Ultrastructure of spermatozoa of the lung fluke, Paragonimus ohirai (Trematoda: Troglotrematidae), in the seminal receptacle

The seminal receptacle of Paragonimus ohirai contains not only mature spermatozoa, but also atypical and degenerate ones, suggesting that abnormal spermatozoa are retained in this organ. The spermatozoon is of a parallel biflagellar type with cortical microtubules, consisting of the anterior region, first mitochondrial region, intermediate (amitochondrial) region, second mitochondrial region, posterior nuclear region (PNR) and tail region (TR). The first third of the spermatozoon exhibits typical undulatory movement, while the middle part shows vibratory movement. At the area between head and midsections (H-M area) the peripheral doublets of axonemes are interrupted, and the external ornamentation is distributed widely around this portion. Throughout the immotile PNR and TR, the axonemes lack the dynein arms of their peripheral doublets. H-M, PNR, and TR ultrastructural characteristics are specific in P. ohirai spermatozoon and seem to be closely related to its pattern of movement.     

Bizarre flagellum of thrips spermatozoa (Thysanoptera,Insecta)

The flagellum of the thysanopteran spermatozoon has been examined by electron microscopy and computer-aided image analysis. The flagellum consists of 27 microtubular elements that probably are formed as outgrowths from three separate basal bodies. Nine of the elements are normal microtubular doublets that carry dynein arms and nine are doublets without dynein arms. The remaining nine elements are microtubular singlets that apparently bear dynein arms and have the same appearance as A-subtubules of microtubular doublets. The 27 elements are arranged in a fixed pattern that consists of nine groups, each of which begins with a microtubular singlet and ends with an arm-less microtubular doublet. Computer-aided image analysis has shown that the A-subtubules of the doublets and the microtubular singlets have lumens with very similar patterns. The sperm tail is known to have some motility; it generates fast waves running along its length. The amalgamated axonemes hence act as a functional flagellum. The thysanopteran sperm tail is the only type of flagellum known to us that consists of microtubules in a highly asymmetric array.     

Characteristics of Spermatozoa from Five Gall-Midge Species (Diptera, Cecidomyiidae)

The gall-midge family Cecidomyiidae is one of the largest within the animal kingdom. Its characteristics include, among others, a chromosome elimination during spermiogenesis and a bewildering diversity in sperm ultrastructure. The sperm tail, in particular, is unusual in that it deviates from the conventional 9+2 pattern of microtubules. We describe here the spermatozoa of five gall-midge species, all belonging to the same supertribe Cecidomyiidi. In Bremia more than 100 microtubular doublets form a tight spiral around a central mitochondrion. In an undetermined binomen many doublets form a spiral around the mitochondria in the distal end of the sperm tail, but a single row along a peripheral cistern in the main part of the tail. In Coquillettomyia caricis a peripheral row of doublets resides in the proximal part and tightly packed doublets distally. In Arthrocnodax sp. the many doublets also form a peripheral single or double row around a central mitochondrion. In Massalongia bachmaieri there are more than 500 doublets which form several rows around the nucleus and tightly packed doublets distally. The nuclear membrane forms bundles of extensive outpocketings. There is no acrosome. The nucleus consists of both condensed and dispersed material. Only outer dynein arms are present in all this species and the spermatozoa are motile. Cecidomyiidi species that have been examined for sperm structure fall into two groups: those where the mitochondria are confined to the centre of the tail and those in which the mitochondria lie in the head region and have a peripheral location. Most species belong to the first group, while Massalongia belongs to the second one.     

