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Buffers: Buffer Capacity01:09

Buffers: Buffer Capacity

2.3K
Buffer capacity is the quantitative measure of a buffer to resist the change in pH. As shown in the following equation, the buffer capacity, denoted by 'beta', is expressed as the number of moles of acid or base needed to change the pH of a one-liter buffer solution by 1 unit. Here, Ca and Cb indicate the number of moles of acid and base, respectively. Note that dpH represents the change in pH.
In the graph, pH is plotted as a function of the number of moles of base (Cb) added to a weak...
2.3K
Buffers02:56

Buffers

172.7K
A solution containing appreciable amounts of a weak conjugate acid-base pair is called a buffer solution, or a buffer. Buffer solutions resist a change in pH when small amounts of a strong acid or a strong base are added. A solution of acetic acid and sodium acetate is an example of a buffer that consists of a weak acid and its salt: CH3COOH (aq) + CH3COONa (aq). An example of a buffer that consists of a weak base and its salt is a solution of ammonia and ammonium chloride: NH3 (aq) + NH4Cl...
172.7K
Buffer Effectiveness02:19

Buffer Effectiveness

55.1K
Buffer solutions do not have an unlimited capacity to keep the pH relatively constant . Instead, the ability of a buffer solution to resist changes in pH relies on the presence of appreciable amounts of its conjugate weak acid-base pair. When enough strong acid or base is added to substantially lower the concentration of either member of the buffer pair, the buffering action within the solution is compromised.
The buffer capacity is the amount of acid or base that can be added to a given volume...
55.1K
Lung Capacity01:47

Lung Capacity

56.3K
The air in the lungs is measured in volumes and capacities. Lung volume measures reflect the amount of air taken in, released, or left over after a lung function, like a single inhalation. Lung capacity measures are sums of two or more lung volume measures.
56.3K
Calculating pH Changes in a Buffer Solution02:45

Calculating pH Changes in a Buffer Solution

58.6K
A buffer can prevent a sudden drop or increase in the pH of a solution after the addition of a strong acid or base up to its buffering capacity; however, such addition of a strong acid or base does result in the slight pH change of the solution. The small pH change can be calculated by determining the resulting change in the concentration of buffer components, i.e., a weak acid and its conjugate base or vice versa. The concentrations obtained using these stoichiometric calculations can be used...
58.6K
Phosphate Buffer01:22

Phosphate Buffer

5.1K
The phosphate buffer system is a critical biological mechanism for maintaining pH stability in the body. This system operates primarily through two components: sodium dihydrogen phosphate (NaH2PO4), which acts as a weak acid, and sodium hydrogen phosphate (Na2HPO4), which serves as a weak base.
Sodium dihydrogen phosphate does not fully dissociate in neutral or acidic solutions. When a strong base, such as sodium hydroxide (NaOH), is introduced into the solution, sodium dihydrogen phosphate...
5.1K

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Dual clumped isotope thermometry resolves kinetic biases in carbonate formation temperatures.

Nature communications·2020
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Seawater temperature and buffering capacity modulate coral calcifying pH.

Weifu Guo1

  • 1Department of Geology and Geophysics, Woods Hole Oceanographic Institution, Woods Hole, MA, 02543, USA. wfguo@whoi.edu.

Scientific Reports
|February 6, 2019
PubMed
Summary

Coral calcifying fluid chemistry is primarily controlled by seawater conditions, not physiological regulation. Ocean warming and acidification will decrease coral calcifying fluid pH, impacting coral skeleton formation.

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Area of Science:

  • Marine biology
  • Biogeochemistry
  • Climate change science

Background:

  • Scleractinian corals precipitate carbonate skeletons by increasing pH and dissolved inorganic carbon (DIC) in their calcifying fluid.
  • Corals possess mechanisms to regulate calcifying fluid chemistry, suggesting potential acclimation to ocean acidification.
  • The degree to which coral regulation can adapt to decreasing ocean pH remains insufficiently understood.

Purpose of the Study:

  • To investigate the relative influence of physiological regulation versus environmental seawater conditions on coral calcifying fluid chemistry.
  • To model the impact of projected ocean warming and acidification on coral calcifying fluid pH.
  • To assess the susceptibility of coral calcification to future ocean changes.

Main Methods:

  • Development of a numerical model to simulate coral pH and DIC regulation.
  • Analysis of the interplay between enzymatic proton pumping, carbon influx, and fluid exchange.
  • Quantitative reproduction of calcifying fluid pH variations in natural Porites coral colonies.

Main Results:

  • Seawater temperature and buffering capacity are the primary drivers of pH elevation in coral calcifying fluid, explaining most observed variability.
  • Physiological regulation contributes to variability but remains relatively stable despite changing seawater conditions.
  • A projected 0.16 unit decrease in Porites calcifying fluid pH by 2100 due to ocean warming and acidification was predicted.

Conclusions:

  • Coral calcification is highly susceptible to future ocean warming and acidification.
  • Seawater conditions, rather than physiological regulation, exert dominant control over coral calcifying fluid chemistry.
  • While supporting coral-based pH proxies, findings emphasize the need to account for multiple influencing factors beyond seawater pH.