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Bombus muscorum

Bombus muscorum, commonly known as the large carder bee or moss carder bee, is a species of bumblebee in the family Apidae. The species is found throughout Eurasia in fragmented populations, but is most commonly found in the British Isles.[2][3] B. muscorum is a eusocial insect. The queen is monandrous, mating with only one male after leaving a mature nest to found its own. Males mate territorially and the species is susceptible to inbreeding and bottlenecks. The species builds its nests on or just under the ground in open grassland and forages very close to the nest. In recent years, populations have significantly declined due to loss of natural habitat. B. muscorum is currently listed as vulnerable in Europe by the European Red List of Bees.[4]

Bombus muscorum
Bombus muscorum agricolae – the Shetland subspecies
Scientific classification
Domain: Eukaryota
Kingdom: Animalia
Phylum: Arthropoda
Class: Insecta
Order: Hymenoptera
Family: Apidae
Genus: Bombus
Subgenus: Thoracobombus
Species:
B. muscorum
Binomial name
Bombus muscorum
Synonyms

Apis muscorum Linnaeus, 1758

Taxonomy edit

 
From top to bottom: A Bombus muscorum Queen, Worker, and Male.

B. muscorum was one of the many insect species originally described in 1758 by Carl Linnaeus in the 10th edition of Systema Naturae. It was given the binomial name Apis muscorum.[5] The species name muscorum is the genitive plural of the Latin mūscus, meaning moss.[citation needed]

B. muscorum is part of the order Hymenoptera, the third largest order of insects, which includes bees, wasps, ants, and sawflies. It is part of the subfamily Apinae, which contains the majority of species within the family Apidae. It is part of the tribe Bombini, which contains a single living genus Bombus, consisting entirely of bumblebees. Within Bombus, B. muscorum is part of the subgenus Thoracobombus, which includes closely relates species such Bombus pauloensis, Bombus dahlbomii, Bombus fervidus, Bombus morio, Bombus pensylvanicus, and Bombus transversalis. The species is further differentiated into at least seven different subspecies.[6] These include B. muscorum sladeni and B. muscorum smithianu, found in the United Kingdom and differentiated on the basis of coat color.[7] Certain forms of this variable taxon are considered separate species by some authors, including B. bannitus and B. pereziellus.[8]

Description edit

 
A male moss carder bee in Deepsyke Forest, Peeblesshire, Scotland on an Aster flower.

B. muscorum is characterized by its oblong face and long tongue. The bristles of the species are ginger in color and cover the head, thorax, and abdomen. The abdomen, however, can have a darker, brownish coloring. In some subspecies, black bristles are intermixed with the ginger bristles that characterize the species. Some subspecies have an entirely black ventral side.[9] The species is similar in appearance to the more common Bombus pascuorum.[10] The queen has a body length 17–19 mm and a wingspan of 32–35 mm. Workers have a body length of 10–16 mm and a wingspan of 26–29 mm. Males have a body length of 13–15 mm and a wingspan of 26–29 mm.[11]

Distribution and habitat edit

 
Bombus muscorum in Gavà, Catalonia, Spain foraging on Cistus albidus.

B. muscorum is widely distributed throughout Eurasia. Populations appear from Ireland in the West to Mongolia in the East. The species has been observed as far north as Scandinavia and Russia and has been spotted as far south as Crete.[12] Populations, however, are fairly rare in all locations.[13] Populations in the United Kingdom have declined sharply since the 1970s. Once widely distributed throughout the British Isles, distributions are now fragmented and predominantly coastal. Populations of other species, such as Bombus pascuorum, appear to be replacing B. muscorum in some parts of Northern Britain.[14] The species is still relatively abundant in Northern Scotland.[15] B. muscorum is classified as vulnerable in Europe by the IUCN.[4]

B. muscorum inhabits moors, grasslands, and salt marshes, where it builds its nest above ground.[16] In the British Isles, B. muscorum nests in open landscapes near coastal areas in the lowlands. Populations are found in moorland and machair in the North. In the South, populations are found in coastal marshes, shingle, and calcareous grasslands.[7] Nests have been found near open regions of fallowed land and man-made ditches.[17] Colonies are small, numbering between 20 and 100 workers.[18]

Diet edit

 
An adult moss carder bee on thistle, covered in pollen

B. muscorum is polylectic, the diet of the species depends on the surrounding area. The species has a strong preference for flowers of the families Fabaceae, Scrophulariaceae, Lamiaceae, and Asteraceae.[3] Common food sources include clover, bird's-foot trefoil, vetches, and thistles.[9] Flowers with long corollas are especially dependent on the long-tongued species.[17]

Colony cycle edit

 
A moss carder bee on the flower of the French marigold in Cradley, Herefordshire, England.

