Fine structure of the excretory system of Amphioxus (Branchiostoma floridae) and its response to osmotic stress

Summary The excretory organs of Amphioxus occur as segmentally arranged structures throughout the pharyngeal region and may be divided into three components: the solenocytes, the renal tubule, and the renal glomerulus.The solenocytes possess foot processes that rest upon the coelomic surface of the ligamentum denticulatum. The tubular apparatus of the solenocytes consists of ten triangular rods surrounding a central flagellum. The distal end of the tubular apparatus enters branches of the renal tubule. The renal tubule eventually opens into the atrial cavity of Amphioxus. The renal glomerulus is a sinus within the connective tissue of the ligamentum dentieculatum where it connects elements of the branchial circulation with the dorsal aorta. The renal glomerulus, like other blood vessels of Amphioxus, lacks an endothelial lining.If Amphioxus is adapted to artificial sea water at different concentrations there is no change in kidney morphology suggesting that Amphioxus is either is osmotic with its environment or is osmoregulating with other organs.This work was supported by U.S. Public Health Service Grant 5-T01-GM 00582.     

The excretory organs in Sphaerodorum flavum (Phyllodocida, Sphaerodoridae): a rare case of co-occurrence of protonephridia, coelom and blood vascular system in Annelida

The excretory organs of Sphaerodorum flavum (Sphaerodoridae) were investigated by TEM and reconstructed from serial ultrathin sections. These organs are segmentally arranged paired protonephridia, which are in close association with a well-developed blood vascular system. Each protonephridium consists of a terminal part made up of two monociliary terminal cells (solenocytes), and a nephridioduct, formed by two cells. The two solenocytes lie close together. Each cilium is surrounded by 12 microvillar rods projecting from the perikaryon of each solenocyte. These rods form a weir-like structure in the coelomic space. The distal part of the weir is embedded in the proximal nephridioduct. The largest part of the cell bodies of the solenocytes, containing the nucleus, is lateral or basal to the weir-like structures. The lumen of the nephridioduct is formed by two multiciliated cells, which enclose the extracellular nephridial canal one behind the other. The canal opens through the nephropore beneath the cuticle without penetrating the cuticle. Both nephridioduct cells are surrounded by a blood vessel, which is partially folded into several layers. The significance of a simultaneous occurrence of protonephridial excretory organs and a well-developed blood vascular system as well as coelomic cavities is discussed. The results of this investigation indicate a close relationship of Sphaerodoridae to Phyllodocidae instead of to Syllidae within the Phyllodocida. Accepted: 27 November 2000     

The nephridia of the interstitial polychaete Hesionides arenaria and their phylogenetic significance (Polychaeta,Hesionidae)

Summary The small hesionid polychaete Hesionides arenaria possesses paired segmental excretory organs that closely resemble solenocytic protonephridia. The nephridium consists of one terminal cell and four tubule cells which form the emission channel. From the terminal cell, up to six flagella arise each surrounded by a weir of ten regularly arranged cytoplasmic rods. The structure of the cytoplasm of three of the following cells suggests that they function in active transport and storage. Because all of the larger, more primitive species of this family are equipped with metanephridia, the possibility is discussed that these organs have been developed out of metanephridia. The Hesionides arenaria nephridium may be a morphological stage in the evolutionary pathway from metanephridia to solenocytes. This would mean that solenocytes can no longer be considered to be homologous in every case with other protonephridial organs in polychaetes and may well be derived several times independently out of metanephridia or true protonephridia.     

The Ultrastructure of the Protonephridium of the Actinotroch Larva (Phoronida)

The actinotroch larva of Phoronis muelleri has a pair of protonephridia located beneath the tentacle ring and draining the blastocoel; each protonephridium is composed of about 25 solenocytes and a nephroduct which opens in a nephropore on the ventral side of the metasome. The neck of the solenocytes consists of bars, mutually interconnected by a fenestration lamina. Inside the neck microvilli originate proximally in the proximal intrachoanal field and extend through the neck into the nephroduct. There is no canal cell. In cross section the nephroduct is composed of 5–7 monociliary cells, with the cilium protruding through a border of microvilli and extending into the nephroduct. The whole protonephridium is surrounded by a basal lamina. Comparisons of the actinotroch protonephridium with those of other groups have not revealed any convincing homologies. The protonephridia of the protostomians are all considered to be of ectodermal origin, while the cyrtopodocytes of Branchiostoma are mesodermal. The protonephridium of the actinotroch is ectodermal.     

