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1 August 2007 Volcanic Ash Deposition and Long-Term Vegetation Change on Subantarctic Marion Island
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A c. 5500 year record of peatland development and vegetation change was generated from a core recovered from an Agrostis magellanica peat bog on subantarctic Marion Island, using palynomorph, plant macrofossil, and tephra analyses. Two tephra horizons (both 17 cm thick) were identified and dated to ca. 2900 cal. BP and ca. 1700 cal. BP. Succession of the vegetation as a consequence of tephra deposition, particularly by the pioneer Azorella selago, appears to have been very slow, lasting as long as c. 700 yr. The slow pace of vegetation succession highlights the sensitivity of the indigenous Marion Island flora to environmental change, and the vulnerability to the spread of alien invasive species.


Owing to their isolation, impoverished biota, and harsh environments, the ecosystems of subantarctic islands are relatively simple and sensitive to disturbance. They can be seen as ‘ecological laboratories’ for studying the response of ecosystems to environmental change (Smith, 2002). Human visitation to the islands has only occurred in the last two centuries; long-term archives of environmental change can therefore show the response of the islands' ecosystems to environmental perturbation in the absence of any human influence.

Marion Island is an intraplate shield volcano located remotely in the subantarctic region of the southern Indian Ocean, c. 2200 km southeast of Cape Town, South Africa (Fig. 1). Ecological surveys and monitoring campaigns have shown that the main drivers of ecological change on the island include the manuring and trampling of vegetation by seals and seabirds in coastal areas. Like other subantarctic islands, there has been a marked change in climate since meteorological recording began in the middle of the 20th century. The increasing temperatures and lower precipitation have been shown to be exacerbating the interaction of indigenous species with invaders such as the grass Agrostis stolonifera. Climate change may also be playing a role in affecting salt spray in coastal ecosystems through changing atmospheric circulation patterns and wind (Bergstrom and Chown, 1999; Smith et al., 2001a; Smith, 2002). On longer time scales, reconstructions of post-glacial environmental change show the impacts of nutrient enrichment and disturbance by animals on vegetation composition in coastal areas, but do not indicate the influence of other factors on long-term ecosystem change (Schalke and van Zinderen Bakker, 1971; Scott and Hall, 1983; Scott, 1985).

Figure 1

Study site location, and location of sites mentioned in the text: (a) Junior's Kop (Schalke and van Zinderen Bakker, 1971); (b) Macaroni Bay (Schalke and van Zinderen Bakker, 1971); (c) Albatross Lakes (Scott, 1985); (d) Kildakey Bay (Scott, 1985).


The effects of tephra deposition from volcanism on local vegetation have been noted in the Pacific Rim (e.g. Bush and Whittaker, 1991; Thornton and Walsh, 1992; Whittaker and Walden, 1992; Horrocks and Ogden, 1998; Hotes et al., 2006), North America (e.g. Blong, 1984), Europe (from paleoecological studies, e.g. Birks and Lotter, 1994; Edwards et al., 2004), and Deception Island in the maritime Antarctic (e.g. Collins, 1969). However, volcanic activity has not been previously recognized as a significant influence on vegetation in the subantarctic. This study is therefore unique in the context of the subantarctic, as it presents a record of vegetation change showing that tephra deposition following volcanic eruptions has been a major driver of long-term ecosystem change and succession at one site on Marion Island during the last 5500 yr.

Marion Island and Its Current Vegetation

40K/39Ar dating suggests the island was formed before 450 ka. 40K/39Ar dating has also shown volcanism to have occurred episodically since this date (McDougall et al., 2001). Geological evidence indicates several glaciations corresponding to marine oxygen isotope stages 2, 4, 6, 8, and 12 (McDougall et al., 2001). Holocene volcanic activity has resulted in the formation of c. 130 scoria cones; with the most recently observed eruptions occurring in 1980 (Verwoerd et al., 1981), 2004, and 2005 (

The island and its nearby, smaller neighbor, Prince Edward Island, have a cool (mean annual temperature, c. 6°C) oceanic climate with a total annual precipitation of c. 2000 mm. Moreover, the climate is exceptionally thermally stable, the difference between the mean temperature of the coldest and warmest months is 3.6°C, and the mean diurnal temperature variation is 1.9°C (Smith, 2002).

The vegetation of the islands has been described and classified using the Braun-Blanquet approach (Gremmen, 1981; Smith et al., 2001b). Salt-spray complexes dominated by Cotula plumosa and Crassula moschata exist in coastal areas. In coastal and some inland areas, disturbance from seals and seabirds maintains biotic herbfield and grassland complexes. Poa cookii and the nitrophiles Callitriche antarctica and Montia fontana are dominant in these habitats.

