erubescens, the latter being widely accepted for the genus Mesoph

erubescens, the latter being widely accepted for the genus Mesophyllum. The addition of M. sphaericum

as new maërl-forming species suggests that European maërl beds are more biodiverse than previously understood. “
“The filamentous, colonial cyanobacterium Trichodesmium has six well-described species, but many more names. Traditional classification was based on field samples using morphological characteristics such as cell width and length, gas vesicle distribution, and colony morphology. We used the Woods Hole Trichodesmium culture collection to identify 21 cultured strains to species using cell morphology; phycobiliprotein absorption spectra; and sequences of the 16S rRNA gene, the 16S–23S internal transcribed spacer (ITS), and the heterocyst differentiation selleck screening library gene hetR. We compared our results to previous studies of field specimens and found similar clades, though not all phylogenetic groups were represented in culture. Our culture collection represented two of the four major clades of Trichodesmium: clade I, made up of Trichodesmium thiebautii Gomont,

Trichodesmium tenue Wille, Katagnymene spiralis Lemmerm., and Trichodesmium hildebrandtii Gomont; and clade III, consisting of Trichodesmium erythraeum Ehrenb. and Trichodesmium contortum Wille. These clades were genetically coherent with similar phycobiliprotein composition, but morphologically selleck chemicals llc Non-specific serine/threonine protein kinase diverse. In the continual revision of cyanobacterial taxonomy, genetic and biochemical information is useful and informative complements to morphology for the development of a functional classification scheme. “
“Many of the genes that control photosynthesis are carried in the chloroplast. These genes differ among species. However, evidence has yet to be reported revealing the involvement of organelle genes in the initial stages of plant speciation. To elucidate the molecular basis of aquatic plant speciation, we focused on the unique plant species

Chara braunii C. C. Gmel. that inhabits both shallow and deep freshwater habitats and exhibits habitat-based dimorphism of chloroplast DNA (cpDNA). Here, we examined the “shallow” and “deep” subpopulations of C. braunii using two nuclear DNA (nDNA) markers and cpDNA. Genetic differentiation between the two subpopulations was measured in both nDNA and cpDNA regions, although phylogenetic analyses suggested nuclear gene flow between subpopulations. Neutrality tests based on Tajima’s D demonstrated diversifying selection acting on organelle DNA regions. Furthermore, both “shallow” and “deep” haplotypes of cpDNA detected in cultures originating from bottom soils of three deep environments suggested that migration of oospores (dormant zygotes) between the two habitats occurs irrespective of the complete habitat-based dimorphism of cpDNA from field-collected vegetative thalli.

Literature search was conducted in English language publications

Literature search was conducted in English language publications using MEDLINE, EMBASE, and the Cochrane Trials Register

in human subjects. Relevant literature from the Asia–Pacific region was of particular interest. Categorization of evidence, classification of recommendation, and voting schema was modified from the Canadian Task Force on the Periodic Health Examination (Table 1).[10] The first vote was conducted electronically by email, without explanation RO4929097 nmr or access to the relevant literature. The second vote was conducted electronically after Web-based access to the provided literature. All feedbacks were collated prior to the face-to-face meeting. Face-to-face meeting of the Consensus group was held on June 30 and July 1, 2012, in Pattaya, Chonburi, Silmitasertib Thailand, to review and discuss the evidence for all statements. All statements were edited and finally

agreed at the concluding plenary session. In addition, some overlapping statements were combined and rewritten before the final vote. Consensus was considered to be achieved when 80% or above of voting members indicated “accept completely” or “accept with some reservation.” A statement was refuted when 80% or above of voting members “reject completely” or “reject with some reservation.” Every accepted statement was then graded to indicate the level of evidence available and the strength of recommendation. Those statements that did not reach consensus were modified to compensate for the rejected reasons and underwent a revote. If the statement still failed to reach the consensus, that statement was dropped from the list.

