Spermiogenesis,sperm structure and fertilization in the palaeonemertean Cephalothrix rufifrons (Nemertini,Anopla)

Summary The spermatozoan from testes of Cephalothrix rufifrons consists of an elongated, straight head 13–14 m long with a flattened anterior acrosome and a 12.5-m-long nucleus. Placed along one side of the nucleus, is a single tubular 7-m-long mitochondrion. There is no midpiece, but immediately posterior to the nucleus are two centrioles. The tail is at least one and a half times the length of the head. Mature sperm cells were also found in the oviducts of mature females which, combined with the modified structure of the sperm cell, indicates that sperm is transferred during pseudocopulation.Abbreviations A acrosome - C centriole - D gonoduct - DC distal centriole - E epidermis - F flagellum - I intestine - LM longitudinal muscle layer - L lateral nerve - M nitochondrion - MT microtubules - N nucleus - O oocyte - PC proximal centriole - R rhynchocoel - S spermatozoa - SC spermatocyte - SP spermatid     

Ultrastructure of spermatids and spermatozoa in the cyclostomatous bryozoan Tubulipora (Bryozoa,Cyclostomata)

Summary Differentiation of spermatids to mature spermatozoa in the bryozoan Tubulipora liliacea was studied by transmission electron microscopy. The spermatozoon of Tubulipora is of a filiform, modified type, and has evolved from the primitive type as an adaptation to a specialized biology of fertilization. The head of the spermatozoon consists of a small, conical acrosome capping an elongated, cylindrical, anteriorly tapering nucleus. A basal invagination in the nucleus contains the proximal portion of the axoneme and a dense attachment matrix. The flagellar axoneme has the typical 9+2 structure. Four elongated rodshaped mitochondria with typical cristae surround the axoneme in the cylindrical middle piece. Granular electron-dense material is accumulated in the form of four columns alternating with four long cylindrical mitochondria. The mitochondrial middle piece is separated externally from the tail region by an involution of the plasma membrane. The tail region contains a cytoplasmic sheath with accessory fibers surrounding the axoneme. Nine outer, coarse fibers extend posteriorly paralleling the nine doublets of the axoneme. The coarse fibers develop from electron-dense plate-like structures associated with the doublets of the axoneme. A characteristic feature in spermiogenesis is that spermatozoa develop in tetrads. There seem to be significant differences in spermatozoan ultrastructure between the three bryozoan classes Stenolaemata, Gymnolaemata, and Phylactolaemata. The differences indicate different lines of evolution of fertilization biology in these groups.Abbreviations used in the figures a acrosome - av acrosomal vesicles - ax axoneme - c coarse fiber - d electron dense rod - m mitochondrion - mp middle piece - Scale bars=0.5 m - mt microtubule - n nucleus - ne nuclear envelope - p nuclear protrusion - pm plasma membrane - t tail     

Ultrastructure of the mature spermatozoon of the musky rat-kangaroo, Hypsiprymnodon moschatus (Potoroidae: Marsupialia)

It is currently accepted that Hypsiprymnodon moschatus is a basal macropod, retaining several primitive features from the ancestral phalangeroid that gave rise both to modern possums and macropods. Sperm ultrastructure is frequently found to provide informative characters for phylogenetic analysis as these features are not strongly selected for and are thus unlikely to be confounded by effects such as convergence. Caudal epididymal biopsies were taken from two male H. moschatus and prepared for transmission and scanning electron microscopy in order to study mature spermatozoan ultrastructure. Within the diprotodont group, several features were found to be unique to H. moschatus. These were an unusual acrosome covering nearly 100% of the dorsal nuclear surface, a midpiece fibre network which is loose, indistinct and extends to the anterior‐most aspect of the midpiece, a nucleus that is very streamlined, while the principal piece is comparatively short, and a mitochondrial helix and annulus which are similar to those of dasyurids. Also reported is the presence of a fibrous network in the connecting piece, not previously reported for any marsupial.     

