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HISTORY AND DEVELOPMENT OF BIOLOGICAL CONTROL

I. The history of Biological Control may be divided into 3
periods:

A. The preliminary efforts when living agents were released 
haphazardly with no scientific approach. Little precise information
exists on successes during this time. Roughly 200 A.D. to 1887 A.D.;

B. The intermediate period of more discriminating BC started with
the introduction the Vedalia beetle, Rodolia cardinalis Mulsant, for
control of the cottony cushion scale in 1888. The period extended from 1888
to ca. 1955; and

C. The modern period is characterized by more careful planning and more
precise evaluation of natural enemies. The period from 1956 to the present.

II. Early History: 200 A.D. to 1887 A.D.

A. 200 A.D. to 1200 A.D: BC agents were used in augmentation

1. The Chinese were the first to use natural enemies to control insect pests.
Nests of the ant Oecophylla smaragdina were sold near Canton in the
3rd century for use in the control of citrus insect pests such as
Tesseratoma papillosa (Lepidoptera)

2. Ants were used in 1200 A.D. for control of date palm pests in Yemen
(south of Saudia Arabia). Nests were moved from surrounding hills
and placed in trees

3. Usefulness of ladybird beetles recognized in the control of aphids and scales
in 1200 A.D.

B. 1300 A.D. to 1799 A.D.: BC was just beginning to be recognized.

1. Aldrovandi noted the cocoons of Apanteles glomeratus on a parasitized
Pieris rapae in 1602 A.D., but thought cocoons were insect eggs

2. Vallisnieri interpreted the phenomenon of insect parasitism (parasitoid)
in 1706 A.D. However the honor of being the first to understand insect
parasitism may belong to the microbiologist Van Leeuwenhoek who
illustrated and discussed a parasite of a sawfly that feeds on willow in a
publication in 1701.

3. The first insect pathogen was recognized by de Reaumur in 1726. It
was a Cordyceps fungus on a noctuid

4. In 1734, de Reaumur suggested to collect the eggs of an “aphidivorous
fly” (actually a lacewing) and place them in greenhouses to control
aphids

5. The mynah bird, Acridotheres tristis, was successfully introduced from
India to Mauritius (off the coast of Madagascar) for control of the red
locust, Nomadacris septemfasciata, in 1762

6. In the late 1700s, birds were transported internationally for insect
control

7. Control of the bedbug, Cimex lectularius, was successfully
accomplished by releases of the predatory pentatomid Picromerus
Bidens in 1776 in Europe

C. 1800 A.D. to 1849 A.D. During this period advances were made in
Europe which was both applied and basic

1. In the 1800’s, Darwin discussed “Ichneumonids” as natural control
factors for cabbage caterpillars

2. Malthus (in England) published Essays on the Principles of
Population in 1803

3. Hartig (Germany) suggested the rearing of parasites from parasitized
caterpillars for mass releases in 1827

4. Kollar (Austria) put forth the concept of “natural control” in 1837

5. Verhulst (1838) described the logistic growth equation but the idea
lay dormant until 1920 when rediscovered by Pearl. Expressed
the idea of “environmental resistance”.

6. During the 1840s releases of predators were used for control of the
gypsy moth and garden pests in Italy

D. 1850 to 1887. During this time the focus on BC switched to the United
States.

1. From 1850 to 1870 enormous plantings of many crops were being
grown in the United States (especially California) and were initially
free of pests. Later farmers saw their crops destroyed by hordes of
alien pests

2. Asa Fitch (New York) suggested importing parasites from Europe
to control the wheat midge, Contarinia tritici, in 1856. No action
was taken. In 1860 parasites were requested from Europe, but none
were received

3. During this period, Benjamin Walsh (Illinois) actively worked
for the importation of natural enemies to control the exotic insects
in the United States but was unsuccessful. Fortunately, he
influenced Charles V. Riley greatly who was in Missouri during
Walsh’s campaign

4. The first practical attempt at BC of weeds occurred in 1863 when
segments of the prickly pear cactus, Opuntia vulgaris, infested with
the imported cochineal insect, Dactylopius ceylonicus, were
transported from northern to southern India

5. Riley conducted the 1st successful movement of parasites for
biological control when parasites were moved from Kirkwood,
Missouri, to other parts of the state for control of the weevil
Conotrachelus nenuphar in 1870

6. LeBaron transported apple branches infested with oyster-shell scale
parasitized by Aphytis mytilaspidis from Galena to Geneva,
Illinois in 1871

7. In 1873 Riley sent the predatory mite Tyroglyphus phylloxerae to
France to control the grape phylloxera. The mite was established
but did not exert control as hoped.

8. Trichogramma sp. (egg parasites) were shipped from the U.S. to
Canada for control of lepidopterous pests in 1882

9. In 1883 the USDA imported Apanteles glomeratus from England
for control of P. rapae (the imported cabbageworm). Parasites
were distributed in DC, Iowa, Nebraska, and Missouri. First
intercontinental shipment of parasites.

III. The Intermediate Period: 1888 to 1955

A. 1888 to 1889: The Cottony Cushion Scale Project

1. Cottony cushion scale, Icerya purchasi Maskell, was introduced into
California in ca. 1868 around the Menlo Park (CA) area (near San
Francisco)

2. It spread to southern California and by 1887 was threatening to destroy
the infant citrus industry

3. C. V. Riley (Chief of the Division of Entomology, USDA) employed
Albert Koebele and D. W. Coquillett in research on control of the
cottony cushion scale

4. No method was working in 1887

5. Koebele was sent to Australia in 1888 to collect natural enemies of the
scale

6. He sent ca. 12,000 individuals of Cryptochaetum iceryae and 129
individuals of Rodolia cardinalis (the vedalia beetle)

7. Within the year, the cottony cushion scale ceased to be a substantial
pest

8. The vedalia beetle controls the scale mainly in the inland desert areas
and C. iceryae controls it in the coastal areas of California.

B. 1890 to 1899: Growing pains for BC

1. Following the success in 1889, California put pressure on Riley to
send Koebele back to Australia in search of parasites for other scales
parasites in California

2. Koebele went on foreign exploration, but on his return, he was recalled
from California. Koebele resigned from his position and went to work for
the Republic of Hawaii in 1893. He worked on BC projects in the
interest of Hawaii until 1912 when he retired due to ill health.

3. Due to the success of the Vedalia beetle, great emphasis was placed on
importation of coccinellids for BC initially in California and Hawaii. It
is believed that California was set back many years by promoting
mostly biological control projects and not researching alternative
control methodologies.

4. L. O. Howard replaced C. V. Riley as Chief of the Division of
Entomology, USDA in 1894. Howard was prejudiced against BC due to
the problems he saw in California

5. George Compere began as a foreign explorer for California in 1899

C. 1900 to 1930: New faces and more BC projects

1. The Gypsy Moth Project in New England (1905-1911). W. F. Fiske
was in charge in Massachusetts. Howard conducted foreign exploration
in Europe and arranged for parasites to be imported to the U.S. Many
prominent entomologists employed on the project: Harry Scott Smith,
W. R. Thompson, P. H. Timberlake.

2. The Lantana Weed Project in Hawaii (1902) First published work on
BC of weeds. Koebele went to Mexico and Central America looking
for phytophagus insects which were sent to R. C. L. Perkins in
Hawaii.

3. The Sugar-cane Leafhopper Project in Hawaii (1904-1920). Hawaiian
Sugar Planters Association (HSPA) created a Division of Entomology
in 1904. R. C. L. Perkins was appointed superintendent. The staff consisted of O. H.

Swezey, G. W. Kirkaldy, F. W. Terry, Alexander
Craw, and Albert Koebele. Later Frederick Muir was employed due to
Koebele’s health problems. Muir found the highly effective predator
Tytthus (= Cyrtorhinus) mundulus (Miridae) in Queensland, Australia,
in 1920.

4. Berliner described Bacillus thuringiensis in 1911 as the causative agent of
bacterial disease of the Mediterranean flour moth

5. Prof. H. S. Smith was appointed superintendent of California State
Insectary, Sacramento, CA, in 1913. The facility moved to the University
of California’s Citrus Experiment Station in 1923 (now UC Riverside).
Smith started another facility in Albany, CA, in 1945. Riverside and
Albany (UC Berkeley) is made up Department of Biological Control, UC.

