The male genital system of the cellar spider Pholcus phalangioides (Fuesslin, 1775) (Pholcidae, Araneae): development of spermatozoa and seminal secretion
© Michalik and Uhl; licensee BioMed Central Ltd. 2005
Received: 07 March 2005
Accepted: 29 June 2005
Published: 29 June 2005
Most arthropods pass through several molting stages (instars) before reaching sexual maturity. In spiders, very little is known about the male genital system, its development and seminal secretions. For example, it is unknown whether spermatozoa exist prior to-, or only after the final molt. Likewise, it is unclear whether sperm are produced throughout male adulthood or only once in a lifetime, as is whether seminal secretions contain factors capable of manipulating female behavior. In order to shed light on these aspects of the reproductive biology of spiders, we investigated the male genital system of the common cellar spider Pholcus phalangioides, with special emphasis on its development and seminal secretions.
Testes already display all stages of spermatogenesis in subadult males (about four weeks before the final molt). Their vasa deferentia possess proximally a very voluminous lumen containing dense seminal fluid and few spermatozoa, whereas the distal part is seemingly devoid of contents. Spermatoza of P. phalangioides are typical cleistospermia with individual secretion sheaths. In male stages approximately two weeks prior to the final molt, the lumina of the testes are wider and filled with a dense secretion. The wide, proximal portion of the vasa deferentia is filled with secretion and a large number of spermatozoa, and the narrow distal part also contains secretion. In adult males, the wide lumina of the testes are packed with spermatozoa and secretions. The latter are produced by the somatic cells that bear microvilli and contain many vesicles. The lumina of the vasa deferentia are narrow and filled with spermatozoa and secretions. We could identify a dense matrix of secretion consisting of mucosubstances and at least three types of secretion droplets, likely consisting of proteinaceous substances.
This study reveals that spermatogenesis begins weeks before maturity and takes place continuously in the long-lived males of P. phalangioides. Possible functions of the various types of secretion in the seminal fluid and previously investigated female secretions are discussed in the light of sexual selection.
When and for how long males produce sperm very likely depends on the mating system of the species in question. Long-lived species in which males can expect several matings probably continue to produce sperm throughout their lifetime. On the other hand, in species with a short reproductive time window or in species that show a considerable drop in female receptivity after a single mating, a male is expected to allocate all resources into sperm production for a single mating. For spiders, both evolutionary scenarios are conceivable: in sexually cannibalistic spiders, males load each of their copulatory organs, the pedipalps, only once and cease to produce sperm after the final molt, which seems to be a consequence of the high incidence of monogamy that is forced upon the male by female cannibalistic attacks [; PM personal observation], whereas in most spider species, males can expect more than one mating. In our focal species, Pholcus phalangioides, adult males are especially long-lived, with life-spans of up to a year [GU personal observation]. In this group of spiders sperm should be produced throughout a male's lifetime.
During mating, males not only transfer sperm, but also seminal fluid [2–6]. The seminal fluid of Drosophila melanogaster contains over 80 proteins and peptides. The few substances that have been identified have marked effects on the reproductive success of males and females: seminal fluid proteins and peptides can decrease female receptivity, increase egg production, facilitate sperm storage, and are necessary for sperm transfer and success in sperm competition. Moreover, antimicrobial agents in the secretions ensure that the female reproductive tract is a hospitable environment during sperm transfer and storage. In some species, even noxious chemicals are transferred and incorporated into developing eggs to protect them from predators and pathogens [reviews: [4–7]]. Similar functions have been reported from other insects such as butterflies  and crickets . In most insects, males produce secretions in separate accessory glands that can be dissected to characterize their products. However, male spiders have not been reported to possess separate accessory glands that are directly connected to the genital tract. The production of seminal secretion is thus very likely to occur within the testes. However, it is conceivable that the effects of the seminal secretions on the reproductive success of males and females may be similar in spiders and insects despite their different origin.