Comparative study of sperm ultrastructure of Donax hanleyanus and Donax gemmula (Bivalvia: Donacidae)

The ultrastructure of bivalve spermatozoa can be species‐specific and often provides important taxonomic traits for systematic reviews and phylogenetic reconstructions. Young individuals of the Donacidae species Donax hanleyanus are often identified as samples of Donax gemmula. Hence, the spermatozoa ultrastructure of both species was described in the present work, aiming to identify characters that could be useful for further taxonomic and phylogenetic analyses. D. hanleyanus and D. gemmula spermatozoa were different especially in relation to acrosomal characteristics and chromatin condensation. The spermatozoon produced by D. hanleyanus had a nucleus (exhibiting granular chromatin with a rope‐like appearance) capped by a long and conical acrosomal vesicle, which extended itself outward beyond the anterior nuclear fossa. Otherwise, the nucleus of the sperm cell of D. gemmula showed well‐compacted chromatin, and its acrosome, which was partially inserted into the anterior nuclear fossa, had a bubble‐like tip. In conclusion, the conspicuous ultra‐structural differences found between the spermatozoan morphologies were helpful for the discrimination of the species. In conclusion, our results suggest that analyses of sperm ultrastructure of the bivalves in the family Donacidae can be valuable to investigate their taxonomic relatedness. The present results also contribute to assess the monophyletic status of the family.     

Ultrastructure and Phylogenetic Significance of Notaspidean Spermatozoa (Mollusca, Gastropoda, Opisthobranchia)

Spermatozoa of five notaspidean opisthobranchs [Berthellina citrina, Berthella ornata, Pleuro-branchus peroni, Pleurobranchaea maculata, Umbruculum sinicum] were examined using TEM. In all five species, the acrosome (sensu lato) consists of an apical vesicle (the acrosomal vesicle) and acrosomal pedestal. The acrosomal pedestal overlaps the nuclear apex, and in P. peroni (and possibly B. ornata) is periodically banded—-the first reported incidence of this type of substructure in any euthyneuran acrosome. Although sperm nuclei of P. peroni, B. ornata and B. citrina differ in length and also the number of keels present (nucleus 7 μm long with four/five keels present in Pleurobranchus; 17 μm long with one keel in Berthella; 15 μm long with a very weak keel in Berthellina), the basal invagination to which the centriolar derivative, axoneme and coarse fibres are attached is always poorly developed, and very little overlap between nucleus and midpiece occurs. In P. maculata and U. sinicum, the nucleus forms a helical cord around the axoneme and mitochondrial derivative such that it is not possible to recognize exclusively ‘nuclear’ and ‘midpiece’ regions of the spermatozoon. In all notaspideans investigated, (1) the axoneme, coarse fibres and glycogen helix are enclosed by the paracrystalline and matrix components of the mitochondrial derivative and (2) a dense ring structure (attached to the plasma membrane) and glycogen piece are observed. While the glycogen piece is very short (0.85–1.43 μm) with a very degenerate axoneme in B. citrina, B. ornata and P. peroni, this region of the spermatozoan is well developed (30–35 μm long) in U. sinicum and exhibits a fully intact 9 + 2 axoneme. The ‘glycogen piece’(or its presumed homologue) in P. maculata spermatozoa is very short (0.65 μm), devoid of any axonemal remnant and constructed of a hollow, internal cylinder attached to an outer (incomplete) shell, and contains scattered (glycogen) granules. Spermatozoal structure supports a close relationship between the genera Berthellina, Berthella and Pleurobranchus. These three genera have more distant links with Pleurobranchaea, while Umbraculum maintains an isolated, specialized position within the Notaspidea.     

Ultrastructure of spermatogenesis and mature spermatozoa in the flatworm Prosthiostomum siphunculus (Polycladida,Cotylea)

