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29 results for “Rutilus rutilus”
Allopatric and sympatric diversification within roach (Rutilus rutilus) of large pre‐alpine lakes
<p>This is the data for the study entitled "Allopatric and sympatric diversification within roach (<em>Rutilus rutilus</em>) of large pre‐alpine lakes" published in the Journal of Evolutionary Biology <a href="https://doi.org/10.1111/jeb.13502">https://doi.org/10.1111/jeb.13502 .</a></p> <p>The dataset consists of three files:</p> <p><strong>Morphology.txt </strong></p> <p>Morphology data from seven Swiss lakes. Given are the individual ID, the respective lake, the habitat classification, grouped habitat classification, length of each fish (mm), and the raw x and y coordinates for 11 landmarks.</p> <p>Geometric morphometric landmarks were set as follow:</p> <p>1) anterior tip of snout, 2) anterior tip of lower jaw, 3) anterior, and 4) posterior point of operculum, 5) junction where the dorsolateral part of the head and body fuse, anterior insertion points of the 6) pectoral, 7) pelvic, and 8) anal fin, 9) ventral and 10) dorsal junction of the caudal peduncle and tail, 11) anterior insertion of the dorsal fin.</p> <p> </p> <p><strong>Stable_isotopes.txt </strong></p> <p>Morphology data from five Swiss lakes. Given are the individual ID, lake, baseline corrected delta 13C values.</p> <p> </p> <p><strong>Stable_isotopes_baselines.txt </strong></p> <p>Morphology data from five Swiss lakes. Given are the lake, the tissue used, delta 13C values.</p> <p> </p>
Fig. 5 in Formation Factors Of Cytogenetic Violation Of Rutilus Rutilus (Cypriniformes, Cyprinidae) In Transformed River Ecosystems
Fig. 5. Distribution of revealed nucleus structural breaking down in R. rutilus individuals of different age: (1+) — one-year-old; (2+) — two-year-old; (3+) –three-year-old; (4+) — four-year-old.
Fig. 1 in Formation Factors Of Cytogenetic Violation Of Rutilus Rutilus (Cypriniformes, Cyprinidae) In Transformed River Ecosystems
Fig. 1. Possible versions of micronuclei and nuclear material in erythrocytes of peripheral fish blood: a — micronuclei of "standart" type; b — "attached"; c — "linked to the nucleus with chromatine thread"; d-I — nonformed nuclear material shaped as small sticks; d-II — non-formed nuclear material in the form of clews; e — rounded formations of nuclear material of big enough sizes.
Fig. 4 in Formation Factors Of Cytogenetic Violation Of Rutilus Rutilus (Cypriniformes, Cyprinidae) In Transformed River Ecosystems
Fig. 4. Distribution of revealed structural breaking down of nucleus in R. rutilus selections from representative alignments of transformed river hydrosystems in the north-western region of Ukraine.
Fig. 2 in Formation Factors Of Cytogenetic Violation Of Rutilus Rutilus (Cypriniformes, Cyprinidae) In Transformed River Ecosystems
Fig. 2. Frequency of nuclear violations of R. rutilus peripheral blood erythrocytes in representative alignments of river hydrosystems in the north-western region of Ukraine.
Fig. 1 Aspidogaster limacoides line drawings from Rutilus rutilus from North Germany. A in Redescription of Aspidogaster limacoides Diesing, 1834 (Aspidogastrea: Aspidogastridae) from freshwater fishes of northern Germany
Fig. 1 Aspidogaster limacoides line drawings from Rutilus rutilus from North Germany. A Dorsal view (scale bar = 500 µm); B ventral view (scale bar = 500 µm); C eggs (scale bar = 50 µm); D cirrus sac (scale bar = 200 µm)
Figure 2 in Infection caused by the tapeworm Ligula intestinalis (Cestoda, Diphyllobothriidae) in the invasive cyprinid Rutilus rutilus (L., 1758), in three man-made lakes in Algeria
Figure 2. – Spatial and temporal variations of parasitic indices of Ligula intestinalis in Rutilus rutilus in Ghrib, Sekkak and Guenitra dams. P%: Prevalence; A: Parasitic abundance; I: Mean intensity of infection.
