Revision of the genus Diclidophora Krøyer, 1838 (Monogenea: Diclidophoridae), with the proposal of Macrouridophora n. g.

The present study re-examines the detailed morphology of the type-species, Diclidophora merlangi (Kuhn, in Nordmann, 1832) Krøyer, 1838, and other Diclidophora species parasitic on gadid fishes: D. denticulata (Olsson, 1876) Price, 1943, D. esmarkii (Th. Scott, 1901) Sproston, 1946, D. luscae (van Beneden & Hesse, 1863) Price, 1943, D. minor (Olsson, 1868) Sproston, 1946, D. palmata (Leuckart, 1830) Diesing, 1850, D. phycidis (Parona & Perugia, 1889) Sproston, 1946, D. pollachii (van Beneden & Hesse, 1863) Price, 1943 and the recently described D. micromesisti Suriano & Martorelli, 1984. An amended generic diagnosis of Diclidophora Krøyer, 1838 (synonym Diclidophora Diesing, 1850) is provided, which includes the presence of a prostatic vesicle in the terminal male genitalia and the distal fusion of the median and peripheral sclerites, a₁ and c₁ in the clamp anterior jaw. Macrouridophora n. g. is herein proposed for species previously considered in Diclidophora, which are parasitic on macrourid and morid fishes. The clamp morphology in Macrouridophora n. g. has distinct lamellate extension attachments to peripheral sclerites c₁ and the distal portion of d₁, with no distal fusion between a₁ and c₁ in the anterior jaw. Macrouridophora macruri (Brinkmann, 1942) n. comb. is chosen as the type-species. Nine other species are herein transferred to Macrouridophora n. g.: M. coelorhynchi (Robinson, 1961) n. comb., M. lotella (Machida, 1972) n. comb., M. nezumiae (Munroe, Campbell & Zwerner, 1981) n. comb. and M. tubiformis (Rohde & Williams, 1987) n. comb. are redescribed, based on the re-examination of type or voucher specimens. Macrouridophora attenuata (Mamaev & Zubtschenko, 1979) n. comb., M. caudata (Mamaev & Zubtschenko, 1984) n. comb., M. papilio (Mamaev & Avdeev, 1981) n. comb., M. paracoelorhynchi (Mamaev & Paruchin, 1979) n. comb. and M. physiculi (Mamaev & Avdeev, 1981) n. comb. have adequately described haptoral clamps in the literature. The clamp morphology in Macrouridophora sp. from Lepidorhynchus denticulatus in Australia is also considered. Diclidophora whitsonii Suriano & Martorelli, 1984 is herein transferred to the genus Macruricotyle Mamaev & Ljadov, 1975, as M. whitsonii (Suriano & Martorelli, 1984) n. comb. D. embiotocae Hanson, 1979 is herein considered a species incertae sedis. D. caudospina Khan & Karyakarte, 1983 and D. paddiforma Deo & Karyakarte, 1979 are herein considered species inquirendae. D. aglandulosa Deo, 1977, D. glandulosa Das, 1972, D. minuta Das, 1972 and D. spindale Deo, 1977 are formally dismissed as nomina nuda. The systematic position of Diclidophora Krøyer, 1838 and Macrouridophora n. g. in the subfamily Diclidophorinae Cerfontaine, 1895 (sensu Mamaev, 1976) is discussed.     

Neotropical Monogenoidea. 32. Cacatuocotyle paranaensis n. g., n. sp. (Dactylogyridae,Ancyrocephalinae) from Characidium spp. (Teleostei,Characidae) from the State of Paraná, Brazil

Cacatuocotyle paranaensis n. sp. (Dactylogyridae, Ancyrocephalinae) is described from the gills of the characid fishes Characidium lanei Travassos and C. pterostictum Gomes collected from two streams on the coast of the State of Paraná, Brazil. Cacatuocotyle n. g. is proposed for species possessing a single cephalic lobe (terminal), one pair of head organs, a convex haptor with thickened muscular anterior margins, one anchor-bar complex (ventral), seven pairs of ventral hooks (one pair associated with the anchor shafts; one central pair anterior to the bar; five submarginal bilateral pairs) and a sinistral vaginal aperture.     

