Secretory products of the haptoral reservoirs and peduncular glands in two species of Bravohollisia (Monogenea: Ancyrocephalidae)

Abstract. Light and electron microscopy were used to characterize the structure of secretory cells and their products involved in attachment of two monogenean parasites of fish, in order to understand their role in the attachment process. In Bravohollisia rosetta and Bravohollisia gussevi , peduncular gland cells with two nuclei, granular endoplasmic reticulum, and Golgi bodies produce dual electron-dense (DED) secretory bodies with a homogenous electron-dense rind and a less electron-dense fibrillar core (oval and concave in B. rosetta and oval in B. gussevi ). The DED secretory bodies are altered as they migrate from the gland cell to the haptoral reservoir, the superficial anchor grooves, and into the gill tissues. The contents of the DED secretory bodies are exocytosed into the reservoirs, fibrillar cores persisting in the matrix, some of which condense, forming highly electron-dense spherical bodies. Small, oval, electron-dense bodies occur in the grooves, while no inclusions are visible in the homogenous exudate within the gill tissues. The single tubular extension of the reservoir enters a bifurcate channel within the anchor via a concealed, crevice-like opening on one side of the anchor. The channel directs secretions into the left and the right grooves via concealed apertures. The secretions, introduced into the tissues by the anchors, probably assist in attachment. The secretions are manifested externally as net-like structures and observed in some cases to be still attached to the point of exudation, on anchors detached from the gill tissues. This suggests that despite having the anchors detached, the worms can still remain anchored to the gill tissues via these net-like structures. Based on this, it is postulated that the net-like secretions probably function as a safety line to anchor the worm during the onset of locomotion and in doing so reduce the risk of tearing host tissues.     

Bucephaline digeneans (Bucephalidae) in <Emphasis Type="Italic">Sphyraena putnamae</Emphasis> Jordan &; Seale (Sphyraenidae) from the lagoon off New Caledonia

Lethrinitrema gibbus n. g., n. sp. and L. dossenus n. sp. are described from the fish Lethrinus rubrioperculatus Sato collected off New Caledonia, South Pacific. Members of Lethrinitrema n. g. (Ancyrocephalidae) are characterised by having two pyriform haptoral reservoirs and ventral anchors with lateral grooves. The elongate tubular distal end of each reservoir bifurcates, draining into a superficial lateral groove on each side of the ventral anchors. The haptoral reservoirs are postulated to store secretory products which assist in attachment to the host. Lethrinitrema spp. also possess tandem gonads, a male copulatory organ without an accessory piece or with thinly sclerotised accessory piece, and a dextrolateral, non-sclerotised vaginal bulb. The two new species have small, poorly demarcated haptors with small haptoral armament and a crown-like piece on the tip of the inner root of the ventral anchors. They differ from each other in the shape and size of the ventral bar and male copulatory organ (40–45 μm in length in L. gibbus vs 24–30 μm in L. dossenus). Three other species, previously included in Haliotrema Johnston & Tiegs, 1922, are transferred to Lethrinitrema, i.e. L. chrysostomi (Young, 1968) n. comb., L. fleti (Young, 1968) n. comb. (both briefly redescribed from paratypes) and L. lethrini (Yamaguti, 1937) n. comb. All species of Lethrinitrema parasitise Lethrinus spp. (Lethrinidae), and there is evidence for the existence of further Lethrinitrema spp. on Lethrinus spp. in the Indo-Pacific region.     

Bravohollisia Bychowsky & Nagibina, 1970 and Caballeria Bychowsky & Nagibina, 1970 (Monogenea: Ancyrocephalidae) from Pomadasys hasta (Bloch) (Pomadasyidae), with the description of a new attachment mechanism

Nine species of monogeneans were collected from the fish Pomadasys hasta (Bloch): Bravohollisia magna Bychowsky & Nagibina, 1970; B. rosetta n. sp.; B. reticulata n. sp.; B. gussevi n. sp.; B. kritskyi n. sp.; Caballeria pedunculata Bychowsky & Nagibina, 1970; C. robusta Bychowsky & Nagibina, 1970; C. liewi n. sp.; and C. intermedius n. sp. The anchors of these species contain a canal beginning in the shaft and ending near the point; ducts of haptoral glands enter the canal in the shaft and are associated with net-like structures near the anchor tip. The net-like structures of Bravohollisia spp. are extensive, while those of Caballeria spp. are smaller and more compact. These nets probably assist the monogeneans in attaching to the gill filaments. Caballeria spp. possess four pairs of extensible haptoral digits. Species of Bravohollisia and Caballeria posses two seminal vesicles.     

