Mackay Whitsunday, Queensland
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Karyotype Variations in the Genus Pollicaria (Caenogastropoda
Zoological Studies 49(1): 125-131 (2010) Karyotype Variations in the Genus Pollicaria (Caenogastropoda: Pupinidae) Bangon Kongim1, Chirasak Sutcharit2, Piyoros Tongkerd2, Shau-Hwai Aileen Tan3, Nguyen Xuan Quynh4, Fred Naggs5, and Somsak Panha2,* 1Department of Biology, Faculty of Science, Mahasarakham University, Kantharawichai District, Maha Sarakham 44150, Thailand 2Animal Systematics Research Unit, Department of Biology, Faculty of Science, Chulalongkorn University, Bangkok 10330, Thailand 3School of Biological Sciences, Universiti Sains Malaysia, Minden, Penang 11800, Malaysia 4Faculty of Biology, Hanoi University of Science, 334 Nguyen Trai, Thanh Xuan, Hanoi, Vietnam 5Department of Zoology, The Natural History Museum, London SW7 5BD, UK (Accepted May 5, 2009) Bangon Kongim, Chirasak Sutcharit, Piyoros Tongkerd, Shau-Hwai Aileen Tan, Nguyen Xuan Quynh, Fred Naggs, and Somsak Panha (2010) Karyotype variations in the genus Pollicaria (Caenogastropoda: Pupinidae). Zoological Studies 49(1): 125-131. The karyotypes of 4 recognized Southeast Asian species of the genus Pollicaria were examined. All 7 populations studied were found to possess the same chromosome pattern: n = 13, 2n = 26. However, the fundamental chromosome number (FN) of both populations of P. elephas from the south (Malaysia) was 46, while those for the other 3 species (5 populations) were all 50. Moreover, although each species had a unique karyotype, the karyotype of the isolated species, P. elephas, differed from the other 3 northern species in exhibiting 3 distinct telocentric chromosomes (2m+6sm+2st+3t). The 3 smaller species, P. mouhoti from northeastern Thailand, P. myersii from Laos, and P. gravida from 2 localities in northern Vietnam, exhibited similar karyotypes of 6m+4sm+2st+1t, 4m+6sm+2st+1t, and (3m+7sm+2st+1t and 2m+8sm+2st+1t) respectively, with only 1 telocentric chromosome. -
Cyclophoridae and Pupinidae of Caroline, Fijian, and Samoan Islands
CYCLOPHORIDAE AND PUPINIDAE OF CAROLINE, FIJIAN, AND SAMOAN ISLANDS BY WILLIAM J. CLENCH BERNICE P. BISHOP MUSEUM BULLETIN 196 HONOLULU, HAWAII PUBLISHED BY THE MUSEUM 1949 ISSUED MAY 18, 1949 FUNDS FOR THE PRINTING OF THIS PAPER WERE CONTRIBUTED BY THE CHARLES M. AND ANNA C. COOKE TRUST. CONTENTS PAGE Introduction , 3 Cyclophoridae 4 Species from the various island groups 5 New Caledonia and Loyalty Islands 5 Santa Cruz Islands 6 Caroline Islands 7 Samoa 9 New Hebrides 19 Fijian Islands 20 Caroline Islands 25 Pupinidae 30 Micronesia and Melanesia 30 Unknown species 48 Literature cited 49 Index 51 Cyclophoridae1 and Pupinidae of Caroline, Fijian, and Samoan Islands By WILLIAM J. CLENCH CURATOR OF MOW.USKS, HARVARD UNIVERSITY INTRODUCTION The following report is based largely upon the extensive collection of Pacific island mollusks in Bernice P. Bishop Museum. The study was made possible by a Yale-Bishop Museum Fellowship which was granted for the winter of 1940-1941. Upon my return to Cambridge, the collection of mollusks in my charge was reviewed for additional data for the two families considered in this paper. I am exceedingly grateful to the Yale University Committee and to the Trustees of Bishop Museum for this fellowship and for the rare opportunity to study in the Hawaiian Islands. The value to the individual scientist of an opportunity of this sort far transcends the published results of a single report. Such an experience with the chance of seeing new and different animals and plants in the field and under totally different conditions naturally tends to shift preconceived viewpoints obtained from other field experience. -
Southern Gulf, Queensland
