Skoči na glavni sadržaj

Izvorni znanstveni članak

https://doi.org/10.37427/botcro-2023-003

Pollen morphology and flower visitors of Leiotulus aureus (Sm.)Pimenov & Ostr.(Apiaceae)

Marina Mačukanović-Jocić ; Faculty of Agriculture, University of Belgrade, Nemanjina 6, 11080 Belgrade - Zemun, Serbia
Danijela Stešević ; Faculty of Natural Sciences and Mathematics, University of Montenegro, Džordža Vašingtona bb, 81000, Montenegro
Dragana Rančić ; Faculty of Agriculture, University of Belgrade, Nemanjina 6, 11080 Belgrade - Zemun, Serbia
Miloje Šundić ; Faculty of Natural Sciences and Mathematics, University of Montenegro, Džordža Vašingtona bb, 81000, Montenegro


Puni tekst: engleski pdf 5.648 Kb

str. 44-51

preuzimanja: 286

citiraj

Preuzmi JATS datoteku


Sažetak

The pollen grains of Leiotulus aureus (syn. Malabaila aurea (Sm.) Boiss.) were examined by light and scanning electron microscopy in order to contribute to the taxonomical and melissopalynological studies of the species. Flower visitors have also been observed and analyzed aiming at the clarification of some pollination aspects including the species contribution to bee pasture. The pollen grains of L. aureusare isopolar, radially symmetrical, medium to large in size, tricolporate and perprolate. They are slightly equatorially constricted with obtuse polar caps and triangular in polar view. The sculpturing patternis rugulate–microperforate. With regard to flower visitors, the following pollination types occurred: melittophily, myophily and sapromyophily and cantharophily. Some insects attracted by L. aureuscannot be considered pollinators but casual visitors. The flowers were the most frequently visited by honey bees during midday.

Ključne riječi

Malabaila aurea, light microscopy - LM, palynomorphology, scanning electron microscopy - SEM, insect pollinators

Hrčak ID:

288166

URI

https://hrcak.srce.hr/288166

Datum izdavanja:

1.4.2023.

Posjeta: 1.079 *




Introduction

According to the latest taxonomic revision, genus Leiotulus Ehrenb., belonging to the Apiaceae tribe Tordylieae Koch., contains 10 species and subspecies, previously mainly assigned to the genera: Malabaila and Pastinaca (POWO 2022). Species Leiotulus aureus is known under the following homotypic synonims: Heracleum aureum Sm. (basionym), Lophotaenia aurea (Sm.) Griseb., Malabaila aurea (Sm.) Boiss., and Pastinaca aurea (Sm.) Calest., while the accepted name is proposed as a new name combination by Pimenov and Ostroumova (1994), based on carpological investigations. The genus included species characterized as intermediate between Pastinaca L. (incl. Malabaila s.str.) and Zosima Hoffm. (e.g. Malabaila involucrata Boiss. & Spruner, M. pastinacifolia Boiss. & Balansa etc.).

L. aureus is a herbaceous biennial, a plant of the native range from SE Europe to NW Turkey (POWO 2022), prefering warm and sunny places along with open rocky habitats. It is caracterised by a semirosette growth form, erect, hollow, striate and somewhat viscid stem up to 50 cm tall, pinnately divided leaves with ovate leaflets near the ground and linear-lanceolate in upper stem ones. Bright yellow flowers are grouped in terminal and subterminal, regularly compound umbels (Tutin et al. 1981). The mature fruit is obcordate - suborbicular, flattened, surrounded by a wide somewhat thickened margin, cordate at the apex, with persistent style (Fig. 1). Although the plant is slightly aromatic, a literature search did not reveal any reference to its local use in traditional medicine or cooking.