This is the first study investigating spermatogenesis and spermatozoan ultrastructure in the polyclad flatworm Prosthiostomum siphunculus. The testes are numerous and scattered as follicles ventrally between the digestive ramifications. Each follicle contains the different stages of sperm differentiation. Spermatocytes and spermatids derive from a spermatogonium and the spermatids remain connected by intercellular bridges. Chromatoid bodies are present in the cytoplasm of spermatogonia up to spermatids. During early spermiogenesis, a differentiation zone appears in the distal part of spermatids. A ring of microtubules extends along the entire sperm shaft just beneath the cell membrane. An intercentriolar body is present and gives rise to two axonemes, each with a 9 + “1” micro‐tubular pattern. Development of the spermatid leads to cell elongation and formation of a filiform, mature spermatozoon with two free flagella and with cortical microtubules along the sperm shaft. The flagella exit the sperm shaft at different levels, a finding common for acotyleans, but so far unique for cotylean polyclads. The Golgi complex produces numerous electron‐dense bodies of two types and of different sizes. These bodies are located around a perinuclear row of mitochondria. The elongated nucleus extends almost along the entire sperm body. The nucleus is wide in the proximal part and becomes narrow going towards the distal end. Thread‐like chromatin mixed with electron‐dense intranuclear spindle‐shaped bodies are present throughout nucleus. The general sperm ultrastructure, the presence of intranuclear bodies and a second type of cytoplasmic electron‐dense bodies may provide characters useful for phylogenetic analysis.     

Fine structure of the germinating cells during the spermiogenesis of Arion rufus (Mollusca,Pulmonate Gastropoda)

Changes in spermatozoan ultrastructure have been studied during spermiogenesis of the slug Arion rufus (Gastropoda, Pulmonata, Stylommatophora). The ovotestis was investigated during the male stage, definite by the presence of spermatozoa. Some peculiar characteristics are shown by early spermatids: Around the nucleus, the nuclear envelope presents two thick layers located on opposite sides, the apical and basal plates, that will determine the antero-posterior axis of the spermatid. The chromatin, first dispersed throughout the nucleoplasm gives later on thick filaments which become attached over the inner surface of these plates. The chromatin filaments are then arranged parallel to the antero-posterior axis as the nucleus elongates. The position of the plates determines the antero-posterior axis of the spermatid. In the mature spermatozoa, the chromatin is more condensed and the nucleus presents an helical organization. The acrosome and flagellum are respectively attached externally to the center of the apical and basal plates. The acrosome consists of a membrane-bound vesicle and forms a column of homogeneous material. In the middle piece, the mitochondria have been transformed into a mitochondrial derivate by the way of a complicated metamorphosis. The axoneme is surrounded by three mitochondrial helices but only one of them contains glycogene granules. © 1996 Wiley-Liss, Inc.     

Fine Structure of Spermiogenesis in Eastern Pacific Species of Hagfish (Myxinidae)

Abstract Spermiogenesis in Eptatretus stoutii, E. deani and E. sp. display great similarities. Minor differences appear in the acrosomal structure. The spermatozoan has a long middle piece in which the axonema is surrounded by a sheath, consisting of a very few mitochondria, a feature usually associated with internal fertilization.     

Spermatozoan ultrastructure and mitochondrial gene sequence of Caryocorbula caribaea (d'Orbigny, 1853) (Corbulidae: Bivalvia), a species with plasticity in shell morphology

Systematics of Corbulidae supported by anatomical and conchological studies remains confused and controversial because of the considerable phenotypic plasticity of their shells. Ultrastructural spermatozoan study and molecular analyses have been performed to contribute valuable information, which could be used in taxonomy. Electron microscopy was used to analyse sperm cells from specimens of Caryocorbula (Gardner, 1926) exhibiting shell differences. The spermatozoon was of the aquasperm type, showing short acrosome, barrel-shaped nucleus, midpiece composed of four spherical mitochondria and simple flagellum. In addition, about 860?base pairs of mitochondrial large ribosomal subunit (16S rRNA) were sequenced from each individual. The consistent similarity shared by spermatozoa and DNA sequences from all studied specimens indicated that they belonged to one coherent unit, Caryocorbula caribaea (d'Orbigny, 1853), despite the extraordinary plasticity exhibited by their shells.     

