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Evaluating tree wētā (Orthoptera: Anostostomatidae: Hemideina species) as bioindicators for New Zealand national biodiversity monitoring

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Abstract

Indicator taxa are increasingly being used to evaluate the natural environment because they provide both quantified and simplified information about complex phenomena and because they result in huge cost savings compared with monitoring entire biotas. In this paper, we examine the suitability of an iconic New Zealand invertebrate, the tree wētā (Orthoptera: Anostostomatidae: Hemideina species), as a bioindicator for invertebrates under a national biodiversity monitoring scheme in New Zealand. Tree wētā are common and widespread in New Zealand, comprising a distinctive component of the native invertebrate fauna, being large-bodied (up to 40 mm in length), relatively long-lived, flightless, and nocturnal. Arboreal tree wētā species are commonly monitored in conservation areas containing scrub or forest, particularly after mammal control, because they can be easily monitored using artificial roosts without harming them and they are readily identified by field workers. We evaluated whether data supported the use of tree wētā as a range of bioindicators for such monitoring and conclude that the arboreal species are good indicators for monitoring the effects of controlling the abundance of insectivorous mammals and that they are likely to be reliable population indicators of taxa sensitive to mammalian predation pressure, especially by rodents. However, it is unlikely that arboreal tree wētā are useful population indicators of habitat change (e.g. degradation and fragmentation) as they commonly survive in exotic vegetation and urban gardens throughout New Zealand. Although poorly studied for indicator value, tree wētā may not be good biodiversity indicators although there are insufficient data to establish this. We recommend further research be undertaken to develop standardised methods for monitoring so that conservation managers and researchers produce results that are consistent and comparable across different locations.

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References

  • Allen RB, Wright EF, MacLeod CJ, Bellingham PJ, Forsyth DM, Mason NWH, Gormley AM, Marburg AE, MacKenzie DI, McKay M (2013a) Designing an inventory and monitoring programme for the Department of Conservation’s Natural Heritage Management System. Landcare Research Contract Report: LC1730

  • Allen RB, Bellingham PJ, Forsyth DM, MacLeod CJ, Wright EF (2013b) Implementing an inventory and monitoring programme for the Department of Conservation’s Natural Heritage Management System. Landcare Research Contract Report: LC1731

  • Andersen AN, Majer JD (2004) Ants show the way down under: invertebrates as bioindicators in land management. Front Ecol Environ 2:291–298

    Article  Google Scholar 

  • Anon (2006) Trounson Kauri Park Mainland Island annual report (Combination of two years work) 2004/05 and 2005/06. Department of Conservation, Kauri Coast Area Office, Dargaville, New Zealand

  • Armstrong DP, Raeburn EH, Lewis RM, Ravine DON (2006) Modelling vital rates of a reintroduced New Zealand robin population as a function of predator control. J Wildl Manag 70:1028–1036

    Article  Google Scholar 

  • Bachand M, Pellerin S, Côté SD, Moretti M, De Cáceres M, Brousseau P-M, Cloutier C, Hébert C, Cardinal É, Martin J-L, Poulin M (2013) Species indicators of ecosystem recovery after reducing large herbivore density: comparing taxa and testing species combinations. Ecol Indic 38:12–19

    Article  Google Scholar 

  • Barker GM (2016) Land snail communities respond to control of invasive rats in New Zealand forests. N Z J Ecol 40:310–320

    Article  Google Scholar 

  • Barrett P (1991) Article 1. Keeping the Wellington weta, Hemideina crassidens (Blanchard, 1851). In: Ramsay GW (ed) Keeping weta in captivity. A series of nine articles for schools and nature-lovers. Wellington Zoological Gardens, Wellington, pp 10–17

    Google Scholar 

  • Bazelet C, Samways M (2011) Identifying grasshopper bioindicators for habitat quality assessment of ecological networks. Ecol Indic 11:1259–1269

    Article  Google Scholar 

  • Bleakley C, Stringer I, Robertson A, Hedderley D (2006) Design and use of artificial refuges for monitoring adult tree weta, Hemideina crassidens and H. thoracica. DOC Research and Development Series 233. Wellington, Department of Conservation

