2.1.1 Investigations at Céide Fields (Behy court tomb) by Smith et al. (1973)

In the early 1970s, investigations that included pollen analysis and ¹⁴C dating were carried out by Smith and colleagues in Queen's University Belfast on a monolith taken in the vicinity of Behy court tomb (see photo in Fig. S8a). The sampling location was most likely close to profiles BHY IV and BHY V (Fig. 1b; probably near to BHY V, i.e. the one nearer to the court tomb).

The results of the ¹⁴C dating were problematic in that the uppermost date, 3930±105 BP (from −36 to −38 cm, fine particulate fraction; the negative depths indicate distance above the mineral soil–peat interface), was the oldest, while the fine particulate and humic fractions of the lowest sample (−24 to −28 cm) yielded distinctly different dates (3890±110 BP and 3245±70 BP, respectively). Smith et al. (1973) concluded that the movement of humic acid in the peat resulted in ages being apparently too young. The sample (bulk sample) from −30 to −34 cm also gave a ¹⁴C date younger than expected that, according to the investigators, was the result of humic-acid movement in the peat.

Using an age–depth curve based on three dates, i.e. 3890±110 BP, 3930±105 BP and a surface point with an estimated date of 1950 CE (peat thickness estimated to be 170 cm), it is estimated that peat initiation began at ca. 3350 BCE. The pollen data (not published) indicated that, in the basal peat, oak-dominated woodland prevailed and, rather significantly, there is no mention of pine (Smith et al., 1973). The base of the record thus seems to postdate the pine flush in the area (see Sect. 5.1). The peat–mineral soil interface in profile BHY V dates to 2500 BCE which would appear to be a more realistic, even if too young, date for initiation of peat accumulation close to the Behy tomb (see Sect. 5.1).

Smith et al. (1973) suggested that, on the basis of a comparison of the pollen data from the monolith with those from a sample from beneath cairn stones (presumably associated with the tomb), construction of the cairn that is associated with the tomb took place as peat at −27 to −28 cm (dating to ca. 2500 BCE) accumulated. From what is known about the age of court tombs (Schulting et al., 2012) and our present understanding of Neolithic and Bronze Age developments in the Céide Fields area, it is doubtful that cairn (and court tomb) construction was so late.

2.1.2 Pollen analytical investigations at Céide Fields by Moore (1979)

Moore (1979) discusses pollen profiles that had probably been constructed about a decade before publication, i.e. Behy I from beside the Behy court tomb and Behy II from 2 km to the west and at lower elevation (profiles Behy I and II are reproduced in Fig. S1a), and a third from Glenamoy (deeper peat; pollen diagram not published). There is no independent evidence of age, but the pollen signature is such that it can be assumed with a high degree of certainty that the base of Behy II predates the start of Neolithic impact and that Behy I starts in the middle to late Neolithic.

Behy I shows high arboreal pollen (AP) levels, including high Pinus values (∼20 %–30 %), in a few spectra at the base after which non-arboreal pollen (NAP) levels and especially Poaceae (initially), Ericoids (presumably mainly Calluna) and Potentilla-type pollen have increased representation. A Plantago lanceolata curve begins when Pinus starts to decline and continues, though frequently interrupted, until mid-profile where the values increase at first modestly but then substantially towards the top. Profile Behy II is longer (230 cm) and the base is older. Noteworthy is a major decrease in Pinus together with the first records for cereal-type pollen and P. lanceolata near the base of the profile (corresponding to Neolithic landnam followed by increased AP (corresponding to woodland regeneration), including a rise in Pinus (i.e. a pine flush) and then the demise of pine and expansion of grasses and heathers. These later changes are comparable to those recorded in Behy I.

2.1.3 Pollen analytical investigations at Belderrig by Bourke (1972)

These investigations resulted in a pollen profile (here referred to as Belderg; for a summary pollen diagram (profile BDG1) see Fig. S1b) from beside a stone wall on peat (wall 3 in Verrill and Tipping, 2010a) that has been dated to the late Bronze Age (it is regarded as the extension of a much earlier wall onto peat; see Sect. 1). The pollen profile is similar to Behy I in that, at the base, AP dominates (mainly Corylus/Myrica). Pinus subsequently increases to achieve 33 % which is regarded as reflecting a pine flush. After that, Pinus decreases to low values and does not recover. Initially Betula expands and then Poaceae. These developments are very similar to those recorded in BHY VI (see results in Sect. 4.1.2) but have little in common with profile BEL by Verrill and Tipping (2010b) which is from less than 250 m away (see Sect. 2.2.2). Interestingly, P. lanceolata values are low (more or less continuously but generally < 2 %), and only a few cereal-type pollen grains are recorded which suggests low levels of farming. Perhaps the investigations are insufficiently detailed to comprehensively reflect farming activity, the evidence for which, including cultivation ridges, ard marks, lynchets and a saddle quern, points to substantial arable activity. The arable activity may have been confined to the vicinity of the Bronze Age house where the ard marks and overlying extensive cultivation ridges were recorded (see Sect. 1 and Fig. S8b). This is ∼190 m downwind from the profile location which, given that cereal pollen is poorly dispersed, is considerable.

2.2.1 Investigations at Céide Fields (Molloy and O'Connell, 1995; O'Connell and Molloy, 2001)

Detailed pollen analytical investigations commenced in 1992 with a view to reconstructing long-term vegetation history, long-term human impact and blanket-bog development at the main stone-wall complex that is usually referred to as Céide Fields. For this purpose, monoliths consisting of blanket peat and underlying mineral soils (BHY III–VI, also monoliths and samples from at and beside the visitor centre), as well as a long core from Glenurla basin (GLU IV) which lies within the field complex, were collected (Figs. 1b and S8a). The main results were published in Molloy and O'Connell (1995). These were later summarised, together with additional details, in a review paper relating to Neolithic impact in Ireland (O'Connell and Molloy, 2001). Since these investigations are still the main evidence for environmental change at Céide Fields, the data are presented below in some detail, together with information that was not available at the time of the earlier publications including additional ¹⁴C dates obtained in 2000, loss-on-ignition (LOI; ashing) measurements and tephra investigations. Details regarding results of the tephra investigations, including geochemical analyses, will be published separately.

2.2.2 Palaeoecological investigations at Belderrig by Verrill and Tipping (2010a, b)

These authors presented information derived from multidisciplinary investigations relating to the Belderrig field system, including a pollen diagram that spanned ca. 3600–2500 BCE. The dates derived from these publications that we cite below, including the age–depth relationship for the profile, are based on the ¹⁴C dates given by the authors that have been recalibrated (the resulting differences are small). Verrill and Tipping (2010b) showed that substantial mineral soil erosion took place after wall construction (in the Neolithic) and that peat initiation was time transgressive, beginning in the basin (wood peat being initially formed rather than blanket bog) and proceeding upslope where blanket-bog peat began to accumulate in the early Bronze Age (ca. 2010 BCE). Interestingly, Dwyer and Mitchell (1997; see Sect. 2.2.4) also report diachronous peat development at Croaghaun East, to the south of Céide Fields, where peat initiation started distinctly later (at ca. 3800 BP, i.e. 2200 BCE) at a downslope location from the main core. It is suggested that blanket-bog expansion coincided with increasing wetness, and at two locations in Croaghaun East it dates to ca. 4200 BP, i.e. ca. 2900 BCE.

