Notes onDiphucephala affinis (Coleoptera:Scarabaeidae) associated with flowers ofHibbertia andAcacia in Western Australia

Notes are provided on the association of the beetleDiphucephala affinis (Scarabaeidae) with yellow flowers ofHibbertia hypericoides, H. huegelii (Dilleniaceae),Acacia pulchella, andA. stenoptera (Mimosaceae). Observations were undertaken during September 9–19, 1979 at S. Perth, Western Australia. They indicated thatD. affinis is not a pollinator ofHibbertia as suggested in the literature, but may play a small role in the pollination of someAcacia species.     

Bee-pollination inHibbertia fasciculata (Dilleniaceae)

In direct contrast to mostHibbertia spp., the flowers ofH. fasciculata R. Br. ex D. C. bear only a single whorl of stamens and these stamens are arranged separately (not in typical bundles). The short filaments are appressed to the three carpels so that the inflated, porose and introrsive anthers form a centralized cluster obscuring the three ovaries. The three slender styles emerge at right angles from between the filaments. These styles curve upward and the stigmas form the three points of a triangle; each stigma is approximately one millimeter outside the centralized cluster of anthers. The flowers are nectarless and bear a bright yellow corolla. A pungent and unpleasant fragrance appears to be concentrated within the pollenkitt. When native bees attempt to forage for the pollen, within the cluster of anthers, the ventrally deposited loads of pollen, on the bees' abdomens, contact the outer triangle of stigmas. The major pollinators ofH. fasciculata are female bees in the polylectic genera,Lasioglossum (subgenusChilalictus, Halictidae) andLeioproctus (Colletidae). These bees carry an average of more than two pollen taxa when they are caught foraging onH. fasciculata. 78% of the 47 bees, captured onH. fasciculata carried the pollen from at least one sympatric taxon bearing nectariferous flowers (e.g., genera in theMyrtaceae, Compositae, andEpacridaceae). The pollination biology ofH. fasciculata is assessed in relation to the known radiation of bee-pollinated flowers in the genusHibbertia, and within theDilleniaceae s. l.     

The pollination biology ofHibbertia stricta (Dilleniaceae)

The exines of pollen grains ofHibbertia stricta (DC.)R. Br. exF. Muell. (Sect.Pleurandra) wear an oily, yellow pollen coat that stains positively for lipids. The pollen is collected by asocial bees, exclusively. The most common floral foragers are members of the genusLasioglossum (subgenusChilalictus;Halictidae) and they harvest pollen via thoracic vibration. As these bees cling to the inflated anthers their pollen smeared bodies come in contact with either of the two wet, nonpapillate stigmas. The stigmas respond positively to cytochemical tests for the presence of esterase immediately following expansion of the corolla, indicating the effective pollination period. The foraging patterns of the bees are narrowly to broadly polylectic. AsH. stricta flowers are nectarless, it is not surprising that bees bearing mixed pollen loads always carry the pollen of at least one nectariferous, coblooming plant. The pollination biology ofH. stricta is compared with otherHibbertia spp. and with pollen flowers in general.     

Chromosome numbers of Western Australian species ofVillarsia (Menyanthaceae)

Chromosome numbers are reported for eight of the nine Western AustralianVillarsia species.Villarsia albiflora, V. calthifolia, V. capitata, V. congestiflora, V. lasiosperma, V. latifolia, andV. violifolia are diploid with n=9. Five populations ofV. parnassiifolia are diploid and three are tetraploid (n=18). The morphological, ecological, and breeding-system diversity of the Western Australian species is largely not associated with the tetraploidy or hexaploidy that characterizes otherVillarsia species in eastern Australia and South Africa. The majority of Western AustralianVillarsia species are restricted to the high rainfall zone of southwestern Western Australia, where favorable climatic and edaphic conditions may have existed since mid-late Tertiary times.     

Open dichotomous venation in the leaves ofUtricularia striatula (Lentibulariaceae)

The open dichotomous pattern of venation in the leaves ofUtricularia striatula is described in detail and compared withCircaeaster andKingdonia. Similar traits of dichotomous venation occur in other species ofUtricularia and may be due to reduction.Studies on IndianUtricularia, 3.     

