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1

Entwisle, Timothy J., and John Huisman. "Algal systematics in Australia." Australian Systematic Botany 11, no. 2 (1998): 203. http://dx.doi.org/10.1071/sb97006.

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Documentation of the algal flora of Australia had its beginnings in the seventeenth century and has progressed sporadically but with increasing vigour ever since. Earlier studies dealing with Australian algae were undertaken by overseas phycologists working with specimens collected during scientific voyages or short visits. Recent floristic studies have concentrated on specific regions, isolated localities, or particular taxonomic or ecological groupings. The algal flora of Australia is unevenly documented: northern Australia remains largely uncollected for seaweeds and marine phytoplankton, f
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2

Field, Ashley Raymond. "Classification and typification of Australian lycophytes and ferns based on Pteridophyte Phylogeny Group classification PPG I." Australian Systematic Botany 33, no. 1 (2020): 1. http://dx.doi.org/10.1071/sb18011.

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The classification and typification of all Australian ferns and lycophytes is updated to reflect the Pteridophyte Phylogeny Group I classification and the International Code of Nomenclature for algae, fungi, and plants, presenting 8 new nomenclatural combinations as well as 85 lectotypifications. The Australian fern and lycophyte flora comprises 2 classes, 14 orders, 32 families, 134 genera and 528 species and subspecies with the addition of 8 newly recorded and 6 newly recognised species since the publication of the Flora of Australia fern volume in 1998. Overall, 208 species are endemic to A
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3

Lucas, A. M. "Assistance at a distance: George Bentham, Ferdinand von Mueller and the production of Flora australiensis." Archives of Natural History 30, no. 2 (October 2003): 255–81. http://dx.doi.org/10.3366/anh.2003.30.2.255.

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George Bentham's seven volume Flora australiensis (1863–1879) was the first continental Flora, and for over a century was the only flora treating the whole of Australia. The work was produced with the “assistance” of Ferdinand Mueller, later von Mueller, the Government Botanist of Victoria from 1853, who loaned his collection, group by group, to Kew, enabling Bentham to compare the specimens with those in British and European herbaria. Mueller, who himself had wished to write the Flora, was stimulated to produce descriptions of the species as they were prepared for shipment, and Bentham's time
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4

Renner, Matt A. M., Margaret M. Heslewood, Simon D. F. Patzak, Alfons Schäfer-Verwimp, and Jochen Heinrichs. "The genera Chiastocaulon, Cryptoplagiochila and Pedinophyllum (Plagiochilaceae) in Australia." Australian Systematic Botany 29, no. 5 (2016): 358. http://dx.doi.org/10.1071/sb16029.

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Molecular and morphological data support the recognition of seven species of Chiastocaulon in Australia, of which four, namely C. braunianum and C. geminifolium comb. nov. from tropical north-eastern Queensland and C. proliferum and C. flamabilis sp. nov. from Tasmania (and New Zealand), represent new records. The other three species accepted for Australia are C. biserialis, C. dendroides and C. oppositum. Chiastocaulon conjugatum is excluded from the Australian flora, because previous Australian records are based on misidentifications of C. braunianum and Plagiochila retrospectans. Pedinophyl
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5

Fensham, R. J., and B. Laffineur. "Defining the native and naturalised flora for the Australian continent." Australian Journal of Botany 67, no. 1 (2019): 55. http://dx.doi.org/10.1071/bt18168.

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The value of distinguishing between plant species regarded as ‘native’ and ‘alien’ has special relevance in the island continent of Australia, where European settlement was a springboard for human-assisted plant dispersal. The year of European settlement is proposed here as providing a distinction between a ‘native’ and ‘naturalised’ flora and is applied for the entire Australian flora of vascular plants. Herbarium collections and ecological criteria were employed to determine the status of 168 species of ambiguous origin. The date of 1788 proved to be a relatively straightforward criterion to
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6

Millar, AJK. "Marine red algae of the Coffs Harbour region, northern New South Wales." Australian Systematic Botany 3, no. 3 (1990): 293. http://dx.doi.org/10.1071/sb9900293.