Fine structure of Lasaea subviridis and Mysella tumida sperm (Bivalvia,Galeommatacea)

Summary Lasaea subviridis and Mysella tumida sperm resemble the primitive spermatozoan type, but exhibit several unique morphological features. L. subviridis sperm heads vary in shape and size owing to differing degrees of nuclear condensation. A fully mature, heterogenous acrosomal vesicle with an associated axial rod is present. Up to 50% of L. subviridis sperm in developing gonads have conspicuously angled flagella that propel the sperm cells in irregular helical paths. This may represent a penultimate stage in sperm development because the remainder of the sperm cells have posteriorly-directed flagella and swim in a nonhelical anterior direction. A trend toward a reduction in both nuclear condensation and swimming ability may be a long-term consequence of increasing degrees of localized, but non-internal self-fertilization in marine invertebrates that brood. Mysella tumida sperm are monomorphic and possess numerous microvilli (30–60 nm in diameter and up to 5.7 m in length) that resemble stereocilia and radiate from the cell membrane surrounding the basal body. In this species, the sperm cell does not have an axial rod, and the complex acrosomal vesicle contains five distinct zones of varying electron opacity. One of these zones is a transverse, electron-opaque band that is apparently composed of rolled-up membrane. Following acrosomal breakdown, this membrane unfolds to cover the anterior tip of the sperm cell. Although both L. subviridis and M. tumida are hermaphroditic, the relative size of their male investments is conspicuously different. Approximately 40–50% of the M. tumida gonadal volume is testis compared with about 5% of that in L. subviridis.     

Ultrastructure of the nephridio-circulatory connections in Tubulanus annulatus (Nemertini,Anopla)

Summary The protonephridial terminal organs in the nemertean Tubulanus annulatus form an integral part of the blood vessel wall. Both endothelial and muscle-cell layers of the vessel's wall are discontinued at the site of each terminal organ. The terminal organs are usually composed of from one to three terminal cells enclosing a central lumen provided with many microvilli and separated from the blood vessel's lumen by a membranous filtration area. The latter is perforated by numerous winding clefts formed by interdigitation of minute cytoplasmic pedicels arising from processes issued by each of the involved terminal cells. Ultrafiltration of blood plasma takes place across a filtration membrane which spans the cleft system and the basal lamina of the terminal cells. Fluid is propelled into the lumen of the terminal organs through the activity of ciliary bundles, one for each terminal cell involved, perhaps supplemented by vascular turgor. All efferent conduits of the protonephridium have profuse infoldings of the luminal cell surfaces and/or numerous pinocytotic pits suggestive of reabsorption of substances from the primary urine.Abbreviations BL basal lamina - C cilium - CP coated pit - CT collecting tubule - CV inzcoated vesicle - D dictyosome - E endothelial cell - F fenestration of endothelial cell - FA filtration area - FM filtration membrane - G glycogen granule - LV lateral vessel - M mitochondrion - MC muscle cell - MV microvillus - N nucleus of terminal cell - NE nucleus of endothelial cell - NP nephridiopore - PC protonephridial capillary cell - PT protonephridial tubule - R rootlet - TC terminal cell     

Megasporogenesis,megagametogenesis, and embryogenesis in Dendrobium nobile (Orchidaceae)

The orchid reproductive strategy, including the formation of numerous tiny seeds, is achieved by the elimination of some stages in the early plant embryogenesis. In this study, we documented in detail the formation of the maternal tissues (the nucellus and integuments), the structures of female gametophyte (megaspores, chalazal nuclei, synergids, polar nuclei), and embryonic structures in Dendrobium nobile. The ovary is unilocular, and the ovule primordia are formed in the placenta before the pollination. The ovule is medionucellate: the two-cell postament and two rows of nucellar cells persist until the death of the inner integument. A monosporic eight-nucleated embryo sac is developed. After the fertilization, the most common central cell nucleus consisted of two joined but not fused polar nuclei. The embryogenesis of D. nobile is similar to the Caryophyllad-type, and it is characterized by the formation of all embryo cells from the apical cell (ca) of a two-celled proembryo. The only exception is that there is no formation of the radicle and/or cotyledons. The basal cell (cb) does not divide during the embryogenesis, gradually transforming into the uninuclear suspensor. Then the suspensor goes through three main stages: it starts with an unbranched cell within the embryo sac, followed by a branched stage growing into the integuments, and it ends with the cell death. The stage-specific development of the female gametophyte and embryo of D. nobile is discussed.

