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Bombus veteranus by John Smit

Bumblebees of the World Blog Series… #11 Bombus veteranus

A bumblebee, Bombus veteranus, feeding on a flower with a large pollen basket

by John Smit, researcher at European Invertebrate Survey – the Netherlands / Naturalis Biodiversity Center, the Netherlands.

This month guest author, John Smit, discusses the conservation of the Sand-coloured carder bee (Bombus veteranus) in the Netherlands, a species which has experienced widespread declines across the country.

Latin nameBombus veteranus

Common name/s: Sand-coloured Carder bee

Colour pattern: Very constant, all yellowish grey (sandy coloured) with a black thoracic band and thin bands of black hairs on abdominal segments 3-5 in queens and workers and 3-7 in males. Freshly emerged specimen can have bright yellow hairs on the second abdominal segment, especially queens.

Favoured flowers: Red clover, white clover, common comfrey and, to a lesser extent, common bird’s-foot trefoil and water mint. Males can frequently be found on Asteraceae like creeping thistle and goldenrod, but also on sea holly (Apiaceae).

Global region: Entire Palearctic, from western France to the Siberian pacific coast, not present in the Mediterranean part of Europe, nor in England

Geographic distribution: Europe: Austria, Belarus, Belgium, Czech Republic, Denmark, Estonia, Finland, France, Germany, Latvia, Lithuania, Luxembourg, the Netherlands, Poland, Romania, Slovak Republic, Sweden, Switzerland, Ukraine. Asia: Russia up to the Pacific coast, including Altai and Sayan mountains and northern Mongolia.

Conservation status: Least Concern

Bombus vetranus is mainly found in the plains of northern Europe, in the southern parts it is confined to slightly higher elevations, with the French Central Massif as the southernmost record. It has disappeared over much of its distribution over the last 100 years, leaving it patchily distributed at present. This is well documented in the Netherlands, where it occurred throughout the country up until the 1970’s, followed by a steep decline. At present it is known from only two areas, along a river and a former estuary.

Evidently, it needs large, open and flower rich areas. The extensive agricultural areas in the Netherlands provided a suitable habitat for this species until agricultural intensification was introduced followed by the use of fertiliser. The borders between the smaller fields and meadows, often consisting of hedgerows, made way for barbed wire and the clover-fields used as a natural fertiliser all but disappeared. There seems to be a strong link between the disuse of red clover as a natural fertiliser and the sharp decline in some of the bumblebee species in the Netherlands. In fact, recent pollen-analyses on Bombus veteranus revealed a strong preference for both red and white clover, as well as common comfrey. Comparison of the pollen load of museum specimens with those of recent specimens revealed a shift in quantity from 64% of both red and white clover together in museum specimens to just 27% in 2017. Conversely common comfrey increased from 24% to 61%, though there are noted differences between the three recent localities surveyed, ranging from 46% at Tiengemeten to 71% at the Biesbosch.

Bombus veteranus is a late appearing species, with queens emerging from hibernation in the end of April or beginning of May and the first workers typically appearing around June, at least in the Netherlands. This is a disadvantage regarding nesting places, compared to the much more common earlier emerging species. It is reported in the literature that nesting typically occurs on the surface, amongst tall grasses or mosses, but can also be underground. The one nest recently found in the Netherlands was situated underground (video below). It consisted of a clump of cells the size of a man’s fist, with no more than 200 to 250 cells. Inside the nest two larvae of the hover fly Volucella bombylans were found, which live as scavengers at the bottom of the nest.

A species action-plan was drawn up for the Netherlands, with measures at the population level. The main goals are to reconnect the two remaining distribution areas and to provide the means for Bombus veteranus to return to the agricultural areas in the Netherlands, where this species can be used as an indicator, or an umbrella species for a more sustainable agricultural system.

Resting bumblebee by Annie Ives

Should you take a bumblebee home?

A bumblebee resting on the ground.

 by Jack Reid, Outreach and Volunteering Officer at Bumblebee Conservation Trust

So, you kidnapped a bumblebee…

Each year, the Trust receives dozens of e-mails and phone calls from well-intentioned beenappers who have been out and about and found a tired-looking lone bumblebee that they’ve rescued and taken home with them to care for. In case you’ve been considering the practicalities of taking a bumblebee home, we have written up this useful guide to caring for your new friend, without taking it home!

Should I take a bumblebee home?

No! Bumblebees have their own homes.

At all times throughout the year, bumblebees have important jobs to be doing – whether it’s queens who are searching for a nest site or gathering pollen for their first clutch of workers; workers who are out, working hard to gather enough pollen and nectar to support their queens and siblings; or males who, despite their work ethic, are vital to ensuring there is a next generation of bumblebees.

For this reason, it’s very important to leave the bumblebees to what they’re supposed to be doing – they can’t support their nests if they can’t get back to them!

What should I feed bumblebees?

Bees need flowers!

Bumblebees are exceptional at identifying the nutrients and foods they need when they are foraging on flowering plants out in the wild. Our knowledge of bumblebee feeding habits is constantly evolving – but nobody knows what they need better than the bumblebees themselves. So we recommend that, rather than taking a tired-looking bumblebee home, you first consider whether they are in danger where they are, or if they’re simply resting!

For more information on if and when to move bumblebees, and when and what to feed them, please click here.

