Broom snakeweed, a perennial rangeland shrub, is highly variable morphologically and can grow under a broad range of environmental conditions. In this study, isozyme analysis using starch gel electrophoresis was used to quantify genetic variability within and among New Mexico populations of broom snakeweed. Eight separate populations of broom snakeweed and one population of threadleaf snakeweed as a comparison were investigated. of the 10 enzyme systems examined, 16 loci were identified in eight populations and two species. Eleven loci were monomorphic in eight populations and two species and five loci were polymorphic in at least one population or species. Genetic variability was large in broom and threadleaf snakeweed populations as determined by isozyme analysis. Genetic variability among broom snakeweed populations was greater than that within populations for the five polymorphic loci. Cluster analysis of genetic distance and identity for the eight populations and two species characterized two major groups. Within broom snakeweed, cluster analysis characterized five groups. The two species shared most common alleles. The genetic variation identified in this research may account for the morphological differences and broad geographical distribution of broom snakeweed.

The importance of seeds in the reproduction and maintenance of yellow nutsedge (Cyperus esculentus L. # CYPES) populations was evaluated. Isozyme analysis using starch gel electrophoresis was performed on 20 individuals of each of 10 widely separate populations in California. Genetic variation among individuals served as an indicator of the relative importance of asexual and sexual reproduction in each population. Eight enzyme systems were assayed from which 12 loci were resolvable, with four of those loci exhibiting variability. A maximum of four isozyme genotypes appeared in any population; only nine of 81 total potential genotypes were identified. Five populations were isozymically uniform, apparently composed of a single genotype. The remaining five populations were genotypically variable; these frequently deviated strongly from the genotype frequencies expected of a sexually reproducing population. These results indicate that sexually produced seeds are unimportant in the maintenance of yellow nutsedge populations in agricultural environments. Although viable seed may be produced, tubers appear to be the primary mode of reproduction in this species.

Genetic diversity within and among populations of yellow nutsedge (Cyperus esculentus L. # CYPES) was analyzed to evaluate and quantify the genetic consequences of the reported predominance of asexually-produced tubers as colonizing agents. Ten populations were examined using starch gel electrophoresis for allozyme analysis. Four populations of purple nutsedge (Cyperus rotundus L. # CYPRO) were surveyed for comparison. Twelve loci were identified in yellow nutsedge among the eight enzyme systems examined; ten of these loci were found in purple nutsedge. Yellow nutsedge showed relatively low genetic diversity. Most of the genetic diversity occurred as differences among individuals within populations (Hs), compared to differences among populations (Dst) for the four variable loci identified in this species. Thus, most genetic distances between its populations were small. Generally, only a few genotypes occurred within each population. Purple nutsedge was found to possess even lower within- and among-population gene and genotypic diversity. This study supports the view that tubers account for most of the establishment of new populations of both species.

Using starch gel electrophoresis, we examined the genetic variability of kikuyugrass collected from three golf course sites within its geographical range in California. These experiments were conducted to determine the method of spread of kikuyugrass in areas where it is considered invasive. Samples from roughs and fairways of each of these locations were compared. of the 354 plants examined, 12 different genotypes were identified by isozyme analysis, and only three of the nine putative loci varied among the genotypes. Two genotypes, representing 73% of the plants examined, were found at all three geographic locations. Our results imply that under common golf course practices, kikuyugrass is maintained by clonal reproduction. We conclude that low genetic variation does not preclude a plant species from being an aggressive invader.

Clonal individuals from 16 hemp dogbane populations with phenotypic variation were analyzed using isozyme and randomly amplified polymorphic DNA (RAPD) analysis. Plants originated from populations in Michigan and Illinois. Three known Apocynum species, spreading dogbane, hemp dogbane, and prairie dogbane, were evaluated. Genetic distance among populations was more pronounced with isozyme analysis compared to RAPD analysis. The combined isozyme and RAPD analysis data separated spreading dogbane from all other plants analyzed. Genetic variation was present among the 16 hemp dogbane populations, but was less than expected based on the phenotypic variation present among the collections. The short genetic distance between the 16 hemp dogbane collections and the three Apocynum species suggests that variation among populations of hemp dogbane may be from outcrossing with other closely related Apocynum species. Isozyme and RAPD analyses were also conducted on plants from two populations in Michigan to determine the level of genetic variation among plants within the same population. Genetic analysis revealed that one population was entirely clonal, while the other population was a mixture of clonal and segregating plants.

Broom and threadleaf snakeweed reduce rangeland productivity throughout the western United States. These closely related species are only distinguishable at flowering and are highly variable in morphology and phenology. The objective of this study was to evaluate the genetic variation among snakeweed populations from Arizona, New Mexico, Texas, and Wyoming using isozyme analysis. Plants from each population were transplanted into pots and maintained in a greenhouse for 6 mo prior to analysis. Protein was extracted from young leaf tissue and separated using starch gel electrophoresis. Genetic variation was assessed based on expressed isozyme patterns of 10 enzymes. Of 10 enzymes tested, 16 loci were identified. Total genetic diversity (HT) was large for the eight polymorphic loci in broom snakeweed and three polymorphic loci in threadleaf snakeweed. Genetic variation among populations (DST) of both species contributed the major portion of diversity, but diversity among individuals within each population (HS) was also present. Phylogenetic analysis using Nei's genetic identity and distance determined broom snakeweed populations from New Mexico and Texas were more alike than those from Wyoming and Texas, or those from Wyoming and New Mexico. Compared to genetic differences among New Mexico broom snakeweed populations defined in a previous study, genetic diversity was greater among populations from different states. In addition, genetic variation was smaller in threadleaf snakeweed populations relative to broom snakeweed populations. Results concurred with previous research designating broom snakeweed as the progenitor of threadleaf snakeweed. Local populations of each species have probably developed due to long-term environmental selection.

