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BioControl

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Grasses as suitable targets for classical weed biological control

  • G. F. SuttonEmail author
  • K. Canavan
  • M. D. Day
  • A. den Breeyen
  • J. A. Goolsby
  • M. Cristofaro
  • A. McConnachie
  • I. D. Paterson
Review
  • 40 Downloads

Abstract

Grasses are amongst the most abundant and environmentally damaging invasive weeds worldwide. Biological control is frequently employed as a sustainable and cost-effective management strategy for many weeds. However, grasses have not been actively pursued as targets for classical weed biological control due to a perceived lack of sufficiently specialised and damaging natural enemies to use as biological control agents. There are also concerns that the risk posed to economically important crop/pasture species and closely-related native species is too great to consider implementing biological control for invasive grasses. In this paper, we review the literature and demonstrate that grasses can possess suitably host-specific and damaging natural enemies to warrant consideration as potential biological control agents. The risk of grass biological control is no greater than for other weedy taxa if practitioners follow appropriately rigorous risk assessments protocols.

Keywords

Invasive grass Arundo donax Phragmites australis Tetramesa Andropogon gayanus Host specificity 

Notes

Acknowledgements

S. Raghu and Martin Hill are thanked for providing valuable feedback on an earlier draft of this manuscript. We thank the editor, and two anonymous reviewers whose comments significantly improved this manuscript. This project is supported by funding from the Australian Government Department of Agriculture and Water Resources as part of its Rural R&D for Profit programme. The authors gratefully acknowledge funding support provided by the Australian Government through AgriFutures Australia, the CSIRO, and the Queensland Department of Agriculture and Fisheries for funding and the provision of this research project, and Rhodes University for logistical support. Part of the funding for this work was provided by the South African Research Chairs Initiative of the Department of Science and Technology and the National Research Foundation of South Africa. Any opinion, finding, conclusion or recommendation expressed in this material is that of the authors and the NRF does not accept any liability in this regard. Funding was also provided by the Working for Water (WfW) programme of the Department of Environmental Affairs: Natural Resource Management programme (DEA: NRM).

Compliance with ethical standards

Conflict of interest

The authors declare that they have no conflict of interest.

Research involving human participants and/or animals

This paper does not contain any studies with human participants or animals performed by any of the authors.

