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Chilean journal of agricultural research

versión On-line ISSN 0718-5839

Chilean J. Agric. Res. v.70 n.3 Chillán sep. 2010

http://dx.doi.org/10.4067/S0718-58392010000300008 

Chilean Journal of Agricultural Research 70(3):408-416 (July-September 2010)

RESEARCH

Effect of Pollen from Different Plant Species on Development of Typhlodromus pyri (Sheuten) (Acari: Phytoseiidae)


Efecto del Polen de Diferentes Especies Vegetales sobre el Desarrollo de Typhlodromus pyri (Sheuten) (Acari: Phytoseiidae).


Paulina Bermúdez1*, Robinson Vargas2, Antonieta Cardemil2, and Eugenio López1

1 Pontificia Universidad Católica de Valparaíso, Facultad de Agronomía, Casilla 4-d, Quillota, Chile. *Corresponding author (paulina.bermudez@ucv.cl).
2Instituto de Investigaciones Agropecuarias INIA, Casilla 3, Quillota, Chile.


ABSTRACT

Typhlodromus pyri (Sheuten) (Acari: Phytoseiidae) is a phytoseiid mite with a high potential in controlling the false Chilean mite (Brevipalpus chilensis Baker; Acari: Tenuipalpidae). The purpose of this study was to determine the effect of different plant species pollen as a complementary food in the development of T. pyri when its prey is in low levels of availability. Mites were individually placed on black plastic boxes with pollen and maintained at a temperature of 26 ± 2 °C, 70 ± 5% relative humidity (RH), and a photoperiod of 16:8 h (L:D). Postembryonic development of T. pyri was studied in 11 pollen species, as well as in a mixed diet of Hirschfeldia incana (L.) and B. chilensis. Results show that H. incana was the only pollen in which there was no mortality (P > 0.05) along with the control (Oxalis pes-caprae L.). Mean duration from egg to adult with H. incana was 8.70 ± 1.66 d, protonymph 3.27 ± 0.21 d, and deutonymph 2.90 ± 1.45 d (P > 0.05). The mix feeding of T. pyri did not show any significant differences neither in the mean time from egg to adult, nor in mortality by feeding only with B. chilensis. Survival curves of T. pyri fed only with H. incana pollen, combined with B. chilensis, and only with B. chilensis are higher in the first 14 d of life. The sex ratio was not significantly affected by being fed only with H. incana pollen, B. chilensis, or by a combination of both.

Key words: phytoseiid mite, complementary food, Hirschfeldia incana, Brevipalpus chilensis, survival curve.


RESUMEN

Typhlodromus pyri (Sheuten) (Acari: Phytoseiidae) es un ácaro que presenta un alto potencial de uso para el control de la falsa arañita roja de la vid (Brevipalpus chilensis Baker; Acari: Tenuipalpidae). El objetivo de este estudio fue determinar el efecto del polen de diferentes especies vegetales como alimento complementario para T. pyri cuando escasea su presa. Los parámetros post-embrionarios de T. pyri se estudiaron en 11 especies de polen, en una dieta mixta de polen de Hirschfeldia incana (L.) y B. chilensis. Los ácaros se colocaron individualmente sobre cajas plásticas negras con polen a una temperatura de 26 ± 2 ºC y 70 ± 5% de humedad relativa y un fotoperíodo de 16:8 h (L:O). Los resultados muestran que el polen de H. incana fue el único en que no hubo mortalidad (P > 0,05) al igual que en el polen testigo (Oxalis pes-caprae L.). Con polen de H. incana la duración promedio de huevo a adulto fue de 8,70 ± 1,66 d, protoninfa 3,70 ± 1,17 d y deutoninfa 2,90 ± 1,45 d (P > 0,05). Con la dieta mixta no hubo diferencias significativas en el tiempo medio de duración de huevo a adulto, ni en la mortalidad con respecto a la alimentación sólo con B. chilensis. Las curvas de supervivencia de T. pyri alimentado sólo con polen H. incana, en combinación con B. chilensis y sólo con B. chilensis, son altas en los primeros 14 d de vida. La proporción de sexos no es afectada significativamente por la alimentación sólo con polen de H. incana, sólo de B. chilensis, o combinados.

Palabras clave: ácaros fitoseidos, alimento complementario, Hirschfeldia incana, Brevipalpus chilensis, curva supervivencia.

