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Fig. 5 in Phylogenetic placement of a new paleoendemic pill scarab from the Udzungwa Mountains, Tanzania, triggers biogeographic interpretations (Coleoptera: Hybosoridae, Ceratocanthinae)
Fig. 5 – Maximum likelihood tree of Ceratocanthinae pill scarabs (Coleoptera: Hybosoridae), as reconstructed by RAxML from the three-fragment concatenated matrix.Balleriodes sphaera gen. et sp. nov. is inside the monophyletic Synarmostes group. Branches with ML bootstrap support percentage ≥90 are marked by black circles; those with bootstrap <90 and ≥75 are marked by open rhombi. Colours of Ceratocanthinae taxa and branches indicate their biogeographical region. Habitus images are to scale; small black arrows indicate imaged specimens.
Fig. 1 – A in Phylogenetic placement of a new paleoendemic pill scarab from the Udzungwa Mountains, Tanzania, triggers biogeographic interpretations (Coleoptera: Hybosoridae, Ceratocanthinae)
Fig. 1 – A, Distribution of Balleriodes sphaera gen. et sp. nov. and potentially related and/or similar pill scarabs in Africa and Madagascar. B-F: Balleriodes sphaera gen. et sp. nov., holotype, habitus (B: left lateral, C: dorsal, D: ventral; E: anterior, F: posterior).
Fig. 4 in Disruption of the leafminer Phyllocnistis citrella (Lepidoptera: Gracillariidae) in citrus: effect of blend and placement height, longevity of disruption and emission profile of a new dispenser
Fig. 4. Pheromone release profiles for DCEPT CLM™ (closed circles) and SPLAT CLM™ (open circles). DCEPT CLM data (top graph) are mean (± SD) percentage of initial amount of (Z,Z,E)-7,11,13-hexadecatrienal remaining in the dispensers (n = 10). SPLAT CLM points are equivalent data previously published (Stelinski et al. 2010). The amount of pheromone released (bottom graph) was calculated as the mean difference in pheromone remaining from the preceding period.
Fig. 1 in Disruption of the leafminer Phyllocnistis citrella (Lepidoptera: Gracillariidae) in citrus: effect of blend and placement height, longevity of disruption and emission profile of a new dispenser
Fig. 1. Mean ± SEM number of male Phyllocnistis citrella captured in pheromone-baited traps in untreated control plots (filled circles, n = 9) and in pheromonetreated plots (open circles, n = 14) of grapefruit at Emerald grove, St. Lucie County, Florida, USA. Triangles are mean ± SEM (n = 14) percentage trap catch disruption (right y axis). Insert: DCEPT CLM dispenser. Rubber disk is 1.2 cm in diameter; white plastic hanger is 3.5 × 4.3 cm.
Fig. 2 in Placement density and longevity of pheromone traps for monitoring of the citrus leafminer (Lepidoptera: Gracillariidae)
Fig. 2. Relationship between the proportional number of Phyllocnistis citrella captures per trap and day of aged lures with respect to unaged lures, and the number of weeks that each lure was exposed to field environmental conditions during spring 2013, for the 2 commercial brands of lures a) ISCA and b) AlphaScents.
Fig. 1 in Placement density and longevity of pheromone traps for monitoring of the citrus leafminer (Lepidoptera: Gracillariidae)
Fig. 1. Mean number of Phyllocnistis citrella adult male captures per trap and day (± standard error) from Apr 2012 to Dec 2013, at the 3 trap densities tested: high: approximately 1 trap per 0.40 ha (1 acre), medium: approximately 1 trap per 1.21 ha (3 acres), and low: approximately 1 trap per 2.02 ha (5 acres).
Fig. 4 in Placement density and longevity of pheromone traps for monitoring of the citrus leafminer (Lepidoptera: Gracillariidae)
Fig. 4. Relationship between the proportional number of Phyllocnistis citrella captures per trap and day of aged lures with respect to unaged lures, and the number of weeks that each lure was exposed to field environmental conditions, with data combined for ISCA and AlphaScents during spring and ISCA during summer/fall 2013.
Fig. 3 in Placement density and longevity of pheromone traps for monitoring of the citrus leafminer (Lepidoptera: Gracillariidae)
Fig. 3. Relationship between the proportional number of Phyllocnistis citrella captures per trap and day of aged lures with respect to unaged lures, and the number of weeks that each lure was exposed to field environmental conditions during summer/fall 2013, for the 2 commercial brands of lures a) ISCA and b) AlphaScents.
species according to Broadley (1994). These may well be the result of continuing confusion over the placement of Keta. Given the localities known from Lunda Norte, it seems likely that the species occurs in other northern regions of Angola. MAP 363. Distribution of Scaphiophis albopunctatus in Angola. in Diversity and Distribution of the Amphibians and Terrestrial Reptiles of Angola Atlas of Historical and Bibliographic Records (1840-2017)
species according to Broadley (1994). These may well be the result of continuing confusion over the placement of Keta. Given the localities known from Lunda Norte, it seems likely that the species occurs in other northern regions of Angola. MAP 363. Distribution of Scaphiophis albopunctatus in Angola.
