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454-sequence data of Iron Age cattle from Althiburos – Tunisia
<p>The Maghreb is a key region for understanding the dynamics of cattle dispersal and admixture with local aurochs following their earliest domestication in the Fertile Crescent more than 10,000 years ago. Here, we present data on mitochondrial <em>D-loop</em> sequences obtained for 12 archaeological specimens of Iron Age (~2,800 cal BP–2,000 cal BP) domestic cattle from the Eastern Maghreb, i.e. Althiburos (El Kef, Tunisia). Maternal lineages were assigned to the elusive R and ubiquitous African-T1 haplogroups found in two and ten Althiburos specimens, respectively. Our results corroborate the introgression of aurochs females into the domestic stock of cattle from Althiburos. </p>
454-sequence data of Iron Age cattle from Althiburos – Tunisia
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Data from: A 454 survey reveals the community composition and core microbiome of the common bed bug (Cimex lectularius) across an urban landscape
Elucidating the spatial dynamic and core constituents of the microbial communities found in association with arthropod hosts is of crucial importance for insects that may vector human or agricultural pathogens. The hematophagous Cimex lectularius (Hemiptera: Cimicidae), known as the human bed bug, has made a recent resurgence in North America, as well as worldwide, potentially owing to increased travel, climate change and resistance to insecticides. A comprehensive survey of the bed bug microbiome has not been performed to date, nor has an assessment of the spatial dynamics of its microbiome. Here we present a survey of internal and external bed bug microbial communities by amplifying the V4–V6 hypervariable region of the 16S rDNA gene region followed by 454 Titanium sequencing using 31 individuals from eight distinct collection locations obtained from residences in Cincinnati, OH. Across all samples, 97% of the microbial community is made up of two dominant OTUs, previously identified as the α-proteobacterium Wolbachia and an unnamed γ-proteobacterium from the Enterobacteriaceae. Microbial communities varied among host locations for measures of community diversity and exhibited structure according to collection location. This broad survey represents the most in-depth assessment, to date, of the microbes that associate with bed bugs.
Data from: Microsatellite markers from the Ion Torrent: a multi-species contrast to 454 shotgun sequencing
The development and screening of microsatellite markers have been accelerated by next-generation sequencing (NGS) technology and in particular GS-FLX pyro-sequencing (454). More recent platforms such as the PGM semiconductor sequencer (Ion Torrent) offer potential benefits such as dramatic reductions in cost, but to date have not been well utilized. Here, we critically compare the advantages and disadvantages of microsatellite development using PGM semiconductor sequencing and GS-FLX pyro-sequencing for two gymnosperm (a conifer and a cycad) and one angiosperm species. We show that these NGS platforms differ in the quantity of returned sequence data, unique microsatellite data and primer design opportunities, mostly consistent with the differences in read length. The strength of the PGM lies in the large amount of data generated at a comparatively lower cost and time. The strength of GS-FLX lies in the return of longer average length sequences and therefore greater flexibility in producing markers with variable product length, due to longer flanking regions, which is ideal for capillary multiplexing. These differences need to be considered when choosing a NGS method for microsatellite discovery. However, the ongoing improvement in read lengths of the NGS platforms will reduce the disadvantage of the current short read lengths, particularly for the PGM platform, allowing greater flexibility in primer design coupled with the power of a larger number of sequences.
Data from: Exploring Symbiodinium diversity and host specificity in Acropora corals from geographical extremes of Western Australia with 454 amplicon pyrosequencing
Scleractinian corals have demonstrated the ability to shuffle their endosymbiotic dinoflagellate communities (genus Symbiodinium) during periods of acute environmental stress. This has been proposed as a mechanism of acclimation, which would be increased by a diverse and flexible association with Symbiodinium. Conventional molecular techniques used to evaluate Symbiodinium diversity lack the sensitivity to capture accurate estimates of diversity and are unable to identify genetic lineages present at background levels below 10%. Next generation sequencing (NGS) offers a solution to this problem and can resolve microorganism diversity at much finer scales. Here we apply NGS to evaluate Symbiodinium diversity and host specificity in Acropora corals from contrasting regions of Western Australia. The application of 454 pyrosequencing allowed for detection of Symbiodinium operational taxonomic units (OTUs) occurring at frequencies as low as 0.001%, offering a 10 000-fold increase in sensitivity compared to traditional methods. All coral species from both regions were overwhelmingly dominated by a single clade C OTU (accounting for 98% of all recovered sequences). Only 8.5% of colonies associated with multiple clades (clades C and D, or C and G), suggesting a high level of symbiont specificity in Acropora assemblages in Western Australia. This contrasts with recent literature that have applied highly-sensitive molecular techniques and identified widespread flexibility in symbiont associations across a number of coral taxa in other geographic regions. While only 40% of the OTUs were shared between regions, the dominance of a single OTU resulted in no significant difference in Symbiodinium community structure, demonstrating that the coral-algal symbiosis can remain stable across more than 15° of latitude and a range of sea surface temperature profiles. This study validates the use of NGS platforms as tools for providing fine-scale estimates of Symbiodinium diversity and can offer critical insight into the flexibility of the coral-algal symbiosis.
