A new tritoniid species (Mollusca: Opisthobranchia) from Bouvet Island

Tritoniid sea slugs (Mollusca, Gastropoda, Opisthobranchia) are reported for the first time from Bouvet Island. Tritonia dantarti sp. n. shows morphological and anatomical differences with regard to the two previously known tritoniids reported from Antarctica and Sub-Antarctica, Tritonia vorax (Odhner 1926) and Tritonia challengeriana Bergh, 1884. Regarding the external morphology, T. dantarti sp. n. is characterized by a very bright orange coloration in the dorsum, white dorsal crests, highly ramified dendritic gills (the largest vertically orientated and the rest laterally orientated), and a quadrangular cross section. The radula presents very long, thin lateral teeth and the jaws present mainly unicuspidate, striated denticles. The seminal receptacle is large, pear-shaped and its grey pigmentation differs from the rest of the genital system. The Antarctic species T. challengeriana was also found in waters off Bouvet Island, while the Subantarctic species T. vorax was not found.     

Transmission of broad bean stain virus and Echtes Ackerbohnenmosaik-Virus to field beans (Viciajaba) by weevils

Sitona lineatus and Apion vorax were the two most common species of weevil on field beans (Vicia faba minor) at Rothamsted between 1970 and 1974. In glasshouse tests, A. vorax was a much more efficient vector than 5. lineatus of broad bean stain virus (BBSV) and Echtes Ackerbohnenmosaik-Virus (EAMV), and both species transmitted EAMV more often than BBSV. Five other species of Apion transmitted the viruses infrequently or not at all. S. lineatus adults transmitted no more often after 8–16 days on infected plants than after 1–2 days. Some A. vorax adults transmitted EAMV, but not BBSV, after feeding on infected leaves for a few minutes. After 4 days on infected plants, A. vorax sometimes remained infective for the following 8 days. No A. vorax collected from woodland plants in spring was infective with BBSV or EAMV, but 4% from bean crops containing seed-borne infection carried BBSV and 17% carried EAMV. BBSV and EAMV were recovered from triturated weevils, but not from weevil haemolymph. Possibly the viruses are transmitted as contaminants of the mouthparts or by regurgitation during feeding, but A. vorax was observed to regurgitate only when anaesthetized. BBSV and EAMV were not transmitted by aphids (Aphis fabae and Acyrthosiphon pisum), nor by pollen beetles {Meligethes spp.). Field observations suggest that infected seed is the main source of BBSV and EAMV in spring-sown crops, and that crops grown from virus-free seed, and isolated from infected crops by 250–500 m, remain free of infection for most of the season.     

An Analysis of Macrostome Production in Tetrahymena vorax Strain V2S-Type*

SYNOPSIS. Tetrahymena vorax is a small polymorphic holotrichous ciliate capable of transforming to macrostomes when microstomes are washed and suspended with prey in distilled water. Extrinsic factors having an effect on this transformation were examined; maximum yields of macrostomes (in excess of 90%) were obtained under the following conditions: populations of both prey, T. pyriformis, and potential predator, T. vorax microstomes, were grown on Loefer's medium for 48 hours prior to washing in distilled water. The density of the prey was adjusted to 300,000 cells/ml and the predator density to 2,000–3,000 cells/ml. Five ml of prey suspension and 5 ml of T. vorax microstome suspension were mixed together in a large petri dish because a high surface-volume ratio is important for high yields of macrostomes. The pH was adjusted to 6.0 and the petri dish was placed at 20 C for 12 hr. Macrostomes then appeared about 6 hr after addition of the prey. A dialyzable, heat stable substance released by the prey which can induce the microstome-macrostome transformation was isolated. This material was effective after being stored for weeks in the cold; its activity was not affected by the protein digesting enzymes pepsin or trypsin. This factor was called stomatin because its first visible effect in producing microstome-macrostome transformation appeared to be to incite reorganization of the oral structures.     

