The effect of pre- and post-harvest sodium nitroprusside treatments on the physiological changes of cut Alstroemeria aurea 'Orange Queen' during vase life.

Cut flowers deteriorate rapidly after harvest, lasting mere days. To extend their vase life, various postharvest techniques are employed. Due to limited knowledge about the postharvest physiology of Alstroemeria cut flowers and the specific role of secondary compounds and antioxidant systems in their protection, this study investigated the optimal dosage of sodium nitroprusside (SNP) as a nitric oxide (NO) donor to enhance quality and antioxidant defenses. Preharvest foliar application of SNP at 0, 50, 100, and 200 µM followed by short-term pulsing treatments upon harvest at the same concentrations were applied in a factorial design. Results revealed that a preharvest 100 µM SNP treatment combined with a 50 µM postharvest pulse significantly increased the total amount of phenols (over 20%), antioxidant capacity (more than doubled), and the activity of two antioxidant enzymes (ascorbate peroxidase by over 35% and guaiacol peroxidase by about 20%). Notably, this combination also diminished ion leakage (by about 20%), ultimately extending the vase life by more than 40% compared to untreated plants. Therefore, SNP application at these specific dosages proves effective in bolstering Alstroemeria cut flower quality and vase life through enhanced total phenols and a strengthened antioxidant system.

AaLaeA targets AaFla1 to mediate the production of antitumor compound in Alternaria alstroemeria.

Endophytic fungi are an important source of novel antitumor substances. Previously, we isolated an endophytic fungus, Alternaria alstroemeria, from the medicinal plant Artemisia artemisia, whose crude extracts strongly inhibited A549 tumor cells. We obtained a transformant, namely AaLaeAOE26 , which completely loses its antitumor activity due to overexpression of the global regulator AaLaeA. Re-sequencing analysis of the genome revealed that the insertion site was in the noncoding region and did not destroy any other genes. Metabolomics analysis revealed that the level of secondary antitumor metabolic substances was significantly lower in AaLaeAOE26 compared with the wild strain, in particular flavonoids were more downregulated according to the metabolomics analysis. A further comparative transcriptome analysis revealed that a gene encoding FAD-binding domain protein (Fla1) was significantly downregulated. On the other hand, overexpression of AaFla1 led to significant enhancement of antitumor activity against A549 with a sevenfold higher inhibition ratio than the wild strain. At the same time, we also found a significant increase in the accumulation of antitumor metabolites including quercetin, gitogenin, rhodioloside, liensinine, ginsenoside Rg2 and cinobufagin. Our data suggest that the global regulator AaLaeA negatively affects the production of antitumor compounds via controlling the transcription of AaFla1 in endophytic A. alstroemeria.

First report of alstroemeria mosaic virus infecting Alstroemeria in Korea.