Data from: Comparison of 454 pyrosequencing methods for characterizing the major histocompatibility complex of nonmodel species and the advantages of ultra deep coverage
Characterization and population genetic analysis of multilocus genes, such as those found in the major histocompatibility complex (MHC) is challenging in nonmodel vertebrates. The traditional method of extensive cloning and Sanger sequencing is costly and time-intensive and indirect methods of assessment often underestimate total variation. Here, we explored the suitability of 454 pyrosequencing for characterizing multilocus genes for use in population genetic studies. We compared two sample tagging protocols and two bioinformatic procedures for 454 sequencing through characterization of a 185-bp fragment of MHC DRB exon 2 in wolverines (Gulo gulo) and further compared the results with those from cloning and Sanger sequencing. We found 10 putative DRB alleles in the 88 individuals screened with between two and four alleles per individual, suggesting amplification of a duplicated DRB gene. In addition to the putative alleles, all individuals possessed an easily identifiable pseudogene. In our system, sequence variants with a frequency below 6% in an individual sample were usually artefacts. However, we found that sample preparation and data processing procedures can greatly affect variant frequencies in addition to the complexity of the multilocus system. Therefore, we recommend determining a per-amplicon-variant frequency threshold for each unique system. The extremely deep coverage obtained in our study (approximately 5000×) coupled with the semi-quantitative nature of pyrosequencing enabled us to assign all putative alleles to the two DRB loci, which is generally not possible using traditional methods. Our method of obtaining locus-specific MHC genotypes will enhance population genetic analyses and studies on disease susceptibility in nonmodel wildlife species.
FIGURES 443–454 in Key to the world species of Holoparasitus Oudemans, 1936 (Acari: Parasitiformes: Parasitidae)
FIGURES 443–454. Males. Holoparasitus excisus: 443 gnathotectum; 444 chelicera, adaxially; 445 pedipalp trochanter and femur, ventrally; 446 Fe II, Ge II and Ti II, anterolaterally. Holoparasitus apenninorum: 447 chelicera, adaxially; 448 chelicera, antiaxially; 449 Fe II, Ge II and Ti II, posterolaterally. Holoparasitus amiatus: 450 genital lamina and anterior part of sternogenital shield; 451 pedipalp trochanter and gnathosoma, ventrally; 452 chelicera, antiaxially; 453 spurs on Fe II, Ge II and Ti II in anteroventral perspective (arrow–anterolateral side); 454 Fe II, Ge II and Ti II, anterolaterally. Scale bars: 0.1 mm.
On following pages: 452. Long-toed Myotis (Myotis secundus); 453. Bornean Whiskered Myotis (Myotis borneoensis); 454. Malaysian Whiskered Myotis (Myotis federatus): 455. Indochinese Myotis (Myotis indochinensis); 456. Peyton's Myotis (Myotis peyton); 457. Burmese Whiskered Myotis (Myotis montivagus); 458. Long-fingered Myotis (Myotis capaccinii); 459. Chinese Water Myotis (Myotis laniger); 460. Csorba's Myotis (Myotis csorbal); 461. Kashmir Cave Myotis (Myotis longipes); 462. Annamit Myotis (Myotis annamiticus); 463. Phan Luong's Myotis (Myotis phanluongi); 464. Himalayan Whiskered Myotis (Myotis siligorensis); 465. Chestnut Myotis (Myotis badius); 466. Ridley's Myotis (Myotis ridley); 467. Thick-thumbed Myotis (Myotis rosseti); 468. Horsfield's Myotis (Myotis horsfieldi); 469. Pallid Large-footed Myotis (Myotis macrotarsus); 470. Stalker's Myotis (Myotis stalkeri); 471. Gray Large-footed Myotis (Myotis adversus); 472. Maluku Myotis (Myotis moluccarum); 473. Southern Myotis (Myotis macropus); 474. Lesser Large-footed Myotis (Myotis hasselti). in Vespertilionidae
