Orientation and withdrawal of pollination drops in Cupressaceae s. l. (Coniferales)

Pollination in the Cupressaceae is studied ex situ, focused on orientation and withdrawal of pollination drops. Orientation of pollination drops is a constant feature in most taxa studied and important for pollen capture. Conspecific pollen causes a withdrawal of pollination drops, varying in time among species from 8 to 24 min, but with little variation within species. Pollination drops of each tested Cupressaceae taxon are also withdrawn when pollinated with foreign, but Cupressaceous pollen. However, they remain unchanged and are not withdrawn immediately when pollinated with pollen of other seed plants. The results clearly indicate that the time for the total withdrawal of pollination drops is strongly influenced by the evolutionary distance of the taxa being involved in the pollination process. Among closely related taxa the withdrawal is much more rapid than in distantly related ones. This points to an effective recognition system regulating the withdrawal of pollination drops, probably controlled by the nucellus. This recognition system can be regarded as an important preadaption for the evolution of a self-incompatibility mechanism. The withdrawal of pollination drops is thus not exclusively a physically induced process as suggested in some earlier studies. Pollination drops of several ovules can fuse to form a large common one, perhaps increasing by this way successful pollen capture.     

国产蔷薇科李亚科的花粉形态

本文报道了国产李亚科（Ｐｒｕｎｏｉｄｅａｅ）１０属１１种植物花粉形态。花粉近球形至长球形,极轴２０００～４４１２μｍ,赤道轴１７８５～３６９５μｍ。极面观三裂圆形,赤道面观椭圆形至圆形。具三孔沟,内孔常为长方形。沟较长,两端较窄。但在Ｓｉｎｏｐｌａｇｉｏｓｐｅｒｍｕｍｕｎｉｆｌｏｒａ中除了３孔沟外,还有周孔沟。花粉外壁明显分化为覆盖层和柱状层,在光学显微镜下表面常模糊,扫描电镜下外壁纹饰均为条纹状。孢粉学结合形态学和细胞学证据说明本亚科为一单系发生的类群。Ｐｒｉｎｓｅｐｉａｕｔｉｌｉｓ和Ｓｉｎｏｐｌａｇｉｏｓｐｅｒｍｕｍｕｎｉｆｌｏｒａ（Ｐｒｉｎｓｅｐｉａｕｎｉｆｌｏｒａ）这两个种在花粉特征和外壁纹饰上差异很大,从而支持将Ｐｒｉｎｓｅｐｉａ和Ｓｉｎｏｐｌａｇｉｏｓｐｅｒｍｕｍ分别处理为两个属但不支持将广义的Ｐｒｉｎｃｅｐｉａ（含Ｐｒｉｎｃｅｐｉａ和Ｓｉｎｏｐｌａｇｉｏｓｐｅｒｍｕｍ）独立为亚科。此外,由于Ｅｘｏｃｈｏｒｄａ的外壁纹饰同Ｐｒｕｎｏｉｄｅａｅ中较原始的类群（如Ｌａｕｒｏｃｅｒａｓｕｓ）相近,结合细胞学和形态学证据,支持将Ｅｘｏｃｈｏｒｄａ移置至Ｐｒｕｎｏｉｄｅａｅ之下     

Changes in forest cover in China during the Holocene

Pollen map data at 2000-year intervals are used to reconstruct changes in Holocene forest cover in China north of the Yangtze River. In almost all regions, the early Holocene from 10 ka b.p. to 6 ka b.p. is characterised by an increase in forest cover although there was a reversal to lower forest cover at 8 ka b.p. in the eastern monsoon regions. A maximum of forest cover was reached at 6 ka b.p. in all regions except for Northeast China where forest cover peaked in the late Holocene. All regions except for Northeast China experienced a marked decline in forest cover after 6 ka b.p. Since 6 ka b.p., forest cover has decreased by about 92% in the middle and lower reaches of the Yellow River, 64% in the easternmost part of the Qinghai-Tibet Plateau and 37% between the Yangtze River and the Huaihe River. In contrast, forest cover in Northeast China increased significantly from 6 ka b.p., but has declined between 2 ka b.p. and the present. Changes in forest cover prior to 6 ka b.p. were probably caused by climate, but the evident drop in forest cover since that time in most regions may have been induced predominantly by human activities.     