First record in South America of Didymosulcus palati and Didymosulcus philobranchiarca (Digenea, Didymozoidae) with new hosts records and pathological alterations

Two species of Didymozoidae, Didymosulcus palati (Yamaguti 1970) and Didymosulcus philobranchiarca (Yamaguti 1970) were reported for the first time in South America, Atlantic Ocean, parasitizing three different tuna species from the coast of Rio de Janeiro, Brazil: Thunnus atlanticus (Lesson), Thunnus albacares (Bonnaterre) and Thunnus obesus (Lowe). Pairs of D. philobranchiarca were found on gill arches of T. albacares and T. obesus, in longitudinal rows of yellow cysts located inside grooves in the hard denticle palate (new site) of the three hosts species studied, and as disperse groups of cysts in the operculum (new site) and gill arches of T. atlanticus (new host record). D. palati occurred as disperse groups of encysted worm pairs in the gill arches of T. albacares and T. obesus and in gill arches and operculum of T. atlanticus (new host record). The pathological alterations induced by D. philobranchiarca in the palate of T. atlanticus are described for the first time. Original measurements and figures are presented.     

On the ontogeny of the haptor and the evolution of the Monogenea

Data on the ontogeny of the posterior haptor of monogeneans were obtained from more than 150 publications and summarised. These data were plotted into diagrams showing evolutionary capacity levels based on the theory of a progressive evolution of marginal hooks, anchors and other attachment components of the posterior haptor in the Monogenea (Malmberg, 1986). 5 + 5 unhinged marginal hooks are assumed to be the most primitive monogenean haptoral condition. Thus the diagrams were founded on a 5 + 5 unhinged marginal hook evolutionary capacity level, and the evolutionary capacity levels of anchors and other haptoral attachement components were arranged according to haptoral ontogenetical sequences. In the final plotting diagram data on hosts, type of spermatozoa, oncomiracidial ciliation, sensilla pattern and protonephridial systems were also included. In this way a number of correlations were revealed. Thus, for example, the number of 5 + 5 marginal hooks correlates with the most primitive monogenean type of spermatozoon and with few sensillae, many ciliated cells and a simple protonephridial system in the oncomiracidium. On the basis of the reviewed data it is concluded that the ancient monogeneans with 5 + 5 unhinged marginal hooks were divided into two main lines, one retaining unhinged marginal hooks and the other evolving hinged marginal hooks. Both main lines have recent representatives at different marginal hook evolutionary capacity levels, i.e. monogeneans retaining a haptor with only marginal hooks. For the main line with hinged marginal hooks the name Articulon-choinea n. subclass is proposed. Members with 8 + 8 hinged marginal hooks only are here called Proanchorea n. superord. Monogeneans with unhinged marginal hooks only are here called Ananchorea n. superord. and three new families are erected for its recent members: Anonchohapteridae n. fam., Acolpentronidae n. fam. and Anacanthoridae n. fam. (with 7 + 7, 8 + 8 and 9 + 9 unhinged marginal hooks, respectively). Except for the families of Articulonchoinea (e.g. Acanthocotylidae, Gyrodactylidae, Tetraonchoididae) Bychowsky's (1957) division of the Monogenea into the Oligonchoinea and Polyonchoinea fits the proposed scheme, i.e. monogeneans with unhinged marginal hooks form one old group, the Oligonchoinea, which have 5 + 5 unhinged marginal hooks, and the other group form the Polyonchoinea, which (with the exception of the Hexabothriidae) has a greater number (7 + 7, 8 + 8 or 9 + 9) of unhinged marginal hooks. It is proposed that both these names, Oligonchoinea (sensu mihi) and Polyonchoinea (sensu mihi), will be retained on one side and Articulonchoinea placed on the other side, which reflects the early monogenean evolution. Except for the members of Ananchorea [Polyonchoinea], all members of the Oligonchoinea and Polyonchoinea have anchors, which imply that they are further evolved, i.e. have passed the 5 + 5 marginal hook evolutionary capacity level (Malmberg, 1986). There are two main types of anchors in the Monogenea: haptoral anchors, with anlages appearing in the haptor, and peduncular anchors, with anlages in the peduncle. There are two types of haptoral anchors: peripheral haptoral anchors, ontogenetically the oldest, and central haptoral anchors. Peduncular anchors, in turn, are ontogenetically younger than peripheral haptoral anchors. There may be two pairs of peduncular anchors: medial peduncular anchors, ontogentically the oldest, and lateral peduncular anchors. Only peduncular (not haptoral) anchors have anchor bars. Monogeneans with haptoral anchors are here called Mediohaptanchorea n. superord. and Laterohaptanchorea n. superord. or haptanchoreans. All oligonchoineans and the oldest polyonchoineans are haptanchoreans. Certain members of Calceostomatidae [Polyonchoinea] are the only monogeneans with both (peripheral) haptoral and peduncular anchors (one pair). These monogeneans are here called Mixanchorea n. superord. Polyonchoineans with peduncular anchors and unhinged marginal hooks are here called the Pedunculanchorea n. superord. The most primitive pedunculanchoreans have only one pair of peduncular anchors with an anchor bar, while the most advanced have both medial and lateral peduncular anchors; each pair having an anchor bar. Certain families of the Articulonchoinea, the Anchorea n. superord., also have peduncular anchors (parallel evolution): only one family, the Sundanonchidae n. fam., has both medial and lateral peduncular anchors, each anchor pair with an anchor bar. Evolutionary lines from different monogenean evolutionary capacity levels are discussed and a new system of classification for the Monogenea is proposed.In agreeing to publish this article, I recognise that its contents are controversial and contrary to generally accepted views on monogenean systematics and evolution. I have anticipated a reaction to the article by inviting senior workers in the field to comment upon it: their views will be reported in a future issue of this journal. EditorIn agreeing to publish this article, I recognise that its contents are controversial and contrary to generally accepted views on monogenean systematics and evolution. I have anticipated a reaction to the article by inviting senior workers in the field to comment upon it: their views will be reported in a future issue of this journal. Editor     

