.
B.
kashmirensis worker robbing Delphinium.
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Alpigenobombus
ecology
and behaviour
HABITAT:
Alpine grassland, meadow, and forest-edge habitats
in mountains.
FOOD-PLANTS:
Short to medium tongue-length bumblebees. Females
are unusual for having six strong mandibular teeth,
which are often used for biting holes in deep
flower corollas in order to rob nectar (e.g. photo
left).
NESTING
BEHAVIOUR:
Nests underground. Pocket-makers only early in
colony development.
MATE-SEARCHING BEHAVIOUR:
Males of B. wurflenii (and probably the
other species) patrol circuits of scent marks.
Males of B. kashmirensis have slightly
enlarged compound eyes relative to females. They
hover and race after potential mates, without
being territorial (Williams, 1991).
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Subgenus
ALPIGENOBOMBUS Skorikov
Alpigenobombus Skorikov, 1914a:128,
type-species Alpigenobombus pulcherrimus Skorikov
(= Bombus kashmirensis Friese) by subsequent
designation of Williams, 1991:65
Bombus (Mastrucatobombus) Krüger,
1917:66, type-species
Bombus mastrucatus Gerstaecker (= Bombus wurflenii
Radoszkowski) by monotypy
Bombus (Alpigenobombus) Frison, 1927:64
[Nobilibombus Skorikov, 1933a:62,
published without fixation of type-species]
[Bombus (Nobilibombus) Bischoff, 1936:12,
type-species Nobilibombus morawitziides Skorikov
(= Bombus nobilis Friese) by monotypy, published
as a junior synonym]
Alpigenibombus Skorikov, 1938a:145,
unjustified emendation
[Pyrobombus (Nobilibombus) Milliron, 1961:54,
type-species Bombus nobilis Friese (cited as
Bombus nobilis Skorikov) by original designation,
published as a junior synonym]
Bombus (Nobilibombus) Richards, 1968:216,222,
type-species Bombus nobilis Friese by original
designation (see Williams, 1991)
[Alpegenobombus Wang, 1979:188,
incorrect subsequent spelling]
Part
of the bumblebee phylogenetic tree including available
Alpigenobombus species from an analysis of DNA
sequence data for five genes (Cameron
et al. 2007
[pdf]).
Values above branches are Bayesian posterior probabilities,
values below branches are parsimony bootstrap values.
Bombus
(Ag.) genalis Friese
genalis Friese, 1918:84,
examined
1 name
TAXONOMIC
STATUS: From COI barcodes, B. genalis appears
to be discrete and is likely to be separate species.
DISTRIBUTION:
Oriental Region.
Bombus
(Ag.) angustus Chiu
angustus Chiu, 1948:59
1 name
DISTRIBUTION:
Oriental Region.
Bombus
(Ag.) grahami (Frison)
grahami (Frison, 1933:334
[Bremus]), examined
3 names
MORPHOLOGY:
photos of male genitalia.
DISTRIBUTION:
Oriental Region.
Bombus
(Ag.) breviceps Smith
nasutus Smith, 1852a:44,
examined
breviceps Smith, 1852a:44,
examined
dentatus Handlirsch, 1888:227
simulus Gribodo, 1892:114,
examined
orichalceus Friese, 1916:107,
examined
rufocognitus Cockerell, 1922:4,
examined
pretiosus Bischoff, 1936:11,
examined, not of Friese, 1911:571
(= B. polaris Curtis)
bischoffiellus (Tkalcu, 1977:224
[Alpigenobombus]) replacement name for pretiosus
Bischoff, 1936:11
22 names
TAXONOMIC
STATUS: Several of these nominal taxa have been
treated as separate species. At least B. dentatus
[Himalaya] may prove to be separate species (e.g. Tkalcu,
1968b, 1989).
However, aside from differences in colour pattern, they
are similar in morphology with a range of variation
(Williams, 1991
[pdf]:67). Until more evidence to the contrary is
available from critical studies of patterns of variation,
I shall treat them as parts of a single variable species.
NOMENCLATURE:
Tkalcu (1968b)
first regarded B. nasutus and B. breviceps
as likely to be conspecific and, following the Principle
of First Reviser (ICZN, 1999:
Article 24), chose B. breviceps as the name for
the species.
MORPHOLOGY:
photos of male genitalia.
DISTRIBUTION:
Oriental Region.