References

  1. Al-Barrak M (2006) Host choice in Tetramesa petiolata (Walker) (Hymenoptera: Eurytomidae). J Entomol 3:55–60CrossRefGoogle Scholar
  2. Anderson FE, Gallego L, Sánchez RM, Flemmer AC, Hansen PV, McClaren D, Barton J (2017) Plant/pathogen interactions observed during host range testing of the rust fungus Uromyces pencanus, a classical biological control agent for Chilean needle grass (Nassella neesiana) in Australia and New Zealand. Biocontrol Sci Technol 27:1096–1117CrossRefGoogle Scholar
  3. Ayres DR, Zaremba K, Strong DR (2004) Extinction of a common native species by hybridization with an invasive congener. Weed Technol 18:1288–1291CrossRefGoogle Scholar
  4. Benoit LK, Askins RA (1999) Impact of spread of Phragmites on the distribution of birds in Connecticut tidal marshes. Wetlands 19:194–208CrossRefGoogle Scholar
  5. Bernays E, Barbehenn R (1987) Nutritional ecology of grass foliage-chewing insects. In: Slansky F, Rodriguez JG (eds) Nutritional ecology of insects, mites, spiders and related invertebrates. Wiley Interscience, New York, pp 147–175Google Scholar
  6. Bernays E, Graham M (1988) On the evolution of host specificity in phytophagous arthropods. Ecology 69:886–892CrossRefGoogle Scholar
  7. Blossey B, Häfliger P, Tewksbury L, Dávalos A, Casagrande R (2018) Host specificity and risk assessment of Archanara geminipuncta and Archanara neurica, two potential biocontrol agents for invasive Phragmites australis in North America. Biol Control 125:98–112CrossRefGoogle Scholar
  8. Briese DT, Evans HC (1998) Biological control of serrated tussock (Nassella trichotoma): is it worth pursuing? Plant Prot Q 13:94–97Google Scholar
  9. Canavan K, Paterson ID, Hill MP, Dudley TL (2018) Testing the enemy release hypothesis on tall-statured grasses in South Africa, using Arundo donax, Phragmites australis, and Phragmites mauritianus as models. Bull Entomol Res 17:1–14Google Scholar
  10. Casagrande RA, Häfliger P, Hinz HL, Tewksbury L, Blossey B (2018) Grasses as appropriate targets in weed biocontrol: is the common reed, Phragmites australis, an anomaly? BioControl 63:391–403CrossRefGoogle Scholar
  11. Charudattan R, deLoach Jr CJ (1988) Management of pathogens and insects for weed control in agroecosystems. In: Altieri MA, Liebman E (eds) Weed management in agroecosystems: ecological applications. CRC Press, Bato Raton, pp 245–264Google Scholar
  12. Claridge M (1961) A contribution to the biology and taxonomy of some Palaearctic species of Tetramesa Walker (= Isosoma Walk.; = Harmolita Motsch.) (Hymenoptera: Eurytomidae), with particular reference to the British fauna. Trans R Entomol Soc Lond 113:175–217CrossRefGoogle Scholar
  13. Cook GD, Dias L (2006) It was no accident: deliberate plant introductions by Australian government agencies during the 20th century. Aust J Bot 54:601–625CrossRefGoogle Scholar
  14. Cornell HV (1989) Endophage-ectophage ratios and plant defense. Evol Ecol 3:64–76CrossRefGoogle Scholar
  15. Cortés E, Goolsby JA, Moran PJ, Marcos-García MA (2011) The effect of the armored scale, Rhizaspidiotus donacis (Hemiptera: Diaspididae), on shoot growth of the invasive plant Arundo donax (Poaceae: Arundinoideae). Biocontrol Sci Technol 21:535–545CrossRefGoogle Scholar
  16. Coughenour MB (1985) Graminoid responses to grazing by large herbivores: adaptations, exaptations, and interacting processes. Ann Mo Bot Gard 72:852–863CrossRefGoogle Scholar
  17. Cowie BW, Venter N, Witkowski ETF, Byrne MJ, Olckers T (2017) A review of Solanum mauritianum biocontrol: prospects, promise and problems: a way forward for South Africa and globally. BioControl 63:475–491CrossRefGoogle Scholar
  18. Crone EE, Marler M, Pearson DE (2009) Non-target effects of broadleaf herbicide on a native perennial forb: a demographic framework for assessing and minimizing impacts. J Appl Ecol 46:673–682CrossRefGoogle Scholar