Taxonomy, host-specificity and biogeography of Symmetrovesicula Yamaguti, 1938 (Digenea: Fellodistomidae) from chaetodontids (Teleostei: Perciformes) in the tropical Indo-west Pacific region

Combined molecular and morphological data demonstrate the presence of two species of Symmetrovesicula Yamaguti, 1938 in chaetodontid fishes from Australian waters. A total of 2,462 individuals of 46 species of chaetodontid at eight localities were dissected. Analysis of the rDNA ITS2 revealed the presence of three genotypes, two separated by a single base difference and the third differed from the other two by 10-11 base differences. Subsequent morphological examination identified a number of variations that supported the presence of two species; however, we found no additional evidence to support the presence of a third species corresponding to the single base variation. Thus, we take the conservative approach of recognising two species of Symmetrovesicula within Australian waters, S. chaetodontis Yamaguti, 1938 from off Ningaloo Reef, Western Australia and S. gracilis n. sp. from off Ningaloo Reef, the Great Barrier Reef, Queensland and New Caledonia. Both species exhibit distinct restrictions to certain clades of chaetodontids.     

<Emphasis Type="Italic">Diplectanocotyla</Emphasis> Yamaguti, 1953 (Monogenea: Diplectanoidea) from <Emphasis Type="Italic">Megalops cyprinoides</Emphasis> (Broussonet) (Teleostei: Megalopidae) off Peninsular Malaysia

Two known and two new species of Diplectanocotyla Yamaguti, 1953 (D. gracilis Yamaguti, 1953, D. megalopis Rakotofiringa & Oliver, 1987, D. langkawiensis n. sp. and D. parva n. sp.) were collected from Megalops cyprinoides (Megalopidae) off Langkawi, Kedah and Matang, Perak, Peninsular Malaysia. All four species possess similar types of sclerotised male and female reproductive structures and similar soft anatomical features. The squamodisc sclerites of all four species have spine-like projections with varying degrees of visibility and shapes (sharp-pointed to triangular). In D. megalopis and D. langkawiensis n. sp. the spines are sharp-pointed and distinct on sclerites from rows 5–6 onwards. In D. gracilis and D. parva n. sp. the sclerite spines are triangular, lightly sclerotised and occur on almost all of the sclerites. D. parva n. sp. has comparatively the smallest set of anchors, bars, squamodiscs and squamodisc suckers. The anchors and bars of the other three species are almost similar in overall size, and the main distinguishing feature is the relative lengths of the inner and outer roots of the ventral anchors. In D. gracilis the outer root is very much smaller than the inner root and they are disposed almost at a right angle to each other. In D. megalopis the outer root is usually about half the length of the inner root and the roots are inclined at c.60° to each other. In D. langkawiensis n. sp. the roots are inclined at c.40° degrees and the outer root is of a similar length or only slightly shorter than the inner root. The openings of the two squamodisc suckers of all four Diplectanocotyla species are surrounded by tiny scale-like spines. Bifid tegumental spines are found in the posterior region of all four species, differing only in their extent: in D. parva n. sp. the tegumental spines are only distributed in the peduncular region and not beyond, whilst in the other three species the tegumental spines extend from the posterior level of the testis to the end of the peduncle. An amended diagnosis of Diplectanocotyla and a key to its species are appended.     

