Grazing rates of bacterivorous protists inhabiting diverse marine planktonic microenvironments

被引:31
作者
Artolozaga, I [1 ]
Valcárcel, M [1 ]
Ayo, B [1 ]
Latatu, A [1 ]
Iriberri, J [1 ]
机构
[1] Univ Basque Country, Fac Ciencias, Dept Microbiol Immunol & Parasitol, E-48080 Bilbao, Spain
关键词
D O I
10.4319/lo.2002.47.1.0142
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Bacterivory on aggregates and bulk seawater by three nanoflagellates and a microciliate was investigated. A new approach to measure bacterivory on the attached bacterial community is proposed. Macroaggregates containing attached fluorescently labeled bacteria (FLB) were obtained by adding labeled planktonic bacteria to rolling tanks filled with natural seawater, and they were used to measure protistan grazing rates on the bacteria attached to aggregates. Protistan grazing on free-suspended bacteria was measured according to the monodispersed FLB uptake technique. The four protists showed low grazing rates when feeding on free-suspended bacteria at the low, densities usually found in seawater. Surprisingly, the analyzed protists also showed low grazing rates when feeding on aggregates despite the very high bacterial densities inhabiting them. The analysis of the influence of prey density on bacterial grazing rates suggests that feeding on bacteria attached to aggregates involves a relevant additional effort when compared to feeding on free-suspended bacteria. The paradox between these results and the very high abundance of protistan communities usually found in aggregates is discussed attending to the view of aggregates as biological reactors. Therefore, marine macroaggregates can be considered as microniches able to support the maintenance of a protistan community without food limitation, as well as to attract protistan colonizers by generating a water layer enriched in organic matter and bacteria.
引用
收藏
页码:142 / 150
页数:9
相关论文
共 62 条
[1]   Bacterial colonization and ectoenzymatic activity in phytoplankton-derived model particles. Part II. Cleavage and uptake of carbohydrates [J].
Agis, M ;
Unanue, M ;
Iriberri, J ;
Herndl, GJ .
MICROBIAL ECOLOGY, 1998, 36 (01) :66-74
[2]   GRAZING OF CILIATED PROTOZOA ON FREE AND PARTICLE-ATTACHED BACTERIA [J].
ALBRIGHT, LJ ;
SHERR, EB ;
SHERR, BF ;
FALLON, RD .
MARINE ECOLOGY PROGRESS SERIES, 1987, 38 (02) :125-129
[3]   PRODUCTION OF HETEROTROPHIC BACTERIA INHABITING MACROSCOPIC ORGANIC AGGREGATES (MARINE SNOW) FROM SURFACE WATERS [J].
ALLDREDGE, AL ;
COLE, JJ ;
CARON, DA .
LIMNOLOGY AND OCEANOGRAPHY, 1986, 31 (01) :68-78
[4]   CHARACTERISTICS, DYNAMICS AND SIGNIFICANCE OF MARINE SNOW [J].
ALLDREDGE, AL ;
SILVER, MW .
PROGRESS IN OCEANOGRAPHY, 1988, 20 (01) :41-82
[5]  
[Anonymous], HETEROTROPHIC ACTIVI
[6]   A NOTE ON THE POSSIBLE ECOLOGICAL SIGNIFICANCE OF CHEMOTAXIS IN CERTAIN CILIATED PROTOZOA [J].
ANTIPA, GA ;
MARTIN, K ;
RINTZ, MT .
JOURNAL OF PROTOZOOLOGY, 1983, 30 (01) :55-57
[7]   Succession of bacterivorous protists on laboratory-made marine snow [J].
Artolozaga, I ;
Santamaria, E ;
Lopez, A ;
Ayo, B ;
Iriberri, J .
JOURNAL OF PLANKTON RESEARCH, 1997, 19 (10) :1429-1440
[8]  
Artolozaga I, 2000, FEMS MICROBIOL ECOL, V33, P191
[9]  
Azam F, 1993, TRENDS IN MICROBIAL ECOLOGY, P410
[10]  
BIDDLE KD, 1995, APPL ENVIRON MICROB, V61, P944