Tag Archives: Pollinators

Garden pollinators for PAW no. 2 – Marmalade hoverfly (Episyrphus balteatus)

Syrphid on lemon balm 1 cropped - 1P1020548 copyOne of the most frequently encountered of hoverfly species in urban gardens is the beautifully named Marmalade hoverfly (Episyrphus balteatus).  This insect is a “true fly” of the order Diptera that is sometimes confused with superficially similar wasps (order Hymenoptera), though (as the common name suggests) the species is translucent orange and black in colour rather than waspish yellow and black.  It also has a very flat abdomen whereas wasps are rounded, and they certainly don’t sting.

Individual insects are relatively ineffective as pollinators – they are small and not very hairy, so carry little pollen compared to bumblebees for instance.  However they can be extremely abundant and that abundance makes up for any individual ineffectiveness.  It’s a real generalist, visiting lots of different types of flowers, and in my garden they visit radishes (as I noted last year) and raspberries.

I often see individuals patrolling crops such as runner beans, not visiting the flowers but laying eggs on leaves and stems: the larvae of the Marmalade hoverfly is carnivorous and feeds on aphids, so it plays an interesting dual role of both pollinator and pest controller.  Definitely a gardener’s friend!

Syrphid on lemon balm 2 - 1P1020548

Pollinator Awareness Week – 13th – 19th July 2015

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Next week has been designated Pollinator Awareness Week (PAW) by Defra and there are events and profile-raising activities going on all over the country.

The motivation behind the PAW is (quote) “to bring attention to the essential needs of pollinators and the simple actions that we can all take to help pollinators survive and thrive”.

With that in mind, next week I intend to produce one blog post a day that highlights, with photographs, a pollinator (or group of pollinators) that I’ve found in my own urban garden in Northampton.  The purpose is to illustrate the diversity of pollinators that even a town garden can support, something about their fascinating life histories, and the different ecological requirements of these pollinators that our gardens can provide.  For some of them I’ll even discuss the garden crops that they pollinate.  First post will be on Monday.

If you, or the group you work with, are doing something for Pollinator Awareness Week feel free to share it in the comments section below.

How can an understanding of plant–pollinator interactions contribute to global food security? A new discussion paper

Megachile on lambs ear 2015-06-29 18.16.49

A new discussion/review paper that I contributed to has just been published in the journal Current Opinion in Plant Biology.  Entitled “How can an understanding of plant–pollinator interactions contribute to global food security?” the paper was written in collaboration with Professor Beverley Glover and her PhD students Emily Bailes and Jonathan Pattrick at the University of Cambridge.

The abstract and highlights are copied below; if anyone wants a PDF of the full paper, send me an email or ask in the comments section.

Abstract:

Pollination of crops by animals is an essential part of global food production, but evidence suggests that wild pollinator populations may be declining while a number of problems are besetting managed honey bee colonies. Animal-pollinated crops grown today, bred in an environment where pollination was less likely to limit fruit set, are often suboptimal in attracting and sustaining their pollinator populations. Research into plant–pollinator interactions is often conducted in a curiosity-driven, ecological framework, but may inform breeding and biotechnological approaches to enhance pollinator attraction and crop yield. In this article we review key topics in current plant–pollinator research that have potential roles in future crop breeding for enhanced global food security.

Highlights:

  • Animals are globally, and increasingly, important for the improved yield and quality of many crops.
  • Floral traits are a promising and little explored avenue for the improvement of crop yields.
  • Work surrounding plant–pollinator interactions can inform us on the best strategies to do this.
  • Coordinating crop flowering time with key lifecycle stages of pollinators could benefit both crop yields and pollinators.

How good is the evidence base for pollinator declines? A comment on the recent Ghazoul and Goulson Science correspondence

In a recent issue of the journal Science, Dave Goulson and colleagues presented a review entitled “Bee declines driven by combined stress from parasites, pesticides, and lack of flowers”.  This stimulated Jaboury Ghazoul to submit a letter to Science criticising the Goulson et al. paper from a number of perspectives, but particularly the paucity of the evidence base for pollinator declines. Dave and his co-authors robustly responded to that letter, as you might imagine. In some respects this was an unsatisfactory exchange, however, as the focus was largely on agricultural pollinators, rather than pollinators of all plants (including the majority non-cultivated species) and I think that (perhaps with more space?) Dave could have outlined the evidence in more depth.

The most striking statement in Jaboury’s letter was that the “evidence for pollinator declines is almost entirely confined to honeybees and bumblebees in Europe and North America”.