  19. Cuda JP, Dunford JC, Leavengood JM Jr (2007) Invertebrate fauna associated with torpedograss, Panicum repens (Cyperales: Poaceae), in Lake Okeechobee, Florida, and prospects for biological control. Fla Entomol 90:238–248CrossRefGoogle Scholar
  20. Cummins GB (1971) The rust fungi of cereals, grasses and bamboos. Springer Science, Berlin, p 570CrossRefGoogle Scholar
  21. Daehler CC (1998) The taxonomic distribution of invasive angiosperm plants: ecological insights and comparison to agricultural weeds. Biol Conserv 84:167–180CrossRefGoogle Scholar
  22. Daehler CC, Strong DR (1995) Impact of high herbivore densities on introduced smooth cordgrass, Spartina alterniflora, invading San Francisco Bay, California. Estuaries 18:409–417CrossRefGoogle Scholar
  23. D’Antonio CM, Vitousek PM (1992) Biological invasions by exotic grasses, the grass/fire cycle, and global change. Annu Rev Ecol Syst 23:63–87CrossRefGoogle Scholar
  24. De Lillo E, Vidović B, Petanović R, Cristofaro M, Marini F, Augé M, Cvrković T, Babić E, Mattia C, Lotfollahi P, Rector B (2018) A new Aculodes species (Prostigmata: Eriophyoidea: Eriophyidae) associated with medusahead, Taeniatherum caput-medusae (L.) Nevski (Poaceae). Syst Appl Acarol 23:1217–1226Google Scholar
  25. Diaz R, Overholt WA, Cuda JP, Pratt PD, Fox A (2009) Host specificity of Ischnodemus variegatus, an herbivore of West Indian marsh grass (Hymenachne amplexicaulis). BioControl 54:307–321CrossRefGoogle Scholar
  26. Domenichini G, Nazzaro C, Mazzoni E (1989) Biological agents limiting the development of Sorghum halepense. In: Delfosse ES (ed) Proceedings of the VII symposium on biological control of weeds. Rome, Italy, pp 581–584Google Scholar
  27. Dubbert M, Tscharntke T, Vidal S (1998) Stem-boring insects of fragmented Calamagrostis habitats: herbivore–parasitoid community structure and the unpredictability of grass shoot abundance. Ecol Entomol 23:271–280CrossRefGoogle Scholar
  28. D’Urso V, Lisi O, Sabella G (2017) The alien leafhopper Balclutha brevis Lindberg, 1954 (Hemiptera Cicadellidae) and its hostplant, the invasive Poaceae Pennisetum setaceum (Försskal) Chiov.: a real risk in the scenario of Mediterranean land biodiversity? Biodivers J 8:145–150Google Scholar
  29. Edwards KM, Schlesinger C, Ooi MKJ, French K, Goeden B (2019) Invasive grass affects seed viability of native perennial shurbs in arid woodlands. Biol Invasions 21:1763–1774CrossRefGoogle Scholar
  30. Ehrlich PR, Raven PH (1964) Butterflies and plants: a study in coevolution. Evolution 18:586–608CrossRefGoogle Scholar
  31. Ellison CA, Evans H (1995) Present status of the biological control programme for the graminaceous weed Rottboellia cochinchinensis. In: Delfosse ES, Scott RR (eds) Proceedings of the VIII international symposium on biological control of weeds. CSIRO Entomology, Melbourne, Australia, pp 493–500Google Scholar
  32. Evans H (1991) Biological control of tropical grassy weeds. In: Baker FWG, Terry PJ (eds) Tropical grassy weeds. CAB International, Wallingford, pp 52–72Google Scholar
  33. Ferdinands K, Beggs K, Whitehead P (2005) Biodiversity and invasive grass species: multiple use or monoculture? Wildl Res 32:447–457CrossRefGoogle Scholar
  34. Firn J (2009) African lovegrass in Australia: a valuable pasture species or embarrassing invader? Trop Grassl 43:86–97Google Scholar
  35. García-Guzmán G, Burdon JJ (1997) Impact of the flower smut Ustilago cynodontis (Ustilaginaceae) on the performance of the clonal grass Cynodon dactylon (Gramineae). Am J Bot 84:1565–1571CrossRefPubMedGoogle Scholar
  36. Gassó MMA, Lovisolo M, Perelló A (2017) Effects of loose kernel smut caused by Sporisorium cruentum on rhizomes of Sorghum halepense. J Plant Prot Res 57:62–71CrossRefGoogle Scholar
  37. Gill G, Blacklow W (1984) Effect of great brome (Bromus diandrus Roth.) on the growth of wheat and great brome and their uptake of nitrogen and phosphorus. Aust J Agric Res 35:1–8CrossRefGoogle Scholar
