Geometric Morphometric Study on Geographic Dimorphism of Codling Moth Cydia pomonella (Lepidoptera, Tortricidae) from North West of Iran

During years 2003—2004, nine geographical populations of codling moth Cydia pomonella (Linnaeus) from 4 north western provinces of Iran were collected. В течение 2003—2004 гг. были собраны экземпляры девяти географических популяций яблонной плодожорки Cydia pomonella (Linnaeus) в 4 северо-западных п...

Full description

Saved in:
Bibliographic Details
Published in:Вестник зоологии
Date:2011
Main Authors: Khaghaninia, S., Mohammadi, S.A., Irani Nejad, K.H., Zahiri, R.
Format: Article
Language:English
Published: Інститут зоології ім. І.І. Шмальгаузена НАН України 2011
Subjects:
Online Access:https://nasplib.isofts.kiev.ua/handle/123456789/65828
Tags: Add Tag
No Tags, Be the first to tag this record!
Journal Title:Digital Library of Periodicals of National Academy of Sciences of Ukraine
Cite this:Geometric Morphometric Study on Geographic Dimorphism of Codling Moth Cydia pomonella (Lepidoptera, Tortricidae) from North West of Iran / S. Khaghaninia, S.A. Mohammadi, K.H. Irani Nejad, R. Zahiri // Вестник зоологии. — 2011. — Т. 45, № 5. — С. 429–437. — Бібліогр.: 25 назв. — англ.

Institution

Digital Library of Periodicals of National Academy of Sciences of Ukraine
_version_ 1859997746186944512
author Khaghaninia, S.
Mohammadi, S.A.
Irani Nejad, K.H.
Zahiri, R.
author_facet Khaghaninia, S.
Mohammadi, S.A.
Irani Nejad, K.H.
Zahiri, R.
citation_txt Geometric Morphometric Study on Geographic Dimorphism of Codling Moth Cydia pomonella (Lepidoptera, Tortricidae) from North West of Iran / S. Khaghaninia, S.A. Mohammadi, K.H. Irani Nejad, R. Zahiri // Вестник зоологии. — 2011. — Т. 45, № 5. — С. 429–437. — Бібліогр.: 25 назв. — англ.
collection DSpace DC
container_title Вестник зоологии
description During years 2003—2004, nine geographical populations of codling moth Cydia pomonella (Linnaeus) from 4 north western provinces of Iran were collected. В течение 2003—2004 гг. были собраны экземпляры девяти географических популяций яблонной плодожорки Cydia pomonella (Linnaeus) в 4 северо-западных провинциях Ирана.
first_indexed 2025-12-07T16:34:12Z
format Article
fulltext UDC 595.782(55) GEOMETRIC MORPHOMETRIC STUDY ON GEOGRAPHIC DIMORPHISM OF CODING MOTH CYDIA POMONELLA (LEPIDOPTERA, TORTRICIDAE) FROM NORTH WEST OF IRAN S. Khaghaninia1, S. A. Mohammadi2, A. M. Srafrazi3, K. H. Irani Nejad1, R. Zahiri4 1 Department of Plant Protection, Faculty of Agriculture, University of Tabriz E-mail: skhaghaninia@tabrizu.ac.ir 2 Department of Agronomy & Plant Breeding, Faculty of Agriculture, University of Tabriz 3 Institute of Plant Pests & Diseases Research, Tehran, Iran 4 Department of Biology, University of Turku, Finland Received 11 May 2010 Accepted 30 March 2011 Geometric Morphometric Study on Geographic Dimorphism of Codling Moth Cydia pomonella (Lepidoptera, Tortricidae) from North West of Iran. Khaghaninia S., Mohammadi S. A., Irani Nejad K. H., Zahiri R. – During years 2003—2004, nine geographical populations of codling moth Cydia pomonella (Linnaeus) from 4 north western provinces of Iran were collected. By preparing 575 images from fore wings and 564 from hind wings, a total of 15 and 11 landmarks were determined for fore and hind wings, respectively. With transforming of landmark’s geometrical data into partial warp scores, 26 and 18 scores were obtained for fore and hind wings, respectively. Canonical correla- tion analysis (CCA) revealed significant correlation between environmental parameters and wing shape variables. Among environmental parameters, wind speed showed the highest correlation with wing shape variables whereas, the correlation between latitude, relative humidity as well as amount of precipitation and wing shape variables was low. Considering the effect of various environmental parameters on wing shape, wind speed was determined as important parameter affecting geographic dimorphism. Among the populations collected from different regions, two geographic population pairs; Meshkinshahr- Mahneshan and Zandjan-Khoramdareh were selected as representative of low and high windy regions, respectively. Relative warp analysis (RWA) of fore and hind wings shape variables in the areas with high and low wind showed shorter and wider fore wings as well as slender and narrower hind wings in pop- ulations from high windy regions compared with populations from low wind regions. Centroid size of fore and hind wings in high windy area populations were smaller compared with those from low windy ones as revealed by t-test. The results showed aerodynamic shape and small size of wings are as adapt- ed traits for powerful flight and its control in high windy regions. Ke y wo r d s: codling moth, Cydia pomonella, geometric morphometry, weather factors, morphologi- cal variation, geographic dimorphism. Ãåîìåòðè÷åñêè-ìîðôîìåòðè÷åñêîå èññëåäîâàíèå ãåîãðàôè÷åñêîãî äèìîðôèçìà ÿáëîííîé ïëîäîæîð- êè Cydia pomonella (Lepidoptera, Tortricidae) â ñåâåðî-çàïàäíîì Èðàíå. Êõàã-õàíèíèà Ñ., Ìîõàììàäè Ñ. À., Èðàíè-Íåäæàä Ê. Í., Çàõèðè Ð. –  òå÷åíèå 2003—2004 ãã. áûëè ñîáðàíû ýêçåìïëÿðû äåâÿòè ãåîãðàôè÷åñêèõ ïîïóëÿöèé ÿáëîííîé ïëîäîæîðêè Cydia pomonella (Linnaeus) â 4 ñåâåðî-çàïàäíûõ ïðîâèíöèÿõ Èðàíà. Âñåãî 15 è 11 ìåòîê ïåðåäíèõ è çàäíèõ êðûëüåâ ñîîòâåòñòâåííî áûëè îïðåäåëåíû ïðè ïîäãîòîâêå 575 èçîáðàæåíèé ïåðåäíèõ êðûëüåâ è 564 èçîáðàæåíèé çàäíèõ êðûëüåâ. 