11-ketotestosterone stimulates putative sex pheromone production in the male peacock blenny, Salaria pavo (Risso 1810)

Male peacock blennies (Salaria pavo) release odors from their anal glands and, possibly, from their gonads that attract reproductive females. The current study investigated the effects of 11-ketotestosterone (KT) on development of the anal glands, testes, and accessory testicular organs as well as the subsequent olfactory potency of their secretions. After 3 wk of KT treatment (5 mg/kg in silastic implants), clusters of cells secreting neutral mucins differentiated in the anal gland of all treated males, whereas this occurred in only one control male. Secretions by anal glands from KT-treated males elicited greater olfactory responses, as assessed by electro-olfactography, than those from controls. Treatment with KT stimulated testicular gland growth and sialomucin secretion but had no clear effect on the germinal region of the testis; KT also stimulated enlargement of, and fluid secretion in, the blind pouches (paired evaginations of the spermatic ducts). Secretions by the testes and fluid in blind pouches from KT-treated males elicited greater olfactory responses than those from controls. In conclusion, KT stimulates development of the anal glands and testicular accessory organs and promotes odorant secretion, the putative multicomponent male peacock blenny pheromone.     

Unusual testicular accessory organs, the testicular blind pouches of blennies (Teleostei, Blenniidae). Fine structure, (enzyme-) histochemistry and possible functions

The testicular blind pouches (TBPs) of Lipophrys canevae and Solaria pavo have an annual reproductive cycle with an active secretion phase during spawning, a regression phase correlated with necrotic processes during post-spawning, an inactive regeneration phase during inter-spawning and prespawning. As revealed by fine structure and enzyme-histochemistry the TBPs of L. canevae and S. pavo are involved in the production of steroid glucuronides, which possibly act as pheromones, Further functions are in the secretion of small amounts of sialomuciri and in lytic activity.     

The spermatic duct of blenniid fish (Teleostei,Blenniidae): Fine structure,histochemistry and function

Summary The annual changes of the spermatic duct ofSalaria pavo and the characteristics of the spermatic ducts of spawningAidablennius sphynx, Lipophrys adriaticus, L. dalmatinus, andParablennius incognitus are described by fine structural and histochemical methods. The spermatic duct ofS. pavo has an inactive phase during the interspawning period, a proliferation phase during the prespawning period, a phase of high secretory activity during the spawning period and a regression phase in the postspawning period. During spawning the spermatic duct ofS. pavo is involved in the secretion of glycogen, lipids, and sulfomucins and has similar fine structural and histochemical characteristics as the spermatic ducts ofA. sphynx, L. adriaticus, L. dalmatinus, andP. incognitus. The spermatic ducts of bleniid fish function (1) in stabilizing and continuation of the final differentiation processes of spermatozoa, (2) in storage of mature spermatozoa, (3) in nutrition of germ cells by glycogen, and (4) in the production of sulfomucins regarded as important for the mode of fertilization. Possible meanings of the varying size of the spermatic ducts in different species of blennies are discussed.     

Morphology of the male reproductive systems of two Indopacific blenniid fishes,Salarias fasciatus and Ecsenius bicolor (Blenniidae,Teleostei)1

The testes and associated accessory organs of two blenniid fishes are described. The testicular organs of Salarias fasciatus consist of a testicular gland adjacent to the testis, chambered seminal vesicles serving as a reservoir for spermatozoa and testicular blind ouches. Ecsenirts bicolor has no testicular gland, has elongated chambered seminal vesicles whii are not used as a reservoir for spermatozoa, and has testicular blind pouches.     

