Further studies of the sieve-element plastids of theCaryophyllales includingBarbeuia,Corrigiola, Lyallia,Microtea, Sarcobatus,andTelephium

The sieve-element plastids of 69 species of theCaryophyllales were investigated by transmission electron microscopy. All contained the specific subtype-P3 plastids characterized by a peripheral ring of protein filaments. The presence or absence of an additional central protein crystal and their shape being either polygonal or globular as well as the average sizes of the sieve-element plastids are useful features in the characterization of some families.—Barbeuia contains sieve-element plastids that confirm its placement within thePhytolaccaceae. Lyallia differs fromHectorella by including small starch grains in their sieve-element plastids, which otherwise by their globular crystals negate a closer connection to theCaryophyllaceae. The lack of a central protein crystal in its form-P3fs plastids placesMicrotea best within theChenopodiaceae. Sarcobatus, a so far uncontested member of theChenopodiaceae, contains form-P3cf plastids, i.e., including a central crystal not found elsewhere in this family.Telephium andCorrigiola, shifted back and forth betweenMolluginaceae andCaryophyllaceae, have form-P3cf(s) plastids with a polygonal crystal which favor their placement within theCaryophyllaceae.     

S-type sieve-element plastids and anthocyanins inVivianiaceae: Evidence against its inclusion intoCentrospermae

The presence of S-type sieve-element plastids and anthocyanins in theVivianiaceae indicates that it is not a member ofCentrospermae (Caryophyllales).     

Elektronenmikroskopische Untersuchungen zur Frage der verwandtschaftlichen Beziehungen zwischenTheligonum undRubiaceae: Feinbau der Siebelement-Plastiden und Anmerkungen zur Struktur der Pollenexine

Theligonum cynocrambe and 13 species ofRubiaceae contain S-type sieve-element plastids, wide-spread in Dicotyledons. Alignment ofTheligonum toCaryophyllales (Centrospermae), especiallyPhytolaccaceae, is unlikely, because this order is characterized by specific P-type plastids. SEM investigations show the pollen exine ofTheligonum to be microreticulate, with additional supratectate spinules.Asperula and other genera of the tribeRubieae have a tectum perforatum (punctitegillate sexine), also with supratectate verrucae or spinulae.—Thus ultrastructure suggests (but not definitely proves) relationships betweenTheligonum andRubiaceae, while affinities betweenTheligonum andCaryophyllales are excluded.

     

Classical morphological features of centrospermous families

The orderCentrospermae (Caryophyllales, Chenopodiales) as treated inA. Englers Syllabus, 12th edition (1964), is compared with several other modern and older systems with the result that no less than 11–13 (and more) families are considered to be centrospermous in the strict sense; to these may be added thePolygonales and, doubtfully, thePlumbaginales andBatidales. As indicated by their name Centrospermae their main character is the central or basal placentation in combination with campylotropy (or amphitropy) of the ovules, seeds with perisperm, and coiled or curved embryos in peripheral position. Other outstanding features are found in the embryology; the ovules are bitegmic-crassinucellate, a nucellar cap is present, as well as an endostome and air spaces; the pollen is trinucleate. Anomalous secondary thickening in stems and roots often occurs. The pollen morphology, specific P-type sieve-element plastids, and the presence or absence of betalains are also important characters. Other floral features, especially the structure of the gynoecium, the androecium, the perianth and the receptacle, as well as the morphology of the inflorescences are of taxonomic importance. The putative relationships of theCaryophyllidae can perhaps best be resolved on the basis of more detailed morphological investigations (e.g. the so-called apocarpy, the development of the androecium, the pollen morphology, chromosome numbers, etc.).Presented in the Symposium Evolution of Centrospermous Families, during the XIIth International Botanical Congress, Leningrad, July 8, 1975.     