Рис. 1. Δинамика чисΛенности меΛких мΛекопитающих в Цасучейском бору: 1 — суммарная чисΛенность (особей / 100 циΛинΑро-суток); Αоминирующие виΑы: 2 — забайкаΛьский хомячок, 3 — бурозубка тунΑряная, 4 — бурозубка крошечная, 5 — поΛёвка монгоΛьская, 6 — поΛёвка РаΑΑе, 7 — красная поΛёвка; A — остепнённый сосняк, B — первичная гарь, С — старая гарь, D — повторная гарь; стреΛка указывает время прохожΑения пожара. Ось X — гг., ось Y — чисΛенность Fig. 1. Population dynamics of small mammals in the Tsasucheysky Pine Forest: 1 — total abundance (individuals / 100 cylinder-days); dominant species: 2 — Cricetulus pseudogriseus, 3 — Sorex tundrensis, 4 — S. minutissimus, 5 — Alexandromys mongolicus, 6 — Lasiopodomys raddei, 7 — Myodes rutilus; A — steppe pine forest, B — primary burns site, С — old burns site; D — repeated burns site; the arrow indicates the time of the fire. The X-axis shows years; the Y-axis shows population density in Population dynamics of small mammals after spring fires in steppe pine forest
Рис. 1. Δинамика чисΛенности меΛких мΛекопитающих в Цасучейском бору: 1 — суммарная чисΛенность (особей / 100 циΛинΑро-суток); Αоминирующие виΑы: 2 — забайкаΛьский хомячок, 3 — бурозубка тунΑряная, 4 — бурозубка крошечная, 5 — поΛёвка монгоΛьская, 6 — поΛёвка РаΑΑе, 7 — красная поΛёвка; A — остепнённый сосняк, B — первичная гарь, С — старая гарь, D — повторная гарь; стреΛка указывает время прохожΑения пожара. Ось X — гг., ось Y — чисΛенность Fig. 1. Population dynamics of small mammals in the Tsasucheysky Pine Forest: 1 — total abundance (individuals / 100 cylinder-days); dominant species: 2 — Cricetulus pseudogriseus, 3 — Sorex tundrensis, 4 — S. minutissimus, 5 — Alexandromys mongolicus, 6 — Lasiopodomys raddei, 7 — Myodes rutilus; A — steppe pine forest, B — primary burns site, С — old burns site; D — repeated burns site; the arrow indicates the time of the fire. The X-axis shows years; the Y-axis shows population density
Figure 1 in Rutilus panosi Bogutskaya & Iliadou, 2006 specimens lacking pelvic fins
Figure 1. Fish specimens of Rutilus panosi lacking pelvic fins caught in Lake Pamvotis (a) and Lake Lysimachia (b–e), western Greece.
FIGURE 4. Pseudochromis rutilus, ZMB 20568 in Two new dottyback species of the genus Pseudochromis from southern Indonesia (Teleostei: Pseudochromidae)
FIGURE 4. Pseudochromis rutilus, ZMB 20568, holotype, 55.0 mm SL, Buyuk, Nusa Penida, Indonesia (photo by M.V. Erdmann).
FIGURE 2 in A revision of the Rutilus complex from Mediterranean Europe with description of a new genus, Sarmarutilus, and a new species, Rutilus stoumboudae (Teleostei: Cyprinidae)
FIGURE 2. Native species of the Rutilus complex in southern Mediterranean Europe: A) Leucos aula, 115 mm SL, R. Bacchiglione, northern Italy, April 1996 (IZA 0425); B) Leucos basak, 95 mm SL, Lake Ohrid, FYROM, August 1987, (IZA 0429); C) Leucos ylikiensis, 120 mm SL, Lake Yliki, April 1987 (IZA 8733); D) Leucos panosi, 130 mm SL, canal to Lake Trichonis, May 1987 (IZA 8766); E) Leucos albus, 98 mm SL, River Moraca, Montenegro, November 1999 (IZA 0421); F) Sarmarutilus rubilio, 100 mm SL, River Ofanto, southern Italy, February 2002 (IZA 02183); G) Rutilus pigus, 230 mm SL, Lake Major, northern Italy, (IZA 0474); H) Holotype of Rutilus stoumboudae new species, 148 mm SL, October 1998, Lake Volvi, Greece (IZA 02107).
FIGURE 3. A in A revision of the Rutilus complex from Mediterranean Europe with description of a new genus, Sarmarutilus, and a new species, Rutilus stoumboudae (Teleostei: Cyprinidae)
FIGURE 3. A) Lectotype of Leucos aula, 74 mm SL (ANSP 6434), Padua Province, northern Italy; B) Lectotype of Leucos basak, 117 mm SL (NMW 50723-1), Vergoraz and Lake Drusino near Imotsky, Croatia; C) Lectotype of Sarmarutilus rubilio, 93 mm SL (ANSP 6509), Lake Nemi, Central Italy.
FIGURE 4 in A revision of the Rutilus complex from Mediterranean Europe with description of a new genus, Sarmarutilus, and a new species, Rutilus stoumboudae (Teleostei: Cyprinidae)
FIGURE 4. Anterior part of body of male Sarmarutilus rubilio showing prominent tubercles at centers of scales (from Bianco & Taraborelli, 1985).
