<Emphasis Type="Italic">Pseudorhabdosynochus hirundineus</Emphasis> n. sp. (Monogenea: Diplectanidae) from <Emphasis Type="Italic">Variola louti</Emphasis> (Perciformes: Serranidae) off New Caledonia

Pseudorhabdosynochus hirundineus n. sp. is described from specimens collected from the gills of Variola louti off Nouméa, New Caledonia, South Pacific. No diplectanid was found on V. albimarginata from the same location. The male sclerotised quadriloculate organ of P. hirundineus is 42 μm in internal length, with a long posterior tube; and the sclerotised vagina, 36 μm in length, is composed of a long tube with anterior open trumpet and two posterior, heavily sclerotised chambers. The two squamodiscs, each with 11–15 rows of rodlets and no central closed row of rodlets, are dissimilar in shape, the ventral being round and the dorsal being oval. By the morphology of its sclerotised vagina, P. hirundineus appears close to P. epinepheli (Yamaguti, 1938) but it is differentiated from it by the shape of its squamodiscs. Pseudorhabdosynochus spp. previously recorded from epinephelines are parasites of species of Epinephelus and Mycteroperca; this is the first species from a species of Variola.

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Résumé Résumé Pseudorhabdosynochus hirundineus n. sp. est décrit de spécimens récoltés sur les branchies de Variola louti au large de Nouméa, Nouvelle Calédonie, Pacifique sud. Aucun Diplectanidae n’a été trouvé chez V. albimarginata de la même origine. L’organe mâle sclérifié tétraloculé de P. hirundineus mesure 42μm de longueur interne et a un long tube postérieur, et le vagin sclérifié, long de 36μm, est composé d’un long tube avec une trompe antérieure et deux chambres postérieures très sclérifiées. Les deux squamodisques, chacun avec 11–15 rangées d’osselets et sans rangée close, sont de formes différentes, le ventral rond et le dorsal ovale. Par la morphologie de son vagin sclérifié, P. hirundineus semble proche de P. epinepheli (Yamaguti, 1938), mais s’en distingue par la forme de ses squamodisques. Les espèces de Pseudorhabdosynochus mentionnées auparavant chez les Epinephelinae étaient parasites d’espèces des genres Epinephelus et Mycteroperca; ceci est la première espèce chez Variola.

     

<Emphasis Type="Italic">Spicocleidus namae</Emphasis> n. g., n. sp. (Monogenea: Dactylogyridae) on <Emphasis Type="Italic">Chanda nama</Emphasis> (Hamilton) from Lucknow,India

Spicocleidus n. g. is proposed for S. namae n. sp., a new monogenean collected from the gills of an ambassid, Chanda nama (Ham.), in the River Sai near Lucknow, Uttar Pradesh, India. The new genus is characterised by a pair of modified dorsal anchors (spikes), the absence of a dorsal bar, alate lateral expansion of the anterior haptor and the post-ovarian position of the testis.     

<Emphasis Type="Italic">Longidorus</Emphasis><Emphasis Type="Italic">kheirii</Emphasis> n. sp. (Nematoda: Longidoridae) from Iran

Longidorus kheirii n. sp., a parthenogenetic species, was found in soil samples collected from the rhizosphere of Rosa sp. growing in a natural mountainous region close to Maragheh city, northwestern Iran. It is characterised by having a long body (6.7-9 mm), a 19.5-23 mum wide head continuous with the body contour, a truncate and slightly concave lip region with convex sides between the anterior end and the guide-ring, an odontostyle 113-130 mum long, an odontophore 69-97.5 mum long, a body width of 90.5-117.5 mum at the mid-body, a long, wide oesophageal bulb (149.5-193.5 x 39.5-48 mum), a tail length of 47-72 mum, a male with 11 ventromedian supplements and spicules of 85 mum in length, and four juvenile stages. The ribosomal 18S rDNA gene of L. kheirii n. sp., L. leptocephalus Hooper, 1961, L. profundorum Hooper, 1966 L. euonymus Mali & Hooper, 1973 and two unidentified species listed as Longidorus sp. 1 and Longidorus sp. 2, all recovered from northwestern Iran in the same survey, and the ITS1 of L. kheirii n. sp. and Longidorus sp. 1 were sequenced in order to investigate the phylogenetic relationships with other previously sequenced Longidorus species.     

