185,865 research outputs found

    Wei L, Songchang S, Huiyu L, Huibin H, Gang C, Junping W. Global characteristics and trends of research on polycystic ovary syndrome from 2004 to 2019: Based on bibliometric analysis combined with information visualization analysis

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    Wei L, Huibin H, Junping W, Gang C, Guangda X.Global characteristics and trends of research on polycystic ovary syndrome from 2004 to 2019: Based on bibliometric analysis combined with information visualization analysi

    Secular variation in the elemental composition of marine shales since 840 Ma: Tectonic and seawater influences

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    Suplemental data for Wei and Algeo_GCA_MS_(08/27/2019

    Secular variation in the elemental composition of marine shales since 840 Ma: Tectonic and seawater influences

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    Suplemental data for Wei and Algeo_GCA_MS_(08/27/2019

    Secular variation in the elemental composition of marine shales since 840 Ma: Tectonic and seawater influences

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    Suplemental data for Wei and Algeo_GCA_MS_(08/27/2019

    The universal planned language of K'ang Yu-wei

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    K’ang Yu-wei był wielkim reformatorem i politykiem, który żył pod koniec epoki Cesarstwa Chińskiego. Był jednocześnie filozofem społecznym i w ramach tejże pracy filozoficznej zajął się ideą uniwersalnego języka dla całego świata.K’ang Yu-wei was a highly important reformer and political figure at the end of the Chinese Empire. He was at the same time a social philosopher, who as part of his philosophy dealt with the concept of a universal world-wide planned languag

    Siobla pseudoplesia Niu & Wei 2012

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    Siobla pseudoplesia Niu & Wei, 2012 (Figs 2 g, 2 h, 5 c, 5 d, 6 j–n, 9 h, 9 u, 10 w, 10 x) Siobla pseudoplesia Niu et al., 2012: 410. f #, type locality: Mt. Shennongjia, Hubei (China). Distribution. China (Ningxia, Shaanxi, Shanxi, Henan, Hubei, Sichuan). Remarks. The species is similar to S. acutitheca Niu & Wei, 2010 but differs from it in the ovipositor sheath distinctly shorter than middle tibia, the apical sheath very narrow in lateral view and acute at apex, the middle breadth of apical sheath about half breadth of the apex of hind tibia; the serrulae weakly sclerotized and almost flat, the 10 th serrula with 10–12 minute teeth; the postocellar area as broad as long; the interspaces between punctures on mesonotum microsculptured, almost mat; the abdominal tergite 1 weakly microsculptured, tergites 2–9 hardly microsculptured; and the first pulvillus small, distinctly shorter than half apical breadth of metabasitarsus.Published as part of Niu, Gengyun & Wei, Meicai, 2013, Revision of the Siobla formosana group (Hymenoptera: Tenthredinidae), pp. 41-68 in Zootaxa 3746 (1) on page 51, DOI: 10.11646/zootaxa.3746.1.2, http://zenodo.org/record/28530

    Siobla pseudoplesia Niu & Wei 2012

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    Siobla pseudoplesia Niu & Wei, 2012 (Figs 2 g, 2 h, 5 c, 5 d, 6 j–n, 9 h, 9 u, 10 w, 10 x) Siobla pseudoplesia Niu et al., 2012: 410. f #, type locality: Mt. Shennongjia, Hubei (China). Distribution. China (Ningxia, Shaanxi, Shanxi, Henan, Hubei, Sichuan). Remarks. The species is similar to S. acutitheca Niu & Wei, 2010 but differs from it in the ovipositor sheath distinctly shorter than middle tibia, the apical sheath very narrow in lateral view and acute at apex, the middle breadth of apical sheath about half breadth of the apex of hind tibia; the serrulae weakly sclerotized and almost flat, the 10 th serrula with 10–12 minute teeth; the postocellar area as broad as long; the interspaces between punctures on mesonotum microsculptured, almost mat; the abdominal tergite 1 weakly microsculptured, tergites 2–9 hardly microsculptured; and the first pulvillus small, distinctly shorter than half apical breadth of metabasitarsus.Published as part of Niu, Gengyun & Wei, Meicai, 2013, Revision of the Siobla formosana group (Hymenoptera: Tenthredinidae), pp. 41-68 in Zootaxa 3746 (1) on page 51, DOI: 10.11646/zootaxa.3746.1.2, http://zenodo.org/record/28530

    FIGURE 4, A–D. Elatostema androstachyum W. T. Wang Y. G. Wei & A in Additions to the Flora of China: three new species of Elatostema (Urticaceae) from Guangxi

