Am. Murphy et Tj. Cowles, EFFECTS OF DARKNESS ON MULTI-EXCITATION IN-VIVO FLUORESCENCE AND SURVIVAL IN A MARINE DIATOM, Limnology and oceanography, 42(6), 1997, pp. 1444-1453
Surveys of the California Current System in 1993 revealed high concent
rations of photosynthetic pigment biomass at similar to 200-m depth, w
ell below the euphotic zone. The deep fluorescence feature contained a
n estimated 2.2 x 10(4) metric tons of carbon and contained similar to
2.5 times the amount of chlorophyll observed in surface waters direct
ly above it. Deep phytoplankton assemblages may be a signature of wate
r mass subduction, suggesting the possibility of using phytoplankton a
s water mass tracers. These field observations led to a laboratory stu
dy of the fluorescence characteristics of autotrophic cells as possibl
e indices of acclimation to extended periods of darkness. In vivo mult
i-excitation Chl a fluorescence of the diatom Thalassiosira weissflogi
i was monitored for 2 months of total darkness. Numbers of living and
dead cells were determined using the vital stain fluorescein diacetate
(FDA). By the end of the dark incubation period, in vivo Chl a fluore
scence and fluorescence per cell had leveled off to similar to 45% and
65% of initial values, respectively. The contribution of accessory pi
gments to Chl a fluorescence, expressed as multi-excitation fluorescen
ce ratios, was higher in the dark than prior to transfer to darkness b
ut showed no significant changes during 2 months of darkness. The FDA
assay indicated that similar to 85% of the cells were alive for at lea
st the first 3 weeks during the first dark experiment and for the enti
re 2 months of a second dark incubation. Cell numbers decreased to 65%
of initial values and then grew exponentially upon reexposure to a li
ght:dark photoperiod. Our results for T. weissflogii suggest that exte
nded light limitation of photosynthesis does not preclude the survival
of subducted phytoplankton assemblages and the consequent accumulatio
n of Chl a at depths below the euphotic zone. If these results extend
to natural assemblages, it is not possible to estimate advective time
scales based on a maximum persistence time of pigment fluorescence bel
ow the euphotic zone. Nevertheless, the deep phytoplankton assemblage
we observed provides evidence for water mass subduction and suggests t
hat large, intermittent pulses of phytoplankton carbon are a part of c
ross-shelf exchange and vertical flux from surface waters to depth in
this region.