Macrosiphum euphorbiae, the potato aphid, is native to North America. It is widespread across the United States and Canada, and the species has spread from the Nearctic region to the Palearctic, Ethiopian, and Neotropical regions. Its range has increased to an almost worldwide distribution, and M. euphorbiae is a significant crop pest. Populations can be found throughout Europe, Asia, Africa, South America, and Australia. (Finlayson, et al., 2009; Le Guigo, et al., 2012; Raboudi, et al., 2011; Stary, et al., 1993; Valenzuela, et al., 2009)
Macrosiphum euphorbiae colonizes over 200 species of host plants throughout temperate and tropical regions. Its host plants, such as potatoes and many other crop species can be found mainly in agricultural fields, but also in grasslands and suburban areas such as greenhouses, gardens, and parks. (Le Guigo, et al., 2012; Petrovic-Obradovic, 2010; van Emden and Harrington, 2007)
Macrosiphum euphorbiae is considered to be a medium-sized aphid. The species has winged and wingless forms. Apterous (wingless) forms typically are 1.7 to 3.6 mm long, and alate (winged) forms are 1.7 to 3.4 mm long. Macrosiphum euphorbiae is spindle or pear-shaped. It has a soft body; long, dark antennae; and a pair of cornicles at the end of its abdomen. Its color can vary among shades of green, pink, or magenta, while its eyes are reddish. Nymphs resemble smaller adults and often are covered in a grayish-white wax. Apterous adults usually appear shinier than nymphs. (Boquel, et al., 2011; Kaplan and Thaler, 2012; Petrovic-Obradovic, 2010; Stoetzel, 1994; van Emden and Harrington, 2007)
Macrosiphum euphorbiae grows through four nymphal instars, each lasting from 1.5 to 3 days, though development time varies with temperature. Total development time from birth to reproductive maturity ranges from about 6 to 12 days. Development times in sexually reproductive and parthenogenetic populations are similar. (Alyokhin, et al., 2011; Boquel, et al., 2011; De Conti, et al., 2011; Macgillivray and Anderson, 1964)
Holocyclic populations of Macrosiphum euphorbiae (where the aphid life cycle includes both parthenogenesis and sexual reproduction) occur only in North America. Anholocyclic populations (in which female aphids reproduce only by parthenogenesis) occur throughout the rest of its global range. Egg-laying females (oviparae) produce a pheromone to attract male mates. The pheromone is produced by a gland on the hind tibia, and the female lifts her legs to release it. (Alyokhin, et al., 2011; Boquel, et al., 2011; Goldansaz and McNeil, 2006)
Holocyclic populations of M. euphorbiae (in which individuals undergo both parthenogenesis and sexual reproduction) are present in North America. In these holocyclic populations, eggs that have overwintered on primary hosts (usually Rosa spp.) hatch in May. In the spring, M. euphorbiae produces several wingless, parthenogenetic generations while colonizing its primary host. Later, winged females are produced; the winged offspring colonize secondary host plants in June and July. Macrosiphum euphorbiae colonizes over 200 secondary host plant species, though it typically prefers plants of the family Solanaceae. Parthenogenesis continues on the secondary host until the fall, at which time males and sexually reproductive females are produced. Males and sexually reproductive females return to the primary host plant species, mate, and lay eggs that overwinter. Anholocyclic populations (in which individuals reproduce only by parthenogenesis) account for the M. euphorbiae populations that are distributed throughout the rest of the world. The life cycle in anholocyclic M. euphorbiae populations is similar, except for the absence of the sexually reproductive stage. Apterous (wingless) females of M. euphorbiae likely overwinter on primary host plants in warmer regions and later produce alate (winged) females that in turn colonize secondary hosts later in the season. One female can give birth to anywhere from a few to 50 offspring in a single day. Macrosiphum euphorbiae nymphs develop to reproductive maturity after about 6 to 12 days. (De Conti, et al., 2011; Lamb, et al., 2009; Raboudi, et al., 2011)
In holocyclic populations of Macrosiphum euphorbiae, eggs are laid on a primary host plant to overwinter, which provides a food source for the offspring when they hatch in the spring. Adults also provision the eggs. Live birth by parthenogenesis is a significant energy investment by the female parent. Because these clones join the colony at birth, interaction with the parent may occur; however, adults provide no parental care. (Macgillivray and Anderson, 1964; van Emden and Harrington, 2007)
