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TABLE 3 in The distribution, specimens and status of Chestnut Owlet Glaucidium (capense) castaneum and Albertine Owlet G. (c.) albertinum
<p>TABLE 3 Details of museum specimens of Albertine Owlet <i>Glaucidium</i> (<i>capense</i>) <i>albertinum</i> and Chestnut Owlet <i>G.</i> (<i>c.</i>) <i>castaneum</i>. Institution acronyms explained in Acknowledgements. M = Male, F = Female.</p><table><tbody><tr><th>Taxon</th><th>Institution</th><th>. no. Reg</th><th>Country</th><th>Region</th><th>Locality</th><th>Mountain range</th><th>Coordinates</th><th>of Elevation Date</th><th>of collection Date</th><th>Collector Sex</th><th>) mm) mm ((Wing Tail</th><th>tail pale. bars No</th><th>pale Predominant of on scapulars colour spots</th><th>on Predominant of spots wing-coverts colour pale</th><th>Notes</th></tr></tbody><tbody><tr><th></th><td>RMCA</td><td>50988</td><td>DR Congo</td><td>N Kivu</td><td>Lundjulu</td><td>West L. Edward</td><td>00°20’S, 28°36’E</td><td>1,120 m</td><td>14/1/50</td><td>Prigogine</td><td>F 131</td><td>72.7</td><td>7 White</td><td>White</td><td>Paratype; bears label with name <i>castaneum</i> 1,2</td></tr><tr><th></th><td>RMCA</td><td>64954</td><td>DR Congo</td><td>N Kivu</td><td>Lundjulu</td><td>West L. Edward</td><td>00°20’S, 28°36’E</td><td>?</td><td>13/1/53</td><td>Schepens</td><td>F 136</td><td>70.8</td><td>8 Buff</td><td>White</td><td>Paratype; bears label with name <i>castaneum</i> 2</td></tr><tr><th></th><td>RMCA</td><td>69589</td><td>Rwanda</td><td>Western Prov.</td><td>Rugege (= Nyungwe)</td><td>Nyungwe)</td><td>02°30’S, 29°09’E</td><td>?</td><td>10/9/53</td><td>Aurélian</td><td>? 129</td><td>69</td><td>8 White</td><td>Buff</td><td>Paratype; bears label with name <i>castaneum</i> 2</td></tr><tr><th><i>albertinum</i></th><td>RMCA</td><td>114546</td><td>DR Congo</td><td>S Kivu</td><td>Musang- akye</td><td>Itombwe</td><td>03°34’S, 28°16’E</td><td>1,690 m</td><td>26/8/66</td><td>Prigogine</td><td>M 130</td><td>68.8</td><td>6 Buff and white</td><td>Buff and white</td><td>Holotype; bears label with name <i>castaneum</i> 3</td></tr><tr><th></th><td>RBINS</td><td>66893</td><td>DR Congo</td><td>S Kivu</td><td>Munga</td><td>Itombwe</td><td>03°35’S, 28°13’E</td><td>?</td><td>26/6/81</td><td>Prigogine</td><td>M 124</td><td>64.7</td><td>7 Buff</td><td>Buff</td><td></td></tr><tr><th></th><td>RBINS</td><td>69998</td><td>DR Congo</td><td>S Kivu</td><td>Munga</td><td>Itombwe</td><td>03°35’S, 28°13’E</td><td>1,960 m</td><td>18/8/87</td><td>Prigogine</td><td>F 132</td><td>?</td><td>? Buff</td><td>Buff</td><td>Tail damaged</td></tr><tr><th></th><td>RBINS</td><td>70229</td><td>DR Congo</td><td>S Kivu</td><td>Munga</td><td>Itombwe</td><td>03°35’S, 28°13’E</td><td>1,870 m</td><td>8/8/87</td><td>Prigogine</td><td>M 126</td><td>70.7</td><td>7 Buff</td><td>Buff</td><td></td></tr><tr><th></th><td>ZMB</td><td>5094</td><td>DR Congo</td><td>N Kivu, Semliki</td><td>Andundi</td><td>-</td><td>00°50’N, 29°54’E</td><td>710 m</td><td>22/12/ 1891</td><td>Stuhlmann</td><td>M 131</td><td>79</td><td>10 White</td><td>White</td><td>Holotype. Specimen examined and measured by N. J. Collar</td></tr><tr><th><i>castaneum</i></th><td>LACM</td><td>70119</td><td>Uganda</td><td>Bwamba</td><td>Ntandi</td><td>-</td><td>00 30 ° ° 49 09 ’ ’ N E,</td><td>700 2,300 m ft (as.)</td><td>as.) 8/12/68</td><td>Glen</td><td>F 130</td><td>76</td><td>10 White</td><td>White</td><td>and Davies Specimen measured examined by G.</td></tr><tr><th></th><td>NHMUK</td><td>1980.20.</td><td>.1 Uganda</td><td>Bwamba</td><td>-</td><td>-</td><td>-</td><td>915 m (as 3,000 ft.)</td><td>as 17/9/58.)</td><td>?</td><td>M 132</td><td>83.8</td><td>11 White</td><td>White</td><td>ex Coryndon Mus, Nairobi (B4385)</td></tr><tr><th></th><td>NMK</td><td>B4386</td><td>Uganda</td><td>Bwamba</td><td>Ntotoro</td><td>-</td><td>00°48’N, 30°07’E</td><td>730 m (as 2,400 ft.)</td><td>as 30/5/56.)</td><td>Mitton</td><td>M 134 imm?</td><td>81</td><td>10 White</td><td>White</td><td>Specimen examined and measured by P. Njoroge and A. S. Kennedy</td></tr></tbody></table><p><sup>1</sup> Schouteden (1950) gave a redescription of <i>castaneum</i> based on this specimen (see text).</p><p><sup>2</sup> Appears as <i>castaneum</i> in Schouteden (1968).</p><p><sup>3</sup> Appears as <i>castaneum</i> in Schouteden (1966).</p><p><sup>5</sup> Coordinates given are for Kamiranzovu Swamp.</p>
TABLE 1 in The distribution, specimens and status of Chestnut Owlet Glaucidium (capense) castaneum and Albertine Owlet G. (c.) albertinum
<p>TABLE 1 Recent taxonomic treatments of the African Barred Owlet <i>Glaucidium capense</i> complex.</p><table><tbody><tr><th>Source</th><th>Genus</th><th>Species</th><th>Subspecies</th></tr></tbody><tbody><tr><th>Kemp (1988)</th><td>Glaucidium</td><td>capense</td><td></td></tr><tr><th>Gill <i>et al</i>. (2022)</th><td></td><td></td><td><i>ngamiense</i></td></tr><tr><th></th><td></td><td></td><td><i>scheffleri</i></td></tr><tr><th></th><td></td><td></td><td><i>castaneum</i></td></tr><tr><th></th><td></td><td></td><td><i>etchecopari</i></td></tr><tr><th></th><td></td><td><i>albertinum</i></td><td></td></tr><tr><th>Holt <i>et al</i>. (1999, 2020)</th><td>Glaucidium</td><td>capense</td><td></td></tr><tr><th>Clements <i>et al.</i> (2021)</th><td></td><td></td><td><i>ngamiense</i></td></tr><tr><th></th><td></td><td></td><td><i>scheffleri</i></td></tr><tr><th></th><td></td><td><i>castaneum</i></td><td></td></tr><tr><th></th><td></td><td></td><td><i>etchecopari</i></td></tr><tr><th></th><td></td><td><i>albertinum</i></td><td></td></tr><tr><th>Dickinson & Remsen (2013)</th><td>Glaucidium</td><td>capense</td><td></td></tr><tr><th></th><td></td><td></td><td><i>ngamiense</i></td></tr><tr><th></th><td></td><td></td><td><i>scheffleri</i></td></tr><tr><th></th><td></td><td></td><td><i>castaneum</i></td></tr><tr><th></th><td></td><td></td><td><i>etchecopari</i></td></tr><tr><th></th><td></td><td></td><td><i>albertinum</i></td></tr><tr><th>König <i>et al</i>. (1999)</th><td>Glaucidium</td><td>capense</td><td></td></tr><tr><th>del Hoyo & Collar (2014)</th><td></td><td></td><td><i>ngamiense</i></td></tr><tr><th>BirdLife International (2022a,b)*</th><td></td><td></td><td><i>scheffleri</i></td></tr><tr><th>Holt <i>et al</i>. (2016)</th><td></td><td></td><td><i>etchecopari</i></td></tr><tr><th></th><td></td><td><i>castaneum</i></td><td></td></tr><tr><th></th><td></td><td><i>albertinum</i></td><td></td></tr><tr><th>König <i>et al</i>. (2008)</th><td>Taenioglaux</td><td>capense</td><td></td></tr><tr><th>Mikkola (2013)</th><td></td><td></td><td><i>ngamiense</i></td></tr><tr><th></th><td></td><td></td><td><i>scheffleri</i></td></tr><tr><th></th><td></td><td><i>castanea</i></td><td></td></tr><tr><th></th><td></td><td><i>etchecopari</i></td><td></td></tr><tr><th></th><td></td><td><i>albertina</i></td><td></td></tr></tbody></table><p>All sources treat races <i>robertsi</i> and <i>clanceyi</i> as synonyms of <i>ngamiense</i>, explicitly or otherwise.</p><p>*Treatment of <i>etchecopari</i> confused: listed under both <i>castaneum</i> and nominate.</p>
Table 1 in Revision of northeast Pacific Paleogene cypraeoidean gastropods, including recognition of three new species: implications for paleobiogeographic distribution and faunal turnover
<p><b>Table 1.</b> Paleogene cypraeoideans from NEP, with author(s), families, subfamilies, geographic distribution, and stage range. Taxa arranged following Lorenz (2017) and Fehse (2021) and listed alphabetically under each genus. Van Is=Vancouver Island, British Columbia, WA=Washington, OR=Oregon, CA=California, BCS Méx= Baja California Sur, México. No=North, So=South, mid=middle, n. comb.=new combination, n. sp.=new species, sp.=species.</p><table><tbody><tr><th>TAXON</th><th><b>LOCATION</b></th><th>NEP "STAGE"</th><th><b>STANDARD STAGE</b></th></tr><tr><th><b>CYPRAEIDAE</b></th></tr></tbody><tbody><tr><th><i>Nucleolaria cowlitziana</i> Groves, 1994</th><td>WA</td><td>upper "Tejon"</td><td>upper Bartonian</td></tr><tr><th><i>Propustularia kemperae</i> (Nelson, 1925)</th><td>So CA</td><td>"Martinez"</td><td>Selandian</td></tr><tr><th><i>Subepona goedertorum</i> (Groves and Squires, 1995)</th><td>WA, So CA</td><td>"Capay" to "Domengine"</td><td>mid to up Ypresian</td></tr><tr><th><i>Subepona leahae</i> Squires and Groves, n. sp.</th><td>So CA</td><td>"Domengine"</td><td>up. Ypres.-low. Lut.</td></tr><tr><th><i>Bernaya grovesi</i> Squires and Demetrion, 1992</th><td>WA?, BC Méx</td><td>"Capay"</td><td>middle Ypresian</td></tr><tr><th><i>Bernaya kaylinae</i> Squires and Groves, n. sp.</th><td>So CA</td><td>"Domengine"</td><td>up. Ypres.-low. Lut.</td></tr><tr><th><i>Bernaya squiresi</i> Groves, 2011</th><td>WA</td><td>"Capay"</td><td>middle Ypresian</td></tr><tr><th><i>Bernaya</i> sp.</th><td>No CA</td><td>"Martinez"</td><td>Thanetian</td></tr><tr><th><i>Protocypraea</i>? <i>simiensis</i> (Nelson, 1925) n. comb.</th><td>So CA</td><td>"Martinez"</td><td>Thanetian</td></tr><tr><th><i>Protocypraea</i>? sp. 1</th><td>Van Is</td><td>"Martinez"?</td><td>Thanetian?</td></tr><tr><th><i>Protocypraea</i>? sp. 2</th><td>No CA</td><td>"Martinez"</td><td>Thanetian</td></tr><tr><th><i>Gisortia clarki</i> Ingram, 1940</th><td>CA, BCS Méx?</td><td>"Capay"</td><td>middle Ypresian</td></tr><tr><th><i>Gisortia</i> sp.