Boelen P, Post A F, Veldhuis M J W, Buma A G J
Department of Marine Biology, Centre for Ecological and Evolutionary Studies, University of Groningen, PO Box 14, 9750 AA Haren, The Netherlands.
Microb Ecol. 2002 Aug;44(2):164-74. doi: 10.1007/s00248-002-1002-7. Epub 2002 Jun 13.
This study focuses on the impact of natural levels of UVBR (ultraviolet-B radiation: 280 to 315 nm) on bacterio- and phytoplankton (<10 microm) from the Gulf of Aqaba, Red Sea. Incident biologically effective doses (BEDs) and attenuation of biologically effective radiation in the water column were measured using a DNA biodosimeter. UVBR-induced DNA damage was measured as cyclobutane pyrimidine dimers (CPDs), using an antibody directed to CPDs followed by chemiluminescent detection. Depth profiles of DNA damage were determined in two plankton size fractions (0.2 to 0.8 microm and 0.8 to 10 microm) collected down to 50 m depth. Furthermore, accumulation and removal of CPDs were monitored in surface plankton samples during several daily cycles. Small plankton (plankton <10 microm) composition was determined by flow cytometry. The plankton community in the Gulf of Aqaba was dominated by nonphototrophic bacteria and the free-living prochlorophyte Prochlorococcus spp. (<0.8 microm). In general, no DNA damage could be detected in dosimeter DNA below 15 m. In contrast, DNA damage (up to 124 CPD Mnucl-1) could be detected in all bacterio- and phytoplankton samples. DNA damage accumulated throughout the day, indicating that plankton in the Gulf of Aqaba undergo UVBR stress via CPD induction. Although the numbers of CPDs decreased during darkness, both size fractions showed some residual DNA damage at the end of the night. This suggests that dark repair processes did not remove all CPDs, or that part of the plankton community was incapable of repair at all. CPD levels in the two size fractions showed no significant differences in situ. During full solar radiation exposures (samples incubated in bags), more CPDs were detected in the smaller (0.2 to 0.8 microm) size fraction as compared to the larger (0.8 to 10 microm) size fraction. In these experiments, initial plankton composition was significantly different from the field samples. This implies that a shift in the population structure or irradiance conditions can lead to a significant change in UVBR sensitivity. In conclusion, the results show that the picoplankton-dominated phyto- and bacterioplankton communities in the clear surface waters from the Gulf of Aqaba undergo UVBR stress. Repair pathways are not sufficient to eliminate damage during or after UVBR exposure hours, suggesting photomortality as a potential loss parameter of the plankton community.
本研究聚焦于红海亚喀巴湾自然水平的UVBR(紫外线B辐射:280至315纳米)对细菌和浮游植物(<10微米)的影响。使用DNA生物剂量计测量入射生物有效剂量(BEDs)以及水柱中生物有效辐射的衰减。通过一种针对环丁烷嘧啶二聚体(CPDs)的抗体,随后进行化学发光检测,将UVBR诱导的DNA损伤测量为CPDs。在采集至50米深度的两个浮游生物大小分级(0.2至0.8微米和0.8至10微米)中测定DNA损伤的深度剖面。此外,在几个每日循环期间监测表层浮游生物样本中CPDs的积累和去除情况。通过流式细胞术确定小型浮游生物(<10微米的浮游生物)的组成。亚喀巴湾的浮游生物群落以非光合细菌和自由生活的原绿球藻属(<0.8微米)为主。一般来说,在15米以下的剂量计DNA中未检测到DNA损伤。相比之下,在所有细菌和浮游植物样本中均可检测到DNA损伤(高达124个CPD Mnucl-1)。DNA损伤在一整天中都在积累,这表明亚喀巴湾的浮游生物通过CPD诱导遭受UVBR胁迫。尽管在黑暗期间CPDs的数量减少,但两个大小分级在夜晚结束时均显示出一些残留的DNA损伤。这表明暗修复过程并未去除所有CPDs,或者部分浮游生物群落根本无法进行修复。两个大小分级中的CPD水平在原位未显示出显著差异。在完全太阳辐射暴露期间(样本在袋中孵育),与较大(0.8至10微米)大小分级相比,在较小(0.2至0.8微米)大小分级中检测到更多的CPDs。在这些实验中,初始浮游生物组成与野外样本有显著差异。这意味着种群结构或辐照条件的转变可能导致UVBR敏感性发生显著变化。总之,结果表明亚喀巴湾清澈表层水域中以微微型浮游生物为主的浮游植物和浮游细菌群落遭受UVBR胁迫。修复途径不足以在UVBR暴露期间或之后消除损伤,这表明光致死亡是浮游生物群落潜在的损失参数。