aE rt aah a ‘earbook cof The Heather s€ar fi sSociety BN 0440-5757 THE HEATHER SOCIETY Registered charity No 261407 Affiliated societies Nederlandse Heidevereniging ‘Ericultura’ Gesellschaft der Heidefreunde North American Heather Society President Mr D. J. Small Vice-Presidents Mr A. Hall Mrs A. Knight Mrs P. B. Lee Mr D. Somer Mr J. Schréder COUNCIL 2004-2005 Chairman Mr A. J. Stow Honorary Secretary Honorary Treasurer Mrs J. Julian’ Mr P. L. Joyner Mr R. Canovan Mr A. R. Collins Mr D. Edge Mrs D. Everett Mrs D. H. Jones JP Mrs S. Kay Mr D. E: Millis Dr R. Nichols Dr B. E. Roberts Mr B. Sellers © The authors & The Heather Society The Heather Society and the editors take no responsibility for the views expressed by authors in papers and notes published in Heathers (Yearbook of The Heather Society). FRONT COVER: Orange-breasted Sunbird on Erica baueri © Peter Steyn (see pp 27-30). Dae Heathers 2 Yearbook of The Heather Society 2005 3 Be : : ye Gaim™ third series Sok a A Se , Pe | fl my : ty! ay Pa BP) 2 pe an 2005 ’ : 4 Ed \ ae x 4 f Ls ry vA =~ AAP PS Editor Dr E. Charles Nelson Assistant Editor B. Sellers ISSN 0440-5757 The Heather Society c/o Denbeigh, All Saints Road, Creeting St Mary, IPSWICH, Suffolk, IP6 8P] Erica junonia vat. junonia from a new locality in the Cold Bokkeveld photographed by Ted Oliver in mid-November 2004. (enlarged c. x2) Heathers 2: 1-12 (2005). © R. Canovan Heathers: coping with the weather and alkaline clay RICHARD CANOVAN 10 Queensborough, Toothill, SWINDON, Wiltshire, SN5 8DU. My first heathers were obtained mainly to give a time-saving groundcover between the roses but were beautiful. Abnormal weather became as much a concern as the soil after an initial test indicated that it had a pH of almost 7.5 with some variation. In one patch it was 8.0, probably due to cement debris and concrete. This was a disappointment. Acid mulches have reduced the pH almost to neutral in the top few centimetres. Having established by good luck that Erica erigena and E. vagans seemed to thrive in my intractably heavy and alkaline (Kimmeridge) clay, the Harlow Carr Trial reports were a valuable guide to what to get next. The results of a potting disaster (Griffiths 1981) also helped. The success of E. vagans suggested a magnesium-rich soil confirmed recently by the spectacular growth of E. erigena ‘Ewan Jones’ reaching over 2.5m (8ft) in six years. After more than two decades of effort, it has become clear that the soil is far from hopeless. For this paper, a professional soil analysis has been undertaken. Soil and site conditions The free lime content of my soil prevented the use of a Morgan’s analysis so the standard ADAS Arable Analysis was carried out by the Scottish Agricultural College. The analysis revealed a pH of 7.8, a phosphorus deficiency and that the magnesium content was slightly lower than expected. The quantities (mg per litre) extractable were: Ca 9,670 Mg 127 Na 25 K 160 P18 Initial preparation involved sedge peat and moss peat mixed with the soil when planting. This worked well for some years but more grit should have been dug in. This imperfect preparation led to a more gluey texture in places than originally! This lesson has been applied to later beds. Those cut out of lawn have had the turf turned upside down and broken up in the second spit, which has proved beneficial. Cracks get filled with compost and grit. Another consideration was shade. As with Karla Lortz (2004) the winter sun does not rise high enough in the sky to reach over the properties uphill. “C vwscneith © Jan FebMar Apr May Jun Jul Aug Sep Oct Nov Dec Figure 1. Daily Central England temperature for 2003 (blue line). The black line shows the 1961-1990 normals after 11-term binomial smoothing. The red lines are the corresponding 1st and 99th percentiles for each day of the year. (Crown copyright: reproduced from Parker et al. (2004) with permission of the Meteorological Office.) The weather and heathers The 1980s saw some extraordinary weather, testing the hardiness of the heathers. The 1990s saw even more extreme conditions. The first extreme year, 1982, opened with floods followed by severe frost, a massive blizzard, then intense cold and fog with record low temperatures. The previous December, E. australis had been killed down to the snow. However in mid-January there was more widespread damage where plants had the snow removed by drifting as temperatures fell to between —-14°C and —18°C nearby: E. xveitchii ‘Exeter’ died. Spring was warm and moist until the night of 5 May which was exceptionally cold. The humid, thundery summer had numerous torrential downpours, rather like 2004. One storm in June washed away the mulch and soil over the young E. vagans to expose the roots to the hot sun but they survived and still thrive. The drought and “hosepipe ban” of 1984 was another test. February 1986 was extremely cold with little snow so many new plants, including E. manipuliflora ‘lan Cooper’, were lost. But this was because they were still 5 | Jan FebMar Apr May Jun Jul Aug Sep Oct Nov Dec Figure 2. Maximum Central England temperature averaged over 1989-2003 (red) against 1961-1990 (black) and its two standard error range (grey shading) and the 20th and 80th smoothed percentiles for 1961-1990 (dotted). All curves smoothed with an 11 term binomial filter. (Crown copyright: reproduced from Parker et al. (2004) with permission of the Meteorological Office.) in pots or just planted. The frost penetration at least converted overturned sods in a newly-dug bed to powder, killing the grass, so it was ready for planting! The three years 1995 to 1997 were a period of “continental” weather with scorching summers (although 1997 was wet) and intervening winters bringing some severe weather, yet the plants survived with nothing more than minor defoliation. The greatest damage was wreaked by lesser events. A theme of the last 15 years has been a trend to warmer conditions. Hot summer weather has become common and the first three months of the year have become much warmer. But December and June have not shared this warming and the autumn and April have had some notable visitations of frost and snow as well as warmth. These trends since 1989 are vividly illustrated in Figure 1. Severe early frost is one source of damage. It was undoubtedly a factor in the December 1981 damage (well summarised for Harlow Carr by Albert Julian (1983)). A sharp frost in early November 1985 caused much damage 4 to buds on E. xdarleyensis ‘Arthur Johnson’. But more damage was caused by a short severe spell after mid-December 1999 when a heavy fall of snow broke the stem of my large E. terminalis and stems on E. erigena ‘Ewan Jones’. E. multiflora ‘Formentor’ was killed while another E. xveitchi ‘Exeter’ was badly damaged. The warmth of November and the first half of December 1994 broke all records but was followed by a cold spell. At Lyneham, four miles away, temperatures on Christmas Eve fell to -9.9°C which was two degrees lower than in 1999. After such warmth it may have been expected to cause great damage, especially without a protective snow-cover, but there was no damage whatever. September had been dull and rather cold, and October also had slightly below-normal temperatures with an air frost on 4 October, so this may have induced early dormancy in the heathers. The worst example of damage in spring was 1989. After a cold November with severe early frosts, the winter and March had been exceptionally mild but April brought unseasonably cold weather. Very locally April or November were colder than any of the intervening months which may be unprecedented. On 25 April, after overnight rain and snow, slight frost fatally damaged E. carnea‘Foxhollow’ and even slightly damaged ‘Pink Spangles’ and E. erigena ‘Brightness’. It seems that this damage may have been partly due to the foliage being encased in ice when the strong morning sun rose and was reflected off the ice-covered drive. The scorching summers of 1989 and 1990 caused great stress to E. erigena ‘Golden Lady’ which has suffered burn on other occasions. But the worst damage from drought was in 2003, also another year with extreme temperatures as shown in Figure 1. This shows that the 99th percentile was exceeded in mid-April, late May, July and August while the October cold spell broke the 1st percentile (Parker, Alexander & Kennedy 2004). On 1 August 2003, the soil was moist throughout its profile after a wet July but that was the start of an intense drought: although Swindon missed the record high temperatures of 10 August, it was very hot. September continued the warm, sunny weather but a short cold snap brought an abnormally early frost on 24 September with the lowest temperatures locally in southern England for more than 70 years. October continued sunny but with cold drying winds and sharp frosts. E. manipuliflora ‘Corfu’ responded to the drought by not fully opening its flowers: instead of a brief display of massed lilac pink bloom it resembled a bud-bloomer for two months. Another problem of this period was a coconut-shell mulch on part of one bed that formed a mat almost impenetrable to water so that the brief heavy rains on both 22 September and 22 October did not reach the roots of some plants 5) which wilted and had to be removed, notably E. xwilliamsii ‘Cow-y-Jack’ and E. erigena ‘Ewan Jones’. Early November was warm and wet but revealed that Chamaecyparis lawsoniana ‘Pygmaea Argentea’ had suffered burn. It is difficult to isolate the effects of the drought, heat and frost, but the conifer damage may have been due to October’s drying winds at a time of a severe soil moisture deficit. Possible explanations of damage by frost Bannister (2001) examined frost resistance of cut shoots of seven heather species. Unfortunately, this did not include E. carnea, but this is likely to behave similarly to Calluna vulgaris and E. tetralix, which showed the maximum resistance to winter frost (down to —22°C). This is supported by the evidence from the damage to the national collection at Cherrybank, Perth, in December 1995 and the cultivars hardy in northeast USA. The latter has a much wider range of temperature than central southern England. But the central England record of the last 250 years reveals 15 occasions when mean temperature in April has been colder than the preceding March, but not in the northeast USA (Burroughs 2002). As in 1989, it can be lower than even the entire winter although that was a very exceptional event. Conversely, E. erigena and E. vagans, while less winter-hardy, were less sensitive to temperature. So there is evidence that the species with the greatest winter hardiness exhibit sharply reduced resistance to frost after high maximum temperatures. This may explain the damage to E. carnea and its hybrids after early and late frosts as in November 1985 five weeks after a heatwave brought maximum temperatures of 27°C, and in October 1997 when more tender varieties have suffered no damage. Although likely to be a factor in the damage in April 1989, that was probably a freak combination of events. Evidence from Sweden does not suggest this is a problem there, although it indicates that E. vagans may be hardier than thought and its tolerance of shade supports my experience (Johansson 1988). Another implication is that global warming with warmer spring weather would reduce frost resistance. Artificial warming of only three degrees Celsius accelerated “dehardening” in Vaccinium myrtillus (Taulavuori et alii 1997). Also, planting of heathers from more southerly latitudes under conditions of different day-length may result in delayed development exposing unhardened tissue to early frost. In October 1993, soft growth on E. terminalis was killed by six successive air frosts. Frost resistance may vary between cultivars of the same species due to differing provenance (Bannister 1996). 