The rhizocephalan Sacculina shiinoi sp. nov. parasitizes three species of Upogebia in Japan. It is described morphologically and compared with another Upogebia parasite, Sacculina upogebiae Shiino, ...1943 from Japan and Korea. These two species are the only sacculinids that parasitize mud shrimps. DNA analyses clearly show the two species to be separate and not closely related. The cuticle differs in being provided with close-set, branched, and spiny excrescences in S. shiinoi, while it lacks excrescences, but forms small scales in S. upogebiae. In S. upogebiae, the bulbous sperm-producing part and the narrow receptacle duct are separated by a compartmentalized mid portion, which is missing in S. shiinoi. A ridge, having a thickened, fluffy cuticle with a U-shaped course, passes across the visceral mass between the two receptacle openings in S. shiinoi. Such a structure has never been described in other rhizocephalans, and its function is uncertain.
A morphological study revealed that the NW American soft-bottom bivalve Nutricola tantilla is dioecious, not a protandric hermaphrodite as previously reported. We base this conclusion on the smaller ...males having highly specialized, glandular sperm ducts, while the larger females have simple oviducts and no transition between the two ducts occurs. The females are brooders and retain their ova in a marsupium within the dorsal part of the inner demibranchs. Sperm cells were present and associated with a mesh-like tissue among the ova or early-stage embryos. How this tissue originates is still unknown. We suggest that sperm cells dissociate from this pool and fertilize the oocytes as soon as they are ovulated. The mode of sperm storage in N. tantilla represents a unique case in that the sperm are presumably nurtured within a nonepithelial tissue. We describe the ultrastructure of the sperm cells in N. tantilla. Large, spherical cytophores become associated with a multitude of acrosomes of spermatozoa and probably represent the precursors of the spermatozeugmata that have been described previously.
Three kidney systems appear during vertebrate development: the pronephroi, mesonephroi and metanephroi. The pronephric duct is the first or primary ureter of these kidney systems. Its role as a key ...player in the induction of nephrogenic mesenchyme is well established. Here we investigate whether the duct is involved in urine modification using larvae of the freshwater amphibian Ambystoma mexicanum (axolotl) as model.
We investigated structural as well as physiological properties of the pronephric duct. The key elements of our methodology were: using histology, light and transmission electron microscopy as well as confocal laser scanning microscopy on fixed tissue and applying the microperfusion technique on isolated pronephric ducts in combination with single cell microelectrode impalements. Our data show that the fully differentiated pronephric duct is composed of a single layered epithelium consisting of one cell type comparable to the principal cell of the renal collecting duct system. The cells are characterized by a prominent basolateral labyrinth and a relatively smooth apical surface with one central cilium. Cellular impalements demonstrate the presence of apical Na+ and K+ conductances, as well as a large K+ conductance in the basolateral cell membrane. Immunolabeling experiments indicate heavy expression of Na+/K+-ATPase in the basolateral labyrinth.
We propose that the pronephric duct is important for the subsequent modification of urine produced by the pronephros. Our results indicate that it reabsorbs sodium and secretes potassium via channels present in the apical cell membrane with the driving force for ion movement provided by the Na+/K+ pump. This is to our knowledge the first characterization of the pronephric duct, the precursor of the collecting duct system, which provides a model of cell structure and basic mechanisms for ion transport. Such information may be important in understanding the evolution of vertebrate kidney systems and human diseases associated with congenital malformations.
