Anthropomorphic representations presuppose

that people th

Anthropomorphic representations presuppose

that people think of humans as forming a referential and distinct category from non-humans. After all, we are not writing this article about how to position species we wish to conserve as panda-morphic, or sea turtle-morphic, or tree-morphic, despite the considerable conservation traction that these taxa may possess. Anthropomorphic representations are transgressive and/or transformative, and thus powerful, in the context #Ferrostatin-1 randurls[1|1|,|CHEM1|]# of Western anthropocentrism and the nature/culture and human/animal dualisms (Ingold 1994; Descola 1996; Fréger 2012). Within this cultural framework, distrust of anthropomorphism as a mode of scientific thinking drew on the idea that non-humans had no mental or emotional states, or that these could not be known (Burkhardt 2005). Anthropomorphism was thus represented as fantasy all across its spectrum (see Fig. 1), firmly on the culture side of the nature/culture dualism. Non-Western cultures, by contrast, display a “seemingly infinite empirical diversity of nature-culture complexes” (Descola 1996 p. 84). Descola divides these complexes into three main types, naturalism (e.g. Western thought), animism (e.g. non-humans speaking to humans), and totemism (e.g. kinship between humans and non-humans). In totemic BAY 11-7082 manufacturer and animistic complexes, anthropomorphism

per se is a non-concept. For example, identification of orangutans as human-like persons by Western visitors to orangutan conservation centers in Malaysia can result in a strong emotional bond that rewards conservation-oriented caring through volunteerism (Parreñas 2012). This empathetic egomorphization constructs a hybrid orangutan/human actor that “disrupts” nature vs. culture while also linking these categories through the “fluid nature of identification” with the orangutan (Sowards 2006; see Descola Sclareol 1996). The emotional bond is arguably motivating and rewarding in part because

it both creates and resolves the problem of orantugan-human similarity. By contrast, indigenous Indonesians already know that orangutans are kin. In their totemic conception, orangutans are humans who went to live in the forest, and they remain human (Sowards 2006). Anthropomorphization of orangutans for conservation outreach to this indigenous community might not produce a similar emotional bond of caring: what would it mean to anthropomorphize a person? The process of anthropomorphization of orangutans could have significantly different meanings across cultures. Many indigenous cultures have some form of totemic or animistic conception of what humans are. For example, in tropical South America monkeys are often a kind of human, or descendants of humans (Cormier 2006). Throughout the Americas, indigenous peoples have been characterized as understanding humans to be what animals and spirits know themselves as when they are at home (de Castro 1998).

Amino acid starvation mainly operates through RelA and the level

Amino acid starvation mainly operates through RelA and the level of ppGpp accumulation was quite similar in all strains (Figure 3b). In contrast in Figure 3a, it is evident that ppGpp response under carbon

starvation was much more heterogeneous, consistent with variations in SpoT or its regulation by carbon starvation. Figure 3 Kinetics of ppGpp accumulation in ECOR strains starved for carbon or amino acid. 32P-labelled cultures of exponentially-growing cells were treated with 2% α-MG (to induce carbon starvation) or 1 mg/ml SH (to induce #EX 527 solubility dmso randurls[1|1|,|CHEM1|]# amino acid starvation). Samples were withdrawn at time intervals and assayed for ppGpp. Values represent the level of ppGpp relative to GTP + ppGpp. Based on the kinetics in Figure 3, the level of ppGpp appeared to stabilise at around 30 min (in agreement with [44]) and a 30 min point was used to survey other ECOR strains. The levels of ppGpp measured under carbon starvation and amino acid starvation respectively are shown in Figure 4a and 4b. Overall, the stringent response with amino acid starvation was present and relatively constant in all strains (collective mean = 0.78, SD = 0.06, SD/mean JNK-IN-8 clinical trial = 0.08). On the other hand, the ppGpp levels triggered by α-MG addition varied over a much greater range (collective mean = 0.24, SD = 0.07, SD/mean = 0.29), consistent with the more heterogeneous kinetics in

Figure 3. Figure 4 ppGpp levels of ECOR strains starved for carbon or amino acid. Cells were treated as in the legend of Figure 3, except that samples were withdrawn 30 minutes following the addition of α-MG or SH. ECORs 50, 51, 53 and 63 carry a T13N substitution in spoT. Bars represent the mean ± SD of three independent measurements.

