ABSTRACT. We give several new characterizations of Riordan Arrays, the most important of which is: if fd nÒk g nÒk2N is a lower triangular array whose generic element d nÒk linearly depends on the elements in a well-defined though large area of the array, then fd nÒk g nÒk2N is Riordan. We also provide some applications of these characterizations to the lattice path theory.

The herd had numerous abortions and premature births with evidence of recent point-source exposure to N caninum. Therefore, to reduce risk of transmission of N caninum to cattle, attempts should be made to prevent canine feces from contaminating feed, especially feedstuffs used to prepare mixed rations for cattle. Cows with evidence of previous exposure to N caninum were less likely to abort or give birth prematurely during the outbreak than cows with primary infections with N caninum; this finding suggests development of protective immunity in previously infected cows.

We compared the accuracy and precision of low-dose insulin administration using various devices including, for the first time, an insulin pump. We dispensed 1, 2, and 5 unit(s) of soluble insulin (100 units/mL) 15 times each from a NovoPen (3.0 mL), a BD-Mini Pen (1.5 mL), a Humalog Pen (100 units/mL), 30G Precision Sure-Dose Insulin Syringes, 30G BD Ultra-Fine II Short Needle Syringes, and a H-TRON-plus V100 insulin pump. Each dose was weighed on an analytical scale, and the delivered and target doses were compared. Accuracy was defined by the absolute percent difference from the target dose. Precision was defined as the absolute percent difference from the group sample mean. Overall, we found that the pen and pump devices were more accurate, and the pump more precise, than the syringes at the 1- and 2-unit doses. Syringes were dangerously inaccurate, clinically, at the 1-unit dose. The use of pens and syringes with very fine increment markings (1/2 unit) did not improve accuracy or precision. Earlier researchers used multiple individuals to draw and weigh the samples. In an effort to eliminate the potential introduction of significant error; our study used only 2 investigators: 1 to draw up the doses and another to weigh them. The conclusions in our study were similar to prior studies.

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Abstract. Abstract. The objective of this study was to determine whether a chlamydial isolate recovered from nasal swabs from swine with pneumonia could cause pneumonia and rhinitis in gnotobiotic pigs. The identity of the isolate currently is unknown, but it shares characteristics with Chlamydia trachomatis. After propagation in Vero cells and preparation of the inoculum (2.5 x 10 10 inclusion-forming units/ml), Chlamydiae were instilled into nostrils (1.0 ml/nostril) and lungs (2.0 ml intralaryngeally) of 15 anesthetized 3-day-old gnotobiotic piglets. Five age-matched gnotobiotic piglets were anesthetized and sham infected with uninfected cell culture lysates. Two treated piglets were moribund and 2 were severely dyspneic prior to necropsy 7 days postinfection (DPI), whereas remaining treated piglets showed mild dyspnea upon exertion throughout the study. All treated piglets developed diarrhea. All treated piglets necropsied 7-21 DPI had extensive consolidation in cranial, middle, and accessory lung lobes; a majority of these piglets also had extensive consolidation in the caudal lobes. Treated piglets necropsied 28 and 35 DPI had a lobular pattern of consolidation in all lung lobes. Histologically, lesions in lungs from treated piglets necropsied 7, 14, and 21 DPI were characterized by bronchointerstitial pneumonia with foci of type II pneumocyte hypertrophy and hyperplasia; pneumocytes and bronchial and bronchiolar epithelial cells were markedly vacuolated. Alveolar macrophages, peribronchitis, peribronchiolitis, and perivasculitis were seen in lungs from treated piglets necropsied 28 and 35 DPI; those necropsied 28 DPI also had foci of lymphohistiocytic and plasmacytic infiltrates. Turbinate lesions in all treated piglets were characterized by mild multifocal lymphoplasmacytic and occasionally neutrophilic rhinitis. Immunohistochemistry detected chlamydial antigen in bronchial and bronchiolar epithelial cells, pneumocytes, and inflammatory cells in treated piglets necropsied 7, 14, and 21 DPI. Positive staining was limited to alveolar macrophages in treated piglets necropsied 28 and 35 DPI. Chlamydial antigen was detected in turbinate epithelial cells at all necropsy intervals. Ultrastructurally, chlamydiae were seen with glycogen particles in vacuoles or free in the cytoplasm of bronchial and bronchiolar epithelial cells and pneumocytes. The results indicated that the chlamydial isolate used in this Chlamydiae have been associated with pneumonia, 17 enteritis, 11,13 conjunctivitis, 14 polyarthritis, 6 pericarditis, 19 perinatal mortality, 22 and reproductive disorders 15,21 in swine; however, the diagnostic and economic significance is unknown. Most of these reports have been based on histopathology, electron microscopy, and in some cases the isolation of chlamydiae. Many of the chlamydial isolates recovered from these disease syndromes are no longer available for study, and only a limited number of these isolates have been characterized.We recently recovered a chlamydial isolate from nasal swabs from pigs...