Management | Beekeeping Information Index
Mid-Atlantic Apiculture
Management of Wild Honey Bees
By: Frank D. Parker and Philip F. Torchio1
(From Beekeeping in the United States)
The term "wild bee" is used commonly for all bees except honey
bees in the genus Apis (hence, apiculture or culturing of honey
bees). Many persons also refer to feral honey bees as wild bees,
so the term is somewhat ambiguous. Bees generally are distinguished
from other flying hymenopterous insects by their characteristic
plumose body hairs. Bees are of many sizes, shapes, and colors.
Some of the smallest bees, Perdita, are less than 3 mm, whereas
our largest leafcutter bee is over 80 mm. Almost the entire range
of colors is found among the brightly marked bees, including many
beautiful metallic species.
Almost anywhere in the United States, one can easily observe many
species of bees actively visiting flowers for nectar and pollen
or engaged in the processes of constructing nests. There are approximately
5,000 species known to occur in North America, plus an estimated
1,500 species not yet described. Wild bee experts agree there
are at least 30,000 species of bees in the world. This number
of species is more than all the fish, bird, and reptile species
combined.
Most bee species construct either single or complex nests in the
ground. Some make earthen, leaf, or resin nests on rocks and plants.
Other bees make or utilize crevices in rocks or plant stems, insect
borings, and plant galls for their nesting sites.
Most bees live a solitary existence-each female after mating locates
and builds her nest without the aid of other bees, and usually
at a distance from her sister bees. However, some bees are quite
gregarious and nest close to one another, sometimes in dense populations
of up to a million nests in a few acres of soil.
Some bees prefer to nest at the same site year after year, but
others relocate their nests each season. A small percentage of
our wild bees are social or semisocial; that is, there is a division
of labor among the bees occupying a single nest. Our total knowledge
of the habits of bees in the United States is quite limited; less
than 10 percent of their biologies have been observed and recorded.
1Research leader and research entomologist, respectively, Science
and Education Administration, Pollinating Insect-Biology Management,
Systematics-Research, Logan, Utah 84322.
Value of Wild Bees as Pollinators
One cannot easily place a dollar figure on the value of wild pollinators,
simply because total impact on the environment is not known. The
potential for utilizing, encouraging, or maintaining populations
of wild bees has been barely researched. It has been calculated
that the mere weight of wild pollinators outnumbers honey bee
populations by hundreds of times. Studies on the impact of each
pollinator species on fruit or seed production of our major crops
is almost nonexistent.
We know that transfer of pollen from one plant to another or from
one plant part to another part of the same plant is essential
for the reproduction of most flowering plants'. Without pollinators,
most of our native flowering plants would decline, disappear,
or be replaced by nonflowering weedy species. Yet, reproduction
each season of the multitude of wild flowering plants is often
taken for granted to aid in maintaining soil moisture and fertility,
and to provide food not only for wild life but for our domestic
livestock as well. How many billions of dollars are these benefits
worth?
It is easy to document the value of crop species visited by bees,
but here again the importance of wild bees as crop pollinators
has been sorely neglected. It has long been the general consensus
that honey bees adequately pollinate crops and there is little
need for wild bees. Unfortunately, such statements are premature
since adequate research on the economic benefits of wild pollinators
has not been done. Conversely, the research completed on the few
wild pollinator species thus far studied has returned much compared
with its investment costs.
The dependence on one species for crop pollination sometimes creates
problems such as now being experienced in our almond industry.
In California, there are not enough colonies of honey bees available
to effectively pollinate the total almond acreage, and it is steadily
increasing. Honey bees must be transported from as far as Minnesota
and Canada, which substantially increases pollination costs and
results in higher costs to the consumer. It seems wise to make
greater efforts to study, conserve, and try to manage as many
species of wild bees as possible.
There are several crops that are underpollinated by the honey
bees, either because the bees are not physically adapted to pollinate
them or the crops are not attractive to honey bees. Some of our
most important crops, valued at billions of dollars, are in this
category. These crops are alfalfa, soybeans, cotton, vegetable
seed, and sunflowers, each of which is adapted to specific types
of pollinators.
Recent research on the utilization of several species of wild
bees as crop pollinators is just beginning to indicate some of
their economic benefits. Currently, there is a viable multimillion
dollar industry centered around the manufacture and sale of equipment,
propagation, and pollination by contract of one of these wild
pollinator species, the alfalfa leafcutter bee.
The alkali bee was the first wild bee to be utilized as a crop
pollinator in the United States beginning in the early 1950's.
Since that time, the alfalfa leafcutter bee and the blue orchard
bee have been domesticated as crop pollinators.