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The marine benthic red algae of the Coffs Harbour region are described and illustrated in detail. The survey constitutes the first ever detailed descriptive and illustrative mainland regional monograph of any area along the entire eastern Australian seaboard. Collections made intertidally and to depths of 20 m have included 119 species in 74 genera, 26 families, and 8 orders of Rhodophyta, of which 54 (45%) were previously unrecorded from eastern Australia, 22 (18%) are new records for the whole of Australia (16 being new Southern Hemisphere records), 1 (Dictyothumnion) constitutes a new genus
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7

Crisp, M. D., S. Laffan, H. P. Linder, and A. Monro. "Endemism in the Australian flora." Journal of Biogeography 28, no. 2 (February 2001): 183–98. http://dx.doi.org/10.1046/j.1365-2699.2001.00524.x.

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Beudel, Saskia, and Margo Daly. "Gallant Desert Flora: Olive Pink’s Australian Arid Regions Flora Reserve." Historical Records of Australian Science 25, no. 2 (2014): 227. http://dx.doi.org/10.1071/hr14016.

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In the mid-1950s Olive Pink campaigned to have an area of land in Alice Springs set aside as a flora reserve. In 1956 the area was gazetted as the Australian Arid Regions Flora Reserve, with Pink appointed as honorary curator. Although Pink was not a professional horticulturalist or botanist, she established a garden that marked itself out from contemporary gardens, such as Maranoa Gardens and the Australian National Botanic Gardens, which were similarly committed to showcasing indigenous Australian plants. Pink's approach was pioneering in that she aimed to create a collection of plants selec
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9

Fleischmann, Andreas. "The huge scientific footprint of Allen James Lowrie (1948 – 2021)." Carnivorous Plant Newsletter 51, no. 1 (March 1, 2022): 22–39. http://dx.doi.org/10.55360/cpn511.af192.

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Allen Lowrie was a not a university trained botanist. He was a botanist by passion. His studies and observations of Australian carnivorous plants and triggerplants for about a half-century will inevitably impact every person with an interest in those plants from the Australian flora. It is not an exaggeration to claim that he was probably the most influential person regarding our recent understanding and knowledge of the carnivorous plant flora of Australia. No other botanist – neither 20th or 21st Century nor before – discovered and described to science more new carnivorous plant species or t
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10

Crawford, Andrew D., Kathryn J. Steadman, Julie A. Plummer, Anne Cochrane, and Robin J. Probert. "Analysis of seed-bank data confirms suitability of international seed-storage standards for the Australian flora." Australian Journal of Botany 55, no. 1 (2007): 18. http://dx.doi.org/10.1071/bt06038.

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The suitability of applying international standards for long-term seed storage to the Australian flora was examined by reviewing seed-storage data from the Western Australian Threatened Flora Seed Centre. The 375 collections examined represented 176 taxa from 44 genera and 16 families. A high proportion of collections, representative of some of the most common genera in Australia, maintained viability in the short (<5 years) and medium (5–12 years) term. Declines in germination were evident for a small number of collections, representing 10 taxa, stored for 5–12 years. However, many of the
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11

Greenwood, DR. "Eocene monsoon forests in central Australia?" Australian Systematic Botany 9, no. 2 (1996): 95. http://dx.doi.org/10.1071/sb9960095.

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The Australian Tertiary plant fossil record documents rainforests of a tropical to temperate character in south-eastern and south-western Australia for much of the Early Tertiary, and also shows the climatically mediated contraction of these rainforests in the mid to Late Tertiary. The fossil record of Australian monsoon forests, that is semi-evergreen to deciduous vine forests and woodlands of the wet-dry tropics, however, is poorly known. Phytogeographic analyses have suggested an immigrant origin for some floral elements of present day monsoon forests in northern Australia, while other elem
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12

Burrett, C., N. Duhid, R. Berry, and R. Varne. "Asian and south-western Pacific continental terranes derived from Gondwana, and their biogeographic significance." Australian Systematic Botany 4, no. 1 (1991): 13. http://dx.doi.org/10.1071/sb9910013.