  • Bowie M, Hodge S, Banks J, Vink C (2006) An appraisal of simple tree-mounted shelters for non-lethal monitoring of weta (Orthoptera: Anostostomatidae and Rhaphidophoridae) in New Zealand nature reserves. J Insect Conserv 10:261–268

    Article  Google Scholar 

  • Bowie MH, Allen WJ, McCaw J, van Heugten R (2014) Factors influencing occupancy of modified artificial refuges for monitoring the range-restricted Banks Peninsula tree wētā Hemideina ricta (Anostostomatidae). N Z J Ecol 38:132–138

    Google Scholar 

  • Brown K, Elliott G, Innes J, Kemp J (2015) Ship rat, stoat and possum control on mainland New Zealand. An overview of techniques, successes and challenges. Department of Conservation, Wellington

  • Bulgerella M, Trewick SA, Minards NA, Jacobson MJ, Morgan-Richards M (2014) Shifting rages of two tree weta species (Hemideina spp.): competitive exclusion and changing climate. J Biogeogr 41:524–535

    Article  Google Scholar 

  • Byrom AE, Innes J, Binny RN (2016) A review of biodiversity outcomes from possum-focused pest control in New Zealand. Wildl Res 43:228–253

    Article  CAS  Google Scholar 

  • Caro TM, O’Doherty G (1999) On the use of surrogate species in conservation biology. Conserv Biol 13:805–814

    Article  Google Scholar 

  • Caro TM, Eadie J, Sih A (2005) Use of substitute species in conservation biology. Conserv Biol 19:1821–1826

    Article  Google Scholar 

  • Carpenter JK, Monks JM, O’Donnell CFJ (2016) Developing indices of relative abundance for monitoring cave and ground weta (Orthoptera) in southern beech forest, New Zealand. N Z J Zool 43:149–162

    Article  Google Scholar 

  • Duthie C, Gibbs G, Burns KC (2006) Seed dispersal by weta. Science 311:1575

    Article  CAS  PubMed  Google Scholar 

  • Elliott GP, Wilson PR, Taylor RH, Beggs JR (2010) Declines in common, widespread native birds in a mature temperate forest. Biol Conserv 143:2119–2126

    Article  Google Scholar 

  • Field LH (ed) (2001) The biology of weta, king crickets and their allies. CABI, Wallingford

    Google Scholar 

  • Field LH, Glasgow S (2001) Defence behaviour. In: Field LH (ed) The biology of weta, king crickets and their allies. CABI, Wallingford, pp 297–316

    Chapter  Google Scholar 

  • Field LH, Jarman TH (2001) Mating behaviour. In: Field LH (ed) The biology of weta, king crickets and their allies. CABI, Wallingford, pp 317–332

    Chapter  Google Scholar 

  • Field LH, Sandlant GR (2001) The gallery-related ecology of New Zealand tree wetas, Hemideina femorata and Hemideina crassidens (Orthoptera, Anostostomatidae). In: Field LH (ed) The biology of weta, king crickets and their allies. CABI, Wallingford, pp 243–258

    Chapter  Google Scholar 

  • Gerlach J, Samways M, Pryke J (2013) Terrestrial invertebrates as bioindicators: an overview of available taxonomic groups. J Insect Conserv 17:831–850

    Article  Google Scholar 

  • Gibbs GW (1998) Why are some weta (Orthoptera: Stenopelmatidae) vulnerable yet others are common? J Insect Conserv 2:161–166

    Article  Google Scholar 

  • Gibbs GW (2001) Habitats and biogeography of New Zealand’s Deinacridine and tusked weta species. In: Field LH (ed) The biology of weta, king crickets and their allies. CABI, Wallingford, pp 35–55

    Chapter  Google Scholar 

  • Gibbs GW (2009) The end of an 80-million year experiment: a review of evidence describing the impact of introduced rodents on New Zealand’s ‘mammal-free’ invertebrate fauna. Biol Invasions 11:1587–1593

