scholarly journals Species-specific phytoplankton growth rates via diel DNA synthesis cycles. I. Concept of the method

1988 ◽  
Vol 43 ◽  
pp. 105-111 ◽  
Author(s):  
EJ Carpenter ◽  
J Chang
PeerJ ◽  
2018 ◽  
Vol 6 ◽  
pp. e5264 ◽  
Author(s):  
Susanne Menden-Deuer ◽  
Caitlyn Lawrence ◽  
Gayantonia Franzè

To assess protistan grazing impact and temperature sensitivity on plankton population dynamics, we measured bulk and species-specific phytoplankton growth and herbivorous protist grazing rates in Disko Bay, West Greenland in April-May 2011. Rate estimates were made at three different temperatures in situ (0 °C), +3 °C and +6 °C over ambient. In situ Chlorophyll a (Chl a) doubled during the observation period to ∼12  µg Chl a L−1, with 60–97% of Chl a in the >20 µm size-fraction dominated by the diatom genus Chaetoceros. Herbivorous dinoflagellates comprised 60–80% of microplankton grazer biomass. At in situ temperatures, phytoplankton growth or grazing by herbivorous predators <200 µm was not measurable until 11 days after observations commenced. Thereafter, phytoplankton growth was on average 0.25 d−1. Phytoplankton mortality due to herbivorous grazing was only measured on three occasions but the magnitude was substantial, up to 0.58 d−1. Grazing of this magnitude removed ∼100% of primary production. In short-term temperature-shift incubation experiments, phytoplankton growth rate increased significantly (20%) at elevated temperatures. In contrast, herbivorous protist grazing and species-specific growth rates decreased significantly (50%) at +6 °C. This differential response in phytoplankton and herbivores to temperature increases resulted in a decrease of primary production removed with increasing temperature. Phaeocystis spp. abundance was negatively correlated with bulk grazing rate. Growth and grazing rates were variable but showed no evidence of an inherent, low temperature limitation. Herbivorous protist growth rates in this study and in a literature review were comparable to rates from temperate waters. Thus, an inherent physiological inhibition of protistan growth or grazing rates in polar waters is not supported by the data. The large variability between lack of grazing and high rates of primary production removal observed here and confirmed in the literature for polar waters implies larger amplitude fluctuations in phytoplankton biomass than slower, steady grazing losses of primary production.


Zygote ◽  
2003 ◽  
Vol 11 (3) ◽  
pp. 261-270 ◽  
Author(s):  
Bong-Ki Kim ◽  
Sun Hong Cheon ◽  
Youn Jeong Lee ◽  
Sun Ho Choi ◽  
Xiang Shun Cui ◽  
...  

The onset of pronucleus formation and DNA synthesis in porcine oocytes following the injection of porcine or murine sperm was determined in order to obtain insights into species-specific paternal factors that contribute to fertilisation. Similar frequencies of oocytes with female pronuclei were observed after injection with porcine sperm or with murine sperm. In contrast, male pronuclei formed 8-9 h following the injection of porcine sperm, and 6-8 h following the injection of murine sperm. After pronucleus formation maternally derived microtubules were assembled and appeared to move both male and female pronuclei to the oocyte centre. A few porcine oocytes entered metaphase 22 h after the injection of murine sperm, but normal cell division was not observed. The mean time of onset of S-phase in male pronuclei was 9.7 h following porcine sperm injection and 7.4 h following mouse sperm injection. Ultrastructural observation revealed that male pronuclei derived from murine sperm in porcine oocytes are morphologically similar to normal male pronuclei in porcine zygotes. These results suggest that species-specific paternal factors influence the onset of pronucleus formation and DNA synthesis. However, normal nuclear cytoplasmic interactions were observed in porcine S-phase oocytes following murine sperm injection.


1971 ◽  
Vol 49 (12) ◽  
pp. 1376-1383 ◽  
Author(s):  
W. G. Verly ◽  
Y. Deschamps ◽  
J. Pushpathadam ◽  
M. Desrosiers

Chalone from rabbit liver has been purified 450-fold; it is a polypeptide of small molecular weight. Its action on liver DNA synthesis is tissue-specific but not species-specific. The dose–effect relationship is in agreement with the theory of receptor sites in the hepatocytes with a low affinity for this hormone.


2008 ◽  
Vol 104 (1) ◽  
pp. 74-85 ◽  
Author(s):  
Abdullah Al Kholaifi ◽  
Abeer Amer ◽  
Brett Jeffery ◽  
Tim J. B. Gray ◽  
Ruth A. Roberts ◽  
...  

1987 ◽  
Vol 9 (5) ◽  
pp. 891-899 ◽  
Author(s):  
Robert M. Dorazio ◽  
James A. Bowers ◽  
John T. Lehman

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