Phylogeny of Australian species of flatheads (Teleostei, Platycephalidae) as determined by allozyme electrophoresis

Phylogenetic relationships of 24 taxa of Platycephalid fish were examined for up to 40 loci using starch and polyacrylarnide gel electrophoresis. Over 400 different enzyme mobilities were scored. The extent of homoplasy was estimated to be between 5 and 12%. Polymorphism at the 1% level was observed at 26 of the 40 loci. The importance of shared polymorphic alleles in cladistic analysis was endorsed by the different results obtained from multistate and binary coding of alleles. Many loci were shown to contain phylogenetically informative ancestral alleles which appear irregularly in extant species. The polymorphism parsimony method provided the most informative results. Genetic similarities between endemic Australian species from each family stem provide the basis for a major revision of subfamilies and genera within the family.     

Biochemical differentiation of two groups within the species-complex Henricia Gray, 1840 (Echinodermata, Asteroidea) using starch-gel electrophoresis

Eighteen specimens from the Henricia pertusa group and 12 from the H. perforata group were examined for biochemical differences at the glucose-1-phosphate isomerase (GPI^* locus). Six alleles were found. Neither group showed deviations from Hardy Weinberg equilibrium (HW) (H. pertusa group: P1, H. perforata group: P=0.07, confidence interval=0.066–0.076). Significant differences in allele frequencies between the two groups (P0), supported previous assertions of reproductive isolation between the two groups based on morphological differences. However, near significance in HW disequilibrium in the H. perforata group indicates possible substructure in this group.     

Detection by allozyme electrophoresis of cryptic species of Hypodontus macropi (Nematoda: Strongyloidea) from macropodid marsupials.

Allozyme electrophoresis of 98 Hypodontus macropi from eight different species of hosts using 24 enzymes revealed a complex of at least six sibling species, with 15-50% fixed genetic differences between taxa. Except for the taxon parasitizing Macropus rufus/M. robustus, pairs of parasite taxa were, in each case, sympatric at each locality examined, thus supporting the conclusion that they represent valid species. The existence of a series of host-specific nematode taxa explains many of the inconsistencies noted previously in the host distribution of H. macropi. Comparison of parasite allozyme phenograms with host phylogeny suggests that four of the speciation events could be attributable to cospeciation and two to host switching. A clear case of host switching between M. rufus/M. robustus and M. fuliginosus was found.     

Isozyme and allozyme markers distinguishing two morphologically similar, medically important Mastomys species (Rodentia: Muridae)

Background  

Two common southern African mice species, Mastomys coucha and M. natalensis, are widely distributed throughout the subregion and overlap in many areas. They also share a high degree of morphological similarity, making them impossible to distinguish in the field at present. These multimammate mice are documented carriers of serious disease vectors causing Lassa fever, plague and encephalomyocarditis, which coupled to their cohabitation with humans in many areas, could pose a significant health risk. A preliminary study reported the presence of isozyme markers at three loci (GPI-2, PT-2, -3) in one population each of M. coucha and M. natalensis. Two additional populations (from the Vaal Dam and Richards Bay) were sampled to determine the reliability of these markers, and to seek additional genetic markers.     

A tropical Atlantic species of Melibe Rang, 1829 (Mollusca,Nudibranchia, Tethyiidae)

A new species of Melibe is described based on two specimens collected in Florida. This new species is well differentiated morphologically and genetically from other species of Melibe studied to date. The four residue deletions in the cytochrome c oxidase subunit 1 protein found in all previously sequenced tropical species of Melibe sequenced (and Melibe rosea) are also present in this new species. These deletions do not appear to affect important structural components of this protein but might have fitness implications. This paper provides the first confirmed record of Melibe in the tropical western Atlantic Ocean.     