Alstroemeria, a member of the Alstroemriaceae family, is a popular cut flower plant with a long-base life and a wide variety of flower colors. It is widely cultivated in many countries, especially in Central and South America. However, numerous viruses such as alstroemeria carlavirus (AlCV), alstroemeria mosaic virus (AlMV), cucumber mosaic virus (CMV), tomato spotted wilt virus (TSWV), alstroemeria streak virus (AlSV), and impatiens necrotic virus (INSV) can infect Alstroemeria and significantly decrease its yield (Kim, 2020). Among these viruses, AlMV is well known to cause an endemic viral disease in the Netherlands (Corine M. et al. 1992). AlMV is a member of the genus potyvirus in the family Potyviridae, one of the most widely distributed families of plant viruses. In 2021, symptomatic alstroemeria plants showing interveinal leaf streaking with elongated light green and chlorosis of leaves were identified from farms in a greenhouse in Gwangju, South Korea. Potyvirus-like particles (approximately 750-800 nm in length) were observed from sap of the symptomatic plants by electron microscope (Supplementary Fig. 1). To confirm virus infection, total RNA was extracted from an alstroemeria leaf using a Beniprep® Super Plant RNA extraction kit (IVT7005, Invirustech Co., Korea). A cDNA library was synthesized and analyzed by high throughput sequencing (HTS) using an Illumina NovaSeq6000 S4 sequencer. A total of 48,072,240 raw reads were obtained after quality filtering with FastQC. Remaining sequences were de novo assembled into contigs with a Trinity assembler. Nucleotide blast analysis of contigs against NCBI viral reference database revealed that 24 assembled contigs (> 1,000 bp) were sequences of AlMV. To confirm AlMV detection, raw reads were mapped to known AlMV complete genome (9,774 bp) using Bowtie2 program. Results showed that a total of 4,698,112 reads were mapped. A consensus sequence (9,778 bp, accession no. LC709275) was then obtained. To verify the presence of AlMV, RT-PCR assay was conducted with AlMV's CP gene-specific primers: AlMV-F (5'-CACGAGGCTGTGAAACAAGC -3') and AlMV-R (5'- CCAGGCGACACGGCTAAATA-3'). PCR products of the expected size (538 bp) were cloned, sequenced, and subjected to GenBank BLASTn search. A 538 bp partial CP sequence was used for BLAST analysis which revealed that it shared 100% identities with the consensus sequence (LC709275) and 96.99~98.76% nucleotide identities with four AlMV isolates (MK440140, NC043135, MT892648, DQ295032). Phylogenetic analysis based on partial CP sequences of representative members of potyviruses (family Potyviridae) using 1,000 bootstrap replicates based on either neighbor-joining or Kimura 2 parameter methods in MEGA-X revealed that AlMV isolate JNU-2 was grouped together with the four known AlMV isolates (Supplementary Fig. 2). To determine the incidence of AlMV in a greenhouse, 30 alstroemeria samples were collected and tested by RT-PCR. Results showed that 23 samples were positive for AlMV by PCR-gel electrophoresis and Sanger sequencing, suggesting a high incidence of AlMV infection. To the best of our knowledge, this is the first report of natural infection with AlMV in Alstroemeria in Korea. Further surveys of AlMV infection in greenhouses will help us prevent the spread of this viral disease in Alstroemeria.

Origin and evolution of highly polymorphic rDNA sites in Alstroemeria longistaminea (Alstroemeriaceae) and related species.

Alstroemeria (Alstroemeriaceae) displays a conserved and highly asymmetric karyotype, where most rDNA sites can be properly recognized by the size and morphology of the chromosomes. We analyzed the intraspecific variation of rDNA sites in A. longistaminea and compared with their distribution in other species (A. caryophyllaea and A. piauhyensis) and a representative of a sister genus, Bomarea edulis. All three species of Alstroemeria presented 2n = 16, and one to six B chromosomes were found in some individuals of A. longistaminea. There was a set of 12 conserved rDNA sites (four 5S and eight 35S) and up to 11 variable sites. B chromosomes were almost entirely covered by 35S signals, coupled with tiny 5S sites. Noteworthy, most rDNA sites found in A. caryophyllaea and A. piauhyensis were localized in chromosome positions similar to those in A. longistaminea, suggesting the existence of conserved hotspots for rDNA accumulation. Some of these hotspots were absent in Chilean Alstromeria as well in B. edulis. We propose that insertions of rDNA sequences on chromosomes do not occur randomly but rather on preferential sites or hotspots for insertions. The maintenance of these arrays, however, may be favored/constrained by different factors, resulting in stable or polymorphic sites.

Molecular characterization and complete genome of alstroemeria mosaic virus (AlMV).

Even though alstroemeria mosaic virus (AlMV) is one of the most important viruses affecting alstroemeria plants, its genome is only partially available in public sequence databases. High throughput sequencing (HTS) of RNA from alstroemeria plants with symptoms of mosaic and streaking, collected in Lasso-Ecuador, indicated the presence of AlMV and lily symptomless virus. In this study, we aimed to assemble and characterize the complete genome sequence of AlMV. Reads from Illumina sequencing of ribosomal RNA-depleted total RNA were assembled into contigs that were mapped to the sunflower chlorotic mottle virus genome, revealing the 9774 [corrected] bp complete genome sequence of AlMV. Multiple sequence alignment of the AlMV polyprotein with close homologs allowed the identification of ten mature proteins P1, HC-Pro, P3, 6K1, CI, 6K2, NIa-VPg, NIa-Pro, NIb and CP. Furthermore, several potyvirus motifs were identified in the AlMV polyprotein including those related to potyvirus aphid transmission 334KMTC337, 592PTK594 and 2800DAG2802. Phylogenetic analysis based in the polyprotein showed that AlMV belongs to the potato virus Y clade and its closest relative is sunflower ring blotch virus. This study describes the first complete genome of AlMV and its placement within the genus Potyvirus, providing valuable information for future studies on this economically important virus.

