMARY
This paper gives an account of the metamorphic and igneous history of the
Rosetta Head area. Regional metamorphism of folded greywdcke and subgreywacke.
types of ? Early Palaeozoic age produced quartz, biotite schists which were later intruded
by granite. The conditions required for metamorphic differentiation were provided by
the presence of the granite magma and andalusite, cordierite, albite and chlorite schists
were formed at the expense of some quartz biotite schists, The material not wanted in
these transfortnations formed andalusite chlorite and andalusite cordierite chlorite
“sweats” and numerotis qttartz and quartz felspar veins, The final intrusion of the granite
recrystallized and partially mobilized some of the albite chlorite schists. A mush con-
sisting of coarse albites and chlorites in a mobile base, which was capable of inttttsion,
was produced. This mush was pushed up along the granite-country rock contact by the
intruding magma atid on cooling gave rise to coarse albite chlorite rocks of igneous
aspect. The formation of the porphyritic granite of Rosetta Head and its unusual features
are explained by the assimilation of albite- and chlorite-rich rocks in a potash-rich
granite magma,
1, INTRODUCTION
(a) Location ann PHyYSIoGRAPHY
Rosetta Head is a promontory at the western extremity of Encounter
Bay, on the south coast of South Australia, about 50 miles south of Adelaide.
This headland—better known as “The Bluff”—juts abruptly out of the sea
to a height of approximately 325 feet. The seaward end is a large granite
mass intrusive into a folded sedimentary series which is now represented by
quartz biotite schists.
Together with West Island to the west and Wright Island, Granite
Island, Seal Island, Pullen Island and Port Elliot Head to the east, Rosetta
Head is part of a chain of granite masses outcropping in the Encounter Bay
area. (Fig. 1 and Plate V., Fig. 1.)
Glacial action during late Palaeozoic times determined much of the
present topography. Rosetta Head itself is a roche moutonnée (Fig. 3.) and
large areas of the rolling hills behind the headland are covered by glacial
till, The glacial topography and deposits have been described and illustrated
by Howchin (1926 and earlier reports listed therein).
* Department of Geology, University College of Swansea
Trans, Roy Soc. S. Aust., 77, July, 1954
183
The coastline features depend on geological factors. The granite mass
rises as sheer cliffs from the sea, but a wave-cut platform with smaller
cliffs behind has been formed where the schists form the coastline (Fig. 10).
This platform has irregular and jagged features owing tu many criss-crossing
veins and the cropping out of irregular bands and lenses of knotted schist.
Where glacial till forms the coastline there is usually a sandy beach.
[+ ]oranrtic Rocks
[v ]coarse aLaire
CHLORITE. ROCKS
ny >}
E-FROSETTA HEAD
&® WEST |,
48 SEAL |.
483 PULLEN
SOUTHERN
Fig. 1
Locality plan showing the outcrops of igneous rocks in the Encounter Bay area.
(b) Previous INVESTIGATIONS
In an account of the igneous rocks-of Encounter Bay, Browne (1920)
discussed the geology of Rosetta Head. The granite mass which forms the
seaward face of the headland was considered an intrusive mass and part
of a large batholith. The associated coarse-grained albite chlorite rock was
termed an “albite mica syenite” and its origin ascribed to the flotation of
carly-formed crystals during the fractional crystallization of the granite
magma, .
The occurrence at Rosetta Head of certain fine-grained, richly albitic
and richly chloritic rocks was recorded by Browne (1920) and their forma-
tion attributed to impregnation of the surrounding quartz biotite schists by
magmatic material. Mawson (1926) suggested that “assimilation of the
intruded schist” had taken place. The presence of “andalusite mica schist”
and “cordierite mica schist” in Petrel Cove was also reported by Browne and
the origin of these rocks attributed to the contact metamorphism of the
quartz biotite schists.
No other contributions to the geology of Rosetta Head have been
published,
(c} PRESENT INVESTIGATIONS
The desirability of a further detailed petrological investigation firstly
of the albite, chlorite, andalusite and cordierite schists and secondly of
the coarse-grained albite chlorite rock was suggested by Professor Mawson
who made available material previously collected from the area. The investi-
gations were carried out during 1946 during the tenure of the James Barrans
Scholarship of the University uf Adelaide and continued during 1947. Further
field and laboratory investigations were performed during 1950-52.
184
A detailed geological map at the seafe of 20 in, =i mile was made
(Fig, 2) and fifteen rack analyses and one mineral analysis were completed.
The specimens referred to in the text are those of the Rock Catalogue.
Department of Geology, University of Adelaide where the specimens. and
corresponding thin sections are housed.
The present investigations have provided evidence to suggest that the
alhite, chlorite, cordietrite schists and most of the andalusite schist were
formed in the aureole of the intrusive granite by contact metasomatism of
the country rock (quartz biotite schist). The metasomatism was not due to
offshoots of the granite penetrating the country rocks but due to the presence
of the requisite conditions to cause metamorphic differentiation.
There is no evidence to suggest the flotation of crystals to giye rise
to the coarse-grained albite chlorite rocks but the evidence indicates thit
these unusual rock types were formed by the partial or complete mobilization
of albite chlorite schists by the intrusion of the granite. The granite over-
rides the country rock and the coarse albite chlorite rocks are mainly found
along the main granite-country rock contact. The unusual features of the
granite are explained by the assimilation of albite- and chlorite-rich maternal,
This paper gives an account of the metamorphic and igneous history af
the area with particular reference to the genesis of the fine-grained albite
chlorite schists and the coarse-grained albite chlorite rocks of igneous aspect.
If. REGIONAL SETTING AND STRUCTURE
(a) Recionar, SETTING
Investigations in south and south-eastern South Australia have revealed
Numerous occurrences of coarse-grained granite. Outcrops at Cape Wil-
loughby, Kangaroo Island (Tilley 1919), in the Encounter Bay area (Browne
1920) and in various parts of south-eastern South Australia (Mawson and
Parkin 1943, Mawson and Dallwitz 1944, and others) have heen described,
but most of these outcrops are either granite islands or completely surrounded
by Tertiary or Recent deposits. At Rosetin Head, however, the intrusive
nature of the granite can be established, the intruded country rock being a
quartz biotite schist, very similar to the unaltered xenoliths in the granite
at Granite Island and Port Elliot.
Howchin (1926) showed that this country rock is portion of the upper
part of a sedimentary series which rests uncomformably on the schists and
gneisses of the Barossian Complex (Older Precambrian). This country rock,
which is largely composed of recrystallized greywackes and subgreywackes
together with some argillaceous and same arenaceous horizons, is well
developed and exposed on the south-eastern und eastern flanks of the Mount
Lofty Ranges. In general it has been metamorphosed to the biotite grade
although in some areas metamorphism has been more intense. Its age and
stratigraphic position have not been definitely determined. Howchin (1926,
1929) heid that this series corresponded to the Adelaide System found on
the western flank of Mount Lofty Ranges but Mawson (1947) suggested
that it was of Mosquito Creek Age, Recent investigations by the South
Australian Geological Survey have suggested that these rocks are part of
the Kanmantoo Series and are of ? Early Palaezuic age.) A general account
of the regional distribution of this series together with the nature and
composition of some of the rock types has been given by Robinson (1946),
Owing to the presence of overlying irregular patches of Permian gtacia!
till, it is mot posstble to trace a continuous sedimentary succession from
Rosetta Head inland, but Howchin (1926) has published a geological map
©) This statement is published by kind permission of the Director of the Geological
Survey of South Australia,
185
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186
of a large area north of Encounter Bay and has described glacial deposits.
Apart from recent superficial deposits, these represent the last episode of
sedimentation in the area,
{b) Structure
The regional structure of the metamorphosed sedimentary series making
up the country rock is simple, From the base of the series some ten miles
inland, the beds dip regularly towards the south-east at moderate angles,
and can be traced in ascending stratigraphic order towards the sea. Close
to the granite intrusion at Rosetta Head the strike varies from N.50°E. to
N.60°E and the dips vary due to folding (Fig. 2).
Fig. 3
Rosetta Head from: the Encounter Bay shore illustrating the distribution and
relationships of the yarious rock formations.
Outside the contact metamorphic aureole but close to the headland,
bedding is a conspicuous feature. Slumped structures, one inch high, are
sometimes seen along the bedding planes as in the cliff at the side of the
road two hundred yards from the wharf, Regional: cleavage, which cuts
across the bedding and which is post-folding is a prominent structural
feature especially on the wave-cut platforms (Fig. 10 and Plate V,, Fig. 2).
Behind the headland the plane of this schistosity strikes N.25°E and dips
70° southerly. It swings gradually to N.35°E near Half Way Rock but the
dip remains constant, The general direction of the granite-country rock
contact and also of the line joining the contact at Rosetta Head to the contact
on Wright Island is approximately that of the strike of the plane of
schistosity.
Withia the area affected by contact metamorphism the bedding is
difficult to detect but the schistosity is a prominent structure. Bands, masses
and lenses of knotted andalusite and cordierite schist and light-coloured
albite chlorite schist are also conspicuous. Although showing no apparent
structural control the bands generally bear about N.50°E. They cut across
and destroy both the schistosity and the bedding. Their presence, together
with numerous associated veins and stringers has resulted in a very confused
structural pattern on parts of the wave-cut platforms.
The dip of the country rock near the granite contaet is approximately
3S°S.E, (i.e. out to sea) and this is the dip of the main granite-country rack
contact, the granite having overridden and intruded over part of the country
rock (Fig, 3). It appears as if the magma stoped its way up the dip during
its intrusion, the bedding exercising a structural control. The frontal advance
of the magma appears to have been structurally controlled by the schistosity
as the direction of the main contact corresponds with the strike of the
achistosity. A vague lineation in the granite parallel to this direction is
shown on the aerial photograph. Roof pendants have not been moved as
the orientation of the schistosity and bedding remains the same, but xenoliths
of country rock, which are common, are disoriented.
137
The granite is cut by several major joint systems which show close rela-
tionship to thuse of West Island (vide Jack 1923). Of the major joint systems
one system strikes N-S and dips 20°W. but the others are verttcal or nearly
so and strike N.10°E, N.40°E., S.70°E, and S. 40°E. respectively.
Ti. THE COUNTRY ROCKS
The country rocks are part of an extensive series now represented by
recrystallized greywackes, quartz biotite schists and impure sandy quartaites
found on the south-eastern and eastern flanks of the Mount Lofty Ranges.
Most of the rock types are dense, fine-grained, dark-grey and composed
essentially of quartz together with biotite. They are generally massive except
for some areas where the parallel orientation of some of the biotite has
produced a schistosity, The age and stratigraphic position of this series has
heen discussed in the previous section and Robinson (1946) has recorded
descriptions of the main rock types.
The composition of the upper part of the series shows little variation
4s is indicated by Kleeman (1937) who, in discussing the origin of the xeno-
liths in the granite of Granite Island states that the “granite was intruded
into a large area of hornfels of fairly uniform composition. The rocks are
well exposed in hills just north of Rosetta Head and to the north of Victor
Harbour itself,”
Two miles inland from Rosetta [lead the country rock is massive,
muicaceous-looking and almost black in colour with no traces of schistosity
(Browne, 1920). Owing to overlying patches of Permian glacial till, it is
not possible to trace a continuous series towards Rosetta Head, but within
the area mapped the country rock is a dark-grey, fine-grained quartz biotite
schist. It consists essentially of quartz and biotite, in varying proportions
together with minor amounts of felspar and muscovite and accessory mag-
netite, apatite and zircon. Some of the biotite flakes show parallel orientation
and, in general, the degree of schisiusily tends lo increase as the headland
is approached.
(a) PeTrocrapuy
The country rock outcropping by the coast at the side of the road in
the most northern part of the area mapped (Fig. 2) is a dark-grey, fine-
grained quartz biotite schist (9590). It consists essentially of uncracked
grains of recrystallized quartz, varying considerably in grain size (from
0:25 mm. to 0:05 mm.}, which form a mosaic in which the less abundant
minerals are dispersed, together with brown biotite flakes (Fig. 4a). Some
of this biotite is present as short stumpy flakes but most of the individuals
are long (up to 1-2 mm. with ratio of elongation 4:1), show parallel orienta-
tion and are pleochroic with x=light yellow. y—=2z—=dark brown. Some
orthoclase, towards which the quartz is idioblastic, is present together with a
few crystallized grains of albite (Ab,,). There are a few stumpy muscovite
flakes, magnetite is fairly abundant, zircon, apatite and tourmaline less so,
This rock ts a greywacke type which has been metamorphosed and is repre-
sentative of much of the surrounding area. Its chemical composition is
set out in Table 1,
Approaching the headland the schistosity tends ta become more pro-
nounced and the size of some of the biotite flakes increases. Two
hundred yards from the granite contact the rock (9591) in the cliffs by the
road leading to the wharf has a pronounced schistosity and consists of vague,
discontinuous bands about i mm. across which are alternately biotite-rich
aud biotite-poor, the biotite fakes generally being 0°35 mm, in length (Fig.
4b). Recrystallized quartz grains together with minor amounts of orthoclase,
188
albite, muscovite, magnetite, apatite, zircon and tourmaline make up a
mosaic which is practically even-grained with an average grain size of
007 mm. This rock represents a belter-sorted, more argillaceous sediment
than the rock previously described but the more pronounced schistosity
suggests that stress was a more important factor in its metamorphism than
int the case of the rock further inland. The chemical composition of this rock
is set aut in Table Ll,
(a) Quartz biotite schist (9599) x 27, with accessory zireda and
magnetite.
(b) Quartz biotite schist (9591) x 27,
(c) Quartz biotite andalusite schist (9593) x 6, showing relics of
schistosity in the andalusite porphyroblasts and a large
chlorite flake which cuts across the schistosity.
Claser to the pranite mass the rocks show a weaker schistosity and the
texture becomes decussate. A few yards from the granite, in the roof pend-
ant just south of the wharf, the country rock (9592) is a quartz biotite
hornfels although a few biotite Hakes showing preferred orientation are still
present. Most of the biotite shows randotm orientation and together with an
equigranular mosaic of recrystallized quartz grains (average prain size
0°15 mm.) makes up the decussate texture, The chemical composition of this
rack is given in Table 1 and this, together with microscopic observations
indicate that it is stmuilar to rock 9590 in mineralogical and chemical com-
position although it represents a better-sorted sediment and has undergone
contact metamorphism following regional metamorphism,
Close ta the margin of parts of the granite mass, 2 natrow zone, up to
fen feet wide, of banded quartz biotite schist has been produced. This is
well shown on the north-western side of the headland where tts schistosity
is paralle), in detail, to the pranite-schist contact, The regional schistosity
has been obliterated in these areas and the directional features of this con-
tact schist often cut across it.
