From 55e9c774483fa7884a6e8bfcf69c046f8bb0f9fb Mon Sep 17 00:00:00 2001 From: ggserver Date: Thu, 2 Jan 2025 15:50:41 +0000 Subject: [PATCH] Add updates up until 2025-01-02 15:45:37 --- .../46/03C44650FF9CFFA057C6FFE3FC5DF951.xml | 81 +- .../46/03C44650FF9CFFA357C6FE64FB56FEF8.xml | 93 +- .../42/939642CE6126517EB38B796B3452C67E.xml | 1520 +++++++++++++++++ 3 files changed, 1606 insertions(+), 88 deletions(-) create mode 100644 data/93/96/42/939642CE6126517EB38B796B3452C67E.xml diff --git a/data/03/C4/46/03C44650FF9CFFA057C6FFE3FC5DF951.xml b/data/03/C4/46/03C44650FF9CFFA057C6FFE3FC5DF951.xml index 2d7086b31f3..ffe2afe5c39 100644 --- a/data/03/C4/46/03C44650FF9CFFA057C6FFE3FC5DF951.xml +++ b/data/03/C4/46/03C44650FF9CFFA057C6FFE3FC5DF951.xml @@ -1,59 +1,58 @@ - - - -On the identity of Cryptothele collina Pocock, 1901, and comment on the preepigyne and pre-vulva in Cryptothele L. Koch, 1872 (Araneae, Zodariidae Cryptothelinae) + + + +On the identity of Cryptothele collina Pocock, 1901, and comment on the preepigyne and pre-vulva in Cryptothele L. Koch, 1872 (Araneae, Zodariidae Cryptothelinae) - - -Author + + +Author -Sankaran, Pradeep M. -Division of Arachnology, Department of Zoology, Sacred Heart College, Thevara, Cochin, Kerala 682 013, India. +Sankaran, Pradeep M. +Division of Arachnology, Department of Zoology, Sacred Heart College, Thevara, Cochin, Kerala 682 013, India. - - -Author + + +Author -Joseph, Mathew M. -0000-0002-6432-9660 -Division of Arachnology, Department of Zoology, Sacred Heart College, Thevara, Cochin, Kerala 682 013, India. & mathewmj @ gmail. com; https: // orcid. org / 0000 - 0002 - 6432 - 9660 -mathewmj@gmail.com +Joseph, Mathew M. +0000-0002-6432-9660 +Division of Arachnology, Department of Zoology, Sacred Heart College, Thevara, Cochin, Kerala 682 013, India. & mathewmj @ gmail. com; https: // orcid. org / 0000 - 0002 - 6432 - 9660 +mathewmj@gmail.com -text - - -Zootaxa +text + + +Zootaxa - -2022 - -2022-04-04 + +2022 + +2022-04-04 - -5124 + +5124 - -3 + +3 - -397 -400 + +397 +400 -journal article -53647 -10.11646/zootaxa.5124.3.9 -d149b4f5-bb0a-4f2a-887a-d005b62b9895 -1175-5326 -6414635 -8717ADB6-ED52-4ADF-9581-086C26AA87FD +journal article +53647 +10.11646/zootaxa.5124.3.9 +d149b4f5-bb0a-4f2a-887a-d005b62b9895 +1175-5326 +6414635 - + - + Cryptothele L. @@ -69,7 +68,7 @@ L. Type species. - + Cryptothele verrucosa L. Koch, 1872 diff --git a/data/03/C4/46/03C44650FF9CFFA357C6FE64FB56FEF8.xml b/data/03/C4/46/03C44650FF9CFFA357C6FE64FB56FEF8.xml index 1b0ce4c8599..f35e3c9203d 100644 --- a/data/03/C4/46/03C44650FF9CFFA357C6FE64FB56FEF8.xml +++ b/data/03/C4/46/03C44650FF9CFFA357C6FE64FB56FEF8.xml @@ -1,59 +1,58 @@ - - - -On the identity of Cryptothele collina Pocock, 1901, and comment on the preepigyne and pre-vulva in Cryptothele L. Koch, 1872 (Araneae, Zodariidae Cryptothelinae) + + + +On the identity of Cryptothele collina Pocock, 1901, and comment on the preepigyne and pre-vulva in Cryptothele L. Koch, 1872 (Araneae, Zodariidae Cryptothelinae) - - -Author + + +Author -Sankaran, Pradeep M. -Division of