Functions of the testicular gland in two blenniid fishes, Salaria (=Blennius) pavo and Lipophrys (= Blennius) dalmatinus (Blenniidae, Teleostei) as revealed by electron microscopy and enzyme histochemistry

The functions of the testicular gland in two different blenniid fishes, Salaria pavo and Lipophrys dulmutinus , are described by fine structural and enzyme histochemical methods. In the testes of the two fishes no mature spermatozoa are found. Sperrniogenesis occurs only until the spermatidal stage. Spermatids are released into the testicular gland. During the spawning period the testicular gland functions in differentiation of spermatids, nutrition of spermatids, and secretion of sialomucins. After spawning, the testicular gland has phagocytotic functions in resorbtion of remaining spermatids, which are transformed into lipids in the gland cells. During the interspawning period the testicular gland is a storage reservoir for lipids and phospholipids which are re-transformed into testicular gland secretion in the next reproductive season. Testicular gland cells themselves do not have steroidogenetic functions, but steroids are synthesized by interstitial cells homologous to Leydig cells in other fish. Possible explanations for the reduction of the testis in L. dalmatinus and implications of the testicular gland in taking over testicular functions are discussed.     

Histological, fine-structural and histochemical differences in the testicular glands of gobiid and blenniid fishes

The testicular gland (t.g.) is a glandular tissue situated adjacent to the testis of blenniid and several gobiid species. In the present study the t.g. of Blennius pavo Risso and Gobius niger L. were compared by histological and histochemical methods. In B. pavo the spermatozoa have to cross the t.g. to reach the vas deferens and thus they come into contact with the gland cells, whereas in G. niger the vas deferens is situated between the testis and the t.g. The fine structure and histo-chemistry of the t.g. cells reveal that in B.pavo the cells of the t.g. have exocrine as well as endocrine functions. The t.g. cells of B. pavo contain large amounts of lipids, form a secretion containing acid mucopolysaccharides, show positive reaction for acid phosphatase, and some cells stain for 3β-HSD and G6PD. The function of the t.g. of G. niger is exclusively endocrine. Characteristics of the gland cells of this species are well developed smooth ER and tubulovesicular or paracristal-line mitochondria. The stainings for 3β-HSD, G6PD and UDPGD give strong positive results in the whole t.g., indicating the presence of steroids and steroid glucuronides.     

Alternative male reproductive strategies in the peacock blenny

A 4-year study (1989–1992) of a population of Lipophrys pavo living in a brackish lagoon (Maugio, France) revealed three types of male during the spawning season (April to September): (i) nest-breeder males which are territorial, and have well-developed secondary sexual characteristics; (ii) non-functional males which were abundant only in 1991 when population density was very high and (iii) 1-year-old kleptogamic males with small body size which possess neither secondary sexual organs nor a testicular gland, although their testes are functional and hyperdeveloped (up to 10.5% of carcass weight). The percentage of kleptogamic males was fairly stable in the population (from 7.9 to 10.0%) and highly variable in their age class (from 8.5 to 51.3%). It is suggested that kleptogamy is a conditional strategy adopted by smaller males.     

Phylogenetic relationships of the north-eastern Atlantic and Mediterranean blenniids

The phylogenetic relationships of 27 north-eastern Atlantic and Mediterranean blennioids are analysed based on a total of 1001 bp from a combined fragment of the 12S and 16S mitochondrial rDNA. The most relevant results with implications in current blenniid taxonomy are: (1) Lipophrys pholis and Lipophrys (=  Paralipophrys ) trigloides are included in a well-supported clade that by the rule of precedence must be named Lipophrys ; (2) the sister species of this clade are not the remaining species of the genus Lipophrys but instead a monotypic genus comprising Coryphoblennius galerita ; (3) the smaller species of Lipophrys were recovered in another well-supported and independent clade, which we propose to be recognized as Microlipophrys ; (4) although some authors included the genera Salaria and Lipophrys in a single group we have never recovered such a relationship. Instead, Salaria is more closely related to the genera Scartella and Parablennius ; (5) the genus Parablennius , which was never recovered as a monophyletic clade, is very diverse and may include several distinct lineages; (6) the relative position of Aidablennius sphynx casts some doubts on the currently recognized relationships between the different blenniid tribes. Meristic, morphological, behavioural and ecological characters support our results and are also discussed. The possible roles of the tropical West African coast and the Mediterranean in the diversification of blenniids are discussed.  © 2005 The Linnean Society of London, Biological Journal of the Linnean Society , 2005, 86 , 283–295.     