26 ïîêàçàòåëåé äëÿ ïåðåäíèõ êðûëüåâ è 18 – äëÿ çàäíèõ áûëè ïîëó÷åíû ïóòåì òðàíñôîðìàöèè èñõîäíûõ ãåîìåòðè÷åñêèõ äàííûõ ìåòîäîì ÷àñòíîé äåôîðìàöèè. Êàíîíè÷åñêèé êîððåëÿöèîííûé àíàëèç îáíàðóæèâàåò çíà÷èòåëüíóþ êîððåëÿöèþ ìåæäó ïàðàìåòðàìè îêðóæàþùåé ñðåäû è âàðèàáåëüíîñòüþ ôîðìû êðûëüåâ. Èç ïàðàìåòðîâ îêðóæàþùåé ñðåäû îòìå÷åíà íàèáîëüøàÿ êîððåëÿöèÿ ñêîðîñòè âåòðà è âàðèàáåëüíîñòè ôîðìû êðûëüåâ, òîãäà êàê êîððåëÿöèÿ ìåæäó øèðîòîé, îòíîñèòåëüíîé âëàæíîñòüþ, êîëè÷åñòâîì îñàä- êîâ è èçìåí÷èâîñòüþ ôîðìû êðûëà áûëà íèçêîé. Ïðèíèìàÿ âî âíèìàíèå âëèÿíèå ðàçíîîá- ðàçíûõ ïàðàìåòðîâ íà ôîðìó êðûëà, ñêîðîñòü âåòðà áûëà îïðåäåëåíà êàê âàæíûé ôàêòîð, äåé- ñòâóþùèé íà ãåîãðàôè÷åñêèé äèìîðôèçì. Íà îñíîâàíèè ýêçåìïëÿðîâ, ñîáðàííûõ â ðàçíûõ Vestnik zoologii, 45(5): 429—437, 2011 ðåãèîíàõ êàê ïðèìåðû ðåãèîíîâ ñ ñèëüíûìè è ñëàáûìè âåòðàìè, ñîîòâåòñòâåííî, áûëè âûáðà- íû äâå ïàðû ãåîãðàôè÷åñêèõ ïîïóëÿöèé: Ìåøêèíøàõð-Ìàõíåøàí è Çàíäüÿí-Êõîðàìäàðåõ. Àíàëèç îòíîñèòåëüíîãî èñêàæåíèÿ ôîðìû ïåðåäíèõ è çàäíèõ êðûëüåâ â îáëàñòÿõ ñ ñèëüíûìè è ñëàáûìè âåòðàìè îáíàðóæèë áîëåå êîðîòêèå è øèðîêèå ïåðåäíèå êðûëüÿ è áîëåå òîíêèå è óçêèå çàäíèå êðûëüÿ â ïîïóëÿöèÿõ èç ðåãèîíîâ ñ áîëåå ñèëüíûìè âåòðàìè ïî ñðàâíåíèþ ñ ïðåäñòàâèòåëÿìè ïîïóëÿöèé èç ðåãèîíîâ ñ áîëåå ñëàáûìè âåòðàìè. Çíà÷åíèÿ öåíòðîèäîâ ïåðåäíèõ è çàäíèõ êðûëüåâ â ïîïóëÿöèÿõ èç ðåãèîíîâ ñ ñèëüíûìè âåòðàìè áûëè ìåíüøå, ïî ñðàâíåíèþ ñ òàêîâûì èç ðåãèîíîâ ñî ñëàáûìè âåòðàìè, êàê áûëî ïðîâåðåíî ïî êðèòåðèþ Ñòüþäåíòà. Ðåçóëüòàòû ïîêàçûâàþò, ÷òî àýðîäèíàìè÷åñêàÿ ôîðìà è ìàëûé ðàçìåð êðûëüåâ – àäàïòàöèîííûå îñîáåííîñòè äëÿ ñèëüíîãî ïîëåòà è óïðàâëåíèÿ èì â ðàéîíàõ ñ ñèëüíûìè âåò- ðàìè. Êëþ÷å âûå ñ ë î â à: ÿáëîííàÿ ïëîäîæåðêà, Cydia pomonella, ãåîìåòðè÷åñêàÿ ìîðôîìåòðèÿ, ïîãîäíûå ôàêòîðû, ìîðôîëîãè÷åñêàÿ âàðèàöèÿ, ãåîãðàôè÷åñêèé äèìîðôèçì. Introduction More than half of the animal described species are insects (Groombridge, 1992). Therefore, under- standing patterns and processes of biological diversification are central importance in evolutionary biology (DeVries et al., 1997). Study of phenotypic plasticity or biodiversity has attracted interest of most biologists ever since Darwin (Hood, 2000 and Bernardo et al., 2007). Morphological diversities including seasonal and geographic dimorphisms can be related to fitness and thus are a possible target of natural selection (Kemp, 2001 and Bernardo et al., 2007). Wing shape deformations have been important subject in studying of geo- graphic forms of intra species evolution (Adams and Funk, 1997 and Kunkel, 2001). Geometric morphometrics offers a new and powerful method for studying of intra species geographic dimorphism or biological forms (Hood, 2000). The shape of organism is very stable and has high heredity, therefore, study of overall shape similarity is known as an accurate way against quantitative estimations for investigating phylogeny as well as study of shape variability in biological forms (Bookstein, 1989; Rohlf, 1990). The population diversity of Neochlamisus bebbianae as well as Chilo suppressalis were studied by means of geometric morphometrics in north part of America and north part of Iran, respectively (Adams and Funk, 1997 and Zahiri et al. 2004). Insect flight performance, dispersal and resource exploitation are pervasively affected by environmen- tal parameters such as wind speed, temperature, relative humidity and elevation (Lambert, 1972, Epila, 1988, Pasek, 1988 and Jones, 2003). The foraging activity of pollinator insects in relation to weather factors like ambient temperature, relative humidity, wind speed and solar radiation was studied through various investi- gations and significant correlations were found between pollination activity and environmental factors (Szabo, 1980 and Narcis and Jordi, 2000). The objectives of the present study were to study the correlation between environment parameters and wing shape variables as well as to estimate wing shape and size deformations in geographic codling moth pop- ulations from northwest of Iran. Material and methods Nine populations were collected from nine regions spanning north west of Iran: East Azarbayjan (four populations), West Azarbayjan (one population), Ardebil (one population) and Zandjan (three populations) during 2003 and 2004. The populations were collected from a number of sites within each region based on the span areas. To eliminate the effect of host in discrimination of populations, all the specimens were col- lected from only golden apple orchards. The specific specimens from each geographical population were ran- domly selected from moths pooled across collecting sites within a given region. Sampling of fifth instar lar- vae was carried out by single face cardboard fastened around the apple trees at 30 cm