Dead wood is those parts of the trees or shrubs where the trunk, branches, twigs or roots have died and become available as substrate for a variety of invasive organisms such as bacteria, lichens and fungi, making it more easily accessible for penetration by animals, both vertebrate and invertebrate, for breeding or shelter. The patterns of degradation over time provide a sequence of habitats which vary from large dry cavities in main trunks and large limbs suitable for nesting birds/mammals or summer roosts for bats, to a proliferation of microhabitats such as detritus and/or water -filled rot holes, assorted burrowings and detaching bark which host a very substantial invertebrate population of central importance in the woodland ecosystem.
In an unmanaged broadleaved forest such as that which covered most of Britain and Northern Europe, and the West Midlands in particular, after the retreat of the ice age some 10,000 years ago, around 17% of all the organic matter present is in the form of deadwood (cf. the extant Primeval Forest of Bialowiesa in Poland).
Our native flora and fauna largely evolved in such conditions and a very high proportion - about 13% - of our native invertebrate animal and fungus species have life cycles making them dependent on the dead wood environment at some stage during their development. In total, almost 5,000 British species are known to be associated with deadwood, but the true total is clearly far higher, as many species undoubtedly remain to be discovered and the life cycles of many others are unknown. Because the public are largely unfamiliar with these species, they are in most cases very poorly recorded, but they contribute enormously to our overall national biodiversity (compare the total known native British vertebrate fauna represented by 210 species of breeding birds, 48 mammals, 12 reptiles/amphibians and 38 freshwater fish). Because of their overwhelming importance in terms of biodiversity in this habitat, this Action Plan concentrates on invertebrates and fungi.
While some species of the deadwood community are relatively numerous and form a significant component of the woodland food chain; others are highly specialised, adapted to living in very specific and limited micro-habitats within the deadwood environment. Many of Britain's rarest and most endangered species are amongst the latter and are particularly susceptible to fragmentation or loss of habitat.
With the increase in human population, the deadwood habitat has been under pressure since prehistoric times, originally as a source of fuel and raw material for handicraft, more recently by a desire for tidiness and an, often exaggerated, perceived threat to public safety and security coupled with a lack of appreciation of its importance to wildlife. Harvesting of mature trees for timber rather than allowing them to mature, die and decay naturally has historically also had a major impact on the proportion of deadwood in woodland.
Dead wood exists not only as completely dead trees, either standing or fallen/felled, but most importantly as a very significant component of mature living trees (particularly pollards and hollow trees) and may be in the form of:
Within these general categories, a number specific primary micro-habitats can be recognised:
Other secondary micro-habitats, particularly important for insects, are formed as a result of colonisation of the primary habitats by bacteria, fungi and other insects:
Although technically not a true deadwood habitat, sap runs from wounds on mature and senescent trees provide an additional very rich habitat for a significant number of particularly scarce insect species in environments where deadwood abounds.
This is eloquently described by Stubbs (1972), but can be summarised as follows. Dead wood is invaded by bacteria, fungi and other micro-organisms which initiate chemical change and produce nutrients (e.g. sugars) that invertebrates can consume. While some invertebrates (particularly beetles) directly attack the unaltered wood itself, others thrive on the bacteria and fungi and the wood they have altered. Still others depend on the bores created by their fellow invertebrates or bore into the softened decayed for shelter or nesting space. Many prey on, or parasitise other invertebrates or live as scavengers in their nests.
A significant proportion of the invertebrates become prey to vertebrates, particularly birds and bats, which are in turn parsitised by other invertebrates or consumed by larger predators.
Dung and dead bodies are returned to the soil where they join the decomposed remains of the original dead wood, creating a habitat for soil organisms. Ultimately, virtually all the deadwood biomass becomes nutrients for the development of new organisms.
From the point of view of dead wood wildlife, there is very little difference between naturally fallen timber and cut/felled timber in the same location. Most species live in damp rather than dry dead wood, so tend to colonise the inner rather than the outer parts of stacked timber piles. Timber stacked in shade (i.e. within the woodland) is a much richer habitat than timber stacked in the open.
Fungi
Fungus spores, carried in the air, are deposited on the wood. If they land on a suitable spot they will germinate and send hyphae into the wood, gradually softening it and breaking it down. Under suitable conditions, as yet not fully understood, fruiting bodies are produced which spread spores to new substrates. The fruiting bodies are the visible signs of fungal activity, but the mycelium, in the form of fine thread like strands through the deadwood, is always there, carrying out the decomposition of the wood. As the wood is broken down, suitable habitats are provided for invertebrates and their larvae. The fruiting bodies of the fungi themselves also provide habitats for some specialised invertebrates, which may lay their eggs on or in the fungus, or "graze" on the spore-bearing surface. The fruiting bodies of the majority of deadwood inhabiting fungi are rather small or insignificant (microfungi), but many are much larger and appear in the form of toadstools or brackets (macrofungi).
Invertebrates
Invertebrates dependent on dead wood at some stage of their life cycle include species of worms, snails, copepods, millipedes, centipedes, pseudoscorpions, spiders, mites and numerous insects. Many other groups of invertebrates, such as woodlice (Isopoda), are common inhabitants of deadwood, but also thrive in other habitats.
