Complete volume with articles 1 to 35 - Cucurbit Breeding - North ...
Complete volume with articles 1 to 35 - Cucurbit Breeding - North ... Complete volume with articles 1 to 35 - Cucurbit Breeding - North ...
Table 4. Seed yield distribution among the center, stylar end, and peduncular end in the fruits of four cultivar groups of Cucurbita pepo. Cultivar-group Cultivar Seed yield (%) Stylar Center Peduncular Pumpkin CIN 25 42 32 Pumpkin ESS 26 43 30 Pumpkin PRQ 36 42 21 Pumpkin TOC 31 58 10 Pumpkin Mean 29 46 23 Vegetable Marrow BEI 55 43 1 Vegetable Marrow BNC 35 49 15 Vegetable Marrow LOG 49 42 8 Vegetable Marrow VPA 44 49 7 Vegetable Marrow Mean 46 46 8 Cocozelle LBS 70 29 0 Cocozelle LCO 65 35 0 Cocozelle LUT 88 12 0 Cocozelle STI 89 10 0 Cocozelle Mean 78 21 0 Zucchini BBU 41 56 3 Zucchini BZU 36 64 0 Zucchini NER 41 56 3 Zucchini NVM 49 47 3 Zucchini Mean 42 56 2 Cucurbit Genetics Cooperative Report 24:82-86 (2001) 85
The four cultivar-groups differed markedly in seedyield distribution in the fruit (Table 4). In the Pumpkin Group, about half of the seed yield was produced in the central portion of the fruit, with about one-quarter of the yield each in the stylar and peduncular portions. In the Vegetable Marrow Group and the Zucchini Group, nearly all of the seed yield was produced in the central and stylar portions of the fruit. In the Cocozelle Group, over threequarters of the seed yield was produced in the stylar portion, with none at all in the peduncular portion. The results (Table 3) indicate that seed yield per fruit in Cucurbita pepo ssp. pepo has decreased over the course of history with highest yield in the most ancient type, the Pumpkin Group, and the lowest yield in the most modern type, the Zucchini Group. The decrease in seed yield per fruit is generally true also over the transition from round (pumpkin) to wedge-shaped (vegetable marrow) to long (cocozelle and zucchini) fruits, except that the Cocozelle Group, even though it has the longest fruits, produced a similar or higher yield than the Vegetable Marrow Group. This can be attributed to the bulbous stylar end of the cocozelles, in which nearly 80% of their seeds are produced. The dominant seed yield component which determined the differences in seed yield among cultivar-groups was the seed number per fruit. The pumpkins had the highest seed number and the most even distribution of seeds in the fruit. In the other cultivar-groups, there was a trend toward decreased seed number, especially in the peduncular end of the fruit. This phenomenon became increasingly apparent as the length-to-width ratio increased, quite consistent with observations made in cucumbers (3). Cucurbit Genetics Cooperative Report 24:82-86 (2001) Literature Cited 1. Andres, T.C. 2000. An overview of the oil pumpkin. Cucurbit Genet. Coop. Rep. 23: 87-88. 2. Nerson, H., H.S. Paris and E.P. Paris. 2000. Fruit shape and seed yield in Cucurbita pepo. In: N. Katzir and H.S. Paris, eds., Proceedings of Cucurbitaceae 2000: The 7 th Eucarpia Meeting on Cucurbit Genetics and Breeding. Acta Hort. 510: 227-230. I.S.H.S., Leuven, Belgium. 3. Nijs, A.P.M. den and P. Miotay. 1991. Fruit and seed set in the cucumber (Cucumis sativus L.) in relation to pollen tube growth, sex type and parthenocarpy. Gartenbauwissenschaft 56(2): 46-49. 4. Paris, H.S. 1989. Historical records, origins and development of the edible cultivar groups of Cucurbita pepo (Cucurbitaceae). Econ. Bot. 43: 423-443. 5. Paris, H.S. 2000. History of the cultivargroups of Cucurbita pepo. In: J. Janick, ed., Horticultural Reviews 25(2001): 71-170, 4 plates. Wiley, New York. 6. Teppner, H. 2000. Cucurbita pepo (Cucurbitaceae) – history, seed coat types, thin coated seeds and their genetics. Phyton 40: 1-42. 7. Whitaker, T.W. and W.P. Bemis. 1964. Evolution in the genus Cucurbita. Evolution 18: 553-559. 86
- Page 45 and 46: Table 1. Percentage of RAPD band pr
- Page 47 and 48: Inodorus Primer Casaba Honeydew Cha
- Page 49 and 50: Frequency of RAPD Polymorphisms in
- Page 51 and 52: BC551 76.6 92.9 38.5 20.5 38.9 42.2
- Page 53 and 54: Powdery Mildew: An Emerging Disease
- Page 55 and 56: Table 1 (continued).z Cultivar Coun
- Page 57 and 58: Disease Severeity Rating Figure 1.