6. The USDA Laboratory for Biological Control was established in France in 1919.

7. The Imperial Bureau of Entomology created the Farnham House
Laboratory for BC work in England in 1927. This was later directed by
W. R. Thompson in 1928.

D. 1930 to 1955: Expansion and decline of BC

1. From 1930 to 1940 there was a peak in BC activity in the world with
57 different natural enemies were established at various places.

2. World War II caused a sharp drop in BC activity.

3. BC did not regain popularity after WW II due to the production of
relatively inexpensive synthetic organic insecticides. Entomological
research switched predominantly to pesticide research.

4. In 1947 the Commonwealth Bureau of Biological Control was
established from the Imperial Parasite Service. In 1951 the name was
changed to the Commonwealth Institute for Biological Control (CIBC).
Headquarters are currently in Trinidad, West Indies.

5. In 1955 the Commission Internationale de Lutte Biologique contre les
Enemis des Cultures(CILB) was established. This is a worldwide
organization with headquarters in Zurich, Switzerland. In 1962 the
CILB changed its name to the Organisation Internationale de Lutte
Biologique contre les Animaux et les Plants Nuisibles.
This organization is also known as the International Organization for
Biological Control (IOBC). Initiated the publication of the journal
“Entomophaga” in 1956, a journal devoted to biological control of
arthropod pests and weed species.

IV. The Modern Period: 1957 to Present.

A. In 1959, Vern Stern et al. (1959) conceived the idea of economic injury
level and economic threshold which would permit growers to make
informed decisions on when they needed to apply control tactices in their
cropping systems and therefore eliminated the need for scheduled pesticide
treatments.

B. Interest developed nationwide in ecology and the environment after 1962
with the publishing of the Rachel Carson’s book “Silent Spring.”

C. “Silent Spring” helped stimulate the implementation of the concept of
Integrated Pest Management (IPM) in the late 1960’s, and biological
control was seen as a core component of IPM by some. More emphasis
was placed on conservation BC than classical BC.

D. In 1964, Paul DeBach and Evert I. Schliner (Division of Biological
Control, University of California, Riverside) publish an edited volume
titled “Biological Control of Insect Pests and Weeds” which becomes a major reference

source for the biological control community. This was a California-based book

with international application.

E. In some areas in the USA (e.g., California, North Carolina, Kansas,
Texas), IPM scouting was commercialized in the 1970’s and natural
enemies were relied upon to suppress pests in crops such as cotton,
alfalfa, citrus, soybeans, and other crops.

F. During the 1970s and 1980’s, Brian Croft and Marjorie Hoy made
impacts by using pesticide-resistant natural enemies in cropping systems.

G. In 1983, Frank Howarth published his landmark paper titled “Biological
Control: Panacea or Pandora’s Box” and significantly impacted classical
BC efforts by concluding that classical BC of arthropods significantly
contributed to extimction of desirable species (e.g., endemic).

1. This eventually forced a rethinking of legislative guidelines as well as
introduction methods which are still being changed today.

2. In Hawaii, BC efforts were diminished significantly and have not risen
to levels before 1985.

3. Research efforts into this area were stimulated with the general results
that many of Howarth’s claims were unjustified, but some impacts
were discovered. No species extinctions have been demonstrated to
have resulted from classical BC efforts to date.

H. In the 1990’s, two additional biological control journals appeared,
“Biological Control – Theory and Application in Pest Management”
(Academic Press) and “Biocontrol Science and Technology” (Carfax
Publishing). Additionally, “Entomophaga” changed its name to
“Biocontrol” in 1997.

 

 

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Balanced mutual use (symbiosis)

Figs and their pollen carriers, fig-wasps have become very popular at least among biologists. Their relationship, in which we can see another extremely complicated relationship in nature, contains one of the hidden keys needed for solving the mysteries of co-evolution and the ecosystem.

This mutual relationship is believed to have begun about 90 million years ago, and approximately 750 varieties of figs (Ficus) now thrive. Amazingly, as a new kind of fig evolves, a fig-wasp corresponding to that new kind of fig appears. But a complicated co-evolution like this can be explained by Darwin’s theory of evolution, just as other happenings in nature can. His theory suggests that every creature evolves to leave the largest number of descendants in the next generation.

Plants, which have animals carry their pollen, offer the carriers a reward such as honey, or provide a carrier’s larva with a place to grow. Cabbage leaves rich in nutrition didn’t evolve to be a salad, but to be host food for larva of butterflies that carry cabbage pollen. Unfortunately, such larva become a horticulturist’s enemies.

The relationship between fig and fig-wasps in which an insect carries pollen and its larva eats the fruit is also seen in the cycad group and the yucca plant, a plant growing in arid areas in America. In this relationship, a contradictory relationship exists; that is, more pollen carriers are active more eggs are laid, and therefore more seeds are eaten even though the carriers help the plant bear fruit.

Fig flowers, which have the egg of a fig-wasp become a gall (an insect’s knot), food for larva, and fig flowers which don’t have an egg become seeds if they are pollinated. The number of female fig-wasps that develop into adults and fly out of the fig plant carrying pollen represents the number of carried pollen; that is, the adaptation rate of the male fig (the rate used to measure the size of the population of a certain genetic model in the next generation).

The number of seeds indicates the adaptation rate of a female fig. On the other hand, to become a host plant for male fig-wasps is fruitless for figs because male fig-wasps don’t have wings and can’t carry pollen. Therefore, figs don’t want to have too many male fig-wasps. Ideally, figs want to produce about the same number of female fig-wasps and seeds to create a balance between the number of female fig-wasps and fruit for themselves. On the other hand, fig-wasps want to lay as many eggs as possible to obtain the greatest possible benefit. Both the figs and fig-wasps co-exist by maintaining this subtly balanced relationship.

If the figs have a pollen carrier in all their flowers, no seeds will be left for the next generation. On the contrary, if figs reject pollen carriers too often, there won’t be enough pollen carried out for pollination. They both need to maintain this relationship. Some figs are heterosexual so male figs raise fig-wasps to carry pollen and female figs fruit seeds. Fig-wasps can’t mate in the female fig syconium, but the wasps can’t distinguish a male syconium from a female syconium. And the wasps that unfortunately come into a female syconium only help the fig pollinate.

Throughout the world, figs grow most abundantly in the forest of Ranbil on Borneo Island in Malaysia, and about 80 varieties of figs can be observed there. While we were studying there in 1998, there was a drought, and no fig flowers bloomed during that time. On that occasion, we made an interesting observation that fig-wasps came back right away as the flowers of the homosexual figs revived, but the wasps took two to three years to come back to the flowers of the heterosexual figs. Who knows when a change of weather in the tropical rainforest will create a new condition and give us clues to solve this mystery? I can’t take my eyes off the Ranbil forest.

 

 

 

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Hard Chaparral


Hard ChaparralHard Chaparral

Chaparral covers about 8.5% of California and is the most characteristic natural vegetative type in the state. It reaches its fullest development in Southern California where it ranges in elevation between 1,000 and 5,000. Annual grasslands and coastal sage scrub occur along its lower limits and its upper limits border on mixed evergreen and coniferous forests. Various types of woodlands bisect hard chaparral in foothill areas and along canyon bottoms.

Chaparral

Chaparral bisected by grassland. The chaparral in the foreground shows a variety of plant species. Soft chaparral is the gray color on the distant hills, and hard chaparral is the dark green color.

The evergreen, stiffly branched shrubs of the true, or hard chaparral are mostly 3 – 10 feet tall. Leaves are small and leathery (sclerophyllous) with thick cuticles. Sometimes the leaves are so reduced as to appear needle-like e.g. Chamise (Adenostoma fasciculatum). These are adaptations to reduce evapotranspiration during the dry summer months. Stands of mature chaparral form a dense, almost impenetrable layer with little or no herbaceous understory.

Hard chaparral occurs in a mosaic reflecting fire history. A twenty-year cycle of fire maintains a community of Chamise. In communities with less frequent or more regular burns, Chamise gives way to Ceanothus, mountain mahogany, Sumac, Toyon, and Manzanita . Dwarfed oaks and drought-resistant, closed-cone pines also occur.

Adaptations to drought

Rain generally falls over the winter months in a few intense storms. The effective moisture is drastically reduced by rapid runoff, low moisture retention by soils, high rates of evaporation, and the protracted rainless period each year. To survive, chaparral plants must be adapted to 5 – 6 inches of rain per year and a drought of 5 – 6 months in duration. The dominant species are mostly spring active – they photosynthesize and grow in the spring when after moisture from the winter rains has penetrated far enough into the soil to become available to their roots.

