ABSTRACT
We describe a primary gas pressure standard based on the measurement of the refractive index of helium gas using a microwave resonant cavity in the range between 500 Pa and 20 kPa. To operate in this range, the sensitivity of the microwave refractive gas manometer (MRGM) to low-pressure variations is substantially enhanced by a niobium coating of the resonator surface, which becomes superconducting at temperatures below 9 K, allowing one to achieve a frequency resolution of about 0.3 Hz at 5.2 GHz, corresponding to a pressure resolution below 3 mPa at 20 Pa. The determination of helium pressure requires precise thermometry but is favored by the remarkable accuracy achieved by ab initio calculations of the thermodynamic and electromagnetic properties of the gas. The overall standard uncertainty of the MRGM is estimated to be of the order of 0.04%, corresponding to 0.2 Pa at 500 and 8.1 Pa at 20 kPa, with major contributions from thermometry and the repeatability of microwave frequency measurements. A direct comparison of the pressures realized by the MRGM with the reference provided by a traceable quartz transducer shows relative pressure differences between 0.025% at 20 kPa and -1.4% at 500 Pa.
ABSTRACT
The need for structures capable of accommodating complex evolutionary signals such as those found in, for example, wheat has fueled research into phylogenetic networks. Such structures generalize the standard model of a phylogenetic tree by also allowing for cycles and have been introduced in rooted and unrooted form. In contrast to phylogenetic trees or their unrooted versions, rooted phylogenetic networks are notoriously difficult to understand. To help alleviate this, recent work on them has also centered on their "uprooted" versions. By focusing on such graphs and the combinatorial concept of a split system which underpins an unrooted phylogenetic network, we show that not only can a so-called (uprooted) 1-nested network N be obtained from the Buneman graph (sometimes also called a median network) associated with the split system [Formula: see text] induced on the set of leaves of N but also that that graph is, in a well-defined sense, optimal. Along the way, we establish the 1-nested analogue of the fundamental "splits equivalence theorem" for phylogenetic trees and characterize maximal circular split systems.