Floral development and systematics ofCistaceae

The floral development of representatives of six genera ofCistaceae has been studied. Calyx development involves the formation of a ring primordium in several taxa. Androecium development in species with intermediate or higher stamen numbers starts with the formation of a ring meristem on which the stamens are initiated in a centrifugal direction. In many taxa five alternipetalous leading stamen primordia can be observed. In the apetalous (cleistogamous) flowers ofTuberaria inconspicua androecium development appears to be unordered; this is probably due to the lack of petals. InLechea intermedia (also cleistogamous) the corolla is trimerous and three complex stamen primordia are produced, which give rise either to one or three stamens. Relationships withinCistaceae are discussed. Floral development inCistaceae is compared with that in otherMalvanae. Among the eight families ofMalvanae from which information on floral development is availableCochlospermaceae andBixaceae exhibit the greatest similarities toCistaceae. InCistaceae the leading stamen primordia are alternipetalous. InBixa the same condition seems to be present. InMalvales s. str. mostTiliaceae also show earliest stamen initiation in alternipetalous sectors, whereas the stamens of the innermost alternipetalous position are retarded early or even suppressed inSterculiaceae, Bombacaceae, andMalvaceae. WithinMalvales s. str. the diversity of androecial developmental patterns seems to decrease inBombacaceae andMalvaceae due to increasing synorganization in the mature androecium. The derivation of polyandry inMalvanae from diplo- or obdiplostemony is discussed by comparison with the sister clades ofMalvanae as shown in recentrbcL studies (i.e.Sapindales, Rutales, the glucosinolate producing clade, andMyrtales).     

Flavonoids ofBignoniaceae from the “cerrado” and their possible taxonomic significance

Flavones and glycosides of flavones and flavonols were obtained from leaves of five species ofBignoniaceae from the cerrado, a savanna ecosystem of Central and Southeast Brazil. A predominance of flavonol glycosides was observed in all samples investigated. Flavones were often found in species of tribeTecomeae and rarely inBignonieae. The species of the former yielded derivatives of 6-hydroxyluteolin. No 6-oxygenated compounds were found in species ofBignonieae. The results point to the flavonoid chemistry evolution ofBignoniaceae following a path of simplification. More complex chemical profiles characterize the more woodyTecomeae rather than the more advancedBignonieae.     

Systematic implications of the flavonoids and chromosomes ofFlyriella (Compositae—Eupatorieae)

The leaves of five species ofFlyriella were found to contain from one to four glycosides of quercetin and its 4- and 7,4-methyl ethers. These patterns are distinct from those observed for more than seventy species ofBrickellia and support morphological and chromosomal data which indicate thatFlyriella should not be treated as an element ofBrickellia. Alternative treatments are briefly considered.     

广西油茶人工林林下植物多样性区域变化规律

为揭示广西油茶林植物多样性的区域变化规律,以广西7个区域具代表性的油茶林为研究对象,采用典型抽样法,对油茶林林下植被进行了调查,并对比分析了群落物种组成、结构特征和物种多样性。结果表明:(1)油茶林林下植被灌草层科数、属数、种数最多的是三江县油茶林(SJ)、较少的是巴马县油茶林(BM)和来宾市油茶林(LB);除巴马县油茶林(BM)灌木层优势种为共有种,其他区域油茶林的灌木层、草本层优势种均为交叉种。(2)多样性指数方面灌木层仅Margalef指数差异显著,草本层Margalef指数、Simpson指数、Shannon-Wiener指数差异显著。(3)通过回归分析,纬度与灌木层(单一种数量)、草本层(科数、属数、种数、单一种数量)以及总数量(属数、种数)、年均温度与草本层(科数、属数、种数、单一种数量)、有效积温与草本层(属数、种数、单一种数量)、年均降雨量与灌木层单一种数量之间的趋势模拟呈二次曲线关系。(4)不同区域油茶林物种相似性不高,通过相似系数矩阵进行聚类分析三江县油茶林(SJ)、贺州市八步区油茶林(HZ)、岑溪市软枝油茶种子园油茶林(CX)、南宁市油茶林(NN)为一类,凤山县油茶林(FS)、巴马县油茶林(BM)和来宾市油茶林(LB)为一类。广西油茶人工林林下植物多样性的区域变化规律可能与不同区域的生境异质性有关。     

