Wang Xuechun, Chen Hao, Lei Kun, Sun Zhong
College of Chemistry and Chemical Engineering, Inner Mongolia University, 235 West University Road, Hohhot, 010021, China.
State Environmental Protection Key Laboratory in Coastal and Estuarine Research, Chinese Research Academy of Environmental Sciences, Beijing, 100012, China.
Environ Sci Pollut Res Int. 2015 Nov;22(21):16969-77. doi: 10.1007/s11356-015-4906-8. Epub 2015 Jun 27.
Exposure of tryptophan (Trp) in aqueous solutions to UVA radiation resulted in decrease of Trp (C1) but generated an unknown fluorescent component (C2) with fluorescence emission maxima extending into wavelength range characteristic of humic substance (HS)-like material. The intensity of the two components (C1 and C2) could be operationally fit to linear functions of the illumination time t (0~40 h). However, C1 and C2 decreased and increased nonlinearly respectively in a mixture (Trp mixed with a reference sample of natural organic matter, i.e., NOM) which was exposed to the same UVA illumination, and the change of both C1 and C2 was faster than that in the absence of NOM. Moreover, the UV-Vis absorption maximum (ex = 278 nm) of Trp was faster removed for the mixture (after 5 h) than for Trp solutions without NOM (after 20 h). These observations suggested NOM-facilitated photobleaching of Trp and photoproduction of a new FDOM component under UVA illumination. Meanwhile, the fluorescence of the NOM in the absence of Trp was well represented by two HS-like components which decayed monotonically upon exposure to UVA light, while the photoinduced decay became nonmonotonic in the presence of Trp, and one component even increased with illumination during certain time window, indicating Trp-facilitated production of HS-like fluorescence signatures from NOM. The findings show that UVA-induced optical signature changes of tryptophan and HS-like materials are coupled and highlight the potential impact of absorption of solar UVA light by natural dissolved organic matter (DOM) on using the optical signatures to trace sources and sinks of DOM.
水溶液中的色氨酸(Trp)暴露于UVA辐射下会导致Trp(C1)减少,但会产生一种未知的荧光成分(C2),其荧光发射最大值延伸到类腐殖质(HS)物质的特征波长范围。这两种成分(C1和C2)的强度可以在操作上拟合为光照时间t(0~40小时)的线性函数。然而,在暴露于相同UVA光照的混合物(Trp与天然有机物参考样品即NOM混合)中,C1和C2分别呈非线性减少和增加,且C1和C2的变化都比不存在NOM时更快。此外,混合物中Trp的紫外可见吸收最大值(ex = 278 nm)在5小时后比不含NOM的Trp溶液在20小时后更快地被去除。这些观察结果表明,在UVA光照下,NOM促进了Trp的光漂白和一种新的FDOM成分的光生成。同时,在不存在Trp的情况下,NOM的荧光可以很好地由两种类HS成分表示,它们在暴露于UVA光时单调衰减,而在存在Trp的情况下,光诱导衰减变得非单调,并且在特定时间窗口内一种成分甚至随光照增加,表明Trp促进了NOM产生类HS荧光特征。研究结果表明,UVA诱导的色氨酸和类HS物质的光学特征变化是相互关联的,并突出了天然溶解有机物(DOM)吸收太阳UVA光对利用光学特征追踪DOM源汇的潜在影响。