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Ancient trees & wildlife

This details the wildlife associated with ancient trees, and the different parts of the tree, click on each section of the contents page to jump to the appropriate section.

Wood decay and 'dead' wood  
Fungi and ancient trees Fungi and trees
  Fungi and the ecosystem
  Fungi and other wildlife
The invertebrate fauna of wood-decay Heartwood decay
  Exposed Heartwood 
  Later stages of heart-rot 
  Other guest species 
  Rot-holes
  Fungal fruiting
  Heart-rotters as keystone species
  Ambrosia beetles
  Bark
  Cobweb beetles
  Deadwood lying in water
  Decaying roots
  Importance of nectar sources
  Changing fauna
Epiphytes Succession
  Lobarion
  Lecanactidetum premneae
  Invertebrates associated with epiphytes
Vertebrates using hollow trees and wood-decay Birds
  Bats
  Other mammals
  Amphibians
   

Wood decay and 'dead' wood  Back »

Dead wood - "the world's largest potential food supply" (Peter Marren).


Each year a woody plant lays down a new annual ring of living tissue. As the plant ages so the inner annual rings of the xylem become dysfunctional, ie cease to have any role in water transport and are effectively dead. Before they die the cells are modified chemically, mobile nutrients are removed and both waste products and other compounds (mainly phenolics) are laid down to reduce the chances of colonisation by potentially damaging organisms. Once dead these tissues are inaccessible to the plant, any potential nutrients are locked up and lost. Eventually, however, they are colonised by non-pathogenic fungi which begin to digest the principle components of the dead tissue - the cellulose and lignin. These heartwood-decay fungi do not affect the living tissues which surround the dead heartwood (Marren, P 1991 Bracket fungi and their role in nature. British Wildlife 3: 1-9; Rayner, ADM 1993 The fundamental importance of fungi in woodlands. British Wildlife 4: 205-215).

As these fungi break down the cellulose and/or lignin, so a whole succession of conditions are created which support the development of a parallel succession of invertebrates. There are two key successions, following the two main types of decay fungi. Some heartrot fungi only digest the cellulose, such as sulphur polypore Laetiporus sulphureus, leaving the lignin as a reddish-brown brittle material - "red-rot". Other fungi digest both cellulose and lignin, leaving a whitish soft, pliable material - "white-rot". The latter include various Ganoderma spp and Inonotus species.

Fungi and ancient trees  Back »

Fungi and trees Back »

In recent years there has been a dramatic change in the way we look at the roles of fungi. No longer is fungal decay and hollowing of ancient trees seen as detrimental, instead they seem to be the key to prolonging the lives of trees.

Although we only perceive the tree, the relationship appears to be so close that every tree has been described as creating a unique and dynamic support system for fungi. Strip away the cellulose and lignin and you are likely to still see the whole tree in ghostly fungal relief. They can also be extremely large organisms - a honey fungus in the USA has been measured at over 50km in diameter. Some fungi can also very long lived; perhaps living forever as some are known to grow continuously.
Fungi fulfil a host of important roles in all parts of the tree - within cells, between cells and on the surface of all parts of the tree, from the leaves in the canopy down to the root hairs. They also occur throughout all stages of a tree's life.

Fungi and the ecosystem  Back »

In the woodland ecosystem many are essential as vital decomposers and recyclers of plant remains others are key transporters of nutrients for the health and optimum growth of plants. Most fungi can be separated into these two main groups: - 

Decomposition [recycling] fungi - associated with wood, leaf litter and other plant and animal matter. The saproxylic fungi are associated particularly with wood decomposition of living standing trees and fallen decaying wood.

Mycorrhizal [food gathering] fungi - forming symbiotic associations with the roots of trees.

In both groups some fungi are associated with a wide range of tree and plant species, others are very specific in their choice of partners. 

The fungal fruiting body is a very tiny part of the organism; much is out of sight as a mycelium growing within and around plants tissues. The presence of fungal fruiting bodies has often led to much concern, however few fungi are major pathogens and in natural systems active pathogens may have a function in glade creation. They pose us a threat only in our dense single stand crops of trees or ornamental areas. 

