Pogonomyrmex occidentalis

Pogonomyrmex occidentalis
Scientific classification
Kingdom: Animalia
Phylum: Arthropoda
Class: Insecta
Order: Hymenoptera
Family: Formicidae
Genus: Pogonomyrmex
Species: P. occidentalis
Binomial name
Pogonomyrmex occidentalis
(Cresson, 1865) [1]

Pogonomyrmex occidentalis is an ant species.

Contents

Phylogeny

The ant genus Pogonomyrmex consists of 16 species (salinus, P. owyheei, P. occidentalis, P. subnitidus, P. subdentatus, P. brevispinosus, P. maricopa, P. californicus, P. comanche, P. badius, P. apache, P. desertorum, P. rugosus, P. barbatus, P. anergismus and P. colei) subdivided into five species complexes (occidentalis, subdentatus, californicus, desertorum and barbatus).[2][3][4] Pogonomyrmex individuals are colloquially known as harvester ants. Pogonomyrmex occidentalis individuals are colloquially known as western harvester ants.

Colonies

Mature colonies consist of up to 20,000 workers[5] and one queen.[6][7] A queen can live up to 40 years, and many colonies survive for 20 years.[5][8][9] Colonies of the close relative, P. owyheei, contain 1000–3000 brood items [7] and can produce 1000 reproductives, or alates, in a year.[7]

Individual workers

Workers' bodies are usually dark red and those in a mature colony are on average 6 mm long.[10] Workers vary in size, but are not subdivided into groups of differently-sized individuals with special roles. A worker lives for an average of 6 months, and as it ages, it usually progresses through different roles within the colony. For example, workers forage towards the ends of their lives.[11] In the field, workers are active when the temperature at the surface of the colony's mound is 25–53 °C (77–127 °F).[12]

Ecosystem

P. occidentalis inhabits the deserts and arid grasslands of the North American west at or below 6,300 feet (1,900 m).[13]

Nest architecture

A colony inhabits a nest that is up to 5 metres (16 ft) deep.[14] The queen stays at the bottom of the nest, and workers usually relocate themselves and brood within the nest, capturing safe levels of heat.[14][15] A colony's nest is topped by an irregularly conical nest mound[15] that can be more than 89 centimetres (35 in) in diameter.[16] The composition, shape, and size of the mound differ across plant environments.[15] The mounds of most colonies are surrounded by an area devoid of vegetation, and so do not burn during fires.[15] The soil in the mound is drier than that in the surrounding denuded area. Bigger P. occidentalis colonies (in number of workers) have bigger mounds.[17]

Nutrition

Workers harvest seeds and pollen directly from plants and gather fallen seeds. Some seeds are sometimes stored in chambers within the nest and are depleted during winter. Workers also gather newly-dead insects. Workers generally forage April–September.[12] Workers generally forage throughout the day during cooler months and only 5–11am and 3–9pm during summer.[12] Genetically diverse colonies forage for more hours daily.[12] Foraging times within a day and foraging temperature range vary consistently among colonies.[12] Given a choice, workers select seeds containing more energy.[18] Given a choice, workers select a diversity of seeds or seeds that are new to the colony.[18] Workers usually forage one kind of item each day, but change their specialty daily.[18] Workers usually forage in one direction over and over, even across days.[11] Colonies recruit more workers (from the total worker pool) to forage at a good food source.[11] Colonies lose foragers in encounters with neighboring colonies.[19] Workers defend foraging territories against neighboring colonies (personal observation). Different plant environments support different densities of colonies. Foragers produce more period mRNA during darkness, the timing of which varies seasonally.[20]

Biomass and brood production

Different developmental stages of ants within a colony process different kinds of food; larvae ingest solids, while adults ingest liquids, including larval excretions (The Ants). Immature individuals cannot pass from one larval stage to another or to adulthood without the help of adults; adults help immature individuals remove their old larval and/or pupal skins during ecdysis (molting). As larvae are relatively immobile, they only interact with nutrients as adults bring the nutrients to the larvae or the larvae to the nutrients. Bigger colonies do not necessarily produce a greater total reproductive biomass.[21] Colonies stop producing brood before they overwinter.[22]

Mating

Colonies release alates synchronously.[16][21] Alates mate in hilltop leks [10][16][23] in swarms.[24][25] Major mating swarms are about 1.4 kilometres (0.87 mi) apart,[26] and queens can fly no more than 800 metres (2,600 ft).[27] Gynes mate with 2–11 (an average of 6.3) genetically distinct males.[28] Females always mate multiply.[10] Queens that mate only a few times are less successful.[29] The colonies of queens that mate with more males grow faster.[28] Males sometimes mate multiply.[10] Females mate nonrandomly.[30] Larger males are more successful at mating (i.e. they are overrepresented among collected maters), but small males can still mate.[23][31] Certain shape characteristics improve male chances of mating success.[23] P. occidentalis populations are effectively small and inbred.[6] Queens pick bare and bright areas to land and then dig where they land.[10]

