25 Tb/s transmission over 5,530 km using 16QAM at 5.2 b/s/Hz spectral efficiency.

We transmit 250x100G PDM RZ-16QAM channels with 5.2 b/s/Hz spectral efficiency over 5,530 km using single-stage C-band EDFAs equalized to 40 nm. We use single parity check coded modulation and all channels are decoded with no errors after iterative decoding between a MAP decoder and an LDPC based FEC algorithm. We also observe that the optimum power spectral density is nearly independent of SE, signal baud rate or modulation format in a dispersion uncompensated system.

16QAM transmission with 5.2 bits/s/Hz spectral efficiency over transoceanic distance.

We transmit 160 x 100 G PDM RZ 16 QAM channels with 5.2 bits/s/Hz spectral efficiency over 6,860 km. There are more than 3 billion 16 QAM symbols, i.e., 12 billion bits, processed in total. Using coded modulation and iterative decoding between a MAP decoder and an LDPC based FEC all channels are decoded with no remaining errors.

Alpha-1 antitrypsin limits neutrophil extracellular trap disruption of airway epithelial barrier function.

Neutrophil extracellular traps contribute to lung injury in cystic fibrosis and asthma, but the mechanisms are poorly understood. We sought to understand the impact of human NETs on barrier function in primary human bronchial epithelial and a human airway epithelial cell line. We demonstrate that NETs disrupt airway epithelial barrier function by decreasing transepithelial electrical resistance and increasing paracellular flux, partially by NET-induced airway cell apoptosis. NETs selectively impact the expression of tight junction genes claudins 4, 8 and 11. Bronchial epithelia exposed to NETs demonstrate visible gaps in E-cadherin staining, a decrease in full-length E-cadherin protein and the appearance of cleaved E-cadherin peptides. Pretreatment of NETs with alpha-1 antitrypsin (A1AT) inhibits NET serine protease activity, limits E-cadherin cleavage, decreases bronchial cell apoptosis and preserves epithelial integrity. In conclusion, NETs disrupt human airway epithelial barrier function through bronchial cell death and degradation of E-cadherin, which are limited by exogenous A1AT.

Lima Bean Downy Mildew Epiphytotics Caused by New Physiological Races of Phytophthora phaseoli.

Before 1995, race D of Phytophthora phaseoli, the causal agent of downy mildew on lima bean (Phaseolus lunatus), was the prevalent physiological race in the mid-Atlantic region of the United States. Since 1995, however, new physiological races of P. phaseoli have been responsible for downy mildew outbreaks in previously resistant cultivars in this region. Cultivar differential testing of 180 isolates of P. phaseoli collected between 1994 and 2005 from Delaware and the eastern shore of Maryland has confirmed the presence of two new physiological races. The detection of race E in 1995 and race F only 5 years later in 2000, plus the lack of resistant cultivars to manage the epiphytotics in lima bean, have led to millions of dollars of crop losses. Intra- and interspecific genetic variation of Phytophthora spp. and isolates were assessed using amplified fragment length polymorphism DNA fingerprinting. Primer groups EcoRI+AG and MseI+C distinguished P. phaseoli and P. capsici from P. infestans but did not distinguish among different races of P. phaseoli.

First Report of Phytophthora capsici Infecting Lima Bean (Phaseolus lunatus) in the Mid-Atlantic Region.

Lima beans are an important crop in Delaware and the Mid-Atlantic Region. In the summer of 2000, five commercial cultivars (3-28, 184-85, C-elite Sel, Butter Bean, and Jackson Wonder) of lima bean in Delaware, Maryland, and New Jersey were observed with white, appressed mycelia on infected pods that appeared distinctly different from signs of downy mildew infection caused by Phytophthora phaseoli. Isolations were made by placing diseased pods between layers of rye media (1). A fungus that produced white mycelia with sporangia was consistently isolated. All Phytophthora isolates from the infected pods were heterothallic, grew at 35°C, had as much as 100 µm long pedicles on varying shapes of caducous sporangia with tapering base and >2 papillae, and were identified as P. capsici (2). Initially, three surface-disinfected pods from cv. Early Thorogreen plants grown in the greenhouse were floated on 20 ml of sterile water in a petri dish, and each was inoculated with a disk of P. capsici. This was repeated for nine isolates obtained from lima bean. After incubation for 7 days at room temperature, all 27 pods were infected, and P. capsici was reisolated from all the pods. A pathogenicity test was performed on the same cultivars from which the original field isolates were collected. Three seedlings and two plants with mature pods were inoculated with a sporangial suspension of each of the nine isolates and placed in a dew chamber for 5 days at 20 to 25°C and 100% relative humidity. White mycelial growth was observed on seedlings and mature pods. One inoculated plant developed brown-to-black stem lesions with white mycelia. All pods on the mature plants showed appressed, white mycelia identical to that observed in the commercial lima bean fields. P. capsici was consistently reisolated from all inoculated plants. In 2000, most infected pods in infested fields were observed low in the plant canopy or touching the soil. However, in 2001, infected pods were mostly in the lower and mid-portion of the plants observed in baby lima bean fields in Kent County, DE. References: (1) C. E. Caten and J. L. Jinks. Can. J. Bot. 46:329, 1967. (2) D. C. Erwin and O. K. Ribeiro. Phytophthora capsici. Page 264 in: Phytophthora Diseases Worldwide. The American Phytopathological Society, St Paul, MN, 1996.

Two New Races of Phytophthora phaseoli from Lima Bean in Delaware.

Downy mildew, incited by Phytophthora phaseoli Thaxt., is the most important disease of lima bean (Phaseolus lunatus L.) on the east coast of the United States. It has been a serious threat to commercial lima bean production in Delaware, Maryland, and New Jersey for the past 5 years. Growers have attempted to manage this disease using resistant cultivars and copper hydroxide fungicides. In August and September 1995, a new pathogenic race of P. phaseoli was isolated from infected pods of the lima bean cv. Packer in a production field near Milton, DE. Races of P. phaseoli are determined using a modification of a cultivar differential developed by Wester (3). The cv. 184-85, which is resistant to races A, B, C, and D (1), is susceptible to the new race, designated as E. In August 2000, another new pathogenic race of P. phaseoli was isolated from infected pods of cv. 184-85 near Middletown, DE. The lima bean line BG2-408, which is resistant to races A, B, C, D, and E, is susceptible to the new race, designated as F. Symptoms produced on lima bean plants infected by races E and F are similar to each other, and to those produced by all other races. All races of P. phaseoli have the same cultural characteristics on lima bean pod agar. Evaluations of in field weather station data and disease occurrence indicate that races E and F may have temperature maxima greater than 32°C, whereas race D has a maximum of less than 32°C (2). During the 2000 growing season, 118 isolates of P. phaseoli were collected from 44 production fields in Delaware and the eastern shore of Maryland, with 86% characterized as race E and 5% as race F. References: (1) C. R. Davidson et al. Biol. Cult. Tests 2001:V80. (2) R. A. Hyre and R. S. Cox. Phytopathology 43:419, 1953. (3) R. E. Wester. Phytopathology 60:1856, 1970.

Long-period fiber-grating-based gain equalizers.

Long-period fiber gratings are used to f latten the gain spectrum of erbium-doped fiber amplifiers. A broadband amplifier with <0.2-dB gain variation over 30 nm is presented. We also show that a chain of amplifiers can be equalized, leading to a bandwidth enhancement by a factor of 3.