Ventrolateral Lobes Research Articles

Mysid subfamily Boreomysinae (Crustacea: Mysida: Mysidae) in the southeast Australian deep-sea

The deep-water mysid crustaceans of Australia have been barely known. Recent explorations of RV Investigator (CSIRO) in the southeast Australian waters discovered a unique fauna. In this special study of the marine subfamily Boreomysinae (family Mysidae) in Australia, five species from both genera Boreomysis and Neobirsteiniamysis are reported, including two new species for science: B. inopinata sp. nov., B. sibogae, B. sphaerops, B. urospina sp. nov. and N. inermis. Among the members of the subfamily, only B. sibogae has been previously known from Australia. The genus Neobirsteiniamysis and its bipolar-amphitropical species N. inermis are firstly recorded in Australia. Boreomysis inopinata sp. nov. has additional spinules on the outer spine of the antennal scale, which are not found in other species of the subfamily. Boreomysis urospina sp. nov. has the longest first segment of the uropodal exopod, laterally terminated by three spiniform setae; and its uropodal endopod is armed with up to five medial spiniform setae, the largest number in the subfamily. This species is included in a newly established subgenus Petryashovia subgen. nov., which unites epi-mesopelagic boreomysines, lacking the rostral projection, having rather small ventrolateral lobes of the carapace, and the 1-segmented propodus of the pereopods. The subfamily and generic diagnoses are updated. Additionally, a fragment of the mtDNA COI gene was sequenced for most of the studied species.

Pseudocapillaria (Ichthyocapillaria) bumpi n. sp. (Nematoda: Capillariidae) Parasitising West African Lungfish Protopterus annectens (Owen, 1839) (Lepidosireniformes: Protopteridae) in Mozambique and Its Phylogenetic Position Within Capillariid Nematodes.

Pseudocapillaria (Ichthyocapillaria) bumpi n. sp. (Nematoda: Capillariidae) is described from specimens infecting the digestive tract of the West African lungfish, Protopterus annectens (Owen) (Lepidosireniformes: Protopteridae). Nematodes were collected in Karingani Game Reserve, Southern Mozambique and studied using light microscopy; obtained sequences of the 18S ribosomal (18S rRNA) gene used for phylogenetic studies. The new species is assigned to Pseudocapillaria Freitas, 1959 by having a stichosome consisting of a single row of stichocytes and ventrolateral lobes on the male tail as well as by lacking spines on the specular sheath, caudal alae, a membranous caudal bursa, and a lateral expansion of the caudal end. It is also assigned to the sub-genus Ichthyocapillaria Moravec, 1982 by having a membrane between the ventrolateral lobes and by lacking a vulvar appendage. Pseudocapillaria (I.) bumpi n. sp. differs from its nominal congeners by having a comparatively large body size with relatively long spicule, bearing the thin membrane non-extending further than ventrolateral lobes in males and relatively smaller eggs without protruding polar plugs. It is the 20th species of the genus, the first from the Afrotropical Realm, and the first from any lungfish species. Phylogenetic analyses suggested that P. (I.) bumpi is deeply nested in a clade that associates species of the genera Pearsonema, Aonchotheca and Baruscapillaria.

New subtribes of Arachnocephalini (Orthoptera: Mogoplistidae) and a new genus and species of this tribe from South Africa

The tribe Arachnocephalini is divided into three subtribes: [1] Pseudomogoplistina subtrib. nov. with one genus lacking ventrolateral lobes on the tarsi and having a massive Y-shaped sclerite in the male genitalia; [2] Bothromogoplistina subtrib. nov. including two genera with similar tarsi but with a different structure of the male genitalia (lacking a Y-shaped sclerite and having a long and thin virga-like sclerotised rachis inside a membranous invagination of the ventral fold); [3] Arachnocephalina Gorochov, 1984 possibly including all the other genera of this tribe (these genera are with a pair of ventrolateral lobes on the second tarsal segment and/or with the male genitalia more or less similar to those of Bothromogoplistina subtrib. nov.). One new genus with one new species (Bothromogoplistes paraproctalis gen. et sp. nov.) are described from a burrow in the arid territory of South Africa. This cricket is probably related to the genera Cycloptiloides Sjöstedt, 1910 and Eucycloptilum Chopard, 1936, but their males differ from each other in the pronotal length, the presence or absence of wings and tympana, and the shape of the paraprocts and genital plate. One species, Cycloptiloides parvum (Chopard, 1961), comb. nov., is transferred from Eucycloptilum to Cycloptiloides.