The main features of the pollen diagram BEL by Verrill and Tipping (2010b) include dominance of Alnus (the pollen was so abundant that it was excluded from the pollen sum), little P. lanceolata apart from a single spectrum near the base where it achieved 2 %–3 %, exceptionally high Ilex (holly) values (for much of the profile 5 %–18 %), and AP taxa consisting mainly of Corylus, Pinus and Quercus. There is a small peak of Pinus near the top that may reflect a pine flush though it is rather late (ca. 2600 BCE) if it is the classical pine flush (see Sect. 5.1). Cereal-type pollen is not recorded. Caulfield (2018, p. 66), in what appears to be a reference to this pollen profile, points to records of cereal pollen in “the upper levels of the core” which he attributes to “the tillage plots to the west”. Only part of the pollen profile may be published in Verrill and Tipping (2010b), which, if correct, is regrettable given the importance of the site. The tillage plots referred to by Caulfield (2018) are presumably those associated with the late Bronze Age house.

On the basis of their investigations, Verrill and Tipping (2010b) draw various conclusions regarding human impact and farming in the area. They suggest that the base of profile BEL, which dates to ca. 3600 BCE, captures the final phase of Neolithic farming and that, outside the field system, a partially wooded landscape persisted. In reality, more data are required, including much higher pollen counts, to enable firm conclusions to be drawn regarding Neolithic farming at Belderrig.

Verrill and Tipping (2010b) emphasise the importance of climate rather than human impact as a driver of landscape change including blanket-bog formation. Humification data relating to core BEL suggest particularly low peat humification in the interval 3000–2900 BCE, this trend having set in as early as 3200 BCE. Lower levels of peat humification are interpreted as signalling wet climatic conditions. Low humification and decomposition are regarded as giving rise to low pollen concentrations as a result of faster peat accumulation, which is plausible but additional independent evidence is desirable. Apart from an interruption in the Calluna curve, the curves for bog and aquatic taxa remain steady. This is not what might be expected if the mire surface became substantially wetter. The evidence for increased wetness due to wetter and stormier conditions at Belderrig is not as well founded as implied by Verrill and Tipping (2010b) and indeed does not agree with the evidence derived from the pine timber record for the north Mayo region (see Sect. 5.1).

In Verrill and Tipping (2010a) attention is focussed on the tillage plots (cultivation ridges and ard marks) associated with the Bronze Age house (Fig. S8b). In thin-soil sections, features associated with the cultivation ridges were clearly distinguishable, but it was not possible to be definitive as to whether the cultivation ridges were made using an ard or spade. Caulfield (1972) assumes the latter which is plausible on the basis of recent ethnographic parallels (Bell and Watson, 2008; see also photographs in Fig. S8b). The ard marks could not be distinguished in thin sections, nor were they distinguishable in the pollen profile (Verrill and Tipping, 2010a). The unnamed pollen profile, derived from mineral soil and overlying peat samples taken in the area with cultivation ridge and ard marks, is here referred to as BEL-S1. As expected, pollen assigned to cereal-type and weeds of arable or disturbed ground and also P. lanceolata are well represented in the spectra from the mineral soil. Calibration of the only available ¹⁴C date, i.e. 2450±35 BP, from the basal peat suggests a terminus ante quem for local peat development of ca. 600–410 BCE (53 % probability), but an older date cannot be ruled out (26 % probability that the ¹⁴C date relates to the interval 750–680 BCE). Given that the ¹⁴C date relates to basal peat and also bearing in mind ¹⁴C dates relating to the site that have become available more recently (Caulfield et al., 2011a; Warren, 2018), it is reasonable to conclude that the final phases of tillage as recorded in the pollen record relate to the late Bronze Age. This conclusion is also supported by the lack of Pinus in profile BEL-S1 though it is unclear if Pinus pollen was actually not recorded; it may be that Pinus records were simply omitted from the pollen diagram (Verrill and Tipping, 2010a). The ard marks, originally regarded as possibly Neolithic (Caulfield, 1972), have been assigned to the late Bronze Age by Verrill and Tipping (2010a), a view that appears to be generally accepted (e.g. Caulfield, 2018). In other words, they are probably not much older than the overlying cultivation ridges.

There is evidence that farming, including cereal cultivation, continued at the site before and after house construction (Caulfield, 1973, 2018) and indeed over a considerable period (Verrill and Tipping, 2010a). Interestingly, Verrill and Tipping (2010a) point to soil features that suggest amelioration practices including the addition of domestic waste (ash and animal bone) to the area under tillage.

2.2.3 Pedological investigations at Belderrig, Céide Fields and Rathlackan by Guttmann-Bond et al. (2016)

These authors report on multidisciplinary investigations carried out on test-pit profiles from the three key archaeological areas in north Mayo listed in the subtitle above. The main test pits within each area are from locations where there was evidence for arable cultivation, mainly in the form of cultivation ridges and/or ard marks. From Belderrig, accelerator mass spectrometry (AMS) ¹⁴C dates – 3563±30, 3649±30 and 3091±29 BP – are provided. These support the idea of activity extending over a considerable duration in the middle to later Bronze Age in the vicinity of the roundhouse. At Céide Fields, test pits were dug near the visitor centre where excavations prior to construction of the centre revealed the presence of ard marks. Here, and also at Rathlackan, the assumption is that the sites investigated relate to the Neolithic. Soil-phosphate and bile-acid data suggest low levels of application of herbivore dung. In one test pit at Céide Fields, the chemical evidence suggests human faecal material. Here also extensive cereal cultivation is postulated for areas adjoining the visitor centre. The authors tentatively suggest that animal manure (dung of herbivores) was used to maintain soil fertility, which is interesting in the context of stable-isotope evidence for the use of livestock manure during the Neolithic in Europe (Bogaard et al., 2013) and recent palaeolimnological evidence for major impact by Neolithic and Bronze Age farming on lake systems, possibly involving animal manure, in nearby County Sligo (Co. Sligo; Taylor et al., 2017). The importance of fires in the context of prehistoric farming in north Mayo is emphasised (based on the abundance of mainly fine charcoal), but it was not possible to determine if firing was natural or human-induced.

2.2.4 Dendrochronology and ¹⁴C dating of pine timbers from north Mayo (Caulfield et al., 1998)

This study reports on the results of a ¹⁴C-dating programme in the later 1990s that involved sampling and dating of pine timbers from north-west Mayo. The numbers of ¹⁴C dates of pine are as follows (Figs. 1, 7 and 8): 19 from Céide Fields (includes six townlands) and 11 (this excludes dates SI-1470, UCD-C47 and C49 that were redated; these are included in Fig. 7 but excluded from Fig. 8) from Belderrig, i.e. Belderg Beg, Belderg More and Geevraun townlands. Additionally, basal peat was dated at Geevraun. From the west of Belderrig – referred to as Erris – there are 17 dates (this excludes a date from intertidal peat but includes two dates of pine stumps by Håkansson, 1974). The above set of pine dates (47 in total) from the north Mayo region shows that pine colonised peat surfaces at various times between ca. 6500 and 1300 BCE but most frequently over a relatively short interval of a few centuries centred on ca. 3000 BCE, which may be regarded as an indicative age for pine flush events in western Ireland (this is regarded here as the classical pine flush to distinguish it from other earlier (and also later) pine flushes in Ireland and also Scotland; e.g. Birks, 1975; Bridge et al., 1990; see Discussion). Significantly from a chronological point of view, stumps that were recorded on stone walls in Belderg More and Annagh More townlands provide a terminus ante quem for these walls (see Discussion). The substantial depth of peat underlying several stumps (10 and 5 timbers on > 50 cm to ≤100 cm, and on > 100 cm, respectively) suggests there was already considerable and extensive peat accumulation at or before the late Neolithic and early Bronze Age in the region. This has led Caulfield et al. (1998, p. 638) to conclude that “blanket bog formation in N. Mayo is early and almost certainly unconnected with human activity”.