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The recent recognition of numerous small geological terranes in the Indo-Pacific region has revolutionised our understanding of geological and biogeographic processes. Most of these terranes rifted from Gondwana. The Shan-Thai terrane rifted from Australia in the Permian and collided with Indo-China in the Triassic. Parts of Sumatra and Kalimantan may have rifted from Australia in the Cretaceous and carried an angiosperm flora north. Other terranes, now dispersed in South-East Asia and in the Pacific were, at various times in the Cenozoic, part of the Australian continent. Faunal and floral mo
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13

Byrne, Margaret, and Daniel J. Murphy. "The origins and evolutionary history of xerophytic vegetation in Australia." Australian Journal of Botany 68, no. 3 (2020): 195. http://dx.doi.org/10.1071/bt20022.

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The xeromorphic vegetation is a significant component of the Australian flora and phylogenetic and phylogeographic analysis of xeromorphic plants provides a basis for understanding the origins and evolutionary history of the Australian vegetation. Here we expand on previous reviews of the origins and maintenance of the Australian flora with an emphasis on the xeromorphic component. Phylogenetic evidence supports fossil evidence for evolution of sclerophyll and xeromorphic vegetation from the Eocene with lineages becoming more common in the Oligocene and Miocene, a time of major change in clima
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14

Pole, M. "Keeping in Touch: Vegetation Prehistory on Both Sides of the Tasman." Australian Systematic Botany 6, no. 5 (1993): 387. http://dx.doi.org/10.1071/sb9930387.

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At the end of the Cretaceous New Zealand broke away from the Australian-Antarctic continental mass and was physically isolated by the Tasman Sea. Early in the Tertiary New Zealand moved a long way north relative to Australia, but with the rapid northward movement of Australia, starting in the Eocene, Australia overtook New Zealand, so that much of the South Island of New Zealand now lies south of Tasmania. The northward and relative movements of the two blocks provide an interesting framework for comparing the development of their vegetation. In the Late Cretaceous, New Zealand and Australia w
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15

Coates, David J., and Stephen D. Hopper. "Preface to 'Genetics and Conservation of Australian Flora'." Australian Journal of Botany 48, no. 3 (2000): I. http://dx.doi.org/10.1071/btv48n3_pr.

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Conservation of Australian plants depends on a spectrum of activities from descriptive and experimental biological studies to active management and restoration of wild ecosystems by local communities who value their native biota. On the basis of the premise that available resources for conservation will not allow for all threatened biodiversity to be saved, some systematists and conservation geneticists argue that phylogenetic relationships should be used to set conservation priorities. The principle advocated is that characters, not species number, should become the currency of conservation,
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16

Miller, G. H., J. W. Magee, M. L. Fogel, and M. K. Gagan. "Detecting human impacts on the flora, fauna, and summer monsoon of Pleistocene Australia." Climate of the Past 3, no. 3 (August 6, 2007): 463–73. http://dx.doi.org/10.5194/cp-3-463-2007.

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Abstract. The moisture balance across northern and central Australia is dominated by changes in the strength of the Australian Summer Monsoon. Lake-level records that record changes in monsoon strength on orbital timescales are most consistent with a Northern Hemisphere insolation control on monsoon strength, a result consistent with recent modeling studies. A weak Holocene monsoon relative to monsoon strength 65–60 ka, despite stronger forcing, suggests a changed monsoon regime after 60 ka. Shortly after 60 ka humans colonized Australia and all of Australia's largest mammals became extinct. B
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17

Martin, Helene A. "The history of the family Onagraceae in Australia and its relevance to biogeography." Australian Journal of Botany 51, no. 5 (2003): 585. http://dx.doi.org/10.1071/bt03033.

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The family Onagraceae is a relatively minor part of the Australian flora but it has a long history in Australia: a probable Ludwigia dates from the Eocene; Fuchsia, not native to Australia today, is present from early Oligocene times; and Epilobium is found only in the Pleistocene. Onagraceae first appears in the Late Cretaceous in northern South America and southern North America, where it is thought to have originated, and Ludwigia dates from the Palaeocene. It is thought that Ludwigia migrated into Australia via a northern route. Fuchsia in Australia predates its first appearance in New Zea
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18

Estes, James A., and Peter D. Steinberg. "Predation, herbivory, and kelp evolution." Paleobiology 14, no. 1 (1988): 19–36. http://dx.doi.org/10.1017/s0094837300011775.