distance of ground. For studying wing shape, the collected larvae were reared in rearing dishes separately for each region under laboratory conditions at 25°C, 60% relative humidity and 16/8 (light/dark) photoperiod. After unisti- tation of emerged adults, they were mounted by 00 mounting needles. Permanent slides of fore and hind wings were prepared following Borror et al. (1989) and transformed to digital images (table 1). By selecting homologous spots as landmarks, 15 and 11 landmarks were chosen from fore and hind wings, respectively (fig. 1). Based on Bookstein’s (1989) classification, all the landmarks were type I repre- senting meeting points of wing veins and their attaching points to wing’s margin. Two-dimentional coordinates data for mentioned landmarks were performed from all the studied spec- imens using a Leica stereoscopic microscope, image analyzing system, and Tpsdig software (Rohlf, 1990). By transforming the row coordinate data into shape variables and partial warp scores, 26 and 18 scores were obtained for fore and hind wings, respectively. Canonical correlation analysis was performed to analyze cor- relation between climate parameters and shape variables of fore and hind wings of both sexes in geographi- cal populations using STATISTICA 5.5 software (Moghaddam et al., 1994). Relative warp analysis (RWA) 430 S. Khaghaninia et al. 431Geometric morphometric study on geographic dimorphism of codling moth Cydia pomonella... Fig. 1. Fore and hind wings of Cydia pomonella with landmarks’ positions on them. Ðèñ. 1. Ïåðåäíåå è çàäíåå êðûëî Cydia pomonella ñ ïîëîæåíèåì îïîçíàâàòåëüíûõ òî÷åê íà íèõ. Ta b l e 1. Number of fore and hind wing images taken from various geographic populations of codling moth Òà á ëèö à 1. Êîëè÷åñòâî èçîáðàæåíèé ïåðåäíèõ è çàäíèõ êðûëüåâ ÿáëîííîé ïëîäîæîðêè èç ðàçëè÷íûõ ãåîãðàôè÷åñêèõ ïîïóëÿöèé Mianeh 24 27 51 21 21 42 Salmas 22 26 48 21 25 46 Zandjan 34 31 65 32 30 62 Zunuz 27 27 54 40 29 69 Khoramdareh 31 18 49 31 24 55 Meshkin Shahr 14 22 36 16 22 38 Shabestar 31 23 54 31 28 59 Marageh 32 28 60 35 35 70 Mahneshan 29 28 57 23 28 51 Total 244 230 474 250 242 492 Population Fore wing Hind wing female male total female male total was carried out and wings relative variations in various geographic populations were determined by software tpsrelw. The wing centroid size of male and females of the studied populations were estimated and t-test was used to test the effect of geographical conditions on wing centriod size by SPSS 14.0. Results and discussion Two-way multivariate analysis of variance (MANOVA) based on all shape vari- ables in fore and hind wings revealed indicated significant differences among popula- tions as well as sexes at least for one the shape variable. The non-uniform variables were more effective in differentiation of geographical population especially due to hind wing compared with uniform one (Khaghaninia et al., 2008). Mean annual weather data of studied areas are indicated in table 2. Canonical cor- relation analysis revealed significant correlation between fore wing shape variables and environment factors in both sexes except relative humidity and longitude in males (table 3). Among environment factors, wind speed showed highest correlation with wing shape variables in both sexes whereas relative humidity and elevation showed low cor- relations with environmental factors. Correlation between environmental factors and fore wing shape variables as well as their effectiveness on fore wing deformations in females was greater than males. Various studies demonstrated longest flight capacity of female codling moth in individual flight as well as life time compared with male. This is in agree with more wing effectiveness and deformations of females in comparison to males (Mani et al., 1995, Schumacher et al., 1997, Dorn et al., 1999 and Voigt et al., 1999) 432 S. Khaghaninia et al. Ta b l e 2. Mean annual climate data of studied regions Ò à á ëèö à 2. Ñðåäíåãîäîâûå êëèìàòè÷åñêèå äàííûå èññëåäîâàííûõ ðåãèîíîâ Sampling area Longitude Latitude Temperature, °C Relative humidity, % Precipitation amount, mm Elevation, m Wind speed, km/h Salmas 38.13 44.51 12.0 57 215.3 1337 6.111 Zunuz 38.45 45.75 11.1 56 415.1 1710 9.863 Marageh 37.24 46.16 12.9 49 322.4 1477.7 10.503 Mianeh 37.27 47.42 13.7 51 282.1 1110 8.711 Shabestar 38.11 45.41 - - - 1452 - Mahneshan 36.46 47.40 14.6 48 275.7 1282 10.558 Zandjan 36.41 48.29 11.0 54 313.1 1663 7.191 Khoramdareh 36.11 49.11 11.9 51 301.1 1575 11.480 Meshkin shahr 38.23 47.40 10.7 60 383.9 1568.5 5.157 Ta b l e 3. Canonical correlation coefficient between environment parameters and shape variables of codling moth fore wing in both sexes Ò à á ëèö à 3. Êîýôôèöèåíò êàíîíè÷åñêîé êîððåëÿöèè ïàðàìåòðîâ îêðóæàþùåé ñðåäû è ôîðìû èçìåí÷è- âîñòè ïåðåäíèõ êðûëüåâ ÿáëîííîé ïëîäîæîðêè îáîèõ ïîëîâ Climate parameters Shape variables of female fore wing Shape variables of male fore wing Rc P value percentage Rc P value percentage Longitude 0.456 0.00891 4.03 0.369 0.347 4.48 Latitude 0.470 0.00371 5.23 0.461 0.0094 4.10 Temperature, °C 0.494 0.00067 4.06 0.440 0.029 3.09 Relative humidity, % 0.494 0.00068 5.70 0.378 0.282 4.30 Precipitation amount, mm 0.469 0.00383 5.52 0.518 0.00016 6.15 Elevation, m 0.520 0.000075 4.68 0.487 0.0017 5.30 Wind speed, km/h 0.719 0.000000 9.93 0.694 0.000000 8.31 The trend of correlations between environmental factors and hind wing shape vari- ables were similar to those for fore wing as revealed by canonical correlation analysis, but the amount of correlation coefficients were higher except for elevation (table 4). 