Biodiversity Summary for NRM Regions Species List What is the summary for and where does it come from? This list has been produced by the Department of Sustainability, Environment, Water, Population and Communities (SEWPC) for the Natural Resource Management Spatial Information System. The list was produced using the AustralianAustralian Natural Natural Heritage Heritage Assessment Assessment Tool Tool (ANHAT), which analyses data from a range of plant and animal surveys and collections from across Australia to automatically generate a report for each NRM region. Data sources (Appendix 2) include national and state herbaria, museums, state governments, CSIRO, Birds Australia and a range of surveys conducted by or for DEWHA. For each family of plant and animal covered by ANHAT (Appendix 1), this document gives the number of species in the country and how many of them are found in the region. It also identifies species listed as Vulnerable, Critically Endangered, Endangered or Conservation Dependent under the EPBC Act. A biodiversity summary for this region is also available. For more information please see: www.environment.gov.au/heritage/anhat/index.html Limitations • ANHAT currently contains information on the distribution of over 30,000 Australian taxa. This includes all mammals, birds, reptiles, frogs and fish, 137 families of vascular plants (over 15,000 species) and a range of invertebrate groups. Groups notnot yet yet covered covered in inANHAT ANHAT are notnot included included in in the the list. list. • The data used come from authoritative sources, but they are not perfect. All species names have been confirmed as valid species names, but it is not possible to confirm all species locations. -
(OUV) of the Wet Tropics of Queensland World Heritage Area
Handout 2 Natural Heritage Criteria and the Attributes of Outstanding Universal Value (OUV) of the Wet Tropics of Queensland World Heritage Area The notes that follow were derived by deconstructing the original 1988 nomination document to identify the specific themes and attributes which have been recognised as contributing to the Outstanding Universal Value of the Wet Tropics. The notes also provide brief statements of justification for the specific examples provided in the nomination documentation. Steve Goosem, December 2012 Natural Heritage Criteria: (1) Outstanding examples representing the major stages in the earth’s evolutionary history Values: refers to the surviving taxa that are representative of eight ‘stages’ in the evolutionary history of the earth. Relict species and lineages are the elements of this World Heritage value. Attribute of OUV (a) The Age of the Pteridophytes Significance One of the most significant evolutionary events on this planet was the adaptation in the Palaeozoic Era of plants to life on the land. The earliest known (plant) forms were from the Silurian Period more than 400 million years ago. These were spore-producing plants which reached their greatest development 100 million years later during the Carboniferous Period. This stage of the earth’s evolutionary history, involving the proliferation of club mosses (lycopods) and ferns is commonly described as the Age of the Pteridophytes. The range of primitive relict genera representative of the major and most ancient evolutionary groups of pteridophytes occurring in the Wet Tropics is equalled only in the more extensive New Guinea rainforests that were once continuous with those of the listed area. -
The Diversity of Land Snail Fauna in Chonburi Province, Eastern Thailand
Kasetsart J. (Nat. Sci.) 42 : 256 - 263 (2008) The Diversity of Land Snail Fauna in Chonburi Province, Eastern Thailand Pratin Boonngam*, Pongrat Dumrongrojwattana and Surin Matchacheep ABSTRACT Land snails diversity were investigated in several habitats in Chonburi Province, Eastern Thailand. Snails were collected from 14 areas throughout Chonburi Province. A total of 16 families 29 genera and 48 species were recorded, 22 of which had been previously reported. The others could be identified into genus level and at least nine of them are being proposed as new to science. Key words: land snail, Gastropoda, Chonburi province INTRODUCTION snail were reported for Chonburi Province previously by Panha (1996) Hemmen and Land snails belong to the Phylum Hemmen (2001) Panha and Burch (2005). The Mollusca, Class Gastropoda and include two present study was undertaken to update the species groups prosobranchs and pulmonates. list of land snails in Chonburi Province. Prosobranchs, frequently have heavily calcified shells and opercula covering the aperture or MATERIALS AND METHODS opening or their shells. Pulmonates, lack opercula and used lung in gas exchange process. As Specimens were collected from several herbivores, snails eat many kinds of fresh and dead habitats in Chonburi Province. Methods consisted leaves and are eaten by many animals such as some of collecting soil samples where shells or predacious insects, snakes, birds and small fragments of shells were found, or where snails mammals. They live under leaves, litter, logs, were suspected to be present. Limestone soils are stones and trash. Some land snails carry serve as by far the richest source of snails in Chonburi hosts for some parasites such as Hemiplecta Province. -
