746 research outputs found
Pari songs
No full textIncludes four prophet songs, fishing songs and chant to wind. Provided to Ian Maddocks by New Zealand author James McNeish
Maddocks, C G, NX13124
No full textThis record was harvested from a previous catalogue system and will be withdrawn in 2025. Information in this record may be superseded or incomplete. Visit this record in UMA's new catalogue at: https://archives.library.unimelb.edu.au/nodes/view/401012Surname: MADDOCKS. Given Name(s) or Initials: C G. Military Service Number or Last Known Location: NX13124. Missing, Wounded and Prisoner of War Enquiry Card Index Number: 9513.220658
Item: [2016.0049.33305] "Maddocks, C G, NX13124
Schedopontocypris Maddocks 1969
No full textGenus SCHEDOPONTOCYPRIS Maddocks, 1969 b 20. * S. ? maculata Schornikov, 1973 Schornikov, 1973: 59 (Propontocypris (S. ?) m.); Aladin & Schornikov, 1986 b: 830, 831 (Propontocypris m.); Aladin, 1987: 820 (Propontocypris m.); Matyushin & Fedotov, 1992: 34 (Propontocypris m.); 1993: 86 (Propontocypris m.); Schornikov, 1997: 95 (Propontocypris (S. ?) m.); Schornikov, 1998: 226 (Propontocypris (S.) m.); Schornikov & Chavtur, 2001: 91; 2002: 94; Schornikov & Zenina, 2004 b: 214. 21. * S. ? postconcava Schornikov, 1973 Schornikov, 1973: 57; 1997: 95 (Propontocypris (S. ?) p.); 1998: 226 (Propontocypris (S.) p.). 22. S. ? sp. 1 Schornikov & Chavtur, 2001: 91; 2002: 94; Schornikov & Zenina, 2004 b: 214.Published as part of Schornikov, Evgeny I., 2006, Checklist of the ostracod (Crustacea) fauna of Peter the Great Bay, Sea of Japan, pp. 29-59 in Zootaxa 1294 on page 34, DOI: 10.5281/zenodo.17351
Sputnik diner
No full textFrom an award-winning writer reminiscent of Richard Russo and Russell Banks: get ready for a heady and heartbreaking stay in Nanticoke, home of the Sputnik Diner. Travelling on Highway 3, along the upper lip of Lake Erie and through a moustache of tobacco fields and sky, we arrive in Nanticoke, Ontario. At the heart of the town is the Sputnik Diner, a smoky grill where the jukebox whirs out an ever-changing soundtrack. Navigating their way through the lies and sexual betrayals are Grace, waitress and self-defeating artist; Buzz, who offers the cook's eye view of the eccentric patrons and staff; and Marcel, the gruff French-Canadian owner who doles out hilarious malapropisms and his own peculiar brand of hospitality. In muscular prose, Maddocks traces the lives of flawed, gutsy, and utterly loveable characters: an immigrant family from Wales, struggling to find their place in the ragged, darkly absurd world of tobacco-belt Ontario; two young brothers who steal the family car and try to come to grips with their father's cancer out on the dinosaur mini-putt course in the pouring rain; and Grace, who seeks out her birth parents only to confront the dizzying epiphanies of that momentous discovery. There are others too, whose stalled dreams, gritty hopes and humour spark through the Sputnik Diner universe. --From publisher description.short stor
Bairdoppilata hirsuta
No full textBairdoppilata hirsuta (Brady, 1880) (Figure 11) 1880 Bairdia hirsuta Brady, n. sp.: 51, pl. 4, figs. 4, 5. 1976 Bairdia hirsuta Brady. —Puri & Hulings, p. 265, pl. 4, figs. 4, 5. Not 1969 Bairdoppilata (Bairdoppilata?) hirsuta (Brady).—Maddocks, p. 79, fig. 43A–I, pl. 2, figs. 1, 2. Not 1973 Bairdoppilata hirsuta (Brady).—Maddocks, p. 42, figs. 5B–G, 6A–E [= B. hirsutella, n. sp., see below]. Not 2009 Bairdoppilata? hirsuta (Brady).