Skip to main content
Log in

The influence of mistletoes on the litter-layer arthropod abundance and diversity in a semi-arid savanna, Southwest Zimbabwe

  • Regular Article
  • Published:
Plant and Soil Aims and scope Submit manuscript

Abstract

Aims

The below-canopy soil moisture content and litter-layer arthropod abundance and diversity of Acacia karroo trees parasitized by each of three mistletoe species (Erianthemum ngamicum, Plicosepalus kalachariensis, and Viscum verrucosum) and uninfected A. karroo trees were investigated in semi-arid savanna, southwest Zimbabwe.

Results

The soils below the canopies of mistletoe-infected trees were significantly low in moisture content compared to those beneath uninfected A. karroo trees. Nevertheless, arthropod species diversity was greater by up to 34 % below the canopies of mistletoe-infected trees than beneath uninfected A. karroo trees, with greater abundances beneath trees infected by E. ngamicum and P. kalachariensis. In addition, the majority of the arthropod species associated with mistletoe-infected trees had litter as their dominant foraging substrate.

Conclusions

Our findings show that mistletoes increase the abundance and diversity of litter-dwelling and –foraging arthropods due to increase in the quality and quantity of litterfall beneath mistletoe-infected trees. By altering the below-canopy arthropod communities and soil moisture content, mistletoes have potential to modify ecosystem processes such as decomposition, soil process rates, and nutrient cycling. Therefore, we suggest that the resulting increase in resource heterogeneity plays an important role in determining the structure and functioning of semi-arid savanna ecosystems.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3

Similar content being viewed by others

References

  • Anderson SJ, Braby M (2009) Invertebrate diversity associated with tropical mistletoe in a suburban landscape from northern Australia. North Territ Nat 21:2–23

    Google Scholar 

  • Barberena-Arias MF, González G, Cuevas E (2012) Quantifying variation of soil arthropods using different sampling protocols: is diversity affected? In: Sudarshana P, Nageswara-Rao M, Soneji JR (eds) Tropical Forest. InTech Online Publisher, www.intechopen.com, pp. 51–70

  • Bardgett RD (2005) The Biology of Soil: A Community and Ecosystem. Oxford University Press, Oxford

    Book  Google Scholar 

  • Bultman TL, Uetz GW (1984) Effect of structure and nutritional quality of litter on abundances of litter-dwelling arthropods. Am Midl Nat 111:165–172

    Article  Google Scholar 

  • Burns AE, Cunningham SA, Watson DM (2011) Arthropod communities in tree canopies: an ordinal comparison between assemblages on mistletoes and their eucalypt hosts. Aust J Entomol 50:221–230

    Google Scholar 

  • Canyon DV, Hill CJ (1997) Mistletoe host-resemblance: a study of herbivory, nitrogen and moisture in two Australian mistletoes and their host trees. Aust J Ecol 22:395–403

    Article  Google Scholar 

  • Cullings K, Hanely J (2010) Dwarf mistletoe effects on soil basidomycete community structure, soil fungal functional diversity, and soil enzyme function: implications for climate change. Soil Biol Biochem 42:1976–1981

    Article  CAS  Google Scholar 

  • Cullings K, Raleigh C, Vogler DR (2005) Effects of dwarf mistletoe infection on the ectomycorrhizal community of a Pinus contorta stand in Yellowstone Park. Can J Bot 83:1174–1180

    Article  Google Scholar 

  • Dye PJ (1983) Prediction of variation in grass growth in a semi-arid induced grassland. PhD thesis, University of the Witswatersrand, Johannesburg, South Africa

  • Dye PJ, Walker BH (1987) Patterns of shoot growth in a semi-arid grassland in Zimbabwe. J App Ecol 24:633–644

    Article  Google Scholar 

  • Ehleringer JR, Marshall JD (1995) Water relations. In: Press MC, Graves DJ (eds) Parasitic plants. Chapman and Hall, London, pp 125–140

