HOST DISCRIMINATION BY A CRUCIFER-FEEDING FLEA BEETLE, PHYLLOTRETA STRIOLATA (F.) (COLEOPTERA: CHRYSOMELIDAE)

1990 ◽  
Vol 122 (5) ◽  
pp. 817-824 ◽  
Author(s):  
R.J. Lamb ◽  
P. Palaniswamy
Keyword(s):  
Small Groups ◽  
Host Selection ◽  
Raphanus Sativus ◽  
Host Plants ◽  
Flea Beetle ◽  
Natural Populations ◽  
Host Discrimination ◽  
Phyllotreta Striolata ◽  
Feeding Experiments ◽  
Cruciferous Plants

AbstractThe flea beetle, Phyllotreta striolata (F.), was attracted to the cruciferous plants Brassica oleracea L. and Raphanus sativus L., but not to B. campestris L. and B. napus L. which are important natural host plants, nor to Pisum sativum (L.), a legume. The presence or absence of attraction was demonstrated by exposing small groups of caged plants to natural populations and trapping beetles near the plants. In choice and no-choice laboratory feeding experiments, P. striolata fed on eight Cruciferae in the genera Brassica, Raphanus, and Sinapis but not on P. sativum. Phyllotreta striolata fed less on S. arvensis L. and S. alba L. than on plants in the other genera. Within Brassica, B. oleracea, B. napus, and B. campestris were preferred over B. juncea (L.) Czern and B. nigra (L.) Koch. Discrimination at the attraction phase of host selection did not account for discrimination shown in laboratory feeding experiments nor in the natural attack of flea beetles on cruciferous crops.

OCCURRENCE OF PHYLLOTRETA STRIOLATA, THE STRIPED FLEA BEETLE, IN OPEN PRAIRIE, FOREST, AND PARKLAND OF SASKATCHEWAN (COLEOPTERA: CHRYSOMELIDAE)

1982 ◽  
Vol 114 (5) ◽  
pp. 439-446 ◽  
Author(s):  
L. Burgess
Keyword(s):  
Host Plants ◽  
Laboratory Experiments ◽  
Flea Beetle ◽  
Forest Edge ◽  
The North ◽  
Phyllotreta Striolata ◽  
Arctic Regions ◽  
Adequate Food ◽  
Laboratory Colony ◽  
Cruciferous Plants

AbstractIn Saskatchewan the range of Phyllotreta striolata (F.), a pest of parkland rapeseed crops, includes the open prairie in the southwest and the boreal forest in the north. The population of P. striolata on the open prairie is small, with cruciferous weeds being the major host plants. Cruciferous crops grown on the open prairie will almost certainly attract some P. striolata. The population of P. striolata in the forest is substantial, and the range extends northward into arctic regions. Although adults of P. striolata feed upon cruciferous plants growing in the forest, these plants do not appear abundant enough to constitute an adequate food supply. In addition, the identity of the major host plants of the larvae in the forest is unknown. In laboratory experiments, adults of P. striolata were attracted to and attempted to feed upon seven species of forest mosses; however, attempts to maintain a laboratory colony of P. striolata on one of the more abundant mosses were unsuccessful. Forest inhabiting P. striolata attacked rape planted in forest clearings, and therefore probably would infest rape crops grown along the forest edge or in newly cleared areas.

MAINTAINING A COLONY OF THE STRIPED FLEA BEETLE, PHYLLOTRETA STRIOLATA (COLEOPTERA: CHRYSOMELIDAE), IN THE GREENHOUSE

1976 ◽  
Vol 108 (1) ◽  
pp. 53-55 ◽  
Author(s):  
L. Burgess ◽  
J. E. Wiens
Keyword(s):  
Life Cycle ◽  
Host Plant ◽  
Flea Beetle ◽  
Natural Populations ◽  
Suitable Host ◽  
Armoracia Rusticana ◽  
Phyllotreta Striolata ◽  
Small Colony

AbstractA small colony of the striped flea beetle, Phyllotreta striolala (F.), has been maintained in a cage in the greenhouse for more than 21/2 years. Horseradish [Armoracia rusticana (Lam) Gaertn., Mey. & Scherb.] was found to be a suitable host plant, and the caged beetle colony has followed a similar life cycle to natural populations in the field.