    Article  Google Scholar 

  • Gibbs GW (2010) Do New Zealand invertebrates reflect the dominance of birds in their evolutionary history? N Z J Ecol 34:152–157

    Google Scholar 

  • Green CJ (2002) Recovery of invertebrate populations on Tiritiri Matangi Island, New Zealand following eradication of Pacific rats (Rattus exulans) [abstract]. In Veitch CR, Clout MN (eds) Turning the tide: the eradication of invasive species. IUCN SSC Invasive Species Specialist Group, Gland

    Google Scholar 

  • Green CJ (2005) Using artificial refuges to translocate and establish Auckland tree weta Hemideina thoracica on Korapuki Island, New Zealand. Conserv Evid 2:94–95

    Google Scholar 

  • Griffin MJ, Morgan-Richards M, Trewick SA (2011) Is the tree weta Hemideina crassidens an obligate herbivore? N Z Nat Sci 36:11–19

    Google Scholar 

  • Harris AC (2009) Further records of Hemideina crassidens (Blanchard) at Anderson’s Bay, Dunedin. Weta 37:13

    Google Scholar 

  • Hellawell JM (1986) Biological indicators of freshwater pollution and environmental management. Elsevier, London

    Book  Google Scholar 

  • Hill J, Hamer K, Lace L, Banham W (1995) Effects of selective logging on tropical forest butterflies on Buru, Indonesia. J Appl Ecol 32:754–760

    Article  Google Scholar 

  • Hoare JM, Adams LK, Bull LS, Towns DR (2007) Attempting to manage complex predator-prey interactions fails to avert imminent extinction of a threatened New Zealand skink population. J Wildl Manag 71:1576–1584

    Article  Google Scholar 

  • Hoare JM, O’Donnell CFJ, Wright EF (2010) Selection of indicator species for State of the Environment reporting: a case study from New Zealand. Pac Conserv Biol 16:76–82

    Article  Google Scholar 

  • Hoare JM, Monks A, O’Donnell CF (2012) Can correlated population trends among forest bird species be predicted by similarity in traits? Wildl Res 39:469–477

    Article  Google Scholar 

  • Hodge S, Vink CJ (2000) An evaluation of Lycosa hilaris as a bioindicators of organophosphate insecticide contamination. N Z Plant Prot 53:226–229

    Google Scholar 

  • Howard PC, Viskanic P, Davenport TRB, Kigenyi FW, Baltzer M, Dickinson CJ, Lwanga JS, Matthews RA, Balmford A (1998) Complementarity and the use of indicator groups for reserve selection in Uganda. Nature 394:472–475

    Article  CAS  Google Scholar 

  • Hutcheson J (1990) Characterization of terrestrial insect communities using quantified, Malaise-trapped Coleoptera. Ecol Entomol 15:143–151

    Article  Google Scholar 

  • Innes J (2005) Ship rat. In: King CM (ed) The handbook of New Zealand mammals. Oxford University Press, Auckland, pp 187–203

    Google Scholar 

  • Innes J, Hay R, Flux I, Bradfield P, Speed H, Jansen P (1999) Successful recovery of North Island kokako (Callaeas cinerea wilsoni) populations, by adaptive management. Biol Conserv 87:201–214

    Article  Google Scholar 

  • Innes J, Kelly D, Overton JM, Gillies C (2010) Predation and other factors currently limiting New Zealand forest birds. N Z J Ecol 34:86–114

    Google Scholar 

  • Jones C, Norbury G, Bell T (2013) Impacts of introduced European hedgehogs on endemic skinks and weta in tussock grassland. Wildl Res 40:36–44

    Article  Google Scholar 

  • Kelly CD (2006a) Movement patterns and gallery use by the sexually dimorphic Wellington tree weta. N Z J Ecol 30:273–278

    Google Scholar 

  • Kelly CD (2006b) Fighting for harems: assessment strategies during male-male contests in the sexually dimorphic Wellington tree weta. Anim Behav 72:727–736

