The spermatozoon of Mengenilla moldrzyki (Strepsiptera,Mengenillidae): Ultrastructure and phylogenetic considerations

Even though the spermatozoa of several strepsipteran species were described earlier, no data were available for the basal family Mengenillidae. Well-fixed material of the recently described Tunisian species Mengenilla moldrzyki was used for a detailed examination of the sperm ultrastructure. The total length is c. 30 μm. The head region contains a conical acrosome vesicle (0.3-0.35 μm) and an elongated nucleus (7.3 μm) with dense chromatin. Some granular material along with a uniformely dense centriole adjunct and two mitochondrial derivatives are visible at the posterior end of the nucleus. The material of the centriole adjunct does not extend along the flagellum and accessory bodies are absent. The mitochondrial derivatives are elongated structures crossed by a longitudinal crista but lacking parallel transverse cristae and paracrystalline material in the dense matrix. The mitochondrial derivatives gradually reduce their size and end at the most posterior tail region. The flagellar axoneme has a 9 + 9 + 2 pattern and originates beneath the nucleus. In the terminal tail region the axoneme gradually disintegrates. Despite the extreme specialization of the endoparasitc group, strepsipteran spermatozoa are mostly characterized by plesiomorphies. The pattern within the order is largely uniform, but Mengenilla displays several apomorphic features compared to the presumptive strepsipteran groundplan (e.g., absence of crystallizations and cristae in the mitochondrial derivatives). The subdivision of the intertubular material into two compartments with a dense beak-like structure adhering to the tubular wall supports a clade Coleopterida (=Strepsiptera + Coleoptera) + Neuropterida.     

Sperm structure of Mecoptera and Siphonaptera (Insecta) and the phylogenetic position of<Emphasis Type="Italic"> Boreus hyemalis</Emphasis>

Sperm ultrastructure has been studied in three species of the taxa Mecoptera and Siphonaptera. The spermatozoon of the scorpion fly Panorpa germanica shows an apical bilayered acrosome, a helicoidal nucleus, a centriolar region and a 9+2 flagellar axoneme helicoidally arranged around a long mitochondrial derivative. A second mitochondrial derivative is very short and present only in the centriolar region. A single accessory body is present and it is clearly formed as a prolongation of the centriole adjunct material. Two lateral lamellae run parallel to the nucleus. The snow fly Boreus hyemalis has a conventional sperm structure and shows a bilayered acrosome, a long nucleus, a centriolar region, two mitochondrial derivatives and two accessory bodies. The axoneme is of the 9+2 type and is flattened at the tail tip. Both P. germanica and B. hyemalis have two longitudinal extra-axonemal rods and have a glycocalyx consisting of longitudinal parallel ridges or filaments. The spermatozoon of the flea Ctenocephalides canis has a long apical bilayered acrosome, a nucleus, a centriolar region, a 9+2 axoneme wound around two unequally sized mitochondrial derivatives, and two triangular accessory bodies. In the posterior tail end the flagellar axoneme disorganises and a few microtubular doublets run helicoidally around the remnant mitochondrial derivative. The glycocalyx consists of fine transverse striations. In all three species, the posterior tail tip is characterised by a dense matrix embedding the disorganised axoneme. From this comparative analysis of the sperm structure it is concluded that Mecoptera, as traditionally defined, is monophyletic and that B. hyemalis is a member of Mecoptera rather than of Siphonaptera.     

Fish germinal cells. I. Comparative spermatology of seven Cyprinid species

The spermatozoa of seven fishes belonging to Cyprinid family are examined. They have no acrosome, like all Teleost fishes, a spheroidal or slightly elliptic nucleus, always eccentrically placed on the tail, two variously oriented centrioles, and a postnuclear cytoplasmic region of various size that contains some mitochondria (2 to 10) and surrounds a periaxonemal postnuclear canal. The tail is of moderate length (from 36 to 60 μm) and contains a “9 + 2” axoneme: both dynein arms are present. Comparative examination of the spermatozoa in the seven species shows that significant differences occur among them, even when they belong to the same genus. These concern the tail length; the position of the centrioles, the proximal with respect to the central one and with respect to the nucleus; the number of mitochondria, which is in relationship to the depth of the postnuclear canal. In the uniform general pattern of the ultrastructure of the Cyprinid spermatozoa, each species is characterized by a particular organization of the sperm organelles; in this respect, the two species examined by us, Leuciscus cephalus and souffia, are more closely related, even if easily recognizable one from the other. From a phylogenetic point of view, the comparative spermatology of the Cyprinid fishes suggests that the mitochondrial number is a good character, which enables us to order them in a phylogenetic arrangement.     

