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.     

Ultrastructure and phylogeny of the spermatozoid ofChara vulgaris (Charophyceae)

At maturity, spermatozoids of the green algaChara vulgaris are biflagellated, contain little cytoplasm, and coil for approximately 2 1/2 gyres within the mother cell wall. The anterior of the cell contains an ovoid headpiece anchoring two slightly staggered basal bodies that are positioned above and directly in front of approximately 30 linearly arranged mitochondria. An elongated stellate pattern occupies the transition zone between the BBs and axonemes. Flagella emerge from the cell just in front of the nucleus and encircle the full length of the spermatozoid. The spline comprises a maximum of 38 microtubules surrounding the anterior mitochondria and gradually decreases posteriorly to a minimum of 11. The dense nucleus is narrow, cylindrical, and occupies the central revolution of the cell. Six starch-laden plastids and associated mitochondria are linearly arranged at the cell posterior. Phylogenetic analyses of charalean taxa and archegoniates based on spermatogenesis strongly support the orderCharales, withNitella as the sister group toChara. Diagnostic features ofChara spermatozoids include absence of a lamellar strip and axonemes embedded in the cell for almost the entire length of the anterior mitochondria. Potential relationships amongCharales, Coleochaetales and archegoniates are evaluated in regards to the probable course of evolution of streamlined biflagellated gametes.     

SPERMATOGENESIS IN COLEOCHAETE PULVINATA (CHAROPHYCEAE): EARLY BLEPHAROPLAST DEVELOPMENT

Transmission electron microscopy of serial thin sections was used to reconstruct several early developmental stages of the blepharoplast in Coleochaete pulvinata spermatids. These were compared to published studies of blepharoplast development in Charales and the closest relatives of charophycean green algae among embryophytes, i.e., hornworts and liverworts. Bicentriolar centrosomes such as occur in bryophytes and fern allies were not observed in Coleochaete. Centriole replication in C. pulvinata was orthogonal as in Charales. The resulting two daughter centrioles were oriented perpendicularly and joined proximally by electron-dense material. Their orthogonal relationship was maintained throughout blepharoplast development by a massive, banded connective which appeared early. In spermatids of hornworts and liverworts, a multilayered structure (MLS) develops in association with two centrioles destined to become flagellar basal bodies. When the MLS of these lower land plants is sectioned at right angles to the long axis of the microtubular layer, the MLS is observed to lie beneath cross sections of both centrioles. In contrast, when developing MLSs of C. pulvinata and Charales are similarly sectioned, they occur beside a cross section of just one of the two centrioles. In C. pulvinata (as in other charophytes), MLS lamellae are oriented at a 90-degree angle to the long axis of the S₁ microtubules from the beginning. This contrasts with the 40–45 degree angle between the MLS lamellae and S₁ microtubules universally reported for archegoniates. In early C. pulvinata spermatids, spline microtubules are closely associated with an anterior mitochondrion having a low stromal density and few cristae. An anterior mitochondrion is typically associated with blepharoplast development in hornworts and liverworts, but has not previously been reported to occur in Coleochaete or any other charophycean alga. In Coleochaete, as in hornworts and liverworts, but unlike Charales, structure of mature blepharoplasts reflects early blepharoplast ontogeny. Very little change in positional relationships among blepharoplast components (flagella, connective, MLS) occurs during development. These character-state differences are of importance in cladistic analyses of charophycean algae and lower land plants.     

Ultrastructural studies of spermatogenesis in the anthocerotales. III. Gamete morphogenesis: From spermatogenous cell through midstage spermatid

An ultrastructural examination of spermatogenesis in Phaeoceros has shown nucleoli to be present in spermatogenous cells and to persist until the centrioles become associated with nuclei of young spermatids. At the onset of multilayered structure (MLS) formation, well-defined aggregations of osmiophilic strands begin to form in the nuclei of young spermatids and disappear shortly after chromatin condensation starts in the midstage spermatids. When the centrioles in the young spermatids are orientated perpendicular to the nuclear envelope, the nucleoplasm immediately in front of them is densely stained. Where the spline tubules of the MLS extend over the nucleus, the nuclear envelope is devoid of pores, and the inner nuclear membrane is contacted internally by the local deposition of dense staining nucleoplasm. Chromatin condensation begins with strands extending perpendicularly from the dense staining nucleoplasm beneath the spline and continues with the nuclear beak becoming filled with condensed chromatin. As the MLS lamellae disappear acropetally, the rear portion of the anterior mitochondrion (AM) extends back under the nuclear beak which now narrows to a size that approximates the anterior end of the nucleus of a spermatozoid. By the end of the mid-spermatid stage, the nucleus has coiled approximately one gyre of a helix and the five or six central slpine tubules extend over the plastid which is now located beneath the front end of the AM. Several profiles of endoplasmic reticulum confluent with the nuclear envelope are present. Possible factors which might play a role in determining the morphology of the mid-spermatids are discussed.     

