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Fig. 4 in Hepatozoon apri n. sp. (Adeleorina: Hepatozoidae) from the Japanese wild boar Sus scrofa leucomystax (Mammalia: Cetartiodactyla)

Fig. 4. Phylogenetic analysis of Hepatozoon apri n. sp. based on 18S rDNA sequences (522-bp). Adelina dimidiata (accession no. DQ096835) was chosen as the outgroup to root the phylogeny. Neighbor-joining (NJ) and maximum likelihood (ML) analysis showing the phylogenetic relationships among boar isolates and two Hepatozoon spp. (KF318170, KF318171) detected in Dermacentor ticks collected from wild boar in Thailand. Sequences included in the comparison were downloaded from the DDBJ/EMBL/GenBank databases. Filled circles indicate Hepatozoon species reported from Japan. Nodal support values based on 1000 bootstrap replicates (NJ/ML) are represented on the ML tree. Scale bar represents 0.01 nucleotide substitutions per site.

opencc-by-4.0Dec 2017View details →
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Fig. 3. a–d in Hepatozoon apri n. sp. (Adeleorina: Hepatozoidae) from the Japanese wild boar Sus scrofa leucomystax (Mammalia: Cetartiodactyla)

Fig. 3. a–d) Various developmental stages of Hepatozoon apri n. sp. detected in the muscles. a) A trophozoite (arrow) in the femoral muscles. The outer layer contains a fibroblast-like nucleus (arrowhead). b–c) Immature meronts found in the heart. d) Mature meront in the femoral muscles. H&E stain. Bar = 20 μm.

opencc-by-4.0Dec 2017View details →
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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).

opencc-by-4.0Mar 2014View details →
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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

opencc-by-4.0Mar 2014View details →
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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)

opencc-by-4.0Mar 2014View details →
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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

opencc-by-4.0Mar 2014View details →
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Figure 3 in Two small species of Cremohipparion (Equidae, Mammalia) from Samos, Greece

Figure 3: Comparison of Samos "Cremohipparion matthewi" species with selected later Miocene Holarctic and Ethiopian smaller horses. A. MC III maximum length (ML) versus distal articular width (DAW). B. MT III ML versus DAW. 1 = "Cremohipparion matthewi" (Samos; AMNH: 23054b—e, 22933,23054, Q5 no numbers, 22893; Bernor, personal observation); 2 = "Hipparion macedonicum" (Ravin de Pluie, Greece; RPL 38; Koufos, Table 9 — insert); 3 = sitifense (Sahabi, Libya; 27P25B, MC III; 1P25B, MT III; Bernor et al., 1987); 4 = gromovae (La Fontana, Spain; Tobien, personal observation); 5 = "S*. platyodus (China; Qiu et al., 1987:95);6 = Calippus (XMAS Quarry, Nebraska AMNH 98 (Bernor, personal observation); 7 = Pseudhipparion sp., XMAS Quarry AMNH 202 (Bernor, personal observation).

opencc-by-4.0Dec 1989View details →
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Figure 2 in Two small species of Cremohipparion (Equidae, Mammalia) from Samos, Greece

Figure 2: Cremohipparion nikosin. sp., BSP 1899 VII31 b. A. Skull fragment, left lateral view; B. Left maxillary cheek tooth series.

opencc-by-4.0Dec 1989View details →
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Fig. 2 in Unusual Age Structure Of The Winter Aggregation Of Nyctalus Noctula (Mammalia, Chiroptera) In Kyiv

Fig. 2. Age of common noctule bats in the examined sample: A — total sample, n = 113, the model of the logarithmic regression is indicated with the line; B — females, n = 31; C — males, n = 77.

opencc-by-4.0Nov 2014View details →
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Figure 2 in A karyotype comparison among 3 species of Allactaga (Mammalia: Dipodidae) from central Iran

Figure 2. Dendrogram of the 3 Allactaga species based on chromosomal characters, using cluster analysis.

opencc-by-4.0Jan 2015View details →
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Figure 5 in The taxonomic status and geographic distribution of the European hare (Lepus europaeus Pallas, 1778) in Turkey (Mammalia: Lagomorpha)

