This document discusses chemical control of insects and classification of insecticides. It defines insecticides and describes their importance in pest management. Insecticides are classified based on origin, mode of entry, mode of action, and chemical nature. Common classifications include inorganic, organic of animal/plant/synthetic origin; contact, stomach, and fumigant modes of entry; and nerve, respiratory, and chitin inhibitor modes of action. Metrics for toxicity evaluation include LD50, LC50, ED50, and knockdown parameters. Bioassays are used to study insecticide effects and determine toxicity values.
Pest control refers to the regulation or management of a species defined as a pest, usually because it is perceived to be detrimental to a person's health, the ecology or the economy.
The principal objective of a pest control is to protect crops by maintaining the attack of the pests and diseases at an acceptable level.
There are various methods of pest control
they are basically non chemical methods and chemical methods
Parasitoids and Predators, their attributes.Bhumika Kapoor
Insect parasitoids have an immature life stage that develops on or within a single insect host, ultimately killing the host, hence the value of parasitoids as natural enemies. Adult parasitoids are free-living and may be predaceous. Parasitoids are often called parasites, but the term parasitoid is more technically correct. Most beneficial insect parasitoids are wasps or flies, although some rove beetles (see Predators) and other insects may have life stages that are parasitoids.
where as the Major characteristics of arthropod predators includes adults and immatures are often generalists rather than specialists, they generally are larger than their prey, they kill or consume many prey males, females, immatures, and adults may be predatory and they attack immature and adult prey.
Pest control refers to the regulation or management of a species defined as a pest, usually because it is perceived to be detrimental to a person's health, the ecology or the economy.
The principal objective of a pest control is to protect crops by maintaining the attack of the pests and diseases at an acceptable level.
There are various methods of pest control
they are basically non chemical methods and chemical methods
Parasitoids and Predators, their attributes.Bhumika Kapoor
Insect parasitoids have an immature life stage that develops on or within a single insect host, ultimately killing the host, hence the value of parasitoids as natural enemies. Adult parasitoids are free-living and may be predaceous. Parasitoids are often called parasites, but the term parasitoid is more technically correct. Most beneficial insect parasitoids are wasps or flies, although some rove beetles (see Predators) and other insects may have life stages that are parasitoids.
where as the Major characteristics of arthropod predators includes adults and immatures are often generalists rather than specialists, they generally are larger than their prey, they kill or consume many prey males, females, immatures, and adults may be predatory and they attack immature and adult prey.
Introduction, Techniques of release of natural enemies, Recovery evaluation of released natural enemies for colonization, Survivorship analysis/ Prediction of Success of released natural enemies for colonization, Conservation of Natural Enemies, Augmentation of Natural Enemies, Ecological manipulations for colonization of natural enemies and colonized natural enemies, Large scale production of bio-control agents.,
The IRAC Mode of Action (MoA) classification provides growers, advisors, extension staff, consultants and crop protection professionals with a guide to the selection of acaricides or insecticides for use in an effective and sustainable acaricide or insecticide resistance management (IRM) strategy.
Rules for inclusion of a compound in the MoA list
Names To be included in the active list, compounds must have, or be very close to having, a minimum of one registered use in at least one country.
when more than one active ingredient in that chemical sub-group is registered for use, the chemical sub-group name is used.
when only one active ingredient is registered for use, the name of that exemplifying active ingredient may be use
Definition of pest and pesticide.
Names of chemically related pesticides.
Description on carbamate insecticide, definition, history and mode of action.
symptoms of carbamate poisoning and it's treatment.
The successful management of a pest by means of another living organism (parasitoids, predators and pathogens) that are encouraged and disseminated by man is called biological
control. In such programme the natural enemies are introduced, encouraged, multiplied by artificial means and disseminated by the man with his own efforts instead of leaving it to nature.
Introduction, Techniques of release of natural enemies, Recovery evaluation of released natural enemies for colonization, Survivorship analysis/ Prediction of Success of released natural enemies for colonization, Conservation of Natural Enemies, Augmentation of Natural Enemies, Ecological manipulations for colonization of natural enemies and colonized natural enemies, Large scale production of bio-control agents.,
The IRAC Mode of Action (MoA) classification provides growers, advisors, extension staff, consultants and crop protection professionals with a guide to the selection of acaricides or insecticides for use in an effective and sustainable acaricide or insecticide resistance management (IRM) strategy.