Arachnology, Department of Zoology, Sacred Heart College, Thevara, Cochin, Kerala 682 013, India. +Sankaran, Pradeep M. +Division of Arachnology, Department of Zoology, Sacred Heart College, Thevara, Cochin, Kerala 682 013, India. - - -Author + + +Author -Joseph, Mathew M. -0000-0002-6432-9660 -Division of Arachnology, Department of Zoology, Sacred Heart College, Thevara, Cochin, Kerala 682 013, India. & mathewmj @ gmail. com; https: // orcid. org / 0000 - 0002 - 6432 - 9660 -mathewmj@gmail.com +Joseph, Mathew M. +0000-0002-6432-9660 +Division of Arachnology, Department of Zoology, Sacred Heart College, Thevara, Cochin, Kerala 682 013, India. & mathewmj @ gmail. com; https: // orcid. org / 0000 - 0002 - 6432 - 9660 +mathewmj@gmail.com -text - - -Zootaxa +text + + +Zootaxa - -2022 - -2022-04-04 + +2022 + +2022-04-04 - -5124 + +5124 - -3 + +3 - -397 -400 + +397 +400 -journal article -53647 -10.11646/zootaxa.5124.3.9 -d149b4f5-bb0a-4f2a-887a-d005b62b9895 -1175-5326 -6414635 -8717ADB6-ED52-4ADF-9581-086C26AA87FD +journal article +53647 +10.11646/zootaxa.5124.3.9 +d149b4f5-bb0a-4f2a-887a-d005b62b9895 +1175-5326 +6414635 - + - + Cryptothele collina Pocock, 1901 @@ -71,7 +70,7 @@ - + Cryptothele collina Pocock, 1901: 498 @@ -119,7 +118,7 @@ leg., repository FIGURE 1. - + Cryptothele collina Pocock, 1901 @@ -130,24 +129,24 @@ leg., repository Diagnosis. Females of - + C . collina are closely related to the females of - + Cryptothele alluaudi Simon, 1893 as the epigyne of both share broad, paired lateral plates and narrow median septum. However, it can be separated from the latter by anterior epigynal hood (vz. absent in - + C . alluaudi ) and epigyne without lateral pockets (vz. present in - + C . alluaudi @@ -203,7 +202,7 @@ The NHM collection has a single female specimen ( FIGURE 2. - + Cryptothele sp. diff --git a/data/93/96/42/939642CE6126517EB38B796B3452C67E.xml b/data/93/96/42/939642CE6126517EB38B796B3452C67E.xml new file mode 100644 index 00000000000..27f569aeca6 --- /dev/null +++ b/data/93/96/42/939642CE6126517EB38B796B3452C67E.xml @@ -0,0 +1,1520 @@ + + + +Cobitis beijingensis, a new spined loach from northern China (Cypriniformes, Cobitidae) + + + +Author + +Sun, Zhi-Xian +0000-0003-0565-2801 +Key Laboratory of Zoological Systematics and Evolution, Institute of Zoology, Chinese Academy of Sciences, Beijing, 100101, China & Shanghai Universities Key Laboratory of Marine Animal Taxonomy and Evolution, Shanghai Ocean University, Shanghai, 201306, China + + + +Author + +Li, Xue-Yuan +Key Laboratory of Zoological Systematics and Evolution, Institute of Zoology, Chinese Academy of Sciences, Beijing, 100101, China + + + +Author + +Li, Xue-Jian +0000-0003-0655-5982 +Institute of Shandong River Wetlands, Jinan, Shandong, 271100, China + + + +Author + +Hao, Jun-Yuan +Key Laboratory of Zoological Systematics and Evolution, Institute of Zoology, Chinese Academy of Sciences, Beijing, 100101, China + + + +Author + +Sheng, Dong +Key Laboratory of Zoological Systematics and Evolution, Institute of Zoology, Chinese Academy of Sciences, Beijing, 100101, China + + + +Author + +Zhao, Ya-Hui +0000-0002-4615-596X +Key Laboratory of Zoological Systematics and Evolution, Institute of Zoology, Chinese Academy of Sciences, Beijing, 100101, China + +text + + +Zoosystematics and Evolution + + +2025 + +2025-01-02 + + +101 + + +1 + + +55 +67 + + + +journal article +10.3897/zse.101.137363 +C3C2A5B2-3CAD-4C86-AACA-1C0E84C0461B + + + + + +Cobitis beijingensis +Sun & Zhao + +sp. nov. + + + + +Figs 2 +, +3 +, +4 +; +Table 2 + + + + +Type material. + + + + + +Holotype + +. + +• + +ASIZB +240630 + +, +male +, 55.0 mm SL; +Shilipu Township +, +Miyun District +, +Beijing +, +from the Chaobaihe River +( + +40.33574769 ° N +, +116.79236588 ° E + +, + +52 m +a. s. l. + +); collected by +Zhixian Sun +, +Junyuan Hao +and +Dong Sheng +; + +13 June 2024 + +. + + + + + + + + +Cobitis beijingensis + +sp. nov. +, holotype, ASZIB 240630, 55.0 mm standard length; +A. +Lateral view; +B. +Dorsal view; +C. +Ventral view; +D. +Original drawing. + + + + + +Paratypes + +. + +Twenty-five specimens +• + + +ASIZB +240631–6 + +, +240689–95 +, +3 males +, +10 females +, +50.2–75.3 mm +SL; same collection information as holotype + +• + + +ASIZB +240697–8 + +, +2 juveniles +, 24.1–27.0 mm SL; same locality and collectors as holotype; + +14 June 2024 + + +• + + +ASIZB +240682–4 + +, +3 males +, +48.8–58.1 mm +SL • + +ASIZB +240685–8 + +, +4 juveniles +, +26.4–33.1 mm +SL; same locality as holotype; collected by +Zhixian Sun +and +Wenli Yu +; + +15 June 2024 + + +• + + +ASIZB +240605 + +, +240680–1 +, +1 male +, +2 females +, +56.1–74.5 mm +SL; +Qiaozi Township +, +Huairou District +, +Beijing +, +from the confluence of the Huaijiuhe River and Huairou Reservoir +( + +40.31521727 ° N +, +116.57391776 ° E + +, + +64 m +a. s. l. + +); collected by +Zhixian Sun +, +Yutian Fang +and +Dong Sheng +; + +10 May 2024 + + +. + + + + + + +Counts and measurements of + +Cobitis beijingensis + +sp. nov. +and + +Cobitis lutheri + +. + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
Counts + +Cobitis beijingensis + +sp. nov. + + +Cobitis lutheri + +
HolotypeAll examined specimens includes types (n = 46)All examined specimens (n = 34)
Mode and RangenMode and Rangen
Branched dorsal-fin rays77 (6–7)407 (7)34
Branched anal-fin rays55 (5)405 (5)34
Branched pectoral-fin rays88 (7–9)408 (7–8)34
Branched pelvic-fin rays66 (5–7)406 (5–6)34
Prepelvic myotomes1515 (14–18)3912 (11–13)34
Vertebrae4 + 374 + 37 (36–38)114 + 39 (38–41)8
MeasurementsMaleMale (n = 11)Female (n = 15)Male (n = 19)Female (n = 15)
Mean and RangeSDMean and RangeSDMean and RangeSDMean and RangeSD
Standard length (mm)55.055.0 (48.8–65.7)64.1 (57.1–71.1)54.8 (48.4–62.8)70.1 (53.8–87.3)
+In percentage of SL +% +
Body depth17.116.7 (12.6–19.8)2.016.4 (13.3–19.3)1.716.5 (14.2–18.8)1.216.5 (14.7–17.9)1.0
Head length21.821.6 (19.7–25.0)1.520.3 (19.0–21.4)0.721.9 (20.2–23.9)1.221.3 (19.4–23.5)1.2
Dorsal-fin length19.918.5 (14.8–20.8)1.917.3 (15.7–19.3)1.118.6 (16.3–20.8)1.417.0 (14.5–18.6)1.0
Dorsal-fin base length10.510.8 (8.0–12.8)1.411.4 (8.3–13.5)1.210.5 (8.6–13.3)1.110.5 (9.4–12.6)0.9
