2009
DOI: 10.1590/s0100-204x2009000800015
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Composition and functional groups of epiedaphic ants (Hymenoptera: Formicidae) in irrigated agroecosystem and in nonagricultural areas

Abstract: -The objective of this work was to evaluate the species composition and functional groups of ants in nonagricultural (NA) and in irrigated areas (S, seasonal irrigation; P, irrigation with well water; W, irrigation with wastewater) in an arid agricultural region in central Mexico, throughout 2005 and2006. A total of 52,358 ants belonging to 6 subfamilies, 21 genera and 39 species was collected using pitfall traps. The species best represented in all plots were: Forelius pruinosus, Pheidole obtusospinosa, Monom… Show more

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Cited by 4 publications
(2 citation statements)
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“…However, the occurrence of ant species under the genus Myrmicaria in all forest types can be associated with their mode of life as it was found in other studies. The species Myrmicaria congolensis and Myrmicaria opaciventris are predators (Andersen & Majer 2004), tropical climate specialist (Hernández-Ruiz et al 2009) and generalized Myrmicinae (Kenne & Dejean 1999), that have the ability to adapt to all environmental conditions (Kenne & Dejean 1999). The occurrence of these species as well as Myrmicaria SP03 in all forest types might be related to their adaptations to different environmental conditions imposed by forest types (Yusuf et al 2013).…”
mentioning
confidence: 99%
“…However, the occurrence of ant species under the genus Myrmicaria in all forest types can be associated with their mode of life as it was found in other studies. The species Myrmicaria congolensis and Myrmicaria opaciventris are predators (Andersen & Majer 2004), tropical climate specialist (Hernández-Ruiz et al 2009) and generalized Myrmicinae (Kenne & Dejean 1999), that have the ability to adapt to all environmental conditions (Kenne & Dejean 1999). The occurrence of these species as well as Myrmicaria SP03 in all forest types might be related to their adaptations to different environmental conditions imposed by forest types (Yusuf et al 2013).…”
mentioning
confidence: 99%
“…bourbonica specimen records from 446 sites (including 396 sites in Florida; Fig 1), documenting the earliest known records for 24 geographic areas (countries, island groups, major islands, and US states), including nine for which I found no previously published records: Anguilla, Antigua, Barbuda, British Virgin Islands, Jamaica, Turks and Caicos Islands, Missouri, and Washington (Table 1). I compiled N. bourbonica from 32 sites on 16 West Indian islands, including published records from Barbados (Wetterer et al, 2016), New Providence (Deyrup et al, 1998), South Bimini (Smith, 1954), North Andros (Deyrup et al, 1998), San Salvador (Deyrup et al, 1998), Cuba (Trager, 1984;LoddoVega et al, 2001), and St Croix (Wetterer & Lombard, 2010) Outside of Florida, I found only 18 North American site records of N. bourbonica, including three from Mexico (Trager, 1984;Hernández-Ruiz et al, 2009;Coronado-Blanco et al, 2013) South Carolina, Summerville (33.0°N; Smith, 1934) South Carolina, Charleston (32.8°N;Smith, 1934) Alabama, Mobile (30.7°N;Trager, 1984) Texas, Harris Co.;Houston, (29.8°N, 30-Jun-1973 In addition to the above records from Jacksonville and Gainesville, I recorded only seven site records of N. bourbonica north of 29.5°N in Florida, all Kallal and LaPolla (2012) presented a map (Figure 205) that purported to show the distribution in North America of N. bourbonica and five other Nylanderia species. Oddly, this map included just three site records for N. bourbonica: one in the Florida Keys, one in Palm Beach County, Florida, and one in eastern Massachusetts.…”
Section: Compiled Published and Unpublished New Worldmentioning
confidence: 98%