Ultrastructural studies on euspermatozoa and paraspermatozoa in Mantispidae (Insecta, Neuroptera)

Previous studies have demonstrated the presence of sperm dimorphism in the Mantispidae Perlamantispa perla. We extended the study on several other mantidflies. In all the examined species the occurrence of euspermatozoa (typical) and paraspermatozoa (atypical) was established. The euspermatozoa are characterized by the presence of a cylindrical nucleus surrounded by an envelope that fans out laterally into two thin wings of different length. The acrosome seems to be missing. The nucleus is surrounded by extracellular material. The flagellum is provided with a 9 + 9 + 2 axonemal pattern; the accessory tubules contain 16 protofilaments and the intertubular material has the distribution typical of the taxon. Two elongated accessory bodies flank partially the axoneme and connect this structure with the mitochondrial derivatives. The flagellar axoneme of paraspermatozoa consists of an axoneme and two giant mitochondrial derivatives filled with large globular units. The axoneme exhibits a 9 + 9 + 2 pattern, in which the central 9 + 2 units have a normal structure, in that the microtubular doublets are provided with both dynein arms and radial links. On the contrary, the nine accessory microtubules have a large diameter and their tubular wall consists of 40 protofilaments. This comparative study provided evidences about the uniformity of sperm ultrastructure in Mantispidae. The function of non-fertilizing giant sperm in mantidflies is discussed.     

Ultrastructural analysis of spermatozoa of Korscheltell us lupulinus L. (Lepidoptera : Hepialidae) and Micropterix calthella L. (Lepidoptera : Micropterigidae)

In Korscheltellus lupulinus (Lepidoptera : Hepialidae), both eusperm and parasperm can be found, whereas Micropterix calthella (Lepidoptera : Micropterigidae) produces only eusperm. The eupyrene sperm in K. lupulinus is 250 μm long. Spermatozoa found in K. lupulinus are very similar to those found in higher Lepidoptera, but the eusperm of M. calthella do not possess similar features. As in other Lepidoptera, the axoneme pattern of K. lupulinus is 9 + 9 + 2. Anteriorly, the axoneme is replaced by a fibrous stem similar to an acrosomal structure; posteriorly it becomes progressively uneven. The sperm of K. lupulinus has other original features. The anterior region of the sperm is rigid and contains the nucleus, which has a longitudinal groove adjacent to the axoneme. The 2 mitochondrial derivatives extend from the posterior end of the nucleus. There are no accessory bodies. Many peripheral cytoplasmic vesicles are present. A thin sheath surrounds the cell. It is thick in the parasperm and made of concentric or spiralling lamellae; it does not have any lacinate appendages.The axoneme of the sperm of M. calthella extends over the entire length of the cell and spirals in a helix around the nucleus. The nucleus is also almost as long as the cell. The 2 mitochondrial derivatives, flanked by accessory bodies, follow this spiralling. The axoneme has a 9 + 2 pattern. The plane, which contains the 2 central microtubules, is at an angle with the median plane of the nucleus.     

Ultrastructure of the spermatozoon ofElenchus japonicus and its bearing on the phylogeny of strepsiptera

The fine structure of the mature spermatozoon of the strepsipteranElenchus japonicus Esaki and Hashimoto (Elenchidae) is described using transmission electron microscopy. The spermatozoon was seen to have an elongated head, a tail containing a 9 + 9 + 2 axoneme, two mitochondrial derivatives and two accessory sheaths. The monolayered acrosome is conical in shape while the nucleus exhibits an internal channel of uncondensed chromatin. The tail is long, and in its final portion, the axoneme, loses its elements progressively. These results are compared with the sperm ultrastructure ofXenos moutoni De Buysson (Stylopidae) and with those of other insect orders, particularly the Coleoptera.     