     

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     

SEXUAL REPRODUCTION,MATING SYSTEM,AND PROTOPLAST DYNAMICS OF SEMINAVIS (BACILLARIOPHYCEAE)1

Cell division, the mating system, and auxosporulation were studied in the marine epipelic diatom Seminavis cf. robusta Danielidis & D. G. Mann. The interphase protoplast contains two girdle‐appressed chloroplasts, each with an elongate bar‐like pyrenoid, and also a central nucleus, located in a bridge between two vacuoles. Before cell division, the chloroplasts divide transversely and translocate onto the valves. The nucleus relocates to the ventral side for mitosis. After cytokinesis and valve formation, the chloroplasts move back to the girdle, showing a constant clockwise movement relative to the epitheca of the daughter cell. Seminavis cf. robusta is dioecious, and sexual reproduction is possible once cells are less than 50 μm. In crosses of compatible clones, gametangia pair laterally, without the formation of a copulation envelope, and produce two gametes apiece. The intensity of sexualization increases as cells reduce further in size below the 50‐μm threshold. At plasmogamy, the gametangia dehisce fully and the gametes, which were morphologically and behaviorally isogamous, fuse in the space between the gametangial thecae. The auxospore forms a transverse and longitudinal perizonium. After expansion is complete, there is an unequal contraction of the protoplast within the perizonium, creating the asymmetrical shape of the vegetative cell. Apart from this last feature, almost all characteristics exhibited by the live cell and auxospores of Seminavis agree with what is found in Navicula sensu stricto, supporting the classification of both in the Naviculaceae. Haploid parthenogenesis and polyploid auxospores were found, lending support to the view that change in ploidy may be a significant mechanism in diatom evolution.     

The ontogeny of the filter apparatus of anuran larvae (Amphibia,Anura)