Rules for inclusion of a compound in the MoA list
Names To be included in the active list, compounds must have, or be very close to having, a minimum of one registered use in at least one country.
when more than one active ingredient in that chemical sub-group is registered for use, the chemical sub-group name is used.
when only one active ingredient is registered for use, the name of that exemplifying active ingredient may be use
Definition of pest and pesticide.
Names of chemically related pesticides.
Description on carbamate insecticide, definition, history and mode of action.
symptoms of carbamate poisoning and it's treatment.
The successful management of a pest by means of another living organism (parasitoids, predators and pathogens) that are encouraged and disseminated by man is called biological
control. In such programme the natural enemies are introduced, encouraged, multiplied by artificial means and disseminated by the man with his own efforts instead of leaving it to nature.
This ppt is about natural pesticides. and how they are better than synthetics. this lecture is helpful for students of pharmacognosy and agriculture.
synthetic pesticides are need to be replaced with natural substances and natural methods to control like biological control etc.
pests are creating a huge economic loss so its the need of the time to focus on natural pest control methods.
if you like the lecture comment and share
Insecticide
An insecticide is a substance used to kill insects. They
include ovicides and larvicides used against insect eggs and larvae, respectively. Insecticides are
used in agriculture, medicine, industry and by consumers. Insecticides are claimed to be a major
factor behind the increase in agricultural 20th century\'s productivity . Nearly all insecticides
have the potential to significantly alter ecosystems; many are toxic to humans; some concentrate
along the food chain.
Insecticides can be classified in two major groups: systemic insecticides, which have residual or
long term activity; and contact insecticides, which have no residual activity.
Furthermore, one can distinguish three types of insecticide. 1. Natural insecticides, such as
nicotine, pyrethrum and neem extracts, made by plants as defenses against insects. 2. Inorganic
insecticides, which are metals. 3. Organic insecticides, which are organic chemical compounds,
mostly working by contact.
The mode of action describes how the pesticide kills or inactivates a pest. It provides another
way of classifying insecticides. Mode of action is important in understanding whether an
insecticide will be toxic to unrelated species, such as fish, birds and mammals.
Insecticides are distinct from insect repellents, which do not kill.
activity
Systemic insecticides become incorporated and distributed systemically throughout the whole
plant. When insects feed on the plant, they ingest the insecticide. Systemic insecticides produced
by transgenic plants are called plant-incorporated protectants (PIPs). For instance, a gene that
codes for a specific Bacillus thuringiensis biocidal protein was introduced into corn and other
species. The plant manufactures the protein, which kills the insect when consumed .Contact
insecticides are toxic to insects upon direct contact. These can be inorganic insecticides, which
are metals and include arsenates, copper and fluorine compounds, which are less commonly
used, and the commonly used sulfur. Contact insecticides can be organic insecticides, i.e. organic
chemical compounds, synthetically produced, and comprising the largest numbers of pesticides
used today. Or they can be natural compounds like pyrethrum, neem oil etc. Contact insecticides
usually have no residual activity.
Efficacy can be related to the quality of pesticide application, with small droplets, such as
aerosols often improving performance.[4][better source needed]
Biological pesticides
Main article: Biopesticide
Many organic compounds are produced by plants for the purpose of defending the host plant
from predation. A trivial case is tree rosin, which is a natural insecticide. Specific, the production
of oleoresin by conifer species is a component of the defense response against insect attack and
fungal pathogen infection . Many fragrances, e.g. oil of wintergreen, are in fact antifeedants.
Four extracts of plants are in commercial use: pyrethrum, rotenone, neem oil, and various
essential oil.
In this presentation I am explaining the different reproductive strategies in Insects and fitness, clutch size, reproductive competition in parasitoids
Cancer cell metabolism: special Reference to Lactate PathwayAADYARAJPANDEY1
Normal Cell Metabolism:
Cellular respiration describes the series of steps that cells use to break down sugar and other chemicals to get the energy we need to function.
Energy is stored in the bonds of glucose and when glucose is broken down, much of that energy is released.
Cell utilize energy in the form of ATP.
The first step of respiration is called glycolysis. In a series of steps, glycolysis breaks glucose into two smaller molecules - a chemical called pyruvate. A small amount of ATP is formed during this process.
