Probing magnetic order and disorder in the one-dimensional molecular spin chains CuF2(pyz) and [Ln(hfac)3(boaDTDA)] n (Ln = Sm, La) using implanted muons.

We present the results of muon-spin relaxation ([Formula: see text]SR) measurements on antiferromagnetic and ferromagnetic spin chains. In antiferromagnetic CuF2(pyz) we identify a transition to long range magnetic order taking place at [Formula: see text] K, allowing us to estimate a ratio with the intrachain exchange of [Formula: see text] and the ratio of interchain to intrachain exchange coupling as [Formula: see text]. The ferromagnetic chain [Sm(hfac)3(boaDTDA)] n undergoes an ordering transition at [Formula: see text] K, seen via a broad freezing of dynamic fluctuations on the muon (microsecond) timescale and implying [Formula: see text]. The ordered radical moment continues to fluctuate on this timescale down to 0.3 K, while the Sm moments remain disordered. In contrast, the radical spins in [La(hfac)3(boaDTDA)] n remain magnetically disordered down to T = 0.1 K suggesting [Formula: see text].

Migrant labor takes a holiday. Reworking modernity and marginality in contemporary Thailand.

This paper examines the practice of working-class group excursions in Thailand, organized by and for rural labor migrants in Bangkok. These trips involve traditional forms of Buddhist ceremonial as well as more self-consciously "modern" sightseeing activities in distant regions of the country. More than just a welcome respite from the drudgery and discipline of factory jobs, these excursions allow labor migrants to make important claims about their experiences as members of the Thai nation-state. As tourist-consumers, migrant workers appropriate powerful signs and symbols of modern Thai identity and status, in doing so they contest (and at least partly rework) their material and ideological marginalization within contemporary Thai society.

Standardization of conjunctival impression cytology.

Lack of standardization limits the potential of conjunctival impression cytology as a clinical and research tool. This may be attributed to the variety of filter paper currently used. MF Millipore membrane filters of pore sizes 8.0, 3.0, 0.45, 0.22, and 0.025 micron were tested. Samples obtained from 30 eyes of rabbits were randomized and scored by four masked observers for cellularity and morphologic preservation. Cellularity was significantly greater with pore sizes 8.0, 3.0, and 0.45 micron versus 0.22 and 0.025 micron (p < or = 0.001), with an 83% correlation among four scorers. In contrast, morphology was better preserved in the smaller pore size papers (0.22 and 0.025 micron) when compared with larger pore sizes (p = 0.048). Using the best two filter papers (0.22 and 0.025 micron) and an ophthalmodynamometer, either 40, 60, or 80 g of pressure was applied for 3 s to each pore size paper to see whether cellularity could be increased. Cellularity was greater with pore size 0.22 than 0.025 micron (42.3 +/- 19.8 versus 8.7 +/- 6.4). Regardless of the pore size of the filter paper, cellularity was significantly improved at 60 g when compared with either 80 or 40 g. The results show that to maximize cell acquisition, a paper with medium pore size (0.22 micron) and a pressure of 60 g may be the best choice.