In various parts of the area there ts local develapment of sericite, mus-
cavite, andalusite and chlorite. Knots of very fine sericite, irregularly
developed over a limited area some 480 yards from the contact arta were
reported by Browne (1920 p, 53). Some muscovite is also present. The
schistosity, which curves around-the knots, is very marked, A spotted anda-
lusite schist (9593) crops out next to the granite mass, just west of the albite
chlorite schist near the wharf (Fig. 11). It is distinctly schistos¢ and is made
up of alternate bands respectively rich in parallel oriented biotite and granu-
lar quartz. The schistosity curves around clear eye-shaped crystals of anda-
189
lusite which are practically free from inclusions (Fig. 4c). Browne (1920)
also reported the sporadic occurrence of rocks containing a few large flakes
of green chlorite that cut across the schistosity although small quartz
inclusions carry the schistosity through the chlorite flakes.
(b) SEDIMENTARY VARIATIONS AND CHEMICAL COMPOSITION
The country rocks in the immediate vicinity of Rosetta Head are now
composed essentially of quartz and biotite in varying proportions with
compositions ranging from subgreywacke to argillaceous greywacke. This
is borne out by the chemical compositions of the analysed rocks and a
comparison with the average composition of greywacke (Table 1). The
variation diagram (Fig. 5) shows that Al,O,, total Fe, MgO, CaO and K,O
increase as Si O, decreases. This. reflects the inverse relations of quartz and
biotite. Felspar is never present in large amounts. Often it is mainly potash
feldspar although albite is usually present as indicated by the Na,O content
of the analysed rocks. The norms of the analysed rocks are given in Table 2.
Taste 1
Analyses of the country rocks and comparisons with greywacke
A B Cc D E F G
510s wre, eee ens “O8B2 63-55 68°76 68-92 72-90 64-2 68-1
TiO ee ee O96 0-86 0-74 0-88 0-56 0°5 0-7
AbOs oo... a. 18°34 16-55 13-79 © 12-65 13-74 14-1 15-4
FesOe on ves vee 096 0-97 0:66 1-60 0-04 1-0 3450
FeQ vac) atin en 5895 4-67 4-60 5:07 3-29 4-2 34
MnO oa ae ee 0°05 0-09 0-07 0-02 n.d. O-1 0-2
MeO 2. ue ee 400 3*12 2°65 2-52 1-85 2-9 1-8
C20 taee pose dat SSS 311 2-81 2:06 2:12 35 2-3
NasO wn a. a = 339 3-33 2-54 2-80 3-02 3-4 2-6
K:0 ieiap wore ees, SON 2S 3-24 2°29 2:10 199 2:0 2-2
HaO+ a ae ae 027 0-50 053 0-96 0-46 2-2 2.1
H,O-(110°C.) 1... 0-10 0-10 0:04 0+04 0-11
POs ee ee = OD 0-19 0-21 0-17 0-15 0-1 02
ZrOy ns ee ee 005 tr. 0-19 = p.n.d. n.d. — —
BaQ ne se 0050058 A OO nd. = 3
SB ae cuee el! bee AP 0+19 0-13 0-18 tid, _ _—
C Os eee aes tare —, ay _— = — 1°6 =
99-95 100+52 100-15 99-98 100-23 100-0 102°4x
LessO .. ws © 0-01 0-08 0-05 0-07 — = _—
for S ee eee eee eee CC
99-94 100-44 100-10 99-91 100-23 100-0 102-4
x Probably in error; FesQ. probably should be 1-00 and the total 100-0.
Quartz biotite schist (9591) in cliff by road, 200 yards from wharf, Rosetta
Head. Analyst: D. R. Bowes,
Inclusion on Breakwater, Granite Tsland, Victor Harbour, Analyst: A. W.
Kleeman, (Kleeman 1937).
Quartz biotite schist (9590) by coast at side of road, half mile north of
Rosetta Head. Analyst: D. R. Bowes.
Quartz biotite hornfels (9592) in toof pendant south of wharf, Rosetta
Head. Analyst: D. R. Bowes.
Sedimentary inclusion, Breakwater Quarry, Granite Island, Victor Harbour.
Analyst: A. W. Kleeman (Kleeman 1937),
Average of greywacke analyses given by Pettijohn (1949, p, 250),
Average of 30 preywackes. Compiled by Tyrrell (1933, p. 26).
>
Ons tM Do &
190
TABLE 2
Norms of the country rocks
A B Cc D E
Quartz sue sets wre nee O15 18+36 32-52 34°14 38°76
‘Orthoclase ce ee ones | 19°46 18:90 13-34 12-23 11-68
Albite (ee eevee pees 2B4B2 28°30 21°48 23°58 25°15
Anorthite 0 a ae oe 16°96 14-18 13-34 9-45 9-73
Corundum wn. ase es ene 2486 2°35 2-24 2°45 3-06
Zircon ay ed ete ane MTB — 0°37 — _—
Hypersthene—En 10-00 7°80 6°60 6°30 4-60
i Fs ou. a = 8°51 6:07 6-60 6:20 §-15
Magnetite ws. wn ae ee 159 1-39 0-93 2°32 —
Iimenite suse! Gare tyerh oe | DBZ 1-67 1+37 1-67 1-06
Pyrite oo. a a eee O12 0°38 0-24 0-30 _
Apatite bdo power pom. “ans O94 0-44 0-34 0-34 0-34
A study of the thin sections and chemical compositions of the rocks,
together with the variation diagram, confirms that no minerals except quartz
and biotite are present in large amounts. The rocks described and analysed
are representative of the country rocks and show the extent of the minera-
logical and chemical variations in the immediate vicinity.
Variations in the conditions during deposition are reflected by changes
in grain-size, Some of the rocks are even-grained and well-sorted although
many are uneven-grained and ill-sorted with the quartz individuals varying
considerably in size,
FIG.5 VARIATION DIAGRAM OF ANALYSES OF
o
x
1
o
E
ae
R
f
T
ae
CST
(c) METAMORPHISM
Two separate episodes of metamorphism are recorded by the courtry
rocks in the area. The first episode was one of regional metamorphism which
took place after the folding but before the intrusion of granite and which
changed the sediments to quartz biotite schists. Shearing stress appears to
have played only a minor role in the metamorphism of the rocks inland, as
evidenced by their lack of recognizable schistosity, but as Rosetta Head is
approached shearing stress became a more important factor and the biotite
shows parallel alignment. All the rocks have been completely recrystallized
and metamorphism reached the biotite grade.
191
The second episode was one of contact metamorphism resultant upan a
magmatic invasion of the area. Close to the granite contact the schistosity
becomes less prominent and, in parts, a hornfels was produced indicating
that heat was the dominant factor. The final emplacement of the granite
mass at Rosetta Head must have been atcompanied by some shearing stress
as andalusite quartz schist and banded qnhartz biotite schist are found in
parts immediately adjacent to the granite. Andalusite, cordiecrite, albite and
chlorite schists were also produced during the phase of contact meta-
morphism but as their formation involved a considerable addition and re-
moval of material, their genesis is discussed separately in the next section.
It is possible that the local development of knots of sericite, muscovite and
chlorite previously described may represent an early stage in these metaso-
matic alterations,
IV. THE ANDALUSITE, CORDIERITE, ALBITE, CHLORITE SCHISTS
Rocks characterized by knots of andalusite or cordierite, wthers by
masses of white albite grains and yet others by the abundance of interwoven
chlorite flakes crop out extensively in parts of the area and their presence
was recorded by Browne (1920). Rocks containing knots of both andalustte
and cordierite are not common, although these two minerals, together with
quartz, are associated in smal! irregular veins and lenses. Albite and chlorite
are commonly associated with each other and together with andalusite or
cordierite. Irregular stringers of fine-grained quartz and felspar and veins
of coarse andalusite transect some of the schists and associated country
rocks.
(a) Distrinution anb FIELD RELATIONS
These schists occur as bands, lenses and irregular masses and are dis-
tributed sporadically on the wave-cut platforms and close to the main granite
contact. There is no regular distribution of any of these types. Generally
they cross-cut and obliterate hath hedding and schistosity (Fig. 2) and are
observed to have replaced the country rock to give a rock having little or
ne directional features. They are best studied in two main localities.
(1) Wave-cut platform west of Rosetta Head
Knotted andalusite and cordierite schists, as well as light-coloured,
granular albite-rich schists crop out in Petrel Cove and to the west (Figs. 2
and 10). They mainly occur as long, narrow bands which generally bear about
N.50°E, and thus cross-cut both hedding and schistosity, although a few do
run parallel to the schistosity, The bands are not very regular and do not
follow one direction continuously although many are approximately parallel
toa prominent joint plane of the country rock, Small lens-shaped masses of
schist also outcrop and relic lenses of country rock are sometimes found
in the schist outcrops.
_ The knotted schists and albite schists are readily distinguished from
the prey schistose country rock by the jagged nature of the weathered surface
(Plate V.. Fig. 3), andalusite and cordierite forming the knots, and by the
light colour respectively, but because of their intimate relations and grada-
tions it has not been possible to separate these types in mapping. Some of
the bands and’ lenses show sharp boundaries which generally cut across both
bedding and schistnsity, but many grade out into the country rock as indi-
cated by the gradual disappearance of the knots or by the gradual change
from the white of the albite schists ta the grey af the country rock,
West of Half Way Rock veins and lenses of pink andalusite occur. They
are short and have sharp baundaries, There are also irregular veins and
masses of coarse-grained rock consisting of knots of blue cordierite (up to
192
half inch across), masses of pink andalusite, colourless anhedral masses of
quartz and greenish flakes of chlorite which wrap around the other minerals,
These tocks are not regularly distributed and are only of limited occurrence.
(2) Chi near wharf
Irregular and interlocking masses of white albite schist and green
chlorite schist make up a large part of the cliff face just south of the wharf
(Fig. 11). “Veins” of chlorite which have no simple, regular shape and no
constant direction cut across the albite schist. Their presence, together with
the presence of irregular veins and masses of coarse albite chlorite rock
(Fig. 12) and veins of granite give the cliff face a very heterogeneous
appearance. No knotted schisig are present in this area
Normally the boundary between the albite-rich and chlorite-tich rovks
is sharp, but in some cases the contact appears a3 a series of distinct steps.
The ratio of albite to chlorite in these rocks varies, and all types from
albite-rich to chlorite-rich schists are found.
The boundary between these schists and the grey schistose country
rack appears sharp and cuts across the bedding and the schistosity, both of
which generally have been obliterated. Some fine parallel banding is, how-
ever, sometimes shown in the albite schists, due to the oriented growth of
smail green chlorite flakes along original bedding planes. The disposition of
these relic bedding planes corresponds with the bedding in the country rock
near the main grantte contact and also that seen in the roof pendant south
of the wharf.
(3) Other localities
Knotted schists crop out on the wave-cut platform on the eastern side
of the headland but they are neither as abundant nor as prominent as in
Petrel Cove and to the west. The rocks are cut by numerous thin, criss-
crossing quartz felspar veins together with some barren quartz veins.
Small outcrops of albite chlorite schist are found along the main granite-
country rock contact (Figs. 2, 10 and 11). In almost every instance they are
separated from the granite by masses of coarse albite chlorite rock elongated
parallel to the contact, The small patch of albite chlorite schist between the
country tock and the coarse albite chlorite rock on the landward side of the
S.W. Tip (Fig. 9) shows the gradual transformation of the country rack to
albite chlorite schist (Plate VI., Fig. 1). This transformation is best seen
near the southern boundary of the roof pendant south of the wharf and is
described in the following section. Small patches of albite chlorite schists
also crop out amongst the country rock.
A mass of chlorite schist is found on the S.W. Tip of the headland
(Fig. 9), It resembles the chlorite sthist near the wharf, but t5 coarser
grained.
{b) Country Rock — Auxerre Cauorttr Scuisr TRANSFORMATION
The transformation of the grey country rock into a white albite chlorite
schist is shown about eighty yards south of the wharf near the southern
boundary of the large roof pendant. Over a distance of twenty-four feet the
tock grades, across the strike, from a grey hornfels, through light-grey
schists in which albite and chlorite have developed, into a light-coloured
albite chlorite schist.
The country rock, a quartz biotite hornfels (9592), has been described
(p. ). With the gradual growth and increase in amount of small individuals
oY albite and flakes of light-green chlorite the character of the rock changes,
Initially the chlorite developed as. thin wisps aligned along. the original
bedding planes, The biotite, which decreased in amount remained randomly
193
oriented together with some larger chlorite flakes. Small grains of albite became
abundant but quartz decreased in amount (9594). With the continued trans-
formation there was a further decrease in the amount of quartz and biotite
and a corresponding increase in albite and chlorite, flakes of the latter being
larger and generally showing no alignment (9595), Flakes of muscovite are
more common than in the country rocks and so are zircon, apatite and tour-
maline. Finally the rock was transformed to an albite chlorite schist (9596)
similar to those described in the following section.
This transformation involved a considerable increase in albite, chlorite
and rutile together with a decrease in quartz and the almost complete dis-
appearance of biotite. Chemical analyses of these rocks set out in Table 3
reflect the mineralogical variations and show the progressive decrease in
SiO, and K,O together with the increase in Na,O, MgO, H,O and A1,Q,.
These chemical changes are graphically set out in the variation diagram,
Fig. 6,
TasLe 3
Analyses showing the country rock—albite chlorite schist transformation
A R Cc D E
SiOe ae ee cee um tee = 68492 60-07 58-45 56-39 58-63
TID: ae tee ee BB 0:96 1-03 0-92 0-73
Al sue eee cee eee eee TBS 17-65. 18*40 18-00 20-10
Fe:Os iad fied tetris «E60 1:29 0-94 2-04 1-01
FeO sade “¥en elgep wide) deed POE 5-50 5°65 4-00 2-08
MnO ye eee cee ee ee = O02 6-05 0-03 0-04 0-04
MeO a eee oe ee ee 25 3+95 4-09 8-14 6-15
CaQ oa aa am ee ue | 206 2°22 2-63 1+29 1-09
NaQO et ee eee | 2 BO 3°88 4-44 5:36 6°95
K,0 Joss -teset vtpen itpee asap “BAG 1/89 1-78 0r15 0-16
HiOF eee ee 096 2+20 2-20 2+96 2°34
HsO-(110°C.) ee O04 0+07 0-12 0-11 0-06
PaOe sass vet tte sete cae O17 0-16 0-15 0-22 0-20
ZrOe wee eee tee nee cae DEL, 0-30 020 0-11 0:22
BaQ ae ey te ee ee O01 0-08 0+08 0+20 0-04
SY dues hie ner pet ane ver Alto 0-16 0-08 0+13 0-11
99-98 100+43 100-27 100-06 99-91
Less O fot S 4. ae ne = 0°07 0-06 0-03 0-05 0-04
99-91 100 +37 100-24 100-01 99-87
A. Quartz biotite hornfels (9592) in roof petidant south of wharf, Rosetta
Head—24 ft. north of schist—coarse albite chlorite rock contact.
