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    TEST FOR DELAYING THE SENESCENCE OF TOMATO

    (Lycopersicum esculentum) USING DIFFERENT LEVEL OFPOTASSIUM

    ALUMINUM SULFATE (ALUM)

    CHAPTER 1

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    INTRODUCTION

    1.1 Background of the Study

    Tomato is one of the most important vegetables in Asia and Africa and these

    countries account for more than 65% of global tomato production. Tomato is rich in

    nutrients such as vitamins, minerals, and antioxidants, which are important to well

    balanced human diets. Tomato is also an important dietary component because it

    contains high level of lycopene, an antioxidant that reduces the risks associated with

    several cancers and neurodegenerative diseases.

    Tomato is susceptible to several insects and mite pests as well as plant

    diseases. Chemical pesticides are being used indiscriminately to manage these pests in

    South and Southeast Asia and part of Africa. In addition, chemical fertilizers and

    insecticides and sometimes overused in tomato production, which may contaminate

    groundwater. Intensive agrochemical use in tomato husbandry substantially increase

    the production cost and may pose serious risks to producers, consumers, and the

    overall health of the environment (Srinivasan R [Ed.] 2010).

    Filipino tomato farmers are often challenged by numerous plant diseases that are

    promoted by warm, and sometime moist climate. The conditions that promote tomato

    diseases also favors the development of tomato rots, in field and even during handling,

    storing and transporting.

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    Tomato fruit rot are generally caused by microscopic opportunistic pathogens

    that live on plant debris. These pathogens can, however, infect tissues that are

    wounded and/or exposed to the environment. The opportunists are ubiquitous in the

    natural environment, in part because they are saprophytes.

    Rhizopus stolonifer, one of postharvest diseases in tomatoes, is mainly

    responsible for significant losses of tomatoes both before and after harvesting

    especially during storage]. Chemical fungicides such as Methyl (1-butylcarbamoyl)-2-

    benzimidazole carbamate (benomyl) are normally utilized to control postharvest

    diseases in tomatoes during storage. Unfortunately, such chemical fungicides may

    induce fungicide-resistant strains. Furthermore, the growing consumer awareness

    and/or demand for healthy foods have increased the quest for more efficient methods

    with minimum health and environmental impact for the control of diseases. Therefore,

    alternative methods to preserve fruits and vegetable have been explored by many

    researchers (Turkhan, 2010).

    Potassium Alum Sulfate (KAl(SO4)212H2O) or alum has shown a good fungicidal

    effect against moulds. Powdered commercial alum, due to its eco-friendly and

    biodegradable nature, has been used as deodorant for a long period of time. Application

    of alum to control fungi in tomatoes has, however, never been examined. The objectives

    of this study were to investigate the antifungal activity of alum against Rhizopus

    stoloniferand to evaluate the potential application of alum to control postharvest

    spoilage on tomatoes during storage (Turkhan, 2010)

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    1.2 Statement of the Problem

    This research was conducted to test the effectiveness of alum sulfate on inhibiting

    the growth of fungi and determine which concentration (1.0mg/L, 2.0mg./L or 3.0mg./L)

    is most effective.

    1.3 General Objectives

    This research is conducted with the end in view of qualifying the possibility of

    using alum sulfate in inhibiting the growth and spread if pathogenic Rhizopus stolonifer

    on commercial tomato. This may likewise help farmers whose products are viable to

    Rhizopus stolonifer infestation to fully protect and preserve the market value of their

    products for more income with less cost on post-harvest crop protection.

    1.4 Specific Objective

    This research will endeavor to come up with a less cost but effective medium in

    controlling the infestation of Rhizopus stolonifer on tomatoes.

    1.5 Hypotheses

    Null Hypothesis: Alum cannot inhibit the growth ofRhizopus stolonifer

    Alternative Hypothesis: Alum inhibit the growth ofRhizopus stolonifer

    1.6 Significance of the Study

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    The current antifungal problems in the society, the study about the antifungal

    effectiveness of alum sulphate will be a very good contribution to the development of

    antifungal medicines or drugs in the near future. It will also compare and determine the

    effect of the different concentrations of alum to bread molds (Rhizopus Stolonifer). This

    research study will also provide a cheaper and easier solution in treating fungal

    infections or diseases especially that drugs for fungal infections are becoming more and

    more expensive. Thus, it will be very beneficial for antifungal research and development

    and also to the people suffering antifungal problems.