Structure of the mouth tube of a parasitic copepod,Isobranchia appendiculata Heegaard, 1947 (Siphonostomatoida:Lernaeopodidae)

The structure and musculature of the mouth tube of the lernaeopodidIsobranchia appendiculata Heegaard is described in detail. Situated on the median eminence, the mouth tube appears to be lodged inside a median longitudinal groove on the ventral wall of the cephalothorax. The components of the mouth tube, the labrum and the labium are loosely held together along their lateral edges. The thin, transparent walls of both the labrum and the labium are reinforced by chitinous rods. The musculature of the mouth tube consists of two pairs ofretractores oris, four pairs ofcompressores labri and two pairs oflevatores labii. The mandibles are operated by a pair of antagonistic muscles, theroto adductor mandibulae androto abductor mandibulae. Like other lernaeopodids,I. appendiculata resorts to a browsing type of feeding.     

Effects of brefeldin A on the endomembrane system and germ tube formation of the tetraspore of Gelidium floridanum (Rhodophyta,Florideophyceae)

Gelidium floridanum W.R. Taylor tetraspores are units of dispersal and are responsible for substrate attachment. This study aimed to examine evidence of direct interaction between germ tube formation and Golgi activity during tetraspore germination of G. floridanum. After release, the tetraspores were incubated with brefeldin A (BFA) in concentrations of 4 and 8 μM over a 6 h period. The controls and treatments were analyzed with light, fluorescence (FM4‐64 dye) and transmission electron microscopy. In the control samples, the Golgi bodies were responsible for germ tube formation. In contrast, BFA‐treated samples were observed to inhibit spore adhesion and germ tube formation. These tetraspores also showed an increase in volume (≥30 μm width). BFA treatment also resulted in the disassembly of Golgi cisternae and the formation of vesiculated areas of the cytoplasm, blocking the secretion of protein and amorphous matrix polysaccharides. When stained with FM4‐64, the control samples showed fluorescence in the apical region of the germ tube, but the treated samples showed an intense fluorescence throughout the cytoplasm. From these results, we can conclude that the germ tube is formed by the incorporation of vesicles derived from Golgi. Thus, vesicle secretion and Golgi organization are basic processes and essential in adhesion and tube formation. By blocking the secretion of protein and amorphous matrix polysaccharides, BFA treatment precluded tetraspore germination.     

Molecular phylogeny of the subgenus Holothuria (Selenkothuria) Deichmann, 1958 (Holothuroidea: Aspidochirotida)

The subgenus Selenkothuria comprises 12 species of tropical shallow water sea cucumbers that share morphological features, such as rods in the body wall and tube feet, modified tentacles for suspension feeding, and cryptic colours. The taxonomic status of this taxon has been controversial, but currently it is accepted as a subgenus of the genus Holothuria. Phylogenetic analyses of mitochondrial genes [cytochrome c oxidase subunit 1 (COI), 16S RNA] of ten species of Selenkothuria and related subgenera showed the polyphyly of this subgenus; monophyly was rejected by a likelihood ratio test. A geographical split divides the species of this subgenus into three different groups: one Indo‐West‐Pacific (IWP) group and two American groups. The IWP group is more closely related to Holothuria (Semperothuria) cinerascens and to other subgenera such as Roweothuria, Holothuria, and Vaneyothuria, whereas the two American groups are more closely related to each other and to some species of the subgenus Halodeima. These results suggest multiple parallel originations and diversification of ossicle morphology within the subgenus Selenkothuria. The current scheme of subgenera for the genus Holothuria is not supported, suggesting the need for a new classification. © 2012 The Linnean Society of London, Zoological Journal of the Linnean Society, 2012, 165 , 109–120.     

