66,518 research outputs found
Blind Per-Survivor Processing-Based Multiuser Detection for Channel-Coded Multi-Carrier DS-CDMA Systems
No full textIn this paper, we present a blind Per-Survivor Processing (PSP)-hased Multiuser Detector (MUD) for synchronous Multicarrier (MC) Direct Sequence (DS) CDMA systems. We modify the branch metric conventionally used for the Single-Carrier (SC) PSP-based MUD in order to detect synchronous MC DS-CDMA signals. Subsequently we characterise the performance of rate R = ½ Low Density Parity Check (LDPC)-coded, Convolutional-based Turbo (CT)-coded and convolutional-coded (CC) MC DS-CDMA systems, which employ four subcarriers. We assume that each subcarrier experienced uncorrelated. narrowband Rayleigh fading and quantified the BER performance, computational complexity and system delay. It is observed that when interleaving is performed over a single transmission burst, it is sufficient to utilise low-complexity CC codes. When the MC DS-CDMA system was not constrained by the tolerable system delay and hence interleaving was performed over several transmission bursts, CT codes yielded the best performance. LDPC codes were also capable of approaching the performance attained by the CT codes, although at a factor of 2.4 higher computational complexity
Going Beyond Counting First Authors in Author Co-citation Analysis
No full textThe present study examines one of the fundamental aspects of author co-citation analysis (ACA) - the way co-citation
counts are defined. Co-citation counting provides the data on which all subsequent statistical analyses and mappings
are based, and we compare ACA results based on two different types of co-citation counting - the traditional type that
only counts the first one among a cited work's authors on the one hand and a non-traditional type that takes into
account the first 5 authors of a cited work on the other hand. Results indicate that the picture produced through this non-traditional author co-citation counting contains more coherent author groups and is therefore considerably clearer. However, this picture represents fewer specialties in the research field being studied than that produced through the traditional first-author co-citation counting when the same number of top-ranked authors is selected and analyzed. Reasons for these effects are discussed
Interphasma leigongshanense Xu, Yang et Guo 2010
No full textInterphasma leigongshanense Xu, Yang et Guo, 2010 Type locality: China (Leigongshan, Guizhou). NOTE. No material examined.Published as part of Li, B. L., Shi, F. M. & Wang, H. J., 2021, Stick insects of the genus Interphasma Chen et He, 2008 (Phasmida: Phasmatidae) from China, pp. 24-32 in Far Eastern Entomologist 422 on page 30, DOI: 10.25221/fee.422.3, http://zenodo.org/record/716634
Dispelling the Myths Behind First-author Citation Counts
No full textWe conducted a full-scale evaluative citation analysis study of scholars in the XML research field to explore just how different from each other author rankings resulting from different citation counting methods actually are, and to demonstrate the capability of emerging data and tools on the Web in supporting more realistic citation counting methods. Our results contest some common arguments for the continued
use of first-author citation counts in the evaluation of scholars, such as high correlations between author rankings by first-author citation counts and other citation
counting methods, and high costs of using more realistic citation counting methods that are not well-supported by the ISI databases. It is argued that increasingly available digital full text research papers make it possible for citation analysis studies to go beyond what the ISI databases have directly supported and to employ more
sophisticated methods
