Student or educator? Sign up with your school email and get 6 months of Pro free.
Cited by 25

The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.

Bioclimatic Modelling Identifies Suitable Habitat for the Establishment of the Invasive European Paper Wasp (Hymenoptera: Vespidae) across the Southern Hemisphere

Howse, Matthew W. F., Haywood, John, Lester, Philip J.·2020·Insects

Abstract

Species distribution models (SDMs) are tools used by ecologists to help predict the spread of invasive species. Information provided by these models can help direct conservation and biosecurity efforts by highlighting areas likely to contain species of interest. In this study, two models were created to investigate the potential range expansion of Polistes dominula Christ (Hymenoptera: Vespidae) in the southern hemisphere. This palearctic species has spread to invade North and South America, South Africa, Australia, and more recently New Zealand. Using the BIOCLIM and MAXENT modelling methods, regions that were suitable for P. dominula were identified based on climate data across four regions in the southern hemisphere. In South America areas of central Chile, eastern Argentina, parts of Uruguay, and southern Brazil were identified as climatically suitable for the establishment of P. dominula. Similarly, southern parts of South Africa and Australia were identified by the model to be suitable as well as much of the North Island and east of the South Island of New Zealand. Based on outputs from both models, significant range expansion by P. dominula is possible across its more southern invaded ranges.

Overview

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Integrity signals

Registry

Crossref · 10.3390/insects11110784

Cites

1 of 1 references verified0 citation errors · 0 not checkable

Statistics

Figures

Figure 1 Global distribution of P. dominula constructed from data retrieved from Global Biodiversity Information Facility database (GBIF) [18]. Red points indicate occurrences in an invaded range. Blue points indicate occurrences in the assumed native range [5,6]. In total 9246 occurrences were used in this study. Of the total, 3028 occurrences were from invaded ranges and 6218 were from the assumed native range.
Figure 1 Global distribution of P. dominula constructed from data retrieved from Global Biodiversity Information Facility database (GBIF) [18]. Red points indicate occurrences in an invaded range. Blue points indicate occurrences in the assumed native range [5,6]. In total 9246 occurrences were used in this study. Of the total, 3028 occurrences were from invaded ranges and 6218 were from the assumed native range.CC BY · PubMed Central
Figure 2 Raw outputs of both prediction models. The left images show the raw output given by BIOCLIM. The raw output of the BIOCLIM prediction is a value between 0 and 1 where the higher the number the more suitable the environment is. The BIOCLIM algorithm compares the environmental values of a cell to the median values of the environmental values of cells containing known occurrences of the target species. Percentile scores closest to 0.5 are most suitable so values over this are subtracted from 1. The resulting score is multiplied by 2 to get a final value between 0 and 1 [30]. The right images show the raw output given by MAXENT where the value is an approximate probability that the species will be present given the local environmental conditions [31,46]. The black crosses indicate known occurrences of P. dominula.
Figure 2 Raw outputs of both prediction models. The left images show the raw output given by BIOCLIM. The raw output of the BIOCLIM prediction is a value between 0 and 1 where the higher the number the more suitable the environment is. The BIOCLIM algorithm compares the environmental values of a cell to the median values of the environmental values of cells containing known occurrences of the target species. Percentile scores closest to 0.5 are most suitable so values over this are subtracted from 1. The resulting score is multiplied by 2 to get a final value between 0 and 1 [30]. The right images show the raw output given by MAXENT where the value is an approximate probability that the species will be present given the local environmental conditions [31,46]. The black crosses indicate known occurrences of P. dominula.CC BY · PubMed Central
Figure 3 Predicted presence/absence plots for each region based on the two model outputs. For both models, thresholds (0.005 and 0.38, respectively) are calculated as the raw output value at which the sum of the true positive and true negative rates is maximized. Locations where the raw output values are over these thresholds are denoted a present status (1) and highlighted in green. Locations where raw output values are lower than the threshold are denoted an absent status (0) and remain grey. Black crosses indicate known occurrences of P. dominula.
Figure 3 Predicted presence/absence plots for each region based on the two model outputs. For both models, thresholds (0.005 and 0.38, respectively) are calculated as the raw output value at which the sum of the true positive and true negative rates is maximized. Locations where the raw output values are over these thresholds are denoted a present status (1) and highlighted in green. Locations where raw output values are lower than the threshold are denoted an absent status (0) and remain grey. Black crosses indicate known occurrences of P. dominula.CC BY · PubMed Central
Figure 4 Area under the receiver operating characteristic curve (AUC) plots for BIOCLIM prediction (a) and MAXENT prediction (b). This value is a number between zero and one and represents how accurately a model predicts presence/absence. A model with an AUC value of 1 predicts presence/absence with 100% accuracy while a model with an AUC score of 0.5 is one that predicts presence or absence correctly 50% of the time [30].
Figure 4 Area under the receiver operating characteristic curve (AUC) plots for BIOCLIM prediction (a) and MAXENT prediction (b). This value is a number between zero and one and represents how accurately a model predicts presence/absence. A model with an AUC value of 1 predicts presence/absence with 100% accuracy while a model with an AUC score of 0.5 is one that predicts presence or absence correctly 50% of the time [30].CC BY · PubMed Central
Figure 5 Histograms showing the distribution of bioclimatic values at known occurrences of P. dominula. Left is the distribution of annual average temperature (Bio1) and on the right the distribution of precipitation of the coldest quarter (Bio19). These two variables were chosen from the full list of 15, based on their high permutation importance in the MAXENT modelling approach.
Figure 5 Histograms showing the distribution of bioclimatic values at known occurrences of P. dominula. Left is the distribution of annual average temperature (Bio1) and on the right the distribution of precipitation of the coldest quarter (Bio19). These two variables were chosen from the full list of 15, based on their high permutation importance in the MAXENT modelling approach.CC BY · PubMed Central
Figure 6 Plot of the average annual temperature (Bio1) bioclimatic layer at each region highlighted in this study. This variable had the highest permutation importance of 37.9%. Black crosses indicate known occurrences of P. dominula.
Figure 6 Plot of the average annual temperature (Bio1) bioclimatic layer at each region highlighted in this study. This variable had the highest permutation importance of 37.9%. Black crosses indicate known occurrences of P. dominula.CC BY · PubMed Central
Figure 7 Plot of the precipitation of the coldest quarter (Bio19) bioclimatic layer at each region highlighted in this study. This variable had the second highest permutation importance of 15.9%. Black crosses indicate known occurrences of P. dominula.
Figure 7 Plot of the precipitation of the coldest quarter (Bio19) bioclimatic layer at each region highlighted in this study. This variable had the second highest permutation importance of 15.9%. Black crosses indicate known occurrences of P. dominula.CC BY · PubMed Central

