Bombus dahlbomii
Bombus dahlbomii | |
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Scientific classification | |
Domain: | Eukaryota |
Kingdom: | Animalia |
Phylum: | Arthropoda |
Class: | Insecta |
Order: | Hymenoptera |
Family: | Apidae |
Genus: | Bombus |
Species: | B. dahlbomii
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Binomial name | |
Bombus dahlbomii Guérin-Méneville, 1835
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Bombus dahlbomii, also known as the moscardón, is a species of
B. dahlbomii is native to southern
B. dahlbomii is an important insect in local
Taxonomy
The species was originally described in 1835 by the French entomologist Félix Édouard Guérin-Méneville.[7]
Description and identification
B. dahlbomii is predominantly red-orange in color. The thorax of the bee is completely red-orange while the abdomen is generally a lighter shade of orange with a small amount of lightening/discoloration towards the end.[4] Like most bumblebees, the abdomen of the bee has a rounded tip. The head, wing and leg region of B. dahlbomii are distinctly black in color. B. dahlbomii has relatively short antennae and a distinct forewing and smaller hindwing that are usually tucked in above the main thorax area (they lie almost flat).[4] Relatively long bristles cover almost the whole thorax and abdomen of B. dahlbomii, giving the bumblebee an extremely furry appearance.[8] The leg and head regions are covered by shorter bristles than the thorax and abdomen. B. dahlbomii queens usually have relatively heavy body masses of around 0.5-1.5 grams and large head-to-tail lengths of up to 4 cm.[8][9] These measurements make B. dahlbomii one of the largest bumblebees in the world and give it the nickname the "flying mouse".[4][8]
Distribution and habitat
B. dahlbomii is the only native bumblebee species in southern South America.[8] Its range extends from 30 degrees southwards to the southern tip of mainland South America.[10] It is endemic to temperate forest regions in central/southern Patagonia.[8] B. dahlbomii is distributed throughout Patagonia, where it coexists with two non-native species that belong to the same genus, Bombus terrestris and Bombus ruderatus.[8] In its distribution in Chile and Argentina, including Patagonia, B. dahlbomii occupies forest environments that have both continuous and fragmented (scattered) distribution of plants, flowers and other resources.[5] Individuals in these two environments have slightly different morphological and behavioral features.[5] Although some reports cite B. dahlbomii outside of southern South America, they fail to substantiate their findings; when compared to other South American bumblebees, B. dahlbomii's range is relatively confined.[2]
Colony cycle
Individual B. dahlbomii queens usually start colonies in the spring by first locating underground cavities, such as rodent burrows.[8] Like many other species in the genus Bombus, the B. dahlbomii colony cycle begins with the production of the egg cell structure inside the underground cavity. This egg cell structure is constructed from a mixture of pollen and wax that the queen forages from the outside environment and brings to the nest site.[11] Eventually, the queen lays her first brood of eggs in this egg cell structure.[11] After a couple of months, in early summer or late spring, this initial brood produces the first B. dahlbomii workers that take over foraging responsibilities from the queen.[8] Males and new queens are subsequently produced to allow the continuation of the colony cycle.[11] The initial period during which the B. dahlbomii queen is alone without workers is referred to as the subsocial phase. The social phase starts when the initial eggs mature into workers that can begin basic foraging activities.[11] Field studies indicate that B. dahlbomii nests can host populations of upwards of 100 workers.[12]
Behavior
Queen behavior
B. dahlbomii queens initiate colonies. Queens forage for nectar and pollen that are used to feed the initial brood of a new colony nest site.[8] The foraging activity of queens usually stops once the first brood develops into fully mature workers that can forage to feed immature siblings and alleviate the queen's need to perform such duties.[8] After this happens, the queen assumes her main role of laying and incubating the brood eggs to further propagate the colony and produce new workers. Once workers begin foraging activities, B. dahlbomii queens seem to venture out of nests less frequently, but are still found in the outside of nests quite often.[8]
Color detection
Scientific research indicates that most bees cannot see the color red, as their photoreceptors are more sensitive to short (UV, blue, green) rather than long wavelengths of light.
