Three new species of the genus Leucon Kröyer, 1846 (Crustacea: Cumacea) from the continental slope off Surinam

Three new, and apparently closely related, species of cumacean are described from the continental slope off Surinam: Leucon turgidulus sp.nov. from about 500 m depth, L. medius sp.nov. from about 1000m and about 1500m, and L.jonesi sp.nov from about 1500m and about 2000m. The species have not been found in extensive collections from other parts of the deep Atlantic. Leucon pallidus G.O. Sars, 1865 is the most closely comparable of the previously known members of the genus.     

The Heart Ultrastructure in Two Species of Pycnogonids, and its Phylogenetic Implications

The heart of the pycnogonids Nymphon (Chaetonymphon) macronyx G. O. Sars and Boreonymphon cf. abyssorum Norman is pseudotubular and lacks an epicardium and an endocardium. The body wall forms the roof over the heart lumen. The myocardium is innvervated, and forms the lateral walls of the heart. Myofibres are absent in the midventral floor. This part is formed by cells of the horizontal septum attached to the gut complex. The myofibres are short. Interdigitating intercalated discs have not been observed, but lateral overlaps are common. Z-, I- and A-bands are seen in the sarcomere. The 2-bands are diffuse and irregular. The sarcolemma invaginates and forms a sparse system of clefts; a poorly developed T-system is indicated. Its presence supports the view that a T-system is inherent in the arthropod myocardium. Couplings are not related to any specific sarcomere band level. It is implied that the thin-walled pseudotubular heart in pycnogonids is a result of a reduction, and that it functions more like a channel than a heart.     

Die Bildung und Differenzierung des postnauplialen Keimstreifs vonDiastylis rathkei (Crustacea,Cumacea)

Zusammenfassung Die Differenzierung der hinter den Mandibeln gebildeten ektodermalen Querreihen des Keimstreifs vonDiastylis wird beschrieben. 4 dieser Querreihen von Zellen werden nicht durch Ektoteloblasten gebildet, sondern lagern sich direkt als Blastodermzellen aneinander. Dahinter werden 12 Reihen durch Ektoteloblasten gebildet. Die Ektoteloblasten teilen sich zum Schlu in die Reihen XIII und XIV. Alle Zellreihen treten in eine Folge von differentiellen Teilungen ein, so da die genaue Differenzierung und Musterbildung der Zellen bis zur Bildung von Ganglienanlagen und ExtremitÄtenknospen zellgenealogisch verfolgt werden kann. Die ersten 2 Reihen hinter den Mandibeln, die Reihen (0) und (1), tragen zur Bildung des vorderen und mittleren Teils des 1. Maxillensegments bei. Der hintere Teil des 1. Maxillensegments wird durch die vorderen Zellabkömmlinge der Reihe (2) gebildet. Die 1. Maxille ist aus Zellen von verschiedenen Zellklonen zusammengesetzt, die zur Reihe (1) und (2) gehören. Die 2. Maxille und die Thorakalbeine werden ebenfalls durch verschiedene Zellklone zusammengesetzt.Die Reihen (2) und (3) haben ein Ähnliches Differenzierungsmuster. Die Unterschiede betreffen hauptsÄchlich den extremitÄtenbildenden Bereich. Die Reihe (3) und die erste ektoteloblastisch gebildete Reihe I sowie die folgenden extremitÄtenbildenden Reihen sind in ihrer Differenzierung fast identisch. Die Ganglien bilden sich durch Neuroblasten, welche Ganglienmutterzellen ins Innere abgeben. Die Neuroblasten haben ein kompliziertes Teilungsmuster. Sie können sich auch nach Abgabe von Ganglienmutterzellen Äqual teilen. Die Intersegmentalfurchen laufen schrÄg durch die Abkömmlinge einer Reihe und markieren nicht die genealogischen Grenzen.Die Ergebnisse werden im Vergleich mit anderen Mandibulaten, besonders mit den Insekten diskutiert. Es ergeben sich interessante Ähnlichkeiten und Unterschiede in der Bildung eines morphologischen Differenzierungszentrums und in der Anlage von ExtremitÄtenknospen, von Ganglien und Intersegmentalfurchen.