  38. Godfree R, Firn J, Johnson S, Knerr N, Stol J, Doerr V (2017) Why non-native grasses pose a critical emerging threat to biodiversity conservation, habitat connectivity and agricultural production in multifunctional rural landscapes. Landsc Ecol 32:1219–1242Google Scholar
  39. Goolsby JA, Moran P (2009) Host range of Tetramesa romana Walker (Hymenoptera: Eurytomidae), a potential biological control of giant reed, Arundo donax L. in North America. Biol Control 49:160–168CrossRefGoogle Scholar
  40. Goolsby JA, Moran PJ, Adamczyk JJ, Kirk AA, Jones WA, Marcos MA, Cortés E (2009a) Host range of the European, rhizome-stem feeding scale Rhizaspidiotus donacis (Hemiptera: Diaspididae), a candidate biological control agent for giant reed, Arundo donax (Poales: Poaceae) in North America. Biocontrol Sci Technol 19:899–918CrossRefGoogle Scholar
  41. Goolsby JA, Spencer D, Whitehand L (2009b) Pre-release assessment of impact on Arundo donax by the candidate biological control agents Tetramesa romana (Hymenoptera: Eurytomidae) and Rhizaspidiotus donacis (Hemiptera: Diaspididae) under quarantine conditions. Southwest Entomol 34:359–376CrossRefGoogle Scholar
  42. Goolsby JA, Moran PJ, Racelis AE, Summy KR, Jimenez MM, Lacewell RD, Perez de Leon A, Kirk AA (2016) Impact of the biological control agent Tetramesa romana (Hymenoptera: Eurytomidae) on Arundo donax (Poaceae: Arundinoideae) along the Rio Grande River in Texas. Biocontrol Sci Technol 26:47–60CrossRefGoogle Scholar
  43. Goolsby JA, Vacek AT, Salinas C, Racelis A, Moran PJ, Kirk AA (2017) Host range of the European leaf sheath mining midge, Lasioptera donacis Coutin (Diptera: Cecidomyiidae), a biological control of giant reed, Arundo donax L. Biocontrol Sci Technol 27:781–795CrossRefGoogle Scholar
  44. Grevstad FS, Strong DR, Garcia-Rossi D, Switzer RW, Wecker MS (2003) Biological control of Spartina alterniflora in Willapa Bay, Washington using the planthopper Prokelisia marginata: agent specificity and early results. Biol Control 27:32–42CrossRefGoogle Scholar
  45. Grice AC, Friedel MH, Marshall NA, van Klinken RD (2012) Tackling contentious invasive plant species: a case study of invasive buffel grass in Australia. Environ Manage 49:285–294CrossRefPubMedGoogle Scholar
  46. Häfliger P, Schwarzlaender M, Blossey B (2005) Biology of Platycephala planifrons (Diptera: Chloropidae) and its potential effectiveness as biological control agent for invasive Phragmites australis in North America. Biol Control 34:302–311CrossRefGoogle Scholar
  47. Häfliger P, Schwarzländer M, Blossey B (2006) Impact of Archanara geminipuncta (Lepidoptera: Noctuidae) on aboveground biomass production of Phragmites australis. Biol Control 38:413–421CrossRefGoogle Scholar
  48. Hardy NB, Cook LG (2010) Gall-induction in insects: evolutionary dead-end or speciation driver? BMC Evol Biol 10:257CrossRefPubMedPubMedCentralGoogle Scholar
  49. Harvey TL, Martin TJ, Seifers DL (2002) Wheat yield reduction due to Wheat Curl Mite (Acari: Eriophyidae) infestations. J Agric Urban Entomol 19:9–13Google Scholar
  50. Hayes L (2015) Pampas project makes progress. Manaaki Whenua Landcare Res 72:5–6Google Scholar
  51. Heidinga L, Wilson SD (2002) The impact of an invading alien grass (Agropyron cristatum) on species turnover in native prairie. Divers Distrib 8:249–258CrossRefGoogle Scholar
  52. Hinz HL, Winston RL, Schwarzländer M (2019) How safe is weed biological control? A global review of direct nontarget attack. Q Rev Biol 94(1):1–27CrossRefGoogle Scholar
  53. Hui C, Richardson DM (2017) Invasion dynamics. Oxford University Press, OxfordCrossRefGoogle Scholar
  54. Johnston MR, Carsten LD, Douglas L, Sands DC (2000) Epidemic development and virulence in 1995-1998 of Puccinia coronata, a potential biocontrol agent of wild oats on San Clemente Island. Biol Control 17:250–257CrossRefGoogle Scholar
  55. Kellogg EA (2015) Flowering plants. Monocots. Springer International Publishing, ChamCrossRefGoogle Scholar