Summary The pharynx ofBufo calamita, Rana temporaria andBombina variegata larvae (larval Types IV and III) changes considerably during the latter part of embryonic development. The entodermal regions between the visceral pockets flatten inward to form the anlagen of the filter plates. The ectoderm thrusts forward from the area of the persistent epidermal gills overlying the anlagen of the filter plates. The esophagus pushes dorsolaterally into the pharynx to give rise to the ciliary cushions. Comparison with the development ofXenopus laevis (larval Type I) reveals shared characters: (1) the filter plates are overlapped by the sensory layer of the epiderm and (2) the ciliary grooves are, like the ciliary cushions of larval Types III and IV, anteriorly directed dorsolateral extensions of the esophagus. In all the species studied an ectodermal-esophageal filter apparatus develops. The evolutionary origin of this filter apparatus is discussed. The epidermalization of gills is suggested as a common character with the sister group of Dipnoi, and is therefore a plesiomorphic character in all amphibians. The tendency of filter plate epidermalization is considered to be the end of a process which is also indicated in the epidermalization of the first visceral pouch in lung fish. The ciliary groove is unique in anuran larvae within the Lissamphibia, and is therefore seen as an autapomorphic character within amphibians. On the basis of the different structure of the ciliary cushion inX. laevis and in the other species of this study, two alternative levels of evolutionary ciliary groove origin are discussed. Derivation from the esophagus took place: (1) in a common anuran larval ancestor, or (2) at two independent levels; the first in the Pipidae (-Rhinophrynidae) ancestor and the second in the ancestor of all the other anuran families. Several larval characters and cladistic aspects make the first alternative more probable than the second. Larval Type II anatomy and Larval Type II truncation from the Larval Type IV of Ranoidea do not contradict these considerations. There is disproportionately early commencement of ingestion activity inR. temporaria (G Stage 23),B. calamita (G Stage 23), andB. bufo (G Stage 24) compared toXenopus. Feeding in the former three species precedes the differentiation of the filter plates, their mucus production, and the exhaustion of the yolk supply in the gut tissue. By contrast, the goblet cells and the ciliary cells of the ciliary cushions are already differentiated when feeding starts. This suggests that ingestion in these early stages requires mucus production by the ciliary cushions and transport by their ciliary cells. Presumably in fully formed larvae, the ciliary cushions are the mucus donors, whereas the filter plates are the mucus depositors. By contrast,X. laevis does not begin active food intake by suspension feeding until after the yolk supply has been used up from the entoderm of the buccal cavity to deep in the esophagus.Abbreviations AAC anlage of apical cell - AC apical cell - ACE anlage of cerebrum - ACG anlage of ciliary groove - AD aorta dorsalis - ADV anlage of dorsal velum - AG anlage of glottis - AFP anlage of filter plates - AFR anlage of filter rows - AFPC anlage of epidermal fold of peribranchial chamber (anlage of operculum) - ant. anterior - AMF anlage of middle fold - AO adhesive organ - APEG anlage of persistent epidermal gills - APOP anlage of postnarial papilla - APSF anlage of primary side fold - ASC1 anlage of Type 1 secretory cell - ATE anlage of tuba Eustachii - ATEG anlage of transient epidermal gills - AVV anlage of ventral velum - B branchial arch - BI-IV branchial arches I–IV - BFA buccal floor arena - BFT branchial food trap - BL basal lamina - BRA buccal roof arena - C cilium, cilia - CA cartilage of visceral arch - CC ciliary cushion - CE cerebrum, brain - CG ciliary groove - CH choana - CHY ceratohyale - CIC ciliary cell - CL capillary vessel - CN centriole, basal body - COC cuboidal cells - CT connective tissue - CTC connective tissue cell - d dorsal - DV dorsal velum - DVI–III dorsal vela I–III - E esophagus - e early - ED edge of filter plate - EN endothelium - ENC entodermal cell - EP epiderm - EPC epidermal cell - ER endoplasmatic reticulum - ET erythrocyte - ETZ ectodermal-entodermal transition zone - EV ear vesicle - EX merocrine extrusion - EY eye - EZ zone of extrusion - FP filter plate - FPII filter plate of the 2nd branchial arch - FPIV filter plate of the 4th branchial arch - FPC epidermal fold of peribranchial chamber (operculum) - FC filter cavity - FN filter niche - FR filter row - GL glottis - GS gill slit - 1. GS first gill slit - GZ glandular zone - H heart - HP hypobranchial plate - HY hyoid arch - IC intercellular space, enlarged by fixation and dehydration - L late - LJ lower jaw - LT larval type - LV lipid vacuole - M mitochondrion - MA mandibular arch - MF middle fold - med. median - MS microvillous stubs - MZ zone of microtubes - NAC nucleus of apical cell - NCIC nucleus of ciliary cell - NCL nucleus of capillary vessel - NCOC nucleus of cuboidal cells - NCT nucleus of connective tissue - NENC nucleus of entodermal cell - NEPC nucleus of epidermal cell - NO external nares - NPEC nucleus of periderm cell - NRC nucleus of random cell - NSC1 nucleus of Type 1 secretory cell - NSC3 nucleus of Type 3 secretory cell - NSLC nucleus of sensory layer cell - NSPC nucleus of supporting cell - NSQC nucleus of squamous epithelial cell - OC oral cavity - OS mouth - P papilla - PC peribranchial chamber - PCW peribranchial chamber wall - PE periderm - PEC periderm cell - PEG persistent epidermal gill - PG pigment granule - post. posterior - PS primary side fold - PH pharynx - RC random cell - RO rootlet - SC1 Type 1 secretory cell - SC2 Type 2 secretory cell, goblet cell - SC3 Type 3 secretory cell - SC4 Type 4 secretory cell - SG secretory groove - SL sensory layer - SLC sensory layer cell - SP secretory pit - SPC supporting cell - SQC squamous epithelial cell - SR secretory ridge - SRC secretory ridge cell - SS secondary side fold - ST. stage - STD stomodeum - SU spiculum of hypobranchial plate - T tentacle - TA anlage of tongue - TEG transient epidermal gill - TZ transitional zone of branchial food trap and ventral velum - UJ upper jaw - v ventral - VA visceral arch - VC vacuole - VPI–IV visceral pockets I–IV - VP visceral pocket - VV ventral velum - YV yolk vacuoles Supported by the Deutsche Forschungsgemeinschaft (DFG)     

Ultrastructure of the spermatozoid of Lycopodium obscurum (Lycopodiaceae)

