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C J Barton

Publications and source records attributed to C J Barton.

15 recordsLinked to original sources
PubMed2006

Stabilization of nuclear isovector valence-shell excitations.

Excited states in 138Ce have been studied via the 12C(138Ce, 138Ce*) Coulomb excitation reaction at 480 MeV. Relative cross sections have been determined from the gamma-ray yields observed with Gammasphere. The E2 and M1 strength distributions between the lowest six 2+ states up to 2.7 MeV enables us to identify the 2(4)+ state in 138Ce as the dominant fragment of the one-phonon 2(1,ms)+ mixed-symmetry state. Mixing between this level and a nearby isoscalar state is observed and is more than 4 times larger than in the neighboring isotone 136Ba. This is direct evidence that the stability of mixed-symmetry states strongly depends on the underlying subshell structure.

Journal Article↗
PubMed2002

B(E2) values in 150Nd and the critical point symmetry X(5).

Lifetimes of states in 150Nd were measured using the recoil distance method following Coulomb excitation of 150Nd by a 132 MeV 32S beam. The experiment was performed at the Yale Tandem accelerator, employing the SPEEDY gamma-ray detector array and the New Yale Plunger Device. Reduced transition probabilities in 150Nd are compared to the predictions of the critical point symmetry X(5) of the phase/shape transition that occurs for the N = 90 rare earth isotones. Very good agreement was observed between the parameter-free (apart from scale) X(5) predictions and the low-spin level scheme of 150Nd, revealing this as the best case thus far for the realization of the X(5) symmetry.

Journal Article↗
PubMed2002

Coulomb excitation of radioactive 132,134,136Te beams and the low B(E2) of 136Te.

The B(E2;0(+)-->2+) values for the first 2+ excited states of neutron-rich 132,134,136Te have been measured using Coulomb excitation of radioactive ion beams. The B(E2) values obtained for 132,134Te are in excellent agreement with expectations based on the systematics of heavy stable Te isotopes, while that for 136Te is unexpectedly small. These results are discussed in terms of proton-neutron configuration mixing and shell-model calculations using realistic effective interactions.

Journal Article↗
PubMed1999

Prenatal diagnosis in factor XIII-A deficiency.

Congenital factor XIII deficiency is a severe bleeding disorder that is inherited as an autosomal recessive trait. The condition is commonly due to absence of the factor XIII-A subunit protein in the plasma. The case of a baby is reported who showed typical clinical features of factor XIII-A deficiency, including recurrent bleeding from the umbilical stump and a life threatening haemorrhage after circumcision. Family studies were performed and molecular analysis, using a Short Tandem Repeat (STR) marker closely linked to the A subunit gene, allowed antenatal exclusion diagnosis to be undertaken in a subsequent pregnancy. The case highlights the importance of seeking a family history of bleeding disorders before surgery in the neonatal period, particularly if the parents are consanguineous.

Consanguinity↗