When should I release them?

The best time to leave your bumblebee alone was before you picked them up. The second best time is now!

Bumblebees navigate using landmarks, like buildings, or rocks, or trees. If they can’t find locations that they recognise, they may struggle to find their way back home to their nest when you release them.

If possible, bumblebees should be released near to where you found them. If not, placing them outside on or near to flowering plants is the next best option.

So what do I do if I find a tired bumblebee?

This is a great question – for information on what to do if you find a tired bumblebee, and when to feed, and/or possibly relocate them, please click here.

Bombus eximius by Chawatat Thanoosing

Bumblebees of the World Blog Series… #8 Bombus eximius

The Orange-legged bumblebee, Bombus-eximius

By Chawatat Thanoosing, PhD student and Paul Williams, researcher at the Natural History Museum London

This month we’ll explore a deep montane tropical forest in Asia, where Chawatat Thanoosing— a PhD student at Imperial College London and the Natural History Museum—is doing his research on the ecology of tropical bumblebees, to see the remarkable giant bumblebee, Bombus eximius.

Latin name: Bombus eximius

Common name/s: Orange-legged bumblebee

Colour pattern: Whole body mainly black with brightly orange tail and legs in all castes.

Favoured flowers: Mid altitude flowering shrubs and trees, and wild orchids

Global region: Oriental region

Geographic distribution: Asia: India, Nepal, Bhutan, Bangladesh, Myanmar, Thailand, Vietnam, China, and Taiwan

Conservation status: Not evaluated

The impressive Bombus eximius is a broadly distributed Asian bumblebee, found across the Himalayas, Southern China, Taiwan island and in the mountain ranges of northern Southeast Asia, at mid altitude, from approximately 1000 m above sea level. Unlike common bumblebees in Europe (eg. B. terrestris), which show black and yellow striped patterns on their abdomen, B. eximius is often a predominantly black bumblebee with orange on their tail and legs, although sometimes the populations in Southern China and Taiwan have extensively orange abdomens as well.. This orange-colouring across the legs is in congruence with the original subgeneric group that this species was attributed to, Rufipedibombus, which means red-legged bumblebees, although it is now included as part of Melanobombus, distantly related to the European B. lapidarius.

Queens of B. eximius are some of the largest bumblebees in the world. The body length of the queen is approximately 3 cm long, similar in size to the Patagonian bumblebee, B. dahlbomii, in South America. Strangely, those big bumblebees show almost the opposite colour pattern between them. They have an orange thorax and abdomen with black legs, whereas B. eximius often has a a black body and orange legs. The two species have evolved independently in different lineages and different geographic regions.

The food preference of B. eximius has rarely been studied. In Thailand, this species has been reported visiting and pollinating some native orchids: Dendrobium infundibulum and Cymbidium insigne. Care is needed when identifying these bees because B. eximius is mimicked very closely by B. flavescens, a relative of B. pratorum. When B. eximius lands on an orchid flower, pollinia (a sticky orchid pollen mass) will either attach to its thorax (in D. infundibulum flowers) or abdomen (in C. insigne flowers). The cross-pollination of the orchids occurs when the bumblebee with attached pollinia visits another orchid flower. In addition, at Doi Inthanon mountain, the highest peak in northern Thailand, B. eximius has been observed to visit Hooker’s St. John’s Worts (Hypericum hookerianum), Som Pae (local Thai name for Vaccinium exaristatum), Rubus chevalieri and Saurauia napaulensis for food.

The IUCN conservation status of this bumblebee has not yet been assessed. This species still flies and hides in the shady forests of the mountains. Despite extreme deforestation, land use changes and heavy pesticide use in this region, no one knows whether the population of this bumblebee is decreasing or not. From the obvious changes in the environment, raising awareness and protecting bumblebees in this region are likely to be urgently needed.

Links to further information:

Natural History Museum species account

Natural History Museum Bombus – Bumblebees of the world homepage

Williams, P. H., Ito, M., Matsumura, T., & Kudo, I. (2010) The bumblebees of the Nepal Himalaya (Hymenoptera: Apidae). Insecta Matsumurana. 66, 115­–151

Williams, P. H., Tang, Y., Yao, J., & Cameron, S. (2009) The bumblebees of Sichuan (Hymenoptera: Apidae, Bombini). Systematics and Biodiversity. 7, 101–190

Kjellsson, G., Rasmussen, F. N. & Dupuy, D. (1985) Pollination of Dendrobium infundibulum, Cymbidium insigne (Orchidaceae) and Rhododendron lyi (Ericaceae) by Bombus eximius (Apidae) in Thailand: A Possible Case of Floral Mimicry. Journal of Tropical Ecology. 1, 289–302

Red-tailed cuckoo bumblebee (Bombus rupestris) by Nick Owens

Bumblebees of the World Blog Series… #6 Bombus rupestris

A Red-tailed cuckoo bumblebee dusted in pollen and feeding from a pink flower.

by Darryl Cox, Senior Science & Policy Officer

Bumblebees of the world would not be complete without delving into the darker side of bumblebee life, and so this month features one of around thirty described parasitic cuckoo bumblebees, the Red-tailed cuckoo (Bombus rupestris).