Peat bogs are abundant on the lowland plains of Marion Island, and mire complexes cover around 50% of the island below 300 m a.s.l. Plant communities of the mires form the Juncus scheuchzerioidesBlepharidophyllum densifolium complex. Graminoid species form an important part of the peat-forming plants, notably Agrostis magellanica, Uncinia compacta, and Juncus scheuchzerioides. Bryophytes also occur on the mires, and the most important of these are Drepanocladus uncinatus, Blepharidophyllum densifolium, Jamesoniella colorata, Racomitrium lanuginosum, and Breutelia integrifolia. The mires have a very even surface and do not possess a pattern of hollows and hummocks. Ranunculus biternatus occurs in bog ponds, and Juncus scheuchzerioides and Agrostis magellanica can form pioneer communities in 20- to 80-cm-deep water.

Well drained lava ridges around the edges of mires are covered in fernbrake vegetation dominated by the pteridophyte Blechnum penna-marina with Acaena magellanica. Exposed ridges and plateaus around the mires, and at higher elevations are covered in a fellfield complex, an open vegetation of isolated, stunted plants, with mosses and lichens. Much of the bare rock and scoria has no vegetation cover except for lichens and cushion dicots including Azorella selago and Colobanthus kerguelensis, on which grow graminoid species such as Agrostis magellanica, Uncinia compacta, and Poa cookii.



Two intersecting transects of peat depth measurements were made across a small bog (135 × 79 m) and are shown in Figure 2. The main peat core, MARI1 (46°52.7303′S, 37°50.9161′E), was taken to a depth of 287 cm. At this depth the Russian corer (7 cm × 50 cm) hit solid lava deposits at the base. The cores were split into contiguous 1 cm slices on Marion Island.

Figure 2

Peat depths along two transects. Light gray rectangles are coring location, black bands indicate tephra deposits; dark gray rectangles are lava ridges/outcrops.


14c Dating

Seven peat samples were AMS radiocarbon dated by the SUERC and Groningen 14C facilities (Table 1). With the exception of the sample at 261.5 cm, which contained Ranunculus biternatus leaf fragments, the samples were composed of roots of Agrostis magellanica and indeterminate humified organic material. The downward growth of these roots would have introduced some contamination, but their ubiquitous presence in the peat samples and the scarcity of other plant macrofossils left no option but to date these components.

Table 1

14C measurements; *weighted average of BCal posterior probability distribution (Buck et al., 1999). With the exception of the sample at 261.5 cm, which contained Ranunculus biternatus leaf fragments, the samples were composed of roots of Agrostis magellanica and indeterminate humified organic material.


Palynomorph and Macrofossil Analyses

Microfossil samples of c. 1 cm3 volume (volume estimated by immersion) were treated with KOH and acetolyzed (Fægri and Iversen, 1989). To estimate microfossil concentrations, tablets with Eucalyptus spores were added to the samples (Stockmarr, 1971). A total of 300 pollen grains was the pollen sum, where possible, for each of the 71 samples. Pollen identifications were made using Schalke and van Zinderen Bakker (1971), Scott and Hall (1983), and Markgraf and D'Antoni (1978). Selected pollen types are shown in Figure 3. The samples also contained a variety of non-pollen palynomorphs. Some of these, including fungi, testate amoebae, and desmids, have already been described in the literature and were identifiable (e.g. van Geel, 1978; Charman et al., 2000). There were a number of unknown structures that were morphologically distinguishable and could be considered as homogeneous entities. These were classified into ‘Types.’ These Types are described in the Appendix and shown in Figure 3. Where possible, a sum of at least 100 palynomorphs was recorded for each sample during the pollen counts, and these are expressed as percentages of the pollen sum for each sample.

Figure 3

Examples of palynomorphs found in the MARI1 profile. (1) Acaena magellanica at three different focal depths; (2a) Cotula plumosa, polar views; (2b) Cotula plumosa, equatorial views; (3) Colobanthus kerguelensis at two focal depths; (4) Hymenophyllum peltatum at two focal depths; (5) Montia fontana at three focal depths; (6a) Azorella selago, polar views; (6b) Azorella selago, equatorial views; (7a) Ranunculus biternatus, polar view; (7b) Ranunculus biternatus, equatorial views; (8) Type 815 fungal spores; (9) Type 816 fungal spores; (10) Type 817 fungal spore; (11) Type 823 fungal spores; (12) Type 818, two examples; (13) Type 819, two examples; (14) Type 820, two examples; (15a) Type 822, polar view; (15b) Type 822, equatorial view; (16) Type 821, two examples.


Macrofossil samples were boiled with 5% KOH and sieved (mesh diameter 150 µm). Macrofossils were identified using a binocular microscope (×10 to ×50), and the abundances of each peat component were expressed using a six point scale: 0, absent; 1, rare; 2, occasional; 3, frequent; 4, common; and 5, abundant. Identifications of plant macrofossils were confirmed using type material of plants collected during fieldwork. Examples of these macrofossils are shown in Figure 4.

