20 research outputs found

    Variation within and between Frankliniella Thrips Species in Host Plant Utilization

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    Anthophilous flower thrips in the genus Frankliniella (Thysanoptera: Thripidae) exploit ephemeral plant resources and therefore must be capable of successfully locating appropriate hosts on a repeated basis, yet little is known of interspecific and intraspecific variation in responses to host plant type and nutritional quality. Field trials were conducted over two seasons to determine if the abundance of males and females of three common Frankliniella species, F. occidentalis (Pergande), F. tritici (Fitch) and F. bispinosa (Morgan), their larvae, and a key predator, Orius insidiosus (Say) (Hemiptera: Anthocoridae) were affected by host plant type and plant nutritional quality. Two host plants, pepper, Capsicum annuum L. (Solanales: Solanaceae) and tomato, Solanum lycopersicum L. that vary in suitability for these species were examined, and their nutritional quality was manipulated by applying three levels of nitrogen fertilization (101 kg/ha, 202 kg/ha, 404 kg/ha). F. occidentalis females were more abundant in pepper than in tomato, but males did not show a differential response. Both sexes of F. tritici and F. bispinosa were more abundant in tomato than in pepper. Larval thrips were more abundant in pepper than in tomato. Likewise, O. insidiosus females and nymphs were more abundant in pepper than in tomato. Only F. occidentalis females showed a distinct response to nitrogen fertilization, with abundance increasing with fertilization. These results show that host plant utilization patterns vary among Frankliniella spp. and should not be generalized from results of the intensively studied F. occidentalis. Given the different pest status of these species and their differential abundance in pepper and tomato, it is critical that scouting programs include species identifications for proper management