; Analyst: D. R. Bowes.
B. Quartz albite chlorite schist (9594), 18 ft. north of contact. Analyst: D. R.
Bowes.
C. Quartz albite chlorite schist (9595), 12 ft. north of contact. Analyst: D. R.
Rowes.
D. Albite chlorite schist (9596), 6 ft. north of contact, Analyst: D. R. Bowes.
E, Coarse albite chlorite rock (9614), 24 ft. souith of contact. Analyst: D. R.
Bowes.
rs
An amalysis of the coarse albite chlorite rock (9614) found between the
albite chlorite schist and the granite is also given in Table 3. This shows the
similarity in composition of the albite chlorite schist and the coarse albite
chlorite rock.
FIG.6 VARIATION DIAGRAM OF ANALYSES OF
o
x
t
i
p |
e
R
¢
f
t
(c) PETROGRAPHY ANB CILEMICAL COMPOSITION
For the pttrpose of description it 1s convenient to divide these schists
into two main groups: (I): those characterized by the presence of andalusite
and/or cordierite and (2) those characterized by an abundance of albite and/or
chlorite. This grouping to a large extent separates those types found in
Petrel Cove and to the west from those that crop out near the granite-
country rock contact, éspeciully at the cliff near the wharf. Detailed rock
descriptions are omitted where they haye been recorded by Browne (1920).
(1) Andalusite and cordierite schists
The knotted andalustte schists consist of irregular andalusite individuals,
which show sieve texture and are crowded with minute inclusions of quartz
and Hmenite, together with abundant smaller grains of quartz and flakes
of biotite, chlorite and muscovite. Some of the micaceous minerals show a
preferred orientation. In parts they curve around the andalusite knots, which
are up to 3 mm. across, but in other parts the andalusite has grown at the
expense of these minerals. Small knots of sericite, showing features similar
to the andalusite, are found in same of the rocks. Much of the chlorite, with
which. rutile is invariably associated, is intergrown with biotite, some of
which has a bleached appearance.
Veins and lenses consisting essentially of andalusite and chlorite are
found west of Hali Way Rock (9597). The large andalusite crystals are
irregularly cracked and contain abundant inclusions while the chlorite occurs
as fakes and rosettes (Fig. 7a). Large and smal! clear colourless masses of
quartz are also present together with biotite Hakes, zircon and ilmenite. The
texture is variable; it is usually coarse but sometimes fine-grained with an
andalusite, biotite, quartz mosaic. Roundish patches of blue cordierite, up
to 1 cm. across are sometimes found in these masses and veins (9598), some
of which now consists of a mosaic of quartz and biotite together with small
crystals of andalusite and cordierite,
The knotted cordierite schists consist of irregular roundish patches. of inter-
locking cordierite crystals, sometimes up to 1 cm. across and either bluc or
195
brownish-yellow in colour, in a fine-grained somewhat schistose base, The
knots show some traces of a preferred orientation parallel to the schistosity
of the base. In thin section (9599-9600), they are seen to be composed of
interlocking crystals, alk im optical continuity, fell of inclusions of quartz,
zircom, chlorite, biotite, muscovite and rutile giving a micro-sieve structure,
and with ragged boundaries which are frayed out into the fine-grained
groundmass (Plate V., Fig. 4). This groundmass is usually made up of
irregular laminae of fine granular quartz and albite alternating with laminae of
parallel oriented biotite flakes. Larger biotite chlorite and muscovite flakes are
present; some of these cut across the schistosity while others sweep around
the cordierite patches. There is a concentration of zircons (all surrounded
by pleochroic haloes) in these biotile flakes and a concentration of red-brown
prisms of rutile in the chlorite. The groundmass in some of the rocks shows
neither laminae nor schistosity and is a mosaic of quartz, biotite and albite
together with some larger biotite, chlorite and muscovite flakes and some
larger quarta individuals. The size and relative concentration of the cordierite
patches varies considerably. Half of some of the rocks are made of cordierite
knots, but in others they are not as common or as Jarge. The grain-size of
the groundmass also varies appreciably amongst the rocks of this group.
There is no microscopic evidence in either the andalusite or cordierite
schists on which to base the order of formation of the constituent minerals.
It appears that all these minerals were formed during the same period and
in no particular order,
A chemical analysis of a knotted cordierite schist (9599) is given in
‘Fable 4 and this indicates the relatively high proportions of Al,O, and MgO
and, the dominance of Na,O over K,O in these rocks and the differences in
their composition compared with that of the country rocks. (Table 1).
"FABLE 4
Analyses of the cordierite, albite, chlorite schists
A B Cc Dp E F
SiOs 58-75 58-91 56-39 46-39 44-33 43°81
TiOy .... 0-70 0°85 0-92 1-28 1-10 1+33
AlLOs wee 20048 21-37 18-00 21-94 16-94 24-60
FesOs . 063 0-82 204 0-65 402 1-20
FeO ..., ‘rt 3-97 1-90 4-00 $-95 4+35 5:14
MnO rt 0-03 0-03 0-04 0-09 0-08 0-08
MgO we = «793 4-50 814 11-61 16-17 12-74
CaQ aw «1578 0-78 1+29 1+28 0-70 0°53
Nav sey ates eee 3+35 8-72 5°36 4-53 1-17 1-80
K,0 1:97 0°16 0-15 O52 4-62 2-62
H,O+ site aat 1-43 1-47 2:96 5+39 4-24 5-74
HyO- (110°C.} 0-15 0-06 O-13 0-05 0-88 O17
PaO. ete mee ee = G60 Q-21 +22 0+23 0-31 0-32
ZrO— os 0-21 0-04 0-11 0-04 0-12 0:08
Bam ee tm 0-13, O13 0-20 0-05 012 0-17
5 «OS 0-06 G13 0-02 0-t5 0-06
F er oom — — _ 0701 . —_ _
LisO ot _ = _ — abs —_
100-24 100-01 100-06 100-03 99-90 100°39
Less O for S&F... 0°06 Or 6-05 0-01 0-06 0-02
100-18 99-99 100-01 106-02 99-84 100-37
196
A. Cordjerite schist (9599) on wave-cut platform at west side of Petre) Cove.
Analyst: D. R. Bowes.
. Albite schist (9601) in cliff by wharf, Rosetta Head. Analyst: D. R. Bowes.
. Albite chlorite schist (9596) in roof pendant south of wharf, Rosetta Head
—6 ft. north of schist-coarse albite chlorite rock contact, Analyst:
D, R. Bowes.
D. Chlorite albite schist (9605) adjoining coatse albite chlorite rock vein
(9606) in cliff by wharf, Rosetta Head. Analyst: D, R. Bowes.
E, Chlorite schist (9609) in cliff by wharf, Rosetta Head. Analyst: D. R.
Rowes,
F. Chlorite schist (9607) in cliff by wharf, Rosetta Head. Analyst: D, R, Bowes,
(2) Albite and chlorite schists
White albite grains and green chlorite flakes occur together in all pro-
portions in these rocks, which show all gradations between an albite schist
and a chlorite schist. The albite in all these rocks has a composition of Ab,,
and has the same composition and optical properties as the larger albite
individuals of the coarse albite chlorite rocks, the mineralogy and chemistry
of which ate discussed later (p, 203 and Table 6). The chlorite is the same
as that found in the knotted schists and in the coarse albite chlorite rocks.
An analysis of this mineral given in Table 5 indicates its richness in MgO.
The mineral is biaxial positive with a small optic axial angle (2E —10°) and
weak birefringence. It is characterized by the presence of many minute
crystals of rutile up to 0-1 mm, in length and the TiO, of the analysis should
be allotted to the rutile and not the chlorite. The derivation of much of the
chlorite from biotite is suggested by the apparent gradations from brown
biotite to a bleached biotite and finally to chlorite with abundant rutile
inclusions.
Tape 5
Analysis of chlorite
SiOs oc. ee tee eee GOST Na.Q wee cer gee 46
+ i a BE 7 FeO 2k ee OS
AlOs wee tee ane 22! BZ H:0+ Au am ane BSS
Fe,Q. Te, ce eanmis 0-21 H.O- Week he wee DNril
FeO a. anu wee oe 11-39 PuOs oe 6 ae TTR
MgO fin ter eee 2G
CaO vn. ne aye | O55 Total ... 98'65xx
« The TiOs of the analysis should be allotted to rutile crystals included in
the chlorite flakes.
xx Low total probably due to low H:O determination.
Analysis of chlorite from chlorite schist in cliff by wharf, Rosetta Head-
Analyst: A. W. Kleeman.@)
The albite schists are dull white in colour and consist essentially of a fine-
grained mosaic of both twinned and untwinned albite (Ab,,) and quartz
together with small chlorite flakes and accessory rutile, zircon, apatite and
biotite (Fig. 7b.). The average grain size is 0-1 mm. although the grain size
varies as does the composition. Chlorite is sometimes more abundant in
certain bands and in parts there are lenses and irregular segregations of larger
quartz crystals and chlorite flakes, Thin stringers of chlorite, biotite and
muscovite cut these rocks and small pockets of chlorite and muscovite are
sometimes present. No rocks consisting wholly of albite haye been dis-
covered; some chlurite is always present. An analysis of an albite schist
(9601) is set ott in Table 4.
©) Published by permission of the analyst.
197
With an increase in the proportion of chlorite and a decrease in albite,
the rocks become albite chlorile schists which are fine-grained and usually
banded (9596, 9602), They consist of irregular wavy bands of chlorite flakes
(up to 2 mm. long) and anhedral quartz individuals with ragged edges
alternating with finer grained bands of albite (Ab,,) and quartz together
with smail chlorite and biotite flakes, Rutile is an abundant accessory; zircon,
apatite and brown tourmaline are also present. Au analysis of an albite
chlorite schist (9596) is given in Table 4.
With a further jnercase in the amount of chlorite and a decrease in
albite, the rock becomes a chlorite albite schist, many of which are patchy
(9603-4), Long chlorite and muscovite flakes make up part of the rock,
These wrap around fine-grained masses consisting of alternating bands of
parallel-oriented chlorite flakes and granular albite and quartz. The relative
abtindance of the larger chlorite and muscovite flakes as compared with the
fine-grained banded part varies considerably amongst rocks of this group,
as does the proportion of each mineraJ. Biotite is sometimes present with
the chlorite and muscovite and often with chlorite alone, but lhe predominant
mineral is abways chlorite. Yeins of randomly oriented chlorite fiakes, up
to 1-5 mm, in length, together with anhedra! quartz containing small chlorite
inclusions sometimes transect these rocks,
(a) (b) (c)
Fig. 7
{a} Andalusite chlorite vem (9597) x LI. ; ; P
(b) Albite schist (9601) x 27, with fakes of chlorite, which
include rutile prisms, and grains of magnetite.
(c) Chlorite bwwtite schist (9608) x 11, with large muscovite
flakes,
In the cliff near the wharf a chlorite alhite schist (9605), the chemical
composition of which is set out in Table 4, is cut by a vein of coarse albite
chlorite ruck (9606) (Plate V1., Fig. 2). This schist consists of smal! chlorete
flakes oriented parallel to the edge of the vein in association with a fine-
grained mosaic of pellucid untwinned albite (Ab,,) and some quartz.
The chlorite schists (9607 -9) are green foliated, crenulated rocks consisting
of parallel oriented Makes of green chlorite and brown biotite, the average
length of the flakes being 0-5 mm. and the ratio of elongation 6:1, Chlorite
is generally the predominant mineral although in some of the rocks it is
subordinate to hietite, Some muscoyite is usually present. Between bundles
of flakes of the micaceous minerals are areas of a fine-grained mosaic of
quartz together with a small but variable amount of alblte (average grain
188
size 0°08 mm.} and accessory rutile, apatite and zircon (Fig. 7c), Analyses of
two chlorite schists are set out in Table 4,
A comparison of the analyses of these albite and chlorite schists (Table
4) with the analyses of the country rocks (Table 1) reveals marked differences
in chemical composition. The high proportion of Na,O associated with the
low proportion of K,O in the albite schists and the high proportion of MgO
in the chlorite schists are distinctive features of these rocks and are far from
the corresponding values for the country rocks.
Fi6.8 VARIATION DIAGRAM OF ANALYSES OF
The mineralogical dominance of albite, the scarcity of biotite and the
presence of some chlorite in the albite schists is reflected in the relatively
high amount of Na,O, the small amount of KO and the presence of MgO
in considerable amounts. As the rocks becotme more chloritic the amounts
of Na,O and SiO, decrease while K,O increases as do H,O and MgO, the
latter constituent to a very marked degree, This reflects the gradually
diminishing amount of albite, the increased Proportion of biotite and the
mineralogical dominance of chlorite. The proportion of TiO, present shows
the greater amount of rutile present in the chloritic rocks as compared with
the albitic types. These chemical changes are graphically represented in the
variation diagram, Fig. 8.
(d) Genesis
Field evidence shows that the parent rock of these andalusite, cordierite,
albite and chlorite schists was the quartz biotite schist of the country rock,
Gradations from quartz biotite schist to albite chlorite schist south of the
wharf have been described (p. 192) and similar gradations, both along and
across the strike, can be seen at the boundaries of many of the albite chiorite
schist masses on the wave-cut platform west of the headland and at the main
country rock-albite schist boundary at the §.W, Tip as illustrated in Plate
VL, Fig. 1. Relics of quartz biotite schist remain within some of the albite
chlorite schist masses although these relics usually consist of an tinaltered
core, with schistosity corresponding with the general schistosity of the
country rocks, and a periphery which grades aut into the albite chlorite
schist. Gradations: from quartz biotite schist to knotted andalusite and
cordierite schist are also shown at the boundaries of many of the knotted
schist masses on the wave-cut platforms and also at the boundaries of relics
of quartz biotite schist within them. As the gradation takes place, sa the
proportion of knots of andalusite or cordierite increases.
199
These bands and masses of andalusite, cordierite, albite and chlorite
schist generally cut across and destroy the bedding, so that their unusual com-
positions cannot be due to original sedimentary bands of tinusual composition.
"They also generally cut across and destroy the regional schistosity indicating
that their formation was after the regional metamorphism which was respon-
sible for the formation of the quartz biotite schists and the regional schistos-
ity. Their distribution is related to the granitic rocks of the area. To the
north and north-west of the contact zone of the granite at Rosetta Head
the country rocks contain no masses of andalusite, cordierite, albite and
chlorite schists, but to the west of the granite outcrop there is a concentration
af these rocks which becomes Jess intense west of Half Way Rock. Half a
mile further west none of these rocks is seen. This asymmetric arrangement
around the outcropping granite mass suggests that these rocks were prodaced
in the aureole of an underlying granite mass which fed the over-riding in-
trusion at Rosetta Head at a late stage in the general process of its emplace-
ment. The small mass of granite now exposed produced a small zone of
contact schists but, in general, it modified rather than was responsible for
the main contact metamorphic changes.