Investigations into the history of pine, involving matching tree rings and investigating pine-pollen concentrations in basal peats, have been carried out by Martin Downes with a view to strengthening the chronological framework for blanket-bog development and settlement history, but the results have not been published (Caulfield, 2018, p. 64). Caulfield (1988), referring to Downes' investigations, indicates that the pine trees preserved in peat close to but at a higher elevation than the archaeological site at Belderrig, i.e. in Geevraun townland (Fig. S8b), grew for about a century and are datable to the main pine flush. Caulfield et al. (2013, p. 99) refer to unpublished investigations that rely on “evidence for a pine flush in the pollen sequence” to support the idea that “peat engulfed Céide Hill from the west” which is plausible given the results from pollen cores BHY III–VI (see Sect. 4.1.2).

2.2.5 Dendrochronology and ¹⁴C dating of pine timbers from Garrynagran (Jennings, 1997)

Garrynagran refers to an area of extensive blanket bog that lies 16 km to the south of the visitor centre, Céide Fields and within 7 km of the nearest pine timbers dated by Caulfield et al. (1998). Pollen analytical and dendrochronological investigations were undertaken here in the mid-1990s in the context of a PhD study by Jennings (1997). Part of the main pollen diagram, GRN I, was published in O'Connell and Molloy (2001). The complete pollen profile and also the results from dendrochronological investigations at Garrynagran are presented here (details below).

Figure 2Locations of (a) ¹⁴C-dated pine timbers and the pollen profile GRN I at Garrynagran (BL is Blanemore) and (b) ¹⁴C-dated pine timbers at Shanvallycahill. Non-filled circles are used to indicate timbers that were not in situ when sampled (1994). The aerial photograph in (a) (accessed using ArcGIS, 22 May 2019) reflects quite well the situation at the time of sampling, especially the extant bog (both exposed cutover surfaces and the relatively intact bog north of centre of the photo). Dark green indicates young conifer plantations on cutover bog. The aerial photograph in (b) is from Bing Maps (©Microsoft), accessed 22 May 2019.

Core GRN I was taken in Ballynagor townland, 3 km north-west of Moygownagh and adjoining Garrynagran townland (Figs. 2a and S8c). Garrynagran derives from Garraí na gCrann, i.e. the garden of the trees, which undoubtedly references the many stumps and tree trunks embedded in the extensive bogs in this part of County Mayo. The place name, Garrynagran, is therefore appropriate when referring to this study area.

Two court tombs (other megaliths including standing stones ascribable to the Bronze Age and also pre-bog stone walls) are known about from within 1.5 km of core GRN I (de Valéra and Ó Nualláin, 1964; see https://moygownagh.ie/, last access: 1 November 2019, for a description of the Blanemore Forest Archaeological Walk; Fig. S8c). The court tombs represent the southern extension of a group of tombs with its main concentration in the area between Céide Fields and Killala and extending south-eastwards but avoiding higher ground (above ∼100 m) to the west (de Valéra and Ó Nualláin, 1964). Given the close geographical and archaeological relationships to Céide Fields, it is appropriate to present data from Garrynagran here. Also included are ¹⁴C dates from pine timbers from Inishbofin (off the west Mayo coast) and the shores of Lough Mask in south Mayo (details in Sect. 4.2.2).

2.2.6 Other palaeoecological investigations in the wider region

Profile Patchico (patch in common) refers to a ∼5 m long Holocene pollen profile from a small bog pool ∼960 m south-west of the Bronze Age house site at Belderrig (Hawthorne and Davis, 2013; Fig. 1c). The record starts in the early Holocene shortly before Corylus expands. Corylus (this pollen taxon may include Myrica) and Pinus dominate the AP component until mid-profile when Pinus declines. This decline is presumably the regional decline in Pinus that occurs shortly after ca. 3000 BCE. According to Hawthorne and Davis (2013), the elm decline, which is not a distinct feature, may be reflected in changes recorded ∼20 cm lower (local pollen assemblage zones (PAZs) Patc-III–Patc-IV boundary) but it may also be reflected still lower in the profile (the available ¹⁴C dates, i.e. 7680±50 and 6070±30 BP, relating to the lower part of the profile, are not helpful in this regard). High ericoid values (curves for both Calluna and Ericoids (unspecified)) are recorded in the lower and upper parts of the profile but surprisingly few Cyperaceae are recorded. The record from the upper part presumably reflects the open bog-covered landscape of recent times, while that from the lower part may reflect heathy vegetation, at the sampling site and/or perhaps also in the wider area, that coexisted with substantial tree cover. Records for cereal-type pollen are not provided (so we assume none were recorded), and P. lanceolata pollen is poorly represented which, at face value, suggests that farming was never important, at least near the site. This is rather at variance with the archaeological and other palaeoecological evidence (e.g. Verrill and Tipping, 2010a, b; also Bourke, 1972). More detailed analyses are required before firm conclusions regarding local vegetation, landscape dynamics and farming history can be drawn.

Sediments from Cregganmore Lake ($\sim \mathrm{350}\times \mathrm{220}$ m; 6.6 ha), situated 4 km to the south-west of the Bronze Age house site at Belderrig (Fig. 1a), have been the subject of various investigations. A pollen profile by McKeever (1984) is summarised in McKeever and Davis (2013). The ∼7.5 m long profile begins in the Late Glacial Interstadial and probably extends to recent or near-recent times. Apart from three ¹⁴C dates from the basal part, an independent chronology is lacking. The pollen data suggest that hazel, pine and oak were the main trees for most of the Holocene. P. lanceolata or other anthropogenic pollen indicators (there are no records for cereal-type pollen) are poorly represented, so it is not possible to draw conclusions regarding human impact, apart from suggesting that it seems to have been unimportant. In subsequent investigations, chironomid, geochemical and geophysical analyses and ¹⁴C dating (10 dates) were carried out on new cores, 6–7 m long, with a view to exploring impact of climate variability on long-term human activity (Holmes et al., 2013). At least half the core is pre-Holocene, so the resolution for the period of greatest interest, i.e. the Holocene, is low. Apart from suggesting that the chironomid-derived Holocene mean July temperature was similar to that of today (an average of 14 vs. 14.9 ^∘C at nearby Belmullet in the period 1981–2010), no firm conclusions were reached regarding climate during the Holocene. The authors cite Caseldine et al. (2005) and O'Connell and Molloy (2001) as indicating that “the decline of Neolithic agriculture was linked to an extreme climatic event ca. 5200 cal BP”. O'Connell and Molloy (2001) nowhere suggest this.

A peat profile from Croaghaun East, which lies 12 km south of Céide Fields and 5 km west of Garrynagran (Fig. 1a), was investigated by Dwyer and Mitchell (1997) with a view to documenting local expansion of blanket bog which they show to be diachronous. The profile spanned the interval ca. 4700–2270 BCE. In core CRST1, seven tephra layers were detected including two closely spaced layers that date to ca. 2100 BCE, i.e. approximately the Hekla 4 (H4) eruption. The chemical composition of these two layers was similar, though not in all respects, to H4. Interestingly, these tephra layers lay above the decline of Pinus (dated to ca. 2200 BCE), and so it is concluded that tephra deposition was not implicated in the decline of pine. The pollen data suggest that, while the vegetation on mineral soil was unaffected, the bog surface became distinctly wetter at the time of tephra deposition. This too is the time when local blanket-bog expansion occurred (Dwyer and Mitchell, 1997). The authors, however, refrain from making a causal connection between tephra deposition and increased bog wetness but, on the other hand, link the pine decline to a transition from dry to wetter bog-surface conditions that preceded tephra deposition. Human activity (based on the P. lanceolata curve) registers at the base of the profile (ca. 3100 BCE) and again towards the top, i.e. after the pine decline. The authors saw no evidence to connect expansion of blanket bog with human activity.

