Olearia arborescens explained

Olearia arborescens, also known as common tree daisy and pekapeka by Māori[1], is a common shrub or small tree of New Zealand. It has also been called the Glossy Tree Daisy and the Forest Tree Daisy[2] . It grows in lowland to alpine scrubland in the North Island from East Cape southwards, and throughout the South and Stewart Islands. Olearia arborescens was previously known as Solidago arborescens.[3]

Description

The Common Tree Daisy is a woody bush/tree-like plant. It has dark green leaves with a light greyish underside [4] . The leaves also display a glossy coat. They usually measure between 4-8cm long. Olearia arborescens has 2cm long petioles. The plant grows to around 4 metres tall. The leaves show pinnate leaf venation, with a smooth leaf margin. They are also arranged in a simple formation [5] . When the plant flowers, clusters of white florets form. These flowers have small fluffy yellow heads. These white flowers develop fluffy seeds that are wind-dispersed ;. There are around 15–20 florets of the white and yellow flowers in each cluster. These clusters form almost spherical shapes. The inner pappus of the flower has hairs up to 5 mm long .

Range

Natural global range

Olearia arborescens is only found in New Zealand, where it is endemic. However, the genus Olearia is not .

New Zealand range

Olearia arborescens is found in both the North and South Island, predominantly areas in the Southern Alps and central Otago;[6] . However, the warmer climates at the top of the North Island, do not seem to be favored by Olearia arborescens[7] .

Habitat

Olearia arborescens lives in lowland areas or alpine shrubland. Predominantly those in mountainous areas like the Southern Alps, or lowland areas like beach forests. These areas predominantly have extreme climates as well as in some instances strong competition with other plants such as grasses and other shrubs. The alpine areas are considered to be isolated areas of flora and fauna diversity[8] . Alpine areas provide a challenge for their inhabitants, with high wind levels, short growing seasons, and poor sunlight levels, all are prominent in Olearia arborescens’s lifespan. Beech forests and lowland areas provide the challenge of sunlight for the Common Tree daisy due to shading out by larger plants, as well as water availability. The Department of Conservation surveyed an area and found Olearia arborescens in riparian areas. These riparian areas were in lowland beach forests. The Common Tree Daisy was only found beside bodies of water like creeks in this study[9] . However, Olearia arborescens only seems to tolerate these low-lying areas, with alpine locations more favored by Olearia arborescens.

Ecology

Life cycle and phenology

Olearia arborescens flowers from around October to January, running from mid-spring to mid-summer. These flowers turn into fruit from December to March. Olearia has winged seeds that come from their white flowers. These wings aid in the wind-blown distribution of the seeds[10] . Success in the plantings of Olearia seedlings in a Landcare Research trial shows us that seeds germinate around October[11] . Olearia seeds are able to survive in the ground for 9–12 months depending on conditions. This is also accompanied by a very low germination rate which may explain the relative rarity of Olearia arborescens recorded around the country.

Diet and foraging

Olearia arborescens typically grows in Gley soils due to this being the predominant soil in alpine shrublands[12] . Overlaying the raw soil map from Landcare Research onto the iNaturalist sightings shows a correlation. These soils usually contain more nutrients and have a higher biochemical composition than areas like meadows and grasslands[13] . Olearia arborescens also prefers high levels of moisture, such as riparian areas and alpine areas where rainfall can be prolific at times.

Predators, parasites and diseases

Olearia arborescens was logged as being a non-threatened species from 2004-2017. According to the New Zealand Plant Conservation Network, Olearia arborescens remains relatively untouched by introduced mammals such as deer, possums, pigs. Olearia arborescens is not considered to be part of their primary food source and are far too uncommon for these species to solely seek out. There was a sampling of the diet of red deer undergone in the Fiordland National Park in mountainous areas[14] . In Fiordland, there have been a large number of Olearia arborescens recordings. The study took place with a group of 426 deer. Out of these individuals, the browse percentage of Olearia was only around 0.4% above the tree line. Browse percentage is the percentage of the deer's diet that Olearia makes up. There was no recording of Olearia spp (several species) below the treeline in deer, further showing the low browse percentage on Olearia arborescens. This included all Olearia subspecies including Olearia arborescens. The study also recorded forage found in the rumen of the animal. Again, the percentage of Olearia found was very low. Around 0.1 in animals recovered below the tree line and around 0.3 in individuals above the tree line had Olearia in their bodies. This shows that the diet of the introduced red deer is not heavily dependant on Olearia arborescens, but this may be due to low Olearia arborescens numbers. The low amount Olearia aborescens makes of a deer's diet may indicate that other ruminants like goats and hind-gut fermenters such as rabbits could have a low impact on Olearia arborescens.