Comparative karyotype analysis of populations in the Alstroemeria presliana Herbert (Alstroemeriaceae) complex in Chile.

Alstroemeria L., one of the most diverse genera of the Chilean flora and of high floricultural value, is represented by 35 species, most of them distributed between 28-38° S in the Mediterranean zone of Central Chile. There are 24 complex-forming taxa, of which 18 have conservation problems (8 are considered "endangered" and 10 as "vulnerable"). One of these complexes is Alstroemeria presliana Herb. with two subspecies: subsp. presliana and subsp. australis Bayer. Alstroemeria presliana grows in Chile and Argentina: subsp. presliana is distributed from Reserva Nacional Siete Tazas (35°27' S, Region of Maule) to Antuco, (37°25' S, Region of Bío-Bío), and is also found in Neuquén, Argentina; subsp. australis is endemic to the Cordillera of Nahuelbuta. A comparative karyotype study was carried out among six populations of A. presliana subsp. presliana and five populations of A. presliana subsp. australis. The eleven populations presented an asymmetric karyotype, with 2n = 2× = 16 chromosomes but with different karyotype formulae. A. presliana subsp. presliana shows the haploid formula 2m + 2m-sat + 1sm-sat + 1st-sat + 1t + 1 t-sat, and A. preslianasubsp. australis presents a formula 1m + 2m-sat + 1sm + 2t + 2t-sat chromosomes. The architecture of the karyotype between the subspecies is very different. The scatter plot among CVCL vs. MCA shows different groupings between populations of the two subspecies. According to the results obtained it is possible to consider raising Alstroemeria presliana subsp. australis at species level.

Alstroemeria Micropropagation in a RITA® Temporary Immersion System.

The use of temporary immersion systems (TIS) for plant micropropagation is an efficient technique for plant production, and we have applied it for the production of alstroemerias. This method involves the cultivation of explants such as rhizomes and axillary buds in a nutrient medium to stimulate shoot growth. TIS offer advantages such as accelerated multiplication processes, uniform production, and cost reduction. This process has shown promise in meeting the growing demand for alstroemeria plants in the market. This chapter describes a specific protocol for temporary immersion bioreactor micropropagation of the "Albatroz" cultivar, with the potential for large-scale automation.

The complete chloroplast genome sequence of the Alstroemeria hybrid variety 'Hanhera'.

Alstroemeria, a member of the Alstroemeriaceae family, is a species from South America. The chloroplast genome of Alstroemeria spp. was completed by de novo assembly using a small amount of whole genome sequencing data. The chloroplast genome of Alstroemeria spp. was 155,672 bp in length consisting of 84,379 bp of large single copy, 17,815 bp of small single copy, and 26,739 bp of a pair of inverted repeat regions. A total of 157 genes were annotated including 103 protein-coding genes (PCGs), 46 tRNA genes, and eight rRNA genes. Maximum likelihood phylogenetic analysis with seven species belonging to the Alstroemeriaceae or Liliaceae family revealed that Alstroemeria spp. is grouped with the species in the Alstroemeriaceae family.

Programmed cell death (PCD) processes begin extremely early in Alstroemeria petal senescence.

• In the Liliaceous species Alstroemeria, petal senescence is characterized by wilting and inrolling, terminating in abscission 8-10 d after flower opening. • In many species, flower development and senescence involves programmed cell death (PCD). PCD in Alstroemeria petals was investigated by light (LM) and transmission electron microscopy (TEM) (to study nuclear degradation and cellular integrity), DNA laddering and the expression programme of the DAD-1 gene. • TEM showed nuclear and cellular degradation commenced before the flowers were fully open and that epidermal cells remained intact whilst the mesophyll cells degenerated completely. DNA laddering increased throughout petal development. Expression of the ALSDAD-1 partial cDNA was shown to be downregulated after flower opening. • We conclude that some PCD processes are started extremely early and proceed throughout flower opening and senescence, whereas others occur more rapidly between stages 4-6 (i.e. postanthesis). The spatial distribution of PCD across the petals is discussed. Several molecular and physiological markers of PCD are present during Alstroemeria petal senescence.

Influence of local floral density and sex ratio on pollen receipt and seed output: empirical and experimental results in dichogamous Alstroemeria aurea (Alstroemeriaceae).