Like other species in the ecology of ancient trees some of the fungi are rare and threatened. Of the 447 macrofungi on the British Red Data Book list nearly 400 are from Ancient Woodland and lowland pasture woodland. Many of those naturally hollowing the heart wood of trees have very restricted distributions. Loss of habitat is still a major concern in the conservation of fungi. Major losses appear to be happening due to acidification and increased nitrogen levels in soils. 

Fungi and other wildife  Back »

It is not only the trees which are dependent on fungi. Many woodland invertebrates could not take advantage of the wood without the fungi ‘softening’ it up first. The invertebrate community changes as the decay process proceeds and some invertebrates are more dependent on the type of decay than of the species of tree. Other invertebrates are dependent on fungi fruiting bodies.

The invertebrate fauna of wood-decay Back »

How many species?


There are more than 1700 different invertebrate species in Britain and Ireland which are dependent on decaying wood in order to complete their life cycles (Alexander, in prep. The invertebrates of living & decaying timber in Britain & Ireland). This represents about 6% of the entire British invertebrate fauna - wood-decay is a major resource! That means more than 1700 different life styles, since each species has very particular requirements. These statistics really bring home just how diverse a habitat wood-decay can be.

The keys to understanding the ecology of these invertebrates is to develop an understanding of the two key processes involved: 
· the aging process of woody plants, and 
· the process of wood decay.

What do they feed on?

Very few invertebrates possess the necessary gut enzymes to break down the principle components of wood - cellulose and lignin. Most rely on fungi and/or micro-organisms to convert these compounds into more digestible materials. The exceptions to this - species which can digest cellulose - include goat moth Cossus cossus, longhorn beetles (Cerambycidae), bark beetles (Scolytidae) and the very rare beetle Lymexlon navale.

The most important wood for wood-decay invertebrates is of course the living tree, for it is the living tissues which generate the wood which will ultimately decay. Dead wood has a limited existence, it decays and is ultimately re-cycled. Conservation of wood-decay communities requires conservation of a diverse age structure of woody plants in order to ensure continuity of wood-decay habitats.

Invertebrates of Heartwood decay
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The single most important wood-decay resource for invertebrates is a large standing living tree with columns of decay in the heartwood.

In the early stages of decomposition, white-rotted heartwood is commonly fed upon by larvae of lesser stag beetle Dorcus parallelepipedus and rhinoceros beetle Sinodendron cylindricum, forming characteristic large and convoluted galleries. White-rot decay supports a very wide range of some of our most colourful insects. Larvae of the beautiful red net-winged beetle Platycis minutus develop in relatively soft moist heartwood, especially beech and ash. The brassy tortoise beetle Thymalus limbatus develops beneath loose bark on decaying broad-leaved timber, especially oak, and in the later stages of white-rot decay when the heartwood is dry and soft. Melandrya caraboides is a large black beetle with a metallic green sheen and develops in relatively soft moist dead heartwood of boughs, trunks and stumps of various broadleaves, but especially ash and beech. The larvae of the bright green beetle Ischnomera cyanea develop in relatively soft white-rotting heartwood of a great variety of broadleaves. The larvae of the spectacular tiger or feather-horned craneflies Ctenophora spp also develop in soft moist white-rot.

Red-rot supports a quite different fauna, including some of the most colourful click beetles. The hairy fungus beetle Mycetophagus piceus feeds directly on the mycelium of the sulphur polypore fungus, deep inside the decaying trunk - it is itself eaten by larvae of the rare click beetle Lacon querceus in Windsor Forest, but nowhere else in Britain. Another very rare heartwood click beetle, the bright red Ampedus cardinalis, also develops in red-rotten heartwood of old oaks, in smaller boughs as well as trunks. Like the Lacon it is an active predator, feeding on the larvae of developing beetles and flies. The red-rot itself is bored by a number of small dark beetles, notably Dorcatoma chrysomelina and Anitys rubens. The larvae of the stiletto fly Pandivirilia melaleuca (Therevidae) is a particularly aggressive predator living in very dry powdery red-rotten heartwood of oak. Scenopinus niger is another scarce fly the larvae of which are specialist predators on dermestid and probably other beetle larvae in dry red-rotting heartwood of various broadleaves.

 The larvae of the rare noble chafer Gnorimus nobilis develop in wood mould within hollowing old trees; often associated with old fruit trees, but also in oaks and willows; it is a speciality of the lower Thames, Severn and Solent Basins.

