Congestion-based routing strategies in multihop TDD-CDMA networks

In this paper, a network topology is investigated that allows both peer-to-peer and nonlocal traffic in a cellular-based time-division duplex code-division multiple-access (TDD-CDMA) system known as opportunity driven multiple access (ODMA). The key to offering appropriate performance of peer-to-peer communication in such a system relies on the use of a routing algorithm which minimizes interference. This paper presents a study of the constraints and limitations on the capacity of such a system using a variety of routing techniques. A congestion-based routing algorithm is presented that attempts to minimize the overall power of the system as well as providing a measure of feasibility. This technique provides the lowest required transmit power in all circumstances, and the highest capacity in nearly all cases studied. All of the routing algorithms studied here allocate TDD time slots on a first come first served basis according to a set of predefined rules. This fact is utilized to enable the development of a combined routing and resource allocation algorithm for TDD-CDMA relaying. A novel method of time slot allocation according to relaying requirements is then developed. Two measures of assessing congestion are presented based on matrix norms. One is suitable for current interior point solution, the other is more elegant but is not currently suitable for efficient minimization and, thus, practical implementation.     

Invited review article: A 10 mK scanning probe microscopy facility

We describe the design, development and performance of a scanning probe microscopy (SPM) facility operating at a base temperature of 10 mK in magnetic fields up to 15 T. The microscope is cooled by a custom designed, fully ultra-high vacuum (UHV) compatible dilution refrigerator (DR) and is capable of in situ tip and sample exchange. Subpicometer stability at the tip-sample junction is achieved through three independent vibration isolation stages and careful design of the dilution refrigerator. The system can be connected to, or disconnected from, a network of interconnected auxiliary UHV chambers, which include growth chambers for metal and semiconductor samples, a field-ion microscope for tip characterization, and a fully independent additional quick access low temperature scanning tunneling microscope (STM) and atomic force microscope (AFM) system. To characterize the system, we present the cooling performance of the DR, vibrational, tunneling current, and tip-sample displacement noise measurements. In addition, we show the spectral resolution capabilities with tunneling spectroscopy results obtained on an epitaxial graphene sample resolving the quantum Landau levels in a magnetic field, including the sublevels corresponding to the lifting of the electron spin and valley degeneracies.     

Adenosine transport inhibition ameliorates postischemic hypoperfusion in pigs

Cerebral ischemia is often followed by a period of delayed hypoperfusion that may contribute to tissue injury. We tested the hypothesis that augmentation of interstitial adenosine can improve tissue perfusion under this condition 10 min global ischemia was produced in two groups of isoflurane-anesthetized newborn pigs by occlusion of subclavian and brachiocephalic arteries, and changes in local cortical blood flow and cortical interstitial purine metabolites were measured using the combined hydrogen clearance-microdialysis technique. In one group, the dialysis probe was perfused with artificial cerebrospinal fluid buffer containing nitrobenzyl-thioinosine (NBT1, 100 mumol/l), a competitive inhibitor of adenosine transport. In the untreated group (n = 9), baseline cortical blood flow (39 +/- 3 ml/min/100 g) was depressed by 51 +/- 5% and 42 +/- 6% at 40 and 60 min, respectively, of postischemic reperfusion. NBTI increased baseline interstitial adenosine levels 2.4-fold which increased baseline cortical blood flow 1.5-fold to 60 +/- 4 ml/min/100 g, and increased both absolute adenosine levels as well as adenosine as a percentage of total purine metabolites throughout ischemia and reperfusion. As a result, the extent of postischemic hypoperfusion was significantly lessened in NBTI-treated animals (n = 9), with reductions in cortical blood flow of only 28 +/- 3% and 24 +/- 5% at 40 and 60 min of reperfusion, respectively. These results indicate that inhibition of adenosine transport by NBTI elevates interstitial adenosine concentration during and following cerebral ischemia, and concomitantly improves cortical perfusion in the post-ischemic period. The latter effect may contribute to the documented neuroprotective efficacy of adenosinergic therapy in cerebral ischemia.