72,200 research outputs found
He Zou yi shi
[著者何諏 ; 編訂者黃天石].Library's copy: Copy 2 is a reproduced copy.[zhu zhe He Zou ; bian ding zhe Huang Tianshi]
Analyse des signaux multicomposante à modulation de fréquence linéaire par la transformation de Teager-Huang-Hough
A novel detection approach of linear FM (LFM) signals, with single or multiple components, in the time-frequency plane of Teager-Huang (TH) transform is presented. The detection scheme that combines TH transform and Hough transform is referred to as Teager-Huang-Hough (THH) transform. The input signal is mapped into the time-frequency plane by using TH transform followed by the application of Hough transform to recognize time-frequency components. LFM components are detected and their parameters are estimated from peaks and their locations in the Hough space. Advantages of THH transform over Hough transform of Wigner-Ville distribution (WVD) are: 1) cross-terms free detection and estimation, and 2) good time and frequency resolutions. No assumptions are made about the number of components of the LFM signals and their models. THH transform is illustrated on multicomponent LFM signals in free and noisy environments and the results compared with WVD-Hough and pseudo-WVD-Hough transforms
Yunte Huang, 35th Annual ODU Literary Festival
Yunte Huang is the author of Charlie Chan: The Untold Story of the Honorable Detective and His Rendezvous with American History (2010), which won the Edgar Award and California Book Award and was also the finalist for the National Book Critics Circle Award. A poet and translator, he has published Transpacific Displacement (2003), Cribs (2005), Transpacific Imaginations (2007), and other books. He is currently a professor of English at the University of California, Santa Barbara
Oscar Huang interview
TaiwanOscar Huang is a University of Washington Bothell student from Taiwan. Huang discusses his life experiences, particularly the challenges he has faced as an international student
Lucanus langi Huang, He & Shi, new species
<i>Lucanus langi</i> Huang, He & Shi new species <p> <i>Lucanus smithii</i> Parry, 1862, <i>sensu</i> Huang & Chen, 2010: 168, Figs. for male clypeolabrum, male habitus and male genitalia (misidentification).</p> <p> <b>Type material. Holotype (Fig. 6): CHINA: Xizang (Tibet):</b> 3, Linzhi Prefecture, Motuo County, 80K, 1800m, VIII.2005. Deposited in the entomological collection of Chongqing Museum, Natural History, Chongqing, China. <b>Paratypes: CHINA: Xizang:</b> 83, 1Ƥ, Linzhi Prefecture, Motuo County, Hanmi Army Station, 1900–2000m, 26.VII.–2.VIII. 2010, Yang He & Zheng Shi leg.; 1 paratype (3) in Natural History Museum, London; 2 paratypes (13, 1Ƥ) in senior author’s collection (Qingdao, China); 2 paratypes (2 3) in Yang He’s collection (Hangzhou, China); 2 paratypes (2 3) in Zheng Shi’s collection (Hangzhou, China); 2 paratypes (2 3) in Peng-Yu Liu’s collection (Fuzhou, China).</p> <p> <b>Holotype description.</b> Body length measured from apex of mandible to terminal tip of elytra: 48.5 mm.</p> <p> <b>Color and pubescence:</b> Head blackish brown, sparsely clad with yellow pubescence on both dorsal and ventral surfaces. Mandible blackish brown, clad with yellow pubescence basally. Pronotum blackish brown, sparsely clad with yellow pubescence laterally. Elytra reddish brown, thinly clad with yellow pubescence along lateral margins. Ventral surface of thorax and abdomen blackish brown, clad with yellow pubescence; pubescence on metasternum markedly longer than on other areas. All femora and tarsi on both dorsal and ventral surfaces blackish brown. All tibiae on both surfaces reddish brown.</p> <p> <b>Head.</b> Shape nearly rectangular; anterior ridge clearly defined and even in elevation; lateral and posterior ridges nearly straight, broadly rounded at posterolateral corners. Clypeolabrum clearly defined by transverse suture in front of frons, about 1.4 times as long as wide, glabrous; labrum and clypeus defined by lateral contraction medially; labrum plate-like, lacking dorsal branch, rounded and not bifurcate apically. Mandible about twice as long as head, evenly incurved, sharply pointed apically, with 1 small subapical ventral tooth; basal part swollen at inner margin, weakly serrate; major inner tooth associated with 1 small tooth in front and 1–2 small teeth behind. Antennal club with four antennomeres; antennomere 7 slender and sharply pointed apically; antennomeres 8–10 lamellate. Maxilla with long setose galea (Fig. 19). Ligula bilobed, with branches rounded at apex (Fig. 20), not pointed as in <i>Lucanus cheni</i> (Fig. 21).