White Pine Blister Rust
Hosts are members of the genus Pinus that have 5 needles per fascicle or bundle. Most taxonomic arrangements break these into two groups, although the fungus seems to disagree with that taxonomy: subgenus Strobus (the white or soft pines, all of which have 5 needles per fascicle) and subgenus Ducampopinus (the piñon, lacebark and foxtail pines; the 5-needle members are two species of bristlecone pine and foxtail pine). Species vary somewhat in susceptibility. The most prominent hosts in North America are Pinus strobus (eastern white pine), P. monticola (western white pine), P. lambertiana (sugar pine), P. albicaulis (whitebark pine), P. flexilis (limber pine) and P. strobiformis (southwestern white pine). Of these, the most effort is currently going into sugar, western white and whitebark pines. Recently, the disease was found for the first time on a bristlecone pine, P. aristata, in Colorado.
Seedlings are in greatest danger. The infection court is needles and almost any infection is likely to hit the stem, where it is lethal, because there is not much distance from the needles to the main stem when the tree is young. In older trees, top-killing can occur, which deforms the tree, and killing of branches can weaken the tree.
White pine blister rust is the only stem rust of white pines in North America.
Cronartium ribicola (Uredinales: Cronartiaceae) is a rust fungus. It is an exotic pathogen in Europe and North America. The life cycle is the most remarkable aspect of the pathogen (see below). The fungus has a macrocyclic, heteroecious life cycle. It seems like a life cycle from another planet, but some students trying to learn it say it is the life cycle from hell!
The disease is often most severe in areas and following years with extended, cool, moist conditions during late summer and early fall. Such conditions facilitate basidiospore production, dispersal and infection in pine needles. Hazard rating systems may be based in part on such weather patterns. Because of the delicacy of basidiospores and their need for good conditions, successful dispersal distances are generally about 300 meters and at most 3-4 kilometers.
Infections of pine are not consistent from year to year, but occur in "wave years," when weather is ideal. For a perennial host, such infrequent infection is sufficient to cause high incidence.
Generally, conditions are more favorable for infection close to the ground because needles stay wet longer. Because trees have branches close to the ground when they are young, infections are more likely in young trees. Infections are also likely to be lethal in young trees because the needles are close the stem, so girdling is more likely, and girdling close to the ground is usually lethal.
In some areas, the moisture that facilitates basidiospore production, survival and infection is often from dew. Conditions in openings, particularly where cool, moist air may settle, are generally considered to be favorable to disease development. Maintaining a partial overstory over developing seedlings reduces dew formation and infection levels.
Let's start with the infected seedlings that were first shipped to North America. They were already infected back in Europe, but there were probably no symptoms. The fungus would have been in the bark of the stem or branch. Eventually the infected area would be discolored and somewhat swollen.
In late summer or early fall, spermogonia appear near the margins of the canker. They produce spores called spermatia. These are like the spores produced by some of the foliage ascomycetes that you have probably learned about — they don't infect, they are only involved in fertilization. Spermatia are produced in tiny drops of sweet liquid which attract insects. The insects carry the spermatia to other spermogonia. Spermatia fuse with receptive hyphae on the spermogonia. They establish the dikaryon (n+n).
Now the fungus is ready to roll. The following spring, aecia appear about where the spermogonia were the year before. The aecia look like swollen white to yellow blisters surrounded by a membrane when young. The bright yellow aeciospores are produced within, eventually pop the blister, and are released into the air.
The aecia break down and the bark dies. The fungus meanwhile has spread into living bark around the margin. It can't survive on dead bark. Every year more aecia are produced in spring, then spermogonia farther out in late summer. It keeps spreading until the branch or stem is girdled and killed. Airborne dispersal of aeciospores is long-range, up to hundreds of kilometers. They may live for months under good conditions. Now comes the amazing part — these spores cannot infect pines, or anything else except Ribes. Ribes (gooseberry) is a genus of shrubs fairly common throughout the white pine areas. The new leaves are infected in spring.
Now mycelium grows in the Ribes leaves. Yellowish leafspots may appear, but they are often not conspicuous. Within 2 weeks, urediniospores are produced in uredinia on the undersides of leaves. They are orange.
The urediniospores are called the "repeating stage" because they reinfect Ribes, leading to production of more uredinia, in a cycle that could go on until the summer ends. Thus infection builds up on the Ribes. The urediniospores cannot infect pine.
In late summer/early fall, telia begin to be produced instead of uredinia. They are like orange-brown rough hairs, also on the underside. They are composed of rows of brick-like teliospores.
When conditions are cool and wet, each teliospore germinates in place to produce a basidium, which produces — can you guess? — basidiospores! The basidiospores are dispersed by air. They are small and quite short-lived, depending on conditions. It is generally considered that a few kilometers is about the upper limit for basidiospore dispersal.