From Achill Island, Caseldine et al. (2005) report on investigations of a pronounced and extensive silty layer in cores from blanket-bog contexts (Fig. 1a; three short profiles are presented that are here collectively referred to as Dooega). The pollen profiles show the typical regional pattern for Pinus in the mid-Holocene, namely strongly elevated pollen values indicative of a pronounced pine flush, which is preceded by (in one of the profiles it coincides with) the well-developed and widespread silty layer that the authors date to ca. 3200 BCE. The silty layer is regarded as indicative of slope erosion caused by an extreme weather event, most likely a storm. Dry conditions, however, which facilitated the pine flush, persisted for a considerable period (till ca. 2850 BCE) after the extreme event. The authors suggest increasing wetness from ca. 2850 BCE onwards, that led to pronounced wetness at and after ca. 2000 BCE (see Discussion). It is suggested that there was a long period (500 years) characterised by dry and warm conditions in the early part of the fourth millennium BCE during which Neolithic farming was introduced and initially expanded strongly in Ireland.

Caseldine et al. (2005) also provide a useful overview of climate-change events in Ireland and elsewhere in Europe at about this time. The evidence includes particularly narrow tree rings in Irish oaks centred on 3200 BCE (Baillie and Munro, 1988) and the cessation of varve formation in the sediments at An Loch Mór (dating to ca. 3300 BCE; cf. Holmes et al., 2019; see also Discussion).

In contrast to the pollen profiles from Achill, pollen profiles from four lakes that lie east of Achill in Co. Mayo, i.e. L. Aisling, L. Clevala, L. Anaffrin and L. Corslieve (Fig. 1a), provide no evidence for a pine flush though Pinus is well represented in the upland lakes, L. Corslieve and L. Aisling (Bradshaw and Browne, 1987). Nor does a pollen profile from L. Doo, 11 km south-west of Carrownaglogh, record a pine flush (O'Connell et al., 1987), probably because of a lack of bog development in the vicinity of the lake.

3.2.1 Pollen analytical methods

In the case of pollen profile GRN I, sampling for pollen, sample preparation, and pollen identification and counting were carried out according to standard procedures as implemented in the Palaeoenvironmental Research Unit, National University of Ireland Galway (NUIG; Molloy and O'Connell, 1995; Jennings, 1997).

All available pollen counts from Garrynagran and Céide Fields were brought into Excel files and replotted in pollen-diagram format using CountPol or Grapher. Short and long profiles were plotted in histogram and curve formats, respectively. A total terrestrial pollen (TTP) sum and a cut-off size for cereal-type pollen of 40 µm (provided the relevant pore and annulus size criteria were fulfilled; see Beug, 2015) were used. Bog taxa (Cyperaceae, Ericoids, etc.) and other taxa such as non-pollen palynomorphs (NPPs) were excluded from the pollen sum (PS). High pollen counts were achieved in most samples. The main exceptions were the pre-elm decline samples in GLU IV and a few levels in GRN I (which were difficult to count due to much debris and low pollen concentration). The average pollen count in respect of the TTP taxa and the associated standard deviation is given in the relevant pollen diagrams. Percentage values for the taxa excluded from the PS are expressed relative to the PS + the sum of taxa relating to the relevant category, e.g. bog taxa, aquatic taxa and NPPs. For calculation purposes, Sphagnum and micro-charcoal particles, etc. are regarded as constituting single-component groups. The datasets are available in the palaeo-database PANGAEA (O'Connell et al., 2020).

In the case of short pollen profiles from Behy (published in Molloy and O'Connell, 1995), minor taxa – e.g. Quercus, Ulmus, Fraxinus and Taxus, and also Alnus and Salix – were summed with a view to reducing the complexity of the diagrams and providing greater visibility for taxa that are of significance for palaeoenvironmental reconstruction appropriate to this paper.

3.2.2 Loss-on-ignition and tephra investigations

LOI measurements were carried out using standard methods (cf. Heiri et al., 2001). Tephra investigations involved the systematic ashing of 4 cm thick blocks of peat taken from monoliths and cores collected at Céide Fields and Garrynagran. The ash so obtained was microscopically searched for tephra shards (cryptotephra). Where concentrations of tephra shards were identified, the peat was resampled by taking 1 cm thick slices. The samples were chemically treated to extract tephra shards. Details will be published elsewhere. For the sake of completeness, the location of tephra layers within the relevant profiles are indicated (see Results).

3.2.3 Dendrochronological investigations

Dendrochronological investigations relate to pine and oak samples from Garrynagran and are fully described in Jennings (1997). Two and, where possible, three radial sections were cut from the timber discs using a bandsaw, avoiding where possible side branches, distortion due to root protrusions and excessive reaction wood. The wedge-shaped samples were pared so as to be able to clearly see the ring boundaries that were highlighted by applying chalk dust.

Ring-width measurements were carried out by placing the wood sample on a moving stage controlled by a screw thread. A Wild M8 binocular microscope with a cross-hair graticule was used, in conjunction with the measuring stage, to measure the distance between ring boundaries. Ring thickness was measured to the nearest 0.01 mm by a digital counter (Heidenhain bidirectional counter VRZ 405) and the values were input directly into a PC. In instances where, after measuring three radii for a particular timber, problems connected with splitting, missing and false rings remained, further radii – up to six radii in some cases – were measured. In some instances, problems were solved by paring larger areas in the region where problems were identified. Also, all wedge-shaped radial sections from problem timbers were prepared, and problem rings were then traced around the circumference of the timber. This normally facilitated the recognition and measurement of annual rings with a high degree of certainty. Though pine is considered to be not as amenable to dendrochronological investigation as oak, P. sylvestris has limited occurrence of missing and double rings compared with other conifers such as juniper (Fritts, 1976).

Cross-dating between trees was attempted visually, by matching the graphed plots of the ring-width measurements, and also statistically, using the cross-dating programs CROS (Baillie and Pilcher, 1973) and CROS84 (Munro, 1984). The latter program provides a more rigorous test of synchroneity and was mainly used. Where anomalies were identified, these were overcome by further replication of measurements and examining the full cross section of the particular timber. The most reliable matches, i.e. those that yielded the highest t values at long overlaps, were used to build up groups of trees with overlapping ring series. A significant match was where t was ≥3.5 (p=0.01). Groups of trees that showed satisfactory cross-dating (both visually and with self-consistent, significant t values, i.e. above 3.5) were combined into working chronologies.

Once all potentially matching trees had been identified and any inconsistencies eliminated, a mean master chronology was constructed. The mean master was extended by the addition of other mean ring series that matched. This process was continued until no further ring series reliably cross-matched with the existing mean masters (details in Jennings, 1997). Before a working master chronology or a site mean was produced, individual series were standardised (Graybill, 1979) so as to remove long-term trends in the data such as those related to the age of a tree.

Samples from three long oak trunks (Fig. S8c) that lay on the cutover peat surface (presumed to be close to where they had been preserved) were measured and matched to the Belfast oak chronology by David Brown, Queen's University Belfast.

