Interactions between meat ants (Iridomyrmex spadius) and bellyache bush (Jatropha gossypiifolia)
F. F. Bebawi A B C and S. D. Campbell A BA Tropical Weeds Research Centre, Queensland Department of Natural Resources and Mines, Charters Towers, Qld 4820, Australia.
B CRC for Australian Weed Management, PMB 1, Waite Campus, Glen Osmond, SA 5064, Australia.
C Corresponding author. Email: Faiz.Bebawi@nrme.qld.gov.au
Australian Journal of Experimental Agriculture 44(12) 1157-1164 https://doi.org/10.1071/EA03194
Submitted: 19 September 2003 Accepted: 10 March 2004 Published: 24 January 2005
Abstract
Understanding the dispersal of weed species is important for the development of effective control strategies. In this study, a series of experiments was conducted to clarify the role that meat ants (Iridomyrmex spadius) play in dispersing bellyache bush (Jatropha gossypiifolia), an exotic shrub currently invading the rangelands of northern Australia. The nutrient composition of food [lipids (fatty acids), fat and soluble carbohydrates] provided by bellyache bush seed components [caruncle, exotegmen and seed (without caruncle and exotegmen)] was identified. Seed components were rich in lipids, particularly palmitic, oleic, stearic, linoleic and eicosenic acids. Oleic and palmitic were most abundant in the caruncle (30% each), linoleic in the seed (61%) and palmitic in the exotegmen (36%). Over all seed components, fat concentration was relatively high (6.3%) compared with soluble carbohydrates (2.3%). The impact of feeding was then determined by comparing germination and viability of intact, non-carunculate (caruncle manually removed) and ant-discarded bellyache bush seeds. Feeding by meat ants significantly increased seed germinability, whilst having no adverse affects on viability. The quantity of seeds dispersed and the seasonal pattern of dispersal was recorded by collecting seed from the middens of randomly selected meat ant nests on a monthly basis. On average, 12 330 ± 603 seeds were retrieved from the middens of individual meat ant nests over 12 months, with highest numbers recorded between February and June (>1200 seeds/ant nest). The effect of this dispersal was determined through comparisons of plant densities within core infestations of bellyache bush, meat ant nest middens and pastures located directly adjacent to core infestations and that were being invaded primarily through localised ballistic dispersal. The density of bellyache bush plants growing from the seed reserves within middens averaged 79 plants/m2, just 18% less than that within core infestations. Seedling survival (1 year) and growth within core infestation and meat ant sites was also quantified. The middens of meat ant nests provided an environment conducive to higher seedling survival and faster growth rates than occurred within core infestations. Mutualistic interaction between bellyache bush and meat ants is likely to build local ‘infestation pressure’ that may be conducive to range extension in years of exceptionally wet seasons. Management of seed dispersal by meat ants may reduce that risk.
Acknowledgments
Special thanks are extended to The Queensland Department of Natural Resources and Mines for providing financial support, and to Dave and Pauline Chapman (Almora Station) and Charlie Truscott (Lynmore Station) for allowing us to use their property for research purposes. We also thank D. Panetta, A. Grice and A. Lindsay for reviewing the manuscript. The technical assistance of M. Madigan, R. Stevenson, C. Dennis and K. Risdale is also acknowledged.
Alpert P, Maron JL
(2000) Carbon addition as a countermeasure against biological invasion by plants. Biological Invasions 2, 33–40.
| Crossref | GoogleScholarGoogle Scholar |
Andersen AN
(1988) Soil of the nest-mound of the seed-dispersing ant, Aphaenogaster longiceps, enhances seedling growth. Australian Journal of Ecology 13, 469–471.
Baskin JM, Baskin CC
(1997) Methods of breaking seed dormancy in the endangered species Iliamna corei (Sherff) Sherff (Malvaceae), with special attention to heating. Natural Areas Journal 17, 313–323.
Beattie AJ, Culver DC
(1983) The nest chemistry of two seed-dispersing ant species. Oecologia 56, 99–103.
| Crossref |
Crossref |
Berg RY
(1975) Myrmecochorous plants in Australia and their dispersal by ants. Australian Journal of Botany 23, 475–508.