Leafcutter Bees
There are many species of leafcutter bees that visit blooming
alfalfa, but for the most part, our native species have not increased
their populations to the point of being manageable. However, several
Eurasian species have become established in the United States,
and Megachile rotundata has become the principal alfalfa pollinator
in several Western States. The alfalfa leafcutter bee, previously
called Megachile pacfica, arrived on our east coast during the
early 1930's and has spread to most parts of the United States
and northern Canada.
In the 1950's, alfalfa seed growers noticed large populations
of leafcutter bees pollinating their fields and began to increase
the bees by providing nest holes in various kinds of wooden objects.
By the 1960's, research at government facilities and western experiment
stations had developed practical means of culturing large populations
of the bees. Seed growers who managed these bees began to see
significant increases in alfalfa seed yields. Leafcutter bees
were particularly effective in areas that had no alkali bees.
During the 1970's, intensive management practices have resulted
in dependable leafcutter bee populations that ensure adequate
pollination of western alfalfa seed fields.
The alfalfa leafcutter bee, about half the size of the honey bee,
is black with white-yellowish bands on the abdomen. These bees
are particularly fond of sweet clover and will visit it to the
exclusion of alfalfa. Other crops visited for pollen are forage
legumes, mints, crucifers and many weeds or garden plants. The
adults commonly are found flying about near outbuildings, fence
posts, cliff banks, or other suitable nesting sites. These leafcutter
bees can utilize almost any small holes and will commonly plug
small tubing, electrical sockets, and nail holes. Other favorite
nesting sites are between the siding on frame homes and between
or under the shakes or shingles on buildings. With such numerous
nesting sites available, it is easy to understand why these bees
became quite common and how large populations can be obtained
for agricultural use.
Biological Features
Leafcutter bees are advantageous for alfalfa pollination because
they:
(1) Usually forage within fields where they nest, making them
less susceptible to being killed by pesticides applied to adjacent
fields, and likely will not pollinate fields owned by other growers;
(2) Collect pollen from and trip the alfalfa flower readily at
the rate of 8 to 10 fiorets per minute;
(3) Forage about the same time alfalfa blooms;
(4) Are predictable in incubation of adult stages;
(5) Have a long field life-up to 9 weeks-and a high rate of reproduction
(maximum of 39 cells);
(6) Are gregarious and nest in manmade objects;
(7) Select older leaves for nesting and are not destructive of
shrubs and trees;
(8) Have sturdy leaf cells and cocoons and thus are suited to
mechanized management operations.
Populations
There are no consistent numbers of leafcutter bees used to pollinate
alfalfa. The rate depends primarily on each seed grower's management
practices. However, it has been calculated that as few as 2,000
females per acre can adequately set up a field. The maximum carrying
capacity has been estimated at 14,000 bees per acre. Early management
recommendations were that small populations of bees be placed
throughout the field for uniform coverage. This practice has changed
gradually to the present concept of "mass pollination," whereby
large populations of leafcutter bees (400,000) are placed on small
acreages (25 to 50 acres) for a few days and then removed. The
primary advantages of this type of management are that adequate
pollination can be obtained in a short period, the bees can be
used to pollinate additional fields, and fields can be treated
regularly for pest insects without harm to the bees.
Nesting Materials and Shelters
Many kinds of nesting media have appeared during the last two
decades of leafcutter bee management, and there are many claims
of success. Substantial population increases have been obtained
in several types of nesting media, but the most commonly used
materials are boxes of soda straws, drilled boards (with or without
removable backs), grooved boards, plastic wafers, and rolled-cardboard
units. There are advantages and disadvantages to each type used.
These characteristics are shown in table 1, although grower choice-unproved
data from bee production-appears to determine which media are
used.
Field shelters have changed from the initial small A-frame capable
of holding a few boards to the large, self-contained, incubation-emergence
type mounted on a trailer and capable of holding several hundred
nesting units. It was assumed that facing the shelters to the
east promoted increased bee activity, but research demonstrated
that this practice actually increases mortality of young bee larvae.
Sunlight penetrates the nesting holes and heats the larvae to
as high as 130 degrees F by 10 a.m. It is recommended that no
sunlight actually strike the nesting units.
Some additional recommendations for shelters are:
(1) Use the conspicuous, larger sizes to attract and keep bees
at the shelters
(2) Ventilate each shelter to prevent an accumulation of heat
at the top or through the sides;
(3) Place chicken wire or grills across the open end of the shelter
to provide protection from birds;
(4) Remove debris from emerging bees, nest cleaning, and leaf
drop from the floor to prevent an increase in scavenger beetles
or moths;
(5) Mount shelters on a trailer with wide tires so movement does
not jar the bees.