<Emphasis Type="Italic">Pseudorhabdosynochus quadratus</Emphasis> n. sp. (Monogenea: Diplectanidae) from the white-streaked grouper <Emphasis Type="Italic">Epinephelus ongus</Emphasis> (Bloch) (Perciformes: Serranidae) off New Caledonia

Gill diplectanid monogeneans from the camouflage grouper Epinephelus polyphekadion (Bleeker) collected in the coral reef lagoon of New Caledonia, South Pacific, comprise four species. Very few monogeneans were found in most fish examined. Pseudorhabdosynochus dionysos n. sp. has a sclerotised vagina with a robust trumpet, a robust primary canal and two chambers of similar size; it is close to P. bacchus Sigura, Chauvet & Justine, 2007. P. viscosus n. sp. has a sclerotised vagina with a robust trumpet, long primary canal with an extremely thin wall and two small chambers, and a male quadriloculate organ with a characteristic thickening at the extremity of its cone. P. crassus n. sp., the most abundant species, has a sclerotised vagina with a thin-walled trumpet, thin-walled primary canal which is always coiled anteriorly and two small chambers. P. huitoe Justine, 2007, P. manifestus Justine & Sigura, 2007 and P. crassus have very similar sclerotised vaginae; however, species of this ‘huitoe complex’ can be distinguished by measurements of the haptoral hard parts. A few diplectanid specimens found in a single specimen of E. polyphekadion were attributed to P. huitoe, a species originally described from E. maculatus (Bloch) and also rarely found in E. cyanopodus Richardson in New Caledonia; specimens from these three fish species are morphologically indistinguishable.     

<Emphasis Type="Italic">Adlardia</Emphasis><Emphasis Type="Italic">novaecaledoniae</Emphasis> n. g., n. sp. (Digenea: Cryptogonimidae) from the fork-tailed threadfin bream <Emphasis Type="Italic">Nemipterus furcosus</Emphasis> (Val.) (Perciformes: Nemipteridae) off New Caledonia

Adlardia novaecaledoniae n. g., n. sp. (Digenea: Cryptogonimidae) is described from the fish Nemipterus furcosus (Val.) (Perciformes: Nemipteridae) from off New Caledonia (South Pacific). Adlardia n. g. is distinguished from all other cryptogonimid genera by the combination of an elongate body, the presence of oral spines, intestinal caeca that open via ani at the posterior end of the body, a highly lobed ovary, oblique testes that are located in the mid-hindbody, vitelline follicles that extend from midway between the testes and ovary to midway between the ovary and ventral sucker, and an excretory vesicle that bifurcates dorsal to the ovary and reunites immediately anterior to the pharynx. A. novaecaledoniae n. sp. is the only cryptogonimid that has been reported with an excretory vesicle that reunites anterior to the pharynx. Siphoderina elongata (Gu &; Shen, 1979) Miller &; Cribb, 2008 is transferred to Adlardia as A. elongata (Gu &; Shen, 1979) n. comb. based on morphological and ecological (host group) agreement with A. novaecaledoniae. Bayesian inference analysis of LSU rDNA revealed that A. novaecaledoniae nested well within a clade containing cryptogonimid taxa known almost exclusively from haemulid and lutjanid fishes, suggesting that host-switching between teleosts of the Haemuloidea, Lutjanoidea and Sparoidea may have been common in the evolutionary history of this system.     