    Article  Google Scholar 

  • King CM (2005) The handbook of New Zealand mammals. Oxford University Press, Melbourne

    Google Scholar 

  • Lambeck RJ (1997) Focal species: a multi-species umbrella for nature conservation. Conserv Biol 11:849–856

    Article  Google Scholar 

  • Landres PB, Verner J, Thomas JW (1988) Ecological uses of vertebrate indicator species: a critique. Conserv Biol 2:316–328

    Article  Google Scholar 

  • Leader-Williams N, Dublin HT (2000) Charismatic megafauna as ‘flagship’ species. In: Entwistle A, Dunstone N (eds) Has the panda had its day? Future priorities for the conservation of mammal diversity. Cambridge University Press, Cambridge, pp 53–81

    Google Scholar 

  • Leathwick J, McGlone MS, Walker S (2004) New Zealand’s potential vegetation pattern. Manaaki Whenua Press, Lincoln

    Google Scholar 

  • Lee W, McGlone M, Wright E (2005) Biodiversity inventory and monitoring: a review of national and international systems and a proposed framework for future biodiversity monitoring by the Department of Conservation. Landcare Research Contract Report LC0405/122, Lincoln, New Zealand

  • Lester PJ, Brown SDJ, Edwards ED, Holwell GI, Pawson SM, Ward DF, Watts CH (2014) Critical issues facing New Zealand entomology. N Z Entomol 37:1–13

    Article  Google Scholar 

  • Lewis RD, York A (2001) Circadian rhythms in tree wetas, Hemideina thoracica. In: Field LH (ed) The biology of weta, king crickets and their allies. CABI, Wallingford, pp 491–508

    Chapter  Google Scholar 

  • Lindenmayer DB, Likens GE (2010) Effective ecological monitoring. CSIRO Publishing, Collingwood

    Google Scholar 

  • Lindenmayer DB, Manning AD, Smith PL, Possingham HP, Fischer J, Oliver I, McCarthy MA (2002) The focal-species approach and landscape restoration: a critique. Conserv Biol 16:338–345

    Article  Google Scholar 

  • Little GA (1980) Food consumption and utilisation in two species of weta (Hemideina femorata, H. maori: Stenopelmatidae). BSc Hons Project, University of Canterbury, Christchurch, New Zealand

  • McGeoch MA (1998) The selection, testing and application of terrestrial insects as bioindicators. Biol Rev 73:181–201

    Article  Google Scholar 

  • McGeoch MA (2007) Insects and bioindication: theory and progress. In: Stewart AJA, New TR, Lewis OT (eds) Insects conversation biology. Proceedings of the Royal Entomological Society’s 23rd symposium. CAB International, Wallingford, pp 144–174

  • McGeoch MA, Sithole M, Samways MJ, Simaika JP, Pryke JS, Picker M, Uys C, Armstrong AJ, Dippenaar-Schoeman AS, Engelbrecht IA, Braschler B, Hamer M (2011) Conservation and monitoring of invertebrates in terrestrial protected areas. Koedoe 53:1–13

    Google Scholar 

  • McGuinness C (2001) The conservation requirements of New Zealand’s nationally threatened invertebrates. Department of Conservation, Wellington

    Google Scholar 

  • McKean NE, Trewick SA, Morgan-Richards M (2016) Little or no gene flow despite F1 hybrids at two interspecific contact zones. Ecol Evol 6:2390–2404

    Article  PubMed  PubMed Central  Google Scholar 

  • Meads M (1990) Forgotten fauna, the rare, endangered and protected invertebrates of New Zealand. DSIR Publishing, Wellington

    Google Scholar 

  • Mills LS, Soulé ME, Doak DF (1993) The keystone-species concept in ecology and conservation. Bioscience 43:219–224

    Article  Google Scholar 

  • Moller H (1985) Tree wetas (Hemideina crassidens) (Orthoptera: Stenopelmatidae) of Stephens Island, Cook Strait. N Z J Zool 12:55–69