THE MICROTUBULAR CYTOSKELETON OF AMPHIDINIUM RHYNCHOCEPHALUM (DINOPHYCEAE)1

The sub-thecal microtubular cytoskeleton of Amphidinium rhynchocephalum Anissimowa was investigated using indirect immunofluorescence microscopy and transmission electron microscopy. The majority of sub-thecal microtubules are longitudinally oriented and radiate from one of two sub-thecal transverse microtubular bands that lie adjacent to the anterior and posterior edge of the cingulum.Both transverse bands consist of 3–5 microtubules and are loop shaped with one end adjacent to the cell's right edge of the sulcus and the other end adjacent to the fibrous ventral ridge. The posterior transverse microtubular band (PTB) defines the posterior edge of the cingulum and gives rise to numerous posteriorly directed longitudinal microtubular bundles that consist of 1–3 microtubules per bundle. These bundles end at the posterior end of the cell. The PTB also gives rise to the cingular longitudinal microtubules that underlie the cingular groove and terminate at the anterior transverse microtubular band (ATB). The ATB defines the anterior edge of the cingulum and loops around the base of the epicone. This band gives rise to anteriorly directed longitudinal microtubular bundles that terminate in the small epicone of the cell. The longitudinal microtubular root of the flagellar apparatus is directed posteriorly and lies immediately beneath the theca but is distinct from the subthecal microtubule system. A narrow fibrous ridge is ventrally located to the cell's left between the exit apertures of the transverse and longitudinal flagella. In this position, the ventral ridge lies between and also connects with the anterior and posterior transverse microtubular bands. The ventral ridge is also associated with three microtubules that are distinct from other cytoskeletal microtubules. Our results demonstrate that the majority of sub-thecal microtubules originate from one of two microtubular bands associated with the cingulum. The possible role of the fibrous ventral ridge and its associated microtubules is also discussed.     

The Ultrastructure of Chaenea teres and an Analysis of the Phylogeny of the Haptorid Ciliates

Chaenea teres has typical haptorid ultrastructure. The somatic monokinetid has two transverse microtubular ribbons, an overlapping postciliary microtubular ribbon, and a laterally directed kinetodesmal fiber. The evered cytopharynx forms a dome at the apical end of the cell. The base of the dome is surrounded by oral dikinetids. The left, anterior kinetosome of the oral pair is not ciliated and has a transverse microtubular ribbon, a nematodesmata and a single postciliary microtubule. The right, posterior kinetosome is ciliated and has only postciliary microtubules. The kinetosomes at the anterior ends of the somatic kinetics are close together and their transverse microtubules and nematodesmata contribute to the support of the cytopharynx. The transverse microtubules of these oralized somatic kinetosomes, together with those from the oral dikinetids, line the cytopharynx. Accessory or bulge microtubules arise perpendicular to the transverse microtubules. A dorsal brush of three kineties of clavate cilia is found on the cell surface just posterior to the oral region. Mucocysts and a single type of toxicyst are present. The toxicysts are confined to the oral region. There are multiple ovoid macronuclei that stain weakly. Micronuclei were not observed. Cladistic analysis indicates the Chaenea may be most closely related to Fuscheria and Acropisthium. The cladistic analysis also suggests that existing taxonomies of the subclass Haptoria need to be revised. We propose some modifications to Foissner & Foissner's classification that include transferring Helicoprorodon, Actinobolina, the buetschiliids, and the balantidiids to the order Haptorida and recognizing the close relationship between pleurostomes and spathidiids.     

Visualization of the funis of Giardia lamblia by high-resolution field emission scanning electron microscopy--new insights

Giardia lamblia is a multiflagellar parasite and one of the earliest diverging eukaryotic cells. It possesses a cytoskeleton made of several microtubular structures-an adhesive disc, four pairs of flagella, median body, and funis. This protozoan displays different types of movements, including a lateral and dorso-ventral dislocation of its posterior region, which has not been completely elucidated. In the present study, high-resolution field emission scanning electron microscopy was used to analyze the funis structure of G. lamblia trophozoites. It was shown that the funis is made of short arrays of microtubules emanating from the axonemes of the caudal flagella, which are anchored to dense rods that run parallel to the posterior-lateral flagella. After emergence of the posterior-lateral flagella, funis microtubules are anchored to the epiplasm, a fibrous layer that underlies the portion of membrane that presents tail contractility. Based on these observations a model for the tail flexion of G. lamblia is proposed.     