</th><td>So CA</td><td>"Capay"</td><td>middle Ypresian</td></tr><tr><th>Cypraeidae, gen. and sp. indeterminate</th><td>Mid CA</td><td>"Martinez"</td><td>Thanetian</td></tr><tr><th><b>EOCYPRAEIDAE</b></th></tr><tr><th><i>Eocypraea batequensis</i> Groves, 2011</th><td>BCS Méx</td><td>"Capay"</td><td>middle Ypresian</td></tr><tr><th><i>Eocypraea crescentensis</i> Groves, 2011</th><td>WA</td><td>"Capay"</td><td>middle Ypresian</td></tr><tr><th><i>Eocypraea jimgoerderti</i> Groves, 2011</th><td>WA</td><td>"Trans." to "Tejon"</td><td>middle Lutetian</td></tr><tr><th><i>Eocypraea judithsmithae</i> Squires and Groves, n. sp.</th><td>So to mid CA</td><td>"Domengine."</td><td>up. Ypres.-low. Lut.</td></tr><tr><th><i>Eocypraea novasumma</i> (Nelson, 1925)</th><td>So CA, BC Méx</td><td>"Martinez"</td><td>Selandian</td></tr><tr><th><i>Eocypraea takeosusukii</i> Groves, 2011</th><td>No CA</td><td>"Martinez"</td><td>Thanetian</td></tr><tr><th><i>Eocypraea</i> sp. cf. <i>E. inflata</i> (Lamarck, 1802)</th><td>So CA</td><td>"Domengine"</td><td>upper Ypresian</td></tr><tr><th><i>Eocypraea</i> sp.</th><td>Mid CA</td><td>"Martinez"</td><td>Thanetian</td></tr><tr><th><i>Grovesia castacensis</i> (Stewart, 1926 [1927]) n. comb.</th><td>WA, So CA</td><td>mid "Tejon" to Galvinian</td><td>Barton.-Priabonian</td></tr><tr><th><i>Grovesia mathewsonii</i> (Gabb, 1869)</th><td>WA, OR, So CA</td><td>"Domeng." to Galvinian</td><td>up. Ypres.-Priabonian</td></tr><tr><th><i>Luponovula maniobraensis</i> (Squires & Advocate, 1986) n. comb.</th><td>So CA</td><td>"Capay"</td><td>middle Ypresian</td></tr><tr><th><b>PEDICULARIINAE</b></th></tr><tr><th><i>Cypraedia</i> sp.</th><td>BCS Méx</td><td>"Capay"</td><td>middle Ypresian</td></tr><tr><th><i>Cypraeogemmula warnerae</i> Effinger, 1938</th><td>WA</td><td>"Capay" to Galvinian</td><td>up. Ypres.-Priabon.</td></tr><tr><th><b>ERATOIDAE</b></th></tr><tr><th><i>Eratotrivia crescentensis</i> (Weaver and Palmer, 1922)</th><td>WA</td><td>"Capay"</td><td>middle Ypresian</td></tr><tr><th><i>NOMINA DUBIA</i></th></tr><tr><th><i>"</i> <i>Bernaya" fresnoensis</i> (Anderson, 1905)</th><td>mid CA</td><td>"Domengine"</td><td>up. Ypres.-low. Lut.</td></tr><tr><th><i>"</i> <i>Eocypraea" bayerquei</i> (Gabb, 1864)</th><td>No CA</td><td>Martinez?</td><td>Paleocene</td></tr><tr><th>" <i>Sphaerocypraea" martini</i> (Dickerson, 1914)</th><td>No CA</td><td>"Martinez"</td><td>Thanetian</td></tr><tr><th>" <i>Sulcocypraea" oakvillensis</i> (Van Winkle, 1918)</th><td>WA</td><td>lower Galvinian</td><td>lower Priabonian</td></tr></tbody></table>
Table 2 in Description Of The Nematode Dirofilaria Repens (Nematoda, Onchocercidae) Parasitic In Dogs In Ukraine
<p><b>Table 2. Metric parameters of</b> ♀ <i>Dirofilaria repens</i>, n = 8 (М ± SD, min–max)</p><table><tbody><tr><th>Parameter</th><th>Present study</th><th>Railliet & Henry, 1911</th><th>Lent & Freitas, 1937</th><th>Sonin, 1975</th><th>Demiaszkiewicz et al., 2011</th><th>Kravchenko & Itin, 2012</th><th>Baisarova, 2021</th></tr></tbody><tbody><tr><th>Body length, mm</th><td>17.2 ± 0.7 16.2–18.1</td><td>10–17</td><td>14–15</td><td>10.6</td><td>15.4 14.7–16.1</td><td>9.8–17.4</td><td>14.5 9.7–17.6</td></tr><tr><th>Body width, μm</th><td>565.2 ± 19.8 541.3–597.9</td><td>450–650</td><td>447–552</td><td>530</td><td>532 490–570</td><td>800–1000</td><td>1140 900–1700</td></tr><tr><th>Body width in the region of, μm:</th></tr><tr><th>nerve ring</th><td>316.1 ± 19.1 294.1–342.6</td><td>–</td><td>–</td><td>–</td><td>290 283–298</td><td>–</td><td>–</td></tr><tr><th>transition from esophagus to intestine vulva</th><td>452.2 ± 26.5</td><td>–</td><td>–</td><td></td><td>417</td><td></td><td>–</td></tr><tr><td>415.6–486.1</td><td></td><td></td><td>–</td><td>411–422</td><td></td><td></td></tr><tr><td>517.1 ± 31.4 463.4–556.1</td><td>–</td><td>–</td><td>–</td><td>503 499–508</td><td>–</td><td>–</td></tr><tr><th>anus</th><td>149.9 ± 9.6 132.2–162.5</td><td>–</td><td>–</td><td>–</td><td>145 128–169</td><td>–</td><td>–</td></tr><tr><th>Esophagus length, mm</th><td>912.7 ± 48.7 831.7–964.2</td><td>–</td><td>1050– 1053</td><td>910</td><td>966 915–1037</td><td>1110</td><td>–</td></tr><tr><th>Esophagus width in the region of, μm:</th></tr><tr><th>nerve ring</th><td>34.6 ± 4.0 30.5–40.2</td><td>–</td><td>–</td><td>–</td><td>–</td><td>–</td><td>–</td></tr><tr><th>middle part</th><td>53.8 ± 3.2 50.2–60.1</td><td>–</td><td>49–54</td><td>–</td><td>–</td><td>–</td><td>–</td></tr><tr><th>the widest part</th><td>71.4 ± 2.8 68.2–77.2</td><td>–</td><td>–</td><td>–</td><td>89 77–102</td><td>–</td><td>–</td></tr><tr><th>Thickness of the cuticle in the region of mouth opening, μm</th><td>10.9 ± 0.8 9.2–11.8</td><td>–</td><td>–</td><td>–</td><td>–</td><td>–</td><td>–</td></tr><tr><th>Thickness of the cuticle in the region of vulva, μm</th><td>12.3 ± 0.77 11.1–13.4</td><td>–</td><td>–</td><td>–</td><td>–</td><td>–</td><td>–</td></tr><tr><th>Distance from anterior end to nerve ring, μm</th><td>258.1 ± 17.8 242.0–296.2</td><td>–</td><td>304–368</td><td>270</td><td>295 291–298</td><td>–</td><td>–</td></tr><tr><th>Distance from anterior end to vulva, mm</th><td>1.4 ± 0.1 1.3–1.6</td><td>1.5–1.9</td><td>1.84–1.92</td><td>–</td><td>1.55 1.45–1.63</td><td>1.6–2.7</td><td>–</td></tr><tr><th>Distance from the vulva to the nerve ring, mm</th><td>1.2 ± 0.1 1.1–1.3</td><td>–</td><td>–</td><td>–</td><td>–</td><td>–</td><td>–</td></tr><tr><th>Distance from the vulva to the tail end, mm</th><td>15.7 ± 0.7 14.7–16.7</td><td>–</td><td>–</td><td>–</td><td>–</td><td>–</td><td>–</td></tr><tr><th>Distance from the vulva to the anus, mm</th><td>15.7 ± 0.7 14.6–16.6</td><td>–</td><td>–</td><td>–</td><td>–</td><td>–</td><td>–</td></tr><tr><th>Tail length, μm</th><td>81.1 ± 8.6 70.4–92.2</td><td>105–126</td><td>–</td><td>90</td><td>85 73–102</td><td>–</td><td>–</td></tr><tr><th>MicroFIlaria length, μm</th><td>208.7 ± 10.2 193.4–224.9</td><td>300–360</td><td>–</td><td>300–360</td><td>329 296–362</td><td>–</td><td>–</td></tr><tr><th>MicroFIlaria width, μm</th><td>5.8 ± 0.4 5.3–6.4</td><td>6–8</td><td>–</td><td>6–8</td><td>7 5–8</td><td>–</td><td>–</td></tr></tbody></table><p>N o t e. Рarameters were not deFIned.</p>
Table 1 in Description Of The Nematode Dirofilaria Repens (Nematoda, Onchocercidae) Parasitic In Dogs In Ukraine
<p><b>Table 1. Metric parameters of</b> Ơ <i>Dirofilaria repens</i>, n = 5 (М ± SD, min–max)</p><table><tbody><tr><th>Parameter</th><th>Present study</th><th>Railliet & Henry, 1911</th><th>Lent & Freitas, 1937</th><th>Sonin, 1975</th><th>Demiaszkiewicz et al., 2011</th><th>Kravchenko & 2012</th><th>Baisarova, 2021</th></tr></tbody><tbody><tr><th>Body length, mm</th><td>57.1 ± 6.5</td><td>48–70</td><td>27.75</td><td>51</td><td>63</td><td>58–71</td><td>87.3 ± 9.6</td></tr><tr><td>48.0–66.5</td><td></td><td></td><td></td><td>56–70</td><td></td><td>71–110</td></tr><tr><th>Body width, μm</th><td>406.7 ± 16.6</td><td>370–450</td><td>–</td><td>320</td><td>325</td><td>800–1000</td><td>1100 ± 0.4</td></tr><tr><td>390.1–432.4</td><td></td><td></td><td></td><td>298–379</td><td></td><td>900–1700</td></tr><tr><th>Body width in the region of, μm:</th></tr><tr><th>nerve ring</th><td>238.5 ± 11.9</td><td>–</td><td>–</td><td>–</td><td>–</td><td>–</td><td>–</td></tr><tr><td>224.1–251.6</td><td></td><td></td><td></td><td></td><td></td><td></td></tr><tr><th>junction between esophagus and intestine – cloaca</th><td>382.7 ± 16.3</td><td>–</td><td>–</td><td>–</td><td>293</td><td>–</td><td>–</td></tr><tr><td>359.4–402.1</td><td></td><td></td><td></td><td>269–317</td><td></td><td></td></tr><tr><td>118.8 ± 15.0</td><td>–</td><td>–</td><td>–</td><td>99</td><td>–</td><td>–</td></tr><tr><td>98.6–137.2</td><td></td><td></td><td></td><td>95–104</td><td></td><td></td></tr><tr><th>Esophagus length, mm</th><td>761.9 ± 39.2</td><td>–</td><td>–</td><td>750</td><td>713</td><td>до 1400</td><td>–</td></tr><tr><td>698.2–797.9</td><td></td><td></td><td></td><td>696–730</td><td></td><td></td></tr><tr><th>Esophagus width in the region of, μm:</th></tr><tr><th>nerve ring</th><td>42.2 ± 2.1</td><td>–</td><td>–</td><td>–</td><td>–</td><td>–</td><td>–</td></tr><tr><td>39.8–44.9</td><td></td><td></td><td></td><td></td><td></td><td></td></tr><tr><th>middle part</th><td>56.3 ± 4.6</td><td>–</td><td>–</td><td>–</td><td>–</td><td>–</td><td>–</td></tr><tr><td>48.2–59.2</td><td></td><td></td><td></td><td></td><td></td><td></td></tr><tr><th>the widest part</th><td>62.1 ± 2.1</td><td>–</td><td>–</td><td></td><td>40</td><td>–</td><td>–</td></tr><tr><td>59.8–64.9</td><td></td><td></td><td></td><td>36–45</td><td></td><td></td></tr><tr><th>Thickness of the cuticle in the region of mouth</th><td>9.2 ± 0.8</td><td>–</td><td>–</td><td>–</td><td>–</td><td>–</td><td>–</td></tr><tr><td>(8.2–10.4)</td><td></td><td></td><td></td><td></td><td></td><td></td></tr><tr><th>opening, μm</th></tr><tr><th>Distance from anterior end to nerve ring, μm</th><td>227.9 ± 10.5</td><td>–</td><td>–</td><td>240</td><td>162</td><td>–</td><td>–</td></tr><tr><td>211.8–241.1</td><td></td><td></td><td></td><td>160–165</td><td></td><td></td></tr><tr><th>Distance from anterior end to cloaca, mm</th><td>57.1 ± 6.8</td><td>–</td><td>–</td><td>–</td><td>–</td><td>–</td><td>–</td></tr><tr><td>47.9–66.4</td><td></td><td></td><td></td><td></td><td></td><td></td></tr><tr><th>Distance from the nerve ring to cloaca, mm</th><td>56.8 ± 6.8</td><td>–</td><td>–</td><td>–</td><td>–</td><td>–</td><td>–</td></tr><tr><td>47.6–66.2</td><td></td><td></td><td></td><td></td><td></td><td></td></tr><tr><th>Tail length, μm</th><td>72.9 ± 7.1</td><td>66–85</td><td>72</td><td>80</td><td>77</td><td>–</td><td>–</td></tr><tr><td>62.2–80.1</td><td></td><td></td><td></td><td>73–82</td><td></td><td></td></tr><tr><th>Long