Time Versus Cost Tradeoffs for Deterministic Rendezvous in Networks

Two mobile agents, starting from different nodes of a network at possibly different times, have to meet at the same node. This problem is known as $\mathit{rendezvous}$. Agents move in synchronous rounds. Each agent has a distinct integer label from the set $\{1,\dots,L\}$. Two main efficiency measures of rendezvous are its $\mathit{time}$ (the number of rounds until the meeting) and its $\mathit{cost}$ (the total number of edge traversals). We investigate tradeoffs between these two measures. A natural benchmark for both time and cost of rendezvous in a network is the number of edge traversals needed for visiting all nodes of the network, called the exploration time. Hence we express the time and cost of rendezvous as functions of an upper bound $E$ on the time of exploration (where $E$ and a corresponding exploration procedure are known to both agents) and of the size $L$ of the label space. We present two natural rendezvous algorithms. Algorithm $\mathtt{Cheap}$ has cost $O(E)$ (and, in fact, a version of this algorithm for the model where the agents start simultaneously has cost exactly $E$) and time $O(EL)$. Algorithm $\mathtt{Fast}$ has both time and cost $O(E\log L)$. Our main contributions are lower bounds showing that, perhaps surprisingly, these two algorithms capture the tradeoffs between time and cost of rendezvous almost tightly. We show that any deterministic rendezvous algorithm of cost asymptotically $E$ (i.e., of cost $E+o(E)$) must have time $\Omega(EL)$. On the other hand, we show that any deterministic rendezvous algorithm with time complexity $O(E\log L)$ must have cost $\Omega (E\log L)$

Time vs. Information Tradeoffs for Leader Election in Anonymous Trees

The leader election task calls for all nodes of a network to agree on a single node. If the nodes of the network are anonymous, the task of leader election is formulated as follows: every node $v$ of the network must output a simple path, coded as a sequence of port numbers, such that all these paths end at a common node, the leader. In this paper, we study deterministic leader election in anonymous trees. Our aim is to establish tradeoffs between the allocated time $\tau$ and the amount of information that has to be given $\textit{a priori}$ to the nodes to enable leader election in time $\tau$ in all trees for which leader election in this time is at all possible. Following the framework of $\textit{algorithms with advice}$, this information (a single binary string) is provided to all nodes at the start by an oracle knowing the entire tree. The length of this string is called the $\textit{size of advice}$. For an allocated time $\tau$, we give upper and lower bounds on the minimum size of advice sufficient to perform leader election in time $\tau$. We consider $n$-node trees of diameter $diam \leq D$. While leader election in time $diam$ can be performed without any advice, for time $diam-1$ we give tight upper and lower bounds of $\Theta (\log D)$. For time $diam-2$ we give tight upper and lower bounds of $\Theta (\log D)$ for even values of $diam$, and tight upper and lower bounds of $\Theta (\log n)$ for odd values of $diam$. For the time interval $[\beta \cdot diam, diam-3]$ for constant $\beta >1/2$, we prove an upper bound of $O(\frac{n\log n}{D})$ and a lower bound of $\Omega(\frac{n}{D})$, the latter being valid whenever $diam$ is odd or when the time is at most $diam-4$. Finally, for time $\alpha \cdot diam$ for any constant $\alpha <1/2$ (except for the case of very small diameters), we give tight upper and lower bounds of $\Theta (n)$

With Great Speed Come Small Buffers: Space-Bandwidth Tradeoffs for Routing

We consider the Adversarial Queuing Theory (AQT) model, where packet arrivals are subject to a maximum average rate $0\le\rho\le1$ and burstiness $\sigma\ge0$. In this model, we analyze the size of buffers required to avoid overflows in the basic case of a path. Our main results characterize the space required by the average rate and the number of distinct destinations: we show that $O(k d^{1/k})$ space suffice, where $d$ is the number of distinct destinations and $k=\lfloor 1/\rho \rfloor$; and we show that $\Omega(\frac 1 k d^{1/k})$ space is necessary. For directed trees, we describe an algorithm whose buffer space requirement is at most $1 + d' + \sigma$ where $d'$ is the maximum number of destinations on any root-leaf path

Impacts of Spatial Resolution and Viewing Angle on Remotely Sensed Estimates of Spartina alterniflora Aboveground Biomass

Coastal salt marshes sequester large quantities of “blue carbon” in plant biomass and sediments, and provide numerous other valuable ecosystem functions and services. However, these ecosystems are increasingly threatened by external stressors, including rising sea levels and a changing climate, which have resulted in large losses of tidal marsh habitat. Measuring plant biomass is critical for understanding how carbon storage may be affected as stressors continue to cause marsh losses, and for improving conservation and management efforts. A number of studies have quantified aboveground biomass (AGB) in salt marshes using remote sensing techniques, and with the development of high resolution sensors there is excellent potential to improve estimates over large scales. However, few studies have evaluated how variability in spatial resolution and viewing angle across platforms impacts AGB estimates, despite the large range of potential imaging systems available. Using 3 cm and 6 cm resolution nadir hyperspectral drone imagery, and 0.5-3 cm oblique imagery collected from a ground-based camera at three viewing angles from two different-aged barrier island salt marshes in Virginia, USA, I evaluated the accuracy of regression models predicting S. alterniflora AGB from vegetation indices across resolution and viewing angle. The overall best performing linear regression models were obtained using the 3 cm nadir drone imagery. However, the best 6 cm regression models demonstrated only minor losses in accuracy relative to 3 cm. AGB estimates from obliquely angled imagery were less accurate than either nadir resolution. The most accurate oblique models were obtained at the highest viewing angle, with performance decreasing as the viewing angle became shallower. These results suggest that not all platforms perform similarly within salt marsh ecosystems, and that both spatial resolution and viewing angle must be considered in choice of imaging systems

The Responses of Normal and Castrate Female Sparrows to Injections of Pregnant Mare Serum

During the winter months, ovaries and oviducts of the sparrows are greatly reduced. Injection of pregnant mare serum during this resting period stimulates the ovary to an activity which simulates that of the breeding season. Oviducts respond to the increased amounts of female hormone released by the ovary