Hemiuridae (Digenea) from marine fishes of the southern Indian Ocean: Genus Lecithochirium Lühe, 1901 (Lecithochiriinae)

The genus Lecithochirium is briefly discussed and a provisional key to species groups is presented. The following species are described, figured and/or recorded from regions of the southern Indian Ocean: Lecithochirium genypteri from Xiphiurus capensis, Cape Province; L. magnus from Gymnothorax woodwardi and G. javanicus, Western Australia; L. parafusiforme n. sp. from G. flavimarginatus, Natal (type-host and locality) and G. woodwardi, Western Australia; L. macrorchis from G. woodwardi; Leithochirium sp. (ghanense-group?) from Platycephalus bassensis, South Australia; L. kawakawa from Euthynnus affinis and Chrysoblephus anglicus, Natal; Lecithochirium sp. (synodi-group?) from Saurida undosquamis, Natal; L. gymnapisti n. sp. from Gymnapistes marmoratus, Western Australia; L. jaffense from Trachichthodes gerrardi, South Australia and Blennioclinus brachycephalus, Cape Province; Lecithochirium sp. (group unknown) from Alectis ciliaris, Natal.     

Hemiuridae (Digenea) from marine fishes of the Great Barrier Reef,Queensland, Australia

The following species are described, figured and/or recorded from the Great Barrier Reef at Heron Island or Lizard Island, Queensland, with comparative material reported from other areas of the ocean around Australia or New Guinea: Dinurus longisinus (new synonym: D. hippuri) from Seriola lalandi, Heron Island and Coryphaena hippurus, Papua New Guinea; Ectenurus trachuri from Caranx sexfasciatus, Diploprion bifasciatus, Pterocaesio marri, Seriola lalandi and Atherinomorus capricorniensis, Heron Island; Erilepturus hamati (with 25 new synonyms) from Lutjanus carponotatus, Lizard Island, Platycephalus bassensis, Coff's Harbour, NSW, P. fuscus, Coff's Harbour, NSW and Moreton Bay, Queensland, P. endrachtensis, Sillago analis, S. maculata, S. ciliata, Pseudorhombus arsius and Polydactylus sp. from Moreton Bay, Queensland and Lates calcarifer, Darwin, Northern Territory; Tubulovesicula angusticauda from Echeneis naucrates and Lethrinus miniatus, Heron Island and Anguilla reinhardtii, Moreton Bay and Bribie Island, Queensland; Elytrophalloides humerus from Trachinotus botla and T. coppingeri, Heron Island; Lecithochirium kawakawa from Euthynnus affinis Heron Island and Lizard Island: Lecithochirium cirrhiti (new synonyms: L. sammarae, L. nohu) from Sargocentron rubrum, Heron Island; Lecithochirium caesionis from Pterocaesio marri, heron Island; Plerurus digitatus (new synonyms: P. cynoglossi, P. atulis, P. scomberomori) from Plectropomus leopardus, Heron Island, Lutjanus erythropterus, Variola louti, Scomberomorus semifasciatus, Grammatorcynus bicarinatus and Carangoides embureyi, C. gymnostethoides, Lizard Island, Scomberomorus commerson, Heron Island, Lizard Island, New Britain, Papua New Guinea, Point Lookout, Queensland and Moreton Bay, Queensland, Euthynnus affinis Heron Island, Lizard Island and New Britain, Papua New Guinea, Sphyraena barracuda, Heron Island and Lizard Island, Scomberomorus munroi, S. queenslandicus and Saurida undosquamis, Moreton Bay, Queensland and Chirocentrus dorab, Bundaberg, Queensland. The Lecithochirium species-group Cirrhiti is considered indistiguishable from the species-group Lotellae.     