Structure and ultrastructure of the spermatozoa of Bephratelloides pomorum (Fabricius) (Hymenoptera: Eurytomidae)

The spermatozoa of Bephratelloides pomorum are very long and fine. Each spermatozoon measures about 620 μm in length by 0.38 μm in diameter and, when seen under the light microscope, appears to be wavy along its entire length. The head, which is approximately 105 μm, comprises a small acrosome and a nucleus. The acrosome is made up of a cone-shaped acrosomal vesicle surrounding the perforatorium and the anterior end of the nucleus. Innumerable filaments radiate from it. The perforatorium has a diameter equal to that of the nucleus at their junction, where it fits with a concave base onto the rounded nuclear tip. The nucleus is helicoidal and completely filled with homogeneous compact chromatin. It is attached to the tail by a very long and quite electron-dense centriolar adjunct that extends anteriorly from the centriole in a spiral around the nucleus for approximately 8.5 μm. The tail consists of an axoneme with the 9+9+2 microtubule arrangement pitched in a long helix, as well as a pair of spiraling mitochondrial derivatives (with regularly arranged cristae) that coil around the axoneme, and two small accessory bodies. As well as the spiraling of the nucleus, mitochondrial derivatives and axonemal microtubules, the sperm of B. pomorum present other very different morphological features. These features include the acrosome and centriolar adjunct, both of which differentiate the spermatozoa from the majority of sperm found in other Hymenoptera. In addition these structural variations demonstrate that the sperm of chalcidoids provide characteristics that can certainly prove useful for future phylogenetic analysis at the subfamily level and, possibly, the genus too.     

A novel membrane specialization in the sperm tail of bug insects (heteroptera)

The sperm tail of bug insects has 9 + 9 + 2 flagellar axonemes and two mitochondrial derivatives showing two to three crystalline inclusions in their matrix. During spermiogenesis, the axoneme is surrounded by a membrane cistern which, at sperm maturity, reduces to two short cisterns on the opposite sides of the axoneme adhering to the mitochondrial derivatives. Filamentous bridges connect the intertubular material of the axoneme to these cisterns. Such bridges, which represent a peculiar feature of bug insects, are resistant to detergent treatment, whereas part of the intertubular material and the inner content of microtubular doublets are affected by the treatment. After freeze‐fracture replicas, at the insertion of the bridges to the cisternal membrane, the P‐face of this membrane shows a characteristic ribbon consisting of four rows of 11 ± 1 nm staggered intramembrane particles, 13 ± 2 nm apart along each row. The bridges could be able to maintain the axoneme in the proper position during flagellar beating avoiding distortion affecting sperm motility. J. Morphol. 2009. © 2009 Wiley‐Liss, Inc.     

Characteristics of the flagellar axoneme in Neuroptera,Coleoptera, and Strepsiptera

Spermatozoa from representatives of the five insect orders in superorder Neuropteroidea were examined by electron microscopy following a new fixation method that includes tannic acid in the primary fixative but has uranyl acetate rather than osmium tetroxide as the secondary fixative. The sperm axoneme was found to be similar in the four orders Megaloptera, Raphidioptera, Neuroptera, and Coleoptera, and is characterized above all by its so-called intertubular material being divided into two portions, one located outside, but in contact with the doublet, and the other projecting from the accessory tubule and having a beak-like shape. These features have not been seen in insects from other orders and may be a synapomorphy for these neuropteroid orders. The accessory tubules in these four orders have 16 protofilaments. The shape of the accessory bodies adjacent to the mitochondrial derivatives is nearly the same in insects from the more primitive neuropteroid orders and in Coleoptera. The sperm tail of the examined strepsipteran deviates in several respects from that of other neuropteroids: the particle row in the wall of accessory tubules is incomplete, an intertubular material is missing, and the mitochondria contain no crystal. © 1994 Wiley-Liss, Inc.     

Sperm structure and spermiogenesis in Coletinia sp. (Nicoletiidae, Zygentoma, Insecta) with a comparative analysis of sperm structure in Zygentoma

The spermatozoon of Coletinia sp. has a bilayered acrosome, a short nucleus (4 microm) and a relatively short sperm tail with two mitochondrial derivatives. The chromatin is uniformly dense except for several electron-lucid channels or strands which permeate the nucleus and which originate in the spermatid as invaginations of the nuclear envelope. The invaginations occur mostly or exclusively along two meridians of the spermatid that are also characterized by the presence of a longitudinal rod of medium electron density. The two rods (designated as 'mid-spermatid rods') evidently are instrumental in the formation of the electron-lucid channels. The significance of this elaborate system of intranuclear channels is not understood. The sperm tail has a 9 + 9 + 2 axoneme with each of the nine microtubular doublets accompanied by an accessory microtubule; scant intertubular material can also be distinguished. Hence, the tail axoneme resembles that of many pterygote insects. Each of the two mitochondrial derivatives contains a crystalline inclusion that has periodically spaced layers going in different directions on either side of the midline. Two synapomorphic traits appear to be shared by Ateluridae and Nicoletiidae, namely the invaginations of the nuclear membrane along two meridians of the nucleus and the shape of the crystalline inclusions of the mitochondrial derivatives. Four species from the family Lepismatidae were also examined as to their sperm ultrastructure. Three of them, Allacrotelsa kraepelini, Ctenolepisma longicaudata and Ctenolepisma sp., were found to be very similar to the two previously examined lepismatids, Thermobia domestica and Lepisma saccharina. On the other hand, spermatozoa of Tricholepisma aurea were aggregated in small groups rather than pairwise joined as seen in the other lepismatids. Sperm characters are also used to reconstruct a phylogenetic hypothesis which suggests a close relationship between Ateluridae and Nicoletiidae.     