Ultrastructural observations reveal that the spermatozoid of Lycopodium obscurum is crescent shaped and contains two posteriorly directed flagella that are inserted at the front of the cell. The nucleus is broad and elongated with a narrow posterior projection or nuclear diverticulum. Spline microtubules (MTs) number 180 at their maximum and provide the framework for the cell. These MTs extend from the anterior of the locomotory apparatus and along the outermost surface of the nucleus, with a central shank of 14–17 MTs encircling the cell for at least one-third gyre beyond the nucleus. The two basal bodies are slightly staggered and positioned at the front of the cell over a highly elongated multilayered structure (MLS). The MLS extends laterally around the cell anterior and curves posteriorly over the nucleus. One large anterior mitochondrion is situated subjacent to the MLS, while numerous small mitochondria are scattered near or among the lobes of the single plastid. The plastid rests on the inner nuclear surface and contains numerous large starch grains. This cell differs from that of L. cernuum, the only other species of Lycopodium examined to date, in that it is more elongated and has an anterior-posterior orientation of the nucleus, basal bodies, MLS, and spline. Comparisons with coiled gametes of bryophytes and Selaginella suggest that some degree of coiling and cell streamlining may be ancestral in archegoniate spermatozoids.     

A comparative analysis of testicular sperm morphology in fossorial and surface-living skinks in South Africa

We described for the first time the spermatozoan ultrastructure of the fully pentadactyl surface-living skink Trachylepis punctatissima, and limbless fossorial skink Acontias meleagris. The spermatozoa of both species follow the general patterns observed within the Squamata. However, several important differences were detected between the two species in the head region (shape of the anterior acrosome, size of acrosome and nucleus) and especially in the midpiece (size of the midpiece, the presence of regular rows of dense bodies, size and number of mitochondria and beginning of the fibrous sheath). Both species shared more characters with the Sphenomorphus + Egernia group than with the Eugongylus group proposed by Jamieson, Oliver, and Scheltinga (Acta Zoologica, 77, 85). Differences in the spermatozoan ultrastructure between T. punctatissima and A. meleagris could be due to distinct ecological and physiological requirements for fertilization, but additional research on these genera and within the Scincidae is required to disentangle this hypothesis, and to disentangle the phylogenetic relationships among skinks.     

Zoospore ultrastructure in species ofTrebouxia andPseudotrebouxia (Chlorophyta)

Zoospore ultrastructure (incl. flagellar apparatus) has been investigated in three species ofTrebouxia (T. glomerata, T. erici, T. pyriformis) and one species ofPseudotrebouxia (P. impressa) using an absolute configuration analysis. Zoospores in all taxa studied are nearly identical in ultrastructure and exhibit a very distinctive disposition of cell organelles: cells are naked, biflagellate and considerably flattened along the plane of flagellar beat, the single contractile vacuole is located anteriorly in the ventral region of the cell, the nucleus is anteriorly to centrally located in the dorsal region of the cell. A single dictyosome is located close to the anterior, ventral edge of the nucleus. The chloroplast occupies a posterior position in the cell and usually has an anterior profile in the left region of the cell. There are two branched mitochondria per cell or a single mitochondrial reticulum with profiles anterior to the nucleus (in the dorsal region of the cell), and posterior to the nucleus. In zoospores ofTrebouxia spp. the posterior mitochondrial profile is associated with a microbody, inP. impressa zoospores the anterior mitochondrial profiles are associated with a microbody. The zoospores contain a distinctive system of three ER-cisternae: one system links to both basal bodies and extends to the nucleus, the other two systems subtend the plasmamembrane on the left and right broad cell surfaces and extend to the posterior region of the cell. The flagellar apparatus is structurally identical to that previously described for zoospores ofFriedmannia israelensis and exhibits basal body displacement by one basal body diameter into the 11/5 o'clock direction, a non-striated distal connecting fiber, a cruciate microtubular root system lacking system I fibers and presence of a single system II fiber which connects the basal bodies with the nucleus and runs parallel to one of the ER-strands. The left flagellar roots (X-roots) are subtended by a complex set of amorphous and striated material that connects each left root with both basal bodies.—This study demonstrates the close systematic relationship between the phycobiontsTrebouxia andPseudotrebouxia and the generaFriedmannia, Pleurastrum, andMicrothamnion and supports recent classification schemes which place all these taxa into a single order separate from otherChlorophyta. Dedicated to Prof. DrElisabeth Tschermak-Woess on the occasion of her 70th birthday.