Figure 4

Examples of macrofossils found in the MARI1 profile. (1a, 1b) Campylopus clavatus leaves; (2) Juncus scheuchzerioides seed; (3) Montia fontana seed; (4a, 4b) Ptychomnion densifolium leaf; (5a) Ranunculus biternatus leaf; (5b, 5c, 5d) Ranunculus biternatus seeds.


Organic Content and Tephra Analyses

The organic content of the peat samples was measured using the loss-on-ignition (LOI) technique (Gale and Hoare, 1991). Oven-dried samples were ignited at 430°C for 24 h, and the change in mass determined.

Visible tephra horizons in the sequence were prepared for geochemical analysis using Wavelength Dispersive Spectrometry (WDS). To avoid migration of some major oxides as a result of heating, the material was not combusted (Turney and Lowe, 2001). Samples were acid digested, following the procedure outlined by Dugmore (1989), and the size fraction 70–15 µm was isolated for analysis. Extracted glass shards were geochemically analyzed on the Jeol 733 Superprobe at the Electron Microscope Unit, Queen's University, Belfast. An accelerating voltage of 15 kV, a beam current of 10 nA, and a slightly defocused beam diameter of c. 8 µm were used, and a lipari standard was analyzed at regular intervals during the analysis period. A ZAF correction was applied to correct for atomic number, absorption, and fluorescence effects (Sweatman and Long, 1969). Counter dead time was also corrected for. All analyses exceeded 95% totals (Hunt and Hill, 1993). The detection limits of the major oxides were of the order of 0.01–0.05 wt%.


14c Chronology

The 14C ages of the samples (Table 1) have been converted to calendar ages by online BCal calibration (Buck et al., 1999) using the Intcal04 calibration data set (Reimer et al., 2004). The probability density plots for each age were then imported into Psimpoll 4.25 (Bennett, 2005), and an age/depth model was constructed by linear interpolation between the weighted averages of the calibrated ages (Figure 5). Owing to the deposition of the tephra layer at 124–107 cm (being assumed to be instantaneous), the 14C date at 117.5 cm was excluded from the age model. Ages are expressed as calibrated radiocarbon years (cal. BP). It is recognized that these dates lie within a range and are not precise; and therefore are rounded to the nearest 100 years.

Figure 5

MARI1 Age-depth model. 14C dates were calibrated using BCal, black lines indicate the 95% confidence interval for each calibrated date. The weighted average of each date was used for the age-depth model produced by Psimpoll 4.25 (Bennett, 2005), using linear interpolation between dated levels.


Palynomorphs and Macrofossils

The pollen spectra are dominated by Poaceae and Azorella selago, in addition to varying proportions of Uncinia compacta, monolete psilate fern spores, Acaena magellanica, and Lycopodium spp. (Fig. 6). Exotic pollen grains were also identified, and these form between 0 and 2% of the whole assemblage. Type 91 and Type 820 palynomorphs were most frequently encountered in addition to varying proportions of Type 821, Type 823, and fungal types (Types 815, 816, 817, 818, 819, and 824). Remains of Corythion-Trinema type testate amoebae (Charman et al., 2000) were only observed in the layers containing tephra. This may be due to special preservation conditions, or the deposition of the ashes producing favorable conditions (relatively dry; see Charman et al., 2000). With the exception of the levels between 263 and 242 cm where macrofossil remains of Ranunculus biternatus and Montia fontana were frequently encountered, very few identifiable macrofossils were present (Fig. 7). Leaves of the moss species Campylopus clavatus and seeds of Agrostis magellanica were restricted to the sample at 3 cm depth, suggesting these macrofossil components do not survive the decomposition processes that occurred in the bog. Zonation of the pollen, palynomorphs, and macrofossils was made by eye and by optimum splitting by information content using Psimpoll version 4.25 (both resulted with similar zone boundaries), and are described in Tables 2 and 3, respectively.

Figure 6

MARI1 Palynomorph stratigraphy. Values of pollen are expressed as percentages based on a sum of 300 pollen grains. Non-pollen palynomorphs are presented as percentages related to the pollen sum for each sample. The total pollen and spore concentration is plotted with a ×20 exaggeration. Montia fontana and Cotula plumosa are plotted with a ×3 exaggeration.


Figure 7

MARI1 Macrofossil stratigraphy. Abundances are expressed using a six point scale: 0: absent, 1: rare, 2: occasional, 3: frequent, 4: common, and 5: abundant.


Table 2

Local Pollen Assemblage Zones (LPAZ).


Table 3

Macrofossil zonation.