Spernathecal morphology,sperm transfer and a novel mechanism of sperm displacement in the rove beetle,Aleochara curtula (Coleoptera,Staphylinidae)

Summary The mechanism by which sperm are transferred from the male's spermatophore to the female's storing cage is described for the rove beetle Aleochara curtula, emphasizing a novel mechanism of sperm displacement by competing males. The cuticular, U-shaped spermatheca is equipped with a valve structure and two sclerotized teeth. The tube of the spermatophore extends into the spermathecal duct through the guidance of the flagellum of the male endophallus. Further elongation of the spermatophore tube, however, occurs only after separation of the pair. A primary tube bursts at its tip after passing through the valve. Within the lumen of the primary tube, a second tube passes through the valve and continues to extend up to the apical bulb of the spermatheca, doubles back on itself and swells to form a balloon filling most of the spermatheca. The balloon of the spermatophore is pierced within the spermatheca by tooth-like structures pressed against the spermatophore through contraction of the spermathecal muscle. The same process of spermatophore growing and swelling is also observed in mated females. Sperm from previous copulations are backflushed through the valve and the spermathecal duct, indicative of last-male sperm predominance.Abbreviations ad adhesive secretion covering the sperm - sac am amorphous secretion of the spermatophore - as ascending portion of the spermatophore - ds descending portion of the spermatophore - end parts of the male endophallus - ext extended tube - f flagellum - gs genital segment - lt large tooth - m muscle of the spermatheca - nsc non sclerotized cuticle - op opening of the spermathecal gland - pt primary tube - sc sclerotized cuticle - sd spermathecal duct - se secretion of the spermathecal gland - sf secretion flowing out of the primary tube - sg spermathecal gland - sm sperm - smt small tooth - sp spermatheca - ss sperm sac - st secondary tube - vm vaginal muscle     

Functional morphology of the mouth tube of a lernaeopodid Pseudocharopinus narcinae (Pillai, 1962) (Copepoda: Siphonostomatoida)

A detailed account of the structure and musculature of the mouth tube and mode of feeding in P. narcinae is presented. The double-walled mouth tube is formed by a close fitting of the lateral, longitudinal ridges of the labium into the longitudinal groove of the inner, lateral edges of the labrum. The musculature of the mouth tube consists of two pairs of retractores oris, four pairs of compressores labri and two pairs of levatores labii. The host tissues are scraped off by the mandibles repeating a very characteristic movement brought about by roto adductor mandibulae and roto abductor mandibulae pair of muscles. The tissue particles are forced into the buccal cavity with the help of labral muscles. The suction is broken by the contraction of levatores labii group of muscles.     

Ultrastructure of Mucocysts in Peranema trichophorum (Euglenophyceae)1

The “mucigenic” or “muciferous” bodies of Peranema trichophorum are further characterized here as unique extrusive organelles, the mucocysts. Intracellular and ejected mucocysts have characteristic shapes that may represent different developmental stages. Mucocysts found near the Golgi apparatus are membrane-bounded, elongate, tubular structures with amorphous contents of low electron density. Subpellicular mucocysts are often aligned with pellicular striae and have dense contents, which are separated by an electron-lucent zone from granular material at the tips. Ejected mucocysts are uniform in structure and consist of an inner tube with helical striations, an outer tube with a diamond-shaped pattern, and a dense middle band. Fine fibrils, visible only after mucocyst discharge, emanate from the tips. Mucocysts may also protrude through the pellicle and discharge mucilaginous materials into the medium. Acid phosphatase activity is localized within the subpellicular mucocysts, suggesting that they may be involved in release of hydrolytic enzymes into the medium.     

Development of excretory organs in <Emphasis Type="Italic">Phoronopsis harmeri</Emphasis> (Phoronida): From protonephridium to nephromixium

Larval protonephridia appear as paired ectodermal invaginations on the posterior body end of the larva (actinotrocha), at early stages of its development. The protonephridium of the early actinotrocha has a straight canal and one group of solenocytes distally. The protonephridium of the late actinotrocha has a U-shaped canal and two (upper and lower) groups of solenocytes. After metamorphosis, solenocytes degenerate and the canal is connected with metacoel. The metanephridial funnel is formed from the upper metacoelomic wall epithelium and the lateral mesentery. The definitive nephridium consists of two parts: the ectodermal canal (derived from the protonephridial canal) and the mesodermal funnel, a derivative of the coelomic epithelium. Thus, the phoronid excretory organ is a nephromixium. Consecutive stages of the evolution of nephridia in phoronids are discussed.     