Two new hemiurine species (Digenea: Hemiuridae) from <Emphasis Type="Italic">Spratelloides robustus</Emphasis> Ogilby (Clupeiformes: Clupeidae) off south-western Australia and records of <Emphasis Type="Italic">Parahemiurus merus </Emphasis>(Linton, 1910) from Australian and New Caledonian waters

Two new species of hemiurine hemiurid are described from Spratelloides robustus off Woodman Point in southern Western Australia. Hemiurus lignator n. sp. differs from its congeners by a combination of similar-sized suckers, long sinus-sac, tandem testes, relatively elongate shape and unthickened seminal vesicle wall. Parahemiurus xylokopos n. sp. differs from its congeners in a combination of its squat form, its distinctly lobed vitellarium and the proximity of the gonads to the ventral sucker. P. merus (Linton, 1910) is reported from Acanthopagrus australis, Pomatomus saltatrix and Trachinotus coppingeri off northern New South Wales, Caranx sexfasciatus, Scorpis lineolata, Siganus nebulosus, Thunnus tonggol and T. coppingeri off southern Queensland, Cephalopholis boenak and Euthynnus affinis off Heron Island, southern Great Barrier Reef, P. saltatrix off southern Western Australia and Priacanthus hamrur off New Caledonia.     

Monostephanostomum georgianum n. sp. (Digenea: Acanthocolpidae) from Arripis georgianus (Valenciennes) (Perciformes: Arripidae) off Kangaroo Island,South Australia,with comments on Monostephanostomum Kruse, 1979 and Stephanostomum Looss, 1899

Monostephanostomum georgianum n. sp. is described from Arripis georgianus off Kangaroo Island, South Australia. It differs from its congeners by the presence of a short second row of oral spines. M. manteri Kruse, 1979 is reported from A. georgianus off southern Western Australia and Kangaroo Island, South Australia and A. trutta off northern Tasmania. It is considered that the other two species, M. yamagutii Ramadan, 1984 and M. krusei Reimer, 1983, should probably be removed from this genus. Two new combinations are formed, M. gazzae (Shen, 1990) n. comb. (from Stephanostomum) and M. mesospinosum (Madhavi, 1976) n. comb. (from Stephanostomum). A key to the four recognised species of Monostephanostomum is given.     

Lepocreadiidae (Digenea) of Australian coastal fishes: new species of Opechona Looss, 1907, Lepotrema Ozaki, 1932 and Bianium Stunkard, 1930 and comments on other species reported for the first time or poorly known in Australian waters

Opechona austrobacillaris n. sp. is described from Pomatomus saltatrix from marine sites off Western Australia and New South Wales, Australia. It differs from O. bacillaris in its elongate outline, small ventral sucker, longer pseudoesophagus (relative to the oesophagus), relatively shorter ventral sucker to ovary distance and the relatively longer post-testicular region. Lepotrema monile n. sp. is described from Pomacentrus wardi from Heron Island, Queensland. It differs from its congeners in the sphincter around the distal metraterm and the more-or-less oval ovary. Bianium spongiosum n. sp. is described from Ostracion cubicus from Lizard Island, Queensland. It differs from its congeners in lacking lateral flaps in the forebody, but in having large, internal spongiform patches in the lateral forebody. The following species are redescribed from Australian sites: Lepocreadium oyabitcha from Abudefduf whitleyi, Lizard Island; Clavogalea trachinoti from Trachinotus botla, Heron Island and T. coppingeri, New South Wales, Stradbroke Island, Queensland and Heron Island; Myzoxenus insolens from Notolabrus parilus, Western Australia; Bulbocirrus aulostomi from Aulostomus chinensis, Heron Island; Lepocreadioides orientalis [new synonyms: Bicaudum interruptum Bilqees, 1973; Lepocreadioides interruptum (Bilqees, 1973) Madhavi, Narasimhulu & Shameem, 1986; Lepocreadioides discum Wang, 1986; Lepocreadioides sp. of Karyakarte & Yadav (1976)] from Cynoglossus bilineata, Moreton Bay, Queensland; Hypocreadium patellare from Sufflamen chrysopterus, Heron Island; Echeneidocoelium indicum from Echeneis naucrates, Heron Island; Multitestis pyriformis from Epinephelus cyanopodus, Heron Island; Pseudopisthogonoporus vitellosus from Naso brevirostris, Heron Island; and Bianium hispidum from Torquigener whitleyi and T. pleurogramma, southern Queensland. Only M. solens and M. pyriformis have been reported from Australian waters before; both are new host records.     