    1.7 Scope and Limitations

    This study was conducted on August 2013 under ambient room conditions.

    Commercial alum sulphate was used as the only experimental chemical with water and

    baking powder as negative and positive control. This research used Rhizopus Stolonifer

    for the antifungal test. Rhizopus stolonifer was procured from the research laboratory of

    Notre Dame Integrated Basic Education Department, General Santos City.

    1.8 Operational Definition of Terms

    In Vitro

    In Vivo

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    Potassium aluminum sulfate (alum), a chemically hydrated aluminum potassium sulfate

    that possesses a specific crystal shape with a chemical formula

    KAl(SO4)2.12H2O. It is no-toxic, has somewhat a sweet acidic taste that

    dissolves easily in water and reacts with acid.

    Tomato,

    Tomato size,

    Post harvest,

    Growth inhibition,

    Rhizopus stolonifer,

    Antifungal

    Radial Infestation

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    Inoculum

    Chapter 2

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    Review of Related Literature

    This chapter places the current study into the context of previous research. It

    consists of both the theoretical and conceptual framework of the present study, the

    critique of both related studies and literature that are related to the present study, as

    well as the operational definition of terms that are based on observable characteristics

    and how it is used in the study.

    Figure 1. Theoretical Framework

    This portion showed the conceptual framework of the research, the major steps

    undertaken towards the desired result.

    Related Literature

    Alum sulfate

    Rhizopus stolonifer

    In Vitro

    a. Growth Inhibition ofRhizopusstoloniferon Commercial Tomato

    b. Color and c. Firmness

    In Vivo

    Anti-fungal Screening ofAlum

    Sulfate

    Recommending the Use of Potassium

    Alum Sulfate Against Rhizopus

    stolonifer

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    Philippine is a tropical country whose climate favoured all sort of microbial

    habitation. Philippine government through its lead agency the Department of Health

    tried to suppress pathogenic microorganism in spreading and contaminating different

    types of diseased be it human or animals. In like manner, the Department of Agriculture

    also heightened their stand to safeguard and help protect Filipino farmers in their effort

    to produce quality and abundant farm products for the end consumers and for their

    livelihood (DA, 2010).

    Seeing the potential of alum in controlling fungal infection in human body ignite

    the researcher scientific thought of exploring the possible application of alum to the

    commercial tomato in order to extend the shelf life to more than two (2) weeks prior to

    its final deterioration caused by fungal infection.

    Potassium Aluminum Sulfate (Alum) is a widely-used and versatile industrial

    chemical, playing an important role in the production of many essentials seen and used

    every day in the home and industry.

    Most of the alum produced today is used in the pulp & paper industry as well as

    water and wastewater treatment. It is inexpensive and effective for a broad range of

    treatment problems because it can function as a coagulant, flocculant, precipitant and

    emulsion breaker. As a coagulant and flocculant, alum removes turbidity, total organic

    carbon (TOC) which can be disinfection byproduct precursors, suspended solids and

    colloidal color, reduces biochemical oxygen demand (BOD) and clarifies potable,

    processes and waste water.

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    Alum is widely used for lake restoration, treatment and nutrient inactivation. It

    also is used in the production of aluminum chemicals, fire extinguisher compounds, soil

    additives and fertilizer, soaps, greases, drugs and cosmetics. It even enters into the

    sports arena, as an additive to give major league baseball covers their hard, tough

    hides. In short, alum touches the lives of just about everyone in many ways.

    http://www.generalchemical.com/aluminum-sulfate.html

    Rhizopus stolonifer (black bread mold) is a widely distributed Mucoralean mold.

    Commonly found on bread surfaces, it takes food and nutrients from the bread and

    causes damage to the surface where it lives.

    Asexual spores are formed within sporangia, which break to release the spores mature.

    Germination of these spores forms the haploid hyphae of a new mycelium. R. stolonifer

    grows rapidly at temperatures between 15 and 30C.