Discussed points on dropped statements are also reported in the most relevant BCKDHA accepted statements. Commentaries on statements were written by the chairmen (RR) and the persons assigned to present the statements during the face-to-face meeting. Co-authors were involved in the final editing of the commentaries. 1. The incidence of cholangiocarcinoma (CCA) varies considerably depending on the geographic region due to the variation in risk factors. The highest incidence is reported in Eastern and Southeastern Asia, and the main risk factor in Asian countries is mostly linked to certain liver fluke infestation. Level of agreement: a—100%, b—0%, c—0%, d—0%, e—0% Quality of evidence: II-1 Classification of recommendation: A There are markedly geographic variations in the incidence of CCA worldwide. The incidence of CCA in the West was reported as much lower (1–2 per 100 000) than in certain parts of Asia (5–71 per 100 000).[11] The highest incidence was reported from Northeastern Thailand (71 per 100 000 in men and 31 per 100 000 in women), followed by Eastern China (10 per 100 000 in men and 5 per 100 000 in women)[1] Table 2.

553-0921) in multivariate analysis

Conclusions: In pati

553-0.921) in multivariate analysis.

Conclusions: In patients with CHB who developed drug resistance, combination therapy with ETV + TDF was superior to ETV + ADV in achieving CVR. We suggest more potent combination therapy was needed in patients who developed drug resistance. Further large-scale prospective study is needed for delineation of these results. Disclosures: Won Young Tak – Advisory Committees or Review Panels: Gilead Korea; Grant/ Research Support: SAMIL Pharma; Speaking and Teaching: Bayer Korea The following people have nothing to disclose: Jung Gil Park, Young Oh Kweon, Se Young Jang, Su Hyun Lee, Soo Young learn more Park Background. Only a subset of chronic hepatitis B patients Palbociclib nmr achieves a response to peginterferon (PEG-IFN) therapy. Methods. A baseline prediction model (EPIC-B Predictor)

for response (HBeAg loss and HBV DNA <2,000IU/mL at 6 months post-treatment) was constructed based on HBV genotype, baseline HBsAg, HBV DNA, ALT and patient age, sex and previous IFN therapy in a training dataset of 822 HBeAg-positive patients treated with PEG-IFN for one year in 3 global randomized trials (Pegasys Phase 3, HBV 99-01 and Neptune) and externally validated in 666 patients treated with PEG-IFN for 24 to 48 weeks in various global studies. Patients were classified according to the predicted probability of response: low (<20%), intermediate (20-30%) or high (>30%). Response was defined as HBeAg loss with HBV DNA <2,000 IU/mL at 6 months post-treatment. Results. The derivation dataset consisted of genotypes A/B/C/D in 112/206/392/112. Genotype specific models were constructed for genotypes A, B and C, but not D because of the limited number of responders. The model

performed well in the training set (AUROC 0.71, p<0.001) and predicted Rebamipide probabilities from the model accurately reflected observed response rates (table). In the validation cohort (genotypes A/B/C in 9/272/385, full year of treatment 33%, response 17%), the model performed well (AUROC 0.67, p<0.01) and the predicted probability strongly correlated with observed response rates (p<0.001). The EPIC-B predictor consistently identified subsets of patients with low (∼40% of patients in both datasets) or high chances of response (∼30% of patients in both datasets). Conclusions. The EPIC-B Predictor accurately estimates the probability of response to PEG-IFN therapy in HBeAg-positive patients and can be used to improve patient counselling and to guide the choice of first-line treatment in HBeAg-positive chronic hepatitis B. Observed response rates by predicted probability Only a subset of patients in the validation dataset received PEG-IFN for one year. Higher EPIC-B predicted probability was associated with higher response rates regardless of therapy duration. Disclosures: Milan J. Sonneveld – Advisory Committees or Review Panels: Roche; Speaking and Teaching: Roche, BMS Vincent W.

However, it is susceptible to fusarium wilt, which causes heavy e

However, it is susceptible to fusarium wilt, which causes heavy economic losses. Forty-eight isolates were isolated from diseased bitter gourd plants that displayed typical fusarium wilt symptoms. Based on the morphological features, the rDNA internal transcribed space (ITS) sequences, pathogenicity and host biotypes, all of the isolates tested were pathogenic to the susceptible bitter gourd plants species (cv. ‘Guinongke No. 2’) and were identified as Fusarium oxysporum f. selleck inhibitor sp. momordicae (FOM). Our results classified different isolates as slightly, moderately or highly virulent. Among the isolates

tested, 43 isolates slightly infected bottle gourd (Lagenaria siceraria Opaganib price var. clavata), whereas they did not infect other species from the family Cucurbitaceae.