Fig. 1 Habitus of Leiotulus aureus (A), inflorescence close up (B), detail of immature fruits (C) (photo: Danijela Stešević).
ABC-82-44-f1

Investigations regarding apiaceaen pollen morphology have been reported by a number of authors, including Erdtman (1971), Van Zeist and Bottema (1977) and Cerceau-Larrival (1981). However, although pollination biology within the Apiaceae has not received much attention, some aspects were studied in a few taxa including Chaerophyllum, Heracleum, Seseli, Thaspium, Zizia and Daucus (Lindsey 1984,Lindsey and Bell 1985,Pimenov and Ostroumova, 1994,Lamborn and Ollerton 2000,Langenberger and Davis 2002a,b,Rovira et al. 2002,Wróblewska 1993,Mačukanović-Jocić et al. 2016). Besides phylogenetic studies (Pimenov and Ostroumova 1994,Ajani et al. 2008,Downie et al. 2010), scientific papers relating to other reproductive aspects of the Leiotulus speciesare rather rare. Although some palynological studies within the genus Leiotulus are modest, except onL. secacul (Mill.) Pimenov & Ostr., L. kotschyi (Boiss.) Pimenov & Ostr.(Van Zeist and Bottema 1977), the pollen features of L. aureus have been unexplored.

The present study aimed to provide palynomorphological features of the species that can be used for the taxon identification and clarification of higher level relationships within the family, as well as to contribute to melissopalynological studies and to the pollen atlas of the region. In addition, the study aimed to examine the attractiveness of this species to the honey bee, in terms of its contribution to honey bee pasture, by providing evidence about flower visitors.

Materials and methods
Study site

The research was focused on L. aureus plant population in the region of Gorica hill (Podgorica), Montenegro (N 42o 26´ 57´´ E 19o 16´ 2´´, elevation 114 m). The population inhabits xerophilous rocky pastures dominated by Salvia officinalis L. and Stipa eriocaulis Borbás, classified within NATURA 2000 as habitat type 62A0 - Eastern sub-mediterranean dry grasslands (Scorzoneratalia villosae). Using D.A.F.O.R. scale for species abundance presence (%): D = Dominant (51-100%), A = Abundant (31-50%), F = Frequent (16-30%), O = Occasional (6-15%), R = Rare (1-5%), L. aureus is observed as "Abundant" in a given area. Pollen collection and insect observations were conducted in 2017 during the blooming period in May. Three mounted and labeled plant voucher specimens (1500402, 1500403, 1500404) were processed and deposited in the herbarium collection of the Faculty of Natural Sciences and Mathematics, University of Montenegro (TGU). Digital photographs of each completed specimen and the accompanying data have also been provided.

Sampling and analysis of pollen

For scanning electron microscopy (SEM) and light microscopy (LM) analysis, the umbels (flowers) at full flowering stage were collected from 10 plants of wild populations.

For SEM study, the pollen grains from fully open flowers were mounted directly on the stub. Aiming to avoid any deformation of the pollen grains or any swelling attributed to solvents, preparation was carried out without the previous acetolysis method (Dustmann and von Der Ohe 1993). Samples were coated with gold (in BAL-TEC SCD 005 Sputter Coater, 100 seconds in 30 mA) and observed using a JEOL JSM- 6390 LV electron microscope at an acceleration voltage of 20 kV. Pollen grains were photographed in polar and equatorial view, and measurements were done on a sample of 50 or more grains for each morphological character. The following features describing pollen grains were examined: size, shape, ornamentation, apertures, polarity, symmetry, length of polar (P) and equatorial axis (E) (in SEM) and exine thickness (in LM). Description of pollen morphology was performed according to Punt et al.(2007) and Erdtman (1971).

For LM, the pollen grains were mounted on slides in a drop of saturated solution of fructose in water, observed without additional staining with a Leica DM2000 microscope equipped with a digital camera (Leica DFC320) and Leica IM1000 software.

