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Journal Article

Distribution and forage use of exotic bumblebees in South Island, New Zealand

01 Jan 2004-New Zealand Journal of Ecology (New Zealand Ecological Society)-Vol. 28, Iss: 2, pp 225-232
TL;DR: Results provide support for the hypothesis that the loss of flower-rich meadows, particularly those containing populations of Fabaceae species with long corollae, is responsible for the decline of bumblebee species across Europe.
Abstract: The rapid decline in bumblebee populations within Europe has been linked to habitat loss through agricultural intensification, and a consequential reduction in the availability of preferred forage plants. The successful introduction of four European Bombus species to the South Island of New Zealand from England (in 1885 and 1906) provides an opportunity to determine how important different forage plants (also introduced from the U.K.) are to two severely threatened European bumblebee species (Bombus ruderatus and B. subterraneus). In January 2003 we conducted a survey of bumblebee populations across 70 sites in the central and southern South Island, recording which plant species were being used as pollen and nectar sources for each Bombus species. All four bumblebee species showed a clear preference for plants of European origin. Only B. terrestris, the most polylectic species, was recorded feeding on native plant species. The longer-tongued bumblebees, B. hortorum, B. ruderatus, and B. subterraneus, foraged predominantly on just two plant species; Trifolium pratense for both nectar and pollen, and Echium vulgare for nectar. These plant species are now declining in abundance in the U.K. Our results provide support for the hypothesis that the loss of flower-rich meadows, particularly those containing populations of Fabaceae species with long corollae, is responsible for the decline of bumblebee species across Europe. Comparison with earlier bumblebee surveys suggests that long-tongued bumblebees may also be in decline in New Zealand, particularly B. subterraneus which is now very localised and scarce.

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Citations
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Journal ArticleDOI
TL;DR: The results showed that female Amegilla are active foragers that make on average 9 pollen foraging flights per day and the number of actively nesting female bees needed for adequate pollination in a commercial greenhouse as 282 per hectare.
Abstract: Blue-banded bees (Amegilla spp.) are Australian native buzz pollinators that are a promising alternative to the introduction of the bumblebee (Bombus terrestris) for use as pollinators of tomatoes in Australian greenhouses. The foraging behaviour of Amegilla chlorocyanea under greenhouse conditions was monitored in detail. Our results showed that female Amegilla are active foragers that make on average 9 pollen foraging flights per day. Using data about flower visitation, we estimated the number of actively nesting female bees needed for adequate pollination in a commercial greenhouse as 282 per hectare.

33 citations


Cites background from "Distribution and forage use of exot..."

  • ...Recent studies in New Zealand and Tasmania have shown that bumblebees are efficient pollinators of some introduced weed species (Hergstrom et al., 2002; Stout et al., 2002; Hanley and Goulson, 2003; Goulson and Hanley, 2004)....

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Journal ArticleDOI
16 Feb 2016-PLOS ONE
TL;DR: A new and more intuitive approach was developed to select the models and evaluate different algorithms based on their performance and predictive convergence, and a comprehensive global map of susceptibility to Bombus terrestris invasion is presented that highlights priority areas for monitoring.
Abstract: The ecological impacts of alien species invasion are a major threat to global biodiversity. The increasing number of invasion events by alien species and the high cost and difficulty of eradicating invasive species once established require the development of new methods and tools for predicting the most susceptible areas to invasion. Invasive pollinators pose serious threats to biodiversity and human activity due to their close relationship with many plants (including crop species) and high potential competitiveness for resources with native pollinators. Although at an early stage of expansion, the bumblebee species Bombus terrestris is becoming a representative case of pollinator invasion at a global scale, particularly given its high velocity of invasive spread and the increasing number of reports of its impacts on native bees and crops in many countries. We present here a methodological framework of habitat suitability modeling that integrates new approaches for detecting habitats that are susceptible to Bombus terrestris invasion at a global scale. Our approach did not include reported invaded locations in the modeling procedure; instead, those locations were used exclusively to evaluate the accuracy of the models in predicting suitability over regions already invaded. Moreover, a new and more intuitive approach was developed to select the models and evaluate different algorithms based on their performance and predictive convergence. Finally, we present a comprehensive global map of susceptibility to Bombus terrestris invasion that highlights priority areas for monitoring.