Invasion history of Lycium ferocissimum in Australia: The impact of admixture on genetic diversity and differentiation

Aim

We investigated the invasion history of Lycium ferocissimum, a spine-covered shrub native to South Africa that was introduced to Australia in the mid-1800s, and has since developed into a damaging invasive plant of undisturbed landscapes and pastures. In addition to identifying the provenance of the Australian plants, we tested for evidence of admixture, and contrasted genetic diversity and structuring across the native and introduced ranges.

Location

Samples were collected across South Africa (24 localities) and Australia (26 localities).

Methods

We used genotyping-by-sequencing (3117 SNPs across 381 individuals) to assess population genetic structuring in L. ferocissimum across Australia and South Africa. Coalescent analyses were used to explicitly test contrasting invasion scenarios.

Results

Clear geographic genetic structuring was detected across South Africa, with distinct clusters in the Eastern and Western Cape provinces. The L. ferocissimum plants in Australia form their own genetic cluster, with a similar level of genetic diversity as plants in South Africa. Coalescent analyses demonstrated that the lineage in Australia was formed by admixture between Eastern Cape and Western Cape plants, with most of the genetic material from the Australian lineage originating from the Western Cape. Our analyses suggest that L. ferocissimum plants were originally introduced to South Australia, though it is unclear whether admixture occurred before or after its introduction to Australia. We detected little evidence of geographic genetic structure across Australia, although many of the populations were genetically distinct from one another.

Main Conclusions

Our results illustrate how admixture can result in genetically diverse and distinct invasive populations. The complex invasion history of L. ferocissimum in Australia poses particular challenges for biological control. We suggest potential biological control agents should be screened against admixed plants (in addition to plants from the Eastern and Western Cape) to test whether they provide effective control of the genetically distinct invasive lineage.     

Bryobartramia schelpei T.A.Hedderson,a new species to accommodate the South African populations of the genus

Abstract

South African populations of Bryobartramia have been treated as B. novae-valesiae, a species otherwise restricted to Australia. However, material from the two regions differs in a number of traits, and the African populations are here described as a new species, B. schelpei. The Cape species differs most obviously from B. novae-valesiae in the markedly prorate-papillose, narrow, thick-walled cells of the calyptra. Nested analysis of variance reveals further morphometric differences, including the relatively narrower, more cylindrical, calyptra with a longer rostrum, and the smaller leaf cells and spores. Bryobartramia schelpii is known only from arid portions of the winter rainfall region in the Northern and Western Cape Provinces of South Africa.     

Capelatus prykei gen. et sp.n. (Coleoptera: Dytiscidae: Copelatinae) – a phylogenetically isolated diving beetle from the Western Cape of South Africa

Capelatus prykei gen. et sp.n. , a distinctive new lineage of copelatine diving beetle, is described from the greater Cape Town area of the Western Cape Province, South Africa, on the basis of both morphological and molecular data. The genus‐level phylogeny of Copelatinae is reconstructed using a combination of nuclear and mitochondrial DNA regions, demonstrating that Capelatus gen.n. has no close relatives within the Afrotropical region, instead forming a clade with the Palaearctic Liopterus and largely Australasian Exocelina. Capelatus gen.n. apparently represents a striking example of a phylogenetically isolated Cape lineage, which also appears to be narrowly endemic and endangered by ongoing habitat loss.     

1. PELICANS BREEDING ON SEAL ISLAND

Clark, A. 1974. The status of the whistling ducks in South Africa. Ostrich 45:1-4. Since the 1920's the status of Dendrocygna viduata and D. bicolor has changed from that of an irregular to that of a regular species in the Transvaal, Zululand, Natal and Orange Free State. In more recent years their numbers have shown a steady increase and breeding has been established. D. viduata numbers built up more quickly than D. bicolor and it has become an established resident whereas D. bicolor is primarily a summer visitor.

In the Western Cape Province there has been little change in the status of either species but there are indications that D. viduata is appearing mote regularly in the Eastern Cape Province. The position in East Griqualand and the Transkei is obscure. In South West Africa, excluding the north east corner, D. viduata remains irregular and D. bicolor rare.