    Factors influencing citrus fruit scarring caused by Pezothrips kellyanus

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    [EN] Kelly s citrus thrips (KCT) Pezothrips kellyanus (Bagnall) (Thysanoptera: Thripidae) is a recently recorded cosmopolitan citrus pest, causing fruit scarring that results in downgrading of fruit. Due to the detrimental effects caused on fruits by KCT, we wanted to study some of the factors influencing fruit scarring. Specifically, the objectives were: (1) to determine the fruit development stage when citrus fruits are damaged by KCT and the population structure of KCT during this period, (2) to study the influence of temperature on intensity of damage, and finally, (3) to identify alternative host plants. KCT populations on flowers and fruitlets and alternate plant hosts were sampled in four citrus orchards from 2008 to 2010. The percentage of damaged fruits was also recorded. The exotic vine Araujia sericifera (Apocynaceae) was recorded as a new host for KCT. Thrips scarring started to increase at 350 650 degree-days (DD) above 10.2 C, coinciding with a peak abundance of the second instar larval stages over all 3 years of the study. The maximum percentage of larval stages of KCT was observed in the 3 years at about 500 DD, a period which corresponds to the end of May or early June. Variation in the severity of fruit scarring appeared to be related to air temperature. Temperature likely affects the synchronisation between the peak in abundance of KCT larvae, and the period when fruitlets are susceptible to thrips damage. Temperature can also influence the survival and development of KCT populations in citrus and other host plants in the citrus agro-ecosystem.The authors thank Alejandro Tena for his valuable suggestions and two anonymous referees for their careful review and helpful comments. We also extend our thanks to the owners of the commercial orchards for giving us permission to use their citrus orchards. The first author was awarded an FPI fellowship from the Polytechnic University of Valencia to obtain her PhD degree.Navarro Campos, C.; Pekas, A.; Aguilar Martí, MA.; Garcia Marí, F. (2013). Factors influencing citrus fruit scarring caused by Pezothrips kellyanus. Journal of Pest Science. (86):459-467. doi:10.1007/s10340-013-0489-7S45946786Baker GJ (2006) Kelly citrus thrips management. Fact sheet. Government of South Australia, primary industries and resources SA. http://www.sardi.sa.gov.au/__data/assets/pdf_file/0010/44875/kctfact_sheet.pdf . Accessed 16 July 2012Baker GJ, Jackman DJ, Keller M, MacGregor A, Purvis S (2002) Development of an integrated pest management system for thrips in Citrus. HAL Final Report CT97007. http://www.sardi.sa.gov.au/pestsdiseases/horticulture/horticultural_pests/kelly_citrus_thrips/research_report_1997-2000 . Accessed 16 July 2012Bedford ECG (1998) Thrips, wind and other blemishes. Citrus pests in the Republic of South Africa. In: Bedford ECG, van den Berg MA, de Villiers EA (eds) ARC-Institute for tropical and subtropical crops, Nelspruit, South Africa, pp 170–183Blank RH, Gill GSC (1997) Thrips (Thysanoptera: Terebrantia) on flowers and fruit of citrus in New Zealand. N Z J Crop Hortic Sci 25:319–332Chellemi D, Funderburk F, Hall D (1994) Seasonal abundance of flower-inhabiting Frankliniella species (Thysanoptera: Thripidae) on wild plant species. Environ Entomol 23:337–342Conti F, Tuminelli R, Amico C, Fisicaro R, Frittitta C, Perrotta G, Marullo R (2001) Monitoring Pezothrips kellyanus on citrus in eastern Sicily, Thrips and tospoviruses. In: Proceedings of the 7th international symposium on Thysanoptera, Reggio Calabria, 1–8 July 2001, Italy, pp 207–210Costa L, Mateus C, zurStrassen R, Franco JC (2006) Thrips (Thysanoptera) associated to lemon orchards in the Oeste region of Portugal. IOBC/WPRS Bull 29:285–291European Plant Protection Organisation Reporting Service [EPPO] (2006) Pezothrips kellyanus. http://www.eppo.org/QUARANTINE/Pest_Risk_Analysis/PRAdocs_insects/06-12760%20DS%20PEZTKE.doc. Accessed 18 June 2012European Plant ProtectionOrganisation Reporting Service [EPPO] (2005) Scirtothrips aurantii, Scirtothrips citri, Scirtothrips dorsalis. EPPO Bull 35:353–356Franco JC, Garcia-Marí F, Ramos AP, Besri M (2006) Survey on the situation of citrus pest management in Mediterranean countries. IOBC/WPRS Bull 29:335–346Froud KJ, Stevens PS, Steven D (2001) Survey of alternative host plants for Kelly’s citrus thrips (Pezothrips kellyanus) in citrus growing regions. N Z Plant Prot 54:15–20Gomez-Clemente F (1952) Un tisanóptero causante de daños en las naranjas de algunas zonas de Levante. Boletín de Patología Vegetal y Entomología Agrícola 19:135–146Grout TG, Morse JG, O’Connell NV, Flaherty DL, Goodell PB, Freeman MW, Coviello RL (1986) Citrus thrips (Thysanoptera: Thripidae) phenology and sampling in the San Joaquin Valley. J Econ Entomol 79:1516–1523Horton J (1918) The citrus thrips. US Dep Agric Bull 616:1–42Kirk WDJ (1987) A key to the larvae of some common Australian flower thrips (Insecta: Thysanoptera), with a host-plant survey. Aust J Zool 35:173–185Lacasa A, Llorens JM, Sánchez JA (1996) Un Scirtothrips (Thysanoptera: Thripidae) causa daños en los cítricos en España. Bol San Veg Plagas 22:79–95Lewis HC (1935) Factors influencing citrus thrips damage. J Econ Entomol 28:1011–1015Lewis T (1997) Distribution, abundance and population dynamics. In: Lewis T (ed) Thrips as crop pests. CAB International, Wallingford, pp 217–258Lovatt C, Streeter S, Minter T, O’connell N, Flaherty D, Freeman M, Goodell P (1984) Phenology of flowering in Citrus sinensis (L.) Osbeck, cv. Washington navel orange. Proc Int Soc Citric 1:186–190Marullo R (1998) Pezothrips kellyanus, un nuovo tripide parassita delle colture meridionali. Informatore Fitopatologico 48:72–75Milne JR, Milne M, Walter GH (1997) A key to larval thrips (Thysanoptera) from Granite Belt stonefruit trees and a first description of Pseudanaphothrips achaetus (Bagnall) larvae. Aust J Entomol 36:319–326Mound LA, Jackman DJ (1998) Thrips in the economy and ecology of Australia, In: Zalucki MP, RAI Drew RAI, White GG (eds) Pest Management: future challenges, Proceedings of the sixth Australian applied entomological research conference, University of Queensland, St. Lucia, pp 472–478Mound LA, Marullo R (1996) The thrips of Central and South America (Insecta: Thysanoptera): an introduction. Mem Entomol Int 6:1–487Mound LA, Walker AK (1982) Terebrantia (Insecta: Thysanoptera). Fauna N Z 1:1–113Navarro-Campos C, Marzal C, Aguilar A, GarciaMarí F (2010) Presencia del microlepidóptero Anatrachyntisbadia en cítricos: descripción, comportamiento y daños al fruto. Levante Agrícola 402:270–276Navarro-Campos C, Aguilar A, Garcia-Marí F (2011) Population trend and fruit damage of Pezothrips kellyanus in citrus orchards in Valencia (Spain). IOBC/WPRS Bull 62: 285–292Navarro-Campos C, Aguilar A, Garcia-Marí F (2012) Aggregation pattern, sampling plan and intervention threshold for Pezothrips kellyanus in citrus groves. Entomol Exp Appl 142:130–139Northfield TD, Paini DR, Funderburk JE, Reitz SR (2008) Annual cycles of Frankliniella spp. (Thysanoptera: Thripidae) thrips abundance on North Florida uncultivated reproductive hosts: predicting possible sources of pest outbreaks. Ann Entomol Soc Am 101:769–778Orphanides G (1997) Thrips on citrus. Annual Review for 1997. Agricultural Research Institute, Nicosia, CyprusPerrotta G, Conti F (2008) A threshold hypothesis for an integrated control of thrips infestation on citrus in South-Eastern Sicily. IOBC/WPRS Bull 38:204–209Reitz S, Yu-lin G, Zhong-ren L (2011) Thrips: pests of concern to China and the United States. Agric Sci China 10:867–892Rhodes AA, Morse JG (1989) Scirtothrips citri sampling and damage prediction on California navel oranges. Agric Ecosyst Environ 26:117–129Schellhorn NA, Glatz RV, Wood GM (2010) The risk of exotic and native plants as hosts for four pest thrips (Thysanoptera: Thripinae). Bull Entomol Res 100:501–510Schweizer H, Morse JG (1997) Estimating the level of fruit scarring by citrus thrips from temperature conditions prior to the end of bloom. Crop Prot 16:743–752Smith D, Beattie GAC, Broadley R (eds) (1997) Citrus pests and their natural enemies: integrated pest management in Australia. Information series Q197030. Queensland Department of Primary Industries, BrisbaneStatgraphics (1994) Version 5.1 Plus. Statistical Graphics System by Statistical Graphics Corporation. Manugistics, RockvilleTanigoshi LK, Nishio JY, Moreno DS, Fargerlund J (1980) Effect of temperature on development and survival of Scirtothrips citri on citrus foliage. Ann Entomol Soc Am 73: 378–338Teksam I, Tunç I (2009) An analysis of Thysanoptera associated with citrus flowers in Antalya, Turkey: composition, distribution, abundance and pest status of species. Appl Entomol Zool 44:455–464Varikou K, Tsitsipis JA, Alexandrakis V, Mound LA (2002) Pezothrips kellyanus (Bagnall) (Thysanoptera: Thripidae), a new pest of citrus trees in Crete, In: Proceedings of the VII European congress of entomology, Thessaloniki, Greece, 7–13 Oct 2002, p 33Varikou K, Tsitsipis I, Alexandrakis V, Hoddle M (2009) Effect of temperature on the development and longevity of Pezothrips kellyanus (Thysanoptera: Thripidae). Ann Entomol Soc Am 102:835–841Varikou K, Birouraki A, Tsitsipis I, Sergentani CHR (2012) Effect of temperature on the fecundity of Pezothrips kellyanus (Thysanoptera: Thripidae). Ann Entomol Soc Am 105:60–65Vassiliou VA (2007) Chemical control of Pezothrips kellyanus (Thysanoptera: Thripidae) in citrus plantations in Cyprus. Crop Prot 26:1579–1584Vassiliou VA (2010) Ecology and behavior of Pezothrips kellyanus (Thysanoptera: Thripidae) on Citrus. J Econ Entomol 103:47–53Vierbergen G, Kucharczyk H, Kirk WDJ (2010) A key to the second instar larvae of the Thripidae of the Western Palearctic region. Tijdschr Entomol 153:99–160Webster KW, Cooper P, Mound LA (2006) Studies on Kelly’s citrus thrips, Pezothrips kellyanus (Bagnall) (Thysanoptera: Thripidae): sex attractants, host associations and country of origin. Aust J Entomol 45:67–74Wiesenborn W, Morse JG (1986) Feeding rate of Scirtothripscitri (Moulton) (Thysanoptera: Thripidae) as influenced by life stage and temperature. Environ Entomol 15:763–76

