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    Carbon in the Planted Aquarium by The Aquarium Shop

    Carbon in the Planted Aquarium

    By: Greg Morin, Ph.D., President/CEO, Seachem Laboratories, Inc.

    Carbon is the backbone of all life. Every organic molecule of every living organism is

    predominantly carbon based. Given this simple fact, it becomes clear why carbon plays a pivotal role in

    the planted aquarium. Aquatic plants extract CO2 (carbon dioxide) from their environment and employ it in

    a process called photosynthesis. Photosynthesis combines CO2, water and light energy to produce simple

    carbohydrates and oxygen (O2) (see Figure 1). The first and simplest carbohydrate produced from

    photosynthesis is 3-phosphoglycerate. It is from this simple molecule that larger and more complex

    carbohydrates arise (by way of a variety of enzymatic processes).

    Growth rates of aquatic plants are strongly correlated1 with availability of carbon and the plant’s

    affinity for carbon uptake. Studies1 have shown that plants with the greatest carbon affinity have the

    greatest growth rates, whereas those with lower carbon affinity have correspondingly slower growth rates.

    Because carbon availability is normally the limiting factor to growth, addition of CO2 to a planted aquarium

    will always result in large increases in growth (assuming other critical elements are not lacking). Without

    additional CO2 the growth rate will be dependent on the rate at which atmospheric CO2 equilibrates into

    the water. CO2 will dissolve into CO2–free water to a degree that is dependent on the air pressure,

    temperature, pH and bicarbonate/carbonate content of the water. The final concentration of CO2 in the

    water depends entirely on those factors. Once that concentration is achieved the level of CO2 will not

    change unless the plants remove it or one of the other factors is altered. Plants remove CO2 at a rate

    much greater than the rate at which it equilibrates into the water. So at the height of CO2 utilization the

    plants limit their own growth by using up all available CO2. Because CO2 is an integral component of the

    bicarbonate buffer system a drop in CO2 will necessarily result in a rise in pH. As the pH rises the influx of

    additional atmospheric CO2 will be diminished by its conversion to bicarbonate. This is offset somewhat

    by hard water plants that can utilize bicarbonate directly. However, without routine water changes or

    buffer additions (Alkaline Buffer™ or Liquid Alkaline Buffer™) this path will eventually lead to complete

    depletion of the KH (carbonate hardness) which will result in dramatic pH swings from day to night (5.7 –

    9.6).1

    CO2 injection bypasses this predicament by delivering a constant source of CO2. Because the

    introduction of CO2 will lower pH one has two options: (1) Monitor and calibrate the rate of CO2 addition to

    precisely match the usage by the plants or (2) use a pH feedback metering system. (2) is ideal because

    as the pH falls below a certain point the CO2 turns off, thus avoiding catastrophic pH drops.

    If one is not quite ready for the initial investment in a CO2 injection system but would still like to

    enjoy some of the benefits of adding additional carbon there is an alternative: Flourish Excel™. Flourish

    Excel™ provides a simple organic carbon molecule (similar to what is described above in the

    photosynthesis discussion) that plants can use as a building block for more complex carbohydrates.

    Because Flourish Excel™ is an organic carbon source it does not impact pH.

    The chemical structure of Flourish Excel™ is quite similar to some of the products of

    photosynthesis (see Figure 2) such as Ribulose 1,5-bisphosphate and 2’-carboxy-3-keto-D-arabinitol 1,5

    bisphosphate. Flourish Excel™ possesses the same basic 5-carbon chain seen in these molecules. The

    route through which Flourish Excel™ is used by plants involves two main processes: a) adsorption and b)

    transformation. Because the active component of Flourish Excel™ (see Figure 2, polycycloglutaracetal) is

    charge neutral and of relatively low molecular weight it is readily adsorbed directly across the cellular

    membranes of most plants. Once present within the cell there are two possible modes of action. It may be

    biologically converted into CO2 and then utilized in that fashion. Or, it may be converted into any number

    of more complex organic compounds needed for the life processes of the plant (e.g. sugars, starch,

    amino acids, etc). These conversions (in either mode of action) are mediated by any of a variety of

    enzymes present (oxygenases, carboxylases, phosphorylases, etc). In order to determine the precise

    mechanism (i.e. down-conversion to CO2, or up-conversion to longer chains) further studies involving

    radioactive C14 tracers would be necessary. However, with that said, our studies to date show that

    Flourish Excel™ imparts a measurable, quantitative growth benefit to plants. Thus, it is clear that the

    plants are utilizing the Flourish Excel™.

    Our research has shown that Flourish Excel™ imparts not only a clear qualitative increase in plant health

    and vitality but also a clearly measurable increase in growth. Recent studies (see Figure 3) have shown

    growth enhancements using Flourish Excel™ that range from 200% - 500% (growth above normal growth

    seen without Flourish Excel™). These are only preliminary results of a currently ongoing studied aimed at

    determining more precisely the relative growth response to Flourish Excel™ in comparison to a standard

    control and a CO2 based control. The anecdotal evidence to date suggests that CO2 injection will promote

    growth enhancements above the growth enhancements seen with Flourish Excel™ alone. However, one

    can still obtain a cumulative benefit by using Flourish Excel™ in conjunction with CO2 as the two work

    quite well together.

    1. Walstad, Diana, Ecology of the Planted Aquarium, Echinodorus Publishing, 1999, pp. 94-97.

    This article was published on Wednesday 13 August 2008.
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