Field monitoring and identification of insect visitors

Field observations were carried out during the peak flowering period of L. aureus, from 7 a.m. to 7 p.m., due to the absence of insect activity outside during the rest of the day. Furthermore, nocturnal insects or those active in the evening (such as sphingid moths) were not recorded. In addition to recording honey bee visits, imaging and sampling of all other flower visitors were performed. The insects were photographed with a Nikon Colorpix P500 digital camera. For the purpose of insect sampling, some insects were identified on sight, but for most species an accurate identification was made only after a specimen had been captured. Specimens were collected by entomological net and exhauster and stored for further determination in the laboratory by experts according to the relevant literature (Bouchard et al. 2011,Cassis and Schuh 2012,Lupoli 2017,Oosterbroek 2006,Sivell 2021,Van Veen 2004,Vazquez 2002).

In order to estimate the frequency of honey bee visits, three plants were randomly chosen and marked at the locality. For diurnal dynamics of frequency of visits, honey bees were monitored five times a day at three-hour intervals. Percentage of visited flowers per plant was calculated as total number of honey bee visits to each marked plant multiplied by the number of umbels visited by one honey bee, divided by the total number of open umbels per plant. The ratio of visited umbels per plant were calculated according to modified formula by Dafni et al. (1988). The following parameters were monitored in the field: A: The total number of bees visiting per marked plant in a time interval of 5 min, B: The number of umbels that each bee visited on the marked plant, C: The total number of umbels per plant. From these data, the percentage of umbels visited by honey bees was calculated according to the formula as follows: (AxB/C)x100. Also, the time each bee spent on the plant was measured.

Results
Pollen morphology

The pollen grains of L. aureusare isopolar, radially symmetrical and at the interface between medium-sized and large, according to Punt et al. (2007). The ratio between the polar axis length (P = 49.4 ± 2.1 μm) and the equatorial diameter (E = 19.5 ± 1.1 μm) amounts to 2.5 ± 0.2 indicating perprolate shape. The grains are slightly equatorially constricted with blunt polar ends (Figs. 2A,3A, B), and in polar view they are triangular with interangular furrows (Fig. 2B). The grains are tricolporate with three straight sunken ectocolpi arranged regularly meridionally, of mean length 28.5 ± 2.2 μm, each with one endopore positioned in the indentations between the mesocolpial lobes (Figs. 2A,3A, B). Mesocolpial width averaged 9.9 ± 1.6 μm. The sculpturing pattern, clearly visible in SEM is rugulate - microperforate (Fig. 2C). Exine is found to be, as observed in LM, 1.22 ± 0.25 μm thick at the poles and twiceas thick in the equatorial region (2.59 ± 0.49 μm) (Fig. 3B).

Fig. 2 Scanning electron microscopy of Leiotulus aureus (Malabaila–type) pollen: the perprolate tricolporate pollen grains are bone-shaped in equatorial (A) and triangular in polar view (B). A detail of exine surface showing rugulate - microperforate ornamentation (C, D).
ABC-82-44-f2
Fig. 3 Light microscopy micrographs of mesocolpial side of Leiotulus aureus (Malabaila–type) pollengrains showing clearlyvisible pores (A) and thicker exine (B) in the area of equatorial constriction.
ABC-82-44-f3

Flower visitors

The golden yellow flowers of this species, arranged in terminally compound umbels, were visited by varyingly efficient pollinator insects. The results of the current study suggest that some floral features are attractive for different insect visitors belonging to four orders: Hymenoptera (Apis mellifera -Fig. 4A), Diptera (Episyrphus balteatus -Fig. 4B, Scaeva pyrastri-Fig. 4C, Sphaerophoria scripta-Fig. 4D, Lucilia sp. -Fig. 4E, Sarcophaga sp. -Fig. 4F, and Bibio sp. -Fig. 4G), Coleoptera (Oedemera lurida-Fig. 4H, Mordella aculeata-Fig. 4I, Malachius bipustulatus -Fig. 4J) and Hemiptera (Closterotomus sp. -Fig. 4K, Graphosoma lineatum -Fig. 4L). These insects are classified as primary and secondary pollinators and or accidental visitors. Regarding the observed flower visitors, pollination types are as follows: melittophily including pollination by honey bees, myophily and sapromyophily including specialized and non-specialized flies, and cantharophily (beetle pollination). Nevertheless, field observations have shown that the plant could be considered melliferous, as the umbels were gladly and frequently visited by honey bees.