Optic glands and the state of the testis in Octopus

If the optic glands are removed from mature male octopuses, the weight of the testis and its ducts decline. Spermatophore production eventually ceases after five or six weeks. The effect of the operation is most marked in the case of large animals. If the glands are activated by removing the source of their nerve supply in the subpedunculate lobe of the suprapesophageal brain, testis and duct enlargement follows enlargement of the glands themselves ; the number of spermatophores found in the male ducts doubles within a month of the operation. Castration of the animals is not followed by a change in the weight of the male ducts, indicating that the optic gland secretion affects the state of the ducts directly rather than through the testis. Octopus vulgaris Cuvier and O. cyanea Gray were used in the experiments.     

Androgen levels and social interactions in breeding males of the peacock blenny

Nest-holder male Salaria pavo have lower circulating concentrations of 11-ketotestosterone (KT) at the beginning of the breeding season than at its peak. At that peak density of nesting males was higher as were the number of visits of sneaker males to nests and of agonistic interactions between nest-holders and sneaker males. There was no difference between the two dates either in the frequency of male-male interactions or in the frequency of courtship episodes. Thus, higher plasma levels in nest-holders might be explained by a more intense sneaking pressure at the peak of the breeding season. At that peak, nest-holders had higher plasma levels of KT and a higher testosterone (T) to KT metabolization index in the gonads than did floater males. Both nest-holders and floaters had higher levels of KT and T in the testicular gland than in the testis. The levels of both androgens in the testicular gland, but not in the testis, were correlated with circulating concentrations of KT. These results suggest that the testicular gland is the major source of circulating KT in blenniids. Nest-holders had higher metabolization indexes than floaters both in the testis and in the testicular gland, which suggests that nest holding status promotes the conversion of T into KT.     

Sexing blennies using genital papilla morphology or ano-genital distance

Information on the genital morphology of male and female Lipophrys pholis is provided, as well as for two other sympatric blenniid species, Coryphoblennius galerita and Lipophrys trigloides. The use of non-invasive sex determination procedures described may be extremely useful not only for ecological studies but also as a proxy for the detection of environmental exposure to endocrine disruptive chemicals, given that blennies have been proposed as potential sentinel species for chemical contamination.     

Morphologie des Gebisses und Nahrungspraferenzen von dreizehn adriatischen Blenniiden (Teleostei, Perciformes)

The morphology and arrangement of the teeth in 13 sympatric species of the genus Blennius were investigated by SEM. All the species were collected in the upper littoral of the Northern Adriatic near Rovinj (Yugoslavia) and represent the total species inventory of the genus Blennius in this area. After analysing the content and length of the intestine, four groups with different feeding habits could be distinguished to which the morphological adaptations of the teeth could be correlated. There is a non-selective omnivorous group of Aufwuchs-grazer which take the inhabiting vagilfauna {Blennius gattorugine, B. incognitas, B. tentacularis ), a herbivorous group ( B. sanguinolentus, B. sphynx, B. canevae ), a carnivorous group ( B. trigloides, B. dalmatinus, B. rouxi ), and a linking group between omnivorous grazers and carnivores (B. adriaticus, B. pavo, B. nigriceps). B. galerita shows a preponderance of comblike teeth and feeds exclusively scraping microscopic algae from the rocky substrate. The morphology and position of the caniniforms vary greatly within the investigated species. The dentition on the vomer is lacking in five species and seems of no consequence in the uptake of food.     

