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Figure 1. A in Diceratocephala boschmai (Platyhelminthes: Temnocephalida) from crayfish farms in Thailand: investigation of the topographic surface and analysis of 18S ribosomal DNA sequences
Figure 1. A) C. destructor harboring adult D. boschmai and eggs of flatworm; B) dorsal view of an extending body; C) diagram of organ structures in dorsal view; D) diagram of reproductive complex; E, F) photomicrograph and diagram of penial stylet, respectively; G) unhatched and hatched eggs. ad, adhesive disc; at, atrium; cv, contractile vesicle; ds, dorsal side; es, ejaculatory sac; ey, eye; ev, excretory vesicle; fi, filament; in, intertentacular flange; ine, intestine; int, introvert; mo, mount; ov, ovary; pe, peduncle; pf, plane of fracture; ph, pharynx; pn, subepidermal pigment network; ps, penial stylet; rv, resorbens vesicle; s, stalk; se, seminal vesicle; sr, seminal receptacle; sp, sclerotized papillae; tc, tentacle; te, testis; tg, tentacular gland; ve, vasa efferentia; vg, vagina; vi, vitellaria; vs, ventral side.
Fig. 6 in Dinoflagellate Cysts Stratigraphy And Palynofacies Of Oligocene Sequences In The Northern Eastern Carpathians
Fig. 6 In a palynological slide under natural light and blue-light fluorescence, the representative palynofacies from the Lower Menilite and Bituminous Marls formations. Scale bar: 30 μm. a - abundant granular AOM with brown color in association with EPS (black arrow, tiny filaments forming an alveolar network), coccoid bodies (bacteria or algae, white arrow), gelified AOM (red arrow) and palynomorphs (blue arrow). The color and abundance of AOM suggest a dysoxic–anoxic environment (P174); b - idem previous image (blue-light fluorescence), AOM exhibits weak fluorescence; c – brown granular AOM (P178); d - idem previous image (blue-light fluorescence), AOM shows a patchy fluorescence.
Fig. 5 in Dinoflagellate Cysts Stratigraphy And Palynofacies Of Oligocene Sequences In The Northern Eastern Carpathians
Fig. 5 Relative abundances of particulate organic matter from the analyzed samples (percentage calculated to Total Sedimentary Organic Matter).
Fig. 1 in Dinoflagellate Cysts Stratigraphy And Palynofacies Of Oligocene Sequences In The Northern Eastern Carpathians
Fig. 1 Geological and tectonic sketch map of the Gura Humorului-Frasin area (after Ionesi, 1971, simplified), with the location of the geological cross-section studied.
Fig. 8 in Dinoflagellate Cysts Stratigraphy And Palynofacies Of Oligocene Sequences In The Northern Eastern Carpathians
Fig. 8 The representative palynofacies from the Bituminous Marls, Lower Dysodilic Shale and Kliwa Sandstone formations. Scale bar: 30 μm. a - abundant AOM (granular and gelified; Bituminous Marls Fm., sample P178) with dark brown color. Granular AOM (blue arrow), gelified AOM (red arrow); b - granular AOM with a light-brown color (black arrow), EPS (red arrow) mixed with continental organic particles such as translucent phytoclasts (yellow arrow), gelified AOM (blue arrow) and palynomorphs (green arrow) (Lower Dysodilic Shale Fm., sample P180); c - brown woody tissue large in size (blue arrow), in association with continental palynomorphs (green arrow) and other terrestrial organic particles (Kliwa Sandstone Fm., sample P185).
Fig. 7 in Dinoflagellate Cysts Stratigraphy And Palynofacies Of Oligocene Sequences In The Northern Eastern Carpathians
Fig. 7. Ternary kerogen plots (Tyson, 1995) for the Lower Menilite Formation up to Kliwa Sandstone Formation, with inferred depositional environments.
