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    Why is the number of primary tunnels of the formosan subterranean termite, Coptotermes formosanus Shiraki (Isoptera: Rhinotermidae), restricted during foraging?

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    https://www.riss.kr/link?id=A104734903

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    Subterranean termites forage by digging a network of tunnels to come into contact with food sources. When 1000 termites (Coptotermes formosanus Shiraki) were placed in a laboratory arena, 6.7 primary tunnels were constructed. The aim of this study was to explain the empirical observation in which termites restrict the number of primary tunnels. To this end, we constructed a model to simulate termite tunnel patterns based on empirical data and to calculate food transportation efficiency, γ, for the tunnel
    patterns. The efficiency was defined as the ratio of the number of encountered food particles to the sum of the shortest length from the location of encountered food particles to the initial position of growth of the tunnel. The γ was maximized when the number of primary tunnels was 5 or 6, which was fairly consistent with the empirical number of primary tunnels. This result indicated that termites may restrict the number of their primary tunnels to improve the transportation efficiency, which is directly related to
    their survival.
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    Subterranean termites forage by digging a network of tunnels to come into contact with food sources. When 1000 termites (Coptotermes formosanus Shiraki) were placed in a laboratory arena, 6.7 primary tunnels were constructed. The aim of this study was...

    Subterranean termites forage by digging a network of tunnels to come into contact with food sources. When 1000 termites (Coptotermes formosanus Shiraki) were placed in a laboratory arena, 6.7 primary tunnels were constructed. The aim of this study was to explain the empirical observation in which termites restrict the number of primary tunnels. To this end, we constructed a model to simulate termite tunnel patterns based on empirical data and to calculate food transportation efficiency, γ, for the tunnel
    patterns. The efficiency was defined as the ratio of the number of encountered food particles to the sum of the shortest length from the location of encountered food particles to the initial position of growth of the tunnel. The γ was maximized when the number of primary tunnels was 5 or 6, which was fairly consistent with the empirical number of primary tunnels. This result indicated that termites may restrict the number of their primary tunnels to improve the transportation efficiency, which is directly related to
    their survival.

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    참고문헌 (Reference)

    1 Su,N.-Y., "Tunneling activity of subterranean termites (Isoptera: Rhinotermitidae) in sand with moisture gradients" 96 : 88-93, 2003

    2 Lee,S.-H., "Rounding a corner of a bent termite tunnel and tunnel traffic efficiency" 77 : 135-138, 2008

    3 Dornhaus,A., "Paying for information: partial loads in central place foragers" 61 : 151-161, 2006

    4 Lee, S.-H, "Optimal length distribution of termite tunnel branches for efficient food search and resource transportation" 90 : 802-807, 2007

    5 Robson,S.K., "Nonrandom search geometry in subterranean termites" 82 : 526-528, 1995

    6 Ydenber,R., "Modelling social insect foraging" 9 : 491-493, 1994

    7 Le Comber,S.C., "Fractal dimension of African mole-rat burrows" 80 : 436-441, 2002

    8 Evans,T.A., "Foraging and building in subterranean termites: task switchers or reserve labourers?" 53 : 56-64, 2006

    9 Lee,S.-H, "Food encounter rates of simulated termite tunnels with variable food size/distribution pattern and tunnel branch l" 243 : 493-500, 2006

    10 Lee, S.-H, "Food encounter rate of simulated termite tunnels in heterogeneous landscapes" 90 : 314-322, 2007

    1 Su,N.-Y., "Tunneling activity of subterranean termites (Isoptera: Rhinotermitidae) in sand with moisture gradients" 96 : 88-93, 2003

    2 Lee,S.-H., "Rounding a corner of a bent termite tunnel and tunnel traffic efficiency" 77 : 135-138, 2008

    3 Dornhaus,A., "Paying for information: partial loads in central place foragers" 61 : 151-161, 2006

    4 Lee, S.-H, "Optimal length distribution of termite tunnel branches for efficient food search and resource transportation" 90 : 802-807, 2007

    5 Robson,S.K., "Nonrandom search geometry in subterranean termites" 82 : 526-528, 1995

    6 Ydenber,R., "Modelling social insect foraging" 9 : 491-493, 1994

    7 Le Comber,S.C., "Fractal dimension of African mole-rat burrows" 80 : 436-441, 2002

    8 Evans,T.A., "Foraging and building in subterranean termites: task switchers or reserve labourers?" 53 : 56-64, 2006

    9 Lee,S.-H, "Food encounter rates of simulated termite tunnels with variable food size/distribution pattern and tunnel branch l" 243 : 493-500, 2006

    10 Lee, S.-H, "Food encounter rate of simulated termite tunnels in heterogeneous landscapes" 90 : 314-322, 2007

    11 Rouland,C., "Experimental manipulation of termites (Isoptera, Macrotermitinae) foraging patterns in a Sahelo–Sudanese savanna: effect of litter quality" 50 : 309-316, 2003

    12 Su,N.-Y., "Directional change in tunneling of subterranean termites (Isoptera: Rhinotermitidae) in response to decayed wood attractants" 98 : 471-475, 2005

    13 King,E.G., "Development of incipient Formosan subterranean termite colonies in the filed" 68 : 355-358, 1975

    14 Su,N.-Y., "Characterization of tunneling geometry of subterranean termites (Isoptera: Rhinotermitidae) by computer simulation" 44 : 471-483, 2004

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    학술지 이력
    연월일 이력구분 이력상세 등재구분
    2023 평가 해외DB학술지평가 신청대상 (해외등재 학술지 평가)
    2020-01-01 등재 등재학술지 유지 (해외등재 학술지 평가) KCI등재
    2010-01-01 등재 등재학술지 유지 (등재유지) KCI등재
    2008-01-01 등재 등재학술지 유지 (등재유지) KCI등재
    2006-01-01 등재 등재학술지 유지 (등재유지) KCI등재
    2003-01-01 등재 등재학술지 선정 (등재후보2차) KCI등재
    2002-01-01 등재 등재후보 1차 PASS (등재후보1차) KCI등재후보
    2001-07-01 등재 등재후보학술지 선정 (신규평가) KCI등재후보
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    기준연도 WOS-KCI 통합IF(2년) KCIF(2년) KCIF(3년)
    2016 1.08 0.26 0.85
    KCIF(4년) KCIF(5년) 중심성지수(3년) 즉시성지수
    0.72 0.62 0.212 0.08
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