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218 results for “Mirabilis”
Data from: Patterns of genomic divergence and signals of selection in sympatric and allopatric northeastern Pacific and Sea of Cortez populations of the sargo (Anisotremus davidsonii) and longjaw mudsucker (Gillichthys mirabilis)
<p><span><span>Studying how isolation can impact population divergence and adaptation in co-distributed species can bring us closer to understanding how landscapes affect biodiversity. The Sargo, </span><i><span>Anisotremus davidsonii </span></i><span>(Haemulidae), and the Longjaw mudsucker, </span><i><span>Gillichthys mirabilis </span></i><span>(Gobiidae), offer a notable framework to study such mechanisms as their Pacific populations cross phylogeographic breaks at Point Conception, California, USA, and Punta Eugenia, Mexico, and are separated to those in the Sea of Cortez by the Baja California peninsula. Here, thousands of loci are genotyped from 48 Sargos and 73 mudsuckers using RADseq to characterize overall genomic divergence, and search for common patterns of putatively neutral and non-neutral structure based on outlier loci among populations with hypothesized different levels of isolation.</span></span><span> </span><span><span>We further search for parallels between population divergence and the total proportion of outliers, outlier </span></span><span><span>F</span><sub><span>ST</span></sub></span><span><span> distribution, and </span></span><span><span>the proportion of outliers matching coding regions in GenBank. This dataset consists of demultiplexed sequence data from Sbf1 single digest RADseq analysis of poulations of both fish species throughout their distributions. </span></span></p>
FIGURES 48–54. Scolopendra mirabilis Porat, 1876 48 in An overview of the extant genera and subgenera of the order Scolopendromorpha (Chilopoda): a new identification key and updated diagnoses
FIGURES 48–54. Scolopendra mirabilis Porat, 1876 48 Locomotory legs of mid-body LBS laterally; Scolopendra cingulata Latreille, 1829; Ad. Rc 8007) 49 ultimate LBS + prefemora of ultimate legs ventrally; Scolopendra canidens Newport, 1844; Ad. Rc 6222 50 forcipular segment ventrally; Scolopendra subspinipes Leach, 1815; Ad. Rc 8010 51 left pleura of LBS 14–15 laterally; Ad. Rc 8010 52 head + LBS 1 dorsally; Sad. CDT 53 forcipular segment ventrally; Ad. Rc 8010 54 LBS 21 + ultimate legs dorso-laterally; (20)—leg 20, (ap)—apical spines of coxopleural process, (csp)—corner spine of ultimate prefemur, (cst)— forcipular coxosternite, (cx)—coxopleuron, (im)—intersclerite membrane, (o)—ocelli, (p)—single pleurites, (pr)—trochantero-prefemoral process, (pts)—pretarsus, (s)—spiracle covered by flap, (su)—ventral spines of ultimate prefemur, (T1)—tergite 1, (T15)—tergite 15, (t1)—tarsus 1, (t2)—tarsus 2, (tas)—tarsal spur, (tp)—forcipular tooth-plate, (ust)—ultimate sternite.
Data from: Taxonomic status and distribution of Mirabilis himalaica (Nyctaginaceae)
Mirabilis himalaica (Nyctaginaceae) is endemic to the Himalayas where it is used in traditional Tibetan folk medicine and is the only Old World representative of a large New World genus. The systematic position of M. himalaica and historical biogeography of Mirabilis and related genera was evaluated using two loci (nrITS, rps16), with divergence times estimated using ITS sequences. All 16 sampled provenances of M. himalaica formed a strongly supported terminal clade and at the sectional level formed a clade with sect. Quamoclidion sensu stricto, despite their morphology. Sect. Oxybaphoides and sect. Oxybaphus were not closely related to M. himalaica, suggesting their apparent morphological similarities are convergent. BEAST analysis and ancestral area reconstruction indicated that M. himalaica separated from related North American species during the late Miocene to early Pleistocene ~5.22 Ma (95 % HPD: 2.53–8.18). Both migration via the Quaternary Bering land bridge (Beringia) and long-distance dispersal may have contributed to the present-day disjunction between M. himalaica and the American species. These results agree with previous studies that suggest Oxybaphus should be merged into Mirabilis. However, although the infrageneric position of M. himalaica is still uncertain, it is not close to sect. Oxybaphus as has been suggested previously.