Tephra Analyses

Two distinct tephra horizons were identified in the Marion Island sequence between 200–183 cm and 124–107 cm using the LOI record (Fig. 8). Samples were extracted from 184 and 121 cm using the methods outlined above and geochemically analyzed using WDS (Tables 4 and 5). None of the glass had any visible phenocrysts. Brown vesicular glass shards (up to sand size particles) were identified in both units. Lavas on the island possess typical oceanic island basalt (OIB) geochemical characteristics (Verwoerd, 1990). There are two types of lavas: ‘older grey lavas’ (Pleistocene) and ‘younger black lavas’ of Holocene age (McDougall et al., 2001). Petrologically, all these lavas have SiO2 values ranging between 45 and 55%, and are overwhelmingly basalt and hawaiite. Trachyte has been found only on nearby Prince Edward Island (Verwoerd, 1990). The two tephra horizons in the MARI1 core can best be characterized as basaltic in composition, at the lower end of the OIB with 46–48% SiO2 content. Although the mean results for both horizons are statistically indistinguishable, the individual data points do, however, record significant differences between the two horizons, suggesting separate eruptions. The horizon at 184 cm has variable Al2O3 values ranging from 19.2 to 14.1 wt%, while the horizon at 121 cm is significantly more limited in its range, with values between 15.8 and 14.2 wt%. Similar differences are seen in most of the other major oxides, while CaO values tend to be higher than those from 121 cm. The two distinct eruptions are dated to ca. 2900 cal. BP and ca. 1700 cal. BP.

Figure 8

Pollen concentrations of selected pollen types, and loss on ignition (LOI) data. Gray shading on pollen concentration diagram indicates ×10 exaggeration.


Table 4

Relative concentrations (wt. %) of oxides of the eight major elements in glass shards from 184 cm depth, as determined by electron microprobe.


Table 5

Relative concentrations (wt. %) of oxides of the eight major elements in glass shards from 121 cm depth, as determined by electron microprobe.


Interpretation of The Local and Regional Vegetation Record

The first stage of organic accumulation in the basin between 274 and 269 cm (ca. 5900–5700 cal. BP in zone MARI1-P1) appears to show the presence of an early successional sequence representing a fellfield/fernbrake habitat, given the high values of monolete psilate fern spores (Blechnum penna-marina) and Acaena magellanica. Free drainage of soils is highly likely to have occurred due to the presence of coarse scoria deposits (up to 9-mm-long axis) identified in this zone.

The pollen spectra in MARI1-P2 (269–258 cm, ca. 5700–5300 cal. BP) are largely composed of Poaceae and Azorella selago and may reflect the slow growth of the latter pioneer species as the lava/scoria deposits were further stabilized. The highest pollen concentrations were identified in this zone, possibly indicating low peat accumulation rates and/or the position of the site in an isolated depression during this interval (Fig. 2).

Mire surface wetness appears to have been consistently high in the overlapping macrofossil and pollen zones MARI1-M2 and MARI1-P3 (263–236 cm, ca. 5500–4400 cal. BP) given the high values of Ranunculus pollen and Ranunculus biternatus seeds and leaves. These remains indicate the presence of a pool forming in the low-lying depression, possibly as a result of organic material accumulation blocking the pores in the lava/scoria deposits and therefore impeding drainage (Smith, 1987). The presence of Montia fontana seeds may indicate the local influence of animals, possibly wandering albatross and/or giant petrels (the site is too far inland for penguins), since this plant occurs in biotic mud habitats (Smith et al., 2001b). Relatively high pollen concentrations were also identified in this zone, again indicating low peat accumulation rates.

The absence of Ranunculus pollen during MARI1-P4 (236–212 cm, ca. 4400–3400 cal. BP) suggests a shift to drier conditions in the mire. Type 91 microfossils are present from the beginning of this zone, indicating oligotrophic conditions in the bog (van Geel, 1978), possibly related to the decline of the mire as an animal habitat.

In zone MARI1-P5 (212–200 cm, ca. 3400–2900 cal. BP), the higher values of Azorella selago may reflect a change from purely local to extra-local pollen deposition, since below c. 220 cm depth the coring site was an isolated depression measuring only c. 5 × 10 m (see Fig. 2). Given the widespread occurrence of Azorella selago from sea level to the limit of vascular plant growth at 765 m elevation (it occurred in 71% of the 457 quadrats examined in the vegetation survey of Huntley, 1972), the increase of its pollen values may indicate an influx of pollen from a greater area around the sampling site.