FIGURE. Mitotic metaphase chromosomes of Thalictrum longistipitatum (A) (2n = 14), T. tsawarungense (B, C) (2n = 14), T. wangii (D) (2n = 14), and T. rostellatum (E, F) (2n = 28), all same scale. A. China, Xizang, Bomi, L. Wang, X.Q. Guo & Y.P. Zeng 3350 (IBSC). B. China, Xizang, Bomi, L. Wang, X.Q. Guo & Y.P. Zeng 3313 (IBSC). C. China, Xizang, Bomi, L. Wang, X.Q. Guo & Y.P. Zeng 3317 (IBSC). D. China, Yunnan, Lijiang, Y.P. Zeng & Y.F. Luo 200 (IBSC). E. China, Xizang, Gyirong, L. Wang, X.Q. Guo & Y.P. Zeng 2732 (IBSC). F. China, Xizang, Mainling, L. Wang, X.Q. Guo & Y.P. Zeng 3295 (IBSC). in Thalictrum hengduanshanense and T. longistipitatum (Ranunculaceae), two new species from southeastern Xizang and northwestern Yunnan, China
No full textFIGURE. Mitotic metaphase chromosomes of Thalictrum longistipitatum (A) (2n = 14), T. tsawarungense (B, C) (2n = 14), T. wangii (D) (2n = 14), and T. rostellatum (E, F) (2n = 28), all same scale. A. China, Xizang, Bomi, L. Wang, X.Q. Guo & Y.P. Zeng 3350 (IBSC). B. China, Xizang, Bomi, L. Wang, X.Q. Guo & Y.P. Zeng 3313 (IBSC). C. China, Xizang, Bomi, L. Wang, X.Q. Guo & Y.P. Zeng 3317 (IBSC). D. China, Yunnan, Lijiang, Y.P. Zeng & Y.F. Luo 200 (IBSC). E. China, Xizang, Gyirong, L. Wang, X.Q. Guo & Y.P. Zeng 2732 (IBSC). F. China, Xizang, Mainling, L. Wang, X.Q. Guo & Y.P. Zeng 3295 (IBSC).Published as part of Zeng, You-Pai, Yuan, Qiong & Yang, Qin-Er, 2022, Thalictrum hengduanshanense and T. longistipitatum (Ranunculaceae), two new species from southeastern Xizang and northwestern Yunnan, China, pp. 1-20 in Phytotaxa 571 (1) on page 16, DOI: 10.11646/phytotaxa.571.1.1, http://zenodo.org/record/727042
Lebertia (Lebertia) abseta Guo, Jin & Asadi 2006
No full text3.4 <i>Lebertia</i> (<i>Lebertia</i>) <i>abseta</i> Guo, Jin <i>&</i> Asadi, 2006 <p> <i>Lebertia</i> (<i>Pseudolebertia</i>) <i>abseta</i> Guo, Jin & Asadi, 2006: 346; Guo & Xu, 2013: 190.</p> <p>Material examined. 3 females, 1 male, Pangquangou Nature Reserve, Jiaocheng County, Shanxi, China (37°30′N, 111°39′E; elev. 1 500 m), 15 August 2002, coll. Jianjun Guo; 6 females, 2 males, Mt. Luya National Nature Reserve, Shanxi, China (37°43′N, 111°51′E; elev. 1 350 m), 17 August 2002, coll. Jianjun Guo; 2 females, Mt. Cangyan, Jingxing County, Hebei, China (38°02′N, 114°08′E; elev. 900 m), 19 August 2002, coll. Jianjun Guo; 3 females, 2 males, Taibaishan National Nature Reserve, Taibai County, Shaanxi, China (37°07′N, 107°53′E; elev. 2 150 m), 9 July 2009, coll. Chengshuai Xu.</p> <p> Remarks. The species was erected by Guo, Jin <i>&</i> Asadi (2006) based on specimens from Iran, and redescribed by Guo <i>&</i> Xu (2013) based on specimens from China. In this paper, the authors agree with the system which proposed by Gerecke (2009) that the subgenus <i>Pseudolebertia</i> should be considered the synonym of the subgenus <i>Lebertia</i>. So that, the species <i>L.</i> (<i>Pseudolebertia</i>) <i>abseta</i> should be <i>L.</i> (<i>Lebertia</i>) <i>abseta</i>.</p> <p>Distribution. Palaearctic Region (Iran (Kerman); China (Shanxi, Shannxi, Hebei)).</p> <p> <b>Founding</b> This research was supported by the National Natural Science Foundation of China (31372161, 31201744), the Program of Science and Technology Innovation Talents Team, Guizhou Province (20144001), the Innovation Team Program for Systematic and Applied Acarology ([2014]33), and the Provincial Outstanding Graduate Program for Agricultural Entomology and Pest Control ([2013]010).</p> <p> <b>Acknowledgement</b> Special thanks to Prof. Shangwei Li (Institute of Entomology, Guizhou University, P. R. China) and Chengshuai Xu (Huantai No. 1 Middle School, Shandong Province, P. R. China) for providing references and advice to the authors.</p>Published as part of <i>Wang, Jialin, Jin, Daochao, Yi, Tianci & Guo, Jianjun, 2016, Water mites of subgenus Lebertia (Lebertia) Neuman from China (Hydrachnidia: Lebertiidae), pp. 54-63 in Zoological Systematics 41 (1)</i> on page 62, DOI: 10.11865/zs.201603, <a href="http://zenodo.org/record/5367272">http://zenodo.org/record/5367272</a>
Stygothrombium garzensis Li & Guo 2021, sp. nov.
