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Research article · 2021 · Full text

International Journal of Biology Sciences

Chromosome studies on some aphid species from two tehsils in Himachal Pradesh's Kangra district

Sarita KumariKanika ChoudharyRajni Rajni

Volume 3(2) · Pages 17–23 · DOI: 10.33545/26649926.2021.v3.i2a.31 ↗

Research areasChromosomal and Genetic VariationsInsect Resistance and GeneticsPlant Virus Research Studies

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Abstract

Author-written

Chromosomes of aphids infesting different host plants from two tehsils namely; Jawali and Kangra in Kangra district of Himachal Pradesh were studied. These aphids species are, zAcyrthosiphon gossypii Mordvilko (2n=6), Aphis punicae Passerini (2n=8), Brachycaudushelichrysi (Kaltenbach) (2n=12), Hyperomyzuslactuae (Linnaeus) (2n=12), Macrosiphoniella sanborni (Gillette) (2n=12), Macrosiphum euphorbiae (Thomas) (2n=10), Myzusascalonicus Doncaster (2n=12), M. ornatus Liang (2n=12), Toxopteraaurantii (Boyer de Fonscolombe) (2n=8), Toxopteraodinae (van der Goot) (2n=8), Uroleuconambrosiae (Linnaeus) (2n=12). The actual lengths, relative lengths and total complement length (TCL) of chromosomes were measured at metaphase. Karyotypes were prepared and idiograms were constructed based on relative lengths data.

Summary

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Plain-language reading of the full paper, prepared with AI and checked against the text. Each point links to the authors' own words.

  1. Why it matters

    • Aphids are harmful pests that damage agricultural and horticultural crops by feeding on sap and transmitting viral infections. View evidence ↗

      Why it matters

      Aphids are harmful pests that damage agricultural and horticultural crops by feeding on sap and transmitting viral infections.

      In the paper's own words

      “Aphids inflict significant harm to a variety of agricultural and horticultural crops by feeding on plant sap and spreading viral infections to various parts of plant”

      Page 1

      Found in: Introduction

      Read it in the full textOpen PDF at page 1 ↗
    • Studying aphid cytogenetics is useful for identifying species-specific chromosomal markers, simplifying otherwise difficult identification work. View evidence ↗

      Why it matters

      Studying aphid cytogenetics is useful for identifying species-specific chromosomal markers, simplifying otherwise difficult identification work.

      In the paper's own words

      “Aphid cytogenetic investigation is beneficial because it aids in the discovery of species-specific chromosomal markers, which makes a work that is now deemed tough much easier”

      Page 1

      Found in: Introduction

      Read it in the full textOpen PDF at page 1 ↗
    • Because aphid species often show karyotype variations, the authors decided to investigate chromosomes of species found on various host plants in the Jawali and Kangra tehsils of Himachal Pradesh. View evidence ↗

      Why it matters

      Because aphid species often show karyotype variations, the authors decided to investigate chromosomes of species found on various host plants in the Jawali and Kangra tehsils of Himachal Pradesh.

      In the paper's own words

      “Keeping this in view the frequent karyotype variations in many species of aphids, it was considered worth to investigate the chromosomes of some species take over different host plants in Jawali and Kangra tehsils of Kangra district of Himachal Pradesh.”

      Page 1

      Found in: Introduction

      Read it in the full textOpen PDF at page 1 ↗
  2. The question

    • The study aimed to examine the chromosomes of various aphid species infesting different host plants in the Jawali and Kangra tehsils of Himachal Pradesh. View evidence ↗

      The question

      The study aimed to examine the chromosomes of various aphid species infesting different host plants in the Jawali and Kangra tehsils of Himachal Pradesh.

      In the paper's own words

      “Chromosomes of aphids infesting different host plants from two tehsils namely; Jawali and Kangra in Kangra district of Himachal Pradesh were studied.”

      Page 1

      Found in: Introduction

      Read it in the full textOpen PDF at page 1 ↗
  3. What they did

    • The researchers collected apterous, viviparous, parthenogenetic female aphids from the twigs, leaves, and inflorescences of several host plants. View evidence ↗

      What they did

      The researchers collected apterous, viviparous, parthenogenetic female aphids from the twigs, leaves, and inflorescences of several host plants.

      In the paper's own words

      “Female aphids infesting twigs, leaves, and influorescence of several host plants were gathered from various locations as apterous, viviparous, parthenogenetic female aphids.”