    Methodology of calculation of construction and hydrodynamic parameters of a foam layer apparatus for mass-transfer processes

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    Промислова реалізація методу стабілізації газорідинного шару дозволяє значно розширити галузь застосування пінних апаратів і відкриває нові можливості інтенсифікації технологічних процесів з одночасним створенням маловідходних технологій. У статті встановлені основні параметри, що впливають на гідродинаміку пінних апаратів, розглянуті основні конструкції та режими роботи пінних апаратів. Виявлено зв'язок гідродинамічних параметрів. Розглянуто гідродинамічні закономірності пінного шару. Вказані фактори, що впливають на процес масообміну, як в газовій, так і в рідкій фазах. Проведений аналіз ряду досліджень показав, що перспективним напрямком інтенсифікації процесу масообміну є розробка апаратів з трифазним псевдозрідженим шаром зрошуваної насадки складних форм із сітчастих матеріалів. Отже, необхідне проведення спеціальних досліджень гідродинамічних режимів роботи апарату з сітчастою насадкою і визначенням параметрів, що впливають на швидкість переходу насадки з одного режиму в інший.Industrial implementation of the stabilization method of the gas-liquid layer can significantly expand the field of use of foaming apparatus and opens up new opportunities for intensifying technological processes with the simultaneous creation of low-waste technologies. The article establishes the basic parameters influencing the hydrodynamics of foam apparatus, considers the basic constructions and operating modes of foam apparatus. The connection of hydrodynamic parameters is revealed. The hydrodynamic laws of the foam layer are considered. The indicated factors affecting the process of mass transfer, both in the gas and in the liquid phases. The conducted analysis of a number of studies showed that the perspective direction of intensification of the mass transfer process is the development of apparatuses with a three-phase fluidized bed of an irrigated nozzle of complex forms with mesh materials

    Trade-offs for butterfly alpha and beta diversity in human-modified landscapes and tropical rainforests

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    Turton, SM ORCiD: 0000-0001-6279-7682The accelerating expansion of human populations and associated economic activity across the globe have made maintaining large, intact natural areas increasingly challenging. The difficulty of preserving large intact landscapes in the presence of growing human populations has led to a growing emphasis on landscape approaches to biodiversity conservation with a complementary strategy focused on improving conservation in human‐modified landscapes. This, in turn, is leading to intense debate about the effectiveness of biodiversity conservation in human‐modified landscapes and approaches to better support biodiversity in those landscapes. Here, we compared butterfly abundance, alpha richness, and beta diversity in human‐modified landscapes (urban, sugarcane) and natural, forested areas to assess the conservation value of human‐modified landscapes within the Wet Tropics bioregion of Australia. We used fruit‐baited traps to sample butterflies and analyzed abundance and species richness in respective land uses over a one‐year period. We also evaluated turnover and spatial variance components of beta diversity to determine the extent of change in temporal and spatial variation in community composition. Forests supported the largest numbers of butterflies, but were lowest in each, alpha species richness, beta turnover, and the spatial beta diversity. Sugarcane supported higher species richness, demonstrating the potential for conservation at local scales in human‐modified landscapes. In contrast, beta diversity was highest in urban areas, likely driven by spatial and temporal variation in plant composition within the urban landscapes. Thus, while improving conservation on human‐modified landscapes may improve local alpha richness, conserving variation in natural vegetation is critical for maintaining high beta diversity.Associated Grant:Wet Tropics Management Authority (WTMA/2017/945) and David Cassells (personal donation

    Trade-offs for butterfly alpha and beta diversity in human-modified landscapes and tropical rainforests