Local density and sexual composition are two aspects of floral neighborhoods thought to influence pollination and seed output of recipient plants. I characterized the floral neighborhood of 436 flowering ramets of Alstroemeria aurea, a southern Andean perennial, distributed among three sites. On each ramet, I measured total pollen receipt and seed output. The long-lived, bumblebee-pollinated flowers of A. aurea are synchronously protandrous with a given ramet being either all male or all female and thus incapable of self or geitonogamous pollination at the ramet level. Even though each ramet changes sex over time, A. aurea forms floral neighborhoods that remain stable with respect to density and sex ratio during the span of a focal ramet female phase. Contrary to expectation, under field conditions neither local density nor sexual identity explained significant amounts of variation in pollen receipt. Density of neighboring flowering ramets marginally affected pollen receipt in two of the three populations but in opposite directions. Despite the absence of strong effects of neighborhood sexual composition on pollen receipt, the sexual identity of neighbors affected seed output which suggests effects on the quality of pollination due to changes in patterns of pollen flow. I also compared pollen loads on the stigmas of artificially isolated ramets (6 m) with those on experimental focal ramets surrounded by six close neighbors (20 cm) that were either all male or all female. Here, pollen receipt by focal ramets in all-male neighborhoods was 1.3 times greater than in isolated ramets, and 3.8 times greater than in ramets in all-female neighborhoods. In these artificial neighborhoods, stigmatic pollen deposition increased significantly over time. In nature, rates of bumblebee visits were higher in female-biased (early-flowering) than in male-biased (late-flowering) co-occurring floral patches. Thus, spatio-temporal shifts in visitation frequencies associated with the sexual composition of floral neighborhoods might compensate for spatial variability in pollen availability within populations and explain the discrepancies between empirical and experimental results.

Early reproductive failure increases nectar production and pollination success of late flowers in south Andean Alstroemeria aurea.

Fertile ramets of bumblebee-pollinated Alstroemeria aurea, a clonal perennial native to the temperate forests of the southern Andes, produce single terminal inflorescences that may bear two or more temporally non-overlapping whorls of flowers. While fruit set is commonly high (>80%) among early-opening flowers, it is usually low (<20%) among late-opening flowers within ramets. Using flowering ramets with two whorls of flowers, we examined experimentally the following related hypotheses. First, late flowers act as a reserve of ovaries, increasing their likelihood of setting seed when early fruits abort due to either pollen or resource limitation. Second, where early fruit abortion has occurred, plants may actively ensure pollination of late flowers by increasing their attractants and rewards. In a natural population, we simulated (1) lack of pollen deposition in early flowers, by excising their stigmas just before receptivity, and (2) resource limitation, by removing all the leaves from an experimental flowering ramet. Treatments were applied to individual ramets according to a 2 × 2 factorial design. We found that when early flowers failed to set fruit due to stigma excision, nectar secretion and particularly pollen receipt strongly increased in late flowers. Higher pollen deposition contributed significantly to the observed five-fold increase in seed output of late flowers. Fruit and seed set from early flowers were more negatively affected by defoliation than that from late flowers. Defoliation did not interfere with a ramet's capacity to increase late reproductive output when early reproduction failed. These results support the assertion that late flowers act as a reserve of ovaries helping a plant to cope with an unpredictable environment. These results also suggest that plants may actively increase pollinator visitation by opportunistically increasing flower rewards.

Development of a plant regeneration system based on friable embryogenic callus in the ornamental Alstroemeria.

Stem segments of seedlings from two Alstroemeria breeding lines, cultured on media supplemented with 4 mg/l 2,4-dichlorophenoxyacetic acid and 0.5-1.0 mg/l 6-benzylaminopurine (BA), initiated soft callus, which became compact after subculture on a medium with only 0.5 mg/l BA. Friable embryogenic calli were initiated from compact callus on a medium supplemented with 10 mg/l picloram. Proembryos developed from friable embryogenic calli via embryos into plants after subculture on medium supplemented with 0.1 mg/l BA. The proembryos formed friable embryogenic calli again after culture on medium supplemented with 10 mg/l picloram. The total time needed to regenerate a complete plantlet from friable callus was approximately 6 months. This system for the production of embryogenic material is considered to have valuable applications for genetic transformation in Alstroemeria.

Conflict between Intrinsic Leaf Asymmetry and Phyllotaxis in the Resupinate Leaves of Alstroemeria psittacina.