Fig. 4 The flower visitors of Leiotulus aureus during the observation period: fam. Apidae (Apis mellifera - A), fam. Syrphidae (Episyrphus balteatus - B, Scaeva pyrastri - C, Sphaerophoria scripta - D), fam. Calliphoridae (Lucilia sp. – E), fam. Sarcophagidae (Sarcophaga sp. - F), fam. Bibionidae (Bibio sp. - G ), fam. Oedemeridae (Oedemera lurida - H), fam. Mordellidae (Mordella aculeata - I), fam. Melyridae (Malachius bipustulatus - J), fam. Miridae (Closterotomus sp. - K), fam. Pentatomidae (Graphosoma lineatum - L) among maturing fruits.
ABC-82-44-f4

During daytime, the average number of honey bees that visited each plant within a 5 minute interval was 2.0 ± 1.7. From 7 a.m. the frequency of honey bee visits increased reaching a maximum between 1-2 p.m., attaining 4.7 ± 1.5 bees per plant, followed by a decreasing tendency toward the evening and no visitors were recorded during the final observing period (7-8 p.m.) (Fig. 5). The average time a bee spent on the inflorescence amounted 6.06 ± 2.64 seconds (ranging from 3.57 ± 0.60 seconds at 7-8 a.m., to 9.47 ± 1.15 seconds at 1-2 p.m.).

The total number of umbels per visited plant averaged 6.3 ± 0.5 and average flower number per umbel amounted 34.4 ± 5.7. The percentage of visited umbels per plant during daytime had a pattern similar to that shown by the diurnal dynamics of honey-bee visiting frequency (Fig. 6), reaching a peak between 1 and 2 p.m., with decreasing tendency towards evening.

Fig. 5 Diurnal dynamics of honey bee visit frequency toLeiotulus aureus.
ABC-82-44-f5
Fig. 6 Percentage of visited umbels per plant during daytime (refers to honey bees). In some periods of the day these values exceed 100%, since it can happen that the same bee during foraging will visit some umbels more than once.
ABC-82-44-f6
Discussion

Pollen grains within the Apiaceaeare usually stenopalynous, radially symmetrical, isopolar and prolate to perprolate in shape (Erdtman 1971). Grains are commonly tricolporate with slit-like ectocolpi and very distinctive and broadband-like costae (Punt 1984,Perveen and Qaiser 2006). The tectum is commonly striate-rugulate or simple striate (Punt 1984), psilate to granulate (Perveen and Qaiser 2006). There are a few different criteria accepted for classification of the pollen grains of the Apiaceae. Various characters have been used, such as polar/equatorial ratio (P/E), exine pattern, etc. For example, Cerceau-Larrival (1962) proposed 5 pollen types occurring within the family based on shape index: sub-rhomboidal (type 1, P/E:1-1.5), sub-circular (type 2, P/E:1-1.5), oval (type 3, P/E:1.5-2), sub-rectangular (type 4, P/E:2), and equatorially constricted (type 5, P/E:over 2). According to this classification, pollen grains of L. aureus in the current study should fit into type 5. In addition, according to Van Zeist and Bottema (1977) the pollen grains of the Apiaceae could be divided into 9 pollen types: Anisosciadium, Bunium, Bupleurum, Eryngium, Ferula, Malabaila, Pimpinella, Sium erectum and Turgenia types. The pollen features characterizing the Malabaila type are as follows: subrectangular to slightly oval shape with rounded poles, P/E is 2, fairly long colpi, transversal furrow oval-rectangular, distinct columellae 0.5 to 0.8 μm in diameter, slight variations in the wall thickness (exine up to 2 μm thick), grain size ranging from 35 to 40 μm. This type comprises Malabaila secacul, M. kotschyi, Orlaya grandiflora, Heracleum maximum, H. lasiopetalum, H. persicum, Ormosciadium aucheri, Scandix iberica, Stenotaenia nudicaulis andTurgeniopsis foeniculacea. Recently, Orlaya has already been described as having its own pollen type (Beug 2015), while Malabaila secacul and M. kotschyi were transferred to genus Leiotulus (as L. secacul (Mill.) Pimenov & Ostr and L. kotschyi (Boiss.) Pimenov & Ostr.)) (Pimenov and Ostroumova 1994,POWO 2022). The results of palynomorphplogical research of L. aureus (which previously also belonged to Malabaila genus) are not completely in accordance with characters described for the Malabaila pollen type, such as P/E ratio and grain size, provided by Van Zeist and Bottema (1977). The pollen grains, described in the current paper, are slightly larger. It is known that the size may vary depending on the liquid medium used to mount samples on microslides for light microscopy (Faegri and Iversen 1989,Pospiech et al. 2021). However, the measurements of pollen size in the present paper are based on micrographs obtained by SEM, without using any mounting media which may cause enlargement of pollen grains. Extensive palynological research provided by Punt (1984), who recognized 50 types of pollen, as well as by Perveen and Qaiser (2006) who distinguished three pollen types based on tectum features within 27 Apiaceae genera, did not cover Malabaila/Leiotulus species.

