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Figure 3 in First record of Hemiclepsis marginata (O.F.Müller, 1773) (Hirudinida: Glossiphoniidae) from the Ferghana Valley, Uzbekistan
Figure 3. Natural habitats of Hemiclepsis marginata marginata: A, Balikkul spring; B, Kaynarbulak spring; D, Uchtepa spring; D, leeches on a stone (photo by Kh. Solijonov).
Figure 2 in First record of Hemiclepsis marginata (O.F.Müller, 1773) (Hirudinida: Glossiphoniidae) from the Ferghana Valley, Uzbekistan
Figure 2. Hemiclepsis marginata marginata: A, dorsal view; B, ventral view; C, eyes; D, posterior sucker; E, juvenile leech (photo by Kh. Solijonov), F, fixed sample (photo by A. Utevsky).
Figure 1 in First record of Hemiclepsis marginata (O.F.Müller, 1773) (Hirudinida: Glossiphoniidae) from the Ferghana Valley, Uzbekistan
Figure 1. Geographic distribution of Hemiclepsis marginata in the Ferghana Valley, Uzbekistan (based on a 10x10 km UTM grid).
Figure 4 in First record of Hemiclepsis marginata (O.F.Müller, 1773) (Hirudinida: Glossiphoniidae) from the Ferghana Valley, Uzbekistan
Figure 4. Phylogenetic relationships of Hemiclepsis marginata from the Ferghana Valley (Uzbekistan) inferred using the maximum likelihood optimality criterion. The analysis is based on a dataset consisting of the newly generated COI sequence of the Uzbekistan leech and previous GenBank sequences. Both ultrafast bootstrapping and SH-like approximate likelihood-ratio test (SHaLRT) values are provided for branches. The newly generated sequence is highlighted in bold, while the entire clade of H. marginata (H. marginata marginata) is highlighted in blue.
Fig. 1. Neighbor-joining tree generated under the Kimura 2 in Cotesia flavipes (Hymenoptera: Braconidae) as a biological control agent of sugarcane stem borers in Colombia's Cauca River Valley
Fig. 1. Neighbor-joining tree generated under the Kimura 2-parameter (K2P) nucleotide substitution model. The percentage of replicate trees in which the associated taxa clustered together in the bootstrap test (1,000 replicates) is shown next to the branches. Abbreviations for sugarcane mills in Colombia's Cauca River Valley are as follows: Manuelita (MN), Mayagüez (MY), Pichichí (PC), Providencia (PV), Riopaila (RP), Risaralda (RS), Sancarlos (SC). GeneBank C. flavipes accessions:Uganda - JQ396735.1, Brazil - DQ232320.1, India - DQ232336.1, Kenya - DQ232317, Thailand - DQ232340.1, USA - DQ232330.1, South Pakistan - JQ396714.1, Jamaica - DQ232321.1, Pakistan - DQ232335.1, Sri Lanka - DQ232327.1, Indonesia - DQ232337.1, Mauritius - DQ232319.1, Reunion - DQ232329.1, Papua New Guinea - DQ232316.1.
Fig. 2 in Cotesia flavipes (Hymenoptera: Braconidae) as a biological control agent of sugarcane stem borers in Colombia's Cauca River Valley
Fig. 2. Distribution of Cotesia flavipes in different sugarcane mills of Colombia's Cauca River Valley.
Fig. 3 in The most northeastern record of the Turkish endemic viper, Pelias barani (Böhme and Joger, 1984), from northeastern Anatolia: two viper species in a valley
Fig. 3. Several views of the habitat of Pelias barani from the Çağlayan Valley, Fındıklı, Turkey. Photos by Serkan Gül.
Fig. 2 in The most northeastern record of the Turkish endemic viper, Pelias barani (Böhme and Joger, 1984), from northeastern Anatolia: two viper species in a valley
Fig. 2. Dorsal (A) and ventral (B) views of typical head pattern, and each side of the head (C–D) in a female specimen of Pelias barani from the Çağlayan Valley, Fındıklı, Turkey. Photos by Serkan Gül.
Fig. 1 in The most northeastern record of the Turkish endemic viper, Pelias barani (Böhme and Joger, 1984), from northeastern Anatolia: two viper species in a valley
Fig. 1. Distribution map of Pelias barani and PelIas kaznakovI (created using ArcGIS 10.4). Red stars: Pelias barani from Mebert et al. (2015), blue star: new locality record for Pelias barani, yellow stars: known localities of PelIas kaznakovI. Inset map indicates previously known localities. Photo by Serkan Gül.
Fig. 4 in The most northeastern record of the Turkish endemic viper, Pelias barani (Böhme and Joger, 1984), from northeastern Anatolia: two viper species in a valley
Fig. 4. Proximity of nearest known Pelias barani and Pelias kaznakovI localities (map generated using Google Earth 7.3.2). Blue pin marker: Pelias barani from Mebert et al. (2015), red pin markers: PelIas kaznakovI from Mebert et al. (2015) and Gül et al. (2016b), yellow pin marker: new locality record of Pelias barani in this study. Distance between blue and yellow pin markers is ~19 km. Note that the short distance between Pelias barani and PelIas kaznakovI localities in the Çağlayan Valley indicates a potential contact zone.
Fig. 2 in First report of Gynmandrosoma aurantianum (Lepidoptera: Tortricidae) in mandarin (Citrus reticulata) in the inter-Andean valleys of Ecuador
Fig. 2. (A) Flattened antenna of male Gymnandrosoma aurantianum; (B) Hairpencil on male hind tibia; (C) Male genitalia - ae: aedeagus, cu: cucullus, co: cornuti, vi: vinculus, ju: juxta; (D) Female genitalia - ob: ostium bursae, db: ductus bursae, ds: ductus seminalis, b: bursae.