Exposed heartwood
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Many of these insects gain access to the hollowing interior of old trees through patches of heartwood which have been exposed to the air through physical damage to the bark, eg through lightning strikes or damage caused by the collapse of a neighbouring tree. The dull brown beetle Ptilinus pectinicornis bores in exposed dry heartwood of old broad-leaves, making the small pin-holes which are so common in areas of exposed heartwood. As with so many of these wood-decay beetles, the female attracts males by release of a pheromone and the males have feathery antennae designed to maximise the sensory area. The females bore breeding passages into the solid outer heartwood to lay eggs, preferring standing tree trunks over fallen ones; only a few females actually leave the old breeding site to initiate new infestation. The bright red and blue beetle Tillus elongatus is a specialist predator of Ptilinus pectinicornis larvae, entering the pin-holes in the exposed heartwood and exploring the galleries below for occupied burrows. Their larvae hunt nocturnally within the galleries and actively explore the trunk surfaces for new prey. Tomoxia bucephala is an example of a species with decay-feeding larvae which is unable to excavate access for itself but uses the vacated Ptilinus galleries to get in to the decay.

Later stages of heart-rot
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In both red- and white-rot the end product is a black wood mould which accumulates in the bottom of the hollow trunk as the fungus works its way into the upper trunk and main boughs. Some of Britain's rarest insects develop in this medium of relatively constant temperature and humidity, protected from the outside world by the surrounding living trunk tissues.

The darkling beetle Prionychus ater is one of the most widespread specialists here. Amongst the rarer species are many of the bright red Ampedus click beetles and the famous violet click beetle Limoniscus violaceus - rare throughout its European range and one of Britain's very few legally protected beetles. The larvae of most of these species appear to develop in hollow trees which have been occupied by cavity-nesting birds such as jackdaw, stock dove or owls. The decayed heartwood is not rich in nutrients, and inputs of bird droppings, feathers, bones, etc, may provide an important source of minerals, etc, which promote successful development. Similar conditions can sometimes develop beneath loose bark on the trunks and main boughs and Prionychus ater can also be found developing in this situation, as well as the much rarer Prionychus melanarius.

The later stages in the decay process of timber are not essentially dissimilar to other decaying organic matter and certain wood-decay inhabiting invertebrates may also be found in other decaying matter. A good example is the click beetle Denticollis linearis, a widespread species developing in decaying timber, but it also develops in peat on moorland. Decaying timber eventually supports what is essentially a soil fauna, dominated by millipedes, woodlice and centipedes.

Heartwood-nesting ants
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There are two ant species which form their nests in the decaying heartwood of trees: brown tree ant Lasius brunneus and jet ant Lasius fuliginosus. Wood is macerated by their jaws and hardened by secretions from the mandibular glands to create the nest itself and intricate passageways are developed through the heartwood to access points in the outer trunk from whence the workers forage over the leaf canopy for food. These ants are of considerable interest for the wide range of other insect species which live specifically in their nests and which are associated with their runs. Good examples are the rove beetles (Staphylinidae) of the genus Zyras which live in the runs and nests of jet ant.

Other guest species
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Other species appear to be associated rather more with the galleries of wood-decay insects than with the wood-decay itself. The rare beetle Aeletes atomarius is usually found in the burrows of lesser stag beetle Dorcus parallelopipedus in moist crumbly decaying heartwood, although also recorded with Sinodendron cylindricum and brown tree ant Lasius brunneus.

Many bees and wasps exploit the exit holes of wood-boring insects and other cavities in timber as nest sites. Hole-nesting digger wasps are good examples. These have their own specialist parasites including certain Sarcophagidae flies such as the rare Macronychia polyodon and Macronychia striginervis.

Rot-holes
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Most of the above discussion relates to hollowing trunks, but similar processes also occur in smaller cavities in the trunk and in the branchwood. These are termed rot-holes and are particularly favoured by Diptera for the moister conditions which prevail. Such rot-holes are open to the elements and particularly rain, creating different conditions to those found in the centre of the main trunk. The gunge which accumulates in these cavities is favoured by a whole host of hoverflies (Syrphidae), moth flies (Psychodidae), wood gnats (Mycetobiidae), long-headed flies (Dolichopodidae), etc. One rare hoverfly Pocota personata is known to develop mainly in rot-holes which are high in the canopy. As with the decaying heartwood, these include species which feed directly on the decaying mulch, others are scavengers, predators and parasites.