Relationship of environmental changes in central Sri Lanka to possible prehistoric land-use and climate changes

A radiocarbon-dated pollen-analysed peat sequence from the Horton Plains (> 2000 m a.s.l.), in central Sri Lanka, together with physical and chemical parameters (organic carbon, mineral magnetics, carbon isotopes and phytoliths), indicates major environmental changes during the last 24,000 years. The results suggest that a mobile life form, i.e. a hunter–forage culture, predominated in an open landscape, associated with xerophytic vegetation, e.g. Chenopodium spp. at  17.5 ka BP. Incipient management of cereal plants and slash-and-burn techniques seem to have prevailed between 17.5 and 13 ka BP, which was indigenous and associated with grazing. Evidence of systematic cereal cultivation in the form of oat and barley pollen grains is found from the late Pleistocene ( 13 ka BP). This is the earliest evidence of farming activities noted in Sri Lanka as well as in south Asia. After 13 ka BP, cereal cultivation was associated with an increase in humidity. With a later abrupt increase in aridity, agricultural land-use decreased from  8 to  3.6 ka BP, when the area appears to have been almost deserted. After a severe middle Holocene arid phase (i.e. 5.4–3.6 ka BP), the agricultural activity with a limited extension was again initiated by  2.9 ka BP. During the next  900 years, cultivation ceased allowing the upper montane rain forest to dominate. Between 0.2 and 0.15 ka BP, new phases of agricultural activities were undertaken and potato cultivation took place lately, between 1950 and 1969 AD.     

The PELPIII glycoproteins in Solanaceae: stylar expression and transfer into pollen tube walls

The class III pistil-specific extensin-like proteins (PELPIII) of Nicotiana tabacum accumulate in the intercellular matrix (IM) of the style transmitting tissue (TT). After pollination, the 110–140 kDa PELPIII is translocated from the IM into the pollen tube walls. PELPIII-like sequences have been found in several solanaceous species. These sequences are expressed in mature non-pollinated styles at both RNA and protein level. Of the genus Nicotiana, the species N. alata, N. x sanderae and N. sylvestris (section Alatae), and N. tomentosiformis and N. otophora (section Tomentosae) showed an expression level of PELPIII homologues similar to that in mature styles of N. tabacum. PELPIII genes were absent in the most ancient species studied, namely N. trigonophylla (section Trigonophyllae). To study the species dependence of the translocation of PELPIII into the pollen tube wall in tobacco, interspecific pollinations on N. tabacum pistils were carried out with pollen from the incongruous species N. rustica, N. trigonophylla and Petunia hybrida, where PELPIII homologues are absent in the style. Immunocytological tests showed that the N. tabacum PELPIII is translocated into the pollen tube walls of all three species. Thus, the pollen tube walls of these species do not form a barrier for IM compounds such as the 110–140 kDa PELPIII and the absence of any possible effect of PELPIII on pollen tube growth cannot be due to failure of PELPIII transport through the wall. The importance of these findings is discussed with respect to the evolutionary origin of PELPIII, the pollen pistil interaction, the function of style TT-specific proteins and the physical properties of pollen tube walls.     

Pollen-pistil size correlation and pollen size-number trade-off in species of Argentinian Nyctaginaceae with different pollen reserves

Data on pollen and pistil traits from 14 Argentinean Nyctaginaceae species with starch or lipids as pollen reserves are presented. We expect differences in the traits between these two groups of species, but the same pattern within each group for (a) the relationship between pollen size and pistil length assuming that pollen tube length is predetermined by provisions in the pollen independently of the pollen reserve type, and for (b) a trade-off between size and number because available resources for male function are not unlimited. In particular we expect that (a) species with longer pistils will have larger pollen grains, (b) pollen grain size and the number of pollen grains per flower will be negatively correlated. Significant differences in the mean pollen number per flower and mean pollen size were observed between species with different pollen reserve type but not for pistil length. Then, correlation analyses were performed for species with starchy pollen or with pollen with lipids separately. Pollen size - pistil length correlation was positive and significant for species with starchy pollen but not for species with pollen with lipids. On the other hand, pollen size - number correlation was not significant for both starchy and oil-rich species. Results suggest that pollen reserve type would be a relevant factor that constraint pollen size in species of Nyctaginaceae, and that this pollen trait should be considered when studying pollen-pistil relationships, mainly between species of those families with mixed pollen reserves.     

Studies on Pollen Morphology and Taxonomy of Lespedeza and Its Allied Genera from NE China