DNA sequencing of the spoT gene from four high- and four low-ppGpp strains in Figure 4 revealed a mutation common in several low-ppGpp strains. A T13N substitution not present in lab strains or high-ppGpp strains was found in ECOR50, 51, 53 and 63. Although there is no direct evidence implicating these substitutions in altered ppGpp levels, these polymorphisms and those found in laboratory strains [21] are possibly consistent with spoT being subject to microevolutionary SPTLC1 pressures. The relationship between ppGpp and RpoS levels in the species E. coli As shown in Figure 5a, a plot of the measured ppGpp and RpoS levels in all the strains does not give a simple relationship in which RpoS concentration is proportional to ppGpp inside cells, as would be expected from extrapolating data on one K-12 strain [9]. Not surprisingly, strains with undetectable RpoS have various ppGpp levels. Some strains, such as ECOR44,36,5,56,17,66 and 69 do exhibit a proportionality between the two measured entities, unlike ECOR14,55,58,65,54 and MG1655, which fall on a plateau with a limited amount of RpoS.

Can J Microbiol 2013, 59:437–441 PubMedCrossRef 21 Paton AW, Pat

Can J Microbiol 2013, 59:437–441.PubMedCrossRef 21. Paton AW, Paton JC: Multiplex PCR for direct detection of Shiga toxigenic Escherichia coli strains producing the novel subtilase cytotoxin. J Clin Microbiol 2005, 43:2944–2947.PubMedCrossRef LY3023414 concentration 22. Wolfson JJ, Jandhyala DM, Gorczyca LA, Qadeer Z, Manning SD, Hadler J, Rudrik JT, Thorpe CM: Prevalence of the operon encoding subtilase cytotoxin in non-O157 Shiga toxin-producing Escherichia coli isolated from humans in the United States. J Clin Microbiol 2009, 47:3058–3059.PubMedCrossRef 23. Kado CI, Liu ST: Rapid procedure for detection and isolation of large and small plasmids. J Bacteriol 1981, 145:1365–1373.PubMed

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methods. Mol Biol Evol 2011, 28:2731–2739.PubMedCrossRef 29. Friedrich AW, Bielaszewska M, Zhang WL, Pulz M, Kuczius T, Ammon A, Karch H: Escherichia coli harboring Shiga toxin 2 gene variants: frequency and association with clinical symptoms. J Infect Dis 2002, fantofarone 185:74–84.PubMedCrossRef 30. Lindgren SW, Samuel JE, Schmitt CK, O’Brien AD: The specific activities of Shiga-like toxin type II (SLT-II) and SLT-II-related toxins of enterohemorrhagic Escherichia coli differ when measured by Vero cell cytotoxicity but not by mouse lethality. Infect Immun 1994, 62:623–631.PubMed 31. Sanchez S, Diaz-Sanchez S, Martinez R, Llorente MT, Herrera-Leon S, Vidal D: The new allelic variant of the subtilase cytotoxin ( subAB ) is common among Shiga toxin-producing Escherichia coli strains from large game animals and their meat and meat products. Vet Microbiol 2013, 166:645–649.PubMedCrossRef 32. Gerhardt E, Masso M, Paton AW, Paton JC, Zotta E, Ibarra C: Inhibition of water absorption and selective damage to human colonic mucosa induced by subtilase cytotoxin produced by Escherichia coli O113:H21. Infect Immun 2013, 81:2931–2937.PubMedCrossRef Competing interests The authors declare that they have no competing interests.

Conclusion In order to detect the changes in M loti between

Conclusion In order to detect the changes in M. loti between Vorinostat manufacturer free-living and symbiotic conditions, we performed proteome analysis of M. loti. We used our LC-MS/MS system, equipped with a long monolithic silica capillary column, to successfully identify 1,658 proteins without bacteroid isolation and prefractionation. This analytical system opens up a new horizon

for symbiotic proteome analysis from small amounts of unpurified crude biological samples. The protein profile indicated some interesting and unexpected results associated with the cell surface structure and metabolism, in accordance with the external environment of each condition (Figure 5). The data set revealed that M. loti under the symbiotic condition simplifies the components of the cell surface, such as flagellum, pilus, and cell wall. In addition, we found that M. loti under the symbiotic condition provided not only a nitrogen source but also FPP, which is a source of secondary metabolism. Our data should be helpful in carrying out