Sieve-element plastids,exine sculpturing and the systematic affinities of theBuxaceae

The sieve-element plastids of members of several genera in theBuxaceae (Buxus, Pachysandra andSarcococca) were found to be of the specific subtype PVI, which contains a central globular protein crystal.Simmondsia (Simmondsiaceae) andDaphniphyllum (Daphniphyllaceae), on the other hand, were found to contain S-type sieve-element plastids. The occurrence of the highly restricted PVI plastids in theBuxaceae mitigates against a close relationship between theBuxaceae andSimmondsia, Daphniphyllum andEuphorbiaceae. Exine sculpturing of theBuxaceae andSimmondsiaceae also shows no close similarities. Both of these EM characters are discussed in connection with other available data and with respect to earlier systematic treatment of these families.     

Contributions to the knowledge of sieve-element plastids inGunneraceae and allied families

P-type sieve-element plastids were found in theGunneraceae, while S-type plastids are present in theHaloragaceae andHippuridaceae. The specific characters of the sieve-element plastids (e.g., their size and the morphology of their contents) are discussed in relation to other taxa of theRosidae containing P-type plastids and to the systematic position of theGunneraceae. Contributions to the Knowledge of P-Type Sieve-Element Plastids in Dicotyledons, III. — For other parts of this series see (I.:)Behnke (1982 b) and (II.:)Behnke (1985).     

Sieve-element plastids ofGymnospermae: Their ultrastructure in relation to systematics

The distribution of S-type and P-type plastids in the sieve elements of 30 species from 13 families of theConiferophytina andCycadophytina is recorded, of which 21 species were studied for the first time with respect to their sieve-element plastids. While starch storing S-type plastids are the most commonly occurring type throughout both taxa, all thePinaceae examined (11 species of 7 genera) contain P-type plastids characterized by a peripheral, ring-shaped bundle of protein filaments, an additional protein crystalloid, and several starch grains. Starch grains of sieve-element plastids in theConiferophytina andCycadophytina are commonly club-shaped. Taxonomic implications of these ultrastructural findings on sieve-element plastids are discussed.     

P-type sieve-element plastids present in members of the tribesTriplareae andCoccolobeae (Polygonaceae) renew the links between thePolygonales and theCaryophyllales

Form-Pfs sieve-element plastids were found inTriplaris, Ruprechtia, andCoccoloba (Polygonaceae) while other genera of the family and those studied from the often associatedPlumbaginaceae contain S-type sieve-element plastids. The rareness of form-Pfs plastids among the angiosperms, their similarity to the peculiar form-P3fs plastids of theChenopodiineae, and the comparatively small plastid diameters measured for all forms present in theCaryophyllales, Polygonales, andPlumbaginales suggest close relationships between these taxa. The restriction inPolygonaceae of form-Pfs plastids to the closely allied tribesTriplareae andCoccolobeae is discussed with regard to both the intrafamilial and ordinal phylogeny, and also considering possible connections to the only magnoliidaean Pfs-taxonCanella. Dedicated to Univ.-Prof. DrF. Ehrendorfer on the occasion of his 70th birthday.     

P-type sieve-element plastids and the systematics of theArales (sensuCronquist 1988)—with S-type plastids inPistia

The sieve-element plastids of 126 species of theArales were investigated by transmission electron microscopy. With the exception ofPistia (with S-type plastids) all contained the monocotyledon specific subtype-P2 plastids characterized by cuneate protein crystals. While the species studied from bothAcoraceae andLemnaceae have form-P2c plastids (i.e., with cuneate crystals only), those of theAraceae belong to either form P2c (14 species), P2cs (the great majority) or P2cfs (Monstera deliciosa, only, with form-P2cs plastids in the otherMonstera species studied). The form-P2cs plastids of theAraceae are grouped into different categories according to the quantity and quality of their protein and starch contents. The subfamilyLasioideae is redefined to comprise all aroid P2c-taxa and those P2cs-genera that contain only one or very few starch grains. Only little starch is also recorded in the sieve-element plastids ofGymnostachys (Gymnostachydoideae), with the other plastid data denying a close relationship toAcorus. While equal amounts of starch and protein are generally present in sieve-element plastids of the subfamiliesPothoideae, Monsteroideae, Colocasioideae, Philodendroideae, andAroideae, maximum starch content and only very few protein crystals are found in form-P2cs plastids ofCalla (Calloideae),Ariopsis (Aroideae), andRemusatia (Colocasioideae?). In the latter, both morphology and size of sieve-element plastids are close to those ofPistia.—In theAraceae the diameters of the sieve-element plastids exhibit a great size range, but are consistent within a species and within a defined part of the plant body. Comparative data are mainly available for stem and petiole sieve-element plastids.—The accumulated data are used to suggest an affiliation of the species to subfamilies and to discuss the phylogeny of theArales. Forms and sizes of their plastids support a separation of bothAcoraceae andLemnaceae from theAraceae. The presence of S-type plastids inPistia does not favour direct and close relationships to the form-P2c genusLemna.—The prevailing form-P2cs plastids might support proposals that place theArales (together with also form-P2cs plastid containingDioscoreales) in the neighbourhood of basal dicotyledons. BesidesAsarum andSaruma (Aristolochiaceae), with monocotyledonous form-P2c plastids,Pistia (with dicotyledonous S-type plastids) gives another example for a link between the two angiosperm classes.     