Colony founding

Individual queens found colonies on their own, without workers or other queens. Survivorship of colonies in the first year is negatively correlated with increasing density of foundresses.[27] Foraging workers kill queens that they encounter aboveground and occasionally excavate queens.[32] Factors independent of colony density are responsible for >90% of foundress mortality.[32] Queens in some populations found colonies claustrally[10] and in others, semi-claustrally. Many of the eggs laid in the first batch die or are unembryonated eggs.[10] During colony founding, larvae may eat eggs.[10] The first workers produced, nanitics, are 2 mm (33% shorter than typical worker).[10] 2/188 founding queens survived from July to March.[16]

Population ecology

Mating swarms that are consistently present and large determine much of the spatial variability in colony density and emerge over the long term.[26] New colonies are founded in a clumped pattern, around the mating sites.[16][27] The population may self-thin through direct interference competition[16] resulting in a uniformly overdispersed distribution pattern.[16] Long-term colony survival is mediated by proximity to older colonies.[33] Smaller colonies have closer nearest neighbors.[16] Smaller nests are more likely to die.[16] The further a colony is from its nearest neighbor (especially for small colonies), the higher the colony's survival probability.[16] Colony age and size are correlated, especially in young colonies.[21]

References

  1. ^ "Pogonomyrmex occidentalis (Cresson, 1865)". Integrated Taxonomic Information System. http://www.itis.gov/servlet/SingleRpt/SingleRpt?search_topic=TSN&search_value=154235. Retrieved February 11, 2011. 
  2. ^ Joel D. Parker & Steven W. Rissing (2002). "Molecular evidence for the origin of workerless social parasites in the ant genus Pogonomyrmex". Evolution 56 (10): 2017–2028. doi:10.1111/j.0014-3820.2002.tb00128.x. JSTOR 3094645. PMID 12449489. 
  3. ^ Steven O. Shattuck (1987). "An analysis of geographic variation in the Pogonomyrmex occidentalis complex. (Hymenoptera: Formicidae)". Psyche 94 (1–2): 159–180. doi:10.1155/1987/24635. 
  4. ^ Christoph Strehl (2005). Evolution of colony characteristics in the harvester ant genus Pogonomyrmex (Ph.D. thesis). Universität Würzburg. http://www.opus-bayern.de/uni-wuerzburg/volltexte/2005/1432/pdf/PhD_CPStrehl_050207.pdf. 
  5. ^ a b Kathleen H. Keeler (1993). "Fifteen years of colony survivorship in the western harvester ant Pogonomyrmex occidentalis". The Southwestern Naturalist 38 (3): 286–289. doi:10.2307/3671438. 
  6. ^ a b Blaine J. Cole & Diane C. Wiernasz (1997). "Inbreeding in a lek-mating ant species, Pogonomyrmex occidentalis". Behavioral Ecology and Sociobiology 40 (2): 79–86. doi:10.1007/s002650050318. JSTOR 4601301. 
  7. ^ a b c R. J. Lavigne (1969). "Bionomics and nest structure of Pogonomyrmex occidentalis (Hymenoptera: Formicidae)". Annals of the Entomological Society of America 62: 1166–1175. 
  8. ^ Sanford D. Porter and Clive D. Jorgensen (1988). "Longevity of harvester ant colonies in southern Idaho". Journal of Range Management 41 (2): 104–107. doi:10.2307/3898942. JSTOR 3898942. 
  9. ^ Keeler, 1982
  10. ^ a b c d e f g h i Harold G. Nagel & Carl W. Rettenmeyer (1973). "Nuptial flights, reproductive behavior and colony founding of the western harvester ant, Pogonomyrmex occidentalis (Hymenoptera: Formicidae)". Journal of the Kansas Entomological Society 46 (1): 82–101. JSTOR 25082548. 
  11. ^ a b c Jennifer H. Fewell (1990). "Directional fidelity as a foraging constraint in the western harvester ant, Pogonomyrmex occidentalis". Oecologia 82 (1): 45–51. doi:10.1007/BF00318532. JSTOR 4219200. 
