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Authors: Rachel Carson

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Sound is also being tested as an agent of direct destruction. Ultrasonic sound will kill all mosquito larvae in a laboratory tank; however, it kills other aquatic organisms as well. In other experiments, blowflies, mealworms, and yellow fever mosquitoes have been killed by airborne ultrasonic sound in a matter of seconds. All such experiments are first steps toward wholly new concepts of insect control which the miracles of electronics may some day make a reality.

The new biotic control of insects is not wholly a matter of electronics and gamma radiation and other products of man's inventive mind. Some of its methods have ancient roots, based on the knowledge that, like ourselves, insects are subject to disease. Bacterial infections sweep through their populations like the plagues of old; under the onset of a virus their hordes sicken and die. The occurrence of disease in insects was known before the time of Aristotle; the maladies of the silkworm were celebrated in medieval poetry; and through study of the diseases of this same insect the first understanding of the principles of infectious disease came to Pasteur.

Insects are beset not only by viruses and bacteria but also by fungi, protozoa, microscopic worms, and other beings from all that unseen world of minute life that, by and large, befriends mankind. For the microbes include not only disease organisms but those that destroy waste matter, make soils fertile, and enter into countless biological processes like fermentation and nitrification. Why should they not also aid us in the control of insects?

One of the first to envision such use of microorganisms was the 19th-century zoologist Elie Metchnikoff. During the concluding decades of the 19th and the first half of the 20th centuries the idea of microbial control was slowly taking form. The first conclusive proof that an insect could be brought under control by introducing a disease into its environment came in the late 1930's with the discovery and use of milky disease for the Japanese beetle, which is caused by the spores of a bacterium belonging to the genus
Bacillus.
This classic example of bacterial control has a long history of use in the eastern part of the United States, as I have pointed out in Chapter 7.

High hopes now attend tests of another bacterium of this genus—
Bacillus thuringiensis
—originally discovered in Germany in 1911 in the province of Thuringia, where it was found to cause a fatal septicemia in the larvae of the flour moth. This bacterium actually kills by poisoning rather than by disease. Within its vegetative rods there are formed, along with spores, peculiar crystals composed of a protein substance highly toxic to certain insects, especially to the larvae of the mothlike lepidopteras. Shortly after eating foliage coated with this toxin the larva suffers paralysis, stops feeding, and soon dies. For practical purposes, the fact that feeding is interrupted promptly is of course an enormous advantage, for crop damage stops almost as soon as the pathogen is applied. Compounds containing spores of
Bacillus thuringiensis
are now being manufactured by several firms in the United States under various trade names.
Field tests are being made in several countries: in France and Germany against larvae of the cabbage butterfly, in Yugoslavia against the fall webworm, in the Soviet Union against a tent caterpillar. In Panama, where tests were begun in 1961, this bacterial insecticide may be the answer to one or more of the serious problems confronting banana growers. There the root borer is a serious pest of the banana, so weakening its roots that the trees are easily toppled by wind. Dieldrin has been the only chemical effective against the borer, but it has now set in motion a chain of disaster. The borers are becoming resistant. The chemical has also destroyed some important insect predators and so has caused an increase in the tortricids—small, stout-bodied moths whose larvae scar the surface of the bananas. There is reason to hope the new microbial insecticide will eliminate both the tortricids and the borers and that it will do so without upsetting natural controls.

In eastern forests of Canada and the United States bacterial insecticides may be one important answer to the problems of such forest insects as the budworms and the gypsy moth. In 1960 both countries began field tests with a commercial preparation of
Bacillus thuringiensis.
Some of the early results have been encouraging. In Vermont, for example, the end results of bacterial control were as good as those obtained with DDT. The main technical problem now is to find a carrying solution that will stick the bacterial spores to the needles of the evergreens. On crops this is not a problem—even a dust can be used. Bacterial insecticides have already been tried on a wide variety of vegetables, especially in California.