A number of new queens are produced in the last brood of the summer colony. These queens mate and then hibernate for an average of 9 months. From March to May, these queens emerge from hibernation to search for nesting sites. After a suitable site is found, the queen lays a small batch of diploid eggs. Once these eggs hatch, the queen tends to the larvae until they are grown and pupate. These pupa emerge as workers. From June onward, the queen will produce a steady supply of workers. From July to September, new males and queens are present and mate.[11]

Reproduction edit

Haplodiploidy edit

B. muscorum, like many bees, exhibit haplodiploidy. The diploid queens produce diploid workers and new queens from fertilized eggs. Haploid males are produced from unfertilized eggs. Workers are also able to lay unfertilized eggs that develop into males.[15] Haploid males produce identical haploid sperm while diploid females produce genetically variant haploid eggs through meiosis. Sex is determined under a single-locus complementary sex determination (sl-CSD) system, where multiple alleles at a single locus determine the sex of an individual. Sex locus heterozygotes develop as females, while hemizygous and homozygous eggs develop as haploid and diploid males.[19]

Mating system edit

B. muscorum is thought to be a monandrous species; the queen mates only once with a single male to start a new colony.[15] This monandrous behavior decreases the amount of genetic variation present in a single colony relative to that of a polygynous or polyandrous species. As a result, B. muscorum has an increased susceptibility to the effects of inbreeding.[18] Queens may possess a distinctive odor that signals relatedness and prevents interbreeding.[15] Studies have shown, however, that mating appears to be random.[18]

Nest surveillance edit

Male mating strategies of bumblebees can be grouped into four broad categories: patrolling, racing, territorial, and cruising. Males of B. muscorum exhibit territorial strategies for mating. In this strategy, males choose a perch outside of a mature nest and pursue potential mates that it spots. Males compete with one another for preferred perches, each attempting to find a spot close to the nest entrance. When another bee flies too close to a perched male, the male sets off in pursuit for several seconds, seeking to either chase away a potential competitor or mount a potential mate. After the chase, one of the males will land back at the perch close to the nest.[15]

Inbreeding edit

As a result of small population sizes and haplodiploidy, B. muscorum has an increased susceptibility to inbreeding. As sex is determined at a single locus, the overall fitness of a population is directly related to the number of different alleles at the sex locus, which in turn is related to the size and isolation of the population.[7] When males mate with related queens, diploid males with reduced fertility and immune response are produced.[18] 10 out of 14 B. muscorum populations in the Hebrides showed significant signs of recent bottlenecking. In recent years, diploid males have come to represent a considerable proportion of males within populations in the British Isles, suggesting an increase in inbreeding among populations.[7]

Behavior edit

Foraging edit

B. muscorum exhibit small foraging ranges, having been recorded going no further than 500 m from their nest to forage. Foraging, however, often takes place within 100 m of the nest. Individuals are often observed foraging at the same spots between 50 and 200 m away from the nest. This variation in individual flight range is attributed to an individual's body size.[20] B. muscorum has been described as doorstep foragers, due to the tendency of workers to use food resources near the nest more frequently than the workers of other species. This restricted radius may be an important factor in the decline of the species.[21]

Nesting edit

B. muscorum build its nest on or just under the ground. It cards together collected moss and dry grass to cover the nest. It is this behavior that gives B. muscorum the name moss carder bee.[10][22] It rarely, if ever, crosses sea barriers greater than 10 km to establish a nesting site. Once a nest is established, the bee is notoriously aggressive, readily attacking intruders that are too close to the nest, which they bite and sting simultaneously.[18]

Parasitism edit

Crithidia bombi edit

B. muscorum may contract infections of Crithidia bombi, a trypanosome parasite, from infected nest mates or from others while foraging on contaminated flowers.[23] Infections have been linked to reduced individual and colony fitness, but the specific relationship between Crithidia bombi and B. muscorum is complex.[24] The presence of Crithidia bombi has been found to be higher in populations with lower genetic diversity. As B. muscorum populations continue to lose heterozygosity, the impact of parasitism increases, pushing already threatened populations closer to extinction.[25]