Latin name: Bombus (formerly Psithyrus) rupestris

Common name/s: Red-tailed cuckoo, Hill cuckoo

Colour pattern: In Britain, females are black with red tails, similar to their host species, the Red-tailed bumblebee (B. lapidarius). However Red-tailed cuckoos are much sparser haired, lack pollen baskets, have large box shaped heads and distinctive black/blue wings. Some females have a faint yellow band which can be seen at the collar. Males can be variable, however usually have a faint yellow collar and bands across the midriff of the lower thorax and upper abdomen, with a red tail. Yellow-banded female forms are found in Asia.

Host species: Red-tailed bumblebee (Bombus lapidarius), Bombus sichelii and likely other species from the subgenus Melanobombus

Favoured flowers: In spring – dandelions, comfrey, oxeye daisies. New females and males in summer – thistles ragwort, brambles and other garden plants like lavender.

Global region: Palaearctic, Oriental regions

Geographic distribution: Europe – Albania, Andorra, Austria, Belarus, Belgium, Bosnia and Herzegovina, Bulgaria, Croatia, Czech Republic, Denmark, Estonia, Finland, France, Germany, Greece, Hungary, Ireland, Italy, Lithuania, Luxembourg, Republic of North Macedonia, Moldova, Montenegro, Netherlands, Norway, Poland, Romania, Russia, Serbia, Slovakia, Slovenia, Spain, Sweden, Switzerland, Ukraine, United Kingdom. Asia – Turkey, Russia, Kazakhstan, Mongolia, Tibet, China.

Conservation status: Least concern

For those that have not heard of cuckoo bumblebees before, they are a fascinating group of bumblebees which have evolved to take advantage of the hard-working nature of social bumblebees. Unlike social bumblebees, cuckoos have no workers of their own. Instead the cuckoo female invades the nest of a social species and either kills or enslaves the resident queen, before using the resident workers to collect food and help her raise her own brood.

In this case (in Britain), the Red-tailed cuckoo will emerge from hibernation between April and June, around six weeks after the first social Red-tailed bumblebee queens have emerged and started setting up their colonies. Timing is key in the world of the cuckoo bumblebees as they search out an established nest. They want to take over a nest which has grown strong enough to raise as many offspring as possible, without being too strong for the cuckoo female to gain control. Once she finds a nest, the cuckoo lies in wait and often digs down into the nest material whilst trying to remain unseen. It is thought she does this to try and take on the scent of the nest, and perhaps to wait for the ideal time to make her move. If the workers and their queen find her, they will attempt to kill her or at very least evict her from their territory. This is the fate for many cuckoo females and nests are often strewn with the carcases of failed usurpers. Nest-stealing behaviour is not limited to cuckoo species though, and many later emerging social queens will also attempt to take over nests of other bumblebees to gain an advantage.

Cuckoos, however, have evolved to be nest-stealing specialists, built for fighting, and once in a position to enter a nest with minimal challenge, they use this to their benefit. Harder exoskeletons, the segments of which fit tightly together (unlike social bumblebees which excrete wax from these points), more powerful mandibles, and a longer sting eventually prove too much for the founding queen, and if she is not killed off she may become subservient to her oppressor, acting in the same manner as her daughter workers.

The workers she leaves behind will continue to forage and provide for the nest, however they will be helping to rear the cuckoo’s brood. The new cuckoo queen keeps her recently acquired workforce in check with the use of pheromones and aggressive behaviour. Any remaining eggs and young larvae are promptly destroyed, although those that are close to adulthood are spared to join the workforce. Some of the original workforce may go rogue and start to lay their own unfertilised eggs, however the new overlord is able to test the eggs to check if they are smooth or ridged. All cuckoo eggs are ridged, which is a useful characteristic for the policing intruder. Any smooth eggs are swiftly devoured. Unlike their social counterparts which lay between 8 and 16 eggs per clutch, cuckoos can lay batches of up to 20-30 eggs at a time, which is important as they only have a limited period of time before their workforce dies off. These eggs are reared into new male and female cuckoos, which then leave the nest to find a mate, before the fertilised females go into hibernation. The cycle then repeats itself in the following season.

After learning about this bumblebee underworld, many people decide they do not like cuckoos and we are often asked if anything should be done to prevent them from invading bumblebee nests. Some people have even gone as far as to devise novel nesting boxes aimed at preventing cuckoos from entering. However, this is not necessary or advisable. It is important to remember that these social parasites are intrinsic parts of nature too and several species are now critically rare due to unrelated declines in their host species. Human-caused drivers of population declines like habitat loss, pesticide use, disease and climate change are the things we should focus on tackling, rather than these naturally evolved brood parasites. There is so much more to discover about these intriguing invaders, but maintaining healthy bumblebee populations by addressing those human-caused problems is key.


Links to further information:

IUCN Redlist page

Natural History Museum species account

Natural History Museum Bombus – Bumblebees of the world homepage

IUCN Bumblebee Specialist Group

Richard Comont’s RSPB Spotlight bumblebees (2017)


Acknowledgements

Many thanks to Paul Williams of the Natural History Museum, London, for his help and advice.