大黄鱼精子的超微结构

大黄鱼的精子由头产和尾部两部分组成。头部结构较为独特,其腹侧有一较大的细胞核,背部有中心粒复合体。头部的后端是袖套。细胞核的腹面稍向外突出背面则稍向内凹。细胞核中的染以质浓缩成致密的团块状。团块状的染色质之间分布着松散的纤维状染色质。植入窝位于细胞核的背部表面,由细胞核背面向内凹陷而成,呈一沟状,其走向与精子的长轴平行。     

The spermatogenesis and sperm structure of Acerentomon microrhinus (Protura, Hexapoda) with considerations on the phylogenetic position of the taxon

The spermatogenesis of the proturan Acerentomon microrhinus Berlese, (Redia 6:1–182, 1909) is described for the first time with the aim of comparing the ultrastructure of the flagellated sperm of members of this taxon with that of the supposedly related group, Collembola. The apical region of testes consists of a series of large cells with giant polymorphic nuclei and several centrosomes with 14 microtubule doublets, whose origin is likely a template of a conventional 9-doublet centriole. Beneath this region, there are spermatogonial cells, whose centrosome has two centrioles, both with 14 microtubule doublets; the daughter centriole of the pair has an axial cylinder. Slender parietal cells in the testes have centrioles with nine doublet microtubules. Spermatocytes produce short primary cilia with 14 microtubule doublets. Spermatids have a single basal body with 14 microtubule doublets. Anteriorly, a conical dense material is present, surrounded by a microtubular basket, which can be seen by using an α-anti-tubulin antibody. Behind this region, the basal body expresses a long axoneme of 14 microtubule doublets with only inner arms. An acrosome is lacking. The nucleus is twisted around the apical conical dense structure and the axoneme; this coiling seems to be due to the rotation of the axoneme on its longitudinal axis. The posterior part of the axoneme forms three turns within the spermatid cytoplasm. Few unchanged mitochondria are scattered in the cytoplasm. Sperm consist of encysted, globular cells that descend along the deferent duct lumen. Some of them are engulfed by the epithelial cells, which thus have a spermiophagic activity. Sperm placed in a proper medium extend their flagellar axonemes and start beating. Protura sperm structure is quite different from that of Collembola sperm; and on the basis of sperm characters, a close relationship between the two taxa is not supported.     

The cytoskeletal architecture of Trypanosoma brucei

The cytoskeleton of Trypanosoma brucei has been analyzed by the high-resolution technique of quick-freeze deep-etch rotary-shadowing electron microscopy. The study provides detailed structural information on the subpellicular array of microtubules, the flagellum, and the interaction of these 2 major structures of the trypanosomal cytoskeleton with each other. The subpellicular microtubules closely interact both with the cell membrane and with each other. At the anterior tip of the cell they converge into a tightly closed structure, whereas at the posterior end the microtubular array remains open ended. The microtubular array is involved also in forming the opening of the flagellar pocket. The microtubular array interacts with the paraflagellar rod of the flagellum through a dense meshwork of fibers that are anchored on the microtubular surface with one end and within the paraflagellar rod structure with the other. The highly ordered, 3-dimensional network of the paraflagellar rod itself is connected tightly to the microtubular axoneme of the flagellum through a regular array of fleur-de-lis-shaped linking structures.     