      Page 1

      Found in: Research Materials and Techniques Identification

      Read it in the full textOpen PDF at page 1 ↗
    • Somatic embryonic tissue from parthenogenetic females was used for the chromosomal analysis. View evidence ↗

      What they did

      Somatic embryonic tissue from parthenogenetic females was used for the chromosomal analysis.

      In the paper's own words

      “For the chromosomal study, somatic embryonic tissue of parthenogenetic females was used.”

      Page 2

      Found in: Research Materials and Techniques Identification

      Read it in the full textOpen PDF at page 2 ↗
    • Chromosome slides and coverslips were stained with 2% Giemsa for a duration of 20 to 30 minutes. View evidence ↗

      What they did

      Chromosome slides and coverslips were stained with 2% Giemsa for a duration of 20 to 30 minutes.

      In the paper's own words

      “20–30 minutes were spent staining chromosome coverslips and slides with 2% Giemsa.”

      Page 2

      Found in: Research Materials and Techniques Identification

      Read it in the full textOpen PDF at page 2 ↗
    • Chromosome lengths were measured using an ocular micrometre. View evidence ↗

      What they did

      Chromosome lengths were measured using an ocular micrometre.

      In the paper's own words

      “Using an ocular micrometre, the lengths of the chromosomes were determined.”

      Page 2

      Found in: Research Materials and Techniques Identification

      Read it in the full textOpen PDF at page 2 ↗
  4. What they found

    • Acyrthosiphon gossypii was found to have a diploid chromosome number of 2n=6. View evidence ↗

      What they found

      Acyrthosiphon gossypii was found to have a diploid chromosome number of 2n=6.

      In the paper's own words

      “Acyrthosiphon gossypii Mordvilko... with six diploid chromosomes (2n=6)”

      Page 2

      Found in: Discussion

      Read it in the full textOpen PDF at page 2 ↗
    • Three species, Aphis punicae, Toxoptera odinae, and Toxoptera aurantii, were found to have a diploid chromosome number of 2n=8. View evidence ↗

      What they found

      Three species, Aphis punicae, Toxoptera odinae, and Toxoptera aurantii, were found to have a diploid chromosome number of 2n=8.

      In the paper's own words

      “Aphis punicae... The number of chromosomes was discovered to be eight (2n=8)”

      Page 3

      “T. odinae... The number of diploid chromosomes in these aphids is eight (2n = 8).”

      Page 5

      “Toxoptera aurantii... The number of diploid chromosomes in this group is eight (2n = 8).”

      Page 5

      Found in: Aphis punicae Passerini

      Read it in the full textOpen PDF at page 3 ↗
    • Macrosiphum euphorbiae was identified as having a diploid chromosome number of 2n=10. View evidence ↗

      What they found

      Macrosiphum euphorbiae was identified as having a diploid chromosome number of 2n=10.

      In the paper's own words

      “Macrosiphum euphorbiae (Thomas)... This species had a total of ten (2n=10) diploid chromosomes”

      Page 4

      Found in: Discussion

      Read it in the full textOpen PDF at page 4 ↗
    • Six species, Brachycaudus helichrysi, Hyperomyzus lactuae, Macrosiphoniella sanborni, Myzus ascalonicus, Myzus ornatus, and Uroleucon ambrosiae, were found to have a diploid chromosome number of 2n=12. View evidence ↗

      What they found

      Six species, Brachycaudus helichrysi, Hyperomyzus lactuae, Macrosiphoniella sanborni, Myzus ascalonicus, Myzus ornatus, and Uroleucon ambrosiae, were found to have a diploid chromosome number of 2n=12.

      In the paper's own words

      “Brachycaudus helichrysi... 2n=12 was discovered to be the chromosomal number”

      Page 3

      “Hyperomyzus lactuae... The number of diploid chromosomes (2n=12) was discovered to be twelve”

      Page 4

      “Macrosiphoniella sanborni... Twelve (2n=12) diploid chromosomes were discovered”

      Page 4

      “Myzus ascalonicus... The number of diploid chromosomes in these aphids is twelve (2n=12)”

      Page 4

      “M. ornatus... The number of diploid chromosomes in these aphids is twelve (2n=12)”

      Page 5

      “Uroleucon ambrosiae... The number of diploid chromosomes was discovered to be twelve (2n=12)”

      Page 5

      Found in: Discussion

      Read it in the full textOpen PDF at page 3 ↗
    • For Acyrthosiphon gossypii, the average total complement length (TCL) of chromosomes was 16.90 µm ±0.30. View evidence ↗

      What they found

      For Acyrthosiphon gossypii, the average total complement length (TCL) of chromosomes was 16.90 µm ±0.30.