detailed studies on the change of these 2 conditions CRT0066101 of rhizobia. Figure 5 Schematic Z-DEVD-FMK cost representation of the lifestyle under the symbiotic condition compared to the free-living condition. The illustration shows the changes in the lifestyles of M. loti: the lifestyle model under the (a) free-living and (b) symbiotic conditions. The central carbon metabolic pathway is essential under both conditions. Under the symbiotic condition, nitrogen is fixed by electrons from the TCA cycle or other energy metabolism and is provided to the host legume or used for amino acid biosynthesis. Moreover, the flagellum and pilus are lost, and the cell wall, which is mainly composed of peptidoglycan, may become thin or disappear. In contrast, FPP is synthesized to provide to the host legume. Under the free-living condition, LPS is secreted extracellularly as a nod factor to infect the host legume. Methods Strains and growth conditions M. loti MAFF303099 was cultured

in tryptone-yeast extract (TY) Oxymatrine medium [35] at 28°C. Cells were harvested in the early stationary phase for 72 h. Cells were subjected to sample preparation in the free-living condition. For the symbiotic condition, L. japonicus MG-20 Miyakojima [36] seeds were sterilized, germinated, and inoculated with M. loti and grown in MM1 [37] medium at 25°C with a 16-h light/8-h dark cycle. Root nodules from several plants were harvested at 7 weeks post-inoculation. Nodules from 3 independently grown pools of plants were collected and processed in parallel. Nodules were frozen with liquid nitrogen, homogenized with an ice-cold mortar, and subjected to sample preparation. Sample preparation Collected cells were resuspended with 500 μL of lysis buffer (2% (w/v) 3-(3-cholamidopropyl)dimethylammonio-1-propanesulfonate, 10 mM dithiothreitol, 1% (v/v) protease inhibitor cocktail (Sigma-Aldrich, St.

J Antimicrob Chemother 2009,64(1):151–8 PubMed 57 Menichetti F,

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of severe sepsis of abdominal origin. Scand J Surg 2007,96(3):184–96.PubMed 60. Osborn TM, Nguyen HB, Rivers EP: Emergency medicine and the surviving sepsis campaign: an international approach to managing severe sepsis and septic shock. Ann Emerg Med 2005,46(3):228–31.PubMed 61. Esteban A, Frutos-Vivar see more F, Ferguson ND, Peñuelas O, Lorente JA, Gordo F, Honrubia T, Algora A, Bustos A, García G, Diaz-Regañón IR, de Luna RR: Sepsis incidence and outcome: contrasting the intensive care unit with the hospital RG7420 solubility dmso ward. Crit Care Med 2007,35(5):1284–9.PubMed

62. Emmi V, Sganga G: Diagnosis of intra-abdominal infections: clinical findings and imaging. Infez Med 2008, (Suppl 1):19–30. 63. Bartolozzi C: Imaging and invasive techniques for diagnosis and treatment of surgical infections. Surg Infect (Larchmt) 2006,7(Suppl 2):S97–9. 64. Foinant M, Lipiecka E, Buc E, Boire JY, Schmidt J, Garcier JM, Pezet D, Boyer L: Impact of computed tomography on patient’s care in non-traumatic acute abdomen: 90 patients. J Radiol 2007,88(4):559–566.PubMed 65. Emmi V, Sganga G: Clinical diagnosis of intra-abdominal infections. J Chemother 2009,21(Suppl 1):12–8.PubMed 66. Puylaert JB, van der Zant FM, Rijke AM: Sonography and the acute abdomen: practical considerations. Am J Roentgenol 1997,168(1):179–86. 67. Doria Tau-protein kinase AS, Moineddin R, Kellenberger CJ, Epelman M, Beyene J, Schuh S, Babyn PS, Dick PT: US or CT for diagnosis of appendicitis in children and adults? A meta-analysis. Radiology

2006, 241:83–94.PubMed 68. TJ, Park KG, Steele RJ, Chung SS, Li AK: A randomized trial of nonoperative treatment for perforated peptic ulcer. N Engl J Med 1989, 320:970–973.PubMed 69. Boey J, Lee NW, Koo J, Lam PH, Wong J, Ong GB: Immediate definitive surgery for perforated duodenal ulcers: a prospective controlled trial. Ann Surg 1982, 196:338–344.PubMed 70. Millat B, Fingerhut A, Borie F: Surgical treatment of complicated duodenal ulcers: controlled trials. World J Surg 2000, 24:299–306.PubMed 71. Crisp E: Cases of perforation of the stomach with deductions therefrom relative to the character and treatment of that lesion. Lancet 1843(2):639. 72. Wangensteen OH: Nonoperative treatment of localized perforations of the duodenum. Minn Med 1935, 18:477–480. 73. XAV939 Taylor H: Peptic ulcer perforation treated without operation. Lancet 1946, 2:441–444.PubMed 74. Crofts TJ, Park KG, Steele RJ, Chung SS, Li AK: A randomized trial of nonoperative treatment for perforated peptic ulcer. N Engl J Med 1989, 320:970–973.PubMed 75.

