Volume 15
Issue 1
Horticulture
JOURNAL OF
POLISH
AGRICULTURAL
UNIVERSITIES
Available Online: http://www.ejpau.media.pl/volume15/issue1/art-04.html
CHARACTERISTICS OF FLOWERS OF SELECTED IRIS SPECIES AND VARIETIES FROM LIMNIRIS SECTION
Magdalena Kulig
Department of Dendrology and Landscape Architecture, University of Agriculture in Krakow
Studies were carried out on seven taxa from beardless (Limniris) section: grassy leaved iris (Iris graminea L.), yellow iris (I. pseudacorus) and Siberian iris (I. sibirica L.), as well as hybrids from Sibiriceae section: I. 'Dreaming Yellow', I. 'Towanda Redflare', I. 'Violet Meer' and I. 'Wiltrud Gissel'. The following parameters were assessed: flower size, the length and width of stamens, the length of pistil, the color of: flower petals, pistil, stamen and pollen. It is considered that tetraploids have twice bigger flowers. The investigations confirmed this opinion. Iris 'Dreaming Yellow', which is tetraploid, has twice bigger individual elements of perianth than diploid taxons. Determining the sizes of individual elements of parental plants' perianth allowed to formulate a standard. It will serve for comparing morphological features of hybrids obtained in future. The identification of colour by means of Royal Horticultural Society Colour Chart occured not enough precise.
Key words: beardless iris, flower size, petals, pistil, color.
INTRODUCTION
Irises are perennials known since the antiquity. At that time they were cultivated mainly for their medicinal and aromatic properties [1, 5]. Initially they were collected on natural sites but with time people started to cultivate them in gardens. Only in modern times, especially in the Renaissance, not only the beauty of iris flowers was appreciated but the diversity of their colors roused general admiration. Iris flowers occur in all colors of rainbow, therefore the Latin name Iris given to the genus in honor of Greek goddess of the rainbow [3, 7, 9, 13]. In modern times not only species were known and identified [7], but also the first varieties of irises [5]. First collections were established in gardens. With time people started to seek the plants with larger flowers and more abundant inflorescences, but also characterized by various shapes of perianth sepals or untypical leafy pistils.
However, the literature lacks detailed data on the sizes or colors of individual flower elements in various species and varieties. Therefore, research was undertaken to investigate this problem. In result of initial investigations, seven taxa were selected for further breeding works within a single Iris genus, from beardless (Limniris) section: grassy leaved iris (Iris graminea L.), yellow iris (I. pseudacorus) and Siberian iris (I. sibirica L.), as well as hybrids from Sibiriceae section: I. ‘Dreaming Yellow’, I. ’Towanda Redflare’, I. ’Violet Meer’ and I. ‘Wiltrud Gissel’. Determining the sizes of individual elements of parental plants’ perianth allowed to formulate a standard. It will serve for comparing morphological features of hybrids obtained in future.
MATERIAL AND METHODS
In August 2005 a collection of beardless irises was started in Bibice. The plants were planted in the native soil, which was a light loam with pH approximate to neutral. The beds were mulched with bark, which was supplemented each year, whereas weeds were removed mechanically. In March 2006 the plants were fertilized with 5–6-month old Osmocote Exact Standard (16 N + 9 P + 12 K + 2.5 MgO + microlements) dosed 20 g per a plant in the ground. In order to protect irises against pests, Diazol preparation was administered for pest control and additionally the plants were sprayed by Confidor preparation at 10-day intervals (from the moment when flower buds first appeared until all flowers faded). Flower characteristics were conducted on three-year-old iris clumps growing in the collection in Bibice.