Directional asymmetry (DA) of the lengths, diameters, and masses of the scapula, humerus, radius, and ulna were analyzed on a sample of 213 harbor porpoises from Denmark and West Greenland. The ...levels of DA were consistent across yearlings and older animals, mature and immature animals, sexes, and populations. All investigated variables showed significant DA favoring the right side. For the pooled sample, DA of lengths ranged from 0.2% SE 0.1 (ulna) to 1.2% SE 0.1 (scapula). DAs of diameters were 1.5% SE 0.2 for the humerus, 0.6% SE 0.1 for the radius, and 1.3% SE 0.2 for the ulna. DA of mass ranged from 2.8% SE 0.5 (humerus) to 4.3% SE 0.7 (ulna). The humerus and ulna had significantly larger mean diameter/ length ratios on the right side than the left, making them more robust. The large DA of scapula length indicates larger muscle mass associated with the right flipper, while the generally more robust right humerii and ulnae may be designed for higher levels of mechanical stress. These DAs and the examples of lateralized behavior recorded in cetaceans, point to the existence of lateralized use of the flippers at the population level in harbor porpoises and possibly other cetacean species.
Males and females of the commensal protandric bivalve
Pseudopythina subsinuata have paired seminal receptacles, the interior of which contains many slender elongate cells. The testis produces small ...euspermatozoa and comparatively few and much larger paraspermatozoa. The ⩽16-μm-long and 3–5-μm-thick paraspermatozoa have a terminally placed irregularly cork-screw-shaped acrosome and a bundle of ca. 16 flagella emerging from behind the nucleus. The role of the paraspermatozoa is obscure. Euspermatozoa are transferred to the seminal receptacles of the females and attach with the tip of the acrosome to the elongate cells. Most females contain one to three “sperm trees”, structures consisting of a short stem and numerous branches. They are firmly implanted in the abfrontal part of the gill filament and protrude into the posterior part of the suprabranchial (brooding) chamber. Implantation of the trees causes the gill tissue to swell around the stem and some of the nearest filaments to coalesce. All branches are densely coated with euspermatozoa that are attached by means of their acrosomes. It is conjectured that the syncytial and multinucleate trees arise from seminal receptacle cells that detach from the receptacle and thereupon fuse. A similar process is known in the allied
P. tsurumaru, but the resulting structure (“sperm-carrying body”) is not attached to the gills.
In
Cristatella mucedo
spermiogenesis occurs in a morula consisting of a large number of spermatids connected with a central cytophore. The mature sperm cell is filiform and consists of a head, a ...midpiece and a tail region, the latter two separated by a deep circular constriction. The comparatively short head contains a drop-shaped, bilaterally symmetrical and pointed nucleus capped by a minute acrosome. The single centriole is placed in a deep posterior invagination of the nucleus followed by the axoneme with the typical 9 + 2 pattern. The elongated midpiece is 0.9–1.1 μm thick and contains several helices of mitochondria surrounding the axoneme. The tail is thicker (1.3 μm) and richer in cytoplasm with many compact accumulations of an electron-dense substance lying peripherally and another less dense material wrapped around the axoneme. The course of the spermiogenesis and the fine structure of the sperm are very similar to that of
Plumatella fungosa
. Comparison with other species shows that the same sperm type is recognizable in four of the five families of Phylactolaemata and, provided it occurs also in the fifth family, the Stephanellidae, is a synapomorphy of the entire class.
The position and structure of paired ‘lateral organs’ in the foot of Arthritica semen and Arthritica bifurca might indicate a chemosensory function. In both species part of the organ is also ...glandular. In A. semen the glandular epithelium is detached piecemeal and, probably by means of the foot, is moved to and grafted upon the gills of the same individual. The transferred epithelia appear as disk‐shaped actively secretory ‘gill bodies’ which, attached to the abfrontal side of the inner demibranch, replace the ordinary unciliated gill epithelium. The secretion is liberated into the suprabranchial chamber, which serves as a marsupium, but its function is uncertain. Arthritica semen is a protandric hermaphrodite and produces very large ova that undergo a direct development that results in a non‐planktonic lecithotrophic crawling juvenile stage. The sperm cells have filiform nuclei that are straight in the euspermatozoa and more or less helicoidal in what is considered to represent paraspermatozoa. By a process of aggregation, spermatozeugmata are formed which consist exclusively either of euspermatozoa or paraspermatozoa. Spermatozoa are stored in the oviduct in A. semen but in paired seminal receptacles in A. bifurca.
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