No full textStygothrombium garzensis Li & Guo, sp. nov. (Figs 1–5) Habitat. Interstitial waters. Material examined. Holotype female, Chaqingsongduo National Nature Reserve, Sichuan, China (31°00′88′′N, 99°24′71′′E, elev. 3523 m), water depth 30–40 cm, located at the hillside, running water with organic detritus, dead wood and leaves on the bottom, collected by Boyan Li, 30.VIII.2020, Slides No. SC-ST-2020080101. Etymology. “ garze -” is derived from the name of the Garze Tibetan Autonomous Prefecture, Sichuan Province, China, where the specimen was collected. Diagnosis. Soft and papillate idiosoma vermiform; eyes completely absent; infracapitulum base approximately 3.5 times as long as rostrum; P-A with two stout subventrodistal harpagones, above harpago seta thicker than other one; on one side of P-B, tibia with one four-pronged odontus claws bulging above tarsus; se about half length of posterior portion of prodorsal plate; one seta and two rather long setae at lateral margin of Cx-I; stalked Ac-1–3 arranging in an almost straight line, glv- 2 between Ac-3 and inner posterior angle of Cx-IV, located at one-third of interval near Ac-3 approximately; empodium considerably smaller than lateral claws. Description. Female (SC-ST-2020080101). Soft and papillate idiosoma vermiform (Fig. 1A); eyes completely absent (Fig. 2A); with eight pairs of gld and seven pairs of gll (gld- 1–8, gll- 1–7 in Fig. 2A), six pairs of glv (glv- 1–6 in Fig. 2B); idiosomal glandularia (or modified stomatoid lyrifissures) without sclerite platelets but surrounded by unpapillate cuticle, a long seta and short seta associated with glandularia except gll -1 with only a short seta (Figs 1B–C); excretory pore placed near posterior end of ventral surface and between glv -5 (Fig. 2B). Gnathosoma retractable into idiosoma; infracapitulum base approximately 3.5 times as long as rostrum; two pairs of setae on rostrum, posterior one longer than anterior one (Fig. 3A); chelicera two-segmented, basal segment expanded and long (Fig. 3B); fused pedipalp two-segmented: first segment including trochanter + femur + genu (P-A); P-A with numerous dorsal setae, a thin ventrodistal seta, two stout subventrodistal harpagones (above harpago seta thicker than other one) and two ventroproximal setae (one normal seta and one long curved seta); tibia + tarsus fused into short second segment (P-B); on one side of P-B, tibia with one four-pronged odontus claws bulging above tarsus, one stout gladius seta, one thick and short lancea seta, one parodontus, and two normal setae on tarsus; P-B with six normal setae on another side, single solenidion on dorsum and alantoid seta with rounded tip at terminus (Figs 3C–D). Prodorsal plate bearing vi, si, ve and se; long and narrow posterior portion of prodorsal plate approximately six times as long as short and wide anterior portion; se about half length of posterior portion, longer than vi, si and ve (Fig. 3E). Coxal plates in four groups; two ACG not fused but close, two PCG widely separated; Cx-I trapezoidal, with numerous setae near inner apical angles and three setae (one seta and two rather long setae) at lateral margin; Cx-II trapezoidal, with one seta near outer posterior angles (Fig. 4A); Cx-III and Cx-IV nearly triangular, with some setae respectively (Fig. 4B). Genital field with about twenty tiny setae; stalked Ac-1–3 arranging in an almost straight line, interval from Ac-1 to Ac-2 and Ac-2 to Ac-3 almost equal; gonopore surrounded by three or four setae on each side; glv- 2 between Ac-3 and inner posterior angle of Cx-IV, located at one-third of interval near Ac-3 approximately (Fig. 4B). Legs without swimming setae but numerous setae present; I-L thicker than other pairs of legs, I-L-3–5 with stomatoid lyrifissures on one side (Figs 