The preference shown by both species for areas where sewage effluent is disposed of and for new storage dams inevitably links their spread and increase with that of the human population.     

The subfamily Aephnidiogeninae Yamaguti, 1934 (Digenea: Lepocreadiidae), its status and that of the genera Aephnidiogenes Nicoll, 1915, Holorchis Stossich, 1901, Austroholorchis n. g., Pseudaephnidiogenes Yamaguti, 1971, Pseudoholorchis Yamaguti, 1958 and Neolepocreadium Thomas, 1960

The status of all of the putative member genera of the subfamily Aephnidiogeninae is reconsidered, based mainly on the morphology of the terminal genitalia. Aephnidiogenes Nicoll, 1915 is the only genus retained in the Aephnidiogeninae. Aephnidiogenes major Yamaguti, 1934 from Diagramma labiosum from the southern Great Barrier Reef is redescribed with particular reference to the terminal genitalia, and is shown to lack a true cirrus-sac, a condition considered to be diagnostic of the Aephnidiogeninae. Holorchis Stossich, 1901 is placed in the subfamily Lepidapedinae. Holorchis pycnoporus Stossich, 1901 from Pagellus acarne from off Spanish Sahara and from Diplodus vulgaris from off Italy and H. legendrei Dollfus, 1946 from Sparodon durbanensis and D. sargus from off eastern Cape Province, South Africa and from Pagellus erythrinus from the Adriatic Sea and Italy are studied and illustrated. The terminal genitalia of H. pycnoporus are found to be enigmatic, but those of H. legendrei are found to fit clearly into the 'Lepidapedon-like' pattern. A new genus Austroholorchis is erected in the Lepidapedinae, with A.sprenti (Gibson, 1987) n. comb. as the type-species. Its diagnostic features are its ani, infundibuliform oral sucker and the position of the ovary at about mid-level of the uterus . A. sprenti is illustrated, its hosts in Queensland waters being Sillago maculata, S. analis and S. ciliata. A. levis n. sp. is described from Sillago bassensis from south-western Western Australia. The genus PseudaephnidiogenesYamaguti, 1971 is placed in the Lepidapedinae. P. rhabdosargi (Prudhoe, 1956) from Rhabdosargus sarba from off Natal, South Africa is illustrated and the terminal genitalia of P. rhabdosargi from R. sarba and from R. holubi from off eastern Cape Province and Pseudaephnidiogenes rossi Bray, 1985 from Caffrogobius nudiceps from off eastern Cape Province, South Africa are illustrated. The genus Pseudoholorchis Yamaguti, 1958 is placed in the subfamily Lepocreadiinae. The terminal genitalia of P. pulcher (Manter, 1954) from Latridopsis ciliaris from New Zealand are illustrated. The genus Neolepocreadium Thomas, 1960 is placed in the Lepocreadiidae.     

Pathotypes of Plasmodiophora brassicae, the cause of clubroot, in Australia

Variation in pathogenicity of Plasmodiophora brassicae in Australia was studied using the European Clubroot Differential series of brassica hosts. From 41 collections of P. brassicae originating from important vegetable brassica production regions in Victoria, Western Australia, Tasmania, Queensland and New South Wales, 23 triplet codes were generated. These were more similar to populations of P. brassicae reported from the USA than those from Europe. The most common Australian pathotypes had triplet codes of 16/3/12 and 16/3/31 and were each assigned seven times to pathogen collections originating from three states of Australia. Other codes that occurred more than once were 16/2/31, which was assigned to six collections from four states of Australia, and 16/19/31, which was assigned twice to collections originating from Western Australia.     

