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276 results for “Myotis myotis”
Fig. 3 in The Subspecies Of Myotis Montivagus - Taxonomic Revision And Species Limits (Mammalia: Chiroptera: Vespertilionidae)
Fig. 3. Detail of the rostral part of skulls: a = M. annectans BM(NH) 78.2355 from Thailand, b = M. borneoensis BM(NH) 83.349 (holotype), c = M. federatus BM(NH) 16.4.20.5 (holotype), d = M. montivagus BM(NH) 76.3.10.5 (holotype), e = M. peytoni BM(NH) 12.8.25.1 (holo-
Fig. 2 in The Subspecies Of Myotis Montivagus - Taxonomic Revision And Species Limits (Mammalia: Chiroptera: Vespertilionidae)
Fig. 2. Lateral view of skulls: a = M. annectans BM(NH) 78.2355 from Thailand, b = M. borneoensis BM(NH) 83.349 (holotype), c = M. federatus BM(NH) 16.4.20.5 (holotype), d = M. montivagus BM(NH) 76.3.10.5 (holotype), e = M. peytoni BM(NH) 12.8.25.1 (holotype). Scale = 5 mm.
Fig. 3 in Contribution To Ecology Of Brandt'S Bat, Myotis Brandtii (Chiroptera, Vespertilionidae) In The North-Eastern Ukraine: Comparison Of Local Summer And Winter Bat Assemblages
Fig. 3. Body mass (g) characteristic of females (F) and (M) of M. brandtii in periods of spring departure April (S_dep) and swarming August (Swarm) from the Tetlega mines (dot — mean value, line — median value, whiskers — min and max values, not filling circles — outliers).
Fig. 2 in Contribution To Ecology Of Brandt'S Bat, Myotis Brandtii (Chiroptera, Vespertilionidae) In The North-Eastern Ukraine: Comparison Of Local Summer And Winter Bat Assemblages
Fig. 2. Forearm length (mm) of females (F) and males (M) of M. brandtii from Tetlega mines (dot — mean value, line — median value, whiskers — min and max values).
Fig. 1 in Contribution To Ecology Of Brandt'S Bat, Myotis Brandtii (Chiroptera, Vespertilionidae) In The North-Eastern Ukraine: Comparison Of Local Summer And Winter Bat Assemblages
Fig. 1. Allocation of M. brandtii (Mbra) and M. daubentonii (Mdau) inside the Tetlega mines from November to April (n — number of counted bats); A — in crevices or open, B — on walls or ceiling.
Fig. 1 in From Greener Times: A New Species Of Thick-Thumbed Myotis From Phnom Penh, Cambodia
Fig. 1. Principal component analysis of 13 craniodental measurements from 122 adult specimens. Symbols represent the position of an individual skull on the first two principal
Fig. 7 in From Greener Times: A New Species Of Thick-Thumbed Myotis From Phnom Penh, Cambodia
Fig. 7. Landcover in Phnom Penh city in February 2003 (left) and February 2021 (right). The central square symbol represents the available coordinates (11°35'N, 104°55'E) for the holotype of Myotis hayesi sp. n., whereas the dashed line encloses the area this was likely captured within (NW to SE corner: 11°36'N, 104°54'E to 11°34'N, 104°56'E). Imagery from Google-Earth Pro (Google Inc.)
Fig. 4 in From Greener Times: A New Species Of Thick-Thumbed Myotis From Phnom Penh, Cambodia
Fig. 4. Lateral view of skulls of Myotis species: A = M. hayesi sp. n. (holotype, HNHM 2005.82.32.) from Cambodia, B = M. rosseti (holotype, RMNH 19629) from Cambodia, C = M. muricola (HNHM 2005.82.20.) from Cambodia, D = M. ater (HZM 10.34188) from Cambodia, E = M. nipalensis (BM(NH) 16.7.29.38) from West Bengal, India, and F = M. alticrania-
Fig. 6 in From Greener Times: A New Species Of Thick-Thumbed Myotis From Phnom Penh, Cambodia
Fig. 6. Bacula (dorsal and right lateral views) of selected Myotis species: A = M. hayesi sp. n. (holotype, HNHM 2005.82.32.), B = M. annatessae (Vietnam, ZMMU S-164989), C = M. ater (Vietnam, ZMMU S-172604), D = M. alticraniatus (Vietnam, ZMMU S-167188), E = M. muricola (Vietnam, ZMMU S-172616). B–E (D as M. siligorensis) after KRUSKOP and BORISSENKO
Fig. 5 in From Greener Times: A New Species Of Thick-Thumbed Myotis From Phnom Penh, Cambodia
Fig. 5. Lateral view of the mandible (scale = 5 mm), and occlusal views of the lower (right) and upper (left) toothrows (scale = 3 mm) of Myotis hayesi sp. n. (holotype, HNHM
Fig. 2 in From Greener Times: A New Species Of Thick-Thumbed Myotis From Phnom Penh, Cambodia
Fig. 2. Right thumb viewed from the leading edge of wing of A) Myotis hayesi sp.n. (holotype, HNHM 2005.82.32.) from Cambodia, B) M. rosseti (HNHM 2869.51.b.1) from Thailand, and C) M. muricola (HNHM 2005.82.20.) from Cambodia. Note the shape of the claw and the relative length of the distal phalanges in relation to the base of the thumb. Scale = 5 mm
Fig. 3 in From Greener Times: A New Species Of Thick-Thumbed Myotis From Phnom Penh, Cambodia
Fig. 3. Plantar view of left hindfoot of A = Myotis hayesi sp. n. (holotype, HNHM 2005.82.32.) from Cambodia, B = M. rosseti (HNHM 2869.51.b.2) from Thailand, and C = M. muricola
Fig. 4 in Is parasite load dependent on host aggregation size? The case of the greater mouse-eared bat Myotis myotis (Mammalia: Chiroptera) and its parasitic mite Spinturnix myoti (Acari: Gamasida)
Fig. 4 Relationship between the size of bat maternity aggregation (a), percentage of forest cover (b), body condition index (c), and parasite infection of the examined bats in the Carpathians Mountains (2007).