Now, even given the fact that Jaboury was possibly referring specifically to agricultural pollinators, that is a very extreme statement to make. Underlying it is the suggestion that global concerns about declining pollinator biodiversity (a subject I’ve discussed repeatedly on this blog) is underpinned by a taxonomically and geographically thin evidence base. Is that really true? I don’t believe so and I think it’s worth presenting a brief overview of the evidence, not least because Dave’s review and the resulting correspondence is pay-walled at the Science site (though if you Google the titles you might, just might, find copies posted on the web…)

Let me state from the outset that I have considerable respect for both Jaboury and Dave, as individuals and as scientists. I’ve known Dave since we were postgrads together in the early 1990s, and have had occasional contact with Jaboury through conferences and via email. So this isn’t meant to be a criticism of either of them.  But I do believe that the evidence for pollinator declines is considerably more robust than Jaboury acknowledges, and even more wide ranging than Dave and colleagues describe in their response (though in fairness, most of the bee evidence was cited in their original review).

Here’s a summary of where I see the evidence base at the moment; it’s not meant to be a full review, by any means, but rather to give a flavour of the taxonomic and geographical breadth and depth of the evidence as it currently stands:

Wild bees (including bumblebees, and solitary and primitively eusocial bees) – significant reduction of abundance and diversity at local, regional and country-levels documented in Britain (Biesmeijer et al. 2006, Ollerton et al. 2014), Holland (Biesmeijer et al. 2006), Europe as a whole (Kosier et al. 2007, the recent IUCN Red List by Nieto et al 2014), North America (Grixti et al. 2007, Cameron et al. 2011, Burkle et al. 2013), South America (Morales et al. 2013; Schmid-Hempel et al. 2013), China and Japan (Xie et al. 2008; Williams et al. 2009; Matsumura et al. 2004; Inoue et al. 2008), and South Africa (Pauw 2007).

Honey bees – colony declines documented in Europe and North America (see reviews by NRC 2007, Potts et al. 2010) and evidence that global demand for honey bee pollination services is outstripping supply (Aizen and Harder 2009).

Hoverflies (Syrphidae) – diversity declines documented in Holland and Britain (Biesmeijer et al. 2006).

Butterflies and moths – diversity and abundance of Lepidoptera has declined in the UK (Gonzalez-Megias et al. 2008, Fox 2013), whilst in North America some 50 species are IUCN criteria Red Listed and there is particular concern about the iconic Monarch butterfly.  Likewise a significant fraction of butterflies in other parts of the world are of conservation concern, e.g. Southern Africa, Australia, and Europe.

Flower-visiting wasps – reduction in country-level diversity in Britain (Ollerton et al. 2014).

Birds and mammals – the major vertebrate pollinators have recently been assessed at a global level by Regan et al. (2015) using IUCN Red List criteria.  They concluded that: “overall, pollinating bird and mammal species are deteriorating in status, with more species moving toward extinction than away from it. On average, 2.5 species per year have moved one Red List category toward extinction in recent decades, representing a substantial increase in the extinction risk across this set of species”.

Of course a number of the studies cited above have shown that some species are doing better than others and a proportion of the taxa they have assessed are stable or even increasing in abundance (including managed honey bee colonies in some parts of the world). But the current evidence base, as I see it, is pointing towards significant declines in pollinator abundance and diversity at multiple spatial scales across all regions that have so-far been assessed with any rigour, for a wide range of taxa.

I’m happy to receive comments on this topic, particularly pointing me to major sources of evidence that I’ve not covered, or if you disagree with my conclusions.

References

Aizen and Harder (2009) The global stock of domesticated honeybees is growing slower than agricultural demand for pollination. Current Biology 19: 915–918.

Biesmeijer et al. (2006) Parallel declines in pollinators and insect-pollinated plants in Britain and the Netherlands. Science 313: 351–354.

Burkle et al. (2013) Plant-pollinator interactions over 120 years: Loss of species, co-occurrence, and function. Science 339, 1611–161.

Cameron et al. (2011) Patterns of widespread decline in North American bumble bees. Proc. Natl. Acad. Sci. U.S.A. 108: 662–667.

Fox (2013) The decline of moths in Great Britain: a review of possible causes. Insect Conservation and Diversity 6: 5–19.

Gonzalez-Megias, A. et al. (2008) Changes in the composition of British butterfly assemblages over two decades. Global Change Biology, 14: 1464-1474.

Grixti (2009) Decline of bumble bees (Bombus) in the North American Midwest. Biol. Conserv. 142, 75–84 (2009).

Inoue et al. (2008). Displacement of Japanese native bumblebees by the recently introduced Bombus terrestris (L.) (Hymenoptera: Apidae). J. Insect Conserv. 12: 135–146.