433Geometric morphometric study on geographic dimorphism of codling moth Cydia pomonella... Ta b l e 4. Canonical correlation coefficient between environment parameters and shape variables of codling moth hind wing in both sexes Ò à á ëèö à 4. Êîýôôèöèåíò êàíîíè÷åñêîé êîððåëÿöèÿ ïàðàìåòðîâ îêðóæàþùåé ñðåäû è ôîðìû èçìåí÷è- âîñòè çàäíèõ êðûëüåâ ó ÿáëîííîé ïëîäîæîðêè îáîèõ ïîëîâ Climate parameters Shape variables of female fore wing Shape variables of male fore wing Rc P Value percentage Rc P Value percentage Longitude 0.528 0.000001 5.09 0.537 0.000001 4.58 Latitude 0.556 0.000000 5.79 0.552 0.000000 4.74 Temperature, °C 0.426 0.000378 4.49 0.453 0.000241 3.89 Relative humidity, % 0.433 0.000743 5.84 0.478 0.000028 5.75 Precipitation amount, mm 0.543 0.000013 5.48 0.545 0.000000 7.32 Elevation, m 0.454 0.000155 4.44 0.456 0.000184 5.24 Wind speed, km/h 0.661 0.000000 10.72 0.578 0.000000 9.42 Fig. 2. Distribution of codling moth geographic populations through RWA by means of landmarks: females (right); males (left). Ðèñ. 2. Ðàñïðîñòðàíåíèå ãåîãðàôè÷åñêèõ ïîïóëÿöèé ÿáëîííîé ïëîäîæîðêè ñîãëàñíî àíàëèçó îòíî- ñèòåëüíûõ îòêëîíåíèé ñ ïîìîùüþ ìåòîê: ñàìêè (ñïðàâà); ñàìöû (ñëåâà). The influence of wind speed on taking off, landing, recognition of flight trout and its control was repetitively reported. In high windy areas or at windy times, the flying insects accumulate leeward of windbreaks as compared with unsheltered sites (Epila, 1988; Pasek, 1988). Lambert (1972) by studying the effect of wind speed and temper- ature on locusts flight found that insect’s flight was inhibited at conditions with high wind speed and the temperature below 19°C. The discrimination of different geographical populations based on RWA using fore and hind wings shape variables were shown in figure 2. Due to various direct and indi- rect effects of environmental factors on wing shape deformations, incomplete discrim- ination between geographical populations was observed. Because of the highest corre- lation between wind speed among environmental factors, the fore and hind wings defor- mations were studied on two pair populations. RWA based on fore and hind wings landmarks of Meshkinshahr (Mes.) and Mahneshan’s (Mah.) populations as candidate of low and high windy areas, respective- ly revealed well discrimination especially for hind wing (fig. 3). The discrimination pat- 434 Samad Khaghaninia et al. Fig. 3. Distribution of Meshkin Shahr and Mahneshan’s codling moth populations through RWA by means of landmarks: females (right); males (left). Ðèñ. 3. Ðàñïðîñòðàíåíèå ïîïóëÿöèé ÿáëîííîé ïëîäîæîðêè èç ïîïóëÿöèé Ìåøêèí Øàõð è Ìàõíåøàí ÷åðåç RWA ñ ïîìîùüþ ìåòîê: ñàìêè (ñïðàâà); ñàìöû (ñëåâà). terns of these populations were different in view point of fore and hind wings land- marks. Overall wings shape deformation compared with reference picture is showed in fig- ure 4. The results showed shorter and wider fore wing and also slender and narrower hind wing in Mah. compared with Mes. population. Because of higher windy condition in Mah. in comparison with Mes. (mean wind speed of 10.558 and 5.157 km/h, respec- 435Geometric morphometric study on geographic dimorphism of codling moth Cydia pomonella... Fig. 4. Overall deformations in fore wing’s (right) and hind wing’s (left) shape of codling moth: A – pop- ulation of Meshkin Shahr; B – reference shape; C – population of Mahneshan, Numbers show the land- marks. Ðèñ. 4. Âñåñòîðîííÿÿ äåôîðìàöèÿ â ôîðìå çàäíèõ êðûëüåâ (ñëåâà) è ïåðåäíèõ êðûëüåâ (ñïðàâà) ÿáëîííîé ïëîäîæîðêè: À – ïîïóëÿöèÿ èç Ìåøêèí-Øàõð;  – ñòàíäàðòíàÿ ôîðìà; Ñ – ïîïóëÿöèÿ èç Ìàõíåøàí, íîìåðà ïîêàçûâàþò îïîçíàâà-òåëüíûå òî÷êè. Ta b l e 5. T-test results of codling moth wing centroid size in Meshkin Shahr and Mahneshan populations Ò à á ëèö à 5. Ðåçóëüòàòû ïðîâåðêè ðàçìåðà öåíòðîèäà êðûëà ó ÿáëîííîé ïëîäîæîðêè èç ïîïóëÿöèé Ìåøêèí Øàõð è Ìàõíåøàí ïî êðèòåðèþ Ñòüþäåíòà Fore Female 14 29 3.40 x 10-2 3.13 x 10-2 1.024ns Male 22 28 3.16 x 10-2 3.11 x 10-2 0.0005ns Hind Female 16 23 4.11 x 10-2 3.85 x 10-2 0.952ns Male 22 28 3.89 x 10-2 3.41 x 10-2 5.226ns Wing Sex Number Centroid size T Meshkin shah Mahneshanr Meshkin shah Mahneshanr No t e . ns – no significant difference. Ïðèìå÷ àíèå . ns – íåò çíà÷èòåëüíûõ îòëè÷èé. A B C tively) presence of this adapted aerodynamic shape of fore and hind wings in Mah. pop- ulation is predictable. Aerodynamic shaped wings enabled insects to powerful flight and well its control in high windy areas (Epila, 1988; Pasek, 1988). Discrimination of Zandjan (Zan.) and Khoramdareh (Kho.) populations as well as their