Observations on the biology and ecology of Apion vorax (Coleoptera: Apionidae), a vector of broad bean stain and broad bean true mosaic viruses

In spring 1974 and 1975 many adult Apion vorax were found at Rothamsted in woods bordering fields that had been cropped with field beans (Vicia faba) the previous season. The weevils were most common on bramble (Rubus spp.), dog's mercury (Mercurialis perennis) and nettle (Urtica dioica). A decrease in the woodland population in May coincided with the appearance of the weevil on field bean crops in neighbouring areas. In laboratory feeding tests, adult weevils fed more on field bean leaves than on leaves of plants on which they were common in woodlands, and they fed more on field beans in May than at other times of the year. No difference was observed in the feeding of male and female weevils. Many A. vorax were caught on sticky traps in woodlands at Rothamsted in 1975, particularly in April and May, but very few were caught on sticky traps in bean crops. The numbers of A. vorax recorded on the upper foliage of bean crops at Rothamsted in June each year from 1970 to 1980 ranged from 0 to 10 per 10-m row. Eggs, larvae and pupae of A. vorax were found in field bean flowers collected from field crops. The larvae were feeding on the tips of the pistils and stamens. Adult weevils that emerged in mid-June from the flowers of autumn-sown beans mated and produced a second generation when caged on glasshouse-grown plants. Some Apion larvae, possibly A. vorax, were found inside flowers of common vetch (Vicia sativa). The name ‘bean flower weevil’ is considered a suitable common name for A. vorax.     

The Effect of 2-Mercapto-1-(Beta-4-Pyridethyl) Benzimidazole (MPB) on Cell Differentiation and RNA Synthesis in the Protozoon Tetrahymena vorax1

SYNOPSIS. Differentiation of small-mouthed cells (microstomes) into large-mouthed, potentially carnivorous cells (macrostomes) in Tetrahymena vorax is prevented by 2-mercapto-1-(β-4-pyridethyl) benzimidazole (MPB). This differentiation, induced by the transforming principle, stomatin, isolated from the potential prey, Tetrahymena pyriformis, is a synchronous process in which 70–95% of the population of T. vorax microstomes transform into macrostomes within 450 min. MPB also inhibits RNA synthesis in transforming microstomes while having little effect on protein synthesis. Finally, the effect of MPB on both transformation and RNA synthesis is reversible.     

Biochemical Comparison of Some Classical Tetrahymena pyriformis and T. vorax Strains*

SYNOPSIS. The classical Tetrahymena pyriformis and T. vorax strains have been classified in antigenic subgroups based on immobilization and agar double diffusion in the presence of specific antisera. The present study utilized disc electrophoresis of proteins and lactate dehydrogenase isozymes for comparison of 11 strains. In agreement with similarities reported for agar diffusion data, close electrophoretic relationships were observed between strains GL and H, and V₂ and W with aniline black staining. Altho LDH isozyme production was more variable and related to cultural growth phase, similarities were recognized between GL and H, and F and PR.     

5S and 5.8S ribosomal RNA evolution in the suborder tetrahymenina (Ciliophora: Hymenostomatida)

Summary The nucleotide sequences of the 5S and 5.8S rRNAs of eight strains of tetrahymenine ciliates have been determined. The sequences indicate a clear distinction betweenTetrahymena paravorax and its suggested conspecificT. vorax, but leave the taxonomic distinction betweenT. vorax andT. leucophrys in doubt. The rRNA sequences of sixTetrahymena species and of three other species of the suborder Tetrahymenina have been used to deduce evolutionary schemes in which ancestral rRNA sequences and changes are proposed. These schemes suggest the predominant acceptance of GA and CT transitions in the 5S rDNA during the evolution of the suborder.     

Protein Similarities in the Genus Tetrahymena and a Description of Tetrahymena leucophrys n. sp.1

The potential utility of protein arrays visualized by SDS-PAGE in taxonomic studies of protozoa has been investigated within the genus Tetrahymena. Matching coefficients have been obtained from one-dimensional separations of cytoskeletal proteins in a study involving 40 strains of Tetrahymena. In separate studies, the method was estimated to be accurate to within 10%, and the limit of intraspecific variation within the genus was estimated at ? 30%. Accordingly, it is suggested that strains showing matching coefficients 0.6 in these preparations probably represent different species. Further tests using strains identified to species by breeding criteria have shown that the 0.6 rule is asymmetric, i.e. although matching coefficients lower than this indicate separate species, values higher than this do not prove identity. Protein comparisons included in the present study indicate that strain Tur, previously identified as a strain of T. vorax, is distinct from all other macrostome-forming species. It is here designated Tetrahymena leucophrys n. sp.     