A structural comparison of cyst and germ tube wall inPhytophthora palmivora

Summary An electron microscopic analysis of germinating cysts ofPhytophthora palmivora involving freeze-etching, thin sectioning, and replica techniques reveals that both cyst and hyphal wall comprise a two-phase system with a fibrillar and an amorphous component. The cyst wall is fibrillar throughout with the fibrils tightly interwoven and embedded in an amorphous matrix on the internal side of the wall. The hyphal wall consists of a fibrillar inner layer with the fibrils lightly covered by some amorphous material and an amorphous outer layer devoid of any fibrillar material. Both cyst and germ tube walls are wholly or partially covered by a fluffy coat of variable thickness. In the zone of germ tube emergence cyst wall and germ tube wall overlap and are tightly apposed. Thus, the germ tube wall is not a simple extension of the cyst wall but a new structural entity separated from the cyst wall by a thin line of demarcation.     

A new species of Spirobrachia (Pogonophora) from the Orkney Trench (Antarctica)

Spirobrachia orkneyensis sp. nov. is described from the Orkney Trench to the east of the South Orkney Islands from a depth of 6130–6420 m. It differs from the congeneric species S. grandis (Ivanov 1952) and S. leospira (Gureeva 1975) in the structure of the tube, i.e. shorter segmental collars, peculiarities of their arrangement throughout the tube, and multi-layered, light-coloured tube wall with wrinkles in its inner layers. Also, the wings of the spermatophores of the new species are much larger than those of the two other species of the genus, while most other size characteristics, including the length of the spermatophores, the size of the cuticular plaques, the number of the tentacles and the diameter of the tube, are intermediate between those of S. grandis and S. leospira. A key to the genera and species of the family Spirobrachiidae is provided. Accepted: 31 January 2000     

The Reissner's Fiber Termination in Some Lower Chordates

The caudal end of the neural tube of the tunicate Oikopleura, the cephalochordate Branchiostoma and newly hatched fry of the clupeiform teleosts Clupea, Engraulis and Sardinops was studied by means of the electron microscope. In Oikopleura and the teleost larvae either Reissner's fiber or an amorphous mass of fiber substance leaks out of the neural tube into the surrounding tissue spaces. In Branchiostoma the disintegrated fiber material is apparently engulfed by the caudal ependymal cells. A relationship seems to exist between the degree of fiber disintegration within the neural tube and the degree of specialization of the caudal neural tube ependymal cells, the two extremes being represented by Branchiostoma with a “closed” Reissner's fiber system with highly specialized caudal ependymal cells and a teleost fry with the intact fiber leaving the neural tube between almost undifferentiated ependymal cells. These observations on lower chordates are in accordance with the hypothesis that Reissner's fiber acts as a detoxicator for the neural tube fluid.     

Structure of wall layers in Selaginella kraussiana microspores (Lycophyta)

A similarity was found in both construction and ultrastructure between the two exospore layers in microspores of Selaginella kraussiana. The exospore is made up of two different kinds of rods. One of the kinds of rods are large, 100–150 nm in width, while the other are tubular rods 10–15 nm in diameter. The large rods are wider at the base of the spines than in the upper part, possibly due to flattening or compression. Both the outer and the inner exospores have a stranded surface that is very pronounced in the microspores of this species. Fibrous strands persisting the scanning electron microscope and transmission electron microscope (TEM) fixations were observed on the spore surface proximally and through perforations (exospore channel openings). This net of fibres penetrates and fills the space of the cavities within large channels through the outer and inner exospore and within the gap. According to our interpretation, these strands would be produced by the tapetum and are probably related to the nourishment of the developing microspores. Contrast varies in TEM sections after cytochemical stains, but this appears to be due to transitory substances, e.g. carbohydrates, rather than to be a substantial difference in basic composition between inner and outer exospore layers.     

Ultrastructure of the lycophora larva of Gyrocotyle urna (Cestoda,Gyrocotylidea)

Summary The ultrastructure of the protonephridial system of the lycophore larva of Gyrocotyle urna Grube and Wagener, 1852, is described. It consists of six terminal cells, at least two proximal canal cells, two distal canal cells and two nephridiopore cells. The terminal cells and the proximal canal cell build up the filtration weir with its two circles of weir rods. The proximal canal cell constitutes a solid, hollow cylinder without a cell gap and desmosome. The distal canal cell is characterized by a strong reduction of the canal lumen by irregularly shaped microvilli. The nephridiopore region is formed by a nephridiopore cell; its cell body is located at some distance proximally within the larva. The connection among different canal cells is brought about by septate desmosomes. Morphological, evolutionary and functional aspects of the protonephridial system within Platyhelminthes are discussed. The structure of the proximal canal cells without a desmosome is considered an autapomorphy of Cestoda.Abbreviations ci cilia of the terminal cell - Co distal canal cell - col lumen of the distal canal cell - Ep epidermis - er outer rods of the filtration weir - il inner leptotriches - ir inner rods of the filtration weir - ld lipid droplets - mt microtubule - mv microvilli - Nc nephridiopore cell - Ne neodermis anlage cells - nu nucleus - pC proximal canal cell - ro ciliary rootlets - sd septate desmosome - Tc terminal cell     

