220,258 research outputs found
Zhou-Nam 2022
Supporting data for Zhou et al. (2022).
A_measured_data contains OCT vibration measurement data for 2-D motion analyses.
B_simulations contains the FE analysis codes for the identification of mechancial properties.</p
MORTUARY ART IN THE NORTHERN ZHOU CHINA (557-581 CE): VISUALIZATION OF CLASS, ROLE, AND CULTURAL IDENTITY
The period of Six Dynasties (221-581CE) has traditionally been thought of as a time when "the Five Barbarians brought disorder to China." During this period, present-day Northern China was ruled by non-Han leaders, including the Xianbei, a pastoral people from China's northern frontier who founded the Northern Zhou Dynasty. In addition, Chinese historical texts from the Six Dynasties refer to "merchant barbarians" generally assumed to be Sogdians, who lived in oasis states in Central Asia in present-day Uzbekistan and came to China across the Silk Road. Most scholarship has assumed that the period of Northern Zhou ruled by non-Chinese leaders was "sinicized," and the adoption of Chinese features in burial and artifacts in foreigners' tombs is evidence of that acculturation process. This dissertation, however, uses newly excavated materials from tombs dated to the Northern Zhou period, including the tombs of Xianbei leaders, Xianbei and Chinese generals, and Sogdian merchants, and proposes that visual arts and mortuary ritual played a role in creating and/or maintaining multiple sociopolitical and cultural identities for these residents of Northern Zhou. The theorization of power, agency, and cultural identity in recent publications has helped me analyze the processes involved in the construction of individual identity, group boundaries, and the interrelationships between socio-cultural groups. Theories of agency have helped me focus on choices made by different social and occupational groups. This dissertation has explored how the patterns of use of mortuary objects documented multiple identities for these three classes listed above with specific ethnic backgrounds: the sovereigns who were Xianbei; the military class of Xianbei and Han-Chinese; and the merchant class of Sogdians. I have discussed how aspects of political, military, and merchant life in the Northern Zhou period created a setting that contributed to multiple roles and identities in each group. My study has demonstrated the construction of multiple identities among elites and how they consistently distinguished themselves from other members of society. This dissertation will be the first contextual analysis focused on the visualization of class, social roles and cultural affiliation by examining mortuary art in the Northern Zhou
Intrinsic Disorder and Semi-disorder Prediction by SPINE-D
Over the past decade, it has become evident that a large proportion of proteins contain intrinsically disordered regions, which play important roles in pivotal cellular functions. Many computational tools have been developed with the aim of identifying the level and location of disorder within a protein. In this chapter, we describe a neural network based technique called SPINE-D that employs a unique three-state design and can accurately capture disordered residues in both short and long disordered regions. SPINE-D was trained on a large database of 4229 non-redundant proteins, and yielded an AUC of 0.86 on a cross-validation test and 0.89 on an independent test. SPINE-D can also detect a semi-disordered state that is associated with induced folders and aggregation-prone regions in disordered proteins and weakly stable or locally unfolded regions in structured proteins. We implement an online web service and an offline stand-alone program for SPINE-D, they are freely available at http://sparks-lab.org/SPINE-D/. We then walk you through how to use the online and offline SPINE-D in making disorder predictions, and examine the disorder and semi-disorder prediction in a case study on the p53 protein.No Full Tex
Cissampelos keniensis Y. D. Zhou & Q. F. Wang
E Cissampelos keniensis Y.D.Zhou & Q.F.Wang — Habit: Liana. Habitat: LMWF; 2 000–2 300 m. Distribution: IIIc. Voucher: Kaburia Track, Alt. 2 241 m, 29 Jun. 2016, Zhou & Mbuni 16/14 (HIB, EA, PE). Reference: Zhou et al. (2017b).Published as part of Zhou, Ya-Dong, Mwachala, Geoffrey, Hu, Guang-Wan & Wang, Qing-Feng, 2022, Annotated checklist of the vascular plants of Mount Kenya, East Africa, pp. 1-108 in Phytotaxa 546 (1) on page 41, DOI: 10.11646/phytotaxa.546.1.1, http://zenodo.org/record/655046