</p> <p> <b>Legs</b>. Protibia with 3–4 small teeth along lateral margin; apex bifurcate with branches blunt at tip. Mesotibia with 3 small lateral spines in addition to terminal spurs and spines. Metatibia with 2 lateral spines in addition to terminal spurs and spines.</p> <p> <b>Male genitalia</b>. Last abdominal tergite with poorly-defined lateral angles. Last abdominal ventrite without apparent membranous area. Ventral plate of 9th abdominal segment with basal part somewhat contracted before terminal expansion, with thin longitudinal membranous stripe along midline of terminal expansion. Aedeagus in dorsal view twice as long as wide. Basal piece in dorsal view triangular, nearly twice as long as parameres, with pair of sclerotized dorsal plates; ventral plate at caudal end of basal piece membranous. Paramere with slender basal process. Penis nearly as long as parameres, with flagellum about 5 times as long as parameres.</p> <p> <b>Male paratypes</b> (Figs. 7–8, 11, 12). Body length measured from apex of mandible to terminal tip of elytra: 41– 57 mm.</p> <p>Variation. Color variable: mandible, head, pronotum and elytra blackish brown to reddish brown; all tibiae on both surfaces entirely reddish brown to entirely blackish brown. Pubescence well marked in fresh specimens but absent in some old specimens. Mandible lacking a subapical tooth in some males. Basal part of mandible weakly to strongly serrate. Lateral spines of tibiae longer and sharper in most male specimens than in holotype. Large-sized males (Fig. 6) with the apical fork of the mandible more opened, and with more secondary teeth. Ventral plate at the caudal end of the basal piece of male genitalia entirely membranous to partly sclerotized.</p> <p> <b>Female paratype</b> (Figs. 9, 15, 16). Body length measured from apex of mandible to terminal tip of elytra: 36.5 mm.</p> <p> <b>Color and pubescence.</b> All structures including femora and tibiae black on both dorsal and ventral surfaces. Head, pronotum and elytra glabrous, only antennal club with yellow pubescence. Ventral surface of the body with yellow pubescence dense on metasternum but sparse elsewhere.</p> <p> <b>Head</b>. Canthus with both anterior and posterior angles clearly defined; anterior angle just inside of eye; lateral margin concave. Frontal and lateral ridges obsolete, not defined. Clypeolabrum in dorsal view transverse, flat at tip, not protruding forwards medially. Both mandibles with distinct dorsal tooth, 2 widely-separated inner teeth and large gap behind apex; lateral margin between 2 inner teeth concave and long.</p> <p> <b>Pronotum.</b> Form about twice as wide as long, widest behind the middle; anterior angle rounded; lateral angles clearly defined but not pointed; posterior angle obtuse; lateral margin before the lateral angle evenly convex.</p> <p> <b>Female genitalia (Figs. 32–35).</b> Last abdominal tergite with poorly-defined lateral angles. Last abdominal ventrite with large semicircular membranous medially. Hemisternite broadly rounded apically, with outer apex not produced beyond inner apex; inner lateral margin of sclerotized part short. Spermatheca sclerotized and J-shaped. Spermathecal duct little more than twice as long as spermatheca. Spermathecal gland slightly longer than spermatheca. Central conjunction of the 9th tergites protruding medially and narrow at tip.</p> <p> <b>Type locality.</b> China, southeastern Tibet, Motuo.</p> <p> <b>Etymology.</b> This species is dedicated to Dr. Song-Yun Lang (Chongqing, China), who kindly sent his lucanid collection to the senior author for study.</p> <p> <b>Diagnosis.</b> This new species is similar to <i>Lucanus smithii</i> Parry, 1862 (Figs. 13, 17, 18), but can be distinguished by the following characters: male mandible with the inner margin of the basal part swollen and serrate (Figs. 12–13), female mandible with two inner teeth and a large gap behind the apex (Figs. 16–18). <i>Lucanus smithii</i> should be placed into the <i>L</i>. <i>fortunei</i> group (<i>sensu</i> Huang & Chen 2010) because of the characters in the female mandible.