The shape of the male genital system in spiders differs enormously across spider taxa, but usually consists of two thick strands of testes, continuing in the thin convoluted vasa deferentia, which fuse distally to form the unpaired ductus ejaculatorius that opens into the genital opening located in the epigastric furrow [for entelegyne araneomorph spiders: [10–13]; but see  for Theraphosidae]. Generally, the male genital system in spiders is embedded in the midgut gland and the testes often extend deeply into the opisthosoma. Additional multicellular glands present in male spiders are the so-called epiandrous (=epigastric) glands, which seem to provide part of the sperm web and release their acinous substances near the genital opening through special spigots (=fusules) [15–17]. For some spider families unicellular glands that open into the epigastric furrow via individual ducts are described, but it is unknown whether the glandular secretion is added to the sperm mass [17, 18]. Unpublished work supports the notion that there is a great diversity of secretions in the male genital tract of spiders, the origin and functions of which are unknown [; PM, GU personal observation].
In the present study, we briefly describe the genital system of the haplogyne spider P. phalangioides. We investigate the organisation and development of the male genital system, the ultrastructure of the different parts, and give a first characterization of the secretions produced in the genital system. Finally, we present some additional findings on spermatogenesis and spermatozoa that complement previous investigations [19–21].
Developmental Stages of the Male Genital System
Stage 1 (about four weeks before the final molt)
These young males are characterized by palpal organs that are bent in the joint of the tibia and patella (Figs. 2a,b). Dark sclerotized areas are present on the femur and tibia. The tarsus has a broad shape without any signs of internal structures or appendages as present in adult males (Figs. 2a,b).
The longitudinal section through the opisthosoma (Fig. 2c) shows that the dimensions of the testis are similar to the final dimensions in adult males (compare Fig. 4a), and all stages of spermatogenesis are observable (Fig. 2f). Spermatogenesis occurs in cysts containing spermatids of the same developmental stage (Fig. 2f, see also Figs. 3e, 4c). The secretory activity within the testis is very low as indicated by the absence of the dark green secretion visible in subadult stage 2 and adults (see below).
The most distal part of the testis becomes thinner and opens into the vas deferens, forming a valve-like structure (Fig. 2e). The proximal part of the vas deferens possesses a thick epithelium and has an extensive lumen that is filled with spermatozoa embedded in a bright green secretion (Figs. 2c,e). In the more distal parts the lumen, the vas deferens is very narrow. It contains neither spermatozoa nor any other recognizable substance (Fig. 2d).
Stage 2 (about two weeks before the final molt)
In this stage the palpal organs are only slightly bent. The tarsus is extended and the internal structures known from the palps of adult males are visible through the cuticle (Figs. 3a,b). Dark sclerotized areas are present on the distal and lateral side of the tarsus (Figs. 3a,b).
The section in Figure 3c displays a similar organization as that in subadult males of stage 1. The testis contains all stages of spermatogenesis (Fig. 3e). Lumina with dark green secretion and several spots with red, roundish secretion are present between the cysts of spermatid (Fig. 3e, arrows). This secretion is produced by the somatic cells of the testis (see below).
The extensive proximal part of the vas deferens is almost completely filled with spermatozoa and secretions (Figs. 3c,d). Distally, the vas deferens becomes thinner and is shaped as a convoluted tube (Figs. 3c,d). Within the lumen a similar material as in the proximal part is present (Fig. 3d, arrows).
Close to the genital opening the thin vasa deferentia fuse and form the ductus ejaculatorius, which is characterized by an extensive lumen with large amounts of spermatozoa and secretions (Fig. 4d). The epithelium near the genital opening and towards the ductus ejaculatorius is prismatic and apically bordered by cuticle (Fig. 4e).
Near the ductus ejaculatorius, epiandrous glands are present which open into small spigots anterior to the genital opening (Fig. 4e). These glands are characterized by large lumina and a prismatic epithelium (Fig. 4e). The secretion of the glands has a granular green appearance as seen in the duct of the epiandrous spigots (Fig. 4e). The lumen of the gland appears empty, though this may be an artifact.
Spermatogenesis and Ultrastructure of the Male Genital System
The spermatozoa of P. phalangioides are characterized by several unique features, as pointed out in detail by Alberti and Weinmann . Apart from additional details, we provide information on the relationship between sperm and secretions in the male genital system.
