Time for change in Portuguese science

There is an almost perfect positive relationship between scientific output and gross domestic product (GDP) in Western Europe (Fig. 1). But two countries — Ireland and Portugal — spoil the relationship

Hormonal control of swimbladder sonic muscle dimorphism in the Lusitanian toadfish, Halobatrachus didactylus

The swimbladder and associated sonic muscle of the Lusitanian toadfish Halobatrachus didactylus increase in size throughout life and are, respectively, 25% and 30% larger in type I (nest-holder) males than females, which may generate sexual differences in sound production. Sexual dimorphism in swimbladder is also evident in the morphological features of sonic muscle fibers. During the breeding season, type I males have smaller myofibril contracting zones surrounded by larger sarcoplasm areas compared with females, possibly an adaptation to speed and fatigue resistance for the production of long mating calls. Type II (floater) males show characteristics that are intermediate, but statistically not significantly different, between type I males and females. Six weeks after castration and androgen (testosterone and 11- ketotestosterone) replacement in type I and type II males there were no alterations either in swimbladder mass or fiber morphology. However, 17b-estradiol induced a significant decrease in swimbladder mass and sarcoplasm area/myofibril area ratio. Six months after castration there was a clear reduction in the seasonal swimbladder hypertrophy in males and induction of sonic fiber morphological characteristics that resemble those occurring in females (low sarcoplasm area/myofibril area ratio). These results suggest that testicular factors are required to initiate sonic muscle hypertrophy and type I sonic fiber phenotype in H. didactylus, but a specific involvement of androgens has not been completely clarified

The swimbladder of the Lusitanian toadfish: sexual dimorphism and hormonal control

The members of the family Batrachoididae produce sounds associated with courtship and agonistic interactions. While long mating calls are only produced by nesting males, agonistic short duration grunts have been recorded from toadfishes and midshipmen in both males (nesting or not) and females. Sound production results from the contraction of paired sonic muscles attached to the walls of the swimbladder, which cause a rapid variation in swimbladder volume and internal pressure. Both sonic muscle growth and sonic fibre morphology have been shown to be androgen sensitive in batrachoidids

Morphometric changes and sex steroid levels during the annual reproductive cycle of the Lusitanian toadfish, Halobatrachus didactylus

The Lusitanian toadfish has group synchronous oocytes, which grow from November until June–July when they are released probably as a single batch. Blood plasma levels of estradiol-17b (E2) and testosterone (T) increase during vitellogenesis and drop rapidly during final maturation and ovulation, when 17,20b, 21-trihydroxy-4-pregnen-3-one (17,20b,21-P) levels increase. The male reproductive apparatus is composed of paired testes and multichambered accessory glands, which secrete mucosubstances and are connected to the spermatic duct. Changes in the gonadosomatic index of males paralleled the females but started to drop slightly earlier. The swimbladder and accessory glands also underwent important seasonal changes in weight reaching a maximum at spawning. T, 11-ketotestosterone (11-KT) and 17,20a-dihydroxy-4-pregnen-3-one (17,20a-P) were generally low except for a sharp peak in June. 17,20b,21-P also peaked in June and then declined slowly. 17,20b-dihydroxy-4-pregnen-3-one (17,20a-P) was undetectable in males and females. As with other species of the family two types of males were identified: type I males with smaller testes (ca. 7-fold) and larger accessory glands (ca. 3-fold) and swimbladders than type II. Type I males also had significantly higher (ca. 6- fold) 11-KT levels than type II males. This suggests a role for 11-KT in the development of structures important for reproductive behaviour

Localization and distribution of nitric oxide synthase and other neuronal markers in the podia ofHolothuria arguinensis

The organization of the nervous system of the holothurian podia-the tentacles, papillae, and tube feet-is still poorly understood, which limits the development of functional studies. Knowledge of nitric oxide (NO) signaling in sea cucumbers is nonexistent, although it is known to play an important role in many essential biological functions, including neurotransmission, throughout the animal kingdom. The objective of this study was to characterize the holothurian podia inHolothuria arguinensis. To this end, we used classical histology, nitric oxide synthase (NOS) distribution, using NADPH-diaphorase histochemistry and NOS immunostaining, and neuronal immunohistochemistry. Our results revealed an abundant distribution of NO in the nervous components of the holothurian podia, suggesting an important role for NO as a neuronal messenger in these structures. Nitrergic fibers were intensely labeled in the longitudinal nerve and the nerve plexus surrounding the stem, but were more weakly labeled in the mesothelium. NOS was also found in scattered cell bodies and abundant fibers in the podia terminal end (i.e., the discs in tentacles and tube feet, and the pointed conical structures in the papillae), with evident neuronal projections to the bud surface, especially in the tentacles. The podia terminal end was the most specialized area and was characterized by a specific nervous arrangement, consisting of a distinct nerve plate, rich in cells and fibers containing potential sensory cells staining positively for neuronal markers, which makes this the most likely candidate to be a chemosensory region and an important candidate for future exploration.Fundacao para a Ciencia e a TecnologiaPortuguese Foundation for Science and TechnologyEuropean Commission [SFRH/BD/90761/2012, UIDB/04326/2020]info:eu-repo/semantics/publishedVersio

Nemo through the looking-glass: a commentary on Desjardins & Fernald

info:eu-repo/semantics/publishedVersio

Follow your nose: chemical communication throughout the European eel (Anguilla anguilla, L.) life-cycle