3.2.4 Radiocarbon dating

Peat samples consisted of peat slices, normally 1 and 2 cm thick in the case of peat monoliths and core GLU IV, respectively. The bulk peat samples were dated by the conventional ¹⁴C dating method. ¹⁴C dates were calibrated using OxCal version 4.3 (Bronk Ramsey, 2009) and the default ¹⁴C calibration curve, IntCal13.14C (Reimer et al., 2013). Age–depth relationships for the peat profiles were constructed using Clam version 2.2 (Blaauw, 2010; http://www.chrono.qub.ac.uk/blaauw/clam.html; downloaded 22 August 2017) and the IntCal13.14C calibration curve. In all instances, several curve-fitting options were tried (linear and polynomial regressions and various spline-fitting options). Usually, many of the options gave results that were obviously unrealistic and so were rejected. The option that gave what was regarded as the most realistic result was accepted.

Pine timbers from Garrynagran were sampled by taking wood from a specific group of rings (details in Fig. 9) that were dendrochronologically investigated (four and two ¹⁴C dates are from timbers included in P1M and P2M, respectively, i.e. the floating pine chronologies referred to as GRN P1M and GRN P2M by Jennings, 1997). The samples – 10 in all from dendrochronologically investigated timbers (two of these timbers could not be matched) and two timbers from pine stumps beside peat core GRN I – were dated by the conventional ¹⁴C dating technique. The midpoint from the calibrated age range of ¹⁴C dates from timbers G30 (4350±25 BP) and G50 (5620±25 BP) was used to fix the floating chronologies P1M and P2M, respectively (Jennings, 1997). These dates were chosen because they relate to steep parts of the calibration curve, and so the uncertainty attached to their calibrated age is correspondingly small.

4.1.1 Core GLU IV (long core from Glenulra basin) (Figs. 3, 4)

This, the main pollen profile from Céide Fields, has an optimal location within the main Céide Fields complex (Fig. 1). It is the longest and most detailed pollen profile and has the greatest temporal span (> 6800 BCE–700 CE). Furthermore, its chronology is well constrained especially in the middle and upper part of the profile, i.e. the most pertinent parts. The age–depth model is derived from a fifth-order polynomial regression curve that uses 20 ¹⁴C dates (two ¹⁴C dates are regarded as outliers and so were not used; Fig. S2b).

The main features of profile GLU IV are summarised below and in Table S2a. Given the small size of the peat-filled basin, especially in the early and mid-Holocene when peat accumulation within the basin was limited, the regional pollen signal is assumed to derive mainly from a ∼1 km radius of the basin. With increasing distance from the basin, the reflection of developments are expected to decrease exponentially in the pollen record (Jacobson and Bradshaw, 1981; Gaillard et al., 2008). In the accounts that follow every effort is made to distinguish between developments in the basin (local, i.e. on the mire surface) and the surrounding landscape (regional, i.e. initially on mineral ground and later on mineral and peaty soils as blanket bog expanded) though this is not always possible given the uncertainties connected with origins of pollen such as those of grasses and bog taxa generally.

Early Holocene development is reflected in the basal part of the profile (PAZs 1–4). Chronological control is weak in this part of the profile (Fig. S2b). The only available ¹⁴C date (5100±80 BP) relates to the upper part of the interval and is clearly an outlier. It is obvious, however, that the record begins relatively early in the Holocene and probably earlier than 6800 BCE. Particularly noteworthy are the high Pinus values. Stumps were frequently encountered during trial corings at about this depth in the basin, and pine wood (pine tracheids) was noted in the pollen samples. The peat-filled basin, which would have been much more limited in extent than today, appears to have supported pine woodland at this time. Calluna, which is strongly represented at the top of PAZs 2 and 3, declines. Given that Calluna pollen is poorly dispersed (Moore et al., 1986), it is probable that ling growing in the basin (it declines as pine expands) rather than on the surrounding mineral ground is reflected here. The precise composition of the woodlands on mineral soil is uncertain but it is likely that, as well as pine, hazel and birch, small populations of oak and elm, willow, rowan, holly, ivy, and honeysuckle were present, all of which are represented in the pollen record (Fig. 3; also Molloy and O'Connell, 1995). The presence of blanket bog in the vicinity of the basin (as distinct from the basin peat) so early in the Holocene cannot be ruled out given the evidence for such a presence provided by pine timbers (see Sect. 4.2.2).

PAZs 5–11 reflect vegetation dynamics within the basin and wider regional contexts. Several influences that vary over time are undoubtedly at play. These include natural processes, e.g. species competition, pedogenesis and climate change, as well as human impact arising mainly from farming activity. Developments in the surrounds of the basin, and especially landscape openness and the role of tall woody species, are, during this time, primarily determined by human activity. This activity is reflected mainly by the NAP component, and especially Poaceae and P. lanceolata. The major expansion of NAP, including Poaceae and P. lanceolata and also Pteridium, and the correspondingly severe decline in AP indicate an intensive landnam, i.e. more or less total woodland removal at least in the general vicinity of the basin. Landnam is at its most pronounced in the interval 3790–3460 BCE (PAZ 5b) and is maintained, but with less intensity, during the following three centuries (PAZ 5c). In the period 3160–2790 BCE (PAZ 6a), woodland (mainly hazel, oak, birch and alder, and small amounts of elm and pine) more or less fully regenerates, a development facilitated by greatly reduced human impact. This phase of development culminates in a small increase in Pinus that is regarded as reflecting the regional (also in the vicinity of the basin) pine flush (PAZ 6b, 2820–2720 BCE). A small increase in P. lanceolata (also Corylus declines) points to a resumption of human activity at this time.

As regards the initiation and spread of blanket bog, bog expansion cannot easily be traced in profile GLU IV since pollen of local mire origin, i.e. within the basin, is expected to dominate and, indeed, is probably dominant in the wetland pollen component. Pollen from any blanket-bog contexts present in the surrounds would thereby be masked. An intriguing aspect is the possibility that increased mire wetness in the basin (cf. Cyperaceae, Sphagnum and Hydrocotyle (marsh pennywort)), coinciding with landnam, is the result of increased runoff that follows on from large-scale woodland clearance (see Discussion).

High values for Calluna and Empetrum in PAZ 6 (3160–2720 BCE) probably reflect ling and crowberry growing locally in the mire basin where dry conditions appear to have prevailed at this time. Given that woodland had regenerated and was dominant, it is unlikely that pollen from pockets of blanket bog in the wider landscape is reaching the coring location in any appreciable quantity.

In the interval 2720–2330 BCE (PAZ 7), i.e. in the late Neolithic, human activity consistently registers, but it is not until the transition to the Bronze Age (PAZ 8) that there is a distinct increase in farming that results in a decrease in woodland and especially a decline in birch, hazel and oak. Fire too increases in importance (cf. micro- and macro-charcoal curves in Figs. 3 and 4, respectively). This strong level of human impact is maintained until 110 CE (particularly high impact in ca. 1650, 850 and the final century BCE; pine ceases to have any importance – locally at least it is probably extinct – from 1650 BCE) when there is a lull in activity that is regarded as the Late Iron Age Lull. This lasts until the beginning of the sixth century CE when an upsurge in farming associated with the early medieval period registers (PAZ 11). From 850 BCE onwards, the mire surface appears to have been particularly dry. Calluna is strongly represented, indicating that ling is dominant, and pollen records for hygrophilous plants, such as Narthecium and Rhynchospora, more or less cease.

4.1.2 Short pollen profiles from Céide Fields

Short pollen profiles from five sites within the Céide Fields complex are presented in Figs. S3–S7. Age–depth curves are given in Fig. S2a. Each profile is independently zoned, mainly on the basis of careful visual inspection of the pollen percentage curves (zones are similar to those in Molloy and O'Connell, 1995). A zone boundary is always placed at the peat–mineral soil horizon to emphasise this important lithological boundary.