Fig. 4 in Dinoflagellate Cysts Stratigraphy And Palynofacies Of Oligocene Sequences In The Northern Eastern Carpathians
Fig. 4 Range chart of the dinoflagellate cysts used in this study. Correlation with previously published dinocyst zonations within Germany (Köthe & Piesker, 2007), the North Sea Basin (Schiøler, 2005), Austria (Soliman, 2012), Italy (Pross et al., 2010), Belgium (Van Simaeys et al., 2005), Northwest Europe (Powell, 1992) and Poland (Barski & Bojanowski, 2010) are shown. Dinocyst biozones and bioevents according to Powell & Brinkhuis (in Vandenberghe et al., 2012).
Fig. 3 in Dinoflagellate Cysts Stratigraphy And Palynofacies Of Oligocene Sequences In The Northern Eastern Carpathians
Fig. 3 Spores and pollen taxa from the studied section (scale bar 30 µm). a. Laevigatosporites gracilis (P180); b. Laevigatisporites nutidus (P180); c. Extrapunctatosporis sp. (P183); d. Pityosporites labdacus (P183); e. Ephedripites sp. (P183); f. Pityosporites alatus (P183); g. Pityosporites microalatus (P183); h. Pityosporites scopulipites (P185); i. Inaperturopollenites concedipites (P180); j. Inaperturopollenites hiatus (P180); k. Cupressacites bockwitzensis (P180); l. Podocarpidites libellus (P183); m. Monocolpopollenites tranquillus (P180); n. Caryapollenites simplex (P183); o. Arecipites sp. (P183); p. Faguspollenites cf. subtilis (P176); q. Tricolporopollenites microhenrici (P180); r. Cyrillaceaepollenites megaexactus (P176); s. Myricipites bituitus (P183); t. Ilexpollenites sp. (P183); u. Coryluspollenites sp. (P183).
Fig. 5. Parsimony splits network constructed from a per and ITS2 concatenated sequence data set. Heterozygous specimens are indicated with A and B in Ecological and geographical speciation in Lucilia bufonivora: The evolution of amphibian obligate parasitism
Fig. 5. Parsimony splits network constructed from a per and ITS2 concatenated sequence data set. Heterozygous specimens are indicated with A and B. 'bufonivora_EUROPE_A' represents a consistent haplotype present in all 12 samples from Europe (Table 1), of which just two were heterozygous ('bufonivora_frog' and 'bufonivora_NLWi'). 'bufonivora_CAN' and 'elongata_CAN' are represented by two samples each, none of which were heterozygous. Scale bar represents expected changes per site.
Text-fig. 4. Electrophoresis after amplification: Electrophoretical analysis of mitochondrial DNA. mtDNA sequences were amplified by primers F15.412 and R16.169 (450 bp), R16.269 (550 bp), R16.519 (800 bp). Lane 1 are primers F15.412 + R16.169, lane 2 primers F15.412 + R16.269, lane 3 primers F15.412 + R16.519, NC – negative control – water, L – 100 bp DNA ladder (band size from 100 bp to 1500 bp). in Genetic Analysis Of Possibly The Oldest Greyhound Remains Within The Territory Of The Czech Republic As Proof Of A Local Elite Presence At Chotěbuz-Podobora Hillfort In The 8 -9 Century Ad
Text-fig. 4. Electrophoresis after amplification: Electrophoretical analysis of mitochondrial DNA. mtDNA sequences were amplified by primers F15.412 and R16.169 (450 bp), R16.269 (550 bp), R16.519 (800 bp). Lane 1 are primers F15.412 + R16.169, lane 2 primers F15.412 + R16.269, lane 3 primers F15.412 + R16.519, NC – negative control – water, L – 100 bp DNA ladder (band size from 100 bp to 1500 bp).
Text-fig. 5. Multiple sequence alignment of mtDNA from ancient bone and recent greyhound, (Gundry et al. 2007) primer pair A – F15.719 and R16.114. in Genetic Analysis Of Possibly The Oldest Greyhound Remains Within The Territory Of The Czech Republic As Proof Of A Local Elite Presence At Chotěbuz-Podobora Hillfort In The 8 -9 Century Ad
Text-fig. 5. Multiple sequence alignment of mtDNA from ancient bone and recent greyhound, (Gundry et al. 2007) primer pair A – F15.719 and R16.114.