Most healthy cells continue the breakdown in a second process, called the Kreb's cycle. The Kreb's cycle allows cells to “burn” the pyruvates made in glycolysis to get more ATP.
The last step in the breakdown of glucose is called oxidative phosphorylation (Ox-Phos).
It takes place in specialized cell structures called mitochondria. This process produces a large amount of ATP. Importantly, cells need oxygen to complete oxidative phosphorylation.
If a cell completes only glycolysis, only 2 molecules of ATP are made per glucose. However, if the cell completes the entire respiration process (glycolysis - Kreb's - oxidative phosphorylation), about 36 molecules of ATP are created, giving it much more energy to use.
IN CANCER CELL:
Unlike healthy cells that "burn" the entire molecule of sugar to capture a large amount of energy as ATP, cancer cells are wasteful.
Cancer cells only partially break down sugar molecules. They overuse the first step of respiration, glycolysis. They frequently do not complete the second step, oxidative phosphorylation.
This results in only 2 molecules of ATP per each glucose molecule instead of the 36 or so ATPs healthy cells gain. As a result, cancer cells need to use a lot more sugar molecules to get enough energy to survive.
Unlike healthy cells that "burn" the entire molecule of sugar to capture a large amount of energy as ATP, cancer cells are wasteful.
Cancer cells only partially break down sugar molecules. They overuse the first step of respiration, glycolysis. They frequently do not complete the second step, oxidative phosphorylation.
This results in only 2 molecules of ATP per each glucose molecule instead of the 36 or so ATPs healthy cells gain. As a result, cancer cells need to use a lot more sugar molecules to get enough energy to survive.
introduction to WARBERG PHENOMENA:
WARBURG EFFECT Usually, cancer cells are highly glycolytic (glucose addiction) and take up more glucose than do normal cells from outside.
Otto Heinrich Warburg (; 8 October 1883 – 1 August 1970) In 1931 was awarded the Nobel Prize in Physiology for his "discovery of the nature and mode of action of the respiratory enzyme.
WARNBURG EFFECT : cancer cells under aerobic (well-oxygenated) conditions to metabolize glucose to lactate (aerobic glycolysis) is known as the Warburg effect. Warburg made the observation that tumor slices consume glucose and secrete lactate at a higher rate than normal tissues.
(May 29th, 2024) Advancements in Intravital Microscopy- Insights for Preclini...Scintica Instrumentation
Intravital microscopy (IVM) is a powerful tool utilized to study cellular behavior over time and space in vivo. Much of our understanding of cell biology has been accomplished using various in vitro and ex vivo methods; however, these studies do not necessarily reflect the natural dynamics of biological processes. Unlike traditional cell culture or fixed tissue imaging, IVM allows for the ultra-fast high-resolution imaging of cellular processes over time and space and were studied in its natural environment. Real-time visualization of biological processes in the context of an intact organism helps maintain physiological relevance and provide insights into the progression of disease, response to treatments or developmental processes.
In this webinar we give an overview of advanced applications of the IVM system in preclinical research. IVIM technology is a provider of all-in-one intravital microscopy systems and solutions optimized for in vivo imaging of live animal models at sub-micron resolution. The system’s unique features and user-friendly software enables researchers to probe fast dynamic biological processes such as immune cell tracking, cell-cell interaction as well as vascularization and tumor metastasis with exceptional detail. This webinar will also give an overview of IVM being utilized in drug development, offering a view into the intricate interaction between drugs/nanoparticles and tissues in vivo and allows for the evaluation of therapeutic intervention in a variety of tissues and organs. This interdisciplinary collaboration continues to drive the advancements of novel therapeutic strategies.
The increased availability of biomedical data, particularly in the public domain, offers the opportunity to better understand human health and to develop effective therapeutics for a wide range of unmet medical needs. However, data scientists remain stymied by the fact that data remain hard to find and to productively reuse because data and their metadata i) are wholly inaccessible, ii) are in non-standard or incompatible representations, iii) do not conform to community standards, and iv) have unclear or highly restricted terms and conditions that preclude legitimate reuse. These limitations require a rethink on data can be made machine and AI-ready - the key motivation behind the FAIR Guiding Principles. Concurrently, while recent efforts have explored the use of deep learning to fuse disparate data into predictive models for a wide range of biomedical applications, these models often fail even when the correct answer is already known, and fail to explain individual predictions in terms that data scientists can appreciate. These limitations suggest that new methods to produce practical artificial intelligence are still needed.