Human impact edit

Habitat destruction edit

Due to recent decades of agricultural intensification in Europe, the natural habitat of B. muscorum has been largely diminished. Many of the permanent flower-rich areas where the bee commonly forages have been destroyed by increased commercial farming.[26] B. muscorum has poor dispersal ability compared to other species of bumblebee, making it more vulnerable to habitat loss. As a result, populations have decreased dramatically in recent decades.[27]

Status edit

B. muscorum is currently listed as vulnerable in Europe by the IUCN.[4] Populations are diminishing in Britain and the species is currently in a species recovery program. Decreasing populations are evident in multiple European countries. Estonia lists the species as vulnerable. Germany and the Netherlands consider the species to be endangered.[28]

Sea walls edit

B. muscorum is often found on sea wall flood defenses managed by the Environment Agency. Nests can be found on the flat grassy area between the sea and the borrowdyke, a brackish pond behind the sea wall. As grasslands on sea walls are predominantly unimproved, they have become an important habitat for rare insect species such as B. muscorum. Current research is examining how these sea walls can be maintained to preserve rare populations.[29]

References edit

  1. ^ "Bombus muscorum". Integrated Taxonomic Information System.
  2. ^ "Map of Bombus muscorum". Discover Life (American Museum of Natural History). Retrieved 24 December 2012.
  3. ^ a b "Bombus muscorum (Linnaeus,1758) | BWARS". www.bwars.com. Retrieved 2015-09-26.
  4. ^ a b c Nieto, Ana (2014). European Red List of Bees. European Commission. p. 12. ISBN 978-92-79-44512-5.
  5. ^ Caroli Linnæi Systema naturæ. Regnum animale. Editio decima, 1758, cura Societatis zoologicæ germanicæ iterum edita. Lipsiæ, sumptibus Guilielmi Engelmann. 1894. Retrieved 2015-09-26 – via www.archive.org.
  6. ^ "NBN Gateway - Taxon". data.nbn.org.uk. Retrieved 2015-09-26.
  7. ^ a b c d Darvill, B.; Ellis, J. S.; Lye, G. C.; Goulson, D. (2006-03-01). "Population structure and inbreeding in a rare and declining bumblebee, Bombus muscorum (Hymenoptera: Apidae)". Molecular Ecology. 15 (3): 601–611. doi:10.1111/j.1365-294X.2006.02797.x. ISSN 1365-294X. PMID 16499688. S2CID 3938575.
  8. ^ Thoracobombus. Bombus: Bumblebees of the World. Natural History Museum, London.
  9. ^ a b Benton, Ted (2006). "Chapter 9: The British Species". Bumblebees. London, UK: HarperCollins Publishers. pp. 384–388. ISBN 978-0007174515.
  10. ^ a b Gittings, Tom. "The Moss Carder Bee (Bombus muscorum)". Tom Gittings: Ecological Consultant. Retrieved 2015-09-20.
  11. ^ a b von Hagen, Eberhard (2003). Hummeln: bestimmen, ansiedeln, vermehren, schützen. Nottuln: Fauna-Verlag. ISBN 978-3-935980-28-9.
  12. ^ Anagnostopoulos, Ioannis Th. (2005). "The bumblebee fauna of Greece: An annotated species list including new records for Greece (Hymenoptera: Apidae, Bombini)" (PDF). Linzer Biologische Beiträge. 37 (2): 1013–1026.
  13. ^ P. Rasmont. "Bombus (Thoracobombus) muscorum (L. 1761)". Université de Mons. Retrieved 24 December 2012.
  14. ^ Plowright, C.M.S. (15 August 1997). "Replacement of Bombus muscorum by Bombus pascuorum in Northern Britain?". The Canadian Entomologist. 129 (6): 985–990. doi:10.4039/ent129985-6.
