Trillium grandiflorum favors well-drained, neutral to slightly
acid soils, usually in second- or young-growth forests. In the Northern parts of its range it shows an affinity for
maple or
beech forests, but has also been known to spread into nearby open areas. Depending on geographical factors, it flowers from late April to early June, just after
Trillium erectum. Like many forest
perennials,
Trillium grandiflorum is a slow growing plant. Its seeds have double dormancy, meaning they normally take at least two years to fully
germinate. The seeds are dispersed in late summer, germinating after a cold and then a warm period, producing a root and after another winter the seedling's cotyledon emerges from the soil. Like most species of
Trillium, flowering age is determined largely by the surface of the leaf and size of the rhizome instead of age alone. Because growth is very slow in nature,
T. grandiflorum typically requires seven to ten years in optimal conditions to reach flowering size, which corresponds to a minimum of of leaf surface area and of rhizome volume. In cultivation, however, wide disparity of flowering ages are observed.
Pollination and seed dispersal Trillium grandiflorum has long been thought to self-pollinate based on the fact that pollinators had rarely been observed visiting the plants and because there is low variation in chromosomal banding patterns. This has been strongly challenged, as other studies have shown high pollination rates by
bumblebees and very low success of self-pollination in controlled experiments, implying that they are in fact self-incompatible.
Trillium grandiflorum has been studied extensively by ecologists due to a number of unique features it possesses. It is a representative example of a plant whose seeds are spread through
myrmecochory, or ant-mediated dispersal, which is effective in increasing the plant's ability to
outcross, but ineffective in bringing the plant very far. This has led ecologists to question how it and similar plants were able to survive glaciation events during the ice ages. The height of the species has also been shown to be an effective index of how intense foraging by deer is in a particular area. s, 3
stigmas, and petals with deep veins Fruits are released in the summer, containing about 16 seeds on average. These seeds are most typically dispersed by
ants, which is called
myrmecochory, but yellow jackets (
Vespula vulgaris) and
harvestmen (order Opiliones) have both been observed dispersing the seeds at lower frequencies. Insect dispersal is aided by the presence of a conspicuous
elaiosome, an oil-rich body attached to the seed, which is high in both
lipids and
oleic acid. The oleic acid induces corpse-carrying behavior in ants, causing them to bring the seeds to their nesting sites as if they were food. As ants visit several colonies of the plant, they bring genetically variable seeds back to a single location, which after germination results in a new population with relatively high
genetic diversity. This has the ultimate effect of increasing
biological fitness. Although myrmecochory is by far the most common dispersal method,
white-tailed deer have also been shown to disperse the seeds on rare occasions by ingestion and defecation. While ants only move seeds up to about , deer have been observed to transport the seeds over . This helps to explain post-agricultural colonization of forest sites by
Trillium grandiflorum, as well as long distance
gene flow which has been detected in other studies. Furthermore, it helps resolve what has been called "
Reid's paradox", which states that migration during
glaciation events must have been impossible for plants with dispersal rates under several hundred meters (yards) per year, such as
Trillium grandiflorum. Thus occasional long distance dispersal events, such as by deer, probably helped save this and other species with otherwise short distance dispersal ability from extinction during the glaciations of the
ice ages. Furthermore, nested
clade analysis of
cpDNA haplotypes has shown that
Trillium grandiflorum is likely to have persisted through the
last glacial period in two sites of refuge in the southeastern
United States and that long distance dispersal was responsible for the post-glacial recolonization of northern areas. In addition to the lateral dispersion (by invertebrates and deer) there is also importance in the fact that burial (vertical dispersion) by ants (or other vectors) increases the survival of new plants by two mechanisms. First, vertical dispersion ensures sufficient depth to preserve the seeds through their dormancy (trillium seeds are normally dormant for their first year). Second, vertical dispersion ensures adequate anchorage of the rhizomes. This is particularly important for young plants because their small rhizomes, with few & short roots, are easily dislodged (e.g. frost heaveal and other erosion factors) and desiccated.
Interaction with deer Trillium grandiflorum as well as other trilliums are a favored food of
white-tailed deer. Indeed, if trilliums are available deer will seek these plants, with a preference for
T. grandiflorum, to the exclusion of others. In the course of normal browsing, deer consume larger individuals, leaving shorter ones behind. This information can be used to assess deer density and its effect on understory growth in general. When foraging intensity increases, individuals become shorter each growing season due to the reduction in energy reserves from less photosynthetic production. One study determined that the ideal deer density in northeastern
Illinois, based on
T. grandiflorum as an indicator of overall understory health, is 4 to 6 animals per square kilometer (10 to 15 per sq. mi.). This is based on a 12 to 14 cm (5" to 6") stem height as an acceptable healthy height.
Disease Trillium grandiflorum is susceptible to a greening disorder caused by bacterial organisms called
phytoplasmas that alter the morphology of infected plants. Symptoms of phytoplasma infection include abnormal green markings on the petals (floral
virescence), extra leaves (
phyllody), and other abnormal characteristics. Infected populations occur throughout the species range but are prevalent in Ontario, Michigan, and New York. For many years, this condition was thought to originate from mutation, and so many of these forms were given taxonomic names now known to be invalid. In 1971, Hooper, Case, and Meyers used
electron microscopy to detect the presence of mycoplasma-like organisms (i.e., phytoplasmas) in
T. grandiflorum with virescent petals. The means of transmission was not established but
leafhoppers were suspected. , the insect
vector for the disorder is unknown. Phytoplasmas were positively identified in
T. grandiflorum and
T. erectum in Ontario in 2016 and later confirmed in 2019.
Phylogenetic analysis supported the grouping of the phytoplasmas isolated from infected plants as a related strain of '
Candidatus Phytoplasma pruni' (subgroup 16SrIII-F) with 99% sequence identity. This subgroup of phytoplasmas is associated with various other diseases, including
milkweed yellows,
Vaccinium witches' broom, and potato purple top. ==Conservation==