Testicular main ducts and spermatic ducts in some cyprinid fishes I. Morphology, fine structure and histochemistry

Alburnus alburnus, Leuciscus cephalus and Vimba vimba efferent duct systems of the male gonads consist of testicular main ducts and spermatic ducts. These have similar histological, fine structural and (enzyme–) histochemical characteristics and function in (1) storage and (2) nutrition of spermatozoa, (3) synthesis of steroid glucuronides, (4) secretion of proteins and enzymes (5) formation of an ionic gradient in the seminal fluid and (6) they have auto– and heterophagocytotic activities. Therefore testicular main ducts and spermatic ducts are important in the formation of the seminal fluid.     

Ectodermal ablation of the third branchial arch in chick embryos and the morphogenesis of the parathyroid III gland.

The parathyroid glands have been classically considered to be derivatives of the third and fourth pharyngeal pouches in most species, including humans. Furthermore, the presence of neural crest-derived cells in the parathyroid glands connective tissue has been apparently established. However, our previous studies have provided a new hypothesis on the origin of these glands in human and chick embryos. To determine the origin of the parathyroid III (P3) gland, ectoderm of the third branchial arch was cauterized in chick embryos at Hamburger and Hamilton's stage 19 (embryonic day 3). Cauterization of the ventral half of the ectoderm was followed by the non-formation, on the same side, of the P3 gland. When the dorsal half of the ectoderm was cauterized, both the right and left P3 glands formed. Our observations suggest that the ectoderm of the ventral half of the third branchial arch is necessary for the organization of the P3 gland.     

Molecular systematics of mantelline frogs from Madagascar and the evolution of their femoral glands

Several genera of frogs from Madagascar, classified in the family Mantellidae, subfamily Mantellinae, possess structures commonly called 'femoral glands' on the ventral side of their shanks. The question arises as to the origin and phylogenetic significance of these glands. A molecular phylogeny based on 3601 nucleotide DNA sequences of three mitochondrial and two nuclear genes of 30 mantellid species provided strong support for monophyly of the included mantellines, all characterized by enlarged femoral gland clusters, as well as for those with gland clusters of coordinated central arrangement of secretion ducts. However, the phylogeny also strongly supported the hypothesis of convergent evolution of structurally similar glands in unrelated frogs ( Indirana , Petropedetes ), and several trends of convergent evolution of gland structure within mantellines. We studied the light microscopic structure of the femoral glands in a representative array of 18 mantellid species. Males of all species of the subfamily Mantellinae were characterized by clusters of distinct single glands. Each was structurally similar to an enlarged granular gland and secreted independently, probably through a single duct. By contrast, the largely semi-aquatic frogs in the genus Mantidactylus had a specialized cluster of glands, in which the secretion ducts led into a macroscopically recognizable central depression. In Boophis opisthodon , a mantellid species of the subfamily Boophinae without externally recognizable femoral glands, we observed a large number of enlarged granular glands of various sizes in the ventral skin of the shank. This observation is consistent with the hypothesis that the large and more uniform organs of mantellines are derived granular glands.  © 2007 The Linnean Society of London, Biological Journal of the Linnean Society , 2007, 92 , 529–539.     

Length–weight relationships of 17 less-studied fish species from Çanakkale, Marmara region of Turkey

This study reports length–weight relationships for 17 cryptic and rare species, Aidablennius sphynx , Arnoglossus kessleri , Callionymus pusillus , Callionymus risso , Clinitrachus argentatus , Echiichthys vipera , Gobius geniporus , Gobius paganellus , Labrus viridis , Lepadogaster lepadogaster , Ophidion barbatum , Pomatoschistus minutus , Pomatoschistus pictus , Salaria pavo , Tripterygion delaisi , Tripterygion tripteronotus and Zebrus zebrus from Çanakkale near shores in the Marmara region of Turkey.     

Hopping locomotion in a nematode: Functional anatomy of the caudal gland apparatus of Theristus caudasaliens sp. n.