As soil moisture supplies become limited, usually by late June, most chaparral plants enter a summer dormancy phase and operate at 5% of their wet season maximums. The plants are most susceptible to fire at this time.

By retaining their leaves, plants of the hard chaparral are physiologically ready to take advantage of a rare summer thundershower. Within minutes of the moisture being absorbed by the roots, the plants will be photosynthesizing. Their evergreenness makes them opportunists who can use soil moisture as soon as it becomes available. The leaves of the evergreen sclerophyll do not wilt so no part of the new water supply needs to be spent in rehydrating the leaves to maximize light absorption.

Succession and Aging

For the chaparral community, disturbance = diversity. It rapidly recovers from disturbance by fire, erosion or man. Chaparral succession is unique in that it succeeds itself rather than being preceded by other vegetative types. However, grasslands will become the dominant community if the previously chaparral-covered area burns many times within a short period. This reduces the chance of regrowth from burls or from seeds germinating, growing to maturity, and casting their seeds. Tje area is also more prone to invasion from non-native colonizing species.

When a chaparral area is prevented from undergoing burns (because of its proximity to a city for example) the accumulated biomass is so great that when the fire eventually occurs it is hot enough to destroy the underground plant structures that would otherwise guarantee the chaparral’s succession by more chaparral. These underground plant structures include buds on woody tap roots (lignotubers), burls, and underground rhizomes. However, the seeds of the chaparral shrubs remain viable after high-intensity burns and the area will eventually again become a stand of mature chaparral.

Immediately after a disturbance the herbs and forbs initially dominate because of their sheer numbers and showy flowers. Within 2 – 5 years the seedlings of chaparral plants and the shrubs resprouting from their crown roots or burls take over. Their more aggressive root systems exploit deeper water reserves and they will eventually shade out the forbs and grasses and replace them.

Productive growth is maintained in the canopy in mature unburned stands of chaparral. Common plants such as scrub oak, toyon, and holly leaf cherry all require a leaf litter that is at least 30 years old before they will germinate successfully. When the fire interval is short, for example between 10 – 15 years, these shrubs may be eliminated and the whole chaparral system replaced by grassland. Plant growth does not occur under the chaparral canopy due to lack of light, the activity of herbivores, and the fact that the seeds contained in the ground covering leaf litter are dormant.

 

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Elderberry Poisoning

Poisoning from Elderberry Juice — California

On August 26, 1983, eight people with acute gastrointestinal and neurologic symptoms were flown by helicopter to a Monterey, California, hospital. Earlier that day, they had attended a gathering for 25 persons of a religious/philosophic group in a remote area of Monterey County. Within 15 minutes after drinking refreshments, 11 persons began to have nausea and vomiting. The eight persons most ill reported nausea, vomiting, abdominal cramps, and weakness. Some also complained of dizziness and numbness; one was stuporous and was hospitalized.

Arterial blood gases were normal for all eight, as were serum cyanide levels (reported later). The San Francisco Bay Area Regional Poison Control Center was promptly consulted regarding treatment for possible cyanide poisoning, but specific treatment was not given because 4 hours had elapsed since exposure, blood gases were normal, and the patients were stable. All recovered quickly, including the patient hospitalized overnight.

Investigation by the Monterey County Health Department revealed that staff at the religious center had gathered local, wild elderberries 2 days before the outbreak and had prepared juice from them the next day. Bunches of berries were crushed with their leaves and branches in a stainless-steel press.

Apple juice, water, and sugar were added, and the mixture was stored overnight. The drink was served the next day in a stainless-steel pot to the group of 25 persons. The severity of illness correlated with the amount of elderberry juice consumed; those who drank only tea remained well. The hospitalized person had consumed five glasses of the juice; the others, much less.

Editorial Note

Editorial Note: The indigenous elder tree of the western United States, Sambucus mexicana, can grow to 30 feet and produces small (1/4-inch), globular, nearly black berries that can be covered with a white bloom at maturity. The berries are juicy and edible when mature. The cooked berries are commonly eaten in pies and jams, and berry juice can be fermented into wine.

The fresh leaves, flowers, bark, young buds, and roots contain a bitter alkaloid and also a glucoside that, under certain conditions, can produce hydrocyanic acid. The amount of acid produced is usually greatest in young leaves. There may be other toxic constituents in this plant. The root is probably the most poisonous and may be responsible for occasional pig deaths; cattle and sheep have died after eating leaves and young shoots.

Although a review of the medical literature revealed no other reports of elderberry juice poisoning in the past 20 years, there are older, anecdotal reports of poisoning in children from the related elder, S. canadensis. The religious center staff has been advised that, while elderberries may be safe to consume, particularly if cooked (uncooked berries may produce nausea), leaves and stems should not be crushed when making juice.

Reported in California Morbidity (February 24, 1984) by S Kunitz, MD, RJ Melton, MD, T Updyke, Monterey County Health Dept, D Breedlove, PhD, California Academy of Sciences, San Francisco, SB Werner, MD, California State Dept of Health Svcs. Bibliography Casarett LJ, Doull J, eds. Toxicology: the basic science of poisons. New York: Macmillan Publishing Company, 1975. Kingsbury JM. Poisonous plants in the United States and Canada. Englewood Cliffs, New Jersey: Prentice-Hall, 1964. Millspaugh CF. American medicinal plants. New York: Dover Publications, Inc. Muenscher WC. Poisonous plants of the United States. New York: Macmillan Company, 1951. Osol A, Farrar GE. The Dispensatory of the United States of America. 25th ed. Philadelphia: JB Lippincott Company, 1955. Pammel LH. A manual of poisonous plants. Cedar Rapids, Iowa: The Torch Press, 1911.

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History of Marshmallow

Marshmallows come from the sweet sap of the ‘Mallow’ Plant that grows in salty marshes near large bodies of water and grows 2 to 4 feet high.

Hence! MARSH + MALLOW = MARSHMALLOW

The ancient Egyptians used the mallow root for making their candied delicacies for their Gods, Nobility, and Pharaohs over 2000 years ago. Since it was a crime for anyone else to eat this sugar-like treat, children looked to honey and figs to cure their sweet tooth.

Egyptian marshmallows were a mixture of Mallow sap, honey, and grains and baked into cakes. The Romans and the Greeks loved the Mallow Plant; they believed that brewed mixtures of the Mallow sap cured soar throats and pains. The sugar mixture was found in Hippocrates’s medical treatments. During the 15th and 16th centuries, marshmallow liquids were given as treatments for toothaches, coughs sore throats indigestion, and diarrhea It was even believed to have been used as a love potion at this time.

It was the French during the 1800s that changed the use of the mallow plant from mainly medicinal to more of a candy consumed by adults. French shop owners discovered that cooking and whipping marshmallow sap with egg whites and corn syrup created an easily moldable substance. This is where the marshmallow as we know it today was born!

In the 1900’s marshmallows were being sold as penny candies in tiny tins. It was at this time that the Boyer Brothers, interested in growing their neighborhood business, started experimenting with marshmallow creme and tried to cover it in chocolate. After many unsuccessful attempts, their mother Emily suggested they put it in a paper cup, using the only thing that they had available- a paper cupcake holder. They tried once more, and… Success! The Mallo Cup was born!

“Do they still make Mallo Cups?” The answer to this is yes and will always be yes! Boyer Candy Company has been proudly making delicious nostalgic candy since the 1930s and has built up a reputation and history just as long and rich as the marshmallow history above! Mallo Cups were the very first cup candy produced in the United States and are still adored by people of all ages. The delicious combination of marshmallow and chocolate has made this nostalgic candy a favorite among all candy lovers.

Mallo Cups have given Boyer Candy Company its place in the wonderful marshmallow history timeline. This delicious and unique candy has been a popular part of candy history since its introduction many, many years ago and remains one of the most popular American-made candies still produced. Some might call Mallo Cups a retro candy, but something this delicious is timeless. Find Mallo Cups and more at BoyerCandies.com today.

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Root fungi turn rock into soil

Trees help to break down barren rocks into soil, but how does that work exactly? It turns out that tiny fungi living on the trees’ roots do most of the heavy work.