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We propose that the kelps (Laminariales) radiated in the North Pacific following the onset of late Cenozoic polar cooling. The evidence is that (1) extant kelps occur exclusively in cold-water habitats; (2) all but one of 27 kelp genera occur in the North Pacific, 19 of these exclusively; and (3) limpets and herbivorous marine mammals obligately associated with kelps or other stipitate brown algae appeared late in the Cenozoic, even though more generalized forms of both groups are much older. We propose, further, that sea otters and perhaps other groups of benthic-feeding predatory mammals, wh
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19

Peacock, Jim, Bryan Barlow, and Roger Carolin. "Spencer Smith-White 1909 - 1998." Historical Records of Australian Science 22, no. 2 (2011): 277. http://dx.doi.org/10.1071/hr11007.

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Spencer Smith-White's research group at the University of Sydney was for many years the foremost laboratory studying the cytology, cytogenetics and cytoevolution of the Australian flora. He pioneered this field with his chromosomal studies on major Australian families, such as the Rutaceae, Myrtaceae, Proteaceae and Epacridaceae. His cytogenetic analyses underpinned his discussions of the origins and distribution of the major elements of the Australian flora.
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20

Lamont, G. P. "AUSTRALIAN NATIVE FLORA AS ORNAMENTAL POTTED PLANTS." Acta Horticulturae, no. 205 (March 1987): 203–6. http://dx.doi.org/10.17660/actahortic.1987.205.29.

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21

Frank, Helen. "Discovering Australia Through Fiction: French Translators as Aventuriers." Meta 51, no. 3 (September 21, 2006): 482–503. http://dx.doi.org/10.7202/013554ar.

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Abstract The translation into French of referents of Australia and Australianness in fiction necessitates a considerable variety of translational tendencies and interpretive choices. This study focuses on French translations of selected passages and blurbs from Australian fiction set in regional Australia to determine how referents of Australian flora, fauna, landscape and people are translated and interpreted in a non-English speaking cultural system. Guided by concerns for the target readers’ understanding of the text, French translators employ normative strategies and adaptive procedures co
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22

Tan, BC, HP Ramsey, and WB Schofield. "A contribution to Australian Sematophyllaceae (Bryopsida)." Australian Systematic Botany 9, no. 3 (1996): 319. http://dx.doi.org/10.1071/sb9960319.

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The family Sematophyllaceae in Australia is narrowly defined to consist of 13 genera and about 36 species. Genera such as Taxithelium, Pseudohypnella and Glossadelphus are excluded. An identification key to the accepted Australian genera of Sematophyllaceae is provided. New additions to the Flora of Australia include Acroporium lamprophyllum var. percaudatum comb. & stat. nov., Clastobryurn epiphyllum, C. conspicuum, Papillidiopsis ramulina, Trichosteleum boschii and T. ruficaule. Trichosteleum elegantulunz is a new synonym of T. ruficaule. Taxa excluded from Sematophyllaceae are Acroporiu
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23

Sala, Samuele, Scott K. Micke, and Gavin R. Flematti. "Marine Natural Products from Flora and Fauna of the Western Australian Coast: Taxonomy, Isolation and Biological Activity." Molecules 28, no. 3 (February 2, 2023): 1452. http://dx.doi.org/10.3390/molecules28031452.

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Marine natural products occurring along the Western Australian coastline are the focus of this review. Western Australia covers one-third of the Australian coast, from tropical waters in the far north of the state to cooler temperate and Antarctic waters in the south. Over 40 years of research has resulted in the identification of a number of different types of secondary metabolites including terpenoids, alkaloids, polyketides, fatty acid derivatives, peptides and arsenic-containing natural products. Many of these compounds have been reported to display a variety of bioactivities. A descriptio
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24

MARTYNYUK, O. "LEXICAL STYLISTIC AND PHONETIC FEATURES OF THE AUSTRALIAN ENGLISH LANGUAGE IN THE CONTEXT OF LINGUISTIC COUNTRY STUDIES." Current issues of linguistics and translation studies, no. 19 (October 30, 2020): 29–34. http://dx.doi.org/10.31891/2415-7929-2019-19-6.