THE OCCURRENCE AND PHYLOGENETIC SIGNIFICANCE OF A MULTILAYERED STRUCTURE IN COLEOCHAETE SPERMATOZOIDS

Spermatozoid-forming cells of Coleochaete scutata were found in packets of four arranged in concentric internal bands. Spermatozoids, which occur singly in antheridial cells, are spherical to ovoid, approximately 7 μm long by about 3.9 μm wide. As compared to relatively unspecialized zoospores, male gametes undergo a number of specialized cellular changes during development. The spherical nuclei and cytoplasm of mature spermatozoids are increased in density. Posterior plastids are reduced and contain large starch grains. Many small mitochondria are clustered near the cell anterior. The plasmalemma is covered with a layer of flattened, diamond-shaped scales, while body scales of zoospores are pyramidal. The two flagella of both zoospores and spermatozoids are covered with flattened, diamond-shaped scales and hairs. The spermatozoids contain an anterior multilayered structure (MLS) structurally similar to, though smaller than, the MLS observed in zoospores. An asymmetrical cytoskeleton consisting of a band of 30–45 microtubules extends from the MLS down one side of the spermatozoid close to the plasmalemma. An immature MLS was observed in an early stage of spermatozoid development. The finding of an MLS and asymmetrical cytoskeleton in specialized male gametes as well as relatively unspecialized zoospores of Coleochaete strengthens assumptions of homology between MLSs of green algal reproductive cells and those found in flagellated spermatozoids of archegoniate plants. The structure of the spermatozoid of Coleochaete supports the hypothesis that this alga may be relatively close to the phylogenetic line which led directly to archegoniates.     

Ultrastructural characterization of the locomotory cytoskeletal system of the spermatozoid inGinkgo biloba

Summary The development of the locomotory cytoskeletal system of sperm is carefully coordinated with the development of the sperm inGinkgo biloba. Here we report further ultrastructural characterization of the locomotory cytoskeletal system in the developing spermatid and mature spermatozoid, particularly with respect to the initiation and early development of the flagellar apparatus. A multilayered structure (MLS) assembles from an electron-dense matrix that self-organizes after blepharoplast breakup and then further elongates. At the tail of the assembling MLS, the spline microtubules connect to an anterior beak of the nuclear envelope. Nuclear-pore complexes are found on the nuclear envelope close to this beak. The mitochondria which elongate and line up one behind the other are tightly associated with the MLS. The MLS ofG. biloba is composed of an upper layer of parallel spline microtubules and a lower layer consisting of a fibrous lamellar strip composed of paralled fibers about 9 nm in diameter. Higher-magnification images show that the fully assembled fibers of the lamellar strip consist of subunits which suggest that protofilaments are involved in the assembly processes. A unique cytoskeletal system of the spermatozoid inG. biloba is given by the anterior bundle of microtubules. This bundle, in which microtubules are arranged parallel to each other, forms between the plasmalemma and the MLS and is about 214–392 nm in cross section. These microtubules expand spirally along the MLS band. Other details of cellular fine structure of the mature spermatozoid are described.     

COMPARATIVE ULTRASTRUCTURAL STUDIES OF SPERMATOGENESIS IN THE METZGERIALES (HEPATICAE). I. THE BLEPHAROPLAST OF PALLAVICINIA LYELLII