Table 1.-- Relative desirability of various nesting materials
for Megachile rotundata 1
| Characteristics |
Drilled boards |
Plastic blocks with holes |
Drilled boards, removable
backs |
Grooved wood |
Grooved polystrene |
Paper straws |
Plastic straws |
Corru-gated paper |
| Low cost |
++
|
-
|
+
|
+-
|
+-
|
+++
|
++
|
+++
|
| Avialibility |
++
|
-
|
++
|
-
|
++
|
+
|
++
|
+
|
Strength
(sturdiness) |
+++
|
++
|
++
|
++
|
+-
|
-
|
+
|
-
|
| Light weight |
-
|
+
|
-
|
-
|
++
|
++
|
++
|
++
|
| Compactness |
+
|
+
|
+
|
+
|
+
|
++
|
++
|
++
|
Insulating
property |
++
|
++
|
++
|
+
|
++
|
+
|
+
|
+
|
Ventilation
qualities |
+
|
-
|
+
|
++
|
-
|
+
|
-
|
+
|
Separability
from cells |
-
|
+
|
++
|
++
|
++
|
-
|
-
|
-
|
Cleanability
for reuse |
-
|
+
|
++
|
++
|
++
|
-
|
-
|
-
|
Inspectability
of contents |
-
|
+
|
++
|
++
|
++
|
+
|
+
|
-
|
| Resistance to chaicids |
++
|
+
|
++
|
2-
|
+-
|
-
|
+
|
-
|
Attractiveness
to bees |
++
|
+-
|
+
|
++
|
+-
|
++
|
+-
|
+-
|
Saftey from
most birds |
++
|
+
|
++
|
++
|
+
|
+-
|
+-
|
(?)
|
Saftey from
most mammals |
++
|
-
|
++
|
++
|
+-
|
-
|
+
|
(?)
|
Ease of
storing 3 |
+
|
+
|
++
|
++
|
++
|
+
|
+
|
+
|
1 +++(excellent), ++(good), +(fair), -(poor), +-(mixed reports).
2 Assuming some warping of boards and poor fit of backing.
3 Principal factor is storage seperately from cells; secondary
factors are compactness. Assumption made that holes are well occupied.
Storage During the Winter
Most growers store their bees as overwintering Jarvac in cold
rooms set at 36 degrees to 40 degrees F. The leaf cells are removed
from the nesting media (loose cells) or are left intact, depending
on the kind of
management used. Cold treatment prevents a buildup of scavenger
beetles, moths, and other nest destroyers that can damage unprotected
nests. Although this practice is widely used, caution is needed
so bee larvae are not stored too early in the season (before they
spin a cocoon and change to the overwintering stage). To prevent
injuring bees by early storage, the nesting media should not be
placed in cold storage for at least 2 weeks after removal from
the field.
Generally, if nests are stored during the summer, larvae destined
for the second generation will die, causing considerable prolems
in the emergence pattern the next season. Also, bee larvae stored
at constant low temperatures for long periods have a higher death
rate (10 percent) than those left at outside temperatures (in
Utah). So growers should determine the abundance of nest destroyers
and their potential for destruction before long-term cold storage
of larvae.
Incubation
Growers must decide when bees will be needed in the spring to
begin incubation of larvae at temperatures averaging 86 degrees
to 90 degrees F approximately 20 days before bee emergence. The
most critical factor during the incubation process is temperature
maintenance. When large lots of bees are incubated, the heat
from bee larvae can be high enough to raise the room temperature
to the point of actually killing the larvae. Therefore, adequate
cooling, as well as heating, is required during the incubation
process. The level of humidity is not nearly as important as maintaining
the temperature level. Newly emerged bees or those still in cocoons
can be held as long as a week at reduced temperatures (55 degrees
to 60 degrees), if inclement weather occurs during the release
schedule.
Protection From Parasites and Predators
Parasite-predator control during incubation should be exercised,
especially in the loose cell method, as a 5-percent infestation
could easily increase to 80 to 90 percent without some type of
control. Most leafcutter bee parasites can complete two generations
during the time required for normal emergence of the bees. Adequate
control of pests during incubation has been obtained through the
use of sprays, repellents, light, or emergence traps.
The leafcutter bee is attacked by numerous insects, and considerable
attention must be given to maintenance of a pest-free population
if an increase in bee populations is to be realized. Table 2 lists
the common insects associated with leafcutter bee nests in some
parts of the United States.
Probably the most important type of parasite-predator control
is the maintenance of clean bee stocks by excluding pest populations
through changing nesting media yearly or by utilizing emergence
traps. Most pest species can be controlled during incubation or
emergence through the use of sprays or traps.