European eels are important in both scientific and economic terms. Unfortunately, current populations are becoming increasingly endangered and urgentmanagement is needed. Several aspects of eel biology, together with their highly developed sense of smell, suggest that chemical communication could be involved at key stages of their life-history. Thus, advances in this area could generate novel tools for stock management

Quantifying dominant bacterial genera detected in metagenomic data from fish eggs and larvae using genus‐specific primers

The goal of this study was to design genus-specific primers for rapid evaluation of the most abundant bacterial genera identified using amplicon-based sequencing of the 16S rRNA gene in fish-related samples and surrounding water. Efficient genus-specific primers were designed for 11 bacterial genera including Alkalimarinus, Colwellia, Enterovibrio, Marinomonas, Massilia, Oleispira, Phaeobacter, Photobacterium, Polarbacerium, Pseudomonas, and Psychrobium. The specificity of the primers was confirmed by the phylogeny of the sequenced polymerase chain reaction (PCR) amplicons that indicated primers were genus-specific except in the case of Colwellia and Phaeobacter. Copy number of the 16S rRNA gene obtained by quantitative PCR using genus-specific primers and the relative abundance obtained by 16S rRNA gene sequencing using universal primers were well correlated for the five analyzed abundant bacterial genera. Low correlations between quantitative PCR and 16S rRNA gene sequencing for Pseudomonas were explained by the higher coverage of known Pseudomonas species by the designed genus-specific primers than the universal primers used in 16S rRNA gene sequencing. The designed genus-specific primers are proposed as rapid and cost-effective tools to evaluate the most abundant bacterial genera in fish-related or potentially other metagenomics samples.info:eu-repo/semantics/publishedVersio

Specific evolution and gene family expansion of complement 3 and regulatory factor H in fish

The complement system comprises a large family of plasma proteins that play a central role in innate and adaptive immunity. To better understand the evolution of the complement system in vertebrates and the contribution of complement to fish immunity comprehensive in silico and expression analysis of the gene repertoire was made. Particular attention was given to C3 and the evolutionary related proteins C4 and C5 and to one of the main regulatory factors of C3b, factor H (Cfh). Phylogenetic and gene linkage analysis confirmed the standing hypothesis that the ancestral c3/c4/c5 gene duplicated early. The duplication of C3 (C3.1 and C3.2) and C4 (C4.1 and C4.2) was likely a consequence of the (1R and 2R) genome tetraploidization events at the origin of the vertebrates. In fish, gene number was not conserved and multiple c3 and cfh sequence related genes were encountered, and phylogenetic analysis of each gene generated two main clusters. Duplication of c3 and cfh genes occurred across the teleosts in a species-specific manner. In common, with other immune gene families the c3 gene expansion in fish emerged through a process of tandem gene duplication. Gilthead sea bream (Sparus aurata), had nine c3 gene transcripts highly expressed in liver although as reported in other fish, extra-hepatic expression also occurs. Differences in the sequence and protein domains of the nine deduced C3 proteins in the gilthead sea bream and the presence of specific cysteine and N-glycosylation residues within each isoform was indicative of functional diversity associated with structure. The diversity of C3 and other complement proteins as well as Cfh in teleosts suggests they may have an enhanced capacity to activate complement through direct interaction of C3 isoforms with pathogenic agents.(FCT) project to CCMAR (UIDB/04326/2020)info:eu-repo/semantics/publishedVersio

Olfactory sensitivity to changes in environmental [Ca2+] in the marine teleost Sparus aurata

Estuarine and/or migratory teleosts may experience large and rapid changes in external [Ca2+]. Previous studies have largely centred on the physiological mechanisms that maintain a constant plasma [Ca2+] in the face of such external fluctuations, but little work has been directed to examining how these changes may originally be detected. We present evidence that the olfactory system of the gilthead seabream (Sparus aurata) is highly sensitive to reductions in environmental [Ca2+] and suggest a possible mechanism by which this may be mediated. Multi-unit extracellular recordings were made from the olfactory nerve of Sparus aurata while the [Ca2+] of artificial sea water flowing over the olfactory epithelium was varied from 10 to 0mmoll-1. Reductions in [Ca2+] caused a large, nonaccommodating increase in the firing rate of the olfactory nerve (apparent IC50=1.67±0.26mmoll-1, apparent Hill coefficient=-1.22±0.14; means ± S.E.M., N=6). This response was not due to the concomitant reduction in osmolality and was specific for Ca2+. During continuous exposure of the olfactory epithelium to Ca2+-free sea water, the apparent IC50 and Hill coefficient in response to increases in [Ca2+] were 0.48±0.14mmoll-1 and -0.76±0.16 (means ± S.E.M., N=6), respectively, suggesting an adaptation of the Ca2+- sensing system to low-[Ca2+] environments. Ca2+ is intimately involved in signal transduction in the olfactory receptor neurones, but our data support a true olfactory response, rather than a non-specific effect to lowering of external [Ca2+]. The absence of Ca2+ from sea water only partially and temporarily blunted the olfactory response to the odorant L-serine; the response amplitude recovered to control levels within 20 min. This suggests that the olfactory system in general is able to adapt to low-[Ca2+] environments. We suggest that the Ca2+ sensitivity is mediated by an extracellular Ca2+-sensing receptor similar to the recently characterized mammalian Ca2+-sensing receptor