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Formation and differentiation of the post-naupliar germ bandm Diastylis rathkei (crustacea, cumacea)II. Differentiation and pattern formation of the ectoderm

Summary The differentiation of ectodermal cell rows arranged on the germ band ofDiastylis behind the presumptive mandibular segment is described. 4 of the cell rows are not budded off from ectoteloblasts, but are formed directly by blastoderm cells. Behind these 4 rows, 12 cell rows are budded off from ectoteloblasts. Eventually, the ectoteloblasts divide to form rows XIII and XIV. All of these cell rows have a fixed sequence of mitoses by which a detailed analysis of the cell-lineage up to the formation of ganglion anlagen and appendage buds is possible. The rows (0) and (1) form the anterior and middle parts of the maxillular segment. The posterior part of this segment is formed by derivatives of the subsequent cell row (2). Thus, the maxillulae are complex structures, composed by cells from different cell clones. The maxillae and the thoracic limbs are complex structures as well. Rows (2) and (3) have a similar differentiation pattern. The differences are mainly found in the appendage-forming parts. The differentiation of row (3) is nearly identical to row I, i.e. the first row budded off from ectoteloblasts, and to the subsequent rows II–VI.Ganglion cells are formed by the division of ganglion mother cells that are budded off from neuroblasts. The neuroblasts have a complicated pattern of divisions. There may be an alternation of unequal and equal mitoses. The intersegmental furrows run in a transverse and slightly oblique plane through the derivatives of one cell row. They do not indicate genealogical boundaries.The results are compared with similar developmental processes in other Mandibulata, especially Insecta. The similarities and differences in the existence of a morphological differentiation center and in the formation of appendage buds, ganglion anlagen, and intersegmental furrows are discussed.

     

Morphology and Differentiation of Non-sensory Cuticular Structures in Mysidacea, Cumacea and Tanaidacea (Crustacea, Peracarida)

The non-sensory cuticular structures of some peracarideans (Mysidacea, Cumacea, Tanaidacea) were examined by scanning electron microscopy. The various types of structures present in the adult specimens are listed and the relation amongst them is elucidated. Three ways of differentiation of the structures can be distinguished: 1) a differentiation in the complexity of the structures themselves, 2) a differentiation of their arrangement on the body. 3) a differentiation of their distribution on the various parts of the body. A highly differentiated type of arrangement (row) of a number of simple structures (e.g. teeth) may lead to a higher complex structure (comb), which is seen to be developed best on special regions of the body (e.g. the distal segments of thoracic legs). The function of the cuticular structures–by analogy with other taxonomic groups–is discussed.     

Die bildung und differenzierung des postnauplialen Keimstreifs von Diastylis rathkei (Crustacea,Cumacea)

Zusammenfassung In diesem 1. Teil der Untersuchungen über die Entwicklung des postnauplialen Keimstreifs bei Diastylis rathkei wird die Furchung, die Blastodermbildung und die Entstehung fast sämtlicher Elemente des postnauplialen Keimstreifs bis zu ihrer Anordnung in Querreihen beschreiben. Die Voraussetzungen für eine solche Arbeit an fixiertem Material werden definiert.

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Formation and Differentiation of the post-Nauphar germ band in Diastylis rathkei (Crustacea, Cumacea)I. Formation of teloblasts and their descendants

The segmentation, first differentiation of the blastoderm, formation of the ectodermal teloblasts and their descendants, the arrangement of nonteloblastic ectodermal cells in rows in front of the ectodermal teloblasts, and the origin of mesodermal teloblasts and their descendants are described. The cell-lineage of nearly all post-naupliar elements is ascertained by recording their mitoses. The results are discussed in the view of a probable analysis of early developmental processes in comparison with Crustaceans and other Arthropods, esp. Insects.