Currently, chalk brood, a disease associated with bee larvae,
is increasing. In some Western States, the incidence of this disease
has increased to as high as 80 percent of the overwintered bee
larvae. However, little is known of the causal organism and its
taxonomic status. We still do not know whether the organism is
the cause or merely a symptom of these bee losses. Until these
questions are adequately researched, control measures cannot be
devised. However, it been shown that growers who use clean nesting
media have less chalk brood than those who reuse infested nesting
media.
Additional Practices
It can be highly advantageous for honey bee keepers to handle
leafcutter bees in addition to their honey bee colonies. The cost
of maintaining and increasing bees is much less than the potential
income from selling bees or their services. New bee boards sell
for about $5 each and are $50 to $70 each when covered with bees.
Cells removed from bee boards or boxes (loose cells) sell at an
average of $100 a gallon (10,000 cells a gal). Many individuals
have made a high profit by setting out bee boards on old outbuildings,
cliff banks, and other likely nesting sites and collecting the
filled boards for resale in the fall. Beekeepers also might consider
custom pollination-providing the pollinators and shelters for
fields during the flowering season for a percentage of the crop.
Other Leafcutter Bees
Megachile concinna, the Pale Leafcutter Bee
This species is quite similar to the alfalfa leafcutter bee; M. rotundata. Except for minor structural differences, they are hard for the
novices to distinguish. In California, these two species often
are confused. The pale leafcutter bee is found in the warmer Southern
and Southwestern States. It is an African species that was accidentally
introduced into North America late in the 19th century. This species
has not been managed like M. rotundata, primarily because its nesting requirements have not been adequately
researched. It is capable of producing almost a complete second
generation, and females have a tendency to nest in places other
than the nesting shelter, such as holes in the ground. However,
recent field tests indicate that M. concinna is an exceptionally good alfalfa pollinator. In field tests M. concinna made more cells and the plants produced more seed than did M. rotundata in similar tests.
M. apicalis and M. leachella
Both of these Eurasian species are found in the United States,
but infrequently. They are potential forage legume pollinators,
and populations of both are being studied as candidate alfalfa
pollinators.
Table 2.-- Characteristics of nest associates of the alfalfa leafcutter
bee.
| |
Native+; introduced 0 |
Predators +;
parasites 0; scavengers - |
Important +; minor 0. |
Control
measures |
| Moths |
|
|
|
|
|
| |
Plodia interpunctella |
0 |
+0 |
0 |
Light traps. |
| |
Vitula edmandsae |
+ |
+0 |
0 |
Light traps. |
| Wasps |
|
|
|
|
|
| |
Sapyga pumila |
+ |
0 |
+ |
Emergence traps. |
| |
Monodontomerus obscurus |
0 |
0 |
+ |
Emergence sprays. |
| |
Monodontomerus montivaga |
+ |
0 |
+ |
Emergence. |
| |
Pteromalus megachilids |
0 |
0 |
+ |
Emergence. |
| |
Tetrastichus megachilids |
+ |
0 |
+0 |
Emergence sprays, traps. |
| |
Melittobia chalybii |
+ |
0 |
0 |
Destroy. |
| |
Dibrachys masculipennis |
0 |
0 |
0 |
Destroy. |
| |
Leucospis affinis |
+ |
0 |
0 |
Nesting media. |
| |
Vespula spp. |
+ |
-+ |
0 |
Traps. |
| |
Formica spp. |
+ |
-+ |
0 |
Barrier. |
| Bees |
|
|
|
|
|
| |
Coelioxys funeraria |
+ |
0 |
0 |
Early emergence? |
| |
Coelioxys gilensis |
+ |
0 |
0 |
(?) |
| |
Coelioxis |
+ |
0 |
0 |
(?) |
| |
Stelis sp. |
+ |
0 |
0 |
(?) |
| Dipera flies |
|
|
|
|
|
| |
Anthrax irroratus |
+ |
0 |
0 |
Emergence. |
| Beetles |
|
|
|
|
|
| |
Nemognatha lutea |
+ |
+ |
0 |
Eliminate host plants. |
| |
Trichodes ornatus |
+ |
+ |
+ |
Traps. |
| |
Ptinus californicus |
+ |
- |
0 |
Sprays, loose cell. |
| |
Trogoderma glabra |
+ |
+- |
0 |
Cold treatment, traps. |
| |
Trogoderma variabile |
+ |
- |
0 |
Baits. |
| |
Tribolium castaneum |
+ |
- |
0 |
Santitation. |
| |
T. audox, T. brevicornis |
+ |
- |
0 |
Santitation. |
| |
Oryzaephilus surinamensis |
0 |
- |
0 |
Santitation. |
| |
Cryptolestes ferrugineus |
0 |
- |
0 |
Santitation. |
| |
Tenebroides maurtanicus |
0 |
- |
0 |
Sanitation. |
| Earwigs |
|
|
|
|
|
| |
Forficula auricularia |
0 |
- + |
0 |
Barriers. |
The Alkali Bee
The alkali bee is brightly colored and nests in the ground in
dense colonies. Each female excavates its own tunnel and cells,
and there is no division of labor among the progeny. The bee was
quite common in many Western States, but populations recently
have declined drastically. Its usefulnes as a crop pollinator
was first noted in the 1940's, when large populations were observed
pollinatiug alfalfa in Utah. By the 1950's, some growers in several
Western States were improving natural nesting sites and constructing
artificial bee beds. In the late 1960's and 1970's, the use of
alkali bees declined in most areas due to replacement by the alfalfa
leafcutter bee. Recently, parasites and diseases of the leafcutter
bee have reduced its advantages, and there is increasing interest
in using the alkali bee for alfalfa pollination. Certain growers
in eastern Washington and the San Joaquin Valley of California
have relied consistently on the alkali bee as an alfalfa pollinator,
and they are convinced that the alkali bee is the best alfalfa
pollinator.