Karyosystematics and evolution of AustralianAnnonaceae as compared withEupomatiaceae,Himantandraceae, andAustrobaileyaceae

Chromosome counts are presented for 12 genera and 20 species of AustralianAnnonaceae (all diploid with 2n = 16 or 18; Table 1) and two species ofEupomatiaceae (2n = 20, partly from Papua New Guinea). Detailed studies on interphase nuclear structure, condensing behaviour of chromosomes, and fluorochrome and Giemsa C-banding patterns also includeHimantandraceae (Galbulimima) andAustrobaileyaceae. — Eupomatiaceae completely correspond withAnnonaceae karyologically, their base number 2n = 20 is interpreted to have evolved from 2n = 18 by ascending dysploidy from common ancestors.Eupomatia laurina andE. benettii differ in DNA and constitutive heterochromatin (hc) quantity; their evolution from high to low DNA content probably corresponds to general progressions inMagnoliidae. Austrobaileya has nuclei of the presumably primitive Tetrameranthus type which is closely related to that ofGalbulimima and several other primitive taxa inMagnoliidae. Karyomorphology and other characters support the maintainance of two main branches within theMagnoliidae, Laurales andMagnoliales, withAustrobaileya probably intermediate; theWinteraceae appear more remote.—InAnnonaceae the reestablishment ofAncana is underlined by its chromosome number (2n = 18) the unexpected and specialized disulcate pollen, and various morphological characters which point to a close alliance with the Australian endemic generaFitzalania andHaplostichanthus (also disulcate) and the American genus pairSapranthus/Desmopsis; they are united in the provisionalSapranthus tribe, with a more distant position toFissistigma s. str. (2n = 16). AustralianAnnonaceae exhibit a high generic and a low species diversity; they can be considered as an ± old and partly impoverished outpost of the family with phytogeographical relationships to Asia, Africa and America.—On the base of field observations three main types of floral development inAnnonaceae are proposed, the most elaborated one found in the fly pollinated genusPseuduvaria. The growth form change from shrubs to lianas during the ontogeny ofDesmos andMelodorum, the vegetative propagation of anAncana species and the ecological and evolutionary patterns of the taxa investigated are discussed.     

Phylogeny of theCyclanthaceae

The affinities ofCyclanthaceae are discussed, and it is concluded that the sister-group to this family is most probablyPandanaceae. A hypothesis of generic relationships inCyclanthaceae, based on cladistic methods, is presented. Bootstrap analysis and Bremer support (decay index) have been used to test the strength of individual clades, and the result is compared with previously made phylogenetic analyses. TheSphaeradenia group (Chorigyne, Stelestylis, Sphaeradenia, andLudovia) is supported as monophyletic and acceptably resolved, while theAsplundia group (remaining genera inCarludovicoideae) may be paraphyletic, with largely uncertain relationships. A formal recognition of these groups is therefore not justified. The probable character evolution inCarludovicoideae is discussed.     

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.     

Comparative studies on the teliospore morphology and ontogeny ofSpumula serispora,spec. nova,andRavenelia texensis (Uredinales,Raveneliaceae)

A new rust fungus,Spumula serispora, is described. The morphology of the teliospores and the telia was studied. In the teliospores ofS. serispora andS. quadrifida, the type species of the genus, sterile cells could be found, which are comparable to apical cells of otherRaveneliaceae. Similar sterile cells were also present in the telial heads ofRavenelia texensis. The ontogeny of the teliospores ofS. serispora and the teliospore heads ofRavenelia texensis was studied and compared. In both species the ontogeny of the spores heads was similar. InR. texensis hygroscopic cysts sustaining the spore heads were produced by division and not by conversion of basal sterile cells of the teliospore heads.Part 114 of the series Studies inHeterobasidiomycetes.     