On following pages: 452. Long-toed Myotis (Myotis secundus); 453. Bornean Whiskered Myotis (Myotis borneoensis); 454. Malaysian Whiskered Myotis (Myotis federatus): 455. Indochinese Myotis (Myotis indochinensis); 456. Peyton's Myotis (Myotis peyton); 457. Burmese Whiskered Myotis (Myotis montivagus); 458. Long-fingered Myotis (Myotis capaccinii); 459. Chinese Water Myotis (Myotis laniger); 460. Csorba's Myotis (Myotis csorbal); 461. Kashmir Cave Myotis (Myotis longipes); 462. Annamit Myotis (Myotis annamiticus); 463. Phan Luong's Myotis (Myotis phanluongi); 464. Himalayan Whiskered Myotis (Myotis siligorensis); 465. Chestnut Myotis (Myotis badius); 466. Ridley's Myotis (Myotis ridley); 467. Thick-thumbed Myotis (Myotis rosseti); 468. Horsfield's Myotis (Myotis horsfieldi); 469. Pallid Large-footed Myotis (Myotis macrotarsus); 470. Stalker's Myotis (Myotis stalkeri); 471. Gray Large-footed Myotis (Myotis adversus); 472. Maluku Myotis (Myotis moluccarum); 473. Southern Myotis (Myotis macropus); 474. Lesser Large-footed Myotis (Myotis hasselti).
On following pages: 423. Tate's Rice Rat (Hylaeamystate); 424. Sowbug Rice Rat (Hylaeamys oniscus); 425. Bolivian Rice Rat (Hylaeamys acritus); 426. Atlantic Forest Rice Rat (Hylaeamys laticeps); 427. Fulvous Pygmy Rice Rat (Oligoryzomys fulvescens); 428. Costa Rican Pygmy Rice Rat (Oligoryzomys costaricensis); 429. Sprightly Pygmy Rice Rat (Oligoryzomys vegetus); 430. Delicate Pygmy Rice Rat (Oligoryzomys delicatus); 431. Grayish Pygmy Rice Rat (Oligoryzomys griseolus); 432. Hairy Pygmy Rice Rat (Oligoryzomys messorius); 433. Tschudi''s Pygmy Rice Rat (Oligoryzomys destructor); 434. Sandy Pygmy Rice Rat (Oligoryzomys arenalis); 435. Andean Pygmy Rice Rat (Oligoryzomys andinus); 436. Small-eared Pygmy Rice Rat (Oligoryzomys microtis); 437. Utiariti Pygmy Rice Rat (Oligoryzomys utiaritensis); 438. Straw-colored Pygmy Rice Rat (Oligoryzomys stramineus); 439. Mato Grosso Pygmy Rice Rat (Oligoryzomys mattogrossae); 440. Moojen's Pygmy Rice Rat (Oligoryzomys moojeni); 441. Highlands Pygmy Rice Rat (Oligoryzomys rupestris); 442. Black-footed Pygmy Rice Rat (Oligoryzomys nigripes); 443. San Javier's Pygmy Rice Rat (Oligoryzomys brendae); 444. Chacoan Pygmy Rice Rat (Oligoryzomys chacoensis); 445. Fornes's Pygmy Rice Rat (Oligoryzomys fornesi); 446. Yellow Pygmy Rice Rat (Oligoryzomys flavescens); 447. Long-tailed Pygmy Rice Rat (Oligoryzomys longicaudatus); 448. Painted Bristly Mouse (Neacomys pictus); 449. Narrow-footed Bristly Mouse (Neacomys tenuipes); 450. Guianan Bristly Mouse (Neacomys guianae); 451. Paracou Bristly Mouse (Neacomys paracou); 452. Dubost's Bristly Mouse (Neacomys dubosti); 453. Large Bristly Mouse (Neacomys spinosus); 454. Pleasant Bristly Mouse (Neacomys amoenus), 455. Vargas Llosa''s Bristly Mouse (Neacomys vargasllosai); 456. Minute Bristly Mouse (Neacomys minutus); 457. Musser's Bristly Mouse (Neacomys musseri). in Cricetidae