Male Bombus inexspectatus by Maurizio Cornalba

Bumblebees of the World Blog Series… #7 Bombus inexspectatus

A male Unexpected bumblebee, Bombus inexspectatus

by Darryl Cox, Senior Science & Policy Officer

July’s Bumblebees of the world blog features the endangered Bombus inexspectatus, literally an unexpected European bumblebee, first described by Tkalcu in 1963, which has been found to parasitize on the Red-shanked carder bee (Bombus ruderarius). This species is one of two bumblebees, outside of the typical cuckoo bumblebee group (discussed in last month’s blog) to have evolved a parasitic way of life.

Latin nameBombus inexspectatus

Common name/s: Unexpected bumblebee

Colour pattern: Males and females have two yellow bands on the thorax, a yellow band at the top of the abdomen and a red tail. The host species (Bombus ruderarius) mainly occurs with similar pattern to the British type (unbanded with a red tail), but can also have similar banding to the Unexpected bumblebee, although the back of the head is larger in B. inexspectatus than B. ruderarius in both males and females.

Host species: Red-shanked carder bee (Bombus ruderarius)

Favoured flowers: Females have been found on Clovers and Rampions, males on Knapweed and Thistles

Global region: Palaearctic

Geographic distribution: Europe – Alpine regions of France, Switzerland, Austria and Italy, and a disjunct population in the Cantabrian Mountains of Spain.

Conservation status: Endangered

When Tkalcu first made his discovery of a new/overlooked European bumblebee species it prompted European bumblebee specialists to resample potential locations and look back in their own collections to reassess potential specimens. As a result, the original four records soon became eighty or so. Interestingly, the original records included two males and two supposed workers, which happen to be the only two workers ever found for this species. The status of these females as workers was called into question by Yarrow in 1970 who proposed that inexspectatus could potentially be a social parasite of the closely-related Red-shanked carder bee (B. ruderarius), which he always found in good numbers wherever inexspectatus was found. He argued that the workers were merely ‘runt’ females which were underdeveloped in comparison to the rest of the female specimens. Close examination of collected specimens revealed that unlike social bumblebees and similar to cuckoos, inexspectatus specimens do not appear to secrete wax from their abdominal segments, which is an essential part of colony building among the social bumblebees. Yarrow noted that none of the specimens he had seen had any evidence of pollen collecting, and that the structures on the legs associated with pollen collection seemed to have degenerated slightly in comparison with social bumblebees, although not to the same extent as the main cuckoo group (Psithyrus subgenus).

It was not until 2005, when Andreas Muller and colleagues stumbled upon a Bombus ruderarius nest in the Swiss Alps, that Yarrow’s suspicions were supported with the first and only evidence of parasitism by inexspectatus. The nest they found was close to completion with no stored nectar, eggs or larvae, a selection of empty cocoons from various generations of workers and four unhatched cocoons, which four ruderarius queens later emerged from. No founding queen/females of either species were found, however two ruderarius workers, two males and one new queen remained in the nest when it was found, as well as one fresh inexspectatus female. This indicated that both the social queen and the parasitic female were co-existing in the nest, which has been found when other cuckoo bumblebees invade nests, but often the social colony does not successfully produce new queens or produces fewer than normal. As this is the only nest that has been found to date – we do not know how common it is for the two species to co-exist or if the invading bees manage to completely take over nests in the same way that some other cuckoo bumblebees do. There are also larger questions about this species’ general ecology and life history still to be answered, for example, whether inexspectatus can invade the nests of other hosts, similar to the other known parasitic bumblebee species.


Links to further information:

IUCN Redlist page

Natural History Museum species account

Natural History Museum Bombus – Bumblebees of the world homepage

IUCN Bumblebee Specialist Group

Hines, H. M., and Cameron, S. A. (2010). The phylogenetic position of the bumble bee inquiline Bombus inexspectatus and implications for the evolution of social parasitism. Insectes Soc. 57, 379–383. doi: 10.1007/s00040-010-0094-1

Müller, Andreas. (2006). A scientific note on Bombus inexspectatus (Tkalců, 1963): Evidence for a social parasitic mode of life. Apidologie. 37. 408-409. 10.1051/apido:2006005.

Yarrow I.H.H. (1970) Is Bombus inexspectatus (Tkalců) a workerless obligate parasite? Insectes Soc. 17, 95–112


Acknowledgements

Many thanks to Maurizio Cornalba of the University of Pavia, Italy, and Paul Williams of the Natural History Museum, London, for their help and advice.

Allotment wildflowers by Katy Malone

Bees find a helping hand on my allotment

Allotment with many colourful wildflowers

23 July 2019

by Katy Malone, Bumblebee Conservation Trust Conservation Officer for Scotland

Being a fully paid-up member of the bumblebee fan club, no-one will be surprised to learn that when I finally got offered an allotment in my village three years ago, I set out to make it as bee-friendly as possible. After all, growing veg and attracting crop pollinators with nectar and pollen-rich flowers – well, it’s just a no-brainer.

That said, my fellow allotmenteers and I each have our own distinctive style of growing, which probably reflect our personalities. The gentleman with the plot next door to mine grows very traditionally in very neat, die-straight rows. Potatoes are earthed up in immaculate V-shaped furrows, all the same height and distance apart. He plots out carrots in a millimetre-accurate grid. Every scratch of ground is used for crops of some sort. One a sunny day in May, he spotted the packets of bulbs I brought for planting in the pre-prepared ground and was intrigued.

“Oh, what’s that you’ve got?”