Sperm Axoneme in Some Apterygote Insects Examined by Computer-aided Image Analysis

Sperm tail axonemes from three insect species, representing the three apterygote orders Diplura, Archeognatha and Zygentoma, have been examined by high resolution electron microscopy. The samples were fixed in a mixture of glutaraldehyde and tannic acid followed by uranyl acetate post-fixation and the electron micrographs were subjected to computer analysis in order better to characterize the minute details of the axonemal microtubules. The dipluran Campodea was seen to have a row of accessory microtubules composed of 13 protofilaments, the archeognath Machilinus to have two rows of accessory microtubules composed of 16 protofilaments. and the zygentoman Lepismodes to have accessory microtubules in contact with the flagellar doublets and with a wall containing 16 protofilaments and an electron-dense lumen. The axonemal structure in Zygentoma is the one most similar to those of the pterygote insects. The protofilaments of the axonemal doublets were seen to have a somewhat widened interspace between some pairs of protofilaments and these ‘gaps’ coincided with the location of the basal parts of the outer dynein arm, the inner dynein arm, the spoke, and the intertubular material. It hence seems that these microtubule-associated structures influence the architecture of the microtubular wall.     

Three‐dimensional organization of flagellar basal apparatus in Ectocarpus gametes

The flagellar basal apparatus of the brown alga Ectocarpus siliculosus was re‐investigated in details using transmission electron microscopy and electron tomography. As a result, three‐dimensional structures with spatial arrangement of bands and microtubular flagellar rootlets were observed. Fibrous structures linking the anterior flagellar basal body to the major anterior rootlet (R3) or the bypassing rootlet was newly discovered in this study. A direct attachment from the minor anterior rootlet (R4) to the anterior and posterior basal bodies was also discovered, as were attachments from the minor posterior rootlet (R1) to the deltoid striated band and from the major posterior rootlet (R2) to the posterior fibrous band. The microtubular flagellar rootlets were connected to the bands and to the anterior or posterior basal body. These bands may have a role in maintaining the spatial arrangement of the anterior and posterior flagellar basal bodies and the microtubular flagellar rootlets. A numbering system of the basal body triplets was established by tracing axonemal doublets in the serial sections. From these observations, the precise position of two flagellar basal bodies, bands, and flagellar rootlets was determined.     

FEEDING APPARATUS OF THE COLORLESS FLAGELLATE KATABLEPHARIS (CRYPTOPHYCEAE)1

The feeding apparatus of Kalablepharis ovalis (isolated from a freshwater impoundment in Colorado) and Katablepharis clone G-2 (isolated from the littoral of the Black Sea near Yalta in the Crimea) consists of inner and outer oval-shaped arrays of microtubules that begin at the anterior end of the cell and pass into the posterior of the cell. Each array of microtubules contains groups of microtubules with two to eight microtubules per group depending on the position of the array in the cell. A specialized area of the plasma membrane, the mouth, occurs at the anterior end of the cell. The mouth is oval with the long axis oriented dorsoventrally and consists of a raised ridge surrounding a central depression. The anterior end of the microtubules of the inner and outer arrays supports the raised ridge of the mouth. In freeze-fracture replicas, the protoplasmic face of the plasma membrane contains intramembrane particles on the raised ridge of the mouth. Three small membrane-cisternae occur on the protoplasmic side of the plasma membrane in the area of the mouth. Katablepharis clone G-2 also has five or six additional large membrane-cisternae associated with the inner microtubular array in the anterior portion of the cell. These larger membrane-cisternae do not occur in K. ovalis. Vesicles with electron-dense contents occur in association with the microtubular arrays. Katablepharis ovalis has a second type of vesicle containing a single-membrane profile associated with the microtubule arrays. The structure of the microtubular arrays in Katablepharis is compared with similar structures in suctorian ciliates and dinoflagellates.     