    Rhizopus stolonifer is a heterothallic species (Kwon, 2001), in that sexual

    reproduction happens only when opposite mating types (designated + and -) come in

    contact. Successful mating results in the formation of durable zygospores at the point of

    contact. Subsequently, the zygospore germinates and forms a sporangiophore whose

    sporangium contains both + and - haploid spores. There are three varieties: R.

    stolonifervar. stoloniferproduces straight, erect sporangiophores, whereas those ofR.

    stolonifer var. lyococcos are curved. A closely related species, Rhizopus sexualis,

    differs primarily in being homothallic (self-compatible).

    http://www.generalchemical.com/aluminum-sulfate.htmlhttp://en.wikipedia.org/wiki/Moldhttp://en.wikipedia.org/wiki/Sporangiumhttp://en.wikipedia.org/wiki/Heterothallichttp://en.wikipedia.org/wiki/Zygosporeshttp://en.wikipedia.org/w/index.php?title=Rhizopus_sexualis&action=edit&redlink=1http://en.wikipedia.org/wiki/Homothallichttp://www.generalchemical.com/aluminum-sulfate.htmlhttp://en.wikipedia.org/wiki/Moldhttp://en.wikipedia.org/wiki/Sporangiumhttp://en.wikipedia.org/wiki/Heterothallichttp://en.wikipedia.org/wiki/Zygosporeshttp://en.wikipedia.org/w/index.php?title=Rhizopus_sexualis&action=edit&redlink=1http://en.wikipedia.org/wiki/Homothallic
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    The Rhiopus stoloniferare opportunists and are ubiquitous (found everywhere) in

    the natural environment, in part because they are good saprophytes. Mechanical

    injuries (e.g., cuts, punctures) that occur during harvest and handling are a frequent site

    for decay development beginning on the fruit surface. By contrast, internalized

    pathogens (those that have entered tissues beneath the fruit surface) cause lesions that

    begin inside the fruit. Internal bruises may occur during harvest, and certain fungi can

    colonize the damaged tissues, producing an internal black rot.

    Green tomatoes are normally resistant to sour rot caused by Geotrichum

    candidum. However, if green fruit have been chill injured or are congested with water,

    sour rot will develop and produce a watery decay often associated with wet boxes.

    Once harvested, fruits and vegetables have a limited postharvest life. They no longer

    receive water or nutrition from the plant. Naturally occurring senescence in produce

    leads to a softening of the tissues and often a loss of preformed antimicrobial

    substances. These changes in the fruit or vegetable also make it less desirable to

    consumers. This correlation between senescence, susceptibility to decay and loss of

    edible quality has a great impact on decay control methods. Therefore, handling

    methods that preserve the freshly harvested quality of the crop, such as cooling, are

    likely to minimize the development of decay. Pathogens are present in all production

    areas and are most numerous when the weather becomes warm and wet. Movement of

    weather fronts or tropical storms through production areas can also affect the

    susceptibility of tomato fruit to decay (Kwon, 2001).

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    The relative perishability and storage shelf life of fresh tomato produce is less

    than two (2) weeks comparable to strawberry asparagus broccoli and lettuce (Kader,

    1978).

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    Chapter 3

    Methodology and Research Design

    This chapter deals with the experimental methods of research used. The techniques

    used under experimental research method as well as the data gathering tools and

    analytical tools used will be further explained in this chapter.

    3.1 Research Design

    The proponent used the experimental research method which involves: In vitro and

    In Vivo Screening of the alum suflate against Rhizopus stolonifer. Data gathering,

    organizing, tabulating, depicting and analyzing using the One Way Analysis of Variance

    and Spearman Product Moment Correlation for homogeneity of data.

    The In Vitro was carried out in five (5) treatments [T1

    as negative control, water; T2

    1.0 mg/L alum; T3 2.0mg/L alum; T4 3.0 mg/L alum and T5 baking powder] and each

    treatment is replicated (3) three times.

    The In Vivo was carried out using a selected tomatoes procured from the Public

    market of General Santos City. The selection was made in order to experiment on similar

    size, color, texture and age of tomatoes under investigation. The same level of

    concentration of alum was employed in the In Vivo Screening.

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    Table 1.0 Experimental Design

    TreatmentsReplication

    Total Mean1 2 3

    Water

    1.0 mg./L Alum2.0 mg./L Alum

    3.0 mg./L Alum

    Baking Power

    Table 1.0 represents the distribution of petri disc containing the agar impregnated

    with Rhizopus stolonifer for growth inhibition protocol by alum sulfate.

    The same arrangement will be followed in the experimental design for the In -

    Vivo investigation.

    Data Gathering:

    In Vitro Screening data will be gathered and recorded 24 hours from the conduct of

    the experimentation. Data such as the minimum zone of inhibition will be measured using

    the micrometer caliper.