Following deposition of a 17-cm-thick tephra layer at 200–183 cm depth, Uncinia compacta and Acaena magellanica initially increase at the expense of Poaceae, and Azorella selago gradually increases throughout the zone (MARI1-P6, 183–152 cm, ca. 2900–2200 cal. BP). This may represent the response of the vegetation to the deposition of the tephra. Concentration data (Fig. 8) reflect this pattern. On the bog surface, there was a decrease in the recruitment of Poaceae above 180 cm, while Uncinia compacta increased in concentration during the interval 178–165 cm. On the slopes around the bog, the cover of Azorella selago increased after tephra deposition and remained high relative to Poaceae (compare with the interval before the tephra deposition, when Poaceae concentrations were higher than A. selago). Type 160 microfossils also increase in this interval. Type 160 is characteristic of mesotrophic moorland pools in Europe (van Dam et al., 1988), and its presence may be related to a change in pH and trophic state of the bog water favoring the organism that produced it.

In zone MARI1-P7 (152–124 cm, ca. 2200–1700 cal. BP), the pollen spectra closely resemble those found in MARI1-5 before the volcanic eruption, with relatively low levels of Azorella selago. The tephra layer above this, in zone MARI1-P8 (124–107 cm, ca. 1700 cal. BP), complicates any vegetation reconstruction.

In the penultimate zone, MARI1-P9 (107–20 cm, ca. 1700–200 cal. BP), there is a gradual increase in the representation of Azorella selago at the expense of Poaceae up to 41 cm depth (ca. 400 cal. BP). On the bog surface, Uncinia compacta shows high values relative to those recorded in MARI1-P7, before the tephra layer. Concentration data (Fig. 8) reflect the increase of Azorella selago cover on the slopes around the bog up to c. 101–90 cm (ca. 1500–1200 cal. BP); which may be a response to the deposition of the tephra. The greatest diversity of exotic pollen was also discovered in MARI1-P9 and is likely to reflect the larger pollen source area of the expanding peatland.

The final zone, MARI1-P10 (20–5 cm, ca. 200 cal. BP to modern), records an increase in monolete psilate fern spores and Acaena magellanica, and may indicate the presence of a fernbrake/dwarf shrub habitat and drier conditions.


The results suggest that tephra deposition has been a major influence on long-term vegetation succession in and around the study site. The effects of tephra deposition close to the source of eruption include the mechanical impact upon the land surface (including the burial or partial burial of plants), the encouragement of erosion in freshly coated surfaces and the chemical ‘scorching’ of leaves (Edwards et al., 2004; Hotes et al., 2006). After volcanic ash deposition ca. 2900 cal. BP, total vegetation cover initially decreased and then Uncinia compacta increased in cover as a pioneer on the disturbed mire surface. On the slopes around the bog, Acaena magellanica, and particularly Azorella selago, increased in cover. Ash deposition can alter topography and therefore influence stream patterns (Collins, 1969); a change in drainage lines would favor Acaena magellanica, since this species occurs where subsurface water flows on slopes (Smith et al., 2001b).

The slow increase of Azorella selago pollen after volcanic ash deposition ca. 2900 cal. BP (MARI1-P6, with a duration of c. 700 yr) represents the long-lived nature and extremely slow growth of Azorella selago (small 15-cm-diameter cushions were estimated to be 83 years old by Huntley [1972], although there are no age estimates for the larger cushions which can exceed 1 m diameter). The volcanic ash itself can also absorb moisture and cause desiccation; resulting in the slow growth of Azorella selago. Furthermore, the exposed periglacial conditions on the island may explain the slow vegetation succession. The low annual temperature ranges experienced on Marion Island combined with high precipitation and cloudiness result in high frequencies of short-duration freeze-thaw cycles with shallow frost penetration. The presence of patterned ground and solifluction features and the incidence of debris flows, peat slides, and frost creep associated with needle ice activity highlight the dynamic nature of geomorphological processes on Marion Island (Boelhouwers et al., 2003; Holness, 2004). The general pattern of long-term vegetation change described in this study may be compared with arctic tundra landscapes, where rates of directional vegetation change are extremely slow, often of the order of a 1000 years or more (e.g. Billings and Peterson, 1980). In the Arctic, episodic environmental events slow or reverse successional development so that the “successional clock” is continually being reset by disturbance (Forbes and Jefferies, 1999). The slow pace of vegetation succession highlights the sensitivity of the indigenous Marion Island flora to environmental change, and the importance of controlling the introduction and spread of alien invasive species, which by contrast, can respond faster. This has been shown by the rapid spread of the grass Agrostis stolonifera between the 1980s and 1990s, possibly as a result of the ongoing climate change (Bergstrom and Chown, 1999). The ongoing climate change may also affect the growth and distribution of Azorella selago both directly through decreased rainfall, and indirectly by increased shading from faster growing grass species (Le Roux et al., 2005).