</p> <p> This new species is sympatric with <i>Lucanus cheni</i> at Motuo and is similar to the latter in some external characters. However the two species can be immediately distinguished from each other by the following characters: male mandible with the apical fork more widely opened in <i>Lucanus cheni</i> than in <i>Lucanus langi</i> (Figs. 10–11); male clypeolabrum bifurcate in <i>Lucanus cheni</i> but rounded in <i>Lucanus langi</i> (Figs. 10–11); ligula of male with the two branches pointed in <i>Lucanus cheni</i> but rounded in <i>Lucanus langi</i> (Figs. 20–21); female canthus with the anterior angle outside of the eye in <i>Lucanus cheni</i> (Fig. 2), but just inside of the eye in <i>Lucanus langi</i> (Fig. 16). The genitalic difference between the two species is slight as in the cases of the other species of the <i>L</i>. <i>lunifer</i> group, but the following points are well marked: the sclerotized part of the penis with the lateral margins more concave in <i>Lucanus cheni</i> than in <i>Lucanus langi</i>; the hemisternite of the female genitalia with the outer apex protruding beyond the inner apex in <i>Lucanus cheni</i>, but with the outer apex not beyond the inner apex in <i>Lucanus langi</i>.</p> <p> This new species has some external characters in common with <i>Lucanus imitator</i> Boucher & Huang, 1991 but differs from the latter by the following characters: male clypeolabrum markedly longer and more rounded at apex; sclerotized part of the penis markedly narrower in front (Figs. 27–30); hemisternite of the female genitalia with basal portion less sclerotized (Figs. 34, 36); spermatheca of the female genitalia with the straight part markedly longer (Figs. 34, 39); central conjunction of the 9th tergites of female markedly narrower (Figs. 35, 42).</p> <p> This new species is also similar to the little known <i>Lucanus singularis</i>, but can be distinguished from the female holotype of the latter by the female clypeolabrum not protruding in the middle. The unique female holotype of <i>Lucanus singularis</i> has not been dissected so that the female genitalic characters remain unknown. However a series of specimens tentatively identified as <i>Lucanus singularis</i> are recently discovered from the Chayu area, southeastern Tibet, which match the most characters of the holotype of <i>Lucanus singularis</i>. A comparison between <i>Lucanus langi</i> and these specimens identified as <i>Lucanus singularis</i> shows more differences as follows: male clypeolabrum with apex rounded in <i>Lucanus langi</i> but pointed in <i>Lucanus singularis</i>; major inner tooth of the male mandible with a few small teeth in <i>Lucanus langi</i> but without any other small teeth in <i>Lucanus singularis</i>; male elytra darker in <i>Lucanus singularis</i> than in <i>Lucanus langi</i>; basal belt of the flagellum of the penis slightly longer in <i>Lucanus singularis</i> (Fig. 31) than in <i>Lucanus langi</i> (Figs. 27–28); hemisternite of the female genitalia markedly longer in <i>Lucanus singularis</i> (Fig. 37) than in <i>Lucanus langi</i> (Fig. 34).</p> <p> This new species can be distinguished from <i>Lucanus dohertyi</i> Boileau, 1911, <i>Lucanus sukkiti</i> Fukinuki, 2004 and other species placed in the <i>L</i>. <i>westermanni</i> group (<i>sensu</i> Lacroix & Bomans 1973) by the basal part of the male mandible strongly swollen and serrate.</p> <p> This new species should be placed in the <i>L</i>. <i>lunifer</i> group (<i>sensu</i> Huang & Chen 2010) with <i>Lucanus cheni, Lucanus imitator</i> and <i>Lucanus singularis</i>.</p>Published as part of <i>Huang, Hao, He, Yang & Shi, Zheng, 2011, Description of two new species of Lucanus Scopoli (Coleoptera: Scarabaeoidea: Lucanidae) from southeastern Tibet, China, pp. 56-64 in Zootaxa 2987</i> on pages 59-63, DOI: <a href="http://zenodo.org/record/278361">10.5281/zenodo.278361</a>
Alex Huang
Dr. Alex Huang received combined B.S./M.S. from University of Chicago, M.D./Ph.D. from Johns Hopkins University, fulfilled his pediatric residency at Johns Hopkins, completed a Pediatric Hematology/Oncology fellowship at Johns Hopkins / NCI, and a postdoctoral fellowship at the National Institute of Allergy and Infectious Diseases. Currently, he is a tenured Professor of Pediatrics, Pathology, Biomedical Engineering and General Medical Sciences at Case Western Reserve University. Dr. Huang holds the endowed Theresia G. & Stuart F. Kline Family Foundation Chair in Pediatric Oncology and serves as Director of the Center for Pediatric Immunotherapy at Rainbow Babies & Children’s Hospital as well as Director of the Medical Scientist Training Program at Case Western Reserve University School of Medicine.
