13 research outputs found

    Strong Ramsey Games in Unbounded Time

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    For two graphs BB and HH the strong Ramsey game R(B,H)\mathcal{R}(B,H) on the board BB and with target HH is played as follows. Two players alternately claim edges of BB. The first player to build a copy of HH wins. If none of the players win, the game is declared a draw. A notorious open question of Beck asks whether the first player has a winning strategy in R(Kn,Kk)\mathcal{R}(K_n,K_k) in bounded time as n→∞n\rightarrow\infty. Surprisingly, in a recent paper Hefetz et al. constructed a 55-uniform hypergraph H\mathcal{H} for which they proved that the first player does not have a winning strategy in R(Kn(5),H)\mathcal{R}(K_n^{(5)},\mathcal{H}) in bounded time. They naturally ask whether the same result holds for graphs. In this paper we make further progress in decreasing the rank. In our first result, we construct a graph GG (in fact G=K6∖K4G=K_6\setminus K_4) and prove that the first player does not have a winning strategy in R(Kn⊔Kn,G)\mathcal{R}(K_n \sqcup K_n,G) in bounded time. As an application of this result we deduce our second result in which we construct a 44-uniform hypergraph G′G' and prove that the first player does not have a winning strategy in R(Kn(4),G′)\mathcal{R}(K_n^{(4)},G') in bounded time. This improves the result in the paper above. An equivalent formulation of our first result is that the game R(Kω⊔Kω,G)\mathcal{R}(K_\omega\sqcup K_\omega,G) is a draw. Another reason for interest on the board Kω⊔KωK_\omega\sqcup K_\omega is a folklore result that the disjoint union of two finite positional games both of which are first player wins is also a first player win. An amusing corollary of our first result is that at least one of the following two natural statements is false: (1) for every graph HH, R(Kω,H)\mathcal{R}(K_\omega,H) is a first player win; (2) for every graph HH if R(Kω,H)\mathcal{R}(K_\omega,H) is a first player win, then R(Kω⊔Kω,H)\mathcal{R}(K_\omega\sqcup K_\omega,H) is also a first player win.Comment: 18 pages, 46 figures; changes: fully reworked presentatio

    Projected differences in isotopic ratios of N (δ<sup>15</sup>N in ‰) between red blood cells and serum fractions in relation to gain or loss of body protein; the gradient of shading indicates the light (low δ<sup>15</sup>N) to heavy N (high δ<sup>15</sup>N).

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    <p>Projected differences in isotopic ratios of N (δ<sup>15</sup>N in ‰) between red blood cells and serum fractions in relation to gain or loss of body protein; the gradient of shading indicates the light (low δ<sup>15</sup>N) to heavy N (high δ<sup>15</sup>N).</p

    Sample sizes (<i>n</i>) of isotopic parameters measured in the blood of adult (≥3 y) female caribou in Denali National Park and Preserve, Alaska.

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    a<p>The isotopic ratios of nitrogen (δ<sup>15</sup>N) in red blood cells.</p>b<p>δ<sup>15</sup>N in serum proteins.</p>c<p>δ<sup>15</sup>N in serum amino acids.</p>d<p>Difference between δ<sup>15</sup>N<sub>RBC</sub> and δ<sup>15</sup>N<sub>Proteins.</sub></p>e<p>Difference between δ<sup>15</sup>N<sub>RBC</sub> and δ<sup>15</sup>N<sub>AAs.</sub></p

    A conceptual model of the routing of isotopes of N within a northern ungulate during winter.

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    <p>The size of each box indicates the relative size of each pool of N. The gradient of shading in each box indicates the range from less to more <sup>15</sup>N. Lighter arrows indicate flows of depleted N when animals are in positive N balance and gaining lean mass, while darker arrows indicate flows of enriched N when animals are losing lean mass.</p

    Winter and late winter locations of adult female caribou in Denali National Park and Preserve (Denali NPP), Alaska; blood was collected (<i>n</i> = 168) for isotopic analyses at late winter locations during March 1993–2007.

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    <p>Winter and late winter locations of adult female caribou in Denali National Park and Preserve (Denali NPP), Alaska; blood was collected (<i>n</i> = 168) for isotopic analyses at late winter locations during March 1993–2007.</p

    Overlapping areas of northern moose distribution (brown outline) [14,15], earlier spring onset (shaded) [74], and documented shrub expansion (green dots) [3,4].

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    <p>Shaded areas indicate trends in spring snow cover duration 1972–2008 (see legend). The green line denotes treeline. Increasing shrub habitat along the northern edge of moose distribution portends northward range extension of moose across the Arctic.</p

    Changes in moose distribution (dashed lines) in northern Alaska since 1880 (exceptions listed in [6]).

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    <p>Map is inset from <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0152636#pone.0152636.g003" target="_blank">Fig 3</a>. Shrub plots were distributed along the Chandler and Colville Rivers (orange ellipse), and temperature records were derived at two locations therein (gray dots) [<a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0152636#pone.0152636.ref033" target="_blank">33</a>]. <sup>a</sup>[<a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0152636#pone.0152636.ref016" target="_blank">16</a>], <sup>b</sup>[<a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0152636#pone.0152636.ref024" target="_blank">24</a>], <sup>c</sup>[<a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0152636#pone.0152636.ref006" target="_blank">6</a>], <sup>d</sup>[<a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0152636#pone.0152636.ref027" target="_blank">27</a>], <sup>e</sup>[<a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0152636#pone.0152636.ref030" target="_blank">30</a>], <sup>f</sup>[<a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0152636#pone.0152636.ref026" target="_blank">26</a>], <sup>g</sup>[<a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0152636#pone.0152636.ref031" target="_blank">31</a>].</p

    Differences in relative flammability of vegetation between the warm (Canadian Center for Climate Modeling Analysis Coupled Global Climate Model 3.1) and hot (Max Planck Institute European Center-Hamburg 5 Model) global circulation models under a moderate emissions scenario (A1B) in the winter ranges of the Central Arctic and Porcupine caribou herds, Alaska and Yukon, 2010–2100.

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    <p>Differences in relative flammability of vegetation between the warm (Canadian Center for Climate Modeling Analysis Coupled Global Climate Model 3.1) and hot (Max Planck Institute European Center-Hamburg 5 Model) global circulation models under a moderate emissions scenario (A1B) in the winter ranges of the Central Arctic and Porcupine caribou herds, Alaska and Yukon, 2010–2100.</p
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