INTRODUCTION

Typhlodromus pyri (Scheuten) (Acari: Phytoseiidae) is a predatory mite adapted to a great diversity of agroecosystems and their surrounding vegetation (Prischmann et al., 2002; Hardman et al., 2006). Male and female development of this predator has been detected in Chile on Brevipalpus chilensis Baker (Acari: Tenuipalpidae) in vineyard (Vitis vinifera L.), reason why it could adapt to climatic conditions of other productive zones of the country (Ragusa and Vargas, 2002). This species are used worldwide due to its effectiveness on Tetranychus urticae Koch and Panonychus ulmi (Koch) populations in countries where they show some resistance to acaricides (Marshall and Lester, 2001; Hardman et al., 2005). Resistant strains of this phytoseiid have been commonly used in vineyards and apple orchards (Malus domestica Borkh.), under integrated pest management by exercising control even when the application of non-selective products is required (Hardman et al., 2000; Bonafos et al., 2007). It is a type III or generalist predator feeding on various species of tetranychidae, tarsonemidae, pollen, fungi, and other mites (McMurtry and Croft, 1997; Luh and Croft, 2001). These characteristics have the potential to control in other agricultural phytophagous mites such as tenuipalpidae.

The Brevipalpus genus has increased its economic importance worldwide possibly due to the limited participation of natural enemies and the techniques employed to avoid them (Gerson, 2008).

Laboratory studies point out that T. pyri has  high regulation of the population level of B. chilensis  with high consumption rate of immature and egg stages (Vargas et al., 2005). Even though generalist predators are limited by the fact that they are more effective with low density phytophagous mite populations, this can be overcome by enhancing the population density (Prischmann et al., 2006).

Generalist phytoseiidae have apreference for feeding on phytophagous mites, however pollen represents the only food source in many crops during spring and summer (Duso et al., 2004). Vargas et al. (2005), determined that T. pyri does not feed on adult stage of B. chilensis, the most predominant stage at the beginning of the spring, which is why the presence of complementary food in the orchard would be a relevant factor in promoting phytoseiidae survival. T. pyri has high mobility and search capacity which would allow it to find complementary food when they are low levels of availability of its prey (Slone and Croft, 2001). At the same time, dispersion of generalist predators is helped by macropredator movement in the orchard (Chuleui and Croft, 2001).

Agricultural systems have usually been managed under the monoculture concept, where the simplified ecosystems are making difficult the balance in the natural enemy/prey relationship. The presence of generalist predators that benefits the diversity of natural ecosystems, as well as other agricultural systems in which the habitat has been manipulated to promote diversity, is among the reasons of contributing to complementary food, such as pollen (Nichols and Altieri, 2004). Tsolakis et al. (1997) studied the frequency of different predators on general vegetation, thus demonstrating that it has a great influence as T. pyri reservoirs. The differences in morphological structures between plant species that keep the pollen can be an influence into the capacity for beneficial mites to persist and establish themselves. Trichomes and a domatium as a refuge in V. vinifera, promote the maintenance of T. pyri in the agroecosystems (Duso and Vettorazzo, 1999; Roda et al., 2003; Loughner et al., 2008). At the same time, leaf morphology provides a microclimate allowing water conservation, a favorable condition for the development of eggs and phytoseiid immature stages which are highly dependent on temperature and relative humidity (Gerson et al., 2003). Overmeer (1981) evaluated the reproductive and biological parameters of T. pyri with pollen from seven plant species under laboratory conditions, detecting differences among them, where Viciafaba L. gave a similar result when fed with phytophagous mites.

Other studies determined that Typhlodromus exhilaratus Ragusa fed with Rosmarinus officinalis L. or Oxalis sp. pollen have a positive influence on the duration of juvenile stages and on the oviposture rate when compare to be fed with Panonychus citri (McGregor) or Tetranychus urticae (Koch) (Ragusa, 1981). Some mites such as Amblyseius hibisci (Chant), have shown a decrease in their predation rate in the presence of pollen (McMurtry and Scriven, 1966), fact also observed in T. pyri fed with Typha latifolia L. pollen (Qingcai and Walde, 1997). Amblyseius victoriensis (Womersley) and Typhlodromus doreenae Schicha, fed with Typha orientalis Presl. pollen efficiently increased their number of mobile stages and eggs (James, 1993; James and Whitney, 1993). Previous studies evaluating the effect of pollen of different species conducted by the Instituto de Investigaciones Agropecuarias INIA, La Cruz (unpublished data), found that Oxalis pes-caprae L. was the one  with the best laboratory results in relation to postembryonic development and reproductive parameters in T. pyri. Oxalis pes-caprae is frequently found in ecosystems of the temperate climate of Chili; however since it is species that blooms in winter, its potential use is limited to habitat management in deciduous crops. This illustrates the necessity to know which species have a positive effect on the development of T. pyri in order to promote them when B. chilensis is not available. The purpose of this research was to study the effect of feeding with pollen from different plant species, developed in an agricultural ecosystem, as an alternative food source for T. pyri.

