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39 results for “endogeic”
Fig. 7 in An unusually elongate endogeic centipede from Sardinia (Chilopoda: Geophilidae)
Fig. 7. Variation in the elongation of legs and the number of legs in a sample of species of Geophilidae, including Endogeophilus ichnusae gen. et sp. nov. The length/width ratio of a leg tarsus was measured at about 20% of the longitudinal series of legs. Full names of species in 'Material and methods'.
Fig. 2 in An unusually elongate endogeic centipede from Sardinia (Chilopoda: Geophilidae)
Fig. 2. Endogeophilus ichnusae gen. et sp. nov., holotype, ♀, forcipular segment, left half. A. Dorsal view. B. Ventral view. Scale bar = 100 µm.
Fig. 1 in An unusually elongate endogeic centipede from Sardinia (Chilopoda: Geophilidae)
Fig. 1. Endogeophilus ichnusae gen. et sp. nov. A–F. Holotype, ♀. A. Anterior part of the body, dorsal view, setae omitted. B. Head, without antennae, and forcipular segment, dorsal view. C. Leg-bearing segment 21, dorsal view. D. Leg-bearing segment 21, ventral view. E. Head, without antennae, ventral view. F. Ultimate leg-bearing segment and postpedal segments, ventral view, setae omitted. G. Paratype B, ³, ultimate leg-bearing segment and postpedal segments, ventral view, setae omitted. Line drawings based on photos taken at the microscope. Scale bars = 200 µm.
Fig. 6 in An unusually elongate endogeic centipede from Sardinia (Chilopoda: Geophilidae)
Fig. 6. Variation in the elongation of a single leg-bearing segment in a sample of species of Geophilidae, including Endogeophilus ichnusae gen. et sp. nov. The length/width ratio was measured on a metasternite at about 20% of the longitudinal series of leg-bearing segments, and the area of the metasternite (length × width, both in µm, log-transformed) has been taken as a proxy for body size. Full names of species in 'Material and methods'.
Fig. 8 in An unusually elongate endogeic centipede from Sardinia (Chilopoda: Geophilidae)
Fig. 8. Variation in the length of setae in a sample of species of Geophilidae, including Endogeophilus ichnusae gen. et sp. nov. The longest seta on the cephalic plate was measured, and the maximum width of the cephalic plate has been taken as a proxy for body size. Full names of species in 'Material and methods'.
Figures 37–40 in Morphological alteration in response to endogeic habitat and ant association in two new planthopper species from New Caledonia (Hemiptera: Auchenorrhyncha: Fulgoromorpha: Delphacidae)
Figures 37–40. Notuchus ninguae sp. nov., male genitalia (holotype). (37) Anal segment, aedeagus, paramere in situ, left lateral aspect. (38–40) Aedeagus, right lateral, dorsal, and left lateral aspects, respectively. Scale bar: 0.1 mm.
Figures 21–23 in Morphological alteration in response to endogeic habitat and ant association in two new planthopper species from New Caledonia (Hemiptera: Auchenorrhyncha: Fulgoromorpha: Delphacidae)
Figures 21–23. Notuchus kaori sp. nov., male genitalia (holotype). (21) Anal segment, aedeagus, paramere in situ, left lateral aspect. (22, 23) Aedeagus, right lateral and dorsal aspects, respectively. Scale bar: 0.1 mm.
Figures 30–36 in Morphological alteration in response to endogeic habitat and ant association in two new planthopper species from New Caledonia (Hemiptera: Auchenorrhyncha: Fulgoromorpha: Delphacidae)
Figures 30–36. Notuchus ninguae sp. nov., male genitalia (holotype). (30, 31) Genital capsule, left lateral and ventrocaudal aspects, respectively. (32–34) Genital segment, left lateral, caudal, and ventral aspects, respectively. (35) Anal segment, dorsal aspect. (36) Parameres, ventrocaudal aspect. Scale bars: 0.1 mm.
Figures 24–29 in Morphological alteration in response to endogeic habitat and ant association in two new planthopper species from New Caledonia (Hemiptera: Auchenorrhyncha: Fulgoromorpha: Delphacidae)
Figures 24–29. Notuchus kaori sp. nov., nymph (5th instar). (24) Habitus, dorsal aspect. (25) Head and prothorax, dorsal aspect. (26) Head, anterior aspect. (27) Frons, anterior aspect. (28) Head and thorax, anterolateral aspect. (29) Distal margin of pedicel. Scale bars in mm.
Figures 14–20 in Morphological alteration in response to endogeic habitat and ant association in two new planthopper species from New Caledonia (Hemiptera: Auchenorrhyncha: Fulgoromorpha: Delphacidae)
Figures 14–20. Notuchus kaori sp. nov., male genitalia (holotype). (14, 15) Genital capsule, left lateral and ventrocaudal aspects, respectively. (16–18) Genital segment, left lateral, caudal, and ventral aspects, respectively. (19) Anal segment, dorsal aspect. (20) Parameres, ventrocaudal aspect. Scale bars: 0.1 mm.
Figures 4–13 in Morphological alteration in response to endogeic habitat and ant association in two new planthopper species from New Caledonia (Hemiptera: Auchenorrhyncha: Fulgoromorpha: Delphacidae)
Figures 4–13. Notuchus kaori sp. nov., adult male (paratype). (4) Habitus, dorsal aspect. (5) Detail: right tegmen, dorsal aspect. (6) Habitus, left lateral aspect. (7) Head, anterolateral aspect. (8) Left antenna. (9) Same, pedicel with sensory plaques and macrosetae. (10) Same as in Figure 9, detail. (11) Post-tibial spur. (12) Same as in Figure 11, detail. (13) Pretarsus (arolium and claws), ventral aspect. Scale bars in mm.