Acacia Spirorbis Subsp. Solandri (Benth.) Pedley
WATTLE Acacias of Australia Acacia spirorbis subsp. solandri (Benth.) Pedley Source: W orldW ideW attle ver. 2. Published at: w w w .w orldw idew attle.com See illustration. Acacia spirorbis subsp. solandri occurrence map. O ccurrence map generated via Atlas of Living Australia (https://w w w .ala.org.au). Family Fabaceae Distribution Occurs on the continental islands off the Qld coast and the immediate mainland between Townsville and Mackay, extending further S on the islands to Rat Is. near Rockhampton, and inland in the Hillborough Natl Park, SW of Townsville. It occurs on margins of rainforest and on drier sites in eucalypt woodland and open forest. Also recorded from the S coast of New Guinea, fide L.Pedley, Contr. Queensland Herb. 18: 20 (1975). The typical subspecies (which includes A. solandri subsp. kajewskii Pedley) occurs on islands of the Pacific, e.g. New Hebrides, New Caledonia and Loyality Is., fide L.Pedley, Contr. Queensland Herb. 18: 20–21 (1975). Description Tree to c. 12 m high; young plants possibly pubescent. Branchlets slender, glabrous. Phyllodes falcately recurved, 9–17 cm long, 6–16 mm wide, dark green, glabrous, with 2 main longitudinal nerves more prominent than the rest and sometimes concurrent with each other near base; minor nerves numerous, 3–5 (–6) per mm, subdistant, 0.1–0.3 mm apart, sparingly anastomosing; pulvinus 2–4 mm long, dark-coloured. Inflorescences simple or rudimentary racemes with axes c. 0.5 mm long; peduncles 2 per axil, 5–10 mm long, glabrous; spikes 3–8 cm long, interrupted, creamy. Flowers 5-merous; sepals united with broadly triangular lobes at apices, glabrous; petals strongly reflexed at anthesis; ovary densely hairy. -
Caenogastropoda
13 Caenogastropoda Winston F. Ponder, Donald J. Colgan, John M. Healy, Alexander Nützel, Luiz R. L. Simone, and Ellen E. Strong Caenogastropods comprise about 60% of living Many caenogastropods are well-known gastropod species and include a large number marine snails and include the Littorinidae (peri- of ecologically and commercially important winkles), Cypraeidae (cowries), Cerithiidae (creep- marine families. They have undergone an ers), Calyptraeidae (slipper limpets), Tonnidae extraordinary adaptive radiation, resulting in (tuns), Cassidae (helmet shells), Ranellidae (tri- considerable morphological, ecological, physi- tons), Strombidae (strombs), Naticidae (moon ological, and behavioral diversity. There is a snails), Muricidae (rock shells, oyster drills, etc.), wide array of often convergent shell morpholo- Volutidae (balers, etc.), Mitridae (miters), Buccin- gies (Figure 13.1), with the typically coiled shell idae (whelks), Terebridae (augers), and Conidae being tall-spired to globose or fl attened, with (cones). There are also well-known freshwater some uncoiled or limpet-like and others with families such as the Viviparidae, Thiaridae, and the shells reduced or, rarely, lost. There are Hydrobiidae and a few terrestrial groups, nota- also considerable modifi cations to the head- bly the Cyclophoroidea. foot and mantle through the group (Figure 13.2) Although there are no reliable estimates and major dietary specializations. It is our aim of named species, living caenogastropods are in this chapter to review the phylogeny of this one of the most diverse metazoan clades. Most group, with emphasis on the areas of expertise families are marine, and many (e.g., Strombidae, of the authors. Cypraeidae, Ovulidae, Cerithiopsidae, Triphori- The fi rst records of undisputed caenogastro- dae, Olividae, Mitridae, Costellariidae, Tereb- pods are from the middle and upper Paleozoic, ridae, Turridae, Conidae) have large numbers and there were signifi cant radiations during the of tropical taxa. -
Accepted Manuscript