      In the paper's own words

      “The total complement length (TCL) was 16.90 µm ±0.30 on average.”

      Page 2

      Found in: Acyrthosiphon gossypii Mordvilko

      Read it in the full textOpen PDF at page 2 ↗
    • Aphis punicae exhibited an average total complement length (TCL) of 17.78 µm ±0.55. View evidence ↗

      What they found

      Aphis punicae exhibited an average total complement length (TCL) of 17.78 µm ±0.55.

      In the paper's own words

      “Total complement length (TCL) was 17.78 µm ±0.55 on average.”

      Page 3

      Found in: Aphis punicae Passerini

      Read it in the full textOpen PDF at page 3 ↗
    • Myzus ornatus had a total complement length of 32.18 µm ±0.70. View evidence ↗

      What they found

      Myzus ornatus had a total complement length of 32.18 µm ±0.70.

      In the paper's own words

      “The length of the total complement was 32.18 µm ±0.70.”

      Page 5

      Found in: M. ornatus Laing

      Read it in the full textOpen PDF at page 5 ↗
  5. What it means

    • The authors conclude that their findings for Aphis punicae (2n=8) are consistent with previous chromosomal reports. View evidence ↗

      What it means

      The authors conclude that their findings for Aphis punicae (2n=8) are consistent with previous chromosomal reports.

      In the paper's own words

      “The diploid chromosome number 2n=8 in A. punicae was in confirmity with earlier chromosomal accounts given by (Panigrahy & Patnaik, 1987)”

      Page 6

      Found in: Discussion

      Read it in the full textOpen PDF at page 6 ↗

Figures & tables

From the original paper
Aphid species along with host plant, place and period of collection. Fig.1.Table 1Page 2Aphids infestind different plantsFigure 1Page 2Figures of KaryotypeFigure 2Page 3Fig 3Figure 3Page 3Fig 4Figure 4Page 4Fig 5Figure 5Page 4Fig 6Figure 6Page 5
FULL TEXT Original article · reflowed for reading

Introduction

Aphids inflict significant harm to a variety of agricultural and horticultural crops by feeding on plant sap and spreading viral infections to various parts of plant (Kennedy et al., 1962) [13] . This group of plant sap sucking insects contains approximately 5000 species described worldwide in about 510 genera infesting about 300 plant families (R L Blackman & Eastop, 2006; Roger L Blackman & Eastop, 2000; Gavrilov-Zimin et al., 2015) [1,2,9] . Aphids have a number of peculiar phenomenon in their life cycle such as polymorphism, viviparity, telescoping of generation, host alternation and holocentric chromosomes. Most of the aphids are heteroecious, exploiting both primary and secondary host plants. Holocyclic aphids have a sequence of parthenogenesis in few generations followed by a single sexual generation, whereas in anholocyclic aphids sexual portion of life cycle lost (Moran, 1992) [20] . In aphids, the XX-XO type of sex determination is used. Aphid X chromosomes have received a lot of interest since they contain a lot of structural limitations (Manicardi et al., 2002) [19] . All fertilized eggs of sexual females produce parthenogenetic females only. To generate a male, an egg must lose half of the sex chromatin of the parent female during a single maturation division. To produce a male, an egg must shed 50% of the parent female's sex chromatin during a single maturation division. During development of the male oocyte, the X chromosomes are coupled end-to-end to create a condensed C-shaped bivalent, according to (Orlando, 1965). When the pairing products split, one X chromosome proceeds to the spindle's end while the other divides equationally with autosomes, leaving just one chromatid of the original X bivalent in the developing male egg. The X chromosomes in presumptive male oocytes form a looping structure and then in middle, a nucleolus like spherical body develops which maintains cohesion between two X chromosomes Blackman (1986). In female developing oocytes, there occurs no such association of X chromosomes. According to scientist (Jaquiéry et al., 2012), evolutionary pressures have a significant influence in evolution of X chromosome in aphids, which have an XO system in which males are hemizygous (XO) and females are homozygous (XX). Aphid cytogenetic investigation is beneficial because it aids in the discovery of species-specific chromosomal markers, which makes a work that is now deemed tough much easier (Rakauskas, 1998) [23] . Classical and molecular cytogenetics work together to investigate the structure and evolutionary history of aphid holocentric chromosomes (Mandrioli & Carlo Manicardi, 2012) [18] . Kangra in Himachal Pradesh is rich in diverse type of vegetation. Keeping this in view the frequent karyotype variations in many species of aphids, it was considered worth to investigate the chromosomes of some species take over different host plants in Jawali and Kangra tehsils of Kangra district of Himachal Pradesh.