Three native iris species: grassy-leaved iris (Iris graminea L.) (Fig. 1), yellow iris (I. pseudacorus L.) (Fig. 2) and Siberian iris (I. sibirica L.) (Fig. 3), together with hybrids from Sibiriceae section: I. ‘Dreaming Yellow’ (Fig. 4), I. ’Violet Meer’ (Fig. 5), I. ’Towanda Redflare’ (Fig. 6) and I. ‘Wiltrud Gissel’ (Fig. 7) were selected for the flower assessment. Each taxon was represented by three clumps. The plants chosen for the analyses were diploids, except for the tetraploid ‘Dreaming Yellow’ species [2, 8]. One of numerous features which must be identified in order to recognize the partners for breeding works is the measurement of individual elements of a flower [6] and determining the flower color. 15 flowers from each clump of a given taxon were gathered to assess the features of reproductive organs. The following parameters were assessed:
- flower size, expressed as the length and width, which in a flower displaying radial symmetry equaled its diameter; the length and width of the inner and outer perianth segments and inflorescence pedicels;
- the length and width of stamens (filaments and anther),
- the length of pistil (from beginning of stigma to the point of leafy style connation, the length of connate style and the length and width of ovary),
- the color of flower petals, pistil (style and ovary), stamen (filament and anthers), pollen.
The tables contains the range of scale, arithmetic mean and the variation coefficient (V%) of every investigated parameter.
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Fig. 1. Three-year-old clumps of grassy leafed iris (I. graminea) in Bibice in 2008 (photo by M. Kulig) |
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Fig. 2. Three-year-old-clumps of yellow iris (I. pseudacorus) in Bibice in 2008 (photo by M. Kulig) |
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Fig. 3. A plot of three-year-old clumps of Siberian iris (I. sibirica) in Bibice in 2008 (photo by M. Kulig) |
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Fig. 4. Iris 'Dreaming Yellow' in Bibice in 2009 (photo by A. Michalik) |
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Fig. 5. Iris 'Violet Meer' in Bibicach in 2009 (photo by A. Michalik) |
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Fig. 6. Iris 'Towanda Redflare' in
Bibicach in 2009 (photo by A. Michalik) |
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Fig. 7. Iris 'Wiltrud Gissel' in Bibicach in 2009 (photo by A. Michalik) |
During the investigation the date of begining and the end of flowering period of each taxon was noted.
Linear measurements were made using Handy Worth caliper with electronic scale and total accuracy of 0.01 mm. The color was identified by means of Royal Horticultural Society Colour Chart [14].
RESULTS
Generative phase and characteristics of irises’ flowering. The irises selected for the analyses differed with their flowering dates. Grassy leaved iris flowered first, in mid-May, followed by yellow iris and then Siberian iris, and hybrids: I. ’Towanda Redflare’, I. ’Violet Meer’ and I. ‘Wiltrud Gissel’, whereas I. ‘Dreaming Yellow’ flowered as the last one, but proved the longest flowering one and single flowers appeared even at the beginning of July. The durability of a single iris flower was between 2 and 5 days, depending on the species and variety. Afterwards the flowers withered and fell together with stamens and leaf-like pistil. Differences in the structure of reproductive organs were observed between the analyzed taxa during the flowering period. Selected morphological traits of the investigated irises were presented in Tables 1–6.
Considering the studied taxa, average length of a single flower pedicle fluctuated from 2.1 cm in I. graminea to 7.3 cm in I. ’Dreaming Yellow’. However, the greatest variability was observed in I. pseudacorus (21.4%) (Tab. 1–3).
The largest flowers with a width of about 12.3 cm had I. ’Dreaming Yellow’. Yellow iris had the smallest flowers (with a diameter of 6.3 cm), but was distinguished by a bigger variability of size (8.1%), as compared with the other species. The diameter of I. sibirica flowers was also variable (9.1%). On the other hand, flowers of I. ‘Violet Meer’, I.’'Wiltrud Gissel’ and I. ‘Dreaming Yellow’ were equalized, with variability of respectively 1.2%, 2.3% and 2.9% (Tab. 3).
The longest flowers between the sudied taxa, had I. ‘Violet Meer’ and I. ‘Wiltrud Gissel’ on average lenght of 7.7 cm. On the other hand the I. ‘Wiltrud Gissel’ had the biggest variability of size equal 13.7%. Iris graminea had the shortest flowers (with mean 3.5 cm) but was also distinguished by smaller variability of size (4.3%). Iris sibirica had the less variable lenght of flower equal 3.0% (Tab. 3).
I. ‘Dreaming Yellow’ had the longest and the widest inner perianth leaves, on average 6.1 cm long and 3.6 cm wide. I. pseudacorus had the narrowest – 0.6 cm and the shortest inner perianth leaves – 2.7 cm. On the other hand, I. graminea revealed the greatest variability of perianth leaves’ width (V% = 20.2) (Tab. 1–3).