Water-filled rot-holes even support a specialist freshwater fauna including the copepod Moraria arboricola, non-biting midges (Chironomidae) such as Metriocnemus martinii, and mosquitoes and gnats such as Anopheles plumbeus. The last develops in water-filled holes on mature trees; the eggs are laid on the sides of tree holes just above waterline and hatch only when flooded. The pale orange beetle Prionocyphon serricornis also develops in water-logged hollows in old trees, especially favouring those hollows amongst roots at the base of the trunk; the larvae are aquatic, feeding on the detritus from the dead leaves which accumulate in the cavities.

Fungal fruiting
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The decay already discussed relates to the activities of the fungal mycelium - the feeding part of the fungus. The fruiting bodies themselves provide specialist habitats for another huge array of invertebrate species.

The larvae of the small moth Morophaga choragella (Tineidae) feed in galleries excavated within the fruiting bodies of various wood-rotting fungi, especially Inonotus and Ganoderma spp, pupating either in the fungus or in deadwood. Elodia ambulatoria is a rare tachinid fly which specialises in parasitism of tineid moth larvae, mainly Morophaga choragella. 

The hard black fruiting bodies of the fungi Daldinia concentrica and Hypoxylon spp are remarkably favoured by insects. The precise species of fungus appears not important, rather the hard black medium provided: the scarce fungus weevil Platyrhinus resinosus develops in Daldinia concentrica on ash trees as well as Hypoxylon fragiforme on beech, and other beetles behave similarly, eg Biphyllus lunatus, Litargus connexus, and Mycetophagus atomarius. 

More typical bracket fungi also have their specialist fauna, eg Inonotus hispidus is where the beetles Triplax russica and Orchesia micans develop, I. radiatus for Abdera flexuosa, and sulphur polypore appears to be the key larval habitat for the beetles Eledona agricola and Hallomenus binotatus. These bracket fungi are fairly long-lived, but even the short-lived brackets of beefsteak fungus Fistulina hepatica are used by a number of species which can develop from egg to adult relatively quickly. The soft-bodied fruits of oyster mushroom Pleurotus ostreatus, for instance, are favoured by the bright red and blue or black Triplax beetles. 

Amongst the many interesting variations on the theme is the small black beetle Dorcatoma ambjoerni which has only been found in the fruiting bodies of the bracket fungus Inonotus cuticularis actually inside hollow beeches rather than growing externally. The larvae of the platypezid fly Agathomyia wankowiczii develop in galls under brackets of Ganoderma applanatum. So far only the galls have been found in Britain and it is currently known from only six localities in the south-east. It is presumed to be a recent establishment from the continent as the galls have only been noticed in recent years and yet are very conspicuous.

Two slugs are particularly associated with old wood-pastures - ash-black slug Limax cinereoniger and slender slug Limax tenellus. The latter is the rarer of the two and a beautiful animal especially when feeding on say black buttons Bulgaria inquinans, when the contrast of the bright yellow slug and the deep matt black of the fungus is very attractive.

Heart-rotters as keystone species
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Basically, the heart-rotting fungi are keystone species - a large number of other species are completely dependent on the conditions which they create. And not just invertebrates. Where would woodpeckers and bats be without hollowing trees?

Ambrosia beetles
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The above species are all opportunistic, colonising suitable wood after fungi have become established. A small group of beetles go one step further and carry their fungal food with them and inoculate the freshly dead timber themselves! The beetle Hylecoetus dermestoides develops in dead timber and root stumps of hard and softwoods. The eggs are laid in batches in wood crevices, in rough bark or in boreholes. The fungal spores are in the eggshells and the larvae feed on the ambrosia fungus which develops on the walls of larval galleries. The other ambrosia beetles known from Britain are all in the bark beetle family (Scolytidae).