The production of andalusite, cordierite, albite and chlorite schists in
the aureole of this granite mass at the expense of the quartz biotite schists
involved a considerable transfer of material as shown by a comparison of the
analyses of Table I with those of Table 4. There is no evidence to suggest
that the granitic magma provided the necessary material and such a postulate
would involve the simultaneous production of offshoots of the granite re-
spectively rich in Na,O, MgO and Al,O, to produce the albite, chlorite,
cordierite and andalusite schists as well as offshoots rich in K,O and 5i0,
tn produce the veinlets of orthoclase and quartz which transect the wave-cut
platforms. The evidence availahle suggests that there has been no intro-
duction of material into the area of the aureole, but that the presence of
the mass of intrusive granite produced the requisite conditions for meta-
morphic differentiation. There has been a cedistribution of some material
resulting in the production of the andalusite, cordierite, albite and chlorite
schists but there has been no bulk introduction of material.
The chemical changes which took place during the formation af these
schists were considerable. In each case there was a decrease in SiO, and,
except in the case of the muscovite- and biotite-rich chlorite schists, of KO.
The excess of these constituents above that remaining in the schists is now
found as yuartz veins and thin quartz orthoclase veins and stringers which
are most abundant in the areas where the schists are most prominent. The
role of AL,Oy varied; it was added to some of the rocks while from others
it was taken away. Any excess Al,O, is found as “sweats” of andalusite
which take the form of veins, Iubes and lenses. Surplus SiO, and MgO was
also concentrated, in parts, in some of these “sweats’ in the furm of quartz,
chlorite and cordierite. Both FeO and MgO were concentrated in the chlorite
schists, the Mg@ especially, while their amounts in the more albitic types
are less than those present in the country rocks. To a lesser extent MgO is
concentrated in the cordierite schists. The albite schists, sotne of which
contain as much as 80% albite, were enriched in Na,O, but the more chloritic
iypes contain a low proportion of this constituent showing that it has been
leached out during the transformations. The ammount of H,O in all the
schists is considerably greater that the amaunt present in the country rocks
and this, together with the presence of numerous “sweats” and veins in the
area suggests that H,O was introduced into the area, possibly from the
magma below, so that the rocks were relatively rich in this consti(uent
during the rock transformations.
200
Varying proportions of andalusite, cordierite, albite, chlorite, biotite.
muscoyite and quartz are found and the various mineral assemblages repre-
sent Stages in the process of metamorphic differentiation. There is no regular
distribution of any of the various types of schist and there is no definite
order of formation of the constituent minerals: Most of the textures and
structures of the country rock’ were destroyed by the transformations but
telics of bedding and schistosity do remain in parts suggesting that the
pracess was one of “soaking” with molecular or ionic exchange. Apart from
the amount of H,O, the bulk composition of the area appears to be the same
as it was before metamorphic differentiation, The process ceased when the
granite mass cooled and the requisite conditions were no longer present.
V. THE COARSE ALBITE CHLORITE ROCKS OF IGNEOUS ASPECT
Rocks of this group—the “albite mica syenite” group of Browne (1920)—
are generally coarse-grained, light-coloured and composed essentially of
white albite crystals, up to 4x 3x3 cm, and green chlorite. In many respects
these rocks resemble plutonic igneous rocks. They are distinguished fram
ALAITE COMORES sDINST
WI PATCH e@ OF Coan
ALDINE CHCORITE MOCA
+++ 4+iHe44
++tettate
GRanite
4+
+
4
= ©
4
+
Pio
a
ap
+
+
+
+
+4
+
+
+
+
oa
+
+
+
+
+
+
+
4
+
+
+
+
+
+
+
+
4
+.
4 +
+
q-
oo
+
+
+
+
a
+
+
+
+ +
4
+
+
+
+
Fig. 9
Geological Map of S.W. Tip of Rosetta Head.
the porphyritic granite by the absence of blue opalescent quartz, the lighter
colour and the abundance of white, twinned albite crystals. The proportions
of albite and chtorite vary considerably from place to place, the rock varying
from an albite-rich rock to a chlorite-rich rock although albite is generally
present in the greater amount. Because of these variations in compositior
the term “coarse albite chlorite rock of igneous aspect” is considered to lie
more appropriate than “albite mica syenite,” as the rock is, in many instances
far from syenitic in composition,
201
(a) Disrrrpution AND FIELp RELATIONS
‘These coarse albite chlorite rocks are mainly found at the main granite-
country rock contact and they crop out almost continuously between the
granite and the country rock (or albite chlorite schist in parts) on the
landward slope of the headland (Fig, 2). Outcrops completely surrounded by
granite and others completely surrounded by country rock are also seetl.
The steep nature of the terrain at the S.W. Tip of the headland and near
the wharf provides good exposures and enables (he field relations of these
rocks to be studied in three dimensions.
(1) South-west Tip of Rosetta Head
The relationships of the cnarse albite chlorite rock with both the albite
chlorite schist and the granite can be seem in this area. In the cliffs close
to the sea, by the main contact with the country rock, veins, stringers and
patches of coarse albite chlorite rock are present in the albite chlorite schist
(Plate VL, Fig. 1). They are not present in the adjoining country rock or in
the relics of country rock in the albite chlorite schist. The veins and stringers
show no ordered arrangement or distribution and in many cases they do not
connect with one another; many of thet are in the form of isolated lenticular
masses. Further from the contact there are “xenoliths” of albite chlorite
schist in the coarse albite chlorite rock. The boundaries of some of these
xenoliths’ are not sharp; a gradation from fine albite chlorite schist to
Aa eat
Ole hSe ALONE Coyonire=e ry :
Ss = _ Stange
GLACIAL a
att AIGTITE SC4iST
=I
S4ACIAL GHAATICS
Toes hes ee pact
wWorres ScHis ine <rabaiye
~ :
SSOUARTZ BIngi7e su
——~ ~
WAVE=CUT DL WTO
= 35 :
SAND uy
.~
~~ O™ ~ a ae
Fig, 10
Rosetta Head from the west, showing the wave-cut platform and Petrel Cove in the
foreground and the granite-country rock contact in the background.
coarse albite chlorite rock by the gradual growth of larger albites and
chlorites is shown, The contact between the coarse albite chlorite rock and
the granite is sharp in each instance, regardless of the composition of the
albite chlorite rock (Plate VL, Fig. 3) and a microscopic examination of a
thin section of this contact (9610) emphasizes its sharpness.
A geological map of the area (Fig. 9) gives the distribution of the
yariotis rocks and the variations in composition of the coarse albite chlorite
rock, Petrographic descriptions of the main types of coarse albite chlorite
rock are given in a following section. The chlorite schist-coarse albite chlorite
rock contact is not a sharp one; there is a gradua) change in rock type with
the disappearance of the large albite crystals.
(2) Along the main gromite contact
Outcrops of coarse albite chlorite rock are found along the main granite-
country rock contact (vie Figs. 2, 10, 11) and in many cases they are
associated with albite chiorite schist. As the granite contact dips 35°S,E.,
the granite mass is above the coarse albite chlorite rock which occurs as
a sheet or a series of masses in the plane of contact between the granite
above and the albite chlorite schist—if present—and the country rock below.
Where the contacts can be observed, they are all sharp—between granite
and coarse albite chlorite rock, between granite and country rock and between
coarse albite chlorite rock and albite chlorite schist.
QUART] BroTire schisT
Fig, 11
Portion of the north-eastern side of Rosetta Head from the north, showing the
granite-country rock contact and the distribution and relationships of both albite
chlorite schists and coarse albite chlorite rocks of igneous aspect.
(3) Cliff near wharf
In this cliff, thin stringers, veins and irregular masses of coarse albite
chlorite rock occur amongst the albite schists, but not amongst the chlorite
schists (Fig. 12). Their distribution, habit and relationship to the surround-
ing rocks are similar to thase of the corresponding rocks at the S.W-. Tip.
Some veins with sharp contacts transect the chlorite albite schists (9611).
Their composition is somewhat more albitic than that of the associated
schist (cf. Table 8, Analysis B, and Table 4, Analysis D) in which the
chlorites in close proximity to the vein are aligned parallel to the boundary
of the vein (Plate VI., Fig. 2). These veins give the appearance of having
been channelways along which material moved although some of the albite
individuals are considerably larger than some of the constrictions in the
veins, There are also outcrops showing a sharp, apparently intrusive contact
between the coarse albite chlorite rock and the country rock.
{4) Other localities
In some patts the coarse albite chlorite rocks crop out as masses sur-
rounded on all sides by granite; in each case the contact is sharp, There
are several such outcrops on the S.W. Tip (Fig. 9) and others on the south-
203
eastern and eastern slopes of the headland, Here, close to sea level, tongues
of coarse albite chlorite rock, ali trending S.70°E. are associated with the
gtanite, with a sharp contact between (Fig. 2). The central part of one of
these tongues is a mass of chlorite schist, three feet wide and extending for
thirty feet. In other parts the coarse albite chlorite rock crops out without
any obvious relation to either the granite or the albite chlorite schists as
small masses surrounded by country rock and bounded by sharp contacts.
Fig. 12
Geological sketch of ihe albite chlorite schist and coarse albite
chlorite rock of igneous aspect seen on the cliff face by the wharf.
(5) Similar outcrops on the neighbouring islands
On Wright Island masses of coarse albite chlorite rocks are found com-
pletely surrounded by granite, the contacts always being sharp. Close to the
sandy beach on the northern end of the island, coarse albite chlorite rock crops
out between the country reck and the granite along the contact {Fig. 2).
On the north-western side of Granite Island, Victor Harbour, and only
visible at very low tide, is a small outcrop of coarse albite chlorite rock
which has sharp contacts with the surrounding granite (Fig. 1).
(b) MInerALocicat. ComPosrTion
The alpite is mostly clear but shows some dusty incipient alteration in
places and contains inclusions of chlorite together with some muscovite,
rutile, zircon and apatile, A mineral analysis (Table 6) of this albite was
done on handpicked material (grains passed through 1 mm. seive) from a
crushed rock collected on the S.W. Tip (9613). The only impurity ef im-
portance was chlorite which could not be separated however fine the crush-
ing. Assuming all the magnesia in the analysis to be in the chlorite, the
requisite amount of the other constituents present in the chlorite was cal-
culated using the analysis of the chlorite given in Tabie 5. All the titania in
the analysis was allotted to the rutile present in the chlorite Aakes. The
calculated composition of the felspar from this analysis is Abg, An, Gry.
204
TABLE 6
Analysis of albite
(i) (ii) (iii) (iv) (v) (vi)
SIOg a eee ee 6543 1:34 64-19 2°93
TiOa oe eee tee ee = O04 _— — 4-01 4
AlsO3 oe ce pee eee 2116 0:94 20:22 1-08
FeQ se ae cee ee O49 0-47 —
MgO ioe see tee nee O86 0-86 _
Ca ce see eee gene 056 0-04 0-52 0-02 (5)
Na2Q ae ae nee ae 10°64 0-02 10:62 0-94 of 0-99 1
KsO oe ae se cee 026 _ 0°26 0-02
HsO oe cee ee O72.
Total oo. wo 100°10
i. Analysis of albite hand picked from coarse albite chlorite rock (9613).
S.W. Tip, Rosetta Head. Analyst: D. R. Bowes,
n. Amounts of constittients present in chlorite impurity.
iii. Resultant composition of albite.
iv. Number of metal atoms on bases of 120.
v. Arrangement in groups.
vi. Ideal composition.
Recalculating column (3) to 100-00 gives:
SiOs sat Stee aay weer GOOD
AkOs bape te Se wae BEAT Proportions of felspar molecules
CaO ee cee ne ee ee OS Ab us uae a 9S
Na.O vee tee cee eee 1109 Dixie cepsay atte) -a0ce 3
K20 gees? tseel ‘atte teien P27 ROE pasate pete canes 2
1¢0-00
Determinations on the Universal Stage gave the optic axial angle of
the mineral as 81° (+2°), the sign positive and maximum extinction in the
symmetrical zone of -14°. Both these measurements indicate a composition
of Aby,. The smaller grains of albite in these rocks also have the same optical
properties and composition.
The chlorite in these rocks has the same properties as the chlorite in
schists (p. 196) and it is assumed to have the same chemical composition
(vide Table 5).
(c) PeTroGRAPHY AND CHEMICAL COMPOSITION
The mineralogical composition of these rocks varies from albite-rich
at one extreme to chlorite-rich at the other. In general quartz is more
common in the albite-rich rocks than in the other types and biotite and
muscovite more common in the chlorite-rich types. The large albite individ-
uals dominate the texture of the albitic types and, to a lesser degree, the
texture of the more chloritic types,
Albite-rich types, which are predominently coarse-grained and composed
almost completely of albite laths up to 3x2 cm. in cross-section, are common
(9612), Fine-grained albite individuals (average grain size 0'3 mm.) fit into
the irregular boundaries of these laths and crystals of albite between these
two extremes of grain size are also present as are smaller crystals of quartz,
chlorite, biotite and muscovite. Rutile, zircon and apatite are accessory.
The texture of such a rock is illustrated in Fig. 13a, It is noticeable that
many of the twin lamallae of the large albites are bent.
205
Browne (1920, p. 21) described a similar rock, the analysis of which is —
included in Table 8, It differs from the rock described above in that mus-
eavite is absent and the amount of chlorite is less. The chlorites are bent,
the felspars fractured and dislocated with considerable granulation and
minerals show undulose extinction, The reason given for these phenomena
is that the “rock mass has been subjected to considerable pressure,”
Albite chlorite types make up the main mass of the S.-W. Tip of the
headland, The rocks are mainly composed of large crystals of albite, many
af which are cracked and granulated while in others the twin lamallae are
bent. Small individuals of albite together with chlorite flakes are present
between the larger albites. Some of the small chlorites wrap around the
large albites but the large chlorites show random orientation and some ate
arranged as rosettes. Both muscovite and biotite are found in parallel inter-
growth with chlorite although the muscovites are often larger than the
chlorites and the biotite is usually found as small crystals pleochroic from
light-brown to almost colourless. Small amhedral crystals of quartz are
present, rutile is a common accessory being especially abundant in the
chlorite flakes, und apatite and zircon are also seen. A micrometric analysis
of one of these types (9613) is given in Table 7, its texture is illustrated
hy Fig. 13b and its chernical composition, together with that of two similar
rocks (9606, 9614), is set out in Table 8.