In the headings used below, the profile name and the time span reflected in the particular profile are indicated. Estimated ages are also given as follows: the age of the base of the profile in brackets where mineral soil has been pollen analysed, followed by the time span represented by the pollen spectra from the overlying peat. In the Discussion, the ages as assigned below to the individual profiles are further considered and, in some instances, modified in the light of the dataset as a whole.

BHY III, [≥2700] 2700–250 BCE, i.e. late Neolithic to mid-Iron Age

The age–depth curve for BHY III is a smooth spline curve (smooth factor = 0.3) that is based on five of the available seven ¹⁴C dates (Fig.  S2a). The ¹⁴C dates 3360±50 BP (Gd-7147) and 3290±60 BP (Gd-7148) (both relate to peat from −6 to −7 cm) have not been included in the analysis as, from the beginning, they were regarded as suspect. The other ¹⁴C dates serve to confirm that these dates are indeed erroneous. Curve fitting that included a surface-age estimate (180 cm of peat, i.e. 50 cm added to compensate for peat shrinkage; top regarded as dating to 1950 CE) was attempted but the age–depth curves that resulted were regarded as unrealistic and so were discarded. Of the BHY series, it is only in this profile that no tephra was recorded.

The pollen data (Fig. S3) indicate that prior to peat growth, and probably for some decades before peat developed, i.e. in the late Neolithic and early Bronze Age, grassland with an ever-increasing heath (ling) component dominated at the sampling site. Peat initiation is estimated to have begun by ca. 2700 BCE. The high Pinus pollen values are presumed to reflect the regional pine flush. A nearby pine stump, on the basis of its stratigraphical position within the peat (we do not have a ¹⁴C date for this stump), may be contributing to the elevated Pinus pollen values. According to the age–depth model, the pine flush had ended by ca. 2210 BCE (subzone 2a–2b boundary), but birch (also Sorbus, presumably S. aucuparia (rowan)) continued to be important, and farming activity remained at a modest level (low P. lanceolata values). At ca. 1500 BCE, there is a switch to a grass-dominated landscape with few trees (little or no pine or birch) or tall shrubs locally and probably also at a regional level (see PAZ GLU IV-9a).

BHY IV, [≥2400] 2400 BCE–20 CE, i.e. early Bronze Age to late Iron Age

The age–depth curve for BHY IV is a smooth spline curve (smooth factor = 0.1) that is based on the three available ¹⁴C dates (Fig. S2a). Two ¹⁴C dates are from near the base and so the lower part is chronologically well constrained. The age–depth model indicates that peat had begun to accumulate by 2400 BCE.

The basal part of the profile (PAZs 1 and 2) reflects the local situation as peat began to accumulate (Fig. S4). Birch is locally dominant; there is a small amount of hazel, but tall canopy trees, including pine, are rare and probably not locally present. From 2000 BCE, i.e. early in the Bronze Age (base of subzone 3a), birch is replaced by grasses probably as a result of increased farming pressures that are maintained until ca. 600 BCE. In subzone 3b, the high values for both Poaceae and Calluna are probably best ascribed to local vegetation on shallow peat that was dominated by grasses, e.g. Molinia caerulea, and ling (Calluna).

BHY V, [≥2600] 2520–210 BCE, i.e. late Neolithic/Chalcolithic to mid-Iron Age

The age–depth curve for BHY V is a smooth spline curve (smooth factor = 0.2) that is based on the five available ¹⁴C dates and a surface age estimate (peat thickness 180 cm, i.e. 50 cm added to compensate for peat shrinkage; top regarded as dating to 1950 CE) (Fig. S2a).

The pollen spectra from the mineral soil (BHY V-1) and immediately overlying peat indicate woody vegetation dominated by birch. Sorbus (probably rowan), holly, ivy and honeysuckle were common. Pine was present regionally, but there is no evidence for a pine flush at least near the site (Pinus at only ∼1 %–2 %) (Fig. S5).

According to the age–depth model, peat initiation at this location began at 2500 BCE. Replacement of birch by grass-dominated vegetation occurred at 2000 BCE. This is somewhat earlier (two centuries) than at nearby BHY IV but about a millennium earlier than at BHY III. The age ascribed to the Betula to Poaceae transition at BHY V may be too old. Contiguous ¹⁴C samples give rather different ages. This and the very sharp change in pollen composition at the PAZs 2–3 boundary raise the possibility of a hiatus or at least exceptionally slow peat accumulation in that part of the profile. On the basis of the low P. lanceolata values in all spectra (but cereal-type pollen is recorded in most spectra), farming activity is subdued. However, the high contribution initially by Betula and subsequently by Poaceae (both presumably of predominantly local origin) undoubtedly depress the P. lanceolata values.

BHY VI, [>2600] 2600 BCE–120 CE, i.e. late Neolithic to late Iron Age

The age–depth model for BHY VI is based on a smooth spline curve (smooth factor = 0.5) that takes into account the four available ¹⁴C dates and a surface age estimate (peat thickness 160 cm, i.e. 40 cm added to compensate for peat shrinkage; top regarded as dating to 1950 CE; Fig. S2a). The exceptionally old date near the base of the peat (4080±50 BP) does not greatly influence the shape of the curve which is assumed to be correct given that what appears to be the regional pine flush is recorded in BHY VI-2a.

The age–depth curve suggests that peat accumulation started at 2600 BCE. Immediately prior to the initiation of peat accumulation, woody vegetation (oak, hazel and especially birch) and heathy grassland (cf. Poaceae and Calluna) were locally common (BHY VI-1; Fig. S6).

In the basal peat (BHY VI-2a; also in the mineral soil), Betula values are exceptionally high which suggests that birch continued to be the main contributor to woody vegetation at and near the sampling site as peat began to accumulate. Elevated Pinus values in BHY VI-2a, which span 2600–2270 BCE according to the age–depth model, reflect the regional pine flush. In subzone BHY VI-2b (2270–1810 BCE), there is an increase in Poaceae, Betula begins to decline, and Pinus values have fallen and do not recover. This corresponds closely as regards pollen (also chronology) with zone 2b in BHY III and zones 1 and 2 in both BHY IV and V.

Zone BHY VI-3 (1810 BCE–120 CE) reflects a treeless landscape at least in the vicinity of the sampling site. High values for Poaceae are probably attributable to grasses growing on the blanket bog (e.g. M. caerulea and/or Nardus stricta) and grasses on mineral soils in the wider region. In subzone BHY VI-3b, Calluna values are exceptionally high and charcoal (micro- and macro-charcoal) values are also high. These changes are probably ascribable to increased farming activity that included cereal growing (cereal-type pollen is rather well represented). The particularly high values for P. lanceolata and cereal-type at the base of BHY VI-3b, i.e. early Iron Age, ca. 400 BCE, which are indicative of intensive farming in the vicinity of the site, are noteworthy.

Pollen profiles and spectra from beside the visitor centre (CF I, CF III and PLM)

Pollen and macrofossil data from short profiles at and beside a stone wall near the visitor centre (CF III and CF I; CF I has also been referred to as CF Ib) are presented in Fig. S7. This figure also includes six pollen spectra (referred to as PLM) relating to soils associated with plough marks that were recorded during excavations conducted on the site of the visitor centre prior to the commencement of construction work (Byrne et al., 2009). Results of calibration of ¹⁴C dates (three dates from CF I and a single date from the plough-mark infill), including an age–depth plot for profile CF1, are provided in Fig. S2a. The material was not searched for tephra.