  56. Kiviat E, Meyerson LA, Mozdzer TJ, Allen WJ, Baldwin AH, Bhattari GP, Brix H, Caplan JS, Kettenring JM, Lambertini C, Weis J, Whigham DF, Cronin JT (2019) Evidence does not support the targeting of cryptic invaders at the subspecies level using classical biological control: the example of Phragmites. Biol Invasions 21:2529–2541CrossRefGoogle Scholar
  57. Lake EC, Minteer CR (2018) A review of the integration of classical biological control with other techniques to manage invasive weeds in natural areas and rangelands. BioControl 63:71–86CrossRefGoogle Scholar
  58. Laska A, Majer A, Szydło W, Karpicka-Ignatowska K, Hornyák M, Labrzycka A, Skoracka A (2018) Cryptic diversity within grass-associated Abacarus species complex (Acariformes: Eriophyidae), with the description of a new species, Abacarus plumiger n. sp. Exp Appl Acarol 76:1–28CrossRefPubMedGoogle Scholar
  59. Le Gac M, Hood ME, Fournier E, Giraud T (2007) Phylogenetic evidence of host-specific cryptic species in the anther smut fungus. Evolution 61:15–26CrossRefPubMedGoogle Scholar
  60. Leonard KJ, Szabo LJ (2005) Stem rust of small grains and grasses caused by Puccinia graminis. Mol Plant Pathol 6:99–111CrossRefPubMedGoogle Scholar
  61. Linder HP, Lehmann CER, Archibald S, Osborne CP, Richardson DM (2017) Global grass (Poaceae) success underpinned by traits facilitating colonization, persistence and habitat transformation. Biol Rev 93:1125–1144CrossRefPubMedGoogle Scholar
  62. Lowe S, Browne M, Boudjelas S, De Poorter M (2000) 100 of the world’s worst invasive alien species: a selection from the global invasive species database. Invasive Species Specialist Group Auckland, http://www.iucngisd.org/gisd/100_worst. Accessed 14 Aug 2019
  63. Marshall M, Goolsby JA, Vacek AT, Moran PJ, Kirk AA, Cortes Mendoza E, Cristofaro M, Bownes A, Mastoras A, Kashefi J, Chaskopoulou A, Smith L, Goldsmith B, Racelis AE (2018) Densities of the arundo wasp, Tetramesa romana (Hymenoptera: Eurytomidae) across its native range in Mediterranean Europe and introduced ranges in North America and Africa. Biocontrol Sci Technol 28:772–785CrossRefGoogle Scholar
  64. McClay AS, Balciunas JK (2005) The role of pre-release efficacy assessment in selecting classical biological control agents for weeds—applying the Anna Karenina principle. Biol Control 35:197–207CrossRefGoogle Scholar
  65. McDaniel B, Boe A (1990) A new host record for Eurytomocharis eragrostidis Howard (Chalcidoidea: Eurytomidae) infesting Eragrostis tef in South Dakota. Proc Entomol Soc Wash 92:465–470Google Scholar
  66. McEvoy PB, Coombs EM (1999) Biological control of plant invaders: regional patterns, field experiments, and structured population models. Ecol Appl 9:387–401CrossRefGoogle Scholar
  67. McFadyen REC (1998) Biological control of weeds. Annu Rev Entomol 43:369–393CrossRefPubMedGoogle Scholar
  68. McFadyen REC, Morin L (2012) Senecio madagascariensis Poir.—fireweed. In: Julien MH, McFadyen REC, Cullen JM (eds) Biological control of weeds in Australia. CSIRO Publishing, Melbourne, pp 526–536Google Scholar
  69. McNaughton SJ, Tarrants JL, McNaughton MM, Davis RD (1985) Silica as a defense against herbivory and a growth promotor in African grasses. Ecology 66:528–535CrossRefGoogle Scholar
  70. Mercadier G, Goolsby JA, Jones WA, Tamesse JL (2009) Results of a preliminary survey in Cameroon, Central Africa, for potential natural enemies of Guineagrass, Panicum maximum. Subtrop Plant Sci 61:31–36Google Scholar
  71. Moore BD, Johnson SN (2017) Get tough, get toxic, or get a bodyguard: identifying candidate traits conferring belowground resistance to herbivores in grasses. Front Plant Sci 7:1925CrossRefPubMedPubMedCentralGoogle Scholar
  72. Moran PJ, Vacek AT, Racelis AE, Pratt PD, Goolsby JA (2017) Impact of the Arundo wasp, Tetramesa romana (Hymenoptera: Eurytomidae), on biomass of the invasive weed, Arundo donax (Poaceae: Arundinoideae), and on revegetation of riparian habitat along the Rio Grande in Texas. Biocontrol Sci Technol 27:96–114CrossRefGoogle Scholar