<Emphasis Type="Italic">Ty</Emphasis>1<Emphasis Type="Italic">/copia</Emphasis>- and <Emphasis Type="Italic">Ty</Emphasis>3<Emphasis Type="Italic">/gypsy</Emphasis>-like DNA sequences in <Emphasis Type="Italic">Helianthus </Emphasis>species

Two repeated DNA sequences isolated from a partial genomic DNA library of Helianthus annuus, p HaS13 and p HaS211, were shown to represent portions of the int gene of a Ty3 /gypsy retroelement and of the RNase-Hgene of a Ty1 /copia retroelement, respectively. Southern blotting patterns obtained by hybridizing the two probes to BglII- or DraI-digested genomic DNA from different Helianthus species showed p HaS13 and p HaS211 were parts of dispersed repeats at least 8 and 7 kb in length, respectively, that were conserved in all species studied. Comparable hybridization patterns were obtained in all species with p HaS13. By contrast, the patterns obtained by hybridizing p HaS211 clearly differentiated annual species from perennials. The frequencies of p HaS13- and p HaS211-related sequences in different species were 4.3x10(4)-1.3x10(5) copies and 9.9x10(2)-8.1x10(3) copies per picogram of DNA, respectively. The frequency of p HaS13-related sequences varied widely within annual species, while no significant difference was observed among perennial species. Conversely, the frequency variation of p HaS211-related sequences was as large within annual species as within perennials. Sequences of both families were found to be dispersed along the length of all chromosomes in all species studied. However, Ty3 /gypsy-like sequences were localized preferentially at the centromeric regions, whereas Ty1/ copia-like sequences were less represented or absent around the centromeres and plentiful at the chromosome ends. These findings suggest that the two sequence families played a role in Helianthusgenome evolution and species divergence, evolved independently in the same genomic backgrounds and in annual or perennial species, and acquired different possible functions in the host genomes.     

<Emphasis Type="Italic">Quinua</Emphasis> and Relatives (<Emphasis Type="Italic">Chenopodium</Emphasis> sect.<Emphasis Type="Italic">Chenopodium</Emphasis> subsect.<Emphasis Type="Italic">Celluloid</Emphasis>)

Traditionally viewed as an Andean grain crop,Chenopodium quinoa Willd. includes domesticated populations that are not Andean, and Andean populations that are not domesticated. Comparative analysis of leaf morphology and allozyme frequencies have demonstrated that Andean populations, both domesticated(quinua) and free-living(ajara), represent an exceptionally homogeneous unit that is well differentiated from allied domesticates of coastal Chile(quingua) and freeliving populations of the Argentine lowlands(C. hircinum). This pattern of relationships indicates that Andean populations represent a monophyletic crop/weed system that has possibly developed through cyclic differentiation (natural vs. human selection) and introgressive hybridization. Relative levels of variation suggest that this complex originated in the southern Andes, possibly from wild types allied withC. hircinum, with subsequent dispersal north to Colombia and south to the Chilean coast. Coastal populations were apparently isolated from post-dispersal differentiation and homogenization that occurred in the Andes. Other data point toward a center of origin in the northern Andes with secondary centers of genetic diversity subsequently developing in the southern Andes and the plains of Argentina. Comparative linkage of South American taxa, all tetraploid, with North American tetraploids of the subsection will eventually clarify this problem. While the possibility of a direct phyletic connection betweenC. quinoa and the Mexican domesticate(C. berlandieri subsp. nuttalliae,) cannot be excluded, available evidence indicates that the latter represents an autonomous lineage that is associated with the basal tetraploid, C. b. subsp.berlandieri, through var.sinuatum, whereas South American taxa show possible affinities to either var. zschackei or var.berlandieri. An extinct domesticate of eastern North America,C. b. subsp.jonesianum, represents either another instance of independent domestication, possibly from subsp. b. var.zschackei, or a northeastern outlier of subsp.nuttalliae.     