wing shape deformations based on RWA were similar to Mes. and Mah. populations with reduced degree because of lower differences at wind speed between Zan. and Kho. areas (with wind speed of 7.191 and 11.480 Km/h, respectively) compared with of Mes. and Mah. areas. In high windy areas (Mah. and Kho.), centroid size of fore and hind wings were smaller than those in low windy ones (Mes. and Mah.) but the differences were not significant as revealed by t-test. (table 5, 6). Insect’s small wing is an adapted charac- teristic for orientation and controlling flight in windy regions (Kemp, 2001). Wing cen- troid size differences between Mes. and Mah. were more than of Zan. and Kho. in agreement with their differences at wind speed. Sadeghi et al. (2005) studied population variation of codling moth in Zanjan and Khorasan regions. They reported smaller wing in Zanjan Population compared with Khorasan population. Increased longitude and decreased latitude (colder and more humid condition) in Zanjan than of Khorasan could be the main reasons of these dif- ferences. Alipanah et al. (1994) found elevation as affecting factor on wing size and limited generations and opportunity for better feeding were known as factors contribut- ing to bigger wing in elevated regions. Adams D. C., Funk D. J. Morphometric inferences on sibling species and sexual dimorphism in Neochlamisus bebbianae leaf beetles: multivariate applications of the thin- plate spline // Systematic Biology. – 1997. – 46. – P. 180—194. Alipanah H., Rezapanah M. R., Sari A. R. Study of the morphometric variations of codling moth (Cydia pomonella L.) in some parts of Iran // Proc. 16th Iranian Plant Protection Congress, 28 Aug.—1 Sept. – 2004. – P. 99. Bernardo U., Pedata P. A., Viggiani, G. Phenotypic plasticity of pigmentation and morphometric traits in Pnigalio soemius (Hymenoptera, Eulophidae) // Bull. Entomol. Res. – 2007. – 97. – P. 101—109. Bookstein F. L. Size and shape: A comment on semantics // Zoological Systematics. – 1989. – 38. – P. 173—180. Borror D. G., Triplehorn C. A., Johnson N. F. An introduction to the study of insects. – 6th ed. – Philadelphia : Saunders College Publishing. – 1989. – P. 761—763. DeVries P. J., Murray D., Lande R. Species diversity in vertical, horizontal and temporal dimensions of a fruit-feeding butterfly community in an Ecuadorian rainforest // Biological J. Linnean Society. – 1997. – 62. – P. 343—364. Dorn, S. Schumacher P. Abivardi C., Meyhofer R. Global and regional pest insects and their antagonists in orchards: spatial dynamics // Agri. Ecos. and Environ. – 1999. – 73. – P. 111—118. Epila J. S. O. Wind, crop pests and agro-forest design // Agri. Sys. – 1988. – 26. – P. 99—110. Groombridge B. Global biodiversity; Status of the Earth’s living resources. – Chapman and Hall / CRC Press, 1992. – 285 p. Hood C. S. Geometric Morphometric approaches to the study of sexual size dimorphism in mammals // Hystrix. – 2000. – 11. – P. 77—90. 436 Samad Khaghaninia et al. Ta b l e 6. T-test results of codling moth wing centroid size in Zandjan and Khoramdareh populations Ò à á ëèö à 6. Ðåçóëüòàòû ïðîâåðêè ðàçìåðà öåíòðîèäà êðûëà â ïîïóëÿöèÿõ Çàíäüÿíà è Êõîðàìäàðåõ ïî êðèòåðèþ Ñòüþäåíòà Note. ns – no significant difference. Ïðèìå÷ àíèå . ns – íåò çíà÷èòåëüíûõ îòëè÷èé. Wing Sex Number Centroid size T Meshkin shah Mahneshanr Meshkin shah Mahneshanr Fore Female 34 31 3.39 x 10-2 3.30 x 10-2 0.0028ns Male 31 18 3.31 x 10-2 3.28 x 10-2 0.0002ns Hind Female 32 31 4.68 x 10-2 3.92 x 10-2 8.043ns Male 30 24 3.04 x 10-2 3.84 x 10-2 0.521ns Jones C. J., Green G. L., Isard S. Dispersal of stable flies: Phenology of dispersing flies // The American Naturalist. – 2003. – 112. – P. 1017—1045. Kemp D. J. Phenotypic plasticity in field populations of the tropical butterfly Hypolimneas bolina (L.) (Nymphalidae) // Biol. J. Lin. Soc. – 2001. – 72. – P. 33—45. Khaghaninia S., Mohamadi S. A., Sarafrazi A. M., et al. Geometric morphometric approach on sexual dimor- phism of Cydia pomonella (Lep.; Tortricidae) in north west of Iran // J. Ent. Soc. Iran – 2008. – 28 (1). – P. 51—62. Kunkel J. G. Shape changes in biology, D’Arcy Thompson’s classic fish transformation // http://www.bio.umass.edu/biology/kunkel. – 2001. Lambert M. R. K. Some factors affecting flight in field populations of the Australian plague locust, Chortoicetes terminifera (Walker), in New South Wales // Animal Behaviour. – 1972. – 20. – P. 205—217. Mani E., Wildbolz T., Riggenbach W. Effect of pheromone trap position in large and small trees and in the open field on the catch of codling moth, Cydia pomonella L. males // Mitt. Schweiz. Entomol. Gesell. – 1995. – 68. – P. 69—78. Moghadam M., Mohammadi S. A., Aghaie Sarborzeh M. Multivariate statistical methods. – Pishtaz Pub. – 1994. – 208 p. Narcis V., Jordi B. Weather-depending pollinatory activity in an apple orchard, with special reference to Osmia cornuta and Apis mellifera (Hymenoptera: Megachilidae and Apidae) // Environ. Entomol. – 2000. – 29. – P. 413—420. Pasek J. E. Influence of wind and windbreaks on local dispersal of insects // Agri. Ecos. & Environ. – 1988. – 22. – P. 539—554. Rohlf F. J. Morphometrics // Annual Review of Ecology and Systematics. – 1990. – 12. – P. 299—316. Sadeghi R., Sari A. R., Sarafrazi A. M., Alipanah H. Study of the morphometric variations of host popula- tions of codling moth (Cydia pomonella L.) in some parts of Iran // M. S. Thesis. University of Thehran. – 2005. – P. 109—119. Schumacher P., Weber D. C., Hagger C., Dorn S. Heritability of flight distance for Cydia pomonella // Entomol. Exp. Appl. – 1997. – 85. – P. 169—175. Szabo T. I. Effect of weather factors on honeybee (Apis mellifera) flight activity and colony weight gain // J. Agri. Res. – 1980. – 19. – P. 164—171. Voigt E. Observations on the flight activity of codling moth, Cidia pomonella L. // IOBC Wprs Bull. – 1999. – 22. – P. 91—98. Zahiri R., Sarafrazi A. M., Salehi L., Kunkel J. G. A geometric morphometric study on populations of Rice Stem Borer, Chilo suppressalis W. (Lep.: Crambidae) in northern Iran // Zoology in the Middle East. – 2004. – 38. – P. 73—84. 437Geometric morphometric study on geographic dimorphism of codling moth Cydia pomonella... << /ASCII85EncodePages false /AllowTransparency false /AutoPositionEPSFiles true /AutoRotatePages /None /Binding /Left /CalGrayProfile (Dot Gain 20%) /CalRGBProfile (sRGB IEC61966-2.1) /CalCMYKProfile (U.S. Web Coated \050SWOP\051 v2) /sRGBProfile (sRGB IEC61966-2.1) /CannotEmbedFontPolicy /Error /CompatibilityLevel 1.4 /CompressObjects /Tags /CompressPages true /ConvertImagesToIndexed true /PassThroughJPEGImages true /CreateJDFFile false /CreateJobTicket false /DefaultRenderingIntent /Default /DetectBlends true /DetectCurves 0.0000 /ColorConversionStrategy /CMYK /DoThumbnails false /EmbedAllFonts true /EmbedOpenType false /ParseICCProfilesInComments true /EmbedJobOptions true /DSCReportingLevel 0 /EmitDSCWarnings false /EndPage -1 /ImageMemory 1048576 /LockDistillerParams false /MaxSubsetPct 100 /Optimize true /OPM 1 /ParseDSCComments true /ParseDSCCommentsForDocInfo true /PreserveCopyPage true /PreserveDICMYKValues true /PreserveEPSInfo true /PreserveFlatness true /PreserveHalftoneInfo false /PreserveOPIComments false /PreserveOverprintSettings true /StartPage 1 /SubsetFonts true /TransferFunctionInfo /Apply /UCRandBGInfo /Preserve /UsePrologue false /ColorSettingsFile () /AlwaysEmbed [ true ] /NeverEmbed [ true ] /AntiAliasColorImages false /CropColorImages true /ColorImageMinResolution 300 /ColorImageMinResolutionPolicy /OK /DownsampleColorImages true /ColorImageDownsampleType /Bicubic /ColorImageResolution 300 /ColorImageDepth -1 /ColorImageMinDownsampleDepth 1 /ColorImageDownsampleThreshold 1.50000 /EncodeColorImages true /ColorImageFilter /DCTEncode /AutoFilterColorImages true /ColorImageAutoFilterStrategy /JPEG /ColorACSImageDict << /QFactor 0.15 /HSamples [1 1 1 1] /VSamples [1 1 1 1] >> /ColorImageDict << /QFactor 0.15 /HSamples [1 1 1 1] /VSamples [1 1 1 1] >> /JPEG2000ColorACSImageDict << /TileWidth 256 /TileHeight 256 /Quality 30 >> /JPEG2000ColorImageDict << /TileWidth 256 /TileHeight 256 /Quality 30 >> /AntiAliasGrayImages false /CropGrayImages true /GrayImageMinResolution 300 /GrayImageMinResolutionPolicy /OK /DownsampleGrayImages true /GrayImageDownsampleType /Bicubic /GrayImageResolution 300 /GrayImageDepth -1 /GrayImageMinDownsampleDepth 2 /GrayImageDownsampleThreshold 1.50000 /EncodeGrayImages true /GrayImageFilter /DCTEncode /AutoFilterGrayImages true /GrayImageAutoFilterStrategy /JPEG /GrayACSImageDict << /QFactor 0.15 /HSamples [1 1 1 1] /VSamples [1 1 1 1] >> /GrayImageDict << /QFactor 0.15 /HSamples [1 1 1 1] /VSamples [1 1 1 1] >> /JPEG2000GrayACSImageDict << /TileWidth 256 /TileHeight 256 /Quality 30 >> /JPEG2000GrayImageDict << /TileWidth 256 /TileHeight 256 /Quality 30 >> /AntiAliasMonoImages false /CropMonoImages true /MonoImageMinResolution 1200 /MonoImageMinResolutionPolicy /OK /DownsampleMonoImages true /MonoImageDownsampleType /Bicubic /MonoImageResolution 1200 /MonoImageDepth -1 /MonoImageDownsampleThreshold 1.50000 /EncodeMonoImages true /MonoImageFilter /CCITTFaxEncode /MonoImageDict << /K -1 >> /AllowPSXObjects false /CheckCompliance [ /None ] /PDFX1aCheck false /PDFX3Check false /PDFXCompliantPDFOnly false /PDFXNoTrimBoxError true /PDFXTrimBoxToMediaBoxOffset [ 0.00000 0.00000 0.00000 0.00000 ] /PDFXSetBleedBoxToMediaBox true /PDFXBleedBoxToTrimBoxOffset [ 0.00000 0.00000 0.00000 0.00000 ] /PDFXOutputIntentProfile () /PDFXOutputConditionIdentifier () /PDFXOutputCondition () /PDFXRegistryName () /PDFXTrapped /False /Description << /CHS <FEFF4f7f75288fd94e9b8bbe5b9a521b5efa7684002000410064006f006200650020005000440046002065876863900275284e8e9ad88d2891cf76845370524d53705237300260a853ef4ee54f7f75280020004100630072006f0062006100740020548c002000410064006f00620065002000520065006100640065007200200035002e003000204ee553ca66f49ad87248672c676562535f00521b5efa768400200050004400460020658768633002> /CHT <FEFF4f7f752890194e9b8a2d7f6e5efa7acb7684002000410064006f006200650020005000440046002065874ef69069752865bc9ad854c18cea76845370524d5370523786557406300260a853ef4ee54f7f75280020004100630072006f0062006100740020548c002000410064006f00620065002000520065006100640065007200200035002e003000204ee553ca66f49ad87248672c4f86958b555f5df25efa7acb76840020005000440046002065874ef63002> /DAN <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> /DEU <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> /ESP <FEFF005500740069006c0069006300650020006500730074006100200063006f006e0066006900670075007200610063006900f3006e0020007000610072006100200063007200650061007200200064006f00630075006d0065006e0074006f00730020005000440046002000640065002000410064006f0062006500200061006400650063007500610064006f00730020007000610072006100200069006d0070007200650073006900f3006e0020007000720065002d0065006400690074006f007200690061006c00200064006500200061006c00740061002000630061006c0069006400610064002e002000530065002000700075006500640065006e00200061006200720069007200200064006f00630075006d0065006e0074006f00730020005000440046002000630072006500610064006f007300200063006f006e0020004100630072006f006200610074002c002000410064006f00620065002000520065006100640065007200200035002e003000200079002000760065007200730069006f006e0065007300200070006f00730074006500720069006f007200650073002e> /FRA <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> /ITA <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> /JPN <FEFF9ad854c18cea306a30d730ea30d730ec30b951fa529b7528002000410064006f0062006500200050004400460020658766f8306e4f5c6210306b4f7f75283057307e305930023053306e8a2d5b9a30674f5c62103055308c305f0020005000440046002030d530a130a430eb306f3001004100630072006f0062006100740020304a30883073002000410064006f00620065002000520065006100640065007200200035002e003000204ee5964d3067958b304f30533068304c3067304d307e305930023053306e8a2d5b9a306b306f30d530a930f330c8306e57cb30818fbc307f304c5fc59808306730593002> /KOR <FEFFc7740020c124c815c7440020c0acc6a9d558c5ec0020ace0d488c9c80020c2dcd5d80020c778c1c4c5d00020ac00c7a50020c801d569d55c002000410064006f0062006500200050004400460020bb38c11cb97c0020c791c131d569b2c8b2e4002e0020c774b807ac8c0020c791c131b41c00200050004400460020bb38c11cb2940020004100630072006f0062006100740020bc0f002000410064006f00620065002000520065006100640065007200200035002e00300020c774c0c1c5d0c11c0020c5f40020c2180020c788c2b5b2c8b2e4002e> /NLD (Gebruik deze instellingen om Adobe PDF-documenten te maken die zijn geoptimaliseerd voor prepress-afdrukken van hoge kwaliteit. De gemaakte PDF-documenten kunnen worden geopend met Acrobat en Adobe Reader 5.0 en hoger.) /NOR <FEFF004200720075006b00200064006900730073006500200069006e006e007300740069006c006c0069006e00670065006e0065002000740069006c002000e50020006f0070007000720065007400740065002000410064006f006200650020005000440046002d0064006f006b0075006d0065006e00740065007200200073006f006d00200065007200200062006500730074002000650067006e0065007400200066006f00720020006600f80072007400720079006b006b0073007500740073006b00720069006600740020006100760020006800f800790020006b00760061006c0069007400650074002e0020005000440046002d0064006f006b0075006d0065006e00740065006e00650020006b0061006e002000e50070006e00650073002000690020004100630072006f00620061007400200065006c006c00650072002000410064006f00620065002000520065006100640065007200200035002e003000200065006c006c00650072002000730065006e006500720065002e> /PTB <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> /SUO <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> /SVE <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> /ENU (Use these settings to create Adobe PDF documents best suited for high-quality prepress printing. Created PDF documents can be opened with Acrobat and Adobe Reader 5.0 and later.) >> /Namespace [ (Adobe) (Common) (1.0) ] /OtherNamespaces [ << /AsReaderSpreads false /CropImagesToFrames true /ErrorControl /WarnAndContinue /FlattenerIgnoreSpreadOverrides false /IncludeGuidesGrids false /IncludeNonPrinting false /IncludeSlug false /Namespace [ (Adobe) (InDesign) (4.0) ] /OmitPlacedBitmaps false /OmitPlacedEPS false /OmitPlacedPDF false /SimulateOverprint /Legacy >> << /AddBleedMarks false /AddColorBars false /AddCropMarks false /AddPageInfo false /AddRegMarks false /ConvertColors /ConvertToCMYK /DestinationProfileName () /DestinationProfileSelector /DocumentCMYK /Downsample16BitImages true /FlattenerPreset << /PresetSelector /MediumResolution >> /FormElements false /GenerateStructure false /IncludeBookmarks false /IncludeHyperlinks false /IncludeInteractive false /IncludeLayers false /IncludeProfiles false /MultimediaHandling /UseObjectSettings /Namespace [ (Adobe) (CreativeSuite) (2.0) ] /PDFXOutputIntentProfileSelector /DocumentCMYK /PreserveEditing true /UntaggedCMYKHandling /LeaveUntagged /UntaggedRGBHandling /UseDocumentProfile /UseDocumentBleed false >> ] >> setdistillerparams << /HWResolution [2400 2400] /PageSize [612.000 792.000] >> setpagedevice
id nasplib_isofts_kiev_ua-123456789-65828
institution Digital Library of Periodicals of National Academy of Sciences of Ukraine
issn 0084-5604
language English
last_indexed 2025-12-07T16:34:12Z
publishDate 2011
publisher Інститут зоології ім. І.І. Шмальгаузена НАН України
record_format dspace
spelling Khaghaninia, S.
