Occurrence of Attributes in Original Text

The text related to the cultural heritage 'Laurisilva of Madeira' has mentioned 'Species' in the following places:
Occurrence Sentence Text Source
The forest is characterized by broadleaf tree species with evergreen, glossy and elongated leaves, known as "laurophyll" or "lauroid".
The canopies are evergreen, dominated by species with glossy- or leathery-leaves, and with moderate tree diversity.
Some species belong to the true laurel family, Lauraceae, but many have similar foliage to the Lauraceae due to convergent evolution.
The scientific names laurina, laurifolia, laurophylla, lauriformis, and lauroides are often used to name species of other plant families that resemble the Lauraceae.
[7] The scientific names Daphnidium, Daphniphyllum, Daphnopsis, Daphnandra, Daphne[8] from Greek: xcex94xcexacxcfx86xcexbdxcexb7, meaning "laurel", laurus, Laureliopsis, laureola, laurelin, laurifolia, laurifolius, lauriformis, laurina, , Prunus laurocerasus (English laurel), Prunus lusitanica (Portugal laurel), Corynocarpus laevigatus (New Zealand Laurel), and Corynocarpus rupestris designate species of other plant families whose leaves resemble Lauraceae.
Laurel forests are typically multi-species, and diverse in both the number of species and the genera and families represented.
[7] In the absence of strong environmental selective pressure, the number of species sharing the arboreal stratum is high, although not reaching the diversity of tropical forests; nearly 100 tree species have been described in the laurisilva rainforest of Misiones (Argentina), about 20 in the Canary Islands.
This species diversity contrasts with other temperate forest types, which typically have a canopy dominated by one or a few species.
Species diversity generally increases towards the tropics.
Some lauroid species that are found outside laurel forests are relicts of vegetation that covered much of the mainland of Australia, Europe, South America, Antarctica, Africa, and North America when their climate was warmer and more humid.
Cloud forests are believed to have retreated and advanced during successive geological eras, and their species adapted to warm and wet conditions were replaced by more cold-tolerant or drought-tolerant sclerophyll plant communities.
Many of the late Cretaceous xe2x80x93 early Tertiary Gondwanan species of flora became extinct, but some survived as relict species in the milder, moister climate of coastal areas and on islands.
[10] Thus Tasmania and New Caledonia share related species extinct on the Australian mainland, and the same case occurs on the Macaronesia islands of the Atlantic and on the Taiwan, Hainan, Jeju, Shikoku, Kyxc5xabshxc5xab, and Ryxc5xabkyxc5xab Islands of the Pacific.
Although some remnants of archaic flora, including species and genera extinct in the rest of the world, have persisted as endemic to such coastal mountain and shelter sites, their biodiversity was reduced.
Isolation in these fragmented habitats, particularly on islands, has led to the development of vicariant species and genera.
Thus, fossils dating from before the Pleistocene glaciations show that species of Laurus were formerly distributed more widely around the Mediterranean and North Africa.
Inner laurel forest ecoregions, a related and distinct community of vascular plants, evolved millions of years ago on the supercontinent of Gondwana, and species of this community are now found in several separate areas of the Southern Hemisphere, including southern South America, southernmost Africa, New Zealand, Australia and New Caledonia.
Most Laurel forest species are evergreen, and occur in tropical, subtropical, and mild temperate regions and cloud forests of the northern and southern hemispheres, in particular the Macaronesian islands, southern Japan, Madagascar, New Caledonia, Tasmania, and central Chile, but they are pantropical, and for example in Africa they are endemic to the Congo region, Cameroon, Sudan, Tanzania, and Uganda, in lowland forest and Afromontane areas.
Associations of Lauraceous species are common in broadleaved forests; for example, Litsea spp., Persea odoratissima, Persea duthiei, etc., along with such others as Engelhardia spicata, tree rhododendron (Rhododendron arboreum), Lyonia ovalifolia, wild Himalayan pear (Pyrus pashia), sumac (Rhus spp.
Some other common trees and large shrub species of subtropical forests are Semecarpus anacardium, Crateva unilocularis, Trewia nudiflora, Premna interrupta, vietnam elm (Ulmus lancifolia), Ulmus chumlia, Glochidion velutinum, beautyberry (Callicarpa arborea), Indian mahogany (Toona ciliata), fig tree (Ficus spp.