Macrosiphum euphorbiae adults typically live for about 10 days to a month. (Kaloshian, et al., 1997)
Like all aphids, Macrosiphum euphorbiae lives in large colonies. These colonies can grow to large sizes quickly due to live birth by parthenogenesis (which eliminates the need and time to find a mate) and the relatively quick maturation time of the offspring. Colonies can be established when alate (winged) aphids fly from primary to secondary host plants. However, because aphids are notoriously weak fliers, they often move on air currents and thus have little control over the direction of flight. Flight and any resulting colonization is largely random. Small-scale dispersal can occur when apterous (wingless) aphids walk from one plant to another. Macrosiphum euphorbiae is diurnal. (Boquel, et al., 2011; Narayandas and Alyokhin, 2006; Pompon, et al., 2010a)
The home range for Macrosiphum euphorbiae has not been reported, but its range is limited significantly by its poor flight ability. Colonization by alate (winged) forms is determined mainly by air currents. Small-scale dispersal range is determined by the distance that M. euphorbiae individuals can walk, likely only to neighboring plants. (Boquel, et al., 2011; Narayandas and Alyokhin, 2006; Pompon, et al., 2010a)
The main sensory organ in aphids is their antennae. The antennae are used for tactile and chemical detection. To determine whether a plant is a suitable host, Macrosiphum euphorbiae uses its antennae to feel along the leaves and detect host-specific odors and other chemical cues. Macrosiphum euphorbiae also uses its stylet mouthparts to probe into plants beneath the epidermis. Color cues can play a role in host plant selection, and M. euphorbiae can detect UV light. In other insects, UV light likely plays a role in flight patterns; however, the detection of UV light by M. euphorbiae likely serves a different purpose, as aphids are weak fliers and instead rely on air currents. Changes in UV light have been shown to alter orientation and colonization in M. euphorbiae. Aphids that are captured or harassed produce an alarm pheromone that alerts other aphids of danger. The alarm pheromone typically elicits evasive behaviors in aphids, such as dropping off the host plant or walking away. In M. euphorbiae, alarm pheromones also cause an increase in the parthenogenetic production of winged individuals, while sexually reproductive females produce a pheromone that attracts male mates. (Goldansaz and McNeil, 2006; Kaplan and Thaler, 2012; Legarrea, et al., 2012; Pompon, et al., 2010a)
Macrosiphum euphorbiae feeds on plant phloem. It uses its stylet mouthparts to pierce the plant tissue and access the phloem. This aphid species is highly polyphagous and has been documented as feeding on over 200 species in 20 different plant families, many of them crop species. Its most notable host plants include plants in the Solanaceae family, particularly potatoes and tomatoes and plants in the Brassicaceae family, including cabbage and lettuce. Macrosiphum euphorbiae individuals (usually dehydrated alate females) also have been observed consuming xylem sap for rehydration. (Atamian, et al., 2013; Le Guigo, et al., 2012; Legarrea, et al., 2012; Pompon, et al., 2010b)
Lady beetles are avid predators of aphids. Many lady beetle species have been documented preying on Macrosiphum euphorbiae, including Harmonia axyridis, Coccinella septempunctata, Hippodamia convergens, Coleomegilla maculata lengi, Coccinella trifasciata perplexa, and Propylea quatuordecimpunctata. Other predators include the carabid beetle, Pterostichus melanarius, which occurs in potato ecosystems, as well as other generalist aphid predators, such as spiders, syrphid flies, green lacewings, and midge larvae. To defend against predators, M. euphorbiae releases an alarm pheromone, as do most aphid species. The alarm pheromone alerts others in the colony of a predation threat and typically elicits evasive behavior such as dropping off the host plant or walking away. Additionally, the European red ant, Myrmica rubra, tends some colonies of M. euphorbiae. The ants protect the aphids from predators and parasitoids in exchange for honeydew produced by the aphids. (Alvarez, et al., 2013; Alyokhin, et al., 2011; Finlayson, et al., 2009; Kaplan and Thaler, 2012; van Emden and Harrington, 2007)