On following pages: 423. Tate's Rice Rat (Hylaeamystate); 424. Sowbug Rice Rat (Hylaeamys oniscus); 425. Bolivian Rice Rat (Hylaeamys acritus); 426. Atlantic Forest Rice Rat (Hylaeamys laticeps); 427. Fulvous Pygmy Rice Rat (Oligoryzomys fulvescens); 428. Costa Rican Pygmy Rice Rat (Oligoryzomys costaricensis); 429. Sprightly Pygmy Rice Rat (Oligoryzomys vegetus); 430. Delicate Pygmy Rice Rat (Oligoryzomys delicatus); 431. Grayish Pygmy Rice Rat (Oligoryzomys griseolus); 432. Hairy Pygmy Rice Rat (Oligoryzomys messorius); 433. Tschudi''s Pygmy Rice Rat (Oligoryzomys destructor); 434. Sandy Pygmy Rice Rat (Oligoryzomys arenalis); 435. Andean Pygmy Rice Rat (Oligoryzomys andinus); 436. Small-eared Pygmy Rice Rat (Oligoryzomys microtis); 437. Utiariti Pygmy Rice Rat (Oligoryzomys utiaritensis); 438. Straw-colored Pygmy Rice Rat (Oligoryzomys stramineus); 439. Mato Grosso Pygmy Rice Rat (Oligoryzomys mattogrossae); 440. Moojen's Pygmy Rice Rat (Oligoryzomys moojeni); 441. Highlands Pygmy Rice Rat (Oligoryzomys rupestris); 442. Black-footed Pygmy Rice Rat (Oligoryzomys nigripes); 443. San Javier's Pygmy Rice Rat (Oligoryzomys brendae); 444. Chacoan Pygmy Rice Rat (Oligoryzomys chacoensis); 445. Fornes's Pygmy Rice Rat (Oligoryzomys fornesi); 446. Yellow Pygmy Rice Rat (Oligoryzomys flavescens); 447. Long-tailed Pygmy Rice Rat (Oligoryzomys longicaudatus); 448. Painted Bristly Mouse (Neacomys pictus); 449. Narrow-footed Bristly Mouse (Neacomys tenuipes); 450. Guianan Bristly Mouse (Neacomys guianae); 451. Paracou Bristly Mouse (Neacomys paracou); 452. Dubost's Bristly Mouse (Neacomys dubosti); 453. Large Bristly Mouse (Neacomys spinosus); 454. Pleasant Bristly Mouse (Neacomys amoenus), 455. Vargas Llosa''s Bristly Mouse (Neacomys vargasllosai); 456. Minute Bristly Mouse (Neacomys minutus); 457. Musser's Bristly Mouse (Neacomys musseri).
On following pages: 446. Glover Allen's Shaggy Rat (Dasymys alleni); 447. Middle Shaggy Rat (Dasymys medius); 448. Rwandan Shaggy Rat (Dasymys rwandae); 449. Tanzanian Shaggy Rat (Dasymys sua); 450. CrawfordCabral's Shaggy Rat (Dasymys cabrali); 451. Angolan Shaggy Rat (Dasymys nudipes); 452. Roberts's Shaggy Rat (Dasymys robertsii); 453. Cape Shaggy Rat (Dasymys capensis), 454. African Shaggy Rat (Dasymys incomtus); 455. Ethiopian Thicket Rat (Grammomys minnae); 456. Arid Woodland Thicket Rat (Grammomys aridulus); 457. Bunting's Thicket Rat (Grammomys buntingi); 458. Western Rainforest Thicket Rat (Grammomys poensis); 459. Albertine Rift Thicket Rat (Grammomys dryas); 460. Eastern Rainforest Thicket Rat (Grammomys kuru); 461. Short-snouted Thicket Rat (Grammomys brevirostris); 462. Gray-headed Thicket Rat (Grammomys caniceps); 463. Mount Kenya Thicket Rat (Grammomys gigas); 464. East African Thicket Rat (Grammomys ibeanus); 465. Macmillan's Thicket Rat (Grammomys macmillani); 466. Selous's Thicket Rat (Grammomys selousi); 467. in Muridae
On following pages: 446. Glover Allen's Shaggy Rat (Dasymys alleni); 447. Middle Shaggy Rat (Dasymys medius); 448. Rwandan Shaggy Rat (Dasymys rwandae); 449. Tanzanian Shaggy Rat (Dasymys sua); 450. CrawfordCabral's Shaggy Rat (Dasymys cabrali); 451. Angolan Shaggy Rat (Dasymys nudipes); 452. Roberts's Shaggy Rat (Dasymys robertsii); 453. Cape Shaggy Rat (Dasymys capensis), 454. African Shaggy Rat (Dasymys incomtus); 455. Ethiopian Thicket Rat (Grammomys minnae); 456. Arid Woodland Thicket Rat (Grammomys aridulus); 457. Bunting's Thicket Rat (Grammomys buntingi); 458. Western Rainforest Thicket Rat (Grammomys poensis); 459. Albertine Rift Thicket Rat (Grammomys dryas); 460. Eastern Rainforest Thicket Rat (Grammomys kuru); 461. Short-snouted Thicket Rat (Grammomys brevirostris); 462. Gray-headed Thicket Rat (Grammomys caniceps); 463. Mount Kenya Thicket Rat (Grammomys gigas); 464. East African Thicket Rat (Grammomys ibeanus); 465. Macmillan's Thicket Rat (Grammomys macmillani); 466. Selous's Thicket Rat (Grammomys selousi); 467.