6 What could grow? Successes and failures With E. erigena ‘Irish Dusk’ flowering as early as November and ‘Superba’ through May, and E. vagans starting in late July through the autumn | already could get bloom for most of the year. E. carnea and E. xdarleyensis cultivars offered many promising variations. By the late 1980s other species and hybrids became available and the hybridisation expertise of Professor John Griffiths and Kurt Kramer opened up new frontiers. Sadly, many of the new “reds” have not succeeded perhaps due to nurseries’ propagation methods. E. xdarleyensis ‘Kramer’s Rote’ has flowered particularly disappointingly not just here but on acid clay as well. Several of the red E. carnea cultivars have not prospered. Some early failures were unrelated to weather events. Among E. carnea, ‘Springwood White’ was found to be rather drought sensitive through drying winds and cracked soil but coped ina moist shady spot where it became too vigorous: ‘Eileen Porter’ was painfully slow. Among Calluna cultivars failure was not surprising with ‘Sunset’ being an anomalous success, although ‘Beoley Gold’ and ‘Serlei’ grew splendidly in 23cms (9 ins) of soil overlying the chalk at the former Chiseldon nursery, south of Swindon. Daboecia gave varied performances but D. cantabrica ‘Atropurpurea’ repeatedly suffered chlorosis and quick death: ‘David Moss’ and D. xscotica ‘William Buchanan’ did well in what was well-prepared soil until my downslope neighbour made the bed a bog by laying a concrete foundation for a greenhouse. This really tested them but they came through unlike D. cantabrica ‘Blueless’, which was clearly lime-tolerant but could not stand frost when the ground was wet. ‘Waley’s Red’ was brilliant but only in autumn. ‘Barbara Philips’ and ‘Hookstone Purple’ coped but the new ‘Cupido’ was very unhappy. It was one battle with nature I have given up. The growth of a weed E. tetralix, probably a seedling brought in with another plant, encouraged me to try ‘Foxhome’. Beautiful cerise flowers were encouraging but not in 2000. Success followed again in 2001. Sequestrene was applied in spring but it seemed essential to catch the start of growth. The soil water was almost certainly a factor, being planted in a wet spot as in nature. Ironically the weed in drier soil did better indicating that a well drained soil may be preferable. Therefore the one bed with reasonably good drainage has to be home for all heathers that prefer such conditions whether they dislike lime, hate it, tolerate it or even prefer it: E. australis, E. bocquetii, E. carnea, E. xgriffithsii, E. xkrameri, E. manipuliflora, E. xoldenbergensis, E. scoparia, E. xwilliamsii and E. spiculifolia x bergiana ‘Edewecht Belle’ all need this rather crowded bed, many planted as trials with no idea of their ultimate dimensions! Figure 3. Erica carnea ‘Rosalie’ Figure 4. Erica carnea ‘Barry Sellers' However, unlike with those gardening over limestone, E. xwilliamsii has not been a success, despite the brilliance of one of the parents. This casts doubt over the new E. xgarforthensis, another hybrid with E. tetralix as a parent: ‘Tracy Wilson’ has made a splendid start but it is too early to be certain of its lime tolerance. } Cultivars: performance I naturally tried the most outstanding cultivars. Some did not give of their best but were still very good and garden-worthy. Others were less reliable, including many of the winter-flowering “reds”. Alongside these, I tried others for time of flowering, colour contrast or taste, and some of these lesser names have done extremely well. E. carnea: the flowers of ‘Myretoun Ruby’ did not have the glow I had seen elsewhere, but that may be because it did not get lit by the winter sun before the flowers deepened. ‘Pink Spangles’ went bare in the centre but was still creditable. However, ‘Praecox Rubra’ was clearly unhappy, even its few flowers seemed to get damaged by hot autumn sunshine and sharp early frosts like October 1997, November 1993 and 2001. Although superficial, such damage is irritating. Some of the late-flowering cultivars of E. carnea such as ‘Rosalie’ (Figure 3) have been rewarding and this applies in general to the newer “pinks” such as ‘Winter Rubin’. ‘Rosantha’ looks promising although with a short season, but ‘Treasure Trove’ was weak. Among foliage cultivars tried, ‘Ann Sparkes’ had too much bare stem. ‘Altadena’ was tried but died back with ‘Barry Sellers’ (Figure 4) being Figure 5. Erica vagans 'Diana Hornibrook' happiest of those with orange foliage tolerating an intractable patch of clay and worth having more of as it flowers quite well. It is fair to say that I tried the plugs of ‘Bell’s Extra Special’ (Wuisky) and it may have been excellent but it was too vigorous a carpeter so had to be removed. Erica bocquetii performed reasonably well until dug up in 1996, but has not flowered since replanting. It does not appear garden-worthy but preferring lime is worth further effort, its very short-lived flowers having the delicacy of a magnolia. Cuttings have been taken to plant elsewhere as it was wrongly located, but it has proved extremely hard to propagate. Erica vagans cultivars performed in line with often high expectations. ‘Birch Glow’, ‘Mrs D. F. Maxwell’, ‘St Keverne’ and ‘Diana Hornibrook’ (Figure 5) thrive: indeed the only failure in this species was ‘Valerie Proudley’, which seemed less tolerant of lime, but ‘Pyrenees Pink’ did not flower as well as usual. Erica erigena ‘Glauca’, ‘Superba’ and ‘W. T. Rackliff’ have been superb shrubs, the latter despite ravaging by foxes, another hazard. Most cultivars tried have been successful, but ‘Irish Salmon’ seemed very weak. Erica xdarleyensis ‘Darley Dale’ and ‘George Rendall’ are among the cultivars that did not disappoint, reliable and trouble-free. Figure 6. Erica vagans ‘Lilacina’, lit by the evening sun, is attractive. The E. carnea cultivar laden with buds is ‘Queen Mary’, with E manipuliflora ‘Don Richards’ behind. Erica manipuliflora generally grows well and is drought resistant. The success of this species in providing good bloom, ‘Korcula’ and ‘Cascades’ apart, contrasts with Arnold Stow’s experience over chalk (Stow 2004). Even unnamed Dalmatian clones and the new golden sport ‘Toothill Mustard’ proved fully garden-worthy. Erica umbellata also flowers well. The tree heaths have generally not found conditions to their liking. E. arborea has not been successful: var. alpina suffered severe chlorosis and ‘Estrella Gold’, while appearing more tolerant of lime could not cope with the cold clay growing only 2.5cm (lin) in six years! E. terminalis and E. xveitchi have been mentioned. The most tolerant appears to be E. australis ‘Holehird’ which is very promising given reasonable drainage. Outperformers But of most interest must be what cultivars seemed to outperform? Even within a species or hybrid there was considerable variation in performance. The preference of E. xdarleyensis ‘Jack H. Brummage’ for a rich clay soil is well known and it was no surprise that it was a super foliage plant until a gale in 1989 flattened my fencing allowing its bed to become an attraction 10 to dogs and a convenience. The brilliant E. erigena ‘Brian Proudley’ and others were finished by that. A real surprise is E. scoparia: the lost ‘Lionel Woolner’ flattened in the same gale and now ‘Madeira Gold’ are not the most garden-worthy plants but their happiness in the adverse conditions is surprising. Others with an indifferent reputation have impressed and good plants excelled. Erica carnea ‘Golden Starlet’, although “recommended”, has probably outperformed. It is an exceptional foliage plant, even rooting into boggy clay when put ina trench to overwinter and showing the same health and vigour! The same may be said of ‘Lake Garda’ which I have largely removed, its pale violet shade seeming to add to the chill of a winter day. But it is certainly happy, not just with the soil but being in a very shady although open spot and flowered profusely. Erica carnea ‘Queen Mary’ (Figure 6) was mentioned by M. G. Frye’s Nurseries as actually preferring lime. This certainly seems to be the case, being a reliable, early and free-flowering carpeter deserving its Boskoop recommendation (Flecken 2004). ‘Rotes Juwel’ failed in those trials but is another free-flowering cultivar that seems remarkably happy, covered with short but crowded spikes of brilliant beetroot even after being run over! These two seem better than ‘Eileen Porter’, ‘Gracilis’ and ‘Jennifer Anne’ for early colour and with the bonus of complementary colours. ‘Winterfreude’ may now be a worthy addition: | like the rich crimson flowers. Erica xdarleyensis ‘Silberschmelze’ was truly outstanding despite a shady spot, eventually spreading so much it had to be removed. ‘Furzey’ under- performed in the same bed. ‘Erecta’ has been excellent in the worst possible soil conditions and is going to be used elsewhere. ‘Aurélie Brégeon’ has certainly proved hardy both against wet, unseasonal frost, drought and heat. Long flowering, it has a little more blue in the colour than ‘Erecta’ but its solid spikes of large flowers are quite effective, and it has been proved not to mind shade given some summer sun. Erica xoldenbergensis ‘Ammerland’ has proved to be a remarkable plant, its massive spikes so smothered in bloom that the orange spring foliage is hardly visible. ‘Oldenberg’ has not been tried. One very good summer flowering cultivar that has been outstanding for bloom and general health is E. vagans ‘Lyonesse’. Like ‘Mrs D. F. Maxwell’, it has found a rather shady spot very much to its liking getting plenty of summer sunshine. It has certainly done far better than ‘Cornish Cream’ although that is long flowering. ‘Lilacina’ may also have exceeded its normal performance, and is going to be tried elsewhere being useful for early bloom. 