    Article  Google Scholar 

  • Monks JM, O’Donnell CF, Wright E (2013) Selection of potential indicator species for measuring and reporting in trends in widespread native taxa in New Zealand. DOC Research and Development Series 338. Department of Conservation, Wellington

  • Monks JM, Monks A, Towns DR (2014) Correlated recovery of five lizard populations following eradication of invasive mammals. Biol Invasions 16:167–175

    Article  Google Scholar 

  • Morgan-Richards M, Gibbs GW (2001) A phylogenetic analysis of New Zealand giant and tree weta (Orthoptera: Anostostomatidae: Deinacrida and Hemideina) using morphological and genetic characters. Invertebr Syst 15:1–12

    Article  Google Scholar 

  • Morgan-Richards M, Trewick SA, Wallis GP (2001) Chromosome races with Pliocene origins: evidence from mtDNA. Heredity 86:303–312

    Article  CAS  PubMed  Google Scholar 

  • Morris JF (1992) Tests of the dual pacemaker model of circadian organisation in the weta (Hemideina thoracica). MSc thesis, University of Auckland, New Zealand

  • New TR (2010) Butterfly conservation in Australia: the importance of community participation. J Insect Conserv 14:305–311

    Article  Google Scholar 

  • Norbury GL, Pech RP, Byrom AE, Innes J (2015) Density-impact functions for terrestrial vertebrate pests and indigenous biota: guidelines for conservation managers. Biol Conserv 191:409–420

    Article  Google Scholar 

  • Noss RF (1990) Indicators for monitoring biodiversity: a hierarchical approach. Conserv Biol 4:355–364

    Article  Google Scholar 

  • O’Donnell CFJ, Hoare JM (2012) Quantifying the benefits of long-term integrated pest control for forest bird populations in a New Zealand temperate rainforest. N Z J Ecol 36:131–140

    Google Scholar 

  • Ordish RG (1992) Aggregation and communication of the Wellington weta H. crassidens (Blanchard) (Orthoptera: Stenopelmatidae). N Z Entomol 15:1–8

    Article  Google Scholar 

  • Paine RT (1966) Food web complexity and species diversity. Am Nat 100:65–75

    Article  Google Scholar 

  • Powlesland RG, Stringer IAN, Hedderley DI (2005) Effects of an aerial 1080 possum poison operation using carrot baits on invertebrates in artificial refuges at Whirinaki Forest Park, 1999–2002. N Z J Zool 29:193–205

    Google Scholar 

  • Pratt RC, Morgan-Richards M, Trewick SA (2008) Diversification of New Zealand weta (Orthoptera: Ensifera: Anostostomatidae) and their relationships in Australasia. Philos Trans R Soc B 363:3427–3437

    Article  Google Scholar 

  • Rainio J, Niemela J (2003) Ground beetles (Coleoptera: Carabidae) as bioindicators. Biodivers Conserv 12:487–506

    Article  Google Scholar 

  • Ramsay GW (1978) The effect of rodents on invertebrates. In: Dingwall PR, Atkinson IAE, Hay C. (eds) The ecology and control of rodents in New Zealand reserves. Department of Lands and Survey Information Series 4, Wellington, NZ, pp 89–95

  • Rate SR (2009) Does rat control benefit forest invertebrates at Moehau, Coromandel Peninsula? DOC Research and Development Series 316, Department of Conservation, Wellington

  • Reardon JT, Whitmore N, Holmes KM, Judd LM, Hutcheon AD, Norbury G, Mackenzie DI (2012) Predator control allows critically endangered lizards to recover on mainland New Zealand. N Z J Ecol 36:141–150

    Google Scholar 

  • Rufaut CG (1995) A comparative study of the Wellington tree weta, Hemideina crassidens in the presence and absence of rodents. Unpublished MSc thesis. Victoria University, Wellington

  • Rufaut CG, Gibbs GW (2003) Response of a tree weta population (Hemideina crassidens) after eradication of the Polynesian rat from a New Zealand island. Restor Ecol 11:13–19