FIGURE 1. A in A revision of the Rutilus complex from Mediterranean Europe with description of a new genus, Sarmarutilus, and a new species, Rutilus stoumboudae (Teleostei: Cyprinidae)
FIGURE 1. A) Collecting localities (L.=lakes, R.=rivers) of Rutilus complex species. 1, R. Thames; 2, R. Danube (Slovakia); 3, R. Danube (Romania); 4, L. Como; 5, L. Maggiore; 6, R. Arno and R. Serchio; 7, R. Albegna and R. Cecina; 8, R. Ombrone and R. Fiora; 9, R. Tiber and R. Mignone; 10, L. Trasimeno; 11, R. Liri and R. Garigliano; 12, R. Volturno and R. Sele; 13, R. Pescara and R. Tavo; 14, R. Trigno; 15, R. Tronto; 16, R. Livenza; 17, L. Pernica; 18, R. Sava; 19, L. Drusino; 20, R. Krupa (R. Neretva basin); 21, L. Besanka (R. Neretva basin); 22, R. Moraca and R. Zeta; 23, L. Skadar; 24, L. Dojran; 25, L. Horid; 26, L. Prespa and L. Micraprespa; 27, L. Vegoritis; 28, L. Volvi; 29, L. Joannina; 30, L. Yliki and L. Paralimni; 31, L. Ambrakia; 32, L. Trichonis. Bold numbers are the different peri-Mediterranean ichthyogeographic districts described in Bianco (1990). B) A schematic temporal reconstruction of the diversification of the genus in southern Mediterranean Europe based on cyt-b is shown (modified from Ketmaier et al., 2008). For each taxon the corresponding number of the district of origin is shown; triangles indicate that multiple populations were analyzed. Numbers at nodes are divergence times in million years; all labeled nodes were robustly supported in the phylogenetic reconstructions (see Ketmaier et al., 2008 for further details).
On following pages: 390. Robert's Arboreal Rice Rat (Oecomys robert); 391. Unicolored Arboreal Rice Rat (Oecomys concolor); 392. Guianan Arboreal Rice Rat (Oecomys auyantepui); 393. King Arboreal Rice Rat (Oecomys rex); 394. Red Arboreal Rice Rat (Oecomys rutilus); 395. Brazilian Arboreal Rice Rat (Oecomys paricola); 396. Foothill Arboreal Rice Rat (Oecomys superans); 397. Dusky Arboreal Rice Rat (Oecomys phaeotis); 398. Mamore Arboreal Rice Rat (Oecomys mamorae); 399. Anderson's Arboreal Rice Rat (Oecomys sydandersoni); 400. Francisco's Arboreal Rice Rat (Oecomys franciscorum); 401. Atlantic Forest Arboreal Rice Rat (Oecomys catherinae); 402. Cleber's Arboreal Rice Rat (Oecomys cleberi); 403. McConnell's Rice Rat (Euryoryzomys macconnelli); 404. Emmons's Rice Rat (Euryoryzomys emmonsae); 405. Big-headed Rice Rat (Euryoryzomys legatus); 406. Russet Rice Rat (Euryoryzomys russatus); 407. Buffy-sided Rice Rat (Euryoryzomys lamia); 408. Elegant Rice Rat (Euryoryzomys nitidus); 409. Long-whiskered Rice Rat (Transandinomys bolivaris); 410. Talamancan Rice Rat (Transandinomys talamancae); 411. Long-nosed Rice Rat (Handleyomys rostratus); 412. Chapman's Rice Rat (Handleyomys chapman); 413. Black-eared Rice Rat (Handleyomys melanotis); 414. Guerrero Rice Rat (Handleyomys guerrerensis); 415. Cloud Forest Rice Rat (Handleyomys saturation; 416. Highland Rice Rat (Handleyomys rhabdops); 417. Alfaro's Rice Rat (Handleyomys alfaroi); 418. Colombian Western Andes Cloud Forest Mouse (Handleyomys fuscatus); 419. Colombian Central Andes Cloud Forest Mouse (Handleyomys intectus). in Cricetidae
On following pages: 390. Robert's Arboreal Rice Rat (Oecomys robert); 391. Unicolored Arboreal Rice Rat (Oecomys concolor); 392. Guianan Arboreal Rice Rat (Oecomys auyantepui); 393. King Arboreal Rice Rat (Oecomys rex); 394. Red Arboreal Rice Rat (Oecomys rutilus); 395. Brazilian Arboreal Rice Rat (Oecomys paricola); 396. Foothill Arboreal Rice Rat (Oecomys superans); 397. Dusky Arboreal Rice Rat (Oecomys phaeotis); 398. Mamore Arboreal Rice Rat (Oecomys mamorae); 399. Anderson's Arboreal Rice Rat (Oecomys sydandersoni); 400. Francisco's Arboreal Rice Rat (Oecomys franciscorum); 