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The article deals with the process of formation and development of the Australian English language, characterizes its present-day lexical, stylistic and phonetic features. It has been found out that the Australian variety of the English language was formed as a result of interaction and development of dialects, colloquialisms, slang, through which the first settlers and emigrants from Great Britain, the United States and other countries of the world communicated. As far as everyday vocabulary is concerned, Australian English shares words and phrases with both British and American English, but
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25

Miller, G. H., J. W. Magee, M. L. Fogel, and M. K. Gagan. "Detecting human impacts on the flora, fauna, and summer monsoon of Pleistocene Australia." Climate of the Past Discussions 2, no. 4 (August 18, 2006): 535–62. http://dx.doi.org/10.5194/cpd-2-535-2006.

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Abstract. All of Australia's largest mammalian vertebrates became extinct 50 to 45 ka (thousand years ago), shortly after human colonization. Between 60 and 40 ka Australian climate was similar to present and not changing rapidly. Consequently, attention has turned toward plausible human mechanisms for the extinction, with proponents for over-hunting, ecosystem change, and introduced disease. To differentiate between these options we utilize isotopic tracers of diet preserved in eggshells of two large, flightless birds to track the status of ecosystems before and after human colonization. δ13C
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Radev, Zheko. "Comparing protein content of pollen and his impact on the lenght of life of honeybees." Journal of the Hellenic Veterinary Medical Society 73, no. 1 (April 29, 2022): 3835–40. http://dx.doi.org/10.12681/jhvms.25905.

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The objective of the research work was to compare the protein content of pollen from some plants visited frequently by honey bees in Bulgarian and Australian flora, and study the length of life of worker honey bees fed by pollen with different protein content. In this study the number of the same floral species, were described nine. Most number of favorite plants for honey bees are from Asteraceae – 5. The percentage of the total protein content in the compared bee-collected pollen grains ranged from: 11.5% for Chondrilla juncea to 25.1% for that of Brassica napus, and the average value was 18
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Cowling, Richard M., Caryl Logie, Joan Brady, Margie Middleton, and B. Adriaan Grobler. "Taxonomic, biological and geographical traits of species in a coastal dune flora in the southeastern Cape Floristic Region: regional and global comparisons." PeerJ 7 (July 31, 2019): e7336. http://dx.doi.org/10.7717/peerj.7336.

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In Mediterranean-Climate Ecosystems (MCEs), Holocene coastal dunes comprise small, fragmented and dynamic features which have nutritionally imbalanced and excessively drained, droughty, sandy soils. These characteristics, along with summer drought and salt-laden winds, pose many challenges for plant colonization and persistence. Consequently, MCE dune floras are likely to be distinctive with a high proportion of habitat specialists and strong convergence in growth form mixes. Very little research has compared the species traits of dune floras within and across MCEs. This paper contributes to f
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Parsons, R. F., and Stephen D. Hopper. "Monocotyledonous geophytes: comparison of south-western Australia with other areas of mediterranean climate." Australian Journal of Botany 51, no. 2 (2003): 129. http://dx.doi.org/10.1071/bt02067.

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Recent data on monocotyledonous geophytes from south-western Australia are compiled and compared with those from other areas of mainly mediterranean climate, especially California, Chile and Victoria, Australia. South-western Australia has a high monocot geophyte diversity of 496 species (7% of an estimated native flora of 7100 vascular species), like Victoria (12%) and the Cape region (14%). As in Victoria, orchids are by far the most important group, with c. 400 species, including those likely to be described once ongoing taxonomic research is completed. South-western Australia has higher ge
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Wulff, Adrien S., Shane R. Turner, Bruno Fogliani, and Laurent L'Huillier. "Smoke stimulates germination in two divergent Gondwanan species (Hibbertiapancheri and Scaevola montana) endemic to the biodiversity hotspot of New Caledonia." Seed Science Research 22, no. 4 (July 30, 2012): 311–16. http://dx.doi.org/10.1017/s0960258512000141.

