HowStriga Parasitizes its Host: a TEM and SEM Study

The cellular contact betweenStriga hermonthica andStriga asiaticaand their hosts,Zea mays andSorghum bicolor , was investigatedby light, transmission electron and scanning electron microscopy.The xylem connections between parasites and hosts involve veryspecific, clustered intrusions into the host's water conductingelements, predominantly into the large vessel elements. A singlehaustorial cell can penetrate a host vessel element with morethan one intrusion. All intrusions become covered by an additionalelectron-opaque wall layer. During subsequent differentiation,a dissolution of specific wall parts of the cell intrusionsoccurs so that open, cup- or trunk-like structures result. Thevessel-like host contact can comprise up to five openings withina single intrusion. Concomitantly, the intrusions and the haustorialcells to which they belong lose their protoplasts and transforminto elements which take up water. The walls of the haustorialcells and both wall parts of their appendages become stronglylignified. The water and nutrient absorbing structures insertedinto the host vessel are named ‘oscula’. Withinthe whole haustorial complex of bothStriga species no phloemelements were detected. Translocation of substances from hostto parasite are briefly discussed. Striga hermonthica ; Striga asiatica ; haustorial anatomy; xylem contact; osculum     

Evaluation of Aerial Cluster Sampling of Double-Crested Cormorants on Aquaculture Ponds in Mississippi

Abstract Concern over increasing numbers of double-crested cormorants (Phalacrocorax auritus) and their impacts on channel catfish (Ictalurus punctatus) aquaculture has resulted in increased need for quantitative information to develop and evaluate depredation management efforts. We evaluated aerial surveys in a stratified cluster sampling (SCS) design to estimate and monitor abundance of cormorants on catfish aquaculture ponds in the Yazoo River Basin of Mississippi, USA (hereafter Yazoo Basin). Twice monthly abundance estimates and coefficient of variation during winter averaged 8,128 (n = 29, SE = 1,233) and 33% (n = 29, SE = 0.02), respectively. Counts of cormorants on catfish aquaculture ponds between survey years were correlated (r = 0.87, n = 28). The correlation between diurnal counts of cormorants on ponds and cormorant night roost counts was 0.64 in 2000–2001 and 0.58 in 2003–2004 (n = 20 in both years). A priori estimates of sample size indicated an average increase in sampling effort of 39% during peak periods of cormorant use would be necessary to detect a ±15% change in cormorant abundance on aquaculture ponds at α = 0.05 and β = 0.80. The sampling design we used has the potential to be an effective tool for providing quantitative information on cormorant abundance on catfish aquaculture ponds in the Yazoo Basin. However, increased sampling effort would be necessary to obtain desired levels of precision. The SCS design we evaluated represents only one of many possible survey methods, and we recommend additional evaluation of this method and related survey methods.