Responses of tropical tree species to urban air pollutants: ROS/RNS formation and scavenging.

Air pollution in an urban environment is the major stress factor for vegetation due to the direct generation of reactive oxygen species (ROS) and reactive nitrogen species (RNS). To quantify urban air pollution-induced ROS/RNS formation, damage and detoxification, nine different biochemical parameters related to free radical formation, scavenging and membrane damage were estimated in twelve tropical tree species. The experiment was performed in three different seasons at four distinct urban environments in Varanasi city located in the Indo-Gangetic plain of India. Redundancy analysis was performed to statistically assess the relationship between air pollutants (PM, NO, SO and O) and temperature with ROS/RNS generation and their detoxification. Significant effects of air pollution exposure and temperature on ROS/RNS formation, scavenging and membrane damage were recorded with increasing pollution load in the city for all the tree species. The extent of variability (47-87%) in responses of different tree species was due to their intrinsic ability to scavenge free radicals which minimized the membrane damage. PM, NO and O were identified as major pollutants that influenced trees to different extents in regulating ROS/RNS. However, the response was maximum against NO (34-72%) followed by PM (16-64%) and O (3-31%), indicating that under urban environment, trees are considerably sensitive to the combined effects of both particulate and gaseous pollutants. Reactive oxygen intermediate release, total free radical scavenging activity, NO scavenging activity and membrane stability index were identified as major parameters which showed distinct responses with increasing pollution load. Caesalpinia sappan, Ficus religiosa and Albizia lebbeck were identified as most tolerant tree species having higher ROS/RNS scavenging potential resulted in lower membrane damage. Thus responses of urban trees to air pollution are governed by their intrinsic defence mechanisms to scavenge ROS/RNS by maintaining the membrane integrity through integrated cross-talk between different antioxidative pathways.