Abstract:The fishes, which have currently named Aphanius Nardo, 1827 are the relict of the ancient ichthyofauna of the Tethys Sea. For a long time since 1827, the genus name has been subjected to revision by several researchers using mainly morphological features. Until recently, no comprehensive single-or multi-locus DNA barcoding study has been conducted on whole members of the family Aphaniidae. In the present study, by applying four conceptually different molecular species delimitation methods, including one distan… Show more
“…Moreover, Ferrito et al (2009) showed that the scale surface microstructures and the lepidonts on the circuli crests of Aphanius species (see Esmaeili, Teimori, Zarei, & Sayyadzadeh, 2020 well as environmental parameters would affect scale morphology (Ibáñez, 2014;Swain & Foote, 1999;Teimori, 2018). Therefore, the characteristics of scale morphology may not be applicable to infer the taxonomic relationships of some fish groups in their local distribution.…”
To study scale based phylogenetic affinity, the ultrastructure and ornamentation characteristics of body key scales were studied for 12 gobiid species from the Iranian coast of the Persian Gulf including Qeshm and Hormuz Islands and the Makran coast of the Oman Sea using scanning electron microscopy (SEM) technique. The scales were removed from below the first dorsal fin, cleaned in potassium hydroxide solution 1%, and were prepared for the SEM imaging. The presence of both ctenoid and cycloid scales in the studied gobiids was revealed. The focus of ctenoid scales was positioned posteriorly, while the focus of cycloid scales was positioned in the postero-central part of the scale. In all the studied species, radii were located only on the anterior part of the scale, and the primary radii were dominant. Also, there were no granules in the inter circular space, but bifurcation was observed in some circuli.In most species, the teeth-like structures called lepidonts were present on the crest of circuli, which functionally help to firmly attach the scales to the epithelium. The dendrogram of the between-groups-linkage method sorted the gobiid species into the two main groups of five distinct clusters: (a) Cryptocentroides arabicus and Cryptocentrus cyanotaenia (the Cryptocentrus-lineage); (b) Bathygobius meggitti and Bathygobius cocosensis (the Glossogobius-lineage); (c) Coryogalops adamsoni and Coryogalops tessellatus (the Gobius-lineage); (d) Acentrogobius dayi, Istigobius ornatus,Favonigobius reichei, Aulopareia ocellata, and Silhouettea ghazalae (the Gobiopsis-lineage). It seems that the dendrogram topology obtained based on the macro-and microscopic structures of scales, reveals phylogenetic lineages of gobies that have already been proposed for these taxa. Hence, the results of this study are largely consistent with the previous molecular studies on the gobiid fishes and implied that besides other data, the analysis of scale shape and scale-surface microstructures could be served to study the diversification of gobiid species.
“…Moreover, Ferrito et al (2009) showed that the scale surface microstructures and the lepidonts on the circuli crests of Aphanius species (see Esmaeili, Teimori, Zarei, & Sayyadzadeh, 2020 well as environmental parameters would affect scale morphology (Ibáñez, 2014;Swain & Foote, 1999;Teimori, 2018). Therefore, the characteristics of scale morphology may not be applicable to infer the taxonomic relationships of some fish groups in their local distribution.…”
To study scale based phylogenetic affinity, the ultrastructure and ornamentation characteristics of body key scales were studied for 12 gobiid species from the Iranian coast of the Persian Gulf including Qeshm and Hormuz Islands and the Makran coast of the Oman Sea using scanning electron microscopy (SEM) technique. The scales were removed from below the first dorsal fin, cleaned in potassium hydroxide solution 1%, and were prepared for the SEM imaging. The presence of both ctenoid and cycloid scales in the studied gobiids was revealed. The focus of ctenoid scales was positioned posteriorly, while the focus of cycloid scales was positioned in the postero-central part of the scale. In all the studied species, radii were located only on the anterior part of the scale, and the primary radii were dominant. Also, there were no granules in the inter circular space, but bifurcation was observed in some circuli.In most species, the teeth-like structures called lepidonts were present on the crest of circuli, which functionally help to firmly attach the scales to the epithelium. The dendrogram of the between-groups-linkage method sorted the gobiid species into the two main groups of five distinct clusters: (a) Cryptocentroides arabicus and Cryptocentrus cyanotaenia (the Cryptocentrus-lineage); (b) Bathygobius meggitti and Bathygobius cocosensis (the Glossogobius-lineage); (c) Coryogalops adamsoni and Coryogalops tessellatus (the Gobius-lineage); (d) Acentrogobius dayi, Istigobius ornatus,Favonigobius reichei, Aulopareia ocellata, and Silhouettea ghazalae (the Gobiopsis-lineage). It seems that the dendrogram topology obtained based on the macro-and microscopic structures of scales, reveals phylogenetic lineages of gobies that have already been proposed for these taxa. Hence, the results of this study are largely consistent with the previous molecular studies on the gobiid fishes and implied that besides other data, the analysis of scale shape and scale-surface microstructures could be served to study the diversification of gobiid species.