Lindera and Litsea species, Himalayan hemlock (Tsuga dumosa), and Rhododendron spp.
Other important species are Magnolia campbellii, Michelia doltsopa, andromeda (Pieris ovalifolia), Daphniphyllum himalense, Acer campbellii, Acer pectinatum, and Sorbus cuspidata, but these species do not extend toward the west beyond central Nepal.
Nepalese alder (Alnus nepalensis), a pioneer tree species, grows gregariously and forms pure patches of forests on newly exposed slopes, in gullies, beside rivers, and in other moist places.
This zone is habitat for many other important tree and large shrub species such as pindrow fir (Abies pindrow), East Himalayan fir (Abies spectabilis), Acer campbellii, Acer pectinatum, Himalayan birch (Betula utilis), Betula alnoides, boxwood (Buxus rugulosa), Himalayan flowering dogwood (Cornus capitata), hazel (Corylus ferox), Deutzia staminea, spindle (Euonymus tingens), Siberian ginseng (Acanthopanax cissifolius), Coriaria terminalis, ash (Fraxinus macrantha), Dodecadenia grandiflora, Eurya cerasifolia, Hydrangea heteromala, Ilex dipyrena, privet (Ligustrum spp.
These forests are distinct in species composition from the lowland tropical forests, which are dominated by Dipterocarps and other tropical species.
Some relict Mediterranean laurel forest species, such as sweet bay (Laurus nobilis) and European holly (Ilex aquifolium), are fairly widespread around the Mediterranean basin.
In the Mediterranean there are other areas with species adapted to the same habitat, but which generally do not form a laurel forest, except very locally in the southernmost tip of the Iberian Peninsula.
This species survives natively in Morocco, Portugal, Italy, Greece, the Mediterranean islands, and some areas of Spain, including the Parque Natural Los Alcornocales in the province of Cxc3xa1diz and in coastal mountains, especially in the Girona Province, and isolated in the Valencia area.
Although the Atlantic laurisilva is more abundant in the Macaronesian archipelagos, where the weather has fluctuated little since the Tertiary, there are small representations and some species contribution to the oceanic and Mediterranean ecoregions of Europe, Asia minor and west and north of Africa, where microclimates in the coastal mountain ranges form inland "islands" favorable to the persistence of laurel forests.
When the Strait of Gibraltar reclosed, the species repopulated toward the Iberian Peninsula to the north and were distributed along with other African species, but the seasonally drier and colder climate, prevented them reaching their previous extent.
In Europe the laurel forest has been badly damaged by timber harvesting, by fire (both accidental and deliberate to open fields for crops), by the introduction of exotic animal and plant species that have displaced the original cover, and by replacement with arable fields, exotic timber plantations, cattle pastures, and golf courses and tourist facilities.
In the Himalayas, in Nepal, subtropical forest consists of species such as Schima wallichii, Castanopsis indica, and Castanopsis tribuloides in relatively humid areas.
The Afromontane laurel forests describe the plant and animal species common to the mountains of Africa and the southern Arabian Peninsula.
These scattered highland laurophyll forests of Africa are similar to one another in species composition (known as the Afromontane flora), and distinct from the flora of the surrounding lowlands.
The main species of the Afromontane forests include the broadleaf canopy trees of genus Beilschmiedia, with Apodytes dimidiata, Ilex mitis, Nuxia congesta, N. floribunda, Kiggelaria africana, Prunus africana, Rapanea melanophloeos, Halleria lucida, Ocotea bullata, and Xymalos monospora, along with the emergent conifers Podocarpus latifolius and Afrocarpus falcatus.
Species composition of the Subsaharan laurel forests differs from that of Eurasia.
Tree species include: Real Yellowwood (Podocarpus latifolius), Outeniqua Yellowwood (Podocarpus falcatus), White Witchhazel (Trichocladus ellipticus), Rhus chirendensis, Curtisia dentata, Calodendrum capense, Apodytes dimidiata, Halleria lucida, Ilex mitis, Kiggelaria africana, Nuxia floribunda, Xymalos monospora, and Ocotea bullata.
As one moves south into central Florida, as well as far southern Texas and the Gulf Coastal margin of the southern United States, the sclerophyll character slowly declines and more tree species from the tropics (specifically, the Caribbean and Mesoamerica) increase as the temperate species decline.