Zehneria subcoriacea Y. D. Zhou & Q. F. Wang
Zehneria subcoriacea Y.D.Zhou & Q.F.Wang — Habit: Climber. Habitat: LMWF, BZ, UMF; 2 000–3 200 m. Distribution: IIIa. Voucher: Naro Moru Track, near Met. Station, Alt. 3065 m, 27 Jun. 2016, Zhou & Mbuni 16/3 (HIB, EA, PE). Reference: Zhou et al. (2016b).Published as part of Zhou, Ya-Dong, Mwachala, Geoffrey, Hu, Guang-Wan & Wang, Qing-Feng, 2022, Annotated checklist of the vascular plants of Mount Kenya, East Africa, pp. 1-108 in Phytotaxa 546 (1) on page 52, DOI: 10.11646/phytotaxa.546.1.1, http://zenodo.org/record/655046
Data for: Mobile sensing of point-source gas emissions using Bayesian inference: the empirical examination of the likelihood function
This dataset is collected during a series of controlled release experiments reported in the manuscript entitled "Mobile sensing of point-source gas emissions using Bayesian inference: the empirical examination of the likelihood function" by Xiaochi Zhou, Amir Montazeri, and John D. Albertson.It includes methane concentrations reported by two analyzers, the GPS coordinate of the mobile measurement platform, and the start and end time of each sensor pass
Diochus ampullaceus Zhou & Zhou, 2016, sp. nov.
2. Diochus ampullaceus sp. nov. (Fig. 3 D; Fig. 5 A–P; Fig. 5 - 1 A–J) Type material. Holotype: male, CHINA: Guangxi: Napo co., Defushuiyuanlin Nature Reserve (E 105.7965 °, N 23.3148 °), 1400 m, 0 4. IV. 1998, Zhou Haisheng collected (IZ-CAS). Paratypes: Guangxi: Napo co., Defushuiyuanlin Nature Reserve (E 105.7965 °, N 23.3148 °), 3 males, 4 females, 1400 m, 0 4. IV. 1998, Zhou Haisheng collected (IZ-CAS). Description. Measurement (n= 5). BL= (4.2–4.3) mm, FL= (2.1–2.2) mm, HL= (0.5–0.6) mm, HW= (0.4– 0.5) mm, PL= (0.7–0.8) mm, PW= (0.6–0.7) mm, EL= (0.6–0.7) mm, EW= (0.8–0.9) mm. Body nearly fusiform shaped, medium sized (Fig. 3 D). Body dark brown, abdominal intersegmental membrane yellowish brown. Legs entirely brown, except tarsi lighter. Antennae light brown. Maxillary and labial palpi yellowish brown. Head (Fig. 5 A, D). Rounded triangular in shape (HL to HW ratio 1.23), tempora (behind eyes) distinctly widened backwards, posterior angles rounded. Dorsal integument shiny, extensively bearing microstriae, without punctures around each eye, but bearing scattered smaller punctures on deflexed portion of tempus and near the posterior margin. Each side of cranium with characteristic punctures: one frontal puncture on frontal region, two anterolateral punctures near antennal insertion, three lateral punctures near dorsal margin of eye, also with occipital puncture at the basal 1 / 4, but temporal puncture unidentified; besides, disc surface bearing two additional paired punctures. Frontal furrows and anteocular furrows absent, a small round elevation present between eyes. Eye medium sized, distinctly protruding laterad, longitudinal diameter slightly shorter than half the length of tempora (eye: tempora = 0.16: 0.34 mm). Epistoma not flattened, abruptly oblique, anterior margin emarginate medially. Distance between antennal insertions 0.17 mm being distinctly longer than distance from antenna to eye (0.09 mm). Ventral surface (Fig. 5 D) with scattered punctures, interspaces between them over 4 punctures’ diameter. Gular sutures deep, gradually convergent, but not confluent, then divergent to neck region. Antennae (Fig. 5 G). Total length 1.2 mm. Scape rod-shaped, slightly thickened apically, 0.17 mm, shorter than two subsequent antennomeres combined; antennomere II elongate, 0.12 mm; III 0.13 mm, slightly longer than II; IV 0.09 mm, IV–X becoming shortened in length; XI 0.14 mm, distinctly longer than X. Mouthparts (Fig. 5 H–J). Labrum not transverse, nearly pentagon; lateral margin straight, not in waved shape; anterior margin distinctly shorter than lateral margins (Fig. 5 H). Mandibles falciform, left one with one sharp tooth on inner edge, right one without tooth (Fig. 5 I–J). Neck (Fig. 5 K–L). Cylindrical, shiny, first half of dorsal surface depressed, with a distinct groove (Fig. 5 K); only bearing shallow microsculpture, width of 0.17 mm, slightly wider than 1 / 3 width of head. Ventral surface with gular sutures to form obvious triangular region, with deep transverse median furrow (Fig. 4 L). Prothorax (Fig. 5 B, E). Pronotum elliptical (PL to PW ratio 1.09), wider and longer than head. Anterior region near anterior angles deflexed, lateral