In this talk, I will discuss our work in (1) building an integrative knowledge infrastructure to prepare FAIR and "AI-ready" data and services along with (2) neurosymbolic AI methods to improve the quality of predictions and to generate plausible explanations. Attention is given to standards, platforms, and methods to wrangle knowledge into simple, but effective semantic and latent representations, and to make these available into standards-compliant and discoverable interfaces that can be used in model building, validation, and explanation. Our work, and those of others in the field, creates a baseline for building trustworthy and easy to deploy AI models in biomedicine.
Bio
Dr. Michel Dumontier is the Distinguished Professor of Data Science at Maastricht University, founder and executive director of the Institute of Data Science, and co-founder of the FAIR (Findable, Accessible, Interoperable and Reusable) data principles. His research explores socio-technological approaches for responsible discovery science, which includes collaborative multi-modal knowledge graphs, privacy-preserving distributed data mining, and AI methods for drug discovery and personalized medicine. His work is supported through the Dutch National Research Agenda, the Netherlands Organisation for Scientific Research, Horizon Europe, the European Open Science Cloud, the US National Institutes of Health, and a Marie-Curie Innovative Training Network. He is the editor-in-chief for the journal Data Science and is internationally recognized for his contributions in bioinformatics, biomedical informatics, and semantic technologies including ontologies and linked data.
Multi-source connectivity as the driver of solar wind variability in the heli...Sérgio Sacani
The ambient solar wind that flls the heliosphere originates from multiple
sources in the solar corona and is highly structured. It is often described
as high-speed, relatively homogeneous, plasma streams from coronal
holes and slow-speed, highly variable, streams whose source regions are
under debate. A key goal of ESA/NASA’s Solar Orbiter mission is to identify
solar wind sources and understand what drives the complexity seen in the
heliosphere. By combining magnetic feld modelling and spectroscopic
techniques with high-resolution observations and measurements, we show
that the solar wind variability detected in situ by Solar Orbiter in March
2022 is driven by spatio-temporal changes in the magnetic connectivity to
multiple sources in the solar atmosphere. The magnetic feld footpoints
connected to the spacecraft moved from the boundaries of a coronal hole
to one active region (12961) and then across to another region (12957). This
is refected in the in situ measurements, which show the transition from fast
to highly Alfvénic then to slow solar wind that is disrupted by the arrival of
a coronal mass ejection. Our results describe solar wind variability at 0.5 au
but are applicable to near-Earth observatories.
Observation of Io’s Resurfacing via Plume Deposition Using Ground-based Adapt...Sérgio Sacani
Since volcanic activity was first discovered on Io from Voyager images in 1979, changes
on Io’s surface have been monitored from both spacecraft and ground-based telescopes.
Here, we present the highest spatial resolution images of Io ever obtained from a groundbased telescope. These images, acquired by the SHARK-VIS instrument on the Large
Binocular Telescope, show evidence of a major resurfacing event on Io’s trailing hemisphere. When compared to the most recent spacecraft images, the SHARK-VIS images
show that a plume deposit from a powerful eruption at Pillan Patera has covered part
of the long-lived Pele plume deposit. Although this type of resurfacing event may be common on Io, few have been detected due to the rarity of spacecraft visits and the previously low spatial resolution available from Earth-based telescopes. The SHARK-VIS instrument ushers in a new era of high resolution imaging of Io’s surface using adaptive
optics at visible wavelengths.
This pdf is about the Schizophrenia.
For more details visit on YouTube; @SELF-EXPLANATORY;
https://www.youtube.com/channel/UCAiarMZDNhe1A3Rnpr_WkzA/videos
Thanks...!
Introduction:
RNA interference (RNAi) or Post-Transcriptional Gene Silencing (PTGS) is an important biological process for modulating eukaryotic gene expression.
It is highly conserved process of posttranscriptional gene silencing by which double stranded RNA (dsRNA) causes sequence-specific degradation of mRNA sequences.
dsRNA-induced gene silencing (RNAi) is reported in a wide range of eukaryotes ranging from worms, insects, mammals and plants.
This process mediates resistance to both endogenous parasitic and exogenous pathogenic nucleic acids, and regulates the expression of protein-coding genes.