5A–D); tarsus of I–IV-L with two pectinate lateral claws and one smooth middle empodium, empodium considerably smaller than lateral claws (Fig. 1D). Male. Unknown. Measurements (holotype). Idiosoma L 3857 (from peak of protrusible integument to bottom), W 1114; excretory pore L 108; Infracapitulum L 783, base L 607, rostrum 176; Chelicera base segment L 477, claw L 102; P-A dL 253, P-B dL 97, alantoid seta L 60, above harpago seta L 64, nether harpago seta L 66; prodorsal plate L 478, anterior portion L 73, posterior portion L 405; ACG L 274; PCG L 346; gonopore L 119, Ac-1 L 76, Ac-2 L 66, Ac-3 L 80; Legs segments dL: Ⅰ-L-1 100, Ⅰ- L-2 164, Ⅰ-L-3 173, Ⅰ-L-4 182, Ⅰ-L-5 189, Ⅰ-L-6 159, claw dL 88; II-L-1 88, II-L-2 134, II-L-3 136, II-L-4 166, II-L-5 190, II-L-6 140, claw dL 84; III-L-1 123, III-L-2 134, III-L-3 139, III-L-4 186, III-L-5 205, III-L-6 153, claw dL 78; IV-L-1 101, IV-L-2 173, IV-L-3 213, IV-L-4 259, IV-L-5 280, IV-L-6 191, claw dL 81. Remarks. The present new species is similar to S. monotrichum Nagasawa & Abé, 2014 from Japan in quantity and location of idiosomal glandularia and pedipalp structures. The new species differs from the latter in the following aspects: (1) idiosoma L 3857 in S. garzensis Li & Guo, sp. nov., but 1560–1830 in S. monotrichum; (2) glv -1 between ACG and PCG in S. garzensis Li & Guo, sp. nov., while absent in S. monotrichum; (3) glv- 2 between Ac-3 and inner posterior angle of CxIV in S. garzensis Li & Guo, sp. nov., but located posteromedially to the posterior acetabula in S. monotrichum; (4) setae on ACG and pedipalp much more multiple than S. monotrichum; (5) P-A dL 253 in S. garzensis Li & Guo, sp. nov., while P-A dL 88 in S. monotrichum. (Nagasawa & Abé 2014) Funding This research was supported by National Natural Science Foundation of China (31772421, 31750002), Guizhou Science and Technology Project (Qiankehe Pingtai Rencai [2017] 5788) and National Key R & D Program of China (2017YFD0201000). Acknowledgements We are grateful to Boyan Li (Institute of Entomology, Guizhou University, P. R. China) for collecting the specimen and processing the photos. Furthermore, we are thankful to Zhuhui Ding (Institute of Entomology, Guizhou University, P. R. China) for helping to take photos of specimen.Published as part of Li, Haitao, Jin, Daochao & Guo, Jianjun, 2021, A new species of the genus Stygothrombium, representing a newly recorded superfamily Stygothrombioidea Mullen & Vercammen-Grandjean, 1980 (Acari: Stygothrombiae) from China, pp. 281-288 in Zoological Systematics 46 (4) on pages 283-287, DOI: 10.11865/zs.2021402, http://zenodo.org/record/717578
Measurement of the ratio of branching fractions B(B0→K∗0γ )/B(B0s→φγ ) and the directCP asymmetry inB 0→K∗0γ
No full textThe ratio of branching fractions of the radiative B decays B0→K⁎0γ and B0s→ϕγ has been measured using an integrated luminosity of 1.0 fb−1 of pp collision data collected by the LHCb experiment at a centre-of-mass energy of s√=7TeV. The value obtained is
B(B0→K⁎0γ)B(B0s→ϕγ)=1.23±0.06(stat.)±0.04(syst.)±0.10(fs/fd),
where the first uncertainty is statistical, the second is the experimental systematic uncertainty and the third is associated with the ratio of fragmentation fractions fs/fd. Using the world average value for B(B0→K⁎0γ), the branching fraction B(B0s→ϕγ) is measured to be (3.5±0.4)×10−5.
The direct CP asymmetry in B0→K⁎0γ decays has also been measured with the same data and found to be
ACP(B0→K⁎0γ)=(0.8±1.7(stat.)±0.9(syst.))%.
Both measurements are the most precise to date and are in agreement with the previous experimental results and theoretical expectations
Fig. 4. Key NOESY correlations for seneciojanine B-D in Pyrrolizidine alkaloids and unusual millingtojanine A-B from Jacobaea vulgaris (syn. Senecio jacobaea L.)