margins paralleled, not widened from anterior angles to the middle, also not convergent backwards, anterior and posterior angles broadly rounded. Dorsal surface glossy extensively with micropunctures, but without any microsculpture. Each side of the midline with symmetrical five large lateral punctures, with additional 13–15 punctures near each margins (including anterior, lateral and posterior margins). Prosternum bearing an observable transverse ridge between basisternum and furcasternum, angularly backwards (Fig. 5 E). Pterothorax (Fig. 5 F, N). Mesoscutellum slightly sharp triangular and small (Fig. 5 N), surface shiny, bearing some light microstriae, but without any punctures. The transverse ridge on mesoventrites substraight (Fig. 5 F); the longitudinal ridge distinct; the paired oblique furrows not distinct; the carina (limiting mesocoxal cavity) possessing wave-shaped median part. The discrimen region on metaventrite distinctly elevated. Elytra (Fig. 5 C). Transverse and short (EL to EW ratio 0.81), shorter and wider than pronotum. Humeri well developed, lateral margins divergent posteriorly, hind margin not rounded, but obliquely truncate. Dorsal integument shiny, flattened, without microsculpture; each elytron with a row of 5 punctures along suture, a row of 5 punctures in median, also with 4–5 rows of punctures on deflexed portion. Legs (Fig. 5 M). First four segments of protarsi stout, wider than those of meso- and metatarsi slender. Last segment of protarsi longer than II–IV together; that of meso- as long as II and III together; that of meta- longer than II and III together. Abdomen (Fig. 5 O). Broadest at segment V. Tergites III–VII covered with dense and obvious transverse microstriae; each tergite with dense and brown pubescence, posterior margin of III–VI without darker and coarser setae. Tergites III–VII with a basal impression near anterior margin, respectively, each one only possessing one basal transverse carina; surface shiny, without any punctures or microsculpture. Tergite VII possessing a transparent palisade fringe on posterior margin. All abdominal sternites shiny, with microstriae and punctures as those on tergites. Male (Fig. 5 - 1 A–G). Posterior margin of tergite VIII arcuate backwards (Fig. 5 - 1 A), that of sternite VIII distinctly bisinuate (Fig. 5 - 1 B). Tergite IX symmetrical, connected mediobasally, sharpened apically. Sternite IX symmetrical, widest near the apical 1 / 3, basal margin deeply emarginate, apical margin nearly subtruncate (Fig. 5 - 1 D). Tergite X symmetrical, in reverse trapezoidal shape (Fig. 5 - 1 C). Aedeagus large sized and bottle-shaped (Fig. 5 E, F), ca. 0.8 mm long, ventral surface normally sclerotized, with part membrane; dorsal surface fully membranous. Parameres symmetrical and soft, extraordinarily thin and long, rolled from ventral to dorsal side (Fig. 5 - 1 E, F). Internal sac membranous, without sclerotized structures. Sperm pump folded basally, spiral toward apex (Fig. 5 - 1 G). Female (Fig. 5 - 1 H–J). Tergite IX bearing numerous setae, elongate and sharply pointed apically. Sternite IX symmetrical, each integrated, and with a deep concaved margin in the middle (Fig. 5 - 1 H). Tergite X broad, basal margin curved (Fig. 5 - 1 I). Sternite X missing. Tube of spermatheca short, with an apical circle (Fig. 5 - 1 J). Distribution. Guangxi. Etymology. The specific epithet is derived from the Latin word “ ampullaceus ” (a flask swelled in middle) and refers to the bottle-shaped aedeagus. Remarks. Although this new species is similar in the round elevation between the eyes to D. pulchellus Cameron, it can be easily recognized by the dilated protarsi. This new species is distinguished from its congeners by the combination of the following characters: 1) sparsely distributed punctures on head; 2) different number of mandible teeth; 3) neck with both a dorsal and ventral groove; 4) transverse elytra; 5) aedeagus large sized and bottle-shaped (Fig. 5 E, F); parameres symmetrical and soft, extraordinarily thin and long, curving from ventral to dorsal side (Fig. 5 - 1 E, F).Published as part of Zhou, Yu-Lingzi & Zhou, Hong-Zhang, 2016, Taxonomy of the genus Diochus Erichson, 1839 (Coleoptera: Staphylinidae, Staphylininae, Diochini) in China with descriptions of four new species, pp. 1-30 in Zootaxa 4127 (1) on pages 10-13, DOI: 10.11646/zootaxa.4127.1.1, http://zenodo.org/record/25826
Medhiama liupanshanensis Zhou & Zhou, sp. n.