The taxonomic status of <Emphasis Type="Italic">Opegaster</Emphasis> Ozaki, 1928 and the description of four new species of <Emphasis Type="Italic">Opecoelus</Emphasis> Ozaki, 1925 (Digenea: Opecoelidae) from marine teleosts in Australian waters

The similarities between Opecoelus Ozaki, 1925, Coitocaecum Nicoll, 1915, Opegaster Ozaki, 1928 and Paropecoelus Pritchard, 1966 and the difficulty of separating Opecoelus and Opegaster are discussed. It is proposed that Opegaster be reduced to synonymy with Opecoelus and the diagnosis of the latter amended to accommodate both forms. Four new species of Opecoelus are described from marine teleosts in Australian waters. These are Opecoelus woolcockae n. sp. from Acanthopagrus butcheri and A. australis from off South Australia, New South Wales and southern Queensland, O. pomatomi n. sp. from Pomatomus saltatrix off New South Wales, O. crowcrofti n. sp. from Atherinomorus ogilbyi off southern Queensland and O. queenslandicus n. sp. from Apogon fasciatus off southern Queensland. The following new combinations are formed: Opecoelus gonorhynchi (Gavrilyuk, 1979) n. comb., O. elongatus (Yamaguti, 1959) n. comb., O. pentadactylus (Manter, 1940) n. comb., O. apogonichthydis (Yamaguti, 1938) n. comb., O. cameroni (Caballero & Caballero, 1969) n. comb., O. dendrochiri (Yamaguti, 1970) n. comb., O. hawaiiensis (Yamaguti, 1970) n. comb., O. jamunicus (Srivastava, 1968) n. comb., O. longivesiculus (Yamaguti, 1952) n. comb., O. mastacembalii (Harshey, 1937) n. comb., O. mehrii (Harshey, 1937) n. comb., O. synodi (Manter, 1947) n. comb., O. tamori (Yamaguti, 1938) n. comb., O. bothi (Yamaguti, 1970) n. comb., O. caulopsettae (Manter, 1954) n. comb., O. beliyai (Pande, 1937) n. comb., O. brevifistulus (Ozaki, 1928) n. comb., O. cryptocentri (Yamaguti, 1958) n. comb., O. dactylopteri (Yamaguti, 1970) n. comb., O. dermatogenyos (Yamaguti, 1970) n. comb., O. ditrematis (Yamaguti, 1942) n. comb., O. gobii (Yamaguti, 1952) n. comb., O. hippocampi (Shen, 1982) n. comb., O. iniistii (Yamaguti, 1970) n. comb., O. lobulus (Wang, 1977) n. comb., O. macrorchis (Yamaguti, 1938) n. comb., O. parapristipomatis (Yamaguti, 1934) n. comb., O. pritchardae (Overstreet, 1969) n. comb., O. syngnathi (Yamaguti, 1934) n. comb., O. lutiani (Bravo-Hollis & Manter, 1957) n. comb., O. ovatus (Ozaki, 1928) n. comb., O. plotosi (Yamaguti, 1940) n. comb. and O. rectus (Ozaki, 1928) n. comb.; all the new combinations were previously species of Opegaster.     