Spiral phyllotactic patterning is the result of intricate auxin transport relationships in the shoot apical meristem (SAM) that act to place auxin maxima at the future sites of leaf initiation. Inherent to this process is a bias in auxin distribution in leaf primordia, such that increased auxin is found on the descending side of the leaf (toward the older neighbor) compared to the ascending side (toward the younger neighbor), creating phyllotactically dependent leaf asymmetry. Separate from phyllotactic-dependent asymmetry is handedness in plants - that is, genetically encoded, fixed chirality, such as the twining of certain vines and the torsions induced by microtubule mutations. Here, we perform a morphometric analysis on the resupinate leaves of Alstroemeria psittacina. Interestingly, the twist in leaves always occurs in a single direction, regardless of the phyllotactic direction of the plant. Because of the resupination, leaves in this species possess an inherent handedness. However, this asymmetry is modulated in a phyllotactic-dependent manner, consistent with the known developmental constraints of phyllotaxis upon leaf morphology. This creates the interesting circumstance in A. psittacina that leaves arising from plants with a counter-clockwise phyllotactic direction are (1) more asymmetric, (2) larger, and (3) possess symmetrical shape differences relative to leaves from plants with clockwise phyllotaxis. The mechanism underlying these differences likely involves a developmental delay in clockwise leaves caused by the conflict between the phyllotaxis-dependent asymmetry and asymmetry resulting from resupination. The evolutionary implications of a dimorphic population without a genetic basis for selection to act upon are discussed.

Comparative karyotypic analysis in the Alstroemeria hookeri Lodd. (Alstroemeriaceae) complex sensu Bayer (1987).

Alstroemeria L. (Alstroemeriaceae) is an American genus of monocots with two principal distribution centers in Chile and Brazil. In Chile, it is represented by about 32 species, most of them in central Chile, an area known for its high level of endemism. The "complex" Alstroemeriahookeri is endemic to Chile, where it is distributed from the Coquimbo to the Bío-Bío Region. We analyzed the karyotypes of 36 populations of this complex along its natural distribution. Ten metaphases per population were used for chromosome measurements. All analyzed subspecies presented a well defined asymmetric karyotype. The populations of A. hookeri subsp. hookeri collected in the coastal range of the Bío-Bío Region and the populations from the Central Valley of this Region (Pangal del Laja) presented striking morphological differences in the karyotype, mainly on chromosome 3. The population of A. hookeri subsp. recumbens from Pichicuy showed a polymorphism on chromosome 7, which differed from the other analyzed populations of this subspecies. Phenetic analysis suggested that A. hookeri subsp. cummingiana, which showed a more symmetrical karyotype and did not grow in sandy soil, should be alocated to A. cummingiana rather than considered as part of the hookeri complex.

Comparative karyotypic analysis in the Alstroemeria hookeri Lodd. (Alstroemeriaceae) complex sensu Bayer (1987)

Alstroemeria L. (Alstroemeriaceae) is an American genus of monocots with two principal distribution centers in Chile and Brazil. In Chile, it is represented by about 32 species, most of them in central Chile, an area known for its high level of endemism. The "complex" Alstroemeria hookeri is endemic to Chile, where it is distributed from the Coquimbo to the Bío-Bío Region. We analyzed the karyotypes of 36 populations of this complex along its natural distribution. Ten metaphases per population were used for chromosome measurements. All analyzed subspecies presented a well defined asymmetric karyotype. The populations of A. hookeri subsp. hookeri collected in the coastal range of the Bío-Bío Region and the populations from the Central Valley of this Region (Pangal del Laja) presented striking morphological differences in the karyotype, mainly on chromosome 3. The population of A. hookeri subsp. recumbens from Pichicuy showed a polymorphism on chromosome 7, which differed from the other analyzed populations of this subspecies. Phenetic analysis suggested that A. hookeri subsp. cummingiana, which showed a more symmetrical karyotype and did not grow in sandy soil, should be alocated to A. cummingiana rather than considered as part of the hookeri complex.