Examination of pollen diagrams from previous studies suggests that increases of Azorella selago after tephra deposition have occurred at other sites around the island. These include Macaroni Bay (at c. 250 cm depth), Albatross Valley on nearby Prince Edward Island (at c. 325 cm, c. 275 cm, and c. 185 cm depth), and Juniors Kop from the early study of Schalke and van Zinderen Bakker (1971), in addition to Albatross Lakes (4th boring) (at c. 175 cm depth) (Scott, 1985). However, these pollen diagrams have relatively low resolution (10 cm), making these changes not so noticeable, and were therefore not discussed in the publications. Schalke and van Zinderen Bakker (1971) used a sum including both pollen and spores, which may have also confused the interpretation of the diagrams. Due to the low number of indigenous taxa (and consequent pollen types) on the island, there has been less motivation to calculate a pollen sum distinguishing local bog pollen types from extra-local taxa. In particular, increases of extra-local A. selago at Albatross Lakes (3rd boring) after the tephra deposition at c. 378 cm (Scott, 1985) may have been masked by the dominance of the pollen spectra by the local aquatic Ranunculus spp.

The evidence for a major effect of volcanic ash deposition on the vegetation of other areas of the island is therefore not entirely conclusive, and this may also be due to the pollen recruitment characteristics of the sites studied. A review of basin characteristics and estimated pollen source area by Davies and Tipping (2004) suggests that the coring site, even at its current dimensions of c. 130 × 80 m, would only record local vegetation mosaics within a radius of c. 1 km. The pollen records reported here and in previous studies are therefore not representative of the entire island's vegetation. However, there are c. 130 volcanic cones on the island marking centers of eruption, and even relatively recently in 1980 (Verwoerd et al., 1981), 2004, and 2005 (, small eruptions have occurred; leading to the speculation that tephra deposition and the consequent effects on the local vegetation have been repeated on numerous occasions around the island since the last glacial. The results of this study outline the sensitivity of ecosystems on Marion Island to disturbance from tephra deposition and associated effects including the burial of plants, chemical ‘scorching’ of leaves, and alteration of trophic status through acidification and nutrient enrichment.


The South African National Antarctic Program provided financial and logistic support for this research, and NERC provided 14C dating support (Allocation No. 987.1002). We thank Jan Boelhouwers for suggesting and encouraging this research in the first instance and for fieldwork assistance with Steve Holness and Werner Nel. We also thank Valdon Smith for collecting additional plant type material and for valuable discussions on Marion Island peatland ecology. Louis Scott offered useful suggestions in the identification and interpretation of the pollen records, and both Melodie McGeoch and Peter Le Roux gave useful advice on the ecology of Azorella selago. Louise Coetzee kindly confirmed the identifications of the mites encountered in the samples. Randy Miller examined possible tardigrade eggs, and identifications of the mosses were made by Ryzard Ochyra. We thank Annemarie Philip for preparing the pollen samples, Jan van Arkel for creating the digital illustrations of the micro/macrofossil samples, and Stephen McFarland for help in operating the electron microprobe at Queen's University Belfast. We also thank Anne Jennings and two anonymous reviewers for constructive comments on the manuscript.

References Cited


K. D. Bennett 2005. Psimpoll manual ( Accessed 6 September 2006. Google Scholar


D. M. Bergstrom and S. L. Chown . 1999. Life at the front: history, ecology and change on southern ocean islands. TREE 14:472–477. Google Scholar


W. D. Billings and K. M. Peterson . 1980. Vegetational change and ice-wedge polygons through the thaw-lake cycle in arctic Alaska. Arctic and Alpine Research 12:413–432. Google Scholar


H. J. B. Birks and A. F. Lotter . 1994. The impact of the Laacher See volcano (11000 yr B.P.) on terrestrial vegetation and diatoms. Journal of Paleolimnology 11:313–322. Google Scholar


R. J. Blong 1984. Volcanic hazards: a sourcebook on the effects of eruptions Sydney, Australia Academic Press. 424. Google Scholar


J. Boelhouwers, S. Holness, and P. Sumner . 2003. The maritime Subantarctic: a distinct periglacial environment. Geomorphology 52:39–55. Google Scholar


C. E. Buck, J. A. Christen, and G. N. James . 1999. BCal: an on-line Bayesian radiocarbon calibration tool. Internet Archaeology 7.( Accessed 6 June 2006. Google Scholar


M. B. Bush and R. J. Whittaker . 1991. Krakatau: colonization patterns and hierarchies. Journal of Biogeography 18:341–356. Google Scholar


D. J. Charman, D. Hendon, and W. A. Woodland . 2000. The identification of testate amoebae (Protozoa: Rhizopoda) in peats. QRA Technical Guide, 9 London Quaternary Research Association. 147. Google Scholar


N. J. Collins 1969. The effects of volcanic activity on the vegetation of Deception Island. British Antarctic Survey Bulletin 21:79–94. Google Scholar