Iris ’Dreaming Yellow’ had the longest and the widest outer perianth leaves, on average 7.5 cm long and 5.3 cm wide. Iris graminea had the narrowest – 1.6 cm and the shortest outer perianth leaves – 3.8 cm. The greatest diversification of of outer perianths leaves’ width was characteristic for I. ‘Towanda Redflare’ (36%) (Tab. 1–3).
Table 1. The sizes and shapes of inner and outer perianth leaves of studied iris species (photo M. Kulig) |
Perianth |
Variety or species |
||
I. graminea |
I. pseudacorus |
I. sibirica |
|
Inner |
|||
Outer |
Table 2. The sizes and shapes of inner and outer perianth leaves of studied iris species (photo M. Kulig) |
I. 'Dreaming Yellow' |
I. 'Towanda Redflare' |
I. 'Violet Meer' |
I. 'Wiltrud Gissel' |
|
Inner |
||||
Outer |
Table 3. Morphological characteristics of flowers and perianth elements of the analyzed iris species and varieties |
Perianth leaves |
|||||||||||||||||||||
outer |
|||||||||||||||||||||
range |
mean |
V% |
range |
mean |
V% |
range |
mean |
V% |
range |
mean |
V% |
range |
mean |
V% |
range |
mean |
V% |
range |
mean |
V% |
|
I. graminea |
2.1–3.1 |
2.8 |
13.9 |
6.5–7.3 |
6.8 |
5.7 |
3.3–3.6 |
3.5 |
4.3 |
3.0–3.4 |
32.0 |
4.6 |
0.8–1.6 |
1.0 |
20.2 |
3.5–4.3 |
3.8 |
6.3 |
1.5–1.8 |
16,0 |
7.0 |
I. pseudacorus |
2.2–4.3 |
3.1 |
214,0 |
5.4–7.0 |
6.3 |
8.1 |
5.4–6.5 |
6.1 |
6.6 |
2.3–3.6 |
2.7 |
10.6 |
0.4–0.8 |
0.6 |
17.6 |
5.9–6.6 |
6.3 |
2.8 |
3.7–4.6 |
4.0 |
5.5 |
I. sibirica |
4.9–5.4 |
5.1 |
4.3 |
6.5–7.5 |
7.1 |
9,1 |
5.6–5.9 |
5.7 |
3.0 |
4.7–5.3 |
5.0 |
4.1 |
1.9–2.3 |
2.2 |
6.0 |
5.0–6.1 |
5.4 |
6.1 |
3.3–4.7 |
3.7 |
12.1 |
I. 'Dreaming Yellow' |
6.9–7.3 |
7.1 |
4.3 |
12.1–12.6 |
12.3 |
2.9 |
6.1–6.5 |
6.3 |
5.2 |
6.0–6.5 |
6.1 |
3.0 |
3.4–3.8 |
3.6 |
3.7 |
7.3–7.6 |
7.5 |
1.8 |
5.1–5.4 |
5.3 |
2.0 |
I. 'Violet Meer' |
5.2–5.5 |
5.3 |
4.0 |
8.9–9.1 |
9.0 |
1.2 |
6.9–8.4 |
7.7 |
4.1 |
5.1–5.9 |
5.5 |
6.3 |
2.4–2.6 |
2.4 |
4.2 |
6.8–7.6 |
7.2 |
3.8 |
4.9–5.1 |
4.9 |
2.2 |
I. 'Towanda Redflare' |
4.7–5.4 |
5.2 |
10.4 |
6.6–7.3 |
7.0 |
6.9 |
5.3–5.9 |
5.6 |
7.6 |
4.5–5.7 |
5.1 |
1.6 |
2.0–2.4 |
2.2 |
15.5 |
5.3–6.4 |
5.6 |
12.9 |
3.0–4.9 |
3.9 |
36.0 |
I. 'Wiltrud Gissel' |
5.2–5.6 |
5.3 |
5.3 |
12.6–13.2 |
12.9 |
2.3 |
8.9–7.3 |
7.7 |
13.7 |
4.9–5.3 |
5.3 |
2.8 |
2.1–2.4 |
2.3 |
4.4 |
6.9–7.5 |
7.0 |
4.1 |
4.7–5.0 |
4.8 |
3.0 |
The stamen was invisible in the studied irises, as it was hidden under the peat-like branching style. The mean length of the whole stamen varied from 2.5 cm in I. ‘Wiltrud Gissel’ to 3.5 cm in I. ’Dreaming Yellow’. I. ‘Wiltrud Gissel’ revealed the highest variability (11.3%). In majority of the irises the filament was longer than the anther, whereas the opposite was noticed only in I. ‘Wiltrud Gissel’. The width of filament and anther was not diversified. The width of filament was between 0.1 cm in I. pseudacorus and I. sibirica to 0.3 cm in I. ’Dreaming Yellow’. The width of anther was 0.1–0.2 cm (Tab. 4).