New findings on sperm ultrastructure of Xenos vesparum (Rossi) (Strepsiptera,Insecta)

The systematic position of insect order Strepsiptera is still under debate. It was, therefore, thought of interest to examine the ultrastructure of a strepsipteran in a search for synapomorphies shared with Coleoptera, Diptera, or any other insect order. The fine structure of spermatozoa and the spermatid from Xenos vesparum (Rossi) was re-examined using scanning and transmission electron microscopy and a fixation technique that permits the visualization of the macromolecular organization of the organelles. The spermatozoon was shown to possess several traits that are characteristics of insects in general, such as a 9 + 9 + 2 axoneme, two mitochondrial derivatives containing a crystalline material and two 'zipper lines' present along the sperm tail. Seventeen protofilaments occurred along most of the accessory tubules, which reduced to 16 posteriorly. An acrosome is absent. The neck region contains a prominent centriolar adjunct, which gives rise to two accessory bodies which adhere to the mitochondrial derivatives, and to slender strands of the so-called intertubular material found between the accessory tubules. Of interest is the finding that the glycocalyx consists of prominent filamentous strands, similar to those found in siphonapterans, mecopterans and basal dipterans.     

Comparative spermatology in Plecoptera (Insecta): an ultrastructural investigation on four species

The ultrastructure of spermatozoa of four Plecoptera species, Leuctra fusca Linnaeus, Brachyptera risi (Morton), Taeniopteryx stankovitchi Ikonomov, T. kuehtreiberi (Aubert), was investigated by light microscopy, scanning and transmission electron microscopy, and immunofluorescence microscopy. The spermatozoa of all the species have a complex acrosome, are filiform and flagellate, with a '9+9+2' axoneme flanked by two mitochondrial derivatives. However, the structure shows a certain interspecific heterogeneity. L. fusca has a short conical nucleus in the apical position and an axoneme flanked by two accessory bodies. In the sperm of the Taeniopterygidae, the nucleus is a long cylindrical body which lies between the two mitochondrial derivatives flanking the axoneme for most of its length. Our results suggest a close phylogenetic affinity between Plecoptera and the other orders of Polyneoptera, although the proposed sister-group relationship between Plecoptera and Embioptera cannot be confirmed.     

Fine structure of the spermatozoon of the strepsipteran Xenos moutoni

Spermatozoa of Xenos moutoni De Buysson belonging to the order Strepsiptera (Insecta) were examined by electron microscopy. The spermatozoon was seen to have an elongated head and a tail containing a 9+9+2 axoneme and two mitochondrial derivatives of equal size. The pear-shaped acrosome is characterised by a mono-layered structure and terminates anteriorly forming two pyramidal evaginations. The nucleus exhibits an external portion of dense chromatin and an internal one of uncondensed material. The latter occupies a central position at the base and becomes progressively peripheral at the apex. The tail is long and in its final portion the axoneme loses its elements progressively. These results have been compared with the ultrastructure of the spermatozoa of Coleoptera which have been considered as a sister group of Strepsiptera.     

Comparative spermatology in Plecoptera (Insecta). II. An ultrastructural investigation on four species of Systellognatha

Sperm structure of four Systellognatha species, Dinocras cephalotes (Curtis, 1827) and Perla grandis (Rambur, 1841), family Perlidae, Siphonoperla torrentium (Pictet, 1841), family Chloroperlidae, and Isoperla grammatica (Poda, 1761), family Perlodidae, was investigated by light microscopy, scanning and transmission electron microscopy, and immunofluorescence microscopy. The spermatozoa of all the species are filiform and flagellate; they have an elongated compact nucleus, topped by either a bi-layered or three-layered acrosomal complex, and a '9+9+2' axoneme flanked by two mitochondrial derivatives. However, some variations have been observed, particularly regarding the morphology of the acrosomal complex, the shape of the nucleus, two more or less evident accessory bodies flanking the axoneme and the degree of crystallisation of the mitochondrial derivatives. Our results support the suggestion that Systellognatha is a monophyletic group, showing a single sperm pattern. Chloroperlidae and Perlodidae retain the plesiomorphic condition of some sperm characters while Perlidae show some autoapomorphies. A phylogenetic affinity between Plecoptera and the other orders of Polyneoptera has been confirmed.     