    The In Vivo Screening data will be gathered and collected on the span of nine (9)

    days or until the tomatoes under study are decomposing due to Rhizopus stolonifer

    invasion. Data to be collected included the following, such as color, texture, and water loss.

    3.2 Materials and Equipments

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    Aluminum sulfate

    Commercially available aluminum sulfate is procured from the supermarket at a

    lower price.

    Tomatoes

    Commercially grown tomatoes (Lycopersicon esculentum Mill.) at the red colour

    stage used in this work were obtained from Public market of General Santos City at

    P15.00 per kilo. Tomatoes were selected to have uniform size, color, and texture.

    Tomatoes with apparent injuries were removed. Before treatments, tomatoes were

    immersed in 70% ethanol for 1 min, washed with ionized water, and then air dried.

    Cultures

    Rhizopus stolonifer was procured from Notre Dame of Dadiangas University,

    Integrated Basic Education Department. R. stolonifer was incubated on Malt Extract

    Agar for 810 days at 25C.

    Preparation of inoculum

    Spores suspensions were obtained from mycelium grown on MEA medium at

    25C for 14 days and were collected by flooding the surface of the plates with ~5 ml

    sterile saline solution (NaCl, 8.5 g/l water) containing Tween 80 (0.1% v/v). After

    counting the spores using a haemocytometer, the suspension was standardized to

    concentrations of 107 spore/ml by dilution with sterile water before using. The viability of

    all strains checked using quantitative colony counts were at 10 7 CFU/ml. (Burton, 2007)

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    Preparation of the Alum concentration

    Alum concentrate is prepared by mass/volume concentration ratio.

    3.3 Anti-fungal Screening

    In vitro test

    The agar dilution method was employed. Each concentration of alum sulfate at

    1.0mg/L, 2.0mg/L, and 3.0mg/L, with water and baking powder as negative and

    positive control respectively. Three replicates were prepared for each treatment. The

    impregnated plates were then incubated at 25 C for 3 days in an incubator. The zone

    of inhibition is then gathered and recorded to statistical analysis.

    In vivo test

    Fruit were dipped for 20 min in the respective alum sulfate concentrations of 1.0mg/L,

    2.0mg/L, 3.0mg/L in distilled water. After drying, they were evenly sprayed with a spore

    suspension ofR. stoloniferand held at 25 C for 9 days. Each treatment was replicated

    three times with 10 fruits per replicate. Following incubation, tomatoes were individually

    rated for mould growth on a scale of 0 to 5, with 0 denoting clean specimens and 5

    representing heavy mould growth (0=clean, 1=20%, 2=40%, 3=60%, 4=80%, 5=100%

    of mould growth). (Matan, 2011)

    2.6 Color Measurement

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    Inset photo is taken from California Tomato Commission. This is the Standard for

    measuring the acceptability of importing tomatoes in California.

    Skin colour values of each of tomatoes at 0th and 9th day were measured

    according to the Color Chart from California Tomato Commission. Corresponding color

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    changed for nine (9) days will be recorded. Extended observation may occur until the

    onset of Rhizopus stolonifer infestation become visible and tomatoes will undergo

    deterioration. Analysis of Variance will be used to determine the significant difference in

    the mean of tomato deterioration.

    2.7 Textural analysis

    Tomatoes firmness was assessed before and after about 9 days of storage at

    25C using a nondestructive tests. The Modified penetrometer deformation apparatus is

    constructed. A 500-g weight was applied (radially) for a constant time period and

    deformation was measured (mm) for a single point.

    Instron axial (vertical) deformation. Fruits were subjected to axial compression of

    an initial pre-load of 0.1 kg and subsequently to a total load of 1.0 kg. Resultant delta

    deformation was measured in millimeters. One data point per fruit was taken. (This

    variation was included because historically most whole fruit firmness studies have been

    in axial mode.)

    A custom brace to gently hold tomatoes in a radial position was designed and the

    Instron method employed a flat disk probe, 3 in. in diameter, and a 2 kg load cell. The

    diameter at each position was measured and recorded prior to compression. The

    crosshead moved at a constant speed of 20 mm/min. Spearmans Rho, which is a

    measure of linear association between ranks of variables, similar to the linear

    regression for parametric statistics, was utilized for analysis of the data. (Matan, 2007)

    Twenty-five replicates were taken per sample. Firmness values were obtained

    from the maximum peak of the first compression.