Genetic studies of human apolipoproteins. XIII. Quantitative polymorphism of apolipoprotein C-III in the Mayans of the Yucatán Peninsula

Apolipoprotein C-III (APO C-III) is a structural component of very-low-density and high-density lipoprotein particles and is an inhibitor of lipoprotein lipase. In a study of genetic variation of apolipoproteins in the Mayan population of the Yucatán peninsula, we observed a quantitative polymorphism in APO C-III levels. This polymorphism is expressed as variation in immunoblot staining intensity following isoelectric focusing and as variation in plasma levels of APO C-III determined by radial immunodiffusion. This variation is consistent with the presence in Mayans of an allele associated with low levels of plasma APO C-III which we have designated APO C-III*D. Analysis of the distribution of APO C-III levels yields a gene frequency estimate for the deficiency allele of 0.59. There is a significant positive correlation between total plasma APO C-III levels and total plasma cholesterol and triglyceride levels, the lowest levels of cholesterol and triglycerides being seen in individuals homozygous for the deficiency allele. This observation is consistent with the proposed role of APO C-III in lipoprotein metabolism. Family data to determine whether this deficiency allele is due to mutation at the APO C-III structural locus were not available. However, molecular analysis using cloned probes from the APO A-I/C-III/A-IV gene cluster revealed no gross DNA rearrangement or deletion of sequences in this region in homozygous deficient individuals.     

Bakkeius moragai n. gen. et n. sp. and Pojmanskia riosae n. gen. et n. sp. (Trematoda: Digenea: Brachylaimoidea) in birds from the Area de Conservación Guanacaste, Costa Rica

We describe 2 new species of leucochloridiid-like brachylaimoid digeneans parasitizing a variety of birds in the Area de Conservación Guanacaste, Costa Rica, each of which we assign to a new genus. According to Pojmanska's (Pojmanska, T. 2002a. Superfamily Brachylaimoidea Joyeux & Foley, 1930. In Keys to the Trematoda, D. I. Gibson, A. Jones, and R. A. Bray [eds.]. CAB International and The Natural History Museum, London, U.K., p. 31-36.) key for the Brachylaimoidea, we are unable to place either species in any family. One species most closely resembles members of Leucochloridium by having well-developed suckers, lacking an esophagus, and having cecal shoulders, gonads at the posterior end, and the genital pore at posterior end of body but differs by having symmetrical testes, a posttesticular ovary, and a terminal genital pore; thus, we propose the genus Bakkeius for it. The second new genus resembles members of Michajlovia by having ventral genital pores but differs by having extracecal uterine loops in the forebody, a cirrus sac containing the pars prostatica and seminal vesicle, and gland cells surrounding the genital pore; thus, we propose Pojmanskia for it. These new genera must currently be treated as incertae sedis according to Pojmanska (op. cit.); however, we feel that future phylogenetic analyses will require emendation of the family diagnosis for Leucochloridiidae to include those taxa with terminal and ventral genital pores and with preovarian testes.     

Paleolimnology of the Petén Lake district,Guatemala

The long-term impact of Maya culture on a lowland tropical watershed is assessed, using data from a 9.2 m sediment core taken from deep water (28 m) in Lake Quexil. Human population growth, estimated by the 1980 archaeological survey, is associated with a shift in the composition of the sediment to a dominance by inorganic material, the Maya clay formation, beginning ca. 3500 B.P. Increasing settlement densities are correlated with accelerated influxes of phosphorus, carbonates, and siliceous sediment. However, chemical data do not track short-term population fluctuations closely. Because much of the sediment is delivered as colluvium, and not by running water, there is a lag between terrestrial disturbance and impact on the aquatic system. As an indication of this lag, contemporary high sedimentation rates are a residual of Maya activity that virtually ceased some 300–400 years B.P. Comparison of the deep-water core with a shallow-water (7 m) section, based on palynological correlation, reveals only minor differences in proximate chemical composition. Chemical influxes are much higher at the deep-water site, however, as a consequence of sediment focusing in this hyperconical basin. Chemical analyses of soil samples from 21 test pits in the Quexil basin support the principal conclusion that bulk soil movement was the mode of nutrient transfer to the lake, following forest clearance by the Maya.     