Phylogenetic relationships of two Salamandrella species as revealed by mitochondrial DNA and allozyme variation (Amphibia: Caudata: Hynobiidae)

We conducted molecular phylogenetic analyses to confirm taxonomic relationships and to delimit distributional ranges of Siberian salamanders, Salamandrella keyserlingii and Salamandrella schrenckii, and to elucidate the origin of the isolated population of this species complex on Hokkaido, Japan. Phylogenetic trees constructed by MP, NJ, ML, and Bayesian methods, using complete sequences of mitochondrial cytochrome b genes, all indicated monophyly of Salamandrella and of each of the two species. Identical relationships were found on UPGMA, NJ, and CONTML trees derived from electrophoretic analysis of variation in 18 inferred allozyme loci. Populations from Hokkaido and northeastern China proved to be S. keyserlingii, while populations from Khabarovsk and Lazovsky are S. schrenckii. Genetic differentiations of S. keyserlingii within Sakhalin, and between Sakhalin and Hokkaido, are substantial. The Hokkaido population is hypothesized to have been isolated on the island since early Pleistocene, much earlier than isolation of sympatric anuran populations from their Sakhalin relatives. In contrast, the continental populations of S. keyserlingii are only slightly differentiated from some Sakhalin populations, and are thought to have expanded their ranges in the late Pleistocene.     

A new species of Armodoris (Mollusca, Gastropoda, Nudibranchia, Akiodorididae) from McMurdo Sound, Antarctica

Recently collected specimens of Armodoris from McMurdo Sound, Antarctica, were morphologically examined and sequenced. Comparison between this new material and literature sources revealed that it belongs to an undescribed species, Armodoris anudeorum. Although this new species is externally very similar to Armodoris antarctica (the only previously known species of Armodoris), these two species differ in several details of their external morphology, and particularly in their reproductive anatomy and radular morphology. This is the second known species of Armodoris; thus, this paper doubles the known diversity of this exclusively Antarctic group.     

Review of the genus Ctenopseustis Meyrick (Lepidoptera: Tortricidae), with reinstatement of two species

Abstract

The genus Ctenopseustis Meyrick (Tortricinae: Archipini) is reviewed. The species C. fraterna Philpot, 1930 and C. servana Walker, 1863 are reinstated, and the concept of C. obliquana (Walker, 1863) is redefined. Synonymies are given for each species, and characteristics are described and illustrated.     

Purification and properties of two endo-1,4-beta-xylanases from Irpex lacteus (Polyporus tulipiferae)

Two different endo-1,4-beta-xylanases [1,4-beta-D-xylan xylanohydrolases, EC 3.2.1.8], named Xylanases I and III, were purified to homogeneity by gel filtration and ion exchange column chromatography from Driselase, a commercial enzyme preparation from Irpex lacteus (Polyporus tulipiferae). The purified enzymes were found to be homogeneous on polyacrylamide disc electrophoresis and their specific activities toward xylan were increased approximately 28.7 and 19.8 times, respectively. The activities of each enzyme were considerably inhibited by Hg2+, Ag+, and Mn2+. Their molecular weights were estimated to be approximately 38,000 and 62,000 by gel filtration and sodium dodecyl sulfate (SDS)-polyacrylamide electrophoresis, respectively. Their carbohydrate contents were 2.5% and 8.0% as glucose, and their amino acid composition patterns resembled each other, showing high contents of acidic amino acids, serine, threonine, alanine, and glycine. Both enzymes were most active at pH 6.0 but Xylanase I was more stable as to pH. Their optimum temperatures were 60 degrees C and 70 degrees C, respectively. Xylanase I split up to 34.5% of larchwood xylan whereas Xylanase III split only 18.9% of it. The products with the former were mainly xylose (X1), xylobiose (X2), and xylotriose (X3), whereas X2 and X3 were the main products with the latter. Both enzymes did not hydrolyze X2. Xylanase I produced almost equal quantities of X1 and X2 from X3, while Xylanase III did not attack this substrate. Both enzymes showed no activity toward glycans, other than xylan, such as starch, pachyman and Avicel (microcrystalline cellulose), except the almost one twentieth activity of Xylanase III toward sodium carboxymethyl cellulose (CMC).     

Discrimination of Cricotopus species (Diptera: Chironomidae) by DNA barcoding

Chironomids (Diptera) typically comprise the most abundant group of macroinvertebrates collected in water quality surveys. Species in the genus Cricotopus display a wide range of tolerance for manmade pollutants, making them excellent bioindicators. Unfortunately, the usefulness of Cricotopus is overshadowed by the difficulty of accurately identifying larvae using current morphological keys. Molecular approaches are now being used for identification and taxonomic resolution in many animal taxa. In this study, a sequence-based approach for the mitochondrial gene, cytochrome oxidase I (COI), was developed to facilitate identification of Cricotopus species collected from Baltimore area streams. Using unique COI sequence variations, we developed profiles for seven described Cricotopus sp., four described Orthocladius sp., one described Paratrichocladius sp. and one putative species of Cricotopus. In addition to providing an accurate method for identification of Cricotopus, this method will make a useful contribution to the development of keys for Nearctic Cricotopus.     

