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Scanning electron microscopy images of teeth in Ophioplocus januarii . A) Dorsalmost tooth. B) Mid-positioned tooth. C) Proximal view of dorsal teeth. D) Proximal view of ventral teeth. E) Detail of B, showing the different calcite compaction. F) Fractured tooth. G) Detail of F, showing the internal differentiation in microstructure. I and II indicate regions of more compaction (I) and more porosity (II) of the calcite, respectively. Scale bars: A, B, C, D = 200 μm; E, G = 50 μm.
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Ophioplocus januarii is a common brittle star on soft and hard substrates along the Argentinian and Brazilian coasts. Based on stomach contents, tooth microstructure and field observations we identified its food. Opposed to previous suggestions, O. januarii appears to be a microphagous species feeding on macroalgal fragments (found in 60.0 % of the...
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Context 1
... microstructure analysis: All teeth in O. januarii revealed a fenestrated stereom microstructure ( Fig. 1). However, it was pos- sible to clearly identify two distinct regions: the basal parts of the teeth which are in contact with the dental plate, are more loosely perfo- rated than the distal parts. There the calcite is much more compacted, presenting a clear different arrangement (Fig. 1 A, B, C, D). This superficial distinction is ...
Context 2
... O. januarii revealed a fenestrated stereom microstructure ( Fig. 1). However, it was pos- sible to clearly identify two distinct regions: the basal parts of the teeth which are in contact with the dental plate, are more loosely perfo- rated than the distal parts. There the calcite is much more compacted, presenting a clear different arrangement (Fig. 1 A, B, C, D). This superficial distinction is visible also internally in the calcite microstructure as can be seen in a fractured tooth (Fig. 1 F, G). The basal surface presents little serrated edges, but at the distal portion these edges are less prominent because of the tightly packed calcite (Fig. 1 ...
Context 3
... basal parts of the teeth which are in contact with the dental plate, are more loosely perfo- rated than the distal parts. There the calcite is much more compacted, presenting a clear different arrangement (Fig. 1 A, B, C, D). This superficial distinction is visible also internally in the calcite microstructure as can be seen in a fractured tooth (Fig. 1 F, G). The basal surface presents little serrated edges, but at the distal portion these edges are less prominent because of the tightly packed calcite (Fig. 1 ...
Context 4
... presenting a clear different arrangement (Fig. 1 A, B, C, D). This superficial distinction is visible also internally in the calcite microstructure as can be seen in a fractured tooth (Fig. 1 F, G). The basal surface presents little serrated edges, but at the distal portion these edges are less prominent because of the tightly packed calcite (Fig. 1 ...
Context 5
... tooth stereom microstructure in O. januarii is distinctly different from that in teeth of macrophagous as well as microphagous spe- cies ( Fig. 1; Table 2). The presently found inter- mediate fenestrated arrangement of the stereom was also here observed for Ophiactis asperula, and confirmed as such when analyzing the teeth with the scanning electron microscope (SEM). The fact that SEM reveals structures which might remain disguised under the light microscope could explain that ...
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... be more specialized than deep-sea counterparts. For example, Ophioplocus januarii found in shallow northern Patagonia appears to be microphagous and omnivorous (Brogger et al., 2015). In intertidal areas of Madagascar, O. venosa feeds on Sargassum densifolium and on organic matter, whereas O. scolopendrina feeds on neuston (Fourgon et al., 2006). ...
... In intertidal areas of Madagascar, O. venosa feeds on Sargassum densifolium and on organic matter, whereas O. scolopendrina feeds on neuston (Fourgon et al., 2006). Many species have been reported to ingest live prey such as molluscs, annelids, crustaceans, or even other ophiuroids (Brogger et al., 2015;Pearson & Gage, 1984;Stöhr et al., 2012;Warner, 1982;Yokoyama & Amaral, 2008). Deep-dwelling ophiuroids display opportunistic and generalist behaviors with a feeding strategy centered on predation or suspension feeding (Gage & Tyler, 1991;Pearson & Gage, 1984). ...
Ophiopholis aculeata is a ubiquitous brittle star (Echinodermata: Ophiuroidea) known to occur from the upper subtidal to the bathyal zone. Individuals from shallow inshore habitats (rhodolith beds and rock fields) and deeper offshore locations in eastern Canada were studied to assess the population structure, habitat selection, diet, and feeding strategies of this species through use of stable isotope analyses, gut contents, and laboratory experiments. Potential drivers of habitat selection such as depth, light conditions, body size, sex, intraspecific competition, and presence of predators were examined. This study highlighted variable population size structures and abundances as well as diversified food sources and feeding strategies (i.e., suspension and deposit feeding, scavenging, predation on live organisms, and even cannibalism) as a function of native depth and habitat. It also revealed that studies on the feeding biology of brittle stars must carefully consider sex and life stage as driving factors.
... Although a relatively extensive amount of literature may be found on this topic (e.g. Deschuyteneer and Jangoux 1978;Chartock 1983;Emson 1990;Emson et al. 1991;Dearborn et al. 1996;Allen 1998;Boos 2012;Brogger et al. 2015), few studies have been conducted in the tropical Atlantic (Davis 1966;Reimer and Reimer 1975;Hendler 1982;Hendler and Miller 1984a;Yokoyama and Amaral 2008). In general, all papers analysing feeding biology in ophiuroids in detail, in both cold and warm waters, recorded a large variety of food items in the diet of these animals. ...
... In general, all papers analysing feeding biology in ophiuroids in detail, in both cold and warm waters, recorded a large variety of food items in the diet of these animals. The most common items are algae, crustaceans, echinoderms, gastropods and polychaetes (Feder 1981;Fratt and Dearborn 1984;Pearson and Gage 1984;Dearborn et al. 1996;Yokoyama and Amaral 2008;Harris et al. 2009;Brogger et al. 2015). ...