—Maddocks et al., Checklist, p. 888. Material Examined: None. Taxonomic Remarks: The species is firmly identified only from the type locality. The lectotype selected by Puri & Hulings (1976) is a somewhat nondescript RV from Challenger Station 300, near Juan Fernandez Island in the Southeast Pacific (33 o 44’0”S, 78 o 10’0” W, depth 1375 fathoms). They reported the dimensions as: RVL 1.46 mm, RVH 0.90 mm (see Fig. 11). Supplemental bairdoppilatan dentition was not mentioned and is not visible in their illustration. The calcified inner lamella (infold) of the lectotype is somewhat narrow, and it may be an instar. The soft parts are unknown. Redescription of a larger, preferably living population from this locality will be needed to recognize this species, and all records of B. hirsuta at other localities require re-examination. Specimens from Eltanin station 25, in the East Pacific were identified as B. hirsuta by Maddocks (1973), but that identification is dubious. For clarity of communication, a new name, B. hirsutella Maddocks, n. sp., is proposed below for that Eltanin population. Maddocks (1969) described and illustrated two adult females as B. (B.?) hirsuta (specimen 468F, USNM 121353; specimen 469F, USNM 121355; both from the Gulf of Mexico, 28 o 15’N, 87 o 02’W, depth 1000 m). Their dimensions agree well with the population described from Eltanin station 25 (Fig. 12), but without males a firm identification is difficult. Maddocks (1969) also reported subfossil valves from numerous Albatross and Anton Bruun stations, but those identifications are even less plausible. Brandão (2008) demonstrated that the diversity of bairdioids has been severely underestimated in the Southern Ocean and in deeper water.Published as part of Maddocks, Rosalie F., 2022, Taxonomic applications of the esophageal flapper valve in Bairdoppilata and Glyptobairdia (Bairdiidae, Ostracoda), with comments on anatomy, ontogeny, and geography, pp. 301-342 in Zootaxa 5175 (3) on pages 321-322, DOI: 10.11646/zootaxa.5175.3.1, http://zenodo.org/record/700358
Bairdiidae Sars 1888
No full textFamily BAIRDIIDAE Sars, 1888 1888 Family Bairdiidae Sars: 288. Nomenclatural Remarks. In an influential review of crustacean classification (Martin & Davis 2001), the author and date of Family Bairdiidae were incorrectly given as “Sars, 1865.” This error has found its way into recent papers and the online World Ostracoda Database (Brand„o et al. 2018). The issue for 1865 actually appeared in 1866 (Kempf 1988, p. 309). In that paper, Sars did name three other families (Conchoeciidae, Polycopidae and Cytherellidae), but he classified the Genus Bairdia in the Family Cypridae Baird, 1845 (Sars 1866, p. 19). The spelling of “ Cypridae ” was validly emended to “ Cyprididae ” by Baird (1850, p. 139; see also Swain 1961, p. Q211; Howe 1955, p. 14; 1962, p. 68). The issue date of Sars’ paper on “ Ostracoda Mediterranea ” was verified as 1888 by Howe (1955, p. 314; 1962, p. 338) during preparation of the Ostracoda volume of the Treatise on Invertebrate Paleontology. The Kraus reprint edition (published in 1969 by Nendeln/ Liechtenstein) states the place and date of publication as “Kristiania 1888.” See also Sylvester-Bradley (1961, p. Q201, Q417), Maddocks (1969, 1995), Maddocks & Iliffe (1986), Maddocks & Wouters (1990), and Brand„o (2008). The date has been erroneously cited as 1887 by Morkhoven (1963, p. 467), Kempf (1988, p. 309), Hartmann (1989, p. 1006), and many others.Published as part of Maddocks, Rosalie F., 2021, Taxonomic applications of the esophageal flapper valve in the Genus Neonesidea (Bairdioidea, Podocopida, Ostracoda), including descriptions of new and poorly known species from the Caribbean and Gulf of Mexico, pp. 451-492 in Zootaxa 4903 (4) on page 454, DOI: 10.11646/zootaxa.4903.4.1, http://zenodo.org/record/443122