11 Erica xgriffithsti ‘Heaven Scent’ is another of the Society’s top 100 that may have exceeded its high standards, with beautiful foliage, even after pruning, in addition to its prolific bloom. ‘Jacqueline’ looks promising and is a superb colour. But they may not have inherited the drought resistance of E. manipuliflora. Erica manipuliflora ‘Don Richards’ smothered in pink flowers every autumn is another plant clearly at home on clay given reasonable drainage. Early summer is the time of least bloom but brilliant new foliage colour on, among others, E. vagans ‘Golden Triumph’, E. carnea ‘Barry Sellers’ (Figure 4) and E. xdarleyensis ‘George Rendall’ providing some compensation to support the late blooms of E. umbellata, its very late cultivar ‘David Small’ and E. erigena ‘Irish Silver’. But it is not long before plants such as E. terminalis, E. vagans ‘Diana Hornibrook’ (Figure 5) or E. xgriffithsii ‘Heaven Scent’ are bursting into bloom, helped by early pruning as soon as safe. In late June 2004, E. terminalis overlapped with E. umbellata ‘David Small’ resulting in year round bloom. Some associated plants that have thrived on this soil have been Chamaecyparis lawsoniana ‘Minima Glauca’ and ‘Minima Aurea’, Picea pungens ‘Globosa’ despite a poor location and, not surprisingly, Thuja plicata ‘Stoneham Gold’. The latter is a magnificent slow-growing shrub. ‘Rogersii’ is being added. Although the trials go on, and now it is E. xkrameri, E. xwilliamsii ‘David Coombe’ and the putative hybrid E. cinerea x terminalis, it is time for some careful design to enjoy the successes. With hot spring weather becoming more common, the risk of blooms fading prematurely can be reduced by planting late flowering E. carnea cultivars such as ‘March Seedling’, ‘Viking’ and ‘Wintersonne’ where there is some shade from the afternoon sun and the early flowering clones like ‘Queen Mary’ and ‘Rotes Juwel’ in the sunny locations. When replanting, I intend bolder plantings of my favourite cultivars. Summary and conclusions It is difficult to draw firm conclusions and evaluations must be partly subjective and a matter of taste. But there is clearly considerable variation in sensitivity to temperature between species and to some extent cultivars. With longer, hotter summers there is a growing risk of damage from sudden falls in temperature in autumn like that of September 2003 given the lengthening nights. Considerable variation in lime sensitivity in Calluna, Daboecia, Erica australis and E. scoparia and perhaps E. tetralix has been found. Some summer-flowering hybrids also appear relatively insensitive to lime, 12 particularly those with E. spiculifolia as a parent. Calluna vulgaris ‘Sunset’, E. spiculifolia x bergiana ‘Edewecht Belle’ and E. scoparia ‘Madeira Gold’ would be rated 1 (moderate impact on growth) or less on the scale used by John Griffiths. Daboecia xscotica ‘William Buchanan’ appears to contradict his experience. More research is needed on this. The failure of many new plants in the last ten years, which appears partly due to modern propagation methods, is compounded by confusion between new cultivars. Therefore taking cuttings regularly is essential to keep a supply. Examples of misnaming include E. carnea ‘Wintersonne’, sold as “Winter Sun” but which has richer flowers and lacks the brown foliage and appears to be ‘Viking’. E. carnea ‘Nathalie’ from several sources is quite distinct from the plant I have of that name which has been so difficult to grow on clay but with its deep reddish purple flowers is worth persevering with. But there is enough evidence to demonstrate that, even on alkaline clay, it is possible to have colour from flower practically every day of the year. References BANNISTER, P., 1996. The frost resistance of heaths and heathers. Yearbook of the Heather Society: 39-42. BANNISTER, P. & POLWART, A., 2002. The frost resistance of ericoid heath plants in the British Isles in relation to their biogeography. Journal of biogeography 28: 589-596. BURROUGHS, W. J., 2002. Gardening and climate change. Weather 57 (5): 151-157. FLECKEN, J. F., 2004. Erica carnea —- a summary of the Royal Boskoop Horticultural Society trials 1999-2002. Heathers 1: 31-38. GRIFFITHS, J., 1981. Observations of lime sensitivity in young plants of some Erica, Calluna and Daboecia cultivars. Yearbook of the Heather Society 2 (10): 65-68. JOHANSSON, B., 1988. Heathers in Sweden. Yearbook of the Heather Society 3 (6): 36-41. JULIAN, T. A., 1983. Damage at Harlow Car during the Winter of 1981-2. Yearbook of the Heather Society 3 (1): 9-12. LORTZ, K., 2004. A woodland heather garden. Heathers 1: 1-3. PARKER, D. E., ALEXANDER, L. V. & KENNEDY, J., 2004. Global and regional climate in 2003. Weather 59 (6): 145-152. STOW, A. J., 2004. Forty years on. Heathers 1: 13-17. TAULAVUORI, K., LAINE, K., TAULAVUORI, E., PALONEN, T. & SAARI, E., 1997. Accelerated dehardening in bilberry (Vaccinium myrtillus L) induced by a small elevation in air temperature. Environmental pollution 98: 91-95. Heathers 2: 13-14 (2005). © Brita Johansson Suggestions for a bed of heathers II: mixed planting BRITA JOHANSSON Musselvagen 3, 468 34 VARGON, Sweden. The first article in this series was published in Heathers 1: 39-41 (2004). KEN 1 5 plants Erica carnea ‘Weisse March Seedling’ 2 7 plants Erica xstuartii ‘Irish Lemon’ 3 4 plants Erica carnea ‘Wintersonne’ 4 7 plants Calluna vulgaris ‘Catherine’ or ‘Gaia’ 5) Opp lants Erica carnea ‘Rosalinde Schorn’ 6 5plants Calluna vulgaris ‘Sirsson’ or ‘Sesam’ 7 7 plants Calluna vulgaris ‘Velvet Fascination’ 8 5 plants Calluna vulgaris ‘Radnor Gold’ 9 plants Calluna vulgaris ‘Easter-bonfire’ 10 5 plants Erica tetralix ‘Helma’ 14 APRIL SEPTEMBER This planting scheme was devised for Swedish conditions, but it should also work in the colder parts of Britain, Ireland and North America. — The planting plan is for an area of about 12 metres? (about 10 x 12 ft). The stones may be replaced by dwarf and miniature conifers. You will need about 55 plants of the cultivars listed. A few alternatives are given. For a smaller area reduce the plantings of each cultivar by two plants. Heathers 2: 15-16 (2005). © C. D. Rogers. Mix and match: a search for year-round colour COLIN ROGERS Ebenezer Chapel, 121 Old Road, Tintwistle, GLOSSOP, Derbyshire, SK13 1JZ. Frustration is . .. doing everything by the book, and still getting it wrong. My only excuse is that, in the beginning, I probably read the wrong books. Furthermore, a cynic might detect different advice from different authors. What none seemed to supply were the advantages and disadvantages of planting winter- and summer-flowering heathers in the same bed, referring to it, if at all, as a matter of personal preference. Whosoever’s fault it was, the result has been something unsatisfactory seen from my lounge window. Sometimes, half a bed will look dead (or, at best, dull); another might look like an irregular chessboard, with patches of colour contrasting with a disfiguring lifelessness. Toogood (and many others) say that dead flowers make an attractive feature over the winter, but my visitors disagree! Recently pruned Calluna vulgaris ‘Beoley Gold’ and ‘Peter Sparkes’ have looked particularly moribund this year, and I still have the spectre of what Maxwell (1927: 22) called “large, flowerless tracts”, supposedly avoided by mixing the seasons in the same bed. Should I, therefore, have surrendered to the inevitable and put all “winter” plants in one bed, and “summer” in another? My earliest enthusiasm had been for flowers “all the year round”, a benefit advocated by most books on the subject, and indeed by being astute (putting, for example, Erica xdarleyensis ‘Kramer’s Rote’ alongside Daboecia xscotica ‘William Buchanan’) this is quite easily achieved with only two cultivars. But a more casual buying of “summer” and “winter” plants for the same bed will often result in fairly colourless areas in May, June and July, just when competition from the rest of the garden is at its height. There are several alternative primary criteria for selection, other than time of flowering. A. T. Johnson, for example, recommends deciding first the ultimate height of plants, particularly in relation to the contours of the ground, within which he suggests an arrangement by which “one will always be in bloom when its neighbour is either over or not yet in flower” (1956: 48). Similarly, the initial plan in Jones (1998: 23) seems to relate essentially to the height of the plants — there is no discussion of seasonality. Chapple, on the other hand, appears to be primarily interested in colour (1964: 62-66), and mixed the seasons in the same bed, as Maxwell did “in roughly equal proportions” (1927: 20-21). Some writers have offered planting schemes which may reveal their 16 attitudes and preferences. Letts (1966: 22-27) and Yates (1985: 22-25) suggest three beds each with a basic design in which either single-season, or mixed season, cultivars can be found. Van de Laar’s examples (1978: 25-29) are almost all “mixed-season” in the same beds, though he is describing whole gardens. None of the above is leading me to that promised land as shown in photographs of heather gardens, which seems as elusive as the permanently blue skies portrayed in all British university prospectuses. I gazed awestruck at some of the photos in Karla Lortz’s book (2002), for example, especially the one on p. 18 which was reproduced in Heathers 1 (2004: 2), and tried to analyse the basis for the beauty she had obtained even in a woodland setting. Asa result, I’ve come round to the Lambies’ advice on the subject — that the prime criterion for planning a