Peat initiation at CF I began at 1000 BCE, i.e. in the late Bronze Age. Locally, the landscape was treeless, and grasslands, in which ling played an increasingly important role, dominated (subzone CF I-2a; 950–710 BCE). The lack of trees is attributed to pastoral farming. In subzone CF I-2b, pastoral farming continues, but there is now a considerable arable component that continues to the top of the profile, i.e. into the early medieval period (cereal-type pollen of all size categories are well represented; details are in Molloy and O'Connell, 1995, Fig. 20).

Pollen profile CF III reflects local conditions at, and immediately prior to, wall construction. AP values are low but higher than in CF I. ¹⁴C dates are not available for this short profile, but conditions at a time prior to that represented in CF I-1 are assumed to be reflected here (Pinus values, though low, are higher than in CF I; this supports the idea of a late fourth millennium BCE date). The high fern values (also in the basal samples of CF I) are assumed to result from differential loss of corrosion-susceptible pollen (e.g. Cyperaceae, etc.) and survival of corrosion-resistant pollen and spores and especially fern spores.

Regarding the spectra that relate to the plough-marks (PLM), the pollen representation is broadly comparable to that in CF 1-2. This, and the single ¹⁴C date (2390±40 BP; calibration indicates an 81 % probability that the age lies between 550 and 390 BCE), suggest that the plough marks relate to the early Iron Age. There are some noteworthy differences within the plough-mark pollen spectra, for instance, the contrasting values for both P. lanceolata and cereal-type pollen in samples 1 and 2 versus 3 and 4. Such differences are not unexpected as the pollen content of soil samples is invariably dominated by pollen of local origin. In samples 5 and 6 (these samples are from the parent soil that contained the plough mark), bog and heath taxa are less well represented, and high values for Poaceae, P. lanceolata and other pastoral pollen indicators suggest that pasture was dominant prior to ploughing and cereal cultivation.

4.2.1 Pollen profile GRN I, ca. 5700–1800 BCE, i.e. early mid-Holocene to mid-Bronze Age

Pollen profile GRN I is from within an extensive bog and hence is expected to reflect, on the one hand, local bog vegetation (cf. bog and heath pollen taxa) and, on the other, vegetation and land use on a wide regional scale (Figs. 5 and 6; Table S2b). Potential complications arise from the distinct possibility, given the high frequency of large timbers (mainly pine, also oak) preserved in the bog, that pollen that would normally be regarded as arising exclusively from vegetation on mineral soils may derive, in part, from mire vegetation. In the latter category are also grasses such as M. caerulea (common on blanket bogs) and Phragmites (pollen of these taxa and other grasses are included in Poaceae as is normally done).

In all, there are 11 ¹⁴C dates directly relevant to core GRN I, i.e. nine from slices of peat and two from outer rings of two pine stumps, both present in the peat bank where core GRN I was taken but laterally separated by ∼1 m (Table S1b, c; Fig. S8c). Timber from the outermost rings of the lower and upper pine stumps gave ¹⁴C dates 5455±15 BP and 4110±20 BP, respectively. The age–depth model for the pollen profile is derived from a smooth spline curve (smooth factor = 0.4) fitted to 10 ¹⁴C dates which includes these two pine dates (Fig. S2b). The uppermost peat-derived ¹⁴C date, 1170±30 BP (from depth 10–8 cm; at least 1 m of peat had been removed by peat cutters), was not used in curve construction as it was regarded as unrealistically young.

The main features of the pollen assemblages are summarised in Table S2b. The lower and middle parts of the profile (zones 1–5a) have high AP values (but much reduced values in 3b) that reflect not only woodland cover on mineral soils but also substantial woodland (mainly pine but also oak) on peat. This is supported by the stomatal pine record (Fig. 5) and also the investigations of pine timbers that are directly associated with GRN I and in the area generally (see Sect. 4.2.2).

The elm decline is a distinct feature (base of 3a) and occurs at the expected age (3880 BCE). An unusual aspect (in an Irish context) is the failure to record P. lanceolata (also there is little change in Poaceae) during the elm decline which suggests that opening up of woodland was minimal and that there was little or no farming in the area during the elm decline. Neolithic landnam registers clearly, however, in subzone 3b. The shape and also the composition of the anthropogenic-indicator pollen component (e.g. Poaceae, P. lanceolata, Ranunculus acris-type and Filipendula) indicate a gradual increase in human impact beginning at 3800 BCE, relatively high and sustained impact from 3700–3300 BCE, and then a gradual decline that continued to the end of subzone 3b (3240 BCE) and into zone 4. Interesting also are the changes in mire conditions during subzone 3b. Sphagnum macrofossils (mainly leaves) are important for the first time (Sphagnum spores and capsules were well represented before this, but no leaves were recorded; Figs. 5 and 6). Initially, the leaves are mainly of S. sect. Acutifolia and, later, S. palustre, and, at the base of zone 4, S. austinii (i.e. S. imbricatum) is recorded, but this species does not become dominant until 2750 BCE (base of zone 5). A trend towards lower ash values (higher LOI) that begins at the base of zone 3 also suggests a change in mire hydrology that probably involved a shift from rheotrophic to ombrotrophic conditions.

Figure 7Results of calibration of ¹⁴C dates from bog-pine wood from Co. Mayo. Sample names include the ¹⁴C laboratory number and, in some instances, the label given by the laboratory that took and submitted the sample for dating is given. In the case of samples for which University College Dublin was responsible (UCD in the number indicates dating by its radiocarbon laboratory), the townland name is given. Note that Lu-774 and Lu-775 relate to Lund University. The curves show the calibrated ages (probability distributions, 95.4 % and 99.7 %) of 68 ¹⁴C dates that relate to the following areas: ¹ CF, Céide Fields; ¹ Agh, Aghoo (5 km south-east of visitor centre (VC), CF); ¹ Ann, Annagh More and Annagh Beg (10 km south-east of VC, CF); ² Bd, Belderrig (6 km west of CV, CF); ³ Err, Erris region; ⁴ Grn, Garrynagran (16 km south of Céide Fields), ⁴ Ck, Carrowkennedy, W. Mayo; ⁵ Inb, Inishbofin (Cloonamore); and ⁶ LM, Shanvallycahill, L. Mask. Replicate ¹⁴C dates are presented from three timbers that relate to Belderrig, i.e. original ¹⁴C dates and later obtained AMS ¹⁴C dates (indicated by * and **, respectively). Calibration results for both sets of dates are plotted; the original dates, which have larger standard deviations, are not included in the compilation shown in Fig. 13. Peat thickness beneath the specimens is indicated schematically, where available. Primary data sources are as follows: ¹ Caulfield et al. (1998); ² Caulfield et al. (1998, 2011a); ³ Caulfield et al. (1998); Håkannson (1974); ⁴ Jennings (1997); ⁵ Ní Ghráinne (1993); O'Connell and Ní Ghráinne (1994); and ⁶ O'Connell (unpubl.). Most of the dates derive from outer tree rings, except MY-002 GrN-33046 (marked by a closed circle) that derives from inner rings. Details of the part of the timbers used for dating by Caulfield et al. (1998) and Håkannson (1974) are mostly not available; in a few instances it is indicated that the outer rings were dated, and so it is assumed that this is generally the case.

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The regional pine flush, on the basis of the pollen record, is of ca. 130 years duration (subzone 5a). The pine timber (P2; Fig. S8c) associated with this feature had a lifespan of ca. 120 years and, based on the ¹⁴C date from the outer rings of the stump (Fig. 7), died shortly before 2600 BCE. Interestingly, most of the stumps in the vicinity of the coring site were stratigraphically related to the lower stump (P1) so that pine stump P2, which was almost 1 m higher in the peat, seemed to be an isolated specimen. However, other pines were probably growing nearby on peat, at about the same time as P2, and were presumably contributing to the pine flush (see Sect. 4.2.2).