Spermatozoa from the supertribes Lasiopteridi and Stomatosematidi (Insecta, Diptera, Cecidomyiidae): ultrastructure data and phylogeny of the subfamily Cecidomyiinae

Spermatozoa from seven gall-midge species, representing the supertribes Lasiopteridi and Stomatosematidi, have been examined by electron microscopy and compared to the spermatozoa of 30 previously examined gall-midge species of the subfamily Cecidomyiinae. Derived characteristics of all examined representatives of this subfamily are the lack of acrosome and the absence of accessory tubules in their axoneme. The sperm axoneme of Didactylomyia has a unique '9 + 5 pattern', i.e. with 9 outer doublets and 5 inner singlet microtubules. Unlike other members of Cecidomyiinae, Didactylomyia has retained some plesiomorphic traits, namely crystal containing mitochondria and a homogeneously condensed nucleus. Stomatosema has a 10 + 0 axoneme and an irregular nuclear condensation. Thus, Didactylomyia may serve as an useful outgroup for phylogenetic analysis within the subfamily Cecidomyiinae. The supertribe Stomatosematidi is a paraphyletic assemblage. Nearly all members of Lasiopteridi, Ozirhincus, Arnoldiola, Brachineura and Ledomyia , have a synapomorphic character in the great number of microtubules in parallel to the axoneme. A notable exception is Rhizomyia , which shares certain apomorphic traits with several genera that have previously been classified within the Cecidomyiidi, i.e. Contarinia, Allocontarinia, Lestodiplosis and Myricomyia. Moreover, these genera have a flat sperm tail and microtubular doublets located close to the cell membrane, both characteristics that differ markedly from the very peculiar sperm tail found in other members of Cecidomyiidi.
Cladistic analysis of sperm characters suggests that the supertribe Cecidomyiidi is a polyphyletic taxon and supports the existence of a sister-group relationship between the supertribe Lasiopteridi and the genera Rhizomyia, Contarinia, Allocontarinia, Lestodiplosis and Myricomyia.     

Morphology and phylogeny of Sainouron acronematica sp. n. and the ultrastructural unity of Cercozoa

Sainouron are soil zooflagellates of obscure taxonomy. We studied the ultrastructure of S. acronematica sp. n. and sequenced its extremely divergent 18S rDNA and that of Cholamonas cyrtodiopsidis (here grouped as new family Sainouridae) to clarify their phylogeny. Ultrastructurally similar, they weakly group together, deeply within Monadofilosa. Sainouron has three cytoplasmic microtubules; all organelles specifically link to them or the nucleus. Mature centrioles have fibrous rhizoplasts. The posterior centriole bearing the motile cilium (with cortical filaments) has a transitional hub-lattice; a dense spiral fibre links its thicker rhizoplast and triplets; its ciliary root has two microtubules: mt1, underlying the plasma membrane, initiates at the spiral fibre; mt2, laterally attached to mt1 and nucleus, initiates in the amorphous centrosomal region. The anterior younger cilium, an immotile stub with submembrane skeleton as in Cholamonas, lacks axoneme, microtubular root, rhizoplasts and spiral fibre, but becomes the posterior one every cell cycle. The nuclear envelope donates coated vesicles directly to the Golgi, which makes kinetocyst-type extrusomes, concentrated at the cell anterior for extrusion into phagosomes. Ciliary transition region proximal hub-lattices (postulated to contain centrin) and distal nonagonal fibres are cercozoan synapomorphies, found with slight structural variation in all flagellate Cercozoa, but not in outgroups.     

The Fine Structure of the Colonial Kinetoplastid Flagellate Cephalothamnium cyclopum Stein

Cell structure, cell adhesion, and stalk formation have been examined by electron microscopy in the colonial flagellate, Cephalothamnium cyclopum. Each cell is obconical or spindle-shaped, pointed posteriorly and truncated anteriorly. The cell membrane is underlain by epiplasm 0.1 μm thick in the posterior region, but bands of microtubules support the anterior region which is differentiated into a flagellar pocket, oral apparatus and contractile vacuole. Each of 2 flagella, joined a short way above their bases by an interflagellar connective, has a paraxial rod and mastigonemes. One flagellum is free and is important in food gathering while the other is recurrent and lies in a shallow groove on the ventral cell surface but projects posteriorly into the stalk. The basal bodies of these flagella are bipartite structures connected by a pair of striated rootlets with accessory microtubular fibers. The oral apparatus consists of a funnel-shaped buccal cavity and cytostome. It is supported by helical and longitudinal microtubules and also has nearby striated and microtubular fibers. Possible roles of associated oral vesicles in relation to ingestion are discussed. A reticulate mitochondrion houses a massive kinetoplast which has a fibrillar substructure resembling that of dinoflagellate chromosomes. Adjacent flagellates adhere by laminate extensions of their posterior regions and attach by their recurrent flagella to a communally secreted stalk composed of finely fibrillar material. This study indicates that Cephalothamnium belongs in the order Kinetoplastida, and has many features in common with members of the family Bodonidae.     