“Gladioli blubs – a lovely mixture of…”

…but he had already turned away in pretend disgust. Of course, I was letting the side down! We joked about it, but I know he’d really prefer me to be grow swedes rather than ‘wasting’ the available space with flowers. He still borrows my rake when I’m not around though.

The plot opposite has lots of flowers as well as crops, in higgledy piggledy rows. She’s a child minder, and her young charges often come down to help her in the allotment.  She grows lovely sweet peas, lilies and cosmos, the veg and the flowers being mostly separate from each other.

My own plot is something of a potager style, with blocks of edible crops interspersed with colourful flowers which attract pollinating insects like bumblebees (of course!) as well as honeybees, wasps, and hoverflies. I get a great sense of satisfaction by growing from seed, and this year almost all my crops are grown this way (except potatoes from sets, and garlic which I grew from cloves saved from last year’s crop).

Cornflowers, self-sown foxgloves and cosmos all attract a variety of beneficial insects. The cornflowers are part of my plan to grow flowers for cutting, but if an insect happens to be feeding on the freshly emerged flower, I leave it alone. I would feel so guilty for depriving any bee of its lunch! If a few crops start bolting, and I don’t need the space immediately, I’ll let them flower. The hoverflies are particularly keen on the towering blooms of Swiss chard, which bloom profusely before flopping over in the wind and need to be propped up or cut back.

Some ‘weeds’ are particularly beneficial and I let them grow amongst my veggies, as long as they don’t start to take over. Red dead-nettle is a favourite with long-tongued bumblebees, which in turn are brilliant pollinators of my runners and broad beans. The shorter-tongued honeybees and hoverflies can’t reach the nectar in these long-flowered crops, and so cannot pollinate them. Encouraging longer tongued species like garden bumblebee and common carder bumblebees by providing a greater diversity of long flowers is good for a quality crop set. I know there are modern F1 crop varieties which are self-setting, but I prefer to grow open-pollinated heritage varieties. For me, it goes against the grain to do anything else.

It would be great to think that all this results in better pollination of my crops – and really, I have no first-hand evidence that supports that. However, a research paper1 published in Nature earlier this year revealed that allotment sites are very valuable spaces in an urban context. The researchers showed that residential gardens and allotments in four different cities across the UK were major hotspots for pollinators, highlighting the value of these places for supporting vital pollinator conservation. In his regular summary of recent science papers ‘Bombus Review’ (Bombus review – Spring 2019) my colleague Darryl Cox wrote of this paper:

“The authors end their report with some really useful and practical suggestions for maximising the pollinator potential of urban areas. They suggest that town planners try to add more allotments to towns and cities as even a small area increase could make a big impact on the robustness of plant-pollinator communities.”

Watching bees work those multi-coloured cornflowers, benefitting from the abundant nectar and pollen from the red dead-nettle and enjoying the late boost of forage from the gladioli and self-sown foxgloves gives me satisfaction beyond words. When I’m enjoying freshly-podded broad beans, lightly steamed with butter and parsley and a squeeze of lemon, I am even more glad to be supporting the bees in my little corner of paradise.


  1. A systems approach reveals urban pollinator hotspots and conservation opportunities. Baldock, KCR et al, Nature Ecology & Evolution volume 3, pages 363–373 (2019)

A brief guide to solitary bee nest boxes

Bex Cartwright, our Making a Buzz for the Coast Conservation Officer, has written this handy guide on how to create or choose a suitable bee box to make a perfect home for solitary bees in your garden!

A bee box for solitary bees attached to a garden fence

Credit: Bex Cartwright

Siting your solitary bee nest box  

To maximise the chances of your solitary bee nest box being occupied, careful siting is important.

  • Position your nest box in full sunshine so facing south east or south
  • Place the nest box at least 1 metre from the ground
  • You can place your nest box near vegetation but ensure that no vegetation will obscure or shade the nest entrances
  • Position the nest box in a stable, fixed position that will not sway in the wind or be easily knocked or dislodged.
  • Remember, one of the reasons for having a bee nest box is so you can observe the fascinating activities of the solitary bees visiting your garden so make sure it is somewhere you will see it regularly.
A leaf-cutter bee entering the hollow tubes of a solitary bee hotel.

Credit: Alison Scimia

Things to consider when choosing or creating a solitary bee nest box

If you are thinking of creating a new bee nest box or buying one of the many commercially available nest boxes there are a number of things to consider. Many are expensive and some are poorly-designed. Some of the most commonly encountered issues are:

  • The length of the nesting tubes or drilled holes is not sufficient. Look for a nest box with nesting tunnels 15cms in length as a minimum.
  • The diameter of the nesting tubes are often too wide. This is because houses manufactured abroad are built to attract larger species than those we have in the UK. It is beneficial to provide a range of diameter nesting tubes as this will attract a range of different species. Provide holes of between 2-10mm in diameter.
  • No protection from wet and windy weather. Ideally the bee house will have a small overhang to prevent nesting tubes becoming damp. To some extent this can be alleviated by careful placing of the bee house. Somewhere sheltered but not shaded is ideal.
  • Avoid the use of plastic straws or containers. Plastic and other ‘non-breathable’ materials prevent the movement of air and moisture and can encourage damp and condensation leading to fungus and mould. This will destroy eggs and larvae.
  • In general tunnel and tube entrances should be smooth and free of splinters although some species will clean out and ‘tidy-up’ a tube before nesting.
  • Nesting tunnels and tubes should have a solid back. Bees will not use nesting tubes which are open at both ends.
  • The nesting tunnels need to be accessible and removable so that the contents can be examined, cleaned and periodically replaced. The most successful bee nest boxes are those that are well-managed.
A female Patchwork leaf-cutter bee flying while holding a small leaf between its legs.