Table 4. Morphological characteristics of stamens of investigated iris species and varieties |
Species or variety |
Length (cm) |
Width (cm) |
|||||||||||||
stamen |
filament |
anther |
filament |
anther |
|||||||||||
range |
mean |
V (%) |
range |
mean |
V (%) |
range |
mean |
V (%) |
range |
mean |
V (%) |
range |
mean |
V (%) |
|
I. graminea |
2.4–2.5 |
2.5 |
3.5 |
1.1–1.7 |
1.3 |
17.7 |
1.2–1.4 |
1.3 |
5.1 |
0.3 |
0.3 |
0.0 |
0.1 |
0.1 |
0.0 |
I. pseudacorus |
2.2–3.0 |
2.6 |
6.9 |
1.0–1.7 |
1.3 |
12.5 |
1.1–1.5 |
1.3 |
7.0 |
0.1–0.2 |
0.1 |
25.5 |
0.2 |
0.2 |
0.0 |
I. sibirica |
2.8–3.0 |
2.9 |
2.8 |
1.9–2.0 |
1.9 |
3.3 |
1.1–1.2 |
1.1 |
4.5 |
0.1–0.2 |
0.1 |
4.0 |
0.1–0.2 |
0.2 |
10.0 |
I. 'Dreaming Yellow' |
3.4–3.6 |
3.5 |
1.4 |
2.0–2.2 |
2.1 |
3.6 |
1.4–1.5 |
1.4 |
3.0 |
0.3–0.4 |
0.3 |
5.7 |
0.2 |
0.2 |
0.0 |
I. 'Violet Meer' |
2.7–2.8 |
2.7 |
3.1 |
1.5–1.5 |
1.5 |
1.9 |
1.4 |
1.4 |
0.0 |
0.2 |
0.2 |
0.0 |
0.1–0.2 |
0.2 |
4.9 |
I. 'Towanda Redflare' |
2.9–3.0 |
2.9 |
3.4 |
1.9–2.0 |
1.9 |
4.8 |
1.0–1.2 |
1.1 |
10.1 |
0.1–0.2 |
0.2 |
9.4 |
0.1–0.2 |
0.1 |
5.1 |
I. 'Wiltrud Gissel' |
2.3–2.8 |
2.5 |
11.3 |
1.1–1.5 |
1.2 |
20.0 |
1.3–1.4 |
1.4 |
4.8 |
0.2 |
0.2 |
0.0 |
0.1–0.2 |
0.1 |
31.5 |
The length of a leafy style in all analyzed taxa ranged from 3.0 cm in I. graminea to 4.8 cm in I. ‘Dreaming Yellow’ (Tab. 5). The highest variability in the length of leafy not connate style and connate (of three leafy branchings) style segment was registered in I. ‘Towanda Redflare’, respectively 12.7% and 18.1%. On the other hand, the length of style from the connation point of three leafy branchings fluctuated from 0.2 cm in I. graminea to 1.1 cm in I. pseudacorus. The longest ovary, on average 2.5 cm was noted in I. pseudacorus and the shortest on average 1.7 cm in I. sibirica. The greatest diversification of ovary sizes was characteristic for I. graminea (15%). The ovary mean width in the examined irises was no larger than 0.7 cm (I. ‘Wiltrud Gissel’ and I. ’Dreaming Yellow’). I. sibirica and I. ’Towanda Redflare’ had the narrowest ovaries, whereas the greatest variability (18.5%) was registered in I. graminea (Tab. 5).