Early stages of spermatogenesis are characterized by a large spherical nucleus surrounded by a manchette of microtubules, an acrosomal vacuole on its anterior pole and an axonemal basis, which migrates into an indentation at the posterior pole of the nucleus. In this early stage, the manchette of microtubules and the nuclear surface possesses a unique arrangement. As seen in cross-sections, the microtubules are not densely packed and the nuclear envelope shows a slightly wave-like outline (Fig. 5a). The quadrangular acrosomal vacuole is tightly connected to the cell membrane, which is indented in this region (Fig. 5a). Within the cytoplasm annulate lamellae are present (Fig. 5a).
During spermiogenesis the chromatin condenses and the nucleus strongly elongates (Fig. 5b). A thin helical band of nuclear material covered by microtubules surrounds the nucleus over its entire length (Figs. 5b,c). The acrosomal vacuole elongates during spermiogenesis, and finally possesses a cylindrical shape (Fig. 5d). A considerable amount of cytoplasm accumulates at the posterior end of the spermatids, forming a big droplet (Figs. 5b,d).
Within the lumen of the testis, only coiled spermatozoa are found embedded in a secretion matrix, which is likely produced by the extensive somatic cells (Figs. 5e,f). The extensions of the somatic cells surround the cysts of spermatids. Apically, the somatic cells bear long microvilli and contain many vesicles, indicative of strong secretory activity (Fig. 5f). Several secretion droplets are visible between the spermatozoa (Figs. 5e,f). The large secretion droplets seem to be produced through fusion of smaller droplets, as indicated by the irregular ring of loose material around the electron-dense center of the droplet (Fig. 5f, arrows).
Within the vas deferens the spermatozoa are densely packed and embedded in a homogenous secretion matrix (Fig. 6a). Each single spermatozoon is surrounded by a secretion sheath forming a so-called cleistosperm (Figs. 6a,b). The secretion sheath is produced within the vas deferens since it is absent in the testis (Fig. 5e). Within the secretion matrix three different kinds of secretions are present (Fig. 6). The first type of secretion consists of small droplets which are densely distributed and characterized by a bright center and a dark border. The second kind is a large electron-dense secretion droplet with a very irregular shape. These droplets often partially surround the spermatozoa (Fig. 6a). The third and rarest type of secretion is a droplet which appears less electron-dense. It is characterized by a heterogeneous content and an irregular surface to which particles may adhere or are partly embedded (Fig. 6c). The epithelium of the vas deferens is flat and bears microvilli in its apical region. A muscle layer surrounds the vas deferens (Fig. 6b).
General Organization of the Male Genital System
The male genital system of P. phalangioides is characterized by thick tube-like testes and thin convoluted vasa deferentia which fuse distally to form the ductus ejaculatorius. This organization is reported from many species of different families, e.g., Cybaeidae, Theridiidae and Agelenidae, and seems to be the general condition in araneomorph spiders (see background). However, theraphosid spiders show no distinct separation between testis and vas deferens [; PM personal observation] and in theraphosid as well as mesothelid spiders the testes themselves are convoluted [[14, 22]; PM personal observation]. In some species, e.g., the cybaeid Argyroneta aquatica, the testes are curved but distinct from the vasa deferentia . Petrunkevitch  suggested that the general organization of the male genital system is not useful for phylogenetic consideration, but the few data available indicate a potential for systematic interpretation. For example, in all theridiid spiders studied thus far, the vasa deferentia lead into a roundish vesicula seminalis (=ductus ejaculatorius?), the storage site of the mature spermatozoa, which is connected via an unpaired duct with the genital opening [; PM personal observation]. Considering the information available to date, it is at least misleading to take the theraphosid type of male genital system as representative for spiders [24, 25].
Development of the Male Genital System
In P. phalangioides, spermiogenesis starts several weeks before the last molt and continues in the adults. In the subadult males approximately four weeks before the final molt, the lumina of the testes are very thin and only a small amount of the dense secretion matrix is observable. The secretory activity increases within the last two weeks of the subadult stage. In adults, the lumina are wide and full of secretion and mature spermatozoa. The two different functions of the testis – the production of sperm cells and different kinds of secretion (see below), are evident. Several authors suggested that these secretions are products of degenerated spermatids and the cytoplasmic droplet discarded at the end of spermiogenesis [20, 26, 27]. However, rough endoplasmic reticulum, Golgi bodies and vesicles in the somatic cells demonstrate that the epithelium itself produces the secretions as was suggested by Alberti et al. .
