Research 10: Special Science Program
Research 10: Special Science Program
Research 10
Quarter 1
Home-Based
Science Investigatory Project
Learning Package
Project TUKLAS
Toolkits for Understanding sKills Leaning to Active Scientific Investigations
What This Module is About
To the parents:
As vital partners in education, your support to your children’s learning at home is a great
factor to ensure that they will become successful in what they do. As parents, you are expected to
monitor your children’s progress while they are accomplishing the tasks in this module while at
the same time, ensuring that they learn independently.
The objectives set for this learning material will be certainly accomplished with your steadfast
guidance and support.
To the learners:
This learning resource hopes to engage you into guided and independent learning
activities at your own pace and time. This also aims to help you acquire the needed 21st century
skills while taking into consideration your needs and circumstances.
Furthermore, it is our objective that you will have fun while going through this material.
Take charge of your learning pace and in no time, you will successfully meet the targets and
objectives set in this module which are intended for your ultimate development as a learner and as
a person.
Multiple Choice: Read the following sentences carefully. Select the best answer from the choices
given. Write your answers on the activity sheet.
The quality of a research paper depends primarily on the quality of the research study it
reports. However, there is also much that authors can do to maximize the clarity and usefulness of
their papers. Journals' instructions for authors often focus on the format, style, and length of
articles. The research question should be stated clearly, along with an explanation of where it
came from and why it is important. The study methods must be reported fully and, where
appropriate, in line with an evidence-based reporting guideline. Any relevant conflicts of interest
should be declared.
Therefore, quality assessment plays many important roles in the research community. It
enlightens crucial decisions on the funding of projects, teams and whole institutions, on how
research is conducted, on what is published or disseminated, and on what researchers and others
choose to read. It makes trust in the work of the research community.
What is It
Many versions of a format for a scientific report can be found in the literature however
most versions have a number of features in common. The following scaffold may be useful for to
you as a student-researcher.
Scaffold Notes
Title Communicate what your investigation is about i.e.
e.g. The effect of UV light on the rate of the title should include: the effect, the independent
growth of mould on bread variable and the dependent variable.
References and acknowledgements Acknowledge the assistance you have received from
other people.
What’s More
Activity 1
Scientific Report Scaffold
Direction. Read three (3) scientific papers in google scholar or any other scholarly search engine.
Each paper is classified as: a) Life Science, b) Physical Science/Applied Science, c)
Robotics. Write a Scientific Report Scaffold of each paper.
Direction. Select one (1) scientific report from Activity 1, and evaluate the paper according to the
requirements/standard presented in table below. Mark / if the items meet the typical
requirements in discussing the research findings and mark X if otherwise. Lastly,
provide annotation or justification of your evaluation.
What I Can Do
Direction: Based from your reasings in scientific reports, what are some problems that you
would like to solve at home, school or in your community.
Scientific Report Scaffold
Life
Scaffold
Title
ANTIOXIDANT ACTIVITY OF METHANOL EXTRACTS OF
DIFFERENT PARTS OF (Lantana Camara)
Introduction
Cancer prevention agent can be extensively characterized as any substance that delays or
hinders oxidative harm to an objective molecules. The quality of a cell reinforcement and its
capacity to trap free extremists. Cancer prevention agent mixes like phenolic acids, polyphenols
and flavonoids search free extremists, for example, peroxide, hydro peroxide or lipid peroxyl
and subsequently hinder the oxidative systems that lead to degenerative diseases. Home grown
plants considered as great cell reinforcement since antiquated occasions.
Lantana camara L (Verbenaceae) (L. camara) is a huge weed of which there are nearly
650 assortments in more than 60 nations or island gatherings. Customary healers have utilized
Lantana species for quite a long time to treat different maladies. Various pieces of L. camara
have been utilized for.
Method
Various samples of Lantana camara were washed with alkaline water and brushed with a
soft brush before drying. The clean plant was transferred to the oven at 50 degrees celcius and
was stayed in the oven for a total of 96 hours. After drying, the Lantana Camara was powdered
by electric blender. Approximately 100g of different parts of Lantana Camara was added to the
400ml methanol and soaked for 4 days. Removal of the plant material from solvent it was done
via filtration method through a cheesecloth, and the filtrate was concentrated using a rotary
evaporator.