spicule, μm:</th></tr><tr><th>length</th><td>432.9 ± 24.0</td><td>465–590</td><td>430</td><td>300</td><td>541</td><td>160–270</td><td>–</td></tr><tr><td>392.1–450.9</td><td></td><td></td><td></td><td>537–547</td><td></td><td></td></tr><tr><th>width of proximal end</th><td>37.2 ± 1.8</td><td>–</td><td>–</td><td>–</td><td>22</td><td>–</td><td>–</td></tr><tr><td>35.2 – 39.9</td><td></td><td></td><td></td><td>20–27</td><td></td><td></td></tr><tr><th>width of distal end</th><td>3.1 ± 0.2</td><td>–</td><td>–</td><td>–</td><td>–</td><td>–</td><td>–</td></tr><tr><td>2.9–3.3</td><td></td><td></td><td></td><td></td><td></td><td></td></tr><tr><th>width in middle part</th><td>18.2 ± 0.7</td><td>–</td><td>–</td><td>–</td><td>–</td><td>–</td><td>–</td></tr><tr><td>17.1–18.9</td><td></td><td></td><td></td><td></td><td></td><td></td></tr><tr><th>width of widening part</th><td>25.2 ± 1.4</td><td>–</td><td>–</td><td>–</td><td>–</td><td>–</td><td>–</td></tr><tr><td>23.6–27.1</td><td></td><td></td><td></td><td></td><td></td><td></td></tr><tr><th>– handle length</th><td>250.3 ± 10.7</td><td>–</td><td>–</td><td>–</td><td>–</td><td>–</td><td>–</td></tr><tr><td>237.1–261.3</td><td></td><td></td><td></td><td></td><td></td><td></td></tr><tr><th>– lamina length</th><td>182.5 ± 32.1</td><td>–</td><td>–</td><td>–</td><td>–</td><td>–</td><td>–</td></tr><tr><td>130.7–209.5</td><td></td><td></td><td></td><td></td><td></td><td></td></tr><tr><th>Ratio of handle to lamina length</th><td>1.42:1</td><td>–</td><td>–</td><td>–</td><td>–</td><td>–</td><td>–</td></tr><tr><td>1.15:1–2.00:1</td><td></td><td></td><td></td><td></td><td></td><td></td></tr><tr><th>Short spicule, μm:</th></tr><tr><th>length</th><td>178.7 ± 9.4</td><td>185–206</td><td>175</td><td>130</td><td>185</td><td>180–200</td><td>–</td></tr><tr><td>170.9–194.1</td><td></td><td></td><td></td><td>181–189</td><td></td><td></td></tr><tr><th>proximal end width</th><td>21.9 ± 4.0</td><td>–</td><td>–</td><td>–</td><td>27</td><td>–</td><td>–</td></tr><tr><td>14.9–25.1</td><td></td><td></td><td></td><td>23–35</td><td></td><td></td></tr><tr><th>distal end width</th><td>14.4 ± 0.7</td><td>–</td><td>–</td><td>–</td><td>–</td><td>–</td><td>–</td></tr><tr><td>13.2–15.1</td><td></td><td></td><td></td><td></td><td></td><td></td></tr><tr><th>middle part width</th><td>31.4 ± 1.2</td><td>–</td><td>–</td><td>–</td><td>–</td><td>–</td><td>–</td></tr><tr><td>30.1–33.1</td><td></td><td></td><td></td><td></td><td></td><td></td></tr><tr><th>Ratio of spicules’ lengths</th><td>2.43:1</td><td>2.5: 1</td><td>2.5: 1</td><td>–</td><td>–</td><td>–</td><td>–</td></tr><tr><td>2.23:1–2.58:1</td><td></td><td></td><td></td><td></td><td></td><td></td></tr></tbody></table><p>N o t e. Рarameters were not deFIned.</p>
Table 1 in A New Record And А Taxonomic Review With Checklist Of Wolf Spiders (Araneae, Lycosidae) From Iraq
<p>Table 1. List of Lycosidae species currently known in Iraq</p><table><tbody><tr><th>No.</th><th>Species</th><th>Previous and present records in Iraq</th><th>Distribution</th></tr></tbody><tbody><tr><th>1</th><td><i>Acantholycosa lignaria</i> (Clerck, 1757)</td><td>Basrah (Najim & Al-Hadlag, 2022)</td><td>Europe, Russia (Europe to Far East), China</td></tr><tr><th>2</th><td><i>Alopecosa albofasciata</i> (Brullé, 1832)</td><td>Dohuk (Fomichev et al., 2018), Basrah (Najim & Al-Hadlag, 2022), Thi Qar (present study)</td><td>Mediterranean to Central Asia</td></tr><tr><th>3</th><td><i>Arctosa cinerea</i> (Fabricius, 1777)</td><td>Baghdad, Salaheddin (Riemoser, 1913)</td><td>Europe, North Africa, Congo, Caucasus, Russia (Europe to Far East), Middle East, Kazakhstan, China, Korea, Japan</td></tr><tr><th>4</th><td><i>Arctosa leopardus</i> (Sundevall,1833)</td><td>Basrah (Najim & Al-Hadlag, 2022)</td><td>Europe, Turkey, Caucasus, Russia (Europe to South Siberia), Iran, Central Asia</td></tr><tr><th>5</th><td><i>Arctosa tbilisiensis</i> Mcheidze, 1946</td><td>Dohuk (Fomichev et al., 2018), Basrah (Najim & Al-Hadlag, 2022), Thi Qar & Basrah (present study)</td><td>Greece, Bulgaria, Turkey, Caucasus (Russia, Georgia, Azerbaijan), Iraq, Iran, Afghanistan</td></tr><tr><th>6</th><td><i>Evippa amitaii</i> Armiach Steinpress, Alderweireldt, Cohen, Chipman & Gavish-Regev, 2021</td><td>Najaf (Zamani and Marusik, 2022), Thi Qar (present study)</td><td>Israel, Iraq, Iran</td></tr><tr><th>7</th><td><i>Hippasa partita</i> (O. Pickard-Cambridge, 1876)</td><td>Basrah (Najim & Al-Hadlag, 2022) as <i>Hippasa cinerea</i> Simon, 1898</td><td>Africa</td></tr><tr><th>8</th><td><i>Hippasa deserticola</i> Simon, 1889</td><td>Basrah (Najim, Seyyar & Demir, 2019)</td><td>Egypt, Saudi Arabia, Iraq, Iran, Uzbekistan, Turkmenistan, Tajikistan, Afghanistan, Pakistan, India, Bangladesh</td></tr><tr><th>9</th><td><i>Hogna effera</i> (O. Pickard-Cambridge, 1872)</td><td>Thi Qar (Al-Khazali, 2020), Najaf (Zamani and Marusik, 2022) Thi Qar (present study)</td><td>Greece (Crete), Cyprus, Turkey, Egypt, Israel, Lebanon, Syria, Yemen (Sokotra), Saudi Arabia, United Arab Emirates, Iraq, Iran</td></tr><tr><th>10</th><td><i>Pardosa aenigmatica</i> Tongiorgi, 1966</td><td>Dohuk (Fomichev et al., 2018)</td><td>Italy, Turkey, Azerbaijan, Israel, Iraq, Iran</td></tr><tr><th>11</th><td><i>Pardosa amentata</i> (Clerck, 1757)</td><td>Karbala (Baker & Ali, 2020)</td><td>Europe, Turkey, Caucasus, Russia (Europe to South Siberia), Kazakhstan?</td></tr><tr><th>12</th><td><i>Pardosa bifasciata</i> (C. L. Koch, 1834)</td><td>Basrah (Najim and Al-Hadlag, 2022)</td><td>Europe, Turkey, Caucasus, Russia (Europe to South Siberia), Kazakhstan, Nepal, China</td></tr><tr><th>13</th><td><i>Pardosa cribrata</i> Simon, 1876</td><td>Dohuk (Fomichev et al., 2018)</td><td>Southern Europe, Algeria, Iraq</td></tr><tr><th>14</th><td><i>Pardosa morosa</i> (L. Koch, 1870)</td><td>Dohuk (Fomichev et al., 2018)</td><td>Europe to Central Asia, Iraq, Iran</td></tr><tr><th>15</th><td><i>Pardosa proxima</i> (C. L. Koch, 1847)</td><td>Baghdad, Thi Qar (Riemoser, 1913)</td><td>Macaronesia, northern Africa, Europe, Caucasus, Russia (Europe to Far East), Kazakhstan, Iran, Central Asia, China</td></tr><tr><th>16</th><td><i>Pardosa roscai</i> (Roewer, 1951)</td><td>Thi Qar (present study)</td><td>Bulgaria, Romania, Cyprus, Turkey, Iran</td></tr><tr><th>17</th><td><i>Wadicosa fidelis</i> (O. Pickard-Cambridge, 1872)</td><td>Salahaddin (Riemoser, 1913), Baghdad, Karbala (Baker & Ali, 2020), Basrah (Najim and Al-Hadlag, 2022), Thi Qar & Basrah (present study)</td><td>Macaronesia, North Africa, Southern Europe, Caucasus, Middle East, Central Asia, China, Japan, Pakistan, India, Bhutan, Bangladesh, Philippines, Indonesia</td></tr></tbody></table>
Table 2 in New observations of Papulifères, putative ciliate cysts, from the plankton of the Chukchi Sea (Western Arctic Ocean) in August of 2023
<p><b>Table 2</b>. The morphological characteristics and sample data (stations and nominal concentrations) of the apparently new Papulifère forms found in the samples taken in 2023. LD refers to longest dimension of the main body (excluding filaments if present). In Morphology Notes, ‘Differs from fig. x.x’ refer to the figures in Dolan et al. 2023; figures are also given in the Supplementary File.</p><table><thead><tr><th>Cyst type</th><th>Morphology Notes</th><th><b>Station</b> (s) found [conc. #L-1] <i># specimens</i></th></tr></thead><tbody><tr><th>2A</th><td><i>Fusopsis sp.,</i> spindle smooth surface/LD 115 µm Differs from fig 6j in larger size and absence of a posterior knob</td><td><b>37</b> [0.01] <i>2</i></td></tr><tr><th>2B</th><td><i>Fusopsis sp</i>., spindle smooth surface/LD 75–85/µm short (3–5µm) filaments Differs from figs 6 f,g,l in larger size and spine lengths & numbers</td><td><b>40</b> [.007] <i>1</i></td></tr><tr><th>2C</th><td><i>Fusopsis sp</i>., spindle smooth surface/LD 50µm/5 long, 25 µm filaments Differs from fig 6c in overall shape small size</td><td><b>54</b> [0.016] <i>1</i></td></tr><tr><th>2D</th><td><i>Fusopsis sp</i>., spindle smooth surface/LD 50 µm/ 3 pairs 30 µm filaments Differs from fig 6g,1 in larger size and filaments in pairs</td><td><b>59</b> [0.007] <i>1</i></td></tr><tr><th>2E</th><td><i>Sphaeropsis sp</i>., oblong smooth surface/ LD 35µm/ 3 10 µm filaments Differs from fig 7f in smaller size and smooth surface</td><td><b>10</b> [0.04] <i>1</i></td></tr><tr><th>2F</th><td><i>Sphaeropsis sp.,</i> oblong smooth surface/LD 70 µm Differs from fig 7h in smaller size and ovoid shape</td><td><b>10</b> [0.01] <i>4</i></td></tr><tr><th>2G</th><td><i>Sphaeropsis sp.,</i> spherical smooth surface/LD 80 µm Differs from fig 7h in smaller size</td><td><b>39</b> [0.08] <i>2</i>, <b>60</b> [0.08] <i>1</i></td></tr><tr><th>2H</th><td><i>Sphaeropsis sp.,</i> oblong smooth surface/LD 105 µm Differs in overall size and shape from other Sphaeropsis in fig7</td><td><b>40</b> [0.004] 1</td></tr></tbody></table>
Table 1. Summary data for the 36 in New observations of Papulifères, putative ciliate cysts, from the plankton of the Chukchi Sea (Western Arctic Ocean) in August of 2023