The identities of two novel perennial nutsedge biotypes collected near Bakersfield, CA, were assessed using isozyme and random-amplified polymorphic deoxyribonucleic acid markers in conjunction with morphological analysis. The two biotypes, designated as CK (Cyperus rotundus cv. ‘Kempeni’) and CR (Cyperus esculentus cv. ‘Robusta’), morphologically resemble purple nutsedge and yellow nutsedge, respectively. Plants from both biotypes exhibited more prolific growth than the typical forms and possessed some traits that are not characteristic of the species they resemble. The morphological study was conducted on a total of 15 purple nutsedge, yellow nutsedge, CK, and CR populations collected in the first year and on 20 additional nutsedge populations were collected in the second year. The genetic analysis was performed on populations from the first year only. In general, there was agreement among the results obtained from the morphometric, isozymatic, and deoxyribonucleic acid studies. Populations of CR clustered with yellow nutsedge populations, indicating that CR is within the normal range of variation of this species and may represent a new introduction. Populations of CK, however, were distinct from both purple nutsedge and yellow nutsedge populations. Considering the low level of genetic variation reported in purple nutsedge and its strict vegetative mode of reproduction, CK might represent a sexually reproducing ecotype of purple nutsedge or a hybrid with yellow nutsedge.

Giant reed is one of the most widespread invasive species in riparian habitats in California and other coastal states of the United States. This species is thought to spread primarily asexually by flood dispersal of stem and rhizome pieces; viable seeds have not been found in the United States. Research was conducted to quantify genetic variation in giant reed along the Santa Ana River in California and to investigate the pattern of distribution of variation along this watershed. Populations at least 3.2 km apart were collected along the length of the Santa Ana River from the headwaters to the Pacific Ocean. One additional population from a different watershed was collected to serve as an out-group. Genetic analyses were conducted using both starch gel electrophoresis for isozyme analysis and random amplified polymorphic DNA (RAPD) analysis. Both isozyme and RAPD analyses revealed levels of genetic diversity comparable with those in the literature for clonal species, suggesting that asexual reproduction is the primary means of spread of giant reed. Most phenotypes were spread along the Santa Ana River, which is expected if water is the primary means of spread of vegetative propagules. Among the unique phenotypes found, two isozyme phenotypes and one RAPD phenotype were dominant and were found spread along the river, which may indicate greater fitness or competitive superiority to the other phenotypes that were less common. The dominant phenotypes were also found in the out-group population, possibly because of spread by humans. Because spread occurs mainly asexually, management efforts should focus on preventing establishment and spread of vegetative propagules. A moderate level of genetic diversity also suggests that biological control of this weed could be successful.

The identity of individual ectomycorrhizas, root colonization patterns and early growth responses of interconnected Scots pine (Pinus sylvestris L.) seedlings were investigated following interactions between local genets of Suillus bovinus (L. ex Fr.) O. Kuntze (SBK4b and SBK5b) and S. variegatus (Swartz ex Fr.) O. Kuntze (SVK3b) and different host–genotype combinations. Three equidistant 39-d-old seedlings, in pots that contained sterile N-limited nursery soil, were each inoculated with one of the three genets in the multiple inoculation treatment (MIT). Single inoculation treatments (SITs), involving inoculation of only one seedling in the triad with one of the three genets, and a similarly configured uninoculated treatment (UIT), were also prepared for comparative analysis. All seedling roots in the inoculated treatments, except for one SIT/SBK4b combination, hosted large numbers (>150) of Suillus-type ectomycorrhizas after 23–25 wk growth without additional fertilization. Esterase (EST) isozyme analysis of individual ectomycorrhizas from all SIT and MIT combinations enabled efficient interspecific and intraspecific typing of fungal (genet) colonization (89 and 72%, respectively) and identification of host genotype variation (Z locus polymorphism) at a lower rate (51%). Species, but not S. bovinus genet, typing within randomly sampled individual ectomycorrhizas from selected SITs was successful (50–70%) following PCR/RFLP analysis of diagnostic sequences of fungal rRNA genes. In the SITs, only the inoculated fungal genet was detected in ectomycorrhizas on all three seedlings. Roots were predominantly colonized by SBK4b in one, and SBK5b in three, of the MIT combinations, although ectomycorrhizas of the former genet were detected at low frequencies on nearly all seedlings. In the remaining MIT combination, both SBK4b and SVK3b were found to co-dominate as ectomycorrhizas on the seedling roots. Small numbers of the latter genet were detected in ectomycorrhizas of two SBK5b-dominated MIT combinations. However, no significant trends in host-mycorrhiza interactions were detected using a log–linear analysis. Compared with the UIT, significant positive mycorrhizal plant growth responses, particularly increased needle length, were recorded in all the heavily colonized seedlings in most SIT and all MIT combinations. Intermediate seedling growth was restricted to the one SIT/SBK4b combination where seedlings supported limited numbers of ectomycorrhizas. The general host-fungal colonization patterns observed provide further below-ground evidence supporting genet interactions previously detected through sporocarp population analyses in young Scots pine reforestation sites.