PHAGODETERRENCY INDUCED BY TWO CRUCIFEROUS PLANTS IN ADULTS OF THE FLEA BEETLE PHYLLOTRETA STRIOLATA (COLEOPTERA: CHRYSOMELIDAE)

1983 ◽  
Vol 115 (9) ◽  
pp. 1209-1214 ◽  
Author(s):  
J. Meisner ◽  
B. K. Mitchell
Keyword(s):  
Flea Beetle ◽  
Chemical Compounds ◽  
Feeding Deterrents ◽  
Thlaspi Arvense ◽  
Phyllotreta Striolata ◽  
Alkaloid Fraction ◽  
Cruciferous Plants

AbstractThe two cruciferous plants Thlaspi arvense and Lunaria annua are largely unacceptable to the striped flea beetle, Phyllotreta striolata, which normally feeds on cruciferous plants. Results suggest that these plants contain chemical compounds that act as feeding deterrents to the beetles. Methanol fractions of the leaves of both plants deterred feeding when added to the surface of acceptable radish leaves. An alkaloid fraction of Lunaria annua was, surprisingly, not deterrent. Evidence suggests that saponins in both Lunaria annua and Thlaspi arvense may be a major reason for the low acceptability of these plants as food for Phyllotreta striolata. Commercial saponins are highly deterrent at concentrations of 0.05% and above.

CHAETOCNEMA CONCINNA (MARSHAM, 1802), A EUROPEAN FLEA BEETLE INTRODUCED IN NORTH AMERICA (COLEOPTERA: CHRYSOMELIDAE: ALTICINAE)

1990 ◽  
Vol 122 (4) ◽  
pp. 647-650
Author(s):  
Laurent Lesage
Keyword(s):  
Nova Scotia ◽  
North America ◽  
Prince Edward Island ◽  
Host Plants ◽  
Flea Beetle ◽  
Collection Data ◽  
First Time

AbstractChaetocnema concinna (Marsham, 1802), a European flea beetle, is reported for the first time from Canada. Preliminary collection data indicate that it may feed on the same host plants as in Europe. It has been collected to date in Prince Edward Island, Nova Scotia, and Maine.

Phyllotreta striolata. [Distribution map].

1994 ◽  
Author(s):  
Keyword(s):  
New York ◽  
North Carolina ◽  
West Bengal ◽  
Flea Beetle ◽  
Peninsular Malaysia ◽  
Distribution Map ◽  
Phyllotreta Striolata ◽  
Kurile Islands ◽  
New Distribution ◽  
Distribution In Europe

Abstract A new distribution map is provided for Phyllotreta striolata (Fabricius) Coleoptera: Chrysomelidae, Alticinae Striped flea beetle, turnip flea beetle. Attacks turnip, cabbage, rape and other Cruciferae. = Phyllotreta vittata(Fabricius) Information is given on the geographical distribution in EUROPE, Albania, Austria, Belgium, Bulgaria, Crete, Czech, Republic Denmark, Estonia, Finland, France, Germany, Greece, Hungary, Irish, Republic Italy, Luxembourg, Netherlands, Norway, Poland, Slovakia, Spain, Sweden, Switzerland, United Kingdom, Yugoslavia, RUSSIA, Amur, Irkutsk, Kamchatka, Karelia, Khabarovsk, Kiev, Leningrad, Magadan, Primorye, Ryazan, Sakhalin, Smolensk, ASIA, Andaman Islands, Bhutan, Burma, China, Anhui, Fujian, Gansu, Guangdong, Guangxi, Hainan, Heilongjiang, Hubei, Hunan, Jiangsu, Xizhang, Hong Kong, India, Assam, Tripura, West Bengal, Indonesia, Java, Sumatra, Japan, Korea, Kurile Islands, Malaysia, Sarawak, Peninsular Malaysia, Mongolia, Myanmar, Nepal, Okinawa, Sikkim, Singapore, Taiwan, Thailand, Tibet, Vietnam, NORTH AMERICA, Canada, Alberta, British Columbia, Manitoba, Ontario, Quebec, Saskatchewan, USA, California, Connecticut, Florida, Illinois, Kansas, Louisiana, Maryland, Mississippi, New Hampshire, New Jersey, New York, North Carolina, Ohio, Pennsylvania, Tennessee, Texas, Virginia, Wisconsin.