FIGURES 453, 454 in Review of Gonatocerus (Hymenoptera: Mymaridae) in the Neotropical region, with description of eleven new species
FIGURES 453, 454. Gonatocerus (Cosmocomoidea) rufescens ♂ (holotype): 453, habitus; 454, dorsellum and propodeum.
Supplementary material 1 from: Mesibov R (2014) The Australian millipede Dicranogonus pix Jeekel, 1982 (Diplopoda, Polydesmida, Paradoxosomatidae): a species with and without paranota. ZooKeys 454: 29-39. https://doi.org/10.3897/zookeys.454.8625
Data table: Explanation note: Known specimen lots of Dicranogonus pix Jeekel, 1982 as of 17 September 2014.
[IO Islamic 454] Bayâḍ
<ul> <li>Bayâḍ</li> <li>This manuscript is now IO Islamic 1767 in the India Office collections.</li> <li>[metadata: Hermann Ethé, Catalogue of Persian Manuscripts in the Library of the India Office, 2 vols. (Oxford: India Office, 1903): volume 1, number 454 here with notations and hyperlinks].</li> </ul> <p><span>1767</span></p> <p><span>Bayâ</span><span>ḍ (</span><span><span><span><span><span>بياض</span></span></span><span> </span></span></span><span>).</span></p> <p><span>An album of Persian poetry and prose, containing miscellaneous pieces in a very confused order, many leaves being turned upside down. The principal contents are:</span></p> <p><span>1.A ḳiṭ’ah by </span><span><span><em>‘</em></span></span><span><em>Alî Ḥ</em></span><span><em>azîn</em></span><span> (died A. H. 1180, see Nos. 1712-1714 above), reproaching Kashmîr (</span><span><span><span><span><span>قطعه در مذمّت كشمير</span></span></span></span></span><span>), on fol. 1</span><sup><span>a</span></sup><span>, and other miscellaneous lyric poems.</span></p> <p><span>2.</span><span><em>Mîr Najât</em></span><span><span><em>’</em></span></span><span><em>s </em></span><span><span><span><span><span>دل كُشتى</span></span></span><span> </span></span></span><span>(a mathnawî on wrestling, composed A.H. 1112= A.D. 1700, 1701; Mîr </span><span><span>‘</span></span><span>Abd-al</span><span><span>’</span></span><span>âl Najât died about A.H. 1126=A.D. 1714, see Bodleian Cat., Nos. 1162-1165; Rieu ii. p. 821; A. Sprenger, Catal., p. 512; W. Pertsch, Berlin Cat., p. 697, No. 10; lithographed at Lucknow (with commentary), A.H. 1258), on fol. 7</span><sup><span>b</span></sup><span>.</span></p> <p><span>3.</span><span><em>Mullâ Nau</em></span><span><span><em>’</em></span></span><span><em>î</em></span><span><span><em>’</em></span></span><span><em>s</em></span><span> </span><span><span><span><span><span>سوز و </span></span></span><span><span><span>گ</span></span></span><span><span><span>داز</span></span></span><span> </span></span></span><span>(see No. 1485 above), on fol. 18</span><sup><span>a</span></sup><span>.</span></p> <p><span>4.A </span><span>ḳaṣîdah, by </span><span><em>Hijrî</em></span><span> (see Nos. 1440 and 1441 above), in homage of Nawwâb Âṣaf-aldaulah Bahâdur, on fol. 19</span><sup><span>b</span></sup><span>.</span></p> <p><span>5.A tarjî</span><span><span>’</span></span><span>band, a mukhammas, and a short mathnawî, by Mîr </span><span><em>Zain-al</em></span><span><span><em>’</em></span></span><span><em>âbidîn</em></span><span> (see No. 20 below), on fol. 24</span><sup><span>b</span></sup><span>.</span></p> <p><span>6.</span><span><span><span><span><span>مناظر</span></span></span><span><span>ۀ </span></span><span><span><span>سرما و </span></span></span><span><span><span>گ</span></span></span><span><span><span>رما</span></span></span></span></span><span>, a dispute between cold and heat, in prose, on fol. 30</span><sup><span>a</span></sup><span>.</span></p> <p><span>7.Poems, by </span><span><em>Mihrî </em></span><span>(died about A.H. 1130), on fol. 35</span><sup><span>b</span></sup><span>.</span></p> <p><span>8.Rubâ</span><span><span>’</span></span><span>iyyât.</span></p> <p><span>9.On the tobacco-pipe (</span><span><span><span><span><span>تعريف قليان تنباكو</span></span></span></span></span><span>), in prose, on fol. 42</span><sup><span>b</span></sup><span>.