Alkali bees collect nectar and pollen from a number of plants.
The main crop plants visited are alfalfa, sweetclover, onions,
and mints. Weedy plants also are visited, and these include saltcedar
(Tamarix), morning glory (Convolvulus), greasewood (Sarcobatus), Russian thistle (Salsola), Rocky Mountain bee plant (Cleome), and several crucifers.
Alkali bees in California usually emerge in May and in Utah as
late as August. Depending on location, these bees may have one
or more generations per season. Males usually emerge a day or
so before the females and begin patrolling the nesting area in
search of newly emerged females, which they pounce upon readily.
The males often are so numerous at nesting sites that they tend
to discourage females from constructing nests.
On warm days, the females visit fields from about 2 hours after
sunrise to 2 hours before sundown. They are capable of tripping
alfalfa flowers at an average rate of 12 per minute. Normally,
they provision at least one cell per day and in their lifetime
provision about 12 cells (maximum 24). This foraging activity
results in about 2,000 alfalfa flowers tripped per day per female
and at least 25,000 flowers per female lifetime. The alkali bee
visits shaded and exposed flowers, thereby increasing its pollination
efficiency. The pollen and nectar provisions are stored in clusters
of cells made 8 to 16 inches beneath the surface of silty loam
soil.
The provisions are formed into a flattened ball with an egg deposited
on the upper surface. The egg soon hatches, and successive stages
of larval forms consume the provisions before entering an overwintering
stage or progressing on to the pupal-adult stages and emerging
to begin another generation.
Nesting Sites
Alkali bees are encouraged to nest in either natural or artificial
nesting sites located in the ground. Generally, the soil is a
silty loam, but the bees will utilize sandy soil or types with
more clay particles. The most critical factor in managing alkali
bee populations is the maintenance of proper soil moisture. Soil
moisture levels can be measured easily by using soil tensiometers.
Soil moisture in the beds and on the surface is maintained by
adding salts, either calcium chloride (CaCl) or sodium chloride
(NaCl), to the water. Natural nesting sites are found in seep
areas where there is a constant supply of moisture extending upwards
to the ground surface. Natural nesting sites can be maintained
by placing a series of blind ditches to grade throughout adjacent
areas and providing water for seepage to the sites.
Fencing is used to prevent packing or destruction of the soil
surface by both farming operations and livestock. Weeds must be
controlled to ensure a bare and attractive surface.
Artificial beds can be made readily by creating a water reservoir
beneath the soil surface. The recipe for artificial beds calls
for the following:
(1) Excavate a hole about 4 feet deep with sloping sides and construct
ridges of soil in the bottom of the excavation to divide it into
compartments;
(2) Line the bottom and side with thick-gage plastic sheeting
and place several inches of soil on the plastic to prevent punctures;
(3) Place several cloth sacks of soil in each compartment;
(4) Add a foot of gravel on top of the soil to hold the water
and install vertical pipes and perforated drain pipe in a radial
pattern from the base of a stand pipe in the gravel layer;
(5) Stretch a layer of burlap on the gravel layer to prevent soil
infiltration;
(6) Fill the remaining hole with soil to the surface level, forming
a gentle crown to prevent ponding;
(7) Add water and salts to the stand pipe and reshape the surface
as soil compaction takes place;
(8) Add brine solution to the soil surface before nesting.