Many of the flying insects involved (e.g. hoverflies) spend their immature stages (egg, larva, pupa) in deadwood, but their adult stages (those familiar to non-naturalists) are found in a wide variety of habitats (e.g. at flowers).
Other species dependent on dead wood
This document addresses primarily invertebrates and fungi, which are relatively well known - even if poorly recorded, but it must be recognised that there are numerous representatives of other groups which are dependent on the dead or dying wood environment and which contribute to the overall biodiversity of the habitat. These include viruses, bacteria, mosses & liverworts (Bryophytes), algae, ferns & horsetails (Pteridophytes) and others.
Some vertebrates are also dependent or largely dependent on the presence of dead wood for survival. These include woodpeckers, which are predaceous on insect dead wood insect larvae, willow tits, tawny owls, nuthatches and several species of bats (particularly the noctule bat) which rely on cavities in tree trunks for nesting or roosting.
Numbers of Species
The following table, derived from the data sources listed in Appendix C, shows the approximate numbers of species of invertebrates and fungi recorded from Birmingham and the Black Country ("B&BC"). A total of over 1100 species believed to be associated with dead wood have so far been recorded, but this is likely to be a significant underestimate of the true total, since many groups are very poorly known and under-recorded. Appendix C contains a table summarising the conservation status of the dead wood invertebrates.
| Group | Total Species Count | Dead Wood Associated | % Dead Wood Associated | |||
| UK | B&BC | UK | B&BC | UK | B&BC | |
| Beetles (Coleoptera) | 4114 | 514 | 754 | 62 | 18.3 | 12.1 |
| Flies (Diptera) | 6668 | 1082 | 737 | 154 | 11.1 | 14.2 |
| Bees, Wasps, Ants etc (Hymenoptera) | 6549 | 264 | 178 | 12 | 2.7 | 4.5 |
| Butterflies & Moths (Lepidoptera) | 2768 | 900 | 46 | 6 | 1.7 | 0.7 |
| Other Insects | 1973 | 317 | 33 | 6 | 1.7 | 1.9 |
| Non-Insects | 1724 | 420 | 25 | 4 | 1.5 | 1.0 |
| Invertebrates Total * | 23796 | 3497 | 1773 | 244 | 7.5 | 7.0 |
| Toadstools etc. (Agaricales) | 1633 | 821 | 204 | 140 | 12.5 | 17.1 |
| Bracket fungi (Aphyllophorales) | 702 | 216 | 519 | 194 | 73.9 | 89.8 |
| Jelly fungi (Tremellales S.L.) | 105 | 21 | 75 | 5 | 71.4 | 23.8 |
| Stomach fungi (Gasteromycetes) | 116 | 27 | 8 | 5 | 6.9 | 18.5 |
| Ascomycetes | 5100 | 904 | 1680 | 284 | 32.9 | 31.4 |
| Slime moulds (Myxomycetes) | 300 | 158 | 267 | 111 | 89.0 | 70.3 |
| Lichens | 1355 | 141 | 223 | 71 | 16.5 | 50.4 |
| Rusts & Smuts | 360 | 111 | 0 | 0 | 0.0 | 0.0 |
| Coelomycetes | 643 | 259 | 40 | 16 | 6.2 | 6.2 |
| Hyphomycetes | 1113 | 196 | 200 | 55 | 18.0 | 28.1 |
| Others | 3573 | 32 | 0 | 0 | 0.0 | 0.0 |
| Fungi Total ** | 15000 | 2886 | 3216 | 881 | 21.4 | 30.5 |
| Invertebrates + Fungi | 38796 | 6383 | 4989 | 1125 | 12.9 | 17.6 |
* Includes a few species also associated with live timber and
species associated with sap runs.
** Includes species recorded from the whole of Warwickshire
- Trim/remove only individual branches, leaving other branches & trunk standing,
- Remove as little of the trunk as possible, leave a stump standing as high above the ground as possible,
- Never remove the stump and roots - always leave them to rot in place. Stump grinders should only be used in the most exceptional circumstances.
- Wherever possible leave it lying where it fell (naturally or by cutting), especially if it is partly submerged in water (pond, lake or stream),
- Move it to similar situation in shade nearby site of origin,
- Stack cut timber in shaded position as close as possible to site of origin,
- Stack cut timber in shaded position at a remote site
- Stack cut timber in poorly shaded position close to site of origin,
- Chip timber and leave it in piles in shaded position around sites of origin,
- Chip timber and leave it in piles at in shaded position at remote site.
- Chip timber and spread it evenly as close to site of origin as possible.
As an alternative to stacking cut timber, consideration may be given to securing it in a (near) vertical position by strapping it to an existing tree trunk or propping it against another tree or a bank etc..
- Propping the suspect limbs/trunks,
- Moving/rerouting the paths away to a safe distance,
- Preventing/limiting public access by fencing, or hedges/boundaries of suitable plants (hawthorn, bramble, etc).