BRAIN Journal-Brain signal analysis using EEG and Entropy to study the effect of physical and mental tasks on cognitive performance-Figure 1. The 10-20 international system electrode placement showing the EEG electrode placement
<p>For the EEG analysis, the average power in the theta band (4 – 8 Hz), and alpha band (8 – 12<br> Hz) were computed at the frontal and parietal electrodes Fz and Pz respectively. Next, the ratio of<br> these two powers was determined, and named the ‘cognitive ratio’ as several researchers found that<br> the fronto-parietal network play important roles in cognitive activities.</p>
Figure 3. Electrode placement diagram-Classification of Human Emotion from Deap EEG Signal Using Hybrid Improved Neural Networks with Cuckoo Search
<p>Reference electrode placed AFz placed in between AF1 and AF2 electrode and ground<br> electrode Oz is placed between O1 and O2 electrodes. The impedance of the electrode range is<br> 5KΩ. The sampling rate was fixed range between 256 samples per second for all the channels.<br> Figure 3 shown in below which is represent the electrode placement diagram. The recorded EEG<br> signal is used to recognize the different level of emotions.</p>
Morphological matrix in NEXUS format - from Klopfstein & Spasejovic, Illustrating phylogenetic placement of fossils using RoguePlots: An example from ichneumonid parasitoid wasps (Hymenoptera, Ichneumonidae) and an extensive morphological matrix
<p>Morphological matrix in NEXUS format - from Klopfstein & Spasejovic, Illustrating phylogenetic placement of fossils using RoguePlots: An example from ichneumonid parasitoid wasps (Hymenoptera, Ichneumonidae) and an extensive morphological Matrix. Preprint published in bioRxiv (doi: https://doi.org/10.1101/425090 ).</p>
Fig. 5 in A redescription of Antispastis clarkei Pastrana (Lepidoptera, Glyphipterigidae) immature stages, with notes on the life history and phylogenetic placement of the genus
Fig. 5. Scanning electron micrographs of Antispastis clarkei fourth (last) larval instar: A–C, head, under lateral, dorsal and ventral views, respectively; D, stemmata, lateral; E, labrum, dorsal; F, antenna, dorsal (asterisk indicates expanded antocoria); G,labium,lateral (asterisk indicates the spinneret); H, prothoracic dorsal shield,dorsal;I, prothoracic upper-coxal plate, lateral; J, spiracle of second abdominal segment, latero-ventral; K, mesothoracic leg, mesal; L, pretarsus in detail, latero-posterior; M, pseudopodium of third abdominal segment, latero-ventral; N, O, last abdominal segments, lateral and posterior, respectively. Scale bars = 200, 150, 200, 30, 50, 40, 10, 200, 80, 40, 100, 20, 80, 150, 150 µm, respectively.
Fig. 4 in A redescription of Antispastis clarkei Pastrana (Lepidoptera, Glyphipterigidae) immature stages, with notes on the life history and phylogenetic placement of the genus
Fig. 4. Scanning electron micrographs of Antispastis clarkei egg (A–C) and first larval instar (D–N): A, general view of egg, latero-dorsal; B, micropylar region on anterior pole, lateral; C, aeropyle, dorsal; D, general view of first instar, lateral; E, F, head, dorsal and anterior, respectively; G, detail of mandible, antenna and maxilla, antero-lateral (asterisk indicates corrugated nature of the mandibular base in association with the antennal antocoria); H, labium, antero-lateral (arrow indicates spinneret); I, stemmata, lateral; J, mesothoracic leg, postero-dorsal; K, tarsal claw in detail, mesal (asterisk indicates associated spatulate seta); L, M, prothoracic and third abdominal spiracles lateral; N, last abdominal segments postero-dorsal. Scale bars = 150, 15, 5, 100, 50, 30, 15, 10, 10, 10, 5, 10, 5, 20 µm, respectively.
Fig. 8 in A redescription of Antispastis clarkei Pastrana (Lepidoptera, Glyphipterigidae) immature stages, with notes on the life history and phylogenetic placement of the genus
Fig. 8. Transverse histological sections of Antispastis clarkei mine on Solanum johannae leaves. A, initial, filiform portion (location indicated by unbroken line in Fig. 7E); B, detail of initial portion (enlarged area marked with a rectangle in A) with cut anticlinal cell wall of palisade parenchyma cells; C, final, blotch portion (location indicated by dashed line in Fig. 7E); D, E, details of blotch portion (enlarged areas marked with rectangles in C) with intact cells in adaxial epidermis and spongy parenchyma. Asterisks indicate intact cells of palisade parenchyma. Open arrows indicate cellular fragments left on palisade parenchyma after insect feeding. Ab, abaxial epidermis; Ad, adaxial epidermis; Lm, leaf mine; Pp, palisade parenchyma; Sp, spongy parenchyma. Scale bars = 50, 40, 100, 50, 50 µm, respectively.
