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Fig. 6 in Morphometric Variation Of Hybridizing Species And Gynogenetic Biotypes Of Spined Loaches (Cobitidae, Cobitis) In River Systems Of Ukraine

Fig. 6. UPGMA clustering of biotypes by Mahalanobis distances calculated for body measurements and indices separately. Rectangles bounds the clusters with more than 90 % AU-support.

Fig 5. 95 in Morphometric Variation Of Hybridizing Species And Gynogenetic Biotypes Of Spined Loaches (Cobitidae, Cobitis) In River Systems Of Ukraine

Fig 5. 95 % confidence ellipses of the biotypes in the morphospace of four between-group principal components calculated for indices. Mean groups of each biotype is marked with black point and designation.

Fig. 3. 95 in Morphometric Variation Of Hybridizing Species And Gynogenetic Biotypes Of Spined Loaches (Cobitidae, Cobitis) In River Systems Of Ukraine

Fig. 3. 95 % confidence interval ellipses of the biotypes in the morphospace of bgPC1 and bgPC2 calculated for log10-transformed absolute traits. Each biotype means are marked with black points and names. The biotypes are explained in table 1.

Fig. 4. 95 in Morphometric Variation Of Hybridizing Species And Gynogenetic Biotypes Of Spined Loaches (Cobitidae, Cobitis) In River Systems Of Ukraine

Fig. 4. 95% confidence interval ellipses of the biotypes in the morphospace of bg PC3 and bgPC4 A calculated for log10 transformed absolute traits. Designations the same as on fig. 3.

Fig. 2 in Morphometric Variation Of Hybridizing Species And Gynogenetic Biotypes Of Spined Loaches (Cobitidae, Cobitis) In River Systems Of Ukraine

Fig. 2. Body measurements for Cobitis. Th e original fish image is from Wilhelm von Wright out of Fries, 1895.

Fig. 1 in Morphometric Variation Of Hybridizing Species And Gynogenetic Biotypes Of Spined Loaches (Cobitidae, Cobitis) In River Systems Of Ukraine

Fig. 1. Collection points of spined loaches in the river systems of Ukraine. Th e decoding of the numbering of samples is given in Material and methods.

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Fig. 1 in Histological And Ultrastructural Studies On The Intestine Of Guntea Loach, Lepidocephalichthys Guntea (Cypriniformes, Cobitidae)

Fig. 1. Photomicrographs of various regions of the intestine of Lepidocephalichthys guntea by scanning electron microscopy (SEM) as well as transmission electron microscopy (TEM) and histological sections stained with Delafield's Haematoxylin-Eosin (HE) and Mallory's triple (MT) stain: a — anterior intestine consists of mucosa (M) with numerous finger like projections (V) toward the lumen (L), submucosa (solid arrows), muscularis (ML) and serosa (arrow heads) (MT) ×100; b — middle intestine exhibits blunt projections lined with tightly packed columnar epithelial cells (CEC) and mucous cells (broken arrows). The submucosa (SM) is distinguished from mucosa (M) by basement membrane (BM) and made up of connective tissue, collagen fibres and blood vessels (solid arrows) forming lamina propria (LP). Note the presence of apical top plate (arrow heads) over the mucosal border (HE) ×400; c — higher magnification of middle intestine showing mucosa (M) packed with CEC having conspicuous nuclei (N) and top plate (arrow heads). Broken arrow marks secreted mucin from mucous cell (HE) ×1000; d — luminal surface of the middle intestine provided with prominent microridges (arrow heads) represent the apical surface of CEC. Note the presence of mucous cells (solid arrows) in between CEC and mucin mass (broken arrows) over CEC (SEM) ×3500; e — folds (V) of middle intestine provided with columnar epithelial cells having numerous microvilli (MV) apically and basally located nuclei (N). Note the presence of scattered mucous cells (broken arrows) in between columnar epithelial cells. Solid arrows indicate blood vessels with erythrocytes (TEM) ×570; f — mucosa of middle intestine showing CEC with microvilli (MV) and nucleus (N) connected with neighbouring cells by tight junctions (broken arrows). Cytoplasm contains tuft of mitochondria (solid arrows), lysosome (arrow head) and lipid droplets (LD). Note the presence of MC and BV (TEM) ×2550.

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Fig. 2 in Reproductive Potentials Of Diploid And Polyploid Representatives Of The Genus Сobitis (Cypriniformes, Cobitidae)

Fig. 2. Ovarium weight variation depend on erythrocytes area size (mµ) of spined loaches of Stugna River with different ploidy levels.

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Fig. 1 in Reproductive Potentials Of Diploid And Polyploid Representatives Of The Genus Сobitis (Cypriniformes, Cobitidae)

Fig. 1. Eggs number variation depend on erythrocytes area size (µm2) of spined loaches of Stugna River with different ploidy levels.