    Article  Google Scholar 

  • Ruscoe WA, Sweetapple PJ, Perry M, Duncan RP (2013) Effects of spatially extensive control of invasive rats on abundance of native invertebrates in mainland New Zealand forests. Conserv Biol 27:74–82

    Article  PubMed  Google Scholar 

  • Samways M, McGeoch MA, New TR (2010) Insect conservation: a handbook of approaches and methods. Oxford University Press, Oxford

    Google Scholar 

  • Sherley GH, Hayes LM (1993) The conservation of giant weta (Deinacrida n. sp. Orthoptera: Stenopelmatidae) at Mahoenui, King Country: habitat use, and other aspects of its ecology. N Z Entomol 16:55–68

    Article  Google Scholar 

  • Smith WW (1931) Ants inhabiting Mount Egmont. N Z J Sci Technol 13:45–47

    Google Scholar 

  • Spurr EB, Berben PH (2004) Assessment of non-target impact of 1080-poisoning for vertebrate pest control on weta (Orthoptera: Anostostomatidae and Rhaphidophoridae) and other invertebrates in artificial refuges. N Z J Zool 28:63–72

    Google Scholar 

  • Spurr EB, Drew KW (1999) Invertebrates feeding on baits used for vertebrate pest control in New Zealand. N Z J Zool 23:167–173

    Google Scholar 

  • Stringer IAN (2001) The reproductive biology and the eggs of the New Zealand Anostostomatidae. In: Field LH (ed) The biology of weta, king crickets and their allies. CABI, Wallingford, pp 379–398

    Chapter  Google Scholar 

  • Stringer IAN, Cary PRL (2001) Postembryonic development and related changes. In: Field LH (ed) The biology of weta, king crickets and their allies. CABI, Wallingford, pp 399–426

    Chapter  Google Scholar 

  • Stringer I, Hitchmough R, Dugdale J, Edwards E, Hoare R, Patrick B (2012) The conservation status of New Zealand Lepidoptera. N Z Entomol 35:120–127

    Article  Google Scholar 

  • Sweetapple P, Barron M (2016) Frass drop for monitoring relative abundance of large arboreal invertebrates in a New Zealand mixed beech forest. N Z J Ecol 40:321–329

    Article  Google Scholar 

  • Thomas BW, Taylor RH (2002) A history of ground-based rodent eradication techniques developed in New Zealand, 1959–1993. In: Veitch CR, Clout MN (eds) Turning the tide: the eradication of invasive species. IUCN SSC Invasive Species Specialist Group, Gland, pp 301–310

    Google Scholar 

  • Towns DR, Atkinson IAE, Daugherty CH (2006) Have the harmful effects of introduced rats on islands been exaggerated? Biol Invasions 8:863–891

    Article  Google Scholar 

  • Townsend JA, Brown B, Stringer IAN, Potter MA (1997) Distribution, habitat and conservation status of Hemideina ricta and H. femorata on Banks Peninsula, New Zealand. N Z J Ecol 21:43–49

    Google Scholar 

  • Trewick SA, Morgan-Richards M (1995) On the distribution of tree weta in the North Island, New Zealand. J R Soc N Z 25:485–493

    Article  Google Scholar 

  • Trewick SA, Morgan-Richards M (2000) Artificial weta roosts: a technique for ecological study and population monitoring of tree weta (Hemideina) and other invertebrates. N Z J Ecol 24:201–208

    Google Scholar 

  • Trewick SA, Morgan-Richards M (2005) After the deluge: mitochondrial DNA indicates Miocene radiation and Pliocene adaptation of tree and giant weta (Orthoptera: Anostostomatidae). J Biogeogr 32:295–309

    Article  Google Scholar 

  • Trewick SA, Morgan-Richards M (2014) NZ wildlife: introducing the weird and wonderful character of natural New Zealand. Penguin, Auckland

    Google Scholar 

  • Waldren A, Mooers AO, Miller DA, Nibbelink N, Redding D, Kuhn TS, Roberts JT, Gittleman JL (2002) Targeting global conservation funding to limit immediate biodiversity declines. Proc Natl Acad Sci USA 110:12144–12148