Mycorrhiza fungi

The fungi first bend the structure of certain minerals, weaken their crystals, and then remove any useful chemical elements to pass on to their host tree. During the process, the rocks change their chemistry, lose their strength, and in the long run, become soil.

These hard-working fungi are called mycorrhiza and cover the roots of trees like gloves. They are extremely small and thin, but they are everywhere: ‘it is estimated that every kilogram of soil contains at least 200 km of fungi strands,’ says Dr Steeve Bonneville, from the University of Leeds.

Bonneville explains: ‘Mycorrhiza has a perfect business relationship with plants and especially trees.’ They help the plant to get nutrients from the soil and in return, they receive part of the carbon produced during photosynthesis.

About 90 percent of tree roots in boreal forests have this symbiotic association with mycorrhiza.

Mycorrhiza plays a major role in soil formation, but how do they do it? ‘We created the first experiment that closely copies a natural system to find out how mycorrhiza helps to break down minerals,’ says Professor Liane G. Benning, the Leeds principal investigator of the project.

Scots Pine seedling growing along a biotite (Bt) flake.
Scots Pine seedling growing along a biotite (Bt) flake.

Together with colleagues at Sheffield, the team planted a Scots pine seedling with the fungi Paxillus involutus, a mycorrhiza species. ‘This is a very common tree-fungi association that occurs naturally in boreal forests,’ says Bonneville. The tree and fungi were allowed to grow together for about 10 weeks and were then placed in a transparent pot with flakes of biotite, a common rock-forming mineral rich in potassium, iron, and magnesium.

The seedling’s roots became covered with fungi, which soon attached to the biotite. After three months, the scientists removed the biotite from the experiment and sampled the crystal along a single strand of fungi-covered root from the tip, middle, and close to the root.

Bend first, steal later

‘The first change we observed in the biotite, at the tip of the mycorrhiza, was mechanical stress,’ says Benning. The fungi can apply pressure onto the minerals that can be as high as the pressure in an average car tyre. This pressure value is ‘very high’, for a tiny organism, but unsurprising to Bonneville: ‘These fungi evolved to penetrate minerals and rocks and some species are capable of even higher pressures.’

As a consequence of the pressure at the tip, the biotite starts to bend and lose its strength. ‘Once the crystal structure is weakened, the chemical changes start,’ explains Benning. The mycorrhiza then proceeds to remove the potassium and other useful nutrients from the biotite, passing them on to the roots and ultimately the tree. Without potassium, the biotite breaks down into vermiculite and ferrihydrate, two minerals common in soils.

The mechanism – bend the structure first, steal nutrients later – is an efficient way for the fungi to break down minerals and at the same time gather essential nutrients for its host tree, write the authors of the report, published in July’s edition of the journal Geology.

‘This is a significant advance on previous simplistic ideas of mineral breakdown,’ says Benning.

S. Bonneville, M.M. Smits, A. Brown, J. Harrington, J.R. Leake, R. Brydson and L.G. Benning. Plant-driven fungal weathering: Early stages of mineral alteration at the nanometer scale Geology July 2009, v. 37, p. 615-618, doi:10.1130/G25699A.1

 

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FARMING A CLIMATE CHANGE SOLUTION

Farmers have a golden solution to global warming largely missed by climate change pundits, right beneath their feet. The innovative Australian Soil Carbon Accreditation Scheme is showing how incentive payments can be received by landholders for measurable increases in soil carbon that soaks up CO2 from the atmosphere. Financial incentives could help fund soil restoration efforts, which in turn bring the bonus of greater productivity, drought resilience and even rain. The action is deep underground.

 

By increasing soil carbon through biologically based techniques, Australian farmers can benefit the environment and their budgets.

Australian soil scientist Dr Christine Jones is frustrated that the world hasn’t fully cottoned on to the important role of healthy crop roots and soils to draw down massive amounts of carbon, buffer drought and re-supply essential nutrients which have been drained from our landscape and farm produce by traditional agricultural practices.

Her 10-year crusade to raise the profile of soil carbon processes and what she calls the microbial ‘carbon highway’ led to the foundation of the organization Amazing Carbon and then to the development and leadership of the Australian Soil Carbon Accreditation Scheme (ASCAS).

ASCAS is a vehicle to demonstrate through farm trials that with biologically based protocols involving perennial (long-lived) deep-rooted pastures and annual crops, measured increases in vital soil carbon can be achieved quickly and rewarded with incentive payments for the CO 2 sequestered. The scheme is the first of its kind in the Southern Hemisphere, making Australia an early leader in the recognition of soils as a verifiable carbon sink.

The ASCAS project is also collecting much-needed hard data on soil carbon accumulation rates across various properties and soil types in the Northern Agricultural Region (NAR) of Western Australia and central Queensland, two of the areas hardest hit by climate change.

After the oceans, the soil is the earth’s largest carbon sink – but plants are the facilitators. Through photosynthesis plants convert CO 2 to sugars to power growth, releasing oxygen into the atmosphere. The activities of symbiotic bacteria and fungi, associated with roots and fed by the sugars, enable the exuded carbon to be combined with soil minerals and made into stable humus1 which locks the carbon away.

The fundamental processes which produce humified soil carbon are part of the microbial bridge – the focus of Dr Jones’ interest – and the key to the formation and maintenance of healthy topsoils with high moisture-holding capacity, which largely determines plant and crop productivity.

‘This can’t happen where farm chemicals kill the essential soil microbes,’ says Dr. Jones. ‘When chemical use is added to intensive cultivation, which exposes and oxidizes the humus already in the soil, it is easy to see why soil has become a huge net source rather than a net “sink” for atmospheric CO2 under current farming practices.’

Alongside this, the removal of groundcover interrupts the important water and climate cycles facilitated by plants. Photosynthesis is a cooling process. Lack of green cover on the land greatly increases heat absorption, causing a dramatic increase in evaporation. Water vapor is a greenhouse gas of greater significance for global warming than CO 2. Lower rainfall can also result from groundcover loss.

Under conventional cropping practices, soil carbon in Australia has declined to one-half to one-third of original levels. CSIRO research has found that the rate of carbon sequestration resulting from good continuous pastures is enough to maintain or increase soil carbon levels, but all other crops/pasture rotations cause a decline of surface soil carbon.

1. A duster applies fungicide to a crop in Virginia in South Australia. While they convey short-term benefits, the application of chemicals to farm soils harms their function and fertility over the long term, causing the release of carbon.2.Carbon-poor farmland after rain (right), showing waterlogging due to poor structure. The denser groundcover of the adjacent stock route (left) results in higher soil carbon, better structure, and improved water-holding capacity.

Dr. Jones claims that conventional approaches to modeling soil carbon, while useful for describing soil carbon loss, are inadequate for determining soil carbon gain. Soil carbon models such as Roth C do not take into account the humification of root exudates or contributions from mycorrhizal fungi. ‘Sequestration rates under regenerative agricultural regimes may be quite a bit higher than estimated by current models,’ she says.

The scheme is the first of its kind in the Southern Hemisphere, making Australia an early leader in the recognition of soils as a verifiable carbon sink.

A cow browses one of many rows of tagasaste planted on Bob Wilson’s property at Lancelin, WA.

Tim Wiley, Development Officer with Western Australia’s Department of Agriculture and Food, was quick to realize the great potential of soil carbon increases with perennials. Wiley has been supporting the ASCAS trials in the NAR of WA. ‘The trend is clear – perennial pastures sequester 5 to 10 tonnes of CO 2 per hectare annually.’ He says with changes to farming practice, landholders in the northern agricultural areas of WA could sequester these amounts of CO 2 over two million hectares of poor sandy soil.

‘If all WA’s agricultural soils were sequestering carbon, we would soak up WA’s current emissions. This would have the potential to significantly decrease Australia’s net emissions and meet our Kyoto obligations.’

Add in the rest of Australia’s agricultural land area – and the world’s – and the impact on global CO2 levels is evident. Wiley pointed to current cost and data limitations to quantitative measurements of soil carbon. ‘We don’t know enough about carbon under different farming systems,’ he said. ‘We have data from farmer sampling before and after perennials were planted and over-the-fence comparisons, but it is not rigorous enough.

‘To trade carbon we need a working model such as Roth C for estimating changes in carbon. The model results would be verified by occasional soil sampling of farmers’ paddocks. Roth C needs to be validated with data from long-term trials in the regions that accurately measure carbon.’ That’s where the ASCAS trials are filling in the picture.