A new species of Crinoniscus P\xe9rez, 1900 (Crustacea: Isopoda: Crinoniscidae) parasitising the pedunculate barnacle Heteralepas newmani Buhl-Mortensen & Mifsud (Cirripedia: Heteralepadidae) with notes on its ecology and a review of the genus

The new species Crinoniscus stroembergi n. sp. belonging to the parasitic isopod family Crinoniscidae Bonnier, 1900, is described from a pedunculate barnacle host collected in the Mediterranean Sea. This is the first species of Crinoniscus Pérez, 1900 described from a host in the genus Heteralepas Pilsbry. The male cryptoniscus larva is distinguished from congeneric species by having a dorsoventrally flattened body with the posterolateral margins of the cephalon scarcely extending beyond the anterior margin of pereomere 1 (in contrast to C. cephalatus Hosie, 2008 with extended margins); articles 1 and 2 of the antennule being subequal in width and the anterodistal angle of antennule article being low and rounded; propodus of pereopods 6 and 7 having a sinuous dorsal margin that is distally narrowing and the posterior margin of the pleotelson being short and rounded. The mature females of species in Crinoniscus are of two basic forms: those with ventrolateral lobes on the pereomeres (C. alepadis (Gruvel, 1901) n. comb., and C. politosummus Hosie, 2008) and those lacking such lobes (C. cephalatus and C. stroembergi n. sp.). The mature females of C. stroembergi n. sp. can be distinguished from other species of Crininiscus based on their lacking lobes on the anterior end. The material examined includes the male and three female developmental stages of the parasite in the host, Heteralepas newmani Buhl-Mortensen & Mifsud. The mouthparts of the immature female are described and the feeding biology and effects on the host are discussed along with a review of feeding modes in species of the Cryptoniscoidea. Leponiscus alepadis is transferred to Crinoniscus; the latter genus now contains five species. A modified diagnosis of Crinoniscus is provided.

Immature Stages and Hosts of Two Plesiomorphic, Antillean Genera of Membracidae (Hemiptera) and a new species of Antillotolania from Puerto Rico

The nymphs of Antillotolania Ramos and Deiroderes Ramos are described for the first time, along with the first host record for the genus Antillotolania, represented by Antillotolania myricae, sp. n. Nymphal features of both genera, such as a ventrally fused, cylindrical tergum IX (anal tube), the presence of abdominal lamellae, and heads with foliaceous ventrolateral lobes confirm their placement in Membracidae and are consistent with phylogenetic analyses placing them in Stegaspidinae but in conflict with a cladistic analysis showing a closer relationship to Nicomiinae. Head processes and emarginate forewing pads in the last instars of both genera support an earlier estimate, based on nuclear genes, that the two genera form a monophyletic group in Stegaspidinae. Distinguishing features of the four species of Antillotolania are tabulated.

Redescription ofEchinocoleus hydrochoeri(Travassos, 1916) (Nematoda: Trichuridae) fromHydrochoeris hydrochaerisLinnaeus, 1766 (Rodentia: Caviidae) from Argentina

Twenty-eight Capillariinae species have been recorded in rodents; 1 of these species was reported from a caviomorph rodent, Hydrochoeris hydrochaeris (capybara), and placed in the genus Echinocoleus by Moravec (1982). However, both original description and subsequent contributions of Echinocoleus hydrochoeri are poor and incomplete. In this paper, this species is redescribed, and a new geographical distribution is reported. The redescription is based on morphologic and morphometrical features; intestine ends in a cloaca beside ejaculatory duct, caudal bursa composed of 2 large ventrolateral lobes with a fleshy internal part and a membranous external part (they are not united dorsally with a membrane), 1 pair of caudal papillae, terminal part of cylindrical cirrus ornamented with thin and thick spines (and particular pattern distribution), sclerotized spicule in male, and vulvar appendage in female, and 3 bacillary bands (1 ventral and 2 lateral). Generic and specific analyses were performed to establish new standards for future studies on the systematic position of Capillariinae species. This study presents new morphological information and a new record of a capillariid species from Argentina.