Genetic diversity among 48 isolates was characterized using amplified fragment length polymorphism (AFLP) analysis. The number of bands amplified by each primer pairs ranged from 41 to 66, with sizes ranging from 200 to 500 bp. A total of 366 bands were observed, out of which 363 were polymorphic (99.14%). The Nei’s genetic identity of the six geographical populations varied from 0.7362 to 0.9707. The mean Nei’s gene diversity index (H = 0.2644) and the mean Shannon’s information index (I = 0.4071) at species level were higher than ones at populations level, indicated that the variation within populations was greater than that among populations. The Nei’s GST (0.5103) and gene flow (Nm = 0.4923) revealed that genetic differentiation was mainly among populations and few gene exchanges. The dendrogram obtained from AFLP marker showed that there was a good

correlation between isolates from different geographical locations and their pathogenicity. The AFLP marker effectively distinguished the high virulent isolates from the less virulent isolates. The highly virulent isolates were distinctly separated in different clusters, which indicated a significantly high correlation with the geographical origin in the AFLP dendrogram. The pathogenicity and molecular marker analysis confirmed the presence of variation in virulence as well Racecadotril as genetic diversity among the FOM isolates studied. “
“Mixed infections of Nicotiana benthamiana plants by Tobacco necrosis virus (TNV) and Turnip crinkle virus (TCV) exhibited an interference interaction. Accumulation of TNV (+)RNA as well as capsid protein in mixed infection were considerably lower than that of singly infected plants. There were also a slight reduction in the levels of TCV (+)RNA and capsid protein in doubly infected plants, which displayed the concentration of both viruses decreased in dually infected plants. Tissue immunoblot analysis of systemic N.

A bimodal mismatch distribution is expected for stable population

A bimodal mismatch distribution is expected for stable populations, whereas expanding populations produce a unimodal distribution (Rogers and Harpending 1992). The values of the mean and mode of the mismatch distribution are relatively high, suggesting that the expansion may have been an old event. From our estimates, the population expansion would have occurred between 511,000 and 110,000 ybp, coinciding with the middle-late Pleistocene. These estimates concur with the findings reported by Amaral et al. (2012). The highly negative Fu Fs value is also supportive of an C59 wnt datasheet expansion event (Ray et al. 2003). Our results also suggest that fine scale population structure may occur

in New Zealand waters. Small but significant genetic differentiation was observed at both nuclear and mtDNA markers. The fact that differentiation between putative Coastal and Oceanic populations was detected with the microsatellites selleck kinase inhibitor but not with mtDNA may suggest that these populations have diverged recently. This is supported by the lack of correlation observed between lineages and populations in the median-joining network, but could also be the consequence of a stochastic effect

considering the high haplotype diversity. The differentiation of the Hauraki Gulf population obtained with mtDNA but not with the microsatellites may be explained by the existence of higher female site-fidelity to this region. Our sex-biased dispersal analysis was too weak to provide reliable results. However, the fact that the Hauraki Gulf retains a notable importance as nursery and feeding ground may support this result (Stockin et al. 2008, 2009a).

Unlike other regions around the New Zealand coast, common dolphins occur in Hauraki Gulf year-round (Stockin et al. 2008), with photo-identification Rebamipide suggesting common dolphins exhibit higher site fidelity in this region compared to other neighboring areas (Neumann et al. 2002). This behavior has also been observed in another small cetacean species in New Zealand waters (Weir et al. 2008). The migration rate estimates showing high directional migration from the Hauraki Gulf to the other populations may also help to explain this discrepancy. These estimates should, however, be considered with caution given the low levels of FST observed for these populations. An alternative interpretation of these results is the potential co-occurrence of two distinct populations/ecotypes that do not coincide with an Oceanic/Coastal subdivision, as revealed by STRUCTURE. The significant positive FIS values detected in the Coastal and Hauraki population also suggest some evidence of Wahlund effect, indicating the presence of subpopulations. The dietary differences identified between Hauraki Gulf individuals and other New Zealand common dolphins further suggest that some degree of dietary specialization could occur in this region (Meynier et al. 2008).