Figure 5. The group centroids obtained from discriminant functions: 1 = Thracian specimen, 2 = Southwest Anatolian population, 3 = Central and East-Central Anatolian population, 4 = Northeast Anatolian population, 5 = Southeast Anatolian population.

opencc-by-4.0Jan 2014View details →
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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).

opencc-by-4.0Feb 2015View details →
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Figure 1 in Reproduction, postnatal development, and social behavior of Ellobius lutescens Thomas 1897 (Mammalia: Rodentia) in captivity

Figure 1. Development of E. lutescens pups (A- newly born, B- 7 days, C- 14 days, D- 21 days, E- 28 days, F- 42 days, G- 56 days, H- 70 days, I- 84 days).

opencc-by-4.0May 2015View details →
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Figure 4 in Karyological and some morphological characteristics of the Egyptian mongoose, Herpestes ichneumon (Mammalia: Carnivora), along with current distribution range in Turkey

Figure 4. Skull morphology of H. ichneumon from Hatay: A) dorsal, B) ventral, C) lateral view of the skull; D) mandible (lingual), E) mandible (labial) view.

opencc-by-4.0May 2015View details →
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Figure 1 in Karyological and some morphological characteristics of the Egyptian mongoose, Herpestes ichneumon (Mammalia: Carnivora), along with current distribution range in Turkey

Figure 1. Distribution of Herpestes ichneumon in Turkey. ▲: Selçuk (Danford and Alston, 1877); ◇◆: Bahçe (Gülen, 1971); ★: current distribution recorded during this study. 1) Göksu Delta; 2) Tarsus, near the Mersin–Adana highway; 3) 1 km west of Tabaklar village; 4) 7 km northeast of Kefeli village; 5) 2 km west of Gölyaka village; 6) 3 km south of Adana; 7) 3 km southeast of Adana; 8) 1 km southeast of Menekşe village; 9) 3 km south of Deveciuşağı village (sample no. 2429); 10) near Sakarcalı village; 11) near Yeniköy village; 12) 1 km east of Cevdetiye village; 13) 2 km north of Ahrazlar village; 14) 1 km east of Hasanlı village (sample no. 19); 15) 1 km west of Kapısuyu village; and 16) 1 km south of Emirler village (Karaisalı).

opencc-by-4.0May 2015View details →
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Figure 2. A in Genetic differentiation of the Meriones tristrami (Mammalia: Rodentia) subpopulations in Turkey - inferring allozyme variations

Figure 2. A dendrogram summarizing the genetic relationships of M. tristrami subpopulations (NTSYSpc options: Coefficient: SM (SimQual), clustering method: UPGMA) (see Nei, 1978) (Mt1 = Gaziantep, Adana, Mt2 = Central Anatolia (Cihanbeyli/Konya, Sivrihisar/Eskişehir), Mt3 = Denizli, Mt4 = Şanlıurfa, Mt5 = Iğdır, Mt6 = Tosya/Kastamonu, Mt7 = Karadağ/Karaman, Mt8 = Turgutlu/Manisa).

opencc-by-4.0May 2016View details →
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Figure. Distribution of Neomys teres and Neomys anomalus species in Turkey (square = Neomys anomalus, triangle = Neomys teres). 1: Ulubey (Ordu), 2: Meryemana (Trabzon), 3: Kutul (Artvin), 4: Yalnızçam (Kars), 5: Bendimahi Canyon (Muradiye, Van), 6: Seyfe (Amasya), 7: Safranbolu (Karabük), 8: Topçam (Ordu), 9: Tamdere (Giresun), 10: Çamlık (Rize), 11: Ovid Mountain (Rize), 12: Lake Abant (Bolu), 13: Kayseri, 14: Erzurum, 15: Samsun, 16: Belgrad Forest (İstanbul), 17: Lake Abant (Bolu), 18: İrve creek (İstanbul), 19: Erçek Mountain (Van), 20: Paşaalandere (Tekirdağ), 21: Lake Terkos (İstanbul), 22: Yeşiloba (Adana), 23: Yenice, Çayır (Zonguldak), 24: Abant (Bolu), 25: Hanyatak village (Sakarya), 26: Longoz forest, Dupnisa cave, Demirköy (Kırklareli), 27: Lake Eber (Afyon), 28: Çırpılar (Çanakkale), 29: Uludağ (Bursa), 30: Balkusan (Karaman). in Taxonomic status of Neomys species (Mammalia: Soricomorpha) and their distribution in Turkey