Detección de geminivirus asociados a la alstroemeria (alstroemeria l.) En villa guerrero, estado de México / Detection of geminivirus associated to alstroemeria (alstroemeria l.) In villa guerrero, state of Mexico / Detecção de geminivírus associados a alstroemeria (alstroemeria l.) Em villa guerrero, estado do México

En plantaciones de alstroemeria (Alstroemeria L.) de Villa Guerrero, Estado de México, se han detectado plantas con síntomas similares a los inducidos por geminivirus en otros cultivos hortícolas. En dichas plantaciones también se ha observado la presencia de la mosquita blanca, considerada como el vector más eficiente de estos virus. El objetivo del presente trabajo fue detectar la presencia de geminivirus en plantas de alstroemeria. Mediante PCR, usando los iniciadores MotCP2118/MotCP2123, se obtuvo un segmento de ~600pb, similar al del control positivo correspondiente a chile infectado con el begomovirus pepper huasteco yellow vein virus (PHYVV, antes pepper huasteco virus) en plantas sintomáticas, mientras que en las asintomáticas la detección fue negativa. Plantas de Nicotiana glutinosa, N. benthamiana, N. rustica, N. tabacum var. xanthi y Datura stramonium inoculadas por biobalística con ADN total obtenido de alstroemerias con síntomas y positivas a PHYVV mediante PCR, mostraron mosaicos leves y deformación de hojas, mientras que en plantas de Capsicum annuum se observaron mosaicos, necrosis en nervaduras y abultamientos en hojas. Con el ADN de estas plantas también se obtuvieron bandas correspondientes al PHYVV, pero en las monocotiledóneas bombardeadas, incluyendo alstroemeria, no fue detectado el fragmento. La secuencia de oligonucleótidos de los productos de PCR mostró 98% de homología con el begomovirus PHYVV. Aunque no fue posible reproducir en alstroemeria los síntomas observados en campo, sí se evidenció mediante PCR la presencia de un geminivirus similar al PHYVV en tejido de plantas sintomáticas.

In alstroemeria (Alstroemeria L.) plantations located in Villa Guerrero, Mexico State, plants with symptoms similar to those induced by geminivirus in other horticultural crops have been detected. In addition, the presence of whiteflies, which are considered the most efficient vectors of these viruses, has been observed in these plantations. The goal of this work was to detect the presence of this geminivirus species in alstroemeria plants. By means of PCR analysis using primers MotCP2118/MotCP2123, a fragment of ~600pb similar to the amplicon obtained from PHYVV-infected positive control was amplified only from symptomatic plants. Nicotiana glutinosa, N. benthamiana, N. rustica, N. tabacum var. xanthi and Datura stramonium plants were inoculated by bombardment with total DNA obtained from symptomatic alstroemerias and positive to PHYVV by means of PCR. Inoculated plants showed mild mosaics and deformation of leaves, whereas in the leaves of Capsicum annum plants, mosaics, vein necrosis and blisters were observed. Using DNA from these plants as template in PCR, amplicons corresponded to PHYVV were also obtained; however, in bombarded monocotyledons, including alstroemeria, this fragment was not detected. The sequence of oligonucleotides from the PCR products showed 98% homology to PHYVV geminivirus. Even though symptoms presented by alstroemeria plants in the field were not reproduced, the presence of a geminivirus similar to PHYVV in tissue of symptomatic plants was evidenced through PCR.

Em plantações de alstroemeria (Alstroemeria L.) de Villa Guerrero, Estado do México, se tem detectado plantas com sintomas similares aos induzidos por geminivírus em outros cultivos hortícolas. Em ditas plantações também tem sido observada a presença da mosquinha branca, considerada como o vetor mais eficiente destes vírus. O objetivo do presente trabalho foi detectar a presença de geminivírus em plantas de alstroemeria. Mediante PCR, usando os iniciadores MotCP2118/MotCP2123, obteve-se um segmento de ~600pb, similar ao do controle positivo correspondente a chile infectado com o begomovírus pepper huasteco yellow vein virus (PHYVV, antes pepper huasteco virus) em plantas sintomáticas, enquanto que nas assintomáticas a detecção foi negativa. Plantas de Nicotiana glutinosa, N. benthamiana, N. rustica, N. tabacum var. xanthi e Datura stramonium inoculadas por biobalística com DNA total obtido de alstroemerias com sintomas e positivas a PHYVV mediante PCR, mostraram mosaicos leves e deformação de folhas, enquanto que em plantas de Capsicum annuum se observaram mosaicos, necrose em nervaduras e protuberâncias em folhas. Com o DNA destas plantas também se obtiveram bandas correspondentes ao PHYVV, mas nas monocotiledóneas bombardeadas, incluindo alstroemeria, não foi detectado o fragmento. A sequência de oligonucleotídeos dos produtos de PCR mostrou 98% de homologia com o begomovírus PHYVV. Embora não foi possível reproduzir em alstroemeria os sintomas observados em campo, sím foi evidenciada, mediante PCR, a presença de um geminivírus similar ao PHYVV em tecido de plantas sintomáticas.