Fig. 1 in Is parasite load dependent on host aggregation size? The case of the greater mouse-eared bat Myotis myotis (Mammalia: Chiroptera) and its parasitic mite Spinturnix myoti (Acari: Gamasida)
Fig. 1 Distribution of greater mouse-eared bat (Myotis myotis) maternity aggregations (grey circles) and single founding individuals (black dots) in the Beskids (Carpathian Mountains, Poland). Data pooled from Kozakiewicz (2003), Szkudlarek et al. (2008), and our data. For the investigated maternity colonies, forested areas within a 10-km radius is shown
Fig. 3 in Is parasite load dependent on host aggregation size? The case of the greater mouse-eared bat Myotis myotis (Mammalia: Chiroptera) and its parasitic mite Spinturnix myoti (Acari: Gamasida)
Fig. 3 Proportions of protonymph (PN), deutonymph (DN), and adult (AD) stages of S. myoti mites, collected from Myotis myotis (bars), and the sex ratios of deutonymph and adult mites (circles)
Fig. 2 in Is parasite load dependent on host aggregation size? The case of the greater mouse-eared bat Myotis myotis (Mammalia: Chiroptera) and its parasitic mite Spinturnix myoti (Acari: Gamasida)
Fig. 2 Micrograph of the adult female Spinturnix myoti, dorsal view. Scanning electron microscopy image, original magnification ×40
Figure 2 in Nucleolus organizer regions of Myotis myotis (Borkhausen, 1797) and Miniopterus schreibersii (Kuhl, 1817) (Mammalia: Chiroptera) from Turkey
Figure 2. Ag-NOR stained metaphase plate of Miniopterus schreibersii (arrow indicates the secondary constriction, inset the NOR-bearing chromosome pairs).
Figure 1 in C-Heterochromatin and nucleolus organizer region distribution of Myotis emarginatus (Chiroptera: Vespertilionidae) from Turkey
Figure 1. Collection sites of Myotis emarginatus in Dubnisa Cave from Kırklareli (1); in old church from Karaisalı, Adana (2); and in Black Cave from Yozgat (3) in Turkey.
Fig. 5 in The natural interaction between Myotis nigricans (Schinz, 1821) and its trematodes: A histopathological analysis
Fig. 5. The parasitized intestine of Myotis nigricans. (A) and (B) Trematodes between the intestinal villi do not invade the intestinal glands. (C) Trematode attached to the villus adjacent to its ventral surface, both by the oral sucker and by the ventral sucker. (D) Oral sucker and (E) ventral sucker attached to the epithelium of the intestine, with the view of goblet cells. (F) Peyer patches with visible lymphoid alteration and intestinal glands. (G) Detail of lymphoid cells with nuclear fragmentation and hyperplasia. Abbreviations: (Ig), intestinal glands; (Os), Oral sucker; (Pp), Payer patches; (T), Trematodes; (Vi), Villi; (Vs), ventral sucker.
Fig. 4 in The natural interaction between Myotis nigricans (Schinz, 1821) and its trematodes: A histopathological analysis
Fig. 4. The liver of Myotis nigricans with a parasitized gallbladder. (A) Hepatic parenchyma with significant hepatocyte impairment and visible centrilobular veins and portal triad. (B) Hepatic lobule with the view of the centrilobular vein surrounded by sinusoids capillaries, bile duct, branches of the portal vein, and hepatic artery. (C) Portal triad: bile duct, branches of the portal vein, and hepatic artery. (D), (E) and (F) Hepatocytes with variation in cytoplasmic granular deposits, from clear vacuoles in basophilic cells to dense basophilic granules or chromophobic voluminous granules in cells of low basophilia. Abbreviations and symbols: (arrow), sinusoid capillaries; (arrowhead), granular deposits; (Bd), bile duct; (Cv), centrilobular vein; (Ha), Hepatic artery; (Pv), Portal vein; (Tp) Portal triad; (Va), vacuoles.
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International Brain Laboratory public data
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OpenNeuro
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