In some areas, the evergreen forests are dominated by species of Live oak (Quercus virginiana), Laurel oak (Quercus hemisphaerica), southern magnolia (Magnolia grandiflora), red bay (Persea borbonia), cabbage palm (Sabal palmetto), and sweetbay magnolia (Magnolia virginiana).
In several areas on the barrier islands, a stunted Quercus geminata or mixed Quercus geminata and Quercus virginiana forest dominates, with a dense evergreen understory of scrub palm Serenoa repens and a variety of vines, including Bignonia capreolata, as well as Smilax and Vitis species'.
The lower shrub layer of the evergreen forests is often mixed with other evergreen species from the palm family (Rhapidophyllum hystrix), bush palmetto (Sabal minor), and saw palmetto (Serenoa repens), and several species in the Ilex family, including Ilex glabra, Dahoon holly, and Yaupon holly.
Several species of Yucca and Opuntia are native as well to the drier sandy coastal scrub environment of the region, including Yucca aloifolia, Yucca filamentosa, Yucca gloriosa, and opuntia stricta.
Typical tree species included oaks ancestral to present-day California oaks, as well as an assemblage of trees from the Laurel family, including Nectandra, Ocotea, Persea, and Umbellularia.
[18][19] Only one native species from the Laurel family (Lauraceae), Umbellularia californica, remains in California today.
Several species of evergreen Quercus forests occur, as well as a mix of evergreen scrub typical of Mediterranean climates.
Species of Notholithocarpus, Arbutus menziesii, and Umbellularia californica can be canopy species in several areas.
Tree species include evergreen oaks, members of the Laurel family, and species of Weinmannia, Drimys, and Magnolia.
The Yungas are typically evergreen forests or jungles, and multi-species, which often contain many species of the laurel forest.
The forest canopy includes species of Lauraceae (Ocotea pretiosa and O. catharinense), Myrtaceae (Campomanesia xanthocarpa), and Leguminosae (Parapiptadenia rigida), with an emergent layer of the conifer Brazilian Araucaria (Araucaria angustifolia) reaching up to 45 metres (148xc2xa0ft) in height.
The laurel forests of Australia, Tasmania, and New Zealand are home to species related to those in the Valdivian laurel forests, including Southern Beech (Nothofagus, fossils of which have recently been found in Antarctica[23]) through the connection of the Antarctic flora.
The laurel forest of Australia, New Caledonia (Adenodaphne), and New Zealand have a number of species related to those of the Valdivian laurel forest, through the connection of the Antarctic flora of gymnosperms like the podocarpus and deciduous Nothofagus.
Beilschmiedia tawa is often the dominant canopy species of genus Beilschmiedia in lowland laurel forests in the North Island and the northeast of the South Island, but will also often form the subcanopy in primary forests throughout the country in these areas, with podocarps such as Kahikatea, Matai, Miro and Rimu.
These forests include species typical of both Northern Hemisphere laurel forests, including Lithocarpus, Ilex, and Lauraceae, and Southern Hemisphere laurel forests, including Southern Beech Nothofagus, Araucaria, Podocarps, and trees of the Myrtle family (Myrtaceae).
The property has great importance for biodiversity conservation with at least 76 vascular plant species endemic to Madeira occurring in the property, together with a high number of endemic invertebrates and two endemic birds including the emblematic Madeiran Laurel Pigeon.
The property provides a wealth of ecological niches, complex food webs and examples of co-evolution of species.
Around 13 liverwort species and 20 moss species are noted as threatened at a European scale, while abundant lichens are indicative of high environmental quality and the absence of pollution.
Vertebrate species include a limited number of species with high endemism, including two rare species of bats, the Madeira Pipistrelle Pipistrellus maderensis and the Leisler's Bat Nyctalus leisleri verrucosus and several birds, such as the Madeira Laurel Pigeon Columba trocaz, the Madeiran Firecrest Regulus madeirensis and the Madeiran Chaffinch Fingilla coelebs madeirensis.
Possibly threats arising from these areas include invasive species and species introductions from both agriculture and forestry.
These multiple layers of protection include status as a special area of conservation under the Habitats Directive of the European Union, which obliges the State Party to protect the area so that both "Madeiran laurel forest" and 39 species of rare and threatened plants and animals remain at, or are restored to, "favourable conservation status".
These include monitoring the potential threat to the property from invasive species including species from former agricultural land at the lower edge of the property.