401. Atlantic Forest Arboreal Rice Rat (Oecomys catherinae); 402. Cleber's Arboreal Rice Rat (Oecomys cleberi); 403. McConnell's Rice Rat (Euryoryzomys macconnelli); 404. Emmons's Rice Rat (Euryoryzomys emmonsae); 405. Big-headed Rice Rat (Euryoryzomys legatus); 406. Russet Rice Rat (Euryoryzomys russatus); 407. Buffy-sided Rice Rat (Euryoryzomys lamia); 408. Elegant Rice Rat (Euryoryzomys nitidus); 409. Long-whiskered Rice Rat (Transandinomys bolivaris); 410. Talamancan Rice Rat (Transandinomys talamancae); 411. Long-nosed Rice Rat (Handleyomys rostratus); 412. Chapman's Rice Rat (Handleyomys chapman); 413. Black-eared Rice Rat (Handleyomys melanotis); 414. Guerrero Rice Rat (Handleyomys guerrerensis); 415. Cloud Forest Rice Rat (Handleyomys saturation; 416. Highland Rice Rat (Handleyomys rhabdops); 417. Alfaro's Rice Rat (Handleyomys alfaroi); 418. Colombian Western Andes Cloud Forest Mouse (Handleyomys fuscatus); 419. Colombian Central Andes Cloud Forest Mouse (Handleyomys intectus).
On following pages: 165. Unstriped Ground Squirrel (Xerus rutilus); 166. Damara Ground Squirrel (Geosciurus princeps davidianus); 169. Forrest's Rock Squirrel (Sciurotamias forresti); 170. Siberian Chipmunk (Tamias sibiricus); 171. Least (Tamias townsendii); 174. Red-tailed Chipmunk (Tamias ruficaudus); 175. Shadow Chipmunk (Tamias senex); 176.); 167. South African Ground Squirrel (Geosciurus inauris); 168. Pere David's Rock Squirrel (Sciurotamias Chipmunk (Tamias minimus); 172. Yellow-pine Chipmunk (7Tamias amoenus); 173. Townsend's Chipmunk Uinta Chipmunk (Tamias umbrinus). in Sciuridae
On following pages: 165. Unstriped Ground Squirrel (Xerus rutilus); 166. Damara Ground Squirrel (Geosciurus princeps davidianus); 169. Forrest's Rock Squirrel (Sciurotamias forresti); 170. Siberian Chipmunk (Tamias sibiricus); 171. Least (Tamias townsendii); 174. Red-tailed Chipmunk (Tamias ruficaudus); 175. Shadow Chipmunk (Tamias senex); 176.); 167. South African Ground Squirrel (Geosciurus inauris); 168. Pere David's Rock Squirrel (Sciurotamias Chipmunk (Tamias minimus); 172. Yellow-pine Chipmunk (7Tamias amoenus); 173. Townsend's Chipmunk Uinta Chipmunk (Tamias umbrinus).
FIGURE 2 in European pondweed in East Siberia: evidence of Potamogeton rutilus (Potamogetonaceae) in Yakutia (Asian Russia) with evaluation of current distribution and conservation status
FIGURE 2. Characters of Potamogeton pusillus from Yakutia (Megino-Kangalasskii district, vicinity of village Maiya, alas lake): A— shoot, B—leaf apex, C—leaf base, D—stipule.
FIGURE 1 in European pondweed in East Siberia: evidence of Potamogeton rutilus (Potamogetonaceae) in Yakutia (Asian Russia) with evaluation of current distribution and conservation status
FIGURE 1. Characters of Potamogeton friesii from Yakutia (Megino-Kangalasskii district, village Pavlovsk, lake Shkolnoe): A—shoot, B—leaf apex, C—leaf base, D—stipule.
FIGURE 4 in European pondweed in East Siberia: evidence of Potamogeton rutilus (Potamogetonaceae) in Yakutia (Asian Russia) with evaluation of current distribution and conservation status
FIGURE 4. Localities of Potamogeton rutilus in the Asian part in context of general distribution. Numbers of localities in accordance with Table 7. Dash line shows preliminary range border due to insufficient data.
FIGURE 3 in European pondweed in East Siberia: evidence of Potamogeton rutilus (Potamogetonaceae) in Yakutia (Asian Russia) with evaluation of current distribution and conservation status
FIGURE 3. Characters of Potamogeton rutilus from Yakutia (Tattinskii district, vicinities of villages Kharbalakh (A, D) and Chychymakh (B, C), lakes): A—shoot, B—leaf apex, C—leaf base, D—stipule.
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