Structure and energy pathways of spermatozoa of the rove beetle Aleochara bilineata (Coleoptera, Staphylinidae)

The morphology of mature spermatozoa of the rove beetle Aleochara bilineata was examined by using scanning and transmission electron microscopy. They are about 1000 mum long and filiform. The acrosome and the nucleus are elongate and each about 20 mum long. A well-developed centriole adjunct region connects the nucleus with the sperm tail. The axoneme reveals the 9 + 9 + 2 pattern of the pterygote sperm flagellum. Two accessory bodies and two mitochondrial derivatives with paracrystalline inclusions are present. Cristae are reduced to the cortical zone of the derivatives. Cytochrome-c oxidase activity was detected within the cristae by DAB-reaction. The energy metabolism of the spermatozoa was investigated by using different inhibitors affecting the mitochondrial and cytoplasmic metabolic pathways. Sperm movement was used as an indicator for the utilization of ATP by the axoneme. In control experiments, the duration of motility was longer than 45 min. In the presence of atractyloside or potassium cyanide the motility duration was not affected. On the other hand, iodoacetic acid in the medium stopped sperm motility within 15 min. This indicates that sperm energy metabolism mainly depends on the glycolytic pathway.     

The sperm structure of Embioptera (Insecta) and phylogenetic considerations

The sperm structure of two species of Embioptera, Embia savignyi Westwood 1837 and Aposthonia japonica (Okajima 1926), was studied. Spermatozoa of both species exhibit a monolayered acrosome and a layer of material surrounding the sperm cells for most of their length. The presence of a 9+9+2 axoneme provided with accessory microtubules with 16 protofilaments, two accessory bodies and two crystallized mitochondrial derivatives are characters shared with other polyneopteran taxa. The supposed close relationship between Embioptera and Phasmatodea is not supported by characters of the sperm ultrastructure.     

Comparative morphology of spermatozoa and reproductive systems of zorapteran species from different world regions (Insecta,Zoraptera)

The male and female reproductive apparatus of Zorotypus magnicaudelli (Malaysia), Zorotypus huxleyi (Ecuador) and Zorotypus weidneri (Brazil) were examined and documented in detail. The genital apparatus and sperm of the three species show only minor differences. The testes are larger in Z. magnicaudelli. Z. huxleyi lacks the helical appendage in the accessory glands. A long cuticular flagellum is present in Z. magnicaudelli and in the previously studied Zorotypus caudelli like in several other species, whereas it is absent in Z. weidneri, Z. huxleyi, Zorotypus hubbardi, Zorotypus impolitus and Zorotypus guineensis. Characteristic features of the very similar sperm are the presence of: a) two dense arches above the axoneme; b) a 9 + 9+2 axoneme with detached subtubules A and B of doublets 1 and 6; c) the axonemal end degenerating with enlarging accessory tubules; d) accessory tubules with 17 protofilaments; e) three accessory bodies beneath the axoneme; and f) two mitochondrial derivatives of equal shape. The first characteristic (a) is unknown outside of Zoraptera and possibly autapomorphic. The sperm structure differs distinctly in Z. impolitus and Z. hubbardi, which produce giant sperm and possess a huge spermatheca. The presence of the same sperm type in species either provided with a sclerotized coiled flagellum in males or lacking this structure indicates that a different organization of the genital apparatus does not necessarily affect the sperm structure. The flagellum and its pouch has probably evolved within Zoraptera, but it cannot be excluded that it is a groundplan feature and was reduced several times. The fossil evidence and our findings suggest that distinct modifications in the genital apparatus occurred before the fragmentation of the Gondwanan landmass in the middle Cretaceous.     