“…Conversely, a sinuous shape of the epural is absent in A. furcatus and it is also absent in the related Paraphanius mento (this study and Teimori et al., 2014). However, Costa (2012a) reported this character also for Aphanius isfahanensis , and two of the Anatolian Aphanius species, which are not closely related according to molecular studies (Esmaeili et al., 2020; Hrbek & Meyer, 2003). It could be that this trait has evolved convergently in different clades of the Aphaniidae.…”
Section: Discussionmentioning
confidence: 99%
“…However, studies by Freyhof, Weissenbacher, and Geiger (2017), Teimori, Esmaeili, Hamidan, and Reichenbacher (2018) and Esmaeili et al. (2020) indicate that A. dispar includes four species ( A. dispar , A. hormuzensis Teimori et al., 2018, A. kruppi Freyhof et al., 2017 , A. stoliczkanus (Day, 1872)), which, together with further five species ( A. furcatus Teimori, Esmaeili, Erpenbeck, & Reichenbacher, 2014, A. ginaonis (Holly, 1929), A. richardsoni (Boulenger, 1907), A. sirhani Villwock et al., 1983, A. stiassnyae (Getahun & Lazara, 2001)) comprise the genus Aphaniops .…”
Section: Introductionmentioning
confidence: 98%
“…Until recently all its representatives were assigned to a single genus, Aphanius Nardo, 1827. However, Esmaeili, Teimori, Zarei, and Sayyadzadeh (2020) separated Aphaniops Hoedeman, 1951 as well as Paraphanius Esmaeili et al., 2020 as own genera. Aphanius and Paraphanius have a geographic distribution along the coasts of the Mediterranean Sea and also occur in inland habitats of Turkey, Jordan, Iran, and Iraq, while Aphaniops lives in coastal and inland habitats in the South‐Eastern Mediterranean and the Dead Sea basins, the Persian Gulf, and all around the Arabian Peninsula south to Ethiopia and east to India (Esmaeili et al., 2020; Wildekamp, 1993).…”
Aphaniops dispar, widespread around the Arabian Peninsula, was recently separated in four species (A. dispar, A. hormuzensis, A. kruppi, A. stoliczkanus) by molecular results and colour patterns, but the morphological differences are small and call for more studies. Here we report differences in skeleton and median fin osteology of these species. In addition, we introduce the term 'modified caudal vertebra' to describe caudal vertebrae that are not directly associated with caudal ray support but are visibly modified from a 'usual' caudal vertebra. Aphaniops hormuzensis, an endemic species to southern Iran, has a significantly higher number of modified caudal vertebrae compared to the more widespread A. stoliczkanus and A. dispar, and also to A. kruppi. This is a surprising result as the caudal skeleton and related structures of the posterior caudal vertebral column have yielded successful results in separating between families or genera, but there are only a few studies that have examined these structures for their role in species diagnosis. Our study also highlights that state‐of‐the‐art methods in X‐raying and improved staining procedures assist in the discrimination of superficially similar species.
“…The members of the family Aphaniidae demonstrate great biological diversity in the old world (Esmaeili et al, 2020). Similar to other killifishes, they have a relatively short generation period, and high endurance in the wild and laboratory conditions (Evans et al, 2011; Schartl, 2014).…”
The potential of central nervous system regeneration was evaluated for the first time in the injured brain of the old world killifish Aphaniops hormuzensis. The histomorphological organization in the regeneration procedure was evaluated using the hematoxylin and eosin (H&E) staining and the bromodeoxyuridine (BrdU) immunohistochemistry technique. The histological tissue sections were sampled daily for 10 days. Based on the H&E staining, a large gliosis reaction was detected along with vacuolization and telencephalon deformation on 1-day post-lesion (dpl). The vacuolated zone declined fast and the telencephalon hemisphere recovered on 3 dpl. The symptoms of injured telencephalon nervous tissue were resolved within 7 dpl in both genders. In the BrdU test of the control group, BrdU-labeled cells were observed in the ventricular zone (VZ), pallium (Pa), and lateral pallium (LPa). On 1 dpl, the BrdU + cells accumulated in the VZ, Pa, and LPa (located near the injury area). From 3 dpl onwards, the BrdU + cells were reduced in the telencephalic VZ, Pa, and LPa. Based on the BrdU + results, the adult brain in A. hormuzensis possesses a remarkable capacity for neuronal regeneration. By taking into account the high neural regeneration potency of A. hormuzensis and its relatively short lifespan, it could be concluded that besides the currently known models, the members of aphaniid fishes could probably be valuable animals to study the regeneration phenomenon in the vertebrates.
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