Bombus
(Ag.) wurflenii Radoszkowski
Wurflenii Radoszkowski, 1860:482,
examined
[Wurfleini Radoszkowski, 1877b:191,
incorrect subsequent spelling]
mastrucatus Gerstaecker, 1869:326,
examined
alpigenus Morawitz, 1874:132
29 names
MORPHOLOGY:
photos of male genitalia.
DISTRIBUTION:
Palaearctic Region.
Bombus
(Ag.) kashmirensis Friese
kashmirensis Friese, 1909[September,
Tkalcu, 1974b]:673,
examined
stramineus Friese, 1909[September,
Tkalcu, 1974b]:673
tetrachromus Cockerell, 1909[November,
Tkalcu, 1974b]:397,
examined
pulcherrimus (Skorikov, 1914a:128
[Alpigenobombus])
14 names
TAXONOMIC
STATUS: Several of these nominal taxa have been
treated as separate species. However, aside from differences
in colour pattern, they are closely similar in morphology
with a range of variation (Williams, 1991
[pdf]:68). Until more evidence to the contrary is
available from critical studies of patterns of variation,
I shall treat them as parts of a single variable species.
NOMENCLATURE:
Tkalcu (1974b)
first regarded B. kashmirensis and B. stramineus
as conspecific and, following the Principle of First
Reviser (ICZN, 1999:
Article 24), chose B. kashmirensis as the name
for the species.
MORPHOLOGY:
photos of male
genitalia.
DISTRIBUTION:
Oriental Region, Palaearctic border.
Bombus
(Ag.) nobilis Friese
nobilis Friese, 1905:513
?sikkimi Friese, 1918:82,
examined
[morawitziides Skorikov, [1923]:159,
published without description]
[moravitziides Skorikov, 1931:203,
published without description]
?morawitziides (Skorikov, 1933a:62
[Nobilibombus]) examined
?xizangensis Wang, 1979:188,
examined
chayaensis Wang, 1979:189,
examined
7 names
TAXONOMIC
STATUS: Several of these nominal taxa have been
treated as separate species.
The type specimens of B. nobilis have also been
in some doubt (Richards, 1968).
In the same publication as the description of B.
validus, Friese (1905)
described the female of B. nobilis as having
a 'quadratisch' malar area and 4-5 teeth on the mandible
(even though he placed it [p. 519] in a group with B.
lapidarius). The
original description lists several females (particularly
from Sichuan), but the only putative type female that
I have been able to examine (although it carries no
Friese 'type' label) is in the Berlin museum collection
and is a specimen of B. friseanus labelled 'Kashgar'
(this locality is outside the known range of either
B. nobilis or B. friseanus). The specimen
does not match the original description of the mandibles
of B. nobilis and so cannot be considered a valid
syntype. Nonetheless, the identity of B. nobilis
is clear from the original description, so the designation
of a neotype is not justified (ICZN, 1999:
Article 75).
B. chayaensis appears to me to be very closely
similar to the yellow banded B. nobilis (in the
strict sense) and I am unaware of any reason to treat
them as separate species.
B. nobilis is interpreted here in the broadest
sense, to include a complex of morphologically closely
similar taxa (Williams, 1991
[pdf]). At least some of the taxa included may prove
to be separate species from B. nobilis. The most
obvious variation is in the colour of the pale thoracic
bands, which may be yellow (B. nobilis), yellow-white
(B. sikkimi), gey-white (B. morawitziides),
or almost completely replaced by black (B. validus).
However, aside from these differences in colour pattern,
they are similar in morphology with a range of variation.
Until more evidence to the contrary is available from
critical studies of patterns of variation, I shall treat
them as parts of a single variable species.
MORPHOLOGY:
photos of male genitalia.
DISTRIBUTION:
Oriental Region.
Bombus
(Ag.) validus Friese
validus Friese, 1905:510,
examined
1 name
TAXONOMIC
STATUS: Friese
(1905) described B.
validus initially (p. 510) as having a quadrate
malar area and untoothed mandibles, but went on (p.
517) to place it within the mastrucatus (= B.
wurflenii) group, which he characterised as having
a short malar area and toothed mandibles. Tkalcu (1987)
designated as lectotype of B. validus a female
with a quadrate malar area and multi-toothed mandibles.
He also synonymised B. morawitziides with
B. validus. From
COI barcodes, B. validus appears to be discrete
and is likely to be separate species (An et al.,
2014). More evidence
is awaited.
DISTRIBUTION:
Oriental Region.
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