Quantification of α-methylene-λ-butyrolactone extracted from different parts ofAlstroemeria wilhelmina and evaluation of it's antigenicity using the guinea-pig maximization test.

To detect the type of contact dermatitis caused due to the handling ofAlstroemeria wilhelmina, 1% α-methylene-λ-butyrolactone (α-MBL) dissolved in physiological alien and a five-fold diluted saline solution of original extracts of flowers, leaves and stems of the flower were applied to guinea-pigs for extracts were applied to the animals as the challenge treatment in compliance with the guinea-pig maximization test (GMT). As a consequence, not only primary irritant dermatitis was observed, but also delayed type allergic contact dermatitis due toAlstroemeria wilhelmina was observed. α-MBL determined in the extracts using high-performance liquid chromatography (HPLC) was found to be the biochemical material cause of the contact dermatitis. the flower region contained α-MBL in the highest concentrations compared with those of the leaves and stems. Therefore, the quantification of α-MBL in the extracts was concluded as being a useful evaluating method for contact dermatitis due to the handling ofAlstroemeria.

Alstroemeriaceae en Perú y áreas vecinas

The family Alstroemeriaceae with special emphasis in Peru is revised using morphological and distributional data. Species in this family were reinvestigated on the basis of all types, material housed in several herbaria and five field trips, each of which lasted several weeks, were undertaken to South America to study the plants in the field. The taxonomic and collection history of the genus is described and for each species the typical growth forms and their variability, habitat preferences and general distribution are discussed. A key to determine the species of Peru in English and Spanish is provided. The study area comprise five geographic units recognised: Amotape-Huancabamba-region (Ecuador, Peru), Cordillera Occidental (Peru), Cordillera Central (Peru), Cordillera Oriental (Bolivia, Peru) and the Altiplano (Bolivia, Peru). The family as here circumscribed comprises two species of Alstroemeria and 68 species of Bomarea, of these 68 species 43 species are members of subgenus Bomarea, 9 species of subgenus Sphaerine and 16 of the subgenus Wichuraea. The fourth and last subgenus into Bomarea genus denominated Baccata cannot be found in the area of this study. Six new species to science of Bomarea are described: B. amazonica, B. libertadensis, B. lopezii, B. macusanii, B. pseudopurpurea, B. weigendii.

Las Alstroemeriaceae peruanas fueron revisadas por última vez por Killip (1936). Es necesaria una nueva revisión. Cinco viajes de campo de varias semanas cada uno fueron emprendidos a Sudamérica con el fin de estudiar las plantas in situ. En el presente trabajo se describe la historia taxonómica y colección de los géneros con especial énfasis en el Perú. El área descrita no considera fronteras políticas sino unidades geográficas de acuerdo a Baumann (1988), Berry (1982), Duellman (1979), Simpson (1975, 1979) y Weigend (2002). Se reconocen cinco unidades geográficas: Región Amotape-Huancabamba (Ecuador, Perú), Cordillera Occidental (Perú), Cordillera Central (Perú), Cordillera Oriental (Bolivia, Perú) y el Altiplano (Bolivia, Perú). Se brinda una clave taxonómica en inglés y español para determinar las especies del Perú. Para cada una de las especies se discute la forma típica de crecimiento y su variabilidad, preferencias de hábitat y distribución general. Se identifican las especies de Ruiz & Pavón (1802). Ellos describieron en su Flora de Chile y Perú 23 especies de Alstroemeria, 18 fueron de Perú, ahora 17 son incluidas en Bomarea, todas proceden de Perú. El género Bomarea está subdividido en 4 subgéneros: Baccata, Bomarea s. str., Sphaerine y Winchurea (Hofreiter & Tillich, 2002). Alstroemeria no es dividido en subgéneros, pero existen dos grupos reconocidos, Alstroemeria de Chile y Brasil. En el área de estudio se encuentran dos especies de Alstroemeria y 68 de Bomarea, de ellas 43 especies pertenecen al subgénero Bomarea, 9 especies al subgénero Sphaerine y 16 especies al subgénero Wichuraea. El subgénero Baccata no se encuentra en el área de estudio. Seis de las especies del género Bomarea son nuevas para la ciencia: B. amazonica, B. libertadensis, B. lopezii, B. macusanii, B. pseudopurpurea, B. weigendii.