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In ~ 50% of the ocean, iron (Fe) limits phytoplankton growth, including that of the diatom Pseudo-nitzschia. Fe-limited Pseudo-nitzschia spp. may produce the potent neurotoxin domoic acid (DA) to acce...
The Eppley curve describes an exponential function that defines the maximum attainable daily growth rate of marine phytoplankton as a function of temperature. The curve was originally fitted by eye as...
Diazotrophic marine cyanobacteria in the genus Trichodesmium contribute a large fraction of the new nitrogen entering the oligotrophic oceans, but little is known about how they respond to shifts in g...
Literature review and synthesis of growth rates of aquatic protists focused on the role of temperature in the formation of massive annual algal blooms in high-latitude ecosystems. Maximal growth rates...
We investigated the relationship between nutritional condition (levels of specific fatty acids) and growth increment (percentage growth per intermoult period, percentage IMP-1) for Antarctic krill (Eu...
Reported estimates of phytoplankton growth rate (μ) in the subtropical gyres range widely from 0.1-0.2 to 1-2 d-1. Dividing chlorophyll a (Chl a)-normalized photosynthesis (PB) by the phytoplankton ca...
Four large, open-ocean diatoms from the Southern Ocean (Actinocyclus sp., Thalassiosira sp., Fragilariopsis kerguelensis, and Corethron pennatum) were grown in natural (low iron) Southern ocean seawat...
Our understanding of the dynamics of phytoplankton communities has been limited by the space and timescales associated with traditional monitoring approaches. To overcome some of these limitations, we...
A simple rapid approach to estimating in situ growth rates of Caridina nilotica (Roux), a small shrimp that plays a pivotal role in Lake Victoria's food web, is described. The approach, potentially ap...

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