The Apiaceae species have a uniform umbel and flower structure, however within the family diverse pollination systems occur varying from completely self-pollination to obligate cross-pollination (Koul et al. 1993). Flowers of umbellifers attract numerous insect taxa from several taxonomic orders supplying them with pollen and nectar (Niemirski and Zych 2011). Hence, umbellifers are often connected with generalized pollination system, indicating that their floral nectar is easily accessible to flower-visiting insects of different pollination efficiency due to the various degree of mouthpart modification for feeding on nectar, pollen or petals (Proctor et al. 1996,Olesen et al. 2007). These include mostly flies, but also hymenopterans and coleopterans (Proctor et al. 1996,Lamborn and Ollerton 2000,Zych 2007,Davila and Wardle 2008,Carvalheiro et al. 2008,Mačukanović-Jocić et al. 2016). In the current study, flowers of L. aureus, representing an open dish-shaped blossom type, were visited by twelve insect species from four taxonomic orders. With regard to the observed flower visitors, the following pollination types occurred: melittophily, myophily, sapromyophily and cantharophily. Dipterans were the most frequent group of visitors. Most of the recorded dipterans were of the “hoverfly type” (i.e. members of the family Syrphidae) and the “muscoid type” (i.e. members of the families Sarcophagidae (flesh flies) and Calliphoridae (blow flies)). Although not highly specialized in pollination, flower-pollinating species have been reported in the Bibionidae in previous research (Goldblatt et al. 2005). Adults of march flies (Bibionidae) are known as pollen-collecting and nectar feeding flower visitors pollinating fruit trees and some other crops (Freeman and Lane 1985,Woodcock et al. 2014). In the present study carrion flies were found to be less important from the pollination point of view, since Leiotulus is an aromatic plant more attractive to Apidae and Syrphidae. Despite a few Coleopteran species observed in the current and similar studies on umbellifers (Zych 2006), they are of minor importance as they are not considered to be efficient pollinators (Mačukanović-Jocić 2010). Hemipterans observed in this study could not be considered as pollinators, since their pollination activity is negligible, except in rare cases (Ishida et al. 2009). Unlike previous research on some other Apiaceae species (Zych 2006,Mačukanović-Jocić et al.2016), in the present study neither moths nor butterflies were observed visiting L. aureus umbels. Low visitation rate of lepidopterans can be explained by the length of their proboscis, which is more adapted to tubular corollas, or by weaker attractiveness of flowers which can be attributed to the scent or floral nectar components. L. aureus could be considered an ecologically generalized species in terms of the need for specialized pollinators. There are many reasons for this. Although L. aureus like many other umbellifers lack any visible or invisible floral signs such as honey guides leading to nectar, the flowers are slightly aromatic and could emit some chemical signals that attract specific groups of pollinators, as previously reported for this family (Tollsten et al.1994,Tollsten and Øvstedal 1994,Niemirski and Zych 2011). Regardless of their floral uniformity, some umbellifers are suggested to exhibit cryptic flower specialization enabling oligolectic relationships with bee pollinators (Lindsey 1984,Lindsey and Bell 1985,Niemirski and Zych 2011). Unlike Zych (2006) who did not observe any honey bee on Heracleum sphondylium, L. aureus flowers were very frequently visited, which is in line with the findings of other authors who pointed out the importance of honey bees in pollinating umbellifers (Langenberger and Davis 2002b,Davila and Wardle 2002). Following the diurnal dynamics of honey bee visits, plants were the most frequently visited about midday. Considering the frequency of honey bee visits L. aureus could be regarded as a melliferous plant contributing to honey bee pasture. However, regarding its rather “unspecialized” floral morphology and its being visited by numerous species of flower visitors, this plant species is without ecological specialization to particular insect species.