A bimodal mismatch distribution is expected for stable population

A bimodal mismatch distribution is expected for stable populations, whereas expanding populations produce a unimodal distribution (Rogers and Harpending 1992). The values of the mean and mode of the mismatch distribution are relatively high, suggesting that the expansion may have been an old event. From our estimates, the population expansion would have occurred between 511,000 and 110,000 ybp, coinciding with the middle-late Pleistocene. These estimates concur with the findings reported by Amaral et al. (2012). The highly negative Fu Fs value is also supportive of an LY2109761 mw expansion event (Ray et al. 2003). Our results also suggest that fine scale population structure may occur

in New Zealand waters. Small but significant genetic differentiation was observed at both nuclear and mtDNA markers. The fact that differentiation between putative Coastal and Oceanic populations was detected with the microsatellites Imatinib datasheet but not with mtDNA may suggest that these populations have diverged recently. This is supported by the lack of correlation observed between lineages and populations in the median-joining network, but could also be the consequence of a stochastic effect

considering the high haplotype diversity. The differentiation of the Hauraki Gulf population obtained with mtDNA but not with the microsatellites may be explained by the existence of higher female site-fidelity to this region. Our sex-biased dispersal analysis was too weak to provide reliable results. However, the fact that the Hauraki Gulf retains a notable importance as nursery and feeding ground may support this result (Stockin et al. 2008, 2009a).

Unlike other regions around the New Zealand coast, common dolphins occur in Hauraki Gulf year-round (Stockin et al. 2008), with photo-identification unless suggesting common dolphins exhibit higher site fidelity in this region compared to other neighboring areas (Neumann et al. 2002). This behavior has also been observed in another small cetacean species in New Zealand waters (Weir et al. 2008). The migration rate estimates showing high directional migration from the Hauraki Gulf to the other populations may also help to explain this discrepancy. These estimates should, however, be considered with caution given the low levels of FST observed for these populations. An alternative interpretation of these results is the potential co-occurrence of two distinct populations/ecotypes that do not coincide with an Oceanic/Coastal subdivision, as revealed by STRUCTURE. The significant positive FIS values detected in the Coastal and Hauraki population also suggest some evidence of Wahlund effect, indicating the presence of subpopulations. The dietary differences identified between Hauraki Gulf individuals and other New Zealand common dolphins further suggest that some degree of dietary specialization could occur in this region (Meynier et al. 2008).

(grade A) The ultrasonographic diagnostic criteria for hepatic ma

(grade A) The ultrasonographic diagnostic criteria for hepatic mass by the Japan Society of Ultrasonics in Medicine specify the following six findings as the B-mode ultrasound findings specific to hepatocellular carcinoma: “sharp and smooth boundary”, “presence of marginal faint hypoechoic zone”, “internal mosaic pattern”, “internal star-shaped anechoic area”, “posterior echo enhancement” and “lateral shadows” (LJ062261 level 6). In particular, for http://www.selleckchem.com/products/erastin.html tumors with a large diameter, these ultrasound findings have a high specificity and correct diagnosis rate for making a diagnosis of hepatocellular carcinoma (LF031202 level 1, LF028483

level 1, LF027844 level 1). Nonetheless, for small tumor sizes, the frequency of obtaining specific findings decreases, and the findings can only be classified as a “low echo pattern” or “high echo pattern”. Because of the decrease in the specificity (LF031202 level 1,

LF030695 level 4), the capacity of this method for differentiation from other liver tumors, such as metastatic liver cancer and hemangioma of the liver, is limited. In contrast-enhanced ultrasonography, tumor vessels are extracted in the early arterial phase (LF019356 level 1, LF020587 level 1, LF109018 level 1, LF110689 level 1). As compared with conventional power Doppler ultrasonography, this method improves the detection capability of tumor blood flow, particularly for small nodules 30 mm or less in diameter,

and the detection capability of tumor blood flow is equivalent to that of CT (LF1031710 level 1, LF1059311 level selleck chemicals 1, LF1004212 level 1, LF1057013 level 1). Contrast ultrasonography using Levovist shows a filling defect in the parenchymal phase (LF0190814 level 1, LF0192115 level 1, LF110689 level 1). As compared with non-contrast-enhanced ultrasonography, contrast-enhanced ultrasonography has been demonstrated to improve the detection capability of lesions (LF1031710 level 1), to enhance the capacity for differentiation between benign Acesulfame Potassium and malignant lesions (LF1078216 level 1, LF1094517 level 1, LF1077718 level 3), and to be useful for determining the degree of differentiation of hepatocellular carcinoma (LF1042519 level 3), however, the diagnostic performance declines for deep lesions (LF020587 level 1). Contrast-enhanced ultrasonography is currently in a situation where advances are being made in the devices, imaging techniques and contrast media used. It is suggested to be useful for determining the degree of malignancy of hepatocellular carcinoma and differentiating hepatocellular carcinoma from benign diseases. There are data to suggest that its diagnostic performance is equivalent to that of CT. As compared with CT, contrast-enhanced ultrasonography has the advantage of not causing radiation exposure and being implementable in patients who are allergic to iodine contrast or decreased renal function.