- Page 59 and 60: In the present study C. lanatus ent
- Page 61 and 62: Lakes, NJ) was a 0.5 cc (50 unit) s
- Page 63 and 64: Characterization of a New Male Ster
- Page 65 and 66: Table 1. Progeny test of male steri
- Page 67 and 68: Progeny Diploid Year Season generat
- Page 69 and 70: elatively small during its developm
- Page 71 and 72: content had no significant effect o
- Page 73 and 74: Stars-N-Stripes 26.3 12.0 35 8.5 5.
- Page 75 and 76: 11. Mozumder, B.K.G, N.E. Caroselli
- Page 77 and 78: Table 1. Vine length of watermelon
- Page 79 and 80: Survey of Watermelon Trialing Metho
- Page 81 and 82: assigned to adjacent plots (Table 2
- Page 83 and 84: Variation among tropical pumpkin cu
- Page 85 and 86: Table 1. Aggressiveness of powdery
- Page 87 and 88: A large variability of aggressivene
- Page 89 and 90: Table 1: Observed reaction of melon
- Page 91 and 92: Same Gene for Bush Growth Habit in
- Page 93 and 94: Relationship between Fruit Shape an
- Page 95: Table 3. Seed yield per fruit and s
- Page 99 and 100: Lee et al. (17) developed a RAPD ma
- Page 101 and 102: 19. Lelley, T and S. Henglmüller,
- Page 103 and 104: Those primers that had strong bands
- Page 105 and 106: Genetic Variability in Pumpkin (Cuc
- Page 107 and 108: those obtained by the ANOVA and the
- Page 109 and 110: Agarose discs were prepared as desc
- Page 111 and 112: Table 4. Effect of different densit
- Page 113 and 114: Isolation and Callus Production fro
- Page 115 and 116: Table 1. Components used for cultur
- Page 117 and 118: 6. Jia, Shi-rong, You-ying Fu and Y
- Page 119 and 120: the preceding one or two days (depe
- Page 121 and 122: Gene List 2001 for Cucumber Jiahua
- Page 123 and 124: Ar - Anthracnose resistance. One of
- Page 125 and 126: de I determinate habit. Short vine
- Page 127 and 128: gi - ginkgo. Leaves reduced and dis
- Page 129 and 130: Mdh-4 Mdh- 3 Malate dehydrogenase-4
- Page 131 and 132: h from 'Gy 2 cp cp', 'Spartan Salad
- Page 133 and 134: wf - White flesh. Intense white fle
- Page 135 and 136: M16056 Cotyledon cDNA Encoding ribu
- Page 137 and 138: (for CsPK2.2) AB001590 Hypocotyl RN
- Page 139 and 140: Caruth, T. F. 1975. A genetic study
- Page 141 and 142: John, C. A. and J. D. Wilson. 1952.
