This paper demonstrates that the sensor cover energy problem in wireless communication can be transformed into a linear programming problem with max-plus linear inequality constraints. Consequently, by a well-developed preprocessing procedure, it can be further reformulated as a 0-1 integer linear programming problem and hence tackled by the routine techniques developed in linear and integer optimization. The performance of this two-stage solution approach is evaluated on a set of randomly generated instances and demonstrates that it is capable of solving large size instances of the sensor cover energy problem.
The Self Organized Mapping (SOM) is a kind of artificial neural network (ANN) which enables the pattern set self-organization in space with Euclidean metrics. Thus, the traditional SOM consists of two layers; input one with n nodes and output one with H ones. Every output node is characterized by its weight vector Wk G in this case. The absence of pattern coordinates in special cases is a good motivation for self-organization in any metric space (U, d). The learning in the metric space is introduced on the cluster analysis problém and a basic clustering algorithm is obtained. The relationship with the traditional ISODATA method and NP-completeness is proven. The direct generalization comes to SOM learning in the metric space, its algorithm, properties and NP-completeness. The SOM learning is based on an objective function and its batch minimization. Three estimates of the proposed objective function are included. They will help to study the relationship with Kohonen batch learning, the cluster analysis and the convex programming task. The Matlab source code for the SOM in the metric space is available in the appendix. Two numeric examples are oriented at self-organization in the metric space of written words and the metric space of functions.
The decapeptide QLNLKEYNLV corresponding to the C-terminus of Gq/G11alpha guanine nucleotide-binding proteins (G-proteins) was synthesized by the solid-phase method and conjugated to keyhole limpet hemocyanin. The rabbits were immunized with these conjugates and an antiserum that reacted specifically with the alpha subunit of Gq/G11 proteins was used in this study. The antiserum exhibited no cross-reactivity with the alpha subunits of stimulatory (Gs) or inhibitory (Gi) G-proteins associated with adenylate cyclase. Immunoblots with the antiserum showed that it specifically recognized the Gq/G11 alpha-proteins in cholate extracts of adipose tissue membranes of goats. Treatment of young castrated male goats with bST had no effect on the quantity of Gq/G11 alpha-subunits in adipose tissue and the results thus obtained did not support the idea that the bST signal in adipose tissue is transmitted via Gq/G11 alpha-proteins., V. Krbeček, H. Kovářů, J. Škarda, T. Barth, J. Velek, V. Žižkovský., and Obsahuje bibliografii
We consider Stanley-Reisner rings $k[x_1,\ldots ,x_n]/I(\mathcal {H})$ where $I(\mathcal {H})$ is the edge ideal associated to some particular classes of hypergraphs. For instance, we consider hypergraphs that are natural generalizations of graphs that are lines and cycles, and for these we compute the Betti numbers. We also generalize some known results about chordal graphs and study a weak form of shellability.
Bothitrema bothi (MacCallum, 1913), a monopisthocotylean monogenean (Bothitrematidae) found on gills and occasionally on the olfactory rosette within the nares of the bothid flounder, Scophthalmus aquosus (Mitchill, 1815), is distributed along the Atlantic coast of the USA from Woods Hole, Massachusetts to Delaware Bay. This study details aspects of the morphology, microecology and biology of the oncomiracidium, juvenile and adult. Adult worms occur almost exclusively between rakers on the first and second gill arches while juveniles occupy secondary gill filaments. Analysis of variance revealed significant arch, side and position effects. Worm attachment and position is maintained largely by suction generated by a circular seal using its 54 radially arranged accessory haptoral sclerotised elements and a marginal valve. A small anterior appendix with two marginal hooks lies dorsal to a deep anteromedian cleft in the haptor, which, together with wall muscles, creates and releases the negative pressure required for attachment. Four pairs of gland openings in the ventrolateral margins of the anterior adhesive area produce secretions for attachment. Operculate eggs with four rounded protuberances and a filament are laid individually at four-minute intervals at 22ºC. Hatching occurs in five days at 20°C. Oncomiracidia have two pairs of eyes, with the posterior pair fused, show both positive and negative phototaxis and swim at a mean rate of 5.2 mm/s at 22°C. Larvae have a circle of 16 hooks and a pair of hamulus primordia. Other accessory haptoral sclerotised structures arise de novo in juveniles after attachment to the host. These data will help to resolve more clearly the relationships of the Bothitrematidae within the Monopisthocotylea.