A. L. Davies and R. Tipping . 2004. Sensing small-scale human activity in the palaeoecological record: fine spatial resolution pollen analyses from Glen Affric, northern Scotland. The Holocene 14:233–245. Google Scholar


A. J. Dugmore 1989. Icelandic volcanic ash in Scotland. Scottish Geographical Magazine 105:168–172. Google Scholar


K. J. Edwards, A. J. Dugmore, and J. J. Blackford . 2004. Vegetational response to tephra deposition and land-use change in Iceland: a modern analogue and multiple working hypothesis approach to tephropalynology. Polar Record 40:113–120. Google Scholar


K. Fægri and J. Iversen . 1989. Textbook of pollen analysis Chichester John Wiley and Sons. 328. Google Scholar


B. C. Forbes and R. L. Jefferies . 1999. Revegetation of disturbed arctic sites: constraints and applications. Biological Conservation 88:15–24. Google Scholar


S. J. Gale and P. G. Hoare . 1991. Quaternary Sediments New York John Wiley & Sons. 323. Google Scholar


N. J. M. Gremmen 1981. The vegetation of the Subantarctic islands Marion and Prince Edward The Hague Junk. 149. Google Scholar


S. D. Holness 2004. Sediment movement rates and processes on cinder cones in the maritime Subantarctic (Marion Island). Earth Surface Processes and Landforms 29:91–103. Google Scholar


M. Horrocks and J. Ogden . 1998. The effects of the Taupo tephra eruption of c. 1718 BP on the vegetation of Mt Hauhungatahi, central North Island, New Zealand. Journal of Biogeography 25:649–660. Google Scholar


S. Hotes, P. Poschlod, and H. Takahashi . 2006. Effects of volcanic activity on mire development: case studies from Hokkaido, northern Japan. The Holocene 16:561–573. Google Scholar


J. B. Hunt and P. G. Hill . 1993. Tephra geochemistry: a discussion of some persistent analytical problems. The Holocene 3:271–278. Google Scholar


B. J. Huntley 1972. Notes on the ecology of Azorella selago Hook. f. South African Journal of Botany 38:103–113. Google Scholar


P. C. Le Roux, M. A. McGeoch, M. J. Nyakatya, and S. L. Chown . 2005. Effects of a short-term climate change experiment on a sub-Antarctic keystone plant species. Global Change Biology 11:1628–1639. Google Scholar


V. Markgraf and H. D'Antoni . 1978. Pollen flora of Argentina Tucson University of Arizona Press. 208. Google Scholar


I. McDougall, W. Verwoerd, and L. Chevallier . 2001. K-Ar geochronology of Marion Island, Southern Ocean. Geological Magazine 138:1–17. Google Scholar


P. J. Reimer, M. G. L. Baillie, E. Bard, A. Bayliss, J. W. Beck, C. J. H. Bertrand, P. G. Blackwell, C. E. Buck, G. S. Burr, K. B. Cutler, P. E. Damon, R. L. Edwards, R. G. Fairbanks, M. Friedrich, T. P. Guilderson, A. G. Hogg, K. A. Hughen, B. Kromer, G. McCormac, S. Manning, C. B. Ramsey, R. W. Reimer, S. Remmele, J. R. Southon, M. Stuiver, S. Talamo, F. W. Taylor, J. van der Plicht, and C. E. Weyhenmeyer . 2004. IntCal04 terrestrial radiocarbon age calibration, 0–26 cal Kyr BP. Radiocarbon 46:1029–1058. Google Scholar


H. J. W. G. Schalke and E. M. van Zinderen Bakker Sr. . 1971. History of the vegetation. In E. M. M. van Zinderen Bakker, J. M. Winterbottom, and R. A. Dyer , editors. eds. Marion and Prince Edward Islands, report on the South African Biological and Geological Expedition 1965–66 Cape Town Balkema. 89–97. Google Scholar


L. Scott 1985. Palynological indications of the Quaternary vegetation history of Marion Island (sub-Antarctic). Journal of Biogeography 12:413–431. Google Scholar


L. Scott and K. J. Hall . 1983. Palynological evidence for interglacial vegetation cover on Marion Island, sub-Antarctic. Palaeogeography, Palaeoclimatology, Palaeoecology 41:35–43. Google Scholar


V. R. Smith 1987. The environment and biota of Marion Island. South African Journal of Science 83:211–220. Google Scholar


V. R. Smith 2002. Climate change in the sub-Antarctic: an illustration from Marion Island. Climatic Change 52:345–357. Google Scholar


V. R. Smith, M. Steenkamp, and N. J. M. Gremmen . 2001a. Terrestrial habitats on sub-Antarctic Marion Island: their vegetation, edaphic attributes, distribution and response to climate change. South African Journal of Botany 67:641–654. Google Scholar