Research Materials and Techniques Identification

Female aphids infesting twigs, leaves, and influorescence of several host plants were gathered from various locations as apterous, viviparous, parthenogenetic female aphids. Key developed by Blackman & Eastop (1984) was used for identification of different aphids species. The detail of aphid species along with host plants, place & collection time are given in Table I. For the chromosomal study, somatic embryonic tissue of parthenogenetic females was used. The aphids dissected by puncturing the posterior part (end) of the abdomen and then processed for 25-30 minutes with a 0.7 percent trisodium citrate solution. For 15 to 20 minutes, these embryos were preserved in a 1:3 acetic-ethanol solution. After stabilising the embryos, they were put for 3 to 5 minutes on a glass slide in a drop of 45 percent acetic acid. A coverslip was placed on the slide. The slide and coverslip then lightly tapped with the blunt end of the forcep between two layers of blotting sheets. With a sharp jerk, the coverslip was thrown off the slide. After that, both the coverslips and the slides were dried in a dustfree environment. 20-30 minutes were spent staining chromosome coverslips and slides with 2% Giemsa. Dipped slides in xylene and mounting them in DPX made them permanent. Photomicrographs were obtained, while the slides were being inspected using a binocular microscop. Using an ocular micrometre, the lengths of the chromosomes were determined.

Actual chromosomal lengths, the total complement lengths, and relative chromosome lengths were determined. Data about relative lengths was used to create the idiograms.

Results

In the current study, the most common diploid chromosomal numbers reported are 8 and 12.

Acyrthosiphon gossypii Mordvilko

Green aphids with bands were discovered infesting the lower side of leaves and flowers, with six diploid chromosomes (2n=6) (Figs. 1a,1b). The mean actual length of chromosomes measured on well dispersed metaphase plates ranged from 2.34 m 0.09 to 3.60 m 0.05. The total complement length (TCL) was 16.90 µm ±0.30 on average. The chromosomes' relative lengths ranged from 11.32µm ±0.30 to 0000. This species' idiogram revealed two pairs of lengthy and two pairs of increasingly shrinking chromosomes (Fig. 1c).

Aphis punicae Passerini

Aphis punicae, a green-colored aphid, was collected from the immature leaves and stem of Punica granatum. The number of chromosomes was discovered to be eight (2n=8) (Figs. 2a,2b). The mean actual length of chromosomes measured on metaphase plates ranged from 1.29 µm ±0.74 to 2.97 µm ±0.05. Total complement length (TCL) was 17.78 µm ±0.55 on average. The chromosomes' relative lengths ranged from 6.87µm ±0.40 to 16.77µm ±0.35. This species' idiogram revealed a pair of lengthy chromosomes and three pairs of increasingly decreasing chromosomes (Fig. 2c).

Hyperomyzus lactuae (Linnaeus)

Hyperomyzus lactuae aphids were collected from the stems, leaves, and flowers of the host plant Sonchus arvensis. The number of diploid chromosomes (2n=12) was discovered to be twelve (Figs. 4a,4b). Chromosome lengths ranged from 1.21 µm ±0.06 to 2.90 µm ±0.05. The length of the total complement was 24.90 µm ±0.52. Chromosome relative lengths varied from 4.87µm ±0.19 to 11.67µm ±0.02. The idiogram revealed a progressive decrease in the length of chromosomes (Fig. 4c).

Macrosiphoniella sanborni (Gillete)

This species of aphid was found on immature apical shoots and stems of plants and was dark reddish brown in colour. Twelve (2n=12) diploid chromosomes were discovered (Figs. 5a,5b). The actual length of chromosomes ranged from 0.45 µm ±0.05 to 2.69 µm ±0.05, according to measurements of well scattered metaphase plates. TCL was 17.60 µm ±0.42. Chromosome relative lengths varied between 2.55 µm ±0.23 to 15.36 µm ±0.49. A pair of long, two pairs of medium, and three pairs of short chromosomes were displayed in the idiogram (Fig. 5c).