     

Phylogenetic analysis of Remipedia (Crustacea)

We present a cladistic analysis of the crustacean class Remipedia, including all 17 extant species currently assigned to the order Nectiopoda, with the Carboniferous fossil Tesnusocaris serving as an outgroup. We applied different methodological approaches and coding options to a basic matrix composed of 26 morphological characters. Our analyses strongly support monophyly of the Godzilliidae and affirm justification of the family Micropacteridae. However, the present taxonomic structure within the Speleonectidae is partly incompatible with our results, and we cannot exclude that the family is paraphyletic.     

Phylogenetic analysis of the Malacostraca (Crustacea)

The Malacostraca comprises about 28 000 species with a broad disparity in morphology, anatomy, embryology, behaviour and ecology. The phylogenetic relationships of the major taxa are still under debate. Is the Leptostraca the sister group of the remaining Malacostraca, or is this taxon more closely related to other Crustacea? Does the Stomatopoda or the Bathynellacea represent the most basal taxon within the remaining taxa? Is the Peracarida monophyletic or are some peracarid taxa more closely related to other ‘caridoid’ taxa? Is the Thermosbaenacea part of the Peracarida or its sister group, and how much support is there for a taxon Amphipoda + Isopoda? To answer these questions a phylogenetic analysis of the Malacostraca combining different phylogenetic approaches was undertaken. In a first step, the monophyly of the Malacostraca including the Leptostraca is shown using the ‘Hennigian approach’. A computer cladistic analysis of the Malacostraca was carried out with NONA and PEE ‐WEE , based on 93 characters from morphology, anatomy and embryology. Nineteen higher malacostracan taxa are included in our analysis. Taxa whose representatives are exclusively fossils were not included. The Leptostraca was used as an operational out‐group. The present analysis supports the basal position of the Stomatopoda. Syncarida and Peracarida (including Thermosbaenacea) are supported as monophyletic, the Eucarida is not. Instead a sister‐group relationship is suggested between Euphausiacea and Peracarida (including Thermosbaenacea), with the Syncarida as the sister group to both taxa. Certain embryonic characters are interpreted as support for the monophyly of the Peracarida (without Thermosbaenacea) because convergences or reversals of these characters seem implausible. Within the Peracarida, the Mysidacea (Lophogastrida + Mysida) represents the sister group to the remaining taxa. A sister‐group relationship between Amphipoda and Isopoda is not supported.     

Vemakylindrus cantabricus, a new species of Diastylidae (Crustacea, Cumacea) from the northern Iberian coasts

Eleven species of the genusVemakylindrus Bacescu, 1961 are known at present. A hitherto unknown species is described herein asV. cantabricus, sp. nov., and is compared with the more closely related congeneric species:V. hastatus (Hansen, 1920) andV. stebbingi Day, 1980.Vemakylindrus cantabricus may be distinguished from its congeners by a combination of the following characters: (1) carapace densely covered by hooked denticles and hairs; (2) pseudorostrum shorter than carapace; (3) telson of “Diastylis type” with 5–6 pairs of lateral spines; and (4) external process of basis of third maxilliped with 4 long plumose setae.     

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 the midgut and hindgut of Derocheilocaris remanei (Crustacea, Mystacocarida)

Ultrastructural features and structure of the midgut and hindgut of Derocheilocaris remanei were studied. The large endodermal midgut is differentiated into an anterior midgut and a posterior midgut separated by a conspicuous constriction. Both circular and longitudinal striated muscle bands surround the midgut, while the hindgut only presents longitudinal muscles. The limit between the midgut and the cuticle-lined hindgut is marked by a rectal valve. In cross-section, the short hindgut is triradiate and has a distinct Y-shaped lumen. The hindgut cuticular lining appears interrupted at the tip of every branch of the Y. Three different cell types are found in the midgut epithelium: basally located undifferentiated cells that give rise to the other two specialized cell types; secretory zymogen-like cells responsible for extracellular digestion and located mainly in the anterior midgut; and vacuolated cells, distributed all along the midgut and appearing to have several functions, including absorption, intracellular digestion, and nutrient transport. A single basic cell type forms the hindgut epithelium. The suggested function for the hindgut is the transport and ejection of waste products.     