heather garden should be overall colour, combining the colour of foliage with that of flower. Admittedly, care has to be taken to give non-green foliage the light it needs to get full advantage — of their contrasts, and to choose cultivars you know to be on sale within travelling distance from home! I also learned from sad experience to buy all cultivars for a new bed from the same source, one half of a bed of Erica cinerea ‘Cindy’ being a distinctly different purple from the other half! Only by looking back does this now seem the obvious solution, yet many of the published plans do not apply it. Letts (1966: 26) for example, has only one yellow-foliage cultivar among his six dark- to mid-green; the Proudleys (1974: 46) have the gold/red foliage of Calluna ‘Robert Chapman’ among seven mid- to dark-green; and van de Laar (1978: 26) has one bright green among seven dark green. So I now believe that the “summer” /“winter” debate is of secondary importance, perhaps almost irrelevant for most gardens, and that any dead or dull patches are the result of my own inadequate design. I might not be able to organise blue skies, even in Tintwistle, but I’m determined that my heather garden will be much more colourful in future. References CHAPPLE, F. J., 1964. The heather garden. Second edition., London; Collingridge. JOHNSON, A. T., 1956. Hardy heaths. Revised edition. London, Blandford. JONES, D., 1998. Conifers and heathers. Oxford, Aura. LAMBIE, D. & LAMBIE, B., not dated. Heathers: a guide to designing a heather garden. Speyside, D. & B. Lambie. LETTS, J. F., 1966. Handbook of hardy heaths and heathers. Ipswich, John F. Letts. LORTZ, K., 2002. Heaths and heathers: color for all seasons. Shelton (Washington), K. Lortz. MAXWELL, D. E,, 1927. The low road. London, Sweet & Maxwell. PROUDLEY, B. & PROUDLEY, V., 1974. Heathers in colour. Poole, Blandford. TOOGOOD, A., 1986. Gardening with conifers and heathers. Greenford, Aura. TOOGOOD, A., 1992. Heathers and heaths. London, HarperCollins. VAN DE LAAR, H., 1978. The heather garden. London, Collins. YATES, G., 1985. Gardener’s book of heathers. London, Warne. 17 Heathers 2: 17-18 (2005). © J. Schréder. The explosion of bud-flowerers JURGEN SCHRODER Gesellschaft der Heidefreunde, Liitjenmoor 66, 22850 NORDERSTEDT, Germany. Some years ago one was inclined to say: “the bud-flowerers are on the advance”. Now it seems that we are experiencing an “explosion”. In the 1980s only a few bud-flowering Calluna cultivars, each one having been collected in the wild, were known: ‘David Eason’ (introduced 1935), ‘Dunwood’ (before 1977) and ‘Underwoodii’ (1936) from Great Britain; ‘Adrie’ (introduced 1974), ‘Ginkel’s Glorie’ (before 1972), ‘Marilyn’ (before 1972), ‘Marleen’ (before 1972) and ‘Visser’s Fancy’ (introduced 1972) from the Netherlands. The best-known of these, and still general in the trade, is ‘Marleen’. In the past ten years a lot of new bud-flowering heathers have been raised in Germany, and breeders now compete with each other to bring more and more cultivars into commercial production, often with the protection of plant breeders’ rights. During the last 20 years marketing has also changed: formerly small nurseries which propagated a limited number of plants of a large number of cultivars sold plants directly to private buyers; today, very large numbers of only a few cultivars are sold at auctions and afterwards garden centres and supermarkets sell these on to private buyers. Correspondingly, nurseries have changed their propagation schemes to producing very large numbers of only a few cultivars. It is almost an industrial process, and every propagator looks for gaps in the market. In 2003 about 80 million Calluna plants were propagated in Germany — about 65 million of these were bud-flowerers — and most were destined for an entirely new market. No longer are the owners of heather gardens the main target group: quite the reverse, for those people now represent the smallest group, buying only about 5% of the production. The new customers are the people who wish to adorn their balconies and terraces in late autumn and early winter with bowls and troughs of flowering plants, and also those who will place heathers as winter decoration on their family graves. The latter bought about 25% of the bud-flowerers in 2003. 18 Figure 1. Left to right Calluna vulgaris 'Aphrodite'; ‘Marlies’; ‘Sandy’; 'Theresa’ and ‘Larissa’. The propagating nurseries put their potted heathers on to the market from September until November at intervals of about a fortnight, so that bud colour lasts from the time of sale until December/January. In this connection, the survival of the plants through the winter is not the aim. On the contrary, the vast majority of these heathers end up in the garbage box, because the sellers hope for lucrative new sales next year. The result of the flood of new bud-flowering Calluna cultivars is that many of them are indistinguishable: differences often exist only in the imagination of the producers! For example, ‘Marlies’, a sport on ‘Marleen’, one of the clones not protected by plant breeders’ rights, has given rise to numerous progeny including ‘Anka’, ‘Bella Rosa’, ‘Bonita’, ‘Cheyenne’, ‘Christin’, ‘Feuerzauber’, ‘Heidegltihen’, ‘Manuel’ and ‘Sphinx’. It would be a wonder if all its “children” are discernably different. At the moment about 80 bud-flowering cultivars, with and without breeders’ rights, have been named, and at least that number again are on trial at the Bundessortenamt in Hannover. Heathers 2: 19-22 (2005). © E. C. Nelson Cultivar names for two remarkable heathers from Kurt Kramer, Edewecht, Germany* E. CHARLES NELSON ee International Cultivar Registrar, The Heather Society, c/o Tippiliwitchet Cottage, Hall Road, Outwell, Wisbech, PE14 8PE, Cambridgeshire, United Kingdom. Among the many novel heathers produced by Kurt Kramer were three seedlings raised from Erica spiculifolia (Balkan heath; formerly Bruckenthalia spiculifolia) that had been artificially fertilized during the Spring of 1987 with pollen from the African (Cape) species E. bergiana (K. Kramer, pers. comm., 23 March 2004). Erica bergiana is a distinctive heath, notable for its urn-shaped flowers (in clusters of four) with reflexed sepals, and hirsute leaves and stems; these characters are clearly demonstrated in the photograph in D. Schumann & G. Kirsten, Ericas of South Africa (1992: 143). E. spiculifolia is also distinctive, unlike any of the other northern hemisphere species. It has tiny, bell-shaped flowers clustered in a leafless, terminal inflorescence (raceme), and leaves that are hairless (apart from some microscopic spicules at the tips). Superficially Kramer’s seedlings resemble E. spiculifolia although they are much more vigorous. They display no morphological evidence that E. bergiana was the pollen parent, so chromosome counts are essential to confirm beyond doubt that they are hybrids (E. spiculifolia has 2n=36 (see McClintock 1979); there is no record of a count for E. bergiana). In 1992, cuttings of this new heather were donated by Kurt Kramer to the late David McClintock, and these were successfully propagated by David Small (Denbeigh Heathers) (the hybrid is noted in Bulletin of The Heather Society 5 (2): 4 (Summer 1994)). Subsequently Denbeigh Heathers provided further cuttings and young rooted plants to heather enthusiasts in various countries; for example, cuttings were made available to members of The Heather Society at the annual conference held at Penrith in 1997 (see Yearbook of The Heather Society 1998: 63). While neither Kurt Kramer Heideztichtung nor Denbeigh Heathers put this plant onthe market, as far asIcan ascertain, ithas now been widely dispersed. During July and August 2004, Isaw mature plants in Ireland and western USA and I am aware of other examples in cultivation in England and France. This paper was originally published in German (translated by Jiirgen Schroder) in Der Heidegarten 56: 52 2-57 (December 2004). 20 Careful examination of these plants indicates that two clones are in cultivation. With Kurt Kramer’s consent, I have published names for these (Der Heidegarten 56: 52-57 (2004)), and the chosen names have been registered with The Heather Society (see Heathers 2: 70 this issue). This should assist in rectifying a serious confusion in nomenclature. In the USA, I saw plants erroneously labelled “Erica xkrameri Unnamed Clone”; E. xkrameri is the name for another of Kramer’s artificial hybrid, between E. spiculifolia and the European species E. carnea, and it is definitely not the name for the plants discussed here. The clone in circulation in the western USA and Canada is identical with that grown by Susie Kay (obtained at Penrith in 1997) in western Ireland (see Yearbook of The Heather Society 2003: 18, Figure 2); this is distinguished (see below) by virtually hairless flower stalks (pedicels) and white (colourless) flowers which appear pink due to the colour of the immature anthers — ‘Edewecht Blush’ is the registered name for this clone. A second clone is cultivated by Allen Hall (Leicestershire, England); this is easily distinguished by its pubescent pedicels and pink flowers — the cultivar name ‘Edewecht Belle’ is registered for this plant. It is most probable that these two clones represent progeny from two of the three seedlings. The cultivar names are derived from Edewecht, the name of the town in northern Germany where Kurt Kramer lives and where he raised these seedlings. Blush refers to the tendency of the flowers, especially in bud, to have a pink tinge, while Belle is an English noun usually applied to handsome (beautiful) women (and there is an underlying pun, an allusion to the bell-shaped flowers). My observations in Ireland and North America suggest that ‘Edewecht Blush’ flowers best when grown in the open; shading reduces the quantity of blossom. It can be in bloom for many months, beginning as early as April and continuing into winter. Pruning delays the onset of the flowering season, because the immature inflorescences are removed. In the mildest areas, where plants are not affected by frost, it may bear flowers for twelve months. ‘Edewecht Belle’ is apparently much less common in cultivation, and I have not seen an example in gardens, although I have examined specimens provided by Allen Hall. Mr Hall has informed me that his plant reaches peak blooming in mid-June. Both clones have malformed stamens; the malformation is not consistent from flower to flower. The filaments are usually broadened and fused, and the anthers are degenerate. Similar malformations have been reported in E. mackaiana (see Yearbook of The Heather Society 1995: 33-40); the clone ‘Maura’ demonstrates the characteristic. 