<p><b>Table 1</b>. Summary data for the 36 stations sampled in 2023. Depth given is the vertical extent of the plankton net tow from the depth indicated to the surface. Chlorophyll <i>a</i> concentration (Chl a) is average integrated concentration (µg L-1) throughout the water column from the surface to approximately the depth of the plankton net tow. Cyst types found refer to the new forms shown in here in Figure 2 (2A-2H), and in the Figures 6 (6A, 6E, 6D) and 7 (7A, 7G, 7H, 7I, 7J, 7K, 7N) in Dolan et al. (2023). For convenience, the supplementary file contains images of all now known Chukchi Sea Papulifère forms in two plates, one showing the 16 spindle-shaped <i>Fusopsis</i> forms, another showing the 18 the spherical and oblong <i>Sphaeropsi</i> s forms.</p><table><thead><tr><th><b>St #</b></th><th><b>Date Aug 2023</b></th><th><b>lat (N°)</b></th><th><b>long (W°)</b></th><th>Tow Depth (m)</th><th><b>Station Depth</b></th><th><b>Chl a</b></th><th><b>SST (C°)</b></th><th><b>cyst types found</b></th></tr></thead><tbody><tr><th>1</th><td>3</td><td>65,17</td><td>–168,69</td><td>45</td><td>55</td><td>1,45</td><td>9,9</td><td>Ø</td></tr><tr><th>2</th><td>3</td><td>66,63</td><td>–168,69</td><td>35</td><td>45</td><td>7,47</td><td>7,8</td><td>Ø</td></tr><tr><th>3</th><td>3</td><td>67,67</td><td>–168,96</td><td>45</td><td>55</td><td>9,92</td><td>6</td><td>Ø</td></tr><tr><th>8</th><td>4</td><td>68,24</td><td>–167,12</td><td>38</td><td>48</td><td>0,74</td><td>12,6</td><td>Ø</td></tr><tr><th>9</th><td>4</td><td>69,17</td><td>–168,67</td><td>43</td><td>53</td><td>0,58</td><td>9,9</td><td>Ø</td></tr><tr><th><b>10</b></th><td><b>5</b></td><td><b>70,50</b></td><td><b>–168,67</b></td><td><b>35</b></td><td><b>45</b></td><td><b>6,48</b></td><td><b>6</b></td><td><b>2E, 2F</b></td></tr><tr><th>11</th><td>5</td><td>71,43</td><td>–168,67</td><td>40</td><td>50</td><td>0,75</td><td>7,9</td><td>Ø</td></tr><tr><th><b>13</b></th><td><b>5</b></td><td><b>72,36</b></td><td><b>–168,66</b></td><td><b>50</b></td><td><b>60</b></td><td><b>6,16</b></td><td><b>1</b></td><td><b>6A</b></td></tr><tr><th>16</th><td>6</td><td>73,89</td><td>–168,19</td><td>100</td><td>183</td><td>1,5</td><td>1</td><td>Ø</td></tr><tr><th>18</th><td>6</td><td>74,80</td><td>–167,90</td><td>100</td><td>195</td><td>0,413</td><td>1</td><td>Ø</td></tr><tr><th><b>21</b></th><td><b>7</b></td><td><b>76,00</b></td><td><b>–170,49</b></td><td><b>100</b></td><td><b>1315</b></td><td><b>1,22</b></td><td><b>–0,5</b></td><td><b>6A, 7H, 7K, 7N</b></td></tr><tr><th><b>23</b></th><td><b>8</b></td><td><b>77,00</b></td><td><b>–170,00</b></td><td><b>100</b></td><td><b>2214</b></td><td><b>0,53</b></td><td><b>–1,1</b></td><td><b>6A</b></td></tr><tr><th>24</th><td>8</td><td>77,00</td><td>–174,99</td><td>100</td><td>2012</td><td>0,34</td><td>–1,3</td><td>Ø</td></tr><tr><th>25</th><td>9</td><td>77,00</td><td>179,95</td><td>100</td><td>1081</td><td>0,09</td><td>–1,2</td><td>OE</td></tr><tr><th><b>27</b></th><td><b>12</b></td><td><b>78,54</b></td><td><b>–177,58</b></td><td><b>100</b></td><td><b>1009</b></td><td><b>0,07</b></td><td><b>–1,2</b></td><td><b>7K</b></td></tr><tr><th><b>28</b></th><td><b>13</b></td><td><b>80,00</b></td><td><b>172,40</b></td><td><b>100</b></td><td><b>2702</b></td><td><b>0,14</b></td><td><b>–1</b></td><td><b>6A</b></td></tr><tr><th>29</th><td>14</td><td>79,00</td><td>172,80</td><td>100</td><td>2561</td><td>0,15</td><td>–0,9</td><td>Ø</td></tr><tr><th>30</th><td>14</td><td>78,00</td><td>173,20</td><td>100</td><td>1133</td><td>0,14</td><td>0,3</td><td>Ø</td></tr><tr><th>31</th><td>15</td><td>77,00</td><td>173,60</td><td>100</td><td>740</td><td>0,4</td><td>0,2</td><td>Ø</td></tr><tr><th><b>32</b></th><td><b>15</b></td><td><b>76,00</b></td><td><b>173,61</b></td><td><b>100</b></td><td><b>265</b></td><td><b>0,2</b></td><td><b>–1,1</b></td><td><b>7H</b></td></tr><tr><th><b>33</b></th><td><b>16</b></td><td><b>75,00</b></td><td><b>173,60</b></td><td><b>100</b></td><td><b>147</b></td><td><b>0,07</b></td><td><b>–0,06</b></td><td><b>6E</b></td></tr><tr><th>36</th><td>16</td><td>74,00</td><td>170,16</td><td>40</td><td>52</td><td>0,1</td><td>–0,8</td><td>Ø</td></tr><tr><th><b>37</b></th><td><b>17</b></td><td><b>74,69</b></td><td><b>174,62</b></td><td><b>60</b></td><td><b>72</b></td><td><b>0,2</b></td><td><b>–1</b></td><td><b>2A</b></td></tr><tr><th><b>39</b></th><td><b>18</b></td><td><b>75,73</b></td><td><b>177,18</b></td><td><b>100</b></td><td><b>499</b></td><td><b>0,15</b></td><td><b>–1,3</b></td><td><b>2G</b></td></tr><tr><th><b>40</b></th><td><b>20</b></td><td><b>75,07</b></td><td><b>176,80</b></td><td><b>100</b></td><td><b>196</b></td><td><b>0,31</b></td><td><b>–1,2</b></td><td><b>2B, 2H, 7I, 7N</b></td></tr><tr><th><b>43</b></th><td><b>21</b></td><td><b>75,16</b></td><td><b>–179,97</b></td><td><b>100</b></td><td><b>539</b></td><td><b>0,35</b></td><td><b>–1,4</b></td><td><b>6D, 6E, 7J</b></td></tr><tr><th>45</th><td>21</td><td>75,15</td><td>–176,00</td><td>100</td><td>327</td><td>1,36</td><td>–1</td><td>Ø</td></tr><tr><th><b>47</b></th><td><b>22</b></td><td><b>75,24</b></td><td><b>–171,97</b></td><td><b>100</b></td><td><b>505</b></td><td><b>2,73</b></td><td><b>–0,7</b></td><td><b>6A, 7J</b></td></tr><tr><th><b>50</b></th><td><b>23</b></td><td><b>75,69</b></td><td><b>–166,64</b></td><td><b>100</b></td><td><b>392</b></td><td><b>3,1</b></td><td><b>–0,9</b></td><td><b>6A, 7H, 7N</b></td></tr><tr><th><b>52</b></th><td><b>23</b></td><td><b>76,57</b></td><td><b>–164,36</b></td><td><b>100</b></td><td><b>550</b></td><td><b>0,019</b></td><td><b>–1,1</b></td><td><b>7G</b></td></tr><tr><th><b>54</b></th><td><b>24</b></td><td><b>77,47</b></td><td><b>–164,10</b></td><td><b>100</b></td><td><b>280</b></td><td><b>0,32</b></td><td><b>–1,3</b></td><td><b>2C, 7J</b></td></tr><tr><th><b>56</b></th><td><b>25</b></td><td><b>77,49</b></td><td><b>–158,73</b></td><td><b>100</b></td><td><b>1323</b></td><td><b>0,02</b></td><td><b>–1,3</b></td><td><b>7H, 7J</b></td></tr><tr><th>57</th><td>26</td><td>76,30</td><td>–156,22</td><td>100</td><td>725</td><td>0,23</td><td>–0,1</td><td>Ø</td></tr><tr><th>58</th><td>26</td><td>76,52</td><td>–159,78</td><td>100</td><td>2113</td><td>0,21</td><td>–1</td><td>Ø</td></tr><tr><th>59</th><td>27</td><td>75,50</td><td>–161,15</td><td>100</td><td>2098</td><td>0,2</td><td>–0,5</td><td>2D, 7A</td></tr><tr><th>60</th><td>27</td><td>74,52</td><td>–162,15</td><td>100</td><td>1596</td><td>0,27</td><td>1,8</td><td>2G, 6A, 7A, 7H</td></tr></tbody></table>
Table 2 in A late Eocene wood assemblage from the Crooked River Basin, Oregon, USA
<p><b>Table 2.</b> Comparison of fossil <i>Fagus</i> woods from Dietz Hill with <i>Fagus dodgei</i> from Post Hammer (UF 279, late Eocene, Wheeler and Manchester 2021) and <i>Fagus manosii</i> (mid-Miocene, Wheeler and Dillhoff 2009). <b>VTD</b> =vessel tangential diameter in µm, mean (SD); <b>V/mm2</b> =number of vessels per square mm; <b>Lrg Ray</b> =large ray, number of cells wide; <b>Cmp</b> =compound ray; <b>Lrg Ray Ht.</b> =large ray height in µm, mean (SD, when known), range.</p><table><tbody><tr><th>Sample</th><th>VTD</th><th>V /mm2</th><th>Lrg Ray</th><th><b>Lrg Ray Ht.</b></th></tr></tbody><tbody><tr><th>UF 278-84869</th><td>59 (8)</td><td>39–53</td><td>6–9, Cmp</td><td>2214 (580), 1269–3102</td></tr><tr><th>UF 278-84903</th><td>49 (13)</td><td>67–82</td><td>7–12, Cmp</td><td>2566 (734), 1974–3948</td></tr><tr><th>UF 278-84873</th><td>44 (6)</td><td>86–103</td><td>to 22, Cmp common</td><td>1875 (500), 1356–2825</td></tr><tr><th>UF 278-84888</th><td>62 (12)</td><td>61–75</td><td>8–11, Cmp common</td><td>2358 (311), 1904–2744</td></tr><tr><th>UF 278-84896</th><td>53 (8)</td><td>87–117</td><td>to 20+, Cmp common</td><td>1967 (815), 705–3666</td></tr><tr><th><i>Fagus dodgei</i></th><td>55 (11)</td><td>39–79</td><td>18–20, Cmp</td><td>1560, 740–2690</td></tr><tr><th><i>Fagus manosii</i></th><td>52 (11)</td><td>110–130</td><td>to 16, Cmp absent</td><td>1700 (max)</td></tr></tbody></table>
Table 1 in A late Eocene wood assemblage from the Crooked River Basin, Oregon, USA
<p><b>Table 1</b>. Comparison of fossil Magnoliaceae woods in chronological order. <b>K</b> =Cretaceous, (<b>C</b>)=Campanian, (<b>M</b>)=Maastrichtian, <b>Eo</b> =Eocene, <b>Olig</b> =Oligocene; <b>Mio</b> =Miocene, <b>e</b> =early, <b>m</b> =middle, <b>up</b> =upper; <b>IVP</b> =intervessel pitting, <b>S</b> =scalariform, <b>O</b> =opposite; <b>Bars/PP</b> =number of bars per scalariform perforation plate; <b>Si</b> =simple perforation plates present; <b>HT</b> =helical thickenings in vessel elements; <b>O/M</b> = oil/mucilage cells; <b>Y</b> =present; <b>N</b> =absent; <b>*</b> =small axis, <b>()</b> =not as common. <b>References</b>. <b>1</b> =Cevallos-Ferriz and Stockey (1990); <b>2</b> = Huang et al. (2020; <b>3</b> = Huard (1967); <b>4</b> = Iamandei et al. (2011); <b>5</b> = Iamandei et al. (2020); <b>6</b> = Page (1970); <b>7</b> = Prakash et al. (1971); <b>8</b> = Sakala et al. (2010); <b>9</b> = Srivastava and Suzuki (2001); <b>10</b> = Suzuki (1976); <b>11</b> = Takahashi and Suzuki (2003); <b>12</b> = van der Burgh (1973); <b>13</b> = Wheeler et al. (1977); <b>14</b> = Wheeler and Manchester (2002).</p><table><tbody><tr><th>Species</th><th>Age</th><th>IVP</th><th>Bars/PP</th><th>Si</th><th>HT</th><th>OM</th><th><b>Reference</b></th></tr></tbody><tbody><tr><th><i>Magnoliaceoxylon hokkaidoense</i></th><td>K (C-M)</td><td>S, O</td><td>12–47</td><td>N</td><td>N</td><td>N</td><td>11</td></tr><tr><th><i>Magnoliaceoxylon panochensis</i></th><td>K (C)</td><td>S, O</td><td>up to 10</td><td>N</td><td>N</td><td>N</td><td>6</td></tr><tr><th><i>Magnoliaceoxylon wetmorei</i></th><td>e m Eo</td><td>S, (O)</td><td>8–26</td><td>N</td><td>N</td><td>Y</td><td>13</td></tr><tr><th><i>Liriodendroxylon mutltiporosum</i></th><td>m Eo</td><td>O</td><td>2–10</td><td>N</td><td>N</td><td>(Y)</td><td>14</td></tr><tr><th><i>Liriodendroxylon princetonensis *</i></th><td>m Eo</td><td>S, O</td><td>8–18</td><td>N</td><td>N</td><td>N</td><td>1</td></tr><tr><th><i>Magnolia pageae</i></th><td>m Eo</td><td>O</td><td>5–20</td><td>N</td><td>N</td><td>Y</td><td>14</td></tr><tr><th><i>Magnoliaceoxylon angulata</i></th><td>m Eo</td><td>S, O</td><td>15–18</td><td>N</td><td>N</td><td>N</td><td>14</td></tr><tr><th><i>Magnoliaceoxylon cutleri</i></th><td>m Eo</td><td>S, (O)</td><td>8–20</td><td>N</td><td>N</td><td>Y</td><td>14</td></tr><tr><th><i>Magnoliaceoxylon longiradiata</i></th><td>m Eo</td><td>S, (O)</td><td>6–20</td><td>N</td><td>N</td><td>(Y)</td><td>14</td></tr><tr><th><i>Magnolia hansnooteboomii</i> sp. nov.