3.3 Site selection
Woodlands are in some ways the most difficult of major ecosystems to deal with in the field of conservation. Although representing the climatic climax over much of Britain, woodland is now highly fragmented and woodlands of native species cover only a small fraction of the total land surface. Moreover, if any natural woodland remains, it is of very small extent. There has, nevertheless, been a great deal of concern about the structure and floristic composition of natural woodland, and many conservationists believe that this is an ideal condition which management should aim to restore on at least some of the important woodland sites. Thus sites which show the closest approach to thepresumptive original state tend to be the most highly valued.
Woods have a dual nature; they are assemblages of trees with value and interest in their own right, and they are also the habitat of other organisms, including plants of quite different life-form and animals of many kinds. The con-servationist is interested in both aspects of woodland, often on the same site, but sometimes separately. Given sufficient time, the tree component of the woodland ecosystem can be manipulated by management into almost any desired state, but the dependent organisms are less easily controlled at will. A desired tree structure and composition could eventually be obtained by planting an open field with appropriate species, but development de novo of the mature woodland with all its associated flora and fauna is likely to take centuries rather than decades, and is to be regarded more as a very long-term possibility.
Trees have a limited life span and unless there is adequate regeneration a wood will eventually die out. Woodland trees are seldom allowed to die of old age, and are usually cut for timber when mature. Coppicing of younger trees may prolong the life of individuals for a very long time, but usually there comes a point in the cycle when tree cover must be perpetuated by the growth of new individuals. In Britain, this regeneration is usually achieved by the planting of seedlings grown in nurseries. On nature reserves, natural regeneration is usually prescribed as a more desirable policy. There has thus been a tendency to rate highly those woods which show good natural regeneration and an uneven age structure of the dominant trees.
Areas where there has been continuity of woodland cover right through the Post-glacial Period are usually richer in dependent communities and organisms than sites where tree cover has been discontinuous during the last few centuries. The persistence of sensitive associates dependent on tree cover may well reflect a rotational cropping and regeneration within one woodland block, which has ensured that parent populations of the sensitive species were always at hand to supply new offspring to the regenerating forest. When species have been entirely lost from a site during a period of woodland clearance, their capacity for recolonisa- tion of re- established forest clearly depends on their powers of spread and establishment. Mobile creatures such as birds, mammals and some insects most readily recolonise reestablished woodland, but this ability varies from species to species. The crested tit is a British forest bird showing a very limited capacity for spread from its established Scottish haunts. Many insects, although theoretically mobile, appear to be remarkably sedentary in distribution over a period. Common plants are able to spread easily, and this is perhaps especially true in general of ferns, bryophytes, lichens and fungi with small, wind-dispersed spores. On the other hand, the rarer members of the flora (including these cryptogams) are usually characterised by an extremely limited capacity for spread, and once they have disappeared from a woodland site, perhaps during the unfavourable conditions of a clearance period, they have gone virtually forever unless they are deliberately reintroduced, and this may be difficult.
Because of their almost complete inability to spread and recover lost ground under the present, fragmented state of our woodlands, many vascular plants, ferns, bryophytes, lichens, fungi, insects, arachnids and molluscs are consistently absent from re-established woodland and are therefore reliable indicators of ancient, permanent woodland.
In general, therefore, re-established woodlands have a lower conservation value than permanent woodlands, in terms of richness of components other than the tree layer, as well as in the historical features discussed earlier. In both types, the tree layer itself may show all degrees of change in composition or reduction in diversity according to the conditions of management.
Woodlands have a great diversity of interest, so that the criteria of evaluation in assessment for conservation are necessarily numerous. They have the most complex organisation of any ecosystem and are the most luxuriant of all living communities; as such they have been a favourite focus for studies of the circulation of nutrients and energy, and of biological productivity. The economic values of trees cannot be divorced from nature conservation and the tree component of native woodland is commercially valuable, provides opportunities for silvicultural research and is an important source of genetic material. Woodlands are also important in demonstrating ecological relationships, including the response of vegetation to climatic change, the effects of spatial differences in soil conditions, plant succession, and the influence of man. Trees have a key position in the understanding of vegetational history, through pollen analysis, subfossil wood remains, dendrochronology, and the long-lasting effects of management practices inscribed in the living trees. Woodlands and trees are important features of the landscape and are of major recreational and educational value.