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AbstractDue to shared geological history and proximity, the flora of New Caledonia is closely linked to other Gondwanan land fragments such as Australia and New Zealand. Many predominant Australian groups are well represented within the New Caledonian flora, including the genera Hibbertia (23 species) and Scaevola (10 species). Previous studies have found that these two genera in particular have a marked positive germination response to smoke products, although all previous studies have centred on Australian species from fire-prone environments. In this present study, we test the hypothesis th
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Broadhurst, Linda, Martin Breed, Andrew Lowe, Jason Bragg, Renee Catullo, David Coates, Francisco Encinas-Viso, et al. "Genetic diversity and structure of the Australian flora." Diversity and Distributions 23, no. 1 (November 13, 2016): 41–52. http://dx.doi.org/10.1111/ddi.12505.

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Burgman, M. A., D. Keith, S. D. Hopper, D. Widyatmoko, and C. Drill. "Threat syndromes and conservation of the Australian flora." Biological Conservation 134, no. 1 (January 2007): 73–82. http://dx.doi.org/10.1016/j.biocon.2006.08.005.

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Christophel, David C. "Evolution of the Australian flora through the Tertiary." Plant Systematics and Evolution 162, no. 1-4 (1989): 63–78. http://dx.doi.org/10.1007/bf00936910.

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Trigger, David S., and Lesley Head. "Restored Nature, Familiar Culture: Contesting Visions for Preferred Environments in Australian Cities." Nature and Culture 5, no. 3 (December 1, 2010): 231–50. http://dx.doi.org/10.3167/nc.2010.050302.

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How are preferences for “native” and “introduced” species of plants and animals given expression in Australian cities? Given the nation's predominantly European cultural heritage, how do urban Australians articulate multiple desires for living environments encountered in everyday life? In examining the cases of inner city parks, backyards, and more general views about flora and fauna appropriate for the city, the paper considers a range of deeply enculturated attachments to familiar landscapes. While residents have considerable interest in the possibilities of urban ecological restoration, our
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34

Froend, Ray. "Rare or Threatened Australian Plants: 1995 Revised Edition." Pacific Conservation Biology 3, no. 4 (1997): 404. http://dx.doi.org/10.1071/pc980404.

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The future of Australia's flora is dependent upon developing an understanding within the community and management of the need for conservation. A vital ingredient in achieving this understanding is the provision of accurate information on how many species are threatened or have already become extinct. Rare or Threatened Australian Plants (ROTAP): 1995 Revised Edition fulfils such a need and represents an up to date list of taxa that are presumed extinct, endangered, vulnerable, rare or poorly known at the national level.
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Gosper, Carl R., Julia M. Percy-Bower, Margaret Byrne, Tanya M. Llorens, and Colin J. Yates. "Distribution, Biogeography and Characteristics of the Threatened and Data-Deficient Flora in the Southwest Australian Floristic Region." Diversity 14, no. 6 (June 17, 2022): 493. http://dx.doi.org/10.3390/d14060493.

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The Southwest Australian Floristic Region (SWAFR) supports an exceptional number of threatened and data-deficient flora. In this study, we: (i) collated statistics on the number, listing criteria and tenure of occurrence of threatened and data-deficient flora; (ii) conducted spatial and biogeographic analyses to address questions concerning patterns of diversity of threatened and data-deficient flora relative to the whole flora and evolutionary and threat drivers; and (iii) examined whether threatened and data-deficient flora richness is evenly distributed across plant lineages. We found that
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Byrne, M. "Phylogeography provides an evolutionary context for the conservation of a diverse and ancient flora." Australian Journal of Botany 55, no. 3 (2007): 316. http://dx.doi.org/10.1071/bt06072.

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Phylogeography can inform conservation strategies through assessment of genetic diversity that incorporates an evolutionary perspective, and allows evaluation within a geographical context, thus providing integration with other biogeographical information. Comparative phylogeography can identify significant historical processes that have had major influences on the biota and provides a historical context for understanding current species distributions. The phylogeographic patterns in the flora of south-western Australia are reviewed. Concordant patterns of lineage divergence in three unrelated
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Spence, JR, and HP Ramsey. "Biogeography of the subfamily Bryoideae (Bryaceae, Musci) in north-eastern Queensland." Australian Systematic Botany 9, no. 2 (1996): 185. http://dx.doi.org/10.1071/sb9960185.