</th><td>l Eo</td><td>S</td><td>8–16</td><td>N</td><td>Y</td><td>N</td><td>This paper</td></tr><tr><th><i>Magnoliaceoxylon palaeogenica</i></th><td>e Olig</td><td>S</td><td>4–15</td><td>N</td><td>N</td><td>N</td><td>9</td></tr><tr><th><i>Michelia oleifera</i></th><td>Olig</td><td>S, O</td><td>7–15</td><td>N</td><td>Y</td><td>Y</td><td>10</td></tr><tr><th><i>Liriodendroxylon tulipiferum</i></th><td>Olig</td><td>O</td><td>~10</td><td>N</td><td>N</td><td>N</td><td>7, 8</td></tr><tr><th><i>Magnolia nanningensis</i></th><td>up Olig</td><td>S, O</td><td>2–11</td><td>N</td><td>Y</td><td>Y</td><td>2</td></tr><tr><th><i>Magnolioxylon</i> c <i>f. transilvanicum</i></th><td>m Mio</td><td>S, O</td><td>short</td><td>Y</td><td>N</td><td>N</td><td>4</td></tr><tr><th><i>Magnolioxylon kräuselli</i></th><td>m Mio</td><td>(S), O</td><td>10–12</td><td>N</td><td>N</td><td>N</td><td>5</td></tr><tr><th><i>Magnolia intermedia</i></th><td>Mio</td><td>S</td><td>15–20</td><td>N</td><td>N</td><td>Y</td><td>3</td></tr><tr><th><i>Magnolioxylon parenchymatosum</i></th><td>Mio</td><td>S</td><td>3–12</td><td>N</td><td>N</td><td>N</td><td>12</td></tr></tbody></table>
Table 1 in A description of the first zoeal stage of Pilumnus vinaceus A. Milne-Edwards, 1880 (Decapoda, Pilumnidae), with a revision of the first zoea morphology of Pilumnus Leach, 1815
<p>Table 1. Larval characters of the first zoeal stage of Indo-West Pacific and Eastern Pacific species of the genus <i>Pilumnus</i> Leach,1815.</p><table><tbody><tr><th></th><th></th><th></th><th><b>Indo-West Pacific</b></th><th></th><th></th><th><b>Eastern Pacific</b></th><th></th><th><b>western Atlantic</b></th><th></th><th><b>eastern Atlantic</b></th></tr></tbody><tbody><tr><th></th><td><i>Pilumnus kempi</i></td><td><i>Pilumnus longicornis</i></td><td><i>Pilumnus minutus</i></td><td><i>Pilumnus scabriusculus</i></td><td><i>Pilumnus sluiteri</i></td><td><i>Pilumnus vespertilio</i></td><td><i>Pilumnus indicus</i></td><td><i>Pilumnus limosus</i></td><td><i>Pilumnus dasypodus</i></td><td><i>Pilumnus reticulatus *</i></td><td><i>Pilumnus vinaceus</i></td><td><i>Pilumnus hirtellus</i></td><td><i>Pilumnus spinifer</i></td></tr><tr><th><b>Size</b></th></tr><tr><th><b>RDL (mm)</b></th><td><b>nd</b></td><td><b>nd</b></td><td><b>0.71</b></td><td><b>0.77</b></td><td><b>nd</b></td><td><b>1.78 (0.98)</b> <b>b</b></td><td><b>0.70</b></td><td><b>0.91</b></td><td><b>1.2</b> <b>b</b></td><td><b>1.02</b></td><td><b>0.83</b></td><td><b>1.5 (1.2)</b> <b>c</b></td><td><b>0.9</b></td></tr><tr><th><b>Carapace</b></th></tr><tr><th><b>posterodorsal s</b></th><td><b>nd</b></td><td><b>0</b></td><td><b>0</b></td><td><b>nd</b></td><td><b>2</b></td><td><b>0</b></td><td><b>nd</b></td><td><b>2</b></td><td><b>0</b></td><td><b>0</b></td><td><b>0</b></td><td><b>0</b></td><td><b>0</b></td></tr><tr><th><b>s on ventral margin</b></th><td><b>1</b> <b>d</b></td><td><b>0</b></td><td><b>0</b></td><td><b>0</b></td><td><b>1</b></td><td><b>0</b></td><td><b>0**</b></td><td><b>0</b></td><td><b>0</b></td><td><b>0</b></td><td><b>0</b></td><td><b>0</b></td><td><b>0</b></td></tr><tr><th><b>Antennule</b></th></tr><tr><th><b>a,s</b></th><td><b>7,1</b></td><td><b>4,2</b></td><td><b>3, 3</b></td><td><b>nd</b></td><td><b>5,2</b></td><td><b>3,2 (4, 2)</b> <b>c</b></td><td><b>2,2 (4)</b></td><td><b>4,1</b></td><td><b>4,1 (4, 3)</b> <b>b</b></td><td><b>4,1</b></td><td><b>4, 2</b></td><td><b>4,2</b></td><td><b>4,1</b></td></tr><tr><th><b>Antenna</b></th></tr><tr><th><b>endopod</b></th><td><b>Present</b></td><td><b>Absent</b></td><td><b>Absent</b></td><td><b>Absent</b></td><td><b>Present</b></td><td><b>Presentb</b></td><td><b>Absent</b></td><td><b>Absent</b></td><td><b>Absent</b></td><td><b>Absent</b></td><td><b>Absent</b></td><td><b>Absent</b></td><td><b>Absent</b></td></tr><tr><th><b>Maxillule</b></th></tr><tr><th><b>s on coxal end.</b></th><td><b>7</b></td><td><b>7</b></td><td><b>7</b></td><td><b>7</b></td><td><b>7</b></td><td><b>7</b></td><td><b>7</b></td><td><b>7</b></td><td><b>7</b></td><td><b>7</b></td><td><b>7</b></td><td><b>6-7</b></td><td><b>7</b></td></tr><tr><th><b>Maxilla</b></th></tr><tr><th><b>s on coxal end.</b></th><td><b>5 + 4</b></td><td><b>6 + 4</b></td><td><b>6 + 4</b></td><td><b>6 + 4</b></td><td><b>6 + 4</b></td><td><b>4 + 3 (6 + 4)</b> <b>c</b></td><td><b>6 + 4</b></td><td><b>5 + 4</b></td><td><b>5 + 4</b></td><td><b>5 + 4</b></td><td><b>5 + 4</b></td><td><b>5 + 4 (4 + 4)</b> <b>c</b></td><td><b>5 + 4</b></td></tr><tr><th><b>s on basial end.</b></th><td><b>4 + 4</b></td><td><b>5 + 4</b></td><td><b>5 + 4</b></td><td><b>5 + 4</b></td><td><b>5 + 4</b></td><td><b>6 + 4 (5 + 4)</b> <b>b</b> <b></b> <b>c</b></td><td><b>5 + 4</b></td><td><b>5 + 4</b></td><td><b>5 + 4</b></td><td><b>5 + 4</b></td><td><b>5 + 4</b></td><td><b>5 + 4</b></td><td><b>5 + 4</b></td></tr><tr><th><b>Maxilliped 1</b></th></tr><tr><th><b>s on basis</b></th><td><b>11 (10)</b> <b>d</b></td><td><b>10</b></td><td><b>10</b></td><td><b>10</b></td><td><b>10</b></td><td><b>9 (10)</b> <b>b</b> <b></b> <b>c</b></td><td><b>10</b></td><td><b>10</b></td><td><b>10</b></td><td><b>10</b></td><td><b>10</b></td><td><b>10</b></td><td><b>10</b></td></tr><tr><th><b>s on end</b></th><td><b>3, 2,1, 2,5</b></td><td><b>3, 2,1, 2,5</b></td><td><b>3,2, 1, 2,5</b></td><td><b>3,2,1, 2,5</b></td><td><b>3, 2,1, 2, 5</b></td><td><b>2 (3)</b> <b>b</b> <b></b> <b>c</b><b>, 2,1, 2, 5</b></td><td><b>3,2,1, 2, 5</b></td><td><b>3,2,1, 2,5</b></td><td><b>3,2, 1, 2,5</b></td><td><b>3, 2,1, 2, 5</b></td><td><b>3,2,1, 2,5</b></td><td><b>3, 2,1, 2, 5</b></td><td><b>3,2,1, 2,5</b></td></tr><tr><th><b>Pleon</b></th></tr><tr><th><b>dorsomedial s (so1)</b></th><td><b>0</b> <b>d</b></td><td><b>0</b></td><td><b>0</b></td><td><b>2</b></td><td><b>1</b></td><td><b>0</b></td><td><b>0</b></td><td><b>0</b></td><td><b>nd</b></td><td><b>0</b></td><td><b>0</b></td><td><b>0</b></td><td><b>0</b></td></tr><tr><th><b>posterodorsal s (so1)</b></th><td><b>0</b> <b>d</b></td><td><b>0</b></td><td><b>0</b></td><td><b>0</b></td><td><b>1</b></td><td><b>0</b></td><td><b>0</b></td><td><b>0</b></td><td><b>nd</b></td><td><b>0</b></td><td><b>0</b></td><td><b>0</b></td><td><b>0</b></td></tr><tr><th><b>dorsolateral processes</b></th><td><b>2</b> <b><b>nd-</b> 3</b> <b>rd</b> <b>so</b></td><td><b>2</b> <b><b>nd-</b> 3</b> <b>rd</b> <b>so</b></td><td><b>2</b> <b><b>nd-</b> 5</b> <b>th</b> <b>so</b></td><td><b>2</b> <b><b>nd-</b> 3</b> <b>rd</b> <b>so</b></td><td><b>2</b> <b><b>nd-</b> 5</b> <b>th</b> <b>so</b></td><td><b>2</b> <b><b>nd-</b> 3</b> <b>rd</b> <b>so</b></td><td><b>2</b> <b>nd</b> <b>so</b></td><td><b>2</b> <b><b>nd-</b> 3</b> <b>rd</b> so</td><td><b>2</b> <b><b>nd-</b> 3</b> <b>rd</b> <b>so</b></td><td><b>2</b> <b><b>nd-</b> 5</b> <b>th</b> <b>so</b></td><td><b>2</b> <b><b>nd-</b> 3</b> <b>rd</b> <b>so</b></td><td><b>2</b> <b><b>nd-</b> 3</b> <b>rd</b> <b>so</b></td><td><b>2</b> <b><b>nd-</b> 3</b> <b>rd</b> so</td></tr></tbody></table><p><b>a = aesthetascs;end.= endopod;nd = not described;RDL = rostrodorsal length;s = setae;so = somite;** = data from figures observation.</b></p><p><b>References: <i>P.kempi</i> (Siddiqui & Tirmizi, 1992; Clark & Ng,2004 <sup>d</sup>); <i>P.longicornis</i> (Clark & Paula, 2003); <i>P.minutus</i> (Terada, 1984; Ko, 1994); <i>P.scabriusculus</i> (Terada, 1990); <i>P.sluiteri</i> (Clark & Ng, 2004); <i>P.verpertilio</i> (Lim & Tan,1981; Terada,1990 <sup>b</sup>; Clark & Paula,2003 <sup>c</sup></b>); <i>P.indicus</i> (Terada,1980); <i>P.limosus</i> (García-Guerrero <i>et al.,</i> 2005).</p>
Table 1 in First Description of Phyllosoma Larva in the Genus Projasus (Crustacea: Decapoda: Palinuridae)