Development of the tentacular apparatus in sipunculans (Sipuncula): I. Thysanocardia nigra (Ikeda, 1904) and Themiste pyroides (Chamberlin, 1920)

The development and arrangement of the tentacular apparatus of Thysanocardia nigra (Ikeda, 1904) and Themiste pyroides (Chamberlin, 1920) are described and illustrated using scanning electron microscopy. In T. nigra, the tentacular apparatus is composed of two crowns: the nuchal arc enclosing the nuchal organ and a crown of numerous oral tentacles arranged in U-shaped festoons. In early juveniles, two dorsal horn-like protrusions develop into the first, or primary, pair of tentacles of the nuchal arc. The second pair of tentacles of the nuchal arc develops dorsolaterally on the bases of the primary tentacles. Two ventrolateral lobes of the oral disk grow and become subdivided by the longitudinal ciliary groove into anlages of one set of dorsal and one set of ventral tentacles, thus forming a first oral festoon. Later, a pair of dorsolateral lobes develop between the first festoons and the nuchal arc to form a second pair of oral festoons. The third and following pairs of oral festoons develop in the dorsolateral growth zones lateral to the borders of the nuchal arc, where they meet the oral crown. The growing festoons extend down the oral disk and run alongside the head. A new oral tentacle appears directly at/on the base of the previous tentacle, thus giving rise to a typical sympodium with an alternating arrangement of tentacles. In T. pyroides, a second pair of tentacles develops from two ciliary lobes that are ventrolateral outgrowths of the circumoral ciliary field around the terminal mouth opening. The third pair of tentacles appears from the dorsolateral lobes at the base of primary tentacles, between the first two pairs of tentacles. These six tentacles determine the position of six main stems of the tentacular apparatus designated the first tentacles in the corresponding stems. The second tentacle in every stem appears as a ventrolateral outgrowth at the base of the first tentacle. The third and following tentacles in the stem are developed between the two previous tentacles according to a sympodial pattern. In both species, the distinct sympodial pattern in the arrangement of tentacles in the tentacular apparatus is well evidenced by the outlines of the ciliary oral grooves. The branched stems of T. pyroides may be homologized structurally and functionally to the oral festoons of T. nigra. J. Morphol. (c) 2006 Wiley-Liss, Inc.

Ultrastructure of the forebody and foregut tegument and eccrine gland cells of Crepidostomum metoecus (Trematoda: Digenea: Allocreadiidae)

The forebody and foregut of Crepidostomum metoecus Braun, 1900 are invested with a tegument bearing regularly arranged surface tubercles comparable with the aspidogastrean surface structures. The tegument of the ventrolateral lobes and of the prepharynx is penetrated by ducts of eccrine gland cells. The frontal and prepharyngeal gland cells, localised in the parenchyma, discharge electron-dense granules. Their ducts are lined by peripheral microtubules and fixed to the tegument plasmalemma by a septate junction. The functional roles of these glands are discussed.

A New Species of the Genus Propedies Hebard (Acridoidea: Acrididae: Melanoplinae) from Northern Argentina

A New Species of the Genus Propedies Hebard (Acridoidea: Acrididae: Melanoplinae) from Northern Argentina

On a new species of Pseudocapillaria (Nematoda: Trichuroidea), P. lepidocephali, from the estuarine fish Lepidocephalus (Lepidocephalichthys) guntea (Hamilton)

Pseudocapillaria lepidocephali n. sp., parasitic in the intestine of the loach Lepidocephalus (Lepidocephalichthys) guntea from the Hooghly estuary at Kalyani, West Bengal, India, is described. The parasite is characterised mainly by its small body size, the structure of the male caudal end (the presence of mediumsized ventro-lateral lobes and the absence of a dorsal membrane), the presence of a non-spinous spicular sheath, the structure of the stichosome (26–34 stichocytes present), and the size and structure of the eggs. This is the first species of the genus Pseudocapillaria described from India and also from the genus Lepidocephalus.

ADDITIONS TO THE SYSTEMATICS AND BIOLOGY OF THE CADDISFLY FAMILY UENOIDAE (TRICHOPTERA)

AbstractA description is given for the male, female, and larva of Farula praelonga sp. nov. and for the female and larva of Neothremma genella Denning. Farula praelonga sp. nov. is distinctive in having an exceptionally long internal branch of segment X. The female of Neothremma genella is the only female yet known in that genus to have greatly reduced ventrolateral lobes of sternum IX. Modifications are made to the keys previously published for adults of Farula and Neothremma to incorporate this new information. These two species occur together in abundance; they are univoltine and have emergence periods 6 months apart.

Development of in vitro fertilized embryos of the polyclad flatworm, Hoploplana inquilina, following blastomere separation and deletion

After in vitro fertilization of naked eggs of the polyclad turbellarian, Hoploplana inquilina, both cell separation experiments and deletions of specific blastomeres are possible. With these techniques one can analyze the developmental potential of isolated blastomeres and determine if the embryonic axes have been established at the four-cell stage in this primitive, equally-cleaving spiralian embryo. Two-cell separation experiments with development of both halves resulted in pairs of larvae 1) neither of which had an eye (29%), 2) both of which had one eye (19%), and 3) one of which was eyeless and the other was one-eyed (43%). Deletion of one blastomere at the four-cell stage resulted in 68% one-eyed, 28% two-eyed and 3% eyeless larvae. The one-eyed larvae were asymmetric with respect to eye position with more having right than left eyes. Abnormal or missing ventrolateral lobes occurred with deletion of any of the macromeres at four cells but were significantly more common when A or C rather than B or D was deleted. The experiments support the hypothesis that eye development is a consequence of cytoplasmic localization of both a specific eye precursor and an inducer which segregate independently of cleavage planes, and indicate that the embryonic axes have been determined at the four-cell stage.