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    Table ____. Relationship between Subjective Firmness Measurements for WholeTomato Fruit Firmness

    2.8 Statistical analyses

    All variables were tested for normality applying the Spearmans Rho for

    homogeneity. Data transformation was done, where necessary. All results were

    expressed as mean standard deviation SD. The data was statistically treated by one-

    way ANOVA and Tukey post hoc test with p < 0.05 was considered to be statistically

    significant.

    Chapter IV

    Results and Discussion

    This chapter presents the data collected during the course of the investigation as

    well as the appropriate statistical used in the analyses of the collected data. Data were

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    presented in tabular form with corresponding graphical presentation for visual

    comprehension.

    There were two sets of data collected and analyzed. The In Vitro and the In vivo

    data as observed during the investigation. Statistical tool used were One Way Analysis

    of Variance and Spearman Rho for correlation of the nonparametric In Vivo observation.

    4.1 In vitro Screening

    Antifungal Screening of the growth inhibitory effect of Rhizopus stolonifer using

    potassium aluminum sulfate in different concentration level. The test is carried out in

    petri disc using agar diffusion method.

    Table xx: Growth Inhibition of Rhizopus stolonifer by Potassium Aluminum Sulfate

    TreatmentReplication

    Total Mean1 2 3

    Water

    0.5 mg/L

    1.0mg/L1.5mg/L

    Baking Powder

    Total

    ANOVA

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    In Vivo Screening Result

    A. Mould Growth Inhibition of Rhizopus stolonifer

    Table ____. Radius ofRhizopus stoloniferGrowth (mm)

    Treatment

    Replication

    Total

    MeanIndex

    1 2 3

    Water

    0.5 mg/L

    1.0mg/L

    1.5mg/L

    Baking Powder

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    B. Color Change

    Table _____ Tomato Fruit Color Index Day 1

    TreatmentsReplication

    Total Mean1 2 3

    Water

    1.0 mg/L

    2.0 mg/L

    3.0 mg/L

    BakingSoda

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    Table _____ Tomato Fruit Color Index Day 3

    TreatmentsReplication

    Total Mean1 2 3

    Water

    1.0 mg/L

    2.0 mg/L

    3.0 mg/L

    BakingSoda

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    Table _____ Tomato Fruit Color Index Day 5

    TreatmentsReplication

    Total Mean1 2 3

    Water

    1.0 mg/L

    2.0 mg/L

    3.0 mg/L

    BakingSoda

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    Table _____ Tomato Fruit Color Index Day 7

    TreatmentsReplication

    Total Mean1 2 3

    Water

    1.0 mg/L

    2.0 mg/L

    3.0 mg/L

    BakingSoda

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    Table _____ Tomato Fruit Color Index Day 9

    TreatmentsReplication

    Total Mean1 2 3

    Water

    1.0 mg/L

    2.0 mg/L

    3.0 mg/L

    BakingSoda

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    Table _____ Tomato Fruit Color Index Day 11

    TreatmentsReplication

    Total Mean1 2 3

    Water

    1.0 mg/L

    2.0 mg/L

    3.0 mg/L

    BakingSoda

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    C. Firmness Index Using Modified Penetrometer Deformation Apparatus

    Table _____ Tomato Fruit Color Index Day 1

    TreatmentsReplication

    Total Mean1 2 3

    Water

    1.0 mg/L

    2.0 mg/L

    3.0 mg/L

    BakingSoda

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    Table _____ Tomato Fruit Color Index Day 11

    TreatmentsReplication

    Total Mean1 2 3

    Water

    1.0 mg/L

    2.0 mg/L

    3.0 mg/L

    BakingSoda

    Spearmans Rho

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    Fungal growth inhibition of citronella oil against Rhizopus stoloniferare shown in

    Table 1. The MIC of citronella oil against R. stoloniferon agar was 5L/mL. Fungal

    resistance of tomatoes dip-treated with various concentrations of citronella oil against

    R. stoloniferis shown in Figures 1 and 2. The results are presented as the average

    ratings of 25 five specimens. It is clear that citronella oil was not active against R.

    stoloniferon tomatoes at the concentration less than 5 L/mL. Above that concentration,

    antifungal activity of citronella oil gradually increased with increasing concentration of

    the oil. A complete protection of tomatoes from R. stoloniferfor up to 9 days was

    achieved at the concentration of citronella oil at 20 L/mL. It should be noted that

    antifungal activity of citronella oil should be inherently arisen from components within

    the oil rather than from the moisture exclusion effect since the control stakes dip-treated

    with vegetable oil showed 100% mold coverage.