  15. ^ a b c d e Darvill, Ben (November 2007). "Aggregations of male Bombus muscorum (Hymenoptera: Apidae) at mature nests. Incestuous brothers or amorous suitors?". Apidologie. 38 (6): 518–524. doi:10.1051/apido:2007032. S2CID 3958083.
  16. ^ "Less common species of bumblebee found in the UK". Bumblebee.org. Retrieved 24 December 2012.
  17. ^ a b Diekötter, Tim; Walther-Hellwig, Kerstin; Conradi, Manuel; Suter, Matthias; Frankl, Robert (2006-01-01). "Effects of Landscape Elements on the Distribution of the Rare Bumblebee Species Bombus muscorum in an Agricultural Landscape" (PDF). Biodiversity & Conservation. 15 (1): 57–68. doi:10.1007/s10531-004-2932-9. hdl:20.500.11850/22878. ISSN 0960-3115. S2CID 21051761.
  18. ^ a b c d e Goulson, Dave (2010). "Chapter 6: Foraging Economics". Bumblebees: behaviour, ecology, and conservation. Oxford, UK: Oxford University Press. p. 95. ISBN 9780199553075.
  19. ^ Wu, Z.; Hopper, K. R.; Ode, P. J.; Fuester, R. W.; Tuda, M.; Heimpel, G. E. (2005-08-03). "Single-locus complementary sex determination absent in Heterospilus prosopidis (Hymenoptera: Braconidae)". Heredity. 95 (3): 228–234. doi:10.1038/sj.hdy.6800720. ISSN 0018-067X. PMID 16077738.
  20. ^ Walther-Hellwig, Kerstin; Frankl, Robert (2000-03-01). "Foraging Distances of Bombus muscorum, Bombus lapidarius, and Bombus terrestris (Hymenoptera, Apidae)". Journal of Insect Behavior. 13 (2): 239–246. doi:10.1023/A:1007740315207. ISSN 0892-7553. S2CID 29303814.
  21. ^ Walther-Hellwig, K.; Frankl, R. (2000-10-01). "Foraging habitats and foraging distances of bumblebees, Bombus spp. (Hym., Apidae), in an agricultural landscape". Journal of Applied Entomology. 124 (7–8): 299–306. doi:10.1046/j.1439-0418.2000.00484.x. ISSN 1439-0418. S2CID 86301677.
  22. ^ "Bumblebee - Moss Carder - Western Isles - Bombus Muscorum". www.virtualheb.co.uk. Retrieved 2015-09-27.
  23. ^ Yourth, Christopher P; Schmid-Hempel, Paul (2006-03-22). "Serial passage of the parasite Crithidia bombi within a colony of its host, Bombus terrestris, reduces success in unrelated hosts". Proceedings of the Royal Society B: Biological Sciences. 273 (1587): 655–659. doi:10.1098/rspb.2005.3371. ISSN 0962-8452. PMC 1560069. PMID 16608683.
  24. ^ Runckel, Charles; DeRisi, Joseph; Flenniken, Michelle L. (2014-04-17). "A Draft Genome of the Honey Bee Trypanosomatid Parasite Crithidia mellificae". PLOS ONE. 9 (4): e95057. Bibcode:2014PLoSO...995057R. doi:10.1371/journal.pone.0095057. PMC 3990616. PMID 24743507.
  25. ^ Whitehorn, Penelope R.; Tinsley, Matthew C.; Brown, Mark J. F.; Darvill, Ben; Goulson, Dave (2011-04-22). "Genetic diversity, parasite prevalence and immunity in wild bumblebees". Proceedings of the Royal Society of London B: Biological Sciences. 278 (1709): 1195–1202. doi:10.1098/rspb.2010.1550. ISSN 0962-8452. PMC 3049068. PMID 20926436.
  26. ^ "Bombus muscorum moss carder bee :: Northern Ireland's Priority Species". www.habitas.org.uk. Retrieved 2015-09-27.
  27. ^ Darvill, B.; S. O'Connor; G.C. Lye; J. Waters; O. Lepais & D. Goulson (2009). "Cryptic differences in dispersal lead to differential sensitivity to habitat fragmentation in two bumblebee species". Molecular Ecology. 19 (1): 53–63. doi:10.1111/j.1365-294x.2009.04423.x. PMID 20002583. S2CID 3943291.
  28. ^ Fitzpatrick, Una (2006). Regional Red List of Irish Bees. Higher Education Authority.
  29. ^ Gardiner, Tim; Benton, Ted (2011). "The importance of sea walls for the moss carder bee Bombus muscorum in Essex" (PDF). Hymettus. Retrieved 4 October 2015.

