Twenty two percent (22/98) of intertidal fishes of 10 species captured in South Africa at Koppie Alleen, De Hoop Nature Reserve (south coast) and Mouille Point, Cape Town (west coast), harboured single or combined infections of haemogregarines, trypanosomes and an intraerythrocytic parasite resembling a Haemohormidium sp. The haemogregarines included the known species Haemogregarina (sensu lato) bigemina (Laveran et Mesnil, 1901) Siddall, 1995 and Haemogregarina (sensu lato) koppiensis Smit et Davies, 2001, while Haemogregarina (sensu lato) curvata sp. n. was observed in Clinus cottoides Valenciennes and Parablennius cornutus (L.) at Koppie Alleen. This last haemogregarine is characterised particularly by its distinctly curved gamonts. Also at Koppie Alleen, squash and histological preparations of 9/10 leeches, Zeylanicobdella arugamensis De Silva, 1963, taken from infected C. cottoides and P. cornutus contained developmental stages of H. curvata and/or trypanosomes, but these were absent from haematophagous gnathiid isopods (Gnathia africana Barnard, 1914) taken from infected fishes. It is suspected that Z. arugamensis transmits the haemogregarine and trypanosomes simultaneously between fishes, a double event unreported previously from the marine environment.
A new species, Gnathia nkulu sp. n. is described from material collected off the South African coast at 80-200m depth. It differs from the intertidal species Gnathia africana Barnard, 1914 in that the mediofrontal process is not deeply divided into two lobes, article 2 of the pylopod is rounded and small wart-like tubercles and long simple setae are present on both the cephalosome and pereon.
Blood films were examined from 154 wild and captive tortoises from four provinces of South Africa, including Gauteng, Kwazulu-Natal, North West and Western Cape. The five species of chelonians studied were Chersina angulata (Schweigger), Kinixys belliana belliana (Gray), K. lobatsiana Power, K. natalensis Hewitt, and Stigmochelys pardalis (Bell). Two species of haemogregarines, previously reported from Mozambique, were identified in blood films, namely Haemogregarina fitzsimonsi Dias, 1953 and Haemogregarina parvula Dias, 1953. Additional stages of development (trophozoites and probable meronts, merozoites and immature gamonts) in blood preparations from South Africa warranted the redescription of H. fitzsimonsi. A variety of hosts and broad host distribution range were observed for this haemogregarine, with all five species of tortoises parasitized, wild and captive, from all four provinces, in all seasons. In contrast, only two individuals of K. b. belliana and one S. pardalis, all three captive in Kwazulu-Natal, contained H. parvula with encapsulated stages resembling those of Hemolivia mauritanica (Sergent et Sergent, 1904). For H. fitzsimonsi, parasite prevalences, but not parasitaemias, were significantly higher in captive than wild S. pardalis; captive female S. pardalis also showed a significantly greater prevalence of infection than males, but younger, lighter hosts were not significantly more heavily parasitized than older, heavier individuals. The ticks, Amblyomma marmoreum Koch, 1844 and A. sylvaticum (De Geer, 1778), found attached to some tortoises, may prove to be definitive hosts for the two species of haemogregarines observed.
A redescription of the adult male and praniza of Gnathia africana Barnard, 1914 is provided from material collected at three localities along the South African coast and from syntypes and other material deposited by the original author. This redescription is based on light and scanning electron microscopy.
A redescription of the adult male of Caecognathia cryptopais (Barnard, 1925) is provided from syntypes and other material deposited in the South African Museum. The generic status of Caecognathia cryptopais is also revised. This redescriplion is based on light and scanning electron microscopy.
During 2001 and 2002, blood smears from 37 of 120 fishes belonging to 10 species captured in the Okavango Delta region of Botswana, were found to harbour trypanosomes. These trypanosomes displayed differing staining properties, were morphometrically variable, and ranged in total length from 29.5 to 80.8 µm. Mixed populations of the smaller and larger trypanosomes were found in most fish examined. Despite variations in size and appearance, these specimens are tentatively identified as Trypanosoma mukasai Hoare, 1932, likely adding another 9 new hosts to those known for this parasite. It is possible that Trypanosoma clariense Pienaar, 1962, described from Clarias gariepinus in South Africa, is also a junior synonym of T. mukasai.
