Genetic variability in high temperature effects on seed-set in sorghum

Sorghum (Sorghum bicolor (L.) Moench) is grown as a dryland crop in semiarid subtropical and tropical environments where it is often exposed to high temperatures around flowering. Projected climate change is likely to increase the incidence of exposure to high temperature, with potential adverse effects on growth, development and grain yield. The objectives of this study were to explore genetic variability for the effects of high temperature on crop growth and development, in vitro pollen germination and seed-set. Eighteen diverse sorghum genotypes were grown at day : night temperatures of 32 : 21 degrees C (optimum temperature, OT) and 38 : 21 degrees C (high temperature, HT during the middle of the day) in controlled environment chambers. HT significantly accelerated development, and reduced plant height and individual leaf size. However, there was no consistent effect on leaf area per plant. HT significantly reduced pollen germination and seed-set percentage of all genotypes; under HT, genotypes differed significantly in pollen viability percentage (17-63%) and seed-set percentage (7-65%). The two traits were strongly and positively associated (R-2 = 0.93, n = 36, P < 0.001), suggesting a causal association. The observed genetic variation in pollen and seed-set traits should be able to be exploited through breeding to develop heat-tolerant varieties for future climates.

Pidyon HaBen 5 Pieces Coin Set

5 Silver coin set in olive-wood box with certificates. Obverse: 25 Silver Lirot coin. In the lower part big emblem of the State of Israel. Reverse: Five pomegranate flowers round a five-pointed star.

David Ben-Gurion Commemorative Coin Set

3 pieces commemorative coin set in a box. 2 silver coins, 1 gold coin. Obverse: 25 Lirot silver coins, 500 Lirot gold coin. In the center the state emblem of the State of Israel. Reverse: Portrait of David Ben-Gurion.

Hanukkah Circulation Coin Set

5 Coin set. 1 Agora; 5 Agorot; 10 Agorot; 1/2 New Sheqel; 1 New Sheqel. All of the coins have Hanukkiyot on the obverse side.

Uncirculated Coin Set, 40th Anniversary of Israel

5 Coin Set: 1 Agora; 5 Agorot; 10 Agorot; 1/2 New Sheqel; 1 New Sheqel. All coins have on the obverse side written 40 Years of Israel. 1 Commemorative coin: Obverse: Menorah inside of number 40. Reverse: Design of a building.

Souvenir from the Lira Period Coin Set

7 coin set. 1 Agora; 5 Agorot; 10 Agorot; 25 Agorot; 1/2 Lira; 1 Lira; 5 Lirot. The motifs are inspired by ancient Hebrew coins which feature the seven species mentioned in the Bible and by vessels from the Temple of Jerusalem.

First Coin Set with 5 New Sheqalim Coin

6 coin set. 1 Agora; 5 Agorot; 10 Agorot; 1/2 New Sheqel; 1 New Sheqel; 5 New Sheqel. The motifs are inspired by ancient Hebrew coins and seals with biblical emblems, and by ornaments from the Holy Temple.

Israel's 41st Anniversary Coin Set, Piefort

5 coin set. 1 Agora; 5 Agorot; 10 Agorot; 1/2 New Sheqel; 1 New Sheqel. Piefort: coins are thicker.

Israel 39th Anniversary Coin Set, Piefort

5 coin set. 1 Agora; 5 Agorot; 10 Agorot; 1/2 New Sheqel; 1 New Sheqel.

Hanukka Israel Coin Set and Official Uncirculated Coin Set

10 coin set. Official Uncirculated coin set (5 coins): 1 Agora; 5 Agorot; 10 Agorot; 1/2 New Sheqel; 1 New Sheqel. Hanukka coin set (5 coins): 1 Agora; 5; Agorot; 10 Agorot; 1/2 New Sheqel; 1 New Sheqel. All Hanukka coins have on the obverse side Hanukkiyot and word Hanukka.

Hanukka Circulation Coins Set

5 coin set: 5 Agorot; 10 Agorot; 1/2 New Sheqel; 1 New Sheqel; 5 New Sheqalim. All of the coins have on the obverse side Hanukkiyot and word Hanukka.