V. R. Smith, M. Steenkamp, and N. J. M. Gremmen . 2001b. Classification of the terrestrial habitats on Marion Island based on vegetation and soil chemistry. Journal of Vegetation Science 12:181–198. Google Scholar


J. Stockmarr 1971. Tablets with spores used in absolute pollen analysis. Pollen et Spores 13:615–621. Google Scholar


T. R. Sweatman and J. V. P. Long . 1969. Quantitative electron microprobe analysis of rock forming minerals. Journal of Petrology 10:332–379. Google Scholar


I. W. B. Thornton and D. Walsh . 1992. Photographic evidence of rate of development of plant cover on the emergent island Anak Krakatau from 1971 to 1991 and implications for the effect of volcanism. GeoJournal 28.2:249–259. Google Scholar


C. S. M. Turney and J. J. Lowe . 2001. Tephrochronology. In W. M. Last and J. P. Smol , editors. eds. Tracking Environmental Changes in Lake Sediments: Physical and Chemical Techniques Dordrecht Kluwer Academic Publishers. 451–471. Google Scholar


H. van Dam, B. van Geel, A. van Wijk, J. F. M. van der Geelen, R. Heijden, and M. D. van der Dickman . 1988. Palaeolimnological and documented evidence for alkalization and acidification of two moorland pools (The Netherlands). Review of Palaeobotany and Palynology 55:273–316. Google Scholar


B. van Geel 1978. A palaeoecological study of Holocene peat bog sections in Germany and the Netherlands. Review of Palaeobotany and Palynology 25:1–120. Google Scholar


W. J. Verwoerd 1990. Marion Island. In W. E. LeMasurier and J. W. Thomson , editors. eds. Volcanoes of the Antarctic Plate and Southern Oceans Washington, D.C American Geophysical Union. Antarctic Research Series no. 48. 411–419. Google Scholar


W. J. Verwoerd, S. Russell, and A. Berruti . 1981. 1980 Volcanic eruption reported on Marion Island. Earth and Planetary Science Letters 54:153–156. Google Scholar


R. J. Whittaker and J. Walden . 1992. Post-1883 ash fall on Panjang and Sertung and its ecological impact. GeoJournal 28.2:153–171. Google Scholar


Appendix—descriptions Of Palynomorphs

Type 815

Two-celled fungal spores, each cell 10–25 µm in length and 5–12 µm in width. Constriction at septum. The spores often show two germ slits running parallel along the long axis of each cell. Some spores have cells that vary in proportion from one another.

Type 816

Three-septate elongate fungal spores, 15–33 µm in length and 5–8 µm in width. Septa are often barely visible and are spaced out evenly along the long axis. Type 816 spores occur in the lower and the upper part of the core only.

Type 817

Elliptical fungal spores, ∼20 µm in length and ∼7.5 µm wide. The spores often show a germ slit along the long axis.

Type 818

Irregular and angular shaped microfossils, 58–220 µm in length and 16–30 µm in width. Appears to be plant cells infested with fungal hyphae. Shows relatively high frequencies of occurrence in the upper 30 cm of the core.

Type 819

‘Winged’ microfossils with a center composed of a double-walled globose object, ∼68 µm in diameter. This is often filled with dark material, frequently smaller globose objects. The wings are relatively thin walled compared to the center. Type 820 appears to be quite fragile, and is more often than not found in a broken state, with two components: (1) the two ‘wings’ joined together, ∼55 µm in length, and ∼33 µm in width; and (2) the double-walled center piece, sometimes filled with dark material.

Type 820

Spores/eggs 28–36 µm in diameter. Covered with small hyaline ridges; ridges often green/white. Objects are sometimes folded. May be a tardigrade egg (R. Miller, personal communication, 2004).

Type 821

Egg-shaped objects, 15–23 µm in length and 8–13 µm in width. Pits on surface at varying depths.

Type 822

Hyaline egg- or cigar-shaped objects, 13–32 µm in length and 8–13 µm in width. A relatively large pore (diameter 2.5–5 µm) and distinct annulus at one end. Possibly a testate amoeba.

Type 823

Fungal spores 20–24 µm in length and 7.5–12 µm in width. Composed of four cells. Two central cells are relatively large. Terminal cells are relatively small and almost hyaline.

Dan Yeloff, Dmitri Mauquoy, Keith Barber, Susannah Way, Bas van Geel, and Chris S. M. Turney "Volcanic Ash Deposition and Long-Term Vegetation Change on Subantarctic Marion Island," Arctic, Antarctic, and Alpine Research 39(3), 500-511, (1 August 2007).[YELOFF]2.0.CO;2
Accepted: 1 September 2006; Published: 1 August 2007

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