Bairdoppilata villosa
No full textBairdoppilata villosa (Brady, 1880) 1880 Bairdia villosa Brady, n. sp.: p. 50, pl. 3, figs. 3a–b; pl. 5, figs. 2a–g; pl. 8, figs. 4a–f. 1976 Bairdia villosa Brady. —Puri & Hulings, p. 266, pl. 2, figs. 1–4. Not (?) 1969 Bairdoppilata (Bairdoppilata?) villosa (Brady).—Maddocks, p. 75, figs. 40A–H, 41A–C. Material Examined: None. Anatomical Remarks: Brady’s drawing of the esophageal flapper valve of B. villosa was the first published illustration of this structure (Brady 1880, pl. 3, fig. 3; Maddocks 2015, fig. 1A). It shows the general relationships of the ring with collar and belt, two thick, symmetrical braces ending in oval aprons, and a fan-shaped plate with concentric light and dark bands, but it does not show whether the posterior margin of the plate is dentate. Taxonomic Remarks: The species is reliably identified only from the subfossil lectotype specimen at the type locality near Kerguelen Island. Brady’s description of soft anatomy should be verified from new material. All reports of this species from elsewhere should be re-examined. It is likely that they comprehend multiple species, as Brandão (2008) showed for B. simplex. For example, the two adult males (specimen 371M, USNM 121344; specimen 194M, USNM 121345) described by Maddocks (1969) were collected from Eltanin station 1418 (54 o 32’S, 159 o 02’E, 113– 92 m), which is thousands of kilometers east of the type locality at Kerguelen Island. They represent a species of Bairdoppilata, but the identification as B. villosa requires re-examination.Published as part of Maddocks, Rosalie F., 2022, Taxonomic applications of the esophageal flapper valve in Bairdoppilata and Glyptobairdia (Bairdiidae, Ostracoda), with comments on anatomy, ontogeny, and geography, pp. 301-342 in Zootaxa 5175 (3) on page 328, DOI: 10.11646/zootaxa.5175.3.1, http://zenodo.org/record/700358
Bairdoppilata simplex
No full textBairdoppilata simplex (Brady, 1880) 1880 Bairdia simplex Brady, n. sp.: 51, pl. 7, figs. 1a–d. 1976 Bairdia simplex Brady. —Puri & Hulings, p. 266, pl. 3, figs. 11–14. Not 1969 Bairdoppilata (Bairdoppilata?) simplex Brady. —Maddocks, p. 77, figs. 42A–H. 2008 ? Bairdoppilata simplex (Brady).—Brandão, p. 379, figs. 3.20a, b; 4, 5G–H; table 3. Material Examined: None. Taxonomic Remarks: The species is firmly identified only from subfossil type specimens at the type locality, and the soft parts are not known. Brandão (2008) demonstrated that, in the Southern Ocean alone, the materials subsequently reported under this name include at least 10 species, and identifications from other regions are even more suspect. For example, two specimens from the materials identified as B. (B.?) simplex by Maddocks (1969) were re-examined by Brandão (2008, p. 387, figs. 8B, E, H–I, L, P, Q): Female specimen 191F, USNM 121347, was collected at Eltanin station 418, 62 o 39–40’S, 56 o 8–10’W, 311– 426 m. Male specimen 205M, USNM 121348, was collected at Eltanin station 1345, 54 o 50–51’S, 129 o 46–48’W, 915–1153 m. Brandão stated that they represent either one or two different species, which she provisionally identified as ? Bairdoppilata sp. 1 aff. ? B. labiata (Müller). The appendages and hemipenis were described, but not the esophageal valve.Published as part of Maddocks, Rosalie F., 2022, Taxonomic applications of the esophageal flapper valve in Bairdoppilata and Glyptobairdia (Bairdiidae, Ostracoda), with comments on anatomy, ontogeny, and geography, pp. 301-342 in Zootaxa 5175 (3) on page 328, DOI: 10.11646/zootaxa.5175.3.1, http://zenodo.org/record/700358
Restricted Quadratic Forms, Inertia Theorems and the Schur Complement.