  12. ^ a b c d e Blaine J. Cole, Adrian A. Smith, Zachary J. Huber & Diane C. Wiernasz (2010). "The structure of foraging activity in colonies of the harvester ant, Pogonomyrmex occidentalis". Behavioral Ecology 21 (2): 337–342. doi:10.1093/beheco/arp193. 
  13. ^ Cole
  14. ^ a b Cole, 1994
  15. ^ a b c d Cole,1932
  16. ^ a b c d e f g h i j Diane C. Wiernasz and Blaine J. Cole (1995). "Spatial distribution of Pogonomyrmex occidentalis: recruitment, mortality and overdispersion". Journal of Animal Ecology 64 (4): 519–527. doi:10.2307/5654. JSTOR 5654. 
  17. ^ Cole and Wiernasz, 1995
  18. ^ a b c Jennifer H. Fewell & Jon F. Harrison (1991). "Flexible seed selection by individual harvester ants, Pogonomyrmex occidentalis". Behavioral Ecology and Sociobiology 28 (6): 377–384. JSTOR 4600566. 
  19. ^ Joseph De Vita (1979). "Mechanisms of interference and foraging among colonies of the harvester ant Pogonomyrmex californicus in the Mojave desert". Ecology 60 (4): 729–737. doi:10.2307/1936610. JSTOR 1936610. 
  20. ^ Krista K. Ingram, Scott Krummey & Michelle LeRoux (2009). "Expression patterns of a circadian clock gene are associated with age-related polyethism in harvester ants, Pogonomyrmex occidentalis". BMC Ecology 9: 7. doi:10.1186/1472-6785-9-7. PMC 2676274. PMID 19374755. http://www.biomedcentral.com/1472-6785/9/7. 
  21. ^ a b c Blaine J. Cole & Diane C. Wiernasz (2000). "Colony size and reproduction in the western harvester ant, Pogonomyrmex occidentalis". Insectes Sociaux 47 (3): 249–255. doi:10.1007/PL00001711. 
  22. ^ A. Cole, Jr. (1934). "The relation of the ant, Pogonomyrmex occidentalis Cr., to its habitat" (PDF). Ohio Journal of Science 32 (2): 133–146. https://kb.osu.edu/dspace/bitstream/handle/1811/2557/V32N02_133.pdf;jsessionid=0199A2DC436E1801AA39CB687D401939?sequence=1. 
  23. ^ a b c Allison J. Abell, Blaine J. Cole, Ruth Reyes & Diane C. Wiernasz (1999). "Sexual selection on body size and shape in the western harvester ant, Pogonomyrmex occidentalis Cresson" (PDF). Evolution 53 (2): 535–545. doi:10.2307/2640789. http://www.bchs.uh.edu/~bcole/pogo/DWEvol1999.pdf. 
  24. ^ J. F. Mull & Thomas O. Crist (1993). "Timing of mating flights in the western harvester ant, Pogonomyrmex occidentalis Cresson (Hymenoptera: Formicidae)". Journal of the Kansas Entomological Society 66: 372–374. 
  25. ^ Wiernasz, 1995
  26. ^ a b Ian Billick, Blaine J. Cole & Diane C. Wiernasz (2004). "Scale of recruitment limitation in the western harvester ant (Hymenoptera: Formicidae)". Annals of the Entomological Society of America 97 (4): 738–742. doi:10.1603/0013-8746(2004)097[0738:SORLIT]2.0.CO;2. ISSN 0013-8746. 
  27. ^ a b c Blaine J. Cole & Diane C. Wiernasz (2002). "Recruitment limitation and population density in the harvester ant, Pogonomyrmex occidentalis" (PDF). Ecology 83 (5): 1433–1442. doi:10.1890/0012-9658(2002)083[1433:RLAPDI]2.0.CO;2. ISSN 0012-9658. http://www.bchs.uh.edu/~bcole/pogo/BCDWEcology.pdf. 
  28. ^ a b Diane C. Wiernasz, Christina L. Perroni & Blaine J. Cole (2004). "Polyandry and fitness in the western harvester ant, Pogonomyrmex occidentalis" (PDF). Molecular Ecology 13 (6): 1601–1606. doi:10.1111/j.1365-294X.2004.02153.x. PMID 15140102. http://citeseerx.ist.psu.edu/viewdoc/download?doi=10.1.1.131.8368&rep=rep1&type=pdf. 
  29. ^ Cole and Wiernasz, 1999
  30. ^ Wiernasz et al., 1995
  31. ^ Diane C. Wiernasz, Amy K. Sater, Allison J. Abell and Blaine J. Cole (2001). "Male size, sperm transfer, and colony fitness in the western harvester ant, Pogonomyrmex occidentalis". Evolution 55 (2): 324–329. JSTOR 2640754. PMID 11308090. 
  32. ^ a b Ian Billick, Diane C. Wiernasz & Blaine J. Cole (2001). "Recruitment in the harvester ant, Pogonomyrmex occidentalis : effects of experimental removal". Oecologia 129 (2): 228–233. doi:10.1007/s004420100721. 
  33. ^ Ryti & Case, 1988

External links