Zur Skulptur der Pollen-Exine bei drei Centrospermen (Gisekia,Limeum, Hectorella), bei Gyrostemonaceen und Rhabdodendraceen

The exine-sculpturing of pollen fromGisekia africana (Gisekiaceae),Limeum argute-carinatum (Molluginaceae) andHectorella caespitosa (Hectorellaceae) with supratectate spinulae and an anulopunctate tectum is in accordance with the manyCentrospermae investigated so far with the SEM. Pollen ofRhabdodendron macrophyllum and three species fromGyrostemonaceae do not exhibit these surface details. WhileRhabdodendron with a finely reticulate exine probably fits intoRutaceae, the unique columellaless exine ofGyrostemonaceae has no direct counterpart, neither inCentrospermae nor inCapparales, the two orders to which this family was allied. The genera ofGyrostemonaceae can be distinguished by different arrangements of minute pollen surface details.

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Zur Skulptur der Pollen-Exine bei drei Centrospermen (Gisekia, Limeum, Hectorella), bei Gyrostemonaceen und Rhabdodendraceen

     

Flavonoids of some controversial members of theCaryophyllales (Centrospermae)

The absence or occurrence of C-glycolsylflavonoids in theAizoaceae andMolluginaceae, respectively, has been utilized to classify several controversial genera of centrospermous plants that have previously been placed in different families by systematists. The presence of these compounds in several further species of theMolluginaceae is reported. Their anomalous presence inGliscrothamnus (Aizoaceae) is discussed.     

Pigment dichotomy and DNA-RNA hybridization data for centrospermous families

The structural types, biogenesis and distribution of betalains and anthocyanins in centrospermous families are reviewed. The implications of the pigment and DNA-RNA hybridization data, along with other evidence, are discussed with respect to the view that the evolutionary line of centrospermous families contains eleven basic or core families of which nine produce betalains and two, theCaryophyllaceae andMolluginaceae, produce anthocyanins; it is suggested that the betalain and anthocyanin families developed from a common ancestor at a time prior to the widespread occurrence of floral pigments in angiosperms.Presented in the Symposium Evolution of Centrospermous Families, during the XIIth International Botanical Congress, Leningrad, July 8, 1975.     

ThePenicillium chrysogenum andAspergillus nidulans wetA developmental regulatory genes are functionally equivalent

Aspergillus nidulans andPenicillium chrysogenum are related fungi that reproduce asexually by forming multicellular conidiophores and uninucleate conidia. InA. nidulans, spore maturation is controlled by thewetA (AwetA) regulatory gene. We cloned a homologous gene (PwetA) fromP. chrysogenum to determine if spore maturation is regulated by a similar mechanism in this species. ThePwetA andAwetA genes are similar in structure and functional organization. The inferred polypeptides share 77% overall amino acid sequence similarity, with several regions having > 85% similarity. The genes also had significant, local sequence similarities in their 5 flanking regions, including conserved binding sites for the product of the regulatory geneabaA.PwetA fully complemented anA. nidulans wetA deletion mutation, demonstrating thatPwetA and its 5 regulatory sequences function normally inA. nidulans. These results indicate that the mechanisms controlling sporulation inA. nidulans andP. chrysogenum are evolutionarily conserved.     