Macrosiphum euphorbiae (Thomas)

This species' aphids had a light green colour to them. This species had a total of ten (2n=10) diploid chromosomes (Figs. 6a,6b). Chromosome lengths varied between 0.94 µm ±0.14 and 3.79 µm ±0.29. 23.05 µm ±0.82 was the total complement length. Chromosomes ranged in relative length from 3.97 µm ±0.36 to 16.57µm ±0.52. This species idiogram revealed a pair of chromosomes that is long, a pair of medium-sized chromosomes, and three pairs of short chromosomes that steadily decreased in size (Fig. 6c).

Myzus ascalonicus Doncaster

This species' aphids ranged in colour from pale yellow to dark green. The number of diploid chromosomes in these aphids is twelve (2n=12) (Figs. 7a,7b). The actual length of chromosomes in these aphids ranged from 1.47 µm ±0.07 to 3.46 µm ±0.08. The length of the total complement was 29.54 µm ±0.66. The chromosomes' relative lengths ranged from 4.88 µm ±0.21 to 11.76 µm ±0.14. This species' idiogram revealed a progressive decrease in chromosomal length (Fig. 7c).

M. ornatus Laing

This kind of aphid is tiny and light green to pale yellow in colour. The number of diploid chromosomes in these aphids is twelve (2n=12) (Figs. 8a,8b). Actual chromosome lengths ranged from 1.57µm ±0.06 in the shortest chromosome to 3.89 µm ±0.04 in the longest chromosome. The length of the total complement was 32.18 µm ±0.70. The chromosomes' relative lengths ranged from 4.89 µm ±0.09 to 12.14 µm ±0.24. This species' idiogram revealed a progressive decrease in chromosomal length (Fig. 8c).

Toxoptera aurantii (Boyer de Fonscolombe)

Aphids had black and white banded antennae, as well as black siphunculi and cauda, and were tiny, round, shiny, brownish red. The number of diploid chromosomes in this group is eight (2n = 8). (Figs. 9a,9b). Actual chromosomal lengths ranged from 1.82 µm ±0.04 to 3.46 µm ±0.07. The length of the total complement was 20.37 µm ±0.22. The chromosomes' relative lengths ranged from 8.92 µm ±0.12 to 16.98 µm ±0.18. This species' idiogram revealed a pair of long, a pair of medium, and two pairs of short chromosomes (Fig. 9c).

T. odinae (van der Goot)

These were little to medium in size, ant-attended and greenish dull or grey brown in colour. The abdomen of alatae is reddish-brown to dark brown in colour. The number of diploid chromosomes in these aphids is eight (2n = 8). (Figs. 10a,10b). Actual chromosomal lengths ranged from 1.82 µm ±0.04 to 2.87 µm ±0.08. The length of the total complement was 18.90 µm ±0.30. The chromosomes' relative lengths varied from 9.64µm ±0.24 to 15.16µm ±0.25. This species' idiogram revealed a progressive reduction in chromosomal length (Fig. 10c).

Uroleucon ambrosiae (Linnaeus)

Uroleucon ambrosiae ranges in colour from dark reddish brown to nearly black. These were taken from the stem leaves and near the flower bud of Sonchus olerceaus, the host plant. The number of diploid chromosomes was discovered to be twelve (2n=12) (Figs. 11a,11b). The mean actual length of chromosomes measured on well dispersed metaphase plates ranged from 1.47µ m ±0.09 to 3.71 µm ±0.06. Total complement length (TCL) was 29.01µm ±2.20 on average. The chromosomes' relative lengths ranged from 4.63µm ±0.09 to 11.99µm ±0.78. This species' idiogram revealed a progressive decrease in chromosomal length (Fig. 11c).