MATERIALS AND METHODS

Postembryonic parameters of the T. pyri predatory mite fed with different types of pollen from dominant plant species in a diverse agroecosystem were evaluated.

Experimental orchard
The study was carried out with organic management in a common vineyard orchard located in the Casablanca Valley

(33º20’ S; 71º20’ W), Valparaíso Region, Chile. Flowers or inflorescences in the pre-anthesis stage of V. vinifera cvs. Chardonnay and Merlot, along with other different associated plant species, were randomly collected between October 2004 and December 2005. Twelve dominant species were detected in the orchard. Four of those where of the Asteraceae family (Anthemis cotula L., Conyza bonariensis (L.) Cronquist, Lactuca serriola L., and Taraxacum officinale (Weber) ex F.H. Wigg., two Brassicacea (Raphanus sativus L. and Hirschfeldia incana (L.) Lagr.-Foss., and a single plant of the followings Chenopodiaceae (Chenopodium album L.), Oxalidaceae (O. pes-caprae), Papaveraceae (Eschscholzia californica Cham.), Poaceae (Poa annua L.), Rosaceae (Rosa sp.), and Umbelifera (Conium maculatum L.). Recollected weeds belonging to the Asteraceae family gave a very little amount of pollen, except for A. cotula, reason why they were not considered in this assay.

Pollen extraction
Pollen was extracted in the INIA La Cruz predator breeding laboratory. Stamens were separated and put on trays to decrease pollen grain moisture content. The drying process took place at a temperature of 26 ± 2 ºC and RH of 60 ± 5% for approximately 5 d. Once dry, thecae were separated with tweezers under a stereomicroscope, sieved, collected in acrylic boxes, and maintained in the same above-mentioned environmental conditions for approximately 3 d for final drying. The acrylic boxes with pollen were put on a silica gel base to avoid excessive humidity and prevent fungus development. They were then stored at 5 ºC, because they do not lose their viability under this conditions, and it is possible to store them for several months in accordance with James and Whitney (1993).

Postembryonic development of T. pyri
Postembryonic development of T. pyri was evaluated with pollen of nine dominant plant species in the orchard and V. vinifera cvs. Chardonnay and Merlot. Each treatment was defined as a type of pollen obtained from a determined plant species. The control was fed with O. pes-caprae pollen. Small, 4-cm-diameter black plastic dishes were employed for each treatment (Swirski et al., 1970), a T. pyri egg, no more than 20 h old, from the laboratory mite breeding was placed on each dish. Each egg corresponded to one replicate for a total of 20 replicates per treatment which were randomly placed on plastic trays. Pollen from a specific plant species, 7 x 10-4 g, was added on a daily basis to each plastic box, old grains were eliminated to avoid fungus development and provide fresh food. Based on similar results with the control, subsequent studies were carried out with H. incana pollen in a mixed diet of eggs and immature mobile stages of B. chilensis. In accordance with the results obtained by Vargas et al. (2005), each mite was daily provided with 15 eggs and 19 immature stages. Along with supplementing the pollen in this daily treatment, predatory mites were eliminated and new individuals added.

They were maintained at a temperature of 26 ± 2 ºC and 70 ± 5% HR, in accordance with the methodology used by Gerson et al. (2003), as well as a 16:8 h (L:D) photoperiod. Observations were carried out with a stereomicroscope 40X (Zeiss Stemi, Göttingen, Germany) every 24 h until dead of the individuals, recording the  molting time-lapse period.

Survival and longevity
H. incana pollen was selected to evaluate survival and longevity, due to the similarity of the control (O. pes-caprae) results, which was evaluated by itself and with a mixed diet of eggs and immature mobile stages of B. chilensis. Methodology was the same as the one applied to determine postembryonic development.

Determination of sex ratio
This parameter was evaluated in H. incana pollen, as well as in a mixed diet combining B. chilensis eggs and mobile stages. Four 7-cm-diameter black plastic dishes were employed for each treatment as described by Swirski et al. (1970). Twenty-five T. pyri eggs, no more than 20 h old, from females previously fed with H. incana pollen or with a mixed diet of H. incana and B. chilensis pollen were placed in each box. On a daily basis, mites born in each treatment were fed a quantity of pollen, 2 x 10-2 g, and old pollen grains were eliminated. In the mixed diet treatment, predatory mites were eliminated along with the pollen, whereas eggs and immature mobile stages of B. chilensis were added. Once they died, the adults were maintained in 75% alcohol to determine the percentage of males and females. Individuals collected were mounted with Hoyer solution and identified with a contrast microscope (Model 473014, Zeiss, West Germany).