Prior to 2023, Dr. Huang served as the Director of Pediatric Hematology-Oncology Fellowship Program at University Hospital’s Rainbow Babies & Children’s for 17 years. Dr. Huang oversees immune-based cancer therapeutics as co-leader of Immune Oncology Scientific Program at Case Comprehensive Cancer Center. Nationally, he is an elected member of the NCI’s Pediatric and Adolescent Solid Tumor Steering Committee (PASTSC) and a steering member of the Coalition for Pediatric Medical Research. Dr. Huang’s research focuses on exploiting the tumor immune microenvironment to control pediatric and AYA cancers.https://openworks.mdanderson.org/kleinermanbios/1003/thumbnail.jp
Racial Replication - Michelle N. Huang in Conversation with Lisa Nakamura and Huan He
Asiatic interchangeability is made, not born. In her talk, Michelle N. Huang discusses how dystopian clone narratives challenge notions of individual racialized identity at both the genetic and generic levels. Drawing on Saidiya Hartman's concept of racial fungibility, Huang will examine Kazuo Ishiguro's Never Let Me Go (2005) and Larissa Lai's Salt Fish Girl (2002) to trace how Asian American interchangeability is produced through reproductive control as well as an economy of character. In rearticulating, rather than rejecting, notions of shared subjectivity, hivemind, and fellow feeling, Asiatic clones ask for experimental alternatives to the ethnic bildungsroman and demonstrate the novel form itself to be a racialized technology of identity. Michelle N. Huang is an Assistant Professor of English and Asian American Studies at Northwestern University. She has research and teaching interests in contemporary Asian American literature, posthumanism, and feminist science studies. Her current project, Molecular Race, examines posthumanist aesthetics in post-1965 Asian American literature to trace racial representation and epistemology at nonhuman, minute scales. Molecular Race argues that a rapprochement with scientific discourse is necessary to fully grasp how the formal and aesthetic qualities of Asian American literature unsettle sedimented structures of racial formation.http://deepblue.lib.umich.edu/bitstream/2027.42/195279/1/racial_replication_flier.jpeghttp://deepblue.lib.umich.edu/bitstream/2027.42/195279/2/Racial_Replication__Michelle_N_Huang_in_Conversation_with_Lisa_Nakamura_and_Huan_He_Transcript.txthttp://deepblue.lib.umich.edu/bitstream/2027.42/195279/3/Racial_Replication__Michelle_N_Huang_in_Conversation_with_Lisa_Nakamura_and_Huan_He_Captioned.mp
Homonemobius brevipennis He & Wang & Huang & Ma 2022, sp. nov.
Homonemobius brevipennis He & Ma, sp. nov. 短D同n'ḋ Figs. 1, 2, 3A–B, 4A–C Holotype. China: Male, Yunnan, Er’yuan, Niuguidan Village, 5.VII.2021, Libin Ma & Wei Yuan coll. Paratypes. 4 males and 4 females, the same data as the holotype; 2 males & 1 female, Yunnan, Lijiang, Gucheng County, Sheshan Park, 5.VIII.2021, Zhixin He & Ning Wang coll. (SNNU). Description. Male (Figs. 2A and 3A). Body size small. Head small and pubescent, slightly wider than the anterior margin of pronotum. Frontal rostrum twice broader than antennal scape. Eyes large. Apical three joints of maxillary palpi distinctly elongated and the 5th joint apically truncated and shaped as horseshoe shaped. Pronotum transverse, both anterior and posterior margins straight and the posterior wider than the anterior. Tegmen short; dorsal field bearing four longitudinal veins and lateral field with four Sc branches. Tympana absent. Hind tibia bears three dorsal external spurs and four internal spurs, and apical spurs comprising two outside and three inside. Genitalia (Figs. 3A–C). Epiphallus relatively short (confined to the basal half of the genitalia complex) and ectoparamere very large (almost similar to epiphallus). Median part of the epiphallus shaped as a bridge and very thin. Ectoparameres clip-shaped (viewed laterally) with an upper branch (large, curved, proximally expanded and apically acute) and lower branch (short and nearly straight). Female (Figs. 2B, 3B). Resemble male. Body size slightly larger than male. Ovipositor needle-like and slightly shorter than cercus. Coloration. Body blackish brown. Four brown longitudinal stripes at the dorsal area of the head. Legs dark brown. Measurements. Male (n=7). BL 4.22±1.29, PL 