A phytosociological analysis of woody species in forest communities of a part of Kumaun Himalaya

This paper reports on a detailed phytosociological analysis of forests in the NW catchment of the Gola River in Kumaun Himalaya, 29°19–29°27N and 79°32–79°42E. Fourteen sites and 56 stands at elevations ranging from 1200 to 2523 m and covering the following five forest types were investigated: Pinus roxburghii, mixed, Quercus leucotrichophora, Q. lanuginosa, and Q. floribunda. The basal cover of the forests differed according to slope position and aspect. The three oak forests had more basal cover than the other two, and Q. lanuginosa had the most. The performance of individual tree and shrub species and the number of saplings and seedlings differed according to slope position and aspect. The mixed forest had the greatest tree diversity, and among the others diversity increased with increasing basal cover. The diversity of trees, saplings, and herb layer was greatest on aspects with intermediate temperature and moisture conditions; whereas that of shrubs and seedlings increased towards the cooler (and wetter) and warmer (and drier) exposures. There was a positive relation between the diversity of shrubs plus seedlings and trees plus saplings in P. roxburghii and mixed forests; whereas this relationship was inverse in the three oak forests. In general, the dominance-diversity curves for the tree layer followed a geometric series conforming to the niche pre-emption situation in communities of low diversity. Among the forests, the regeneration was best in Q. lanuginosa and worst in Q. leucotrichophora.Nomenclature follows: Osmaston (1926).Finacial support from the Council of Scientific and Industrial Research, New Delhi and the Indian Space Research Organisation, Banglore is gratefully acknowledged.     

Karyotaxonomic analysis of the genusBunium (Umbelliferae)

Chromosome numbers are reported for 23 species of the genusBunium, distributed mainly in Middle Asia and Transcaucausia. The great diversity of basic chromosome numbers is unusual for a genus ofUmbelliferae: x = 11, 10, 9, 8, 7, and 6. This series obviously has to be interpreted as descending dysploidy. Infraspecific aneuploidy was found in three species, but there are no B-chromosomes or polyploidy. The karyotypes of 18 species are described, using two morphometric chromosome parameters, centromere position and relative length (Table 2), and illustrated (Figs. 2–4). Species vary greatly in their karyotype asymmetry (20.4–45.9%). Chromosome numbers and structures appear to be useful in the karyotaxonomical and biogeographical analysis of the genus.     

Die Homologie des Perigons der Zingiberaceen Ein Beitrag zur Morphologie und Phylogenie des Monokotylen-Perigons

Nicolaia elatior is used as an example to demonstrate that the mucronate tepals ofZingiberaceae correspond to hypsophylls (bracts) consisting of a leaf sheath and a rudimentary Oberblatt (= leaf petiole + lamina) represented by the mucro. Evidence for this interpretation is furnished by all available criteria: leaf sequence (exhibiting a complete continuum of forms from foliage leaves over cata- and hypsophylls to the tepals), nervature, and ontogeny.The present conception is compared with the well-founded thesis ofLeinfellner that the perigone ofLiliaceae is derived from the androecium. The different morphological status of the perigone in both families is not regarded as the result of different phylogenetic origin, but as a manifestation of morphogenetic transgressions from one phyllome category to an adjacent one: In theLiliaceae the perigone is under a strong morphogenetic influence of the androecium, and therefore displays staminal characters, in theZingiberaceae it is under the dominating influence of the extrafloral region, and thus appears as a hypsophyllous structure. If this assumption of a morphologically oscillating perigone is correct, it will be fundamentally impossible to demonstrate unequivocally the phylogenetic origin of the monocotyledonous perigone.

Im wissenschaftlichen Werk Prof. Dr.Walter Leinfellners steht an erster Stelle die Morphologie der Blütenorgane. Als sein dankbarer Schüler möchte ich ihm aus Anlaß seines 70. Geburtstages die folgende Studie zu einem Thema zueignen, das ihn wie mich gleichermaßen angesprochen hat und schon Gegenstand der Forschungsarbeit des Jubilars war: die Homologie des Monokotylen-Perigons.     

