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Information on the diversity of marine fungi in polar environments is lacking, especially marine fungi colonizing wood. During visits to Tromsø and Longyearbyen, Norway, drift and trapped wood was collected to provide a preliminary account of lignicolous marine fungi in Arctic waters. Six marine fungi were recorded from 24 and 27 samples of wood from Tromsø and Longyearbyen, respectively. Among these, four marine fungi new to science were identified from wood collected at Longyearbyen. To shed light on the ecological role of this group of fungi in the Arctic, a physiological study of one of the collected fungi, Havispora longyearbyenensis, was conducted. H. longyearbyenensis grew at 4 °C, 10 °C, 15 °C and 20 °C in all salinities tested (0 0/00, 17 0/00, 34 0/00). However, growth was significantly reduced at 4 °C and 0 0/00 salinity. The optimal condition for growth of H. longyearbyenensis was at 20 °C in all salinities tested

Phthalate esters (PAEs) are important industrial compounds mainly used as plasticizers to increase flexibility and softness of plastic products. PAEs are of major concern because of their widespread use, ubiquity in the environment, and endocrine-disrupting toxicity. In this study, two fungal strains, Fusarium sp. DMT-5-3 and Trichosporon sp. DMI-5-1 which had the capability to degrade dimethyl phthalate esters (DMPEs), were isolated from mangrove sediments in the Futian Nature Reserve of Shenzhen, China, by enrichment culture technique. These fungi were identified on the basis of spore morphology and molecular typing using 18S rDNA sequence. Comparative investigations on the biodegradation of three isomers of DMPEs, namely dimethyl phthalate (DMP), dimethyl isophthalate (DMI), and dimethyl terephthalate (DMT), were carried out with these two fungi. It was found that both fungi could not completely mineralize DMPEs but transform them to the respective monomethyl phthalate or phthalate acid. Biochemical degradation pathways for different DMPE isomers by both fungi were different. Both fungi could transform DMT to monomethyl terephthalate (MMT) and further to terephthalic acid (TA) by stepwise hydrolysis of two ester bonds. However, they could only carry out one-step ester hydrolysis to transform DMI to monomethyl isophthalate (MMI). Further metabolism of MMI did not proceed. Only Trichosporon sp. was able to transform DMP to monomethyl phthalate (MMP) but not Fusarium sp. The optimal pH for DMI and DMT degradation by Fusarium sp. was 6.0 and 4.5, respectively, whereas for Trichosporon sp., the optimal pH for the degradation of all the three DMPE isomers was at 6.0. These results suggest that the fungal esterases responsible for hydrolysis of the two ester bonds of PAEs are highly substrate specific.