<p>Table 1. Main larval characteristics in the final or latest stages of phyllosoma in 10 palinurid genera.*</p><table><tbody><tr><th></th><th></th><th>Cephalic shield</th><th></th><th></th><th>Maxillue</th><th>Mxp 2</th><th>Mxp 3</th><th>Pereiopod</th><th>Pleon</th><th></th></tr></tbody><tbody><tr><th>Genus</th><td>outline</td><td>rostrum</td><td>overlap on thorax</td><td>overlap on Mxp 3 coxa</td><td>CW/TW ratio <b>**</b></td><td>stout spines on BE</td><td>exopod</td><td>exopod</td><td>chelate</td><td>DMS on pleonite</td><td>References</td></tr><tr><th>‘Silentes’ group</th></tr><tr><th><i>Projasus</i></th><td>circular</td><td>+</td><td>No</td><td>Yes</td><td>2.33</td><td>5</td><td>+</td><td>+</td><td>?</td><td>1</td><td>This study</td></tr><tr><th><i>Sagmariasus</i></th><td>circular</td><td>−</td><td>No</td><td>Yes</td><td>1.93</td><td>4</td><td>r</td><td>−</td><td>No</td><td>—</td><td>1</td></tr><tr><th><i>Jasus</i></th><td>circular</td><td>−</td><td>No</td><td>Yes</td><td>2.25</td><td>3</td><td>r</td><td>−</td><td>No</td><td>—</td><td>1</td></tr><tr><th><i>Palinurellus</i></th><td>rectangular</td><td>+</td><td>Yes</td><td>Yes</td><td>2.25</td><td>3</td><td>+</td><td>+</td><td>No</td><td>—</td><td>2, 3</td></tr><tr><th>‘Stridentes’ group</th></tr><tr><th><i>Palinurus</i></th><td>oval</td><td>−</td><td>No</td><td>Yes</td><td>1.71</td><td>3</td><td>+</td><td>+</td><td>No</td><td>—</td><td>4, 5, 6</td></tr><tr><th><i>Panulirus</i></th><td>oval</td><td>−</td><td>No</td><td>Yes</td><td>0.83</td><td>3</td><td>+</td><td>+</td><td>No</td><td>—</td><td>7</td></tr><tr><th><i>Justitia</i></th><td>oval</td><td>−</td><td>No</td><td>No</td><td>1.06</td><td>2</td><td>+</td><td>+</td><td>Yes (P1,P3)</td><td>—</td><td>8, 9</td></tr><tr><th><i>Nupalirus</i></th><td>oval</td><td>−</td><td>No</td><td>Yes</td><td>0.91</td><td>2</td><td>+</td><td>+</td><td>Yes (P1,P3,P4)</td><td>—</td><td>8, 9</td></tr><tr><th><i>Palinustus</i></th><td>subrectangular</td><td>−</td><td>No</td><td>Yes</td><td>1.76</td><td>2</td><td>+</td><td>+</td><td>Yes (P1,P3,P4)</td><td>2</td><td>10</td></tr><tr><th><i>Puerulus</i></th><td>circular</td><td>−</td><td>Yes</td><td>Yes</td><td>1.98</td><td>2</td><td>+</td><td>+</td><td>No</td><td>1</td><td>11</td></tr></tbody></table><p><b>*</b> No late stage phyllosoma with evident identification has been described in the genera <i>Palibythus</i> and <i>Linuparus</i> to date. <b>**</b> Latest stage. BE: basial endite; CW:cephalic shield width; DMS:dorsal median spine; Mxp: maxilliped; P: pereiopod; r: rudimentary bud; TW: thoax width; “−” means absent; “+” means present. References: <sup>1</sup> McWilliam and Phillips (1987); <sup>2</sup> Sims (1966); <sup>3</sup> Michel (1970); <sup>4</sup> Gurney (1936); <sup>5</sup> Berry (1974); <sup>6</sup> Bouvier (1914); <sup>7</sup> Goldstein et al. (2008); <sup>8</sup> Johnson and Robertson (1970); <sup>9</sup> Konishi et al. (2021); <sup>10</sup> Palero et al. (2010); <sup>11</sup> Sekiguchi et al. (1996).</p>
TABLE 1 in Molecular phylogeny and morphology reveal a new species of genus Rhodocybe sensu stricto Maire (Entolomataceae; Agaricales) from Pakistan
<p>TABLE 1. — Voucher/strain/isolate, country, GenBank/UNITE accession number, and reference for the specimens included in nrITS and combined ITS-28S phylogenetic analysis. The sequences produced during this study are shown in <b>bold font</b>.</p><table><tbody><tr><th></th><th><b>GenBank/UNITE</b></th><th></th><th></th></tr></tbody><tbody><tr><th></th><td><b>accession no.</b></td><td></td><td></td></tr><tr><th><b>Taxon name Voucher/strain/isolate</b></th><td><b>nrITS</b></td><td><b>28S</b></td><td><b>Country</b></td><td><b>Reference</b></td></tr><tr><th><i>Calocybe carnea</i> (outgroup) CBS552.50</th><td>AF357028</td><td>AF223178</td><td>–</td><td>Hofstetter <i>et al.</i> 2002</td></tr><tr><th><i>Clitocella fallax</i> CBS605.79</th><td>AF357018</td><td>AF223165</td><td>–</td><td>Hofstetter <i>et al.</i> 2002</td></tr><tr><th><i>Clitocella fallax</i> CBS129.63</th><td>AF357017</td><td>AF223166</td><td>–</td><td>Hofstetter <i>et al.</i> 2002</td></tr><tr><th><i>Clitocella mundula</i> TJB7599</th><td>DQ494694</td><td>AY700182</td><td>–</td><td>Matheny <i>et al.</i> 2006</td></tr><tr><th><i>Clitocella mundula</i> HMJAU 7275</th><td>MN061331</td><td>MN065723</td><td>China</td><td>Jian <i>et al.</i> 2020</td></tr><tr><th><i>Clitocella orientalis</i> KUN-HKAS 75664 (Liu53)</th><td>MN061332</td><td>MN065726</td><td>China</td><td>Jian <i>et al.</i> 2020</td></tr><tr><th><i>Clitocella orientalis</i> KUN-HKAS 75548 (Cai794)</th><td>MN061333</td><td>MN065727</td><td>China</td><td>Jian <i>et al.</i> 2020</td></tr><tr><th><i>Clitopilopsis albida</i> KUN-HKAS 104519 (JSP224)</th><td>MN061335</td><td>MN065730</td><td>China</td><td>Jian <i>et al.</i> 2020</td></tr><tr><th><i>Clitopilopsis albida</i> KUN-HKAS 104520 (JSP225)</th><td>MN061336</td><td>MN065731</td><td>China</td><td>Jian <i>et al.</i> 2020</td></tr><tr><th><i>Clitopilopsis hirneola</i> MEN 199956</th><td>KC710132</td><td>GQ289211</td><td>–</td><td>Morgado <i>et al.</i> 2013</td></tr><tr><th><i>Clitopilopsis hirneola</i> CBS 126.46</th><td>MH856141</td><td>AF223163</td><td>France</td><td>Vu <i>et al.</i> 2019</td></tr><tr><th><i>Clitopilus passeckerianus</i> CBS 299.35</th><td>MH855682</td><td>MH867198</td><td>Austria</td><td>Vu <i>et al.</i> 2019</td></tr><tr><th><i>Clitopilus scyphoides</i> KRAM5</th><td>MN744420</td><td>MN744422</td><td>India</td><td>-</td></tr><tr><th><i>Clitopilus scyphoides</i> CBS 127.47</th><td>MH856181</td><td>MH867707</td><td>France</td><td>Vu <i>et al.</i> 2019</td></tr><tr><th><i>Clitopilus sinoapalus</i> KUN-HKAS 77037 (Wu865)</th><td>MN061321</td><td>MN065713</td><td>China</td><td>Jian <i>et al.</i> 2020</td></tr><tr><th><i>Clitopilus sinoapalus</i> KUN-HKAS 101191</th><td>MN061322</td><td>MN065711</td><td>China</td><td>Jian <i>et al.</i> 2020</td></tr><tr><th>(Yang6002)</th><td></td><td></td><td></td><td></td></tr><tr><th><i>Clitopilus umbilicatus</i> KUN-HKAS 80310 (Han79)</th><td>MN061324</td><td>MN065716</td><td>China</td><td>Jian <i>et al.</i> 2020</td></tr><tr><th><i>Clitopilus umbilicatus</i> KUN-HKAS 104509</th><td>MN061327</td><td>MN065719</td><td>China</td><td>Jian <i>et al.</i> 2020</td></tr><tr><th>(Wu2506)</th><td></td><td></td><td></td><td></td></tr><tr><th><i>Entoloma caccabus</i> MEN 200324</th><td>KC710063</td><td>GQ289155</td><td>–</td><td>Morgado <i>et al.</i> 2013</td></tr><tr><th><i>Entoloma conferendum</i> MEN 200330</th><td>KC710055</td><td>KC710133</td><td>Slovakia</td><td>Morgado <i>et al.</i> 2013</td></tr><tr><th><i>Entoloma serrulatum</i> LE254361</th><td>KC898447</td><td>KC898501</td><td>Russia</td><td>Morozova <i>et al.</i> 2014</td></tr><tr><th><i>Entoloma</i> sp. Sulzbacher 433/1-D-1</th><td>LT594987</td><td>–</td><td>Brazil</td><td>-</td></tr><tr><th><i>Entoloma tjallingiorum</i> LE254318</th><td>KC898411</td><td>KC898510</td><td>Russia</td><td>Morozova <i>et al.</i> 2014</td></tr><tr><th><i>Lyophyllum decastes</i> (outgroup) JM87/16(T1)</th><td>AF357059</td><td>AF042583</td><td>–</td><td>Hofstetter <i>et al.</i> 2002</td></tr><tr><th><i>Rhodocybe asanii</i> KATO:Fungi:3657</th><td>KX834265</td><td>–</td><td>Türkiye</td><td>Sesli & Vizzini 2017</td></tr><tr><th><i>Rhodocybe asanii</i> KATO:Fungi:3659</th><td>NR_154442</td><td>NG060176</td><td>Türkiye</td><td>Sesli & Vizzini 2017</td></tr><tr><th><i>Rhodocybe asyae</i> KATO:Fungi:3653</th><td>KX834268</td><td>–</td><td>Türkiye</td><td>Sesli & Vizzini 2017</td></tr><tr><th><i>Rhodocybe asyae</i> KATO:Fungi:3640</th><td>NR_154443</td><td>NG060177</td><td>Türkiye</td><td>Sesli & Vizzini 2017</td></tr><tr><th><i>Rhodocybe brunneoaurantiaca</i> CUH AM720</th><td>MW023201</td><td>MW023223</td><td>India: West Bengal</td><td>Dutta <i>et al.</i> 2021</td></tr><tr><th><i>Rhodocybe brunneoaurantiaca</i> CAL 1825</th><td>MW031906</td><td>MW031916</td><td>India: West Bengal</td><td>Dutta <i>et al.</i> 2021</td></tr><tr><th><i>Rhodocybe caelata</i> JVG 1070904-2</th><td>KU862855</td><td>–</td><td>Spain</td><td>Vizzini <i>et al.</i> 2016</td></tr><tr><th><i>Rhodocybe formosa</i> Herb. B. Picillo 12/208</th><td>KU862858</td><td>–</td><td>Italy</td><td>Vizzini <i>et al.</i> 2016</td></tr><tr><th><i>Rhodocybe formosa</i> LIP JVG 1061015</th><td>KU862856</td><td>–</td><td>Spain</td><td>Vizzini <i>et al.</i> 2016</td></tr><tr><th><i>Rhodocybe fumanellii</i> MCVE:29550</th><td>NR_166243</td><td>NG068264</td><td>Italy</td><td>Vizzini <i>et al.</i> 2018</td></tr><tr><th><i>Rhodocybe fusipes</i> DLK 587</th><td>MN306210</td><td>–</td><td>Brazil</td><td>Silva-Filho <i>et al.</i> 2020</td></tr><tr><th><i>Rhodocybe fusipes</i> DLK 298</th><td>MN306209</td><td>–</td><td>Brazil</td><td>Silva-Filho <i>et al.</i> 2020</td></tr><tr><th><i>Rhodocybe incarnata</i> REH5369</th><td>MT254071</td><td>–</td><td>Venezuela</td><td>Silva-Filho <i>et al.</i> 2020</td></tr><tr><th><i>Rhodocybe luteobrunnea</i> CAL:1322</th><td>NR_154434</td><td>NG060167</td><td>India</td><td>–</td></tr><tr><th><i>Rhodocybe matesina</i> MCVE:29261</th><td>KY629962</td><td>KY629964</td><td>Italy</td><td>–</td></tr><tr><th><i>Rhodocybe matesina</i> MCVE:29262</th><td>NR_154455</td><td>NG060184</td><td>Italy</td><td>–</td></tr><tr><th><i>Rhodocybe mellea</i> JBSD127402</th><td>MN784993</td><td>–</td><td>Dominican Republic</td><td>Baroni <i>et al.</i> 2020</td></tr><tr><th><i>Rhodocybe mellea</i> CORT013885</th><td>MN784992</td><td>–</td><td>Dominican Republic</td><td>Baroni <i>et al.</i> 2020</td></tr><tr><th><i>Rhodocybe mellea</i> NYBG815044</th><td>MN784995</td><td>–</td><td>Costa Rica</td><td>Baroni <i>et al.</i> 2020</td></tr><tr><th><i>Rhodocybe mellea</i> CORT014470</th><td>MN784994</td><td>–</td><td>Belize</td><td>Baroni <i>et al.</i> 2020</td></tr><tr><th><i>Rhodocybe mellea</i> var. <i>depressa</i> F. Wartchow 08-2019</th><td>MT408926</td><td>OL687341</td><td>Brazil</td><td>Xavier <i>et al.</i> 2022</td></tr><tr><th><i>Rhodocybe minutispora</i> LIP JVG 1071101</th><td>KU862860</td><td>–</td><td>Spain</td><td>Vizzini <i>et al.</i> 2016</td></tr><tr><th><b><i>Rhodocybe pakistanica</i> sp. nov. LAH37948</b></th><td><b>OR606544</b></td><td><b>OR606542</b></td><td><b>Pakistan</b></td><td><b>This study</b></td></tr><tr><th><b><i>Rhodocybe pakistanica</i> sp. nov. LAH37949</b></th><td><b>OR606545</b></td><td><b>–</b></td><td><b>Pakistan</b></td><td><b>This study</b></td></tr><tr><th><b><i>Rhodocybe pakistanica</i> sp. nov. LAH37947</b></th><td><b>OR606543</b></td><td><b>OR606541</b></td><td><b>Pakistan</b></td><td><b>This study</b></td></tr><tr><th><b>(holotype)</b></th></tr><tr><th><i>Rhodocybe pallidogrisea</i> CORT 013944</th><td>KX271752</td><td>–</td><td>Australia</td><td>–</td></tr><tr><th><i>Rhodocybe roseiavellanea</i> PBM4056 (TENN)</th><td>MF686525</td><td>–</td><td>United States</td><td>–</td></tr><tr><th><i>Rhodocybe rubrobrunnea</i> CAL 1387</th><td>KX951452</td><td>–</td><td>India</td><td>–</td></tr><tr><th><i>Rhodocybe</i> sp. Sulzbacher 340</th><td>LT594979</td><td>–</td><td>Brazil</td><td>Sulzbacher <i>et al.</i> 2017</td></tr><tr><th>(UFRN-fungos 2557)</th><td></td><td></td><td></td><td></td></tr><tr><th><i>Rhodocybe</i> sp. Sulzbacher 413</th><td>LT594984</td><td>–</td><td>Brazil</td><td>Sulzbacher <i>et al.</i> 2017</td></tr><tr><th>(UFRN-fungos 2062)</th><td></td><td></td><td></td><td></td></tr><tr><th><i>Rhodocybe truncata</i> CBS482/50</th><td>EF421110</td><td>AF223167</td><td>–</td><td>–</td></tr><tr><th><i>Rhodocybe tugrulii</i> IMG-7316</th><td>MG050105</td><td>MG050111</td><td>United States</td><td>–</td></tr><tr><th><i>Rhodocybe tugrulii</i> KATO:Fungi:3340</th><td>NR_154436</td><td>NG060175</td><td>Türkiye</td><td>–</td></tr><tr><th><i>Rhodophana griseobrunnea</i> LUG 19799</th><td>MT580804</td><td>MT580803</td><td>France</td><td>–</td></tr><tr><th><i>Rhodophana nitellina</i> TU106939</th><td>UDB015654</td><td>–</td><td>Estonia</td><td>–</td></tr><tr><th><i>Rhodophana nitellina</i> TU106585</th><td>UDB011813</td><td>–</td><td>Estonia</td><td>–</td></tr><tr><th><i>Rhodophana squamulosa</i> CAL:1262</th><td>KT180329</td><td>NG060152</td><td>India</td><td>Raj <i>et al.</i> 2016</td></tr></tbody></table>