In the subadult stages, the vasa deferentia possess a very extensive lumen in which the mature spermatozoa and secretion from the testes accumulate continuously. The thick epithelium of the vasa deferentia also shows secretory activity. It may be responsible for the formation of the secretion sheath surrounding each spermatozoon, as suggested for other spider species [20, 28–32]. In adults, several kinds of secretion are present in the vasa deferentia, whereas in young subadult stages only a dense secretion matrix is present. Thus, it is evident that secretory activity increases in subadults when approaching the final molt. Furthermore, in adult male spiders the epithelium of the vasa deferentia is very thin and secretory activity is low as was stated for the cybaeid Argyroneta aquatica .
In adult males of P. phalangioides cleistospermia and secretions are transferred into the palpal copulatory organ soon after the final molt. Sperm uptake by the male can occur repeatedly after each mating and may require a continuous production of sperm cells. In fact, P. phalangioides males mate several times  and refill their pedipalp sperm stores after each mating [GU unpublished observation]. To do so successfully, cellar spider males begin sperm production in the subadult phase and continue production throughout adulthood, as demonstrated by our study. In contrast, studies on short lived spider males with only a single mating opportunity showed that males do not refill their sperm stores and probably cease to produce sperm after the final molt , instead using their resources for rigorous mate selection [Pauly A, Uhl G, Schneider JM unpublished data].
Three different kinds of secretion droplets could be identified in the dense secretion matrices of the testes and vasa deferentia of P. phalangioides. According to Romeis , the Goldner staining method results in a green coloration of acidic mucosubstances and in red coloration of proteinaceous substances. It cannot be ruled out that the seemingly different kinds of secretion represent different steps of a single secretory pathway. However, since we also found different secretion droplets within the palpal organ, we conclude that different secretory pathways result in a variety of secretions with potentially different functions. Morphologically, the secretions are clearly different from those found in two other spider species, a mesothelid spider  and the related pholcid spider Holocnemus pluchei . The obvious difference in seminal secretory products in closely related species suggests that there is rapid divergence of seminal fluid substances that may originate from the process of sexual selection. It has been assumed that the rapid evolution of reproductive proteins is a motor in the speciation process .
In spiders, sperm and the seminal secretions are not directly transferred into the female genital tract, but taken up into the palpal organ before mating. Within the pedipalps, glandular epithelia adjacent to the sperm storage site seem to be widespread and also occur in P. phalangioides and other spider species [[37, 38]; Rose W, unpublished data]. It has been assumed that their products serve to release the sperm into the female genital tract during copulation or to serve as a protective matrix for sperm storage within the male palp [e.g., [37, 39, 40]]. During mating, sperm are transferred to the storage site within the female together with the secretions originating from both genital tract and pedipalp. Finally, inside the female cellar spider, sperm and male secretions encounter secretion that is produced by the female. The only non-morphological investigation existing to date identified proteinaceous substances and glyco- and lipoprotein components in the sperm storage site of virgin female P. phalangioides using gel-electrophoretic methods .
For spiders, a nutritive and protective function (desiccation and pathogens) has mainly been attributed to either male or female secretions since the sperm cells are often stored for extended periods of time [e.g., [41–45]], but secretions may also serve as lubricants and promote physical uptake or release of sperm inside the male palp (see above). Female secretory products have been suggested to control sperm activation [18, 46–48]. However, male secretions may also play an important role in this process.