About 300 species belonging to four superfamilies (Gnathostomatoidea, Habronematoidea, Physalopteroidea and Thelazioidea) of the nematode suborder Spirurina are known as the adult parasites of freshwater, brackish-water and marine fishes. They are placed in four families, of which the Gnathostomatidae, including Echinocephalus with a few species and the monotypic Metaleptus, are parasites of elasmobranchs, whereas Ancyracanthus contains one species in teleosts; the Physalopteridae is represented in fish by four genera, Bulbocephalus, Heliconema, Paraleptus and Proleptus, each with several species in both elasmobranchs and teleosts. The majority of fish spirurines belongs to the Rhabdochonidae, which includes 10 genera (Beaninema, Fellicola, Hepatinema, Heptochona, Johnstonmawsonia, Megachona, Pancreatonema, Prosungulonema, Rhabdochona and Vasorhabdochona) of species parasitizing mainly teleosts, rarely elasmobranchs, and the Cystidicolidae with about 23 genera (Ascarophis, Caballeronema, Capillospirura, Comephoronema, Crenatobronema, Cristitectus, Ctenascarophis, Cyclozone, Cystidicola, Cystidicoloides, Johnstonmawsonoides, Metabronema, Moravecnema, Neoascarophis, Parascarophis, Prospinitectus, Pseudascarophis, Pseudoproleptus, Salvelinema, Similascarophis, Spinitectoides, Spinitectus, Sterliadochona), with many species parasitic in teleosts only. Because of difficulties in studying fish spirurines, associated with their morphological and biological peculiarities, most species of these parasites are poorly known. It is apparent that their present classification system does not reflect phylogenetic relationships and a taxonomic revision of this nematode group, based on detailed morphological (including SEM and TEM), life history and molecular studies of individual species, is quite necessary. In Cystidicolidae, several genera have been based on details in the cephalic structures visible only with the aid of SEM, but it will be evident whether or not these tiny features are of generic importance only when more cystidicolids are described using SEM and comparative molecular data become available. Data on the biology of fish spirurines are scarce. In known cases, their life cycles involve aquatic arthropods (crustaceans or insects) as intermediate hosts, in which, sometimes, the larvae undergo a precocious development and may even attain adulthood and become gravid in these invertebrates; sometimes, fish paratenic hosts are known to occur in cystidicolids parasitizing as adults piscivorous definitive hosts. Some spirurine species are pathogenic and are known as causative agents of serious fish diseases. and Consequently, further detailed studies on fish spirurines are significant not only from the theoretical viewpoint, but they may also have practical implications.
The nematode superfamily Dracunculoidea includes 166 recognized species, of which 150 (90%) are parasitic in about 300 species of freshwater, brackish-water and marine fishes. Fish dracunculoids are placed in 31 genera (86% of all dracunculoid genera) belonging to eight of the nine dracunculoid families: Anguillicolidae, Daniconematidae, Guyanemidae, Lucionematidae, Micropleuridae, Philometridae, Skrjabillanidae, and Tetanonematidae; the genus Lockenloia is considered incertae sedis. Because of difficulties in studying fish dracunculoids, associated with their morphological and biological peculiarities, most species of these largely histozoic parasites are poorly known and males of the majority of species and of eight genera have not yet been discovered. It is apparent that the present classification system of dracunculoids as a whole does not reflect phylogenetic relationships and a taxonomic revision of this nematode group, based on detailed morphological (including SEM and TEM), life history and molecular studies of individual species, is quite necessary. Data on the biology of fish dracunculoids is scarce. In known cases, their life cycles involve copepods, ostracods or branchiurids as intermediate hosts and, sometimes, fish paratenic hosts are known to occur in dracunculoid species parasitizing as adults piscivorous definitive hosts. However, nothing is known about the life cycles of representatives of 20 genera. Some species of dracunculoids, particularly of philometrids, are highly pathogenic and are known as agents of serious fish diseases. During recent years, especially the importance of Philometra spp. parasitizing the gonads of many species of marine fishes has increased due in particular to the rapid development of marine aquaculture, because they may significantly decrease fish reproduction or even cause full parasitic castration. Therefore, further detailed studies on fish dracunculoids are significant not only from the theoretical viewpoint, but they may also have practical implications.