The blepharoplast in the young spermatid of Pallavicinia is similar to that of other hepatics in that it comprises a four-layered multilayered structure (MLS) and two staggered, dimorphic basal bodies. The spline, approximately 40 μm in length and extending through nearly two full gyres, comprises 20 parallel microtubules at its anterior end and narrows to 17 at the posterior limit of the subjacent lamellar strip (LS). Behind this, the spline shank, approximately 32 μm in length, is reduced to six tubules. The LS curves around the spermatid, following the anterior one-third of the first gyre of the spine, and is approximately 7.5 μm in length, the longest yet recorded for the bryophytes. It is spatulate in outline, equaling the width of the spline anteriorly but tapering steeply from the right-hand side behind the anterior basal body (ABB). It then extends posteriorly as a narrow strip beneath the left-hand margin of the spline. The basal bodies of the greatly staggered flagella are nonoverlapping and separated by a distance of about 4.4 μm. The subapical ABB and PBB measure (including the ventral triplet extensions and transition zones) 1.2 μm and 2.4 μm in length, respectively. A short, narrow aperture equaling one tubule-diameter in width is located in the spline directly beneath the ABB. The anterior mitochondrion is about 7 μm long and follows the outline of the overlying LS, while a cupshaped posterior mitochondrion is appressed to the plastid. Comparisons with other taxa indicate that major distinguishing features of metzgerialian blepharoplasts are highly staggered, nonoverlapping basal bodies, greatly elongate anterior mitochondria, and six-tubule shanks. Great differences between the spermatids suggest wide phylogenetic discontinuities between the genera of the Metzgeriales.     

Spermatogenesis in Polytrichum juniperinum

Summary Spermatogenesis in Polytrichum juniperrinum includes a series of precise and coordinated morphogenetic movements among the organelles of the androcyte. The basal bodies, the underlying microtubules, and the multilayered structure (MLS) are positioned as an integrated unit at the periphery of the cell, and the nucleus migrates into contact with them. The shape of the nucleus begins to change, with the formation of an anterior projection, or beak. The mitochondrial sheath that has coalesced on the plastid divides to form the apical body, and elongation of the nucleus begins. The posterior basal body and one microtubule undergo lateral displacement from the rear forward, as elongation of the nucleus and the microtubules continues. The mitochondrial mass that is now the apical body grows rearward along the side of the elongated nucleus, and the two groups of microtubules in the MLS rearrange themselves. The lower elements of the MLS also participate in the morphogenetic rearrangement. By the time the nucleus has elongated once around the cell and the apical body has begun it s rearward growth, the lower elements of the MLS are found only beneath the anterior basal body. Subsequently these layers disappear from this location also.     

Ultrastructural studies of mutant spermatozoids in ferns. I. The mature nonmotile spermatozoid of mutation 230X in Ceratopteris thalictroides(L.)Brongn

Electron microscopy reveals that nonmotility in the spermatozoids of mutant 230X of the fern Ceratopteris thalictroides results from highly aberrant flagella. With respect to its mitochondrial complement, amyloplasts, condensed chromatin within the nucleus and the multilayered structure (MLS), the mutation is almost indistinguishable from the wild-type spermatozoids. In contrast to flagellar mutations in other organisms (man, mouse, Drosophila, Chlamydomonas), which principally affect the microtubules of the axoneme, the basal body cartwheel is lacking in 230X. In its absence, compound microtubules with shared walls are still present, but in highly disorganized arrays. Since the amount of polymerized tubulin in the spermatozoids of 230X is approximately the same as in the wild type, the mutation does not seem to affect microtubule synthesis or assembly. Centriolar cartwheels appear to be essential templates for the alignment of triplet and doublet tubules in regular radial arrays. The MLS in 230X is almost normal, whereas the flagella are aberrant, indicating that there are two distinct functional classes of microtubules in archegoniate spermatozoids. In contrast to the helix of 3½ gyres found in the wild type, nuclear morphology in 230X exhibits profound distortions ranging from deep channels and holes to supernumerary attenuated arms. Parts of nuclei associated with the MLS are almost normal, but malformations are in variably associated with the presence of microtubules of the aberrant flagella that are in close proximity t o the nuclear surface. The shapes of the teratologies are directly related to the number and configuration of the adjacent perinuclear tubules. From these findings, it is argued that microtubules have a crucial role in nuclear shaping in archegoniates; and that the precise form of the nucleus is closely related to the geometry and development of the MLS. On the other hand, it is difficult to envisage how microtubules growing in the chaotic arrays found in 230X could themselves generate shaping forces, More likely, the actual force-generating system, situated in or near the nuclear envelope, has become misaligned and severely restricted by the perinuclear arrays of flagellar tubules, which function as cytoskeletal elements additional to those of the normal MLS. Archegoniate plants are particularly advantageous for the detection of basal body mutants, since centrioles are absent from the mitotic apparatus. Cytological and hybridization studies of 230X affirm the nuclear basis of the mutation, and provide no support for the possible genetic autonomy of centrioles.     