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The biogeography of Bryum and its relatives in the tropical and subtropical regions of north-eastern Queensland is analysed. The flora is small compared to other tropical areas, with six genera and 30 species. This low diversity results from the lack of high mountains in the study area. The principal floristic affinities are widespread – cosmopolitan (20%), pantropical (20%), and Australian endemic (17%). The strongest floristic affinities are with Indonesia-Malaya and New Guinea among tropical regions. Tropical-subtropical elements make up 50% of the flora, with Paleotropical and Indo-Malesia
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38

Moore, Sally. "Trituration Proving of Australian Acacias (WA)." Homœopathic Links 32, no. 03 (September 2019): 167–73. http://dx.doi.org/10.1055/s-0039-1700876.

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AbstractTo date, a few Australian plants have been proven and used as homoeopathic remedies.We believe that the Australian native flora provides a yet untapped reservoir of healing potential.Four Australian Acacia species were used in the trituration: Acacias dentifera, pulchella, floribunda and longifolia.Potencies are available in the 3C, 4C and 5C range.
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39

van Ee, Benjamin W., Paul I. Forster, and Paul E. Berry. "Phylogenetic relationships and a new sectional classification of Croton (Euphorbiaceae) in Australia." Australian Systematic Botany 28, no. 4 (2015): 219. http://dx.doi.org/10.1071/sb15016.

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A molecular phylogeny, morphological descriptions, species lists and a key to the sections of Croton L. (Euphorbiaceae) recognised for Australia are presented. The molecular phylogenetic results supported the recognition of six sections, to account for the 29 native Australian species. The monophyly of each of these sections was highly supported in the Bayesian and maximum-likelihood analyses of nuclear ITS and plastid trnL–F DNA sequences, whereas their relationships to each other and to other groups were less well resolved. Croton may represent one, two or three separate arrivals to Australi
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40

Keating, J. M. "Palynology of the Lachman Crags Member, Santa Marta Formation (Upper Cretaceous) of north-west James Ross Island." Antarctic Science 4, no. 3 (September 1992): 293–304. http://dx.doi.org/10.1017/s0954102092000452.

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Palynomorph assemblages from the Lachman Crags Member of the Santa Marta Formation, north-west James Ross Island, Antarctic Peninsula are described. By basis of comparison with other Southern Hemisphere localities, particularly southern Australia, an early Santonian–early Campanian age is indicated. The results broadly corroborate previous stratigraphical interpretations based on macrofaunal evidence, although the presence of a significant thickness of Santonian strata, not previously recognized, is suggested. The dinoflagellate cyst floras allow the recognition of the local equivalents of the
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James, Sidney H. "Genetic systems in the south-west flora: implications for conservation strategies for Australian plant species." Australian Journal of Botany 48, no. 3 (2000): 341. http://dx.doi.org/10.1071/bt99016.

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Is genetic diversity a reliable indicator of evolutionary capability? A comparative study of genetic systems in Australian native plants, particularly from south-west Australia, suggests the primitive condition to be recombinationally capable with low allelic diversity. Diversity has accumulated in some nursery lineages in association with lethal equivalent polymorphisms. This generated an elevated evolutionary capability which allowed escape from the benign nursery into the demanding arid playground. Lethal equivalent polymorphisms also generate a high genetic load which drives genetic system
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42

Silcock, J. L., A. R. Field, N. G. Walsh, and R. J. Fensham. "To name those lost: assessing extinction likelihood in the Australian vascular flora." Oryx 54, no. 2 (August 29, 2019): 167–77. http://dx.doi.org/10.1017/s0030605318001357.