    Chapter 5

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    SUMMARY OF FINDINGS, CONCLUSIONS AND RECOMMENDATION

    This chapter presents the summary of findings and conclusions made from the study and

    recommendations given by the researcher.

    5.1 Summary of Findings

    The water reservoirs we have these days are being contaminated with many different

    chemicals from either industrial wastes and it may be naturally occurring. These chemicals can

    therefore be harmful to living things. This study was conducted to test if Sphagnum moss

    (Sphagnum flexuosum) can absorb the heavy metals used in this project.

    In conducting this study, the proponents collected some Sphagnum moss and placed it

    equally upon containers with contaminated waters with Copper and Lead with 3 replications

    each. After an observation of 7 days, the water in the contaminated water changed and can be

    concluded that there was an effect. To prove this, water in the containers was removed and

    placed separate containers to be studied. It was discovered and confirmed that the moss had an

    effect and greatly reduced the amount of contaminants that was originally present in the water.

    Though no study was conducted to test if the heavy metals were transferred to the

    moss, it can be already directly concluded that the moss absorbed it because there could not be

    another explanation to how the heavy metals were removed from water.

    5.2 Conclusions

    Based on the experimentation performed, results and information drawn together, the

    researcher was able to formulate the following conclusions:

    http://en.wikipedia.org/w/index.php?title=Sphagnum_flexuosum&action=edit&redlink=1http://en.wikipedia.org/w/index.php?title=Sphagnum_flexuosum&action=edit&redlink=1
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    5.2.1. Sphagnum moss was proven to remove copper and lead in water.

    5.2.2. Sphagnum moss was effective in adsorbing copper and lead content in water

    5.2.3. The proponents determined the change in amount of copper and lead when using

    Sphagnum moss from the color change of the contaminated water in all replications.

    5.3 Recommendations

    From the findings of the study, it can be observed that there were research gaps. Results

    can be improved and further benefits can be disclosed with the following recommendations:

    5.3.1. People shall cultivate Sphagnum moss as a plant in the surroundings to ensure that

    water surrounding them shall be free from chemicals such as copper, and lead.

    5.3.2. Further research will be conducted to determine the amount of the said chemicals

    absorbed day by day in the experimentation.

    5.3.3. Another study shall be conducted using another kind of moss to test the effects on

    the said chemicals.

    5.3.4. Another experimentation shall be conducted with other contaminants.

    5.3.5. The government will conduct the study to improve the research.

    5.3.6. A further study shall be conducted to prove that the moss absorbed the

    Heavy metals

    BIBLIOGRAPHY

    Books

    Burton and Engelkirk,. 2007. Burtons Microbiology for the Health Science

    Siegel, S. 1998. Nonparametric Statistics for Behavioral Sciences

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    Journals

    Bartz, J.A, Steven, R.A and Mahovic, M. Guide t0 Identifying and ControllingPostharvest Tomato Diseases in Florida, J, p.23

    Barrett, D. M.et all. 1998.Textural Modification of Processing Tomatoes, 185 190

    Kader, A. A. 1978, American Society of Horticultural Science Vol. 103, p.101

    Kwon, J.H, et all. 2001. Rhizopus Soft Rot on Cherry Tomato by Rhizopus stolonifer inKorea, Mycobiology 176-178.

    Matan, N, W., 2011. Postharvest Control of Rhizopus stolonifer on Tomato by CitronellaOil, Thailand. p 23

    Radzevicius, A. et all. 2012. Tomato Ripeness Influence on Fruit Quality, World

    Academy of Science and Technology Vol. 64 J, 653

    Turkhan, H.A et all. 2010. The Effect of Head Rot Disease (Rhizopus stolonifer)On Sunflower Genotype at Two Different Growth Stages, Turkish Journal offiled Crops Vol. 15(1), p. 94

    www.lagorio.com, California Tomato Commission

    http://www.lagorio.com/http://www.lagorio.com/
  • 7/27/2019 Test for Delaying the Senescence of Tomato

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  • 7/27/2019 Test for Delaying the Senescence of Tomato

    35/35