Dynamics of spermiogenesis in Drosophila melanogaster: III. Relation between axoneme and mitochondrial derivatives

In cross sections of developing spermatid tails of D. melanogaster, the angular positions of the mitochondrial derivatives relative to the axoneme are precisely defined at each stage of development. Nearly mature sperm in the coiling stage, however, exhibit a variable angular relation between the axonome and the rest of the tail. A similar variation is also found among cross sections of mature sperm tails. These observations, together with other morphological evidence, are interpreted as indicating limited rotational freedom between the axoneme and the rest of the tail in mature sperm. Such a freedom seems to be related to the swimming pattern of sperm and the fertilization process. It is suspected that specific shapes and natures of mitochondrial derivatives in sperm tails of insects are related to a particular swimming pattern of sperm, which must be highly precise in order to meet the requirements of species-specific modes of fertilization.     

The giant sperm of a minute beetle

The mature sperm of Ptinella aptera is a helically coiled, flagellate gamete ca. 1.4 mm long—twice the length of the beetle itself. The rod-like acrosome, comprising the anterior part of the sperm, is 0.4 μm thick but is expanded as a flange around the nucleus and the base of the tail, increasing the diameter of the sperm to 2 μm. The bulk of the tail consists of a pair of bodies with a characteristic ultrastructure of longitudinal tubules beneath a lamellar cortical layer. These bodies are probably homologous with the mitochondrial derivatives of other insect sperm. The axoneme is helically coiled and is flanked by a single accessory body. One of the ‘structured bodies’ is connected to the acrosome and the other to the accessory body. The sperm move actively in the female reproductive tract. The functional significance of this behaviour and of the evolution of the large gamete itself is discussed in relation to existing hypotheses.     

Spermatozoa and phylogeny of Curculionoidea (Coleoptera)

In the examined families of Curculionoidea (Coleoptera), the sperm, although characteristic of typical pterygote insects, shows a few peculiarities that suggest Curculionoidea to be a homogeneous group. The curculionid sperm, in fact, always follows a similar structural design, without any variation. For example, it has 2 mitochondrial derivatives of different sizes, the larger of which is almost completely filled with a crystalline protein, the other being more moderately crystallized and almost completely occupied by cristae, and 2 accessory bodies of different sizes that are made up of a crystalline portion, crescent-shaped in section, and a “puff”-like expansion that is of different consistency, shape, and symmetry in various cases. The different extensions of the accessory bodies seem, therefore, to compensate for the high degree of asymmetry due to the largely different sizes of the 2 mitochondrial derivatives.The examined families and subfamilies can be arranged in 2 groups: Rhynchitidae appear drastically isolated, because they have a peculiar “9 + 9 + 0” axoneme, and show, moreover, a limited degree of asymmetry in the tail organelles. The remaining families and subfamilies are more closely related to one another by the presence of a “9 + 9 + 2” classical axoneme and by the same degree of asymmetry in the tail, typical of curculionid sperm. Among them, Apionidae are distinguished for the space containing the extraacrosomal layer, which may be hollow or absent, a twice-stepped nucleus-tail connection, and a thick glycocalyx at the end of the tail.The Curculionidae conserve primitive characters, such as the 3-layered acrosomal complex and “9 + 9 + 2” axoneme, but also present a high degree of differentiation in the shape of the asymmetrical tail organelles. There appear to be 3 clusters: the first cluster includes Brachyderinae, Leptopiinae, Gymnetrinae, Cryptorhynchinae, Rhynchophorinae. The second cluster includes Scolytidae, Cleoninae, Hylobiinae. The third cluster is more numerous and heterogeneous and shows 3 subgroups. The first of these includes only Otiorhynchinae. The sum of their characters shows that they have most of the common features of primitive curculionids; however the differences between a genus and another are so large that they could be assigned to different subfamilies. The second subgroup includes Hyperinae, Pissodinae, Magdalinae, Ceutorhynchinae and Cossoninae, and the third group includes Cioninae, Anthonominae, and Barimae.It is difficult to arrange these subfamilies (frequently recognizable for a different combination of the same recurrent characters) in a phylogenetic tree. However, we observed signs of primitiveness in Brachyderinae (small crescents) and their cluster; advanced ones in the third and fourth clusters all evolved with different patterns of the puff-like expansion of one of the accessory bodies, the latter being the most peculiar character of the superfamily. A tentative reconstruction is given.The functional significance of the variations seems to be that Rhynchitidae seem to be evolving towards immotility (their spermatozoon, in fact, is able to produce only a series of vibrations, not the progressive series of waves as in all other species studied), while all the other families and subfamilies show no signs of alterations in axonemal pattern and motility. The main evolutionary pathways observed in them are towards compensating for an exaggerated lengthening and a greater degree of asymmetry in the tail organelles: one of them, the major mitochondrial derivative, acts as a rigid axis, while the axoneme produces undulations in the opposite portion of the axonemal section.