The median age of the cohort was 56 years and the majority were m

The median age of the cohort was 56 years and the majority were male. As expected, HCV was the predominant etiology of liver disease in this U.S. cohort. Selleck Pictilisib Most patients (88%) had evidence of cirrhosis. The median MELD score was 9.2 and most patients had normal performance status and were ambulatory. A majority of patients had a single lesion with a wide range in the size of the tumors with half of the patients meeting the so-called Milan criteria. Vascular invasion or extrahepatic spread was relatively infrequent. Curative therapy was employed including resection in 17% (n = 71) and liver transplantation in 31% (n = 133). Local ablation was used in 9%

(n = 37), transarterial therapy in 25% (n = 106), and systemic chemotherapy in 5% (n = 22). In 56 patients (13%), only comfort care was possible. In patients who underwent liver transplantation, their median MELD score were

9 (interquartile range [IQR] = 7-13). As expected, nearly all (88%) were within the Milan criteria. The median follow-up was 23 months and 295 (62%) died during the follow-up. The univariate Cox proportional hazards analysis was performed in the derivation cohort (Table 2a). All of the data elements that represent liver disease severity and tumor extent were significantly associated with risk of mortality, whereas age had a marginal effect. Galunisertib research buy Family history and liver disease etiology (HBV or HCV) had no apparent impact on survival. When variables with univariate significance were considered in a multivariate model, age, Selleck Cetuximab MELD, serum albumin, and the four radiographic variables that reflect the tumor extent (the size of the largest tumor nodule, the number of nodules, vascular invasion, and metastasis) as well as AFP were selected as independent predictors of survival. Figure 1 illustrates the relation between MELD and risk of death after adjusting for other variables in the multivariate model.

There was little change in mortality risk with low MELD scores. The risk started to increase demonstrably at a score of 13, beyond which a one-point increase in the MELD score was associated with a 10% rise in mortality in a largely linear fashion. For this reason, we instituted a lower bound of MELD score at 13 in the development of the survival model. Results of similar analysis on age, albumin, serum AFP, tumor size, and tumor numbers are illustrated in Supporting Figures 2-6. Based on the multivariate model, a risk score (MESIAH; Model to Estimate Survival in Ambulatory HCC patients score, MESIAH henceforth) can be calculated using the formula shown in Table 2b. Further, Table 2c illustrates expected survival for patients with the median MESIAH score in the derivation cohort. Application of the risk score in individual patients allows calculation of expected survival. For example, the 1- and 3-year survival probability in patients in the lowest quartile (MESIAH score <3.62), was 85.8%, 68.1%, respectively. In the highest quartile (MESIAH score >5.05), survival decreased to 52.

In particular, the breakage of chromosomes 1, 5, 6, 7, and 12 may

In particular, the breakage of chromosomes 1, 5, 6, 7, and 12 may represent an early event during hepatocarcinogenesis, while the deletions of chromosomes 4, 12, 14, and X appear during HCC progression.12 Of note, the breakpoints described on c-myc/TGF-α chromosomes 1, 4, 7, and 12 correspond to human 1q, 1p, 11p, and 14q that are also rearranged in human HCC.4, 13 In human liver specimens, loss of heterozygosity (LOH) was found to be uncommon in cirrhosis, focal nodular hyperplasia, and hepatocellular selleck chemicals llc adenomas, but detectable

in high-grade dysplastic nodules (DN), which are putative precancerous lesions.13 Importantly, the frequency and pattern of genetic alterations detected in DNs highly resembled those in HCCs. Gains of DNA were found to cluster in chromosome arms 1p, 1q, 7q, 15q, 16p, 17q, and 20q and losses of DNA at 3p, 4q, 9p, and 11q in both lesion types. Also, chromosomal alterations responsible for HCC progression and metastasis were found to be located on chromosome arms 4q, 6q,