Mohammadi, S.A.
Irani Nejad, K.H.
Zahiri, R.
2014-07-03T17:21:46Z
2014-07-03T17:21:46Z
2011
Geometric Morphometric Study on Geographic Dimorphism of Codling Moth Cydia pomonella (Lepidoptera, Tortricidae) from North West of Iran / S. Khaghaninia, S.A. Mohammadi, K.H. Irani Nejad, R. Zahiri // Вестник зоологии. — 2011. — Т. 45, № 5. — С. 429–437. — Бібліогр.: 25 назв. — англ.
0084-5604
https://nasplib.isofts.kiev.ua/handle/123456789/65828
595.782(55)
During years 2003—2004, nine geographical populations of codling moth Cydia pomonella (Linnaeus) from 4 north western provinces of Iran were collected.
В течение 2003—2004 гг. были собраны экземпляры девяти географических популяций яблонной плодожорки Cydia pomonella (Linnaeus) в 4 северо-западных провинциях Ирана.
en
Інститут зоології ім. І.І. Шмальгаузена НАН України
Вестник зоологии
Экология
Geometric Morphometric Study on Geographic Dimorphism of Codling Moth Cydia pomonella (Lepidoptera, Tortricidae) from North West of Iran
Геометрическое морфометрическое исследование географического диморфизма яблонной плодожерки Cydia pomonella (Lepidoptera, Tortricidae) северо-западного Ирана
Article
published earlier
spellingShingle Geometric Morphometric Study on Geographic Dimorphism of Codling Moth Cydia pomonella (Lepidoptera, Tortricidae) from North West of Iran
Khaghaninia, S.
Mohammadi, S.A.
Irani Nejad, K.H.
Zahiri, R.
Экология
title Geometric Morphometric Study on Geographic Dimorphism of Codling Moth Cydia pomonella (Lepidoptera, Tortricidae) from North West of Iran
title_alt Геометрическое морфометрическое исследование географического диморфизма яблонной плодожерки Cydia pomonella (Lepidoptera, Tortricidae) северо-западного Ирана
title_full Geometric Morphometric Study on Geographic Dimorphism of Codling Moth Cydia pomonella (Lepidoptera, Tortricidae) from North West of Iran
title_fullStr Geometric Morphometric Study on Geographic Dimorphism of Codling Moth Cydia pomonella (Lepidoptera, Tortricidae) from North West of Iran
title_full_unstemmed Geometric Morphometric Study on Geographic Dimorphism of Codling Moth Cydia pomonella (Lepidoptera, Tortricidae) from North West of Iran
title_short Geometric Morphometric Study on Geographic Dimorphism of Codling Moth Cydia pomonella (Lepidoptera, Tortricidae) from North West of Iran
title_sort geometric morphometric study on geographic dimorphism of codling moth cydia pomonella (lepidoptera, tortricidae) from north west of iran
topic Экология
topic_facet Экология
url https://nasplib.isofts.kiev.ua/handle/123456789/65828
work_keys_str_mv AT khaghaninias geometricmorphometricstudyongeographicdimorphismofcodlingmothcydiapomonellalepidopteratortricidaefromnorthwestofiran
AT mohammadisa geometricmorphometricstudyongeographicdimorphismofcodlingmothcydiapomonellalepidopteratortricidaefromnorthwestofiran
AT iraninejadkh geometricmorphometricstudyongeographicdimorphismofcodlingmothcydiapomonellalepidopteratortricidaefromnorthwestofiran
AT zahirir geometricmorphometricstudyongeographicdimorphismofcodlingmothcydiapomonellalepidopteratortricidaefromnorthwestofiran
AT khaghaninias geometričeskoemorfometričeskoeissledovaniegeografičeskogodimorfizmaâblonnoiplodožerkicydiapomonellalepidopteratortricidaeseverozapadnogoirana
AT mohammadisa geometričeskoemorfometričeskoeissledovaniegeografičeskogodimorfizmaâblonnoiplodožerkicydiapomonellalepidopteratortricidaeseverozapadnogoirana
AT iraninejadkh geometričeskoemorfometričeskoeissledovaniegeografičeskogodimorfizmaâblonnoiplodožerkicydiapomonellalepidopteratortricidaeseverozapadnogoirana
AT zahirir geometričeskoemorfometričeskoeissledovaniegeografičeskogodimorfizmaâblonnoiplodožerkicydiapomonellalepidopteratortricidaeseverozapadnogoirana