common name: small carpenter bees
scientific name: Ceratina spp. (Insecta: Hymenoptera: Apidae: Xylocopinae)
In America north of Mexico, Ceratina (small carpenter bees) is one of two genera of the
subfamily Xylocopinae, the other being Xylocopa, (large carpenter
bees). Of the 21 species of Ceratina in America north of Mexico, only two are known to
occur in Florida: C. cockerelli H.S. Smith and C. dupla Say. Mitchell (1962) described the
subspecies C. dupla floridanus from Florida, but Daly (1973) synonymized it simply as a more
densely punctate, brighter blue population of the typical eastern C. dupla.
Ceratina cockerelli is found throughout Florida and most of the southern coastal states from
Texas to Georgia (Daly 1973). Specimens have not been reported from Alabama or Mississippi,
but probably occur there. Ceratina dupla is found throughout Florida as well as most of the
eastern United States (Daly 1973).
At various times carpenter bees have been placed in the families Anthophoridae, Xylocopidae, or
Apidae. Hurd and Moure (1963) traced the history of the placement of these bees in various
families; the most recent placement is within the Apidae (Krombein 1967). This family is
characterized, in part, by the jugal lobe of the hindwing being absent or shorter than the
submedian cell and by the forewing having three submarginal cells. Within the family, carpenter
bees are distinguished most easily by the triangular second submarginal cell, and by the lower
margin of the eye almost in contact with the base of the mandible (i.e., the malar space is absent).
The easiest method of separating Ceratina from Xylocopa is by
size: Ceratina are less than 8 mm in length whereas Xylocopa are 20 mm or larger. In addition,
Ceratina has the second submarginal cell about as high as wide basall, whereas in Xylocopa it is about half as high as wide basally.
wing venation of Ceratina and Xylocopa
Small carpenter bees are black, bluish green, or blue, and often have yellowish or whitish
markings on the clypeus, pronotal lobes, and legs. The two Florida species of Ceratina may be
separated as follows:
C. cockerelli (both sexes): body length 3 to 4.5 mm; head and thorax mostly black, abdomen
black with brownish or tawny areas; head and scutum (dorsum of thorax) mostly polished,
without punctures for the most part.
C. dupla (both sexes): body length 6 to 8 mm; body dark metallic blue; head and scutum with
numerous distinct punctures, not polished.
adult C. dupla
In general, members of this genus excavate nests with their mandibles in the pith of broken or
burned plant twigs and stems. Females overwinter as adults in partially or completely excavated
stems. In the spring, this resting place (hibernaculum) is modified into a brood nest by further
excavation. Rau (1928) reported several nests of C. calcarata Robertson that ranged
from 20 to 30 cm deep. Daly (1966) measured 126 nests of C. dallatorreana Friese which ranged
from 3 to 19 cm deep. When a desired depth is reached, the female collects pollen and nectar,
places this mixture at the base of the burrow, lays an egg on the provision, and then caps off the
cell with masticated plant material. Several cells are constructed end to end in each plant stem,
the absolute number depending upon the depth to which the nest was excavated. Daly (1966)
found a range of two to 12 cells (19 completed nests examined) for C. dallatorreana.
nest diagrams
The female works at a single stem until it is filled with cells, each of which contains provisions
and an egg or larva, except for the last cell near the nest entrance. Here the bee rests and,
according to Malyshev (1936) and Daly (1966), presumably defends her nest from intruders. The
female bee remains with the nest until her progeny emerge. Since the nest has been under
construction for some time, the oldest progeny (at the base of the nest) mature and begin to gnaw
their way out before the others above them are ready. This poses a special problem because the
bees do not emerge laterally through the side of the stem, but vertically through all the other
cells. Rau described this process thoroughly for C. calcarata (1928). Essentially the oldest bee
chewed apart the cell cap above and packed it at the base of its own cell. If the bee above was not
mature it was carefully moved down to rest on the new "floor." If the bee above was mature, the
eldest passed it by and worked on the cell cap above, passing the pithy material to the younger
bee or bees beneath. These bees packed the material at the base of the nest, moving and adjusting
any pupae which remained. Thus the mature bees at the base of the nest gained freedom by "... a
process of displacement, gradually shifting the material behind them as they make their way to
the top" (Rau 1928: 390). The process observed by Rau took eight days for the eldest bees to
make their way to the entrance; several days later all the bees emerged.
Special biological references to the Ceratina occurring in Florida are scarce. Extensive flower
visitation records were given by Mitchell (1962) and Daly (1973). The only biological record for
C. cockerelli was given by Daly (1973) who cited Sage (in litt.) as reporting nests "... in dead,
cut stems of sea-oats, Uniola paniculata L., on the beach of Mustang Island, Texas." References
to C. dupla are not in abundance, but Daly (1973) cited what was known at that time. The
more important papers, though wholly inadequate, are Ashmead (1894), Comstock and
Comstock (1895), and Graenicher (1905).
Unlike their larger relatives in the genus Xylocopa, the small carpenter bees in the genus
Ceratina are not known to be of economic importance.
- Ashmead WH. 1894. The habits of the aculeate Hymenoptera. I. Psyche 7: 19-26.
- Borror DJ, Triplehorn CA, Johnson NF. 1989. An Introduction to the Study of Insects.
6th Ed. Harcourt Brace, New York. 875 p.
- Comstock JH, Comstock AB. 1895. A Manual of the Study of Insects. The Comstock
Publishing Company, Ithaca, NY. p. III-VII, 1-701 (reprinted in many editions without change).
- Daly HV. 1966. Biological studies on Ceratina dallatorreana, an alien bee in California which
reproduces by parthenogenesis. Annals of the Entomological Society of America 59: 1138-1154.
- Daly HV. 1973. Bees of the genus Ceratina in America north of Mexico. University of California Publications Entomology 74: 1-113.
- Graenicher S. 1905. On the habits of two ichneumonid parasites of the bee Ceratina dupla Say.
Entomological News 16: 43-49.
- Grissell EE, Sanford MT. (July 1999). Large Carpenter Bees, Xylocopa spp. Featured Creatures. EENY-100. http://creatures/misc/bees/xylocopa.htm (July 1999).
- Malyshev SI. 1936. The nesting habits of solitary bees. A comparative study. Eos 11: 201-309,
pl. III-XV.
- Mitchell TB. 1962. Bees of the Eastern United States. Vol. II. North Carolina Agricultural Experiment Station Technical Bulletin 152: 1-557.
- Rau P. 1928. The nesting habits of the little carpenter-bee, Ceratina calcarata. Annals of the Entomological Society of America 21: 380-397.
Authors: E.E. Grissell, Florida Department of Agriculture and Consumer Services, Division of
Plant Industry; and Malcolm T.
Sanford, University of Florida
Originally published as DPI Entomology Circular 167. Updated for this publication.
Drawings and Photographs: Division of Plant Industry
Project Coordinator: Thomas R. Fasulo, University of Florida
Publication Number: EENY-101
Publication Date: July 1999. Revised October 2002.
Copyright 1999-2002 University of Florida
Featured Creatures
Department of Entomology and Nematology
Division of Plant Industry
Extension Data Information Source