By immunohistochemistry, greater expression of MMP-9 and less exp

By immunohistochemistry, greater expression of MMP-9 and less expression of TIMP-1 in ectopic selleck products endometrium than in eutopic endometrium was also observed [10]. Recently, it was demonstrated in mice that the treatment of 15-Epi-lipoxin A4 (LXA4) may inhibit the progression of endometriosis possibly by lowering the concentrations and the activities of MMP-2 and MMP-9

[38]. In our model, MMP-9 mRNA expression, as expected, was greater in endometriotic lesions than in eutopic endometrium. selleckchem Our results indicate a direct role for MMPs in the ability of rat endometrium to establish ectopic lesions within the peritoneum. By other hand, it is known that proteoglycans play an important role in the maintenance of vascular integrity. Kirn-Safran et al. (2008) [39] showed that proteoglycans are involved in angiogenesis by presenting and modulating a wide range of growth factors such as fibroblast growth PP2 price factor-2 and -10 and VEGF on their glycosaminoglycan (GAG) side-chains. Recently, we have demonstrated that chondroitin sulfate (CS) GAG was the dominant sulfated GAG present in stroma of deeply infiltrating endometriosis lesion foci [40], as also observed in eutopic endometrium [41]. Taken together, these studies suggest that the high concentration of CS in endometriosis could be related to the angiogenesis process, and reinforce the importance of extracellular

matrix metalloproteinases in the progression of endometriosis. Animal models of endometriosis are of extreme value and indispensable for the evaluation of pathophysiological mechanisms underlying the development of this prevalent gynaecological disease. Other possible and important use for this method is to test the angiogenic

therapy for endometriosis. Although there are disadvantages in extrapolating data across species, it is still possible to utilize animal models to study events involved in the pathogenesis of endometriosis that are not accessible in humans. Rat endometriotic tissues and cells perform similarly to human endometriotic cells, as revealed in this study. While the rat model for endometriosis has been used to identify effects of ectopic endometrial tissue adhesion and growth, the mechanisms eliciting these effects remain elusive. In general, animal models will help to develop novel non-invasive diagnostic tools and improved therapeutical approaches for improved treatment of endometriosis Org 27569 in women. Conclusions Here we originally showed that the pattern of angiogenic process in rat endometriosis is very similar to human disease. Despite recent advances in the field, there is still only a limited amount of knowledge about the mechanisms regulating the complex dynamic process of blood-vessel development in endometriotic lesions. The introduction of sophisticated in vivo models of peritoneal and extra-peritoneal endometriosis, which allow for detailed monitoring of angiogenesis within endometriotic lesions under standardized conditions, certainly will help to clarify these mechanisms.

The data pre-computing process is illustrated in Figure 1; web-ba

The data pre-computing process is illustrated in Figure 1; web-based and stand-alone tools learn more were used separately. Web-based localization prediction tools were requested via a Web automat, a python automatic submission

workflow using both “”httplib”" and “”urllib”" libraries. A different script was created for each tool. For web-tools with no equivalent (such as “”TatP”" for Tat-BOX and “”LIPO”" for Lipoprotein-BOX) and incompatible with automatic requests, we collected results manually. CoBaltDB also provides a platform with automatically pre-filled forms for additional submissions to a selection of fifty recent or specific web tools (Table 4). The stand-alone tools selleck compound were installed on a Unix platform (unique common compatible platform) and included in a global python pipeline with the HTTP request scripts. We selected information from a up-to-date collection of 20 databases and integrated this data within CoBaltDB; these databases were retrieved by simple downloading or creating an appropriate script which navigates on the web databases to collect all protein information. The global python pipeline used multi-threading to speed up the pre-computation of the 784 proteomes. Figure 1 A schematic view of the CoBaltDB