Kosior (2007) The decline of the bumble bees and cuckoo bees (Hymenoptera: Apidae: Bombini) of Western and Central Europe. Oryx 41, 79–88.

Matsumura et al. (2004) Invasion status and potential ecological impacts of an invasive alien bumblebee, Bombus terrestris L. (Hymenoptera: Apidae) naturalized in Southern Hokkaido, Japan. Glob. Environ. Res. 8, 51–66.

National Resource Council (2007) Status of Pollinators in North America.  National Academies Press, Washington, DC.

Nieto et al. (2014) European Red List of Bees.  Publication Office of the European Union.

Ollerton et al. (2014) Extinction of aculeate pollinators in Britain and the role of large-scale agricultural changes.  Science 346: 1360-1362.

Pauw (2007) Collapse of a pollination web in small conservation areas. Ecology 88: 1759-1769.

Potts et al. (2010) Declines of managed honey bees and beekeepers in Europe. Journal of Apicultural Research 49: 15–22.

Regan et al. (2015) Global Trends in the Status of Bird and Mammal Pollinators. Conservation Letters DOI: 10.1111/conl.12162

Schmid-Hempel et al. (2013) The invasion of southern South America by imported bumblebees and associated parasites. Journal of Animal Ecology 83: 823–837.

Williams et al. (2009) The bumblebees of Sichuan (Hymenoptera: Apidae, Bombini). Syst. Biodivers. 7: 101–189.

Xie et al. (2008) The effect of grazing on bumblebees in the high rangelands of the eastern Tibetan Plateau of Sichuan. Journal of Insect Conservation 12: 695–703 (2008).

All pollinators are equal, but some pollinators are more equal than others

The infamous line from George Orwell’s Animal Farm asserting that “All animals are equal, but some animals are more equal than others” nicely captures an ecological view of pollinators and their relationships with plants.  “Pollinators” by definition move pollen between flowers, but not all pollinators are equally good at transferring pollen of any particular plant: some are more effective than others. I’ll illustrate this with examples from the urban garden that Karin and I are developing, which I’ve discussed before.

As you can see from that link, the garden is modest in size, but nonetheless this year it contains a significant biodiversity of edible plants that require pollinators for some or all of the fruit and seed set, including: strawberries, apples, greengages, cherries, blackcurrants, squashes, courgettes, blackberries, fennel, runner beans, french beans, passion fruit, tomatoes, raspberries, and radishes.

Radishes?!”  I hear you ask.  “But they are grown for their edible swollen roots which don’t require pollination!”  True, usually.  But we let our radishes flower because we mainly grow them for their seed pods which, picked young, are delicious in salads and stir fries, like mustardy mange tout.  They look like this:

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The radish flowers are pollinated by a diversity of insects including butterflies, bees, and small flies:

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These insects will vary in their effectiveness as pollinators of radish, depending on the frequency of visits, how often they move between flowers, and the amount of pollen on their bodies.  This last factor is largely a function of size and hairiness (bigger, hairier insects carry more pollen as a rule), though cleanliness also plays a part: insects often groom the pollen from their bodies and, in the case of bees, may pack it into their pollen baskets where it’s not available for pollination.

The size and behaviour aspect is best illustrated by some recent photos that I took of visitors to the flowers of passion fruit (Passiflora caerulea var.).  We have a large, sprawling plant growing up a fence which is currently being visited by honey bees, hoverflies, solitary bees and bumblebees.  In comparison to the size of the flower and the position of the anthers (male, pollen producing parts) and stigmas (female, pollen receiving parts), the hoverflies, honey bees and solitary bees are relatively small.  These two images are of honey bees (Apis mellifera):

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Here’s an unidentified solitary bee:

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These bees were occasionally touching the anthers, mainly with their wings, so some pollen will be moved around.  But from what I observed it’s likely to be a relatively small amount in comparison to bumblebees, which are usually much larger and hairier, and don’t groom themselves as often as honey bees.  Here’s a Buff-tailed bumblebee (Bombus terrestris):

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They were actively collecting pollen as well as nectar.  Much of this pollen is packed into the pollen baskets on the rear legs and will go back to the nest to feed the developing larvae, but some will be involved in pollination:

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So it seems to be the bumblebees we have to mainly thank for the deliciously sweet-sour fruit we will enjoy later in the season. Of course to test this properly we would need to set up an experiment in which we excluded larger bumblebees from the flowers and only allowed smaller bees to forage, with appropriate experimental controls.  Would make a great project if any of my students are interested!  But it should give you a sense of just how complex the interactions between flowers and their pollinators are: the ecology of pollination is far from simple, despite what some would have us believe.

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