Diplectanum yamagutii sp.n.(Monogenea, Monopisthocotylea, Diplectanidae), Parasite de Kyphosus cinerascens (Forsskål) à Hawaii

Diplectanum yamagutii sp.n., a gill parasite of Kyphosus cinerascens (Forsskål, 1775) off Hawaii is described from amongst the type-material deposited by Professor S. Yamaguti in the National Parasite Collection of the United States National Museum of Natural History at Beltsville (Maryland, USA). Diplectanum yamagutii sp.n., D. diplobulbus Yamaguti, 1968, D. nenue Yamaguti, 1968, D. spiculare Yamaguti, 1968 and D. kyphosi (Yamaguti, 1968) comb.n. are sympatric parasites of Kyphosus cinerascens off Hawaii. These five species are distinguished by the shape and size of the armature of both the cirrus and the haptoral sclerotised pieces.     

Weight–length relationships of 22 fish species from Paraíba do Sul River in Rio de Janeiro State,southeastern Brazil

The present study reports the weight–length relationships of 22 fish species from middle stretches of the Paraíba do Sul River, a riverine system located in the most important economic regions of Brazil and which is under great pressure due to damming and others ventures. Data were collected quarterly in 2010 and 2011 from three reservoirs and the adjoining downstream by using three different mesh sizes of gill nets. Of the 22 species, eight had no records in the FishBase WLR database; new maximum lengths are given for eight species.     

Fine structural aspects of silk secretion in a spider. II. Conduction in the pyriform glands

The excretory duct of pyriform glands in Araneus diadematus is connected to the secretory sac through an intermediary cell ring. Apices of these cells bear thick, long microvilli and cytoplasmic extensions containing microtubules in bundles, some of which are derived from normal basal bodies. These finger-like extensions lie between the cuticular intima and the secretory product; they are thought to protect the intima and to initiate moulding of the silk thread. Structural features of the duct cells suggest that the latter play a role in the control of the water content of the silk glue which is restricted to the last portion of the duct where numerous nerve endings are inserted between cells. It is evident that duct structure and chemical and physical characteristics of silk are correlated in all spider silk glands.     

Microstructure of the silk apparatus of the comb-footed spider, Achaearanea tepidariorum (Araneae: Theridiidae)

The microstructural organization of the silk‐spinning apparatus of the comb‐footed spider, Achaearanea tepidariorum, was observed by using a field emission scanning electron microscope. The silk glands of the spider were classified into six groups: ampullate, tubuliform, flagelliform, aggregate, aciniform and pyriform glands. Among these, three types of silk glands, the ampullate, pyriform and aciniform glands, occur only in female spiders. One (adult) or two (subadult) pairs of major ampullate glands send secretory ductules to the anterior spinnerets, and another pair of minor ampullate glands supply the median spinnerets. Three pairs of tubuliform glands in female spiders send secretory ductules to the median (one pair) and posterior (two pairs) spinnerets. Furthermore, one pair of flagelliform glands and two pairs of aggregate glands together supply the posterior spinnerets, and form a characteristic spinning structure known as a “triad” spigot. In male spiders, this combined apparatus of the flagelliform and the aggregate spigots for capture thread production is not apparent, instead only a non‐functional remnant of this triad spigot is present. In addition, the aciniform glands send ductules to the median (two pairs) and the posterior spinnerets (12–16 pairs), and the pyriform glands feed silk into the anterior spinnerets (90–100 pairs in females and 45–50 pairs in males).     

Effect of artificial baits on the catch efficiency of monofilament gill nets

Greater success in catching fish with gill nets is possible if more the fish are attracted to the nets. Bait has been successfully used to lure fish into the gill nets. With the aim of increasing the catch efficiency of monofilament gill nets, a study was conducted between January 2009 and December 2010 to test the effect of artificial baits on the efficiency of 40, 50 and 55 mm monofilament gill nets in the Keban Dam Lake (Elaz??/Turkey). The catch rate of the baited nets was compared to similar nets without bait. Baited nets caught 482 fish (71.8% of the total, seven species). Non‐baited nets caught 189 fish (28% of the total, seven species). The majority of fish (238) were caught using baited gill nets with 40 mm mesh. The most commonly caught species was Capoeta trutta. The differences between the baited gill nets and non‐baited gill nets were statistically significant (P < 0.05). Finally, it was understood that artificially baited monofilament gill nets had higher catch efficiencies than non‐baited monofilament gill nets. Unlike most natural baits, artificial baits are re‐usable and thus more economical in the long term.     