The nature conservation value of woods composed partly or wholly of alien species is a difficult subject. The present review is concerned essentially with assessing their value in relation to the selection of a series of nationally important woodland sites. The boundary between indigenous and non-indigenous species is not always clearly defined but, in general, it is accepted that alien trees have a lower conservation value than native species, both in themselves and with particular reference to invertebrates, as habitats for dependent organisms. However, well-established and freely regenerating aliens such as sycamore are of considerable ecological interest, and introduced poplars are important food plants for a number of interesting moths. Scots pine, outside its native range, is a common component of many woods dominated by deciduous trees, and is, for example, often preferred as a nest site by sparrowhawks. The pine rows and clumps are an artificial but characteristic feature of the East Anglian Breckland and are here largely responsible for the occurrence of the interesting population of breeding crossbills. The feeling that the purity and therefore quality of a native woodland is in some way diminished by the presence of alien trees cannot always be substantiated in reason. The presence of a certain proportion of non-native trees can add to the interest of a woodland, and may
Criteria for key site assessment and selection enhance the faunal diversity. The undesirable state is reached when alien trees cover such a large part of a wood that it cannot be regarded as a good example of the native type, or when vigorously competitive aliens are spreading at the expense of native species and creating unfavourable habitats for associated organisms. A good example of the second situation is the spread of rhododendron in some oak- woods, and the resulting virtual elimination of the field and ground layers.
Much depends on the species. Those which cast deep shade, such as rhododendron, sycamore and spruce tend to be regarded as undesirable, whereas Turkey oak, common lime and sweet chestnut are viewed with more favour. Some species are native in part of their range and introduced elsewhere (e.g. Scots pine, beech and hornbeam) and, while the presence of these is not regarded as objectionable, they are not usually rated so high in conservation interest in non- native localities. This does not always hold, as the entirely planted woods around Stornoway Castle, Lewis, are of very considerable regional interest. It is generally felt, however, that woods composed largely of introduced species do not merit grade i or 2 status. This is particularly so in the case of commercially grown species; it is pointless to give this grading to a wood of Sitka spruce or lodgepole pine at this time, when such large areas of these species are being planted every year.
Plantations of non-native trees, notably conifers, are of considerable conservation value. Especially in their younger stages, some have proved to be important habitats for rare breeding birds such as short-eared owl, hen harrier and Montagu's harrier (see subsection on birds, p. 89). These non-indigenous and recently created forests are so widespread and cover such a large total area that they are a major wildlife habitat in Britain. Nevertheless, most of these artificial forests, especially when mature, are so fundamentally different from the native woodlands that they can never represent the most important attributes of the latter or take their place as conservation sites. Much of the artificial woodland is re- established on ground which has had a long period without trees, and the associated communities which develop within, especially of plants and invertebrates, are usually of minor interest in that they are composed of common, rapidly spreading species, or those remaining from the treeless phase. Many conifer forests have such a high stocking density of trees that the subsidiary vegetational component is virtually eliminated and the fauna becomes greatly reduced, though some woodland birds thrive. Much can be done to improve the nature conservation value of commercial conifer forests by modifications in management, but it would be inappropriate to develop this theme here. Moreover, where native deciduous woodland is cleared and replanted with alien conifers, considerable subsequent impoverishment of the field and ground communities and the invertebrate fauna occurs, and this change in management involves greater conservation losses than gains. Native woodlands in Britain are a rapidly diminishing resource and the conservation of a representative series is a matter of the greatest urgency.
Comparative site evaluation
With these considerations in mind, the following attributes in particular are weighed in the comparative evaluation of the individual sites:
Size
Diversity
 
Permanence

Lack of modification

Rarity

Requirements for the national series

Implications for conservation
3.3.1 Size
The nature conservation value of a woodland tends to increase with size. Only in a large wood may it be possible to encompass the local range of diversity or to achieve diversity by means of different silvicultural systems or management practices. Large size is also a safeguard against accidental destruction, e.g. by fire. Experiments may need homogeneous conditions over an area of adequate size or they may be concerned with ecological diversity; both requirements are more likely to be satisfied in a large area than a small one. Some organisms, e.g. large birds, require a fairly large minimum area, depending on their territory size, so that a substantial area may be needed to contain a reasonable population.
3.3.2 Diversity
Diversity in woodland is of several kinds. There is structural diversity, including different age of the trees. Ecological diversity involves floristic and faunal variability within any part of a wood especially in response to varying soil conditions and topography, and also relationships in space and time such as the catena, serai stages and succession. 