  73. Muniappan R, McFadyen R (2005) Gall-inducing arthropods used in the biological control of weeds. In: Raman A, Schaefer CW, Withers TM (eds) Biology, ecology, and evolution of gall-inducing arthropods, vol 1–2. Science Publishers Inc., Enfield, pp 709–730Google Scholar
  74. Nartshuk EP (2014) Grass-fly larvae (Diptera, Chloropidae): diversity, habitats, and feeding specializations. Entomol Rev 94:514–525CrossRefGoogle Scholar
  75. Nestory S (2016) Biological and mechanical control of Japanese stiltgrass (Microstegium vimineum). MSc Thesis, University of Delaware, USAGoogle Scholar
  76. Overholt WA, Hidayat P, Le Ru B, Takasu K, Goolsby JA, Racelis A, Burrell AM, Amalin D, Agum W, Mjaku M, Pallangyo B, Klein PE, Cuda JP (2016) Potential biological control agents for the management of cogongrass (Cyperales: Poaceae) in the southeastern USA. Fla Entomol 99:734–739CrossRefGoogle Scholar
  77. Paterson ID, Hoffmann JH, Klein H, Mathenge CW, Neser S, Zimmermann HG (2011) Biological control of Cactaceae in South Africa. Afr Entomol 19:230–246CrossRefGoogle Scholar
  78. Paynter Q, Fowler SV, Gourlay AH, Peterson PG, Smith LA, Winks CJ (2015) Relative performance on test and target plants in laboratory tests predicts the risk of non-target attack in the field for arthropod weed biocontrol agents. Biol Control 80:133–142CrossRefGoogle Scholar
  79. Pearson DE, Callaway RM (2003) Indirect effects of host-specific biological control agents. Trends Ecol Evol 18:456–461CrossRefGoogle Scholar
  80. Pemberton RW (1996) The potential of biological control for the suppression of invasive weeds of southern environments. Castanea 61:313–319Google Scholar
  81. Pemberton RW (2002) Selection of appropriate future target weeds for biological control. In: van Driesche R, Lyon S, Blossey B, Hoddle M, Reardon R (eds) Biological control of weeds in the Eastern United States. United States Department of Agriculture, Forest Service, FHTET-2002-04, Morgantown, pp 375–386Google Scholar
  82. Piątek M, Lutz M, Jacobs A, Villablanca F, Wood A (2015) Epitypification of Tilletia ehrhartae, a smut fungus with potential for nature conservation, biosecurity and biocontrol. Eur J Plant Pathol 143:151–158CrossRefGoogle Scholar
  83. Powles SB, Yu Q (2010) Evolution in action: plants resistant to herbicides. Annu Rev Plant Biol 61:317–347CrossRefPubMedGoogle Scholar
  84. Pyšek P, Jarošík V, Hulme PE, Pergl J, Hejda M, Schaffner U, Vilá M (2012) A global assessment of invasive plant impacts on resident species, communities and ecosystems: the interaction of impact measures, invading species’ traits and environment. Glob Change Biol 18:1725–1737CrossRefGoogle Scholar
  85. Quirion B, Simek Z, Dávalos A, Blossey B (2018) Management of invasive Phragmites australis in the Adirondacks: a cautionary tale about prospects of eradication. Biol Invasions 20:59–73CrossRefGoogle Scholar
  86. Racelis AE, Davey RB, Goolsby JA, Perez de Leon AA, Varner K, Duhaime R (2012) Facilitative ecological interactions between invasive species: Arundo donax stands as favorable habitat for cattle ticks (Acari: Ixodidae) along the U.S.–Mexico border. J Med Entomol 49:410–417CrossRefPubMedGoogle Scholar
  87. Raman A (1993) Chemical ecology of gall insect–host plant interactions: substances that influence the nutrition and resistance of insects and the growth of galls. In: Ananthakrishnan TN, Raman A (eds) Chemical ecology of phytophagous insects. Oxford & IBH Publishing Co., New Delhi, pp 227–250Google Scholar
  88. Randall RP (2017) A global compendium of weeds, 3rd edn. R.P. Randall, PerthGoogle Scholar
  89. Ray CA, Sherman JJ, Godinho AL, Hanson N, Parker IM (2018) Impacts and best management practices for Erect Veldtgrass (Ehrharta erecta). Invasive Plant Sci Manag 11:40–48CrossRefGoogle Scholar
