• 제목/요약/키워드: 6/8 structure

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백두대간 남덕유산∼소사재 구간의 능선부 식생구조 (Vegetation Structure of Mountain Ridge from Namdeogyusan to Sosajae in the Baekdudaegan)

  • 최송현;오구균;강현미
    • 한국환경생태학회지
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    • 제18권2호
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    • pp.131-141
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    • 2004
  • 백두대간의 남덕유산∼소사해 구간 능선부에 대해 16개 조사지(단위면적 500$m^2$)를 설정하여 식생구조를 조사하였다. Classification(TWINSPAN)기법에 의한 군락분리를 실시 한 결과, 군락 I 에서 군락 IV는 모두 신갈나무가 우점종인 가운데 부수종별 차이가 있었으며, 군락V는 신갈나무-소나무군락으로 최종 5개 군락으로 분리되었다. 각 군락은 층위별 상대우점치를 이용하여 군락구조를 밝혔다. 기술통계분석결과 단위면적당(500$m^2$)평균출현종수는 27.8$\pm$7.5종, 평균출현개체수는 687.6$\pm$326.8주이었다.

남산자연공원(南山自然公園)의 식물군집구조(植物群集構造) 및 8년간(年間)의 식생변화분석(植生變化分析) (Analysis of Vegetational Community Structure and Phytosociological Changes During Eight Years of the Namsan Nature Park in Seoul)

  • 이경재;박인협;오구균
    • 한국산림과학회지
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    • 제76권3호
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    • pp.206-217
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    • 1987
  • 서울의 남산자연공원(南山自然公園)의 식물군집구조(植物群集構造)를 분석하기 위하여 30개의 조사구(調査區)를 선정, 각 조사구에 $10{\times}10m$의 방형구(方形區) 5개씩을 설치 조사하였고, 또한 1978년과 1986년의 8년간의 식생군집변천(植生群集變遷)을 조사하기 위하여 17개 지점에 $5{\times}50m$의 "트란섹트"를 설치, 조사하였다. 남산(南山)의 현존식생(現存植生)의 비율은 아까시나무군집(群集) 29.39%, 신갈나무군집(群集) 21.25%, 소나무군집(群集) 17.58%이었다. 신갈나무림은 북사면(北斜面), 아까시나무림은 도로(道路) 등 시가지(市街地)와의 경계부(境界部), 소나무림은 동(東) 남사면(南斜面)에 주로 분포(分布)하였다. 녹지자연도(綠地自然度) 8, 7, 6의 비율은 각각 43.2, 7.8, 30.8%이었다. 남산삼림(南山森林)에서 소나무개체군(個體群)은 신갈나무, 팥배나무, 아까시나무, 산벚나무 등의 활엽수와의 경쟁에서 도태 되어 가고 있으며, 천이계열분석(遷移系列分析)에서도 소나무림은 신갈나무림으로 천이(遷移)가 진행되고 있었다. 지난 8년간의 식생구조(植生構造)의 변화(變化)는 종다양도(種多樣度)와 균재도(均在度)는 증가하였고, 우점도(優占度)는 감소(減少)하여, 하층(下層)의 종구성(種構成)이 다양(多樣)하여졌다. Raunkiaer 빈도계급(頻度階級)에서는 1986년이 1978년보다 A, E 급(級)이 증가하고, B 급(級)이 감소하여 남산(南山)의 식생(植生)은 동질화(同質化)되어 가고 있었다.

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초광대역 개방형 스터브 대역통과 여파기의 설계 (Design of an Ultra Wide Band Band-pass Filter with Open-Stubs)

  • 윤기철;강철호;홍태의;이종철
    • 한국ITS학회 논문지
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    • 제12권6호
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    • pp.37-43
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    • 2013
  • 본 논문에서는 SIR(Stepped Impedance Resonator) 구조를 이용한 초광대역(UWB:Ultra Wide Band) 개방형 스터브 대역통과 여파기를 제안한다. 제안한 개방형 스터브 대역통과 여파기는 초광대역을 구현하기 위해 스터브 위치에 SIR 구조를 적용하였으며 낮은 삽입손실을 갖는다. 제안된 대역통과 여파기의 대역폭은 중심 주파수 5.8GHz에서 103% 이고, 삽입 및 반사손실은 각각 0.17dB 및 13.1dB이며 전체의 크기는$21.6{\times}17.8mm^2$ 이다.

Protonation and Stability Constants for $Co^{2+},\;Ni^{2+},\;Cu^{2+},\;and\;Zn^{2+}$ of the Open-Chain Polyamine 1-Amino-13-(2-pyridyl)-3,6,9,12-tetraaza-tridecane. Crystal Structure of Its Nickel(Ⅱ) Complex

  • 김선덕;김준광;정우식
    • Bulletin of the Korean Chemical Society
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    • 제18권6호
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    • pp.653-656
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    • 1997
  • The new unsymmetric $N_6$ ligand 1-amino-13-(2-pyridyl)-3,6,9,12-tetraazatridecane (aptatd) containing one pyridyl group has been synthesized and characterized by EA, IR, and NMR. Its proton association constants $(log K_H^n)$ and stability constants $(log K_{ML})$ for Co(Ⅱ), Ni(Ⅱ), Cu(Ⅱ), and Zn(Ⅱ) ions were determined at 298.1 K and ionic strength 0.100 mol $dm^{-3}$ (KNO₃) in aqueous solution by potentiometry: log $K_H^1$=8.80, log $K_H^2$=8.49, log $K_H^3$=6.84, log $K_H^4$=4.17, log $K_H^5$=3.47; log $K_{ML}(Co^{2+})$=18.00, log $K_{ML}(Ni^{2+})$=21.31, log $K_{ML}(Cu^{2+})$=23.62, log $K_{ML}(Zn^{2+})$=15.60. The X-ray structure of its nickel(Ⅱ) complex [Ni(aptatd)]$(ClO_4)_2$ are reported: orthorhombic space group Pbca, a=15.715(1) Å, b=14.280(2) Å, c=19.443(2) Å, V=4363.4 (9) ų with Z=8. The geometry around nickel is a distorted octahedron with the pyridine nitrogen atom being cis to the nitrogen atom of the terminal primary amine.