Statistical analysis
Data were processed by analysis of variance (ANOVA). When statistical differences were detected due to the treatment effect, media separation was carried out by the Tukey multiple comparison range test with the SAS (SAS Institute, 2001) computer program.

RESULTS AND DISCUSSION

Postembryonic development
The lowest mean duration of the T. pyri larval stage was obtained with P. annua and the highest with H. incana (P < 0.05) with all species in a short or transition period (Table 1). Schausberger and Croft (1999)  established that T. pyri is classified as a non-feeding larva fed although it could be done occasionally. It was observed in this study that the time prolongation of the larval stage in relation to the rest of the treatments was possibly due to have been fed on H. incana and V. vinifera cvs. Chardonnay and Merlot when they were provided. Regardless of the type of pollen made available, it was observed that all larvae were able to molt and reach the protonymph stage in all treatments.

Table 1. Effect of feeding pollen from 11 plant species on the development (d) and survival rate of Typhlodromus  pyri.


The highest and lowest time in the protonymph stage was obtained with H. incana and E. californica, respectively. T. pyri only reached the deutonymph stage when fed with O. pes-caprae, H. incana, and R. sativus showing that if the pollen has no nutritional value, it dies shortly after the first molting (Table 1).

Broufas and Koveos (2000) determined that cherry (Prunus avium L.), apricot (Prunus armeniaca L.), and walnut (Juglans regia L.) pollen have a high nutritional value for Euseius finlandicus Oudemans because the mortality rate of immature stages was lower and mean longevity was higher. Papadopoulos and Papadoulis (2008) were also able to satisfactorily develop Typhlodromus foenilis Oudemans on apple pollen (Malus pumila Mill.), pear (Pyrus comunis L.), cherry, plum (Prunus domestica L.), walnut, almond (Prunus amygdalus L.), and apricot, where the last two species had the highest nutritional value. However, in this study V. vinifera cvs. Chardonnay and Merlot pollen would not have any nutritional value for T. pyri since it would not be used as a complementary food even when there was no other food available, demonstrated by a  high mortality after reaching the protonymph stage.

Sazo et al. (2006) demonstrated that Neoseiulus californicus (McGregor) fed with E. californica could have a survival rate similar when fed with T. urticae. However, it was observed in this study that when T. pyri was fed with E. californica, individuals avoid approaching this pollen and if they came in contact with it, they energetically eliminated it from their bodies. That is because this type of pollen could contain toxic elements for some phytoseiid mite species.

When the T. pyri deutonymph is fed with O. pes-caprae, its deutonymph stage has the same mean duration as with H. incana and R. sativus (P > 0.05) (Table 1).

T. pyri reached the adult stage when it was provided with O. pes-caprae, H. incana, or R. sativus and did not differ in mean duration from egg to adult. Only with O. pes-caprae pollen it was possible to determine that all individuals reached the adult stage. It had a survival rate of 70% with H. incana pollen and 40% with R. sativus pollen (Table 1). This makes R. sativus less attractive than the other species evaluated belonging to the same botanical family.

Carotenoids pollen posess the indispensable nutrients for the female phytoseiid predators entering diapause (Overmeer and Van Zon, 1983). In consecuence, if there is enough pollen, they would not respond exclusively to the availability of the existing prey. Dicke (1988) and Fitzgerald and Solomon (1991) determined that there would be no carotenoid effect for T. pyri entering diapause. Females do not need them, or if they did, they would be able to extract enough from the pollen and use it as a complementary food in presence of short day length conditions (Dicke, 1988; Fitzgerald and Solomon, 1991). Entering diapause would be conditioned by the photoperiod, which is why the presence of pollen would only be important at the beginning of the season when the B. chilensis population is essentially female.

Analysis of the intestinal content of T. pyri by electrophoresis revealed that the main nutrition components are pollen in spring, eriophyidae and thrips larvae in summer, mites in summer until autumn (Engel and Ohnesorge, 1994). Qingcai and Walde (1997) reaffirm this by pointing out that the presence of pollen would be of great importance when prey density is low. An increase in T. pyri numeric response early in the summer, would allow better control of B. chilensis during the season.

Table 2 shows that T. pyri postembryonic parameters with a H. incana diet and a mixed diet with B. chilensis. Furthermore, results are compared with those from studies published by the Instituto de Investigaciones Agropecuarias INIA La Cruz in which this mite is fed with both eggs and mobile stages of B. chilensis.