Macrosiphum euphorbiae is a significant crop pest with an almost worldwide distribution. It colonizes over 200 host plant species. Its primary host often is cited to be Rosa spp. Its preferred secondary host is potato, though M. euphorbiae feeds on other plant species in the family Solanaceae. Other significant host plants include tomatoes, lettuce, and plants in the Brassicaceae family, such as cabbage. All aphids, including M. euphorbiae, contain a bacterial endosymbiont, Buchnera aphidicola. These bacteria live within the bodies of aphids and synthesize amino acids that the aphids cannot get from their nutrient-poor phloem diet. The European red ant, Myrmica rubra, has been documented tending colonies of M. euphorbiae in a mutualistic relationship. The ants eat the honeydew produced by the aphids; in return, the ants protect, clean, and transport the aphids. Macrosiphum euphorbiae is prey to many species of lady beetle and many other insect species, such as syrphid flies and green lacewings. Many species of wasp parasitoids lay eggs inside aphids, which causes aphid death when the wasp offspring hatch. These wasp species can be used to control aphid populations. Aphidius ervi and Praon volucre are two of the major wasp species that use M. euphorbiae as a host. Pathogenic fungi in the genus Entomophthora can cause disease and death in M. euphorbiae. (Alyokhin, et al., 2011; Atamian, et al., 2013; Boquel, et al., 2011; Finlayson, et al., 2009; Francis, et al., 2010; Le Guigo, et al., 2012; Legarrea, et al., 2012; Lins, et al., 2013; Petrovic-Obradovic, 2010; Thi, et al., 2013)
There are no known positive effects of Macrosiphum euphorbiae on humans.
Macrosiphum euphorbiae, the potato aphid, is described as one of the most harmful aphid species in the world. It feeds on many plant species and causes significant crop damage in potatoes, tomatoes, lettuce, and cabbage. The aphid also is a vector of many plant diseases, including 40 non-persistent viruses and several persistent viruses (e.g., yellow net virus, pea leaf roll virus, and potato leaf roll virus). To prevent as much crop damage as possible, substantial research has been and continues to be conducted to find the most effective insecticides, biological control methods, and resistant plants. (Legarrea, et al., 2012; Raboudi, et al., 2011; van Emden and Harrington, 2007)
Macrosiphum euphorbiae has no special conservation status.
Angela Miner (author), Animal Diversity Web Staff, Elizabeth Wason (author, editor), Animal Diversity Web Staff, Leila Siciliano Martina (editor), Animal Diversity Web Staff.
Living in Australia, New Zealand, Tasmania, New Guinea and associated islands.
living in sub-Saharan Africa (south of 30 degrees north) and Madagascar.
living in the Nearctic biogeographic province, the northern part of the New World. This includes Greenland, the Canadian Arctic islands, and all of the North American as far south as the highlands of central Mexico.
living in the southern part of the New World. In other words, Central and South America.
living in the northern part of the Old World. In otherwords, Europe and Asia and northern Africa.
living in landscapes dominated by human agriculture.
reproduction that is not sexual; that is, reproduction that does not include recombining the genotypes of two parents
having body symmetry such that the animal can be divided in one plane into two mirror-image halves. Animals with bilateral symmetry have dorsal and ventral sides, as well as anterior and posterior ends. Synapomorphy of the Bilateria.
uses smells or other chemicals to communicate
used loosely to describe any group of organisms living together or in close proximity to each other - for example nesting shorebirds that live in large colonies. More specifically refers to a group of organisms in which members act as specialized subunits (a continuous, modular society) - as in clonal organisms.
animals which must use heat acquired from the environment and behavioral adaptations to regulate body temperature
union of egg and spermatozoan
An animal that eats mainly plants or parts of plants.
having a body temperature that fluctuates with that of the immediate environment; having no mechanism or a poorly developed mechanism for regulating internal body temperature.
fertilization takes place within the female's body
referring to animal species that have been transported to and established populations in regions outside of their natural range, usually through human action.