Ultrastructure of the labrum and foregut of Derocheilocaris remanei (Crustacea,Mystacocarida)

The cuticle-lined foregut of Derocheilocaris remanei consists of the mouth with its associated labrum, and an undifferentiated esophagus. It is separated from the midgut by an esophageal valve. The labrum is a conspicuous structure moved by five pairs of muscles (four dorsoventral and one longitudinal). Four pairs of subcuticular glands open to its inner face forming two longitudinal, lateral rows of cuticular pores. Each secretory unit is composed of a glandular component (with one or two secretory cells), a neck cell, and a duct cell. In addition, a single gland cell opens mesially into the buccal cavity. The ventrally located mouth is a complex structure characterized by a filter-like system, a sensory organ, and epithelial cells with highly developed microvilli. The esophagus is a simple tube with a characteristic curvature following the mouth. It has a rounded cross section and a triradiate lumen. A layer of circular musculature surrounds this region. The end of the esophagus protrudes into the midgut lumen forming the so-called esophageal valve. The ultrastructural features of the foregut, with the presence of a mucus-trapping mechanism, a relatively well-developed filter system and associated structures and an esophagus lacking glands confirm the microphagic feeding habits of mystacocarids. © 1996 Wiley-Liss, Inc.     

哺乳动物朊蛋白基因序列变异及其系统发育意义

以朊蛋白基因(PRNP)为研究对象,从GenBank中选取代表哺乳动物的17目61属共84个物种PRNP的编码区序列,分析了该基因的结构及其在不同层次分类阶元间的进化关系.发现由于在基因内序列重复区存在插入或缺失,PRNP的编码区长度在哺乳动物不同目的物种间存在差异.在终止密码子的使用上不同目的物种之间存在明显的偏好性, TGA和TAG是哺乳动物PRNP最常用的终止密码子,只有奇蹄目的5个种和有袋目袋鼠科的2个种是使用TAA终止.所有84条序列呈现了较高的核苷酸多样性(10.54%).以PRNP为分子标记构建的系统进化树总体上是和以往研究一致的,结果表明PRNP可以应用于哺乳动物较高分类单元的系统进化研究,但对于能否用于种间和种内不能肯定.最后应用系统进化树对尚未有患病报道的哺乳动物的患病可能性进行了预测.     

Ultrastructure of CaCO3 deposits of terrestrial isopods (Crustacea, Oniscidea)

 The ultrastructure of the sternal CaCO₃ deposits of 3 species of the Diplochaeta and 15 of the Crinochaeta was investigated by means of scanning electron microscopy of fractured surfaces. In the Diplochaeta Li-gia italica and L. oceanica, the deposits consist exclusively of individual spherules with diameters between 0.2 and 1.4 μm. No material was observed within the spaces between the spherules. In Ligidium hypnorum, two structurally distinct regions exist. A proximal layer resembling the deposit of Ligia italica and L. oceanica and a distal layer in which the spherules appear to be fused with each other. In the species of the Crinochaeta, the CaCO₃ deposits comprise a spherular region which resembles the deposits of Ligidium hypnorum, and a homogeneous layer located between the spherular part of the deposit and the hypodermal cell layer. In some species the diameters of the spherules may be up to 3.1 μm. In the homogeneous layer and the distal spherular layer more calcium per volume can be stored than in the proximal spherular layer in which the spaces between the spherules are devoid of CaCO₃. This suggests that the multiple layered deposits are an adaptation to terrestrial life, as a consequence of the need for increased resorption of cuticular calcium. Accepted: 7 January 1997     

Phylogenetic relationships between spiny, slipper and coral lobsters (Crustacea, Decapoda, Achelata)