What are small ncRNAs?
micro RNA (miRNA)
short interfering RNA (siRNA)
Properties of small non-coding RNA:
Involved in silencing mRNA transcripts.
Called “small” because they are usually only about 21-24 nucleotides long.
Synthesized by first cutting up longer precursor sequences (like the 61nt one that Lee discovered).
Silence an mRNA by base pairing with some sequence on the mRNA.
Discovery of siRNA?
The first small RNA:
In 1993 Rosalind Lee (Victor Ambros lab) was studying a non- coding gene in C. elegans, lin-4, that was involved in silencing of another gene, lin-14, at the appropriate time in the
development of the worm C. elegans.
Two small transcripts of lin-4 (22nt and 61nt) were found to be complementary to a sequence in the 3' UTR of lin-14.
Because lin-4 encoded no protein, she deduced that it must be these transcripts that are causing the silencing by RNA-RNA interactions.
Types of RNAi ( non coding RNA)
MiRNA
Length (23-25 nt)
Trans acting
Binds with target MRNA in mismatch
Translation inhibition
Si RNA
Length 21 nt.
Cis acting
Bind with target Mrna in perfect complementary sequence
Piwi-RNA
Length ; 25 to 36 nt.
Expressed in Germ Cells
Regulates trnasposomes activity
MECHANISM OF RNAI:
First the double-stranded RNA teams up with a protein complex named Dicer, which cuts the long RNA into short pieces.
Then another protein complex called RISC (RNA-induced silencing complex) discards one of the two RNA strands.
The RISC-docked, single-stranded RNA then pairs with the homologous mRNA and destroys it.
THE RISC COMPLEX:
RISC is large(>500kD) RNA multi- protein Binding complex which triggers MRNA degradation in response to MRNA
Unwinding of double stranded Si RNA by ATP independent Helicase
Active component of RISC is Ago proteins( ENDONUCLEASE) which cleave target MRNA.
DICER: endonuclease (RNase Family III)
Argonaute: Central Component of the RNA-Induced Silencing Complex (RISC)
One strand of the dsRNA produced by Dicer is retained in the RISC complex in association with Argonaute
ARGONAUTE PROTEIN :
1.PAZ(PIWI/Argonaute/ Zwille)- Recognition of target MRNA
2.PIWI (p-element induced wimpy Testis)- breaks Phosphodiester bond of mRNA.)RNAse H activity.
MiRNA:
The Double-stranded RNAs are naturally produced in eukaryotic cells during development, and they have a key role in regulating gene expression .
2. ENTO 231 (1+1): FUNDAMENTALS OF
ENTOMOLOGY II & IPM
Course In-Charge
Mr.S.Srinivasnaik
Assistant Professor
Department of Entomology
LECTURE NO.11
CHEMICAL CONTROL - CLASSIFICATION OF
INSECTICIDES-TOXICITY EVALUATION OF
INSECTICIDES - LC50, LD50, ED50, LT50,
KD50 AND KT50-
INORGANIC INSECTICIDES - ARSENIC
COMPOUNDS - FLUORINE AND SULPHUR
3. CHEMICAL CONTROL
Chemical control is one of unavoidable component in the IPM
Control of insects with chemicals is known is chemical
control. The term pesticide is used to those chemicals which kill
pests and these pests may include insects, animals, mites,
diseases or even weeds. Chemicals which kill insects are called
as insecticides.
4. Definition
Insecticide may be defined as a substance or mixture of
substances intended to kill, repel or otherwise prevent the insects.
Similarly pesticides include nematicides – which kill nematodes,
miticides or Acaricides which kill mites, Rodenticides – which kill
rats, weedicides- that kill weeds, Fungicides- that kill fungus etc.
5. Importance of chemical control
•Insecticides are the most powerful tools available for use in
pest management.
•They are highly effective, rapid in curative action, adoptable to
most situations, flexible in meeting changing agronomic and
ecological conditions and economical. Insecticides are the only
tool for pest management that is reliable for emergency action
when insect pest populations approach or exceed the economic
threshold.
•A major technique such as the use of pesticides can be the very
heart and core of integrated systems.
6. General Properties of Insecticides
•Pesticides are generally available in a concentrated from which
are to be diluted and used except in ready to use dust and
granules.