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AbstractExtinction is a profound biological event, yet despite its finality it can be difficult to verify and many frameworks have been proposed to define formally that extinction has occurred. For most taxonomic groups and regions there is no reliable list of species considered to be probably or possibly extinct. The record of plant extinctions in Australia is no exception, characterized by high turn-over within lists, low transparency of attribution and lack of consistency between jurisdictions. This makes it impossible to evaluate how many plant taxa have become extinct in Australia. We pre
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Wright, Boyd R., Donald C. Franklin, and Roderick J. Fensham. "The ecology, evolution and management of mast reproduction in Australian plants." Australian Journal of Botany 70, no. 8 (December 20, 2022): 509–30. http://dx.doi.org/10.1071/bt22043.

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Australia is home to a diverse assemblage of plant species that display marked population-level variation in inter-annual flower or seed output (i.e. masting). These include a semelparous bamboo with an estimated inter-crop period of 40–50 years, numerous iteroparous masting gymnosperms, angiosperms that include landscape-dominant eucalypts, arid-zone wattles and spinifex (Triodia spp.) grasses, and a rich selection of species that display disturbance-related forms of masting such as pyrogenic flowering and environmental prediction. Despite the prevalence of masting in the Australian flora, th
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Bowman, D. M. J. S., and L. D. Prior. "Why do evergreen trees dominate the Australian seasonal tropics?" Australian Journal of Botany 53, no. 5 (2005): 379. http://dx.doi.org/10.1071/bt05022.

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The northern Australian woody vegetation is predominantly evergreen despite an intensely seasonal climate and a diversity of deciduous species in the regional flora. From a global climatic perspective the dominance of evergreen rather than deciduous trees in the Australian savannas is apparently anomalous when compared with other savannas of the world. However, this pattern is not unexpected in light of existing theory that emphasises photosynthetic return relative to cost of investment between deciduous and evergreen species. (a) Climatically, monsoonal Australia is more extreme in terms of r
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Pócs, Tamás. "Contribution to the Bryoflora of Australia. VI. The Genus Cololejeunea (Spruce) Steph. (Lejeuneaceae, Marchantiophyta)." Polish Botanical Journal 61, no. 2 (December 1, 2016): 205–29. http://dx.doi.org/10.1515/pbj-2016-0031.

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AbstractThirty-eight species of the genus Cololejeunea (Spruce) Steph. (Lejeuneaceae, Marchantiophyta) are reported for the whole of Australia, more than doubling the number of taxa known since the first account of the Australian members of the genus. Cololejeunea cairnsiana Pócs, Cololejeunea heinari Pócs and Cololejeunea floccosa var. fraseriana Pócs are described as new to science. The records of Cololejeunea diaphana A. Evans, Cololejeunea gottschei (Steph.) Mizut., Cololejeunea longifolia (Mitt.) Benedix ex Mizut. Cololejeunea verrucosa Steph. and Cololejeunea floccosa (Lehm. & Linden
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Beard, J. S., A. R. Chapman, and P. Gioia. "Species richness and endemism in the Western Australian flora." Journal of Biogeography 27, no. 6 (November 2000): 1257–68. http://dx.doi.org/10.1046/j.1365-2699.2000.00509.x.

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Southwell, Ian A., and Joseph J. Brophy. "Essential Oil Isolates from the Australian Flora. Part 3." Journal of Essential Oil Research 12, no. 3 (May 2000): 267–78. http://dx.doi.org/10.1080/10412905.2000.9699514.

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Lyons, M. N., N. Gibson, G. J. Keighery, and S. D. Lyons. "Wetland flora and vegetation of the Western Australian wheatbelt." Records of the Western Australian Museum, Supplement 67, no. 1 (2004): 39. http://dx.doi.org/10.18195/issn.0313-122x.67.2004.039-089.

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Gibson, N., G. J. Keighery, M. N. Lyons, and A. Webb. "Terrestrial flora and vegetation of the Western Australian wheatbelt." Records of the Western Australian Museum, Supplement 67, no. 1 (2004): 139. http://dx.doi.org/10.18195/issn.0313-122x.67.2004.139-189.

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Irish, Julie, Shona Blair, and Dee A. Carter. "The Antibacterial Activity of Honey Derived from Australian Flora." PLoS ONE 6, no. 3 (March 28, 2011): e18229. http://dx.doi.org/10.1371/journal.pone.0018229.

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