</span></p> <p><span>10.Several mukhammasât and other miscellaneous poems, on ff. 48</span><sup><span>b</span></sup><span> and 63</span><sup><span>a</span></sup><span>.</span></p> <p><span>11.Admonitions, by </span><span><span>‘</span></span><span><em>Abdallâh An</em></span><span><em>ṣârî</em></span><span> (</span><span><span><span><span><span>نصائح عبد الله انصارى</span></span></span></span></span><span>), the great mystic Shaikh, who died A.H. 481 (A.D. 1088), see No. 1778 sq. below, in prose, on fol. 68</span><sup><span>b</span></sup><span>. </span></p> <p><span>12.A few poems, by </span><span><em>Ḥ</em></span><span><em>azîn</em></span><span>, on fol. 71</span><sup><span>a</span></sup><span>.</span></p> <p><span>13.Ghazals, by </span><span><em>Shaukat</em></span><span> (died A.H. 1107, see Nos. 1628-1633), </span><span><em>Mihrî</em></span><span>, etc., on fol. 79</span><sup><span>a</span></sup><span>.</span></p> <p><span>14.Historical incidents from Nâdirshâh</span><span><span>’</span></span><span>s time, beginning with A.H. 1149 (A.D. 1736), on fol. 80</span><sup><span>a</span></sup><span>.</span></p> <p><span>15.A </span><span>ḳaṣîdah by </span><span><em>Nâṭiḳ</em></span><span> (</span><span><span><span><span><span>قصيد</span></span></span><span><span>ۀ </span></span><span><span><span>ناطق</span></span></span><span> </span></span></span><span>), and other poetry, on fol. 84</span><sup><span>a</span></sup><span>.</span></p> <p><span>16.</span><span><span><span><span><span>چ</span></span></span><span><span><span>ار اندر </span></span></span><span><span><span>چ</span></span></span><span><span><span>ار</span></span></span></span></span><span>, a prose-piece by </span><span><span><em>‘</em></span></span><span><em>Ubaid Zâkânî</em></span><span> (died A.H. 772), on fol. 89</span><sup><span>a</span></sup><span>, and another </span><span><span><span><span><span>چ</span></span></span><span><span><span>ار در </span></span></span><span><span><span>چ</span></span></span><span><span><span>ار</span></span></span></span></span><span>, likewise in prose, by Maulânâ </span><span><em>Mushf</em></span><span><em>iḳî</em></span><span> (of Bukhârâ, died A.H. 994), on fol. 87</span><sup><span>a</span></sup><span>.</span></p> <p><span>17.Miscellaneous pieces in prose and verse.</span></p> <p><span>18.</span><span><span><span><span><span>قضا و قدر</span></span></span><span> </span></span></span><span>, a mathnawî on predestination, by Mirzâ </span><span><em>Ṭ</em></span><span><em>âhir</em></span><span>, on fol. 117</span><sup><span>b</span></sup><span>.</span></p> <p><span>19.A </span><span>ḳaṣîdah, by Mirzâ </span><span><em>Ṭ</em></span><span><em>âhir</em></span><span>, on fol. 119</span><sup><span>b</span></sup><span>.</span></p> <p><span>20.</span><span>Ḳaṣîdas, by Mîr </span><span><em>Zain-al</em></span><span><span><em>’</em></span></span><span><em>abidîn</em></span><span>, with the takhallu</span><span>ṣ Hijrî, on fol. 133</span><sup><span>b</span></sup><span>.</span></p> <p><span>21.</span><span><span><span><span><span>قضا و قدر</span></span></span></span></span><span>, a second mathnawî of the same title, by </span><span><em>Hijrî</em></span><span>, on fol. 143</span><sup><span>b</span></sup><span>.</span></p> <p><span>22.A short mathnawî</span><span><span><span><span><span>قضا و قدر</span></span></span></span></span><span>, by Mu</span><span>ḥammad </span><span><em>Salîm</em></span><span> (see No. 1558, 5 above), on fol. 148</span><sup><span>b</span></sup><span>.</span></p> <p><span>23.A fourth mathnawî </span><span><span><span><span><span>قضا و قدر</span></span></span></span></span><span>, by </span><span>Ḥ</span><span>akîm </span><span><em>Ruknâ</em></span><span> (see No. 1572 above), on fol. 150</span><sup><span>b</span></sup><span>; a fifth mathnawî of the same title, by Amîrbeg Wâlih, is quoted in the Bodleian Cat., col. 768, e.