SUMMARYThe anatomical structures of the sound-producing organ in Ophidion rochei males present an important panel of highly derived characters: three pairs of putatively slow sonic muscles; a neural arch that pivots; a rocker bone at the front pole of the swimbladder; a stretchable swimbladder fenestra; a swimbladder plate; and an internal cone that terminates in a pair of membranes in the caudal swimbladder. Male courtship calls are produced nocturnally and consist of trains of 10 to 40 pulses that increase in amplitude and decrease in rate before exhibiting alternating periods of ca. 84 and 111ms. Each pulse includes an unusual waveform with two parts. Pulse part 1 is a single cycle followed by a longer duration pulse part that exhibits gradual damping. Sounds and morphology suggest two hypotheses on the sound-producing mechanism. The 'pulley' hypothesis would require an alternate contraction of the ventral and dorsal muscles to form the two parts of each pulse. The 'bow' hypothesis involves a release mechanism with the sustained contraction of the dorsal muscle during all of the call, and the rapid contraction/relaxation of the ventral muscle to form each pulse.
BackgroundMany Ophidiidae are active in dark environments and display complex sonic apparatus morphologies. However, sound recordings are scarce and little is known about acoustic communication in this family. This paper focuses on Ophidion rochei which is known to display an important sexual dimorphism in swimbladder and anterior skeleton. The aims of this study were to compare the sound producing morphology, and the resulting sounds in juveniles, females and males of O. rochei.ResultsMales, females, and juveniles possessed different morphotypes. Females and juveniles contrasted with males because they possessed dramatic differences in morphology of their sonic muscles, swimbladder, supraoccipital crest, and first vertebrae and associated ribs. Further, they lacked the ‘rocker bone’ typically found in males. Sounds from each morphotype were highly divergent. Males generally produced non harmonic, multiple-pulsed sounds that lasted for several seconds (3.5 ± 1.3 s) with a pulse period of ca. 100 ms. Juvenile and female sounds were recorded for the first time in ophidiids. Female sounds were harmonic, had shorter pulse period (±3.7 ms), and never exceeded a few dozen milliseconds (18 ± 11 ms). Moreover, unlike male sounds, female sounds did not have alternating long and short pulse periods. Juvenile sounds were weaker but appear to be similar to female sounds.ConclusionsAlthough it is not possible to distinguish externally male from female in O. rochei, they show a sonic apparatus and sounds that are dramatically different. This difference is likely due to their nocturnal habits that may have favored the evolution of internal secondary sexual characters that help to distinguish males from females and that could facilitate mate choice by females. Moreover, the comparison of different morphotypes in this study shows that these morphological differences result from a peramorphosis that takes place during the development of the gonads.
Refined baseline inventories of non-indigenous species (NIS) are set per European Union Member State (MS), in the context of the Marine Strategy Framework Directive (MSFD). The inventories are based on the initial assessment of the MSFD (2012) and the updated data of the European Alien Species Information Network, in collaboration with NIS experts appointed by the MSs. The analysis revealed that a large number of NIS was not reported from the initial assessments. Moreover, several NIS initially listed are currently considered as native in Europe or were proven to be historical misreportings. The refined baseline inventories constitute a milestone for the MSFD Descriptor 2 implementation, providing an improved basis for reporting new NIS introductions, facilitating the MSFD D2 assessment. In addition, the inventories can help MSs in the establishment of monitoring systems of targeted NIS, and foster cooperation on monitoring of NIS across or within shared marine subregions.
In the present article, new records are given for 15 species (4 native and 9 alien and 2 cryptogenic), belonging to 6 Phyla (i.e. Chlorophyta, Ctenophora, Cnidaria, Mollusca, Arthropoda, and Chordata), from 10 Mediterranean countries: Morocco: the finding of the crab Callinectes sapidus represents the westernmost one of the species in the Mediterranean; Italy: first records of the nudibranch Polycera hedgpethi from the harbour of La Spezia, and first finding of the invasive ctenophore Mnemiopsis leidyi in the Fiora River; Tunisia: Caulerpa taxifolia var. distichophylla is recorded for the first time, showing an even wider distribution in the Mediterranean; Greece: the finding of the jellyfish Pelagia benovici represents the first record of the species in the Ionian Sea, while the finding of the smallscale codlet Bregmaceros nectabanus in the Ionian Sea is another interesting first report for the area; Malta: the cryptogenic scleractinian coral Oculina patagonica was recorded; Slovenia: the parasitic copepod Demoleus heptapus was recorded from a sixgill bluntnose shark, Hexanchus griseus; Croatia: the Lessepsian cephalaspidean mollusc Haminoea cyanomarginata is recorded for the first time from the area; Bulgaria: the Asian date mussel Arcuatula senhousia was recorded from the Black Sea; Cyprus: the Lessepsian gastropod Viriola sp. [cf. corrugata) was recorded for the first time from the area, while two decapod species were recorded also for the first time from Cyprus, i.e. the caridean shrimp Pasiphaea sivado and the anomuran Munida curvimana; Turkey: the acari Lohmannella falcata is recorded for the first time from Antalya and the Lessepsian fish Priacanthus sagittarius in the Levantine coasts of Turkey (off Hatay/Arsuz) showing that this species has extended its range in a very short time.
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