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FIGS. 77–84 in Implications of the tympanal hearing organ and ultrastructure of chaetotaxy for the higher classification of Embioptera
FIGS. 77–84. Chaetotaxy and middle bladder: 77, slender hook of Oligotoma saundersi (Oligotomidae); 78, slender hook of Archembia lacombea (Archembiidae); 79, middle bladder with sculpture on Archembia lacombea (Archembiidae); 80, middle bladder with few microtrichia of Gibocercus chaco (Archembiidae); 81, middle bladder without sculpture or michrotrichia Pachylembia unicincta (Archembiidae); 82, small middle bladder with microtrichia Pararhagadochir trachelia (Archembiidae); 83, mechanoreceptor on middle bladder Antipaluria urichi (Clothodidae); 84, detail of mechanoreceptor (circle in fig. 83) on middle bladder of Antipaluria urichi (Clothodidae).
FIGS. 85–90 in Implications of the tympanal hearing organ and ultrastructure of chaetotaxy for the higher classification of Embioptera
FIGS. 85–90. Apical bladder of hind tarsus midsegment: 85, Clothoda longicauda (Clothodidae) left leg; 86, Notoligotoma hardyi (Notoligotomidae) right leg; 87, Gibocercus chaco (Archembiidae) left leg; 88, Dihybocercus femorata (Embiidae) right leg; 89, Oligotoma saundersii (Oligotomidae) left leg; 90, Teratembia geniculata (Teratembiidae) right leg.
FIGS. 71–76 in Implications of the tympanal hearing organ and ultrastructure of chaetotaxy for the higher classification of Embioptera
FIGS. 71–76. Chaetotaxy of hind basitarsus: 71, broad setae of Antipaluria urichi (Clothodidae); 72, broad setae of Clothoda longicauda (Clothodidae); 73, jagged setae of Chelicerca barbara (Anisembiidae); 74, jagged setae of Saussurembia calypso (Anisembiidae); 75, serrate hairs on lateroapical surface of Clothoda longicauda (Clothodidae); 76, three-pronged setae on lateroapical surface of Dihybocercus femorata (Embiidae); an enlarged section of this type of setae is shown in the adjacent circle.
FIGS. 63–70 in Implications of the tympanal hearing organ and ultrastructure of chaetotaxy for the higher classification of Embioptera
FIGS. 63–70. Hind tarsus, ventral view: 63, broad setae in Antipaluria caribbeana (Clothodidae) left leg; 64, broad setae in Australembia incompta (Australembiidae) left leg; 65, jagged setae in Chelicerca barbara (Anisembiidae) left leg: an enlarged section of this seta is shown in the adjacent circle; 66, broad setae in Notoligotoma hardy (Notoligotomidae) right leg; 67, broad setae in Dihybocercus femorata (Embiidae) right leg; 68, broad setae in Gibocercus chaco (Archembiidae) left leg; 69, broad setae in Oligotoma saundersii (Oligotomidae) left leg; 70, jagged setae in Teratembia geniculata (Teratembiidae) right leg.
FIGS. 57–62 in Implications of the tympanal hearing organ and ultrastructure of chaetotaxy for the higher classification of Embioptera
FIGS. 57–62. Comb setae on ventral surface of foretarsus basal segment: 57, Clothoda longicauda (Clothodidae); 58, Haploembia solieri (Oligotomidae); 59, Oligotoma saundersii (Oligotomidae); 60, Pararhagadochir trachelia (Archembiidae); 61, Saussurembia calypso (Anisembiidae); 62, Gibocercus chaco (Archembiidae).
FIG. 52 in Implications of the tympanal hearing organ and ultrastructure of chaetotaxy for the higher classification of Embioptera
FIG. 52. Optimization of the silk ejectors length: state 0, short as in Embiidae (less than 80 μm); state 1, long (more than 100 μm).
FIGS. 45–50 in Implications of the tympanal hearing organ and ultrastructure of chaetotaxy for the higher classification of Embioptera
FIGS. 45–50. Ventral view of basal segment of foretarsus: 45, Australembia incompta (Australembiidae) left leg; 46, Saussurembia calypso (Anisembiidae) left leg; 47, Notoligotoma hardy (Notoligotomidae) right leg; 48, Pararhagadochir trachelia (Archembiidae) right leg; 49, Embia ramburi (Embiidae) right leg; 50, Teratembia geniculata (Teratembiidae) right leg.
FIGS. 30–32 in Implications of the tympanal hearing organ and ultrastructure of chaetotaxy for the higher classification of Embioptera
FIGS. 30–32. Silk ejectors and combs on basal segment of foretarsus: 30, detail of ventral left margin view of Gibocercurs chaco (Archembiidae): A, silk ejector Type I, B, silk ejector Type II, C, comb setae; 31, silk ejector Type I of Oligotoma saundersii (Oligotomidae), slightly curved; 32, silk ejector Type I of Gibocercus chaco, erect and slender.
FIGS. 39-44 in Implications of the tympanal hearing organ and ultrastructure of chaetotaxy for the higher classification of Embioptera
FIGS. 39-44. Ventral view of basal segment of foretarsus: 39, Haploembia solieri (Oligotomidae), left leg; 40, Clothoda longicauda (Clothodidae), right leg; 41, Antipaluria caribbeana (Clothodidae), left leg; 42, Oligotoma saundersii (Oligotomidae), left leg; 43, Dihybocercus femorata (Embiidae), right leg; 44, Chelicerca barbara (Anisembiidae), left leg.