The interstitial nematode Theristus caudasaliens n. sp. normally locomotes by hopping on the left side of its tail tip, a mode of locomotion that is unique among nematodes. The animal uses its caudal glands and caudal musculature to perform the hops, attaching itself momentarily between hops with the glands and executing the hops by straightening and curling the posterior part of its body. The caudal gland apparatus can be seen by electron microscopy to consist of five gland cells of two different types. Three of these cells, termed viscid glands, are involved in adhesion of the animal to substrates and produce ovoid granules with a central dense band. The other two cells are characterized by smaller, lessdense granules and presumably function in releasing the animal from substrates. The ducts of both gland types extend to the tail tip where they terminate in a common crescent-shaped space. Their secretions are released to the outside through two pores on the left side of the tail tip. There is no spinneret valve in this nematode. The muscles of the tail and of the mid-body region are developed to the same extent. The caudal gland apparatus can be compared with the duo-gland adhesive organs of other interstitial animals, but its homology with either these organs or the caudal glands of other nematodes is uncertain. Theristus caudasaliens is described as a new species.     

Morphology, fine structure, biochemistry, and function of the spermatic ducts in marine fish

The spermatic ducts and the testicular efferent ducts were investigated in different marine teleost fish species (Diplodus sargus, Mullus barbatus, Thalassoma pavo, Trachinus draco, Uranuscopus scaber, Sparisoma cretense, Synodon saurus). From the morphological, histological, fine structural and biochemical investigations it appeared that the testicular main ducts and spermatic ducts of the investigated marine fish have the following functions: storage of spermatozoa, monosacharide synthesis for nutrition of spermatozoa, synthesis of steroid glucuronides, synthesis of seminal plasma proteins, formation of a ionic gradient in the seminal fluid and phagocytotic activity. Species-specific differences were only found in the morphology of the gonads and in the histology of the spermatic duct epithelium.     

Hypophysectomy and hemivasectomy can inhibit the testicular hemicastration response of the mature rat

Three questions were asked in an attempt to understand how testosterone (T) concentration in the veins of the remaining testis can double within 24 h after hemicastration in the mature rat without a change in plasma luteinizing hormone (LH) levels. These three questions (and their answers) were: 1) Can the testicular hemicastration response occur in hypophysectomized rats? Answer, No. 2) Does LH binding to the testis increase after hemicastration? Answer, No. 3) Is there a neural route to the testis alternate to the superior spermatic plexi? Answer, Yes, apparently there is, since hemivasectomy contralateral to the excised testis partially suppressed the testicular hemicastration response (150.4 +/- 13.2 ng/ml in hemicastrated, sham- hemivasectomized rats [n = 18] vs. 109.4 +/- 11.6 ng/ml in hemicastrated, hemivasectomized rats [n = 18], P less than 0.026). It was concluded that LH was probably necessary to the testicular hemicastration response but that its presence did not provide a mechanism. The response was mediated at least partly through the inferior spermatic nerves associated with the vas deferens. A possible reason, although highly speculative, for failure to previously block the testicular hemicastration response by bilateral denervation of the superior spermatic plexi (Mock and Frankel , 1982) was that during the 12-wk interval between denervation and hemicastration, testicular innervation functionally transferred from the superior spermatic to the inferior spermatic nerves.     

Larval development of three blenniid species Aidablennius sphynx, Coryphoblennius galerita and Lipophrys canevai (Pisces: Blenniidae: Blenniini) in the western Mediterranean

The early stages of development of three blenniid species, Aidablennius sphynx (6.7–15.8 mm BL), Coryphoblennius galerita (4.3–13.9mm BL), and Lipophrys canevai (3.5–10.4 mm BL) are described from specimens collected in the western Mediterranean. The characteristics used for identification included meristic, developmental, morphological and pigmentation characters. Distinguishing characters of these species useful in differentiating them from other species of blenniids for which early stages are known in the Mediterranean are presented. Information on the occurrence of larvae and juveniles of these species off the Catalan coast (north-western Mediterranean) is also given.