Identification of Anguilla japonica and A. mavmovata elvers by allozyme electrophoresis

In Taiwanese waters, the morphologically similar elvers of Anguilla japonica and A. marmorata can be distinguished easily at the following loci examined: CK-D *, LDH-B *, sMDH-A * and sMDH-B *. Among these, CK-D * and LDH-B * have fixed allelic differences which can be used as a synoptic key for easy discrimination of the elvers of these two species.     

Identification of life cycle stages of the nematode Echinocephalus overstreeti by allozyme electrophoresis

Data presented in this study highlight the potential of allozyme electrophoresis in providing unequivocal genetic evidence for the identification of life cycle stages, particularly where species have complex life cycles. Adults of the nematode Echinocephalus overstreeti parasitize the elasmobranch Heterodontus portusjacksoni. The putative larval form which is morphologically dissimilar is found in two species of marine molluscs, Chlamys bifrons and Pecten albus. Electrophoretic analysis indicated that the adult and larval forms shared alleles at all of the 34 enzyme loci established. Furthermore, there were no fixed allelic differences between larval forms from different mollusc species.     

Assessment of allozyme variation among New Zealand populations of Gracilaria chilensis (Gracialiares,Rhodophyta) using starch-gel electrophoresis

New Zealand populations of Gracilaria chilensis are uniform in anatomical reproductive characteristics but vary morphologically and have been found to separate into two distinct groups with respect to agar methylation level, namely low (24–30%) and high (43–47%). To investigate the genetic variation within New Zealand populations of this species, 14 isozyme loci detected by starch-gel electrophoresis were examined in 17 wild populations from a wide range of localities, and in cultures derived from these populations. Five of these loci were polymorphic, but the genetic variation within populations was low: of the 17 populations examined, 15 were fixed at all loci (heterozygosity 0.000) and in the remaining two populations the observed heterozygosity was still low (0.004 and 0.011). The genetic distances between the populations ranged from 0.00 to 0.43. UPGMA cluster analysis separated the populations into two groups, a northern group and a group found throughout the country. Although these two groups do not correlate with the two groups based on agar methylation level at every locality, the correlation is sufficiently striking to merit further investigation.     

A new species of Trapania (Nudibranchia: Goniodorididae) from the Pacific coast of Central America

A new marine gastropod species of the genus Trapania Pruvot-Fol, 1931, is described from Cabo Blanco, Puntarenas, Costa Rica and from Islas Secas, Panamá. Trapania inbiotica sp. nov. has a white body with red patches, white rhinophores with some little red patches, yellow appendages with partially red bases. The radula is composed of 28 rows of teeth. Each tooth has a large conical cusp with 21-24 denticles. Two or three of those denticles on the inner side of the cusp are smaller than the others. There are also 1-3 small denticles on the outside of the cusp. The jaw elements are very irregular.     

Ultrastructure of the renopericardial complex in Hypselodoris tricolor (Gastropoda, Nudibranchia)

The histology and ultrastructure of the renopericardial complex of Hypselodoris tricolor (Gastropoda, Nudibranchia, Doridoidea) have been investigated by means of semithin serial sections and transmission electron microscopy (TEM). The examinations revealed a functional metanephridial system comprising a monotocardian heart with ventricle and auricle in a spacious pericardium that is linked with the single, large kidney by a renopericardial duct with prominent ciliation towards its opening. Podocytes as the site of ultrafiltration were not only detected in the auricular epicardium, but also line the entire outer pericardial epithelium. The cuboidal, highly vacuolated excretory cells of the kidney epithelium with extensive basal infoldings and an apical microvillous border indicate secretory and reabsorptive activity. Solitary rhogocytes (pore cells) of the connective tissue and haemocoel represent additional loci of ultrafiltration with a fine structure identical to that of the podocytes (slits between cytoplasmic processes, bridged by fine diaphragms and covered by extracellular matrix). The presence of podocytes situated in the epicardial wall of the auricle is regarded as plesiomorphic for the Mollusca and is confirmed for the Nudibranchia. An additional, extensive and separate ultrafiltration site in the outer pericardial wall is not known from any other taxon of the Mollusca and strongly suggests a significantly increased ultrafiltration activity in H. tricolor.