•They are highly toxic and available in different formulations
7. Properties of an ideal insecticide or pesticide
1.It should be freely available in the market under different formulations.
2.It should be toxic and kill the pest required to be controlled.
3.It should not be phytotoxic to the crops on which it is used.
4.It should not be toxic to non target species like animals, natural enemies etc.
5.It should be less harmful to human beings and other animals.
6.It should not leave residues in crops like vegetables.
7.It should have wide range of compatibility.
8.It should not be toxic to bees and fish and other beneficial organisms.
9.It should have higher tolerance limits.
10.It should possess quick known down effect.
11.It should be stable on application.
12.It should not possess tainting effects and should be free from offensive odour.
13.It should be cheaper
8. Different Classifications of Insecticides
Insecticides are classified in several ways taking into consideration
their origin, mode of entry, mode of action and the chemical nature of the
toxicant
I. Based on the origin and source of supply
A. Inorganic insecticides: comprise compounds of mineral origin and
elemental sulphur. This group includes arsenate and fluorine compounds as
insecticides. Sulphur as acaricides and zinc phosphide as rodenticides.
B. Organic Insecticides:
1. Insecticides of animal origin: Nereistoxin isolated from marine annelids,
fish oil rosin soap from fishes etc.
2. Plant Origin insecticides or Botanical insecticides: Nicotinoids, pyrethroids,
Rotenoids etc.
3. Synthetic organic insecticides: Organochlorines, Organophosphorous,
Carbamate insecticides etc.
4. Hydrocarbon oils etc.
9. II. Based on the mode of entry of the insecticides into the body of the
insect
A. Contact poisons
These insecticides are capable of gaining entry into the insect body
either through spiracles and trachea or through the cuticle itself. Hence, these
poisons can kill the insects by mere coming in contact with the body of the
insects.
Eg. DDT and HCH (Banned), Chlorpyriphos 20EC, Profenophos 50 EC.
B. Stomach poisons
The insecticides applied on the leaves and other parts of plants when
ingested act on the digestive system of the insect and bring about the kill of the
insect. Eg: Calcium arsenate, lead arsenate.
10. C. Fumigants
A fumigant is a chemical substance which is volatile at ordinary
temperatures and sufficiently toxic to the insects. Fumigation is the process of
subjecting the infested material to the toxic fumes or vapours of chemicals or
gases which have insecticidal properties. Chemical used in the fumigant and a
reasonably airtight container or room is known as fumigation chamber or
“Fumigatorium”. Fumigants mostly gain entry into the body of the insect
through spiracles in the trachea
Commonly used Fumigants and their doses
1.Aluminium phosphide, marketed as Celphos tablets used against field rats
groundnut bruchids etc
2. Carbon disulphide: 8-20 lbs/1000ft3 of food grains
3. EDCT (Ethylene Dichloride Carbon Tetrachloride) 20-30 lbs/1000cft of
food grains
4. EDB: Ethylene dibromide 1 lb/1000ft3 of food grains.
5. SO2: By burning sulphur in godowns SO2 fumes are released
11. D. Systemic insecticides
Chemicals that are capable of moving through the vascular systems of
plants irrespective of site of application and poisoning insects that feed on the
plants.
Ex: Methyl demeton, Phosphamidon, Acephate
‘Non systemic insecticides’ are not possessing systemic action are
called non systemic insecticides. Some non-systemic insecticides, however,
have ability to move from one surface leaf to the other. They are called as
‘trans laminar insecticides’. Eg. Malathion, Diazinon, spinosad etc.
12. An ideal systemic insecticide quality are
1.It should have high intrinsic pesticidal activity
2.The toxicant must be adequately liposoluble for it to be absorbed by the plant
system and water soluble for it to be translocated in the plant system.
3.The toxicant or its metabolites should be stable for sufficiently long period to
exercise residual effect.
4.Sufficiently soluble in water for translocation through vascular system
5.Should degrade to nontoxic form in reasonable time to avoid toxicity to
consumer
13. III. Based on mode of action
A. Physical poisons
It brings about the kill of insects by exerting a physical effect. Eg:
Heavy oils, tar oils etc. which cause death by asphyxiation. Inert dusts effect
loss of body moisture by their abrasiveness as in aluminium oxide or absorb
moisture from the body as in charcoal.