Gries-llosary Method
Superoxide levels were used using gries-llosary method. Superoxide levels were
estimated by the Griess-Ilosvay method. In an acidic arrangement, nitrite particles are changed
over to nitrosonium particles; a diazotizing reagent (sulfanilic corrosive) is added to frame a
diazonium particle, and this diazonium particle ties with N-(1-naphthyl) ethylenediamine
dihydrochloride to create an azo compound, which is noticeable as a fuchsia dye. Same method
as xanthine oxidase hindrance measure was applied. In the wake of halting the response by HCl,
the shading reagent comprising 200 µL sulfanilic corrosive (last focus 300 µg/mL), 200 µL of
N-(1-naphthyl)- ethylenediamine dihydrochloride (last focus 5 µg/mL), also, 1 mL frigid acidic
corrosive (last fixation 16.7% (v/v) was included. The blend was permitted to represent 30 min
at room temperature, and the absorbance at 550 nm was estimated by spectrophotometer. The
test was done in three-fold. Superoxide rummaging impact was determined as following recipe.
The antioxidant activity of the extracts was measured. Using the described DPPH Free
Radical Scavenging Assay With others, Alterations. The universal bottle was, in short, included.
With 50 μL of L. Extracts from camera in concentrations of 1 to 1 The 0.004 percent (w / v)
solution of DPPH was 5 mg / mL and 5 mL. Appended. Vortexed was the obtained mixture,
incubated for 30 minutes in a relatively dark location at room temperature and It was then read
at 517 nm using a spectrophotometer. THE The 80% (v / v) methanol was blank. (Vitamin C)
ascorbic acid For contrast, was used. Measurements were performed in To triple.
The xanthine oxidase inhibitation assay was done through the method of xanthanine
oxidase. The uric acid production was calculated according to the increasing absorbance. The
uric acid production was calculated from the differential absorbance with a blank solution in
which the xanthine oxidase was replaced by buffer solution. A test mixture containing no extract
was prepared to measure the total uric acid production
Data Analysis
The data was analyzed via SPSS. The values were obtained by linear regression statistics
based on the least squares method. Following one way analysis of variance (ANOVA)
treatments were compared using post hoc comparisons test. Kruskal-wallis H non parametric
test. It was used for examining superoxide scavenging effect data.
The DPPH radical scavenging activity results are shown in Figure 1 as comparable with
known antioxidant Vitamin C. From the analysis of Figure 1, we can conclude that the
scavenging effects of leaves, flower, root and stem extracts on DPPH radicals were excellent,
especially in the case of L. camara leaves. The RSA values were also remarkably good for
flower, root and stem, but L. camara fruits revealed a low value of antioxidant activity. Figure 1
shows antioxidant activity with IC50 values of L. camara Vitamin C, leaves, flower, root, stem
and fruit measured by DPPH radicalscavenging assays. Overall, L. camara leaves revealed the
At
concentrations of 2.00-20.00 µg/mL, all extracts from leaves, stem and root displayed the
inhibition of superoxide formation greater than that of other parts and the xanthine oxidase
inhibition effect of all samples was in the order of allopurinol > leaves > stem > root > fruit >
flower. In the xanthine-xanthine oxidase system, the IC50 value of all leaves extract was found
the highest. Hence, leaves also showed a stronger xanthine inhibition activity than other parts
after allopurinol. Figure 2 shows the relationship between xanthine oxidase inhibition and final
The extract showed potent scavenging activity of nitric oxide with IC50 values in the
order of root > leaves >allopurinol > flower > stem > fruit. Figure 3 showed the relationship
between nitric oxide scavenging and final concentration of the extracts from various parts of L.
camara.
Acknowledgements
This work was partly supported by USM Incentive Grant (Grant Number: 2009/167)
References
Abou-Karam M, Shier WTA. Simplified plaque reduction assay for antiviral agents from
plants. Demonstration of frequent occurrence of antiviral activity in higher plants. J Nat Prod
1990; 53: 340-344.
Das DK, Engelman RM, Clement R, Otani H, Prasad MR, Rao PS. Role of xanthine
oxidase inhibitor as free radical scavenger: a novel mechanism of action of allopurinol and
oxypurinol in myocardial salvage. Biochem Biophys Res Commun 1987; 148: 314-319.
Hernández T, Canales M, Avila JG, Duran A, Caballero J, Vivar AR, et al. Ethnobotany
and antibacterial activity of some plants used in traditional medicine of Zapotitlán de las
Salinas, Puebla (México). J Ethnopharmacol 2003; 88: 181-188.