Molecular data can aid in the resolution of conflicting hypotheses generated through difficulties in the interpretation of morphological data and/or an incomplete fossil record. Moreover, the reconstruction of phylogenetic relationships using molecular data may help to trace back the origin of morphological innovations which had a major impact on the radiation of a taxonomical group. In this work, different nuclear (18S, 28S, and H3) and mitochondrial (16S and COI) gene regions were sequenced in a total of 35 Achelatan species to test conflicting hypotheses of evolutionary relationships within the Achelata infraorder and solve the taxonomic disagreements in the group. The combined molecular dataset strongly supports the hypothesis that Achelata is a monophyletic group composed of two main families: Palinuridae and Scyllaridae. Synaxidae is found to be a polyphyletic group, which should be included within Palinuridae. Consequently, our results indicate that the origin of the stridulating organ occurred only once during Achelata evolution. Finally, the two main clades found within the Scyllaridae are in agreement with previous inferences based on adult morphological data. The dating of divergence of Achelata obtained with a relaxed-clock model is compatible with previous hypotheses of a Triassic origin of the Achelata.     

Global diversity of cumaceans &; tanaidaceans (Crustacea: Cumacea &; Tanaidacea) in freshwater

Cumacea and Tanaidacea are marginal groups in continental waters. Although many euryhaline species from both groups are found in estuaries and coastal lagoons, most occur only temporarily in non-marine habitats, appearing unable to form stable populations there. A total of 21 genuinely non-marine cumaceans are known, mostly concentrated in the Ponto-Caspian region, and only four tanaids have been reported from non-marine environments. Most non-marine cumaceans (19 species) belong in the Pseudocumatidae and appear restricted to the Caspian Sea (with salinity up to 13‰) and its peripheral fluvial basins, including the northern, lower salinity zones of the Black Sea (Sea of Azov). There are nine Ponto-Caspian genera, all endemic to the region. Only two other taxa (in the family Nannastacidae) occur in areas free of any marine–water influence, in river basins in North and South America. Both seem able to survive in waters of raised salinity of the lower reaches of these fluvial systems; but neither has been recorded in full salinity marine environments. The only non-marine tanaidacean thus far known lives in a slightly brackish inland spring in Northern Australia. The genus includes a second species, from a brackish-water lake at the Bismarck Archipelago, tentatively included here as non-marine also. Two additional species of tanaidaceans have been reported from non-marine habitats but both also occur in the sea. Guest editors: E. V. Balian, C. Lévêque, H. Segers & K. Martens Freshwater Animal Diversity Assessment     

Relationship of Homolidae and Dromiidae: Evidence from Spermatozoal Ultrastructure (Crustacea,Decapoda)

Abstract The homolid spermatozoon, as exemplified by Homolasp., Paromolasp. and Paromola petterdi, differs markedly from spermatozoa of crabs of the Heterotremata–Thoracotremata assemblage but agrees with the sperm of dromiids, in the strongly anteroposteriorly depressed acrosome (apomorphy?) and the capitate form of the perforatorium (a major synapomorphy seen nowhere else in the Crustacea). These similarities support inclusion of the Dromiidae and Homolidae in a single grouping, the Podotremata. The homolid perforatorium differs from that of dromiids in the autapomorphic spiked–wheel form of the anterior expansion. Homolid spermatozoa show nuclear arms symplesiomorphic of all investigated crabs (small or questionably sometimes absent in Dromiidae), and corresponding loss of purely microtubular arms seen in other reptants. Homolid sperm agree with those of dromiids (synapomorphy?), raninids, higher heterotremes and thoracotremes (homoplasies?) but differ from lower heterotremes, in lacking microtubules in the nuclear arms. A posterior median process of the nucleus in homolids, not seen in dromiids, is shared with anomurans and lower heterotremes. No features in the ultrastructure of homolid or dromiid sperm have been detected which associate them exclusively with either the Raninidae or the heterotreme and thoracotreme Brachyura.     