Credit: Jean Baird

Which bee species will the nest box attract?

The most common resident of garden bee nest boxes is the Red Mason Bee (Osmia bicornis), this species flies in early spring. Later in summer your bee nest box may also attract leafcutter bees such as Patchwork Leafcutter (Megachile centuncularis) (image above) and Willughby’s Leafcutter (Megachile willughbiella). These species play host to cuckoo bees Coelioxys, also known as ‘sharp-tailed bees’ (image right), fascinating bees which lay their own eggs in the provisioned leafcutter nests. Smaller bees such as Harebell bees (Chelostoma sp.) and Masked or Yellow-faced bees (Hylaeus spp.) are also attracted to nest boxes

A range of solitary wasps may also use the nest box, these will act as a great natural pest control in your garden, collecting flies, small caterpillars and aphids to provision their nests.

Managing your bee hotel

Periodic maintenance and cleaning will result in a more successful nest box and a healthier population of bees in your garden. With no cleaning, fungi, debris and parasites tend to build up which can be damaging to the bees.

  • Bring your nest box into an unheated shed or garage during the autumn and winter to protect it from damp and wet weather. If you don’t have either then a porch or any covered area will do. It is damp not cold that destroys larvae. Not only will this protect the larvae and adult bees waiting to emerge in the spring but it will mean that your nest box will last longer. You can place the box outdoors in the spring, from March onwards.
  • If you notice birds predating your nest box or removing nest tubes (woodpeckers and tits often do this) then you can place a piece of mesh or chicken wire across the front. This does not appear to deter the bees.
  • If your nest box is built of stacked & routed wooden sheets or you use paper nest tube liners you can clean it out in winter, remove the cocoons (image left) and store them until spring.
  • At least every couple of years replace all of the tubes and blocks in the nest box with fresh ones. In spring leave the old tubes in an upturned box or bucket on the ground with a hole at the top (bees naturally orientate towards light) so that the previous year’s bees can emerge but so that they won’t reoccupy the old tubes.

For further information on all of the above Marc Carlton of ‘The Pollinator Garden’ has produced an excellent guide to ‘Making and Managing a Bee Hotel’. A pdf. version can be downloaded from www.foxleas.com

George Pilkington also has a fantastic website and blog ‘Nuturing Nature’ www.nurturing-nature.co.uk which has a wealth of information on managing bee houses.

For photos and more information about the bees and wasps that are attracted to nest boxes the website of The Bees, Wasps and Ants Recording Society ‘BWARS’ is very helpful  www.bwars.com

 

Bombus fraternus by J C Jones

Bumblebees of the World Blog Series… #4 Bombus fraternus

The Southern Plains bumblebee, Bombus fraternus

by Darryl Cox, Senior Science & Policy Officer

The Southern Plains bumblebee (Bombus fraternus) features in this month’s Bumblebees of the World blog, with a particular focus on how the species’ endangered conservation status was classified by the  IUCN’s Bumblebee Specialist Group (BBSG).

Fact File

Latin name: Bombus fraternus

Common names: Southern Plains bumblebee

Colour pattern: Queens and workers are predominantly pale straw-coloured yellow with a black band between the dark wings and an extensive black tail. Males look similar, although can be more extensively yellow between the wings and have very large eyes.

Favoured flowers: Milkweed (Asclepias), Prairie clovers (Dalea), Blazing stars (Liatris), Sweet clovers (Melilotus), Prairie coneflowers (Ratibida) and Goldenrod (Solidago)

Global region: East Nearctic region, West Nearctic border

Geographic distribution: North America – Central to South-eastern US (Virginia, Texas, Minnesota, Massachusetts, Louisiana, Kansas, Iowa, Indiana, Illinois, Georgia, Florida, Colorado, Arkansas, Alabama, Mississippi, Missouri, Nebraska, New Jersey, New Mexico, North Carolina, North Dakota, Ohio, Oklahoma, South Carolina, South Dakota, Tennessee)

Conservation status: Endangered

The Southern Plains bumblebee is found to the east of the Rockies, across the prairie lands in the south of the Great Plains, stretching to the coastal plains of central Florida and New Jersey. With pale yellow and black banding, this short-tongued bumblebee has a similar colour form to a number of North American species, however it is has a very distinctive look, with extremely short and even hair across its body. This gives the bee a very close-cropped and neat look overall – almost like a bumblebee with a (forgive me) buzz cut! Some of the hair on the abdomen is completely flattened to the body making the abdomen look slim and sleek in comparison to other fuzzier bumblebees.

The IUCN-BBSG last assessed the conservation status of this species in 2014, when it was classified as endangered. Their justification came down to three main factors – relative abundance, which is a measure of how many records of this species there are in relation to the total number of species recorded, a change in its extent of occurrence, which relates to the species’ overall distribution, and the loss of suitable habitat within the species’ known range.