21 Key to cultivars Flowers colourless but appearing pink (“blushing”) when young due to colour of immature stamens inside; flower-stalks usually entirely without hairs............. ‘Edewecht Blush’ Flowers pink; flower-stalks covered with very short hairs, some of which have glands at the tips Gaisilenwitunancd=lens)iic. ents elas ea a Gas. oe. a ee ‘Edewecht Belle’ ‘Edewecht Blush’ This clone is in cultivation in Ireland (Susie Kay), Great Britain and western USA; the description was prepared from specimens provided by S. Kay. Bushy, vigorous shrub, to 0.5m tall. Shoots densely puberulous. Foliage bright green. Leaves scattered, almost spirally arranged or in pairs or in “disarticulated” whorls of 3 or 4; linear, with parallel sides, to 6.5mm long, 0.5mm wide; sulcate; with a few, scattered microscopic hairs on the margins; apex pointed, with spicules (microscopic hairs). Flowers in contracted, terminal racemes, 8—14(—20) per cluster, central peduncle to c. 20mm. Pedicels straight or curving, usually slightly bent towards apex so that the flowers are held at an angle, 3-5mm long, tinged red, hairless (or with a very few, scattered, minute hairs), with 1 bract at base (leaf-like, <3mm long, <0.4mm wide), or occasionally with the bract 4 way from base; very rarely with 1 or 2 proximate bracteoles. Calyx cup-shaped, clasping base of corolla, hairless, c. 1.25mm long, 4-lobed; lobes c. 0.75mm long, pale green with colourless, fringed margins, fused irregularly for up to 0.5mm (but sometimes one sulcus extending almost to base). Corolla bell-shaped (campanulate) or broad funnel-shaped, white (colourless) but “blushing” pink when young (due to colour of the immature stamens visible inside), hairless, c. 3.5mm long, c. 1.25mm in diameter-in lower part, costricted in middle, to c. 1.8mm diameter towards apex, 4-lobed; lobes erect, rounded, c. Imm wide, c. 0.8mm long (4 length of tube); buds can be pink. Stamens 8, not manifest (included), with very broad, irregularly fused, colourless filaments which coallesce to form a “pseudocorolla”, c. 0.7mm long; anthers degenerate, bright red when young, turning golden brown, oval in lateral view, papillose, often remaining fused in a collar, without awns, c. 0.45mm long; pore oval, lateral towards apex, c. 0.1mm long; pollen observed. Ovary indistinctly 4-celled (4-locular), glabrous, inversely pear-shaped (narrow (stipitate) at base, expanding towards top) with style continuous with apex; style usually prominently manifest, to c. 4.5mm long (but sometimes malformed, and then very much shorter), straight, slightly expanded towards apex, and at base broadening and merging with the ovary; eas stigma simple, truncate, with 4 dark-red ovoid Fig. 1. Inflorescence of ‘Edewecht Blush’: carpels (see H.A. Baker & E.G.H. Oliver (1967) Ericas enlarged (© David Plumridge). of southern Africa: xlvi, fig. 11). Ovules numerous. pe ‘Edewecht Belle’ This clone is in cultivation in Great Britain (Allen Hall) and probably in France; the description was prepared from specimens provided by A. Hall. Like ‘Edewecht Blush’, but distinguished most easily by the dark red pedicels being noticeably pubescent with minute, straight hairs (without glands) mixed with shorter, gland-tipped hairs. Bushy, vigorous shrub; when not pruned to 0.5m tall. Corolla pink (H9), campanulate (bell-shaped) to conical so broadening gradually towards lobes (not constricted in middle), c. 4.5mm long. Stamens variously malformed, not manifest (included); some are simple, petaloid staminodes; others have broadened filaments; some filaments and staminodes may be fused, and in some flowers they may fuse entirely into an inner “pseudocorolla”. Ovary 8-celled, not distinctly stipitate, but broadly obovoid to barrel-shaped with emarginate apex (so style base is recessed); style to 3.7mm long, only slightly broader at base. Leaves with hairs along the margins and on the under-rolled sides; terminal hair usually with gland at tip. Figure 2. Photograph by Kurt Kramer (reproduced by courtesy ©); note the shape of the individual florets and the appearance of the “pseudocorolla” at the mouth of the florets. Author’s footnote (not included in Der Heidegarten) The photograph (Figure 2) of the flowers of one of the original seedlings, taken c. 1990 by Kurt Kramer, very clearly shows “double” flowers. In these the malformed stamens are obvious at mouth of the corolla, appearing as an inner cluster of closely-packed “petals”; thus the internal “pseudocorolla” is as long as, ora little longer than, the corolla, not shorter as in ‘Edewecht Blush’ and ‘Edewecht Belle’. None of the flowers I have examined resembled this state, and so I conclude that the third seedling was distinct too. I would welcome any information that could lead to its rediscovery and propagation. Heathers 2: 23—26 (2005). © R. B. Stewart & C. W. N. Anderson. Erica andevalensis, a unique “copper flower” from Spain ROBERT B. STEWART & CHRISTOPHER W. N. ANDERSON Soil and Earth Sciences, Institute of Natural Resources, Massey University, PALMERSTON NORTH, New Zealand. Professor Robert Brooks (1926-2001) was a leading figure in the international fields of geochemistry and biogeochemistry throughout much of the second half of the twentieth century. His work on the ecology, distribution and the potential uses for metal-accumulating plants gave him great notoriety during the final years of his academic career. In 1977 Robert and colleagues published a paper in the Journal of geochemical exploration describing how areas of nickel-rich rock around the world could be identified by analysing small pieces of plant material, obtained from the world’s herbaria, that had originally been collected from their respective areas of mineralisation. Robert realised that some plant species had unexpectedly high concentrations of nickel, and in a fit of imagination invented the term hyperaccumulator to describe this abnormally high accumulation of metal. Little did he know of the interest this discovery would make in the future. _Robert’s research during the 1990s saw development of a practical use of the hyperaccumulator plants he identified during his frequent expeditions around the globe — the concept of phytoextraction. This is a technique whereby certain plants are grown over a contaminated site or low-grade ore body, and used to clean up the site (phytoremediation) or to grow an economic crop of metal (phytomining or phyto-reclamation). Robert's research into gold accumulation in plants in particular captured global attention. Academic and industry groups around the world continue to closely follow the work he pioneered. Many regard his last book, Plants that hyperaccumulate heavy metals, as the benchmark to describe the subject area to new readers. His involvement with a mining company in South Africa during 1995 saw the first ever, working example of a phytoremediation phytomining operation through to fruition. One of the plants Robert identified as endemic to areas of copper mineralization was a heather from Spain, Erica andevalensis. It sparked his curiosity as to whether it too was a hyperaccumulator, and so we became involved in an investigation to check this out. 24 Erica andevalensis was first described by Cabezudo and Rivera in 1980. E. andevalensis is an edaphic-endemic of the Andévalo, a 3,500 sq. km area within Huelva Province, southwestern Spain, where it is an excellent geobotanical indicator of copper. The region has a history of metal mining going back to Roman times when it was a source of copper, silver and gold extracted from pyrite. As a result of these mining activities the local environment has been severely affected by both metal contamination and acidity. Some soils in the mining areas have a pH as low as 3 and have high concentrations of copper (Cu), zinc (Zn) and iron (Fe). Stream waters can be dark red from dissolved Fe at the low pHs present and it is in wet, humus-rich, highly metal-contaminated areas along the banks of these streams that E. andevalensis naturally occurs. Since E. andevalensis occurs only on older, weathered and highly toxic spoil heaps and highly contaminated soils it cannot be indigenous but rather has adapted to life on contaminated sites. Copper levels in some of these soils range from about 20-3,500 ppm. It will only colonise these heaps after pyrite oxidation has lowered the pH to a point where the toxic conditions exclude other species. Another heather, Calluna vulgaris, grows on contaminated soils around the abandoned Parys Mountain copper mine on Anglesey, North Wales, but, although Calluna, and other Erica species, grow in the Huelva area, none is found with E. andevalensis on the most toxic spots. Our interest in E. andevalensis was to determine if it were a true hyperaccumulator plant for copper. If it were it would join an elite group of copper hyperaccumulating plants previously only described from the Democratic Republic of Congo (Haumaniastrum katangense) and Hubei Province in China (Elsholtzia haichowensis). Our experimental results showed that E. andevalensis was in fact not a hyperaccumulator but, intriguingly, exhibited one of the highest tolerances to Cu of any known plant. Cu levels in plants from natural populations were <50¢g g"!, well below the 1,000g ¢" threshold for hyperaccumulation. In the experiments we carried out, even with the addition of EDTA to enhance the solubility and uptake of Cu, the concentration in the plant was <500g ¢". A further observation was that the correlation between total Cu in the soil and that in the plant was not as good as expected. The correlation was significantly improved by determining the plant-available Cu, which made the data from natural and artificial substrates consistent. This outcome showed that the organic matter present in the soil has bound the Cu tightly and rendered it unavailable for plant uptake, explaining in part why E. andevalensis is able to survive in the organic-rich, high total Cu soils of the Andévalo. 25 Figure 1. The valley of Rio Odiel is one of the principal natural habitats of Erica andevalensis; the dark shrubberies on both sides of the river on the valley floor are dense stands of the heather (photographed during the expedition by David McClintock, David Small and Charles Nelson in 1982; see Nelson et alii 1985) (E. C. Nelson). 