No full textFig. 4. Key NOESY correlations for seneciojanine B-D (2–4).Published as part of Jumai, Aikebaier, Rouzimaimaiti, Ruxianguli, Zou, Guo-An & Aisa, Haji Akber, 2021, Pyrrolizidine alkaloids and unusual millingtojanine A-B from Jacobaea vulgaris (syn. Senecio jacobaea L.), pp. 1-9 in Phytochemistry (112862) 190 on page 4, DOI: 10.1016/j.phytochem.2021.112862, http://zenodo.org/record/825741
Torrenticola pseudoalargada Gu & Guo 2023, sp. nov.
No full text<i>Torrenticola pseudoalargada</i> Gu & Guo sp. nov. (Figures 5–8) <p> <b>Type Materials.</b> <b>Holotype</b> male: No. CQ-TO-2022081301, China, Chongqing, Wuxi, Yintiaoling National Nature Reserve, Lanying Grand Canyon (31°26′19′′N, 109°50′46′′E, 870 m a.s.l.), collected by Yuhao Zhang, 13-VIII- 2022. <b>Paratypes</b>: 1/3/0, No. CQ-TO-2022081106 – CQ-TO-2022081109, Yintiaoling National Nature Reserve, Linkouzi (31°28′35′′N, 109°53′18′′E, 1250 m a.s.l.), collected by Yuhao Zhang, 11-VIII-2022.</p> <p> <b>Diagnosis</b>. Dorsal plate arrangement: 4+1; Infracapitular bay U-shaped; P-2 with four dorsal setae, and one ventral seta at the base of a serrated extension; P-3 with one serrated rectangular extension on ventrum, at the base of which with one ventral seta; P-4 with two dorsal setae, and two setae on two ventral extensions.</p> <p> <b>Description. Male (n = 2):</b> Idiosoma elliptical, L 690 (813), W 438 (538), L/W ratio 1.6 (1.5). Dorsal plate arrangement: 4+1 (Fig. 5A); dorsal shied L 558 (626), W 391 (467), dorsal plate L 526 (571), frontal platelets L 118 (129), W 53 (65), L/W ratio 2.2 (2.0); shoulder platelets L 169 (202), W 61 (85), L/W ratio 2.8 (2.4). Infracapitular bay U-shaped, L 131 (156); Cx-I L 256 (300), mL 126 (144), Cx-II+III mL 78 (112); genital field ellipse, L 152 (185), W 106 (140); <i> C 4</i> at the same level as the 4 th pair of acetabula; the posterior margin of Cx-IV relatively indistinct; <i> V 1</i> anterior to <i> V 2</i> , <i> V 2</i> almost at the same level of Ap (Fig. 5B). Gnathosoma: dL 206 (266), vL 281 (350); rostrum long and dorsal apodeme short, ventral apodeme long and blunt; chelicera bs L 281 (356), claw L 41 (47), (Fig. 5D). Palp (Fig. 5C): P-1 short, with one dorsodistal seta; P-2 with four dorsal setae, and one ventral seta at the base of a serrated extension; P-3 with two dorsal setae and one serrated rectangular extension on ventrum, at the base of which with one ventral seta; P-4 with two dorsal setae, and two ventral setae on two ventral extensions. L of palp segments: P-1, 30 (39); P-2, 85 (105); P-3, 52 (55); P-4, 63 (70); P-5, 15 (19). Legs (Fig. 6): L of leg segments: I-L-1–6: 33 (36), 78 (84), 66 (72), 70 (88), 79 (97), 80 (91); II-L-1–6: 31 (36), 77 (89), 57 (69), 79 (83), 87 (99), 94 (101); III-L-1–6: 45 (42), 78 (94), 65 (72), 90 (101), 106 (118), 108 (117); IV-L-1–6: 89 (98), 87 (104), 95 (116), 124 (133), 136 (137), 123 (131). Ejaculatory complex (Fig. 5E), L 156 (-), aL 118 (-).</p> <p> <b>Female (n = 3).