3.3.3 Permanence
A site which has been continuously occupied by woodland is usually more valuable than one where woodland has been re-established after a break in continuity, especially in regard to subsidiary elements of the flora and fauna. Its value will be further enhanced if a good historical record is available. Such woods are historical monuments, embodying many aspects of past rural life and organisation. Climax woodlands are to be preferred to serai types, for though examples of the latter are valuable in demonstrating dynamic processes, they can be more easily and rapidly created. The few examples of woodlands which appear to approach a 'natural' state are regarded as especially important, though they are usually fragments on islands, landslips, cliffs and ravine sides.
3.3.4 Stability
While the tree layer usually reflects the silvicultural system used (and the range of system requires representation), the quality of the shrub and herb layers is particularly dependent on the absence of such influences as grazing by large herbivores. The permanence of tree cover may be especially important in maintaining the floristic richness of the subsidiary layers. 
3.3.5 Rarity
The presence and abundance of rare species of trees, shrubs, herbs, pteridophytes, bryophytes and lichens, and of animals, gives an added value to a woodland site selected on other criteria, but rarity is usually taken as a major criterion for selection only when a group of such species is involved. A very few sites are selected for the rarity of one species.
3.3.6 Representation
Selection of the national series of key woodland sites has involved an attempt to represent adequately the most important types within the total field of variation. When the many directions of variation in woodlands are considered, especially in relation to the partial independence of the separate structural layers, the number of possible combinations of different character, i.e. the number of different woodland types, is extremely large. However, it is more realistic to lump small, closely related differences, and thus to reduce greatly the number of different woodland types required in the national series. Certain highly modified or degenerate types of woodland have deliberately been omitted, and a wide range of types with high nature conservation value has been included.
Choice of sites has been based first on the different major woodland types as identified by the dominant tree species (oakwood, pinewood and so on), and then on the range of diversity within the other components of the wood and ecosystem, i.e. the other layers, flora and fauna. Within each major woodland type the number of sites chosen has depended on the relative geographical extent and variability of the type. Mixed deciduous woodland is the most widespread and variable British woodland type and so is represented by the largest number of sites, whereas a local type such as pinewood is represented by a much smaller number. In addition, particular attention has been paid to representation of the following features.
1 Major silvicultural systems which influence the structural character of a woodland, especially in the tree and tall-shrub layers, e.g. high forest, coppice, coppice with standards, park woodland. These are represented under separate ftoristic woodland types, as relevant, e.g. oak high forest, oak-hazel coppice with standards, hornbeam coppice.
2 Other structural variations, related mainly to variations in development of the tall-shrub and field layers.
3 Topographic variations. These apply mainly in hilly country where differences in angle of slope, aspect and rocki-ness give different types of wood associated with plateaux, steep slopes (hanging woods), valley bottoms and river gorges. In some districts, e.g. the Vale of Ffestiniog, north Wales, and Borrowdale, Lakeland, the number of sites chosen within the same area is an attempt to represent this range of diversity, which seldom falls within the compass of a single woodland block, although it does so in the Wye valley, south Wales.
4 Local diversity in soil conditions. This is often associated with feature 3 above, especially in sites representing a catena, where both nutrient status and wetness of soil are affected by topography. Base-status is also strongly influenced by the nature of the parent rock and where there are non-calcareous and calcareous rocks within the same wood or in the slope above, the effect on woodland floristic composition is usually very marked. Where this situation obtains, it is often possible to have good examples of different major woodland types represented within the same site. A classic case is Roudsea Wood, north Lancashire.
5 Woodland succession. Colonisation of acidic mire or heath by birch and pine, and of base-rich fen by alder and willow, is well represented on many peatland and heathland sites. There are also many examples of the changes associated with the coppice cycle. The replacement of one or more dominant tree species by others is a rarer condition, but examples have been chosen which may throw light on some species relationships not yet fully understood, e.g. oak- beech, beech-ash, birch-oak, birch-pine and oak-pine.
6 Natural woodland. This is so fragmentary that it has a considerable scarcity value and examples are difficult to find. Indeed, it has been said that there is no woodland in Britain completely unmodified by man. Woods which approach most closely to the presumptive original condition are in relatively inaccessible situations, and in remoter parts of Britain. A range of types has been included in the national series but none is extensive.
