Accumulation and removal of UVBR-induced DNA damage in marine tropical plankton subjected to mixed and simulated non-mixed conditions

被引:29
作者
Boelen, P
Veldhuis, MJW
Buma, AGJ
机构
[1] Univ Groningen, Dept Marine Biol, NL-9750 AA Haren, Netherlands
[2] NIOZ, Dept Biol Oceanog, NL-1790 AB Den Burg, Netherlands
关键词
cyclobutane pyrimidine dimers; DNA damage; DNA repair; Caribbean Sea; marine bacteria; mixing; phytoplankton; ultraviolet-B radiation; UVBR;
D O I
10.3354/ame024265
中图分类号
Q14 [生态学(生物生态学)];
学科分类号
071012 ; 0713 ;
摘要
Accumulation and removal of UVBR (ultraviolet-B radiation: 280 to 315 nm)-induced DNA damage (cyclobutane pyrimidine dimers; CPDs) were studied in 2 size fractions (0.2 to 0.8 and 0.8 to 10 mum) of natural populations of tropical marine bacterio- and phytoplankton off Curacao, Netherlands Antilles. Plankton was either directly sampled from the surface layer (mixed situation), or incubated in UVR-transparent bags at 2 water depths (simulated non-mixed situation). A DNA dosimeter was used to measure biologically effective UVBR doses as well as attenuation of biologically effective radiation in the surface layer. A significant difference in CPD level between the 2 plankton size fractions could not be measured. In the mixed as well as in the non-mixed situation, DNA damage was accumulated between 09:00 and 14:00 h irrespective of the variability in incident UVBR. Surface layer samplings on consecutive days showed a clear diel pattern of increase and decrease, indicating that, in the field, DNA damage is repaired or diluted during the afternoon or at night. No significant repair of DNA damage could be measured in samples that were incubated during the afternoon at 0.2 or 10 m depth. The UVBR sensitivity of surface-incubated plankton was expressed as the ratio between damage induced in the cells to damage induced in (unshielded and unrepaired) bare DNA. In both plankton size classes this ratio fluctuated around 0.32, In conclusion, the results show that plankton cells present in the clear waters off Curacao undergo UVBR stress despite the fact that they are subjected to vertical mixing. No significant difference in CPD levels between 2 size fractions of plankton could be measured, suggesting that in this plankton population other aspects, e.g. repair capacities or cell morphology, were more important than cell size.
引用
收藏
页码:265 / 274
页数:10
相关论文
共 42 条
[1]   Inhibition of bacterial activities by solar radiation in nearshore waters and the Gulf of Mexico [J].
Aas, P ;
Lyons, MM ;
Pledger, R ;
Mitchell, DL ;
Jeffrey, WH .
AQUATIC MICROBIAL ECOLOGY, 1996, 11 (03) :229-238
[2]   EFFECTS OF ULTRAVIOLET-B RADIATION ON PRIMARY PRODUCTION ALONG LATITUDINAL TRANSECTS IN THE SOUTH-PACIFIC OCEAN [J].
BEHRENFELD, M ;
HARDY, J ;
GUCINSKI, H ;
HANNEMAN, A ;
LEE, H ;
WONES, A .
MARINE ENVIRONMENTAL RESEARCH, 1993, 35 (04) :349-363
[3]   UVBR-induced DNA damage in natural marine picoplankton assemblages in the tropical Atlantic Ocean [J].
Boelen, P ;
de Boer, MK ;
Kraay, GW ;
Veldhuis, MJW ;
Buma, AGJ .
MARINE ECOLOGY PROGRESS SERIES, 2000, 193 :1-9
[4]   Attenuation of biologically effective UV radiation in tropical Atlantic waters measured with a biochemical DNA dosimeter [J].
Boelen, P ;
Obernosterer, I ;
Vink, AA ;
Buma, AGJ .
PHOTOCHEMISTRY AND PHOTOBIOLOGY, 1999, 69 (01) :34-40
[5]   Depth distributions of DNA damage in Antarctic marine phyto- and bacterioplankton exposed to summertime UV radiation [J].
Buma, AGJ ;
de Boer, MK ;
Boelen, P .
JOURNAL OF PHYCOLOGY, 2001, 37 (02) :200-208
[6]   MONITORING ULTRAVIOLET-B-INDUCED DNA-DAMAGE IN INDIVIDUAL DIATOM CELLS BY IMMUNOFLUORESCENT THYMINE DIMER DETECTION [J].
BUMA, AGJ ;
VANHANNEN, EJ ;
ROZA, L ;
VELDHUIS, MJW ;
GIESKES, WWC .
JOURNAL OF PHYCOLOGY, 1995, 31 (02) :314-321
[7]   Dead or alive? A large fraction of ETS-inactive marine bacterioplankton cells, as assessed by reduction of CTC, can become ETS-active with incubation and substrate addition [J].
Choi, JW ;
Sherr, BF ;
Sherr, EB .
AQUATIC MICROBIAL ECOLOGY, 1999, 18 (02) :105-115
[8]  
Fekete A, 1998, PHOTOCHEM PHOTOBIOL, V68, P527, DOI 10.1562/0031-8655(1998)068<0527:AOTEOV>2.3.CO
[9]  
2
[10]  
FRIEDBERG EC, 1995, DNA REPAIR MUTAGENES