Table 5. Morphological characteristics of pistils of the studied iris species and varieties |
Species or variety |
Length of pistil elements (cm) |
Width (cm) |
||||||||||
leafy style |
connate style |
ovary |
ovary |
|||||||||
range |
mean |
V (%) |
range |
mean |
V (%) |
range |
mean |
V (%) |
range |
mean |
V (%) |
|
I. graminea |
3.00–3.6 |
3.2 |
5.8 |
0.2–0.3 |
0.3 |
14.6 |
1.7–2.2 |
1.9 |
15.0 |
0.5–0.7 |
0.6 |
18.5 |
I. pseudacorus |
3.9–4.7 |
4.3 |
4.3 |
0.9–1.4 |
1.1 |
12.6 |
2.1–2.7 |
2.5 |
6.2 |
0.5–0.6 |
0.5 |
6.6 |
I. sibirica |
3.4–4.2 |
4.1 |
8.9 |
0.8–1.0 |
0.9 |
12.5 |
1.7–1.8 |
1.7 |
4.1 |
0.4–0.5 |
0.4 |
4.6 |
I. 'Dreaming Yellow' |
3.8–4.8 |
4.2 |
10.8 |
0.7–0.8 |
0.8 |
6.5 |
2.3–2.4 |
2.3 |
3.1 |
0.7–0.8 |
0.7 |
3.8 |
I. 'Violet Meer' |
3.7–4.2 |
3.9 |
5.9 |
0.6 |
0.6 |
0.0 |
2.1–2.4 |
2.3 |
12.3 |
0.6 |
0.6 |
0.0 |
I. 'Towanda Redflare' |
3.5–4.2 |
3.8 |
12.7 |
0.8–1.0 |
0.9 |
18.1 |
1.8–1.9 |
1.8 |
5.8 |
0.4–0.5 |
0.4 |
4.8 |
I. 'Wiltrud Gissel' |
3.8–3.9 |
3.9 |
1.8 |
0.39–0.4 |
0.4 |
1.5 |
1.9–2.3 |
2.1 |
8.9 |
0.7 |
0.7 |
0.0 |
Table 6. Colors of the perianth elements, pistils, stamens and pollen of the studied iris species and varieties according to Royal Horticultural Society Color |
Species or variety |
Flower color |
Pistil color |
Stamen color |
Pollen color |
||||||||||
leafy style |
connate style |
ovary |
filament |
anthers |
||||||||||
RHS CC |
RHS CC |
RHS CC |
RHS CC |
RHS CC |
RHS CC |
RHS CC |
||||||||
I. graminea |
purple-yellow |
no equivalent |
blue-purple |
no equivalent |
light green |
154C |
green |
134A |
amaranth |
80B |
amaranth-yellow |
no equivalent |
dark yellow |
9A |
I. pseudacorus |
yelow |
158D |
yellow |
9B |
light green |
142A |
green |
134A |
light yellow |
8C |
yellow-brown |
no equivalent |
yellow |
9C |
I. sibirica |
purple |
96C |
purple |
96C |
light green |
142B |
green |
134B |
purple |
96D |
dark purple |
89B |
blue |
100C |
I. 'Dreaming Yellow' |
white-yellow |
155D/9B |
cream white |
no equivalent |
light green |
154C |
green |
134A |
white |
155C |
cream white |
11D |
cream white |
155D |
I. 'Violet Meer' |
puple |
95C |
light blue |
101C |
light green |
142B |
green |
134B |
purple |
96D |
dark purple |
89B |
cream |
158D |
I. 'Towanda Redflare' |
amaranth |
78B |
amaranth |
10B |
light green |
154C |
green |
134B |
cream |
150D |
amaranth |
80B |
yellow |
10B |
Iris flowers differed with the color of perianth, filament, anthers and the color of pollen. Most flowers were unicoloured, only I. graminea and I. ‘Dreaming Yellow’ stood out with their double colored flowers, respectively purple-yellow and white-yellow. The pistil (the style and ovary) were of a similar color but of different shades, respectively light green and green (Tab. 6).