Discussion

The chromosome number 2n=8 was found in three species in this investigation, while 2n=12 was found in six species. In addition, 2n=10 and 2n=6 were identified in one species each. In the current study, Acrythosiphon gossypii with the lowest chromosome number 2n=6 was found in Abelmoschus esculentus. However, earlier variations have been recorded in this species with 2n=6, 8, 10, 12, 14 and 16. Many workers reported 2n=8 in A. gossypii but from different host plants (Kulkarni & Kacker, 1979; Kurl, 1978) [14,15] . Gautam reported karyotypes of 21 species of aphids and various chromosomes were studied (Gautam, 2002, 2003) [7] . Gautam and Kumar reported karyotypes of aphids infesting Quercus and Rhododendron (Gautam, 2006) [8] . The chromosome number (2n=8) was reported in 3 species of present study, Aphispunicae (Passerini) collected from Punica granatum, Toxoptera aurantii and T. odinae collected from Citrus medica and Duranta erecta. The diploid chromosome number 2n=8 in A. punicae was in confirmity with earlier chromosomal accounts given by (Panigrahy & Patnaik, 1987) [22] . (Samkaria et al., 2010) [25] Same diploid chromosome number in T. aurantii also reported. T. odinae had the same diploid chromosomal number (2n = 8) as Kurl (1980) [15] . Macrosiphum euphorbiae has the diploid chromosomal number 2n=10. Macrosiphum is a polyphagous North American species that eats up to 200 different plant species from 20 different families (Le Roux et al., 2010) [17] . In the present investigation, M. euphorbiae was collected from Malva parviflora revealed the diploid chromosome number as 2n=10.

In present investigation chromosome number as 2n=12 was observed in six species namely; Brachycaudus helichrysi (Kaltenbach) collected from Ageratum sp., Hyperomyzus lactuae collected from host plant Sonchus, Macrosiphoniella sanborni was collected from Chrysanthemum, Myzus ascalonicus collected from Dahlia pinnata, M. ornatus collected from Ajuga bracteosa and Uroleucon ambrosiae collected from host plant Sonchus olerceaus. 2n=12 in B. helichrysi confirmed by earlier reports of (Dutta, 1993) [5] from Artemisia vestita, (Kuznetsova, 1968) reported 2n + 10 in aphids from Prunus sp. While (Raychaudhuri & Das, 1987) [24] reported 2n=10 in B. helichrysi collected from Brassica napus. In M. sanborni, the same diploid chromosomal number (2n=12) was reported by (R L Blackman & Eastop, 2006; Boschetti, 1963; Dutta, 1993) [1,3,5] . 2n=10 has also been found in M. sanborni by (Chen, 1985) [4] . The number of diploid chromosomes in the genus Myzus ranges from 8 to 20 in different species. Here, two species of Myzus has been investigated. M. ascalonicus collected from Dahlia pinnata and M. ornates collected from Ajuga bracteosa. Uroleucon ambrosiae collected from host plant Sonchus olerceaus. Diverse researchers have counted the number of diploid chromosomes in this genus's diverse member (Gut, 1976; Kar et al., 1990) [10] .

Acknowledgement

AcknowledgmentsKanika Choudhary acknowledges CSIR-JRF New Delhi, Council of Scientific & Industrial Research. Authors duly acknowled Professor of Department of Biosciences, Himachal Pradesh University for providing facilities to carry out the work. This research did not receive any specific grant from funding agencies in the public, commercial, or not-for-profit sectors.

Figures and tables from the paper

Table 1. Aphid species along with host plant, place and period of collection. Fig.1.
Species of AphidsHost plantsCollection siteCollection time
Acyrthosiphon gossypiiAbelmoschus esculentusNagrota Surian, KangraOctober, 2017
Aphis punicaePunica granatumNagrota Surian, KangraOctober, 2017
Brachycaudus helichrysiAgeratum houstonianuNagrota Surian, KangraOctober, 2017
Hyperomyzus lactuaeSonchus arvensisNurpur, KangraApril, 2017
Macrosiphoniella sanborniChrysanthemum indicumAnsoli, KangraOctober, 2017
Macrosiphum euphorbiaeMalva parvifloraIchhi, KangraSeptember, 2017
Myzus ascalonicusDahlia pinnataAnsoli, KangraSeptember, 2017
M. ornatusAjuga bracteosaAnsoli, KangraSeptember, 2017
Toxoptera aurantiiCitrus medicaMatour, KangraOctober, 2017
T. odinaeDuranta erectaIchhi, KangraOctober, 2017
Uroleucon ambrosiaeSonchus olerceausJawali , KangraApril, 2017

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Table 1
Aphid species along with host plant, place and period of collection. Fig.1.

Aphid species along with host plant, place and period of collection. Fig.1.

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Figure 1. Aphids infestind different plants
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Aphids infestind different plants

Aphids infestind different plants

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Figure 2. Figures of Karyotype
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Figures of Karyotype

Figures of Karyotype

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References

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