Phylogenetic position,systematic status,and divergence time of the Procarididea (Crustacea: Decapoda)

Bracken, H. D., De Grave, S., Toon, A., Felder, D. L. & Crandall, K. A. (2009). Phylogenetic position, systematic status, and divergence time of the Procarididea (Crustacea: Decapoda). —Zoologica Scripta, 39, 198–212. Ever since discovery of the anchialine shrimp, Procaris ascensionis Chace & Manning 1972 , there has been debate as to its systematic position in relationship to other shrimp‐like decapods. Several morphological characters have suggested a close affinity among Procarididae, Dendrobranchiata and Stenopodidea, whereas other physical features unite Procarididae with Caridea. Few molecular studies have examined the phylogenetic position of procaridid shrimp due to limited available material for genetic analyses. Those studies show procaridids as sister to carideans but lack sufficient taxon and locus sampling to validate the relationship. Here, we present a molecular phylogeny of selected individuals across decapod infraorders and superfamilies to clarify the phylogenetic position of procaridid shrimp. One mitochondrial (16S) and three nuclear genes (18S, 28S, H3) have been chosen to elucidate relationships. We used Bayesian molecular dating methods implemented in multidivtime to estimate and compare the divergence times among procaridids and other lineages. Findings secure the placement of the procaridids as a sister clade to carideans. Results provide evidence for the recognition of procaridids as a separate infraorder (Procarididea Felgenhauer & Abele 1983 ) within the Decapoda on the basis of molecular and morphological data.     

Ultrastructure of the spermatozoa of Aristaeopsis edwardsiana and Aristeus varidens (Crustacea, Dendrobranchiata, Aristeidae)

The acrosome-less spermatozoon of Aristaeopsis edwardsiana (Crustacea, Aristeidae), which consists of a central non-membrane bound nuclear region surrounded by a thin peripheral cytoplasm, much resembles that of the previously studied aristeid Aristaeomorpha foliacea. The marked spermatozoal similarities between these two species appear to indicate a close phylogenetic proximity. A considerably different spermatozoal pattern is observed in aristeids from the genus Aristeus (A. varidens and A. antennatus), whose spermatozoa possess an anterior spherical acrosome, lacking a spike, and partially embedded in (instead of capping) the main sperm body. The two distinct sperm types found in the Aristeidae differ significantly from the spiked sperm typically found in most penaeoids (Penaeidae, Solenoceridae and Sicyoniidae), thus suggesting a phylogenetic separation of the Aristeidae from the remaining Penaeoidea.     

Ultrastructure of Prorodon (Ciliophora, Prostomatida) Ii. Oral Cortex and Phylogenetic Conclusions

ABSTRACT. The ultrastructure of the oral region and the ultrastructural architecture of the basket of Prorodon aklitolophon and Prorodon teres are described. the oral region of Prorodon consists of: 1) A circumoral kinety at the anterior pole of the cell surrounding the typically slit-shaped cytostomial funnel. This kinety is composed of inversely oriented dikinetids in which both kinetosomes are ciliated and are associated with a very short postciliary microtubular ribbon and a few transverse microtubules; 2) Three brush rows aligned in parallel and extended meridionally in the anterior part of the cell. the individual brush rows consist of dikinetids, but in contrast to the dikinetids around the cytopharynx they are not inverted and only the anterior kinetosomes bear specialized short brush cilia and are associated with a divergent-tangential transverse microtubular ribbon. the posterior kinetosome is non-ciliated and bears a prominent convergent postciliary microtubular ribbon. Schematized dikinetid patterns of both oral regions of Prorodon are provided. In addition, a three-dimensional reconstruction of the basket of the genus Prorodon based on serial thin sections is presented. A phylogenetic tree, mainly based on stomatogenic data, is given to show the phylogenetic relationships of some prostomatid genera as well as the hypothesized sistergroup relationship of colpodid and prostomatid ciliates.