Factors affecting the response ofLongitarsus jacobaeae(Coleoptera: Chrysomelidae) to upwind plant odours

1996 ◽  
Vol 86 (3) ◽  
pp. 307-313
Author(s):  
Zhi-Qiang Zhang ◽  
Peter B. McEvoy
Keyword(s):  
Wind Tunnel ◽  
Host Plants ◽  
Local Density ◽  
Flea Beetle ◽  
Late Summer ◽  
Developmental State ◽  
Early Summer ◽  
Directed Movement ◽  
Factors Affecting ◽  
Plant Odours

AbstractFactors (developmental state, starvation time, host local density and host distance from insects) affecting the response of the ragwort flea beetle,Longitarsus jacobaeae(Waterhouse), to upwind plants of tansy ragwort,Senecio jacobaeae(Compositae), were examined in a wind tunnel. There was seasonal variation in beetle response to host odours. Individuals collected during spring and early summer (6 May to 14 July 1993) showed directed movement toward the upwind plants. However, individuals collected in mid-summer (23 July 1993) showed no significant response to upwind host plants and walked randomly in the wind tunnel. Individuals collected during late summer to autumn (4 August to 23 October 1994) once again showed response to upwind plants, whereas those collected in winter (January 1994) walked randomly in the wind tunnel. The absence of beetle response to plant odours coincided with potential summer aestivation and winter ‘hibernation’. For spring and early summer beetles that responded to plant odours, the strength of the response did not change significantly with the number of plants (1, 2, 4 or 6) presented upwind in the tunnel nor with the starvation time (2, 6, 10, 12, 24 or 36 h) of the tested beetles, and these patterns were consistent for male and female beetles. Individuals responded to plants from a distance of 60 and 300 cm. The speed of movement, similar for males and females, increased slightly asL. jacobaeaeoriented more directly toward host plants.

scholarly journals The Bacterial Flora Associated with the Polyphagous Aphid Aphis gossypii Glover (Hemiptera: Aphididae) Is Strongly Affected by Host Plants

2019 ◽  
Vol 79 (4) ◽  
pp. 971-984 ◽  
Author(s):  
Shifen Xu ◽  
Liyun Jiang ◽  
Gexia Qiao ◽  
Jing Chen
Keyword(s):  
Host Plant ◽  
Host Plants ◽  
Statistical Tests ◽  
Bacterial Flora ◽  
Aphis Gossypii ◽  
Natural Populations ◽  
Aphid Species ◽  
Ecological Specialization ◽  
Cotton Aphid ◽  
Symbiotic Associations

AbstractAphids live in symbiosis with a variety of bacteria, including the obligate symbiont Buchnera aphidicola and diverse facultative symbionts. The symbiotic associations for one aphid species, especially for polyphagous species, often differ across populations. In the present study, by using high-throughput 16S rRNA sequencing, we surveyed in detail the microbiota in natural populations of the cotton aphid Aphis gossypii in China and assessed differences in bacterial diversity with respect to host plant and geography. The microbial community of A. gossypii was dominated by a few heritable symbionts. Arsenophonus was the most dominant secondary symbiont, and Spiroplasma was detected for the first time. Statistical tests and ordination analyses showed that host plants rather than geography seemed to have shaped the associated symbiont composition. Special symbiont communities inhabited the Cucurbitaceae-feeding populations, which supported the ecological specialization of A. gossypii on cucurbits from the viewpoint of symbiotic bacteria. Correlation analysis suggested antagonistic interactions between Buchnera and coexisting secondary symbionts and more complicated interactions between different secondary symbionts. Our findings lend further support to an important role of the host plant in structuring symbiont communities of polyphagous aphids and will improve our understanding of the interactions among phytophagous insects, symbionts, and environments.

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