    Google Scholar 

  • Holt JA, Coventry RJ (1990) Nutrient cycling in Australian savannas. J Biogeogr 17:427–432

    Article  Google Scholar 

  • Irish J (1992) The Hetrodinae (Orthoptera: Enisfera: Bradyporidae) of Southern Africa: Systematics and Phylogeny. Navors Nas Mus Bloemfontein 8:394–434

    Google Scholar 

  • Kareiva P (1987) Habitat fragmentation and the stability of predator–prey interactions. Nature 326:388–390

    Article  Google Scholar 

  • Krebs CJ (1999) Ecological methodology. Benjamin Cummings, Menlo Park

    Google Scholar 

  • Kuijt J (1969) The biology of parasitic flowering plants. University of California Press, Berkeley

    Google Scholar 

  • Malaka SLO (1996) Termites in West Africa. University of Lagos Press, Lagos

    Google Scholar 

  • Mapaura A, Timberlake J (2004) A checklist of Zimbabwean vascular plants. Southern African Botanical Diversity Network Report No. 33. SABONET, Pretoria and Harare

  • March WA (2007) The impact of an Australian mistletoe, Amyema miquelii (Loranthaceae), on nutrient cycling in eucalypt forests and woodlands (PhD Thesis). Charles Sturt University, Thurgoona

  • March WA, Watson DM (2007) Parasites boost productivity: effects of mistletoe on litterfall dynamics in a temperate Australian forest. Oecologia 154:339–347

    Article  PubMed  Google Scholar 

  • March WA, Watson DM (2010) The contribution of mistletoes to nutrient returns: evidence for a critical role in nutrient cycling. Aust Ecol 35:713–721

    Article  Google Scholar 

  • Mueller RC, Gehring CA (2006) Interactions between an above-ground plant parasite and below-ground ectomycorrhizal fungal communities on pinyon pine. J Ecol 94:276–284

    Article  Google Scholar 

  • Ndagurwa HGT, Dube JS, Mlambo D (2013) The influence of mistletoes on nitrogen cycling in a semi-arid savanna, southwest Zimbabwe. J Trop Ecol 29:147–159

    Article  Google Scholar 

  • Ndagurwa HGT, Dube JS, Mlambo D, Mlambo D (2014) The influence of mistletoes on nutrient cycling in a semi-arid savanna, southwest Zimbabwe. Plant Ecol 215:15–26

  • Ndagurwa HGT, Mundy PJ, Dube JS, Mlambo D (2012) Patterns of mistletoe infection in four Acacia species in a semi-arid southern African savanna. J Trop Ecol 28:523–526

    Article  Google Scholar 

  • Picker M, Griffiths C, Weaving A (2004) Field Guide to Insects of South Africa. Struik, South Africa

    Google Scholar 

  • Press MC (1998) Dracula or Robin Hood? A functional role of root hemiparasites in nutrient poor ecosystems. Oikos 82:609–611

    Article  Google Scholar 

  • Press MC, Phoenix GK (2005) Impacts of parasitic plants on natural communities. New Phytol 166:737–751

    Article  PubMed  Google Scholar 

  • Rattray JM (1957) The grasses and grass associations of southern Rhodesia. Rhod Agric J 54:197–234

    Google Scholar 

  • Razeng E, Watson DM (2012) What do declining woodland birds eat? A synthesis of dietary records. Emu 112:149–159

    Article  Google Scholar 

  • Room PM (1972a) The constitution and natural history of the fauna of the mistletoe Tapinanthus bangwensis (Engl. & K. Krause) growing on cocoa in Ghana. J Anim Ecol 41:519–535

    Article  Google Scholar 

  • Room PM (1972b) The fauna of the mistletoe Tapinanthus bangwensis (Engl. & K. Krause) growing on cocoa in Ghana: relationships between fauna and mistletoe. J Anim Ecol 41:611–621