Table 2. Effect of feeding Hirschfeldia incana and Brevipalpus chilensis pollen on the development (d) and survival rate of Typhlodromus pyri.


T. pyri in the larval stage shows the highest time when provided with H. incana pollen (1.40 d) and show no difference from when it is fed only with eggs or mobile stages of B. chilensis. On the other hand, a mixed diet has the lowest value and does not differ from data obtained only with the phytophagous mite (P > 0.05). The protonymph stage maintains the tendency of longest duration with an exclusive pollen diet, and is significantly different from the rest. There were no differences among treatments with mixed diet and only B. chilensis. No differences were observed at the deutonymph stage (P > 0.05) (Table 2).

When T. pyri was fed with a mixed diet, it showed a lower duration from egg to adult (6.13 d) and was different from the rest of the treatments (P < 0.05). Mean duration from egg to adult of T. pyri fed with mobile stages of B. chilensis were 7.6 and 8.8 d on an egg diet, with no observation of mortality (Vargas et al., 2005) (Table 2). Duso and Camporese (1991) obtained a mean duration from egg to adult of 7.1 d with Mesembryanthemum criniflorum L. f. pollen and 6.6 d with P. ulmi. The mean time in this study from egg to adult using exclusively H. incana pollen was greater (P > 0.05) than the one obtained by Vargas et al. (2005). Overmeer (1981) determined that when T. pyri was fed with T. urticae, the mean duration was 9 to 12.5 d and 9 to 12 d with V. faba. On the other hand, feeding this mite with H. incana combined with B. chilensis, the mean duration was similar to that obtained by Vargas et al. (2005) (Table 2).

Survival and longevity
The behavior of the three kind of feeding shows a 100% survival rate during the first 7 d of life. As for T. pyri fed exclusively with H. incana, a decrease in survival rate starts on day 7 as compared to when it is fed with a mixed diet or only with B. chilensis with a decrease reaching days 21 and 29, respectively (Figure 1). Survival rate gradually decreases with H. incana in comparation with the other two diets, which showed an abrupt drop between day 21 and 35. The 50% mortality for T. pyri fed with H. incana and with the mixed diet is reached at about the age of 49 d, whereas this occurs before (33 d) when it is fed only with B. chilensis (Figure 1). In studies carried out with another generalist species, Iphiseius degenerans (Berlese), it was determined that feeding with castor pollen progressively decreased mortality from day 20 and the 50% mortality rate was reached around day 45 (Van Rijn and Tanigoshi, 1999). This shows that the presence of H. incana pollen in V. vinifera orchards is an alternative of supplementary food for T. pyri which would allow it to survive at the beginning of the season when activated overwintering B. chilensis females move to the shoots to oviposit and initiate the birth of juveniles. Adisson et al. (2000) observed that T. pyri has a higher correlation with population growth at the beginning of the spring and pollen supply than with the presence of prey.

Figure 1. Survival rate of Typhlodromus pyri in length of time (d) fed on a exclusive diet of Hirschfeldia incana and Brevipalpus chilensis, and with a mix diet of both.

Longevity or average age of T. pyri fed only with H. incana is 58 and 56 d with a mixed diet including B. chilensis (Figure 1). This contrasts with the results obtained when it is fed only with B. chilensis, averaging 29.6 d (Vargas et al., 2005). It is not possible to generalize that exclusive pollen diets produce greater longevity than feeding with mites. Camporese and Duso (1995) determined that T. talbii fed with Tydeus caudatus has a similar duration as T. pyri fed with H. incana. It was observed in this study that high longevity decreases activity. Therefore, a decrease in the feeding rate occurs as a undesirable characteristic since it could lead to lower depredation. Qingcai and Walde (1997) determined that the presence of T. latifolia pollen significantly reduces the depredation rate of T. pyri on P. ulmi. Nevertheless, the presence of pollen as an alternative food does not change the functional response of the consumption curve of P. ulmi over time. There was a permanent consumption of mites  despite the pollen availability in mixed feeding with H. incana and B. chilensis.

Determination of sex ratio
There are 98.9% females and 1.1% males when T. pyri is fed only with H. incana. When B. chilensis is added, 92.23% are females and if it is only fed B. chilensis (unpublished data), 93% are females (Figure 2). The high ratio of females early in spring is a frequent reproductive behavior in predatory species that do not require a large number of mating events to produce total egg production (Bounfour and McMurtry, 1987). Ferragut et al. (1987) determined that temperature is another factor in the sexual expression of these predators; increasing temperature between 18 and 32 ºC in Euseius stipulatus (Athias-Henriot) decreased the female ratio while the opposite occurred in T. phialatus. Studies carried out with Typhlodromus athiasae Porath and Swirski and T. negevi (Swirski and Amitai), established that there is a direct relation between the increase in the number of available prey and female production in a progeny (Momen and El-Borolossy, 1999).