Up at Lancelin, about 140 km north of Perth, things have been tough during the last 10 years of below-average rainfall. But cattle farmer Bob Wilson hasn’t been too fazed; since changing his farming system over the past 20 years from traditional annual pastures to the fast-growing fodder shrub, tagasaste, and subtropical perennial (permanent) grasses, his farm has ridden out the dry far better than most, producing good returns.

As a member of the Evergreen Farming Group, he hasn’t been surprised by the exciting results of the ASCAS trials. His band of farmers advocates growing hardier perennial plants which improve the soil and help stave off salinity. Two decades ago the view to the future of farming opened up for Wilson and his colleagues, and it looked much greener.

Unlike some of the other farmers involved in the ASCAS trials, Wilson has been growing perennials for some time. Using the scheme’s protocols he has been able to measure soil carbon on his land and quantify to some extent how it can improve yields, increase water and nutrient retention for greater farm vigour, and now, potentially bring useful credit income for sequestering carbon dioxide.

He now has half his 2000 ha under tagasaste in wide rows with annual pastures in between. ‘I changed my farming system because of concern for the environment, wind erosion, and our need for an extended grazing season. We have doubled our carrying capacity.’

But he points out that while subtropical perennials provide an extended period of green feed, they grow slowly during winter and are susceptible to frosts. ‘We need annuals as well for winter feed. A mixture of pasture types is best, on a case by case basis,’ he says. When Tim Wiley dug soil pits in Bob Wilson’s paddocks, he found perennial grass roots at the bottom of a 2.5 m deep pit and tagasaste roots at the bottom of a 3 m pit. He calculated from the soil test and other results that the perennial grasses and tagasaste were sequestering 7 t/ha of CO2 per year more than traditional annual
pastures.

Department of Primary Industries and Fisheries Extension Agronomist Stuart Buck and Principal Technical Officer Maurie Conway drill sample soil cores as part of ASCAS trials northeast of Clermont in central Queensland. Testing is repeated in the same place each year to determine annual changes in soil carbon content. The soil under this crop contained over 3% carbon at the surface and 4% total carbon at 110 cm.

The group of 12 farmers involved in ASCAS ‘benchmarking’ in the Northern Agricultural Region of WA over the last year will later in 2008 be completing calculations to see how much carbon has been sequestered under their perennial pastures. Baseline soil carbon levels in five increments in the 110 cm soil profile were determined during August 2007 within Defined Sequestration Areas on their properties.

Results from the first 12 months of field trials in Queensland will also be known later this year. Dr. Jones says the initial findings have been exciting. ‘One of the broadacre cropping properties north-east of Clermont in Queensland that is participating in the ASCAS project has more than three times the amount of carbon in the farmed soil than there is under the surrounding native vegetation (149 tonnes of carbon/ha under native vegetation versus 516 tonnes of carbon/ha under the crop). As a result, the soil is far more productive. The wheat crop yielded 4 tonnes per hectare of grain with 13.5 percent protein this year – well above the district average.

‘This demonstrates that with the right kind of farming (in this case zero till with microbial stimulants in place of harsh fertilizers) we can dramatically improve soil health. I’m not saying we should replace native vegetation with farmed land – far from it. What I am saying is there is still hope for much of the land that we have inadvertently almost totally destroyed,’ she observes.

1. Carbon-rich topsoil from beneath perennial grass (left hand) compared to adjacent carbon-poor soil (right hand). By holding more air, sustaining moisture, and having higher bioavailabilities of soil nutrients, carbon-rich soils benefit plants and soil biota.2.Plant roots provide habitat for soil biota and exude carbon, both of which are important for humification and soil-carbon stabilization. Continuous grazing stunts grass root systems (left), which are more robust under rest-rotation grazing (right).

Under the Australian Soil Carbon Accreditation Scheme, participating farmers will receive Soil Carbon Incentive Payments (SCIPS) calculated at one-hundredth the 100-year rate ($25 per tonne CO 2 sequestered).

The incentive payments made to farmers are a private donation from Rhonda Willson, Executive Chairman, John While Springs (S) Pte Ltd and Director, Gilgai Australia.

Receipt of Soil Carbon Incentive Payments will be similar to being paid ‘on delivery’ for livestock or grain, with the bonus being that sequestered carbon remains in the soil, conferring multiple landscape health and productivity advantages.

Agricultural soils have short-, medium, and long-term potential to mitigate climate change by sequestering atmospheric carbon as beneficial humified organic matter. Results from overseas studies indicate that the carbon sequestration potential of appropriately managed farmlands can be higher than that of tropical forests. In countries such as Brazil, Colombia, Costa Rica, Mexico, and Cuba, the science of soil carbon is the subject of active research and development.

Dr. Jones says the rationale for the ASCAS trials was to demonstrate that significant quantities of soil carbon could be sequestered on Australia’s commercial properties, even under difficult environmental conditions, provided appropriate land management technologies were employed.

Dr. Christine Jones is advocating more focus on the role of soil carbon mechanisms in restoring landscapes and sequestering atmospheric carbon.

Apart from needing to be rapid, stable, and applicable to large areas, soil carbon sequestration as an effective climate mitigating tool must involve low-cost, easily implemented, innovative land management techniques that differ substantially from ‘business as usual. There also needs to be effective monitoring, evaluation, and verification, particularly when measures of carbon sequestered might be linked to a financial mechanism.

At present, an emissions trading scheme does not operate in Australia, although a national scheme is planned in line with the government’s recent ratification of the Kyoto accord. Rio Tinto Coal Australia is currently one of the organizations funding research into soil carbon and its potential for a future carbon trading scheme under ASCAS.

Recent good news is that Australian agricultural products company Incitec Pivot Ltd has also come on board as a supporter of the Queensland field trials. Of the estimated 3060 gigatonnes of carbon in the terrestrial biosphere, 82 percent is in soils.2 That’s over four times the amount of carbon stored in the world’s vegetation. Dr. Jones asks, ‘If only 18 percent is stored in vegetation, why all the emphasis on biomass, rather than soil, as a carbon sink?

‘The answer is that people – including most of our top scientists – simply don’t understand soil carbon sequestration or the role of the microbial bridge and have therefore overlooked it.

‘ASCAS was established so that farmers could receive incentive payments for increases in their soil carbon. We’re demonstrating the incredible rates at which carbon can be put into soil by roots in biologically based sustainable cropping and grazing systems,’ she says.

‘Effective soil carbon management is a key factor for productive farms, revitalized catchments, and a greener planet.

‘Incentive payments for regenerative land management would help to “cash flow” the multiple natural resource management and environmental benefits that accompany increased levels of carbon in soils.’

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Mycorrhizal Fungi Nitrogen Transfer Discovery

Another source of nitrogen uptake unique to mycorrhizal symbiosis has recently been discovered – it involves the direct transfer of nitrogen-laden amino acids from the fungus into the cereal plant roots. 1. Amino acids inside mycorrhizal hyphae 2. Amino acids have entered the root from mycorrhizal hyphae

Let’s begin with a topic that interests all farmers and one to which nearly all the other benefits of mycorrhizae are inherently linked: improving crop yields. Typically, mycorrhizae’s single most prominent contribution to a crop plant is improved access to and uptake of phosphorus (P).

All farmers are intensely familiar with the importance of this elemental nutrient to essential plant functions, which include energy transfer, photosynthesis, the transformation of carbohydrates, systemic nutrient mobilization, and genetic transfers. Given that often one of the most noticeable evidence of P deficiency in a crop is reduced yield (or in forage and pasture reduced quantity), it is no wonder that P is such a critical (and expensive) component in crop fertilizers.

Much of the naturally-occurring P in soils is found bound tightly with elements such as iron or aluminum in the form of recalcitrant compounds. Similarly, P inputs derived from fertilizers often react with ambient soil cations to form insoluble salts. In natural ecosystems, plant communities rely on mycorrhizal fungi to access these forms of phosphorus.

Mycorrhizal hyphae produce enzymes, including phosphatase to convert phosphorus into soluble, plant-usable forms. This same process can be valuable in agriculture, maximizing the availability of natural soil P as well as dramatically enhancing the efficient uptake of P derived from fertilizers. With greater P uptake, costs go down and yields frequently increase as well.

The availability of nitrogen can also be a factor in limiting crop productivity for reasons opposite to those limiting P. Available nitrogen in the forms of nitrates (N03), nitrites (N02), and ammonium (NH4) are very soluble and can flow past the root zone before roots can absorb it. This means they are often lost to run-off or groundwater or trapped in subsoil beyond the access of roots.

