15 research outputs found
On Optimal Coverage of a Tree with Multiple Robots
We study the algorithmic problem of optimally covering a tree with mobile
robots. The tree is known to all robots, and our goal is to assign a walk to
each robot in such a way that the union of these walks covers the whole tree.
We assume that the edges have the same length, and that traveling along an edge
takes a unit of time. Two objective functions are considered: the cover time
and the cover length. The cover time is the maximum time a robot needs to
finish its assigned walk and the cover length is the sum of the lengths of all
the walks. We also consider a variant in which the robots must rendezvous
periodically at the same vertex in at most a certain number of moves. We show
that the problem is different for the two cost functions. For the cover time
minimization problem, we prove that the problem is NP-hard when is part of
the input, regardless of whether periodic rendezvous are required or not. For
the cover length minimization problem, we show that it can be solved in
polynomial time when periodic rendezvous are not required, and it is NP-hard
otherwise
Descripción del perfil ontogénico de hormonas esteroides sexuales e intermediarios en testÃculos del ratón de orejas negras (Peromyscus melanotis, Allen y Chapman, 1897)
Se analizó por radioinmunoanálisis (RIA) el contenido de esteroides sexuales (ES), dos hormonas (progesterona –P4-y
testosterona -T-) y tres intermediarios (pregnenolona -P5-; 17a-hidroxi-progesterona –17P4-y androstendiona –A-), en
cuatro categorÃas de edad de Peromyscus melanotis, asà como la histologÃa de sus testÃculos y epidÃdimos. Cuando se
compararon las concentraciones de los ES entre su correspondiente categorÃa de edad (CE) se encontraron diferencias
significativas (P < 0.0001), pero cuando la comparación se hizo entre P5, P4, 17P4 y A en las cuatro CE no hubo diferencias
(P > 0.05). Al comparar el contenido de T entre subadultos (CE II) y adultos jóvenes (CE III) la diferencia fue significativa (t1,7
= 30.80, P
0.05); en cambio sà existieron (t1,7 = 14.05, P < 0.0001) cuando la comparación se hizo entre adultos (CE IV) y viejos (CE V). El
ciclo ontogénico de la testosterona, asà como la espermatogénesis aumentan a partir de la pubertad, alcanzando su máximo
en la edad adulta y decrecen progresivamente con el envejecimiento
Separability, Boxicity, and Partial Orders
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To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/A collection S = {Si,..., Sn} of disjoint closed convex sets in Rd is separable if there exists
a direction (a non-zero vector) −→v of Rd such that the elements of S can be removed, one
at a time, by translating them an arbitrarily large distance in the direction −→v without hitting
another element of S. We say that Si ≺ Sj if Sj has to be removed before we can remove Si .
The relation ≺ defines a partial order P(S, ≺) on S which we call the separability order of S
and −→v . A partial order P(X, ≺
) on X = {x1,..., xn} is called a separability order if there
is a collection of convex sets S and a vector −→v in some Rd such that xi ≺ x j in P(X, ≺
) if
and only if Si ≺ Sj in P(S, ≺). We prove that every partial order is the separability order of
a collection of convex sets in R4, and that any poset of dimension 2 is the separability order
of a set of line segments in R3. We then study the case when the convex sets are restricted to
be boxes in d-dimensional spaces. We prove that any partial order is the separability order
of a family of disjoint boxes in Rd for some d ≤ n
2 + 1. We prove that every poset of
dimension 3 has a subdivision that is the separability order of boxes in R3, that there are
partial orders of dimension 2 that cannot be realized as box separability in R3 and that for
any d there are posets with dimension d that are separability orders of boxes in R3. We also
prove that for any d there are partial orders with box separability dimension d; that is, d is
the smallest dimension for which they are separable orders of sets of boxes in Rd