The start of the pine flush coincides with the beginning of the continuous dominance of S. austinii and also a record for Racomitrium moss (Fig. 6). Whether or not this shift preceded, coincided with, and was subsequent to, the local presence of pine trees on the bog surface is difficult to say. The stratigraphy suggests that the stump may have predated these changes.

Bearing in mind the more or less continuous pine-stomata record and the results of ¹⁴C and dendrochronological investigations of pine timbers from elsewhere on the bog (see Sects. 4.2.2 and 5.1; also Jennings, 1997), it can be concluded with confidence that pine grew in at least some places on the mire over the entire period, apart from the youngest interval, i.e. apart from subzone 5b and zone 6 (from 2600 BCE onwards; Figs. 5 and 6).

4.2.2 Radiocarbon dating of bog pine in north Mayo and dendrochronological investigations at Garrynagran

The results of ¹⁴C dating of pine-wood samples from north-west, west and central Co. Mayo are shown graphically in Figs. 7 and 8, and details are provided in Table S1b. In Fig. 7, probability curves from calibration of 68 ¹⁴C dates (these including three replicate dates from Belderrig) of pine timbers are plotted. Provenance and stratigraphic context of the timbers involved are also indicated. In Fig. 8, histograms are used to show age frequencies (200-year bins) for all pine dates (Fig. 8a; in the case of the replicate dates from Belderrig, the UBA rather than UCD dates are included). The dates are grouped according to geographical areas, i.e. Céide Fields together with nearby Aghoo and Annagh More and Annagh Beg (referred to as Annagh Tds), Belderrig, Garrynagran and Carrowkennedy and Inishbofin, and Shanvallycahill, i.e. a cutover peatland on the south-west shore of Lough Mask (Fig. 8b–f). The thickness of peat beneath the timbers is schematically indicated (details in Table S1b).

Figure 8Histograms showing age–frequency distribution (calibrated medium ages derived from OxCal) of pine stumps from Co. Mayo (for sources see legend to Fig. 12). Fill patterns are used to show the depth of peat on which the ¹⁴C-dated pine stumps occurred; a schematic representation of the relationships of the pine stumps to the mineral soil or peat and stone walls is provided in the inset.

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The ¹⁴C dates are decidedly concentrated in the interval 3400–2400 BCE, with the greatest concentration in the interval 3200–2600 BCE which can be regarded as the period characterised by widespread growth of pine on bog and peaty surfaces, i.e. the regional pine flush. The widest span of dates is recorded from the Erris region (ca. 6400–1350 BCE) but here too most of the dates are concentrated in the interval 3400–2200 BCE.

As regards thickness of peat beneath the timbers, not surprisingly many (20) are associated with a thin layer of peat (≤50 cm; these statistics include the 47 pine ¹⁴C dates discussed in Caulfield et al., 1998; information was not provided for C52). Relatively few pine stumps (9) rest on mineral ground which again is not too surprising as peat growth is expected to have commenced during the lifetime of the tree or shortly after death; otherwise the chances of preservation would have been small. Rather surprisingly, however, several timbers were recorded on substantial thicknesses of peat (51–100 cm, 10; >100 cm, 13) which may have taken several centuries to accumulate. This suggests that blanket bog was already present as Neolithic culture spread though it remains unclear how widespread blanket bog was (extensive areas without megaliths, however, may be indicative of widespread presence of bog in parts of the region at the time of expansion of Neolithic peoples) and the degree of landscape openness, particularly at a local level, due to presence of bog as farming commenced (evidence supporting landscape openness at a local level is lacking). As emphasised by Caulfield et al. (1998), the two pine stumps recorded on a stone wall (see Discussion; presumably drainage resulting from the stone wall created a locally favourable environment for these trees to germinate, establish and grow) are important indicators of age of wall construction. The walls in question date to ca. 3000 BCE at the latest, and, most likely, are a couple of centuries older if allowance is made for the inherent age of the tree (outer rings dated). So, with confidence, construction of these walls can be justifiably imputed to the Neolithic; i.e. they are much older than the late Bronze Age dating argued for by Whitefield (2017).

The results of the dendrochronological investigations at Garrynagran are presented in Fig. 9. The age span of individual pine and oak timbers that have been dendrochronologically dated (the pine chronologies are floating; the oak chronology is fixed) are plotted as well as ¹⁴C dates from pine timbers including the date used to “fix” the two floating pine chronologies, P2M and P1M.

Figure 9Overview of data relating to pine and other developments in north Mayo in the interval 5700–1700 BCE plotted on a calendar–calibrated timescale (BCE and cal. BP; both calibrated]. (a) Pinus percentage data from pollen profiles that show a pine flush. The curves are weighted averages of three values; the central value is accorded double weighting. Data are plotted as follows (PAZs are specified): GLU IV-3 to -8, BHY III-1 to -2b and BHY VI-1 to -2b); the beginnings and ends of curves where values are low ($<\sim \mathrm{1}$ %) are not shown; for GRN I the complete profile is plotted. Peat initiation dates are indicated for BHY profiles; that the age may be underestimated is suggested by an arrowhead pointing towards older ages (see text). Pine stomatal data (%; silhouette indicates ×10 exaggeration) for GRN I are shown. (b) Master chronologies from Garrynagran, i.e. two floating pine chronologies and one fixed oak chronology (three timbers). Time intervals represented by individual oak timbers, G32, G36 and G37, are indicated. (c) Chronologies for individual pine timbers from Garrynagran (dendrochronological data and results of ¹⁴C dating; r  is ring nos.) that are included in the floating pine chronologies GRN P1M and GRN P2M. Probability curves for calibrated dates from pines G42 and G43 (dendrochronologically investigated but without matches) and pines W1 and W2 (also referred to as P2 and P1, respectively) from beside pollen profile GRN I are also shown.

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Centres of the five trees included in P1M were preserved, but sapwood was not present in any sample. Matching of G49M with G50M gave a t value of 12.02 (this was the maximum t value for the pine timbers). There is the possibility that the samples relate to the same tree (the samples came from stumps removed from the surrounding bog and stacked) but it is also possible that the trees grew in close proximity which could explain the high correlation (Fritts, 1976). The G40M ring series is only 66 years in length, and hence t values are low. However, visual comparison of the plotted ring widths suggested that it matched well, and so G40M has been included in master chronology P1M.

The floating chronologies P1M and P2M, each of which was fixed on the basis of a calibrated ¹⁴C date from a selected timber (see Methods; Fig. 9c), have a duration of 438 and 183 years, and span the intervals ca. 3135–2700 and 4530–4350 BCE, respectively (Jennings, 1997). Pine timbers G43 and G42 yielded ring patterns that could not be matched, and ¹⁴C dating confirmed that these were older than P1M and P2M, respectively. Pine timbers P2 and P1, that were ¹⁴C dated but not dendrochronologically investigated, are interesting in that the former fits in well with P1M (pine flush), while P1 relates to the younger part of P2M and could potentially extend that chronology forward by some years (Fig. 9c). The eight pine trees that constitute P1M were all alive at ca. 2950 BCE and possibly also pine P2 that was not dendrochronologically investigated. The three oak trees also began life at about this time (Fig. 9b). Thus an interval centred on 3000 BCE, and including a century or so on either side of that date, is highly significant as regards the final phase of tree growth on peat surfaces at Garrynagran.