Neotropical Monogenoidea 64. Cosmetocleithrum falsunilatum sp. n. (Monogenoidea,Dactylogyridae) parasite of the gills of Megalodoras uranoscopus (Siluriformes,Doradidae) from the Solimões river,near Iquitos,Peru

Systematic Parasitology - Megalodoras uranoscopus (Eigenmann & Eigenmann) (Siluriformes, Doradidae) (the giant-talking catfish or the giant-raphael catfish), from the...     

Morphogenesis in the marine spirotrichous ciliate Apokeronopsis crassa (Claparède & Lachmann, 1858) n. comb. (Ciliophora: Stichotrichia), with the establishment of a new genus, Apokeronopsis n. g., and redefinition of the genus Thigmokeronopsis

Morphogenetic events during the division of the marine spirotrichous ciliate, Apokeronopsis crassa (Claparède & Lachmann 1858) n. comb. were investigated. Compared with members of the well-known genera Thigmokeronopsis, Uroleptopsis, and Pseudokeronopsis, A. crassa has one row of buccal cirri, high number of transverse cirri, clearly separated midventral rows, lacks thigmotactic cirri and a gap in adoral zone, its undulating membranes (UMs) anlage forms one cirrus and marginal rows and dorsal kineties form apokinetally during division. All these characteristics indicate that this organism represents a new taxon at the generic level, and hence a new genus is suggested, Apokeronopsis n. g. It is defined as thus: Pseudokeronopsidae with Pseudokeronopsis-like bicorona of frontal cirri and one marginal row on each side; one row of two or more buccal cirri in ordinary position; two midventral rows distinctly separated, hence of cirri that are not in a typical zig-zag pattern; high number of transverse cirri, caudal cirri absent, and frontoterminal cirri present; thigmotactic cirri absent, many macronuclear nodules fuse into many masses as well as marginal and dorsal kineties form apokinetally during morphogenesis. At the same time, the genus ThigmokeronopsisWicklow, 1981 is redefined, and one new combination, Apokeronopsis antarctica (Petz, 1995) n. comb. is proposed. The morphogenetic events of A. crassa are characterized as follows: (1) In the proter, the adoral zone of membranelles and UMs are completely renewed by the oral primordium. The UM anlage is formed apokinetally on the dorsal wall of the buccal cavity and is hence clearly separated from the frontoventral-transverse (FVT) cirral anlagen in the proter. (2) Frontoventral-transverse cirral anlagen are generated de novo in the outermost region of the cortex to the right of the old UMs. (3) A row of buccal cirri arises from FVT cirral streak I. (4) The marginal rows and dorsal kineties originate de novo in both dividers; no caudal cirri are formed. (5) The last FVT-streak contributes two frontoterminal cirri. (6) The many macronuclear nodules fuse into many masses (about 50 segments) during division, unlike a singular or branched mass as described in other urostylids.     

At the end of the rope: Geophilus hadesi sp. n. – the world’s deepest cave-dwelling centipede (Chilopoda,Geophilomorpha, Geophilidae)

A new geophilomorph centipede, Geophilus hadesi sp. n., is described from caves in the Velebit Mountain, central Croatia. Together with Geophilus persephones Foddai & Minelli, 1999, described from Pierre Saint-Martin cave in France, they are the only two remarkably troglomorphic geophilomorphs hitherto known. The new species apparently belongs to a group of Geophilus species inhabiting mainly Western and Southern Europe, with a uniquely modified pretarsus in the second maxillae. Geophilus hadesi sp. n. shows unusual traits, some of which commonly found in troglobitic arthropods, including exceptionally elongated antennae, trunk segments and leg claws. The species is described upon specimens found in two caves at a depth below -250 m. Another two specimens apparently belonging to the same species have been recorded in another deep vertical cave at -980 m and -1100 m. The latter represents the world’s deepest record of Chilopoda as a whole.     