Ultrastructure of the gametes ofCoelomomyces dodgei Couch (Blastocladiales,Chytridiomycetes)

Summary As part of an investigation on the developmental biology ofCoelomomyces dodgei Couch (Blastocladiales, Chytridiomycetes), the ultrastructure of the male and female gametes was studied. The nucleus is central and conical in shape except for a basal spur that curves back towards the large plate-like mitochondrion. A nuclear cap of ribosomes sits on the flat anterior end of the nucleus. Approximately seven lipid globules are partially embedded in the mitochondrion and are interconnected by membrane cisternae. The lipid globules are covered by a single fenestrated microbody and a backing membrane lies between the microbody and the gamete plasma membrane. The kinetosome is at the base of the nucleus and is connected to a single, posterior, whiplash flagellum. A nonkinetosomal centriole is absent. In the peripheral cytoplasm of both mating types there is a paracrystalline body of unknown composition and function. No significant ultrastructural differences were found between the male and female gametes.     

INFLUENCE OF THE MULTILAYERED STRUCTURE ON THE MORPHOGENESIS OF MARCHANTIA SPERMATIDS

The multilayered structure (MLS) in a spermatid of Marchantia is the morphogenetic blueprint of the headpiece in a mature sperm. As the nucleus begins elongation, a curved, tapered nuclear projection follows the path of microtubules extending from the MLS and becomes inserted into an indented zone at the rear of the asymmetric organelle. The indented zone defines the most forward penetration of the nucleus into the sperm headpiece. Partial disorganization of MLS lower strata nearest the nuclear projection facilitates overlapping of the nucleus with the rearward part of the anterior mitochondrion. At the front of the nascent headpiece, the mitochondrion is stabilized against microtubules following total disorganization of intervening MLS strata. Penetration of the nuclear projection along the MLS and directed disorganization of MLS lower strata control ultimate disposition of headpiece components. The headpiece is isolated and molded into final shape by undercutting and constriction of the cell membrane.     

SPERMATOGENESIS IN LYCOPODIUM: THE MATURE SPERMATOZOID

The mature spermatozoid of Lycopodium cernuum is a blunt ended, fusiform cell, 8–10 μm long by 4–5 μm wide. A multilayered structure (MLS) and a subtending anterior mitochondrion are located at the anterior of the cell. The MLS is coiled through 1–1.5 gyres in a shallow sinistral helix around the periphery of the cell. The MLS would be triangular in outline if unwound and laid flat, about 1.4 μm wide, 7.5–8 μm long, and 80 nm thick. The MLS comprises four layers, S₁–S₄. The S₁ forms the spline, a supportive sheet of microtubules; the S₂, lamellate in younger stages, is an homogeneous, darkly staining layer in the mature sperm; the S₃ and S₄ retain their lamellate appearance and are delimited by lateral connections. Approximately 200 S₁ microtubules extend posteriorly from the MLS at about 45° to the MLS long axis and form a partial sheath around the nucleus. The two basal bodies are located on opposite sides of the cell external to the MLS. Each is tangential to the curve of the MLS and surrounded by a globular matrix. At their attachment, the axonemes are oriented laterally and are antiparallel to each other. Distally, the flagella, each about 38 μm long, trail behind the cell as it swims. The nucleus is roughly ovoid, about 4 μm diam, and centrally or sometimes laterally located. The greater volume of the nucleus is occupied by condensed, amorphic chromatin. Cavities within the chromatin are often seen to contain spheroidal inclusions that have two differently staining regions. The inclusions are also located at the periphery of the chromatin. The posterior of the cell is occupied by several small mitochondria and an amyloplast, about 2 μm diam containing numerous starch grains.     

Ultrastructure of spermatids and spermatozoa in three polychaetes with modified biology of reproduction: Autolytus sp., Chitinopoma serrula,and Capitella capitata

Unlike the primitive type of spermatozoon found in most polychaetes, the spermatozoon of Autolytus has a bilateral symmetry with elongated nucleus, and the mitochondria surround the posterior part of the nucleus. A rather large disk-shaped acrosome is situated along one side of the anterior part of the nucleus. From the anterior margin of the distal centriole emerge long striated rootlets, which run along the nuclear envelope to the anterior part of the nucleus. The spermatozoon of Chitinopoma serrula has an elongated, slightly bent nucleus, a thimble-like acrosome apically on the anterior surface of the nucleus, and an elongated middle piece containing 4 rod-like mitochondria developed from spherical mitochondria surrounding the basal part of the tail flagellum. In the spermatozoon of Capitella capitata, both nucleus and middle piece are elongated compared to the primitive type. The large and conical acrosome is placed asymmetrically at the nucleus and consists of an acrosomal vesicle and subacrosomal substance. The greater part of the middle piece forms a collar around the initial part of the tail flagellum. The cytoplasm of the collar contains granular material. One or two small mitochondria lie around the 2 centrioles at the base of the nucleus.