bombus, muscorum, commonly, known, large, carder, moss, carder, species, bumblebee, family, apidae, species, found, throughout, eurasia, fragmented, populations, most, commonly, found, british, isles, muscorum, eusocial, insect, queen, monandrous, mating, with. Bombus muscorum commonly known as the large carder bee or moss carder bee is a species of bumblebee in the family Apidae The species is found throughout Eurasia in fragmented populations but is most commonly found in the British Isles 2 3 B muscorum is a eusocial insect The queen is monandrous mating with only one male after leaving a mature nest to found its own Males mate territorially and the species is susceptible to inbreeding and bottlenecks The species builds its nests on or just under the ground in open grassland and forages very close to the nest In recent years populations have significantly declined due to loss of natural habitat B muscorum is currently listed as vulnerable in Europe by the European Red List of Bees 4 Bombus muscorumBombus muscorum agricolae the Shetland subspeciesScientific classificationDomain EukaryotaKingdom AnimaliaPhylum ArthropodaClass InsectaOrder HymenopteraFamily ApidaeGenus BombusSubgenus ThoracobombusSpecies B muscorumBinomial nameBombus muscorum Linnaeus 1758 1 SynonymsApis muscorum Linnaeus 1758 Contents 1 Taxonomy 2 Description 3 Distribution and habitat 4 Diet 5 Colony cycle 6 Reproduction 6 1 Haplodiploidy 6 2 Mating system 6 3 Nest surveillance 6 4 Inbreeding 7 Behavior 7 1 Foraging 7 2 Nesting 8 Parasitism 8 1 Crithidia bombi 9 Human impact 9 1 Habitat destruction 9 2 Status 9 3 Sea walls 10 ReferencesTaxonomy edit nbsp From top to bottom A Bombus muscorum Queen Worker and Male B muscorum was one of the many insect species originally described in 1758 by Carl Linnaeus in the 10th edition of Systema Naturae It was given the binomial name Apis muscorum 5 The species name muscorum is the genitive plural of the Latin muscus meaning moss citation needed B muscorum is part of the order Hymenoptera the third largest order of insects which includes bees wasps ants and sawflies It is part of the subfamily Apinae which contains the majority of species within the family Apidae It is part of the tribe Bombini which contains a single living genus Bombus consisting entirely of bumblebees Within Bombus B muscorum is part of the subgenus Thoracobombus which includes closely relates species such Bombus pauloensis Bombus dahlbomii Bombus fervidus Bombus morio Bombus pensylvanicus and Bombus transversalis The species is further differentiated into at least seven different subspecies 6 These include B muscorum sladeni and B muscorum smithianu found in the United Kingdom and differentiated on the basis of coat color 7 Certain forms of this variable taxon are considered separate species by some authors including B bannitus and B pereziellus 8 Description edit nbsp A male moss carder bee in Deepsyke Forest Peeblesshire Scotland on an Aster flower B muscorum is characterized by its oblong face and long tongue The bristles of the species are ginger in color and cover the head thorax and abdomen The abdomen however can have a darker brownish coloring In some subspecies black bristles are intermixed with the ginger bristles that characterize the species Some subspecies have an entirely black ventral side 9 The species is similar in appearance to the more common Bombus pascuorum 10 The queen has a body length 17 19 mm and a wingspan of 32 35 mm Workers have a body length of 10 16 mm and a wingspan of 26 29 mm Males have a body length of 13 15 mm and a wingspan of 26 29 mm 11 Distribution and habitat edit nbsp Bombus muscorum in Gava Catalonia Spain foraging on Cistus albidus B muscorum is widely distributed throughout Eurasia Populations appear from Ireland in the West to Mongolia in the East The species has been observed as far north as Scandinavia and Russia and has been spotted as far south as Crete 12 Populations however are fairly rare in all locations 13 Populations in the United Kingdom have declined sharply since the 1970s Once widely distributed throughout the British Isles distributions are now fragmented and predominantly coastal Populations of other species such as Bombus pascuorum appear to be replacing B muscorum in some parts of Northern Britain 14 The species is still relatively abundant in Northern Scotland 15 B muscorum is classified as vulnerable in Europe by the IUCN 4 B muscorum inhabits moors grasslands and salt marshes where it builds its nest above ground 16 In the British Isles B muscorum nests in open landscapes near coastal areas in the lowlands Populations are found in moorland and machair in the North In the South populations are found in coastal marshes shingle and calcareous