Verification

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

Citations

Cites

Show all 1 references

Research works printed but not linked: 66

  1. Pearson, 2007, Species’ distribution modeling for conservation educators and practitioners, Lessons Conserv., 3, 54
  2. Leathwick, 2005, Using multivariate adaptive regression splines to predict the distributions of New Zealand’s freshwater diadromous fish, Freshw. Biol., 50, 2034, 10.1111/j.1365-2427.2005.01448.x · DOI
  3. Moor, 2015, Predicting climate change effects on wetland ecosystem services using species distribution modeling and plant functional traits, Ambio, 44, 113, 10.1007/s13280-014-0593-9 · DOI
  4. Curry, 2020, The potential tropical island distribution of a temperate invasive snail, Oxychilus alliarius, modeled on its distribution in Hawaii, Biol. Invasions, 22, 307, 10.1007/s10530-019-02091-w · DOI
  5. Buck, 2008, Identification atlas of the Vespidae (Hymenoptera, Aculeata) of the northeastern Nearctic region, Can. J. Arthropod Identif., 5, 1
  6. Carpenter, 1996, Distributional checklist of species of the genus Polistes (Hymenoptera: Vespidae; Polistinae, Polistini), Am. Mus. Novit., 3188, 1
  7. Brown, 2012, Prey capture and caste-specific payload capacities in the European paper wasp Polistes dominulus, Insectes Sociaux, 59, 519, 10.1007/s00040-012-0246-6 · DOI
  8. Baker, 2020, Invasive paper wasp turns urban pollinator gardens into ecological traps for monarch butterfly larvae, Sci. Rep., 10, 1, 10.1038/s41598-020-66621-6 · DOI
  9. Jeon, 2019, Prey diversity of Polistes rothneyi koreanus in different landscapes using DNA barcoding, J. Appl. Entomol., 143, 1052, 10.1111/jen.12681 · DOI
  10. Ward, 2013, Molecular identification of the prey range of the invasive Asian paper wasp, Ecol. Evol., 3, 4408, 10.1002/ece3.826 · DOI
  11. Kasper, 2004, Assessment of prey overlap between a native (Polistes humilis) and an introduced (Vespula germanica) social wasp using morphology and phylogenetic analyses of 16S rDNA, Mol. Ecol., 13, 2037, 10.1111/j.1365-294X.2004.02193.x · DOI
  12. Cervo, 2000, Polistes dominulus (Hymenoptera, Vespidae) invading North America: Some hypotheses for its rapid spread, Insectes Sociaux, 47, 155, 10.1007/PL00001694 · DOI
  13. Schenk, 2002, Functional response of a generalist insect predator to one of its prey species in the field, J. Anim. Ecol., 71, 524, 10.1046/j.1365-2656.2002.00620.x · DOI
  14. Roets, 2019, Better colony performance, not natural enemy release, explains numerical dominance of the exotic Polistes dominula wasp over a native congener in South Africa, Biol. Invasions, 21, 925, 10.1007/s10530-018-1870-5 · DOI
  15. Pickett, 2000, High productivity in haplometrotic colonies of the introduced paper wasp Polistes dominulus (Hymenoptera: Vespidae; Polistinae), J. N. Y. Entomol. Soc., 108, 314, 10.1664/0028-7199(2000)108[0314:HPIHCO]2.0.CO;2 · DOI
  16. Gamboa, 2002, The comparative biology of two sympatric paper wasps, the native Polistes fuscatus and the invasive Polistes dominulus (Hymenoptera, Vespidae), Insectes Sociaux, 49, 45, 10.1007/s00040-002-8278-y · DOI
  17. GBIF.org (2020, February 28). GBIF Occurence Download. Available online: https://doi.org/10.15468/dl.jzezgu. · DOI
  18. Liebert, 2006, Genetics, behavior and ecology of a paper wasp invasion: Polistes dominulus in North America, Ann. Zool. Fenn., 43, 595
  19. Taylor, R.W., Brown, D.R., and Cardale, J.C. (1985). Hymenoptera: Formicoidea, Vespoidea and Sphecoidea. · DOI
  20. Elgueta, 1989, Antecedentes sobre especies de reciente introducción a Chile (Diptera: Stratiomyidae; Hymenoptera: Vespidae), Rev. Chil. Entomol., 17, 97
  21. Sackmann, 2003, Presencia de una nueva avispa social exótica, Polistes dominulus (Hymenoptera: Vespidae) en la Patagonia Argentina, Rev. Soc. Entomológica Argent., 62, 68
  22. Eardley, 2009, Polistes dominulus (Christ, 1791)(Hymenoptera: Polistinae: Vespidae) newly recorded from South Africa, Afr. Entomol., 17, 226, 10.4001/003.017.0214 · DOI
