scholarly journals Studies on Procamallanus (Spirocamallanus) pereirai Annereaux, 1946 (Nematoda: Camallanidae), with new host records and new morphological data on the larval stages

1999 ◽  
Vol 94 (5) ◽  
pp. 635-640 ◽  
Author(s):  
Cláudia Portes Santos ◽  
Melissa Querido Cárdenas ◽  
Herman Lent
2002 ◽  
Vol 16 (2) ◽  
pp. 237 ◽  
Author(s):  
R. A. Campbell ◽  
I. Beveridge

The onchobothriid tetraphyllidean cestode genus Acanthobothrium van Beneden, 1849, parasitic in the spiral intestine of elasmobranch fishes, was investigated in the Australian region. Thirty-three species are recognised, including 27 that are new. Diagnoses compare the morphological taxonomic characters of all congeners. New species are: Acanthobothrium adlardi; A. angelae; A. arlenae; A. bartonae; A. blairi; A. brayi; A. cannoni; A. chisholmae; A. clarkeae; A. cribbi; A. edmondsi; A. gasseri; A. gibsoni; A. gloveri; A. jonesi; A. lasti; A. laurenbrownae; A. martini; A. mooreae; A. ocallaghani; A. odonoghuei; A. pichelinae; A. robertsoni; A. rohdei; A. stevensi; A. thomasae; and A. walkeri. Additional morphological data are provided for A. australe Robinson, 1965, A. pearsoni Williams, 1962, A. heterodonti Drummond, 1937 and A. urolophi Schmidt, 1973, reported previously from Australia. Acanthobothrium rhynchobatidis Subhapradha, 1955 and A. semnovesiculum Verma, 1928 are reported from Australia for the first time and are redescribed. Additional morphological details are provided for A. ijimae Yoshida, 1917 and A. grandiceps Yamaguti, 1952. Acanthobothrium wedli Robinson, 1959 is redescribed from the type host from New Zealand waters and considered a sister species of A. blairi from Tasmania. Seven new host genera for Acanthobothrium are reported: Hypnos Duméril, 1852 (Hypnidae); Pristiophorus MÜller & Henle, 1837 (Pristiophoridae); Sutorectus Whitley, 1939 (Orectolobidae); Aptychotrema Norman, 1926 and Trygonorrhina MÜller & Henle, 1838 (Rhinobatidae); Parascyllium Gill, 1862 (Parascylliidae); and Aetomylaeus Garman, 1908 (Myliobatididae). Species of Acanthobothrium are reported from the families Hypnidae, Pristiophoridae and Parascylliidae for the first time. New host species for Acanthobothrium are: Pristiophorus cirratus (Latham, 1794); Parascyllium ferrugineum McCulloch, 1911; Sutorectus tentaculatus (Peters, 1865); Aptychotrema vincentiana (Haacke, 1885); Trygonorrhina fasciata MÜller & Henle, 1841; Raja whitleyi Iredale, 1938; Raja cerva Whitley, 1939; Hypnos monopterygium (Shaw & Nodder, 1795); Dasyatis annotata Last, 1987; Urolophus cruciatus (Lacépède, 1804); Urolophus expansus McCulloch, 1916; Urolophus lobatus McKay, 1966; Urolophus paucimaculatus Dixon, 1969; Gymnura australis (Ramsay & Ogilby, 1886); Aetomylaeus nicofii (Schneider, 1801); and Myliobatis australis Macleay, 1881 (Myliobatididae). New host records for Australia include the above 16 elasmobranch species and the following three host species also known to harbour Acanthobothrium in other geographic localities: Rhynchobatis djiddensis (Forsskål, 1775) (Rhynchobatidae); Himantura uarnak (Forsskål, 1775); and Pastinachus sephen (Forsskål, 1775) (Dasyatidae). Four additional records for hosts previously reported for Acanthobothrium from Australian waters are Squalus megalops (Macleay, 1881) (Squalidae), Heterodontus portusjacksoni (Meyer, 1793) (Heterodontidae), Orectolobus maculatus (Bonnaterre, 1788) (Orectolobidae) and Trygonoptera ‘testacea’ MÜller & Henle, 1841 (Urolophidae). An emended diagnosis of the genus, key to Australian species, host-parasite checklist, phylogenetic analysis of the Australian species and an updated world list of all species of Acanthobothrium are provided.


1985 ◽  
Vol 63 (9) ◽  
pp. 2224-2229 ◽  
Author(s):  
John Brattey ◽  
Robert W. Elner ◽  
Leslie S. Uhazy ◽  
Anne E. Bagnall

Seven hundred and twenty-one brachyuran crabs (Cancer borealis, Cancer irroratus, Carcinus maenas, Chionoecetes opilio, Geryon quinquedens) were collected in waters off eastern Canada during 1980–1982 and the prevalences of metazoan parasites and commensals determined. The survey revealed larval stages of three species of parasite, Microphallus sp. (Platyhelminthes: Digenea), Polymorphus sp. (Acanthocephala: Palaeacanthocephala), Nectonema sp. (Nematomorpha: Nectonematoidea), and five species of ectocommensal, Eteonopsis geryonicola (Annelida: Polychaeta), Johanssonia arctica (Annelida: Hirudinea), Ectocotyla paguri and Ectocotyla multitesticulata (Platyhelminthes: Turbellaria), and Carcinonemertes sp. (Nemertea: Monostilifera). New host records are reported for E. geryonicola in the branchial chambers of C. opilio and for Carcinonemertes sp. on egg masses of ovigerous G. quinquedens. All of the larval parasites, except Nectonema sp., and all of the ectocommensals, except J. arctica and Ectocotyla spp., are previously unreported from crabs off eastern Canada. Our findings suggest that the crab species studied do not support a diverse community of metazoan parasites or commensals.