grasslands 7 Nests have been found near open regions of fallowed land and man made ditches 17 Colonies are small numbering between 20 and 100 workers 18 Diet edit nbsp An adult moss carder bee on thistle covered in pollenB muscorum is polylectic the diet of the species depends on the surrounding area The species has a strong preference for flowers of the families Fabaceae Scrophulariaceae Lamiaceae and Asteraceae 3 Common food sources include clover bird s foot trefoil vetches and thistles 9 Flowers with long corollas are especially dependent on the long tongued species 17 Colony cycle edit nbsp A moss carder bee on the flower of the French marigold in Cradley Herefordshire England A number of new queens are produced in the last brood of the summer colony These queens mate and then hibernate for an average of 9 months From March to May these queens emerge from hibernation to search for nesting sites After a suitable site is found the queen lays a small batch of diploid eggs Once these eggs hatch the queen tends to the larvae until they are grown and pupate These pupa emerge as workers From June onward the queen will produce a steady supply of workers From July to September new males and queens are present and mate 11 Reproduction editHaplodiploidy edit B muscorum like many bees exhibit haplodiploidy The diploid queens produce diploid workers and new queens from fertilized eggs Haploid males are produced from unfertilized eggs Workers are also able to lay unfertilized eggs that develop into males 15 Haploid males produce identical haploid sperm while diploid females produce genetically variant haploid eggs through meiosis Sex is determined under a single locus complementary sex determination sl CSD system where multiple alleles at a single locus determine the sex of an individual Sex locus heterozygotes develop as females while hemizygous and homozygous eggs develop as haploid and diploid males 19 Mating system edit B muscorum is thought to be a monandrous species the queen mates only once with a single male to start a new colony 15 This monandrous behavior decreases the amount of genetic variation present in a single colony relative to that of a polygynous or polyandrous species As a result B muscorum has an increased susceptibility to the effects of inbreeding 18 Queens may possess a distinctive odor that signals relatedness and prevents interbreeding 15 Studies have shown however that mating appears to be random 18 Nest surveillance edit Male mating strategies of bumblebees can be grouped into four broad categories patrolling racing territorial and cruising Males of B muscorum exhibit territorial strategies for mating In this strategy males choose a perch outside of a mature nest and pursue potential mates that it spots Males compete with one another for preferred perches each attempting to find a spot close to the nest entrance When another bee flies too close to a perched male the male sets off in pursuit for several seconds seeking to either chase away a potential competitor or mount a potential mate After the chase one of the males will land back at the perch close to the nest 15 Inbreeding edit As a result of small population sizes and haplodiploidy B muscorum has an increased susceptibility to inbreeding As sex is determined at a single locus the overall fitness of a population is directly related to the number of different alleles at the sex locus which in turn is related to the size and isolation of the population 7 When males mate with related queens diploid males with reduced fertility and immune response are produced 18 10 out of 14 B muscorum populations in the Hebrides showed significant signs of recent bottlenecking In recent years diploid males have come to represent a considerable proportion of males within populations in the British Isles suggesting an increase in inbreeding among populations 7 Behavior editForaging edit B muscorum exhibit small foraging ranges having been recorded going no further than 500 m from their nest to forage Foraging however often takes place within 100 m of the nest Individuals are often observed foraging at the same spots between 50 and 200 m away from the nest This variation in individual flight range is attributed to an individual s body size 20 B muscorum has been described as doorstep foragers due to the tendency of workers to use food resources near the nest more frequently than the workers of other species This restricted radius may be an important factor in the decline of the species 21 Nesting edit B muscorum build its nest on or just under the ground It cards together collected moss and dry grass to cover the nest It is this behavior that gives B muscorum the name moss carder bee 10 22 It rarely if ever crosses sea