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    The accelerating expansion of human populations and associated economic activity across the globe have made maintaining large, intact natural areas increasingly challenging. The difficulty of preserving large intact landscapes in the presence of growing human populations has led to a growing emphasis on landscape approaches to biodiversity conservation with a complementary strategy focused on improving conservation in human‐modified landscapes. This, in turn, is leading to intense debate about the effectiveness of biodiversity conservation in human‐modified landscapes and approaches to better support biodiversity in those landscapes. Here, we compared butterfly abundance, alpha richness, and beta diversity in human‐modified landscapes (urban, sugarcane) and natural, forested areas to assess the conservation value of human‐modified landscapes within the Wet Tropics bioregion of Australia. We used fruit‐baited traps to sample butterflies and analyzed abundance and species richness in respective land uses over a one‐year period. We also evaluated turnover and spatial variance components of beta diversity to determine the extent of change in temporal and spatial variation in community composition. Forests supported the largest numbers of butterflies, but were lowest in each, alpha species richness, beta turnover, and the spatial beta diversity. Sugarcane supported higher species richness, demonstrating the potential for conservation at local scales in human‐modified landscapes. In contrast, beta diversity was highest in urban areas, likely driven by spatial and temporal variation in plant composition within the urban landscapes. Thus, while improving conservation on human‐modified landscapes may improve local alpha richness, conserving variation in natural vegetation is critical for maintaining high beta diversity

    Plant species composition alters the sign and strength of an emergent multi-predator effect by modifying predator foraging behaviour

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    The prediction of pest-control functioning by multi-predator communities is hindered by the non-additive nature of species functioning. Such non-additivity, commonly termed an emergent multi-predator effect, is known to be affected by elements of the ecological context, such as the structure and composition of vegetation, in addition to the traits of the predators themselves. Here we report mesocosm experiments designed to test the influence of plant density and species composition (wheat monoculture or wheat and faba bean polyculture) on the emergence of multi-predator effects between Adalia bipunctata and Chrysoperla carnea, in their suppression of populations of the aphid Metopolophium dirhodum. The mesocosm experiments were followed by a series of behavioural observations designed to identify how interactions among predators are modified by plant species composition and whether these effects are consistent with the observed influence of plant species composition on aphid population suppression. Although plant density was shown to have no influence on the multi-predator effect on aphid population growth, plant composition had a marked effect. In wheat monoculture, Adalia and Chrysoperla mixed treatments caused greater suppression of M. dirhodum populations than expected. However this positive emergent effect was reversed to a negative multi-predator effect in wheat and faba bean polyculture. The behavioural observations revealed that although dominant individuals did not respond to the presence of faba bean plants, the behaviour of sub-dominants was affected markedly, consistent with their foraging for extra-floral nectar produced by the faba bean. This interaction between plant composition and predator community composition on the foraging behaviour of sub-dominants is thought to underlie the observed effect of plant composition on the multi-predator effect. Thus, the emergence of multi-predator effects is shown to be strongly influenced by plant species composition, mediated, in this case, by the provision of extra-floral nectar by one of the plant species

    The identity of belowground herbivores, not herbivore diversity, mediates impacts on plant productivity

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    Across many ecosystems, increases in species biodiversity generally results in greater resource acquisition by consumers. Few studies examining the impacts of consumer diversity on resource capture have focused on terrestrial herbivores, however, especially taxa that feed belowground. Here we conducted field mesocosm experiments to examine the effects of variation in species richness and composition within a community of wireworm herbivores on wheat plant productivity. Our experiments involved wireworm communities consisting of between one and three species, with all possible combinations of species represented. We found that the presence of wireworms reduced plant biomass and seed viability, but wireworm species richness did not impact these plant metrics. Species identity effects were strong, as two species, Limonius californicus and Selatosomus pruininus, had significantly stronger impacts on plants compared to L. infuscatus. Communities with either of the two most impactful species consistently had the greatest impact on wheat plants. The effects of wireworms were thus strongly dependent on the particular species present rather than the overall diversity of the wireworm community. More broadly, our study supports the general finding that the identity of particular consumer species within communities often has greater impacts on ecosystem functioning than species richness
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