Antigenic Differences Among Some Classical Tetrahymena pyriformis and T. vorax Strains*

SYNOPSIS. Suspensions of whole, killed ciliates were diffused against rabbit antisera for the respective strains to observe cross precipitation. The strains fell into the following groups: I. GL, H, ChS, GP, Aq, L-I, L-II, L-2, and V₁; II. W, L-3, Gl-R, and V₂; III. PR and F; and IV. BF and Lava. T. vorax strains V₁ and V₂ each resembled certain T. pyriformis strains more closely than they resembled each other. The same grouping of strains emerged in comparing antigenic suspensions and in comparing antisera and was confirmed by comparing absorption properties of antigens from the different strains.     

Morphological,Biometric, and Morphogenetic Comparison of Two Closely Related Species,Stylonychia vorax and S. pustulata (Ciliophora: Oxytrichidae)1

Differences in the morphology of Stylonychia vorax Stokes, 1885 and S. pustulata (Müller, 1786) Ehrenberg, 1838 recognizable in vivo are the shape, the ventral cirral pattern, the caudal cirri, and the mode of moving. The dorsal-bristle complexes are distinguishable by the length of dorsal kinety four and the spaces among the pairs of basal bodies. When the ranges of variation of different populations and clones are compared by biometric analyses, S. vorax shows a relatively stable cortical pattern whereas in S. pustulata the cortical elements are regulated depending on the size of the body and the number of adoral membranelles. In S. vorax morphogenesis begins with a proliferation of basal bodies close to the transverse cirri. In contrast, in S. pustulata, the oral primordium appears de novo between the left marginal row and the postoral cirri. All other morphogenetic events are the same for both species. In proters and opisthes the six anlagen of the frontal-ventral-transverse cirri are of different origin and evolve independently. Three anlagen of the opisthe separate from the oral primordium, two originate from the right, and one from the left postoral cirrus. Three anlagen of the proter evolve from the posteriormost cirrus in the frontal area, one from the parental undulating membranes, one from the buccal cirrus, and one from the cirrus below the buccal cirrus. The anlagen one to six generate one, three, three, three, four, and four cirri. The characteristic arrangement of the undulating membranes and the participation of only two postoral cirri in the formation of primordia provide features that distinguish between the often confused genera Oxytricha and Stylonychia.     

Phytoplankton/zooplankton relationships during spring in the brackish Lake Grevelingen 1976–1978 (III)

Summary Rotifer species of the genusSynchaeta represent the dominating zooplankton organisms during early spring (BAKKERet al., 1977).Reproductive capacity of the rotifers (sensu EDMONDSON, 1965) was always significantly correlated with algal densities, cryptomonad flagellates being the main food. The slope of the curve representing the feeding relationSynchaeta-Cryptomonas was significantly steeper than forSynchaeta and the diatomSceletonema. Positive influences of increasing temperature forSynchaeta cf.vorax were only found within the range of 2–7°C. When temperature rose above 10°CS. vorax was succeeded byS.triophthalma. Negative temperatures, occurring in brackish lakes during periods of strong frost, caused a decrease of the egg ratio (numbers of eggs per animal) and of the population density.Development times ofS. vorax eggs were determined (VAN DAMet al., 1978) in order to calculate birth rates and production. Egg development time amounted to 3 days at 5°C and to 2 days at 10°C. Birth rates declined strongly when maximum population densities were reached. Mortality was approached by subtracting the actual rate of increase of population density from the birth rate. Sometimes negative mortalities were found, presumably caused by the development of resting eggs.Population dynamics of the rotifers were related to phytoplankton biomass and to primary productivity. Grazing effects of the rotifers on the algal population became evident during the final stage of the spring bloom (April). In the beginning (February–March) the mortality of the algal population could not be explained by grazing, other factors (cf. JASSBY and GOLDMAN, 1974) being responsible.     