Figure. Distribution of Neomys teres and Neomys anomalus species in Turkey (square = Neomys anomalus, triangle = Neomys teres). 1: Ulubey (Ordu), 2: Meryemana (Trabzon), 3: Kutul (Artvin), 4: Yalnızçam (Kars), 5: Bendimahi Canyon (Muradiye, Van), 6: Seyfe (Amasya), 7: Safranbolu (Karabük), 8: Topçam (Ordu), 9: Tamdere (Giresun), 10: Çamlık (Rize), 11: Ovid Mountain (Rize), 12: Lake Abant (Bolu), 13: Kayseri, 14: Erzurum, 15: Samsun, 16: Belgrad Forest (İstanbul), 17: Lake Abant (Bolu), 18: İrve creek (İstanbul), 19: Erçek Mountain (Van), 20: Paşaalandere (Tekirdağ), 21: Lake Terkos (İstanbul), 22: Yeşiloba (Adana), 23: Yenice, Çayır (Zonguldak), 24: Abant (Bolu), 25: Hanyatak village (Sakarya), 26: Longoz forest, Dupnisa cave, Demirköy (Kırklareli), 27: Lake Eber (Afyon), 28: Çırpılar (Çanakkale), 29: Uludağ (Bursa), 30: Balkusan (Karaman).

opencc-by-4.0Dec 2015View details →
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Figure 1 in Genetic differentiation of the Meriones tristrami (Mammalia: Rodentia) subpopulations in Turkey - inferring allozyme variations

Figure 1. Map of the locations of the M. tristrami specimens in Turkey (Gaziantep, Adana: Mt1; Central Anatolia (Cihanbeyli/Konya, Sivrihisar/Eskişehir): Mt2; Denizli: Mt3; Şanlıurfa: Mt4; Iğdır: Mt5; Tosya/Kastamonu: Mt6; Karadağ/Karaman: Mt7; Turgutlu/ Manisa: Mt8).

opencc-by-4.0May 2016View details →
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Figure 1 in Distribution and current status of Cricetulus migratorius (Mammalia: Cricetidae) in Bulgaria, with comments on its status in the Balkans

Figure 1. Degree of fragmentation of Cricetulus migratorius mandibles found in the diets of different avian predators; from left to right: A. heliaca, A. noctua, and T. alba.

opencc-by-4.0Jan 2016View details →
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Figure 2 in Distribution and current status of Cricetulus migratorius (Mammalia: Cricetidae) in Bulgaria, with comments on its status in the Balkans

Figure 2. Distribution of Cricetulus migratorius in Bulgaria (1- Straka, 1962; 2- Simeonov, 1964a, 1964b; this study; 3–6- Milchev, 2009; 7–8- Markov, 1964; 9- Markov, 1960; 10- Peshev et al., 1960; 11- Peshev et al., 1960; this study; 12- Georgiev, 2004; this study; 13–14- Georgiev, 2004; 15- this study).

opencc-by-4.0Jan 2016View details →

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Allen Brain Atlas

Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.

allen-brain-atlas
neuroscienceopenDocumentation, web resources, and API references are available online.
Last verified 2026-04-30Open record

Annotated Behaviour and Observability Dataset (ABODe)

ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.

abode-home-cage
behavioral-neuroscienceopenThe DataShare record exposes download links for annotations, documentation, license text, and the zipped per-snippet data directory.
Last verified 2026-04-30Open record

DANDI Archive for NWB datasets

DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.

dandi-nwb
electrophysiologyopenPublished Dandiset metadata and archive endpoints are available through the production DANDI API.
Last verified 2026-04-30Open record

International Brain Laboratory public data

The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.

ibl
behavioral-neuroscienceopenPublic sessions can be searched and loaded from the IBL public data server through ONE.
Last verified 2026-04-29Open record

OpenNeuro

OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.

openneuro
neuroscienceopenPublished datasets are available on demand over the internet.
Last verified 2026-04-29Open record