Two new, one known and three unidentified species of the nematode family Camallanidae are reported and described from the intestines of marine perciform fishes off the southwestern coast of New Caledonia, South Pacific: Camallanus carangis Olsen, 1952 from the forked-tailed threadfin bream Nemipterus furcosus (Nemipteridae), the yellowstriped goatfish Upeneus vittatus and the whitesaddle goatfish Parupeneus ciliatus (both Mullidae) (new host records); Procamallanus (Spirocamallanus) variolae sp. n. from the white-edged lyretail Variola albimarginata (type host) and the blacktip grouper Epinephelus fasciatus (both Serranidae); Procamallanus (Spirocamallanus) longus sp. n. from the twotone tang Zebrasoma scopas (Acanthuridae); Procamallanus (Spirocamallanus) sp. 1 (female tail with 2 terminal spikes on a digit-like projection) from the speckled sandperch Parapercis hexophtalma (Pinguipedidae); Procamallanus (Spirocamallanus) sp. 2 (female tail with 1 spike on a digit-like projection) from the drab emperor Lethrinus ravus (Lethrinidae) and Procamallanus (Spirocamallanus) sp. 3 (female tail with a smooth digit-like protrusion) from the two-lined monocle bream Scolopsis bilineata (Nemipteridae). Camallanus paracarangis Velasquez, 1980 is synonymized with C. carangis. Several additional species of Camallanus from marine fish of the Indo-Pacific region may be synonymous with C. carangis as it has a poorly sclerotized left spicule and 3 small caudal projections on the tail of young (i.e., non-gravid) females. The fourth-stage larva of C. carangis is described for the first time. P. (S.) variolae differs from most similar species of this region mainly in the position (i.e., at level or posterior to the nerve ring) and shape of deirids. P. (S.) longus differs from the similar P. (S.) chaimha mainly in a different arrangement of postanal papillae, shape of the female tail, much longer right spicule (429 µm) and longer body of gravid females (38-55 mm). All Camallanus and Procamallanus (Spirocamallanus) spp. reported here represent the first records of camallanids from marine fishes in New Caledonian waters.
For ordered (= partially ordered) sets we introduce certain cardinal characteristics of them (some of those are known). We show that these characteristics—with one exception—coincide.
A closed convex set $Q$ in a local convex topological Hausdorff spaces $X$ is called locally nonconical (LNC) if for every $x, y\in Q$ there exists an open neighbourhood $U$ of $x$ such that $(U\cap Q)+\frac{1}{2}(y-x)\subset Q$. A set $Q$ is local cylindric (LC) if for $x,y\in Q$, $x\ne y$, $z\in (x,y)$ there exists an open neighbourhood $U$ of $z$ such that $U\cap Q$ (equivalently: $\mathrm bd(Q)\cap U$) is a union of open segments parallel to $[x,y]$. In this paper we prove that these two notions are equivalent. The properties LNC and LC were investigated in [3], where the implication ${\mathrm LNC}\Rightarrow {\mathrm LC}$ was proved in general, while the inverse implication was proved in case of Hilbert spaces.