The examination of eight spotted skates, Raja straeleni Poll, resulted in the discovery of four new species of Acanthobothrium van Beneden, 1849, namely A. microhabentes sp. n., A. microtenuis sp. n., A. crassus sp. n., and A. dolichocollum sp. n., located off the Western Cape of South Africa. With a total of over 200 valid species of Acanthobothrium recognised worldwide, the use of an integrative approach becomes imperative in the interest of simplifying interspecific comparisons between congeners. In accordance with this, the four new species were incorporated into the category classification system established by Ghoshroy and Caira in 2001, where they were identified as category 2 species, which, at present, includes 47 recognised species of Acanthobothrium. Nevertheless, each of the four new species exhibits postovarian testes, a most intriguing and highly unusual feature among Acanthobothrium, instantly differentiating them from most congeners. This feature has been reported in 12 congeners, which have previously been considered to be restricted to waters of the Indo-Pacific Ocean. Not only do the four new congeners represent the first species of Acanthobothrium reported from southern Africa, but they also represent the first reported species with postovarian testes from the southern Atlantic Ocean. and Regarding the legitimacy of the four new species, only two other category 2 species are reported to exhibit this feature, namely A. popi Fyler, Caira et Jensen, 2009, and A. bobconniorum Fyler et Caira, 2010, to which the four congeners were compared to. Acanthobothrium microhabentes sp. n. is the smallest of the congeners and differs from A. popi and A. bobconniorum by having fewer testes and postovarian testes, a shorter body, fewer proglottids, a shorter scolex, and longer cephalic peduncle. Acanthobothrium microtenuis sp. n. differs from A. popi and A. bobconniorum by having fewer testes and postovarian testes, a shorter scolex, longer cephalic peduncle, and the possession of columnar spinitriches on the anterior region of the terminal proglottid. Acanthobothrium crassus sp.n. differs from A. popi and A. bobconniorum by having fewer postovarian testes, a narrower cirrus-sac, larger vitelline follicles, and a longer cephalic peduncle. Acanthobothrium dolichocollum sp. n. is the longest of the four new species and differs from A. popi and A. bobconniorum by having fewer postovarian testes, more postporal testes, a larger body, more proglottids, larger testes and vitelline follicles, and an exceptionally long cephalic peduncle. Apart from differences in overall size, the four new species differ in a combination of measurements for the scolex, vitelline follicles, muscular pad and cephalic peduncle, and the number of proglottids and testes. The four species were recovered from a previously unexplored host and locality, expanding the host associations and geographical distribution of the genus.
Haematophagous larvae of a gnathiid isopod were collected from the gills, nares and buccal cavity of a single leopard catshark Poroderma pantherinum (Smith, 1838) at Jeffreys Bay and five puffadder shysharks Haploblepharus edwardsii (Voight, 1832) and one blackspotted electric ray Torpedo fuscomaculata Peters, 1855, at the De Hoop Nature Reserve on the South African south coast. Larvae were kept in fresh seawater until their moult into adult stages. The morphology of the adult males did not conform to that of any known species and they are therefore described as Gnathia pantherina sp. n. The descriptions of the adult male, female and praniza larva are based on light and scanning electron microscopy observations. Characteristic features of this species include the large size of all the final life-cycle stages, the deeply divided mediofrontal process of the male, the morphology of the pylopods and maxillipedes of the female, and the number of teeth on the mandibles (eight) and maxillules (seven) of the praniza larvae.
This paper reviews past, current and likely future research on the fish haemogregarine, Haemogregarina bigemina Laveran et Mesnil, 1901. Recorded from 96 species of fishes, across 70 genera and 34 families, this broad distribution for H. bigemina is questioned. In its type hosts and other fishes, the parasite undergoes intraerythrocytic binary fission, finally forming mature paired gamonts. An intraleukocytic phase is also reported, but not from the type hosts. This paper asks whether stages from the white cell series are truly H. bigemina. A future aim should be to compare the molecular constitution of so-called H. bigemina from a number of locations to determine whether all represent the same species. The transmission of H. bigemina between fishes is also considered. Past studies show that young fish acquire the haemogregarine when close to metamorphosis, but vertical and faecal-oral transmission seem unlikely. Some fish haemogregarines are leech-transmitted, but where fish populations with H. bigemina have been studied, these annelids are largely absent. However, haematophagous larval gnathiid isopods occur on such fishes and may be readily eaten by them. Sequential squashes of gnathiids from fishes with H. bigemina have demonstrated development of the haemogregarine in these isopods. Examination of histological sections through gnathiids is now underway to determine the precise development sites of the haemogregarine, particularly whether merozoites finally invade the salivary glands. To assist in this procedure and to clarify the internal anatomy of gnathiids, 3D visualisation of stacked, serial histological sections is being undertaken. Biological transmission experiments should follow these processes.