</span></p> <p><span>24.A mathnawî, by </span><span><em>Mihrî</em></span><span>, entitled </span><span><span><span><span><span>سرا</span></span></span><span><span><span>پ</span></span></span><span><span><span>اى</span></span></span><span> </span></span></span><span>(description of the human figure, see Bodleian Cat., No. 1168), on fol. 153</span><sup><span>b</span></sup><span>.</span></p> <p><span>25.</span><span>Ḳaṣidas, rubâ</span><span><span>’</span></span><span>s, and fards, on fol. 164</span><sup><span>b</span></sup><span>.</span></p> <p><span>It might have been better to page the MS. from the back, as most of the poems are running in that way.</span></p> <p><span>Therefore in using this copy the reader must read backward. A short index of the more prominent pieces of this album is found twice, both on ff. 165</span><sup><span>b</span></sup><span> and 166</span><sup><span>b</span></sup><span>.</span></p> <p><span>No. 454, ff. 166; written in Nasta’lîḳ and Shikasta; size 9¼ in. by 4½ in.</span></p> <p> </p>
Trento 1936 - Building 454
<u>Coordinates</u>: N/A <br><u>Length</u>: 12.97 m<br><u>Width</u>: 14.48 m<br><u>Height</u>: 16.68 m<br><u>Points</u>: 13 <br><u>Vertices</u>: 69 <br><u>Primitives</u>: 23 <br><br><u>Main Files:</u><br><table><tbody><tr><th>Filename</th><th>.glb</th><th>.xml</th><th>.obj</th></tr><tr><td><a href="https://zenodo.org/api/records/12696146/files/building_454.glb/content">building_454.glb</a></td><td><a href="https://zenodo.org/api/records/12696146/files/building_454.glb/content">Link</a></td><td></td><td></td></tr><tr><td><a href="https://zenodo.org/api/records/12696146/files/building_454.obj/content">building_454.obj</a></td><td></td><td></td><td><a href="https://zenodo.org/api/records/12696146/files/building_454.obj/content">Link</a></td></tr><tr><td><a href="https://zenodo.org/api/records/12696146/files/11575244_edm.xml/content">11575244_edm.xml</a></td><td></td><td><a href="https://zenodo.org/api/records/12696146/files/11575244_edm.xml/content">Link</a></td><td></td></tr><tr><td><a href="https://zenodo.org/api/records/12696146/files/11575244_metsmods.xml/content">11575244_metsmods.xml</a></td><td></td><td><a href="https://zenodo.org/api/records/12696146/files/11575244_metsmods.xml/content">Link</a></td><td></td></tr></tbody></table><br><br><u>Thumbnails:</u><br><table><tbody><tr><th>Perspective</th><th>1000x1000</th><th>512x512</th><th>256x256</th><th>128x128</th></tr><tr><td>Perspective 1</td><td><a href="https://zenodo.org/api/records/12696146/files/building_454_perspective_1.png/content">Link</a></td><td><a href="https://zenodo.org/api/records/12696146/files/building_454_perspective_1_512x512.png/content">Link</a></td><td><a href="https://zenodo.org/api/records/12696146/files/building_454_perspective_1_256x256.png/content">Link</a></td><td><a href="https://zenodo.org/api/records/12696146/files/building_454_perspective_1_128x128.png/content">Link</a></td></tr><tr><td>Perspective 2</td><td><a href="https://zenodo.org/api/records/12696146/files/building_454_perspective_2.png/content">Link</a></td><td><a href="https://zenodo.org/api/records/12696146/files/building_454_perspective_2_512x512.png/content">Link</a></td><td><a href="https://zenodo.org/api/records/12696146/files/building_454_perspective_2_256x256.png/content">Link</a></td><td><a href="https://zenodo.org/api/records/12696146/files/building_454_perspective_2_128x128.png/content">Link</a></td></tr><tr><td>Perspective 3</td><td><a href="https://zenodo.org/api/records/12696146/files/building_454_perspective_3.png/content">Link</a></td><td><a href="https://zenodo.org/api/records/12696146/files/building_454_perspective_3_512x512.png/content">Link</a></td><td><a href="https://zenodo.org/api/records/12696146/files/building_454_perspective_3_256x256.png/content">Link</a></td><td><a