Fig. 1 in First report of Gynmandrosoma aurantianum (Lepidoptera: Tortricidae) in mandarin (Citrus reticulata) in the inter-Andean valleys of Ecuador
Fig. 1. (A) Gymnandrosoma aurantianum larvae infesting mandarin (Citrus reticulata) fruit; (B) Larva at fifh instar; (C) Pupae (ventral, lateral, and dorsal views); (D) Adult of Gymnandrosoma aurantianum.
Figure 3 in Temporal dynamics of the recruitment of glass eels in two valleys of French Polynesia (Tahiti and Moorea Islands)
Figure 3. – Annual monitoring of glass eels recruitment for each of the three species in: A: Moorea; B: Tahiti; C: Moorea and Tahiti, given in number of specimens per month.
Figure 4 in Temporal dynamics of the recruitment of glass eels in two valleys of French Polynesia (Tahiti and Moorea Islands)
Figure 4. – Composition of the recruitment of Anguilla species from Moorea and Tahiti Islands given in percent; * test chiº, p-value <0.001.
Figure 5 in Temporal dynamics of the recruitment of glass eels in two valleys of French Polynesia (Tahiti and Moorea Islands)
Figure 5. – Mean length (in mm) of the glass eel specimens at recruitment, for the three species in Moorea and Tahiti islands; * test chiº, p-value <0.001.
Figure 2 in Temporal dynamics of the recruitment of glass eels in two valleys of French Polynesia (Tahiti and Moorea Islands)
Figure 2. – Annual monitoring of glass eels recruitment in the Opunohu River on the Moorea Island and in the Vaituoru River on the Tahiti Island per year, given in number of specimens caught per day.
Рис. 17–23. Carabus (Alipaster) semenoviellus Breuning, 1934, самцы (17–20 – общий виÃ, 21–23 – меÃиаΛьная ÃоΛя эÃеагуса, виà сбоку). 17, 21 – C. semenoviellus semenoviellus, экземпΛяр с гор ТагымбеΛь; 18–20, 22–23 – C. semenoviellus tokkuztaraensis subsp. n.: 18, 22 – гоΛотип, 19, 23 – паратип из ÃоΛины реки Эрботу, 20 – паратип из ÃоΛины реки Актуюк. Figs 17–23. Carabus (Alipaster) semenoviellus Breuning, 1934, males (17–20 – general view, 21–23 – median lobe of the aedeagus, lateral view). 17, 21 – C. semenoviellus semenoviellus from the locality in Tagymbel Mountains; 18–20, 22–23 – C. semenoviellus tokkuztaraensis subsp. n.: 18, 22 – holotype; 19, 23 – paratype from the locality in the Erbotu Valley; 20 – paratype from the locality in the Aktuyuk Valley. in New data on the taxonomy of the genus Carabus Linnaeus, 1758 (Coleoptera: Carabidae) from the Ili River basin (China)
Рис. 17–23. Carabus (Alipaster) semenoviellus Breuning, 1934, самцы (17–20 – общий виÃ, 21–23 – меÃиаΛьная ÃоΛя эÃеагуса, виà сбоку). 17, 21 – C. semenoviellus semenoviellus, экземпΛяр с гор ТагымбеΛь; 18–20, 22–23 – C. semenoviellus tokkuztaraensis subsp. n.: 18, 22 – гоΛотип, 19, 23 – паратип из ÃоΛины реки Эрботу, 20 – паратип из ÃоΛины реки Актуюк. Figs 17–23. Carabus (Alipaster) semenoviellus Breuning, 1934, males (17–20 – general view, 21–23 – median lobe of the aedeagus, lateral view). 17, 21 – C. semenoviellus semenoviellus from the locality in Tagymbel Mountains; 18–20, 22–23 – C. semenoviellus tokkuztaraensis subsp. n.: 18, 22 – holotype; 19, 23 – paratype from the locality in the Erbotu Valley; 20 – paratype from the locality in the Aktuyuk Valley.
Fig. 6 in Jurassic rhynchonellide brachiopods from the Jordan Valley
Fig. 6. Serial sections of rhynchonellide brachiopod Pycnoria magna Cooper, 1989. AMNH FI−72403. Bed 25, Hamam Formation, Arda, Jordan. Numbers describe sectional distance from apex. Abbreviations: c, crus; cb, crural base; dms, dorsal median septum; dp, dental plate; isr, inner socket ridge; osr, outer socket ridge; pf, pedicle foramen; s, socket; t, tooth.
Fig. 5 in Jurassic rhynchonellide brachiopods from the Jordan Valley
Fig. 5. Serial sections of rhynchonellide brachiopod Daghanirhynchia susanae sp. nov. AMNH FI−72410. Bed 21b, Hamam Formation, Arda, Jordan. Numbers describe sectional distance from apex. Abbreviations: c, crus; cb, crural base; dms, dorsal median septum; dp, dental plate; isr, inner socket ridge; osr, outer socket ridge; s, socket; sp, septalial plate; ssm, secondary shell material; t, tooth; vms, ventral median septum.
Fig. 4 in Jurassic rhynchonellide brachiopods from the Jordan Valley
Fig. 4. Serial sections of the rhynchonellide brachiopod Cymatorhynchia quadriplicata (Zieten, 1830). AMNH FI−72369. Bed 21a, Hamam Formation, Arda, Jordan. Numbers describe sectional distance from apex. Abbreviations: c, crus; cb, crural base; dms, dorsal median septum; dp, dental plate; isr, inner socket ridge; osr, outer socket ridge; s, socket; sp, septalial plate; ssm, secondary shell material; t, tooth.
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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.
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.
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.
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.
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.