Acknowledgements

The authors express gratitude to Ivan Bošković for assistance in the fieldwork, as well as to Miloš Bokorov, graduate biologist, for performing SEM. The research is financed by Ministry of Education, Science and Technological Development, Republic of Serbia, Grant no. No: 451-03-68/2022-14/200116.

References

 

Ajani, Y.; Ajan, A.; Cordes, J.M.; Watson, M.F.; Downie, S.R. 2008: Phylogenetic analysis of nrDNA ITS sequences reveals relationships within five groups of Iranian Apiaceae subfamily Apioideae. Taxon 57, 383- 401.

 

Beug, J.-H. 2015: Leitfaden der Pollenbestimmung für Mitteleuropa und angrenzende Gebiete, 2nd Edition, Verlag Dr. Friedrich Pfeil, München.

 

Bouchard, P.; Bousquet, Y. Davies, A.E., Alonso-Zarazaga, M.A., Lawrence, J.F., Lyal, C.H.C., Newton, A.F., Reid, C.A.M., Schmitt, M., Ślipiński, S.A., Smith A.B.T. 2011: Family-group names in Coleoptera (Insecta). ZooKeys 88, 1- 972.

 

Carvalheiro, L.G.; Barbosa, E.R.M.; Memmott, J. 2008: Pollinator networks, alien species and the conservation of rare plants: Trinia glauca as a case study. Journal of Applied Ecology 45, 1419- 1427.

 

Cassis, G.; Schuh, R.T. 2012: Systematics, biodiversity, biogeography, and host associations of the Miridae (Insecta: Hemiptera: Heteroptera: Cimicomorpha). Annual Review of Entomology 57, 377- 404.

 

Cerceau-Larrival, M.T. 1962: Le pollen d'Ombellifères Méditerranéennes. Pollen et spores 4, 955- 104.

 

Cerceau-Larrival, M.T. 1981: World Pollen and Spore Flora 9. Umbelliferae Juss. Hydrocotyloideae Drude/Hydrocotyleae Drude. Almqvist and Wiksell, Stockholm.

 

Dafni, H.; Lenski, Y.; Fahn, A. 1988: Flower and nectar characteristics of nine species of Labiatae and their influence on honeybee visits. Journal of Apicultural Research 27, l03- 114.

 

Davila, Y.C.; Wardle, G.M. 2002: Reproductive ecology of the Australian herb Trachymene incisa subsp incisa (Apiaceae). Australian Journal of Botany 50, 619- 626.

 

Davila, Y.C.; Wardle, G.M. 2008: Variation in native pollinators in the absence of honeybees: implications for reproductive success of an Australian generalist pollinated herb Trachymene incia (Apiaceae). Botanical Journal of the Linnean Society 156, 479- 490.

 

Downie, S.R.; Spalik, K.; Katz-Downie, D.S.; Reduron, J.-P. 2010: Major clades within Apiaceae subfamily Apioideae as inferred by phylogenetic analysis of nrDNA ITS sequences. Plant Diversity and Evolution 128, 111- 136.