Zootaxa ◽  
2012 ◽  
Vol 3227 (1) ◽  
pp. 54 ◽  
Author(s):  
ANKITA GUPTA ◽  
BLAISE PEREIRA

A new species, Glyptapanteles hypermnestrae Gupta and Pereira, is described from Maharashtra, India, and comparedwith closely allied species. This new species was bred from parasitized larvae of Elymnias hypermnestra (Linnaeus) (Lep-idoptera: Nymphalidae). In addition to this, two hymenopteran parasitoids, Apanteles folia Nixon (Braconidae: Microgas-trinae) and Brachymeria indica (Krausse) (Chalcididae), are for first time reported parasitizing larvae of Arhopalaamantes (Hewitson) (Lepidoptera: Lycaenidae) and pupae of Pareronia valeria (Cramer) (Lepidoptera: Pieridae) respectively.


Mycoses ◽  
2009 ◽  
Vol 25 (11) ◽  
pp. 638-640 ◽  
Author(s):  
S. C. Sati ◽  
G. S. Mer ◽  
R D. Khulbe

1969 ◽  
Vol 47 (6) ◽  
pp. 1411-1411
Author(s):  
W. A Webster ◽  
R. R. MacKay

Nematodirus spathiger (Railliet, 1896) Railliet and Henry, 1909 from a horse, and Nematodirus odocoilei Becklund and Walker, 1967 from the white-tailed deer Odocoileus virginianus, constitute new host–parasite records.


1988 ◽  
Vol 83 (4) ◽  
pp. 437-440 ◽  
Author(s):  
Anna Kohn ◽  
Cláudia Portes Santos

Mazocraeoides georgei price, 1936 and mazocraeoides opisthonema Hargis, 1955 are reported for the first time in Brazil in Brevoortia aurea (Spix, 1829) and in Harengula clupeola (Cuvier, 1829) respectively, clupeid fishes from the littoral of Rio de janeiro State, which represent new host records. Mazocraeoides olentangiensis Sroufe, 1958 and mazocraeoides hargisi Price, 1961 are considered new synonyms for Mazocraeoides georgei.


2013 ◽  
Vol 22 (1) ◽  
pp. 6-12 ◽  
Author(s):  
Gustavo Seron Sanches ◽  
Thiago Fernandes Martins ◽  
Ileyne Tenório Lopes ◽  
Luís Flávio da Silva Costa ◽  
Pablo Henrique Nunes ◽  
...  

In the present study, we report tick infestations on wild birds in plots of the Atlantic Forest reforested fragments with native species and plots reforested with Eucalyptus tereticornis in the municipality of Rio Claro, State of Sao Paulo, Brazil. A total of 256 birds were captured: 137 individuals of 33 species, in planted native forest; and 128 individuals of 37 species, in planted Eucalyptus tereticornis forest. Nymphs of two tick species were found on the birds: Amblyomma calcaratumand Amblyomma longirostre, the former was more abundant in the fragments reforested with Atlantic forest native species, and the latter in the fragment reforested with E. tereticornis. New host records were presented for A. calcaratum.


2007 ◽  
Vol 67 (4) ◽  
pp. 759-763 ◽  
Author(s):  
WO Almeida ◽  
A Vasconcellos ◽  
SG Lopes ◽  
EMX Freire

This study aimed to evaluate the infection rates of snakes by pentastomids in the semi-arid region of Brazil. Fifteen snakes (four Micrurus ibiboboca (Merrem, 1820) and eleven Philodryas nattereri Steindachner, 1870) were collected between January and April of 2005, in the municipality of Crato (07° 14' S and 39° 24' W), State of Ceará, Brazil. Laboratorial analysis of the respiratory tracts of the sampled snakes indicated differences in host infection rates: four individuals of P. nattereri (36.4%) were infected by Cephalobaena tetrapoda Heymons, 1922 (mean infection intensity 1.5 ± 0.28, 1-2) and three specimens (27.3%) by Raillietiella furcocerca (Diesing, 1863) (2.3 ± 1.32, 1-5). Only one individual of M. ibiboboca (25%) was infected by a non-identified species of Raillietiella sp. These are the first data on pentastomid infection in snakes in Northeastern Brazil and both snake species comprise new host records for the pentastomids. The results also indicate that the generalist parasites C. tetrapoda and R. furcocerca share their definitive hosts.


2013 ◽  
Vol 13 (3) ◽  
pp. 74-79 ◽  
Author(s):  
Mario Fernando Garcés-Restrepo ◽  
Alan Giraldo ◽  
John L. Carr ◽  
Lisa D. Brown

This study provides an update on the ectoparasites (ticks and leeches) associated with Rhinoclemmys annulata and provides new accounts on the ectoparasites associated with R. nasuta, R. melanosterna andKinosternon leucostomum from the Pacific coast of Colombia. The presence ofAmblyomma sabanerae on R. nasuta and R. melanosterna provided two new host records for the tick species. Also, the documentation ofA. sabanerae from the Department of Valle del Cauca represents a new department record for the species in Colombia. Placobdella ringueleti was identified fromR. nasuta and K. leucostomum, which represents a new host record for the leech species, as well as a significant extension of the known range.


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