Systematics,evolution, and biogeography of the Pliocene stem meline badger Ferinestrix (Carnivora: Mustelidae)

Ferinestrix vorax is an extinct mustelid carnivoran of enigmatic relationships, known from a partial mandible and femur collected from the 3.2‐ and 3.6‐Myr‐old deposits of Hagerman Fossil Beds National Monument, Idaho, USA. Here, we report Ferinestrix rapax sp. nov. based on 80 remains of skull and dentition from a 3.1–3.6‐Myr‐old deposit of Udunga, Transbaikal, Russia. We demonstrate that Ferinestrix is a stem genus of the badger subfamily Melinae. This genus is distinctly larger and more carnivorous than any other total‐clade meline. We show that Ferinestrix originated in Asia and immigrated to North America no later than at the early (Zanclean) to late (Piacenzian) Pliocene transition, and that the North American F. vorax and Asian F. rapax underwent parallel evolution toward increased carnivory. © 2013 The Linnean Society of London, Zoological Journal of the Linnean Society, 2013, 167 , 208–226.     

Structure and formation of the feeding apparatus in Aporcelaimus and Aporcelaimellus (Nematoda: Dorylaimida)

The structure of the adult feeding apparatus in Aporcelaimus vorax and Aporcelaimellus is described. An account is given of the odontostyle formation in juvenile stages.     

Life-history consequences of resource allocation of two bdelloid rotifer species

Two bdelloid species,Macrotrachela quadricornifera (aquatic species) andPhilodina vorax (terrestrial moss species), with similar survival but different age-specific fecundity schedules, were analyzed daily to determine growth rates and the volume invested in reproduction. The two species had similar growth patterns and started reproduction while still growing. In both, the size at maturity was independent of age.M. quadricornifera resumed growth after reaching a size plateau when reproduction was over, whileP. vorax continued to reproduce until death. Although the net reproductive rate ofP. vorax was consistently lower than that ofM. quadricornifera, the same percent of adult volume was invested in reproduction over its life time because its eggs were relatively bigger. The difference in reproductive rates is probably related to different partitioning of equal amounts of relative biomass: more small eggs for the aquatic rotifer vs. fewer big eggs for the terrestrial rotifer. Egg size might be related to the selective pressures of the environments.     

Growth Kinetics of Three Species of Tetrahymena On Solid Agar*

A nutrient-agar method without liquid overlay has been developed for cultivation of ciliates. Three species of Tetrahymena-T. pyriformis strain W, T. rostrata strain UNI, and T. vorax strain V₂S, representing the 3 main groups of Tetrahymena species, were used; however the method should apply to other ciliates. Growth on the surface of the agar was facilitated by an optimal surface-to-volume ratio yielding a high density of ciliates (5.8 × 10₅ cells/cm² for T. pyriformis at 25 C) and short generation times (3 h for T. pyriformis at 30 C). At the highest density achieved, the cells became irregularly hexagonal and formed a monolayer “tissue” on the agar. Ciliates grown on agar were like those in liquid culture, typical oral ciliature, food-vacuole formation, and typical cortical patterns being retained. Advantages of this method include high cell density, easy recovery, and optimal O₂ supply. the organisms can also be cultivated on the surface of sterile cellulose-nitrate filters, facilitating in situ fixation and staining as well as transfer into different media by transfer of filters with cells, without prior centrifugation and resuspension.     

Morphological and Molecular Differences in Two Strains of <Emphasis Type="Italic">Ustilago esculenta</Emphasis>