Pectoral-fin length19.418.4 (14.7–21.2)1.913.6 (12.1–16.3)1.217.1 (14.6–20.0)1.413.0 (10.7–15.7)1.0
Pectoral-fin base length4.54.1 (2.6–5.3)0.93.1 (2.5–3.9)0.34.2 (3.5–5.0)0.43.4 (2.8–3.9)0.3
Pelvic-fin length15.614.4 (12.0–16.1)1.411.5 (10.1–12.7)0.813.6 (11.1–15.1)1.111.3 (9.6–13.1)1.0
Pelvic-fin base length3.83.5 (2.6–4.9)0.73.1 (2.5–3.9)0.43.4 (2.9–4.3)0.33.1 (2.8–3.9)0.3
Anal-fin length14.714.0 (13.0–15.1)0.812.9 (11.2–14.6)1.015.3 (11.5–15.1)1.413.4 (12.8–14.6)0.6
Anal-fin base length7.27.3 (5.3–8.5)0.97.7 (5.9–8.7)0.68.2 (6.5–10.3)1.08.0 (6.9–9.7)0.8
Pre-dorsal length58.356.1 (41.3–61.1)5.456.9 (52.9–61.6)2.154.7 (52.4–56.8)1.554.9 (52.4–58.4)1.7
Post-dorsal length44.245.6 (41.3–56.5)4.046.6 (42.6–50.5)2.147.2 (43.7–49.5)1.947.8 (43.1–50.6)1.8
Pre-pectoral length23.023.7 (21.8–26.0)1.421.9 (21.0–23.8)0.924.1 (20.5–27.5)2.122.0 (19.5–24.2)1.6
Pre-pelvic length60.561.3 (58.1–65.1)2.358.8 (53.5–63.1)2.553.7 (50.2–58.1)2.253.5 (49.7–55.9)1.6
Pre-anal length85.185.0 (81.0–89.8)3.183.7 (80.0–88.3)2.281.8 (77.1–86.1)2.581.4 (78.6–84.8)2.0
Caudal peduncle length8.010.1 (8.0–12.7)1.410.5 (8.6–13.5 ))1.511.1 (8.9–13.1)1.310.8 (9.5–13.6)1.1
Caudal peduncle depth10.49.9 (8.0–11.3)1.09.3 (8.6–10.0)0.49.2 (8.0–11.0)0.79.0 (7.6–10.0)0.7
Head length (mm)12.011.8 (11.0–12.9)19.6 (12.6–26.6)12.0 (10.6–13.6)14.9 (12.2–17.7)
+In percentage of HL +% +
Head depth62.061.7 (56.5–66.8)3.362.2 (57.2–68.3)3.262.1 (57.1–71.9)3.361.1 (54.7–69.1)4.0
Head width40.543.1 (35.2–52.7)6.044.0 (37.1–51.7)3.842.5 (35.8–49.5)4.345.6 (37.7–56.1)5.2
Eye diameter15.816.8 (14.2–20.3)2.213.3 (11.2–16.7)1.517.6 (14.0–22.2)2.415.3 (12.0–17.9)1.9
Interorbital width27.924.2 (18.3–28.1)3.823.1 (19.9–27.8)1.921.5 (16.6–26.8)2.622.2 (15.9–27.5)3.2
Snout length43.943.2 (36.9–49.3)3.446.9 (41.7–50.1)2.239.6 (35.6–45.4)2.642.7 (37.7–48.1)3.2
+
+
+ + +Additional materials examined. + + +Twenty-five specimens +• + + +ASIZB +62425–8 + +, +1 male +, +3 females +, 42.0–67.0 mm SL; +Niulanshan Township +, +Shunyi District +, +Beijing +, +from the Chaobaihe River +; collected by +Chunguang Zhang +; 1992 + +• + + +ASIZB +192934 + +( + +FMZB +3861 + +), +female +, 53.0 mm SL; +Shahe Township +, +Changping District +, +Beijing +; + +1 June 1929 + + +• + + +ASIZB +16918 + +, +female +, +92.2 mm +SL; +Beijing + +• + + +ASIZB +17732 + +, +female +, +75.8 mm +SL; +Beijing + +• + + +ASIZB +17388 + +( + +FMZB +6030 + +), 17390 (6032), from one lot of specimens ( + +ASIZB +17388–99 + +), +1 male +, +1 female +, 51.4–54.0 mm SL; +Changxindian Township +(originally in Hebei Province), +Fengtai District +, +Beijing +, +from the Yongdinghe River +; collected by +Yingxiang Du +; + +9 May 1930 + + +• + + +ASIZB +17297–802 + +, gender unidentified, +6 specimens +, +59.4–68.5 mm +SL; +Liulihe Township +, +Fangshan District +, +Beijing +, +from the Liulihe River + +• + + +ASIZB +103008–10 + +, +2 males +, +1 female +, +50.5–65.7 mm +SL; +Anxin County +, +Baoding City +, +Hebei Province +, +from the Baiyangdian Lake system +; collected by +Shiyi Zhang +and +Wenbin Wang +; + +October 1959 + + +• + + +ASIZB +16917 + +, +female +, +116.3 mm +SL; +Xinji Township +, +Sanhe City +, +Langfang City +, +Hebei Province +, +from the Juhe River +; + +13 June 1930 + + +• + + +ASIZB +79421–5 + +, +5 females +, +58.3–109.4 mm +SL; +Anxin County +, +Baoding City +, +Hebei Province +, +from the Baiyangdian Lake system + +• + + +ASIZB +170316 + +, +female +, +62.4 mm +SL; +Xisiduhe Village +, +Jiuduhe Township +, +Huairou District +, +Beijing +, +from the Huaijiuhe River +; + +1 June 1974 + + +• + + +ASIZB +240696 + +, +male +, +54.5 mm +SL; Lvhu local market, +Qiaozi Township +, +Huairou District +, +Beijing +, +from the Huairou Reservoir +; collected by +Zhixian Sun +, +Junyuan Hao +and +Dong Sheng +; + +15 June 2024 + + +. + + + + +Diagnosis. + + +The new species can be distinguished by the combination of the following characters: Lamina circularis on pectoral fin elongated, posterior margin slightly serrated; 14–18 (mode 15) prepelvic myotomes; pelvic fin inserted below 3 +rd +– 5 +th +branched dorsal-fin ray; total vertebrae 4 + 36–38 (mode 37); the second Gambetta line (L +2 +) does not exist or is fused with the first line (L +1 +). + + + + +Description. + +Body elongated, laterally compressed. Dorsal body profile rising smoothly from nostrils to occiput, almost horizontal between occiput and dorsal-fin insertion, gradually sloping along dorsal-fin base, then horizontally extending to caudal-fin base. Maximum body depth at dorsal-fin origin, body depth 12.6–19.8 % of standard length. Lower surface of head flattened, abdomen rounded. Caudal peduncle short, depth almost equal to length, laterally compressed, with fleshy keels on dorsal and ventral sides. Head length greater than body depth (101.0–156.7 % of head length); snout elongated and blunt, snout length 36.9–50.1 % of head length; eye small, 11.2–20.3 % of head length, superior and laterally positioned, near gill opening than tip of snout; nostrils positioned close together, anterior nostril with short tube; interorbital region ridged and narrow. Anus positioned near anal-fin insertion. +Mouth inferior, lips fleshy. Upper lip without affiliated apparatus; lower lip two lobed, medial side elongate-oval shaped. Three pairs of barbels: rostral barbels shorter than maxillary and mandibular barbels; maxillary barbels length equal to mandibular barbels length; mandibular barbels not or almost reaching under the anterior edge of the orbit. + +Body covered with tiny cycloid scales. Prepelvic myotomes 14 ( +3 specimen +), 15 (26), 16 (7), 17 (2), 18 (1). + +Dorsal fin with three unbranched and six (1) or seven (39) branched rays; distal margin slightly convex, inserted nearer to caudal-fin base than snout. Pectoral fin with one unbranched and seven (3), eight (32) or nine (5) branched rays. Pelvic fin with one unbranched and five (1), six (38) or seven (1) branched rays, inserted below third to fifth branched dorsal-fin ray. Anal fin with 3 unbranched and 5 (40) branched rays; inserted nearer to caudal-fin base than to pelvic-fin insertion. Caudal fin slightly truncated, with one unbranched principle ray and seven