    Article  Google Scholar 

  • Walker K (2003) Recovery plans for Powelliphanta land snails 2003–2013. Threatened species recovery plan 49. Department of Conservation, Wellington, New Zealand

  • Ward-Smith T, Sullivan W, Nakagawa K, Abbott P, MacDonald P, Stephenson B (2005) Boundary Stream Mainland Island 2003-04 Annual Report. Department of Conservation, East Coast Hawke’s Bay Conservancy, Gisborne, New Zealand

  • Watts CH (2015) Review of tree wētā (Hemideina species) as potential indicator species for Department of Conservation’s Tier 1 national indicator and monitoring framework. Unpublished contract report LC2362

  • Watts CH, Thornburrow D (2009) Where have all the weta gone? 2009. Results after two decades of transferring a threatened New Zealand giant weta, Deinacrida mahoenui. J Insect Conserv 13:287–295

    Article  Google Scholar 

  • Watts C, Armstrong DP, Innes J, Thornburrow D (2011) Dramatic increases in weta (Orthoptera) following mammal eradication on Maungatautari—evidence from pitfalls and tracking tunnels. N Z J Ecol 35:261–272

    Google Scholar 

  • Watts CH, Stringer I, Gibbs G (2012) Insect conservation in New Zealand: an historical perspective. In: New T (ed) Insect conservation: past, present and prospect. Springer, Dordrecht, pp 213–243

    Chapter  Google Scholar 

  • Watts C, Thornburrow D, Cave V, Innes J (2014) Beetle community changes following pest mammal control at two biodiversity sanctuaries in Wellington, New Zealand. J R Soc N Z 44:61–87

    Article  Google Scholar 

  • Watts C, Ranson H, Thorpe S, Cave V, Clarkson B, Thornburrow D, Bartlam S, Bodmin K (2015) Invertebrate community turnover following control of an invasive weed. Arthropod-Plant Interact 9:585–597

    Article  Google Scholar 

  • Wehi PM, Hicks BJ (2010) Isotopic fractionation in a large herbivorous insect, the Auckland tree weta. J Insect Physiol 56:1877–1882

    Article  CAS  PubMed  Google Scholar 

  • Wehi PM, Jorgensen M, Morgan-Richards M (2013) Sex- and season-dependent behaviour in a flightless insect, the Auckland tree weta (Hemideina thoracica). N Z J Ecol 37:75–83

    Google Scholar 

  • Wyman T, Trewick SA, Morgan-Richards M, Noble ADL (2010) Mutualism or opportunism? Tree fuchsia (Fuchsia excorticata) and tree weta (Hemideina) interactions. Austral Ecol 36:261–268

    Article  Google Scholar 

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Acknowledgements

This review was originally done for a Landcare Research contract report (LC2362) prepared for and funded by the New Zealand Department of Conservation. Its metamorphosis into a paper was supported by a writing scholarship funded by MBIE Core Funds to Landcare Research. We thank Kate McNutt (Department of Conservation) for her discussion on DOC’s Tier 1 national monitoring programme and her constructive review of the report. John Early (Auckland War Memorial Museum), Ricardo Palma and Phil Sirvid (Museum of New Zealand Te Papa Tongarewa), Cor Vink and Matthew Shaw (Canterbury Museum) kindly provided locality data for tree wētā specimens in the collections they manage used in Fig. 1. Steve Trewick and Mary Morgan-Richards (Massey University) generously provided distributional data included in Fig. 1. We thank Danny Thornburrow who helped collect the Mahoenui giant wētā data and for the photo of a wētā in Fig. 1, and thanks to Robbie Price for preparing Fig. 1. George Gibbs, William Lee, Anne Austin, James Pryke and two anonymous reviewers provided useful comments that improved this manuscript.

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Watts, C., Stringer, I., Innes, J. et al. Evaluating tree wētā (Orthoptera: Anostostomatidae: Hemideina species) as bioindicators for New Zealand national biodiversity monitoring. J Insect Conserv 21, 583–598 (2017). https://doi.org/10.1007/s10841-017-9997-8

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