Figure 2. Percentage of Typhlodromus pyri males and females fed on a exclusive diet of Hirschfeldia incana and Brevipalpuschilensis, and with a mix diet of both.


A high presence of female at the beginning of the season could initially benefit the predatory mite population growth rate and thus have a high number of individuals when the pest occurs. Therefore, reproductive parameters should be studied as a complement in order to determine aspects such as oviposture rate and egg viability.

Species of the Brassicaceae family, R. sativus and H. incana, would show greater potential for use in orchard habitat management, and the latest species is the one which could have a better response as a complementary or supplementary food. Biodiversity is undoubtedly a powerful tool for integrated pest management, but is not consistently beneficial if there is no ecological engineering process associated with it (Gurr et al., 2004). Therefore, species compatible with crop health must be considered, those that should be shown early in autumn so that pollen is available in the spring and can be combined with late blooming species.

CONCLUSIONS

The best food source for T. pyri was H. incana pollen which provided the highest survival percentage comparing to the others diets including only pollen. This result suggests that the presence of H. incana, which blooms when spring begins because B. chilensis is not yet available as food source, needs to be promoted.

Regarding the duration of the cycle and survival rate, a diet with H. incana pollen has an effect on T. pyri which is similar to that obtained with mixed feeding or exclusively with B. chilensis.

Survival curves of this predatory mite fed with H. incana in a mixed diet and with B. chilensis showed that the number of death of the individual was constant over time.

It is possible to reduce development time from egg to adult when T. pyri is fed with mites as well as with H. incana pollen. On the other hand, this pollen could benefit T. pyri development in the absence of tenuipalpidae mites.

Feeding exclusively with H. incana or B. chilensis pollen or with a mixed diet, does not significaly affect the T. pyri sex ratio, maintaining a high proportion of females.

Pollen of the Asteraceae family does not contribute as a complementary food for T. pyri due to the scarcity of pollen in its anthers. Similarly, S. californica is not a food alternative due it could contain toxic elements for predatory mites.

LITERATURE CITED

Addison, J.A., J.M.J. Hardman, and S.J. Walde. 2000. Pollen availability for predaceous mites on apple: spatial and temporal heterogeneity. Experimental and Applied Acarology 24:1-18.         [ Links ]

Bonafos, R., E. Serrano, P. Auger, and S. Kreiter. 2007. Resistance to deltamethrin, lambda-cyhalothrin and chlorpyriphos-ethyl in some populations of Typhlodromus pyri Scheuten and Amblyseius andersoni (Chant) (Acari: Phytoseiidae) from vineyards in the south-west of France. Crop Protection 26(2):169-172.         [ Links ]

Bounfour, M., and J.A. McMurtry. 1987. Biology and ecology Euseius scutalis (Athias-Henriot) (Acarina: Phytoseiidae). Hilgardia 55(5):1-23.         [ Links ]

Broufas, G.D., and D.S. Koveos. 2000. Effect of different pollens on development, survivorship and reproduction of Euseius finlandicus (Acari: Phytoseiidae). Environmental Entomology 29:743-749.         [ Links ]

Camporese, P., and C. Duso. 1995. Life history and life table parameters of the predatory mite Typhlodromus talbii. Entomologia Experimentalis et Applicata 77:149-157.         [ Links ]

Chuleui, J., and B.A. Croft. 2001. Ambulatory and aerial dispersal among specialist and generalist predatory mites (Acari: Phytoseiidae). Environmental Entomology 30:1112-1118.         [ Links ]

Dicke, M. 1988. Prey preference of the phytoseiid mite Typhlodromus pyri. I. Response to volatile kairomonas. Experimental and Applied Acarology 4:1-13.         [ Links ]

Duso, C., and P. Camporese. 1991. Development times and oviposition rates predatory mites Typhlodromus pyri and Amblyseius andersoni (Acari: Phytoseiidae) reared on different foods. Experimental and Applied Acarology 13:117-128.         [ Links ]

Duso, C., V. Malagnini, A. Paganelli, L. Aldegheri, M. Bottini, and S. Otto. 2004. Pollen availability and abundance of predatory phytoseiids mites on natural and secondary hedgerows. Biological Control 49:397-415.         [ Links ]