Spermatozoa and Spermatogenesis
It has been known since the study of Alberti and Weinmann  that P. phalangioides possesses very aberrant spermatozoa with several unique characters (e.g., an elongated proximal centriole and a central nuclear canal containing the acrosomal filament), but the most conspicuous character is the band of nuclear material spirally surrounding the nucleus. As shown in the present study, the first signs of this peculiar transformation of the helical band are present in very early spermatid stages: microtubules are loosely arranged around the nucleus resulting in a wave-like outline of the nuclear envelope. The functional implications of the band are still unknown. It may influence the mobility of the spermatozoa or play a role during fertilization. The phylogenetic value of the peculiar spermatozoa of P. phalangioides remains uncertain as well, as the sperm ultrastructure of only one further pholcid spider, H. pluchei, is known [34, 49]. The spermatozoa of these two species however do markedly differ in accord with the present ideas on systematic relationships within the Pholcidae . On the other hand, a helical band of nuclear material is also present in Spermophora senoculata [PM personal observation], a species closely related to P. phalangioides . It therefore seems that sperm characteristics may be successfully applied successfully in phylogenetic considerations.
Our study demonstrates that sperm production in males of a long-lived spider species begins weeks before the final molt and continues throughout adulthood. Within the male genital tract, there are at least three different types of proteinaceous secretion droplets apart from a basic matrix secretion containing acidic mucosubstances. The different secretions may serve functions similar to those found in insects, such as oviposition stimulants or manipulators of female receptivity, and clearly warrant future investigation. Moreover, since secretory glands of the female are known to discharge their products into the sperm storage site, their effect on sperm storage, activation and sperm competition should also be investigated. Further, both male and female secretions may interact in as yet unexpected ways. If males have evolved manipulative substances that are against female interests, or if they offer a platform for cryptic female choice, we expect a similar divergence in female secretions and in their interactions with male derived substances.
Light Microscopy (LM)
Males of P. phalangioides were collected in houses and cellars within the city of Freiburg i.Br., Germany at an early juvenile stage and reared in the laboratory in individual containers on a diet of fruitflies. During the last intermolt interval, males were classified into two developmental stages according to the external morphology of their developing palpal organs. Young subadult males (stage 1, N = 5) were fixed approximately four weeks before the final molt and older subadult males (stage 2, N = 5) were fixed about two week before the final molt. Adult males (N = 5) were examined one to two days after their final molt.
Male specimens were fixed in Bouin solution according to Gregory , dehydrated in a graded series of ethanol or isopropanol and embedded in Paraplast. Sections (7 μm) were made with a Reichert 1150 Autocut microtome, stained according to Goldner , and mounted with Eukitt medium. Examination was performed with an Olympus BX 60 and pictures were taken with an Olympus DP 10.
Transmission Electron Microscopy (TEM)
Elder male specimens (N = 2) were dissected in 0.1 M phosphate buffer supplemented with 1.8% sucrose. The isolated genital system was fixed in 2.5% glutaraldehyde in the same buffer followed by postfixation in buffered 2% osmium tetroxide. After washing, the tissue pieces were dehydrated in graded ethanols and embedded in Spurr's resin . Ultrathin sections (50 nm) were made with a Leica ultramicrotome and stained with uranyl acetate and lead citrate . Examination was performed with a Zeiss EM 10A electron microscope.
Scanning Electron Microscopy (SEM)
The isolated genital system of elder males (N = 3) was split open in a droplet of phosphate buffer (see above) with thin needles on glass coverslips covered with 1% poly-L-lysin. After 10 min sedimentation the adhering material was fixed in 2.5% glutaraldehyde buffer for 1 h at 4°C. Samples were then rinsed in buffer and post-fixed in buffered 1% osmium tetroxide, dehydrated in ethanol, dried in a Balzers CPD 030 critical point dryer, coated with gold in a Balzers MED 010 sputtering device and examined in a Philips XL20 scanning electron microscope.
We are indebted to Gerd Alberti and Michael Schmitt for useful comments on the manuscript. For the help with the SEM, the authors are grateful to David Mercati, Fabiola Giusti and Eugenio Paccagnini from the lab of Romano Dallai (University of Siena, Italy). PM acknowledges a grant from the German National Merit Foundation and from the VIGONI-program (German Academic Exchange Service, DAAD). Furthermore, the financial support of the German Research Council (DFG, Al 138/11-1) is greatly appreciated. The histological investigations were performed by GU during her doctoral studies at the University of Freiburg, supported by the German National Merit Foundation. GU thanks Peter Weygoldt, Claudia Gack and Gerhard von der Emde for support.