Stresses analyses of shell structure with large holes

  • Tian, Zongshu;Liu, Jinsong
    • Structural Engineering and Mechanics
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    • 제6권8호
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    • pp.883-899
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    • 1998
  • The strength, deformation and buckling of a large engineering structure consisting of four ellipsoidal shells, two cylindrical shells with stiffening ribs and large holes, one conical shell and three pairs of large flanges under external pressure, self weight and heat sinks have been analysed by using two kinds of five different finite elements - four assumed displacement finite elements (shell element with curved surfaces, axisymmetric conical shell element with variable thickness, three dimensional eccentric beam element, axisymmetric solid revolutionary element) and an assumed stress hybrid element (a 3-dimensional special element developed by authors). The compatibility between different elements is enforced. The strength analyses of the top cover and the main vessel are described in the paper.

Crystal Structure of Pentapotassium Disodium Hexatungstoantimonate(V) Dodecahydrate, $K_5Na_2[SbW_6O_{24}]\cdot12H_2O$

  • Lee, Uk;Sasaki, Yukiyoshi
    • Bulletin of the Korean Chemical Society
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    • 제8권1호
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    • pp.1-3
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    • 1987
  • The crystal structure of $K_5Na_2[SbW_6O_{24}]{\cdot}12H_2O$ has been determined. Final R = 0.081 for 890 observed independent reflections collected by diffractometry. Crystal data as follows; trigonal, space group R3m, a = 9.794(1) ${\AA},\;{\alpha}$ = 84.72$(1)^{\circ}$, Z = 1. The heteropolyanion has a structure with point symmetry $D_{3d}$ (3m), of the ideal Anderson-type heteropolyanion. The Sb-W and W-W distances are 3.259(2) and 3.259(3) ${\AA}$. Three types of W-O ($W-O_t,\;W-O_b\;and\;W-O_c$) distances are 1.73(2), 1.95(4) and 2.20(3) ${\AA}$. The Sb-O distance is 1.97(3) ${\AA}$.

Crystal Structure of Antiinflammatory Sulindac

  • 구정회;김상헌;신완철
    • Bulletin of the Korean Chemical Society
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    • 제6권4호
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    • pp.222-224
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    • 1985
  • The crystal structure of sulindac, $C_{20}H_{17}Fo_3S$, one of the nonsteroid antiinflammatory agents, has been determined by the X-ray diffraction techniques using diffractometer data obtained by the $\varpi-2{\theta}$ scan technique with Cu $$K_{\alpha}$$ radiation from a crystal with space group symmetry Pbca and unit cell parameters a = 8.166(1), b = 18.291(8), c = 23.245(10) ${\AA}.$ The structure was solved by direct methods and refined by full-matrix least-squares to a final R = 0.11 for the 1153 observed reflections. The carboxyl group is nearly perpendicular to the indenyl ring as observed in indomethacin. The dihedral angle between the indenyl and phenyl rings is $35^{\circ}while$ the corresponding angle in indomethacin is $67^{\circ}.$ Crystal packing consists of a hydrogen bond and partial ring stacking between the indenyl rings.

소결조제 첨가에 따른 $0.6TiTe_3O_8-0.4MgTiO_3$ 세라믹스의 jdhs 소결 특성 (Low Temperature Sintering Properties of the $0.6TiTe_3O_8-0.4MgTiO_3$ Ceramics with Sintering Adds)

  • 김재식;류기원;고중혁;이영희
    • 대한전기학회:학술대회논문집
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    • 대한전기학회 2007년도 Techno-Fair 및 추계학술대회 논문집 전기물성,응용부문
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    • pp.114-115
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    • 2007
  • In this study, low temperature sintering property of the $0.6TiTe_3O_8-0.4MgTiO_3$ ceramics with sintering adds were investigated for LTCC application which enable to cofiring with Ag electrode. $TiTe_3O_8$ mixed with $MgTiO_3$ to improve the temperature property. In the X-ray diffraction patterns, the columbite structure of $TiTe_3O_3$ phase and ilmenite structure of $MgTiO_3$ phase were coexisted in all specimens. In the case of $H_3BO_3$ addition, the bulk density and dielectric constant were decreased but quality factor was increased with amount of $H_3BO_3$ additions. The TCRF of the $0.6TiTe_3O_8-0.4MgTiO_3+xwt%H_3BO_3$ ceramics were moved to positive direction. In another case, SnO addition, the bulk density and dielectric constant were increased but Quality factor was decreased with amount of SnO additions. The TCRF of the $0.6TiTe_3O_8-0.4MgTiO_3$+ywt%SnO ceramics were shifted to negative direction. The dielectric constant, quality factor and TCRF of the $0.6TiTe_3O_8-0.4MgTiO_3$ ceramics with $2wt%H_3BO_3$ and 2.5wt%SnO sintered at $830^{\circ}C$ for 1h, were 28.5, 39,570GHz, $+9.34ppm/^{\circ}C$ and 29.86, 35,80000z, $-0.58ppm/^{\circ}C$, respectively.

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