Authors and Theories - Comparative table (Update October 2024)
<p>This Excel file features a comparative chronological table/report including data on authors, theories, discoveries, inventions, major events, studies, and the preliminary results of my research work carried out through the outgoing phase of my MSCA Fellowship at Johns Hopkins University and Ca' Foscari University Venice (Horizon 2020 – MGA MSCA-IF – Grant agreement No. 101019781 – SOUNDEPTH).</p>
Table 1 in Review Of Bryophyte Functional Traits In Ecological Studies
<p><b>Table 1.</b> Overview of main bryophyte functional traits according to van Zuijlen et al. (2023).</p><table><tbody><tr><th>Biological traits</th><th><b>Ecological traits</b></th></tr></tbody><tbody><tr><th>generation length</th><td>aquatic species</td></tr><tr><th>growth form</th><td>epiphytic species or not</td></tr><tr><th>life form</th><td>how strong species are bound to forest habitats</td></tr><tr><th>life strategy</th><td>major habitat class “Artificial/Terrestrial”</td></tr><tr><th>peristome</th><td>major habitat class “Forest”</td></tr><tr><th>permanent protonema</th><td>major habitat class “Grassland”</td></tr><tr><th>rhizoids</th><td>major habitat class “Rocky areas”</td></tr><tr><th>r or K strategy</th><td>major habitat class “Shrubland”</td></tr><tr><th>length of the seta</th><td>major habitat class “Wetlands”</td></tr><tr><th>sexual condition</th><td>indicator value – moisture</td></tr><tr><th>sporophyte frequency</th><td>indicator value – heavy metal tolerance</td></tr><tr><th>shoot size</th><td>indicator value – continentality</td></tr><tr><th>spore size</th><td>indicator value – light</td></tr><tr><th>deciduous branches or stem tips</th><td>indicator value – nutrients</td></tr><tr><th>bulbils</th><td>indicator value – salt tolerance</td></tr><tr><th>gemmae</th><td>indicator value – temperature</td></tr><tr><th>deciduous leaves or leave fragments</th><td>substrate class: dead animal carcass or dung</td></tr><tr><th>tubers</th><td>substrate class: bark of living phanerophyte</td></tr><tr><th>size of vegetative propagule</th><td>substrate class: epiphytic on non­woody living substrate</td></tr><tr><th></th><td>substrate class: rock</td></tr><tr><th></th><td>substrate class: soil</td></tr><tr><th></th><td>substrate class: deadwood</td></tr></tbody></table>
Dataset: A review of methods to trace material flows into final products in dynamic material flow analysis - from industry shipments in physical units to monetary input-output tables (p
<p>Dynamic material flow analysis (dMFA) is widely used to model stock-flow dynamics. To appropriately represent material lifetimes, recycling potentials, and service provision, dMFA requires data about the allocation of economy-wide material consumption to different end-use products or sectors, that is, the different product stocks, in which material consumption accumulates. Previous estimates of this allocation only cover few years, countries, and product groups. Recently, several new methods for estimating end-use product allocation in dMFA were proposed, which so far lack systematic comparison. We review and systematize five methods for tracing material consumption into end-use products in inflow-driven dMFA and discuss their strengths and limitations. Widely used data on industry shipments in physical units have low spatio-temporal coverage, which limits their applicability across countries and years. Monetary input–output tables (MIOTs) are widely available and their economy-wide coverage makes them a valuable source to approximate material end-uses. We find four distinct MIOT-based methods: consumption-based, waste input–output MFA (WIO-MFA), Ghosh absorbing Markov chain, and partial Ghosh. We show that when applied to a given MIOT, the methods’ underlying input–output models yield the same results, with the exception of the partial Ghosh method, which involves simplifications. For practical applications, the MIOT system boundary must be aligned to those of dMFA, which involves the removal of service flows, sector (dis)aggregation, and re-defining specific intermediate outputs as final demand. Theoretically, WIO-MFA, applied to a modified MIOT, produces the most accurate results as it excludes massless and waste transactions. In part 2 of this work, we compare methods empirically and suggest improvements for aligning MIOT-dMFA system boundaries.</p>
Table 1 in Revision of the enigmatic South African Cryptolaryngini (Coleoptera, Curculionidae), with description of a new genus and twenty-two new species
<p><b>Table 1.</b> List of species and host plant associations of the species of <i>Cryptolarynx</i> Van Schalkwyk, 1966 and <i>Hadrocryptolarynx</i> Haran gen. nov. * = reared from bulbs of host plant; + = sequences available for at least one population of the species.</p><table><tbody><tr><th><b>Genus</b></th><th><b>species</b></th><th><b>Host associations</b></th><th><b>COI</b></th><th><b>EF1</b></th></tr></tbody><tbody><tr><th><i>Cryptolarynx</i></th><td><i>armatus</i> sp. nov.</td><td><i>O. obtusa</i>, <i>O.</i> cf. <i>suteroides</i></td><td></td><td>+</td></tr><tr><td><i>carinatus</i> sp. nov.</td><td><i>O. purpurea</i></td><td>+</td><td>+</td></tr><tr><td><i>cederbergensis</i> sp. nov.</td><td><i>O. obtusa</i></td><td>+</td><td>+</td></tr><tr><td><i>endroedyi</i> sp. nov.</td><td><i>_</i></td><td></td><td></td></tr><tr><td><i>estriatus</i> (Marshall, 1957)</td><td><i>_</i></td><td></td><td></td></tr><tr><td><i>falciformis</i> sp. nov.</td><td><i>_</i></td><td></td><td></td></tr><tr><td><i>hirtulus</i> sp. nov.</td><td><i>O. obtusa *</i></td><td>+</td><td>+</td></tr><tr><td><i>homaroides</i> sp. nov.</td><td><i>_</i></td><td></td><td></td></tr><tr><td><i>luteipennis</i> sp. nov.</td><td><i>Oxalis</i> spp.</td><td>+</td><td>+</td></tr><tr><td><i>marshalli</i> sp. nov.</td><td><i>O. imbricata</i></td><td>+</td><td>+</td></tr><tr><td><i>muellerae</i> sp. nov.</td><td><i>_</i></td><td></td><td></td></tr><tr><td><i>namaquanus</i> sp. nov.</td><td><i>O. obtusa</i></td><td>+</td><td>+</td></tr><tr><td><i>oberlanderi</i> sp. nov.</td><td><i>O. depressa</i></td><td>+</td><td>+</td></tr><tr><td><i>oberprieleri</i> sp. nov.</td><td><i>O. glabra</i></td><td>+</td><td>+</td></tr><tr><td><i>pilipes</i> sp. nov.</td><td><i>_</i></td><td></td><td></td></tr><tr><td><i>pyrophilus</i> sp. nov.</td><td><i>O. pes-capreae</i></td><td>+</td><td>+</td></tr><tr><td><i>robustus</i> sp. nov.</td><td><i>Oxalis</i> spp.</td><td>+</td><td>+</td></tr><tr><td><i>san</i> sp. nov.</td><td><i>O. luteola</i>, <i>O. obtusa</i>, <i>O.</i> cf. <i>hirta</i></td><td>+</td><td>+</td></tr><tr><td></td><td><i>O.</i> cf. <i>luteola</i>, <i>O. obtusa</i>,</td><td></td><td></td></tr><tr><td><i>spinicerus</i> sp. nov.</td><td><i>O.</i> cf. <i>odorata</i></td><td></td><td>+</td></tr><tr><td><i>squamulatus</i> sp. nov.</td><td><i>O. obtusa</i></td><td>+</td><td>+</td></tr><tr><td><i>subglaber</i> sp. nov.</td><td><i>O. lanata</i>, <i>O. purpurea</i>, <i>O. tenuifolia</i></td><td>+</td><td>+</td></tr><tr><td><i>variabilis</i> sp. nov.</td><td><i>O. pes-capreae *</i>, <i>O. purpurea *</i></td><td>+</td><td>+</td></tr><tr><td><i>vitis</i> (Marshall, 1957)</td><td><i>O. glabra</i></td><td>+</td><td>+</td></tr><tr><td>sp. 1</td><td><i>O. obtusa</i></td><td>+</td><td>+</td></tr><tr><td>sp. 2</td><td><i>O.</i> cf. <i>purpurea</i></td><td>+</td><td>+</td></tr><tr><td>sp. 3</td><td><i>O. obtusa</i></td><td>+</td><td>+</td></tr><tr><td>sp. 4</td><td><i>_</i></td><td></td><td></td></tr><tr><td>sp. 5</td><td><i>O. obtusa</i></td><td></td><td>+</td></tr><tr><td>sp. 6</td><td><i>_</i></td><td></td><td></td></tr><tr><th><i>Hadrocryptolarynx</i> gen. nov.</th><td><i>major</i> gen. et sp. nov.</td><td><i>O. luteola</i>, <i>O. obtusa</i>, <i>Oxalis</i> spp.</td><td></td><td></td></tr></tbody></table>
TABLE 1 in A sabre-tooth predator from the Neotropics: Cranial morphology of Anachlysictis gracilis Goin, 1997 (Metatheria, Thylacosmilidae), based on new specimens from La Venta (Middle Miocene, Colombia)