No full textThe starting point of this investigation is the properties of restricted quadratic forms, x^TAx, x {IS A MEMBER OF} S {IS A SUBSET OF} {m DIMERNSIONAL SPACE}, where A is an m x m real symmetric matrix, and S is a subspace. The index theory of Heatenes (1951) and Maddocks (1985) that treats the more general Hilbert space version of this problem is first specialized to the finite-dimensional context, and appropriate extensions, valid only in finite-dimensions, are made. The theory is then applied to obtain various inertia theorems for matricea and positivity tests for quadratic forms. Expressions for the inertial of divers symmetrically partitioned matrices are described. In particular, an inertia theorem for the generalized Schur complement is given. The investigation recovers, links and extends several, formerly disparate, results in the general area of inertia theorems
Macroscapha INAEQUATA MADDOCKS 1990
No full text<i>MACROSCAPHA INAEQUATA</i> MADDOCKS, 1990 <p>(FIGS 34, 37A–C, 37H–J, 38A–C, 38H–J, 39D, 39H, 40A–G, 41A–C, 41Z, 64G–H)</p> <p> 1979 <i>Macrocyprina</i> sp. nov. 7, Maddocks, 1979, pl. 2.11.</p> <p> 1990?in part <i>Macroscapha inaequata</i> Maddocks, 1990: 99–100. Numerous figures and plates.</p> <p> 1997 <i>Macroscapha inaequata,</i> Hartmann, 1997: 246– 247, fig. 104.</p> <p> <i>Material:</i> 61 live specimens.</p> <p>2 A F (SNB 0054), 6 A M (SNB 0021, 0034, 0052, 0053), 1 A, 1 (A-1), EASIZ II, # 48-107, ZMH K- 40819;</p> <p>1 A F (SNB 0752), EASIZ II, # 316, ZMH K-40821; 1 A M (SNB 0753), EASIZ II, # 323, ZMH K-40822; 17 A F, 13 A M (SNB 0099 -DNA 2, SNB 0100-DNA 12, SNB 0580-DNA 287, SNB 0581-DNA 288, SNB 0582- DNA 289), six juveniles, three live specimens (SNB 0098 -DNA 1, SNB 0778-0784), ANDEEP III, 74-6-E; 5 A F, 5 A M (SNB 0575-0579 -DNA 283-286), ANDEEP II, # 74-6-S, ZMH K-41487.</p> <p> <i>Distribution (Fig. 34):</i> Recent. Atlantic Sector of the SO, 311-2452 m.</p> <p> <i>Right valve measurements (Fig. 34):</i> A F L 1.80– 1.94 mm, H 0.70–0.79 mm; A M L 1.80–1.90 mm, H 0.71–0.76 mm; (A-1) L 1.48–1.56 mm, H 0.56– 0.61 mm.</p> <p> <i>Remarks:</i> Considering the material studied herein, the hemipenis of the only adult male of <i>Mh. inaequata</i> collected from the continental slope (no. 323) presents a more sinuous posterior margin (Fig. 40A–D) than that of specimens collected on the shelf, which present a subhemispherical outline (Fig. 40E). Variation in hemipenis outline and in the copulatory process (bilobated versus elongated) can also be observed amongst previously studied specimens (Maddocks, 1990: pl. 92. 3, 92.7). Additionally, the only abyssal record of <i>Mh. inaequata</i> (collected from the Pacific Sector of the SO) involves a teratological specimen of considerably larger size (~ 2.3 mm) and more rectilinear outline than the other specimens (Maddocks, 1990: 100, graph 47); this record is therefore not considered herein. Consequently, similar to <i>Mk. glacierae</i> and <i>Mh. opaca</i>, I think that <i>Mh. inaequata</i> is most probably a group of closely related species, instead of one species with such a large morphological variation, geographical and bathymetrical distribution.</p> <p> <i>Adult chaetotaxy:</i> Antenna I 1(0/0), 2(0/.2)+3(.1/.1), 4(.1/.1), 5(.1/.1), 6(.2/.3), 7(0/0:4). Antenna II 1(0/.0-1:1), 2(0/0:1), Exopodite (0/0:2,1r), 3(0/.5-6.4), 4[female (.1r./.1r.1c,2)] [male (.1r./.1r.1c,2mod,1)], 5(0/1c,1:3-4c,1-2), 6(0/0:2c,2-3). Mandible 1(.1/0: 5-6t,+8), 2(0/.2:1), Exopodite (1r,5-7), 3(0/.4:-4), 4(.3.2/.4), 5(0./0:2-3c,2-3). Maxilla I vibratory plate (2strahlen,+16), palp 1(.1/0), 2(.4-5/0), 3(0/0:6). Appendage V 1(0/0:1-2.0-1.1), Exopodite (0/0:7-10), [female 2(0/0), 3(0/0), 4(0/.1), 5(.1./ 0:1c,1)] [male 2(0/2mod,1:1r), 3(0/0:1mod)]. Appendage VI 1(.1-2./0), 2(.2.1./.1), 3(.1/0), 4(.1/0), 5(.1,1r/0), 6(0/ 0:1,2c). Appendage VII 1(0/0:1), 2(.1.1.1/.1.), 3(.1/0), 4(.1/0), 5(.2/0), 6(0/0:2,1mod). Furca (0/0:1,4r).