Basidiospores can only infect pine. They enter through stomata into the needles. Within a month or so a small yellowish spot can be seen where infection occurred. The fungus grows down the needle into the bark, and the cycle is complete. Here is a summary:
Note several aspects of the disease cycle:
On pines, the first symptom may be a small, yellow or red spot on a needle, but this is difficult to find. Within a year or two, perennial cankers can be found on branches. These may become somewhat swollen and may have a yellowish margin. Cankers close to the stem may invade the stem. When a stem or branch is girdled (killed around the entire circumference) by the canker, it is killed beyond that point.
From a distance, symptoms seen are chlorotic, stunted, or dead branches (flagging) and dead tops.
On Ribes spp., yellowish leafspots may appear but these are often inconspicuous. Usually no significant impact occurs to Ribes.
White pine blister rust is apparently native to Asia. It has been introduced to Europe and then North America (see Other Issues below). In North America it has invaded most white pine areas and is still making progress into the Southwest and into southern California.
Many management approaches are available to combat white pine blister rust, but none is completely satisfactory.
Resistance. Active programs are underway to select and/or breed for resistance to white pine blister rust in P. lambertiana, P. monticola and P. albicaulis.
Ribes eradication. Pine can only be infected by basidiospores produced on Ribes plants. These spores are somewhat delicate and short-lived, so spores typically are not dispersed from Ribes to pine more than about 300 meters. For up to about 50 years in the middle of the 20th century there were substantial programs in parts of the United States to eradicate Ribes species in areas where white pine growth was important. The project was military in its size, scope and organization. It probably succeeded somewhat in the East. In the West, however, the Ribes species proved too elusive, difficult to kill and resilient, and the approach was abandoned.
Quarantine. In the past, especially in the Northeast, a major source of inoculum was from cultivated Ribes species. Many states have quarantines to prevent cultivation of such species. In some cases only the most susceptible cultivated species, Ribes nigrum, European black currant, is prohibited, and in some cases putatively resistant or immune varieties of R. nigrum are permitted. For instance, Maine law prohibits the planting and cultivation of currants and gooseberries in most of southern Maine, and prohibits the planting and cultivation of European black currants and their hybrids anywhere within the state. However, enforcement of such regulations is sometimes lax and there are increasing initiatives from growers to repeal or relax such regulation.
Transport of infected pines may spread the disease to uninfested areas. Unfortunately, white pines are becoming quite popular for landscape plantings in many parts of the West. In some cases, forests have rules prohibiting the transplanting of white pines from infested areas, and broader regulatory control over plant movement may be needed.
Hazard rating of sites. Sites likely to have good conditions for basidiospore production, dispersal and infection are high-hazard sites. Basidiospore dispersal distances tend to be longer in such sites, and conditions for infection are more frequent. These tend to be low-lying areas where cool air settles, although hazard ratings are usually unique for each geographic region. Once hazard rating is accomplished, management of white pine can be focussed on low-hazard sites.
Raising trees under understory. In some areas, a recommendation is to avoid regenerating white pines in small openings. Dew that forms on seedlings under open conditions is likely to persist in smaller openings, creating better conditions for basidiospore infection. Maintaining a partial overstory over developing seedlings reduces dew formation and infection levels.
Pruning. Branch infections are not too serious; stem infections are — they are often lethal. However, stem infections usually arise from branch infections. Pruning infected branches can prevent infections near the stem from growing into the stem, where they are likely to girdle and kill the tree. If the branch dies before the fungus reaches the next larger branch or stem, the fungus is done for. If it colonizes the stem, especially when it is small, the tree is done for.
Pruning healthy trees can also be a benefit because it decreases the occurrence of new infections, especially on young trees. It is best to prune early, prune up to 50% of tree height from the ground, and repeat until pruning extends up to about 3 meters.
This is one of the most important diseases in the history of forest pathology in North America and it continues to be a major focus for research and management. It is one of the most famous forest diseases in the world. A student of forest pathology should be intimately familiar with the life cycle and disease cycle.
The pathogen moved to Europe in the early days of plant movements. It was introduced on seedlings of Pinus strobus (eastern white pine) from Germany into eastern North America about 1898 and on eastern white pine seedlings from France into Vancouver in 1910. Why on earth, you might ask, were seedlings of a species from North America being grown in Europe and then shipped to America for planting? The United States had been cutting its forests rapidly and rapaciously, and was just beginning to realize that it needed to focus more effort on forest management and reforestation. Because Europeans had long-established nurseries and knew how to produce seedlings, much of the early production was done there. Unfortunately, some of the seedlings were infected before being shipped back.
White pine blister rust is a premier example of an introduced pathogen. Pathogens evolve with their hosts to strike some kind of balance, especially obligate parasites. There is clearly selection for ability to infect and cause disease. But if they kill too many hosts, they are biting the hand that feeds them. So in natural systems these fungi tend not to completely destroy a population of their hosts.
When you bring a pathogen in from Asia to North America, the trees are similar enough to Asian white pines to become infected, but there is no sophisticated genetic balance. The host has evolved no good mechanisms of resistance because there was never selection for them. So the disease may be more serious than similar, native diseases. That is an important concept.
You can learn more about this topic on the the Invasive Species page.