Accepted Manuscript Plastid and nuclear DNA markers reveal intricate relationships at subfamilial and tribal levels in the soapberry family (Sapindaceae) Sven Buerki, Félix Forest, Pedro Acevedo-Rodríguez, Martin W. Callmander, Johan A.A. Nylander, Mark Harrington, Isabel Sanmartín, Philippe Küpfer, Nadir Alvarez PII: S1055-7903(09)00017-7 DOI: 10.1016/j.ympev.2009.01.012 Reference: YMPEV 3130 To appear in: Molecular Phylogenetics and Evolution Received Date: 21 May 2008 Revised Date: 27 November 2008 Accepted Date: 23 January 2009 Please cite this article as: Buerki, S., Forest, F., Acevedo-Rodríguez, P., Callmander, M.W., Nylander, J.A.A., Harrington, M., Sanmartín, I., Küpfer, P., Alvarez, N., Plastid and nuclear DNA markers reveal intricate relationships at subfamilial and tribal levels in the soapberry family (Sapindaceae), Molecular Phylogenetics and Evolution (2009), doi: 10.1016/j.ympev.2009.01.012 This is a PDF file of an unedited manuscript that has been accepted for publication. As a service to our customers we are providing this early version of the manuscript. The manuscript will undergo copyediting, typesetting, and review of the resulting proof before it is published in its final form. Please note that during the production process errors may be discovered which could affect the content, and all legal disclaimers that apply to the journal pertain. ACCEPTED MANUSCRIPT Buerki et al. 1 1 Plastid and nuclear DNA markers reveal intricate relationships at subfamilial and tribal 2 levels in the soapberry family (Sapindaceae) 3 4 Sven Buerki a,*, Félix Forest b, Pedro Acevedo-Rodríguez c, Martin W. Callmander d,e, 5 Johan A. -
I Is the Sunda-Sahul Floristic Exchange Ongoing?
Is the Sunda-Sahul floristic exchange ongoing? A study of distributions, functional traits, climate and landscape genomics to investigate the invasion in Australian rainforests By Jia-Yee Samantha Yap Bachelor of Biotechnology Hons. A thesis submitted for the degree of Doctor of Philosophy at The University of Queensland in 2018 Queensland Alliance for Agriculture and Food Innovation i Abstract Australian rainforests are of mixed biogeographical histories, resulting from the collision between Sahul (Australia) and Sunda shelves that led to extensive immigration of rainforest lineages with Sunda ancestry to Australia. Although comprehensive fossil records and molecular phylogenies distinguish between the Sunda and Sahul floristic elements, species distributions, functional traits or landscape dynamics have not been used to distinguish between the two elements in the Australian rainforest flora. The overall aim of this study was to investigate both Sunda and Sahul components in the Australian rainforest flora by (1) exploring their continental-wide distributional patterns and observing how functional characteristics and environmental preferences determine these patterns, (2) investigating continental-wide genomic diversities and distances of multiple species and measuring local species accumulation rates across multiple sites to observe whether past biotic exchange left detectable and consistent patterns in the rainforest flora, (3) coupling genomic data and species distribution models of lineages of known Sunda and Sahul ancestry to examine landscape-level dynamics and habitat preferences to relate to the impact of historical processes. First, the continental distributions of rainforest woody representatives that could be ascribed to Sahul (795 species) and Sunda origins (604 species) and their dispersal and persistence characteristics and key functional characteristics (leaf size, fruit size, wood density and maximum height at maturity) of were compared. -
Section 8-Maggie-Final AM
KEY TO GROUP 8 Shrubs or trees usually more than 1.5 m tall. A. flower B. phyllode and C. leaf D. leaf E. leaf margins F. leaf margins spike pod lobed dissected crenate serrate NOTE: The following trees and shrubs, which are deciduous when flowering, will not come out in this key unless you can find a leaf. There are usually some old ones on the ground or even a few hanging on the tree. These plants are: Brachychiton (Group 8.G), Cochlospermum (Group 8.G), Cordia (Group 8.K), Gyrocarpos (Group 8.G), Sterculia (Group 8.O), Terminalia (Group 8.M), Turraea (Group 8.R), and the mangrove, Xylocarpus (Group 1.H). 