 

Dustmann, JH.; von Der Ohe, K. 1993: Scanning electron microscopic studies on pollen from honey IV Surface pattern of pollen of Sapium sebiferum and Euphorbia spp (Euphorbiaceae) . Apidologie 24, 59- 66.

 

Erdtman, G. 1971: Pollen morphology and plant taxonomy (Angiosperms). Hafner Publishing Company, New York.

 

Faegri, K.; Iversen, J. 1989: Textbook of pollen analysis. In: Faegri, K.; Kakand, P.E.; Krzywinski, K. (eds.), 4th Edition. John Wiley and Sons, Chichester.

 

Freeman, P.; , Lane, R.P., , authors. 1985: Bibionid and scatopsid flies. Diptera: Bibionidae & Scatopsidae. Handbook for the Identification of British Insects 9/7: 1–74.

 

Goldblatt, P.; Manning, J.C.; Bernhardt, P. 2005: Observations on the floral biology of Melasphaerula (Iridaceae): Is this monotypic genus pollinated by march flies (Diptera: Bibionidae)? Annals of the Missouri Botanical Garden 92, 268- 274.

 

Ishida, C.; Kono, M.; Sakai, S. 2009: A new pollination system: brood-site pollination by flower bugs in Macaranga (Euphorbiaceae). Annals of Botany 103, 39- 44.

 

Koul, P.; Sharma, N.; Koul, A.K. 1993: Pollination biology of Apiaceae. Current Science 65, 219- 222.

 

Lamborn, E.; Ollerton, J. 2000: Experimental assessment of the functional morphology of inflorescences of Daucus carota (Apiaceae): testing the ‘fly catcher effect’. Functional Ecology 14, 445- 454.

 

Langenberger, M.W.; Davis, A.R. 2002a: Temporal changes in floral nectar production, reabsorption, and composition associated with dichogamy in annual caraway (Carum carvi, Apiaceae). American Journal of Botany 89, 1588- 1598.

 

Langenberger, M.W.; Davis, A.R. 2002b: Honey bee pollen foraging in relation to flowering phenology of biennial caraway (Carum carvi L ). Canadian Journal of Plant Science 82, 203- 215.

 

Lindsey, A.H. 1984: Reproductive biology of Apiaceae I Floral visitors to Thaspium and Zizia and their importance in pollination. American Journal of Botany 71, 375- 387.

 

Lindsey, A.H.; Bell, C.R. 1985: Reproductive biology of Apiaceae II Cryptic specialization and floral evolution in Thaspium and Zizia. American Journal of Botany 72, 231- 247.

 

Lupoli, R. 2017: Graphosoma lineatum (L , 1758) and G italicum (O F Müller, 1766), two valid and distinct species, probably derived from the Zanclean mediterranean transgression (Hemiptera Pentatomidae). L'Entomologiste 73, 19- 33.

 

Mačukanović-Jocić, M. 2010: The Biology of Melliferous Plants with an Atlas of Serbian Apiflora. Monographic Study. Faculty of Agriculture University of Belgrade, Belgrade.

 

Mačukanović-Jocić, M.; Stešević, D.; Rančić, D.; Dajić Stevanović, Z. 2016: Pollen morphology and the flower visitors of Chaerophyllum coloratum L. (Apiaceae), Acta Botanica Croatica 76, 1- 8.

 

Menemen, Y.; Jury, S. 2001: A systematic study of the genus Malabaila Hoffm. (Umbelliferae) comparing with the closely related genera. In: Gozukkimizi, N. (ed.), The Proceedings of the 2nd Balkan Botanical Congress, 299- 312. Marmara University, Istanbul.

 

Niemirski, R.; Zych, M. 2011: Fly pollination of dichogamous Angelica sylvestris (Apiaceae): How (functionally) specialized can a (morphologically) generalized plant be? Plant Systematics and Evolution 2294, 147- 158.

 

Olesen, J.M.; Bascompte, J.; Dupont, Y.L.; Jordano, P. 2007: The modularity of pollination networks. Proceedings of the National Academy of Sciences of the United States of America 104, 19891- 19896.