  23. Stringer, 2012, Assessing the conservation status of New Zealand’s native terrestrial invertebrates, N. Z. Entomol., 35, 77, 10.1080/00779962.2012.686309 · DOI
  24. Lester, 2014, Critical issues facing New Zealand entomology, N. Z. Entomol., 37, 1, 10.1080/00779962.2014.861789 · DOI
  25. Sands, 2018, Important issues facing insect conservation in Australia: Now and into the future, Austral Entomol., 57, 150, 10.1111/aen.12342 · DOI
  26. Booth, 2014, bioclim: The first species distribution modelling package, its early applications and relevance to most current MaxEnt studies, Divers. Distrib., 20, 1, 10.1111/ddi.12144 · DOI
  27. Longmore, 1986, A biogeographic analysis of Australian elapid snakes, Atlas of Elapid Snakes of Australia, Volume 7, 16
  28. Elith, 2011, A statistical explanation of MaxEnt for ecologists, Divers. Distrib., 17, 43, 10.1111/j.1472-4642.2010.00725.x · DOI · Paper page
  29. Elith, 2006, Novel methods improve prediction of species’ distributions from occurrence data, Ecography, 29, 129, 10.1111/j.2006.0906-7590.04596.x · DOI · Paper page
  30. Phillips, 2006, Maximum entropy modeling of species geographic distributions, Ecol. Model., 190, 231, 10.1016/j.ecolmodel.2005.03.026 · DOI · Paper page
  31. Sumner, 2019, Mapping species distributions in 2 weeks using citizen science, Insect Conserv. Divers., 12, 382, 10.1111/icad.12345 · DOI
  32. Fick, 2017, WorldClim 2: New 1-km spatial resolution climate surfaces for global land areas, Int. J. Climatol., 37, 4302, 10.1002/joc.5086 · DOI · Paper page
  33. Beckham, 2017, An updated understanding of Texas bumble bee (Hymenoptera: Apidae) species presence and potential distributions in Texas, USA, PeerJ, 5, e3612, 10.7717/peerj.3612 · DOI
  34. Ward, 2007, Modelling the potential geographic distribution of invasive ant species in New Zealand, Biol. Invasions, 9, 723, 10.1007/s10530-006-9072-y · DOI
  35. Rodder, D., Schmidtlein, S., Veith, M., and Lotters, S. (2009). Alien invasive slider turtle in unpredicted habitat: A matter of niche shift or of predictors studied?. PLoS ONE, 4. · DOI
  36. Raghavan, R.K., Peterson, A.T., Cobos, M.E., Ganta, R., and Foley, D. (2019). Current and future distribution of the lone star tick, Amblyomma americanum (L.)(Acari: Ixodidae) in North America. PLoS ONE, 14. · DOI
  37. Dudaniec, 2018, Signatures of local adaptation along environmental gradients in a range-expanding damselfly (Ischnura elegans), Mol. Ecol., 27, 2576, 10.1111/mec.14709 · DOI
  38. Jiguet, 2012, Selecting pseudo-absences for species distribution models: How, where and how many?, Methods Ecol. Evol., 3, 327, 10.1111/j.2041-210X.2011.00172.x · DOI · Paper page
  39. Merow, 2013, A practical guide to MaxEnt for modeling species’ distributions: What it does, and why inputs and settings matter, Ecography, 36, 1058, 10.1111/j.1600-0587.2013.07872.x · DOI · Paper page
  40. Muscarella, 2014, ENMeval: An R package for conducting spatially independent evaluations and estimating optimal model complexity for ecological niche models, Methods Ecol. Evol., 5, 1198, 10.1111/2041-210X.12261 · DOI · Paper page
  41. Liu, 2016, On the selection of thresholds for predicting species occurrence with presence-only data, Ecol. Evol., 6, 337, 10.1002/ece3.1878 · DOI
  42. Liu, 2013, Selecting thresholds for the prediction of species occurrence with presence-only data, J. Biogeogr., 40, 778, 10.1111/jbi.12058 · DOI
  43. Hosmer, D.W., Lemeshow, S., and Sturdivant, R.X. (2013). Assessing the fit of the model. Applied Logistic Regression, John Wiley & Sons, Inc.. [3rd ed.]. · DOI · Paper page
  44. Veldtman, 2014, Rapid range expansion of the invasive wasp Polistes dominula (Hymenoptera: Vespidae: Polistinae) and first record of parasitoids on this species and the native Polistes marginalis in the Western Cape province of South Africa, Afr. Entomol., 22, 220, 10.4001/003.022.0104 · DOI
  45. Beggs, 1999, Restructuring of Lepidoptera communities by introduced Vespula wasps in a New Zealand beech forest, Oecologia, 119, 565, 10.1007/s004420050820 · DOI