Bark
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The outer parts of the trunk and branches - the bark - also has a whole succession of invertebrates associated with it. Freshly dead or even dying bark is rapidly colonised by bark beetles (Scolytidae) and with them come a series of scavengers which exploit the beetle galleries, plus predators and parasites. The ant beetle Thanasimus formicarius is a specialist predator of bark beetles, and larvae of the long-headed flies (Dolichopodidae) Medetera spp are also found in the burrows of bark beetles and other beetles on whose larvae and pupae they feed. The adult flies are very characteristic of the surfaces of exposed heartwood on the trunks where they court, mate and catch their prey.

Larvae of the oak jewel beetle Agrilus pannonicus tunnel in and under thick oak bark where dying and dead. Its main refugia are ancient woodlands and pasture-woodlands, but this beetle spreads more widely on occasion. Numbers were already building up in the south-east when the Great Storm of 1987 gave the species a bonanza of freshly dead oaks. This event was closely followed by Oak Dieback Disease, which has boosted the species ever further to the point that it is now being implicated in this worrying oak condition, albeit on very questionable grounds.

Larvae of Wood Snipe Fly Xylophagus ater develop beneath bark on branchwood of a wide variety of dead broadleaves in the early stages of decay. They feed on the larvae of larger beetles such as longhorn beetles and possibly other insects although it is not known quite how they overcome their large prey - these are by no means defenceless since they have large jaws used for breaking up hard wood! It is suspected that they use their large toughened beak to puncture the waterproof coating of a potential prey larva and then retire and wait for the prey to loose vigour as it dehydrates and then to come back for the kill once the victim is more or less moribund. It has even been suggested that the dense rings of wood-dust with which longhorn beetles surround themselves before pupating is intended as a defensive stockade to protect this vulnerable stage specifically from Xylophagus. The larvae of snakeflies such as Xanthostigma xanthostigma are more conventional predators which pursue more defenseless prey beneath the bark. 

Many fungi exploit dead wood on the outer surfaces of the tree or on smaller branchwood and it is not surprising that there are many further invertebrates which specialise on them. Good examples are species such as the beetles Phloiophilus edwardsii and Tetratoma ancora which develop in the fruits of the fungus Phlebia merismoides. A number of scarce species develop particularly in the dead lower limbs of trees, branches which have become shaded out by the tree's own canopy, presumably feeding on fungi such as Stereum spp. Examples include the beetles Tetratoma desmaresti and Abdera biflexuosa.

Britain's largest false scorpion Dendrochernes cyrneus lives beneath loose bark on tree trunks. It is mainly a southern species and prefers timber heated by the sun. It not only feeds on small wood-decay invertebrates but also explores the outside surfaces of the trunk on calm warm summer evenings - exploiting the epiphyte communities as well as the saproxylics! 

Cobweb beetles
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Four species of cobweb beetle have larvae which live in the crevices beneath dead bark on the trunks of large old living trees, or under the dry loose bark of dead standing trees, where they are associated with the webs of bark-frequenting spiders. They feed on the remains of insects eaten and left over by the spiders. The larvae are covered with long bristles which protect them from the jaws of the spiders. They pupate within the larval skin, which splits along the back and affords protection for this vulnerable stage in their life cycle. Ctesias serra is the most widespread and to be found on just about any ancient tree in the countryside. In contrast Trinodes hirtus is a rarity found only on ancient oaks in old wood-pastures.

Deadwood lying in water
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Deadwood lying in water provides yet another range of niches to be exploited by invertebrates. The beetle Cyanostolus aeneus only occurs under bark on trunks and boughs which have been saturated with water, occurring along rivers and streams subject to spates. Larvae of the non-biting midge (Chironomidae) Orthocladius lignicola specialise in submerged rotten wood, and the rare hoverfly Chalcosyrphus eunotus develops in deadwood which is semi-submerged in freshwater.

Decaying roots
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So far discussion has focused on the aerial parts of the trees. Decay in the roots is a further important habitat for invertebrates. The most famous species is the Stag Beetle Lucanus cervus, the larvae of which develop in moist decaying wood below the soil surface, especially the decaying roots of old stumps, but also in the base of fenceposts. The rare metallic green hoverfly Caliprobola speciosa develops in wet-rot in underground roots of beech stumps, and Criorhina spp and Xylota spp hoverflies also specialise in decaying roots.