(a) (b) (c)
Fig. 13
(a) Coarse albite-rich rock (9612) x5 showing large Branulated
albite individuals in a matrix of albite together with small
amounts of chlorite and quartz.
(b) Coarse albite chlorite rock (9613) x 5 showing large, granu
lated, bent and fractured albite individuals in am albite
chlorite matrix.
{c) Coarse chlorite albite rock (9615) x 5 showing large albite,
chlorite and biotite individtals in a chlorite albite matrix.
TABLE 7
Micrometric analysis of a coarse albtte chlorite rock
Albtte aus pan ner SOO Biotite tie wine anne | (OF
Chlorite a se ae 3087 Apatite 4, .. .. 5
Museovite = oy eS Zircon sue pe -wiee Ord
Quart. wes ae ee
Rutile see ee ee OD Total vee ee aes TODO
Micrometric analysis of coarse albite chlorite rock (9613), S. W. Tip of Rosetta
Hence,
266
Taste &
Analyses of the coarse albite chlorite rocks.
A B Cc D
SiOs ee see oe 64°60 59-00 58°63 56:24
TiOy ee cee seen ws = 1404 0+72 0:73 0-98
AleOg oe cee vee ee 20°37 19°41 20-10 19-75
FresOp oe vee see eee OSL 0-34 1-01 0+76
FeO ise tse vee ane 067 359 2:08 1-63
MnO soe seit ontse _ 0-04 0-04 0-01
MEO™ 240 Gin sacs wee D5 6°44 6-15 7:00
CaQ sec ue ee ee 4D 1-60 1-09 0-75.
NasO say atte see D4 6-42 6:95 8-62
DO eer | CG) 0-09 0:16 0:49
H,0O+ wee ue oe 0885 2:47 234 2/90.
HzO— (110° C) ae vee OTS 0-09 0-06 0-09
On (L774 0-18 0+20 0+19
ZrOn se ee ee ee = 003 0°08 0-22 0-15
BaO oa ae ae ue) Oa 0-08 0-04 0-13
5 man span ths 0-03 Olt 0°03
99-98 99-91 99-63
Less O for Su uy 0-01. 0-04 0-01
99-90 99-97 99+87 99-62
“Albite mica syenite’ (coarse albite-rich rock). Rosetta Head. Analyst:
W. R. Browne (Browne 1920).
Coarse albite chlorite rock (9606). Vein next to chlorite albite schist €9605)
in cliff by wharf, Rosetta Head. Analyst: D. R. Bowes,
Coarse albite chlorite rock (9614), 24 ft. south of south side of roof pendant
south of wharf, Rosetta Head. Analyst: D. R. Bowes.
Coarse albite chlorite rock (9613), S.W. Tip of Rosetta Head. Analyst:
D, R. Bowes,
9 no eB p>
Chlorite albite types contain less albite and quartz and more chlorite, biotite
and muscovite than the rocks described above. The amount of micaceous
minerals is greater than the amount of albite which still occurs as large
crystals (9615-6). ‘These albites tend to weather out and from a distance
the rock has, at first sight, the appearance of a vesicular lava (Plate VI,
Fig. 3), Litle granulation is evident in these types although many of the
large albites are cracked and show displacement of the twin lamellae along
the cracks. The texture of one of these rocks is illustrated in Fig. 13c. These
rocks grade into chlorite-rich types. which appear to be identical with the
chlorite schists and have been mapped as such.
A comparison of the analyses of these coarse albite chlorite rocks (Tahle
8) with the analyses of the albite chlorite schists (Table 4) reveals very
marked similarities in chemical composition and the variations shown. As
in the case of the schists, there is a high proportion of Na,O associated with
a low proportion of K,O, especially in the more albitic types, and a high
proportion of MgO in the chloritic types. The mineralogical dominance of
albite and the scarcity of biotite in the albitic types is again reflected in
the high amount of Na,O and the low amount of K,O, The small amount
of chlorite present is reflected in the MgO: percentage. As the rocks become
207
more chloritic, the amounts of Na,O and SiO, decrease while MgO, H.O
and to a lesser extent K,O, increase. As in the case of the schists, this reflevts
the gradually diminishing amount of albite, the importance of chlorite and
the increased proportion of biotite. These chemical changes are graphically
represented im the variation diagram Fig. 14.
FIG.I4 VARIATION DIAGRAM OF
ANALYSES OF TABLE 8
(d) Genesis
The present investigations have shown that these coarse albite chlorite
rocks are related in the field to both the albite chlorite schists and to the
granite. The salient points concerning their relationship with the albite
chlorite schists are as follows: (1) Much of the coarse albite chlorite rock
is found in association with albite chlorite schists, This is the case when
granite is associated with the albite chlorite schists but not when granite
is not associated with the schists. (2) At the 5.W. Tip and in the cliff near
the wharf, lenses and masses of coarse albite chlorite rock appear to have
been developed in site at the expense of the albite chlorite schists and both
rock types have the same mineralogical and chemical compositions. (3) In
some places, veins of coarse albite chlorite rock cut the albite chlorite schist
and jin these cases, the veins are usually more albitic than the schist. (4)
Variations in both mineralogical and chemical compositions are parallel even
in respect of many details. The salient features concerning the relationship
of the coarse albite chlorite rock with the granite are as follows: (1) Coarse
albite chlorite rocks crop out almost contunuously along the main granite-
country rock boundary. Their form is .as a sheet or a series of isolated fiat
bodies in the plane of the contact {1e. dipping 35°S.E.) with the granite
above and the country rock—or albite chlorite schist—below. (2) There is
always a sharp contact between the two rocks, regardless of the composition
of the coarse albite chlorite rock. (3) In some cases the granite tongues in
and out of the coarse albite chlorite rock but in other cases the coarse albite
chlorite rock tongues in and out of the granite or is found as small plug-like
masses in the granite.
The salient features of the coarse albite chlorite rock itself are as follows:
(1) Tt shows intrusive relations with the granite and the country rock and
in some but not all cases, with the albite chlorite schists {as stated above).
(2) Many of the albites are strained, cracked and broken and show con-
siderable peripheral granulation. This is most pronounced in the albitic types
and is not common in the chlorite types. (3) Some of the chlorite flakes
208
are bent, some wrap around the large albites, and yet others are found as
rosettes of large crystals, (4) A few of the albite individuals in the veins
of coarse albite chlorite rock are considerably larger than the narrowest
parts of the veins, (5) The shapes of the walls on either side of the veins
often do not match.
This evidence suggests that the parent of the coarse albite chlorite rock
Was the albite chlorite schists and that the rock was formed during, and
because of the intrusion of the granite by recrystallization and partial
mobilization, In the eatly stages of the process, large albites and chlorites
grew in the albite chlorite schist in favourable areas, which were probably
those containing most moisture and those most affected by the heat from
the magma. Hence there developed irregular lenses, masses and stringers
of coarse albite chlorite rock in albite chlorite schist of the same composition.
As the processes proceeded there was loss of cohesion hetween some af
the smaller grains and the rock hecame capable of movement and intrusion,
The more albitic rocks were most susceptible and so a semt-mobile coarse
albite chlorite rock containing large albites and some large chlorites in a
mobile base veined the surrounding rocks. This provided the heat and Auid
necessary for parts of the vein walls to become semi-mobile and so the veins
widened and the size of the crystals increased, The more chloritic types were
not sa readily mobilized, but large albite crystals developed in them and the
grain-size of the chlorites increased. The chlorite-rich schists were not
mobilized but were recrystallized to give coarse chlorite-rich rocks.
A considerable amount of semi-mobile coarse albite chlorite rock was
farmed at the expense of albite chlorite schist along the main gramite contact
during the over-riding intrusion of the granite up the dip of the strata. This
miush of albite and chlorite crystals in a Huid base was forced along beneath
the intruding granite and incorporated into itself mare albite chlorite schist
over which it pushed, Thus the coarse albite chlorite rocks are found as a
sheet or a series of flat bodies in the plane of the main granite-country rock
contact and show sharp, intrusive relations with the vranile, the country
rocks and some of the albite chlorite schists.
With this type of intrusion the large albites were cracked, broken,
strained and granulated and the chlorites were bent and pushed arptind the
albites. With the cooling of the granite mass, the fluid base crystallized
forming some large rosettes of chlorite, but mainly the finer grained base
of albite and chlorite with some quartz.
VI. THE GRANITIC ROCKS
(a) Distaiution ann Pirin RELATIONS
The scaward part of Rosetta Head is a mass of grey porphyritic granite
(Fig. 3) which is similar in mode of outcrop, appearance and composition to
the granite found on West Island, Wright Island and in some Jocalilies
at Port Elliot (Fig. 1). Sharp contacts are shown at Lhe junction of the
granite with the country rock, the albite chlorite schist and the coarse albite
chlarite rock of igneous aspect. Small tongues of pranite are injected into
the country tock at the contact, much of the nearby rock is a hornfels and
a narrow zone of contact schist follows the contact, The granite overlies
the country rock as the main contact dips 35° S.E.
Angular disoriented xenoliths of metamorphosed and metasomatised
country rock are present in the granite anc these are concentrated near
its margins, The metasomatic alteration of the xenoliths of country rock
in the granile of Granite Island has been studied by Kleeman (1937) and
209
similar stages of alteration to those described in that area aré shown in
the xenoliths at Rosetta Head.
Two small masses of even-grained granite (9617) with sharp intrusive
contacts, outcrop on the landward side of the main granite-country tock
boundary, Directional features due to the parallel orientation of biotite
flakes are shown in some of these rocks. Small, angular disoriented xenoliths
of country rock are enclosed in the granite and some of these have dark
rims enriched in biotite (9618) due to teaction between xenolith and magma
(Plate VL. Fig. 4), There ts a small outcrop of graphic quartz felspar granite
just east of the old mine shaft,
The prophyritic granite is cut by dolerite dykes which are now uralitized.
One dolerite on the south-eastern side of the headland intrudes into both
the coarse albite chlorite rock and the granite and has a fine-grained margin
which shows parallel flow banding through four or five inches within the
contact, The associated granite shows directional features, with the orienta-
tion of biotite flakes parallel to the edge of the dyke. The dolerite itself
is cut by small quartz tourmaline veins.
(b) MINERALOGICAL COMPOSITION
Soda-microcline microperthite, The felspar phenocrysts from the granite of
Granite Island were described by Gartrell (1903) who classed them as
anorthoclase. Later Browne (1920) suggested they were microcline mucro-
perthite. The mineral shows microcline crass-hatching, has two cleavages
at right angles and measurements on the Universal Stage have shown that
it has an optic axial angle of 74° (+1°), a negative optical sign and an extinction
angle YA(010) of 54°. This suggests a composition intermediate hetween
microcline and anorthoclase. A section parallel to (010) shows intergrown
streaks of plagioclase which are roughly parallel to (100), This plagioclase
has an optic axial angle of &2° (+1°), is optically negative, has a maximum
extinction angle on a section normal to (010) of +14° and has a composition
of acid andesine (Ab,.).
The mitieral is thus. a soda-microcline microperthite, the chemical com-
position of which was recorded by Gartrell (1903) and the above determina-
tions show why the CaO percentage is high for a perthite and why the Na,O
pereentage is high for microcline and low for anorthoclase. The proportions
4 the various felspar molecules calculated from the analysis are Org,, ADag,
Nij-
Plagioclase. Albice and pericline twinning is offen shown and many of
the crystals are strongly zoned, The centre of some of the zoned. ctystals
is andesine (Ab,,} but the composition becomes progressively more albitic
towards the outer zones which are usually Ab,, although some are Ab,,.
A few small crystals in the ground muss also huve a composition pf Aby,,.
(c) Tetrocrapuy, CHEMICAL COMPOSITION AND CLASSIFICATION
The porphyritic granite (9619) consists of large, tabular, subhedral
phenocrysts of soda-mirocline microperthite up to 4x3 cm,, together with
some large plagioclase and quartz individuals set in a coarse-grained ground-
mass, with hypidiomorphic texture, of quartz, microcline, acid plagioclase
and biotite, Muscovite, apatite, zircon, ilmenite and pyrite are accessory,
The potash felspar phenacrysls are studded with inclusions of irregularly
distributed biotites, up to 3. mm. in length, small laths of andesine and ragged
or rounded grains of quartz together with smaller biotite flakes and small
apatite prisms. All these inclusions are primary and of earlier crystallization
than the felspar, but some later quartz and muscovite fills cracks. As
a
210
described by Browne (1920, p. 13) a “fairly constant characteristic of these
felspar phenocrysts is the presence of a rim of variable width composed of
quartz granules graphically intergrown with felspar . . . ‘The inter edge
of the rim is usually straight. There are outgrowths of felspar beyond the
rim, the phenocrysts having as a result irregular boundaries against the other
minerals of the rock. These outgrowths are usvially notably free from
perthitic intergrowths . . .” This rim often shows up megascopically as
an outer, whiter zone, giving the appearance of a zoned felspar.
TABLE 9 P
Analyses of granites
A 8 Cc D E F
SIGq eg ee tee eee nee PS 71°44 68°20 75 +8 70-18 65-01
TiOn ae ce ee ee ee OSA OSB DH 0-39 0-57
AlsO,s vue te eee eee 1G7B 15-09 18509 12-90 14g? 15.04
FesOn 0. ce cae ee ee O80 0-86 0-39 0-25 1°57 1-74
REO i cas tai ake ats ER 2-58 0-85 1-78 2-65
MnO wee ee O01 0-02 0-04 = 0-12 0-07
MgO wn ue ke ae ee NY 8) 0-80 0-13 0-88 1-9)
CaO... n., oer ys Os F: | 0+74 1-99 4-42
NasO oo. ee ee ene cee 2h 2-09 285 231 3-48 3-70
Katd= oe co. ein pine 4035 4-46 4-60 6°06 4-11 2:75
H,O+ tin ate one cet DSS 0-24 0-64 0:60 >
HiO-(#10°C) a OE 04 et eee O84 1-04
PrOw ee cee ee OT 0-22 O14 _ 49 ‘0-20
Zr Qe ve cece cess cee aeee EB — pad. _ = —
BaO cee ay ree ee OD mil 0:04 — —_ —
Ss wets tins aork atte en "OOS —_— — _ _— —
HeSy fen can, od xine) Ane — 0-04 O11 = ~ Sn,
Cl sagh | Hite wane Yqi'e _ 0-05 — —_ ~ ~
100, +52 GO-41 =100+28 99-70 «106-00 =: 180-00
Less O for S ou. an a. =©002 _ — um ee —
100°50 99-41 10028 99-70 100-00 100-00
A. Porphyritic granite (9619), Rosetta Head (bulk analysis), Analyst: D, R.
Bowes,
B, Porphyritic granite, West Island. Analyst: W. S. Chapman (Jack, 1923).