Neotropical Monogenoidea. 49. Four new species of the Diplectanidae (Dactylogyrinea) from the gills of some pachyurines (Teleostei: Sciaenidae) from the Rio Tocantins and Rio Doce Basins, with the proposal of Anoplectanum n. g. and Spinomatrix n. g.

Four new species of the Diplectanidae from the gills of freshwater sciaenid species (Pachyurinae) in Brazil are described and two new genera, Anoplectanum n. g. and Spinomatrix n. g., are proposed. These are: Diplectanum copiosum n. sp. from Pachyurus junki and Petilipinnis grunniens; Anoplectanum haptorodynatum n. g., n. sp. from Pachyurus junki and Petilipinnis grunniens, and A. microsoma n. g., n. sp. from Petilipinnis grunniens, all in the Tocantins Basin; and Spinomatrix penteormos n. g., n. sp. from Pachyurus adspersus in the Rio Doce Basin. Anoplectanum is proposed to accommodate diplectanids lacking squamodiscs and having a superficial root of the ventral anchor as long or longer than the deep root. Spinomatrix is proposed for species having a haptoral and peduncular armature composed of spines, hooks, anchors, squamodiscs and armed muscular pads.     

Three new species of Protogyrodactylus Johnston & Tiegs, 1922 (Monogenoidea: Dactylogyridae) from the gills of the longtail silverbiddy Gerres longirostris (Teleostei: Gerreidae) in the Red Sea

Twenty-one specimens of the longtailed silverbiddy Gerres longirostris (Gerreidae) were examined for dactylogyrid parasites from the Nabq Managed Resource Protected Area, Ras Mohammed National Park (Red Sea) near Sharm El-Sheikh, South Sinai, Egypt. The diagnosis of Protogyrodactylus Johnston & Tiegs, 1922 was amended, and three new species, P. federicae n. sp., P. zullinii n. sp. and P. alatus n. sp., were recovered and described; the prevalence of each species was 100%. P. federicae most closely resembled P. alienus Bychowsky & Nagibina, 1974, but differed from it by possessing two anteromedial projections on the ventral bar, a claw-like ventral anchor sclerite and spatulate dorsal bars. P. zullini was most similar to P. quadratus Johnston & Tiegs, 1922, from which it differed by having a distal hook on the superficial root of the dorsal anchor, an evenly curved ventral anchor shaft and point, and a flange on the bulbous base of the male copulatory organ. P. alatus was closest to P. youngi Bychowsky & Nagibina, 1974, from which it differed by having delicate anchors and two prominent anteromedial processes on the ventral bar.     

Life cycles of the trematodes Parasymphilodora japonica (Yamaguti, 1938) and P. markewitschi (Kulakowskaja, 1947) (Monorchidae) in the conditions of Primorye land

In contrasts to formerly known data, it is found that two species of the Parasymphilodora trematodes, Parasymphilodora japonica (Yamaguti, 1938) and P. markewitschi (Kulakowskaja, 1947) are actually distributed in the territory of Primorye land. The first intermedial hosts of the former species are snails of the genus Parafossarulus; in the second species, these hosts are snails of Boreoelona. A life cycle and stages of development of both trematodes are described.     

Modified method for external attachment of transmitters to birds using two subcutaneous anchors

ABSTRACT Of the transmitter attachment techniques for birds, the subcutaneous anchor provides a secure attachment that yields relatively few secondary effects. However, the use of subcutaneous anchors has been limited by transmitter size and retention time. Using a modified method of attachment that utilized two subcutaneous anchors, we deployed 69 GPS transmitters, plus 13 VHF transmitters that were similar in size and weight to GPS models, on Pacific Black Brant (Branta bernicla nigricans). Prior to our study, only harnesses were used for attaching GPS transmitters on birds, mainly because GPS transmitters are too large for other external attachment techniques and implantation in the body cavity attenuates the GPS signal. Thus, to increase the size capacity of anchor attachment and to avoid the well‐documented negative effects of harnesses on behavior and survival, we added a second anchor at the transmitter's posterior end. The double‐anchor attachment technique was quickly and easily accomplished in the field, requiring bird handling times of <10 min. Incidental recoveries of tagged Brant indicate a high degree of transmitter retention. Five recaptured birds (4–6 weeks after deployment) and eight killed by hunters (3–6 mo after deployment) retained their GPS transmitters. For studies involving the use of relatively large transmitters, the double‐anchor method appears to provide a viable alternative for external attachment.     