Figures 2, 3 in Morphological alteration in response to endogeic habitat and ant association in two new planthopper species from New Caledonia (Hemiptera: Auchenorrhyncha: Fulgoromorpha: Delphacidae)
Figures 2, 3. Notuchus kaori sp. nov., adult male. (2) Habitus with colour pattern, dorsal aspect, paratype male. (3) Colour pattern of abdomen, ventrolateral aspect (genital capsule removed), holotype male. Scale bar: 0.2 mm.
Figures 41, 42 in Morphological alteration in response to endogeic habitat and ant association in two new planthopper species from New Caledonia (Hemiptera: Auchenorrhyncha: Fulgoromorpha: Delphacidae)
Figures 41, 42. Paratrechina spec. (Formicidae), worker. (41) Habitus, lateral aspect. (42) Head, frontal aspect.
Figures 43, 44 in Morphological alteration in response to endogeic habitat and ant association in two new planthopper species from New Caledonia (Hemiptera: Auchenorrhyncha: Fulgoromorpha: Delphacidae)
Figures 43, 44. (43) Hypochthonella caeca China and Fennah (Hypochthonellidae), endogeic species (from Hoch 1994, used with permission). (44) Notuchus larvalis Fennah (Delphacidae), obligately cavernicolous (troglobitic) species (from Hoch 1994, used with permission). Scale bars: 0.5 mm.
FIGURES 25 in Baezia vulcania sp. n., an endogeous weevil from La Palma I. (Canary Is.) (Coleoptera: Curculionidae: Molytinae)
FIGURES 25. Baezia vulcania sp. n. 2: Penis, dorsal and side view. 3: Tegmen, dorsal view. 4. Ovipositor, dorsal view. 5. Spiculum ventrale, ventral view. Scale: 23: 100 m; 45: 47 m.
ENDOG_NGS data related to article "Biallelic variants in ENDOG associated with mitochondrial myopathy and multiple mtDNA deletions" submitted to Cells
<p>vcf file of the targeted NGS; csv of the top 50 rare variants from WES prioritized by eVAI software; csv of WES rare variants prioritized by eVAI software using patient's phenotype information.</p>
Bioturbation by endogeic earthworms facilitates entomopathogenic nematode movement toward herbivore-damaged maize roots
<p>Entomopathogenic nematodes (EPNs) have been extensively studied as potential biological control agents against root-feeding crop pests. Maize roots under rootworm attack have been shown to release volatile organic compounds, such as (E)-β-caryophyllene (Eβc) that guide EPNs toward the damaging larvae. As yet, it is unknown how belowground ecosystems engineers, such as earthworms, affect the biological control capacity of EPNs by altering the root Eβc-mediated tritrophic interactions. We here asked whether and how, the presence of endogeic earthworms affects the ability of EPNs to find root-feeding larvae of the beetle Diabrotica balteata. First, we performed a field mesocosm experiment with two diverse cropping systems, and revealed that the presence of earthworms increased the EPN infection potential of larvae near maize roots. Subsequently, using climate-controlled, olfactometer-based bioassays, we confirmed that EPNs response to Eβc alone (released from dispensers) was two-fold higher in earthworm-worked soil than in earthworm-free soil. Together our results indicate that endogeic earthworms, through burrowing and casting activities, not only change soil properties in a way that improves soil fertility but may also enhance the biocontrol potential of EPNs against root feeding pests. For an ecologically-sound pest reduction in crop fields, we advocate agricultural practices that favour earthworm community structure and diversity.</p>
Figure 3 in Shedding light on species boundaries in small endogeic animals through an integrative approach: species delimitation in the centipede Clinopodes carinthiacus (Chilopoda: Geophilidae) in the south-eastern Alps
Figure 3. Subdivision of specimens into candidate species according to a model-based cluster analysis through normal mixture models on ten morphological characters (Table 2). The ventral view of the forcipular segment is illustrated for representative specimens of the candidate species. Denticles are indicated by arrowheads. The lower panel shows Bayesian information criterion (BIC) values of different models (coded as in the paper by Scrucca et al., 2016) in relation to the hypothetical number of candidate species.
Figure 2 in Shedding light on species boundaries in small endogeic animals through an integrative approach: species delimitation in the centipede Clinopodes carinthiacus (Chilopoda: Geophilidae) in the south-eastern Alps
Figure 2. Subdivision of 16S, COI and 28S haplotypes into candidate species according to different species delimitation methods. The ultrametric trees used for the general mixed Yule coalescent (GMYC) analyses are illustrated for the haplotypes of 16S and COI (all nodes: bootstrap supports ≥ 81% for 16S and ≥ 71% for COI). The median-joining network is illustrated for the 28S haplotypes (see also Supporting Information, Fig. S2). Mountain ranges where the haplotypes were found are also indicated.
Figure 6 in Shedding light on species boundaries in small endogeic animals through an integrative approach: species delimitation in the centipede Clinopodes carinthiacus (Chilopoda: Geophilidae) in the south-eastern Alps
Figure 6. Geometric morphometric analysis of between-population variation of the shape of the forcipular coxosternite in Clinopodes carinthiacus s.s.. The left panel shows landmarks (circles) and semilandmarks (diamonds) on a representative specimen (PD-G 7787, from population GUI). The right panel shows the distribution of 40 specimens from eight populations (codes as in Table 1) on the first and second principal components (bgPC 1 and bgPC 2) obtained from a between-group principal components analysis of the symmetric component of the shape. Polygons indicate populations. The wireframes along the components represent the variation in shape (dark blue) in comparison to the average shape (light blue).
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Allen Brain Atlas
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Annotated Behaviour and Observability Dataset (ABODe)
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