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    FIGURE 4, A–D. Elatostema androstachyum W. T. Wang Y. G. Wei & A. Monro: A, Habitat; B, Habit with staminate (centre) and pistillate inflorescences (bottom-right) visible; C, Pistillate inflorescence; D, Staminate inflorescence. (A–D by Yi-Gang Wei from the isotype)Published as part of Wei, Yi-Gang, Monro, A.K. & Wang, Wen-Tsai, 2013, Additions to the Flora of China: three new species of Elatostema (Urticaceae) from Guangxi, pp. 1-12 in Phytotaxa 147 (1) on page 7, DOI: 10.11646/phytotaxa.147.1.1, http://zenodo.org/record/510017

    A Higher-Order Energy Expansion to Two-Dimensional Singularly Neumann Problems

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    Of concern is the following singularly perturbed semilinear elliptic problem \begin{equation*} \left\{ \begin{array}{c} \mbox{ϵ2Δuu+up=0{\epsilon}^2\Delta u -u+u^p =0 in Ω\Omega}\\ \mbox{u>0u>0 in Ω\Omega and uν=0\frac{\partial u}{\partial \nu}=0 on Ω\partial \Omega}, \end{array} \right. \end{equation*} where Ω\Omega is a bounded domain in RN{\mathbf{R}}^N with smooth boundary Ω\partial \Omega, ϵ>0\epsilon>0 is a small constant and 1<p<(N+2N2)+1< p<\left(\frac{N+2}{N-2}\right)_+. Associated with the above problem is the energy functional JϵJ_{\epsilon} defined by \begin{equation*} J_{\epsilon}[u]:=\int_{\Omega}\left(\frac{\epsilon^2}{2}{|\nabla u|}^2 +\frac{1}{2}u^2 -F(u)\right)dx \end{equation*} for uH1(Ω)u\in H^1(\Omega), where F(u)=0uspdsF(u)=\int_{0}^{u}s^p ds. Ni and Takagi (\cite{nt1}, \cite{nt2}) proved that for a single boundary spike solution uϵu_{\epsilon}, the following asymptotic expansion holds: \begin{equation*} (1) \ \ \ \ \ \ \ \ J_{\epsilon}[u_{\epsilon}]=\epsilon^{N} \left[\frac{1}{2}I[w]-c_1 \epsilon H(P_{\epsilon})+o(\epsilon)\right], \end{equation*} where I[w]I[w] is the energy of the ground state, c1>0c_1 >0 is a generic constant, PϵP_{\epsilon} is the unique local maximum point of uϵu_{\epsilon} and H(Pϵ)H(P_{\epsilon}) is the boundary mean curvature function at PϵΩP_{\epsilon}\in \partial \Omega. Later, Wei and Winter (\cite{ww3}, \cite{ww4}) improved the result and obtained a higher-order expansion of Jϵ[uϵ]J_{\epsilon}[u_{\epsilon}]: \begin{equation*} (2) \ \ \ \ \ \ J_{\epsilon}[u_{\epsilon}]=\epsilon^{N} \left[\frac{1}{2}I[\omega]-c_{1} \epsilon H(P_{\epsilon})+\epsilon^2 [c_2(H(P_\epsilon))^2 +c_{3} R(P_\epsilon)]+o(\epsilon^2)\right], \end{equation*} where c2c_2 and c3>0c_3>0 are generic constants and R(Pϵ)R(P_\epsilon) is the scalar curvature at PϵP_\epsilon. However, if N=2N=2, the scalar curvature is always zero. The expansion (2) is no longer sufficient to distinguish spike locations with same mean curvature. In this paper, we consider this case and assume that 2p<+ 2 \leq p <+\infty. Without loss of generality, we may assume that the boundary near P\in\partial\Om is represented by the graph {x2=ρP(x1)} \{ x_2 = \rho_{P} (x_1) \}. Then we have the following higher order expansion of Jϵ[uϵ]:J_\epsilon[u_\epsilon]: \begin{equation*} (3) \ \ \ \ \ J_\epsilon [u_\epsilon] =\epsilon^N \left[\frac{1}{2}I[w]-c_1 \epsilon H({P_\epsilon})+c_2 \epsilon^2(H({P_\epsilon}))^2 ] +\epsilon^3 [P(H({P_\epsilon}))+c_3S({P_\epsilon})]+o(\epsilon^3)\right], \end{equation*} where H(P_\ep)= \rho_{P_\ep}^{''} (0) is the curvature, P(t)=A1t+A2t2+A3t3P(t)=A_1 t+A_2 t^2+A_3 t^3 is a polynomial, c1c_1, c2c_2, c3c_3 and A1A_1, A2A_2,A3A_3 are generic real constants and S(P_\epsilon)= \rho_{P_\ep}^{(4)} (0). In particular c3<0c_3<0. Some applications of this expansion are given
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