<Emphasis Type="Italic">Malalophus jensenae</Emphasis> n. g., n. sp. (Monogenea: Monocotylidae) from the gills of <Emphasis Type="Italic">Aetomylaeus vespertilio</Emphasis> (Myliobatidae) off northern Australia

Malalophus jensenae n. g., n. sp. is described from the gills of the ornate eagle ray Aetomylaeus vespertilio (Bleeker) collected off the eastern coast of the Gulf of Carpentaria, northern Queensland. The new genus is similar to Heliocotyle Neifar, Euzet & Ben Hassine, 1999, with which it shares a haptor bearing seven peripheral loculi and a single dorsal haptoral accessory structure. M. jensenae can be distinguished from species of Heliocotyle by the presence of numerous sclerotised sinuous ridges covering the ventral surfaces of the peripheral loculi of the haptor. It also lacks pseudosepta which are present on the haptor of Heliocotyle species. This is the first published record of a monogenean from an elasmobranch in the Gulf of Carpentaria, Australia.     

<Emphasis Type="Italic">Kretzschmaria varians</Emphasis> sp. nov., <Emphasis Type="Italic">Xylaria coremiifera</Emphasis> sp. nov. and <Emphasis Type="Italic">Xylaria umbonata</Emphasis> sp. nov. from Costa Rica

Kretzschmaria varians, a species apparently related to K. micropus, is described as new. It is distinguished primarily by having asci with 2 to 8 ascospores with inconstant germination slit length and remains of synnemata on stromata and surrounding substrate. Xylaria coremiifera, described here as new, bears small fragile coremia on pulvinate stromata and the surrounding substrate. Asci often have fewer than 8 ascospores, most frequently 4. Xylaria umbonata, described here as new, produces perithecia around a central umbo that appears to be the remains of a synnema. Ascospores have long spiralling germination slits.     

<Emphasis Type="Italic">Neolebouria blatta</Emphasis> n. sp. (Digenea: Opecoelidae) from <Emphasis Type="Italic">Pristipomoides argyrogrammicus</Emphasis> (Valenciennes) and <Emphasis Type="Italic">Etelis carbunculus</Emphasis> Cuvier (Perciformes: Lutjanidae) off New Caledonia

Neolebouria blatta n. sp. is described from Pristipomoides argyrogrammicus (Valenciennes) and Etelis carbunculus Cuvier in waters off New Caledonia. It differs from all other species of Neolebouria Gibson, 1976 but one, N. georgenascimentoi Bray, 2002, in the extension of the cirrus-sac to the ovary or nearly so. It differs from N. georgenascimentoi in its continuous, rather than interrupted, vitelline distribution. N. blatta belongs to a small group of similar Neolebouria species reported in deep-water lutjanids, which includes N. longisacculus (Yamaguti, 1970) n. comb., N. rooseveltiae (Yamaguti, 1970) n. comb. and N. ulaula (Yamaguti, 1970).     

<Emphasis Type="Italic">Steinernema costaricense</Emphasis> n. sp. and <Emphasis Type="Italic">S. puntauvense</Emphasis> n. sp. (Rhabditida: Steinernematidae), two new entomopathogenic nematodes from Costa Rica

Steinernema costaricense n. sp. and S. puntauvense n. sp. were recovered during a survey for native entomopathogenic nematodes in Costa Rica. Morphological data, molecular (28S rDNA sequence data) studies and cross-hybridisation tests were used for diagnostic and identification purposes. Additionally, 28S rDNA sequence data were used to assess the evolutionary relationships of the new species with other Steinernema spp. Morphological diagnostic features for S. costaricense n. sp. include: the body size of the infective juvenile (av. 1,696); the presence of protruding 'horn-like' cephalic papillae; the position of the excretory pore in the infective juvenile (av. 77 microm) and the first generation male (av. 117 microm); the D% value of the infective juvenile (av. 53) and the first generation male (av. 56); the E% value of the infective juvenile (av. 85); and the morphology of the spicules and gubernaculum of the first generation male. Diagnostic traits for S. puntauvense n. sp. are: the position of the excretory pore in the infective juveniles (av. 25 microm); the shape and size of the spicules and gubernaculum of the first generation male; and the shape of the tail of the first generation female. In addition to these traits, 28S rDNA sequences analysis and hybridisation tests showed that both new Steinernema species are distinct and unique entities.     