7 Floristic richness of the subsidiary layers. Selection for a wide range of tree and tall shrub species is implicit in what has been said above (except perhaps for rare and local shrubs such as Sorbus spp.), but this does not necessarily take equal account of variety in the field and ground layers. Care has been taken to represent the full range of floristic richness, especially on the calcareous rock formations, where the herbaceous component of the woodland flora is often very varied and rare species (e.g. certain orchids) are well represented. In a few instances woods which are of no particular interest for their tree and shrub component have been chosen for their rich herbaceous flora (e.g. Conistone Old Pasture and Bastow Wood, Yorkshire).
In western Britain many woods, especially those with rocky floors or stream ravines, are extremely rich in bryo-phytes, which grow in great abundance and luxuriance. There is a strong component of Atlantic mosses and liverworts forming an interesting phytogeographical element for which Britain and Ireland form the European headquarters. This Atlantic bryoflora changes somewhat in composition latitudinally, especially in representation of southern, thermophilous species, and there are also differences in richness according to degree of humidity. A series of sites (especially sessile oakwoods, since most Atlantic species are calcifuge) has been chosen to cover the range of variation in south-west England, west Wales, north-west England and western Scotland. Stream gorge woodlands are well represented.
Britain has a rich Atlantic lichen flora, in parallel with the bryophytes, though there is a different bias in habitat preference, and epiphytic lichen interest is only partly covered in the selection of woods rich in Atlantic bryophytes. Selection of additional sites for their rich lichen flora has thus paid special attention to the park woodlands which are an optimum habitat for some species and are so especially a feature of Britain.
8 Vertebrate interest. Selection of woodlands for botanical features automatically includes a wide range of variation in species of vertebrates, especially birds. Ornithological interest has often been used as a secondary criterion in the choice of woodland sites primarily for botanical reasons. In some instances, however, ornithological interest may rate more strongly. The important and distinctive avifauna of the central Scottish pinewoods, and the extremely diverse and large bird populations of the New Forest have already been mentioned.
9 Invertebrate interest. Several woodlands have been chosen especially for the richness of their insect fauna, notably the Lepidoptera, e.g. Monks Wood, Huntingdonshire; Waterperry Wood, Oxfordshire; and Craigellachie Wood, Inverness-shire. This has also been a strong supporting criterion in many other cases, e.g. the New Forest. The other groups of woodland invertebrates have been much less fully surveyed, and it is not known how adequate the present selection of sites will be for the conservation of this very large group of organisms.
10 Features of international importance. These are mainly floristic features associated with the strongly oceanic climate of Britain. Particularly noteworthy woodland species and communities in Britain are ash as a tree dominant, holly and various whitebeams in the tall-  shrub layer, bluebells and various ferns as field layer dominants, bryophytes in general and Atlantic species in particular in the ground layer, and lichens (especially Atlantic species) as epiphytes. All these features are well represented in the selection of woodland sites now to be described.
3.3.7 Management issues
A major problem in the conservation of woodlands is the high degree of fragmentation to which this ecosystem has been subjected. Ideally, one would wish to safeguard a large continuous block of woodland containing the whole range of local environmental diversity that is characteristic of the particular region. Separate blocks would then be chosen to represent the major regional environmental differences, which would be mainly climatic but partly geological. This ideal situation hardly exists anywhere in Britain at present, and it is usually necessary to select several discrete sites in attempting to conserve the woodland diversity characteristic of any particular district; sometimes these sites are not widely separated, however, and there is a case for treating them as a single aggregate site (e.g. Borrowdale Woods, Cumberland). Even the limited range of diversity peculiar to a single local woodland type (e.g. oak-lime woods in Lincolnshire) may not be represented in one site, and it is necessary to include two or more adjacent sites in order to encompass adequately this variability. The sites selected and delimited are often only part of a more extensive block of woodland, which also has features of ecological importance. Though every attempt has been made to delimit precisely the area of importance, the boundaries of some sites may, on further inspection, require alteration. Similarly, as our knowledge of the flora, and more particularly
the fauna, increases it may be necessary to revise this list of key sites.
In many cases where numerous woods of biological importance occur in a restricted geographical area it is perhaps inappropriate to select a few particular sites and more appropriate to achieve conservation through prescriptions aimed at the management of the woods as a whole. Examples of such areas are the western Weald, New Forest, Forest of Dean, Dartmoor woodlands, Wye valley, north Wales, Lincolnshire, Lake District, Loch Sunart and Spey-Dee Valleys (see also Chapter 13). Selection of separate sites in such areas is difficult, but an attempt has been made to do this, to maintain uniformity of treatment throughout the Review.