B. Protoplasmic poisons
A toxicant responsible for precipitation of protein especially destruction
of cellular protoplasm of midgut epithelium.
Eg. Arsenical compounds.
C. Respiratory poisons
Chemicals which block cellular respiration as in hydrogen cyanide
(HCN), carbon monoxide etc.
D. Nerve poisons
Chemicals which block Acetyl cholinesterase (AChE) and effect the
nervous system. Eg. Organophosphorous, carbamates.
14. E. Chitin inhibitors
Chitin inhibitors interfere with process of synthesis of chitin due to
which normal moulting and development is disrupted.
Ex Novaluron, Diflubenzuran, Lufenuron, Buprofezin
F. General Poisons
Compounds which include neurotoxic symptoms after some period and
do not belong to the above categories.
Eg. Chlordane, Toxaphene
15. IV. Based on stage specificity
1. Ovicides
2. Larvicides
3. Pupicides
4. Adulticides
17. First generation Inorganics and Botanicals
Second
generation
Synthetic organics
Third generation Recent chemicals for reproductive control, IGRs (Insect
Growth Regulators) like MH & JH mimics
Fourth generation Synthetic pyrethroids
Fifth generation A. Synthetic pyrethroids
Examples
1.Alfamethrin - Alfaguard/ Fartac 10 EC
2.Fenpropathrin – Danitol 10 EC
3.Bifenthrin – Taletar 10 EC
4.Fluvalinate – Mavrik
5.Ethofenpron – Treban 10 EC
B. Novel insecticides
Neonicotinoids
Phenyly pyrazoles
Diamides
Oxadizines
Avermectins etc.
VI. Generation wise:
18. VII. IRAC Classification
•IRAC: Insecticide Resistance Action Committee
•It is based on the mode of action of the insecticides
•It is also called as the modern classification of insecticides based on the mode
of action
•According to this there are 21 classes of insecticide groups are present.
19. Toxicity evaluation of insecticides
1. LD 50 (Lethal Dose):
In 1952 Finney has given the computation methods. It is the amount of
toxicant required to kill 50% of the test population and is expressed in terms of
milligrams of the substance of toxicant per kilogram body weight (mg/kg) of the
test animal (usually rat, when treated orally). As the test animals usually rat and
some times rabbit it is also referred to as the mammalian toxicity. This forms the
general criteria for acute toxicity and is also known acute oral LD50.
In case of insects the LD50 (Median Lethal Dose) value is expressed in terms
of micrograms of the toxicant per one gram body weight of the insect.
Eg. Phosphamidon – 28; Parathion 3.6 to 13; Malathion 2800; Hydrogen
cyanide 1.0
20. Acute dermal LD50: The amount of toxicant required to be placed on the skin to cause
death of 50% of test population is known as acute dermal LD50. It must be understood
that higher the LD50.value lesser is the toxic nature of the chemical and vice - versa.
Acute toxicity refers to the toxic effect produced by a single dose of a toxicant where
as chronic toxicity is the effect produced by the accumulation of small amounts of
toxicant over a long period of time. Here the single dose produces no ill-effect.
21. 2. LC 50 (Median Lethal concentration): It is expressed in terms of percentage of
the toxicant required (concentration) to cause 50% kill of the population of a test animal
and is usually determined by potters tower and probit analysis.
3. ED50/ EC50 (Effective Dose/Concentration 50): Chemicals that gives desirable
effects in 50% of test animals.
4. LT 50 (Lethal time 50): Time required to produce effect in 50% of population
5. KD50/ KT50 (Knockdown Dose /Time 50) Dose / Time required for 50% of
population having knockdown effect
22. Bioassay of insecticides
Study of response of individual or group of organisms exposed to the
toxicant is called ‘Bioassay’ or Any quantitative procedure used to determine the
relationship between the amount (dose or concentration) of an insecticide
administered and the magnitude of response in a living organism.
Potter spraying tower apparatus is required for studying the biological effects
of contact poisons on organisms. This air operated spraying apparatus applies an even
deposit of spray over a circular area of 9 cm diameter. Suitable for studying the
biological effects of chemicals, both when applied as direct spray on organisms or as a
residual film. Bioassays are used for screening of potential insecticides, for
determination of valuesLD50 and LC 50. Estimation of residues, and quality testing of
formulated insecticides.