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Review: Preparing Journal-Format Graphs

The document provides guidelines for preparing graphs in journal format for biochemistry lab reports, including how to construct graphs with properly labeled axes using appropriate scales and units. Key aspects that are covered include using good quality graph paper, providing a descriptive title or caption, determining slopes and intercepts of lines, and representing data points on the graph. An example graph and caption are also provided following the guidelines.

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Wendy Cohen
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© © All Rights Reserved
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Download as PDF, TXT or read online on Scribd
45 views

Review: Preparing Journal-Format Graphs

The document provides guidelines for preparing graphs in journal format for biochemistry lab reports, including how to construct graphs with properly labeled axes using appropriate scales and units. Key aspects that are covered include using good quality graph paper, providing a descriptive title or caption, determining slopes and intercepts of lines, and representing data points on the graph. An example graph and caption are also provided following the guidelines.

Uploaded by

Wendy Cohen
Copyright
© © All Rights Reserved
Available Formats
Download as PDF, TXT or read online on Scribd
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REVIEW: PREPARING JOURNAL-FORMAT GRAPHS

Graphs are a very useful way of expressing experimental data in biochemistry. Understanding the
information contained in graphs will be important in understanding data in biochemical experiments. In this
review, we will outline the preparation of a graph including the how numbers are represented and how axes
are labelled. In many of your labs, you will be preparing graphs for presentation of your data. Several of
your labs will be written in journal format. For these reports, we want you to prepare your graphs an
acceptable "journal format". These graphs, if done by hand on graph paper, will not be publicaion quality
but at least the format will be publication quality. If you do the graphs through spreadsheet programs, it
may be possible to have not only a journal format graph but also a publication quality graph. Do not do
your graphs on the computer unless you get approval from your instructor.

Construction of a graph:
Each graph has a vertical axis (y-axis) that expresses the range of values for the dependent variable
and a horizontal axis (x-axis) that expresses the range of values for the independent variable. The quality
of your graph depends upon your following a set of simple rules. ALL HAND-DRAWN GRAPHS ARE
TO BE DONE IN INK.

Quality of graph paper:


Good quality graph paper is required for all graphs in reports in biochemistry. This paper must be
one of two types of engineering paper: 1 cm ruled in 1 mm divisions or 1 inch paper ruled in 20 (not 10)
divisions. No other graph paper will be acceptable. Make the plot as large as possible using as much of
graph paper as possible.
If you are using a spreadsheet program such as EXCEL to create graphs, you should consult with
the instructor and review the information provided on EXCEL (short version and long version).

Title or caption for graph:


You will be required to give a title or a caption for your graphs. In scientific publications graphs
have captions but no titles are given. Check with your instructor as to what will be required for your
reports.
Titles are placed at the top of the graphs. They should be descriptive with enough information so
the reader knows exactly what the graph is about. For example, for the buffer lab where histidine is
titrated, an appropriate title could be, "Titration of the Side Chain of Histidine to Determine its pKa Value".
A title that would not be acceptable would be "pH vs mole OH-\mole histidine". This latter title just repeats
the axis which are obvious anyway.

PREPARING JOURNAL-FORMAT GRAPHS, continued


Captions are to be at the bottom of the graphs which includes a figure number. The caption
contains all the relevant information to describe the graph. The first line is ususally an incomplete sentence.
If followed by any further information, complete sentences must be used. For example, in the buffer lab
for the histidine titration, the following caption would be appropriate:
Figure 1.

Titration of histidine hydrochloride. The pKa value of the


side chain determined from these data is 6.05.

Scale factors for the axes:


You must use a constant scale factor along the distance on each axis. For example, if you decide
1.0 cm = 0.010 min-1, then 5.0 cm = 0.050 min-1. A common error that some students make is not paying
attention to this constant factor. Linear graphs will be nonlinear or have breaks in them at inappropriate
values if the axes are constructed incorrectly.

Placement of zero on one axis or both axes:


It may not be necessary to have one (or both) axis start at 0.0. This is determined by the kind of
experiment that you are doing. For instance, in the titration of hisitidine in the buffer experiment, you will
have pH values as the dependent values on the y-axis that range from about 5 to about 8. In this case, the
y axis should reflect the observed ranges of the measured pHs and not start at 0 (or end at 14). In this
titration, the x-axis values will start at 0.0 moles of added NaOH so that a 0.0 value on the x-axis is
appropriate. Ask your instructor if you have any trouble deciding about any graph you are about to
prepare.