Fig. 5 in Phylogenetic placement and microthrix pattern of Paranybelinia otobothrioides Dollfus, 1966 (Trypanorhyncha) from krill Nyctiphanes simplex Hansen, 1911
Fig. 5. Maximum Likelihood tree under the General Time Reversible model of selected trypanorhynchs including Paranybelinia otobothrioides. Major families, superfamilies, and orders are indicated. Numbers on the branches show nodal support.
Fig. 2 in Phylogenetic placement and microthrix pattern of Paranybelinia otobothrioides Dollfus, 1966 (Trypanorhyncha) from krill Nyctiphanes simplex Hansen, 1911
Fig. 2. Surface ultrastructure of the scolex and tentacular armature of Pa. otobothrioides. (A) Dorso-ventral view of the scolex dissected from the blastocyst showing the distal bothrial surface without complete median separation. (B) Pedunculus scolecis showing 2 bothria with free lateral and posterior margins. (C) Apical view of the scolex bothrial surfaces. (D) Capilliform filitriches. (E) External tentacle surface, metabasal armature with solid uncinate hooks. (F) Distal bothrial surface showing (G) hamulate spinitriches and (H) lineate spinitriches. Scale bars: (A,C) 100 μm; (D–H) 50 μm.
Figure. Location of the study area in the Czech Republic near Nové Losiny village (marked by star), delimitation of the studied meadows and placement of pan-traps transects within them. in Comparison of two methods for sampling orthopterans in grassland: differences in species representation and sex ratios
Figure. Location of the study area in the Czech Republic near Nové Losiny village (marked by star), delimitation of the studied meadows and placement of pan-traps transects within them.
FIGURE 5 in Population level genetic divergence and phylogenetic placement of Mexican shortfin mollies (Mollienesia: Poecilia: Poeciliidae)
FIGURE 5 | Cytochrome b (1,140 bp) mitochondrial gene Bayesian phylogeny, parsimony haplotype network, and sampling distribution of Atlantic taxa Poecilia limantouri (Turqouise-North of the Trans Mexican Volcanic Belt, forest green-South of the Trans Mexican Belt), P. sulphuraria/P. thermalis (yellow-South of the Isthmus of Tehuantepec), and P. mexicana (baby blue-North of the Trans Mexican Volcanic Belt, light green-South of the Trans Mexican Volcanic Belt, purple-North of the Isthmus of Tehuantepec, orange-South of the Isthmus of Tehuantepec) across geographic barriers along the Atlantic coast of Mexico. The phylogeny has Bayesian posterior values followed by bootstrap values with asterisks representing support of 95% or above. The Parsimony network values correspond to the haplotype values and are colored according by geographic locations separated by barriers; circle sizes correspond to the number of individuals with that haplotype (larger circles reflect more individuals), and black circles indicate unsampled haplotypes. The capital letters at the end of each sample represents the state of origin in Mexico, from North to South: NVL = Nuevo Leon, T = Tamaulipas, V = Veracruz, H = Hidalgo, Tb = Tabasco, C = Chiapas.
FIGURE 3 in Population level genetic divergence and phylogenetic placement of Mexican shortfin mollies (Mollienesia: Poecilia: Poeciliidae)
FIGURE 3 | Cytochrome b (1,140 bp) mitochondrial gene Bayesian phylogeny, parsimony haplotype network, and sampling distribution of Poecilia sphenops (aqua-Atlantic North of the Trans Mexican Volcanic Belt, pink- Balsas River Drainage, purple- Atlantic North of the Isthmus of Tehuantepec, red- Pacific North of the Isthmus of Tehuantepec, orange- Atlantic South of the Isthmus of Tehuantepec, and yellow- Pacific South of the Trans Mexican Volcanic Belt) across geographic barriers along the coasts of Mexico. The phylogeny has Bayesian posterior values followed by bootstrap values with asterisks representing support of 95% or above. The Parsimony network values correspond to the haplotype values and are colored according by geographic locations separated by barriers; circle sizes correspond to the number of individuals with that haplotype (larger circles reflect more individuals), and black circles indicate unsampled haplotypes. The capital letters at the end of each sample represents the state of origin in Mexico, from North to South: V = Veracruz, H = Hidalgo, M = Michoacan, G = Guerrero, O = Oaxaca, C = Chiapas.
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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.