2. <i>Medhiama liupanshanensis</i> Zhou & Zhou, sp. n. <p>(Fig. 4 A–H)</p> <p> <b>Type material.</b> Holotype: male, <b>CHINA</b>: <b>Ningxia</b>: <b>JingYuan co.:</b> Liupan Shan: Shanpo Linchang, 2200 m, 06.VII.2008, Zhou Haisheng & Zhao Zongyi collected (IZ-CAS); Paratypes: 1 female, same data as holotype; Xixia Linchang, 1 male, 2100 m, 26.VI.2008, Zhou Haisheng & Zhao Zongyi collected; Erlonghe Linchang, 1 female, 2050 m, 22.VI.2008, Zhou Haisheng & Zhao Zongyi collected (IZ-CAS).</p> <p> <b>Description. Measurement.</b> BL= 5.89 mm, FL= 3.23 mm, HL = 1.08 mm, HW= 0.80 mm, PL= 1.10 mm, PW= 0.70 mm, EL= 0.95 mm, EW= 0.95 mm.</p> <p>Body nearly cylindrical and medium sized. Entirely brown, except legs, apical 1/2 of last antennomere, last segment of maxillary and labial palpi lighter in color.</p> <p> <b>Head</b>. Oblong (HL to HW ratio 1.36), tempora substraight, not widened, posterior angles rounded. Dorsal integument entirely bearing microsculpture composed of shallow polygonal reticulum, and extensively distributed relatively small punctures, puncture intervals not wide, being equal about puncture diameter. Median longitudinal region impunctate, width equals to 4–5 puncture diameters; frontal region with shallow microstriae, and 3 pairs of tiny punctures. Each side of cranium without anterolateral puncture, with midlateral puncture far from dorsal margin of eye (5–6 puncture diameters to eye), temporal puncture rather near lateral margin (at lateral 1/6) and occipital puncture rather near posterior margin (at posterior 1/6). Frontal furrows deep and long, convergent backwards; anteocular furrows indistinct, scarcely observable. Eye quite small and rather flat, diameter not over 1/5 of temporal length (eye: tempora = 0.13: 0.82 mm). Epistoma relatively wide, subrectangular and flat, with a pair of tiny punctures. Distance between antennal insertions 0.24 mm, longer than distance from antenna to eye (0.19 mm).</p> <p> <b>Antennae</b>. Scape stout, thickened apically, much longer than three subsequent antennomeres combined, 0.44 mm; antennomere II elongate, 0.11 mm; III elongate, slightly shorter than II, 0.10 mm; IV and V subequal in length, 0.080 mm; last antennomere of medium length, 0.19 mm, subequal to two preceding antennomeres combined.</p> <p> <b>Mouthparts</b>. Labrum bilobed, with a median longitudinal groove. Maxillary palpus elongate, segment III longest, last segment slender and obconical and shorter than the penultimate. Labial palpus distinctly slender, last segment longest.</p> <p> <b>Neck</b>. Medium width (0.29 mm), nearly 1/3 of head width, with a transverse substraight ridge on anterior 1/3.</p> <p> <b>Pronotum</b>. Relatively shorter (PL to PW ratio 1.57), of same length as head, but narrower. Widest at anterior 1/3, narrowest at posterior 1/3. Anterior angles widely rounded and slightly protruding, lateral margins sinuate from middle, posterior angles rounded. Integument bearing shallow microstriae, and a pair of admedian row of 12–14 punctures, smaller than those on head. Areas outside admedian rows with additional, irregular, sparsely set punctures.</p> <p> <b>Mesoscutellum.</b> Shiny, extensively bearing polygonal reticulum and with a pair of small punctures on apical 1/4.