Stocking of new or replenished nesting sites can be accomplished
by two methods. The most common method involves digging cubic-foot
blocks of undisturbed soil from a densely populated bee bed and
incorporating the blocks into a new or revitalized bed before
emergence of the bees in the spring. These soil blocks often contain
200 larvae each and can be purchased from growers, especially
in the State of Washington. Another method of seeding an artificial
bed is to sweep up newly emerged adults from natural nesting sites
and release them after dark at the new site. Holes are prepared
in the bed for the bees to crawl into and be protected during
the night. Better results are obtained also by transplanting adults
to a bed where alkali bees are active. The adults cannot be transferred
to a new bed if the new area is within the old flight range (5
to 9 miles).
The area for the bee bed depends on the acreage to be pollinated.
Millions of alkali bees can be produced in an area of less than
1 acre. The most ideal situation is for a community-based operation,
since these bees can fly great distances and growers who build
bee beds generally have no control of where their bees will forage.
Alkali bees easily can fly several miles to the fields of another
grower, and this long flight range makes them especially susceptible
to pesticides applied in densely cultivated farming areas.
The population of alkali bees needed to set seed is highly variable
and depends on the condition of the field. Most recommendations
are for saturation at the level available forage can support,
but it has been calculated that an acceptable level of alkali
bee females per acre is between 3,500 to 5,000.
Protecting Bees from Parasites
Alkali bees are attacked by a number of insects and animals. Among
the more common are the bombyliid (Heterostylum robustum), a sarcophagid fly (Euphytomina nomivora), and conopid flies (Zondion obliquefasciatum). Generally, high populations of these flies indicate the bed
is not adequately populated with bees, since well-populated sites
provide good defense by limiting oviposition by the flies. Some
fly control has been obtained by traps or sprays.
A recent nest predator found in some areas is the black blister
beetle (Meloe nigra). This beetle is easily controlled, since the flightless females
must crawl from the site to deposit their eggs.
Various methods are used to discourage vertebrate predators such
as birds and skunks. Federal laws now protect most animals, so
growers must seek information at the local level before using
control measures.
Heavy rain also can contribute to the destruction of bee cells
by creating a favorable environment for soil pathogens to develop
and destroy the pollen. No effective control measures have been
developed to protect bees from infrequent drenching by summer
rains.
Blue Orchard Bee
During the last 25 years, orchard acreages planted to stone and
pome species increased dramatically. The major pollinator species
for these crops is the honey bee, but-unfortunately-its colony
numbers steadily decreased during the same 25-year period. We
decided, therefore, to search for alternative pollinator species
of these crops. A survey was initiated in 1970 and by 1972 we
found a most promising species, Osmia lignaria Say, that was named the blue orchard bee. We have worked since
to develop an effective management program for its use in orchards.
Research on this species is nearing completion, and growers are
rapidly becoming aware of its real potential as an alternate pollinator
of orchard crops.
The blue orchard bee is a native species widely distributed across
most of the contiguous United States and southern Canada. It has
been collected in diverse habitats from sea level to elevations
of 7,000 ft, but it is not found in low deserts or sub-tropical
areas. Two allopatric subspecies are recognized, and these are
isolated by the Rocky Mountains.
This robust bee flies early in the spring when few other species
are active, and its size (slightly shorter than the honey bee)
and color (blue-black) are diagnostic. Like the alfalfa leafcutter
bee, it carries light-colored pollen on the underside of its abdomen.
Females have a flat-tipped, brilliant-green prong protruding from
the head directly above each mandible.
Biology
This bee nests in existing holes and fills them with a series
of cells. Each female collects mud, carries it to her nest, and
constructs a thin-walled partition that completely seals the cavity
near its terminus. She subsequently collects nectar and pollen
on each foraging trip and deposits these materials directly in
front of the mud partition until the lower half of the horizontal
cavity is filled with a loaf-shaped provision. An egg is deposited
on the surface of the provision, and the cell is sealed by a second
mud partition in front of the provision. A series of cells is
thus constructed until the cavity is filled. Finally, the nest
entrance is sealed with a thick plug of mud.
Eggs hatch within a week, and each larva consumes its provision
for a month. A characteristic cocoon is spun, after which the
larva enters a "rest" period for approximately a month. Pupation
occurs in late summer, and the resultant adult remains in the
cocoon through the winter. As the temperature rises in the spring,
adults chew through cocoons and nest partitions, take flight,
mate, and reestablish nesting.
Nesting Materials
Three nesting materials (straws, drilled holes in wood, and drilled
holes in stryofoam) have been tested for trapping populations
and establishing them in orchards. The blue orchard bee will nest
in all three materials, but drilled wood is the most attractive
for nests. The preferred hole depth is 5 to 6 inches, and the
most attractive size of hole is 9/32-in. diameter.