A large change in the shape or structure of an animal that happens as the animal grows. In insects, "incomplete metamorphosis" is when young animals are similar to adults and change gradually into the adult form, and "complete metamorphosis" is when there is a profound change between larval and adult forms. Butterflies have complete metamorphosis, grasshoppers have incomplete metamorphosis.
having the capacity to move from one place to another.
the area in which the animal is naturally found, the region in which it is endemic.
reproduction in which eggs are released by the female; development of offspring occurs outside the mother's body.
development takes place in an unfertilized egg
chemicals released into air or water that are detected by and responded to by other animals of the same species
"many forms." A species is polymorphic if its individuals can be divided into two or more easily recognized groups, based on structure, color, or other similar characteristics. The term only applies when the distinct groups can be found in the same area; graded or clinal variation throughout the range of a species (e.g. a north-to-south decrease in size) is not polymorphism. Polymorphic characteristics may be inherited because the differences have a genetic basis, or they may be the result of environmental influences. We do not consider sexual differences (i.e. sexual dimorphism), seasonal changes (e.g. change in fur color), or age-related changes to be polymorphic. Polymorphism in a local population can be an adaptation to prevent density-dependent predation, where predators preferentially prey on the most common morph.
reproduction that includes combining the genetic contribution of two individuals, a male and a female
living in residential areas on the outskirts of large cities or towns.
uses touch to communicate
that region of the Earth between 23.5 degrees North and 60 degrees North (between the Tropic of Cancer and the Arctic Circle) and between 23.5 degrees South and 60 degrees South (between the Tropic of Capricorn and the Antarctic Circle).
Living on the ground.
the region of the earth that surrounds the equator, from 23.5 degrees north to 23.5 degrees south.
A terrestrial biome. Savannas are grasslands with scattered individual trees that do not form a closed canopy. Extensive savannas are found in parts of subtropical and tropical Africa and South America, and in Australia.
A grassland with scattered trees or scattered clumps of trees, a type of community intermediate between grassland and forest. See also Tropical savanna and grassland biome.
A terrestrial biome found in temperate latitudes (>23.5° N or S latitude). Vegetation is made up mostly of grasses, the height and species diversity of which depend largely on the amount of moisture available. Fire and grazing are important in the long-term maintenance of grasslands.
uses sight to communicate
reproduction in which fertilization and development take place within the female body and the developing embryo derives nourishment from the female.
Alvarez, J., R. Srinivasan, F. Cervantes. 2013. Occurrence of the Carabid Beetle, Pterostichus melanarius (Illiger), in Potato Ecosystems of Idaho and its Predatory Potential on the Colorado Potato Beetle and Aphids. American Journal of Potato Research, 90/1: 83-92.
Alyokhin, A., F. Drummond, G. Sewell, R. Storch. 2011. Differential Effects of Weather and Natural Enemies on Coexisting Aphid Populations. Environmental Entomology, 40/3: 570-580.
Atamian, H., R. Chaudhary, V. Dal Cin, E. Bao, T. Girke, I. Kaloshian. 2013. In Planta Expression or Delivery of Potato Aphid Macrosiphum euphorbiae Effectors Me10 and Me23 Enhances Aphid Fecundity. Molecular Plant-Microbe Interactions, 26/1: 67-74.
Boquel, S., P. Giodanengo, A. Ameline. 2011. Probing Behavior of Apterous and Alate Morphs of two Potato—Colonizing Aphids. Journal of Insect Science, 11/164: 1-10.
De Conti, B., V. Bueno, M. Sampaio, J. Lenteren. 2011. Development and survival of Aulacorthum solani, Macrosiphum euphorbiae and Uroleucon ambrosiae at six temperatures. Bulletin of Insectology, 64/1: 63-68.
Finlayson, C., A. Alyokhin, E. Porter. 2009. Interactions of Native and Non-Native Lady Beetle Species (Coleoptera: Coccinellidae) With Aphid-Tending Ants in Laboratory Arenas. Environmental Entomology, 38/3: 846-855.
Francis, F., F. Guillonneau, P. Leprince, E. De Pauw, E. Haubruge, L. Jia, F. Goggin. 2010. Tritrophic interactions among Macrosiphum euphorbiae aphids, their host plants and endosymbionts: Investigation by a proteomic approach. Journal of Insect Physiology, 56/6: 575-585.
Goldansaz, S., J. McNeil. 2006. Effect of wind speed on the pheromone-mediated behavior of sexual morphs of the potato aphid, Macrosiphum euphorbiae (Thomas) under laboratory and field conditions. Journal of Chemical Ecology, 32/8: 1719-1729.