Labels for both axes:


Both axes must be labelled properly with appropriate significant figures and dimensions (units).
Numbers must have the number of significant figures appropriate to the experiment. The units required
varies from one journal to another. However, we require you to use a format which is simple and accepted
by all scientific journals.
Significant figures:

Number on axes:
(in correct sig. figs.)

Appropriate for measurements. This is usually 2 or 3. For example, for the buffer
lab, pH measurements between 1 and 9 should be expressed in 3 significant
figures.
0 to 1.0 in 0.1 or 0.2 increments
0 to 10.0 in 1.0 or 2.0 increments

For the maximum numbers on your axes, use ones that are divisible by 2 or 5 or 10. This makes
points easier to locate. It is recommended to use the 0.2 (2.0) increments since the graph axes are less
crowded.
2

PREPARING JOURNAL-FORMAT GRAPHS, continued

Dimensions:

EXPONENTIAL NOTATION IS NOT ALLOWED


IN INDICATING NUMBERS ALONG EITHER
AXIS.
The order of magnitude for a number is indicated in the
axis title:
Example:

$-CAROTENE (10-4 M)

This means that each number along the axis is to be


multiplied by 10-4 M. This format alleviates confusion.
The following example is one which is correctly written
but is often interpreted by students as 104 M which is
impossible(!):

$-CAROTENE x 104 M
For example: 0.235 x 10-4 x 104 M = 0.235
(actual concentration) (factor for graph) (value on graph)
Data points:
Data points are indicated using a circled dot. The size of the circle is an indication of the magnitude
of the error in the data point. In journal articles, the data points are often indicated with a symbol only
whose size is indicative of the magnitude of the error.

Lines or smooth curves?


Depending upon the experiment, you will have data points that define straight lines as well
as data points that define a smooth curve with a well-defined mathematical function. You
should know whether a line or curve is required for your graph.
For a straight line, use a clear plastic ruler and draw the best straight line that goes through
the points. If the points do not all fit on the straight line, adjust the line so that you have as
many points above the line as below it. Your eye will give you nearly the same line as the
computer would do with a linear regression analysis.
For a curved line, you should use a flexible ruler and draw the best curve. If you are using
a spreadsheet to create your graph, discuss with your instructor what mathematical function
best describes the data points. Using this function, you will be able to have the computer
draw the best curved line through your data. This is done very easily in EXCEL or
QUATTRO PRO.
3

PREPARING JOURNAL-FORMAT GRAPHS, continued

Determining the slope, y-intercept, and x-intercepts of a straight line:


To determine the slope of a straight line, pick two points ([x1 ,y1 ] and [x2,y2]) as far apart as
possible on the line. The slope is defined as follows:

)Y
=

y1 - y2
-----------x1 - x2

Slope

= --------------)X

y-intercept

y value on line when line crosses y axis


(y value when x = 0)

x-intercept

x value on line when line crosses x axis


(x value when y = 0)

INVERSE RATE
(10 5 M -1 min)

LINEWEAVER-BURK PLOT FOR LACTATE DEHYDROGENASE


(This is not a publication quality graph - why?)
10.0
Y

y-intercept = 3.4 x 105 M-1 min

slope =

9.0

= 10.4 min

(4.00, 7.57)

8.0
7.0
6.0
5.0
Y

4.0

= ( 7.57 - 1.35 ) x 105


= 6.22 x 10 5 M-1 min

3.0
(-2.00, 1.35)

2.0
1.0

= ( 4.00 - ( -2.00 ) ) x 104


= 6.00 x 104 M-1

0.0
-4.00 -3.00 -2.00 -1.00 0.00 1.00 2.00 3.00 4.00 5.00
x-intercept = - 3.3 x 104 M-1

Figure 1.

INVERSE PYRUVATE (104 M-1 )

Lineweaver-Burk plot for rabbit muscle lactate dehydrogenase. The Km was found
to be 3.0 x 10-5 M and the Vmax 2.9 x 10-6 M min-1.
4

Sample Graph
and Caption

9.00

8.00

7.00

pH

pKa

6.00

5.00

4.00

3.00
0.00

0.20

0.40

0.60

0.80

1.00

1.20

mol OH- / mol HIS.HCl

Figure 1.

Titration of histidine monohydrochloride with NaOH at


room temperature. The pKa determined from these
data is 6.20.

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