Trapping
In Utah, the best areas for trapping this species are in undisturbed
drainages with mixed stands of maple and aspen interrupted by
open meadows. Trapping is also good on the periphery of agricultural
areas in habitats that include a ready supply of mud, early bloom,
and dead trees with beetle holes.
Trap nests, each having 30 to 60 holes, are attached horizontally
to old stumps eafly in the year before nesting activities. The
traps are removed 1 month following the initiation of nesting
and stored until the following year in shaded, outdoor areas having
good ventilation.
Nest Shelters
Experiments completed to date in commercial orchards indicate
that the best size for nest shelters is a boxlike structure approximately
32 by 16 by 12 inches (wooden military foot lockers serve as ideal
shelters). The shelters are attached to metal fence posts and
faced in a southeast direction to catch the morning sun. Each
shelter is filled with trap-nest materials. Several shelters should
be used for each acre pollinated.
Population
Cage studies on almond demonstrate that fewer than 10 female lignaria bees will adequately pollinate a tree. While this cannot be applied
directly to open pollination conditions, the information can be
used to indicate the approximate number of blue orchard bees required
to pollinate each acre. Since males of this species also visit
blooms frequently and are proved pollinators, we estimate that
600 nesting females will adequately pollinate 1 acre of fruit
trees.
Commercial Utilization
Field populations of the blue orchard bee have been tested only
recently, but results of such studies justify comments on the
advantages of this species as an orchard crop pollinator. These
are:
(1) Nesting is completed during the short period of orchard bloom
when pesticides normally are not applied. As a consequence, growers
can easily schedule post-bloom pesticide schedules without affecting
their pollinator force.
(2) The blue orchard bee initiates daily flight at temperatures
2 to 5 degrees lower than for the honey bee, and individuals visit
orchard bloom consistently throughout the daylight hours. This
can be of much significance during "bad" weather years.
(3) Both sexes of 0. lignaria visit orchard bloom throughout their adult lives. Therefore,
the entire population serves as a pollinator force.
(4) This species increases its nesting efficiency by flying short
distances to collect pollen and nectar provisions when bloom is
adequate. Proper management, therefore, can be applied to better
guarantee full pollinator utilization on individual properties.
(5) The normal adult flight periods of this species are short
in comparison to those of other pollinators, and its annual appearance
is early in the spring when inclement weather conditions are common.
Nevertheless, this species is successful because females rapidly
collect pollen over long daily flight periods. These facts, together,
indicate the bee can serve as an effective pollinator of massive
plants, such as orchard crops, that have short flower life.
(6) The blue orchard bee has its complement of nest associates,
but these species have been nearly eradicated in field population
tests by applying proper management techniques.
(7) The nests and nesting materials used for this species are
relatively light. Therefore, management of large field populations
will require fewer pieces of expensive equipment designed to move
and transport heavy pollinator units.
(8) Few worker-hours, relatively, are needed for management of
the species and this is restricted to a short period annually.
(9) Necessary transport of nesting populations throughout the
summer months is eliminated in managing the blue orchard bee because
it is an obligatory one-generation species.
(10) Osmia lignaria can successfully nest and pollinate crops
in competition with other pollinator species visiting the same
crops.
If the acreage of orchard crops continues to expand as it has
in the last 25 years, it soon will be impossible to supply enough
pollinators for these crops, regardless of the species used. This
problem can be resolved, however, by using a multiple-species
approach. Further, those presently involved in honey bee pollination
could easily adapt their operations to accommodate management
of additional species for concomitant use. The management of multiple
species already has proved successful for several western honey
bee suppliers who have added the alfalfa leafcutter bee to their
operations.
Related Species
Sibling species of the blue orchard bee occur in other parts of
the world. One of these, Osmia cornifrons, occurs in Japan and is an established pollinator of apple in
that country. We cooperated with Japanese scientists recently
in working with this species in Utah. While the study population
nested well under Utah conditions, its progeny did not overwinter
successfully. Another SEA scientist is working with this species
in the Washington, D.C., area to determine if climatic conditions
on our east coast (similar to Japan's) will permit successful
overwintering of 0. cornifrons.
Populations of the European species, Osmia cornuta, have been received from a Spanish collaborator, and we have
completed studies of its biology and pollinator potential. Unlike
the Japanese species, cornuta overwintered well under Utah conditions, and we are increasing
our greenhouse-reared populations for possible field release in
the near future.
Other European species are being established in our Utah greenhouses,
and their status as potential pollinators has yet to be deciphered.