1.08±0.24, TL 1.27±0.83, HFL 2.79±0.62; Female (n=5). BL 4.45±1.10, PL 1.03±0.14, TL 1.03±0.56, OL 2.42±0.43. Etymology. The name refers to the species’ short tegmen. Distribution (Fig. 1). China (Yunnan). Remarks. This species is similar to Homonemobius curifolis Zhang et al., 2020 in color,but differin the shape of epiphallus. Of the known species, H. curifolis has a short and thick clip-like ectoparamere, which this structure is long and thin on H. brevipennis sp. nov. This new species also resembles Homonemobius amare He & Ma, 2021. The differences are: shorter tegmen, and more acute lower branch of the ectoparameres. It differs from Homonemobius nigrus Li et al., 2010 in ectoparameres (bifurcated vs. not bifurcated), and differs from H. monomorphus in coloration of body (dark brown vs. yellowish brown) and tegmen’s length (reached the 3 rd vs. 6 th segment of abdomen).Published as part of He, Zhixin, Wang, Ning, Huang, Huateng & Ma, Libin, 2022, Two new species of ground crickets (Orthoptera: Trigonidiidae; Nemobiinae) from China, pp. 473-479 in Zootaxa 5092 (4) on pages 474-475, DOI: 10.11646/zootaxa.5092.4.6, http://zenodo.org/record/588651
Zu ben Su Huang chi du he ke
蘇東坡, 黃山谷先生著."埽葉山房石印."線裝, 一函.Su Dongpo, Huang Shangu xian sheng zhu."Sao ye shan fang shi yin."Xian zhuang, yi han
Pteronemobius osuviridis He & Wang & Huang & Ma 2022, sp. nov.
Pteronemobius osuviridis He & Ma, sp. nov. fl尾异n'ḋ Figs. 1, 3C–D, 4D–F, 5 Holotype. China: Male, Yunnan, Lincang, Linxiang County, Datian Village, 16.VIII.2021, Zhixin He, Ning Wang & Wei Yuan coll. Paratypes. 4 males and 4 females, the same data as holotype (SNNU). Description. Male (Figs 2C, 4A). Body size medium. Head round, slightly wider than pronotum. Rostrum approximately equal to antennal scape in width. Ocelli oval-like, median ocellus smallest. The apical joint of maxillary palpi longer than the third one, and it depressed, widened and with rounded apex; apical joint of labial palpi rod-like, longer than remaining sections, depressed and widened. Pronotum transverse, bearing bristles. Anterior and posterior margin straight, posterior margin wider than the anterior, both lateral edges slightly concaved in the middle. Tegmen reaching 7th abdominal segment, bearing one oblique vein and three chord veins. Dividing vein longitudinally separates the mirror as two cells. Apical region degraded. The Fore tibia only possesses a long oval-like external tympanum. Hind tibia bearing four dorsal spurs and three apical spurs on each side. Genitalia (Figs. 4D–F). Epiphallus large and dorsally broad, with apical margin broadly and medially concaved and armed with short lateral lobes. Ectoparamere clip-like (laterally viewed) and conspicuously shorter than epiphallus. In lateral view, ectoparamere aremedwith similar upper and lower branches and the upper one significantly and proximally expanded. Female (Figs 3D, 5B). Resembles male. Body size slightly smaller than male. Tegmen short, bearing five regular veins on the dorsal field. Ovipositor is sword-like and slightly shorter than cercus. Coloration. Body yellowish-brown. Four dark longitudinal stripes at the dorsal area of head. Anterior half of the abdomen colored dark brown. The apex of the hind femur bears small dark spots on two sides. The basal part of cercus greenish. Measurements. Male (n=5). BL 6.43±1.43, PL 1.42±0.46, TL 3.75±0.97, HFL 4.69±0.99; Female (n=4). BL 6.03±1.45, PL 1.49±0.31, TL 2.93±0.76, OL 4.10±0.66. Etymology. The name refers to the greenish color of the male's cercus. Distribution (Fig. 1). China (Yunnan). Remarks. This species is very similar to Pteronemobius nitidus (Bolívar, 1901) in appearance and coloration but different in body size and shape of ectoparamere. P. nitidus is larger than the new species (BL 8 mm vs. 6 mm). The male genitalia of the known species is armed with an upper branch nearly two times longer than the lower one, while the branches of the new species are similar in length.Published as part of He, Zhixin, Wang, Ning, Huang, Huateng & Ma, Libin, 2022, Two new species of ground crickets (Orthoptera: Trigonidiidae; Nemobiinae) from China, pp. 473-479 in Zootaxa 5092 (4) on pages 476-477, DOI: 10.11646/zootaxa.5092.4.6, http://zenodo.org/record/588651
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