- Herberstein ME, Gaskett AC, Schneider JM, Vella NGF, Elgar MA: Limits to male copulation frequency: sexual cannibalism and sterility in St Andrew's Cross spiders (Araneae, Araneidae). Ethology.
- Leopold R: The role of male accessory glands in insect reproduction. Ann Rev Entomol. 1976, 21: 199-221. 10.1146/annurev.en.21.010176.001215.View ArticleGoogle Scholar
- Marchini D, Del Bene G, Cappelli L, Dallai R: Ultrastructure of the male reproductive accessory glands in the medfly Ceratitis capitata (Diptera: Tephritidae) and preliminary characterization of their secretions. Arthropod Struct Dev. 2003, 31: 313-327. 10.1016/S1467-8039(03)00003-3.View ArticlePubMedGoogle Scholar
- Gillot C: Male accessory gland secretions: Modulators of female reproductive physiology and behavior. Ann Rev Entomol. 2003, 48: 163-184. 10.1146/annurev.ento.48.091801.112657.View ArticleGoogle Scholar
- Wolfner MF: Tokens of love: functions and regulation of Drosophila male accessory gland products. Insect Biochem Mol Biol. 1997, 27: 179-192. 10.1016/S0965-1748(96)00084-7.View ArticlePubMedGoogle Scholar
- Wolfner MF: The gifts that keep on giving: physiological functions and evolutionary dynamics of male seminal proteins in Drosophila. Heredity. 2002, 88: 85-93. 10.1038/sj.hdy.6800017.View ArticlePubMedGoogle Scholar
- Chapman T, Davies SJ: Functions and analysis of the seminal fluid proteins of male Drosophila melanogaster fruit flies. Peptides. 2004, 25: 1477-1490. 10.1016/j.peptides.2003.10.023.View ArticlePubMedGoogle Scholar
- Jin ZY, Gong H: Male accessory gland derived factors can stimulate oogenesis and enhance oviposition in Helicoverpa armigera (Lepidoptera: Noctuidae). Arch Insect Biochem Physiol. 2001, 46: 175-185. 10.1002/arch.1027.View ArticlePubMedGoogle Scholar
- Wagner WE, Harper CJ: Female life span and fertility are increased by the ejaculates of preferred males. Evolution. 2003, 57: 2054-2066.View ArticlePubMedGoogle Scholar
- Bertkau P: Ueber den Generationsapparat der Araneiden. Arch Naturgesch. 1875, 41: 235-262.Google Scholar
- Crome W: Die grobe Morphologie des männlichen Genitalapparates einiger Araneen. Dtsch Zool Z. 1951, 1: 169-186.Google Scholar
- Kim JK, Kim TH, Moon MJ: Ultrastructure of the testis in the spider, Pardosa astrigera L. Koch. Korean Arachnol. 1993, 9: 43-53.Google Scholar
- Knoflach B: Mating in Theridion varians Hahn and related species (Araneae: Theridiidae). J Nat Hist. 1998, 32: 545-604.View ArticleGoogle Scholar
- Melchers M: Zur Biologie der Vogelspinnen (Fam. Aviculariidae). Z Morph Oekol Tiere. 1964, 52: 517-536. 10.1007/BF00408073.View ArticleGoogle Scholar
- Marples BJ: The spinnerets and epiandrous glands of spiders. J Linn Soc Lond. 1967, 46: 209-223.View ArticleGoogle Scholar
- Lopez A, Emerit M: New data on the epigastric apparatus of male spiders. Bull Br arachnol Soc. 1988, 7: 220-224.Google Scholar
- Lopez A: Glandes épigastrique et classification des araneides. Bull Ass Anat Paris. 1974, 58: 899-904.Google Scholar