Mercury Tolerance of Thermophilic <Emphasis Type="Italic">Bacillus</Emphasis> sp. and <Emphasis Type="Italic">Ureibacillus</Emphasis> sp

Although resistance of microorganisms to Hg(II) salts has been widely investigated and resistant strains have been reported from many eubacterial genera, there are few reports of mercuric ion resistance in extremophilic microorganisms. Moderately thermophilic mercury resistant bacteria were selected by growth at 62 °C on Luria agar containing HgCl₂. Sequence analysis of 16S rRNA genes of two isolates showed the closest matches to be with Bacillus pallidus and Ureibacillus thermosphaericus. Minimum inhibitory concentration (MIC) values for HgCl₂ were 80 μg/ml and 30 μg/ml for these isolates, respectively, compared to 10 μg/ml for B. pallidus H12 DSM3670, a mercury-sensitive control. The best-characterised mercury-resistant Bacillus strain, B. cereus RC607, had an MIC of 60 μg/ml. The new isolates had negligible mercuric reductase activity but removed Hg from the medium by the formation of a black precipitate, identified as HgS by X-ray powder diffraction analysis. No volatile H₂S was detected in the headspace of cultures in the absence or presence of Hg²⁺, and it is suggested that a new mechanism of Hg tolerance, based on the production of non-volatile thiol species, may have potential for decontamination of solutions containing Hg²⁺ without production of toxic volatile H₂S.     

<Emphasis Type="Italic">Ligophorus llewellyni</Emphasis> n. sp. (Monogenea: Ancyrocephalidae) from the redlip mullet <Emphasis Type="Italic">Liza haematocheilus</Emphasis> (Temminck &; Schlegel) introduced into the Black Sea from the Far East

Ligophorus llewellyni n. sp. (Ancyrocephalidae: Ligophorus Euzet & Suriano, 1977) is described from the gills of Liza haematocheilus (Temminck & Schlegel) introduced into the Black Sea from the Far East. Ligophorus llewellyni is closely related to L. pilengas Sarabeev & Balbuena, 2004, which parasitises the same host species. The two species differ in the morphology of the accessory piece of the copulatory organ and in some of the characters of the haptoral hard-parts. The morphometric variability of L. llewellyni and in its morphologically most similar congeners from the Black Sea is studied. Correlations between 30 morphometric characters of the haptoral hard-parts and the significance of each for species differentiation are examined. It is suggested that only 22 characters are useful as diagnostic criteria permitting the differentiation of morphologically similar species of Ligophorus.     

<Emphasis Type="Italic">Agrobacterium</Emphasis><Emphasis Type="Italic">tumefaciens</Emphasis>-mediated transformation of callus cells of <Emphasis Type="Italic">Crataegus</Emphasis><Emphasis Type="Italic">aronia</Emphasis>

A genetic transformation system has been developed for callus cells of Crataegus aronia using Agrobacterium tumefaciens. Callus culture was established from internodal stem segments incubated on Murashige and Skoog (MS) medium supplemented with 5 mg l⁻¹ Indole-3-butyric acid (IBA) and 0.5 mg l⁻¹ 6-benzyladenine (BA). In order to optimize the callus culture system with respect to callus growth and coloration, different types and concentrations of plant growth regulators were tested. Results indicated that the best average fresh weight of red colored callus was obtained on MS medium supplemented with 2 mg l⁻¹ 2,4-dichlorophenoxyacetic acid (2,4-D) and 1.5 mg l⁻¹ kinetin (Kin) (callus maintenance medium). Callus cells were co-cultivated with Agrobacterium harboring the binary plasmid pCAMBIA1302 carrying the mgfp5 and hygromycin phosphotransferase (hptII) genes conferring green fluorescent protein (GFP) activity and hygromycin resistance, respectively. Putative transgenic calli were obtained 4 weeks after incubation of the co-cultivated explants onto maintenance medium supplemented with 50 mg l⁻¹ hygromycin. Molecular analysis confirmed the integration of the transgenes in transformed callus. To our knowledge, this is the first time to report an Agrobacterium-mediated transformation system in Crataegus aronia.     