Gene flow of the canker pathogen Botryosphaeria australis between Eucalyptus globulus plantations and native eucalypt forests in Western Australia

Abstract The eucalypt plantation industry in Western Australia provides a unique opportunity to study the movement of pathogens between closely related host taxa. Eucalyptus globulus, a native to Tasmania and south‐eastern Australia, is the predominant species in Western Australian plantations, often being planted adjacent to native forest containing Eucalyptus marginata and Eucalyptus diversicolor. Since the commencement of the plantation industry 20 years ago, several fungal species, previously known only to eastern Australia or overseas, have been reported on E. globulus in Western Australia. Botryosphaeria australis is a newly described species, recently found causing cankers on Acacia spp. in eastern Australia. However, during a routine survey, B. australis was found to be the predominant species associated with E. globulus plantations and native Eucalyptus spp. in Western Australia. In this study, six short simple repeat markers were used to evaluate genetic diversity and gene flow between collections of B. australis from native eucalypt forest and E. globulus plantations at two locations in south‐western Australia. In both cases, there was no restriction to gene flow between the plantations and the adjacent native forest. Botryosphaeria australis has now been isolated from a wide range of hosts across south‐western Australia and was not isolated from E. globulus in Tasmania or South Australia. This extensive distribution and host range suggests B. australis is native to Western Australia. This study demonstrates the ability of a pathogen to move between plantation and forests.     

Historical biogeography of Australian Rhamnaceae, tribe Pomaderreae

Aim To discover the pattern of relationships of areas of endemism for Australian genera in the plant family Rhamnaceae tribe Pomaderreae for comparison with other taxa and interpretation of biogeographical history. Location Australian mainland, Tasmania and New Zealand. Methods A molecular phylogeny and geographic distribution of species within four clades of Pomaderreae are used as a basis for recognition of areas of endemism and analysis of area relationships using paralogy‐free subtrees. The taxon phylogeny is the strict consensus tree from a parsimony analysis of 54 taxa, in four clades, and sequence data for the internal transcribed spacer regions of ribosomal DNA (ITS1‐5.8S‐ITS2) and the plastid DNA region trnL‐F. Results The biogeographical analysis identified five subtrees, which, after parsimony analysis, resulted in a minimal tree with 100% consistency and seven resolved nodes. Three sets of area relationships were identified: the areas of Arnhem and Kimberley in tropical north Australia are related based on the phylogeny of taxa within Cryptandra; the moister South‐west of Western Australia, its sister area the coastal Geraldton Sandplains, the semi‐arid Interzone region and arid Western Desert are related, based on taxa within Cryptandra, Spyridium, Trymalium and Pomaderris; and the eastern regions of Queensland, McPherson‐Macleay, south‐eastern New South Wales (NSW), Victoria, southern Australia, Tasmania and New Zealand are related based on Cryptandra, Pomaderris and Spyridium. Tasmania and NSW are related based entirely on Cryptandra, but the position of New Zealand relative to the other south‐eastern Australian regions is unresolved. Main conclusions The method of paralogy‐free subtrees identified a general pattern of geographic area relationships based on Australian Pomaderreae. The widespread distribution of clades, the high level of endemicity and the age of fossils for the family, suggest that the Pomaderreae are an old group among the Australian flora. Their biogeographical history may date to the early Palaeogene with subsequent changes through to the Pleistocene.     

Acaulonopsis,a new moss genus of the Pottiaceae from Western Cape Province of South Africa,and comments on Vrolijkheidia

Abstract

A new genus, Acaulonopsis (Pottiaceae, Bryophyta), including two new species, A. fynbosensis and A. eureka, is described from the Western Cape Province of South Africa. Together with the similarly much reduced pottiaceous genus Acaulon, Acaulonopsis is unique in the family with a very short seta and spherical capsule, which lacks the apiculus found in other genera. The new genus is also distinguished by short plant stature, and a total of about five ovate leaves that clasp closely the capsules in nearly spherical leaf bases. Continuing bryological study of the fynbos region has recently resulted in a number of startling discoveries of bryophytes new to science and distinct at the genus level. A new combination is made for the South African endemic genus Vrolijkheidia (Pottiaceae) with discussion of its dimorphic habitus.     

