Cell wall components, especially arabinogalactan proteins (AGPs) and pectins as the source of signaling molecules active in cell-to-cell communication, are involved in many biological processes, including plant growth and development. Understanding the mechanisms of intercellular communication is particularly important in the context of reprogramming cell fate and transition from somatic to germline identity. The present study focuses on immunodetection of some pectic epitopes and AGPs in young ovules of selected Hieracium, Pilosella and Taraxacum species. The purpose of this research was to answer the questions: (1) whether the distribution of pectins and AGPs is related to the mode of reproduction and (2) whether their spatial and temporal distribution in young ovules may herald a later differentiation of the nutrient tissue present in the integument of mature ovules. We analyzed the localization of low and highly methyl-esterified pectins and AGP epitopes using monoclonal antibodies, i.e., LM19, LM20, JIM13, respectively. Our research found no significant differences in the localization of pectins and AGPs in young ovules of sexual and apomictic species, and the initial distribution pattern of these compounds did not appear to be related to the subsequent differentiation of the periendothelial nutrient zone. The presented findings may confirm the existence of a general developmental trend in the spatial and temporal distribution of pectins and AGPs during the maturation of ovules in angiosperms.

Chromosome numbers of 46 Hieracium L. and Pilosella Vaill. taxa from Austria, Bulgaria, Czech Republic, Macedonia, Montenegro, Poland, Romania, Serbia and Slovakia are presented. Chromosomes numbers are given for the first time for Hieracium amphigenum Briq. 2n = 3× = 27, H. bohatschianum Zahn 2n = 4× = 36, H. borbasii R. Uechtr. 2n = 4× = 36, H. cernuum Friv. 2n = 2× = 18, H. hazslinszkyi Pax 2n = 3× = 27, H. mirekii Szeląg 2n = 4× = 36, H. polyphyllobasis (Nyár. & Zahn) Szeląg 2n = 3× = 27, H. porphyriticum A. Kern. 2n = 4× = 36, H. racemosum Waldst. & Kit. ex Willd. subsp. racemosum 2n = 3× = 27, H. scardicum Borm. & Zahn 2n = 4× = 36, H. sparsum subsp. ipekanum Rech. fil. & Zahn 2n = 4× = 36, H. sparsum subsp. peristeriense Behr & Zahn, H. sparsum subsp. squarrosobracchiatum Behr & al. 2n = 3× = 27, H. tomosense Simk. 2n = 4× = 36, H. tubulare Nyár. 2n = 4× = 36, H. werneri Szeląg 2n = 3× = 27 and Pilosella fusca subsp. subpedunculata (Zahn) Szeląg, as well as five species of Hieracium sect. Cernua R. Uechtr. not described to date and a hybrid between H. bifidum s. lat. and H. pojoritense Woł

The authors report the first discovery of diploid populations of Hieracium naegelianum Panč. subsp. naegelianum and H. naegelianum subsp. ljubotenicum Behr & Zahn., and give the first chromosome counts for H. cernuum Friv., H. gymnocephalum Griseb. ex Pant., H. sparsum Friv., Pilosella pavichii (Heuff.) Holub and P. serbica (F. W. Schultz & Schultz-Bip.) Szeląg from Macedonia and/or Montenegro. A diploid chromosome count for Hieracium renatae Szeląg is confirmed based on material from the whole distribution range of the species. An emasculation experiment showed that all the analyzed diploid Hieracium taxa reproduce sexually.