</p> <p> MACROSCAPHA WALTERAE <b>SP.</b> <b>NOV.</b> (FIGS 34, 37K–M, 38K–M, 39E–G, 39J–K, 39P–Q, 40H–P, 41D–I, 412, 42, 64A, 64I–J)</p> <p> <i>Etymology:</i> In honour of Renate Walter (University of Hamburg) for her valuable technical assistance for three generations of ostracodologists.</p> <p> <i>Material:</i> 43 live specimens plus 43 valves.</p> <p>Holotype: 1 A M (SNB 0745) (soft parts in glass slide, valves in micropalaeontological slide), ANDEEP II, #132-2-S, ZMH K-41484.</p> <p>Paratypes: 6 A F (SNB 0047, 0048), 9 A M (SNB 0051, 0748, 0749, 0750, 0751), 6 (A-1), EASIZ II, # 89, ZMH K-40818; 2 A F, 3 (A-1), 6 RV, 7 LV, 5 RLV, 4 V, ANDEEP II, # 132-2-S, ZMH K-41486; 1 A M (SNB 0574), 7 RV, 5 LV, 2 RLV, ANDEEP II, # 133-3, ZMH K-41481; 1 A M (SNB 0119 -DNA 22) ANDEEP III, # 121-7, ZMH K-41480; 3 A F (SNB 0421 -DNA 128, SNB 0462-DNA 169, SNB 0611-DNA 318), 3 A M (SNB 0419 -DNA 126, SNB 0422-DNA 129, SNB 0746), 4 (A-1) (SNB 0420 -DNA 127, SNB 0612-DNA 319, SNB 0613-DNA 320), three live specimens (SNB 0799, 0800), ANDEEP III, # 133-2, ZMH K-41485.</p> <p> <i>Distribution (Fig. 34):</i> Recent. Weddell Sea, 1123– 2666 m.</p> <p> <i>Valve measurements (Fig. 34):</i> Holotype, RV L 2.01 mm, H 0.80 mm; LV L 1.96 mm, H 0.80 mm. Paratypes, A L 1.90–2.16 mm, H 0.76–0.88 mm; (A–1) L 1.60–1.72 mm, H 0.62–0.68 mm.</p> <p> <i>Diagnosis:</i> Carapace fairly large (for the genus); lateral outline subhemispherical to subtriangular with faint dorsal angle; posterior margin rounded. Female appendage V with one short and three medium-sized, terminal setae, medial and ventral ones subequal in length and thickness. Male appendage V very asymmetrical; terminal podomere strongly sclerotized, and pointed at 90° in right appendage, but smoothly curved in left one. Furca very asymmetrical. Hemipenis</p> <p>·</p> <p>subhemispherical to elongated, strongly sclerotized, with V-shaped copulatory process, maximum height posterior to mid-length. Zenker’s organ with very thin, weakly sclerotized central tube and very large terminal bulb; vas deferens arranged as several loops as long as the Zenker’s organ’s central tube.</p> <p> <i>Description:</i> Carapace fairly large (for the genus), lateral outline subhemispherical to subtriangular, with faint dorsal angle; posterior margin obtusely rounded; ventral margin fairly straight, anterior margin protruded and narrowly rounded. Vestibules medium-sized, zone of concrescence thin, except by the medium-sized anteroventral region; radial pore canals mostly straight, very few slightly ramified. RV always larger than and overlapping LV.</p> <p>Podomere IV of antenna I and podomere II of antenna II elongated. Mandible with one conical plus four tricuspidate teeth. Female appendage V with podomere II (= palp podomere I) more than two times longer than podomere III; podomere V with one medial and one ventral, subequal, medium-sized setae, dorsal seta short. Male appendage V strongly asymmetrical, podomere I (basis) with long setae; right appendage with podomere II bearing one long and one short modified setae (= pegs) plus one short seta, and podomere III strongly sclerotized and pointed at 90°; left appendage with podomere II