Meanwhile, other perhaps less spectacular work is concerned with viruses. Here and there in California fields of young alfalfa are being sprayed with a substance as deadly as any insecticide for the destructive alfalfa caterpillar—a solution containing a virus obtained from the bodies of caterpillars that have died because of infection with this exceedingly virulent disease. The bodies of only five diseased caterpillars provide enough virus to treat an acre of alfalfa. In some Canadian forests a virus that affects pine sawflies has proved so effective in control that it has replaced insecticides.

Scientists in Czechoslovakia are experimenting with protozoa against webworms and other insect pests, and in the United States a protozoan parasite has been found to reduce the egg-laying potential of the corn borer.

To some the term microbial insecticide may conjure up pictures of bacterial warfare that would endanger other forms of life. This is not true. In contrast to chemicals, insect pathogens are harmless to all but their intended targets. Dr. Edward Steinhaus, an outstanding authority on insect pathology, has stated emphatically that there is "no authenticated recorded instance of a true insect pathogen having caused an infectious disease in a vertebrate animal either experimentally or in nature." The insect pathogens are so specific that they infect only a small group of insects—sometimes a single species. Biologically they do not belong to the type of organisms that cause disease in higher animals or in plants. Also, as Dr. Steinhaus points out, outbreaks of insect disease in nature always remain confined to insects, affecting neither the host plants nor animals feeding on them.

Insects have many natural enemies—not only microbes of many kinds but other insects. The first suggestion that an insect might be controlled by encouraging its enemies is generally credited to Erasmus Darwin about 1800. Probably because it was the first generally practiced method of biological control, this setting of one insect against another is widely but erroneously thought to be the only alternative to chemicals.

In the United States the true beginnings of conventional biological control date from 1888 when Albert Koebele, the first of a growing army of entomologist explorers, went to Australia to search for natural enemies of the cottony cushion scale that
threatened the California citrus industry with destruction. As we have seen in Chapter 15, the mission was crowned with spectacular success, and in the century that followed the world has been combed for natural enemies to control the insects that have come uninvited to our shores. In all, about 100 species of imported predators and parasites have become established. Besides the vedalia beetles brought in by Koebele, other importations have been highly successful. A wasp imported from Japan established complete control of an insect attacking eastern apple orchards. Several natural enemies of the spotted alfalfa aphid, an accidental import from the Middle East, are credited with saving the California alfalfa industry. Parasites and predators of the gypsy moth achieved good control, as did the
Tiphia
wasp against the Japanese beetle. Biological control of scales and mealy bugs is estimated to save California several millions of dollars a year—indeed, one of the leading entomologists of that state, Dr. Paul DeBach, has estimated that for an investment of $4,000,000 in biological control work California has received a return of $100,000,000.

Examples of successful biological control of serious pests by importing their natural enemies are to be found in some 40 countries distributed over much of the world. The advantages of such control over chemicals are obvious: it is relatively inexpensive, it is permanent, it leaves no poisonous residues. Yet biological control has suffered from lack of support. California is virtually alone among the states in having a formal program in biological control, and many states have not even one entomologist who devotes full time to it. Perhaps for want of support biological control through insect enemies has not always been carried out with the scientific thoroughness it requires—exacting studies of its impact on the populations of insect prey have seldom been made, and releases have not always been made with the precision that might spell the difference between success and failure.

The predator and the preyed upon exist not alone, but as part of a vast web of life, all of which needs to be taken into account. Perhaps the opportunities for the more conventional types of biological control are greatest in the forests. The farmlands of modern agriculture are highly artificial, unlike anything nature ever conceived. But the forests are a different world, much closer to natural environments. Here, with a minimum of help and a maximum of noninterference from man, Nature can have her way, setting up all that wonderful and intricate system of checks and balances that protects the forest from undue damage by insects.

In the United States our foresters seem to have thought of biological control chiefly in terms of introducing insect parasites and predators. The Canadians take a broader view, and some of the Europeans have gone farthest of all to develop the science of "forest hygiene" to an amazing extent. Birds, ants, forest spiders, and soil bacteria are as much a part of a forest as the trees, in the view of European foresters, who take care to inoculate a new forest with these protective factors. The encouragement of birds is one of the first steps. In the modern era of intensive forestry the old hollow trees are gone and with them homes for woodpeckers and other tree-nesting birds. This lack is met by nesting boxes, which draw the birds back into the forest. Other boxes are specially designed for owls and for bats, so that these creatures may take over in the dark hours the work of insect hunting performed in daylight by the small birds.