The profoundly dense network of tiny hyphae filaments in a mycorrhizal system typically extends 45 to 60 centimeters beyond the roots themselves, increasing the absorptive surface area of colonized roots hundreds to thousands of times. A teaspoon of mycorrhizal soil can easily contain several kilometers of hyphae, all of which are highly absorptive of soluble nitrogen ions, ensuring optimum uptake and the associated nitrogen-related cropping benefits.

Another source of nitrogen uptake unique to mycorrhizal symbiosis has recently been discovered by scientists at the University of California, Irvine, US. The researchers set out to explore how nutrients, including nitrogen, are mobilized through the environment. Using cutting-edge technology, nanometre-sized bits of a semiconducting material called quantum dots were attached to organic compounds such as nitrogen-laden amino acids.

Nutrient transfer discovery

When energised by an ultraviolet laser, the tiny dots emitted light, becoming detectable by special cameras positioned in the root zone of plants. In this manner, the scientists could track nutrients as they were absorbed into the microscopic mycorrhizal hyphae and follow their subsequent movement into the tissue of the host plant.

For more than 100 years conventional scientific wisdom held that root absorption of nitrogen was restricted to inorganic forms of nitrogen such as N03, N02, and NH4. But to their surprise, the scientists saw the illuminated dots attached to amino acids enter the mycorrhizal hyphae and observed them as entire molecules moved into the root cell vacuoles and then continued systemically to the chloroplasts (in which nitrogen is used for photosynthesis).

MYCORRHIZAE

In non-mycorrhizal rhizospheres, amino acids, which are the primary components of proteins, must undergo extensive and time-consuming decomposition processes by bacteria and other soil organisms before nitrogen is released in inorganic, plant-usable forms. In many cases, much of the nitrogen is consumed by the organisms, further delaying its plant availability.

This research demonstrates that mycorrhizal fungi allow their plant hosts to bypass this process, implementing quick and effective access to organic nitrogen sources. What this means to the farmer is that utilizing mycorrhizal fungi, naturally occurring and introduced sources of organic nitrogen (such as found in fish-based fertilizers, green manures, and compost) can provide a readily available source of nitrogen to promote crop growth and enhance yields.

In addition to phosphorus and nitrogen, the mass of hyphal filaments in the soil surrounding mycorrhizae-colonized roots is also capable of mobilizing an array of other important plant nutrients, including calcium, iron, magnesium, and critical micro-nutrients such as manganese, zinc, and copper. Just as a lack of vitamins can impair human or animal health, crop yields and forage production are sometimes limited by insufficient supplies of these minor- and micro-nutrients, even when N-P-K is abundant.

Mycorrhizae’s ubiquitous presence throughout the surrounding soil can access these relatively scarce resources and, in many cases, can release them from insoluble compounds via the production of specialized enzymes. The management of micro-nutrients is becoming increasingly recognized as an important component of modern cropping science. Mycorrhizal fungi can serve as a useful tool to ensure that both natural and introduced sources of these nutrients are transferred efficiently from the soil to the plant.

When moisture becomes limiting in a dryland period the mycorrhizal plant utilizes the water stored in root cell vesicles.

Help find water

Mycorrhizae’s significant assistance with nutrient uptake is important, but it is not the only crop-enhancing benefit offered by these amazing fungi. Another valuable feature is water management. The expanded and enormous absorptive surface area connected to the roots is going to ensure that nearly all moisture in a plant’s surrounding soil is accessed. But what then? Once the soil is dry, how can the plant survive?

Mycorrhizae provide a mechanism inside the root cells that addresses this problem. When a root cell becomes colonized by a mycorrhizal fungus, a special shared organ called a vesicle grows inside the root cell. The vesicle is essentially a storage container for water and dissolved nutrients that can be utilized in times of deficiencies, such as drought periods.

When moisture and nutrients are abundant in the soil, surplus supplies are stored in the vesicle. When moisture and/or nutrient shortages occur, the plant begins to utilize the resources stored in the vesicles to avoid stress for extended periods – often weeks or even months longer than non-mycorrhizal plants.

When moisture or nutrients again become available, the plant is able to return to normal, healthy respiration and growth without shock or other negative symptoms. Of course, the reservoir provided by the vesicle cannot last indefinitely and the plant will suffer stress and ultimately death if sufficient moisture or nutrients remain unavailable for too long.

However, in most cases the extra non-stressed time provided via the vesicle allows the plant to survive until the next rainfall. This is great news for the dryland farmer. Australia’s recent excessive rainfall notwithstanding, drought is a serious risk encountered by all dryland farmers. Although not infallible, mycorrhiza inoculation offers inexpensive crop insurance as one of its many benefits.

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Our soils, our future

Introduction

There has been a notable ‘climate shift’ in many of the arable regions of eastern, southern and western Australia. A trend to less reliable autumn, winter and spring rainfall has increased production risks for annual cereal crops, while the greater incidence of episodic high intensity rainfall events in summer has heightened the vulnerability of bare fallows to erosion. Declining rainfall experienced over the last 7-10 years has severely impacted on the financial viability of cropping and grazing enterprises and disrupted the social fabric of rural communities.

These events have highlighted a fundamental lack of resilience in current agricultural production systems.

Historical losses of soil and soil carbon

In little over 200 years of European settlement, more than 70 percent of Australian agricultural land has become seriously degraded. Despite efforts to implement ‘ best practice’in soil conservation, the situation continues to deteriorate.

On average, 7 tonnes of topsoil is lost for every tonne of grain produced. This situation has worsened in recent years due to an increased incidence of erosion on unprotected topsoils, coupled with declining yields.

The most meaningful indicator for the health of the land, and the long-term wealth of a nation, is whether soil is being formed or lost. If soil is being lost, so too is the economic and ecological foundation on which production and conservation are based.

In addition to the loss of soil itself, there has been a reduction of between 50% and 80% in the organic carbon content of surface soils in Australia since European settlement (2, 3, 4, 11, 12).

Losses of carbon of this magnitude have immeasurable economic and environmental implications. Soil carbon is the prime determinant of agricultural productivity, landscape function and water quality.

Further, the carbon and water cycles are inextricably linked. Humus holds approximately four times its own weight in water (8). The most beneficial adaptation strategy for climate change would therefore be one that focuses on increasing the levels of both carbon and water in soils.

Discussions on adapting to climate change are irrelevant unless they focus on rebuilding healthy topsoil.

Building new topsoil

Healthy groundcover, active root growth and high levels of microbial association (7), are fundamental to the success of any endeavour to build new topsoil. These factors are absent from conventionally managed broadacre cropland.

Current ’best practice’, that is, chemically-based zero-till broadacre cropping (Fig.1) does not provide a suitable environment for high levels of biological nitrogen fixing, nutrient cycling, hydraulic redistribution, active sequestration of humified soil carbon, or soil building.

 

Fig.1. Current ‘best practice’. Chemically based zero-till farming lacks essential requirements for biological N-fixing, sequestration of humified soil carbon, and building of new topsoil.

Fortunately, the highly effective land management technique of ‘perennial cover cropping’ (Figs. 2, 3, and 4) has become more widely adopted in recent years. This practice involves the direct drilling of annual grain or fodder crops into ‘out-of-phase’ dormant perennial groundcover.

Fig.2. The ‘new face of agriculture. Annual grain crop direct-drilled without herbicide into dormant perennial groundcover enhances plant-microbial associations, vastly improves rates of biological N fixation, stimulates nutrient cycling, facilitates sequestration of highly stable, humified soil carbon, and promotes the formation of new topsoil.

The essential first step to rebuilding topsoil is to maximize photosynthetic capacity. A permanent cover of perennial plants provides an ongoing source of soluble carbon for the soil ecosystem, buffers soil temperatures, inhibits weeds, reduces erosion, improves porosity, enhances aggregate stability and water infiltration, slows evaporation, and ‘conditions’ the soil for the production of healthy, high quality, over-sown annual crops.

The soluble carbon exuded into the rhizosphere by perennial groundcover plants and/or transported deep into the soil by mycorrhizal fungi provides energy for the vast array of microbes and soil invertebrates that produce sticky substances enabling soil particles to be glued together into lumps (aggregates). When soil is well aggregated, the spaces (pores) between the aggregates allow the soil to breathe, as well as absorb moisture quickly when it rains. Healthy topsoil should be ‘more space than stuff’, that is, less than 50% solid materials and more than 50% spaces.