Brew CR,
O’Dowd DJ, Rae ID
(1989) Seed dispersal by ants: behaviour releasing compounds in elaiosomes. Oecologia 80, 490–497.
| Crossref |
Crossref |
Burke MJW, Grime JP
(1996) An experimental study on plant community invasibility. Ecology 77, 776–796.
Culver DC, Beattie AJ
(1978) Myrmecochory in Viola: dynamics of seed-ant interactions in some West Virginia species. Journal of Ecology 66, 53–72.
Culver DC, Beattie AJ
(1980) The fate of Viola seeds dispersed by ants. American Journal of Botany 67, 710–714.
Czerwinski Z,
Jakubczyk H, Petal J
(1971) Influence of ant hills on meadow soils. Pedobiologia 11, 277–285.
Danin A, Yom-Tov Y
(1990) Ant nests as primary habitats of Silybum marianum (Compositae). Plant Systematics and Evolution 169, 209–217.
Davidson DW, Morton SR
(1981) Myrmecochory in some plants (F. Chenopodiaceae) of the Australian arid zone. Oecologia 50, 357–366.
| Crossref |
Crossref |
Gramshaw D
(1972) Germination of annual ryegrass seeds (Lolium rigidum Gaud.) as influenced by temperature, light, storage environment, and age. Australian Journal of Agricultural Research 23, 779–787.
| Crossref |
Crossref |
Handel SN
(1976) Dispersal ecology of Carex pedunculata (Cyperaceae), a new North American myrmecochore. American Journal of Botany 63, 1071–1079.
Hanzawa FM,
Beattie AJ, Culver DC
(1988) Directed dispersal: demographic analysis of an ant–seed mutualism. American Naturalist 131, 1–13.
| Crossref | GoogleScholarGoogle Scholar |
Horvitz CC
(1981) Analysis of how ant behaviours affect germination in a tropical myrmecochore Calathea microencephala (P. and E.) Koernicke (Marantaceae): microsite selection and aril removal by neotropical ants, Odontomachus, Pachychondyla and Solenopsis (Formicidae). Oecologia 51, 47–52.
| Crossref |
Crossref |
Kjellsson G
(1985) Seed fate in a population of Carex pilulifera L. l. Seed dispersal and ant–seed mutualism. Oecologia 67, 416–423.
| Crossref |
Crossref |
Kjellsson G
(1985) Seed fate in a population of Carex pilulifera L. ll. Seed predation and its consequences for dispersal and seed bank. Oecologia 67, 424–429.
| Crossref |
Crossref |
Kusmenoglu S,
Rockwood LL, Gretz MR
(1989) Fatty acids and diacylglycerols from elaiosomes of some ant-dispersed seeds. Phytochemistry 28, 2601–2602.
| Crossref | GoogleScholarGoogle Scholar |
Lanza J,
Schmitt MA, Awad AB
(1992) Comparative chemistry of elaiosomes of three species of Trillium. Journal of Chemical Ecology 18, 209–221.
| Crossref |
Crossref |
Levey DJ, Byrne MM
(1993) Complex ant–plant interactions: rain forest ants as secondary dispersers and post-dispersal seed predators. Ecology 74, 1802–1812.
Lush WA,
Kaye PE, Groves RH
(1984) Germination of Clematis microphylla seeds following weathering and other treatments. Australian Journal of Botany 32, 121–129.
Miller IL, Pitt JL
(1990) Is Jatropha gossypiifolia the next Mimosa pigra? Australian Weed Research Newsletter 39, 1–6.
Skidmore BA, Heithaus ER
(1988) Lipid cues for seed-carrying by ants in Hepatica americana. Journal of Chemical Ecology 14, 2185–2196.
| Crossref |
Crossref |
Soukup VG, Holman RT
(1987) Fatty acids of seeds of North American pedicillate Trillium species. Phytochemistry 26, 1015–1018.
| Crossref | GoogleScholarGoogle Scholar |
Vitelli JS
(2000) Options for effective weed management. Tropical Grasslands 34, 280–294.
Zettler JA,
Spira TP, Allen CR
(2001) Ant–seed mutualisms — can red imported fire ants sour the relationship? Biological Conservation 101, 249–253.
| Crossref | GoogleScholarGoogle Scholar |