Importance of nectar sources
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The requirement of the adults of some of the insects which develop in wood-decay for access to blossom is widely appreciated. Nectar provides an energy-rich food which can rapidly be assimilated and used to fuel flight, and pollen is a protein-rich food which aids egg production. Flowering trees and shrubs are by far the most important sources, although other plants can also be very popular, notably hogweed and Angelica. Hawthorn provides the classic insect blossom, partly due to its flowering in late spring when so many wood-decay insects are in the adult stage. But really, blossom can important right through the season, and the presence of species such as sallow, holly, privet, rowan, crab apple, wild pear, guelder rose, bramble, and so on, are all beneficial. Even elder, with its poor reputation amongst entomologists, can be important for a select few species - it is particularly favoured by the nationally scarce beetle Aderus oculatus, for instance, which develops in red-rot in old oaks.

Changing fauna
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Today's fauna is unique in time. The fauna of the ancient Wildwood of Britain and Ireland would have been particularly species-rich. Extinction has been a continuing process, in relation to a variety of factors but particularly fluctuating climate and as a result of the activities of people since prehistoric times. The fossil record includes many species which nowadays require visits to continental Europe to see them: Rhysodes sulcatus is a relict species of primary, wholly undisturbed forest, ie before it has been disturbed by human activity, and is most recently known in Britain at c3000 BP. The click beetle Porthmidius austriacus appears to have become extinct during the Neolithic period. There is evidence for the presence in Britain of another species of stag beetle Platycerus caraboides up until the Bronze Age. And so on.

Even many of our currently rare species were once much more widespread here. The rare chafer Gnorimus variabilis, for instance, used to occur in old trees on Tooting Common, London, now so long gone that none of the residents can remember there ever having been old trees there! It is currently confined in Britain to Windsor Forest
An interesting quirk is the story of the lime bark beetle Ernoporus caucasicus which was described in Britain from fossil remains found in the Somerset Levels long before anyone noticed that it was still alive and well and widespread across the Midlands!

But it is not all decline. Species have been colonising too, although mostly in response to the activities of people! Many species have been accidentally introduced through commerce and others through the introduction of exotic plants for gardens and hothouse collections. Some of today's commonest wood-decay insects came originally from long away. Good examples are the weevil Euophryum confine and the small fungus beetle Cis bilamellatus which originate from New Zealand. The jewel beetle Agrilus sulcicollis is one of the latest arrivals, having been expanding its range across Europe in recent years and was first noticed in Britain in 199 - did it fly the channel or did it hitch a lift on a timber lorry? 

Some species have established themselves in Britain firstly within buildings, but with global warming are not being able to live out of doors. An example is Alphitobius diaperinus, known as the Lesser Mealworm Beetle for many years as it has been exploiting stored products and especially deep litter poultry houses, but now its other name of Black Fungus Beetle is becoming more appropriate as it colonises old trees in the countryside.

Epiphytes
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The various plants which exploit the bare wood surfaces of trees as a place to grow includes mosses, liverworts, lichens and algae. The gradual build-up of these species into recognisable communities, as species colonise, grow and reproduce, is a very extended process, taking decades and even centuries to reach the full expression of diversity that can be achieved in this country. So the richest sites tend to be those with the oldest trees - depending on local conditions of course, notably air pollution levels as most are intolerant. A combination of adequate light levels, humidity, shelter and so also contribute. the need for good lighting means that it is the large old open-grown trees which support the richest epiphyte communities, rather than trees in closed canopy woodland.

Succession 
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Two year old twigs support different associations of species to say older branches and the ultimate species-richness of old trunks. Smooth-barked trees support different communities to heavily ridged trees, involving variability due to genetics, position, life history, etc, as well as due to different species.

Lobarion 
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The Lobarion is the famous community of ancient wood pastures, and occurs on the trunks and major boughs. It comprises the dramatic foliose species such as the tree lungwort Lobaria pulmonaria and rarer closely-related species such as Lobaria virens. the reddish liverwort Frullania tamarisci is a good indicator of the community as it is often very visible from a distance.

The Lobarion is confined to large old oak, ash and beech over much of lowland Britain, but the further west one travels then increasingly it may be found on younger trees. It is also more widespread in the west, due to the higher levels of air pollution in the east. Even with reduced air pollution it will take a very long time for this community to return to eastern woods.