<p>TABLE 1. — Dental measurements of the specimens of <i>Anachlysictis gracilis</i> Goin, 1997. Abbreviations: <b>C/c</b>, upper/lower canines; <b>P/p</b>, premolars; <b>L</b>, length; <b>M/m</b>, molars; <b>Tal.</b>, talonid; <b>Trg</b>, trigonid; <b>W</b>, width. Measurements expressed in millimeters.</p><table><tbody><tr><th><b>Specimen</b></th><th></th><th><b>C</b></th><th><b>P2</b></th><th><b>P3</b></th><th></th><th><b>M1</b></th><th><b>M2</b></th><th><b>M3</b></th><th><b>M4</b></th></tr></tbody><tbody><tr><th>VPPLT 1612 (right)</th><td>L</td><td>20.63</td><td>3.47</td><td>6.46</td><td></td><td>12.3</td><td>13.22</td><td>12.99</td><td>3.99</td></tr><tr><th></th><td>W</td><td>6.74</td><td>1.88</td><td>4.42</td><td></td><td>6.97</td><td>8.83</td><td>10.2</td><td>10.8</td></tr><tr><th>VPPLT 1612 (left)</th><td>L</td><td>?</td><td>?</td><td>6.41</td><td></td><td>12.5</td><td><i>c.</i> 12.60</td><td><i>c.</i> 13.18</td><td>4</td></tr><tr><th></th><td>W</td><td>?</td><td><i>c.</i> 2.60</td><td>2.56</td><td></td><td>6.45</td><td>8.67</td><td>10.3</td><td><i>c.</i> 10.70</td></tr><tr><th></th><td></td><td><b>c</b></td><td><b>p2</b></td><td><b>p3</b></td><td></td><td><b>m1</b></td><td><b>m2</b></td><td><b>m3</b></td><td><b>m4</b></td></tr><tr><th>IGM 184247 (right)</th><td>L</td><td>?</td><td><i>c.</i> 6.00</td><td><i>c.</i> 7.20</td><td></td><td><i>c.</i> 9.50</td><td>11.45</td><td>13.6</td><td>13.4</td></tr><tr><th></th><td>W</td><td>?</td><td><i>c.</i> 3.00</td><td><i>c.</i> 3.30</td><td>Trg</td><td><i>c.</i> 4.45</td><td>5.25</td><td>6</td><td>6</td></tr><tr><th></th><td></td><td></td><td></td><td></td><td>Tal.</td><td><i>c.</i> 4.00</td><td>4.75</td><td>5.05</td><td>1.75</td></tr><tr><th>IGM 184247 (left)</th><td>L</td><td>?</td><td>?</td><td>?</td><td></td><td>?</td><td>11.3</td><td>13.6</td><td>?</td></tr><tr><th></th><td>W</td><td>?</td><td>?</td><td>?</td><td>Trg</td><td>?</td><td>5</td><td>5.8</td><td>?</td></tr><tr><th></th><td></td><td></td><td></td><td></td><td>Tal.</td><td>?</td><td>4.45</td><td>5.1</td><td>?</td></tr><tr><th>VPPLT 1612 (right)</th><td>L</td><td>?</td><td><i>c.</i> 4.25</td><td><i>c.</i> 6.70</td><td></td><td>9.38</td><td>11.81</td><td>13.38</td><td>13.6</td></tr><tr><th></th><td>W</td><td></td><td><i>c.</i> 2.26</td><td><i>c.</i> 3.91</td><td>Trg</td><td>4.25</td><td>5.6</td><td>6.59</td><td>6.73</td></tr><tr><th></th><td></td><td></td><td></td><td></td><td>Tal.</td><td>3.6</td><td>4.85</td><td>5.41</td><td>2.5</td></tr><tr><th>VPPLT 1612 (left)</th><td>L</td><td>8.94</td><td>3.39</td><td>6.7</td><td></td><td>9.24</td><td><i>c.</i> 12.05</td><td><i>c.</i> 13.35</td><td><i>c.</i> 14.00</td></tr><tr><th></th><td>W</td><td>5.32</td><td>1.76</td><td>2.5</td><td>Trg</td><td>3.88</td><td>5.29</td><td><i>c.</i> 6.46</td><td>6.23</td></tr><tr><th></th><td></td><td></td><td></td><td></td><td>Tal.</td><td><i>c.</i> 3.20</td><td>4.55</td><td><i>c.</i> 5.62</td><td>2.5</td></tr></tbody></table>
TABLE 2 in A sabre-tooth predator from the Neotropics: Cranial morphology of Anachlysictis gracilis Goin, 1997 (Metatheria, Thylacosmilidae), based on new specimens from La Venta (Middle Miocene, Colombia)
<p>TABLE 2. — Body mass estimations. Abbreviations: <b>Log</b>, common logarithm (with base 10); <b>ln</b>, natural logarithm (with base e); <b>M2A</b>, second upper molar area; <b>M2L</b>, second upper molar length; <b>m2A</b>, second lower molar area; <b>m3L</b>, third lower molar length; <b>%PE</b>, percent prediction error; <b>R2</b>, ratio estimate; <b>SE</b>, smearing estimate correction factor; <b>X</b>, selected variable. Body mass expressed in kilograms. Equation source references: <b>1</b>, Myers 2001, ‘All species’ data-set; <b>2</b>, Myers 2001, Dasyuromorphian data set; <b>3</b>, Zimicz 2012.</p><table><tbody><tr><th></th><th></th><th></th><th></th><th></th><th></th><th><b>Body</b></th><th></th></tr></tbody><tbody><tr><th><b>Species</b></th><td><b>Equation</b></td><td><b>X</b></td><td><b>%PE</b></td><td><b>R2</b></td><td><b>SE</b></td><td><b>mass</b></td><td><b>Ref.</b></td></tr><tr><th>“ <i>A. gracilis</i> (IGM 184247)”</th><td>log(y) = 1.005 + 1.857 log(x)</td><td>m2A</td><td>7.00</td><td>0.951</td><td>1.119</td><td>22.77</td><td>1</td></tr><tr><th></th><td>log(y) = 0.567 + 3.400 log(x)</td><td>m3L</td><td>12.00</td><td>0.945</td><td>1.035</td><td>27.29</td><td>2</td></tr><tr><th></th><td>ln(y) = 1.76 + 3.17 ln(x)</td><td>m3L</td><td>12.08</td><td>0.950</td><td>1.110</td><td>25.29</td><td>3</td></tr><tr><th>“ <i>A. gracilis</i> (VPPLT 1612)”</th><td>log(y) = 0.426 + 1.890 log(x)</td><td>M2A</td><td>7.00</td><td>0.989</td><td>1.029</td><td>22.15</td><td>2</td></tr><tr><th></th><td>log(y) = 1.005 + 1.857 log(x)</td><td>m2A</td><td>7.00</td><td>0.951</td><td>1.119</td><td>27.19</td><td>1</td></tr><tr><th></th><td>ln(y) = 1.89 + 3.14 ln(x)</td><td>M2L</td><td>7.03</td><td>0.950</td><td>1.160</td><td>25.47</td><td>3</td></tr><tr><th></th><td>log(y) = 0.567 + 3.400 log(x)</td><td>m3L</td><td>12.00</td><td>0.945</td><td>1.035</td><td>25.82</td><td>2</td></tr><tr><th></th><td>ln(y) = 1.76 + 3.17 ln(x)</td><td>m3L</td><td>12.08</td><td>0.950</td><td>1.110</td><td>24.02</td><td>3</td></tr><tr><th>“ <i>P. goini</i> (MLP 07-VII-1-1)”</th><td>log(y) = 0.426 + 1.890 log(x)</td><td>M2A</td><td>7.00</td><td>0.989</td><td>1.029</td><td>25.93</td><td>2</td></tr><tr><th></th><td>ln(y) = 1.89 + 3.14 ln(x)</td><td>M2L</td><td>7.03</td><td>0.950</td><td>1.160</td><td>19.79</td><td>3</td></tr><tr><th>“ <i>T. atrox</i> (P14531)”</th><td>log(y) = 0.426 + 1.890 log(x)</td><td>M2A</td><td>7.00</td><td>0.989</td><td>1.029</td><td>42.50</td><td>2</td></tr><tr><th></th><td>ln(y) = 1.89 + 3.14 ln(x)</td><td>M2L</td><td>7.03</td><td>0.950</td><td>1.160</td><td>41.12</td><td>3</td></tr></tbody></table>
Table 2 in Five new species of Enchytraeidae (Annelida: Clitellata) from Mediterranean woodlands of Italy and reaffirmed validity of Achaeta etrusca, Fridericia bulbosa and F. miraflores
<p>Table 2. Key morphological characters distinguishing <i>Fridericia rara</i> sp. nov. from <i>F. bulbosa</i> sensu stricto, the only known quadrisetose congener possessing adiverticulate spermathecae, hyaline coelomocytes and short, simple peptonephridia. Measurements in this table refer to live specimens, except where specified by (f), meaning fixed material.</p><table><tbody><tr><th>Species</th><th><i>F. rara</i> sp. n.</th><th><i>F. bulbosa</i> sensu Rota, 1995</th><th><i>F. bulbosa</i> – urban SI</th><th><i>F. bulbosa</i> – urban NA</th></tr></tbody><tbody><tr><th>Length</th><td>5 mm</td><td>7–9 mm</td><td>6 mm</td><td>5–7 mm</td></tr><tr><th>Width (at clitellum)</th><td>0.25 mm</td><td>0.23–0.28 mm</td><td>0.23 mm</td><td>0.22–0.26 mm</td></tr><tr><th>Segments</th><td>27–32</td><td>39–41</td><td>27–37</td><td>24–36</td></tr><tr><th>Chaetal formula</th><td>0,2 – 2: 2,3,4 – 2</td><td>2,3,4– 4,3,2: 2,3,4–4,3,2</td><td>2,3,4 – 2: 2,3,4 – (4,3),2</td><td>2,3,4 – 2: 2,3,4 – 4,3,2</td></tr><tr><th>Chaetal length precl.</th><td>24–27 μm (lat.); 27-35 μm (v.)</td><td>up to 45 μm</td><td>up to 42 μm</td><td>up to 40 μm</td></tr><tr><th>length postcl.</th><td>26–35 μm (lat. & v.)</td><td>50 μm</td><td>up to 42 μm</td><td>40 μm</td></tr><tr><th>Clitellar pattern</th><td>regular rows, chequered, interr. ventrally in XII; cells mostly hyaline, large</td><td>regular rows, ventr. absent between ♂ pores, granular behind them, mosaic in XIII; hyaline cells large</td><td>regular rows, absent between ♂ pores, granular behind them, mosaic in XIII; hyaline cells large</td><td>regular rows, absent between ♂ pores, granular behind them, mosaic in XIII; hyaline cells large</td></tr><tr><th>Male openings</th><td>longitudinal, glandular duct end</td><td>longitudinal</td><td>longitudinal</td><td>longitudinal</td></tr><tr><th>Peptonephridia</th><td>Type a</td><td>Type a</td><td>Type a</td><td>Type a</td></tr><tr><th>Coelomocytes:</th></tr><tr><th>nucleated</th><td>Type a,.24–30 μm long(f)</td><td>Type a, up to 30 μm long</td><td>Type a</td><td>Type a, 32–40 μm long</td></tr><tr><th>anucleate</th><td>small (2.5–6 μm)(f)</td><td>small (4–10 μm)</td><td>small</td><td>small (4–6 μm)</td></tr><tr><th>Chylus cells</th><td>XII–XIV</td><td>XIII–XIV</td><td>XIII–XIV</td><td>XIII–XIV</td></tr><tr><th>Dorsal vessel from</th><td>XV</td><td>XVI–XVII</td><td>XVI</td><td>XV–XVII</td></tr><tr><th>Preclitellar nephridia</th><td>3 pairs (6/7–8/9) midventral</td><td>5 pairs (6/7–10/11)</td><td>5 pairs (6/7–10/11) subterminal</td><td>5 pairs (6/7–10/11)</td></tr><tr><th>Sperm funnels l: w</th><td>88: 50 μm</td><td>152–184: 65 μm 112: 50(f)</td><td>80: 32 μm (f)</td><td>75–100: 42–50 μm</td></tr><tr><th>Penial bulb length</th><td>50 μm(f)</td><td>120 μm, soft, 80(f)</td><td>50–58 μm(f)</td><td>60–64 μm(f)</td></tr><tr><th>Spermathecal ampulla w;</th><td>45 μm; 32(f)</td><td>30 μm; 26(f)</td><td>30 μm; 26–28(f)</td><td>32 μm; 24–29(f)</td></tr><tr><th>ental ducts;</th><td>adjacent;</td><td>adjacent;</td><td>adjacent, on one side;</td><td>merging;</td></tr><tr><th>ectal duct l: w;</th><td>112: 10 μm(f);</td><td>245: 12 μm;</td><td>225: 15 μm;</td><td>175: 15 μm;</td></tr><tr><th>glands at pore</th><td>one, small, 8 μm long(f)</td><td>one, 28 μm long</td><td>one, small, 13 μm long</td><td>one, small, 10 μm long(f)</td></tr></tbody></table>
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Allen Brain Atlas
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Annotated Behaviour and Observability Dataset (ABODe)
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OpenNeuro
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