Neurohemal-Endocrine Organs in the Camel Tick, Hyalomma Dromedarii (Acari: Ixodoidea: Ixodidae)123

The neurohemal-endocrine organs of female Hyalomma dromedarii consist of (a) 2 pairs of lateral segmental organs (LSO) innervated by hemal nerves originating from the 1st and 2nd pedal nerve roots and (b) the neurohemal organ (NHO) of 1 dorsal lobe and 2 ventrolateral lobes innervated by compound nerves. The LSO are most active in feeding females and in inseminated, fully engorgd females. The NHO enlarges when virgin and inseminated females feed. Neuronal cell secretion is most abundant in partly fed virgin females.

The nervous system and ciliary band of Müller's larva.

The newly hatched Müller’s larva of the polyclad Pseudoceros canadensis is described at the electron microscopical level with attention to the arrangement and innervation of the ciliary band and the organization of the larval nervous system. Distinctive ultrastructural features allow the trochal cells of the band to be distinguished from general epithelium of the body surface and the specialized oral field epithelium. The band comprises a ventral and a dorsal marginal loop that run along the margins of the six projecting lobes of the larva, and a suboral plate that forms a bridge between these behind the mouth. These three components are joined asymmetrically to form a single, but discontinuous, band: on the left the ventral loop and suboral plate are joined, but these fail to connect with the dorsal loop; on the right it is the ventral and dorsal loops that join, but there is no connection between these and the suboral plate. A system of intraepithelial nerves is associated with the ciliary band, the largest nerves being those in the ventrolateral lobes and the intraepithelial commissure that connects these across the oral field. The system is truly peripheral: it lies outside the basement membrane and is separated by it from the central nervous system, which at this stage comprises a brain and four radiating nerve cords. The peripheral and central nervous systems are in direct contact only at two points, located just behind the ventrolateral lobes on either side of the larva, where a few neurites pass through the basement membrane from one system to the other. The neurites of the peripheral system arise mainly from bipolar sensory cells located in the ciliary band. These are concentrated along the ventrolateral lobes, and their projecting cilia face incoming water currents. Observations on larval swimming behaviour do not, however, suggest any obvious function for these cells. The ciliary band is thus organized as a self-contained unit supplying its own innervation. Other primitive invertebrate larvae have ciliary bands that are similar to some extent in their organization and ultra­structure. This, added to what is already known about Müller’s larva, supports the idea that it is primitive and is closely related to at least several other larval types, but it is not clear how the overall arrangement of the band in Müller’s larva as described here relates to what is seen in other larvae. Several ways in which the pattern might have originated from simpler patterns in hypothetical ancestral forms are, however, discussed.

Prostatic hyperplasia and neoplasia in aging F344 rats.

The prostates of 1775 (614 control and 1161 experimental) 2-year-old F344 rats from 12 different carcinogen bioassays conducted by the Bioassay Program of the NCI and the NTP were evaluated histologically. The incidence of prostatic lesions including (atypical) hyperplastic foci, adenomas, and carcinomas was 6.8%. There was no difference in the type or incidence of the lesions between treated and untreated animals. Adenomas or carcinomas were found in 71 (4.0%) of the rats, primarily as incidental findings. The number of tumors and hyperplastic foci varied from laboratory to laboratory depending on the anatomical localization of the plane of the section. Most of the neoplasms were found in the ventrolateral lobes of the prostate (ventral prostate). When adequate sections were prepared of the ventral lobe, 10-20% of the prostates had these proliferative lesions. The lesions were usually small and originated in the epithelium of the alveoli and small ducts and were usually small and originated in the epithelium of the alveoli and small ducts and were not associated with the common inflammatory lesions of the rat prostate. Thin fibrous capsules were formed in a few of the larger tumors. Metastases were not observed but there was local invasion into alveoli, ducts and interstitial connective tissue. Evidence is presented that the atypical hyperplasias progress to adenoma and carcinoma. The F344 rat offers a potential model for the study of latent prostatic preneoplastic and neoplastic lesions.