FIGURES 1–9 in A new Friesea of the mirabilis- group from Algeria (Collembola: Neanuridae: Frieseinae)
FIGURES 1–9. Friesea major sp. nov.: 1, dorsal chaetotaxy (S: S-chaetae); 2, dorsal ordinary chaeta of Abd. VI; 3, labium and four distal chaetae of the labrum; 4, labrum and prelabral chaetae; 5, right antenna in dorsal view (1 to 4, 7, 8: thickened S-chaetae; ms: S-microchaeta; i: chaeta i; large «mou» chaetae of Ant. IV are represented by their sockets); 6, abdominal sternite chaetotaxy; 7, Abd. V–VI in dorso-lateral view; 8, pretarsus, tibiotarsus and femur of leg II; 9, furcal vestige.
FIGURES 3–5 in Leptogenopapus mirabilis, a new genus and species of Lomechusini (Coleoptera: Staphylinidae, Aleocharinae) from Papua New Guinea associated with ants of the genus Leptogenys Roger
FIGURES 3–5. Details of Leptogenopapus mirabilis sp. n. (holotype). 3, head ventral; 4, head dorsal; 5, thorax, ventral.
FIGURES 11–15 in Leptogenopapus mirabilis, a new genus and species of Lomechusini (Coleoptera: Staphylinidae, Aleocharinae) from Papua New Guinea associated with ants of the genus Leptogenys Roger
FIGURES 11–15. Details of Leptogenopapus mirabilis sp. n. (holotype). 11, right maxilla, ventral; 12, right mandible, ventral; 13, left paramera, dorsal; 14, median lobe of aedegus, dorsal; 15, median lobe of aedegus, lateral.
FIGURES 6–10 in Leptogenopapus mirabilis, a new genus and species of Lomechusini (Coleoptera: Staphylinidae, Aleocharinae) from Papua New Guinea associated with ants of the genus Leptogenys Roger
FIGURES 6–10. Legs and antenna of Leptogenopapus mirabilis sp. n. (holotype). 6, right fore leg, dorsal; 7, right mid leg, dorsal; 8, right hind leg, dorsal; 9, left antenna, dorsal; 10, hind tarsus, dorsal.
FIGURES 3–18. Peyrierocoris mirabilis n in Peyrierocoris a new genus of Harpactorinae (Hemiptera: Heteroptera: Reduviidae) from Madagascar
FIGURES 3–18. Peyrierocoris mirabilis n. sp.: 3. pygophore, ventral view; 4. pygophore, middle process, frontolateral view; 5. pygophore, middle process, lateral view; 6. pygophore, frontal view; 7. right clasper, outer view; 8. right clasper, lateral view; 9. left clasper, outer view; 10. left clasper, lateral view; 11. aedeagus, dorsal view; 12. aedeagus, frontal view; 13. scutellum, dorsal view; 14. aedeagus, left lateral view; 15. aedeagus, right lateral view; 16. valvifer 1, inner view; 17. valvula 3, outer view; 18. valvula 1, inner view.
FIGURE 5. a. Darevskia rudis mirabilis ssp.nov. Holotype. Dorsal view. b. D. r. mirabilis ssp. nov. Holotype. Ventral view. c. Darevskia rudis bolkardaghica ssp. nov. Holotype. Dorsal view. d. D. r in External morphology and osteology of Darevskia rudis (Bedriaga, 1886), with a taxonomic revision of the Pontic and Small-Caucasus populations (Squamata: Lacertidae)
FIGURE 5. a. Darevskia rudis mirabilis ssp.nov. Holotype. Dorsal view. b. D. r. mirabilis ssp. nov. Holotype. Ventral view. c. Darevskia rudis bolkardaghica ssp. nov. Holotype. Dorsal view. d. D. r. bolkardaghica ssp. nov. Holotype. Ventral view.
FIGURES 12, 13. Dobrodesmus mirabilis. Fig 12 in A millipede missing link: Dobrodesmidae, a remarkable new polydesmidan millipede family from Brazil with supernumerary rings (Diplopoda, Polydesmida), and the establishment of a new suborder Dobrodesmidea
FIGURES 12, 13. Dobrodesmus mirabilis. Fig 12, ventral view of right lateral part of midbody segment, showing positions of spiracles. Abbreviations: as, anterior spiracle; ps, posterior spiracle. Fig 13. Posterior spiracle.
FIGURES 8–10. Dobrodesmus mirabilis. Fig 8 in A millipede missing link: Dobrodesmidae, a remarkable new polydesmidan millipede family from Brazil with supernumerary rings (Diplopoda, Polydesmida), and the establishment of a new suborder Dobrodesmidea
FIGURES 8–10. Dobrodesmus mirabilis. Fig 8, Ozopore, lateral view. Fig 9, intercalary microscutes of metazonital dorsum, dorsal view. Fig 10, same.