workflow. CoBaltDB integrates the results of 43 localization predictors for 784 complete bacterial and archaeal proteomes. Each complete NCBI prokaryotic genome implemented in CoBaltDB was classified as: archaea, or monoderm or diderm bacteria. 101 protein subcellular location predictors were evaluated and few were rejected. Selected tools were classified as: feature localization tools (Specialized), localization meta-tools (Global) or databases. The data recovery process was performed manually or via a Web automat using a python automatic submission workflow for both stand-alone and web-based tools. Databases were downloaded. For each protein, ouptuts collected were parsed and selected items were stored in particular CoBaltDB formatted

files (.cbt). The parsing pipeline creates one “”.cbt”" file per replicon to compose the final CoBaltDB repository. The client CoBaltDB Graphical User Interface communicates with the Phospholipase D1 server-side repository via web services to provide graphical and tabular representations of the results. Database Creation and Architecture For each protein, every output collected (a HTML page for web tools and a text file for standalone applications) was parsed and selected items were stored in a particular format: Selleckchem AZD8186 binary “”marshal”" files. The object structure obtained by parsing tool output was directly saved into a marshal file, allowing a quick and easy opening by directly restoring the initial parsing object.

When

DNA extracts from bovine blood were added to the tem

When

DNA extracts from bovine blood were added to the templates, both pCS20 and sodB LAMP could not detect 10 copies in two samples, which is in accordance with real-time PCR (Table 2). When DNA extracts from A. variegatum were added to the templates, both pCS20 and sodB LAMP failed in detecting 10 copies in all five samples, while real-time PCR could detect in four. The pCS20 PCR using the KAPA Blood PCR kit detected more positives than the pCS20 PCR using the AmpliTaq Gold PCR kit in the templates with 102 and 103 copies (Table 2). Table 2 Inhibitory effects of DNA

extracts from field Selleck IWR1 samples on pCS20 PCR, pCS20 real-time PCR, pCS20 LAMP, and sodB LAMP     No. of samples: Sample type No. of plasmid Screening Library copies per reaction Tested pCS20 PCR positive pCS20 real-time PCR positive pCS20 LAMP positive sodB LAMP positive DNA extracts from bovine blood 1 5 0 (0)a 0 0 0   10 5 0 (0) 3 3 3   102 5 2 (0) 5 4 5   103 5 5 (0) 5 5 5   104 5 5 (5) 5 5 5 DNA extracts from Amblyomma variegatum 1 5 0 (0) 0 0 0   10 5 0 (0) 4 0 0   102 5 5 (0) 5 BGB324 price Rho 5 5   103 5 5 (3) 5 5 5   104 5 5 (5) 5 5 5 aTotal no. of samples positive

by using the KAPA Blood PCR kit (Total no. of samples positive by using the AmpliTaq Gold PCR kit). Detection of E. ruminantium DNA in field samples A total of 140 A. variegatum ticks were collected in 7 sites in Uganda and individually analyzed for the presence of E. ruminantium DNA. Out of 140 ticks, including 96 males and 44 females, 12 ticks (11 male and 1 female) were found positive with both pCS20 LAMP and sodB LAMP. The pCS20 real-time PCR detected 13 positives, including the 12 LAMP-positive ticks and an additional tick from Dokolo, while pCS20 PCR could detect only 8 positives (Table 3). All the samples found positive with PCR were also positive with LAMP. The percent positive with LAMP (8.57%) was higher than with PCR (5.71%) but slightly lower than with real-time PCR (9.29%). Of the 150 bovine, 35 goat, and 19 lamb blood samples analyzed, two lamb samples were positive using PCR, real-time PCR, and LAMP (Table 3). Table 3 Comparison of pCS20 PCR, pCS20 real-time PCR, pCS20 LAMP, and sodB LAMP for the detection of E. ruminantium in various field samples     No.

However, previous reports have indicated that carotenogenesis may

However, previous reports have indicated that carotenogenesis may be regulated by some type of feedback mechanism, by which the relative proportion of astaxanthin regulates the total amount of carotenoids synthesized [27]. Given our observations, the feedback mechanism mediated by astaxanthin in the carotenoid biosynthesis pathway may involve regulatory mechanisms at the transcriptional level, and the presence and composition of pigments may affect the transcriptional response triggered by the addition of glucose to the medium. To test this hypothesis, we performed glucose addition experiments using homozygous mutant strains that are incapable of synthesizing astaxanthin.