branched principle rays on upper part and seven branched principle rays and one unbranched principal ray on lower part. + +Total vertebrae 4 + 36 (1), 37 (6), 38 (4). Suborbital spine bifurcated (Fig. +3 +), posteriorly reaching under the center of the orbit. + + + + + + +Right suborbital spine of + +Cobitis beijingensis + +sp. nov. +A. +Lateral view; +B. +Dorsal view. + + + + + +Coloration in live. + + +Dorsal side of head and body yellowish brown, mid-lateral side light yellowish brown, ventral side grayish white. A clear black stripe or “ tear mark ” runs from tip of snout, crossing the eye, to the occiput; two dark grey stripes distributed parallel to the clear black stripe, one on the dorsal side of the head; one runs across the nostrils; several vague and irregular patterns located under the eye and opercula, sometimes forming one or two grey stripes parallel to the clear black stripe. Four obvious lines of Gambetta’s pattern. The L +1 +of Gambetta’s pattern on the dorsal of body, 7–10 black blotches before dorsal-fin insertion, 7–11 black blotches after dorsal-fin base end; L +2 +not exist or fused with L +1 +; L +3 +linear, interrupted into several small irregular blotches and fused with L +1 +at caudal peduncle; L +4 +linear, consisted of many tiny spots; L +5 +obvious, extending along the mid-lateral side of body, consisted of 9–15 different sized black blotches, sometimes connected with each other with black strip. Three or four rows of pigmentation on dorsal-fin rays; three or four arcuate black bars on caudal fin. One big jet-black oval-shaped spot on upper caudal-fin base, size comparable to the eye diameter (Fig. +4 +). + + + + + + +Live individuals of + +Cobitis beijingensis + +sp. nov. +A. +Holotype, +ASIZB +240630, male; +B. +Uncatalogued, female; +C. +Paratype, +ASIZB +240682, male, photographed in aquarium. + + + + + +Coloration in preservation. + +Dorsal side of head and body yellow, mid-lateral side light yellow, ventral side pale. All patterns same position as living specimen. + + + +Sexual dimorphism. + + +Males with elongated lamina circularis derived from the base of the first branched pectoral-fin ray; tip of the lamina circularis almost reaching the mid-point of the first branched ray; posterior margin of the lamina circularis usually serrated (Fig. +5 A +). The L +4 +of Gambetta’s pattern in males, usually thin and short, sometimes disappeared. The blotches on L + +5 +in + +males usually merged into a line. Females usually larger and slender than males. The L + +4 +in + +females usually exceeds over dorsal fin insertion, sometimes reaching the caudal peduncle. The blotches on L + +5 +in + +females not fully merged into one line. + + + + + + +Lamina circularis of + +Cobitis beijingensis + +sp. nov. +( +A +) and + +C. lutheri + +( +B +). + + + + + +Distribution. + + +Based on our field collections and the historic specimens, + +Cobitis beijingensis + +is distributed in the Haihe River basin in northern +China +, including rivers in +Beijing +and the Baiyangdian Lake in +Hebei Province +. This species can be currently