  46. Toft, 1998, Reducing predation of orb-web spiders by controlling common wasps (Vespula vulgaris) in a New Zealand beech forest, Ecol. Entomol., 23, 90, 10.1046/j.1365-2311.1998.00100.x · DOI
  47. Kirkpatrick, 2018, The effects of introduced vespid wasps (Vespula germanica and V. vulgaris) on threatened native butterfly (Oreixenica ptunarra) populations in Tasmania, J. Insect Conserv., 22, 521, 10.1007/s10841-018-0081-9 · DOI
  48. Beaumont, 2005, Predicting species distributions: Use of climatic parameters in BIOCLIM and its impact on predictions of species’ current and future distributions, Ecol. Model., 186, 251, 10.1016/j.ecolmodel.2005.01.030 · DOI
  49. Stamp, 1988, Direct and indirect effects of predatory wasps (Polistes sp.: Vespidae) on gregarious caterpillars (Hemileuca lucina: Saturniidae), Oecologia, 75, 619, 10.1007/BF00776428 · DOI
  50. Pilowsky, 2018, Displacement and replacement in real time: Polistes dominula’s impact on P. fuscatus in the northeastern U.S, Biol. Invasions, 20, 1161, 10.1007/s10530-017-1617-8 · DOI
  51. Parent, C.E., Peck, S.B., Causton, C.E., Roque-Albelo, L., Lester, P.J., and Bulgarella, M. (2020). Polistes versicolor (Hymenoptera: Vespidae), an introduced wasp in the Galapagos Islands: Its life cycle and ecological impact. Environ. Entomol. · DOI
  52. Beggs, 2011, Ecological effects and management of invasive alien Vespidae, BioControl, 56, 505, 10.1007/s10526-011-9389-z · DOI
  53. Lefort, M.-C., Beggs, J.R., Glare, T.R., Saunders, T.E., Doyle, E.J., and Stephane, B. (2020, August 17). A Molecular Approach to Studying Hymenoptera Diets Using Polistine Wasps. Available online: https://www.biorxiv.org/content/10.1101/2020.04.06.024422v1. · DOI
  54. Stringer, 2012, The conservation status of New Zealand Lepidoptera, N. Z. Entomol., 35, 120, 10.1080/00779962.2012.686316 · DOI
  55. Tautz, 2015, Nesting behavior of the paper wasp Polistes dominula in Central Europe-a flexible system for expanding into new areas, Ecosphere, 6, 1
  56. Schapheer, 2018, Pest Cockroaches May Overcome Environmental Restriction Due to Anthropization, J. Med Entomol., 55, 1357
  57. Cranshaw, 2011, Notes on fruit damage by the European paper wasp, Polistes dominula (Christ) (Hymenoptera: Vespidae), Southwest. Entomol., 36, 103, 10.3958/059.036.0110 · DOI
  58. Wisz, 2013, The role of biotic interactions in shaping distributions and realised assemblages of species: Implications for species distribution modelling, Biol. Rev., 88, 15, 10.1111/j.1469-185X.2012.00235.x · DOI · Paper page
  59. Giannini, 2013, Improving species distribution models using biotic interactions: A case study of parasites, pollinators and plants, Ecography, 36, 649, 10.1111/j.1600-0587.2012.07191.x · DOI
  60. Godsoe, 2012, How do species interactions affect species distribution models?, Ecography, 35, 811, 10.1111/j.1600-0587.2011.07103.x · DOI
  61. Bulgarella, 2014, Shifting ranges of two tree weta species (Hemideina spp.): Competitive exclusion and changing climate, J. Biogeogr., 41, 524, 10.1111/jbi.12224 · DOI
  62. Mpakairi, K.S., Ndaimani, H., Tagwireyi, P., Gara, T.W., Zvidzai, M., and Madhlamoto, D. (2017). Missing in action: Species competition is a neglected predictor variable in species distribution modelling. PLoS ONE, 12. · DOI
  63. Pellissier, 2010, Species distribution models reveal apparent competitive and facilitative effects of a dominant species on the distribution of tundra plants, Ecography, 33, 1004, 10.1111/j.1600-0587.2010.06386.x · DOI
  64. Gamboa, 2004, The comparative biology of two sympatric paper wasps in Michigan, the native Polistes fuscatus and the invasive Polistes dominulus (Hymenoptera, Vespidae), Insectes Sociaux, 51, 153, 10.1007/s00040-003-0721-1 · DOI
  65. Miller, 2013, A ten-year comparative study of the population dynamics and parasitoidism in the native paper wasp Polistes fuscatus and the invasive P. dominulus, Insectes Sociaux, 60, 49, 10.1007/s00040-012-0264-4 · DOI
  66. Kearney, 2010, Correlative and mechanistic models of species distribution provide congruent forecasts under climate change, Conserv. Lett., 3, 203, 10.1111/j.1755-263X.2010.00097.x · DOI