Friable, porous topsoils make it easier for plant roots to grow and for small soil invertebrates to move around. Well-structured soils retain the moisture necessary for microbial activity, nutrient cycling, and vigorous plant growth and are less prone to erosion. Soil structure is very fragile and soil aggregates are continually being broken down. An ongoing supply of energy in the form of carbon from the rhizosphere exudates of actively growing plants and, to a lesser extent, decomposing organic materials, enables soil organisms to flourish and produce adequate amounts of the sticky secretions required to maintain soil structure and function.

Healthy, chemical-free soils also create appropriate conditions for humification (conversion of soluble carbon to humus), a process that does not occur in most conventionally managed agricultural soils.

Fig. 3. Modern machinery is well suited to sowing annual grain crops into dormant perennial groundcover, a technique known as perennial cover cropping.

Cropping into dormant perennial groundcover is a one-pass operation that markedly reduces fuel costs and largely eliminates the need for fossil-fuel-based herbicides, fungicides, and pesticides. Perennial cover cropping has many similarities to annual cover cropping but brings with it the ecosystem benefits of perennial groundcover. The practice of perennial cover cropping was inspired by the highly innovative integrated cropping and grazing technique of ‘pasture cropping’ initiated by Darryl Cluff over a decade ago and further developed by Colin Seis (1, 5, 6).

The use of ‘biology friendly’ fertilizers, particularly those based on humic substances, in combination with Yearlong Green Farming (YGF) techniques such as perennial cover cropping, can have a protective effect on soil carbon, slowing or preventing its decomposition and further reducing the carbon footprint of agriculture.

There is no valid reason for the Australian agricultural sector to be a net emitter of CO2.

The world’s soils hold three times as much carbon as the atmosphere and over four times as much carbon as the vegetation. With 82% of terrestrial carbon in soil (compared to only 18% in vegetation), soil represents the largest carbon sink over which we have control. Soil is also the world’s largest store of terrestrial diversity, with over 95% of life forms being underground (that is, only 5% of biodiversity is above ground).

Sequestering humified carbon in soils represents a practical, permanent and productive solution to removing excess CO2 from the atmosphere. By adopting regenerative soil-building practices, it is practical, possible, and profitable for broadacre cropping and grazing enterprises to record net sequestration of carbon in the order of 25 tonnes of CO2 per tonne of product sold (after emissions accounted for).

Australia’s annual emissions of CO2 are predicted to reach 603 million tonnes in 2008.

There are therefore 603 million good reasons for agriculture to be a net sequester of CO2.

It would require only a 0.5% increase in soil carbon on 2% of agricultural land to sequester all Australia’s emissions of carbon dioxide (1). That is, the annual emissions from all industrial, urban, and transport sources could be sequestered in farmland soils if the incentive was provided to landholders for this to happen.

This would provide Australia with a 50-year window of opportunity to be carbon neutral while implementing viable technology to meet future energy needs.

Australian Soil Carbon Accreditation Scheme (ASCAS)

Dr. Christine Jones launched the Australian Soil Carbon Accreditation Scheme (ASCAS) in March 2007. ASCAS is a stand-alone incentive scheme with voluntary involvement, which encourages the adoption of innovative soil building practices (9). Widespread implementation of techniques developed by leading-edge landholders (as depicted in Figs. 2, 3, and 4) will transform the agricultural sector. Adoption of these processes needs to be fast-tracked.

ASCAS is the first incentive payments scheme for soil carbon in the Southern Hemisphere, placing Australia among world leaders in the recognition of soil as a verifiable carbon sink.

Incentive payments for annual measured increases in soil carbon above baseline levels have been sourced from a private donation by Rhonda Willson, Executive Chairman, John While Springs (S) Pte Ltd, Singapore. Receipt of Soil Carbon Incentive Payments (SCIPs) is similar to being paid ‘on delivery’ for livestock or grain, with the bonus being that sequestered carbon remains in the soil, conferring multiple landscape health and productivity advantages. Soil Carbon Incentive Payments are calculated at one-hundredth the 100-year rate ($25/tonne CO2-e).

A 0.5% increase in soil carbon across only 2% of agricultural land would sequester 685 million tonnes of CO2, well above the country’s annual emissions. (Assumptions: 0-30cm soil profile, bulk density 1.4 g/cm3, land area 2% of 445 million hectares).

Annual payments to landholders based on measured soil parameters provide an incentive for maximizing soil carbon sequestration and maintaining the permanency of sinks.

The amount of humified carbon in soil is directly related to nutrient bioavailability, soil structural stability, soil water-holding capacity, agricultural productivity, and landscape function. One of the aims of the ASCAS project is to collect data that will enable rigorous scientific evaluation of soil carbon, water, nutrients, and crop yield under regenerative regimes.

Adapting to climate change

There is an urgent need for Australian agricultural industries to adapt to climate change. To be effective, the strategies employed will require radical departures from ‘business as usual.

It is possible that global warming could accelerate even more rapidly than observed to date. Fundamental redesign of agricultural production systems will enable the sequestration of more carbon and nitrogen than is being emitted, as well as enhancing soil water retention, improving the resilience of the resource base, and restoring richness to farmed soils. These much-needed changes will assist the agricultural sector to deal confidently with a changing climate.

Rather than increase costs, mitigation of climate change via the adoption of regenerative soil building practices would bring net financial benefits to landholders and rural communities (the sectors hardest hit by climate change).

Fig 4. Emerging wheat crop one month after sowing into the dormant perennial pasture. Large volumes of soluble carbon are fixed in green leaves during photosynthesis, transferred to roots, and thence to soils via the hyphae of mycorrhizal fungi. After grain harvest, the warm-season native perennial pasture will activate and continue the sequestration process, building soil carbon over the summer period.

Yearlong Green Farming (YGF) techniques such as perennial cover cropping rapidly build humified soil carbon, improving the capacity of soil to hold water and increasing the resilience of farming systems to climatic extremes.

Farming in a perennial base

A change to farming in a perennial base has many advantages, including

  1. same or better yield than chemical fallow or cultivation-style farming

2. fewer inputs, resulting in higher gross margins per hectare

3. less reliance on fossil fuel-based fertilizers and farm chemicals

4. enhancement of natural soil building processes

5. ‘reverse’ carbon footprint – more carbon sequestered than emitted

6. ‘reverse’ nitrogen footprint – more nitrogen fixed than emitted

7. increased water use efficiency due to lower evaporative demand

8. improved soil water balance due to hydraulic lift and hydraulic redistribution

9. no bare soil for weeds to grow – paddocks virtually weed-free

10. reduced financial risk – no expenditure if a crop is not sown

11. an additional income stream from harvest and sale of perennial grass seed

12. more time for family – little or no requirement for cultivation or herbicide application

13. higher biodiversity of plants and animals (eg bettongs returning on some farms)

14. incentive for all members of the farm family, including children, to become involved

The new face of agriculture

Widespread adoption of productive and resilient agricultural practices that enhance net sinks for atmospheric carbon would have a revitalizing effect on the natural resource base and provide a financial benefit to the government, individuals, and rural and regional communities.

Furthermore, farming in a perennial base would enhance the resilience of the agricultural landscape to a wide range of climatic extremes, some of which may not even have been encountered to date.

The development of an appropriate incentives framework for regenerative agricultural activities would reverse the farm sector’s carbon and nitrogen footprints (more C and N sequestered than emitted) and improve food security in a warming, drying environment.

An overview of the Australian Soil Carbon Accreditation Scheme (ASCAS) has been provided as an example of an incentive-based (rather than regulatory) approach. The ASCAS project is an initiative designed to provide proof of concept that: –

  1. innovative soil management practices exist for sequestering soil carbon

2. improvements in soil carbon and soil health can be measured

3. landholders can be financially rewarded for building soil carbon

The ASCAS project supports soil restoration by providing financial incentives for landholders to move away from ‘business as usual’ (that is, carbon depleting activities) and by improving community knowledge on effective methods for building soil carbon.

Irrespective of climate change, it would be of enormous economic benefit to the agricultural sector to rebuild soils by implementing practices that increase levels of humified soil carbon and reduce reliance on fossil fuels.