Text-fig. 3. Simplified geological map of the Krkonoše Piedmont Basin (based on Blecha et al. 1997) with the palaeogeographic outline of the Rudník lake deposits. The site of Vrchlabí – road cut represents the complete Rudník "Horizon" sequence with record of various developmental stages of the lake. Numbers of sites are simplified. in Permian Fauna Of The Krkonoše Piedmont Basin (Bohemian Massif, Central Europe)
Text-fig. 3. Simplified geological map of the Krkonoše Piedmont Basin (based on Blecha et al. 1997) with the palaeogeographic outline of the Rudník lake deposits. The site of Vrchlabí – road cut represents the complete Rudník "Horizon" sequence with record of various developmental stages of the lake. Numbers of sites are simplified.
Figure 6. Four most parsimonious phylogenetic trees for 12S in New insight into the systematic position of the endemic Madagascan genus Amberiana (Hemiptera: Heteroptera: Dinidoridae) using 12S rDNA sequences
Figure 6. Four most parsimonious phylogenetic trees for 12S rDNA sequences of 28 species used in this study generated using the maximum parsimony method. Bootstrap support is indicated at nodes; the frame shows the clade consisting of Amberiana montana and Sehirus luctuosus.
Figure 5. Phylogenetic tree for 12S in New insight into the systematic position of the endemic Madagascan genus Amberiana (Hemiptera: Heteroptera: Dinidoridae) using 12S rDNA sequences
Figure 5. Phylogenetic tree for 12S rDNA sequences of 28 species used in this study generated by using the maximum likelihood method. Bootstrap support is indicated at nodes; the frame shows the clade consisting of Amberiana montana and Sehirus luctuosus.
Figure 2 in Investigation of genetic variation among Turkish populations of Andricus lignicola using mitochondrial cytochrome b gene sequence data
Figure 2. Bayesian analysis tree. Posterior probability values are given on the branches. Outgroup haplotypes: Ac (Andricus caliciformis) and Ak (Andricus kollari).
Figure 9 in New insight into the systematic position of the endemic Madagascan genus Amberiana (Hemiptera: Heteroptera: Dinidoridae) using 12S rDNA sequences
Figure 9. Phylogenetic tree obtained from the Bayesian inference analysis of the 12S rDNA sequences of 28 species used in this study. The Bayesian posterior probabilities are indicated at each node; the frame shows the clade consisting of Amberiana montana and Sehirus luctuosus.
Figures 1−3. 1 in New insight into the systematic position of the endemic Madagascan genus Amberiana (Hemiptera: Heteroptera: Dinidoridae) using 12S rDNA sequences
Figures 1−3. 1: Amberiana montana. 2: A. major (from Lis, 1990). 3: Location of known records for the 2 Amberiana species.
Figure 4. Phylogenetic tree for 12S in New insight into the systematic position of the endemic Madagascan genus Amberiana (Hemiptera: Heteroptera: Dinidoridae) using 12S rDNA sequences
Figure 4. Phylogenetic tree for 12S rDNA sequences of 28 species used in this study generated by using the minimum evolution method. Bootstrap support is indicated at nodes; the frame shows the clade consisting of Amberiana montana and Sehirus luctuosus.
Figure 7 in New insight into the systematic position of the endemic Madagascan genus Amberiana (Hemiptera: Heteroptera: Dinidoridae) using 12S rDNA sequences
Figure 7. Strict consensus tree of 4 most parsimonious trees for 12S rDNA sequences of 28 species used in this study generated by using the maximum parsimony method. The frame shows the clade consisting of Amberiana montana and Sehirus luctuosus.
Figure. Interferon alpha-A based phylogenetic tree (neighbor joining method) constructed by MEGA 6.1 for Punjab urial in comparison with other mammalian species sequences available from GenBank (NCBI). in Characterization of interferon alpha of major histocompatibility complex class I in Punjab urial (Ovis vignei punjabiensis)
Figure. Interferon alpha-A based phylogenetic tree (neighbor joining method) constructed by MEGA 6.1 for Punjab urial in comparison with other mammalian species sequences available from GenBank (NCBI).
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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.