The IUCN-BBSG team took historical national bumblebee records and plotted the Southern Plains bumblebee’s relative abundance at 10 year intervals to understand how it had changed from 1912 to 2012. The figure below shows a historical downward trend which is close to being statistically significant. If the trajectory were to continue at this rate, the assessors warn the species could potentially be extinct within the next 80-90 years.

The decline in relative abundance since 2002 was consistent with a decline in distribution. The team mapped historical records and compared them with records post 2002 to understand the extent that the species still occurs across its known range. After taking care to avoid statistically overestimating range loss (by randomly rarefying the much larger number of pre-2002 records), they found that the species had reduced its area of occupancy by 28.62% since 2002. A heat map depicts the amount of surveying that took place between 2002 and 2012. This shows that some of the areas the species has declined from have also been well surveyed in recent times, which gives the team confidence in their assessment that Bombus fraternus has declined in range.

The third area of justification relates to severe changes that have occurred in the Southern Plains bumblebee’s habitat range, particularly since 2002. This period has seen native grasslands converted into agricultural land and increased use of agricultural pesticides. Identifying the negative impact that these changes have had is useful as it helps indicate what needs to change for this species to recover. The IUCN-BBSG identify the following general actions to conserve Bombus fraternus: restoring, creating and preserving natural grasslands, restricting harmful pesticide use within or close to their habitats, and protecting them from diseases introduced by managed bees.  However, more research is needed to fully understand the specific requirements of this distinctive species and how best to help it. For those wishing to get involved with Bumblebee Conservation in the U.S. check out the IUCN Bumblebee Specialist Group.


Links to further information:

IUCN Redlist page

Natural History Museum species account

Natural History Museum Bombus – Bumblebees of the world homepage

The Bumble bees of North America: An Identification guide. By Williams, P.H., Thorp, R.W., Richardson, L.L. and Colla, S.R. (2014) Princeton University Press, Princeton

IUCN Bumblebee Specialist Group

Xerces Society Bumblebee conservation page

Acknowledgements

Many thanks to Paul Williams of the Natural History Museum, London, for his help and advice.

Bombus cullumanus by Natural History Museum, London

Bumblebees of the World Blog Series… #5 Bombus cullumanus

Cullum’s bumblebee, Bombus cullumanus pinned as a museam exhibit

by Paul Williams, Researcher at the Natural History Museum, London, and Darryl Cox, Senior Science & Policy Officer.

This month, Bumblebees of the world returns from across the Atlantic to feature Cullum’s bumblebee (Bombus cullumanus), a Eurasian species which is sadly no longer found in the UK and has experienced drastic declines across the rest of Western Europe.

Latin name: Bombus cullumanus

Common name/s: Cullum’s bumblebee

Colour pattern: In Western Europe, queens and workers are black with red tails and look very similar to Red-tailed bumblebees (B. lapidarius), although queens are smaller and sometimes have a very faint yellow band that can be seen at the collar.

Males have a dull yellow collar and bands across the lower thorax and majority of the upper abdomen with a red tail (similar to some brighter Ruderal bumblebee (B. ruderarius) males).

Favoured flowers: older male specimens are described as feeding on Knapweed, White clover, Wild marjoram, Musk and Dwarf thistles. Workers are thought to favour legumes.

Global region: Palaearctic

Geographic distribution: Europe – Moldova, Montenegro, Romania, Russia, Serbia, Spain, Ukraine. Asia – Russia, Turkey, Armenia, Iran, Afghanistan, Uzbekistan, Turkmenistan, Tadzhikistan, Kyrgyzstan, Kazakhstan, China, and Mongolia.

Conservation status: Critically Endangered in Europe

Cullum’s bumblebee, named after 7th Baronet, Sir Thomas Cullum, a medical doctor and well-respected natural historian from Suffolk, was described as new to science by William Kirby in 1802 after an interesting striped and red-bottomed male was spotted in Suffolk. It was not until 1926 that the connection was made between the yellow-banded males and the black females with red tails, which are difficult to separate from the similar, more widespread Red-tailed bumblebee (Bombus lapidarius).

Bombus cullumanus belongs to a broader species group of closely related species known as the cullumanus­-group. The species group has been the source of much debate amongst taxonomists and there have been several interpretations of the number of species within the cullumanus-group, but DNA barcoding has been able to provide a much clearer answer.

It turns out that Cullum’s bumblebee can be exceptionally variable in terms of colour pattern and because of this it has been classified as several separate species from different geographic locations. Williams et al. (2012) set out to sequence the DNA of some bumblebee specimens within the cullumanus-group and found that four bumblebees which had been classified as separate species are actually parts of Bombus cullumanus, which is known to be declining steeply in Western Europe (described in the fact file). The following ‘species’ have therefore been reclassified as parts of Bombus cullumanus:

  • Bombus serrisquama – a yellow banded bumblebee found in Spain, Russia and Central Asia
  • Bombus apollineus – a white banded bumblebee found in Turkey and Armenia.
  • Bombus tenuifasciatus – darker yellow bands found in Central Asia
  • Bombus nigrotaeniatus – also Central Asia and with no yellow band on the abdomen

The last confirmed sighting of Bombus cullumanus in the UK was a male on the Berkshire downs in 1941, making it one of two species that have likely gone extinct from the UK in the last 80 years (the other being the Short-haired bumblebee, Bombus subterraneus). It has similarly vanished from the Netherlands, Belgium, France, Germany, Sweden and Denmark.