Cited by

See all 25

Metadata

Authors
Howse, M. W. F., Haywood, J., & Lester, P. J.
Affiliations
  • School of Biological Sciences, Victoria University of Wellington, Wellington 6140, New Zealand
  • School of Mathematics and Statistics, Victoria University of Wellington, Wellington 6140, New Zealand
Venue
Insects
Publisher
MDPI AG
Published
2020-11-11
Volume
11
Issue
11
Pages
784
ISSN
2075-4450
Cited by
25
References
1
Language
en

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review

How to cite

Cite CoChat for the checks on this page, and the paper for its own findings.

This page
CoChat. (2026). Citation check: Bioclimatic Modelling Identifies Suitable Habitat for the Establishment of the Invasive European Paper Wasp (Hymenoptera: Vespidae) across the Southern Hemisphere. https://app.cochat.ai/papers/10.3390/insects11110784
The paper
Howse, M. W. F., Haywood, J., & Lester, P. J. (2020). Bioclimatic Modelling Identifies Suitable Habitat for the Establishment of the Invasive European Paper Wasp (Hymenoptera: Vespidae) across the Southern Hemisphere. Insects. https://doi.org/10.3390/insects11110784

Data sources

Bibliographic data: Semantic Scholar, OpenAlex, Crossref.

Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.