DISCUSSION
Irises are valued for diversity of their colors and sizes of flowers. The species belonging to Limniris section deserve particular attention. Their flowers are smaller but the clumps bloom more abundantly. Studies on the flower size allowed to classify the flowers of examined taxa to the iris group with large or medium flowers [4, 10].
Iris flowers differed with the size and structure of their reproductive organs. Tetraploid I. ‘Dreaming Yellow’ had visibly larger perianth segments, as has been confirmed by the studies conducted by McEwen [11, 12]. The Author’s own investigations of pistil and stamen length confirmed iris heterostyly, which was described by Strassbourger [15]. All iris taxa were characterized by protandry. Pollen matured and poured out from the stamens placed under the leafy style immediately when the flowers opened.
The color of flowers and leaves was assessed in the irises selected for breeding works. A method of comparison of the individual flower elements with RHS CC standard was applied. The investigations revealed that the analysis the colors of iris perianth parent forms using RHS CC standard was difficult due to an extended area of the elements and numerous veinings and copigmentation of flowers. In some cases it was impossible to establish the color. The standards obtained in Author’s own investigations will serve to compare the perianth color of F1 hybrids in further breeding works.
CONCLUSIONS
- The investigated iris flowers were of medium and large size.
- Diploid taxons were characterized by a similar size of individual perianth elements.
- Tetraploid species stood out by their twice larger individual perianth elements.
- A more precise method than comparing the colours with RHCC standards should be used to determine the precise color of the perianth elements, e.g. determining flower colors using spectrophotometer.
REFERENCES
- Actes et Comptes-Rendus de la 1re Conférence Internationale des iris Tenue á Paris en 1922. Société Nationale D'horticulture de France. Comiision des Iris. ss. 95.
- Brookins H.L. (red.), 1991. The 1991 cumulative check list of siberian irises. The Society for Siberian Irises (A Section of the American Iris Society). ss. 57.
- Goldblatt P., Manning J.C., 2008. The iris family. Timber Press. London. ss. 290.
- Köhlein F., 1989. Iris. Timber Press. Portland, Oregon ss. 370.
- Komarnicki L., 1993. Irysy (Irises). PWRiL. Warszawa (in Polish).
- Korzonek D., 2001. Biologia kwitnienia i tworzenie mieszańców międzygatunkowych różaneczników (Rhododendron L.) (Biology of flowering and creating an intespecifics hybrids of rhododendrons (Rhododendron L.)). Praca doktorska. Kraków (in Polish).
- Kresánek J., Krejča J., 1982. Atlas liečivých rastlin a lesných plodov. Osveta. Martin.
- Kulig M. 2010. Biologia kwitnienia i tworzenie mieszańców międzygatunkowych kosaćców bezbródkowych z sekcji Limniris (Biology of flowering and creating an interspecific hybrids of beardless irises from section Limniris). Praca doktorska. Kraków (in Polish).
- Lubowicka H., 1977. Kosaćce (Irises). PWRiL. Warszawa (in Polish).
- Marcinkowski J., 2002. Byliny ogrodowe (Garden's perennials). PWRiL. Warszawa (in Polish).
- McEwen C., 1966. Tetraploidy in siberian irises.Year Book. British Iris Society, 77.
- McEwen C., 1978. Methods for inducing tetraploidy in siberian and japanese irises. Bulletin American Iris Society. 223, 20–23.
- Rejewski M., 1996. Pochodzenie łacińskich nazw roślin polskich (The origin of latin names of polish plants). KiW. Warszawa (in Polish).
- Royal Horticultural Society Colour Chart (RHS CC), 1995. Royal Hort. Soc., London, UK.
- Strassbourger E., 1960. Botanika (Botanic). PWRiL.Warszawa, 793–796 (in Polish).
Accepted for print: 20.02.2012
Magdalena Kulig
Department of Dendrology and Landscape Architecture, University of Agriculture in Krakow
al. 29 Listopada 54,
31-427 Kraków, Poland
email: mkulig@ar.krakow.pl
Responses to this article, comments are invited and should be submitted within three months of the publication of the article. If accepted for publication, they will be published in the chapter headed 'Discussions' and hyperlinked to the article.