</p> <p> <b>Elytra</b>. Subquadrate (EL to EW ratio 1.0), shorter but distinctly wider than pronotum. Humeri well developed, lateral margins widened posteriorly, hind margin rounded. Integument slightly wrinkled, without microsculpture; each side symmetrically with regular rows of punctures, interspaces between rows 1–2 puncture diameters; deflexed portion of each elytron with 3–4 rows of punctures.</p> <p> <b>Legs</b>. First four segments of protarsi stout, not dilated, those of mesotarsi relatively slender; each last segment as long as the II–IV combined. Protibia with apical ctenidium and subapical ctenidia, meso- and metatibia only with apical ctenidium.</p> <p> <b>Abdomen.</b> Cylindrical, broadest at segment VII. Tergites III–VII shiny, surface entirely covered with a distinct mixture of extensive microstriae and polygonal reticulum; punctures small, sparsely scattered, interspace between them 3–4 puncture diameters, but much denser on tergite VI and VII. Each tergite with median longitudinal impunctate region, width about 3–4 puncture diameters, without distinct basal impression near anterior margin. Surface between two basal transverse carinae of tergites III–VII bearing distinct polygonal reticulum. All abdominal sternites shiny, with microstriae and setiferous punctures as those on tergites.</p> <p> <b>Male</b> (Fig. 4 A–F). Abdominal segment VIII entirely covered with setiferous punctures, posterior margins of tergite VIII and sternite VIII both slightly emarginated (Fig.4 A, B). Tergite IX symmetrical, connected mediobasally. Sternite IX, with long linear-shaped base and rounded in right margin (Fig.4 D). Tergite X symmetrical and broadest at anterior 1/4, anterior 1/4 sharply narrowed and with obtusely rounded apex (Fig.4 C). Aedeagus elliptical and large (Fig. 4 E, F), basal bulb 1.16 mm long. Parameres symmetrical and simple, 0.34 mm and slightly shorter than 1/3 of basal bulb length. Internal sac broadly bag-like, gradually widened and with cellshaped structure in median portion (Fig. 4 E).</p> <p> <b>Female</b> (Fig. 4 G, H). Sternite VIII not distinctly oblong, and posterior margin sharply protruding posteriorly (Fig. 4 G). Genital segment with a large pair of subtriangular supplementary sclerites, and a broad sternite with not distinctly protruding anterior margin (Fig. 4 H).</p> <p> <b>Distribution.</b> China (Ningxia).</p> <p> <b>Etymology</b>. The specific epithet is the Latinized adjective derived from the Chinese name (Pin-yin) of the type locality: Liupan Shan.</p> <p> <b>Remarks.</b> This new species can be easily distinguished from its congeners by the following character combination: sparsely punctate head, emarginated posterior margin of male sternite VIII, special form of sternite IX, tergite X, unique shape of inner sac and a broad sternite with slightly protruding anterior margin in female genital segment.</p>Published as part of <i>Zhou, Yu-Lingzi & Zhou, Hong-Zhang, 2012, Taxonomy of the genus Medhiama Bordoni, 2002 (Coleoptera: Staphylinidae, Staphylininae, Xantholinini) with descriptions of three new species, pp. 169-191 in Zootaxa 3478</i> on pages 175-178, DOI: <a href="http://zenodo.org/record/282239">10.5281/zenodo.282239</a>
Dendrolycopodium verticale comb. nov (Lycopodiopsida: Lycopodiaceae) from China
A new combination in the lycophyte genus Dendrolycopodium (Lycopodiacae) from Lycopodium, D. verticale (Li Bing Zhang) Li Bing Zhang & X. M. Zhou, for a Chinese species is made
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