- Page 143 and 144: Ohkawa, J., A. Shinmyo, M. Kanchana
- Page 145 and 146: Shimizu, S., K. Kanazawa, and A. Ka
The four cultivar-groups differed markedly in seedyield<br />
distribution in the fruit (Table 4). In the<br />
Pumpkin Group, about half of the seed yield was<br />
produced in the central portion of the fruit, <strong>with</strong><br />
about one-quarter of the yield each in the stylar and<br />
peduncular portions. In the Vegetable Marrow<br />
Group and the Zucchini Group, nearly all of the seed<br />
yield was produced in the central and stylar portions<br />
of the fruit. In the Cocozelle Group, over threequarters<br />
of the seed yield was produced in the stylar<br />
portion, <strong>with</strong> none at all in the peduncular portion.<br />
The results (Table 3) indicate that seed yield per fruit<br />
in <strong>Cucurbit</strong>a pepo ssp. pepo has decreased over the<br />
course of his<strong>to</strong>ry <strong>with</strong> highest yield in the most<br />
ancient type, the Pumpkin Group, and the lowest<br />
yield in the most modern type, the Zucchini Group.<br />
The decrease in seed yield per fruit is generally true<br />
also over the transition from round (pumpkin) <strong>to</strong><br />
wedge-shaped (vegetable marrow) <strong>to</strong> long (cocozelle<br />
and zucchini) fruits, except that the Cocozelle Group,<br />
even though it has the longest fruits, produced a<br />
similar or higher yield than the Vegetable Marrow<br />
Group. This can be attributed <strong>to</strong> the bulbous stylar<br />
end of the cocozelles, in which nearly 80% of their<br />
seeds are produced. The dominant seed yield<br />
component which determined the differences in seed<br />
yield among cultivar-groups was the seed number per<br />
fruit. The pumpkins had the highest seed number and<br />
the most even distribution of seeds in the fruit. In the<br />
other cultivar-groups, there was a trend <strong>to</strong>ward<br />
decreased seed number, especially in the peduncular<br />
end of the fruit. This phenomenon became<br />
increasingly apparent as the length-<strong>to</strong>-width ratio<br />
increased, quite consistent <strong>with</strong> observations made in<br />
cucumbers (3).<br />
<strong>Cucurbit</strong> Genetics Cooperative Report 24:82-86 (2001)<br />
Literature Cited<br />
1. Andres, T.C. 2000. An overview of the oil<br />
pumpkin. <strong>Cucurbit</strong> Genet. Coop. Rep. 23:<br />
87-88.<br />
2. Nerson, H., H.S. Paris and E.P. Paris. 2000.<br />
Fruit shape and seed yield in <strong>Cucurbit</strong>a pepo.<br />
In: N. Katzir and H.S. Paris, eds.,<br />
Proceedings of <strong>Cucurbit</strong>aceae 2000: The 7 th<br />
Eucarpia Meeting on <strong>Cucurbit</strong> Genetics and<br />
<strong>Breeding</strong>. Acta Hort. 510: 227-230.<br />
I.S.H.S., Leuven, Belgium.<br />
3. Nijs, A.P.M. den and P. Miotay. 1991. Fruit<br />
and seed set in the cucumber (Cucumis<br />
sativus L.) in relation <strong>to</strong> pollen tube growth,<br />
sex type and parthenocarpy.<br />
Gartenbauwissenschaft 56(2): 46-49.<br />
4. Paris, H.S. 1989. His<strong>to</strong>rical records, origins<br />
and development of the edible cultivar<br />
groups of <strong>Cucurbit</strong>a pepo (<strong>Cucurbit</strong>aceae).<br />
Econ. Bot. 43: 423-443.<br />
5. Paris, H.S. 2000. His<strong>to</strong>ry of the cultivargroups<br />
of <strong>Cucurbit</strong>a pepo. In: J. Janick, ed.,<br />
Horticultural Reviews 25(2001): 71-170, 4<br />
plates. Wiley, New York.<br />
6. Teppner, H. 2000. <strong>Cucurbit</strong>a pepo<br />
(<strong>Cucurbit</strong>aceae) – his<strong>to</strong>ry, seed coat types, thin<br />
coated seeds and their genetics. Phy<strong>to</strong>n 40: 1-42.<br />
7. Whitaker, T.W. and W.P. Bemis. 1964.<br />
Evolution in the genus <strong>Cucurbit</strong>a. Evolution<br />
18: 553-559.<br />
86