Ultrastructural,micromorphological and phytochemical evidence for a “Central Position” ofMacarthuria (Molluginaceae) within theCaryophyllales

Subtype PIII sieve-element plastids, anthocyanins, spinulose, perforate-tectate pollen grains and the specific seed-coat sculpturing found in twoMacarthuria species (M. australis, M. neocambrica) consolidate their placement withinMolluginaceae. The unique form of the sieve-element plastids, i.e. with cubic crystals and starch grains (PIIIc″fs), finds its closest counter-part inLimeum. The multiple intertwinement of different genera of theMolluginaceae with many other centrospermous families led to a consideration of their more central position withinCaryophyllales.     

Chromosome numbers and differentiation of centrospermous families

The patterns of variation of chromosome numbers in theCentrospermae suggest a common ancestry of centrospermous anthocyanin and betalain families. Phylogenetic divergence in the order may have originated with progenitors similar to extantMolluginaceae, Aizoaceae orPhytolaccaceae taxa with x = 9. Evolutionary radiation and advancement in several lines then seems to have been paralleled by trends for increasing chromosome base numbers through dysploidy and polyploidy, e.g. towardsCaryophyllaceae, Portulacaceae-Basellaceae, Hectorellaceae, Cactaceae, Didieraceae, Nyctaginaceae andChenopodiaceae-Amaranthaceae. Presented in the Symposium Evolution of Centrospermous Families, during the XIIth International Botanical Congress, Leningrad, July 8, 1975.     

Sieve-element plastids ofTriticum andAegilops (Poaceae)

Fourteen taxa of the Triticum-Aegilops group have been investigated for their sieve-element plastids. At maturity they contain dense and thin crystalloid inclusions and are classified into the PIIc' plastid type; onlyAe. comosa var.biaristata lacked the thin crystalloids and thus conforms to the PII c type. The proteinaceous nature of the crystalloids was demonstrated by application of proteolytic enzymes. Ultrastructural evidence suggests that both kinds of crystalloid inclusions are involved in the sealing of sieve-plate pores of injured sieve tubes. Measurements and calculations of the spacings and angles carried out on crystalloid prints permitted the construction of a two- and three-dimensional pattern forT. aestivum thin crystalloids.     

Eine blütenmorphologische Analyse derLagoecieae (Apiaceae)

An analysis of the morphology, anatomy and ontogeny of the flowers, particularly of the gynoecium ofLagoecieae is presented. 1. The gynoecial model of angiosperms can be applied to all three generaArctopus, Lagoecia andPetagnia. 2. In the case ofArctopus an additional Apikalseptum is developed. 3. In the synascidiate region of the gynoecium the adaxial carpel is reduced inArctopus andPetagnia, the abaxial inLagoecia. 4. The reduced carpel produces either one mature ovule inArctopus, a rudimentary ovule inPetagnia, or none inLagoecia. 5.Petagnia andLagoecia have a completely pseudomonomerous gynoecium. 6.Arctopus displays many flower characteristics which lack in theSaniculoideae but occur in theHydrocotyloideae. 7. ForPetagnia andLagoecia an independent phylogenetic development within theSaniculoideae is assumed.

Herrn Univ.-Prof. Dr.Walter Leinfellner zum 70. Geburtstag gewidmet.     

Sieve-element plastids and evolution of monocotyledons, with emphasis on Melanthiaceae sensu lato and Aristolochiaceae-Asaroideae, a putative dicotyledon sister group