    Article  Google Scholar 

  • Sala A, Carrey EV, Callaway RM (2001) Dwarf mistletoe affects whole-tree water relations of Douglas fir and western larch primarily through changes in leaf to sapwood ratios. Oecologia 126:42–52

    Article  Google Scholar 

  • Scholtz CH, Holm E (1985) Insects of Southern Africa. Butterworths, Durban

    Google Scholar 

  • Schuurman G (2005) Decomposition rates and termite assemblage composition in semiarid Africa. Ecology 86:1236–1249

    Article  Google Scholar 

  • Seastedt TR, Crossley DA (1981) Microarthropod response following cable logging and clear-cutting in the southern Appalachians. Ecology 62:126–135

    Article  Google Scholar 

  • Shaw DC, Watson DM, Mathiason RL (2004) Comparison of dwarf mistletoes (Arceuthobium spp., Viscaceae) in the western United States with mistletoes (Amyema spp., Loranthaceae) in Australia – ecological analogs and reciprocal models for ecosystem management. Aust J Bot 52:481–498

    Article  Google Scholar 

  • Skaife SH (1979) African insect life. Struik, Cape Town

    Google Scholar 

  • Swift MJ, Heal OW, Anderson JM (1979) Decomposition in Terrestrial Ecosystems. University of California Press, Berkeley

    Google Scholar 

  • Van der Putten WH, Van Dijk C, Peters BAM (1993) Plant-specific soil-borne diseases contribute to succession in foredune vegetation. Nature 362:53–56

    Article  Google Scholar 

  • Ward HK, Richardson FD, Denny RP, Dye PT (1979) Matopos research station: a perspective. Rhod Agric J 76:5–18

    Google Scholar 

  • Wardle DA (2002) Communities and ecosystems. Linking the aboveground and belowground components. Princeton University Press, Princeton, p 57

    Google Scholar 

  • Watson DM (2001) Mistletoe—a keystone resource in forests and woodlands worldwide. Ann Rev Ecol Syst 32:219–249

    Article  Google Scholar 

  • Watson DM (2002) Effects of mistletoe on diversity: a casestudy from southern New South Wales. Emu 102:275–281

    Article  Google Scholar 

  • Watson DM (2009) Parasitic plants as facilitators: more Dryad than Dracula? J Ecol 97:1151–1159

    Article  Google Scholar 

  • Watson DM (2011) A productivity-based explanation for woodland bird declines: poorer soils yield less food. Emu 111:10–18

    Article  Google Scholar 

  • Watson DM, Herring M (2012) Mistletoe as a keystone resource: an experimental test. Proc R Soc B 279:3853–3860

    Article  PubMed  PubMed Central  Google Scholar 

  • Watson DM, McGregor HW, Spooner PG (2009) Hemiparasitic shrubs increase resource availability and multi-trophic diversity of eucalypt forest birds. Funct Ecol 150:889–899

    Google Scholar 

  • Whittake PL (1982) Community ecology of Phoradendron tomentosum in southern Texas. PhD thesis, University of Texas, Austin, Texas

Download references

Acknowledgments

This research was supported by a grant from the National University of Science and Technology Research Board (Grant RB/11/10). We are grateful to the people who assisted with fieldwork, particularly Alford Magwizi, Kudzanai Dhliwayo, and Obey Sonono. Laboratory work was carried out at the Natural History Museum of Zimbabwe, and were are grateful to the Department of Entomology specifically, Kudzai Mafuwe and staff. We also thank David M Watson and another anonymous reviewer for their time and effort that allowed us to increase the clarity and quality of our work.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Hilton G. T. Ndagurwa.

Additional information

Responsible Editor: Duncan D. Cameron.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Ndagurwa, H.G.T., Dube, J.S., Mlambo, D. et al. The influence of mistletoes on the litter-layer arthropod abundance and diversity in a semi-arid savanna, Southwest Zimbabwe. Plant Soil 383, 291–299 (2014). https://doi.org/10.1007/s11104-014-2176-8

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s11104-014-2176-8

Keywords

Navigation