8p, 13q, 16q, and 17p.14 Thus, the data from transgenic mice and human HCC together with those obtained by Aleksic et al. strongly support the hypothesis of the need of specific genomic alterations “dictating,” more than simply accompanying, the histopathological and molecular changes along hepatocarcinogenesis. The authors’ findings also have important clinical implications. Indeed, the data from Aleksic et al. further substantiate the unfavorable prognostic role of genomic instability in HCC. In this regard, it is worthwhile noting that gene expression patterns from DEN-initiated/PB-fed selleck mice and

c-Myc/TGF-α transgenic mice, both exhibiting elevated genomic instability,5, 7, 12 were highly similar to those of human HCCs characterized by a short survival of the patients.15 The latter human HCC subgroup also displays elevated genomic instability, thus linking a specific gene signature to genomic instability and poor prognosis. A Sodium butyrate chromosomal instability gene signature predicting the patient’s outcome has been previously described in a vast collection of lung, breast, and brain tumors.16 Noticeably, among the genes that were positively correlated with genomic instability was the forkhead box M1b (FoxM1b) transcription factor and its target genes CYCLIN B1 and B2, CDC2, NEK2, KIF20A, TOP2A, CDC25B, AURORA KINASE A, and AURORA KINASE B.16 Given that FoxM1b is overexpressed in HCC and directly correlates with patient survival,17 it would be significant to determine whether the same chromosomal instability gene signature predicts the prognosis of HCC patients as well. Also, since preliminary data show that FoxM1b can be inhibited pharmacologically,18 it would be of high importance to assess whether HCC with elevated genomic instability would benefit from therapies aimed at suppressing FoxM1b expression. Aleksic et al.

2008) with empirical amino acid frequencies and rate heterogeneit

2008) with empirical amino acid frequencies and rate heterogeneity (LG + F  +  G) model for protein

parts. ML analyses were performed using the RAxML v.7.2.8 (Stamatakis 2006). We used “-f a” option for rapid bootstrap analysis and the best likelihood tree searching using “-# 1000” with default “-i” (automatically optimized SPR rearrangement) and “-c” (25 distinct rate categories) options of the program. The independent evolution model for all partition were unlinked by using “-m GTRGAMMA” and “-q” options. Bootstrap values (MLBS) were calculated using Y-27632 research buy 1,000 replications under the same evolution model used for the best tree search. For DNA barcoding analysis, cox1 and ITS sequences were aligned with related phaeophycean sequences using BioEdit™ and MAFFT™

(Katoh et al. 1995). Phylogenetic analyses were conducted in MEGA5 (Tamura et al. 2011). For pairwise distance calculations, both uncorrected p-distances and kimura 2- parameter (Kimura 1980) models were calculated by MEGA5 and were found to be almost identical. The number of base differences per site was calculated from averaging over all sequence pairs within each species group. For cox1 and ITS, 556 and 447 positions were analyzed, respectively, in the final data set. The analysis involved 324 and 253 sequences for buy Cilomilast cox1 and ITS respectively. Codon positions included were 1st, 2nd, 3rd, and noncoding. All positions containing gaps and missing data were eliminated. Species were defined based on clades obtained from phylogenetic analyses using all molecular markers in combination with nonmolecular

characters (see ‘Results’ and ‘Discussion’). Within species and between species pairwise distances were categorized into discrete bins and measured against their frequency. The barcoding cut-off was determined as the smallest distance that encompassed all within-species distances. Minimum genus-level distances were defined as the smallest pairwise distance observed between two species. This distance was applied to species to categorize them into barcode groups. The barcode groups were cross-compared with the combined morphological and DOK2 multigene phylogenies to determine species-and genus level boundaries for each barcode marker. Desmarestia japonica sp. nov. Ligulate Desmarestia is fairly common in northern Japan and an ecologically important component of seaweed communities. It grows on rocks of more or less exposed coasts in the shallow subtidal to 5–6 m (Fig. 1) and is distributed around Hokkaido and along the Pacific coast of Northern Honshu. The sporophytic thalli are annual, growing from winter to late summer, becoming fertile in late spring. The holdfast is cushion-shaped, bearing one to a few erect thalli. The erect thalli are light olive brown to brown in color, 0.6–1 (-2) m in length, with a conspicuous main axis 2–6 (-20) mm in width, oppositely branched in 2–3 orders.