- Lopez A: Glandular aspects of sexual biology. Ecophysiology of spiders. Edited by: Nentwig W. 1987, Berlin: Springer, 121-132.View ArticleGoogle Scholar
- Rosati F, Baccetti B, Dallai R: The spermatozoon of Arthropoda. X. Araneids and the lowest Myriapods. Comparative Spermatology. Edited by: Baccetti B. 1970, New York, London: Academic Press, 247-254.Google Scholar
- Alberti G, Weinmann C: Fine structure of spermatozoa of some labidognath spiders (Filistatidae, Segestriidae, Dysderidae, Oonopidae, Scytodidae, Pholcidae; Araneae; Arachnida) with remarks on spermiogenesis. J Morphol. 1985, 185: 1-35. 10.1002/jmor.1051850102.View ArticleGoogle Scholar
- Dallai R, Afzelius BA, Witalinski W: The axoneme of the spider spermatozoon. Boll Zool. 1995, 62: 335-338.View ArticleGoogle Scholar
- Haupt J: The Mesothelae – a monograph of an exceptional group of spiders (Araneae: Mesothelae). Zoologica. 2003, 154: 1-102.Google Scholar
- Petrunkevitch A: An inquiry into the natural classification of spiders, based on a study of their internal anatomy. T Connecticut Acad Arts Sci. 1933, 31: 299-389.Google Scholar
- Foelix RF: Biology of Spiders. 1996, New York: Oxford University PressGoogle Scholar
- Felgenhauer BE: Araneae. Microscopic anatomy of invertebrates. Edited by: Harrison FW, Foelix RF. 1999, New York: Wiley-Liss, 8A: 223-266.Google Scholar
- Wagner J: Einige Beobachtungen über die Spermatogenese bei den Spinnen. Zool Anz. 1896, 19: 188-190.Google Scholar
- Bösenberg H: Beiträge zur Kenntnis der Spermatogenese bei den Arachnoiden. Zool Jb Anat. 1905, 21: 515-570.Google Scholar
- Alberti G, Afzelius BA, Lucas SM: Ultrastructure of spermatozoa and spermatogenesis in bird spiders (Theraphosidae, Mygalomorphae, Araneae). J Submicrosc Cytol. 1986, 18: 739-753.Google Scholar
- Michalik P, Gray MR, Alberti G: Ultrastructural observations of spermatozoa and spermiogenesis in Wandella orana Gray, 1994 (Araneae: Filistatidae) with notes on their phylogenetic implications. Tissue Cell. 2003, 35: 325-337. 10.1016/S0040-8166(03)00054-5.View ArticlePubMedGoogle Scholar
- Michalik P, Haupt J, Alberti G: On the occurrence of coenospermia in mesothelid spiders (Araneae: Heptathelidae). Arthropod Struct Dev. 2004, 33: 173-181. 10.1016/j.asd.2004.02.001.View ArticlePubMedGoogle Scholar
- Michalik P, Dallai R, Giusti F, Alberti G: The ultrastructure of the peculiar synspermia of some Dysderidae (Araneae, Arachnida). Tissue Cell. 2004, 36: 447-460. 10.1016/j.tice.2004.08.001.View ArticlePubMedGoogle Scholar
- Michalik P, Sacher P, Alberti G: Ultrastructural observations of spermatozoa of some tetragnathid spiders and their phylogenetic implications (Araneae, Tetragnathidae). J Morphol. 2005,Google Scholar
- Uhl G: Mating behaviour and female sperm storage in Pholcus phalangioides (Fuesslin) (Araneae). Memoirs of the Queensland Museum. 1993, 33: 667-674.Google Scholar
- Michalik P, Dallai R, Giusti F, Mercati D, Alberti G: The spermatozoa and spermiogenesis of Holocnemus pluchei (Scopoli, 1763) (Pholcidae, Araneae).