  90. Scheirs J, Bruyn LD, Verhagen R (2003) Host nutritive quality and host plant choice in two grass miners: primary roles for primary compounds? J Chem Ecol 29(6):1373–1389CrossRefGoogle Scholar
  91. Schwarzländer M, Hinz HL, Winston RL, Day MD (2018) Biological control of weeds: an analysis of introductions, rates of establishment and estimates of success, worldwide. BioControl 63:319–331CrossRefGoogle Scholar
  92. Setterfield SA, Rossiter-Rachor NA, Hutley LB, Douglas MM, Williams RJ (2010) Turning up the heat: the impacts of Andropogon gayanus (gamba grass) invasion on fire behaviour in northern Australian savannas. Divers Distrib 16:854–861CrossRefGoogle Scholar
  93. Showler AT, Osbrink WLA (2018) The arundo wasp, Tetramesa romana, does not control giant river reed, Arundo donax, in Texas, USA. Entomol Exp Appl 166:883–893CrossRefGoogle Scholar
  94. Sileshi G (1997) Potential biocontrol agents for the blue couch grass, Digitaria abyssinica (A. Rich.) Stapf., in East Africa. Int J Pest Manage 43:173–176CrossRefGoogle Scholar
  95. Simmonds FJ (1972) Biological control in the tropics. CIBC Trop Bull 15:159–169Google Scholar
  96. Skoracka A, Smith L, Oldfield G, Cristofaro M, Amrine JW (2010) Host-plant specificity and specialization in eriophyoid mites and their importance for the use of eriophyoid mites as biocontrol agents of weeds. Exp Appl Acarol 51:93–113CrossRefPubMedGoogle Scholar
  97. Smith MC, Reeder RH, Thomas MB (1997) A model to determine the potential for biological control of Rottboellia cochinchinensis with the head smut Sporisorium ophiuri. J Appl Ecol 34:388–398CrossRefGoogle Scholar
  98. Smith L, De Lillo E, Amrine JW (2010) Effectiveness of eriophyid mites for biological control of weedy plants and challenges for future research. Exp Appl Acarol 51:115–149CrossRefPubMedGoogle Scholar
  99. Spears BM, Barr WF (1985) Effect of jointworms on the growth and reproduction of four native range grasses of Idaho. J Range Manag 38:44–46CrossRefGoogle Scholar
  100. Strong DR, Lawton JH, Southwood SR (1984) Insects on plants. Community patterns and mechanisms. Blackwell Scientific Publications, OxfordGoogle Scholar
  101. Takasu K, Yoshiyasu Y, Burrell AM, Klein PE, Racelis A, Goolsby JA, Overholt WA (2014) Acrapex azumai Sugi (Lepidoptera, Noctuidae) as a potential biological control agent of the invasive weed Imperata cyclindrica (L.) Beauv. (Poaceae) in the United States. Lepid Sci 65:30–35Google Scholar
  102. Tewksbury L, Casagrande R, Blossey B, Häflinger P, Schwarzländer M (2002) Potential for biological control of Phragmites australis in North America. Biol Control 23:191–212CrossRefGoogle Scholar
  103. Tosiah S, Kadir J, Sariah M, Juraimi AS, Lo NP, Soetikno S (2009) Survey and evaluation of native fungal pathogens for biocontrol of barnyard grass (Echinochloa crus-galli complex). J Trop Agric Fd Sc 37:119–128Google Scholar
  104. Tracy JL, DeLoach CJ (1998) Suitability of classical biological control for giant reed (Arundo donax) in the United States. University of California Cooperative Extension, Holtville, pp 73–109Google Scholar
  105. Tscharntke T, Greiler HJ (1995) Insect communities, grasses, and grasslands. Annu Rev Entomol 40:535–558CrossRefGoogle Scholar
  106. van Klinken RD, Friedel MH (2017) Unassisted invasions: understanding and responding to Australia’s high-impact environmental grass weeds. Aust J Bot 65:678–690CrossRefGoogle Scholar
  107. van Loan A, Meeker J, Minno M (2002) Cogongrass. In: van Driesche R, Lyon S, Blossey B, Hoddle M, Reardon R (eds) Biological control of weeds in the Eastern United States. United States Department of Agriculture, Forest Service, FHTET-2002-04, Morgantown, pp 353–364Google Scholar
  108. Vánky K (2003) The smut fungi (Ustilaginomycetes) of Sporobolus (Poaceae). Fungal Divers 14:205–241Google Scholar
  109. Vicari M, Bazely DR (1993) Do grasses fight back? The case for antiherbivore defences. Trends Ecol Evol 8:137–141CrossRefPubMedGoogle Scholar