bearing two short modified setae (= pegs) plus one short seta, and podomere III smoothly curved. Podomere II of appendage VI with three long, dorsal setae; podomere VI with one long claw, one medium-sized seta, and one short seta. Reflexed seta of appendage VII long. Furca very asymmetrical, shorter ramus three-quarters as long as longer ramus, suture between rods and terminal setae conspicuous. Hemipenis subhemispherical to elongated, strongly sclerotized; maximum height posterior to mid-length; copulatory process V-shaped. Zenker’s organ with very thin, weakly sclerotized, central tube and very large terminal bulb; vas deferens arranged as several loops as long as the Zenker’s organ’s central tube.</p> <p> <i>Adult chaetotaxy:</i> Antenna I 1, 2(0/.2), 3(.1/.1.), 4(.1/.1.), 5(.1/.1), 6(.2/.3), 7(0/0:4). Antenna II 1(0/0:1), 2(0/ 0:1), Exopodite (0/0:2,1r), 3(0/6.4), 4[female (.2./.2.1c,3)] [male (.1r./.2r.1c,2mod,1)], 5(0/.1c,1:4c,1), 6(0/ 0:2c,2). Mandible 1(0/ 5t,+5.1.), 2(0/.2:1), Exopodite (0/0:1r,7), 3(0/.4-5:3-4), 4(.4-5/4), 5(0/0:3c,3). Maxilla I vibratory plate(2re,19), palp 1(.1/0), 2(.4/0), 3(0/0:6). Appendage V 1(0/.2.1.1), Exopodite (0/0:3.4-7), [female 2, 3, 4(0/.1) 5(.1./0:1,1)]; [male 2(0/2mod,1:0-1r), 3(0/.1r:1mod)]. Appendage VI 1(.1-2/0), 2(.2.1/.1), 3(.1/.0), 4(.1/0), 5(1,1r/0) 6(0/0:1,2c). Appendage VII 1(0/0:1), 2(.1.1.1/1) 3(.1/0), 4(.1/0), 5(.2/0), 6(0/0:2,1re). Furca 1(0/0:3-4r.1).</p> <p> <i>Remarks:</i> Genetic distances (marker COI, model of evolution HKY85) amongst specimens of the same station (no. 133-2, average 0.0008) are considerably larger than genetic distances between specimens of different stations – nos 133-2 and 121-11, average 0.0090. Such a picture indicates that the depth or any factor related to it (e.g. water masses) plays an important role in hindering genetic flux. This finding is in accord with Dingle <i>et al.</i> (1990), who found relationships between Atlantic deep-sea ostracod distribution and water masses.</p> <p> Similarly, genetic distances between specimens of <i>Mh. walterae</i> (Weddell Sea) and <i>Macroscapha</i> sp. aff. <i>Mh. walterae</i> (from the Scotia Sea, see below) are even greater (0.055).</p> <p> The valve lateral outline of <i>Mh. walterae</i> sp. nov. is very similar to <i>Mh. inaequata</i>, but the former species is larger (Figs 34, 37, 38) and displays a more elongated hemipenis, with a shovel-shaped (instead of rod-shaped) copulatory process.</p> <p> Concerning the lateral outline of the valves (1) <i>Macroscapha atlantica</i>, <i>Mh. heroica</i>, <i>Mh. jiangi, Mh. sinuata</i>, and <i>Mh. turbida,</i> have more sinuous outlines than <i>Mh. walterae</i>; (2) <i>Mh. gyreae</i>, <i>Mh. inaequalis, Mh. rehmi,</i> and <i>Mh. tensa</i> are more elongated, less high in relation to length; (3) <i>Mh. scotia</i> is more subtriangular, higher in relation to length; (4) <i>Mh. opaca</i> presents a more acute posterior angle; (5) <i>Mh. marchilensis</i> is similar in valve outline to <i>Mh. walterae</i> but the Zenker’s organ of the former species presents a medium-sized (instead of very large) terminal bulb.</p>Published as part of <i>Brandão, Simone N., 2010, Macrocyprididae (Ostracoda) from the Southern Ocean: taxonomic revision, macroecological patterns, and biogeographical implications, pp. 567-672 in Zoological Journal of the Linnean Society 159 (3)</i> on pages 622-632, DOI: 10.1111/j.1096-3642.2009.00624.x, <a href="http://zenodo.org/record/4890076">http://zenodo.org/record/4890076</a>
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