 

Oosterbroek, P. 2006: The European families of the Diptera: identification, diagnosis, biology Utrecht: KNNV, Publishing. 205. pp.

 

Perveen, A.; Qaiser, M. 2006: Pollen Flora of Pakistan XLVIII Umbelliferae. Pakistan Journal of Botany 38, 1- 14.

 

Pimenov, M.; Ostroumova, T. 1994: The genus Malabaila Hoffm (Umbelliferae:Tordylieae): A carpological investigation and taxonomic implication. Feddes Repertorium 105, 141- 155.

 

Pospiech M, Javůrková Z, Hrabec P, Pospiech M, Ljasovská S, Bednář J 2021: Identification of pollen taxa by different microscopy techniques. PLoS One 16(9), e0256808.

 

POWO 2022: Plants of the World Online. Facilitated by the Royal Botanic Gardens, Kew. Retrived 19 September 2022 from http://www.plantsoftheworldonline.org/ .

 

Proctor, M.; Yeo, P.; Lack, A. 1996: The natural history of pollination. HarperCollins Publishers, London, UK.

 

Punt, W. 1984: The Northwest European Pollen Flora, 37 Umbelliferae. Review of Palaeobotany and Palynology 42, 155- 364.

 

Punt. W., Hoen, P.P., Blackmore, S., Nilsson, S., Le Thomas 2007: Glossary of pollen and spore terminology. Review of Palaeobotany and Palynology 143, 1- 81.

 

Rovira, A.M.; Bosch, M.; Molero, J.; Blanche, C. 2002: Pollination ecology and breeding system of the very narrow coastal endemic Seseli farrenyi (Apiaceae) Effects of population fragmentation. Nordic Journal of Botany 22, 727- 740.

 

Sivell, O., , author. 2021: Blow flies (Diptera: Calliphoridae, Polleniidae, Rhiniidae). Handbook for the Identification of British Insects 10/16, 1–206.

 

Tollsten, L.; Knudsen, J.T.; Bergström, LG. 1994: Floral scent in generalistic Angelica (Apiaceae) — an adaptive character. Biochemical Systematics and Ecology 22, 161- 169.

 

Tollsten, L.; Øvstedal, D.O. 1994: Differentiation in floral scent chemistry among populations of Conopodium majus (Apiaceae). Nordic Journal of Botany 14, 361- 368.

 

Tutin, T.G.; Heywood, V.H.; Burges, N.A.; Moore, D.M.; Valentine, D.H.; Walters, S.M.; Webb, D.A. 1981: Flora Europaea. Volume 2. Rosaceae to Umbelliferae (3rd ed.). Cambridge University Press, Cambridge.

 

Van Veen, M.P. 2004: Hoverflies of Northwest Europe, Identification Keys to the Syrphidae (Hardback). KNNV Publishing, Utrecht.

 

Van Zeist, W.; Bottema, S. 1977: Palynological investigation in western Iran. Paleohistoria 19, 19- 85.

 

Vazquez, X. A. 2002: European Fauna of Oedemeridae. Argania editio, Barcelona.

 

Woodcock, T.S.; Larson, B.M.H.; Kevan, P.G.; Inouye, D.W.; Lunau, K. 2014: Flies and flowers II: floral attractants and rewards. Journal of Plant Ecology 12, 63- 94.

 

Wróblewska, A. 1993: Flowering and pollen value of selected species of umbelliferous family - Umbelliferae Juss (Apiaceae Lindl ) in Lublin region Part II Pollen efficiency and insect visit Acta Agrobotanica 46, 51- 65, (in Polish).

 

Zych, M. 2006: Diurnal activity of the key pollinators of Heracleum sphondylium L (Apiaceae). Acta Agrobotanica 59, 279- 288.

 

Zych, M. 2007: On flower visitors and true pollinators: The case of protoandrous Heracleum spondylium L. (Apiaceae), Plant Systematics and Evolution 263, 159- 179.


This display is generated from NISO JATS XML with jats-html.xsl. The XSLT engine is libxslt.