The Mouth Cone and Mouth Ring of Echiniscus viridissimus Peterfi, 1956 (Heterotardigrada) with Comparisons to Corresponding Structures in Other Tardigrades

The mouth cone and mouth ring of the tardigrade Echiniscus viridissimus are described and their primary homology is assessed by comparing them to structures considered to be homologous in other heterotardigrades, eutardigrades, and ecdysozoans. In E. viridissimus the mouth cone is divided into anterior and posterior regions that differ in the ultrastructure of their cuticle. The mouth ring of the buccopharyngeal apparatus lies just anterior to the buccal tube. It is connected to it by a narrow flange or ridge of cuticle that allows the rostral end of the mouth tube to telescope part way into the mouth ring. Sensilla innervating the mouth cone and mouth ring in E. viridissimus correspond to sensilla of the circumoral and suboral sensory regions described for eutardigrades. The sensory fields, of both the mouth cone and mouth ring, exhibit two planes of mirror image or biradial symmetry. Although the relative dimensions of mouth ring differ markedly between E. viridissimus and eutardigrades, homologous areas can be identified easily. For example, the supporting rods of the mouth ring in E. viridissimus appear to be homologous to the supporting plates in the lamellae of eutardigrades. The widespread occurrence of the mouth cone and mouth ring in hetero- and eutardigrades suggests that these structures were present in the last common ancestor of all tardigrades. Expression of these characters in other ecdysozoans is more problematic. Tentatively the mouth cone and mouth ring are considered to be homologous to the circumoral plates of onychophorans and the ring of radiating plates found in the ‘Peytoia’ apparatus of Cambrian arthropods. These structures are not thought to be homologous to the introverts of scalidophorans or the circumoral structures of nematodes or nematomorphs, and are considered to be absent in these taxa. Thus, the mouth cone and mouth ring are potentially key synapomorphies for Panarthropoda.     

The feeding activity of Echinostrephus molaris (de Blainville) in the central red sea

Echinostrephus molaris (de Blainville) is a small Indo‐pacific echinoid which burrows in coral reef limestone. Normally individuals do not leave the burrows so they cannot graze on algae growing around the burrow mouth. E. molaris catches floating algal particles with its long aboral spines. When a particle touches one of these organs or a tube‐foot in the area, the surrounding spines converge and grip it. Captured fragments are lowered to the test by further tube‐foot and spine action and are then passed across the ambitus towards the mouth. They are held by the oral tube‐feet and the shorter curved oral spines which aid ingestion. The behavioural and structural modifications shown for this habit are discussed. Burrowing and particle collecting have allowed E. molaris to occupy a particular niche on the reef. A similar method of food gathering is reported for Echinometra mathaei (de Blainville).     

Experimental Colonization and Alteration of Orthopyroxene by the Pleomorphic Bacteria Ramlibacter tataouinensis

The colonization of orthopyroxene crystals by a pleomorphic bacterium and the mineralogical products resulting from a prolonged interaction have been studied. We used Ramlibacter tataouinensis (strain TTB310), which is an aerobic β-Proteobacterium moving over surfaces by gliding motility and whose life cycle includes rods and spherical cysts. Analysis of cultures grown on solid media with micrometer-sized pyroxene and quartz crystals scattered over the surface revealed a taxis of the bacteria toward the crystals. Given the mineralogical non-specificity of the interaction, a mechanism of elasticotaxis is inferred. After the rods had adhered to the pyroxene surface, they differentiated into cysts leading to the formation of microcolonies that were centered on a crystal grain. This suggests an original coupling between the life cycle of R. tataouinensis and the interaction with the crystals. The alteration of orthopyroxene was studied by high-resolution transmission electron microscopy at the interface between cysts and pyroxene crystals. The pyroxene surface showed an amorphous layer that was more developed than that of abiotic control samples processed under the same conditions. Moreover, chemical analyses showed that the dissolution of pyroxene was reduced in the presence of R. tataouinensis. The origin and the significance of the amorphous layers is discussed.