Israel Official Uncirculated Coins Set

8 coin set. 1 Sheqel; 5 Sheqalim; 10 Sheqalim; 2 times 50 Sheqalim-one with a portrait of David Ben-Gurion on the reverse side, one normal coin; 3 times 100 Sheqalim-one with a portrait of Ze'ev Jabotinsky on the reverse side, one with Hanukkah lamp on the obverse side, one normal plain coin.

Low temperature exposure of root system and inflorescence affected flowering and fruit set in 'Chardonnay' grapevines (Vitis vinifera)

The mechanisms by which low temperature affects flowering and fruit set of grapevines are poorly understood, as is the specific response of the grapevine root system and inflorescence to low temperature effects that reduce fruit set. This study aimed to determine the responses of the root system and inflorescence of the grapevine 'Chardonnay' to low temperature (10 degrees C) during flowering, and considered the possible mechanisms of low temperature effects on those parts. Temperature treatments of 10 degrees C or 20 degrees C were imposed to potted 'Chardonnay' grapevines in a glasshouse for up to two weeks during the early stages of flowering. When the root system alone was exposed to 10 degrees C (with the rest of the plant at 20 degrees C) during flowering, the number of attached berries and percentage fruit set were significantly reduced by 50 % than when the root system alone was exposed to 20 degrees C. Whereas, exposure of the inflorescence alone to 10 degrees C (with the rest of the plant at 20 degrees C) delayed flowering, allowed rachis to grow longer, and increased both the number of attached berries (from 22 to 62 per vine) and fruit set (from 8 % to, 20 %), than when the inflorescence alone was exposed to 20 degrees C. This study will enhance our understanding of the possible mechanisms of low temperature effects on grapevine fruit set and productivity.

Sorghum genotypes differ in high temperature responses for seed set

Significant genotypic differences in tolerance of pollen germination and seed set to high temperatures have been shown in sorghum. However, it is unclear whether differences were associated with variation in either the threshold temperature above which reproductive processes are affected, or in the tolerance to increased temperature above that threshold. The objectives of this study were to (a) dissect known differences in heat tolerance for a range of sorghum genotypes into differences in the threshold temperature and tolerance to increased temperatures, (b) determine whether poor seed set under high temperatures can be compensated by increased seed mass, and (c) identify whether genotypic differences in heat tolerance in a controlled environment facility (CEF) can be reproduced in field conditions. Twenty genotypes were grown in a CEF under four day/night temperatures (31.9/21.0 °C, 32.8/21.0 °C, 36.1/21.0 °C, and 38.0/21.0 °C), and a subset of six genotypes was grown in the field under four different temperature regimes around anthesis. The novelty of the findings in this study related to differences in responsiveness to high temperature—genotypic differences in seed set percentage were found for both the threshold temperature and the tolerance to increased maximum temperature above that threshold. Further, the response of seed set to high temperature in the field study was well correlated to that in the CEF (R2 = 0.69), although the slope was significantly less than unity, indicating that heat stress effects may have been diluted under the variable field conditions. Poor seed set was not compensated by increased seed mass in either CEF or field environments. Grain yield was thus closely related to seed set percentage. This result demonstrates the potential for development of a low-cost field screening method to identify high-temperature tolerant varieties that could deliver sustainable yields under future warmer climates.

Validation of a new spot form of net blotch differential set and evidence for hybridisation between the spot and net forms of net blotch in Australia

A recently developed spot form of blotch differential set of 16 barley lines was tested for reaction response to 60 Pyrenophora teres f. maculata isolates from geographically disperse barley crops of Australia. Twelve barley lines (Arimont, Barque, Chebec, CI5286, CI5791, CI9214, CII6150, Dairokkaku, Esperance Orge 289, Galleon, Keel, Skiff, Torrens and TR250) provided differential response between the isolates. The susceptible controls Gairdner and Kombar provided indication of isolate virulence or avirulence. Abundant pathogenic diversity was revealed with 33 designated pathotypes, some of which related to geographic region. AFLP analysis also revealed abundant diversity with each of the isolates representing a unique genotype and one isolate that contained both AFLP bands unique to P. teres f. maculata and P. teres f. teres, the cause of spot form and net form of net blotch respectively, suggesting that sexual recombination between the net form and spot form isolates may have occurred naturally in the field.