26 Erica andevalensis is therefore an excluder plant; it tolerates high metal levels by excluding the metal from its tissues. Its Cu uptake follows the typical pattern of metal-excluder plants with restricted uptake until the threshold of tolerance is exceeded. At this point, there is rapid, exponential growth of uptake until the plant dies. Thus Erica andevalensis is an excellent indicator of copper mineralization, having adapted to a very specific and highly toxic environment, and is so specialised that it cannot survive in ordinary sites. Although not a hyper- ee) Bees oo a ae accumulator, E. andevalensis does Figure 2. Erica andevalensis shrubs in the Rio belong to the unique group of Odiel valley; note the dark red colour of the plants, “copper flowers”, that have water which is due to contamination with iron g special relationship to copper (E. C. Nelson). : ; ; mineralization. Sources ANSENSL, A., BENNETT, F., BROOKS, R. R., ROBINSON, B. & STEWART, R., 1999. Copper uptake studies on Erica andevalensis, a metal tolerant plant from southwestern Spain. Commun. Soil Sci. Plant Anal. 30: 1615-1624. BROOKS, R. R., LEE, J., REEVES, R. D. & JAFFRE, T., 1977. Detection of nickeliferous rocks by analysis of herbarium specimens of accumulator plants. Journal of geochemical exploration 7: 49-57. BROOKS, R. R. & MAILASSE, F., 1985. The heavy metal tolerant flora of southcentral Africa. Balkema, Rotterdam. BROOKS, R. R., 1977. Copper and cobalt uptake by Haumaniastrum species. PI. soil 48: 541-545. BROOKS, R. R., BAKER, A. J. M & MAILASSE, F., 1992. Copper flowers. Nat. geogr. res. explor. 8: 338-351. CABEZUDO, R. & RIVERA, J., 1980. Notas taxonomicas y corologicas sobre la flora de Andalucia Occidental: Erica andevalensis Cabezudo and Rivera sp. nov. Lagascalia 9: 223-226. NELSON, E. C., McCLINTOCK, D. C., & SMALL, D. J., 1985. The natural habitat of Erica andevalensis in south-western Spain. Kew magazine 2: 324-330. SE, S-T. & SJUJ, B-L., 1953. Elsholtzia haichowensis Sun - a plant that can reveal the presence of copper-bearing strata. Dichzi Sjuozheo 32: 360-368. Heathers 2: 27-30 (2005). © P. Steyn. Focus on sunbirds: the art of sunbird photography ge | PETER STEYN P. O. Box 54, NEWLANDS, 7725 South Africa. (peregrine@mweb.co.za) There are 21 species of sunbird in southern Africa and they occur in a wide variety of habitats. My favourite is the Orange-breasted Sunbird, Nectarinia violacea (front cover and p. 28), which I first photographed at Kirstenbosch as a schoolboy in 1952. I still have this nostalgic black-and-white picture of a female at her nest feeding chicks, but since then I have lost track of the number of times I have photographed this species which I consider — with my bias freely admitted — the most beautiful of all our sunbirds. The specific name of this exquisite sunbird refers to a small band of violet on the upper breast which is very difficult to portray in a photograph. Like hummingbirds, to which sunbirds are not in any way related, the colours are the result of the refraction of light on the iridescent feathers and are constantly changing —- in deep shade the glossy green on the head of an Orange-breasted Sunbird appears almost black. How then does the photographer capture the range of variable iridescent colours on a sunbird? The answer is to supplement sunlight by the use of flash, sometimes even using two flash-heads attached to a powerful pack that can give multiple exposures in quick succession. However, even a small flash attached to a camera will enhance any sunbird picture. As a rule the power output of the flash is balanced to the normal daylight exposure selected, a technique known as fill-in flash. The Orange-breasted Sunbird illustrated here (Figure 1, p. 28) used this method to capture not only the green on the head but also the elusive violet on the throat. All the sunbird pictures accompanying this article used flash to ensure that the iridescent plumage was correctly portrayed. Photographing sunbirds in flight requires a lot of preparation and powerful electronic flash equipment to freeze the extremely rapid wing beats. The Lesser Double-collared Sunbird, Nectarinia chalybea, depicted here (Figure 2, p.29) was taken after many months and numerous failures. In order to achieve a very high speed, the flash-heads needed to be placed close to the Erica which was arranged in such a way that the sunbird was unable to alight to probe the flowers. Figure 1. An Orange-breasted Sunbird feeding on Erica baueri with the elusive violet on its throat revealed by the use of fill-in flash. © P. Steyn. 29 Figure 2. A Lesser Double-collared Sunbird hovers beneath Erica versicolor flowers are in such a way that it could not alight to feed. © P. Steyn. Early attempts failed as there was too much ambient light with the result that the wings were blurred because the daylight was also recording an exposure, an effect known as ghosting. The problem was eventually solved by photographing in very dull light once the sun was below the horizon so that only the high-speed flash was effective. Another useful tip for photographers is to use a telephoto lens, and a focal length of 400 mm is ideal. The reason for this choice is that from a normal working distance of about two metres any distracting background is thrown out of focus and the bird itself is etched in sharp contrast. Finally, how does one ensure that the sunbird will perch where one wants it to? The solution is to condition the birds to visit an Erica or similar plant with long tubular flowers that have been filled with glucose water (Figure 3). A hypodermic syringe with a blunted needle (so as not to pierce the flowers) is used to inject the solution and the viscosity of the fluid ensures that it remains in place. My fellow photographer Nico Myburgh is an expert on attracting sunbirds and some have become virtual glucose addicts. In one remarkable instance an Orange-breasted Sunbird was so enthusiastic that it alighted on Nico’s finger and tried to drink from the syringe before he could inject the flower! 30 Figure 3. This Lesser Double-collared Sunbird returned repeatedly to this cluster of Erica regia because the flowers were filled with a glucose solution. © P. Steyn. Although sunbirds are usually tame it is not always easy to photograph them to best advantage and it is hoped that these few guidelines, based on many years of experience, will enable potential sunbird photographers to depict these colourful pollinating jewels in a new light. Originally published in Veld & Flora 90 (2) June 2004), and reprinted here by kind permission of the Editor, Caroline Voget, Botanical Society of South Africa. Two photographs, showing sunbirds feeding on Chasmanthe and Aloe species, have been omitted. The scans were supplied by Rothko International, Cape Town. Heathers 2: 31-34 (2005). ©R. Arruda Humming and feeding on the Pacific Rim RON ARRUDA Curator of South African Collections, The Arboretum, University of California at Santa Cruz, SANTA CRUZ, California, USA. The Arboretum at UC Santa Cruz is pretty famous for birds of all kinds — it’s on the Pacific Coast Flyway. But hummingbirds are the ones that attract the most attention, both from serious birders and the general public, especially children. In fact, we have an annual Hummingbird Day here during their mating season in March, with hundreds of youngsters overrunning the place, learning about this rambunctious corner of the natural world. And for hummer photography, educational walks, or for just plain visual enjoyment, there’s no place in our garden like the South African Erica (Cape heaths) beds. For humans, the big draw is the many plants in wide-open arrangement and the head-high flowers that make for easy bird viewing. For the birds, it’s the © abundance of high-quality nectar year round. Hummingbird metabolism is about the highest in the animal kingdom, and they use an extravagant amount of energy to keep themselves going. Their body temperature hovers around 40°C (104°F), with heart rates close to 1,000 beats a minute! Though they spend quite a bit of time perching, they have to feed often. Hummers are the only birds that have (or need) a “dormancy” phase, mainly on cold nights, when their body temperature can fall as low as 21°C (70°F). This torpor, known as “noctivation” slows their metabolic rate to a crawl and makes it possible for them to survive the night without feeding, otherwise they would literally starve to death on the roost! Besides a wealth of sugar to burn, the other reason these birds like our heather garden is the way we water it, with overhead oscillating sprinklers: it’s the only bed that gets watered this way. No rain falls between May and October here, and we give the Cape heaths plenty to drink to keep them blooming around the year, and the birds are very appreciative. They dart in and out of the spray and bathe in the wet vegetation — a real treat in our long, dusty summers. Summer can also bring erratic spells of morning fog rolling in off the bay, and we don’t irrigate then, as these conditions provide quite a lot of moisture for the plants and the wild life. Figures 1 and 2 (opposite). Anna’s Hummingbird feeding on Erica discolor. The flowers are about 2.5-3cm (1-1'/ ins) long whereas the bird is around 8.5cm (3¥ins) long. S)e) Fm Here, smack in the middle of the central coast of California, we only see , a few of the fifty or so North American species of hummingbird, and only two are common — Anna’s and Allen’s — but these are present in great numbers where food and nest sites afford. Hummers are all very small: Anna’s weighs about 4 grams, a tiny bit more than a British 1p piece, and a whole gram less than our American 5¢ coin. They’re mostly hollow bones and feathers, and their breast muscles make up 30% of their body weight. Anna’s is by far the more abundant species, and it hardly migrates at all in this mild climate, where only light frosts are common in the winter. This bird has a vivid rose-red forehead and “gorget” (the feathers on the throat and upper chest). Allen’s is a bit smaller in the body (just over 3 grams), with rusty under-parts rearward, and a scarlet to orange-red gorget. The brilliant colors around the head for which hummingbirds are justly famous are “physical” colors, like the spectrum you get when a prism breaks up a beam