1 Leaves with oil glands, readily visible with a hand lens if not to the naked eye, aromatic when crushed, eucalypt or citrus smell. (Chiefly eucalypts, paperbarks, bottlebrushes and similar) go to 2 1* Leaves lacking easily seen oil glands, if aromatic when crushed, then smell not of an eucalypt; citrus or even an apple smell go to 5 Oil glands/dots as seen with a good hand lens 2 Trees; petals fused to form an operculum or cap, stamens numerous and free (eucalpyts) go to 3 2* Shrubs or trees, petals not fused to form an operculum or cap, stamens if numerous then usually united into bundles or stamens are fewer than 10 (Myrtaceae-Rutaceae) go to 4 3 Bark smooth throughout but occasionally some rough fibrous or persistent bark at base go to Group 8.A 3* Persistent, fibrous bark for at least 2-3 m or usually more from the base go to Group 8.B 4 Flowers clustered into spikes (see sketch A), old capsules usually remain on the old wood -
Types of Vegetation Occuring on Santo
in BOUCHET P., LE GUYADER H. & PASCAL O. (Eds), The Natural History of Santo. MNHN, Paris; IRD, Marseille; PNI, Paris. 572 p. (Patrimoines naturels; 70). Types of Vegetation Occurring on Santo Jérôme Munzinger, Porter P. Lowry II & Jean-Noël Labat The Santo 2006 expedition was Table 5: Vegetation types in Vanuatu proposed by Mueller- designed to carry out detailed explo- Dombois and Fosberg. ration of the botanical diversity 1. Lowland rain forest present on the island. A wide diver- sity of vegetation types were there- a. High-stature forests on old volcanic ash fore studied, covering the full range b. Medium-stature forest heavily covered with lianas extending from what can be regarded c. Complex forest scrub densely covered with lianas as "extremes" on a scale from natu- d. Alluvial and floodplain forests ral, nearly undisturbed areas to those e. Agathis-Calophyllum forest that have been profoundly modified f. Mixed-species forests without gymnosperms and by man. Large areas have been trans- Calophyllum formed by humans — partially or completely — through clearing, fire, 2. Montane cloud forest and related vegetation Principal and other means, in an effort to meet basic needs for food, shelter, fiber, 3. Seasonal forest, scrub and grassland grazing land for livestock, etc., although such a. Semi-deciduous transitions forests habitats exist only because they are created and b. Acacia spirorbis forest maintained by man or by domesticated animals. c. Leucaena thicket, savanna and grassland At the other extreme, Santo’s vegetation includes nearly pristine formations that result from the 4. Vegetation on new volcanic surfaces natural processes of evolution and succession and are self-maintaining, provided they are not subject 5. -
Acacia Spirorbis Subsp. Solandri (Benth.) Pedley Family: Fabaceae Pedley, L
Australian Tropical Rainforest Plants - Online edition Acacia spirorbis subsp. solandri (Benth.) Pedley Family: Fabaceae Pedley, L. (1990) Austrobaileya 3(2): 216. Common name: Wattle Stem Dead bark layered. Inner and outer blazes very fibrous. Leaves Leaves phyllodineous. Leaf blades about 9-17 x 0.6-16 cm. Veins longitudinal, parallel, not Leaves and inflorescences. © R.L. anastomosing, generally 2-3 more prominent than the rest. A small gland normally visible on the Barrett upper side of the leaf blade-petiole junction. Flowers Spikes about 3-8 cm long, on glabrous peduncles about 5-10 mm long, in axillary pairs. Calyx cylindrical, glabrous, about 0.8-1 mm long, apex sinuate. Corolla about 1.8-2.5 mm long, glabrous, lobes strongly reflexed, about as long as the tube. Stamens about 2.5-3.5 mm long. Ovary densely pubescent. Fruit Pod +/- flat, sometimes raised over the seeds, coiled, up to 10 x 0.3-0.5 cm. Seeds (colour unknown) longitudinally or slightly obliquely oriented in the pod, about 3.5-5 x 2.5-3.5 mm. Funicle (colour unknown) folded many times beneath the seed to form an aril-like structure nearly as long as Scale bar 10mm. © CSIRO the seed. Seedlings Features not available. Distribution and Ecology Endemic to Queensland, occurs in the southern extremity of NEQ (near Townsville) and CEQ. Altitudinal range from sea level to 600 m. Grows in monsoon forest, dry rain forest and beach forest. A. spirorbis ssp. spirorbis occurs in Vanuatu and New Caledonia. Synonyms Racosperma spirorbe subsp. solandri (Benth.) Pedley, Austrobaileya 2(3): 355(1984).