Kaloshian, I., M. Kinsey, D. Ullman, V. Williamson. 1997. The impact of Meu1-mediated resistance in tomato on longevity, fecundity and behavior of the potato aphid, Macrosiphum euphorbiae. Entomologia Experimentalis et Applicata, 83/2: 181-187.
Kaplan, I., J. Thaler. 2012. Phytohormone-mediated plant resistance and predation risk act independently on the population growth and wing formation of potato aphids, Macrosiphum euphorbiae. Arthropod-Plant Interactions, 6/2: 181-186.
Lamb, R., P. MacKay, S. Migui. 2009. Measuring the performance of aphids: fecundity versus biomass. Canadian Entomologist, 141/4: 401-405.
Le Guigo, P., A. Rolier, J. Le Corff. 2012. Plant neighborhood influences colonization of Brassicaceae by specialist and generalist aphids. Oecologia, 169/3: 753-761.
Legarrea, S., B. Diaz, M. Plaza, L. Barrios, I. Morales, E. Vinuela, A. Fereres. 2012. Diminished UV radiation reduces the spread and population density of Macrosiphum euphorbiae (Thomas) [Hemiptera: Aphididae] in lettuce crops. Horticultural Science, 39/2: 74-80.
Lins, J., V. Bueno, L. Sidney, D. Silva, M. Sampaio, J. Pereira, Q. Nomelini, J. van Lenteren. 2013. Cold storage affects mortality, body mass, lifespan, reproduction and flight capacity of Praon volucre (Hymenoptera: Braconidae). European Journal of Entomology, 110/2: 263-270.
Macgillivray, M., G. Anderson. 1964. Effect of photoperiod + temperature on production of gamic + agamic forms in Macrosiphum euphorbiae (Thomas). Canadian Journal of Zoology, 42/3: 491-510.
Narayandas, G., A. Alyokhin. 2006. Diurnal patterns in host finding by potato aphids, Macrosiphum euphorbiae (Homoptera : Aphididae). Journal of Insect Behavior, 19/3: 347-356.
Petrovic-Obradovic, O. 2010. 14.35 - Macrosiphum euphorbiae (Thomas, 1878) - potato aphid (Hemiptera, Aphididae). BioRisk, 4: 930-931.
Pompon, J., D. Quiring, P. Giordanengo, Y. Pelletier. 2010. Role of host-plant selection in resistance of wild Solanum species to Macrosiphum euphorbiae and Myzus persicae. Entomologia Experimentalis et Applicata, 137/1: 73-85.
Pompon, J., D. Quiring, P. Giordanengo, Y. Pelletier. 2010. Role of xylem consumption on osmoregulation in Macrosiphum euphorbiae (Thomas). Journal of Insect Physiology, 56/6: 610-615.
Raboudi, F., H. Makni, M. Makni. 2011. Genetic Diversity of Potato Aphid, Macrosiphum euphorbiae, Populations in Tunisia Detected by RAPD. African Entomology, 19/1: 133-140.
Stary, P., M. Gerding, H. Norambuena, G. Remaudiere. 1993. Environmental-research on aphid parasitoid biocontrol agents in Chile (Hym, Aphidiidae, Hom, Aphidoidea). Journal of Applied Entomology, 115/3: 292-306.
Stoetzel, M. 1994. Aphids (Homoptera: Aphididae) of potential importance on citrus in the United States with illustrated keys to species. Proceedings of the Entomological Society of Washington, 96/1: 74-90.
Thi, T., I. Magnoli, C. Cloutier, D. Michaud, F. Muratori, T. Hance. 2013. Early presence of an enolase in the oviposition injecta of the aphid parasitoid Aphidius ervi analyzed with chitosan beads as artificial hosts. Journal of Insect Physiology, 59/1: 11-18.
Valenzuela, I., M. Carver, M. Malipatil, P. Ridland. 2009. Occurrence of Macrosiphum hellebori Theobald & Walton (Hemiptera: Aphididae) in Australia. Australian Journal of Entomology, 48: 125-129.
van Emden, H., R. Harrington. 2007. Aphids as Crop Pests. Trowbridge, United Kingdom: CABI.