The strains used were T-YBHH2 (crtYB – ), T-I21H1H (crtI -) and T-SHH2 (crtS – ), as described in a previous work [28]. First, we determined that the response of grg2 and PDC expression to glucose was similar in all of the strains studied and check details did not depend on the synthesis of STI571 manufacturer pigments (data not shown). In contrast, different results were observed for the mutants of the carotenogenesis pathway genes. For the crtYB gene, the 6-fold repression of mature messenger observed in the wild-type strain in response to glucose completely disappeared and was replaced by a slight induction in both, the mutant that accumulates phytoene (crtI -) and

the mutant that accumulates β-carotene (crtS – ) (Figure 5a). However, the levels of alternative transcripts in both mutant strains exhibited a glucose-mediated decrease that was less than the one observed in the wild-type strain (Figure 5b). A similar phenomenon was observed for the crtI gene; both, the mutant incapable of synthesizing carotenoids (crtYB triclocarban – ) and the mutant that accumulates β-carotene (crtS – ) showed a complete lack of glucose repression of the mature Entospletinib cell line transcript (Figure 5c) and a very diminished response of the alternative transcript levels (Figure 5d). Finally, in the case of the crtS gene, the slight repression by glucose observed

in the wild-type strain was replaced by a slight induction in the crtYB – and crtI – mutants (Figure 5e). These results indicate that the expression of the crtYB, crtI and crtS genes in response to the addition of glucose depends, at least in part, on the normal synthesis of astaxanthin or on the presence of this compound in the cell. Figure 5 Effect of glucose on the expression of carotenogenesis genes in mutant strains incapable of synthesizing astaxanthin. Strains: T-YBHH2 (crtYB-/-, white inverted triangle), T-I21H1H (crtI-/-, black square) and T-SHH2 (crtS-/-, white diamond). Levels of mRNA for mature crtYB (a), alternative crtYB (b), mature crtI (c), alternative crtI (d) and crtS (e) in glucose-treated cultures (20 g/l) were determined for each strain relative to the control.

The baseline hazard is multiplied by an exponential function that

The baseline hazard is multiplied by an exponential function that expresses the multiplicative effect of the 1 to p covariates, multiplied by the corresponding

regression parameters \( \beta_i \). If a particular covariate \( x_i \) does not influence the observed hazard rate, then \( \beta_i \) does not differ significantly from 0. The estimates for the regression coefficients are used to compute a hazard ratio (HR), which describes the effect of the covariate (Kalbfleisch and Prentice 2002). Its significance is assessed with a Z score. Covariates used in the analysis NVP-BSK805 datasheet were coded as categorical since the measurements were unevenly spread over the ranges: temperature (°C; T), radiation (°C; R), cloudiness (% cloud cover; C), wind speed (m/s; W), gender (G; male Torin 1 mouse versus baseline female), and year (Y; 2007 versus baseline 2006; representing unmeasured factors changing between years,

e.g. food supply). Weather variables were clustered into ‘low’, ‘intermediate’, and ‘high’ categories to distinguish optimum or unidirectional effects of weather variables on the duration of bouts (Table 2). We based the clustering of covariates on Kaplan–Meier plots. A Kaplan–Meier survival curve is a step function that decreases from 1 (all individuals are still flying MEK162 supplier at time t) toward a minimum value >0 due to termination of flying bouts. Kaplan–Meier survival curves O-methylated flavonoid should be parallel for all covariate categories, i.e. should not cross (Kalbfleisch and Prentice 2002),in order to be able to assume proportionality estimating the effect size in Cox model(s). We plotted Kaplan–Meier survival curves for flying bouts for all covariate values separately, to see under what values curves do not cross (for an example see Appendix Fig. 4). Clustering was subsequently based on best Kaplan–Meier plot appearance. Next, we tested for pairwise differences in behavioural response under

low, intermediate and high weather categories. The effects of single weather variables were estimated simultaneously with other weather variables. We used R 2.7.0 software (Ihaka and Gentleman 1996) to perform the survival analysis. For P. argus, temperature, cloudiness, and wind speed were highly correlated, and differed strongly between years (see Appendix Table 8). Therefore, only radiation was used in the analysis, together with gender and year. Table 2 Clustering of weather variables into ‘low’, ‘intermediate’, and ‘high’ categories per species, resulting from Kaplan–Meier survival curves for flying bouts Weather variable Category C. pamphilus M.