</b> Body features same as the male except: genital field pentagonal; <i> C 4</i> at the same level as the 4 th pair of acetabula; the posterior margin of Cx-IV relatively obvious (Fig. 7B); P-3 with three dorsal setae (Fig. 7C). Idiosoma L 937 (771–937), W 627 (502–627), L/W ratio 1.49 (1.49–1.54). Dorsal shield L 738 (621–738), W 556 (453–556), L/W ratio 1.3 (1.3–1.4); dorsal plate L 675 (568–675), frontal platelets L 178 (130–178), W 71 (57–71), L/W ratio 2.5 (2.3–2.5), shoulder platelets L 218 (171–218), W 90 (60–90). Infracapitular bay depth 174 (153–174); Cx-I L 348 (293–348), mL 171 (142–171), Cx-II + III mL 76 (48–76). Genital field L 191 (161–191), W 178 (134–178), L/W ratio 1.1 (1.1–1.2); distance between genital field and Ap 202 (177–202). Gnathosoma vL 412 (308–412), dL 309 (231–309), chelicera bs L 433 (330–433), claw L 53 (51–53). L of palp: P-1, 43 (34–43); P-2, 125 (95–125); P-3, 66 (55–66); P-4, 81 (66–81); P-5, 13 (13–17). L of leg segments: I-L-1–6: 43 (30–43), 100 (85–100), 85 (70–85), 94 (76–94), 112 (81–112), 101 (81–101); II-L-1–6: 40 (34–40), 96 (85–96), 79 (64–79), 99 (83–99), 114 (88–114), 112 (99–112); III-L-1–6: 40 (35–40), 108 (83–108), 85 (69–85), 122 (98–122), 139 (115– 139), 129 (122–129); IV-L-1–6: 120 (101–120), 102 (102–118), 122 (113–122), 157 (132–157), 159 (143–159), 144 (139–144).</p> <p> <b>Habitat.</b> Streamlet, about 0.3–0.5 <i>m</i> in depth, is so clear that you can see many small stones at the bottom.</p> <p> <b>Remarks.</b> The present species is similar to <i>T. alargada</i> Goldschmidt, 2007, a species from Latin American (Goldschmidt 2007). Both species have a serrated ventral extension on P-2, two setae-bearing projections on ventral margin of P4, and a similar gnathosoma. The new species differs from <i>T. alargada</i> in: (1) <i>T</i>. <i>pseudoalargada</i> Gu & Guo <b>sp. nov.</b> with a U-shaped infracapitular bay, but V-shaped in <i>T. alargada</i>; (2) <i>T</i>. <i>pseudoalargada</i> Gu & Guo <b>sp. nov.</b> without color pattern, but posterior two-thirds of dorsal plate red to pale reddish in <i>T. alargada</i>; (3) P-4 with two ventral setae in <i>T</i>. <i>pseudoalargada</i> Gu & Guo <b>sp. nov.</b>, but with four ventral setae in <i>T. alargada</i>.</p> <p> In addition, the new species resembles <i>T. malaisei</i> (Lundblad, 1941) (Wiles 1997; Pešić <i>et al</i>. 2012) in: P-3 with a short, subrectangular, apically serrated ventrodistal projection, and a long seta laterally at the base of the projection and a comparatively short P-4. But two species have obvious differences in: (1) P-2 with a flat blade-like ventral extension in <i>T. malaisei</i> but with a serrated extension in <i>T. pseudoalargada</i>; (2) posterior suture line of Cx-IV obvious and long in <i>T. malaisei but</i> retrogressive in <i>T. pseudoalargada</i>; (3) <i>Cx-I</i> –II exceeding to the anterior margin of idiosoma in <i>T. malaisei</i>, but only Cx-I and Cx-II exceeding to it in <i>T. pseudoalargada.</i></p> <p> <b>Etymology.</b> This species is named after its similar species, <i>T</i>. <i>alargada</i>. And the specific name, <i>pseudoalargada</i>, is from the Latin affix: “ <i>pseudo</i> -”, which means fake or simulated; used as a noun in apposition.</p> <p> <b>Distribution.</b> Known only on the type locality (Wuxi, Chongqing of China).</p>Published as part of <i>Gu, Xinyao, Zhang, Yuhao, Zheng, Yuling & Guo, Jianjun, 2023, First collection of Torrenticolidae (Hydrachnidiae, Acari) from Yintiaoling National Nature Reserve, China, with descriptions of two new species, pp. 131-142 in Zootaxa 5257 (1)</i> on pages 136-138, DOI: 10.11646/zootaxa.5257.1.10, <a href="http://zenodo.org/record/7765695">http://zenodo.org/record/7765695</a>
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