  110. Vitelli JS, Tan YP, Riding N, Holdom DG, Chamberlain A, Shivas RG (2017) First record of Ustilago sporoboli-indici in Australia. Australas Plant Dis Notes 12:52CrossRefGoogle Scholar
  111. Wapshere A (1990) Biological control of grass weeds in Australia: an appraisal. Plant Prot Q 5:62–75Google Scholar
  112. Wells MJ (1977) Progress with research on Nassella tussock. In: Balkema AA (ed) Proceedings of the second national weeds conference of South Africa. Stellenbosch, South Africa, pp 48–55Google Scholar
  113. Widmer TL, Sforza R (2004) Exploration for plant pathogens against Taeniatherum caput-medusae (medusahead ryegrass). In: Cullen JM, Briese DT, Kriticos DJ, Lonsdale WM, Morin L, Scott JK (eds) Proceedings of the XI international symposium on biological control of weeds. CSIRO Entomology, Canberra, Australia, pp 193–197Google Scholar
  114. Williams DG, Baruch Z (2000) African grass invasion in the Americas: ecosystem consequences and the role of ecophysiology. Biol Invasions 2:123–140CrossRefGoogle Scholar
  115. Williams JL, Crone EE (2007) The impact of invasive grasses on the population growth of Anemone patens, a long-lived native forb. Ecology 87:3200–3208CrossRefGoogle Scholar
  116. Winder RS, van Dyke CG (1990) The pathogenicity, virulence, and biocontrol potential of two Bipolaris species on Johnsongrass (Sorghum halepense). Weed Sci 38:89–94CrossRefGoogle Scholar
  117. Winston RL, Schwarzländer M, Hinz HL, Day MD, Cock MJW, Julien MH (2014) Biological control of weeds: a world catalogue of agents and their target weeds, 5th edn. USDA Forest Service, Forest Health Technology Enterprise Team, FHTET-2014-04, MorgantownGoogle Scholar
  118. Witt A, McConnachie AJ (2004) The potential for classical biological control of invasive grass species with special reference to invasive Sporobolus spp. (Poaceae) in Australia. In: Cullen JM, Briese DT, Kriticos DJ, Lonsdale WM, Morin L, Scott JK (eds) Proceedings of the XI international symposium on biological control of weeds. CSIRO Entomology, Canberra, Australia, pp 198–202Google Scholar
  119. Wu M-Y, Hacker S, Ayres D, Strong DR (1999) Potential of Prokelisia spp. as biological control agents of English cordgrass, Spartina anglica. Biol Control 16:267–273CrossRefGoogle Scholar
  120. Yobo KS, Laing MD, Palmer WA, Shivas RG (2009) Evaluation of Ustilago sporoboli-indici as a classical biological control agent for invasive Sporobolus grasses in Australia. Biol Control 50:7–12CrossRefGoogle Scholar
  121. Youtie BA, Stafford M, Johnson JB (1987) Herbivorous and parasitic insect guilds associated with Great Basin wildrye (Elymeus cinereus) in southern Idaho. Great Basin Nat 47:644–651Google Scholar
  122. Zachariades C, Paterson ID, Strathie LW, Hill MP, van Wilgen BW (2017) Assessing the status of biological control as a management tool for suppression of invasive alien plants in South Africa. Bothalia 47:a2142CrossRefGoogle Scholar

Copyright information

© International Organization for Biological Control (IOBC) 2019

Authors and Affiliations

  • G. F. Sutton
    • 1
    Email author
  • K. Canavan
    • 1
  • M. D. Day
    • 2
  • A. den Breeyen
    • 3
  • J. A. Goolsby
    • 4
  • M. Cristofaro
    • 5
    • 6
  • A. McConnachie
    • 7
  • I. D. Paterson
    • 1
  1. 1.Department of Zoology and Entomology, Centre for Biological ControlRhodes UniversityGrahamstownSouth Africa
  2. 2.Department of Agriculture and FisheriesBrisbaneAustralia
  3. 3.ARC-Plant Health and Protection, Weed Pathology UnitStellenboschSouth Africa
  4. 4.United States Department of Agriculture, Agricultural Research Service, Plains Area, Knipling-Bushland U.S. Livestock Insects Research Laboratory, Cattle Fever Tick Research LaboratoryEdinburgUSA
  5. 5.Biotechnology and Biocontrol AgencyRomeItaly
  6. 6.ENEA, C. R. CasacciaRomeItaly
  7. 7.Weed Research Unit, New South Wales Department of Primary Industries, Biosecurity and Food SafetyOrangeAustralia

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