C. Porphyritic granite, Granite Island, Victor Harbour. Analyst: W. R.
D
E
Browne (Browne, 1920).
Even-grained granite, Port Elliot. Analyst: W. R. Browne (Browne, 1920).
. Granite of all periods: average of 546 analyses (Daly, 1933).
F. Granodiorite: average of 40 analyses (Daly, 1933).
The analysis of the porphyritic granite shows that its composition is
comparable with those of the corresponding rocks from West Island and
Granite Island (Table 9). A comparison with averages of compositions of
granite and grandiorite (Daly 1933) shows that the SiO,, MgO, CaO and
K,O percentages of the porphyritic granite from Rosetta Head are similar
to those of the average of granite, while the TiO, and FeO percentages are
similar to those of the average of granodiorite. The rock contains considerably
less Na,O than the average of either granite or granodiorite and much more
K,O than the latter, whereas the even-grained granite from Port Elliot is
even poorer in Na,O but very rich in KO. Apart from an abnormally high
241
amount of corundum in the norm of the West Island granite, the norms of
the granites (Table 10) reflect the variations shown in the different granites
in the variations of the percentages of the standard minerals.
Potash ‘felspar and acid plagioclase are present in approximately equal
proportions with quartz and biotite being abundant and the only other
‘essential minerals. Hence, petrographically, the rock should be classified
as-an adatnellite, whereas its chemical composition is similar to granite in
some respects and granodiorite in others. Field and internal evidence reveals
that the rock is a contaminated one, hence it is best termed a contaminated
granite.
Taste 10
Norms of granites
A B Cc D
Quartz ever) EYL | 37-2 26°28 36-48
Orthoclase cue wee 26713 26°69 27-24 36.14
Albite sae un pee 2308 17-82 24-30 19.39
Anorthite 2... sa. wo 8°34 4-45 11-95 361
Corundum oe ve 1+43 5-10 1-94 1-22
Zircon car wee we = O37 _ — —_
Hypersthene—En ... 2°80 2-00 2-00 0-30
” Fe .. 3:43 2:64 3-04 1-19
Magnetite 0 1. sn. 1716 1-16 1°39 0-46
Timeniteé 0 =. a 1°08 1-06 1-06 0-23
Pyrite oa eee nee 0-12 _— = —
Apatite Hiss eons ony WDA 0-50 0-4 —
ee a ee ne ee sees ee
(d) GENESIS
‘The intrusive, magmatic origin of this granite is clearly demonstrated
on field evidence. It contains hornfelsed and metasomatized disoriented
xenoliths of country rock, the granite-country rock boundary is sharp with
small veins and stringers of the granite penetrating the country rock, and
the granite mass has an associated contact metamorphic aureole. Hence it
is considered that in this area, a granite magma stoped its way upwards
and blocks of displaced country rock are strewn ahout as xenoliths.
The gtanite is in close association with the albite chlorite schists which
it veins and cuts near the wharf. It would thus appear that the granite now
occupies space formerly taken by these schists, but no remains of the albite
chlorite schists are found as xenoliths and no grains of albite or flakes of chlorite
are strewn about in the granite, As albite and chlorite are lower in the ‘reaction
series (Bowen 1928) than the plagioclase and biotite of the granite, these minerals
are thought to have been reactively dissolved by the magma. It is considered that the
assimilation of such albite- and chlorite-rich rocks into potash-rich granite
magma, possibly similar to that represented by the even-grained granite of
Port Elliot (vide Table 9), would explain the formation of the porphyritic
granite and its unusual mineralogical and textural features. The following
is an elaboration of this hypothesis,
With the incorporation of blocks of albite- and chlorite-rich rock into
the granite magma, the albite was dissolved and its heat equivalent of ande-
sine (Abg,)—the plagioclase with which the magma was saturated—was
precipitated. The chlorite, together with the associated muscovite, was alsa
dissolved with the concomitant precipitation of its heat equivalent of biotite.
Any quartz individuals present in the incorporated rock were reacted upon
by the magma giving them ragged outlines. These processes enriched the
212
magma in soda, magnesia and titania and from this melt the snda-microcline
microperthites were precipitated, The phenocrysts probably grew quickly
inclnding within themselyes crystals of the previously precipitated andesine
and biotite and the ragged-edged quartzes. The plagioclase intergrowth is
more albitic (Ab,,) than the previously precipitated crystals.
Following the formation of the phenocrysts, crystallization proceeded
normally with falling temperature, The composition of the plagioclase became
more albitic and a coarse-grained groundmass of quartz, bictite, microcline
and acid-plagioclase, together with accessory minerals, crystallized. The rim
of graphically intergrown quartz and felspar which forms a zone around the
phenocrysts grew during this period; the inner edge is straight against the
erystal face. but the outer edge dovetails inta the grotindmuss.
The occurrence of coarse albite chlorite rock on both Wright Island
and Granite Island suggests that the granite in these areas may have assimi-
lated albite- and chlorite-rich rocks during intrusion and that the genesis
suggested above is applicable to the porphyritic granite of these islands and
in othet areas of the Encounter Bay region.
The small masses of even-grained and graphic granite cropping out on
the landward slope of Rosetta Head are taken to represent two of the final
stages of crystallization of the contaminated granite magma.
VII. THE PETROLOGY OF THE SERIES
The earliest effects of metamorphism in this area were of a regional
nature with the isochemical metamorphism of greywacke and subgreywacke
types to quartz biotite schists, This was post-folding but during the period
in which stress was an active agent, The other metamorphic and igneous
events were post-tectonic and alse after all regional stresses had ceased
to operate. They were connected with the upward intrusion of magmatic
gtanite into rocks which had previously only reached the biotite grade of
regional metamorphism.
A mass of intrusive granite just below the present level of the wave-cut
platforms produced an aureole of contact metamorphism and metasotnatism.
Metamorphic differentiation took place with the exchange of material and
the production of andalusite, cordierite, albite and chlorite schists at the
expense of the quartz biotite schists, The bulk composition of the area
Temained essentially the same and “sweats” of andalusite, chlorite, cordierite
and quartz, veins of quartz and stringers of quartz and felspar represent
the material thrown out during the formation of the contact schists.
The granite intrusion reached its highest level in the crust at Rosetta
Head and this cupola-mass weakly hornfelsed the surrounding area but
partially mobilized the albite chlorite schists with which it came in contact.
The granite made its way up the bedding planes, using bedding and schist-
osity as structural controls, and over-rode both quartz biutite schists and
contact schists, Any albite chlorite schists along this gtanite contact were
made mobile and pushed as a mush along the dipping boundary of the
intrusion by the intruding granite above. This mush was capable of intrusion
and crystallized as a coarse albite chlorite rock of igneous aspect. The
original granite magma is considered ta have assimilated considerable
quantities of albite- and chlorite-rich rocks and its composition, porphyritic
nature and other features are thought ta be due to this cause,
‘A final movement in the emplacement af the granite at Rosetta Head
was either associated with, or caused some local stresses, as a zone of contact
schists up to Len feet wide, follows the main contact in must parts. These
rocks modify the hornfelsed quartz biotite schists and there was local devel-
213
opment of andalusite schists by isochemical contact metamorphism under
some stress,
Hence four periods of metamorphism and three phases of the granite
intrusion have been separated by this study. The first period of meta-
morphism was associated with regional factors, but the other three stages
are connected with one another and with the main emplacement, the emplace-
ment of the cupola-mass of Rosetta Head and the final movement of the
intfusive granite, respectively. Dolerite dykes—now uralitized—were injected
later, followed by a small amount of pegmatitic activity,
VIII. EXTENT AND AGE OF THE INTRUSION
There are many outcrops of granite in the Encounter Bay area (Browne
1920) all of which appear to be part of the same intrusion. The granite at
Cape Willoughby, Kangaroo Island, is considered by Tilley (1919) to be
part of the same batholith and a suite of similar rocks from south-eastern
South Australia has been described by Mawson and Parkin (1943) who
assume that the rocks are “an eastward extension of the Encounter Bay and
Cape Willoughby intrusions.”
As previously suggested (Bowes, 1953), it is considered that there was
a period of granite formation and intrusion in South Australia during early
Palaezoic times. At this fime the granitic rocks of southern and south-castern
South Australia formed upon the collapse of the eugeosyncline which ex-
tended to the east and south-east of the miogeosyncline in which the sedi-
ments of the Adelaide System were deposited, This period is correlated with
the migmatization and granite intrusions which took place in the North-
eastern Flinders Ranges, the final stages of which have been dated as
mid-Ordovician by an age determination of 400+ 50 million years on a
samarskite from a granite pegmatite (Kleeman, 1946), The postulated (?)
Early Palaeozoic age of the intruded and altered country rocks at Rosetta
Head appears compatible with the correlations.
ACKNOWLEDGMENTS
I wish to record my thanks to Professor Sir Douglas Mawson for
suggesting the area and for making available specimens and data previously
collected; to Mr, A, W. Kleeman for his advice and he)pful criticism and
to the University of Adelaide for the assistance made available by the award
of the James Barrans Scholarship.
BIBLIOGRAPHY
Bowen, N.L. 1928 The Evolution of the Igneous Rocks. Princetown
Bowes, D, R. 1953 The Genesis of Some Granitic and Associated Rocks in the
North-eastern Flinders Ranges, South Australia, Trans. Roy. Soc,
S. Aust. 76
Browne, W, R. 1920 The Igneous Rocks of Encounter Bay, South Australia.
Trans. Roy. Soc. S. Aust., 44
Day, R. A. 1933 Igneous Rocks and the Depths of the Earth. New York
Gartretr, H.W. 1903 The Port Victor Granite. Trans. Roy Soc. S, Aust., 27
Howenin, W. 1926 The Geology of the Victor Harbour, Inman Valley and
Yankalilla Districts, with special reference to the Great Inman Valley
Glacier of Permo-Carboniferous Age. Trans. Roy. Soc. S: Aust., 50
Howcutx, W. 1929 The Geology of South Australia, Adelaide
Jacx, R. L, 1923 The Building Stones of South Australia. Geol, Surv., S. Aust.,
Bull. 10
214
Kireman, A. W. 1937 The Nature and Origin of the so-called Diorite Inclu-
sions in the Granite of Granite Island. Trans, Roy. Soc. S. Aust., 61
Kreeman, A. W. 1946 An Age Determination on Samarskite fram Mount
Painter, South Australia. Trans, Roy. Soc. S. Aust., 70, (2)
Mawson, D. 1926 A Brief Resumé of Present Knowledge Relating to. the
Igneous Rocks of South Australia. Aust. Assn. Adv. Sci., 18
Mawson, D. 1947 The Adelaide Series as Developed along the Western Mar-
gin of the Flinders Ranges. Trans. Roy. Soc. S. Aust., 71, (2)
Mawson, D. and Datiwitz, W. B. 1944 Palaeozoic Igneous Rocks of Lower
South-eastern South Australia, Trans. Roy. Soc, S. Aust., 68, (2)
Mawson, D., and Parxrn, L. W. 1943 Some Granitic Rocks of South-eastern
South Australia. Trans. Roy. Soc. S. Aust., 67, (2)
Pertiyoun, F. J. 1949 Sedimentary Rocks. New York
Rozinson, E, J. 1946 The Hornfels Series of the Eastern Mt. Lofty Chain.
Portion of Thesis, University of Adelaide,
Tittey, C. E. 1919 The Petrology of the Granite Mass of Cape Willoughby
Kangaroo Island, Part I. Trans. Roy. Soc. S, Aust., 43
TYRRELL, S W. 1933 Greenstones and greywackes. Bull. Comm. géol. Finlande,
102
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1953/84 (Istinstlt) ‘350 0 041,750 0 0 ” Tibrarian 5 ear
—<————— » Printing an St:
» Sale of Publications and ” Postage, a ationery ic i i
Reprints ike Seden i413 2 . Filing Cabinets du 6716 4
” Interest Saop) ge -eegen Qeees 214 8 9 ” Insurance nese Bn 1210 O
» Lighting bes stk 12 8 8
» Cleaning Rooms x: 38 7 0
4 Sundries 717 0
» Balance 30th Sept., 1953:
A. and N.Z.
Bank Ltd..... 672 11 5
Less Out-
standing
Chqus6 5 0
100
3 8 0 1013 0 661 18 5
Savings Bank
of S.A.:
General A/c. 536 0 0
Ex Endow-
ment Fund 11 7 9 547 7 9
Cash on Hand ay 215 61,212 1 8
£2,996 1 9 £2,996 1 9
ENDOWMENT FUND
Receipts and Payments for the Year ended 30th September 1953
£sda € a a £sd4a £ s. d.
1952—October 1 1952—Sept. 20
To Balance— By Revenue A/e. wo 214 8 9
Commonwealth Inscribed » Balance
Stock 6,010 90 0 Commonwealth In-
Savings Bank of S.A, 62 18 76,072 18 7 scribed Stock ....6,010 0 Q
————— Savings Bank of S. A. | 6218 7 6,072 18 7
1953—Sept. 30
Inscribed Stock aw =199 14 6
Savings Bank of S.A... 1414 3 214 8 9
£6,287 7 4 | £6,287 7 4
rewire oo I
Audited and. found correct. The stock and Bank Balances have been verified by certificate
from the respective institutions.
M. ANGEL Ul _-Hona.
N. ANGEL, A.U.A.Com. § Auditors T. R. N. LOTHIAN, Hoa Treasurer
Adelaide, 6th October, 1953
216
AWARDS OF THE SIR JOSEPH VERCO MEDAL
1929 Pror. Warrer Howcuin, F.G.S.
1930 Jown McC. Brack, A.LS.
1931 Prov. Sin DoucLas Mawsos, O.B,E., D.Sc. B-E,, F.R.S.
1933 Pror. J. Burtow Crzranp, M.D.
1935 Pror. T. Harvey Jonnston, M.A., D.Sc,
1938 Por. J. A. Prescott, D.Sv., F.A.LC.
1943 Herpert Womenstey, A.L,S,, F.R.E.S.
1944 Paor, J. G. Woon, D.Sc. Ph.D,
1945 Crem T. Manicax, M.A., B.E., D.Sc. F.G.S.
1946. Hervent M, Hare
LIST OF FELLOWS, MEMBERS, ETC.
AS AT 30 MARCH 1953
Those marked with au asterisk (*) have contributed papers pyblished in the Society’s
Transactions. Those marked with a dagger (t+) are Life Members,
Any change in address or any other changes should be totified to the Secretary,
Noie—Yhe publications of the Society are not sent to those members whose subscriplians
are in arrear.
Bates, Honorary Feccows
1945, *Fenner, C. A. E., D.Sc., 42 Alexandra Avenue, Rose Park, Adelaide—Fellow, 1917-45;
Council, 1925-28; President, 1930-31; Vice-President, 1928-30; Secretary, 1924-25;
Treasurer, §932-33; Editor, 1934-37.