barriers greater than 10 km to establish a nesting site Once a nest is established the bee is notoriously aggressive readily attacking intruders that are too close to the nest which they bite and sting simultaneously 18 Parasitism editCrithidia bombi edit B muscorum may contract infections of Crithidia bombi a trypanosome parasite from infected nest mates or from others while foraging on contaminated flowers 23 Infections have been linked to reduced individual and colony fitness but the specific relationship between Crithidia bombi and B muscorum is complex 24 The presence of Crithidia bombi has been found to be higher in populations with lower genetic diversity As B muscorum populations continue to lose heterozygosity the impact of parasitism increases pushing already threatened populations closer to extinction 25 Human impact editHabitat destruction edit Due to recent decades of agricultural intensification in Europe the natural habitat of B muscorum has been largely diminished Many of the permanent flower rich areas where the bee commonly forages have been destroyed by increased commercial farming 26 B muscorum has poor dispersal ability compared to other species of bumblebee making it more vulnerable to habitat loss As a result populations have decreased dramatically in recent decades 27 Status edit B muscorum is currently listed as vulnerable in Europe by the IUCN 4 Populations are diminishing in Britain and the species is currently in a species recovery program Decreasing populations are evident in multiple European countries Estonia lists the species as vulnerable Germany and the Netherlands consider the species to be endangered 28 Sea walls edit B muscorum is often found on sea wall flood defenses managed by the Environment Agency Nests can be found on the flat grassy area between the sea and the borrowdyke a brackish pond behind the sea wall As grasslands on sea walls are predominantly unimproved they have become an important habitat for rare insect species such as B muscorum Current research is examining how these sea walls can be maintained to preserve rare populations 29 References edit Bombus muscorum Integrated Taxonomic Information System Map of Bombus muscorum Discover Life American Museum of Natural History Retrieved 24 December 2012 a b Bombus muscorum Linnaeus 1758 BWARS www bwars com Retrieved 2015 09 26 a b c Nieto Ana 2014 European Red List of Bees European Commission p 12 ISBN 978 92 79 44512 5 Caroli Linnaei Systema naturae Regnum animale Editio decima 1758 cura Societatis zoologicae germanicae iterum edita Lipsiae sumptibus Guilielmi Engelmann 1894 Retrieved 2015 09 26 via www archive org NBN Gateway Taxon data nbn org uk Retrieved 2015 09 26 a b c d Darvill B Ellis J S Lye G C Goulson D 2006 03 01 Population structure and inbreeding in a rare and declining bumblebee Bombus muscorum Hymenoptera Apidae Molecular Ecology 15 3 601 611 doi 10 1111 j 1365 294X 2006 02797 x ISSN 1365 294X PMID 16499688 S2CID 3938575 Thoracobombus Bombus Bumblebees of the World Natural History Museum London a b Benton Ted 2006 Chapter 9 The British Species Bumblebees London UK HarperCollins Publishers pp 384 388 ISBN 978 0007174515 a b Gittings Tom The Moss Carder Bee Bombus muscorum Tom Gittings Ecological Consultant Retrieved 2015 09 20 a b von Hagen Eberhard 2003 Hummeln bestimmen ansiedeln vermehren schutzen Nottuln Fauna Verlag ISBN 978 3 935980 28 9 Anagnostopoulos Ioannis Th 2005 The bumblebee fauna of Greece An annotated species list including new records for Greece Hymenoptera Apidae Bombini PDF Linzer Biologische Beitrage 37 2 1013 1026 P Rasmont Bombus Thoracobombus muscorum L 1761 Universite de Mons Retrieved 24 December 2012 Plowright C M S 15 August 1997 Replacement of Bombus muscorum by Bombus pascuorum in Northern Britain The Canadian Entomologist 129 6 985 990 doi 10 4039 ent129985 6 a b c d e Darvill Ben November 2007 Aggregations of male Bombus muscorum Hymenoptera Apidae at mature nests Incestuous brothers or amorous suitors Apidologie 38 6 518 524 doi 10 1051 apido 2007032 S2CID 3958083 Less common species of bumblebee found in the UK Bumblebee org Retrieved 24 December 2012 a b Diekotter Tim Walther Hellwig Kerstin Conradi Manuel Suter Matthias Frankl Robert 2006 01 01 Effects of Landscape Elements on the Distribution of the Rare Bumblebee Species Bombus muscorum in an Agricultural Landscape PDF Biodiversity amp Conservation 15 1 57 68 doi 10 1007 s10531 004 2932 9 hdl 20 500 11850 22878 ISSN 0960 3115 S2CID 21051761 a b c d e Goulson Dave 2010 Chapter 6 Foraging Economics Bumblebees behaviour ecology and conservation Oxford UK Oxford University Press p 95 ISBN 9780199553075 Wu Z Hopper K R Ode P J Fuester 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