of sunlight, rather than pigment colors, like say in a robin red-breast: “jewel-like colors” may be a cliché, but absolutely describes them! It’s staggering to remember that Aztec chiefs had magnificent cloaks made from thousands of hummingbird pelts: the effect must have been jaw-dropping! Of native California plants, these little birds feed particularly on species of Penstemon and Salvia (sages), and the floral shape of many of the South African Erica species we grow is very similar. Much favored by the hummers are Erica baueri, E. mammosa, E. hebecalyx, E. brachialis, E. cerinthoides, E. cruenta, E. abietina, E. curviflora, and E. discolor, all with good-size straight or curving 34 Figure 3. The cape heath garden at The Arboretum, University of California at Santa Cruz, August 2004. (Allen Hall). tubes and abundant nectar. Hummers also eat a fair quantity of small insects and spiders, especially during nesting season, and some of these come up with the nectar as they feed. Our garden’s Australian collection, with its eucalypts and Grevillea, is also a concentrated hummingbird area with generous winter bloom — another instance of trans-hemisphere cooperation! These plants are also nest sites for the birds, whereas the Erica shrubs are usually not. Hummingbirds are only found in the Americas — the New World, so- called — and Erica only in the Old World. This doesn’t stop the pair from getting along famously in California, where Erica pollination is very successful: witness our tiny forest of seedlings that spring up unbidden on every hand, especially near Erica baueri! Due to human occupance, and the unbridled way we garden in coastal California’s benign climate, this place is a hybrid ecosystem, a riot of color and ad-hoc adaptation. It offers ever-new niche opportunities, and undreamed of combinations of plants and animals in an exuberant and complicated dance of happy, peppy, mutual exploitation. Heathers 2: 35-44 (2005). ©E.C. Nelson & J. V. Aubrey. Fred Esgate (1911-2003): the last breeder of Cape heaths in Britain E. CHARLES NELSON! & JOHN V. AUBREY? ' Tippitiwitchet Cottage, Hall Road, Outwell, WISBECH, PE14 8PE Figure 1. Fred Esgate (centre, with hat) with Dr Violet Gray (left) and Mr E. R. Turner (Treasurer of The Heather Society), in Dr Violet Gray’s garden, Southcote, Hindhead, Surrey, 7 April 1973, on the occasion of the Cape Heath Party (J. V. Aubrey). Frederick Esgate, a true Cockney, was born on 24 November 1911 within the “sound of Bow bells” in southwest London. He died on 30 July 2003. Without doubt Fred Esgate was the last specialist breeder of Cape heaths, on a commercial scale, working in Great Britain. He did not start life as a horticulturist. When he was 15 years old, early in 1926 Fred found employment with a Tunbridge Wells hosier and glover, Sidney H. Bailey, “Indian & Colonial Outfits a speciality”, and remained there for 13 months. “During his employment”, wrote Bailey, “I have always found him to be strictly honest, painstaking, and a very willing Boy ... a 36 hard worker, he is sharp & quick at picking up any work entrusted to him.” “Thoroughly” recommending Fred to any future employer, Bailey continued: “He leaves at his own wish as I understand he is anxious to learn a trade.”! It is evident that Fred soon moved into horticulture; there is a gap of about a year and a half in our knowledge of his career, and it is possible that during those months he obtained horticultural experience, if not training. By March 1931 he had been working for two and a half years as assistant propagator in R. Wallace & Co., Tunbridge Wells, under J. Marchand. The firm specialized in hardy trees and shrubs, including many members of the Ericaceae, especially rhododendrons. When Fred left Wallace’s employ, Marchand wrote as complimentary a reference as Sidney Bailey had composed four years earlier, noting that Esgate was “good at grafting Rhododendrons, Clematis, Camellias, Conifers, etc. etc. ... he is a hard and painstaking worker ...”.* Esgate’s next employer was Geo. I. Adams Ltd, “Florists, nurserymen and seedsmen, garden artists”, also of Tunbridge Wells. One of their catalogues, which Fred Esgate kept, includes a long list of hardy heather cultivars. He remained there for four years, and again, on leaving of his own accord, was characterised as “very active, intelligent, painstaking, and trustworthy ...”.> He moved to work for C. Willett, anurseryman specializing in fruit and tomatoes, at Hayes in Middlesex. Fred received 50 shillings (£2. 10s. 0d) a week, and Willett offered him lodgings, “with good food and room to yourself” for 20 shillings (£1) a week.‘ In February 1938, Fred moved to work for Ryder & Son, “Seed specialists and makers of beautiful gardens”, St Albans, Hertfordshire, but only remained there for about three months, leaving in late April 1938 to join Milton Hutchings Ltd. Dear Sir, Confirming conversation over the telephone last evening in which you and your friend accepted employment here, the rate being for yourself £2. 10. 0, and your friend £2. 5. 0, for a week of 53% hours, the hours being 6.30 a.m. to 5.30 p.m. with the usual meal times, over time required when necessary during the Summer. Please let me know the date you will be able to commence work. Yours faithfully for MILTON HUTCHINGS, LIMITED Milton H. Hutchings? It is not known what Fred Esgate worked at during 1938, but in 1939 he was in charge of “20,000 Chrysanthemums grown in ten inch pots”, and after the Second World War commenced he was given charge of several 37 acres planted with tomatoes and lettuces. There seems to have been some bother between the nursery foreman, Mr J. Whipp, and Esgate; Fred resented receiving “directions” from the foreman. He was formally reminded (by a letter dated 3 January 1940°) that it was “quite impossible to make any distinction between Tomatoes and other crops on the Nursery, and make your Department independent of ... supervision from Mr. Whipp.” A reference dated 5 April 1941’ suggests that Esgate had decided to leave Milton Hutchings Ltd, but in fact he enlisted in the Home Guard, and continued working in the nursery throughout the Second World War. After the end of the war, Fred Esgate was given more responsibility within Milton Hutchings’ nursery, as the firm set about establishing its reputation as one of the major producers of ornamental pot-grown plants, especially chrysanthemums, including Cape heaths and azaleas. “New hybrid azaleas”, tolerant of low light levels and air-conditioning, were first propagated at Milton Hutchings in 1970, under Fred Esgate’s “careful eye” (Mannington 1981): by March 1980 the stock of these shrubs numbered 875,000 plants, ranging from rooted cuttings to saleable 3-year old plants. As for Cape heaths, by the early 1980s, Milton Hutchings grew more winter-flowering Capes . than any other British nursery (Brandham & McClintock 1985). In the same decade “Hillingdon Heaths” were being exported to Holland and Denmark. “In the early fifties ... Fred Esgate embarked upon a sixteen year hybridisation programme of Cape Ericas. He was able to raise in excess of forty new varieties, many of which have won him accolades [sic] from the Royal Horticultural Society” (Worsfold 1981). Some of the resulting seedlings were selected and named, and during the late 1960s these were shown at the RHS, and a few gained awards of merit (see Appendix). For his hybrids, Esgate used, among other plants, a nineteenth-century hybrid named E. xhiemalis (often spelled “hyemalis”; a name of very dubious application), which typically has pink-purple, tubular flowers with white tips — a colour picture published in Amateur gardening on 26 November 1983 (see page 43) shows a range of these plants including one with apricot- coloured bells (Sheppard 1983). E. gracilis was also one of the Cape heaths Esgate worked on. He had access to some of the new introductions including E. pageana, from which came the cultivar ‘Limelight’, and E. oatesii, one of the parents of ‘Gaiety’. But apart from these, no detailed records of his crossings has been traced, and we are left to guess at his techniques. It is interesting that among Fred’s possessions were Practical plant breeding (Lawrence 1937) and two booklets entitled Protected wild flowers of the Cape Province (Anonymous 1953, 1956), which included colour illustrations of some Cape heaths. Seated (from right): Fred Esgate; Mabel Turner; Constance McLeod; Gary Fitzgerald (Milton Hutchings Ltd); Dr Violet Gray; unknown (Dr Gray’s companion). Standing (from right): Ron Cleevely; John Aubrey (Milton Hutchings Ltd); Anne Small; David Small; Roy Turner; Ros Cleevely; Phil Joyner. (Reproduced by courtesy of Ron Cleevely.) The only other evidence we have about how Fred conducted the Milton Hutchings’ breeding programme comes from a brief article by Brandham and McClintock (1985). They stated that “It was learnt in late 1978 that Mr. F. Esgate, who has for long been in charge of their [Milton Hutchings Ltd] hybridising, has been using colchicine in an attempt to get better plants.” Colchicine, an organic compound extracted originally from the autumn crocus (Colchicum spp), can disrupt cell division in newly fertilized ovules, leading sometimes to a doubling of chromosome numbers, and the production of tetraploid plants (with twice the normal number of chromosomes). Esgate treated two cultivars, ‘Majestic’ and ‘Pink Gem’, and obtained seedlings with larger flowers (these were referred to as “ “Grandiflora” forms ...”*) which were sent to the Jodrell Laboratory, Royal 39 Botanic Gardens, Kew, for investigation of their chromosome complements. Whatever these new, larger-flowered plants were they were shown not to be tetraploids (Brandham & McClintock, 1985). Fred Esgate was appointed Joint Managing Director of Milton Hutchings Ltd, with responsibility for the nursery, on 31 May 1976; he resigned from this post on 17 August 1979 but remained in charge of the nursery and continued working for Milton Hutchings Ltd into the early 1980s. For his services to Milton _ Hutchings Ltd, Fred was awarded the Royal Horticultural Society’s : : Long Service Medal. He moved to Figure 3. Fred Esgate (1911-2003) Iver Flowerland Production Nursery, (By courtesy of Derek Jordan) Iver, Buckinghamshire, where he worked into the 1990s. Fred Esgate was never a member of The Heather Society, but he was present on the occasion when the Society’s short-lived Cape Heath Group visited Dr Violet Gray’s garden on 7 April 1973 (McLeod 1973). Notes 'S. H. Bailey ms, 26 March 1927 (all the documents quoted here, unless otherwise stated, have been made available by Mr Derek Jordan, nephew of Fred Esgate). 