1949. *Cretann, Pror. J, B, M.D., Dashwood Road, Beaumont, S,A.—Fellow, 1895-1949;
Verco Medal, 1933; Council, 1921-26, 1932-37; President, 1927-28: 1940-41; Vice-
President, 1926-27, 1941-42.
Frttows.
194, Appre, Prov A. A., M.D., D.Sc, Ph,D., University. of Adelaide,
1953. Apcock, Miss A., 4 Gertrude Street, Norwood, $.A.
1951. Arrcaison, G, D., B.E,, Waite Research Institute (Private Mail Bac), G.P°0.,
Adelaide.
1927. *AcperMaAK, A. R., Ph.D., D.Sc, F.G.S. , Div. Indus, Chemistry, C.S.LR.O., Box 4331,
G.P.0., Melbourne, Victoria—Couneil, 1937-42.
1951. Anpvrrson, Mrs, S. H., B.Sc., Zoology Dept., University of Adelaide, S.A.
1931. Anorew, Rev. J. R., c/o Methodist Manse, Maitland.
1951, Awprews, J., M.B., B.S., 40 Seafield Avenue, Kingswood, S.A,
1935. *Anprewarrma, H. G, M.Agr.Sc., D.Sc., Waite Institute (Private Mail Bag),
Adelaide—Counctl, 1950; Vice-President, 1950-51; President, 1951-.
1935, *AnprewarrHa, Mrs. H. V., B.Agr.Sc., M.S. (nee H. V. Steele), 29 Claremont
Avenue, Netherby, S.A.
1929. *Ancer, F. M,, 34 Fullarton Road, Parkside, S.A,
1939, *AncEL, Miss L, M,, M.Sc., c/o University of Adelaide.
1945. *Bartrert, H. K., L.Th., 15 Claremont Avenue, Netherby, S.A,
1950. Brastey, A. K,, Harris Street, Marden, S.A.
1950, Brcr, R. G, B.Ag.Se., R.D.A,, Linewood Park, Mittel, S.A.
1932. Brce, P, KR. D.D.Se., L.D.S., Shell House, 170 North Terrace, Adelaide.
1928. Best, R, J., D.Sc, F.A.C.1., Waite Institute (Private Mail Bag), Adelaide,
1953. Bro, A. F., B.Sc., Zoology Department, University, Adelaide,
1934, Bracx, E. C, M.B., B.S. Magill Road, Tranmere, Adelaide.
1950. Bonnin, N. J.. MB, B.S., FRCS. (Eng:), FR.A.CS,, 144 Hil Street, North
Adelaide, S.A.
1945, *Bonyrsoy, C. W., B.Sc, A.A.C.I.; Romalo House, Romalo Avenue, Magill, S.A.
1940. BonytHon, Sir J. Lavincron, B.A, (Camb,), 263 East Terrace, Adelaide.
1945. *Boomsma, C, D,, M.Sc., B.Sc.For., 2 Celtic Avenue, South Road Park, S.A.
1947, Bowes, D. R,, Ph.D., M.Sc,, D.1.C, F.G.S., 51 Eton Street, Malvern.
1939. Brookman, Mrs. R. D. (nee A. Harvey), B.A., Meadows, S.A,
1945. Brovucuton, A. C, Farina, S.A,
1948. Brownine, T: O., B.Sc. (Syd.), Waite Institute (Private Mail Bag), Adelside.
1944. *Burpipcr, Miss N. T., M.Sc, C.S.LR.O., Div. Plant Industry, P.O.. Box 109, Cat:-
berra, A.C.T.
Bunvon, R, S., D.Sc., University of Adelaide—Coyncil, 1946,
2
Oate of
Election,
1922. *Cameseir, T. D, D.DSe, D.Sc, Dental Dept, Adelaide Hospital, Adelaide—
Council, 1928-32, 1935, 1942-45; Vice-President, 1932-34; President, 1934-35, '
1953. Canten, A. N., B.Sc., 70. Madeline Street, Burwood F 13, Vict.
1951. areata, R. G, B.Sc, c/o CS.LR.O,, Div. of Fisheries, 1 Museum Street,
Perth, W.A.
1929. Curistre, W., M.B., B.S., Education Department, Social Services, 51 Pirie Street
Adelaide—Treasurer, 1933-38,
1950, Coatsran, 5. T, BSc, 6 Iampton Street, Hawthorn, S.A,
1949. Cortiver, FP, S., Geology Department, University of Queensland.
1930. *Corgunoun, T. Ty MSc., 10 French Street, Netherby, S.A. Secretary, 1942-43.
1907. *Cooxr, W. T., D.Sc, AA.C.L, 4 South Terrace, Kensington Gardens, S.A.—Counell,
1938-41; Mice-President, 1941-42, 1943-44: President, 1942-43,
1942, *Coorsr, H. M,, 51 Hastings Street, Glenelg, S_A,
1929. *Corrox, B, ©, SA, Museum, Adelaide—Connei, 1943-46, 1948-49; Fire-President,
1949-50, 1951; President, 1950-51.
1953, Dawe, D. M. S. MB. B.Chin, M.R.CS., L.RC.P., B.A,, Institute of Medical and
Veterinary Science, Frome Road, Adelaide;
1951, Dayne, AGL, PLD, B.Sc, Waite Research Institute, Private Mail Bag, G.P.G,
co
1950, Detanp, C. M, MB, BS, DPD, DJ, 29 Gilbert Street, Goodwood, S.A.
1941. Dicxtnson, S. B., M.Sc, 51 Moseley Street, Glenelg, S.A. Council, 1949-51; Vice-
President, 1951-.
1930. Dix, E. V., Hospitals Department, Rundle Street, Adelaide, $.A.
1944. Duxstows, S. M. L, M.B., B.S., 124 Payneham Road, St. Peters, Adelaide.
1931, Dwyer, Ff, M,, M.B., B,S., 105 Port Road, Hindmarsh, 5.A.
1933. *Earpizy, Mrss C. M., M.Sc. University of Adelaide—Council, 1943-46.
1945. *Enmonns, S. J, B.A. M.Sc. Zoology Department, University, Adelaide,
1902. *Epouist, A. G, 19 Farrell Street, Glenelg, S.A—Couneil, 1949-,
1944. Freres, Mrss H. M., M.Sc., 8 Taylor's Road, Mitcham, S.A.
1927. *Fintayson, H. H,, 305 Ward Street, North Adelaide—Council, 1937-40.
1951. Fismer, R. H., 265 Goexdwood Road, Kings Park, SA. |
1923. *Fry, H. K., O.S.0., M.D, B.S., B.Sc, F.R.A,C.P,, Town Hall, Adelaide—Council,
1933-37: Wier-President, 1937-38, 1939-40; President, 1938-39,
1951. Futon, Cor, D, C.MG.,, CB.E., Aldgate, S.A.
1954. Greson, A. A., A.W.A.S.M., Geologist, Mines Department, Adelaide.
1932. *Greson, E. S, H., M.Se., 297 Cross Roads, Clarence Gardens, Adelice.
1927, Goorrev, F, K,, Box 951H, G,P.O,, Adelaide,
1935. }Go.nsacx, H., Coromandel Val'ey, S.A.
1925. Gosse, Sm James H., Gilbert House, Gilbert Place, Adelaide.
1910. *Gaant, Prov. Sin Kerr, M-Sc., F.LP., 56 Fourth Avenue, Se. Peters, S.A,
1930. Gray, J. T,, Orroroo, SA,
1933, Greaves, H., 12 Edward Street, G'ynde, S.A. |
1951, Green, J, W. 4 Holden Street, Kensington Park, S.A.
1904, Grirrivn, H. B,, Dunrobin Road, Rrighton, 5.4,
1948, Gross, G F,, B.Sc, South Australian Museum, Adelaile--Secretury, 1950-—
1944, Guevy, D, J., B.Sc. Mineral Resources Survey, Canberta, A,C,T.
1922. *Hacr, H- M., Director S.A. Museum, Adelaide—Ferro Medal, 194; Council, 1931-34,
1950-; Vice-President, 1934-36, 1937-38; Presides?, 1936-37; Treasurer, 1938-1950.
1949, Hatt, D, R,, Mern Merna, via Quorn, S.A.
1953. Hansen, I. V., B.A., 34 Herbert Road, West Croydon, §.A.
1946, *Harvy, Mrs, J. E. (nee A. C. Beckwith), M.Sc., Box 62, Smithton, Tas.
1944. Harars, J. R., B.Sc, 94 Archer Street, North Adelaide, S.A.
1947. Henperson, D. L. W., P-M.B., 20 Bourke, N.S.W.
1944. Herrror, R. 1, B.Agr.Sc,, Soil Conservator, Dept. of Agriculture, S.A.
1954. Hinroy, F. J., B.AgSe., Botanist, 298 Miugill Road, Benlaly Park
1951. Hoeexrne, L. J., 57 Marino Parade, Seacliff, S.A.
1949, Horioway. B. W., B.Sc., 33 Kyre Avenue, Kingswood, S.A,
1924. *Hossrernn, P_S, MSe, (322 Fisher Street, Fullarton, S.A.
1950. Howarp, P. F., USe., c/o Great Western Consolidated, Bullfitch, W.A,
1944, Humere, D. S, W~ 238 Payneham Road. Payneham, 5.A.
1947, Hurron, J. T.. B.Sc, 18 Emily Avenue, Clapham,
1928, Irounn, P. Kurralta, Burnside, SA,
1942, Jenxins, C F. H., Department of Agriculture, St. George’s Terrace, Perth, W.A,
1918 “Jenwison, Rev. J, C., 7 Frew Street, Fuilarton, S.A
1945, *Jessur, R, W,, M.Sc. 3 Alma Road, Fullartan, 5.4.
1910. *Jonnson, FE. A., M.D. MRCS, 1 Baker Street, Glenelg.
1950. Jouns, R. K., B.Sc, Department of Mines, Flintlers Street, Adelaide, S.A.
1951, Kavarovic, D., B.A‘Sc, (Mun), 22 Grandview Road, Toorak Gardens, S.A
21g
Date of
Eleeslon,
1954. Kaars, A. L., BE, prey C/o. North Broken Hill Led, srolaope Hi
1951. KxsTine, YN. fe Dept. Ar and Ed., P.A.C, Preparatary School, 3 Hartley R
‘esp Brightan,
tKeaamy i Mi, Ph.D., MB, F.R.GS., Khakhar Buildings, C.P, Tank Read, Rom-
*Kine, D,, M.Sc. 44 een Avenue, Blair Athol, S.A.
. *KLEEMAN, A. W., M.Ses University of Adelaide—Secretary, 1945-49: [ice-Prest-
deni, 1948-49, 1950-51; President, 1949-50.
Lenpow, G. A., M. es B, Sc E.R.C. P., A.M.P, Building, King William Street, Adelaide,
Loratan, T. R. N,, N.D. i, cN. 2). er Botanic Garderis, Adelaide.
Lowek, H, F., 7 Averue Road, Highgate, S.
*Luveroor, Mrs. N. H., M.A., Pn.D. D.LC., Fo. S., Department of Mines, 31 Flinders
Street, Adelaide,
McCurtocn, R, N., M.B.E., B.Sc. (Oxon.), B.Agr.Sci. (Syd.), Roseworthy Agricul-
tural College, S.A.
Maporen, C, B., B.D.S,, D.BiSe, Shell House, North aierrace, Adelaide,
Maszeg, D. A, B.Sc. (Hons.), Waite Institute, Adelaide,
Mann, E. A., C/o Bank of Adelaide, Adelaide,
MARSHALL, T. J. M.Aer.Se, Ph,D., Waite Institute (Private Mail Bag}, Adelaide—
Council, 1948
*Mawson, "Prov. ‘Sin Doors, 0.8.E, D.Sc, BE, PRS, University of Adelaide-~
Vereo Medal, 1931; President, 1924- 25, 1944-45: ¥ ice-President, 1923-24, 1925-26;
Council, 1941-43.
May, L. H., BSc, 691 Esplanade, Grange, S.A,
Mayo, THe "Hon, Me: Justice, LL.B., K.C., Supreme Court, Adelaide,
Mayo, G, M. E,, B,AgSc., Waite 2 Instimte (Private Mail Bag), Adelaide, S.A.
McCauray, Misa D, BA. & B.Sc., 70 Halton Terrace, Kensington Park,
McCautnezy, J. E,, MD. D Sc. (Edin), Institute of Medical and Veterinary Science,
rome Road, Adelaide.
F: , .
. tMmes, K. R, D.Sc. FES. Mines. Department, Flinders Street, Adelaide,
Mries, J. A. K, MA, y BChie. (Cant), 48 Gladys Strest, Edwardstown, S.A.
Mincuam, V. H. ee ene
tMrecuent, Peor. Sie W., CMC, M.A, D.Se., Fitzroy Ter, Prospect, SA.
Mitcee1, Paor, M. L, a. M Se. University, A
MitcHeiw, F. J., c/o The South Austrafian Museum, North Terrace, Adelaide,
Moonnouse, F, W., M.Sc., Chief Inspector of Fisheries, Flinders Street, Adelaide.
*MounTFoRD, Cc. P., 25 First Avenue, St. Peters, Adelaide.
Mourrew., J. W., Engineering and Water Supply Dept, Port Road, Thebarton, S.A
Neat-Suirtna, C. A., B.Agr.Sci., 16 Gooreen Street, Reid, Canberra, A,C,T.
Niwnes, A. R,, B.A, 62 Shetheld Street, Malvern, 5.A.
*Nortucore, K. H,, B.Agr.Sc., A.T.A.S., Waite Institute Cena Mail Bag), Adelaide.
Ocxenoen, G. P., "B.A, Schoal House, Box 63, Kimba, S.A.
*Orpner, I. L., 65 Fifth Avenue, St. Peters, S.A.
*Oszonn, Pror. T. G. B., D. Se., Department of Botany, Oxford, England—Counedl,
1915-20, Ba President. $925-26-- Vice-President, 1924-25, 1926-27,
*Paruin, L. Me Sc, ¢/o North Broken Hill Mining Co., Melbourne, Victoria.
Parxinsox, K ‘a B. Sc, 8 Mooreland Avenue, Beverley, SIA.
Patrrson, G., 68 Partridge Street, Glenelg, S.A-
PAuLL, A. G, 10 Millon Avenue, Fulfarton Estate, S.A
. *Prrra, C. S,, 'D.Sc.. Waite Institute (Private Mail Bag}, Adelaide—Council, 1941-435;
Vice-President 1943-45, 1946-47 President. 1945-46.
Powrtr, J. K. . BSc, CSIRO., Division of Biochemistry, University, Adelaide.
