Multimodal Imaging of Cotton Wool Spots in Branch Retinal Vein Occlusion.

PURPOSE: To describe and follow cotton wool spots (CWS) in branch retinal vein occlusion (BRVO) using multimodal imaging. METHODS: In this prospective cohort study including 24 patients with new-onset BRVO, CWS were described and analyzed in color fundus photography (CF), spectral domain optical coherence tomography (SD-OCT), infrared (IR) and fluorescein angiography (FA) every 3 months for 3 years. The CWS area on SD-OCT and CF was evaluated using OCT-Tool-Kit software: CWS were marked in each single OCT B-scan and the software calculated the area by interpolation. RESULTS: 29 central CWS lesions were found. 100% of these CWS were visible on SD-OCT, 100% on FA and 86.2% on IR imaging, but only 65.5% on CF imaging. CWS were visible for 12.4 ± 7.5 months on SD-OCT, for 4.4 ± 3 months and 4.3 ± 3.4 months on CF and on IR, respectively, and for 17.5 ± 7.1 months on FA. The evaluated CWS area on SD-OCT was larger than on CF (0.26 ± 0.17 mm(2) vs. 0.13 ± 0.1 mm(2), p < 0.0001). The CWS area on SD-OCT and surrounding pathology such as intraretinal cysts, avascular zones and intraretinal hemorrhage were predictive for how long CWS remained visible (r(2) = 0.497, p < 0.002). CONCLUSIONS: The lifetime and presentation of CWS in BRVO seem comparable to other diseases. SD-OCT shows a higher sensitivity for detecting CWS compared to CF. The duration of visibility of CWS varies among different image modalities and depends on the surrounding pathology and the CWS size.

Abundance of microplankton in the eastern Mediterranean Sea in March and April 2008 during SES_GR1

The dataset is based on samples taken from 12 stations in Southern Aegean Sea, Northern Aegean Sea, Ionian Sea and Libyan Sea during March-April 2008. 12 Niskin bottles (8lt) made by PVC with rubber coated o rings and stainless steel ss springs. Seawater samples (150 ml) were collected from selected depths of the water column (2, 20, 50, 75, 100 m) for the identification and enumeration of phytoplankton cells (>=5 µm). The samples were fixed with Lugol solution and concentrated to 25 ml by sedimentation. Phytoplankton species abundance was determined with an inverted light microscope (OLYMPUS IX70) according to the Utermohl method (Utermohl, 1958).