- Swanson WJ, Vacquier VD: Reproductive protein evolution. Ann Rev Ecol Syst. 2002, 33: 161-179. 10.1146/annurev.ecolsys.33.010802.150439.View ArticleGoogle Scholar
- Romeis B: Mikroskopische Technik. 1989, München: Urban und SchwarzenbergGoogle Scholar
- Lopez A, Juberthie-Jupeau L: Ultrastructure compare du tube séminifére chez les males d'araignées. Mém Biospéol. 1985, 12: 97-109.Google Scholar
- Huber BA: Evolutionary transformation from muscular to hydraulic movements in spider (Arachnida, Araneae) genitalia: a study based on histological serial sections. J Morphol. 2004, 261: 364-376. 10.1002/jmor.10255.View ArticlePubMedGoogle Scholar
- Kraus O: Male Spider Genitalia: Evolutionary Changes in Structure and Function. Verh Naturwissenschaftl Ver Hamburg. 1984, 27: 373-382.Google Scholar
- Suhm M, Thaler K, Alberti G: Glands in the male palpal organ and the origin of the mating plug in Amaurobius species (Araneae: Amaurobiidae). Zool Anz. 1996, 234: 191-199.Google Scholar
- Uhl G: Sperm storage secretion of female cellar spiders (Pholcus phalangioides: Araneae): Agel-electrophoretic analysis. J Zool. 1996, 240: 153-161.View ArticleGoogle Scholar
- Engelhardt V: Beiträge zur Kenntnis der weiblichen Kopulationsorgane einiger Spinnen. Z Wiss Zool. 1910, 96: 32-117.Google Scholar
- Coyle FA, Harrison FW, McGimsey WC, Palmer JM: Observation on the structure and function of spermathecae in haplogyne spiders. Trans Am Microsc Soc. 1983, 102: 272-280.View ArticleGoogle Scholar
- Uhl G: Sperm storage and repeated egg production in female Pholcus phalangioides Fuesslin (Araneae). Bull Soc Neuchâteloise Sci Nat. 1993, 116: 245-252.Google Scholar
- Michalik P, Reiher W, Suhm-Tintelnot M, Coyle FA, Alberti G: The female genital system of the folding-trapdoor spider Antrodiaetus unicolor (Hentz, 1842) (Antrodiaetidae, Araneae) – an ultrastructural study of form and function with notes on reproductive biology of spiders. J Morphol. 2005, 263: 284-309. 10.1002/jmor.10309.View ArticlePubMedGoogle Scholar
- Uhl G: Genital morphology and sperm storage in Pholcus phalangioides (Fuesslin, 1775) (Pholcidae; Araneae). Acta Zool Stockholm. 1994, 75: 1-12.View ArticleGoogle Scholar
- Uhl G: Ultrastructure of the accessory glands in female genitalia of Pholcus phalangioides (Fuesslin, 1771) (Pholcidae; Araneae). Acta Zool Stockholm. 1994, 75: 13-25.View ArticleGoogle Scholar
- Berendonck B, Greven H: Genital structures in the entelegyne widow spider Latrodectus revivensis (Arachnida; Araneae; Theridiidae) indicate a low ability for cryptic female choice by sperm manipulation. J Morphol. 2005, 263: 118-132. 10.1002/jmor.10296.View ArticlePubMedGoogle Scholar
- Lopez A, Boissin L: La spermatide d'Holocnemus pluchei (Scop.) (Arachnida, Araneida, Pholcidae): Étude ultrastructurale. Bull Soc Zool France. 1976, 101: 423-431.Google Scholar
- Huber BA: High species diversity in one of the dominant groups of spiders in east african montane forests (Araneae: Pholcidae: Buitinga n. sp., Spermophora Hentz). Zool J Linn Soc. 2003, 137: 555-619. 10.1046/j.1096-3642.2003.00053.x.View ArticleGoogle Scholar
- Gregory RE: Alcoholic Bouin fixation of insect nervous systems for Bodian silver staining. II. Modified solutions. Stain Technol. 1980, 55: 151-160.PubMedGoogle Scholar
- Goldner J: A modification of the Masson trichrome technique for routine laboratory purposes. Am J Pathol. 1938, 14: 247-249.Google Scholar
- Spurr AR: A low-viscosity epoxy resin embedding medium for electron microscopy. J Ultra Mol Struct Res. 1969, 26: 31-43.View ArticleGoogle Scholar
- Reynolds ES: The use of lead citrate at high pH as an electron-opaque stain in electron microscopy. J Cell Biol. 1963, 17: 208-10.1083/jcb.17.1.208.PubMed CentralView ArticlePubMedGoogle Scholar
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.