31 citations

Journal ArticleDOI
TL;DR: It is concluded that B. sassaricus remains inconspicuous in France and competition from the three native subspecies may have prevented it from becoming invasive, however, genetic interference through introgression cannot be ruled out.
Abstract: The natural diversity of Bombus terrestris subspecies could be under threat from the commer- cialisation of bumblebees. Therefore, to determine whether commercially imported bumblebees are able to establish and spread, we carried out long-term observations of bumblebees in southern France. Our surveys occurred before, during, and after the importation (between 1989 and 1996) of thousands of colonies of the Sardinian subspecies B. t. sassaricus. Queens and males of B. t. sassaricus were observed foraging outside commercial greenhouses in 1991, 1993, and 1994 and feral workers were observed foraging on native veg- etation nearly two years after the importation of B. t. sassaricus ceased. However, no B. t. sassaricus ,o r F1 hybrids were observed after 1998. We conclude that B. t. sassaricus remains inconspicuous in France and competition from the three native subspecies may have prevented it from becoming invasive. However, genetic interference through introgression cannot be ruled out.

31 citations


Cites background from "Distribution and forage use of exot..."

  • ...Furthermore, it has been suggested that introduced bumblebees in these countries rely heavily on plants introduced from Europe that are not utilised by the native bee fauna (Stout et al., 2002; Goulson and Hanley, 2004)....

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Journal ArticleDOI
TL;DR: Using pan-trap records from the Mid-Atlantic US, catch abundance is examined of two exotic and six native Osmia species over the span of fifteen years (2003–2017) to estimate abundance changes, and it is discussed how disease spillover and enemy release in this system may result in the patterns.
Abstract: A potential driver of pollinator declines that has been hypothesized but seldom documented is the introduction of exotic pollinator species. International trade often involves movement of many insect pollinators, especially bees, beyond their natural range. For agricultural purposes or by inadvertent cargo shipment, bee species successfully establishing in new ranges could compete with native bees for food and nesting resources. In the Mid-Atlantic United States, two Asian species of mason bee (Osmia taurus and O. cornifrons) have become recently established. Using pan-trap records from the Mid-Atlantic US, we examined catch abundance of two exotic and six native Osmia species over the span of fifteen years (2003-2017) to estimate abundance changes. All native species showed substantial annual declines, resulting in cumulative catch losses ranging 76-91% since 2003. Exotic species fared much better, with O. cornifrons stable and O. taurus increasing by 800% since 2003. We characterize the areas of niche overlap that may lead to competition between native and exotic species of Osmia, and we discuss how disease spillover and enemy release in this system may result in the patterns we document.

29 citations

Book ChapterDOI
01 Jan 2013

26 citations

References
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Book
30 Sep 1988
TL;DR: In this paper, the authors define definitions of diversity and apply them to the problem of measuring species diversity, choosing an index and interpreting diversity measures, and applying them to structural and structural diversity.
Abstract: Definitions of diversity. Measuring species diversity. Choosing an index and interpreting diversity measures. Sampling problems. Structural diversity. Applications of diversity measures. Summary.

10,957 citations


"Distribution and forage use of exot..." refers background in this paper

  • ...This index is insensitive to sample size (Magurran, 1988), important because samples are inevitably larger for the more common species....

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Journal ArticleDOI
01 Jan 1949-Nature
TL;DR: In this article, the authors define and examine a measure of concentration in terms of population constants, and examine the relationship between the characteristic and the index of diversity when both are applied to a logarithmic distribution.
Abstract: THE 'characteristic' defined by Yule1 and the 'index of diversity' defined by Fisher2 are two measures of the degree of concentration or diversity achieved when the individuals of a population are classified into groups. Both are defined as statistics to be calculated from sample data and not in terms of population constants. The index of diversity has so far been used chiefly with the logarithmic distribution. It cannot be used everywhere, as it does not always give values which are independent of sample size ; it cannot do so, for example, when applied to an infinite population of individuals classified into a finite number of groups. Williams3 has pointed out a relationship between the characteristic and the index of diversity when both are applied to a logarithmic distribution. The present purpose is to define and examine a measure of concentration in terms of population constants.

10,077 citations


"Distribution and forage use of exot..." refers methods in this paper

  • ...To compare the diet breadth of the species recorded, a Simpson’s index was calculated for the diversity of flowers visited (Simpson, 1949):...

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  • ...To compare the diet breadth of the species recorded, a Simpson’s index was calculated for the diversity of flowers visited (Simpson, 1949): where ni is the number of flowers of the ith species that were visited, N is the total number of flowers visited, and s is the total number of flower species…...