<Emphasis Type="Italic">Galleria</Emphasis><Emphasis Type="Italic">mellonella</Emphasis> are Resistant to <Emphasis Type="Italic">Pneumocystis</Emphasis><Emphasis Type="Italic">murina</Emphasis> Infection

Studying Pneumocystis has proven to be a challenge from the perspective of propagating a significant amount of the pathogen in a facile manner. The study of several fungal pathogens has been aided by the use of invertebrate model hosts. Our efforts to infect the invertebrate larvae Galleria mellonella with Pneumocystis proved futile since P. murina neither caused disease nor was able to proliferate within G. mellonella. It did, however, show that the pathogen could be rapidly cleared from the host.     

Revision of the <Emphasis Type="Italic">Serrulati</Emphasis> species of <Emphasis Type="Italic">Penstemon</Emphasis> section <Emphasis Type="Italic">Saccanthera</Emphasis> subsection <Emphasis Type="Italic">Serrulati</Emphasis>

A revision of Penstemon sect. Saccanthera subsect. Serrulati includes a new species (P. salmonensis), a new variety (P. triphyllus var. infernalis), and the elevation of a subspecies to species (P. curtiflorus), bringing the total number of species to eight, which are keyed and described, complete with nomenclature and type citations.     

In planta transformation of <Emphasis Type="Italic">Notocactus scopa</Emphasis> cv. <Emphasis Type="Italic">Soonjung</Emphasis> by <Emphasis Type="Italic">Agrobacterium </Emphasis><Emphasis Type="Italic">tumefaciens</Emphasis>

Notocactus scopa cv. Soonjung was subjected to in planta Agrobacterium tumefaciens-mediated transformation with vacuum infiltration, pin-pricking, and a combination of the two methods. The pin-pricking combined with vacuum infiltration (20-30 cmHg for 15 min) resulted in a transformation efficiency of 67-100%, and the expression of the uidA and nptII genes was detected in transformed cactus. The established in planta transformation technique generated a transgenic cactus with higher transformation efficiency, shortened selection process, and stable gene expression via asexual reproduction. All of the results showed that the in planta transformation method utilized in the current study provided an efficient and time-saving procedure for the delivery of genes into the cactus genome, and that this technique can be applied to other asexually reproducing succulent plant species.     

<Emphasis Type="Italic">Pseudodiplectanum syrticum</Emphasis> n. sp. (Monogenea: Diplectanidae), a parasite of <Emphasis Type="Italic">Synapturichthys kleinii</Emphasis> (Teleostei: Soleidae) from off Tunisia

Pseudodiplectanum syrticum n. sp. (Monogenea: Diplectanidae) is described from the gills of Synapturichthys kleinii (Risso) collected from the Gulf of Gabès in the Mediterranean Sea off Tunisia. The new species differs from the congeneric species by the morphology of the penis and vagina. It resembles the Mediterranean species P. kearni Vala, Lopez-Roman & Boudaoud, 1980 from Solea vulgaris Quensel and P. gibsoni Oliver, 1987 from Michrochirus variegatus (Donovan) in its tubular penis, but it differs from these two species by having a vagina with a long tube presenting two loops and a male copulatory organ ending in a curved point. It also differs in the morphology and size of the transverse bars of the haptor. In P. syrticum the ventral transverse bar and dorso-lateral bars are longer than those of P. gibsoni (114 vs 69.5-89 microm and 48 vs 33-44 microm, respectively).