Ultrastructure of Prorodon (Ciliophora, Prostomatida) I. Somatic Cortex and Some Implications Concerning Kinetid Evolution In Prostomatid and Colpodid Ciliates

ABSTRACT. This study describes the ultrastructure of the somatic cortex of Prorodon aklitolophon and Prorodon teres. the meridionally arranged somatic kineties of both species can be separated into two parts: a short anterior part, which consists of a few somatic dikinetids (in which both kinetosomes are ciliated), and a longer posterior consisting of monokinetids. the somatic monokinetids are associated with a convergent postciliary microtubular ribbon, a transverse microtubular ribbon flatly inserted in front of the kinetosome, a short and steeply extending kinetodesmal fibre attached to kinetosomal triplet 5 and 7, and a desmose anterior to triplet 3. From this desmose, two to five prekinetosomal microtubules originate and extend anteriorly. the posterior kinetosome of the somatic dikinetids is associated with the same microfibrillar and microtubular structures as the somatic monokinetid, except that no prekinetosomal microtubules originate from the desmose. the anterior kinetosome has a single postciliary microtubule and a tangentially oriented transverse microtubular ribbon. the permanent collecting canals of the unique contractile vacuole system extend parallel and adjacent to the somatic kinetics of Prorodon . the collecting canals are supported by the prekinetosomal microtubules. A similarly organized contractile vacuole system is not yet known from any other ciliate group. One of the most surprising results of this investigation was finding a significant similarity between the somatic dikinetid pattern of Prorodon and the colpodid dikinetid pattern. A hypothesis is presented to illustrate the evolution of the somatic kinetid patterns in colpodid and prostomatid ciliates.     

Cortical organellar complexes,their structure,formation, and bearing upon cell shape in a ciliate,Dileptus

Summary Ciliary complexes termed the kinetids, contain fibres of several kinds attached to the proximal end of a basal body. One of these fibres, the long microtubular fibre running in the endoplasm ofDileptus, is of special interest for this study. The fibres when attached to oral kinetids are orientated towards the cell posterior, and are numerous in the proboscis endoplasm. The fibres anchored at locomotor kinetids are orientated towards the cell anterior and penetrate the endoplasm of the tail. The endoplasm of both proboscis and tail appears transparent when viewed in the light microscope, and is deprived of many organelles: nuclei, lipid droplets, and food vacuoles. During regeneration proboscis and tail reconstitution is simultaneous, with an increase in transparency and in the density of microtubular fibres within the regenerating region. In posterior fragments ofDileptus which contain locomotor kinetids only, oral kinetids form as an offspring of locomotor ones. During differentiation of oral structures oral kinetids rotate until their endoplasmic fibres point posteriorly. It is this rotation that supplies the cell with a posteriorly directed set of endoplasmic fibres. The possibility that the translocation of endoplasmic organelles along the microtubular fibres may be one of mechanisms in shaping cells is discussed. Since the direction of endoplasmic translocation depends upon fibre orientation, the MTOCs which govern this orientation are likely candidates to be bearers of information concerning cell shape inDileptus.     