Foraging
B. dahlbomii forages both nectar and pollen from a wide variety of plants, including Lapageria rosea, Alstroemeria aurea, Eucryphia cordifolia, Crinodendron hookerianum and Embothrium coccineum.[6][13] B. dahlbomii individuals show both short and relatively long distance foraging patterns.[5] Short distance foraging patterns arise in continuous, resource rich situations where workers can gather the necessary nectar from plants that exist close to the nest site.[5] Long distance foraging patterns develop in resource poor environments such as fragmented forests; long distance foragers usually have to deal with harsher environmental/temporal conditions as well, including faster wind gusts.[5] In general, B. dahlbomii spends more time foraging on each flower than other related species of bumblebees.[14] Researchers attribute this slower foraging behavior to B. dahlbomii's bigger size and heavier body, which partially precludes it from fast movements. B. dahlbomii's relatively short tongue may also prevent it from performing rapid foraging patterns.[5]
Interaction with other species
Invasive species
In regions of South America (Chile, Patagonia), B. dahlbomii coexists and competes with two other species,
Invasive species induced population decline
Although the population decline can be linked to the introduction of alien species, B. terrestris and B. ruderatus, the exact mechanisms that account for the decline in B. dahlbomii population are not completely understood. Research indicates that exploitative/competitive advantage and pathogen introduction account for some part of the population decline in Patagonia.[8] The aliens’ competitive advantage results from their relatively high migration ability, foraging ranges, polylectic foraging strategies and gyne production rate when compared to B. dahlbomii.[8] Moreover, B. dahlbomii queens emerge and colonize nests later in the season than their B. terrestris counterparts, which provides B. terrestris a colony-cycle advantage over B. dahlbomii and accounts for further decline.[8]
Pathogen incidence
Populations of B. dahlbomii have been greatly affected by the highly pathogenic
Pathogen mechanism and effect
B. dahlbomii individuals, both workers and queens, initially are infected by A. bombi when they ingest
Batesian mimicry
Syrphid flies in Patagonia and the Southern parts of Chile (Aneriophora aureorufa) seem to use B. dahlbomii as a Batesian mimicry template. A. aureorufa thus, resembles/mimics certain aspects of B. dahlbomii morphology and behavior.[13] In particular, B. dahlbomii and A. aureorufa have similar color and size, and are sometimes difficult to distinguish when observed in the wild because of similar flight motion patterns.[13] The fact that such marked similarities exists illustrates how A. aureorufa morphology must have evolved rapidly, as B. dahlbomii speciation only occurred approximately 7.5 million years ago.[13] The mimicry demonstrates how B. dahlbomii has a competitive advantage in avoiding predation that A. aureorufa lacks (A. aureorufa mimics B. dahlbomii to falsely “steal” this competitive advantage and increase fitness).[13]
Interaction with environment
Pollination
B. dahlbomii is an important pollinator to a number of plant species such as
Current events
B. dahlbomii is now in danger of extinction.[17] In 2014, The Independent reported that this species is endangered by the arrival of the two invasive species detailed above.[17] Researchers are worried that further imports of European species to South American countries could lead to complete destruction of native species within the next couple of years.[17] This bee is an endangered species on the IUCN Red List.[18]
References
- ^ Morales, C., Montalva, J., Arbetman, M., Aizen, M.A., Smith-Ramírez, C., Vieli, L. & Hatfield, R. 2016. Bombus dahlbomii. The IUCN Red List of Threatened Species 2016: e.T21215142A100240441. https://dx.doi.org/10.2305/IUCN.UK.2016-3.RLTS.T21215142A100240441.en. Accessed on 19 November 2022.
- ^ PMID 20118307.
- ^ a b c King, A. (September 14, 2012) Plight of the Bumblebee. ScienceNow.
- ^ a b c d e f Johnston, Ian (6 July 2014). "Bye bye big bee: In South America, the world's largest bumblebee is at risk from imported rivals". The Independent. Retrieved 23 February 2015.
- ^ .
- ^ a b c d Morales, C. L., et al. (2004). "Potential displacement of the native bumblebee Bombus dahlbomii by the invasive Bombus ruderatus in NW Patagonia, Argentina", pp. 70-76 in Proceedings of the 8th IBRA International Conference on Tropical Bees and VI Encontro sobre Abelhas, Ribeirão Preto, Brasil, September 6–10, 2004.
- ^ "Bombus dahlbomii Guérin-Méneville, 1835". ITIS. Retrieved 15 October 2015.
- ^ PMID 25499798.
- ^ "Bombus Dahlbomii". RedList. IUCN. Archived from the original on 17 September 2015. Retrieved 15 October 2015.
- ^ doi:10.1007/s10530-012-0311-0. Archived from the original(PDF) on 2017-01-09. Retrieved 2015-10-15.
- ^ a b c d "The bumblebee lifecycle". BumbleBee Conservation Trust. Retrieved 16 October 2015.
- ^ Bernard, Bernard. "Evaluation of Bombus dahlbomii (guer.) as a pollinating agent for tomato". Akimoo. Archived from the original on 23 November 2015. Retrieved 15 October 2015.
- ^ hdl:10261/126136.
- ^ PMID 18443825.
- ^ . Retrieved 15 October 2015.
- PMID 18164709.
- ^ a b c "World's largest bumblebee is at risk from imported rivals". The Independent. 2014-07-05. Retrieved 2015-11-23.
- ^ Morales, C., et al. 2015. Bombus dahlbomii. The IUCN Red List of Threatened Species. Downloaded on 04 March 2016.