The pollen morphology of 11 species and 1 variety in the genus Lespedeza and its allied genera (Campylotropis, Kummerowia) from NE China was examined under light and scanning electron microscopes. 1. Lespedeza Michx. (plate 1:1-6; 2:1-6; 3:1-6; 4:1-2) Pollen grains prolate, rarely subprolate or spheroidal, elliptic or rarely suborbicular in equatorial view, 3-lobed-rounded in polar view, tricolporate, colpus margins smooth or jagged. Polar axis 20.7-33.1μm long, equatorial axis 15.4-20.9 μm long. Exine reticulate or foveolate, lumina verrucose or smooth under SEM. 2. Campylotropis Bge. (plate 4:3-4) One species in NE China, C. macrocarpa (Bge.) Rehd. Pollen grains prolate, elliptic in equatorial view, 3-lobed-rounded in polar view, 3-colporate, colpus linear, 25.1μm long, 1.79μm broad, colpus margins jagged, with a series of verrucae equal in size along one side visible under SEM. Polar axis 19.7μm long, equatorial axis 14.6μm long. Exine reticulate, lumina nearly rounded, verrucose at periphery under SEM. 3. Kummerowia Schindl. (plate 4:5-6) Pollen grains spheroidal, oblate or prolate, elliptic in equatorial view, obtuse-triangular in polar view, tricolporate, colups linear, 25.1μm long, 2.01μm broad, colpus margins sinuate. Polar axis 24.7-27.9μm long, equatorial axis 19.7-26.6μm long. Exine reticulate or subreticulate, lumina nearly rounded, with verrocae visible under SEM. According to the pollen morphology of Lespedeza and its allied genera, the division of Lespedeza (s. lat.) into Lespedeza (S. str.), Campylotropis and Kummarowia by Schindler (1912) is reasonable. The subdivision of Lespedeza (s. str.) into Sect. Macrolespedeza and Sect. Lespedeza by many botanists, and the treatment of Lespedeze juncea (L. f.) Pers. var. inschanica Maxim. as an independent species (i.e. Lespedeza inschanics (Maxim). Schindl.) are also supported by the pollen morphology shown in the present work.     

Accumulation of Japanese cedar pollen allergen,Cry j 1, in the protein body I of transgenic rice seeds using the promoter and signal sequence of glutelin GluB-1 gene

Recombinant Cry j 1, a Japanese cedar pollen allergen, was produced in rice seeds for potential use for oral immunotherapy. Cry j 1 cDNA was divided into two parts, an N-terminal half and a C-terminal half, and each was fused downstream to glutelin GluB-1 gene containing sequences of the promoter, 5 untranslated region and signal peptide. A gene for green fluorescent protein was also fused to the 3 end of the Cry j 1 fragment. Recombinant Cry j 1 of up to 16.6 g per mg total protein of the seeds was expressed in transgenic rice seeds. Although the recombinant Cry j 1 was expected to be accumulated in protein body II because of the employment of glutelin signal peptide, it was demonstrated to be accumulated exclusively in protein body I. The recombinant Cry j 1 was not shown to react with IgE of allergic patients, indicating the reduction of the risk of anaphylactic reaction. These results demonstrate that the transgenic rice seeds with the recombinant Cry j 1 would be useful for the study of oral immunotherapy.     

Pollen Morphology of Neottianthe (Orchidaceae) and Its Taxonomic Significance

The genus Neottianthe (Orchidaceae) consists of about 12 species in the world, of which all are found in China and nine are endemic to China. The pollen morphology of this genus is very specific in shape and composition. All pollen grains in Neottianthe are of a compound pollen grain, called massula, in which of many monad pollen grains adhere togeth er. A massula is usually long and narrow trigonous cone in shape. Pollen grains can be divid ed into five types according to ornamentation, of exine surface: (A) pollen surface almost smooth, or very obscurely fossete, (B)perforate, (C) fossulate or foveolate, (D) reticuloid, and (E)typically reticulate. Neottianthe. calcicola, N. monophylla, N.pseudo-diphylax and N. cucullata have been merged into one species, N. cucullata, by some taxonomists. This treatment is not supported by the pollen morphological data, because pollen morphological characteristics of above-mentioned four species are different from each other. Therefore, pollen morphology shows that they are all independent at the specific level. Finally, it must be stressed that N. camptoceras is uniquite in the genus Neottianthe for its pollen shape,size and surface ornamentation of pollen exine.     

水稻台中65与其花粉不育近等基因系的杂种F1的裂药性研究

以台中65及其7个F1花粉不育近等基因系为材料,对水稻亚种间杂种F1裂药性及其与小穗育性的关系进行了研究。结果表明,杂种F1的裂药性受花粉不育基因互作控制。不同杂合座位内等位花粉不育基因互作导致杂种F1花药不开裂的程度不同,S-b座位导致杂种F1部分花药不开裂;不同杂合座位问非等位花粉不育基因互作明显降低杂种F1的裂药程度;杂种F1中含杂合花粉不育基因座位数越多,其裂药指数越小,裂药程度越低,含三个杂合花粉不育基因座位的杂种F1裂药指数为2．27,35．3％的花药不开裂。杂种F1花药不开裂的原因随其所含的杂合花粉不育基因座位种类和数目不同而异。杂种F1裂药程度的下降显著减少落在其柱头上的花粉总数和萌发的花粉数。杂种F1裂药指数和结实率呈极显著的正相关关系。