Lecanactidetum premneae 
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This is the other classic ancient tree epiphyte community and is normally only found on trees at least 250-300 years old, and is mainly known from old pollard oaks, whose bark has become dry and brittle with age. The community is named for the major species in southern Britain...the crustose Lecanactis premnea. It is truly the ancient tree lichen community!

Further reading: Francis Rose Ancient British woodlands and their epiphytes (British Wildlife 1993 5: 83-93)

Invertebrates associated with epiphytes
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Most people are aware that epiphytes - lichens, mosses and liverworts - are of great interest in their own right, but remarkably few appreciate that the epiphytic vegetation itself supports a very interesting invertebrate fauna. As with all vegetation types, there are specialist communities of herbivores, detritivores, predators and parasites. These communities are relatively poorly known in Britain. The best known invertebrates are the moth species which have larvae which feed on the lichens and bryophytes. These include spectacular species such as the red-necked footman and merveille-du-jour, as well as a host of smaller and drabber moths.

A particularly interesting group are the barkflies (Psocoptera). The best known of this group are the infamous booklice, but the majority of the native species actually live on the bark or foliage of woody plants where they feed on algae, lichens and fungal spores. Although not well-studied, species richness appears greatest on large open-grown trees with varied epiphyte communities. It is in this situation where the scarcer species tend to be found, particularly those of the family Psocidae, eg the smoky-winged Metylophorus nebulosus and the various speckled-winged Trichadenotecnum spp.

Amongst the predators are the better-known carabid beetles of the genus Dromius, including the common and widespread D.quadrimaculatus and D.quadrinotatus, as well as scarcer species. The predatory minute bugs (Microphysidae) are also a characteristic inhabitant of epiphytes as well as fruiting fungi - the widespread Loricula elegantula and the scarcer Loricula pselaphiformis, as well as flowerbugs such as Temnostethus gracilis. 

Jumping spiders (Salticidae) are amongst the more noticeable inhabitants of the tree trunk outer surfaces. The common zebra spider Salticus scenicus is widespread on open-grown trees with sunny trunks, but a good range of other species also occur including the scarce Marpissa muscosa and the rare Salticus zebraneus. These predatory species overlap to some extent with the true wood-decay predatory communities - food is food wherever it develops! But they are not directly dependent on wood-decay organisms even though they will exploit them to some extent.

Molluscs are great grazers of these communities although, in contrast to the barkflies, tend to prefer the more humid conditions of closer-grown trees. They therefore tend to form the more diverse communities in ancient woodlands rather than the wood pastures. Tree snail Balea perversa lives up to its name by preferring more isolated trees.

Vertebrates using hollow trees and wood-decay
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Breeding birds 
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A wide range of birds nest inside tree cavities, some adopting existing cavities with little or no modification - such as owls, kestrels, marsh tit, tree-creeper - while others modify the cavity and its access considerably, eg woodpeckers and nuthatch.

Some are directly dependent on the trees for the bulk of their food, including foliage gleaners such as titmice and warblers, while others are specialists on wood-decay invertebrates plus invertebrates which are merely sheltering in the wood, eg overwintering or nocturnal insects. Generally the bird does not concern itself with why the particular invertebrate is where it is, merely eating it! The woodpeckers are the main birds specifically breaking into decaying wood in search of food - even nuthatch and treecreeper are mainly gleaning prey from the external surfaces and shallow cavities.

Bats
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Tree cavities provide very important roost sites for bats and a high proportion of our local bats are dependent on them - from the commoner noctule (in Britain) and Leisler's bat (in Ireland) right through to our rarer old forest bats, barbastelle and Bechstein's. Bechstein's is believed to mainly use rot-holes in the larger boughs high in the canopy, whereas barbastelle may be more characteristic of hollow trunks.

The impacts of the accumulation of bat droppings and urine within the tree have not been studied. Bat guano makes good garden compost so presumably the tree is able to benefit from its degradation within its cavities. The guano probably supports an interesting invertebrate fauna, but this too has not been studied.

Other mammals
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Other mammals also use tree cavities, particularly squirrels, but also foxes, mink, and anything else seeking dry sheltered conditions for resting, sleeping or even hibernation.

Amphibians
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Amphibians are also known to use old trees and decaying wood as places of shelter. The best known user is the protected great crested newt