Other Pollinators
Bumble Bees
Bumble bees are important pollinators of many of our native plants,
especially those growing at high elevations. Also, bumble bee
species are associated with our crop plants, but no successful
attempts have been made to utilize them on a large scale. The
number of workers per colony is quite low (50-100), and the profitability
of using such small colonies of bumble bees is unknown. Researchers,
however, are studying means of increasing colony size and extending
the life of colonies to more than a single season.
The generalized life cycle of a colony of bumble bees is as follows:
the mated queen overwinters in some type of hybernaculum. In the
spring, she becomes active and begins searching for a nesting
site to make cells, lay eggs, and begin a colony. After nest establishment
and the emergence of the first workers, the queen enlarges the
colony with the aid of the numerous workers so that its size increases
during the season. By fall, new queens, drones, and workers are
being produced. Then the new queens mate, leave the colony for
overwintering sites, and the old queen, workers, and drones gradually
die.
Bumble bees are quite cyclic in their abundance, and this periodicity
has been linked to cycles of rodent populations in whose old nests
many of these bees find suitable nesting sites. Several bumble
bees are quite common, and can be trapped by placing nesting boxes
out in spring or by catching overwintered females before they
begin to build their nests in the spring. Many of the captured
females will begin to make colonies in these boxes, if pollen
and nectar are provided. After the queen begins making cells and
the first workers appear, the box can be opened and the bees allowed
to forage in the field.
Anthophorids
Several species of Anthrophoridae have the potential of being
used as crop pollinators. Although they nest in the ground, artificial
nesting sites have been made from blocks of adobe, which are readily
accepted by these bees. Excellent nesting and reproductions by
some native species such as Anthophora urbana, A. pacifica, and A. bomoides have been obtained in greenhouses, but these species have not
yet been field tested. A Polish species, A. parietina, has been successfully tested in hairy vetch in that country.
Other anthophorid bees are potential pollinators of such crops
as cotton (Diadasia and Ptilothrix) and sunflowers (Diadasia and Melissodes). These bees possess characteristic habits such as gregarious
nesting and restricted floral visitation, which make them potential
crop pollinators. No research, however, has been done on utilizing
them as such.
There are several genera of bees, such as Peponapis and Xenoglossa, whose sole host plants are species of native and cultivated
squash. Some species nest in dense aggregations and might be managed
somewhat like our ajkali bees. However, no management programs
have been developed to utilize these efficient pollinators on
a commercial scale.
Introduction of Foreign Pollinators
There have been only two intentional introductions of pollinators
from other countries to the United States. The most obvious and
successful is the honey bee. Its introduction has been so successful
that additional introductions have been largely ignored. The other
example is a group of fig wasps without which hybrid figs cannot
be produced (except with hormonal sprays).
Several additional species of bees and wasps have become established
in the United States, mostly inadvertently via our numerous vehicles
of commerce. One, the alfalfa leafcutter bee, has become the most
important of these adventive species. Many other species of potential
crop pollinators are known to exist in foreign countries and might
be valuable supplements to our existing species.
A principal shortcoming of the honey bee as a pollinator of specific
crops is its wide host range. This results in a large share of
each colony's population not pollinating the desired crop. Thus,
the best means of obtaining specific pollinators would be the
introduction of oligotrophic species that have a principal host
plant.
There are many examples of foreign species that have definite
affinities for certain of our important crop plants. For example,
alfalfa in its native home in Eurasia is effectively pollinated
by several genera and species of bees that do not occur in the
United States. All these species are excellent choices for an
introduction program to increase seed yields in areas of poor
alfalfa seed production. Promising species of tomato and red clover
pollinators are known to exist in Central America and South America,
but no populations have been imported for preliminary trials.
With the origin of a large number of our cultivated crops being
other countries, an expanded program for the introduction and
establishment of exotic pollinators should be expanded rapidly.
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Kansas Entomological Society 49(4) :475-482.
----------- and F. D. PARKER.
1975. FIRST GET THE SEEDS. Utah Science 39:26-30.
WATERS, N. D.
1971. INSECT ENEMIES OF THE ALFALFA LEAF-CUTTER BEE AND THEIR
CONTROL. 4 p. Univ. of Idaho Current Information Ser. 163.
H.W. HOMAN, and D. W. SUTHERLAND.
1973. RAISING ALFALFA LEAFCUTTER BEES IN IDAHO. 12 p. University
of Idaho Cooperative Extension Service Bull. 538.
WILSON, E. F.
1968. LEAF-CUTTING BEE STORAGE. 5 p. Washington State University
Extension Service EM 2909.
Management | Beekeeping Information Index
Mid-Atlantic Apiculture