Duso, C., and E. Vettorazzo. 1999. Mite population dynamics on different grape varieties with or without released (Acari: Phytoseiidae). Experimental and Applied Acarology 23:741-763.         [ Links ]

Engel, R., and B. Ohnesorge. 1994. The role of alternative food and microclimate in the system Typhlodromus pyri Scheuten (Acari, Phytoseiidae) and Panonychus ulmi Koch (Acari, Tetranychidae) on grapevines. I. Laboratory investigations. Journal of Applied Entomology 118:129-150.         [ Links ]

Ferragut, F., F. Garcia-Marí, J. Costa-Comelles, and R. Laborda. 1987. Influence of food and temperature on development and oviposition of Euseius stipulatus and Typhlodromus phialatus (Acari: Phytoseiidae). Experimental and Applied Acarology 3:317-329.         [ Links ]

Fitzgerald, J.D., and M.G. Solomon. 1991. Diapause induction and duration in the phytoseiid mite Typhlodromus pyri. Experimental and Applied Acarology 12:135-145.         [ Links ]

Gerson, U. 2008. The Tenuipalpidae: An under-explored family of plant-feeding mites. Systematic and Applied Acarology 13:83-101.         [ Links ]

Gerson, U., R.L. Smiley, and R. Ochoa. 2003. Mites (Acari) for pest control. Blackwell, Oxford, UK.         [ Links ]

Gurr, M., S. Wratten, and M. Altieri. 2004. Ecological engineering for enhanced pest management: towards a rigorous science. p. 219-225. In Gurr, G., S. Wratten, and M. Altieri (eds.) Ecological engineering for pest management. CSIRO Publishing, Collingwood, Australia.         [ Links ]

James, D.G. 1993. Pollen, mould mites and fungi: improvements to mass rearing of Typhlodromus doreenae and Amblyseius victoriensis. Experimental and Applied Acarology 17:271-276.         [ Links ]

James, D.G., and J. Whitney. 1993. Cumbungi pollen as a laboratory diet for Amblyseius victoriensis and Typhlodromus doreenae Schicha (Acari: Phytoseiidae). Australian Journal of Entomology 32:5-6.         [ Links ]

Hardman, J.M., J. Franklin, K. Jensen, and D. Moreau. 2006. Effects of pesticides on mite predators (Acari, Phytoseiidae) and colonization of apple trees by Tetranychus urticae. Phytopatarasitica 34:449-462.         [ Links ]

Hardman, J.M., K. Jensen, J. Franklin, and D. Moreau. 2005. Effects of dispersal, predators (Acari, Phytoseiidae), weather, and ground cover treatments on populations of Tetranychus urticae (Acari, Tetranychidae) in apple orchards. Journal of Economic Entomology 98:862-874.         [ Links ]

Hardman, J.M., D. Moreau, M. Snyder, S. Gaul, and E. Bent. 2000. Performance of a pyrethroid-resistant strain of the predator Typhlodromus pyri (Acari, Phytoseiidae) under different insecticide regimes. Journal of Economic Entomology 93:590-604.         [ Links ]

Loughner, R., K. Goldman, G. Loeb, and J. Nyrop. 2008. Influence of thrichomes on predatory mite (Typhlodromus pyri). Experimental and Applied Acarology 45:111-122.         [ Links ]

Luh, H., and B. Croft. 2001. Quantitative classification of life-style types in predaceous phtytoseiid mites. Experimental and Applied Acarology 25:403-424.         [ Links ]

Marshall, D.B., and P.J. Lester. 2001. The transfer of Typhlodromus pyri on grape leaves for biological control of Panonychus ulmi (Acari: Phytoseiidae, Tetranychidae) in vineyards in Ontario, Canada. Biological Control 20:228-235.         [ Links ]

McMurtry, J.A., and B.A. Croft. 1997. Life styles of phytoseiids mites and their roles in biological control. Annual Review of Entomology 42:291-321.         [ Links ]

McMurtry, J.A., and G.T. Scriven. 1966. The influence of pollen and prey density on the number of prey consumed by Amblyseius hibisci (Acarina: Phytoseiidae). Annals of the Entomological Society of America 59:147-149.         [ Links ]

Momen, F.M., and M. El-Borolossy. 1999. Fertility and sex ratio of Typhlodromus athiasae and T. negevi under experimental conditions: Influence of prey density (Tetranychus urticae). Acarology 40(3):227-230.         [ Links ]

Nichols, C.I., and M.A. Altieri. 2004. The agroecological engineering: for pest management. p. 33-54. In Gurr, G., S. Wratten, and M. Altieri (eds.) Ecological engineering for pest management. CSIRO Publishing, Collingwood, Australia.         [ Links ]