FIGURES 2–7. Dobrodesmus mirabilis. Fig 2, collum. Fig 3, sensilla from sixth antennal article. Fig 4 in A millipede missing link: Dobrodesmidae, a remarkable new polydesmidan millipede family from Brazil with supernumerary rings (Diplopoda, Polydesmida), and the establishment of a new suborder Dobrodesmidea
FIGURES 2–7. Dobrodesmus mirabilis. Fig 2, collum. Fig 3, sensilla from sixth antennal article. Fig 4, midbody segment, dorsal view. Fig 5, midbody segment, ventral view. Fig 6, anterior right corner of midbody segment, dorsal view. Fig 7, posterior right corner of nonporiferous midbody segment, dorsal view.
FIGURE 6 in A new species of lithistid sponge hiding within the Isabella mirabilis species complex (Porifera: Demospongiae: Tetractinellida) from seamounts of the Norfolk Ridge
FIGURE 6. Specimens of Isabella tanoa, clockwise from the bottom left the holotype MNHN DCL 4111 (QM G318737), then paratypes QM G318803, G318765 and G335130.
FIGURE 7 in A new species of lithistid sponge hiding within the Isabella mirabilis species complex (Porifera: Demospongiae: Tetractinellida) from seamounts of the Norfolk Ridge
FIGURE 7. Outer surface and desma skeleton of the holotype MNHN DCL 4111 (QM G318737) of Isabella tanoa n. sp. A, outer surface showing bundles of oxeas protruding through the surface, with abundant centrotylote microacanthoxeas and ectosomal dichotriaenes. B, minute oscules surrounded by ectosomal streptasters and microxeas. C, loose open architecture of the dicranoclone desmas in the upper choanosome. D, increased thickness of the desmas and increased complexity of the articulation between the desmas deeper in the choanosome. E and F, details of articulation between choanosomal desmas.
FIGURE 8. Spicules from the holotype MNHN DCL 4111 in A new species of lithistid sponge hiding within the Isabella mirabilis species complex (Porifera: Demospongiae: Tetractinellida) from seamounts of the Norfolk Ridge
FIGURE 8. Spicules from the holotype MNHN DCL 4111 (QM G318737) Isabella tanoa n. sp. A to C, centrotylote microacanthoxeas. D, close up of the tip of the centrotylote microacanthoxeas. E, long ectosomal dichotriaenes. F, short-shafted ectosomal dichotriaenes. G to J, spirasters with long thin thorny arms. K to Q, streptasters with short thick thorny arms of variable number, length and termination.
FIGURE 5 in A new species of lithistid sponge hiding within the Isabella mirabilis species complex (Porifera: Demospongiae: Tetractinellida) from seamounts of the Norfolk Ridge
FIGURE 5. Dichotriaenes of Isabella mirabilis. A to H, showing the variability of dichotriaenes. I, triaene.
FIGURE 3 in A new species of lithistid sponge hiding within the Isabella mirabilis species complex (Porifera: Demospongiae: Tetractinellida) from seamounts of the Norfolk Ridge
FIGURE 3. One of the 'warts' from Isabella mirabilis budding off from specimen G318751, with the large oxeas, dichotriaenes and microscopic oscules clearly visible.
FIGURE 2 in A new species of lithistid sponge hiding within the Isabella mirabilis species complex (Porifera: Demospongiae: Tetractinellida) from seamounts of the Norfolk Ridge
FIGURE 2. Preserved specimens of I. mirabilis. Back row, from left to right: G318751, G329916 and G329917. Middle row: G329919, G329920, G329921 and G329924. Front row: G329925, G329922 and G329923.
FIGURE 1 in A new species of lithistid sponge hiding within the Isabella mirabilis species complex (Porifera: Demospongiae: Tetractinellida) from seamounts of the Norfolk Ridge
FIGURE 1. Specimens of I. mirabilis, on the left, the Holotype MNHN DCL 3903 (QM G318560), and on the right G318751.
FIGURE 4 in A new species of lithistid sponge hiding within the Isabella mirabilis species complex (Porifera: Demospongiae: Tetractinellida) from seamounts of the Norfolk Ridge
FIGURE 4. Spicules of Isabella mirabilis. A, microacanthoaxeas. B, centrotylote microacanthoxeas. C, centrotylote microacanthoxeas with thorns. D and E, smooth centrotylote microxeas. F, tip of microacanthoxeas. G to I, tip of smooth microxeas. J, range of smooth microxeas. K to M, Spirasters with long thin thorny arms. N to R, streptasters with short thick thorny arms of variable number, length and termination.
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