Sierra M M D, Giovanela M, Parlanti E, Soriano-Sierra E J
Departamento de Química, Universidade Federal de Santa Catarina, 88040-900 Florianópolis, SC, Brazil.
Chemosphere. 2005 Feb;58(6):715-33. doi: 10.1016/j.chemosphere.2004.09.038.
Excitation/emission matrix (EEM), single-scan excitation and synchronous fluorescence spectra of a series of FA and HA from distinct environments are presented. The EEM plots show at least four spectral features whose corresponding Ex/Em pairs relate to the alpha', alpha, beta and gamma (or delta) fluorophores previously found in natural waters spectra. The alpha' and alpha peaks, which identify typical humic-like components, are present in all samples, independently of the organic matter (OM) source. In FA, their Ex/Em pairs are approximately 260 nm/460 nm and approximately 310 nm/440 nm, respectively. In HA their excitation and emission maxima are red-shifted, the corresponding Ex/Em pairs being located at approximately 265 nm/525 nm and approximately 360 nm/520 nm, respectively. The appearance of beta and gamma (or delta) peaks is dependent both on the OM origin and on HS aging. The former (Ex/Em approximately 320 nm/430 nm), that has been associated with the incidence of marine humic-like material, is present only in a few marine and estuarine HA. It emerges as a shoulder on the alpha peak and its detection is dependent on a balance between its magnitude and the magnitude and emission maxima location of the alpha peak. The gamma (or delta) peak (Ex/Em approximately 275 nm/315 nm in FA, and approximately 275 nm/330 nm in HA), on the other hand, is better visualized in FA than in HA diagrams. It has typical protein-, mainly tryptophan-like, fluorescence properties and appears with varied significance in a few marine and estuarine samples being hardly detected in samples from exclusively terrestrial environments. It is also shown in this study that with selected lambda(ex), lambda(em) and (delta)(lambda) values, regular emission, excitation and synchronous spectra can, together, provide a good picture of the OM sources and aging for extracted HS.
本文展示了一系列来自不同环境的富里酸(FA)和腐殖酸(HA)的激发/发射矩阵(EEM)、单扫描激发光谱和同步荧光光谱。EEM图显示至少有四个光谱特征,其相应的激发/发射对与先前在天然水体光谱中发现的α'、α、β和γ(或δ)荧光团有关。识别典型类腐殖质成分的α'峰和α峰存在于所有样品中,与有机物质(OM)来源无关。在FA中,它们的激发/发射对分别约为260 nm/460 nm和约310 nm/440 nm。在HA中,它们的激发和发射最大值发生红移,相应的激发/发射对分别位于约265 nm/525 nm和约360 nm/520 nm处。β峰和γ(或δ)峰的出现既取决于OM的来源,也取决于腐殖质(HS)的老化程度。前者(激发/发射约为320 nm/430 nm)与海洋类腐殖质物质的存在有关,仅在少数海洋和河口HA中出现。它作为α峰上的一个肩峰出现,其检测取决于它的强度与α峰的强度和发射最大值位置之间的平衡。另一方面,γ(或δ)峰(在FA中激发/发射约为275 nm/315 nm,在HA中约为275 nm/330 nm)在FA图中比在HA图中更明显。它具有典型的蛋白质荧光特性,主要是类色氨酸荧光特性,在少数海洋和河口样品中以不同的显著程度出现,而在仅来自陆地环境的样品中几乎检测不到。本研究还表明,通过选择特定的激发波长(λ(ex))、发射波长(λ(em))和波长差(δ(λ))值,常规发射光谱、激发光谱和同步光谱可以共同提供提取的HS的OM来源和老化的良好图景。