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Fig. 3 in Reproductive Potentials Of Diploid And Polyploid Representatives Of The Genus Сobitis (Cypriniformes, Cobitidae)

Fig. 3. Eggs weight (mg) variation depend on erythrocytes area size (mµ) of spined loaches of Stugna River with different ploidy levels.

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Fig. 2 in Absorbing Hybridization Of Cobitis Taenia And Sabanejewia Aurata (Cypriniformes, Cobitidae) In Water Reservoirs Of Northern Ukraine Connected With Diploid-Polyploid Complex Formation

Fig. 2. Electrophoretic spectra of enzymes coding by allozymic loci: aspartate amynotransferase (1 — Aat- 1100/100, 2 — Aat-1100/110-110, 3 — Aat-195/110-110, 4 — Aat-1100-100/110, 5 — Aat-195-95/110, 6 — Aat-195-100/110), lactate dehydrogenase (1 — Ldh-B90/90, 2 — Ldh-B100/100, 3 — Ldh-B90/100-100, 4 — Ldh-B90/100/110), malate dehydrogenase (1 — Mdh-1A100/100, 2 — Mdh-1A100/110-110, 3 — Mdh-1A100-100/110).

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Рис. 4. МоΛоΔой вьюн Àабри Paramisgurnus dabrianus (Dabry de Thiersant, 1872) Fig. 4. Young Paramisgurnus dabrianus (Dabry de Thiersant, 1872) in Cobitidae And Balitoridae Of The Middle Part Of Amur In The Jewish Autonomous Region And The Adjacent Border Territories Of China

Рис. 4. МоΛоΔой вьюн Àабри Paramisgurnus dabrianus (Dabry de Thiersant, 1872) Fig. 4. Young Paramisgurnus dabrianus (Dabry de Thiersant, 1872)

Fig. 11 in Lepidocephalichthys balios, a new species of loach from central Laos (Teleostei: Cobitidae)

Fig. 11. Lepidocephalichthys hasselti; a, CMK 19805, 37.2 mm SL; Laos: Mekong drainage: Nam Theun; b, MHNG 1372.40-50, 28.4 mm SL; Indonesia: Java: Sukabumi.

Fig. 10 in Lepidocephalichthys balios, a new species of loach from central Laos (Teleostei: Cobitidae)

Fig. 10. Lepidocephalichthys berdmorei; a, CMK 25927, 71.1 mm SL; Laos: Mekong drainage: Nam Youan; b, CMK 25430 59.3 mm SL; Myanmar: Tenasserim: Lenya drainage.

Fig. 8 in Lepidocephalichthys balios, a new species of loach from central Laos (Teleostei: Cobitidae)

Fig. 8. Lepidocephalichthys balios; CMK 13249, pectoral fin, in dorsal view. a, male, 27.4 mm SL, with adjacent rays 7 and 8; b, female, 32.6 mm SL, with separate rays 7 and 8.

Fig. 9 in Lepidocephalichthys balios, a new species of loach from central Laos (Teleostei: Cobitidae)

Fig. 9. Laos: Nam Leuk, pool at confluence with Nam Gnong; type locality of Lepidocephalichthys balios. 24 February 1997. Scanned from an old slide.

Fig. 6 in Lepidocephalichthys balios, a new species of loach from central Laos (Teleostei: Cobitidae)

Fig. 6. Lepidocephalichthys balios; CMK 13249, 32.6 mm SL; mouth in ventral view. Abbreviations: mb, maxillary barbel; ml, mental lobe of lower lip; pf, postlabial flange of lower lip; rbi, inner rostral barbel; rbo, outer rostral barbel; ul, upper lip.

Fig. 5. Lepidocephalichthys balios, CMK 13249 in Lepidocephalichthys balios, a new species of loach from central Laos (Teleostei: Cobitidae)

Fig. 5. Lepidocephalichthys balios, CMK 13249, paratype, 28.1 mm SL; Laos: Nam Leuk. Shortly after fixation, scanned from a slide prepared in 1997. Right side, reversed.

Fig. 3 in Lepidocephalichthys balios, a new species of loach from central Laos (Teleostei: Cobitidae)

Fig. 3. Lepidocephalichthys balios; MHNG 2792.020, holotype, 28.8 mm SL; Laos: Nam Leuk (right side, reversed).

Fig. 2 in Lepidocephalichthys balios, a new species of loach from central Laos (Teleostei: Cobitidae)

Fig. 2. Laos: Nam Ngum, Nam Mang, Nam Ngiep, and Nam Xan watersheds, showing type locality of Lepidocephalichthys balios (black dot).