The structure of the flagellar apparatus of the swarm cells ofPhysarum polycephalum

Summary Flagellation ofPhysarum polycephalum amoebae (Myxomycete) involves the formation around the two kinetosomes of a flagellar apparatus leading to a modification in the shape of the amoeba and its nucleus. A tridimensional ultrastructural model of the flagellar apparatus is proposed, based upon observation of the isolated nucleo-flagellar apparatus complex. The flagellar apparatus is composed of a non-microtubular structure (the posterior para-kinetosomal structure), five microtubular arrays and two flagella: a long anterior flagellum and a short flagellum directed backwards. The asymmetry of the flagellar apparatus is due mainly to the presence of the posterior para-kinetosomal structure on the right side of the posterior kinetosome and of the two asymmetrical microtubular arrays 3 and 4. Thus, the flagellar apparatus is right-handed. This asymmetry implies also some spatial constraints on two other microtubular arrays (2 and 5). Except in the case of the microtubular array 1 which links the proximal end of the anterior kinetosome to the nuclear membrane, the number of microtubules of each microtubular array seems to be well defined: 39, 5–6, 7–9, and 2+2 for the microtubular arrays 2, 3, 4, and 5 respectively. All the elements of the nucleo-flagellar apparatus complex are linked either directly or indirectly through bridges. Furthermore, the microtubules which composed the microtubular array 3 are linked through bridges while the microtubules of the microtubular arrays 2, 3, and 4 seem to be linked through a reticulate material. All these spatial relationships lead to a great cohesion of the nucleo-flagellar apparatus complex which appears to be a well defined structure. This suggests thatPhysarum amoebal flagellation can be a promising system to study the morphogenesis of an eucaryotic cell.Abbreviations PIPES Piperazine-N,N-bis [2-ethane-sulfonic acid] - EGTA [Ethylenebis(oxyethylenenitrile)]tetraacetic acid - DMSO Dimethyl sulfoxide     

The microtubular cytoskeleton of three dinoflagellates: an immunofluorescence study

Summary The sub-thecal microtubular cytoskeleton of the dinoflagellatesAmphidinium rhynchocephalum, Gymnodinium sanguineum, andGymnodinium. sp has been investigated by indirect immunofluorescence microscopy. In these cells, the majority of cytoskeletal microtubules lie in the anterior-posterior plane. These longitudinal microtubules clearly originate from one of two radially arranged microtubular bands that correspond in location with the anterior and posterior edge of the cingolar depression. Despite the morphological variability of these gymnodinioid dinoflagellates, our data indicate that the microtubular cytoskeleton perfectly reflects the spatial patterning of the epicone and hypocone in each cell.Abbreviations ALB Anterior longitudinal microtubular bundles - ATB Anterior transverse microtubular bands - C cingulum - CLB Cingular longitudinal microtubular bundles - E Epicone - H Hypocone - PLB Posterior longitudinal microtubular bundles - PTB Posterior transverse microtubular bands - S Sulcus     

ULTRASTRUCTURE OF SWARMERS IN THE LAMINARIALES (PHAEOPHYCEAE). I. ZOOSPORES1

Zoospores of 17 species in 14 genera of Laminariales, collected in the northeast Pacific Ocean, were studied by electron microscopy. These zoospores are unique in the brown algae in lacking both an eyespot in the single chloroplast and any associated swelling at the base of the shorter, posterior flagellum. Spores of all species examined possess a distal whiplash portion on the longer, mastigoneme-bearing anterior flagellum. This appendage may sometimes be as long as the mastigoneme-bearing portion of the flagellum, but it is only seldom preserved in the preparations for electron microscopy. A microtubular cytoskeleton is probably responsible for maintaining the shape of the spore. It consists of a short band of about 10 microtubules between the two basal bodies, scattered tubules converging at the anterior of the spore, a band of 7–9 tubules directed anteriorly from the anterior basal body, and a band directed posteriorly from the posterior basal body. These anterior and posterior bands may form one continuous band looping around the periphery of the spore. Variation with possible taxonomic significance was found in the ultrastructure of vesicles which apparently contain adhesive material, and which are extruded through the plasmalemma when the zoospores settle.