The British Red Data Books provide an assessment ("RDB category") of the rarity and vulnerability of most (the better known) species of insects (Shirt, 1987) and fungi. The reader is referred to those publications for a full definition of each category.
| Red Data Book Status | Total Species Count | Deadwood Species | % Species in Deadwood | |||
| UK | B&BC | UK | B&BC | UK | B&BC | |
| Presumed Extinct - Not recorded since 1900 | 148 | 0 | 25 | 0 | 17.0 | 0.0 |
| K - Insufficiently Known | 456 | 1 | 56 | 0 | 12.0 | 0.0 |
| 1 - Endangered | 587 | 4 | 95 | 0 | 16.0 | 0.0 |
| 2 - Vulnerable | 397 | 5 | 54 | 1 | 14.0 | 20.0 |
| 3 - Rare (found in<16 10km squares) | 811 | 15 | 95 | 1 | 12.0 | 6.7 |
| Notable - Known from 15-100 10km squares | 2739 | 129 | 356 | 17 | 13.0 | 13.2 |
| Unclassified | 15395 | 3343 | 1092 | 247 | 6.0 | 7.4 |
| Total | 20533 | 3497 | 1773 | 266 | 8.6 | 7.6 |
The invertebrate species counts in tables 1.1 and B1.1 were derived from a following sources:
Counts of overall numbers of British species and those known to be associated with dead wood were derived for each systematic group using a variety of published reference works. This has been compared with the published list of species recorded in Warwickshire (updated with some unpublished more recent data) to derive figures representative of the local area. It must be emphasised that records for the whole of Warwickshire are included, incorporating some areas not strictly within B&BC.
Technical terminology has been avoided as far as possible in the main text of this BAP. Nevertheless, anyone reading the recommended references will quickly come across such terms. A summary of the more common terms is given here to assist in understanding those references.
| Term | Meaning |
| Saproxylic | Species that depend on wood, usually but not always dead wood, for some part of their life-cycles. Typically used in reference to invertebrates. |
| Saprophytic | Organisms living on dead organic matter. Typically used in reference to species of fungi |
| Pollarding | The (ancient) practice of lopping off the top of a tree 2.5 to 4m above ground level (above the level browsed by grazing animals). New shoots grow at the point of cutting or below. The process is repeated at regular intervals and seems to act in a rejuvenating fashion. Many pollarded trees reach a considerable age, much older than maidens of the same species. Their trunks typically grow thick and gnarled with zones of dead timber. |
| Coppicing | Similar to pollarding, but the lopping is carried out close to the ground. The coppice stool contains relatively little volume of over-mature timber and so constitutes a relatively poor dead wood habitat |
| Name | Location | Speciality Interest |
| Dr. D. Antrobus | Birmingham | Fungi |
| Mr. T. Bird | Walsall | Tree management |
| Mr. M. Bloxham | West Bromwich | Invertebrates |
| Mr. E. Browne | Wolverhampton | Coeloptera (beetles) |
| Mr. S. Hinton | Birmingham | Tree management |
| Mr. P. Millett | Wolverhampton | Reserve & Park Management |
| Dr. J. Sadler | Birmingham | Coeloptera (beetles) |
| * Dr. M.J. Smart | Wolverhampton | Diptera (flies) |
| Mr. N. Williams | Birmingham | Fungi |
| Mr. N. Wilde | Wolverhampton | Fungi |
| Mr. W. Moodie | Birmingham | Fungi |
* facilitator & editor
The following people have contributed advice and assistance to the committee during the preparation of this document:
| Name | Location | Subject |
| Dr. K. Alexander | NT, Cirencester | Pre-publication access to saproxylic invertebrate list |
| Mr. P. Chandler | Burnham | Information and references on dead wood diptera |
| Dr. P. Coxhead | Aston University | Access to Sutton Park record database |
| Mr. S. Falk | Coventry Museum | Access to pre-publication information on Sutton Park Survey |
| Mr. T. Hextall | Birmingham | Advice about birds associated with dead wood |
| Dr. M. Hull | Liverpool Museum | Information on dead wood microlepidoptera |
| Mr. S. Judd | Liverpool Museum | Loan of reference books |
| Dr. R. Key | EN, Peterborough | Reference list |
| Ms. B. Pederson | RES Library, London | Help with obtaining obscure references |
| Mr. S. Phipps | Walsall | Advice about bats associated with dead wood |
| Mr. J. Preston | Saltwells LNR | Loan of reference books |
| Dr. M. Speight | Eire Wildlife Service | Permission to use material from SYRPH-THE-NET database |
| Mr. P. Stephenson | B&BCWT | Considerable general guidance |
| Mr. A. Stubbs | Peterborough | General information, advice |
| Mr. D. Sumner | Leicester Museum | References |
| Mr. D. Whiteley | Sheffield City Museum | Loan of reference books |
Biodiversity Action Plan for Birmingham and the Black Country © 2000
Printing of this publication for educational purposes is permitted, provided that copies are not made or distributed for commercial gain, and the title of the publication and its date appear. To copy otherwise, or to republish, requires specific permission from the Steering Group.