Poynton, J. “O., MD. MA. ChE, MRCS, LRCP, Institute Medicine, Vet
Science, Frome Road, Adelaide.
Pratrr, R. G., 81 Park Terrace, North Unley, S
’ *Paescorr, “PROF. j. A, CBE, DSe., ALC, PES. Waite Instinite (Private Mail
Bag), Adelaide—V’erco Medai, 1938; Council, 1927-30, 1935-39; Wice-President,
1930-32; Evendent 1932-33,
Parcs, A. G., M.G., M.A., Litt.D., F.R.GS,, 46 Pennington Tersate, North Adelaide,
Pryor, L. D., se Dip. For., 32 La Perouse Street, Griffith, N.S.W.
*Rarmcay, J. H, B.Sc., Bureau of Mineral Resources, Melbourne Building. Canberra,
Raysen, P., B. Se) Bos, 111, SA.
Riceman, D. S., M.Sc., B.Agr. Sc, CSLRO, Division of Nutrition, Adelaide,
Rienen, Ww. R, BSc, Oceanographic Institute, Gettenburg, Syeeden.
*Rimes, ‘ D., B.Sc., 24 Winston Avenue, Clarence Gardens, S.A.
Rex, C. E., 42 Waymouth Avenue, Glandore, S.A,
*Restnson, E.G, M.Sc. 42 Riverside Drive, Sudbury, Ontario, Canada.
2
Date of
Election
1953, Rocers, W. P., Ph,D., Zoo! ent University, Adelaide,
ter Baath, LD cfg Huh Scawl, Port Pita, SA
195%, Rows, S.A, 22 Shelley Street, Firle, SA.
1951. E,, B.Sc, 22 Shelley Street, Firle, S.A.
1950. voo, Pror. E A. B.Sc, A.M,, University, Adelaide, S.A.
1945. Rv, J. R,, ne Penola Estate, Penola, S.A.
1944, *Sannars,,. Miss D B,, M.Se,, University of Queens; vie Brisbane, Queeosland.
1950, Saunneys, F. L., ‘99, Winchester Street, Malvern,
1933. Scuwmmex, M., MB, B.S, 175 North Ter, Adel
1951, Seorr, T. D,, Be c/o S.A. Museum, North. Terrace, Adelaide, S.A.
1946. *Sranrt, E. R, M.Sc., C.S.LR.O., Division. of Industrial Chamistry, Box 4331, G.P.0,
1924, *5 Metbbunie, Viet BSc, En and Water. Supply Vi
‘ EGNIT, G5 gwineer ater, Supp! trnent, ictoria
Square, Adelaide—Se feretary, 1930- recone 1937-38; Vice Bes ident, 1938-39,
1940-41; President, 1939-40,
1925. *Sueaap, H., Port Elliot, $.4.
1936. *SHkaAgy, K., Fisheries Research Div, C_S.1.R.0., Universi a De of on Medians, W.A,
1945. SHEPHERD, ‘T. H,, M.Sc, B.A, ¢/o Anglo-Weatralian
1934. Suinxrievo, R. Cc. Salisbury, 5-A-
1924. Simpson, F. N., Pirie Street, Adelaide.
1949. Simpson, dD, A, M.B., B.S., 42 Lockwood Road, Burnside, S.A.
1941. *Suire, T. 1, B.Sc, Regional Planning Section, Department of National Develop-
ment, Canberra, A, CT
1M]. *5ourecoir, R. V., M.B., B.S., D.T,M. & H., 13 Jasper Street, Hyde Park, S.A—
Couneil, "1948-51; Treasurer, 1951-_
1936. Sourn won, A.R, ‘M.D., M.S. (Adel), M.R.C.P., Wootestig Ter., Glen Osmond, §.A,
1947, ean K 1. Ly MSc., 15 Main Ro d, Richmo nd, S:A.—Council, 1951+.
1936. +*Spzicc, RC. "MSc. ” Mines Menarinent Flinders Street, Adelaide.
1951. STEADMAW, Rev. W. R, 8 Blairgowrie Road, St. Georges, S.A,
1947. Spurinc, ML. B., BA Sc, Agricultural College, Roseworthy, 5.A.
1949, *Spry, A. H., B.Sc., 63 LeFevre Terrace, North Adelaide, S.A.
1938. *STEPHENS, ¢ at D.Se,, Waite Institute (Private Mail Pag), Adetaid
1935. Srrickianp, A. G, M.Agr. Sc., 11 Wootoona Terrace, Glen Osmond, SA —Council,
1947,
1932. Swan, D. C, M.Sc, Waite Institute (Private Mail Bag). Adelaide—Secretary,
1940-42 ; Vie Eeeeleaet, 1946-47, 1948-49; President, 1947-48,
1M8, Swann, F. J. W., 38 Angas Road, Lower Mitcham, S.A.
1931. Swirsxt, P,, Mag. Sc, 22a Henry Street, Croydon, $.A-
1934. Symons, 1, G. 35 anreas Street, Lower Mitcham, S.A—Editor, 1947-,
1929. *Taveor, J. K., B.A, MSc., Waite Institute (Private Mail Bag), Adelaide—Counecsl,
1940-43, 1947-505 "Librarian, 1951.
1950. Tavuor, G. H., BSc, Department of Mines, Old Legislative Council Building, North
Terrace, Ads S.A.
1948. eons, I. M, M.Sc. (Wales), University, Adelaide—Seerelary, 1948-50; Council,
1938, *THomas, Mrs, I, M. Mn e P, M. Mawson), M.Sc., 36 King Street, Brighton.
1940, THomson, Capt. J. M. 138 Military Road, Semaphore South,
1923. *Tinnare, N. B., BSc, South Australian Museum, Adelaide—Seeretary, 1935-36;
Corned, 1946-47 : Vice-President, 1947-48, 1949-50; President, 1948-49
7945, . §, M.Sc, B.AgrSc., Waite Institute (Private Mail Bas), Adelaide.
1937. *TRUMILE, Prov. H. Cy D.Sc, M.Agr.Sc., Waite Institute (Private Mail Bag),
Adelaide—Council, 1942-1945 ; Pice-President, 1945-46, 1947-48; President, 1946-47.
1925. Turner, D, C, Brookman ' Buildings, Grenfell Street, Adelaide,
1950. Vuerca, S, T, Port Lincola, 8 S.A.
1912. *Warp. L. K., 1.S.0., B.A., B.E. D.Se.. 22 Northumberland Avenue, Tusmore—Counciél,
1924-27, 1033, 353 Vice- President, 1927-28: President, 1922-3),
1941. *Warr, D. C., Agr. Se, Div, Plant Industry, C.S.LR.0,, Canberra, A.C.T,
1936, WATERHOUSE, Miss L. M, 35 King Street, Brighton, S.A
1953, Waterman, R, A, BA., M.A., PhD.. North-western University, Evanston,
Thinois, As S.A,
1954. Wens, B. P., B.Sc., Geologist, Mines Departs, onaee
1954. Wetns, C. B., ae Sc, Research Officer, C.S.LR Soils ‘Division, Adelaide.
2939, *Wrenrnc, Rev. B J. 5 York Street, Henley Beac .
1949, *Weoener, C. F., B. Se, Department Mines, Flinders Street, Adelaide, S.A.
1954. Warrecaw, A. I, B.Sc., C/o. Adelaide Boys High School, Adelaide.
16, WHrTLe, A. W. G., B.Sc., Mities Departenenit Flinders Street, Adelaide,
1950. Wruaams, L. D,, *Duntosa,” Meningie, S.
1946. *Wrison, A. FP. MSe., University of W.A., edtands, W.A.
220
Date of
Election ease se R
1938. *Wizson, J. O., C.S.LR.O., Division of Nutrition, Adelaide.
1930. *Womerstry, H., F.R.ES, ALS. (Hon. causa), S.A. Museum, Adelaide—Verco
Medal, 1943; Secretary, 1936-37; Editor, 1937-43, 1945-47; President, 1943-44; Vice-
regnient, 1944-45: Rep. Fauna and Flora Protection Committee, 1945; Treasurer,
1950-51.
1944, *Womerstey, H. B. S., M.Sc., University of Adelaide.
1944. Womerstey, J. S., B.Sc, Lae, New Guinea,
1923. *Woon, Pror. J. t, D.Sc, Ph.D., University of Adelaide—Verco Meaal, 1944;
Council, 1938-40; Vice-President, 1940-41, 1942-43; Rep. Fauna and Flora Board,
1940-; President, 1941-42; Council, 194448.
1950. Woopnarp, G. D., 20 Kensington Road, Leabrook, S.A.
1953. WoopHouse, L. R., 15 Robert Street, North Unley, S.A.
1943. Wooptanps, Harotp, Box 989 H, G.P.O., Adelaide.
1945. Worruuey, B. W., B.A. M.Sc., A. Inst. P., University, Adelaide,
1948. *Wymonp, A, P., B.Sc., 4 Woodley Road, Glen Osmond, S.A.
1949. Yeates, J. N., L.S. AM.LE, A.M.LM.E, Richards Buildings, 99 Currie Street,
Adelaide, S.A.
1944, Zier, W. J., Dip.For., F.L.S. (Lon.), 7 Rupert Street, Footscray West, W.12, Vict.
221
GENERAL INDEX
[Names in italics indicate that the forms classified are new to science]
Centenary Addresses, i-xiy
Angel, L. Madeline: Parorchis acanthits var.
australis, n. var., with an Account of the
Life Cycle in South Australia
Australonereis ehlersi, 19
Babiangia bulbifera, 98
Bowes, D. R.: The Metamorphic and Igneous
History of Rosetta Head, South Aus-
tralia, 182-214.
Boydaia derricki, 65
Ceratocephala edinondst, 23
Cleland, J. B., and N, B. Tindale: The Eco-
Jogical Surroundings of the WNealia
Natives in Central Australia, and Native
Names and Uses of Plants, 81-86
Eight New Species of Trombiculidae (Aca-
ra) from Queensland: H. Womersley,
67-80
Fuschongastia parva, 74; E. popet, 76; E.
procang, 77; E. andromeda, 80
Hansen, Tan V.: An Account of the Negalia
Initiation Ceremonies at Yuendumu, Cen-
tral Australia, January 1953, 175-181
Hartman, Olga: Australian Nereidae, 1-41
Hossfeld, Paul §.: Stratigraphy and Struc-
ture of the Northern Territory of Aus-
tralia, 103-161
ichthyostrongylus clelandi n,g., n.sp., from
an Australian Shark: Patricia M. Maw-
son, 162
Ludbrook, N. H.: The Molluscan Fauna of
the Pliocene Strata underlying the Ade-
laide Plains, Part I, 42-64
Mawson, Patricia M.: Ichthyostrongylus cle-
lendt nog, nosp, fromm an Australian
Shark, 162
Metamorphic and Igneous History of Rosetta
Head, South Austraha: D. R, Bowes,
182-214
Micromereis halei, 25
Molluscan Fauna of the Pliocene Strata
underlying the Adelaide Plains, Part I:
N, H. Ludbrook, 42-64
Mountford, Charles P.: A Carved Human
Figure from the Durack Range, north-
western Australia, 87
Nercidae, Australian; Olga Hartman, 1-41
Nealia Natives in Central Australia, Ecologi-
cal Surrotindings of: J. B. Cleland and
N. B. Tindale, 81-86
Negalia Initiation Ceremonies at Ytrendumu,
Central Australia, January 1953; An
Account of the: Ian V. Hansen, 175-181
Neotrombidium barringunense, 89-97
Northern Territory of Australia, Strati-
graphy and Structure of: Paul S. Hoss-
feld, 103-161
Parorchis acanthus var. australis, n. var.,
with an Account of the Life Cycle in
South Australia; L. Madeline Angel,
164-174
Rosetta Head, South Australia: The Meta-
morphic and Igneous History of: D. R.
Bowes, 182-214
Stratigraphy and Structure of the Notthern
Territory of Australia: Paul S. Hoss-
feld, 103-161
Sauthcatt, R. V.: The Genus Neotrombidium
(Acarina: Leeuwenhoekiidae), I, Descrip-
tion of the Ovum and Larva of Neo-
frombidium barringunense Hirst 1928,
with an Account of the Biology of the
Genus, 89-97
Southcott, R. V.; Description of a New
Genus and Species of Larval Trombiculid
Mite from New Guinea, 98-102
Trombicula derricki, 67; T. antechinus, 69;
T. thylogale, 71; T. Mackayensis, 72
Tindale, N. B., J. B. Cleland and: The Eco-
logical Surroundings of the Nealia
Natives in Central Australia and Native
Names and Uses of Plants, 81-86
Womersley, H.: Atother New Species of
Boydaia (Speleognathidae, Acarina) from
Australia, 65
Womertsley, TI: light New Species of
Trombiculidae (Acarina) from Queens-
land, 67-79
CONTENTS
CENTENARY MEETING, 24 September 1953—
Dickinson, 5. B.: Centenary of the Society
Rocers, W. P.: The Biological Sciences ....
Prescorr, J. A.:-Agricultural Sciences
Mawson, D.; The Role of Geology in the Activities of the Society
HartMan, Orca: Australian Nereidae
Lupsroox, N. H.: Molluscan Fauna of the Pliocene Strata underlying the Adelaide
; Plains
Womerstey, H.: Another New Species of Boydaia (Speleognathidae : Acariua)
from Australia
Womerstey, H.: Eight New Species of Trombiculidae (Acarina) from Queens-
land
CieLann, J. B., and Trxnare, N. B.: Ecological Surroundings of the Ngalia
Natives in Central Australia and Native Names and Uses of Plants ...
Mountrorp, C. P.: A Carved Human Figure from the Durack Ranges, North-
western Australia i Pe:
Sourncorr, R. V.: The Genus Neotrombidium (Acarina :_Leeuwenhoekiidae)
I, Description of the Ovum and Larva of Neotrombidium Barringun-
ense Hirst 1928, with an Account of the Biology of the Genus ....
Soutucorr, R. V.: Description of a New Genus and Species of Larval Trom-
biculid Mite from New Guinca
Hossrerp, P. S.: Stratigraphy and Structure of the Northern Territory of
Australia
Mawson, Partricra M.: Ichthyostrongylus clelandi, n.g., n.sp., from an Aus-
tralian Shark
ANGEL, L, Mapettne: Parorchis acanthus var. australis, n.var., with an Account
of the Life Cycle in South Australia
Hansen, tan V.: An Account of the Ngalia Initiation Ceremonies at Yuendumu,
Central Australia, January 1953
Bowes, D. R.: The Metamorphic and Igneous History of Rosetta Head, South
Australia
eee
Page
i—iii
iv—vi
Vii—xi
xii—xiv
1—41
81—86
87—88
89—97
98—102
103—161
162—163
164—174
175—181
182—214
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