Ophioderma appressum is a common and abundant ophiuroid species in tropical reef
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... This is consistent with the hypothesis claiming that madreporites are ecologically informative (Ezhova et al. 2016). The differences among species in the type of teeth are relevant if we consider that teeth types have been used as an indicator of feeding preferences (uniform teeth for macrophagous feeders and compound for microphagous) (Medeiros-Bergen 1996;Brogger et al. 2015). Five ophionereidids have been reported to possess only compound teeth (Medeiros-Bergen 1996), while O. commutabilis shows both compound and uniform teeth, which could represent an adaptation, increasing the importance of omnivorous feeding in this cave system (as suggested by Bribiesca-Contreras et al. (2019) for other food sources). ...
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... The numbers in parentheses refer to the following comments: (1) The microstructure of type A and B tooth types has been described and illustrated with scanning electron micrographs by Medeiros-Bergen [36][37][38]. Most examined type B teeth have a cap consisting of imperforate stereom (Fig 1Cc), which has been described variously in the literature as "enamelled", "hyaline" or "glassy"; a cap consisting of more densely fenestrated stereom has been observed in Ophiopholis aculeata (Ophiopholidae), Ophiactis asperula (Ophiactidae), ophiolepidids have type A dental plates, one species has an "imperfect" perforation and another has distinctly type B perforations. ...
... https://doi.org/10.1371/journal.pone.0202046.g010 Acrocnida brachiata, Amphiura chiajei (both Amphiuridae) and Ophioplocus januarii (Hemieuryalidae) ( [37,39]; Wilkie pers. obs.) (Fig 1Dc). ...
... There are no comparable data on any type B IF. It is, however, intriguing that, even taking into account the trophic versatility demonstrated by many ophiuroids [67][68][69][70], suspension feeding features prominently and consistently in all clades with type B IFs (as shown in Fig 10), but sporadically, or not at all, in those with type A IFs (see inter alia [37,63,68,69,[71][72][73]). It has also been suggested that the capped teeth of type B IFs are an adaptation for the efficient comminution of material obtained by suspension or deposit feeding [36,64]. ...
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... This may indicate the broad food spectrum, unselective feeding behaviour and dependence of Ophiothrix spp. feeding preference to its habitat diversity (Brogger et al. 2015). Feeding preferences of brittle star is approximated by Brogger et al. (2015) as relatively poorly developed both on hard substrates and on soft sediments rich in detritus. ...
... feeding preference to its habitat diversity (Brogger et al. 2015). Feeding preferences of brittle star is approximated by Brogger et al. (2015) as relatively poorly developed both on hard substrates and on soft sediments rich in detritus. As a deposit feeder, Ophiothrix spp. ...
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Les algues brunes du genre Cystoseira sensu lato forment les écosystèmes marins, comptant parmi les plus productifs de Méditerranée, mais aussi parmi les plus menacés par les facteurs anthropiques et phénomènes globaux ; elles comptent aujourd’hui 45 espèces reconnues taxonomiquement, avec un nombre soumis à évolution, en raison des confusions taxonomiques récurrentes et de l’apport de la biologie moléculaire. Cette dernière a permis grâce aux récents travaux de distinguer trois genres : Cystoseira, Carpodesmia et Treptacantha. Notre étude qui a concerné un total de 29 Stations de la région centre, s’étendant du littoral de Chlef à l’Ouest au Littoral de Bejaia à l’est, ainsi que 3 stations additives à l’extrême est et ouest, a permis de recenser un total de 12 espèces, parmi les 16 citées dans la littérature. Le Treptacantha barbata, classé taxa excludenda, et signalé par de rares auteurs n’a été observé ni par Sellam (2018), ni par nous-mêmes, nous suggérons une confusion taxonomique avec le Cystoseira compressa subsp. Compressa ou le Cystoseira humilis. Un intérêt particulier a par ailleurs été dévolu à l’espèce endémique stricte Cystoseira sedoides, car très peu étudiée, elle a été recensée à 14 stations, où elle forme des faciès monospécifiques et 2 autres où elle est rare. L’analyse historique de son observation a révélé une tendance à la diminution, voire à la disparition dans les stations les plus urbanisées. Les résultats des mesures de densité et de matière sèche moyennes ont corroboré la nécessité de reconsidérer son statut écologique, d’espèce fondatrice, au même titre que le Cystoseira amentacea var. stricta et le Carpodesmia crinita. L’étude de la faune et de la flore associées a concerné les 4 formations clés du littoral algérien, l’association en mode battu à Cystoseira amentacea var. stricta, moyennement battu à Cystoseira sedoides et l’association à
Carpodesmia crinita et à Cystoseira humilis, en mode calme. L’examen de la diversité
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The detailed study of arm ossicles, particularly the lateral arm plates, is providing valuable information in the elucidation of ophiuroid taxonomy. The present study describes in detail 16 species of brittle stars from Araçá Bay, Brazil. This information is used to construct the first interactive electronic key, providing a valuable resource for a broad range of researchers. Brittle stars families were divided into three groups based on their spatial distribution: i) infaunal species of intertidal and shallow subtidal belonging to Amphiuridae and Ophiactidae, ii) epizoic species belonging to Amphiuridae, Ophiactidae, and Ophiotrichidae and, iii) epifaunal species of the subtidal belonging to Ophiodermatidae and Hemieuryalidae. In the global context of recent revisions of ophiuroid taxonomy, the present work provides additional characters for use in future phylogenetic studies.