Interesting information

Olearia hybrid species discovered:

A hybridization derived from Olearia arborescens and Celmisia gracilenta was described in 1988 by Clarkson[15] . This hybrid was found on Mount Tarawera, continuing the Common Tree Daisy’s preference for Montaine environments. At that stage, the total hybrids between the Olearia sub-species and Celmisia was now up to four. The report hypothesizes that these hybridization events would be due to intense selection pressures such as the harsh alpine environment inhabited by Olearia arborescens. This hybrid species had different characteristics presenting, such as tailed anthers which are an elongated part of the stamen that contains pollen and undersides of leaves densely covered in hairs. This hybrid was considered to have no evolutionary potential unless the habitat it was located in changes in a way that would allow these new characteristics to give the hybrid a competitive advantage against other species and the ancestral parent species. The report also stated that this hybrid was more closely related to the Celmisia gracilenta than to Olearia arborescens.

Scientific name meaning:

The “Olearia” of Olearia arborescens was named after Johann Gottfried Olearius who authored Specimen Florae Hallensis . He was a prominent figure in the etymology field in 17th-century Germany. The “arborescens” aspect of the name is a for “tree forming” or “tree-like.”

Evolution of Olearia arborescens:

The Common Tree Daisy evolved from a long lineage of plants. Olearia arborescens is one of 15 species descended from a common ancestor[16] . This includes all four species of Commidendrum and Melanodendron integrifolium. The phylogeny also included five species from the Felicia genus which is common to areas in South Africa. The remaining five species were also from the Asteraceae family. This shows that relatives of Olearia arborescens are found throughout the world, including the small, tropical Island of St Helena.

Etymology timeline:

The final scientific naming of Olearia arborescens took from 1846 to 1911. These scientific names varied greatly from each other. The first name that was given to the Common Tree Daisy was Steiractis arborescens by Augustin de Candolle in 1836[17] .  The name changed a further ten times before it was given the final name Olearia arborescens by Cockayne and Laing[18] . This indecisiveness shows a clear struggle in identifying what group Olearia arborescens belongs. Leonard Cockayne was one of the two final botanists who named Olearia arborescens. He is a well-known figure in the botany world especially in the Canterbury region where he lived[19] .

Chromosome count: The number of chromosomes present in a 2n diploid cell is recorded at 108, meaning that a haploid cell will contain half this number, 54.

Notes and References

  1. Web site: Nz Flora . Olearia arborescens (G.Forst.) Cockayne & Laing . Landcare Research . 6 March 2024.
  2. Book: Allan . H . Flora of New Zealand . 1961 . Government Printer, New Zealand.
  3. Book: Richard . T . New Zealand and its inhabitants . 1855 . Renaissance Books . 430-457.
  4. Web site: de Lange . P . Olearia arborescens . New Zealand Plant Conservation Network . 6 March 2024.
  5. Web site: Forst . G . Olearia arborescens (G. Forst.) Cockayne and Laing . Te Papa . 6 March 2024.
  6. Web site: Walker . S . The woody vegetation of Central Otago, New Zealand: its present and past distribution and future restoration needs . 6 March 2024 . Department of conservation.
  7. Web site: Stephen . S . Common Tree Daisy (Olearia arborescens) . INaturalist. . 6 March 2024.
  8. Web site: NZPCN . Alpine ecosystems . New Zealand Plant Conservation Network . 6 March 2024.
  9. Web site: DOC . Lowland flats and alluvial terraces plant list . 6 March 2024 . . Department of Conservation.
  10. Web site: DOC . Seed collection and propagation guide for native trees and shrubs . Department of Conservation . 6 March 2024.
  11. Web site: Ledgard . N . Visit to the Sherry River, October 20-23, 2008 . Landcare research . 6 March 2024.
  12. Web site: Drewry . J . Distribution of raw soils . . Landcare research . 6 March 2024.
  13. Web site: Quiyun . F . Yang . Y . Geng . Y . Wu . Y . Niu . Z . Biochemical composition and function of subalpine shrubland and meadow soil microbiomes in the ilian Mountains, Quinghai-Tibetan plateau, China . Proquest . 6 March 2024.
  14. Web site: Lavers . J . Spatio-temporal feeding selection of red deer in a mountainous landscape . Wiley, Online library . 6 March 2024.
  15. Web site: Clarkson . B . A natural intergeneric hybrid, Celmisia gracilenta × Olearia arborescens (Compositae) from Mt Tarawera, New Zealand . ResearchGate . 6 March 2024.
  16. Web site: Eastwood . M . Gibby . M . Cronk . B . Evolution of St Helena arborescent Astereae (Asteraceae): relationships of the genera Commidendrum and Melanodendron. Oxford academic . Botanical Journal . 6 March 2024.
  17. Book: De Candolle . A . Prodromus Systematis Naturalis Regni Vegetabilis . 1836 . Treuttel et Wurtz . 345 .
  18. Book: Cockayne . L . The Mount Arrowsmith district: A Study in Physiography and Plant Ecology. Part II: Plant Ecology . Laing . R . 1911 . Transactions and Proceedings of the New Zealand Institute . 342-378 .
  19. Web site: Partridge . T . Leonard Cockayne – the Legacy, how we celebrate Cokayne today . New Zealand plant conservation network . 6 March 2024.