These types of spermatozoa represent early steps in the evolution of modified spermatozoa combined with changed biology of reproduction. The modified spermatozoa are larger than the primitive ones.     

ULTRASTRUCTURAL STUDIES OF SPERMATOGENESIS IN THE ANTHOCEROTALES. II. THE BLEPHAROPLAST AND ANTERIOR MITOCHONDRION IN PHAEOCEROS LAEVIS: LATER DEVELOPMENT

Chromatin condensation begins as the multilayered structure (MLS) in Phaeoceros reaches its maximally structured differentiation. As nuclear elongation and chromatin condensation proceed, the S_2–4 strata disappear, and the nuclear beak extends between the S₁ and the nearly spherical anterior mitochondrion. In a mature sperm the mitochondrion is elongate and lies completely anterior to the blunt front end of the nucleus. The 12 S₁ tubules extend over the anterior mitochondrion and nucleus, but their number becomes reduced to five at the level where the nucleus' midportion is constricted. The anterior ends of the S₁ tubules lie embedded in a rather conical osmiophilic crest. Flagellar insertion is restricted to the extreme anterior tip of the S₁ tubules. The locomotory apparatus in Phaeoceros is compared with that of other bryophytes.     

Morphology and development of rhabdovirus-like particles inCuscuta odorata (Convolvulaceae) simultaneous infected with virus and mycoplasma-like organisms

Summary Electron microscopic examination ofCuscuta odorata, used for transmission trials, revealed mycoplasma-like organisms (MLO) as well as rhabdovirus-like particles, unknown toCuscuta. The virus infection is confined to certain phloem-parenchyma cells and a 1–2 cell thick layer of parenchyma cells with thickened walls surrounding the central cylinder. Virus particles, mostly bacilliform, could be detected mainly in the nucleus but also in the cytoplasm. They reach a length of 350–400 nm and a diameter of approximately 75 nm. Virus assembly takes place exclusively in the nucleus. Virus maturation occurs in membrane bound areas within the nucleus, which have no connection with the perinuclear space. Formation of nucleocapsids is always associated with a nuclear viroplasm. Envelopment of virus particles occurs in these membrane bound areas. Budding into the perinuclear space does not occur. Virus infection leads to degeneration and finally to death of the protoplast.Abbreviations cy cytoplasm - m membrane stacks - mt mitochondria - my mycoplasma-like organisms - nc nucleocapsid - ncp nucleocapsid particles - nf nuclear filaments - np nucleoplasm - nu nucleus - nvp nuclear viroplasm - oc obliterated cells - p plastid - pc passage cells - ph phloem - ps perinuclear space - spc strand of parenchymatous cells - v virus particle - x xylem     

Flagellar apparatus ultrastructure inMesostigma viride (Prasinophyceae)

The ultrastructure of the flagellar apparatus ofMesostigma viride Lauterborn (Prasinophyceae) has been studied in detail with particular reference to absolute configurations, numbering of basal bodies, basal body triplets and flagellar roots. The two basal bodies are interconnected by three connecting fibers (one distal fiber = synistosome, and two proximal fibers). The flagellar apparatus shows 180° rotational symmetry; four microtubular flagellar roots and two system II fibers are present. The microtubular roots represent a 4-6-4-6-system. The left roots (1s, 2s) consist of 4 microtubules, each with the usual 3 over 1 root tubule pattern. Each right root (1d, 2d) is proximally associated with a small, but typical multi-layered structure (MLS). The latter displays several layers corresponding to the S₁ (the spline microtubules: 5–7), and presumably the S₂—S₄ (the lamellate layers) of the MLS of theCharophyceae. At its proximal origin (near the basal bodies) each right root originates with only two microtubules, the other spline microtubules being added more distally. The structural and positional information obtained in this study strongly suggest that one of the right roots (1d) ofMesostigma is homologous to the MLS-root of theCharophyceae and sperm cells of archegoniate land plants. Thus the typical cruciate flagellar root system of the green algae and the unilateral flagellar root system of theCharophyceae and archegoniates share a common ancestry. Some functional and phylogenetic aspects of MLS-roots are discussed.Dedicated to Prof. DrLothar Geitler on the occasion of his 90th birthday.     