NEW ARRENURUS SPECIES (ACARI,HYDRACHNELLAE, ARRENURIDAE) FROM SOUTHERN AFRICA

SUMMARY

Five new Arrenurus spp, from Southern Africa are described: A. amoenus sp. nov. from Natal, A. agnewi sp. nov., A. curtipalpus sp. nov., A. pedatus sp. nov. and A. cavatus sp. nov. from Botswana. The species from Natal came from an older collection belonging to the National Institute for Water Research. The species from Botswana were collected recently by Dr J.D. Agnew¹

The water mite fauna of South Africa is only partly known. Therefore it is important that collectors should know that alcohol and formalin are not suitable fixatives. Fixing and storing is most successful in the following mixture: 5 parts glycerin, 2 parts glacial acetic acid and 3 parts water.     

The Saurida undosquamis group (Aulopiformes: Synodontidae), with description of a new species from southern Japan

Four lizardfishes of Saurida (family Synodontidae), S. undosquamis, S. umeyoshii sp. nov., S. macrolepis, and S. longimanus, are described. All are recognized here as the Saurida undosquamis group, characterized by having dark dots on the upper margin of the caudal fin, pectoral fin exceeding origin to pelvic fin, anterior rays of dorsal fin neither elongate nor filamentous, predorsal length greater than distance between dorsal-fin and adipose-fin origins, 46–55 pored lateral-line scales, and vomer with 0–8 teeth. Saurida undosquamis, from northern West India and West Pacific, excluding East Asia, differs from others in having lateral-line scales ridged on the caudal peduncle, conspicuously concave posterior margin of the pectoral fin, 51–55 pored lateral-line scales, and 50–53 vertebrae. Saurida umeyoshii sp. nov., from southern Japan and the East China Sea, is defined by three rows of indistinct dark blotches on, above, and below the lateral line, distribution of scale pockets with melanophores on their posterior part extending over the entire abdominal region from the lateral line in specimens over ca. 130 mm SL, lateral-line scales not ridged on caudal peduncle, 49–52 pored lateral-line scales, and 48–50 vertebrae. Saurida macrolepis, from the Indo-West Pacific, is characterized by 46–49 pored lateral-line scales and 45–48 vertebrae. Saurida longimanus, from northern West India, northwest Australia, and southern Indonesia, differs from the others in having a long pectoral fin extending past the origin of the dorsal fin. Some geographic variations are found in S. macrolepis. Saurida grandisquamis is confirmed as a junior synonym of S. undosquamis, based on examination of the type specimens. A key to species in the S. undosquamis group is included.     

Gracilaria species (Gracilariaceae, Rhodophyta) from southeastern Australia, including a new species, Gracilaria perplexa sp. nov.: Morphology, molecular relationships and agar content

Select species of the agarophyte Gracilaria were studied from southeastern Australia. The morphology and anatomy of species is described and molecular relations are inferred based on plastid and mitochon‐drial DNA sequence data. Agar yields and qualities are determined for each species. Gracilaria chilensis, found in Tasmania and Victoria, is morphologically and molecularly similar to G. chilensis from New Zealand and Chile and has low agar yields of 11–16%. Gracilaria cliftonii from Victoria, has high crude agar yield (52%) and is molecularly uniform. Gracilaria perplexa sp. nov., known only from Botany Bay, New South Wales, has an agar yield of 39%. The agar of G. perplexa is unusual in requiring the addition of 0.1 mol L^?1 NaCl for alcohol precipitation and is cold‐water (25°C) soluble because of the very high sulfate ester content. Molecular phylogeny shows that G. perplexa is closely related to Gracilaria preissiana from western Australia, but differs from the latter in its reduced branching and narrower more terete axes.     

Tasmanian rotifera: Affinities with the Australian fauna

Plankton was collected from more than 100 lentic and lotic habitats in Tasmania. Of the 131 rotifer taxa identified, 126 are first records for the island, and 9 are first records for Australia. Three new species, Aspelta tilba, sp. nov., Lepadella tyleri sp. nov., and Testudinella unicornuta sp. nov. are described and figured. Horaëlla brehmi, which has a disjunct distribution (equatorial regions and southeastern Australia), also occurs in Tasmanian waters. The morphology and development of this rare species are discussed. Geographical affinities of the Tasmanian assemblage are considered. There appears to be a significant tropical component in the Tasmanian Rotifera.