Ustilago esculenta is a fungal endophyte of Zizania latifolia that plays an important agricultural role in this vegetable crop. The purpose of this study was to characterize sporidial (T) and mycelial (M-T) strains of U. esculenta isolated from sporulating and non-sporulating galls on plants growing in Zhejiang province, China. Morphological comparisons of the T strain and M-T strain were made by optical and scanning electron microscope observation. Genetic differences were examined by sequencing the ITS region of the fungus and examining differential protein expression by two-dimensional gel electrophoresis and MALDI-TOF-MS/MS. The sporidial (T) and mycelial (M-T) strains differed in morphological characteristics of their in vitro single colony formations and in cell shape. Alignment of ITS sequences of the T strain and M-T strain revealed a single mutation between the T strain and M-T strain, but the sequences were the same within strains. A total of 146 proteins were only expressed in the M-T strain, and 242 proteins were only expressed in the T strain isolated from infected plants. A total of 222 proteins were up-regulated or down-regulated in the T strain when compared with the M-T strain. Of these, 18 proteins were identified and eight were associated with processes involving energy metabolism and the cytoskeleton. Two morphology-related proteins, MAP kinase kinase and actin, were differentially expressed. The differences noted in the T strain and M-T strain may lead to a better understanding of the life cycle and morphogenesis in U. esculenta.     

Morphology and Phylogeny of Two Species of Loxodes (Ciliophora,Karyorelictea), with Description of a New Subspecies,Loxodes striatus orientalis subsp. n.

The morphology and phylogeny of Loxodes vorax and L. striatus orientalis subsp. n. were investigated based on infraciliature and small subunit (SSU) rRNA gene sequence data. Loxodes striatus orientalis subsp. n. was separated from L. striatus striatus stat. n. by having fewer dikinetids in the intrabuccal kinety (35–55 vs. 50–70) and a variable number of macronuclei (2–4 vs. 2). In addition, the SSU rRNA gene sequence of the new subspecies differs in 13 and 11 nucleotides from that of two populations of the nominotypic subspecies. We also summarized the morphological differences between Loxodes and Remanella based on the data available. Phylogenetic analyses revealed that the genus Loxodes was monophyletic and nested within Remanella species. This study might, therefore, support the hypothesis that the freshwater genus Loxodes evolved from the marine genus Remanella.     

The cultivation and predator-prey relationships Chænæ vorax and Cyclidium sp.

Chaenea vorax, a predatory marine gymnostome, was established in laboratory culture using Cyclidium sp. as a food source. The respective cultures were used to study the predator-prey relationships of these organisms. In addition, the feeding specifics of Chaenea vorax were studied and a possible sexual phenomenon, herein called “coupling”, was observed. Whenever Chaenea vorax is introduced into a laboratory culture of Cyclidium sp. the predator brings about a decimation of the prey population. Other food sources were offered to the predator, but only those organisms having a long caudal cilium were used and/or grasped. The phenomenon of “coupling” is proposed to be conjugation, but the nuclear events have not been established.     

Electrophysiological Properties of the Microstome and Macrostome Morph of the Polymorphic Ciliate Tetrahymena vorax

Polymorphic ciliates, like Tetrahymena vorax, optimize food utilization by altering between different body shapes and behaviours. Microstome T. vorax feeds on bacteria, organic particles, and solutes, whereas the larger macrostome cells are predators consuming other ciliates. We have used current clamp and discontinuous single electrode voltage clamp to compare electrophysiological properties of these morphs. The resting membrane potential was approximately ?30 mV in both morphs. The input resistance and capacitance of microstomes were approximately 350 MΩ and 105 pF, whereas the corresponding values for the macrostomes were 210 MΩ and 230 pF, reflecting the larger cell size. Depolarizing current injections elicited regenerative Ca²⁺ spikes with a maximum rate of rise of 7.5 Vs^?1 in microstome and 4.7 Vs^?1 in macrostome cells. Depolarizing voltage steps from a holding potential of ?40 mV induced an inward Ca²⁺ ‐current (I_ca) peaking at ?10 mV, reaching approximately the same value in microstome (?1.4 nA) and macrostome cells (?1.2 nA). Because the number of ciliary rows is the same in microstome and macrostome cells, the similar size of I_Ca in these morphs supports the notion that the voltage‐gated Ca²⁺ channels in ciliates are located in the ciliary membrane. In both morphs, hyperpolarizing voltage steps revealed inward membrane rectification that persisted in Na⁺‐free solution and was only partially inhibited by extracellular Cs⁺. The inward rectification was completely blocked by replacing Ca²⁺ with Co²⁺ or Ba²⁺ in the recording solution, and is probably due to Ca²⁺ ‐activated inward K⁺ current secondary to Ca²⁺ influx through channels activated by hyperpolarization.