Although this is undeniably sad news, the new understanding that the species is much more widely distributed than initially thought (albeit in different colour forms) means that in conservation terms, it is doing better than initially feared, especially in Russia and Central Asia where it can be common in grasslands. In fact, the genetic work by Williams and colleagues indicated that another species within the wider cullumanus-group, Bombus unicus, may actually be worse off. They are calling for urgent surveys to help assess the status of Bombus unicus, which seems restricted to the far East of Russia and has only ever been found in very low numbers.


Links to further information:

IUCN Redlist page

Williams, P.H., Byvaltsev, A., Sheffield, C., Rasmond, P., Bombus cullumanus—an extinct European bumblebee species? Apidologie (2013) 44: 121.

Natural History Museum species account

Natural History Museum Bombus – Bumblebees of the world homepage

IUCN Bumblebee Specialist Group

Bombus dahlbomii by Michael Usher

Bumblebees of the World . . . #1 Bombus dahlbomii

The Patagonian bumblebee or Flying Mouse, Bombus dahlbomii, feeding on a flower

by Darryl Cox, Senior Science & Policy Officer

There are around 250 species of bumblebees across planet Earth, stretching across most of the Northern Hemisphere, from the arctic, right down to the southern-most tip of South America in the Southern Hemisphere. Each bumblebee species has a different distribution and all are an important part of life within their ecosystems. By transferring pollen that helps plants set fruit and reproduce, they are involved in the base layers of numerous food chains, which provide food and shelter for a great multitude of living things (including ourselves).

This year, we have decided to show our appreciation for some of the most beautiful and diverse bumblebees from across the world in our monthly Bumblebees of the World blog series, and what better way to start our series than with one of the world’s largest and most iconic bumblebees: Bombus dahlbomii.

Fact File

Latin name: Bombus dahlbomii

Common names: Patagonian bumblebee, Flying Mouse

Colour pattern: Deep orange/ginger thorax and abdomen, with black underside, legs and wings. (Queens, workers and males)

Favoured flowers: Chilean bellflower (Lapageria rosea), Peruvian lily (Alstroemeria aurea)

Global region: Southern Neotropical, Eastern Neotropical

Geographic distribution: South America – Chile, Patagonia, Argentina

Conservation status: Endangered

Commonly known as the Patagonian bumblebee or the Flying Mouse, the South American Bombus dahlbomii is a giant among bumblebees. With queens that can grow as large as 3 cm long – you definitely know when you’ve seen one of these ginormous ginger bees! These majestic bumblebees are not only iconic based on their size, they are also known globally for their story, which sadly, is one of human-caused decline.

The decline has been rapid and can be attributed to the introduction of two non-native invasive European bumblebees, Bombus ruderatus and Bombus terrestris. These bees were originally imported to Chile for commercial pollination in agriculture. In 1982 and 1983, hundreds of Bombus ruderatus queens were brought over from New Zealand (from the population originally exported from the UK in the 1800’s) to aid with pollination of red clover, which subsequently led to their invasive establishment in the wild. Bombus terrestris colonies are still regularly imported into the country, where they are deployed in greenhouses and in open fields to pollinate tomatoes, avocados and blueberries. Astonishingly, since 1997, over a million colonies of Bombus terrestris have been imported into Chile. They are now firmly established in the wild and have invaded Patagonia and Argentina.

Not only do these invasive bees compete for food resources, but they have also brought novel diseases with them which have likely had a profound negative impact on the native species, much like when the Spanish unleashed a host of new human diseases on the native South American people throughout their colonization of the Americas. Unfortunately for Bombus dahlbomii, the consequences of this introduction have been great and the species is now classed as internationally endangered. Sightings of the legendary Flying Mouse are now much rarer across its once large distribution in southern South America; it has all but disappeared from the north of its known range, coinciding with the range expansion of the two invasive species. With Bombus terrestris expanding further and further south, there is grave concern that Bombus dahlbomii may not be far away from extinction. This is not only bad for Bombus dahlbomii, but also has wider ecological consequences for the plants it pollinates, many of which are now subject to nectar robbing by the alien species, and also means that non-native invasive plants, such as Scotch broom, are able to spread as their preferred European pollinator is now there to help them reproduce.

The damage caused by these alien bees entering South America is now irreversible because the alien species cannot be eradicated. However there are crucial lessons to be learned: animals do not respect international borders and so decisions made by one country’s government can have unintended consequence for neighbouring countries (in this case Argentina did not import non-native bumblebees). This has led scientists to argue for international cooperation on the global trade of species, something which is vital to prevent further cross-border invasions. The global commercial bumblebee trade has been growing rapidly over the last three decades and it is imperative that governments, traders and farmers act responsibly to avoid the consequences of allowing commercial bumblebees to freely enter non-native environments.


Links to further information:

IUCN Redlist page

Natural History Museum species account

Natural History Museum Bombus – Bumblebees of the world homepage

British Ecological Society Article

Aizen et al. Coordinated species importation policies are needed to reduce serious invasions globally: The case of bumblebees in South America (Journal of Applied Ecology)


Acknowledgements

Many thanks to Paul Williams of the Natural History Museum, London, for his help and advice.