Ingrid ALP, Karin P, Staffan H, Rolf GGA. Effects of cocoa extract and dark chocolate
on angiotensin-converting enzyme and nitric oxide in human endothelial cells and healthy
Wu YY, Li W, Xu Y, Jin EH, Tu YY. Evaluation of the antioxidant effects of four main
theaflavin derivatives through chemiluminescence and DNA damage analyses. J Zhejiang Univ
Sci B. 2011; 12: 744-751.
Appendix
Scientific Report Scaffold
Physical
Scaffold
Title
Effect Of Rice-Husk Ash On Durability Of
Cementitious Materials
Introduction
The Food and Agriculture Organization’s forecast of global rice production over the 2009
season was 678 million tones about 20% of which is rice husk which is typically a waste material
from the point view point of industrial and agricultural processes. Even after its incineration, 20%
of rice husk’s weight remains as a waste material in the form of rice-husk ash (RHA) As an
example, in Uruguay, where rice production has had a dramatic increase over the past ten years
(becoming the most important crop since 2001), the main use of rice husk is as fuel in the rice
paddy milling process. But the use of this fuel generates a huge volume of ash which has no
immediate useful application and is usually dumped into water streams causing pollution and
contamination of springs.
As a result, the use of RHA has aroused great interest. The chemical composition of RHA
depends on temperature and burning time, but the variations in the components are not significant.
The ash from open-field burning (or from non-controlled combustion in industrial furnaces)
usually contains a higher proportion of non-reactive silica minerals such as cristobalite and
tridymite, and it should be ground into very fine particles to develop pozzolanic activity. In
addition, highly pozzolanic ash can be produced by means of controlled combustion when silica is
kept in non-crystalline form. Such silica can react when added to cement in the presence of water
(with calcium hydroxide) resulting in cementitious compounds Most research confirms the fact
that burning temperature is a critical point in the production of amorphous reactive ash.
Method
The materials below were used in the preparation of the Specimens: type I (normal
Portland cement) of Portland cement; Natural river sand of siliceous natural sand with optimum
aggregate size 4.75 mm; coarse aggregate with a maximum of (crushed granite) 12.5 mm
aggregate size; and a superplasticizer based on sulfonated naphthalene formaldehyde condensate
(42 percent solid content). Two RHA sources were considered: a residual RHA that was generated
Not successfully in the burning temperature parboiling process Managed (from the only parboiled
rice factory in Uruguay); And a homogeneous ash from controlled incineration provided by the
United States (CRHA). In this study, the residual RHA used A refined waste that has been dry-
milled for the required purposes A given specific specific time to obtain a median particle size of 8
lm, Surface by absorption of nitrogen and maximum index of operation according to ASTM C311-
98b. The procedure for residual In previous RHA optimization is discussed. THE Optimization
Air permeability: on concrete cylinders of 150 300 mm at 28 days of age was determined
by the ‘‘Torrent Permeability Tester” method [40,41] according to the Swiss Standard SIA 262/
1:2003. The particular features of the Torrent method are a two chamber vacuum cell and a
pressure regulator, which ensure that air flows at right angles to the surface directed towards the
inner chamber; this allows the calculation of the permeability coefficient Kt on the basis of a
simple theoretical model.
Acid attack: the influence of RHA in the chemical deterioration of concrete was studied
according to Mehta and Folliard and ASTM C267 on mortar cylinders of 50 100 mm exposed to
1% HCl solution. The mass of the cylinders from each of the mixtures, after 7 days of moist-curing
(temperature of 20 C and a relative humidity of 100%), was determined in the saturated surface dry
(SSD) condition, before immersion in the HCl solution.
Alkali-silica expansion: to study the influence of the two RHAs behavior concerning the
ASR, tests were performed according to the ASTM C1260 method on mortar bars. Water–
cementitious materials ratio of 0.47 was used with 10%, 20%, 30% and 40% of RRHA
replacement by mass, and 10% and 20% of CRHA, respectively.
Acknowledgements
The author acknowledges the financial support of CSIC and INIA, Uruguay. The author
would like to express her appreciation to M. Arq. Carola Romay and M.Sc. Stela Sabalsagaray for
their assistance in carrying out the experimental program; and to the companies ARROZUR S.A.,
ANCAP, Canteras Montevideo and SIKA Uruguay for the materials supplied.
References
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Appendix