Unique positioning of mitochondria in developing microspores and pollen grains inPharbitis nil: mitochondria cover the nuclear surface at specific developmental stages

Summary Changes in the number and distribution of mitochondria in microspores and pollen grains during male gametogenesis inPharbitis nil were examined with Technovit sections stained with 3,3-dihexyloxacarbocyanine iodide. The number of mitochondria per microspore or pollen grain ofP. nil increased constantly and dramatically during male gametogenesis. During this process, mitochondria exhibited characteristic localizations: subpopulations of mitochondria covered the surface of the microspore and vegetative nuclei before and again just after postmeiotic mitosis I (9 and 5 days before flowering, respectively). The mitochondria also surrounded the generative nucleus 2 days after postmeiotic mitosis I (5 days before flowering), although the density of mitochondria on the nuclear surface was lower. Electron microscopy showed that the mitochondria were about 30 nm from the nuclear envelope and that each mitochondrion was located near a nuclear pore. The characteristic localization of mitochondria inP. nil pollen may serve as a model to analyze the mechanisms that control mitochondrial positioning within a cell and interactions between mitochondria and nuclei.Abbreviations DAPI 4,6-diamidino-2-phenylindole - DiOC₆ 3,3-dihexyloxacarbocyanine iodide - PM I postmeiotic mitosis I     

A cytoskeletal system predicts division plane in meiosis ofSelaginella

Summary An ultrastructural investigation of the monoplastidic microsporocytes ofSelaginella arenicola revealed a unique cytoskeletal array that predicts the future division plane before nuclear division takes place. By midprophase of the first meiotic division, the single plastid has divided once and the two plastids lie on opposite sides of the nucleus which is elongated in the plane of the incipient metaphase I spindle. A cytoplasmic structure, the procytokinetic plate (PCP), predicts the division plane of of both plastid and cytoplasm. The PCP consists of a distinct concentration of vesicles lying in the future division plane and an elaborate system of microtubules aligned parallel to the long axis of plastids and nucleus. Microtubules of the axially aligned system appear to terminate in clusters of vesicles in the central zone of the PCP. The PCP with axially aligned microtubules is as predictive of the division plane in these meiotic cells as is the girdling preprophase band of microtubules in mitotic cells.     

Morphological aspects of fertilization in Phallusia (Ascidia) nigra (Ascidiacea,Tunicata)

The spermatozoa of Phallusia (Ascidia) nigra have an elongated head (approximately 5 m in length) in which a nucleus and a single mitochondrion are located side by side. There is no midpiece. The apex of the head is wedge-shaped. Acrosomal vesicles (approximately 55–65 nm in diameter) and moderately electron-dense material (MEDM) are present between the plasmalemma and the nuclear membranes in the anterior tip of the head. The MEDM occupies a central position and three or four acrosomal vesicles are seen in a line alongside it. The acrosomal vesicles disappear as the sperm makes contact with the surface of the chorion. Gamete fusion most likely occurs between a small process extending from the peripheral margin of the sperm apex and the egg surface, resulting in incorporation of the sperm into the egg from the anterior region of its head.     

Monoclonal antibodies to surface and cytoskeletal components of the spermatozoid ofPteridium aquilinum

Summary Detergent extracted spermatozoids of the fernPteridium aquilinum were used as mixed antigen preparations for raising monoclonal antibodies in order to obtain reagents for detecting as yet uncharacterized components of the plant cytoskeleton. Selected antibodies were studied by immunofluorescence microscopy of developing spermatids and mature spermatozoids. Some reacted directly with fixed cells, others required permeabilization treatments with cold methanol or Triton X-100. AntibodiesPas2D9 andPas6D7 bind to glycoprotein antigenic determinants that are exposed on the surface of the plasma membrane. Several antibodies interact with cytoskeletal components.Pas1D3,Pas5D8 andPas5F4 bind to the cytoskeleton of permeabilized cells including the flagella. Three react specifically with the flagellar band or associated components:Pas2G6 reacts with the whole flagellar band but shows a prominent binding to basal bodies,Pas5E2 binds exclusively to basal bodies, andPas5E7 detects mitochondria associated with the flagellar band. Cross-reactions to wheat root tip cells at different stages of the cell cycle are described inMarc andGunning (1988).Abbreviations MLS multilayered structure - MT microtubule - MAb monoclonal antibody - MAP microtubule associated protein