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Book
01 Jan 1988

1,150 citations


"Distribution and forage use of exot..." refers background in this paper

  • ...In addition to T. pratense and L. corniculatus, both of which are highly dependent on insects for pollination (Grime et al., 1988), we found substantial numbers of bumblebees visiting lupin (Lupinus arboreus and L. polyphyllus), thistles (Cirsium vulgare), and broom (Cytisus scoparius)....

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  • ...Although H. perforatum is believed to be increasing in abundance in the U.K., the other main forage plants we identified in New Zealand (E. vulgare, L. corniculatus and T. pratense) are all declining (Grime et al., 1988; Rich and Woodruff, 1996)....

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  • ...Each of these species is known to depend substantially or wholly on bee pollinators in order to reproduce (Grime et al., 1988; Stout, 2000; Stout et al., 2002)....

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  • ...corniculatus, both of which are highly dependent on insects for pollination (Grime et al., 1988), we found substantial numbers of bumblebees visiting lupin (Lupinus arboreus and L....

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Journal ArticleDOI
TL;DR: Negative impacts of exotic bees need to be carefully assessed before further introductions are carried out.
Abstract: Bees are generally regarded as beneficial insects for their role in pollination, and in the case of the honeybee Apis mellifera, for production of honey. As a result several bee species have been introduced to countries far beyond their home range, including A. mellifera, bumblebees (Bombus sp.), the alfalfa leafcutter bee Megachile rotundata, and various other solitary species. Possible negative consequences of these introductions include: competition with native pollinators for floral resources; competition for nest sites; co-introduction of natural enemies, particularly pathogens that may infect native organisms; pollination of exotic weeds; and disruption of pollination of native plants. For most exotic bee species little or nothing is known of these possible effects. Research to date has focused mainly on A. mellifera, and has largely been concerned with detecting competition with native flower visitors. Considerable circumstantial evidence has accrued that competition does occur, but no experiment has clearly demonstrated long-term reductions in populations of native organisms. Most researchers agree that this probably reflects the difficulty of carrying out convincing studies of competition between such mobile organisms, rather than a genuine absence of competitive effects. Effects on seed set of exotic weeds are easier to demonstrate. Exotic bees often exhibit marked preferences for visiting flowers of exotic plants. For example, in Australia and New Zealand many weeds from Europe are now visited by European honeybees and bumblebees. Introduced bees are primary pollinators of a number of serious weeds. Negative impacts of exotic bees need to be carefully assessed before further introductions are carried out.

648 citations


"Distribution and forage use of exot..." refers background or result in this paper

  • ...It seems likely that, in Europe at least, agricultural intensification is primarily responsible for the decline of many bumblebee species (Rasmont, 1988; Osborne and Corbet, 1994; Goulson, 2003a), although it is difficult to provide unequivocal evidence....

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  • ...of many bumblebee species (Rasmont, 1988; Osborne and Corbet, 1994; Goulson, 2003a), although it is difficult to provide unequivocal evidence....

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  • ...Our results lend further support to the claim that exotic (bumble- and honey-) bees are important pollinators of various weeds (Sugden et al., 1996; Stout et al., 2002; Goulson, 2003b; Hanley and Goulson, 2003)....

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  • ...Both B. terrestris and B. hortorum, by contrast, remain common throughout most of Northwestern Europe (Goulson, 2003a)....

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Book
01 Jan 2003
TL;DR: This book discusses social organisation and conflict in bumblebee communities, foraging economics, and the effects of introduced bees on native ecosystems.
Abstract: 1. Introduction 2. Thermoregulation 3. Social organisation and conflict 4. Finding a mate 5. Natural enemies 6. Foraging Economics 7. Foraging range 8. Exploitation of patchy resources 9. Choice of flower species 10. Intraspecific floral choices 11. Communication during foraging 12. Competition in bumblebee communities 13. Bumblebees as pollinators 14. Conservation 15. Bumblebees abroad effects of introduced bees on native ecosystems

360 citations


"Distribution and forage use of exot..." refers background or result in this paper

  • ...It seems likely that, in Europe at least, agricultural intensification is primarily responsible for the decline of many bumblebee species (Rasmont, 1988; Osborne and Corbet, 1994; Goulson, 2003a), although it is difficult to provide unequivocal evidence....

    [...]

  • ...Our results lend further support to the claim that exotic (bumble- and honey-) bees are important pollinators of various weeds (Sugden et al., 1996; Stout et al., 2002; Goulson, 2003b; Hanley and Goulson, 2003)....

    [...]

  • ...Both B. terrestris and B. hortorum, by contrast, remain common throughout most of Northwestern Europe (Goulson, 2003a)....

    [...]