2J. Marchand, 13 March 1931. > Geo. I. Adams, Ltd., typewritten letter, 8 March 1935; F. Taylor, ms., 8 March 1935. *C, Willett to F. Esgate, 1 April 1935. > M. H. Hutchings to F. Esgate, 14 April 1938. ° [Milton Hutchings Ltd] to F. Esgate, 3 January 1940: incomplete typewritten letter. ’ C. E. Lunn “For and on behalf of Milton Hutchings, Ltd.”, 5 April 1941: Lunn was one of the company’s directors. § Brandham and McClintock (1985) did not intend that “Grandiflora” should be used as a name, or part of aname. Unfortunately, they employed the ambiguous phrase “... “Grandiflora” forms ...”: “The larger flowers of the “Grandiflora” forms are presumably the result of selection of gene mutations ...”. As the plants raised following colchicine treatment must have been seedlings, each one should have been given a unique cultivar epithet, unless they were individually indistinguishable; tagging the word “grandiflora”, or the phrase “grandiflora form”, on to the names of the parent clones contravenes the International code of nomenclature of cultivated plants. 40 Acknowledgements We are most grateful to Mrs Pamela Lee, Mr Ron Cleevely and to Mr Ernie Jordan and Mr Derek Jordan for their assistance with this article. Derek Jordan was especially helpful, making available copies of documents about his uncle’s career. References ANONYMOUS, 1953, 1956. Protected plants of the Cape Province. Cape of Good Hope: Department of Nature Conservation. BRANDHAM, F. & McCLINTOCK, D., 1985. The chromosome number of four hybrid heaths. Yearbook of The Heather Society 3 (3): 55. LAWRENCE, W. J. C., 1938. Practical plant breeding. London: George Allen & Unwin. McLEOD, C. I., 1973. The Cape Heath Party, April 7th, 1973. Bulletin of The Heather Society [1] (19): 5-6. MANNINGTON, L., 1981. Christmas azaleas - looking for something different. Floral trades journal: 36. SHEPPARD, E. A., 1983. A bunch of Capes. Amateur gardening (26 November): 36-37. WORSFOLD, M., 1981. Specialist Erica producer looks to the future. Floral trades journal: 33, 36. Appendix: Cultivars of Cape heaths associated with Fred Esgate and Milton Hutchings Ltd, extracted from International register of heather names. ‘Bow Bells’ Listed 1969 to 1978. ““Bow Bells’, as I recall, was the nearest Fred came to naming one of his hybrids after himself, as he was born in S. W. Hackney” (J. Aubrey to ECN, 11 March 2004), thus he was raised within the sound of Bow bells, and therefore a true Cockney; the peal of bells of St Mary-le-Bow, Cheapside, London, have long been famous, to direct travellers on the road to London town. ref.: no printed source traced; [D. McClintock record card]. ‘Daybreak’ Introduced (as ‘Dawn’) by 1967; exhibited (as ‘Dawn’) at the RHS on 31 October 1967. ref.: Proceedings of the Royal Horticultural Society 93: 25 (1968); — 94: 85 (1969). ‘Dawn’ — see ‘Daybreak’ Figure 4. ‘Daybreak’ in production in Milton Hutchings early in 1972. 41 ‘Delight’ Exhibited at the RHS on 14 March 1967: Cultural Certificate. ref.: Proceedings of the Royal Horticultural Society 92: 23 (1967) [name only]; Bulletin of The Heather Society 2 (11): 4 (1977); [Yearbook of The Heather Society 2 (6): 11 [erroneously called ‘Gaiety’ ] (1977)]; Amateur gardening 94 (23-30 December): 60 (1978). ‘Dusky Maid’ Flowers lcm long, mauve base with yellow lobes, December to February. 60cm high. Artificial hybrid, between two unnamed seedlings; raised by Fred Esgate and introduced by 1967; shown at RHS on 31 October 1967: Award of Merit. ref.: Proceedings of the Royal Horticultural Society 93: 21 (1968) [name only]; Yearbook of The Heather Society 2 (2): 14 (1973); — 2 (11): 17, 18 (1982); — 3 (1): 15, 16 (1983); Catalogue, Denbeigh Heather Nurseries, Creeting St Mary, 23 (not dated [1976]); Bulletin of The Heather Society 2 (16): 5 (Spring 1979). ws . Ai nm A ty ee Oe Figure 5. ‘Gaiety’ in production at Milton Hutchings early in 1973. ‘Gaiety’ Flowers “large deep pink, bell-like”; “even larger pinkish bells than” E. oatesii; “deep rosy version of E. oatesii”. Selected from E. oatesii crossed with an unnamed seedling; raised by Fred Esgate and introduced by 1967; shown at the RHS on 14 March 1967: Award of Merit. ref.: Journal of the Royal Horticultural Society 92: 236 (1967); Proceedings of the Royal Horticultural Society 92: 24 (1967); Bulletin of The Heather Society 1 (19): 5 (1973); — 2 (11): 4* (1977); [Yearbook of The Heather Society 2 (6): 11 [erroneous] (1977)]. 42 Figure’ 5) = GuERe being srown at Denbeigh, CEE St = Teewicht January 2005. ‘Ghislaine’ Flowers tubular to clavate, 3 x 9 mm, “deep H14 with white lobes”. Possibly raised at Milton Hutchings Ltd, Uxbridge, Middlesex, before 1980. Rescued from a nursery in Iver Heath, Berkshire, in 1994; introduced by Denbeigh Heathers in late 1997. ref.: Yearbook of The Heather Society 1998: 70 [as E. xhyemalis]. ‘Limelight’ Flowers pale sulphur yellow, 2.5cm long, pitcher-shaped’; tightly packed in long inflorescences; (October)—December—February; to 0.5m tall. Introduced by 1967; shown at the RHS on 20 November 1967 and 20-21 February 1973 (Heather Competition, Class 5, Ist). ref.: Proceedings of the Royal Horticultural Society 93: 22 (1968) [name only]; Yearbook of The Heather Society 2 (1): 37* (1972); — 3 (6): 48-49 (1988); Bulletin of The Heather Society 1 (19): 5, 6 (Summer 1973);— 1 (20): 1-2 (Autumn 1973);— 2 (16): 5 (Spring 1979); Catalogue, Denbeigh Heather Nurseries, Creeting St Mary, 23 (not dated [1976)]). ‘Majestic’ Large tubular deep magenta flowers, white portion of the corolla is confined to the lobes. “E. hyemalis hybrid”; raised by Fred Esgate and introduced by 1967; shown at RHS on 31 October 1967: Award of Merit. ref.: Proceedings of the Royal Horticultural Society 93: 21 (1968) [name only]; Yearbook of The Heather Society 2 (2): 14 (1973); — 3 (3): 55 (1985) [chromosome counts]; Bulletin of The Heather Society 2 (16): 5 (Spring 1979). 43 Figure 6. 'Limelight'’ grown at Denbeigh, Creeting St Mary, Ipswich, c. 1976. ‘Pink Gem’ Introduced by 1967 (as ‘Pink Pearl’); shown (as ‘Pink Pearl’) at the RHS on 31 October 1967. ref.: Proceedings of the Royal Horticultural Society 93: 21 (1968); — 94: 85 (1969) [name only]; Yearbook of The Heather Society 3 (3): 55 (1985) [chromosome counts]; [www.collinaexport.com accessed 12 October 2003]. (Erica stock list, Ericaflora, Monbulk (Victoria, Australia), not dated [c.2000] [name only]; Catalogue, Larkman Nurseries, (Lilydale, Victoria, Australia), 32* (July 2002) both ‘Pink Pearl’) ‘Pink Pearl’ — see ‘Pink Gem’ ‘Pink Splendour’ Exhibited at the RHS on 31 October 1967; withdrawn by 1978. ref.: Proceedings of the Royal Horticultural Society 93: 21 (1967) [name only]. ‘Pink Superb’ At Milton Hutchings Ltd by 1969, but withdrawn or discarded by 1978. ref.: no printed source traced; [D. McClintock record card]. ‘Pink Supreme’ Exhibited at the RHS on 21 November 1967. ref.: Proceedings of the Royal Horticultural Society 93: 22 (1967) [name only]. ‘Redbreast’ Raised and selected by Fred Esgate and introduced by 1968; shown at the Royal Horticultural Society on 20 February 1968. ref.: Proceedings of the Royal Horticultural Society 93: 23 (1968) [name only]. 44 ‘Rosea’ — see ‘Rosita’ ‘Rosita’ Introduced by 1967; shown (as ‘Rosea’) at the RHS on 31 October 1967. ref.: Proceedings of the Royal Horticultural Society 93: 21 (1968); — 94: 85 (1969) [name only]. ‘Salmon Supreme’ Raised before 1969; withdrawn by 1978. ref.: no printed source traced; [D. McClintock record card]. ‘Silver Pink’ Said to be a selection from the hybrid Erica “willmorei” x “hyemalis”; exhibited at the RHS on 14 March 1967: Cultural Certificate. ref.: Proceedings of the Royal Horticultural Society 92: 23 (1967) [name only]. ‘Snowfall’ Foliage mid-green (RHS 143B); flowers short (5-8mm long, 0.25mm wide), tubular, white (RHS 155D). 60cm high. Selected from a cross between E. gracilis var. nivalis and an unnamed seedling; raised in 1955 by Fred Esgate and introduced in 1965; shown at the RHS on 20 February 1968 — Award of Merit — and 21 November 1968; and on 17-18 February 1976 (Heather Competition, Class 13, 3rd). ref.: Proceedings of the Royal Horticultural Society 93: 22 (1968); Journal of the Royal Horticultural Society 94: 318 (1969); Catalogue, Denbeigh Heather Nurseries, Creeting St Mary, 23 (not dated [1976]); Bulletin of The Heather Society 2 (8): 3 (Summer 1976); — 2 (16): 5 (Spring 1979); Amateur gardening 94 (23-30 December): 60 (1978); W. Martensson (editor), The homemaker’s library — houseplants, 68 (1979); Yearbook of The Heather Society 3 (1): 16 (1983). ‘Sunburst’ Exhibited at the RHS on 21 November 1967. ref.: Proceedings of the Royal Horticultural Society 93: 22 (1968) [name only]. ‘White Spray’ Selected from a cross between E. pageana and an unnamed seedling; raised by Fred Esgate and introduced by 1967; shown at the RHS on 14 March 1967: Preliminary Commendation. ref.: Journal of the Royal Horticultural Society 92: 236 (1967); Proceedings of the Royal Horticultural Society 92: 24 (1967); Bulletin of The Heather Society 1(19): 5. Heathers 2: 45-48 (2005). © J. V. Aubrey. Milton Hutchings Ltd: a brief history JOHN V. AUBREY Redlands, Ellis Avenue, Chalfont Heights, GERRARDS CROSS, Buckinghamshire, SL9 9UA. Milton Henry Hutchings was born on 2 December 1872 (The advertiser and gazette, 1 December 1939), and was the fourth son of James Hutchings of Cowley, Middlesex. He established his nursery at Kingston Lane, Hillingdon, in 1894 and within ten years had transferred it to Pield Heath Road where it became known as Pield Heath Nurseries. This site subsequently occupied 20 acres to the east of the River Pinn and 10 acres to the west. To the north and adjacent to this area was the already established nursery of Lowe and Shawyer which by the mid-1930s had become Britain’s, if not Europe’s, biggest range of greenhouses. Mr Milton Hutchings always strived to produce high-quality produce and was awarded several medals by the National Chrysanthemum Society Figure 1. Cape heaths in 9cm pots at Milton Hutchings; the blocks were positioned to take Dutch lights; autumn 1972 (J. V. Aubrey). J -Q (40) — oO > (40) aa de 6D oe ‘S MY je) = (e) iS WN + oO > 5 5} U 2 3 8 NM love) ita] oD e oe ne} > U S = nn to fe)