In 1937, Franklin Roosevelt (10) stated “The nation that destroys its soil destroys itself”. The future of Australia depends on the future of our soil.

REFERENCES CITED

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Hand In Hand With The Soil

Mycorrhizae are tiny, beneficial organisms that live in the soil and connect to plant roots, providing them with moisture and nutrients. The tiny fibers are called hyphae.

Living Soil is very important to plant care. It is no surprise then that nursery professionals continue to increase their understanding of it.

Living soil includes a myriad of soil-dwelling organisms, including bacteria, fungi, soil arthropods, and a wide variety of others. One of the most intensive studies groups in recent years also has the most potential for use by nursery professionals; mycorrhizal fungi.

My-Co-Rise-ee

There is a special relationship that exists between plant roots and certain types of fungi. Which are called mycorrhizae. The name is pronounced by my-co-rise-ee. Its literal meaning is “Fungus Roots”(“myco” meaning fungus “rhiza” meaning root).

These fungi are a major component of a multitude of hardworking armies of beneficial soil organisms largely invisible to us beneath the soil surface.

The mycorrhizal relationship is a symbiotic relationship. Both the plant and the fungus benefit. Nearly all horticulturally important plants and approximately 90 percent of all higher plants depend on the mycorrhizal relationships in their natural habitats.

Mycorrhizal fungi attach themselves to plant roots and radiate out into the soil, helping their host plants absorb water and nutrients. In return, the host plant feeds the fungi with sugars, proteins, amino acids, and other needed substances. The relationship is mutually beneficial to both fungi and host plants.

MYCORRHIZAE

These hard-working fungi provide the cornerstone for sustainability of our plant communities. They provide the moisture and nutrients needed to keep plants in our natural areas healthy and functioning through tiny absorptive threads called hyphae.

We could not survive a day without them. Without their diligent munching in the soil, plants in native ecosystems all over the world would go hungry and die of thirst.

Ancient workers

Since the early days, 460 million years ago, these mycorrhizal fungi have been amazingly prolific. Miles of fungal filaments can explore a single thimbleful of healthy soil. They pluck phosphorus, nitrogen and micronutrients out of the soil with a specific arsenal of designer enzymes just right for the job.

Mycorrhizal fungi process waste and make it usable again, purify our water, and keep our plant communities productive. The wide variety of nursery plants will thrive when given the right source of mycorrhizal inoculum in areas where it has been lost to disturbance or not present in sterile soil mixes.

Mycorrhizal fungi attach themselves to the roots of plants and radiate out into the soil, helping their host plants absorb water and nutrients. In return, the host tree feeds the fungi with sugars, proteins, amino acids and other organic substances.

Fungi are made up of filaments called hyphae. A mass of hyphae is a mycelium, which can grow very rapidly. A fungus colony can produce more than a kilometer of new mycelium in 24 hours!

This growth form has a very high surface area. This is one of the attributes that makes the symbiotic relationship so successful. Mycorrhizae can spread their net of hyphae far and wide in the soil, penetrating tiny spaces in the soil where plant roots can’t go.

In addition, fungi are also capable of breaking down, or converting, some nutrients such as nitrogen and phosphorus to forms usable by plants.

The good news and the bad news

The good news is when water and soluble nutrients are amply provided, non-mycorrhizal plants can grow well under nursery conditions. However, until they form mycorrhizae, they don’t efficiently take up water and nutrients at the nursery or upon being planted in the ground.

Routine nursery practices such as fumigation, sterile soilless growing media and chemical use produce non-mycorrhizal plants. The bad news is that target plants do not utilize much of the fertilizer used in the nursery industry because the root/mycorrhizal system is underdeveloped.

In addition, many nursery-grown plants (and their roots) are adapted to nursery conditions and not to the highly disturbed and sometimes hostile environment found in many urban and suburban settings. In these settings, the chance of a beneficial mycorrhizal fungus colonizing the roots can be low because there may be no source of inoculum readily available.

To confirm the effectiveness and benefits of mycorrhizal treatment, I conducted a test of a mycorrhizal inoculant for four important horticultural species at Village Nursery in Sacramento, Calif.

My hypothesis was that mycorrhizal fungi could be established under nursery conditions and would increase the plants’ root system capacity to effectively uptake nutrients at levels considered by conventional standards to be lower than optimum rates. I wanted to test whether inoculated plants’ growth and development would be adversely affected as a result of reduced fertilizer inputs.

The experiment

Four plant families were tested because of their popularity in the landscape industry: 1) Cotoneaster apiculata, 2) Trachelospermum jasminiodes, 3) Pinosponim uariegate, and 4) Escallonia fradesii. The experiment had three fertilizer treatments. 

1) Grower standard practice (GSP). For this control group, I applied 8 pounds Apex 23-6-12 per cubic yard (equivalent to 0.23 pounds nitrogen per cubic yard over an 8 month period). Because this was the control group, there was no mycorrhizal inoculation.

2) Apex mixed at 20 percent less than GSP. I added a fertilizer ratio of 6.5 pounds Apex 23-6-12 per cubic yard (equivalent to 0.19 pounds nitrogen per cubic yard over an 8 month period) with mycorrhizal inoculation.

3) Apex mixed at 30 percent less than GSP. I fertilized with 5.5 pounds 23-6-12 per cubic yard (equivalent to 0.15 pounds nitrogen per cubic yard over an 8 month period) with mycorrhizal inoculation.

How the experiment was conducted

For each plant species and fertilizer/mycorrhizal treatment there were 50 replications. Mycorrhizal inoculum was watered in (drenched), until water began dripping from the bottom of the 2-inch liner pots. Mycorrhizal inoculum was used at a rate of 1 pound per 200 gallons of water. Each pound treated approximately 2,000 square feet of nursery plants.

The standard fertilization (GSP) rate was not inoculated. The plots with Apex mixed at 20 percent below standard and 30 percent below standard were inoculated with Mycorrhizal inoculum. For all treatments, lime was added to the soil at the standard 7 pounds per cubic yard of soil. A premix containing other nutrients was added. It included 1 pound Nitroform fertilizer, 1 pound FeSO4 (iron sulfate) , 0.75 pounds Tiger-90 sulfur fertilizer, and 1 pound triple phosphate (fertilizing supplemental blend) per cubic yard.

All plants were allowed to continue growing for 90 days. At the end of 90 days, root systems were sampled, cleared, and stained to determine the presence of mycorrhizal colonization of the plant root systems. Afterward, plants were transplanted as 2-inch liner pots into 1-gallon containers. Plants were set up aside the GSP in the grow grounds under the typical Rain Bird irrigation system. These plants were monitored for visual differences in growth and development. Random subsamples of Rscallonia Weir were selected for biomass measurements.

Results

Mycorrhizal colonization averaged 48 percent and 56 percent for the Mycorrhizal inoculum treatments with fertilization reductions of 20 percent and 30 percent. In the untreated, or control plants, there was only 3 percent mycorrhizal root colonization. No significant visual differences were detected in plant growth development between standard growing practices and 20 and 30 percent reduction in fertilizer with Mycorrhizal inoculation. In fact, in nearly all cases, plants are grown with fertilizer reduction treatments with mycorrhizal inoculation looked as good or better than the GSP.

A subsampling of Rscallonia species biomass indicated that the plants treated with 20 percent less fertilizer had 15 percent greater biomass than plants receiving the GSP treatment.

Conclusions

Mycorrhizal inoculants are not a silver bullet but are another valuable tool available to the nursery professional. Mycorrhizal colonization was achieved by a simple inoculum drenching of the plant material. In this experiment, a significant reduction of fertilizer inputs accompanied by mycorrhizal inoculation of a plant’s root system achieved a high level of mycorrhizal colonization. The plants that received mycorrhizal inoculations and were treated with 20 percent or 30 percent less fertilizer than standard practice did not suffer adverse plant growth or development.

Establishing nursery plants on disturbed sites requires an understanding of the many soil processes important in facilitating uptake, storage, and cycling of nutrients and water. In natural areas, these activities are largely performed by a diversity of beneficial soil organisms. These include mycorrhizal fungi working hard below the living soil surface.

In past decades, clearing of natural areas, compaction, and disturbances in suburban and urban environments have substantially reduced mycorrhizal populations. Reestablishing these beneficial fungi can occur at the nursery.

The result can be substantial fertilizer savings without adversely affecting plant growth and development. The resulting will have root and mycorrhizal systems that are well suited for the out-planted environment.