But this is only the beginning. Some of the most fascinating control work in European forests employs the forest red ant as an aggressive insect predator—a species which, unfortunately, does not occur in North America. About 25 years ago Professor Karl Gösswald of the University of Würzburg developed a method of cultivating this ant and establishing colonies. Under his direction more than 10,000 colonies of the red ant have been established in about 90 test areas in the German Federal Republic. Dr. Gösswald's method has been adopted in Italy and other countries, where ant farms have been established to supply colonies for distribution in the forests. In the Apennines, for example, several hundred nests have been set out to protect reforested areas.

"Where you can obtain in your forest a combination of birds' and ants' protection together with some bats and owls, the biological equilibrium has already been essentially improved," says Dr. Heinz Ruppertshofen, a forestry officer in Mölln, Germany, who believes that a single introduced predator or parasite is less effective than an array of the "natural companions" of the trees.

New ant colonies in the forests at Mölln are protected from woodpeckers by wire netting to reduce the toll. In this way the woodpeckers, which have increased by 400 per cent in 10 years in some of the test areas, do not seriously reduce the ant colonies, and pay handsomely for what they take by picking harmful caterpillars off the trees. Much of the work of caring for the ant colonies (and the birds' nesting boxes as well) is assumed by a youth corps from the local school, children 10 to 14 years old. The costs are exceedingly low; the benefits amount to permanent protection of the forests.

Another extremely interesting feature of Dr. Ruppertshofen^ work is his use of spiders, in which he appears to be a pioneer. Although there is a large literature on the classification and natural history of spiders, it is scattered and fragmentary and deals not at all with their value as an agent of biological control. Of the 22,000 known kinds of spiders, 760 are native to Germany (and about 2000 to the United States). Twenty-nine families of spiders inhabit German forests.

To a forester the most important fact about a spider is the kind of net it builds. The wheel-net spiders are most important, for the webs of some of them are so narrow-meshed that they can catch all flying insects. A large web (up to 16 inches in diameter) of the cross spider bears some 120,000 adhesive nodules
on its strands. A single spider may destroy in her life of 18 months an average of 2000 insects. A biologically sound forest has 50 to 150 spiders to the square meter (a little more than a square yard). Where there are fewer, the deficiency may be remedied by collecting and distributing the baglike cocoons containing the eggs. "Three cocoons of the wasp spider [which occurs also in America] yield a thousand spiders, which can catch 200,000 flying insects," says Dr. Ruppertshofen. The tiny and delicate young of the wheel-net spiders that emerge in the spring are especially important, he says, "as they spin in a teamwork a net umbrella above the top shoots of the trees and thus protect the young shoots against the flying insects." As the spiders molt and grow, the net is enlarged.

Canadian biologists have pursued rather similar lines of investigation, although with differences dictated by the fact that North American forests are largely natural rather than planted, and that the species available as aids in maintaining a healthy forest are somewhat different. The emphasis in Canada is on small mammals, which are amazingly effective in the control of certain insects, especially those that live within the spongy soil of the forest floor. Among such insects are the sawflies, so-called because the female has a saw-shaped ovipositor with which she slits open the needles of evergreen trees in order to deposit her eggs. The larvae eventually drop to the ground and form cocoons in the peat of tamarack bogs or the duff under spruce or pines. But beneath the forest floor is a world honeycombed with the tunnels and runways of small mammals—whitefooted mice, voles, and shrews of various species. Of all these small burrowers, the voracious shrews find and consume the largest number of sawfly cocoons. They feed by placing a forefoot on the cocoon and biting off the end, showing an extraordinary ability to discriminate between sound and empty cocoons. And for their insatiable appetite the shrews have no rivals. Whereas a vole can consume about 200 cocoons a day, a shrew, depending on the species, may devour up to 800! This may result, according to laboratory tests, in destruction of 75 to 98 per cent of the cocoons present.

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