“…List of harpacticoids and their localities determined in these study and comparison with the previous records from Turkey. A: Noodt [8], B: Karaytuğ & Huys [25], C: Huys et al [26], D: Karaytuğ & Sak [27], E: Sak et al [28], F: Pulat et al [29], G: Alper et al [22], H: Sönmez et al [30], I: Kaymak et al [31], J: Sönmez et al [32], K: Köroğlu et al [33], L: Alper et al [34], M: Sönmez et al [35], N: Karaytuğ & Koçak [11], O: Yıldız & Karaytuğ [12], P: Sönmez et al [36], Q: Alper et al [13]. ---------- ---------- ).…”
Section: Resultsmentioning
confidence: 99%
“…As a result, a total of 72 species/subspecies belonging to 44 genera in 15 families were identified. All identified taxa except Tryphoema gallipoliensis Alper et al, 2018 are new records for the study area, besides 16 species were also recorded for the first time from the Turkish seas.…”
mentioning
confidence: 81%
“…After that the studies have accelerated and many literatures about harpacticoids were published in Turkey (see [11]) thus the number of harpacticoid species identified from the Turkish Seas was raised to 210 [12]. Recently six new species were added by several authors [13][14][15][16][17] so the number of species has reached to 216. Although the taxonomical researches about harpacticoids of Turkey have increased in the last 15 years, it would not be wrong to say that these studies are quite far from to reveal the real harpacticoid diversity.…”
The study was aimed to reveal interstitial harpacticoid copepod fauna of the Gulf of Saros (Turkey), where no detailed research has been done before on this subject. The samples were collected from 30 stations located along the mediolittoral zone of the gulf between 2013 and 2014. As a result, a total of 72 species/subspecies belonging to 44 genera in 15 families were identified. All identified taxa except Tryphoema gallipoliensis Alper et al., 2018 are new records for the study area, besides 16 species were also recorded for the first time from the Turkish seas.
“…List of harpacticoids and their localities determined in these study and comparison with the previous records from Turkey. A: Noodt [8], B: Karaytuğ & Huys [25], C: Huys et al [26], D: Karaytuğ & Sak [27], E: Sak et al [28], F: Pulat et al [29], G: Alper et al [22], H: Sönmez et al [30], I: Kaymak et al [31], J: Sönmez et al [32], K: Köroğlu et al [33], L: Alper et al [34], M: Sönmez et al [35], N: Karaytuğ & Koçak [11], O: Yıldız & Karaytuğ [12], P: Sönmez et al [36], Q: Alper et al [13]. ---------- ---------- ).…”
Section: Resultsmentioning
confidence: 99%
“…As a result, a total of 72 species/subspecies belonging to 44 genera in 15 families were identified. All identified taxa except Tryphoema gallipoliensis Alper et al, 2018 are new records for the study area, besides 16 species were also recorded for the first time from the Turkish seas.…”
mentioning
confidence: 81%
“…After that the studies have accelerated and many literatures about harpacticoids were published in Turkey (see [11]) thus the number of harpacticoid species identified from the Turkish Seas was raised to 210 [12]. Recently six new species were added by several authors [13][14][15][16][17] so the number of species has reached to 216. Although the taxonomical researches about harpacticoids of Turkey have increased in the last 15 years, it would not be wrong to say that these studies are quite far from to reveal the real harpacticoid diversity.…”
The study was aimed to reveal interstitial harpacticoid copepod fauna of the Gulf of Saros (Turkey), where no detailed research has been done before on this subject. The samples were collected from 30 stations located along the mediolittoral zone of the gulf between 2013 and 2014. As a result, a total of 72 species/subspecies belonging to 44 genera in 15 families were identified. All identified taxa except Tryphoema gallipoliensis Alper et al., 2018 are new records for the study area, besides 16 species were also recorded for the first time from the Turkish seas.
“…Previously, both genera had already undergone a changeful assignment into different categories; for example, their optional assignment to the Canthocamptidae Sars, 1906, and subsequently to the Cletodidae T. Scott, 1904, the synonymising of Tryphoema with the genus Adelopoda Pennak, 1942, or the transfer of Tryphoema as a subgenus to Rhizothrix. For a detailed historical outline, see [2,4,[17][18][19]]. Por's [2] revision was therefore a valuable contribution to clarifying the systematic ambiguities.…”
During expedition EMB-238 of RV EM BORGESE to the Fehmarn Belt (Baltic Sea, Germany) in 2020, specimens of a new species of the Rhizothrichidae Por (Crustacea, Copepoda, Harpacticoida) were found. Currently, Rhizothrichidae enclose two genera: Rhizothrix Sars and Tryphoema Monard. The assignment of the new species is based on the following commonly derived characters: the formation of a strong spinulose (sub)apical element on the last segment of the female A1, and the formation of a long brush seta on the last exopodal and endopodal segments of the P1. The new species could not be assigned to either Rhizothrix or Tryphoema because it lacks their autapomorphies but presents exclusive derived characters, including the absence of the abexopodal seta on the A2 allobasis, the possession of only one seta on the endopods of P2–P4, and the fusion of the female P5 exopod and baseoendopod. Therefore, it is assigned to a new genus. Besides the species description, its phylogenetic position in the Rhizothrichidae as well as its possible relationship with Rhizothrix and Tryphoema are discussed. Furthermore, the affiliation of the Rhizothrichidae with the Cletodoidea is justified on the basis of 17 apomorphies. A key to the rhizothrichid genera is provided.
“…In addition, Doolia gen. nov. has superficial similarities with Rhizothrix Sars G.O., 1909, and they share the following character sets: the presence of pinnate setae on the antennule and its segmentation, the segmentation of exopods and endopods in P1-P4, lack of sexual dimorphism in legs P1-P4, and lack of ornamentation on P6 in the male. Tryphoema Monard, 1926 shares similar characters with Doolia except for the segmentation of the legs [14]. Based on previous reports [15] and the present study, Rhizothrix has clear discrepancies from Doolia: clearly separated rostrum with anterior row of long setules (spinules) in Doolia ara (fused to cephalosome and lacking the spinules in Rhizothrix), the well-developed comb-shaped hyaline frill on the body somites in D. ara (all frills serrulate in Rhizothrix), the long and cylindrical caudal rami in D. ara (short and robust, or ovoid in Rhizothrix), absence of the brush setae in the exopod and endopod in P1 in D. ara (present in Rhizothrix), and presence of setae on the P6 of female in D. ara (absent in Rhizothrix).…”
A new harpacticoid copepod is described from the waters off Jeju Island, Korea. This species displays a unique set of characteristics including a rostrum that is clearly demarcated from the cephalosome, a setular (spinular) row on the rostrum, a well-developed frill along the posterior margins of each body segment except for the cephalosome, long and cylindrical caudal rami, four segmented female antennules, paired genital apertures in the female, the absence of sexual dimorphism in legs P1–P4, and highly reduced P5 and P6 in the male. This combination of characteristics allocates the specimen to the family Nannopodidae Por, 1986, but the new species belongs to none of the extant genera within the family. A new genus, Doolia, is proposed. Nannopus is suggested as a sister taxon of the new genus based on shared plesiomorphic characteristics in the maxilliped, legs P1–P4, and P5. Doolia gen. nov. is the eighth genus of Nannopodidae, and an amended key for the genus is provided herein.
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