Evolution of thedec-1 eggshell locus inDrosophila. I. Restriction site mapping and limited sequence comparison in themelanogaster species subgroup

Summary We have analyzed 18 kb of DNA in and upstream of thedefective chorion-1 (dec-1) locus of the eight known species of themelanogaster species subgroup ofDrosophila. The restriction maps ofD. simulans, D. mauritiana, D. sechellia, D. erecta, andD. orena are shown to have basically the restriction map ofD. melanogaster, whereas the maps ofD. teissieri andD. yakuba were more difficult to align. However, the basic amount of DNA and sequence arrangement appear to have been conserved in these species. A small deletion of varying length (65–200 bp) is found in a repeated sequence of the central transcribed region ofD. melanogaster, D. simulans, andD. erecta. Restriction site mapping indicated that thedec-1 gene is highly conserved in themelanogaster species subgroup. However, sequence comparison revealed that the amount of nucleotide and amino acid substitution in the repeated region is much larger than in the 5 translated region. The 5 flanking region showed noticeable restriction site polymorphisms between species. Based on calculations from the restriction maps a dendrogram was derived that supports earlier published phylogenetic relationships within themelanogaster species subgroup except that theerecta-orena pair is placed closer to themelanogaster complex than toD. teissieri andD. yakuba.     

Chemogeography ofAniba (Lauraceae)

A comparison between geographical distribution and secondary metabolites of 18 species ofAniba (Lauraceae) leads to a coherent picture of spatial and chemical evolution of these species. In chemical evolution, general mechanisms as blocking of reaction steps leading to primary metabolites and diversification of secondary metabolites within biogenetic groups are found to be operative. Sympatric distribution of closely related species seems to imply chemical diversity. The relation between size of distribution area and evolutionary status of individual species showsAniba to be an evolutionarily more recent, actively evolving genus.Part XIV in the series Plant Chemosystematics and Phylogeny. For Part XIII seeGottsberger & Gottlieb 1981).     

Seed oil fatty acid patterns of theAconitum-Delphinium-Helleborus complex (Ranunculaceae)

Many members ofRanunculaceae contain unusual fatty acids in their seed oils. This leads to rather typical genus-specific fatty acid patterns or fingerprints in these seed oils. The members of theDelphinioideae and/orHelleboroideae, however, do not contain highly unusual fatty acids. Nevertheless, their seed oil fatty acid fingerprints are also fairly typical and genus-specific, and the patterns found are rather consistent throughout several species of one genus. It was found that species ofAconitum do not contain fatty acids with 20 carbon atoms.Delphinium, Consolida, Helleborus, Nigella and others do contain C₂₀ fatty acids. In allHelleborus species, for example, there was a consistent C₂₀ fatty acid pattern of 20:020:120:2>20:3. Species ofNigella andGaridella contain high levels,Helleborus low levels, of 20:2n-6 in their seed oils.Delphinium andAconitum both contain low levels of 18:3n-3, whereasHelleborus spp. consistently show high levels of this fatty acid. The genus-specific fatty acid patterns found are discussed, and a correlation with the subfamily and tribe affiliation of the genera investigated here is attempted.     

Recombination protein A gene,recA, fromSpirulina platensis IAM-M135

We report the cloning and sequencing of therecA gene fromSpirulina platensis. A genomic library ofSpirulina was constructed in pUC19 and screened by PCR using oligonucleotides corresponding to the conserved amino acid sequences ofAnabaena variabilis andSynechococcus RecA proteins. TheSpirulina recA gene consists of an open reading frame (ORF) of 1095 nucleotides encoding a protein (365 residues) which shares an identity of 79%, 70% and 57% with the RecA proteins ofAnabaena variabilis, Synechococcus andEscherichia coli respectively. TherecA gene is located close to one end of the clonedBglII fragment and has only 53 bp of 5 nucleotides. The isolation of this gene has implications for the development of gene transfer system(s) forSpirulina.