Monocotyledons are distinguishable from dicotyledons by their subtype P2 sieve-element plastids containing cuneate protein crystals, a synapomorphic character uniformly present from basal groups through Lilioids to Commelinoids. The dicotyledon generaAsarum andSaruma (Aristolochiaceae-Asaroideae) are the only other taxa with cuneate crystals, but their sieveelement plastids include an additional large polygonal crystal, as is typical of many eumagnoliids. New investigations in Melanthiaceae s.l. revealed the same pattern (polygonal plus cuneate crystals) in the sieve-element plastids ofJaponolirion osense (Japonoliriaceae/Petrosaviaceae), ofHarperocallis flava, Pleea tenuifolia, andTofleldia (all: Tofieldiaceae). InNarthecium ossifragum a large crystal, present in addition to cuneate ones, usually breaks up into several small crystals, whereas inAletris glabra andLophiola americana (Nartheciaceae) and in all of the 15 species studied and belonging to Melanthiaceae s.str. only cuneate crystals are found. Highresolution TEM pictures reveal a crystal substructure that is densely packed in both cuneate and polygonal forms, but in Tofieldiaceae the polygonal crystals stain less densely, probably as a result of the slightly wider spacing of their subunits. The small crystals ofNarthecium are “loose”; that is, much more widely spaced. Such “loose” crystals are commonly found in sieve-element plastids of Velloziaceae, present there in addition to angular crystals, and together with cuneate crystals in a few Lilioids and many taxa of Poales (Commelinoids). Ontogenetic studies of the sieve elements ofSaruma, Aristolochia, and several monocotyledons have shown that in their plastids cuneate crystals develop very early and independent from a polygonal one present in some taxa. Therefore, a conceivable particulation of polygonal into cuneate crystals is excluded. Consequently, mutations of some monocotyledons that contain a lone, large, polygonal crystal in their sieve-element plastids are explained as the result of a complex genetic block. The total result of all studies in sieve-element plastids suggests thatJaponolirion and Tofieldiaceae are the most basal monocotyledons and that Aristolochiaceae are their dicotyledon sister group.     

Phylogeny and divergence of basal angiosperms inferred from<Emphasis Type="Italic"> APETALA3</Emphasis>- and<Emphasis Type="Italic"> PISTILLATA</Emphasis>-like MADS-box genes

The B-class MADS-box genes composed of APETALA3 (AP3) and PISTILLATA (PI) lineages play an important role in petal and stamen identity in previously studied flowering plants. We investigated the diversification of the AP3-like and PI-like MADS-box genes of eight species in five basal angiosperm families: Amborella trichopoda (Amborellaceae); Brasenia schreberi and Cabomba caroliniana (Cabombaceae); Euryale ferox, Nuphar japonicum, and Nymphaea tetragona (Nymphaeaceae); Illicium anisatum (Illiciaceae); and Kadsura japonica (Schisandraceae). Sequence analysis showed that a four amino acid deletion in the K domain, which was found in all previously reported angiosperm PI genes, exists in a PI homologue of Schisandraceae, but not in six PI homologues of the Amborellaceae, Cabombaceae, and Nymphaeaceae, suggesting that the Amborellaceae, Cabombaceae, and Nymphaeaceae are basalmost lineages in angiosperms. The results of molecular phylogenetic analyses were not inconsistent with this hypothesis. The AP3 and PI homologues from Amborella share a sequence of five amino acids in the 5 region of exon 7. Using the linearized tree and likelihood methods, the divergence time between the AP3 and PI lineages was estimated as somewhere between immediately after to several tens of millions of years after the split between angiosperms and extant gymnosperms. Estimates of the age of the most recent common ancestor of all extant angiosperms range from ~140–210 Ma, depending on the trees used and assumptions made.     

Accumulation of seed storage proteins and the taxonomy ofPoaceae

The accumulation of specific seed proteins is a taxonomically valuable feature and can be used to additionally characterize plant taxa. To date, mainly crop proteins have been analysed in thePoaceae. In this investigation seed proteins from 147 species were screened with emphasis on legumin-like proteins and prolamins. The groups resulting from evaluation of the protein profiles correspond with well-known subfamilies and tribes.Panicoideae are clearly separated fromPooideae. WithinPooideae, theBromeae plusTriticeae tribes revealed obvious similarities.Lolium, Festuca andVulpia, generally included in the tribeFestuceae, revealed a protein profile similar to the profile of theBromeae/Triticeae. Legumin-like proteins are accumulated abundantly inBambusoideae andPooideae exceptBromeae/Triticeae, however, only the species included in theAveninae subtribe produce soluble (globulin-type) legumins as already known fromAvena sativa. Dedicated to emer. Univ.-Prof. DrFriedrich Ehrendorfer on the occasion of his 70th birthday