href="https://zenodo.org/api/records/12696146/files/building_454_perspective_3_128x128.png/content">Link</a></td></tr><tr><td>Perspective 4</td><td><a href="https://zenodo.org/api/records/12696146/files/building_454_perspective_4.png/content">Link</a></td><td><a href="https://zenodo.org/api/records/12696146/files/building_454_perspective_4_512x512.png/content">Link</a></td><td><a href="https://zenodo.org/api/records/12696146/files/building_454_perspective_4_256x256.png/content">Link</a></td><td><a href="https://zenodo.org/api/records/12696146/files/building_454_perspective_4_128x128.png/content">Link</a></td></tr><tr><td>Perspective Top</td><td><a href="https://zenodo.org/api/records/12696146/files/building_454_perspective_top.png/content">Link</a></td><td><a href="https://zenodo.org/api/records/12696146/files/building_454_perspective_top_512x512.png/content">Link</a></td><td><a href="https://zenodo.org/api/records/12696146/files/building_454_perspective_top_256x256.png/content">Link</a></td><td><a href="https://zenodo.org/api/records/12696146/files/building_454_perspective_top_128x128.png/content">Link</a></td></tr></tbody></table><br><br><br><u>Changelog</u>: <br> - v<a href="https://doi.org/10.5281/zenodo.12544232">0.0.2</a>: Thumbnails added, Description updated with Link Tables.<br> - v<a href="https://doi.org/10.5281/zenodo.12696146">0.0.3</a>: Added XMLs for Europeana Data Model (EDM) and MetsMods.<br>
FIGURES 453–454 in Studies on the Australian Muscidae (Diptera). VIII. The genus Lispe Latreille, 1797
FIGURES 453–454. Lispe bengalensis (Robineau-Desvoidy), ♂. 453. Hypopygium, lateral view. 454. Cercal plate, dorsal view. (NSW, Merrimbula.)
finals_2019_07_454
Log and boot files of game 454
FIGURES 449–454 in The morphology and molecular phylogenetics of some marine diatom taxa within the Fragilariaceae, including twenty undescribed species and their relationship to Nanofrustulum, Opephora and Pseudostaurosira
FIGURES 449–454. Scanning electron micrographs of Serratifera takanoi (culture s0308). Figs 449–450. External views, showing narrowly-linear sternum and each stria consisting of a single slightly transapically-elongate areola on both valve face and mantle. Fig. 451. Internal view, showing the absence of rimoportulae. Figs 452–453. Girdle views, showing plain copulae and much wider valvocopulae. Fig. 454. Close up of a girdle view, showing open (indicated by arrowhead) copula.
FIGURES 450–454 in Rearing mining flies (Diptera: Agromyzidae) from host plants as an instrument for associating females with males, with the description of seven new species
FIGURES 450–454. Chromatomyia gentianae Hering; 450: cephalopharyngeal skeleton; 451: frontal view of head; 452: head viewed from the side; 453: oviscape, ventral receptacle and spermatheca proportionally; 454 a–b: spermatheca and ventral receptacle proportionally; a: spermatheca; b: ventral receptacle.
FIGURES 447–454. 447–454. Mallinella zebra, from New Guinea. 447. Male palp, ventral. 448 in Systematics and biogeography of the spider genus Mallinella Strand, 1906, with descriptions of new species and new genera from Southeast Asia (Araneae, Zodariidae) 3369
FIGURES 447–454. 447–454. Mallinella zebra, from New Guinea. 447. Male palp, ventral. 448. TA, retrolateral. 449. Ditto, ventral. 450. Ditto, prolateral. 451. Right spermatheca, dorsal. 452. Ditto, anterior. 453. Left spermatheca, lateral. 454. Anterior portion of left spermatheca, posteriror.
FIGURES 452–454 in Additions to the knowledge on the genus Tiphia Fabricius (Hymenoptera: Tiphiidae: Tiphiinae) from India with the description of ten new species
FIGURES 452–454. Tiphia (Tiphia) pulchaukiae Allen, ♂. 452. Genitalia, ventral view; 453. Genitalia, dorsal view; 454. Genitalia, lateral view.
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Allen Brain Atlas
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OpenNeuro
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