found in the Chaobaihe River system in Huairou and Miyun District, +Beijing +(Fig. +6 +). + + + + + + +Distribution of + +Cobitis beijingensis + +sp. nov. +and + +C. lutheri + +; the zoom-in map shows detailed distribution (i. e., specimen locality records) of the new species in Beijing and the adjacent area. + + + + + +Habitat and biology. + + +This species usually inhabits slow-flowing water or still water with plenty of submerged plants or filamentous algae. The benthic microhabitat is usually sand and silt mixed with some gravel. Coexisting species include + +Rhodeus ocellatus + +, + +Carassius auratus + +, + +Misgurnus anguillicaudatus + +, + +Oryzias latipes + +, + +Rhinogobius giurinus + +, etc. + + + + +Etymology. + + +The species name + +“ +beijingensis + +” was referred to the type locality of this species, +Beijing +, the capital city of +China +. The Chinese name for the new species is “ 北京花鳅 ”. + + + + +Genetic comparisons. + + +A total of 24 haplotypes from 30 + +Cobitis + +individuals were included in the analyses. The molecular phylogenetic results ( +BI +and + +ML + +trees in Fig. +7 +) based on mitochondrial Cyt +b +sequences show that the new species + +C. beijingensis + +forms a monophyletic group itself, which is sisters to the group consists of + +C. lutheri + +, + +C. tetralineata + +, + +C. nalbanti + +, and + +C. hankugensis + +. The interspecific genetic distances between + +C. beijingensis + +and four congeners, + +C. lutheri + +, + +C. tetralineata + +, + +C. nalbanti + +, and + +C. hankugensis + +, are 13.1 %, 8.0 %, 12.5 %, and 8.3 %, respectively (Table +3 +). The intraspecific genetic distances in + +C. beijingensis + +, + +C. lutheri + +, + +C. tetralineata + +, + +C. nalbanti + +, and + +C. hankugensis + +are 0.2 %, 0.5 %, 0.0 %, 0.6 %, and 0.0 %, respectively (Table +3 +), which are much lower than the interspecific genetic distances. The molecular phylogenetic results support + +C. beijingensis + +to be a distinct species. + + + + + + +Genetic distances of the Cyt +b +gene computed by MEGA 6.0 amongst nine analyzed species of + +Cobitis + +, + +Sabanejewia aurata + +was used as the outgroup. + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
-Intraspecific123456789
1 + +C. beijingensis + +sp. nov. +0.002---------
2 + +C. lutheri + +0.0050.131--------
3 + +C. nalbanti + +0.0060.1230.125-------
4 + +C. hankugensis + +00.1000.0980.083------
5 + +C. tetralineata + +00.1180.1210.0390.080-----
6 + +C. choii + +0.0060.1570.1770.1720.1750.161----
7 + +C. melanoleuca + +0.0030.1710.1760.1640.1640.1530.128---
8 + +C. gracilis + +0.0060.1580.1710.1610.1660.1550.1240.077--
9 + +C. granoei + +0.0040.1750.1810.1620.1650.1560.1300.0150.076-
10 + +S. aurata +(Outgroup) + +NA0.1950.1980.2010.1880.1910.2090.1910.1940.198
+
+ + + + + +Molecular phylogenetic trees of + +Cobitis beijingensis + +sp. nov. +and other phylogenetically close related congeners based on Cyt +b +sequence (1140 bp). +A. +Bayesian Inference method; +B. +Maximum Likelihood method. + + +
+
+
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