海南岛海水鱼类单殖吸虫研究及宽海盘虫二新种记述

记述了采自海南岛后水湾的眶棘双边鱼Ambassis gymnocephalus Lacépéde鳃上寄生的宽海盘虫2新种.张氏宽海盘虫Euryhaliotrema zhangjianyingi sp nov.以其边缘小钩明显长于两对中央大钩,支持器的套环状特殊结构,两对中央大钩和联结片而不同于属内的已知种;双边鱼宽海盘虫,Euryhaliotrema ambassisi sp.nov.以其交接器的量度,后吸器中央大钩内突基部较宽,外突较小,钩基部较直,钩尖短而不同于相似种和属内已知种.文中量度μm,模式标本保存在海南师范学院生物系.     

Dactylogyrids (Monogenea: Dactylogyridea) with an unusual number of anchors,their origin and phylogenetic significance. Reference data

It is considered that in Anacanthorinae, Markewitschiana and Pseudacolpenteron pavlovskii (Dactylogyridae s. s.) the anchors are absent originally. In the other dactylogyrids (s. l.) without anchors (Pseudacolpenteron ignotus; Acolpenteron; Anonchohaptor-Icelanchohaptor; Kritskyia-Telethecium-Pavanelliela) these structures are lost. In related genera Rhinoxenus and Nanotrema the dorsal pair of anchors is transformed into the "spikes"; in Heteronchocleidinae there is one anchor; in Trinigyrus and Schilbetrematoides are two anchors; and in Urogyrus three anchors are reduced. But in Rhinonaster, Cacatyocotyle, Callceostomella, Neocalseostoma elongatum and Pseudodactylogyridae the presence of one pair of ventral "peduncular" or "haptoral" anchors appear to be the original state. For Anacanthorinae and Dactylogyridae s. s. the presence of 18-16 hooks, original lacking of anchors, appearance of one pair of them, evolutionary development and subsequent reduction of these structures are characteristic. In the dactylogyrids (s. l.) having two pairs of anchors and 14 hooks, one pair of the anchors is present originally, then usually the second dorsal pair grows up, and finally, the reduction of a part of anchors or all the anchors is possible. In the 16-hooked dactylogyrids (s. l.) having two pairs of anchors (Tetraonchinea, Amphibdellainea, Neodactylodiscinea) the original lacking or reduction of the anchors is not reported. The author considers, that it is unwarranted to unite all dactylogyrids (s. l.) without anchors into the superorder Ananchorea Malmberg, 1990 or to postulate the original presence of the two pairs of ventral anchors in this group. It is also impossible to unit all dactylogyrids (s. l.) having 0-4 anchors and 18-14 hooks into Dactylogyridae sensu Boeger et Kritsky, 1993.     

Rosette glands in the gills of the grass shrimp,Palaemonetes pugio. I. Comparative morphology,cyclical activity,and innervation

Two types of exocrine rosette glands (called type A and type B), located in the gill axes of the grass shrimp Palaemonetes pugio, are described. The type A glands are embedded within the longitudinal median septum of the gill axes, whereas the type B glands typically project into the efferent hemolymph channels of the gill axes. Although both glands have certain common characteristics (i.e., a variable number of radially arranged secretory cells, a central intercalary cell, and a canal cell that forms the cuticular ductule leading to the branchial surface), they differ in the following respects. The type B gland is innervated, but the type A gland is not; axonal processes, containing both granular (ca. 900–1300 Å) and agranular (ca. 450–640 Å) vesicles, occur at a juncture between adjacent secretory cells and the central cell of the type B gland. The secretory cells of type A and type B glands differ in their synthetic potential and membrane specializations. These differences are more pronounced in well-developed, mature glands, most frequently encountered in larger (24–28 mm, total length) grass shrimp, than in the underdeveloped, immature glands that are most abundant in smaller (14–18 mm, total length) grass shrimp. Thus, in mature glands, the secretory cells of the type A rosette glands are characterized by extensive RER, abundant Golgi, and numerous secretory granules, whereas the secretory cells of the type B gland are characterized by extensively infolded and interdigitated basal plasmalemmas and by the presence of numerous mitochondria. In general, both types of glands exhibit increased secretory activity soon after ecdysis. The central and canal cells in both glands seem to have a role in the modification of the secreted materials. The possible functions assigned to the type A gland and the type B gland include phenol-oxidase secretion and osmoregulation, respectively.