Physical-chemical features and determination of pesticides in the lagoon water in Gandoca, Limón, Costa Rica.

Nutrients and chlorophylls concentrations, as well as salinity, temperature and Secchi disk depth were determined from November 1999 to April 2000, at three stations and two depths, at Gandoca lagoon, Gandoca-Manzanillo National Wildlife Refuge, Limón, Costa Rica. Salinity profiles indicated that the lagoon was a salt wedge estuary with a partially mixed region near the mouth. No processes of eutrophication were found. The distribution and abundance of nutrients and chlorophylls showed a slight influence of continental water and water circulation patterns in the lagoon. A preliminary study was done in order to analyze the presence of 20 organochlorated and organophosphorated pesticides along the Gandoca lagoon in February 2000. None of the pesticides were detected by the analysis of residues from liquid-liquid extractions. The absence of the pesticides may be due to the fact that they did not reach the lagoon or, if they did, they were washed away by the strong rains during the sampling period.     

First isolation and molecular characterization of Cryptococcus neoformans var. grubii in excreta of birds in the urban perimeter of the Municipality of Popayán,Colombia

Background

Cryptococcosis is a systemic opportunistic mycosis, caused by Cryptococcus neoformans and Cryptococcus gattii, which affects mainly the central nervous system of immunocompromised patients; no reports have been made on the isolation of the fungus from the environment of Popayán, Colombia.

Lichen biodeterioration of the Convento de la Peregrina, Sahagún, Spain

Lichen encrustations from Diploschistes scruposus involved in the biodeterioration of the 13th Century Convento de la Peregrina in Sahagún Spain, have been analyzed using Raman spectroscopy. The vibrational spectra are characteristic of calcium oxalate monohydrate, beta-carotene, chlorophyll, and para-depside phenolic acids such as atranorin, lecanoric acid, and diploschistesic acid. The destructive colonization of the monumental stonework is highlighted and evidence presented for deleterious lichen invasion of the wall paintings inside the Convent.     

Dichelyne (Dichelyne) bonacii n. sp. (Nematoda: Cucullanidae) from the grey snapper Lutjanus griseus and the black grouper Mycteroperca bonaci off the coast of Yucatán,Mexico

A new cucullanid, Dichelyne bonacii n. sp., is described from the intestine of the grey snapper Lutjanus griseus and the stomach of the black grouper Mycteroperca bonaci off the coast of Yucatán. The absence of a ventral precloacal sucker and the presence of 11 pairs of caudal papillae in males allocate it to the subgenus Dichelyne. It differs from its congeners in body dimensions and by having two almost equal spicules (left 712-950 and right 722-945m), two intestinal caeca and in the position of the deirids and excretory pore. Apparently, L. griseus acts as definitive host of this species, whereas M. bonaci may be considered as a postcyclic host. This new species represents the first record of a nematode of the subgenus Dichelyne in marine fishes of Mexico.     

Ilyocryptus smirnovi n. sp. (Branchiopoda,Anomopoda) – a new member of the species group Ilyocryptus brevidentatus s. lat. from Australia

All representatives of the genus Ilyocryptus with short lateral setae at the postanal margin of the postabdomen may be separated into the compact species group I. brevidentatus s. lat. A new species of Ilyocryptus from this group is described from the Lake Numalla, Queensland, Australia. I. smirnovi n. sp. shows clear morphological differences in the armature of the valve, postabdomen, and several other structures, from all other species of the group. Differences between members of the above-mentioned species group are analogous with those between European species, listed by Štifter (1991). This revised version was published online in July 2006 with corrections to the Cover Date.