Overmeer, W.P.J. 1981. Notes on breeding phytoseiids mites form orchards (Acarina: Phytoseiidae) in the laboratory. Med. Fac. Landouww Rijsuniv. Gent 43(2):503-509.         [ Links ]

Overmeer, W.PJ., and A.Q. Van Zon. 1983. The effect of different kind of food on the induction of diapause in the predacious mites Amblyseius potentilliae. Experimental and Applied Acarology 33:27-30.         [ Links ]

Papadopoulos, G.D., and G.Th. Papadoulis. 2008. Effect of seven different pollens on bio-ecological parameters of the predatory mite Typhlodromus foenilis (Acari: Phytoseiidae). Environmental Entomology 37:340-347.         [ Links ]

Prischmann, D.A., B.A. Croft, and H.K. Luh. 2002. Biological control of spider mites on grape phytoseiids mites (Acari: Tetranychidae, Phytoseiidae): Emphasis on regional aspects. Journal of Economic Entomology 95:340-347.         [ Links ]

Prischmann, D.A., D.G. James, L.C. Wright, and W.E. Snyder. 2006. Effects of generalist phytoseiid mites and grapevine canopy structure on spider mite (Acari: Tetranychidae). Environmental Entomology 35:56-67.         [ Links ]

Qingcai, W., and S.J. Walde. 1997. The functional response of Typhlodromus pyri to its prey, Panonychus ulmi: The effect of pollen. Experimental and Applied Acarology 21:677-684.         [ Links ]

Ragusa, S. 1981. Influence of different kinds of food substances on the developmental time in young stages of the predacious mite Typhlodromus exhilaratus Ragusa (Acarina: Phytoseiidae). Redia 64:237-243.         [ Links ]

Ragusa, S., and R. Vargas. 2002. On some phytoseiid mites (Parasitiformes, Phytoseiidae) from Chile. Phytophaga 12:129-139.         [ Links ]

Roda, A., J. Nyrop, and G. English-Loeb. 2003. Leaf pubescence mediates the abundance of non-prey food and the density of the predatory mite Typhlodromus pyri. Experimental and Applied Acarology 29:193-211.         [ Links ]

SAS Institute. 2001. SAS system for Windows 98. Version 8.2. SAS Institute, Cary, North Carolina, USA.         [ Links ]

Sazo, L., J.E. Araya, y P. Iturriaga. 2006. Efecto del tipo de polen sobre la supervivencia, fertilidad y viabilidad de los huevos de Neoseiulus californicus (McGregor) (Acarina: Phytoseiidae) en laboratorio. Boletin de Sanidad Vegetal. Plagas 32:619-623.         [ Links ]

Schausberger, P., and B.A. Croft. 1999. Activity, feeding and development among larvae of specialist and generalist phytoseiid mite species (Acari: Phytoseiidae). Environmental Entomology 28:322-329.         [ Links ]

Slone, D.H., and B.A. Croft. 2001. Species associations among predacious and phytophagous apple mites (Acari: Eriophydae, Phytoseidae, Stigmaeidae, Tetranychidae). Experimental and Applied Acarology 25:109-126.         [ Links ]

Swirski, E., S. Amitai, and N. Dorzia. 1970. Laboratory studies of the feeding habits, post-embrionic survival, and oviposition of the predaceous mites Amblyseius chilenensis Dosse and Amblyseius hibisci Chant (Acarina: Phytoseiidae) on various kinds of foods substances. Entomophaga 15:93-106.         [ Links ]

Tsolakis, H., E. Ragusa, and S. Ragusa Di Chiara. 1997. Importanza della flora spontanea ai margini degli agroecosistemi per gli acari fitoiseidi (Parasitiformes, Phytoseidae). Naturalista Siciliano S. IV, (suppl) p. 159-173.         [ Links ]

Vargas, R., N. Olivares, y A. Cardemil. 2005. Desarrollo postembrionario y parámetros de tablas de vida de Typhlodromus pyri Scheuten, Cyndodromus californicus (McGregor) (Acarina: Phytoseiidae) y Brevipalpus chilensis (Acarina: Tenuipalpidae). Agricultura Técnica (Chile) 35:147-156.         [ Links ]

Van Rijn, P.C, and L.K. Tanigoshi. 1999. Pollen as food for the predatory mites Iphiseius degenerans and Neoseiulus cucumeris (Acari: Phytoseiidae): dietary range and life history. Experimental and Applied Acarology 23:785-802.        [ Links ]
Accepted: 27 October 2009.

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