FIGS. 14–23 in Implications of the tympanal hearing organ and ultrastructure of chaetotaxy for the higher classification of Embioptera
FIGS. 14–23. Shapes of auditory organ on middle femur: 14, Chelicerca wheeleri (Anisembiidae) right leg; 15, Mesembia chamulae (Anisembiidae) right leg; 16, Teratembia geniculata (Teratembiidae) left leg; 17, Clothoda longicauda (Clothodidae) right leg; 18, Chelicerca barbara (Anisembiidae) left leg; 19, Australembia nodosa (Australembiidae) left leg; 20, Biguembia copo (Archembiidae) left leg; 21, Machadoembia angolica (Embiidae) right leg; 22, Dihybocercus femorata (Embiidae) right leg; 23, Aposthonia indica (Oligotomidae) right leg.
FIG. 29 in Implications of the tympanal hearing organ and ultrastructure of chaetotaxy for the higher classification of Embioptera
FIG. 29. Optimization of the shape of tympanal organ in the hind femur: state 0, small and semicircular; state 1, small disk depressed area; state 2, absent.
FIGS. 33–38 in Implications of the tympanal hearing organ and ultrastructure of chaetotaxy for the higher classification of Embioptera
FIGS. 33–38. Ventral view of midsegment of foretarsus: 33, Saussurembia calypso (Anisembiidae) left leg: A, silk ejector Type I, B, comb setae, C, serrate hairs; 34, Haploembia solieri (Oligotomidae); 35, Notoligotoma nitens (Notoligotomidae); 36, Australembia incompta (Australembiidae) left leg; 37, Pararhagadochir trachelia (Archembiidae); 38, Teratembia geniculata (Teratembiidae).
FIGS. 6–12 in Implications of the tympanal hearing organ and ultrastructure of chaetotaxy for the higher classification of Embioptera
FIGS. 6–12. Shapes of auditory organ on forefemur: 6, Chelicerca barbara (Anisembiidae) right leg; 7, C. wheeleri right leg; 8, Machadoembia angolica (Embiidae) right leg; 9, Teratembia geniculata (Teratembiidae) left leg; 10, Australembia nodosa (Australembiidae) right leg; 11, Clothoda longicauda (Clotodidae) left leg; 12, Aposthonia indica (Oligotomidae) right leg.
FIG. 13 in Implications of the tympanal hearing organ and ultrastructure of chaetotaxy for the higher classification of Embioptera
FIG. 13. Optimization of the shape of the forefemora tympanal organ: state 0, semicircular with well-defined edges; state 1, a curved, slender band, elongated along the femoral axis; state 2, a tiny triangle. Arrows (>>>) in some parts of the cladogram represent higher groups, with several species included in the dataset, but the internal resolution of which is not relevant for this level of analysis (hence, for clarity, the groups are collapsed and replaced by the corresponding name).
Figs. 272–274. Himalcoelotes martensi, new species. 272. Trichobothrium. 273. Tarsal organ. 274 in A Generic-Level Revision Of The Spider Subfamily Coelotinae (Araneae, Amaurobiidae)
Figs. 272–274. Himalcoelotes martensi, new species. 272. Trichobothrium. 273. Tarsal organ. 274. Tarsus, showing position of tarsal organ (double arrows) and distalmost trichobothrium (single arrow).
Figs. 23–27. Anatomical organs. 23–26 in Classification, Natural History, and Evolution of Epiphloeinae (Coleoptera: Cleridae). Part V. Decorosa Opitz, a New Genus of Checkered Beetles from Hispaniola with Description of Its Four New Species
Figs. 23–27. Anatomical organs. 23–26. Decorosa iviei Opitz (23, metathoracic wing; 24, elytra, ventral view; 25, cluster of elytral punctations; 26, elytra, lateral view). 27. Madoniella dislocata (Say) elytra, lateral view.
Figs. 39–43. Anatomical organs and habitus. 39. Decorosa aladecoris Opitz elytra, ventral view. 40–41. D in Classification, Natural History, and Evolution of Epiphloeinae (Coleoptera: Cleridae). Part V. Decorosa Opitz, a New Genus of Checkered Beetles from Hispaniola with Description of Its Four New Species
Figs. 39–43. Anatomical organs and habitus. 39. Decorosa aladecoris Opitz elytra, ventral view. 40–41. D. neiba Opitz (40, aedeagus; 41, habitus). 42. D. aladecoris, pronotum. 43. D. neiba, pronotum.
Text-fig. 1. Torres Vedras site. Arrow point to the organic rich horizon where the fossils described here were collected. in The Early Cretaceous Mesofossil Flora Of Torres Vedras (Ne Of Forte Da Forca), Portugal: A Palaeofloristic Analysis Of An Early Angiosperm Community
Text-fig. 1. Torres Vedras site. Arrow point to the organic rich horizon where the fossils described here were collected.
Figure 3 in Oribatid mites of conventional and organic vineyards in the Valencian Community, Spain
Figure 3 Detrended correspondence analysis (DCA) in studied plots in El Poble Nou de Benitatxell: Tr – zone between rows driven by a tractor, Vi– zone between vines, Bo – border; 12 most abundant species (withD> 5) are underlined; eigenvalues for axes 1 and 2 are 0.54 and
Figure 2 in Oribatid mites of conventional and organic vineyards in the Valencian Community, Spain
Figure 2 Mean temperature (°C) and sum of precipitation (mm) in all months of years 2014 and 2015 in El Poble Nou de Benitatxell (data
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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.