We welcome contributions that elucidate deep history and those th

We welcome contributions that elucidate deep history and those that address contemporary processes; we especially invite manuscripts with potential to guide and inform humanity into the future. While Anthropocene emphasizes publication of research and review articles detailing human interactions

with Earth systems, the Journal also provides a forum for engaging global discourse on topics of relevance and interest to the interdisciplinary communities. We therefore seek short essays on topics that include policy and management issues, as well as cultural aspects of bio-physical phenomena. We also welcome communications that debate the merits and timing of the Anthropocene as a proposed geologic epoch. While we encourage these discussions, the Journal will remain neutral in its position with regards to the proposal to name a new epoch within the Geological Time Scale. The title of the journal, Anthropocene, is intended as a

MEK activation broad metaphor to denote human interactions with Earth systems and does not imply endorsement for a new geologic epoch. We are pleased to highlight the first issue of Anthropocene comprising contributed and invited articles reporting studies from different parts of the world and different components of Earth’s systems. The editorial team is committed to producing a quality journal; we look forward to selleck working together with the research communities to facilitate advancement of the science of the Anthropocene. “
“The nature, scale and chronology of alluvial sedimentation is one of the most obvious geological elements in the identification and demarcation of the Anthropocene (sensu Zalasiewicz et al. (2010)) – the proposed geological period during which humans have overwhelmed the ‘forces of nature’ ( Steffen et al., 2007). The geological record is largely composed of sedimentary rocks which reflect both global and regional Earth surface conditions. Although the geological record is dominated by marine enough sediments there are substantial intervals of the record where fluvial sediments are common (such as the Permo-Trias and much of the Carboniferous). The constitution of the rock record fundamentally reflects plate tectonics and global climate with the

two being inter-related through spatiotemporal changes in the distribution of land and oceans, astronomical forcing (Croll-Milankovitch cycles) and oceanic feedback loops. However, even marine sediments are the result of a combination of solutional and clastic input both of which are related to climate and Earth surface processes such as chemical weathering and erosion. Geomorphology is therefore an integral part of the rock-cycle and so fundamentally embedded within the Geological record both in the past and today ( Brown, 2008 and Brown et al., 2013). It is in this context that we must consider the role of humans both in the past and under the present increasingly human-driven global climate. Since pioneering work in North America after the dust-bowl of the 1930s by Happ et al.

75 vs 0 80 in Cazorzi et al , 2013) We deemed, therefore, approp

75 vs 0.80 in Cazorzi et al., 2013). We deemed, therefore, appropriate to apply the same width-area class definition considered by the authors (0.4 m2 cross-sectional

areas for widths lower than 2 m, 0.7 m2 for widths up to 3 m and 1.5 m2 for sections larger than 3 m). In addition to the agricultural network storage capacity, we also considered the urban drainage system, adding the storage capacity of the culverts. The major concerns for the network of the study area arise for frequent rainfall events having high intensity. We decided therefore to provide a climatic AZD8055 supplier characterization of the area, focusing on a measure of the aggressivity and irregularity of the rainfall regime, to quantify the incidence of intense rainfall events on the yearly amount of precipitation. This climatic characterization is accomplished by the use of a precipitation Concentration Index (or CI) according to Martin-Vide (2004). This index evaluates the varying weight of daily precipitation, that is the contribution of the days of greatest rainfall to the total amount. The CI is based on the computation of a concentration curve that relates the accumulated percentages

of precipitation contributed by the accumulated percentage of days on which it took place, and it considers the relative separation between this concentration curve and an ideal case (represented by the bisector of the quadrant, or equidistribution line) where the distribution mafosfamide of the daily precipitation www.selleckchem.com/products/AZD2281(Olaparib).html is perfect (Fig. 5). The area enclosed by the equidistribution line and the actual concentration curve, in fact, provides a measure of the concentration itself, because the greater the area, the greater is the concentration. The concentration curve can be represented according to the formulation equation(1) y=a⋅x⋅ebxy=a⋅x⋅ebxwhere y is the accumulated amount of precipitation and x is the accumulated number of days with precipitation, and a and b are two constants that are computed by means of the least square method ( Martin-Vide,

2004). Once the concentration curve is evaluated, it is possible to evaluate the area under the curve, as the definite integral of the curve itself between 0 and 100. The area compressed between the curve and the equidistribution line is then the difference between 5000 (the area under the equidistribution line) and the area under the curve. Finally, the Concentration Index (CI) is computed as the ratio between the area enclosed by the equidistribution line and the actual concentration curve, and 5000. To evaluate the concentration curve, we considered cumulative rainfall data that are available publicly (ISPRA, 2012) for the station of Este, located about 10 km from the study area, whose rainfall measurements cover the years from 1955 up to 2012.

T cells from Vav1AA/AA mice also show a proliferative defect when

T cells from Vav1AA/AA mice also show a proliferative defect when injected into MHC-mismatched recipient animals in a mechanistic GvH mouse model (Fig. 3). The

total number of Vav1AA/AA T cells after 3 days was strongly reduced compared to WT T cells, and 18% of the cells did not divide at all. Interestingly, the majority of Vav1AA/AA T cells reached 6 division cycles, showing that there was no complete block in proliferation. Rather, Vav1AA/AA T cells seemed to have divided more slowly compared to WT T cells, which led to the reduced total numbers of cells. This is in contrast to T cells treated with the strong immunosuppressant CsA, where the majority of T cells did not divide at all. However, in a previous study, T cells from Vav1−/− mice also did not show a complete block in proliferation but a similar delay in proliferation, which was enhanced in T cells from mice deficient in both learn more Vav1 and Vav2 [23]. These findings suggest that disruption of Vav1 function only partially affects the TCR-induced proliferative signals which can be overcome by a stronger costimulatory environment in vivo. Vav1 GEF activity seems to be important for the Vav1-mediated proliferative response, as Vav1 GEF inactivation and total Vav1 deficiency have comparable effects. CsA, however, might affect Vav-independent TCR-induced signals CP-868596 supplier and also different stimuli

in addition to TCR engagement such as cytokines and costimulatory signals, which also contribute to T cell proliferation [28]. Furthermore, CsA has effects on other cell types and tissues resulting in strong general immunosuppression, which may explain the stronger response compared to Vav1 inactivation. Vav1AA/AA mice show prolonged cardiac allograft survival with a mean survival time of 22 days compared to WT animals which reject the allograft after 7 days (Fig. 4). These findings confirm

the previously observed central role for Vav1 in allograft rejection [23]. Vav1AA/AA as well as Vav1−/− mice have reduced numbers of peripheral T cells due to a defect in thymic development [20], and we cannot exclude a partial effect of this reduction on allograft survival. However, Vav1AA/AA T cells showed a strong defect in allogeneic T cell proliferation and activation in vitro and in vivo when SSR128129E equal numbers of T cells were used, indicating that the prolonged allograft survival in Vav1AA/AA mice is likely to be caused by defective T cell activation. However, to fully confirm these findings, inducible genetic systems or specific Vav1 inhibitors will be needed. Graft survival in Vav1AA/AA mice is not as pronounced as in Vav1−/− mice which lack the whole Vav1 protein, indicating that the GEF function of Vav1 affects only part of the processes mediating rejection [23]. This could also account for the high variation in allograft survival time observed for the Vav1AA/AA mice.

In C  elegans, RNA-dependent RNA polymerase (RdRP) amplifies the

In C. elegans, RNA-dependent RNA polymerase (RdRP) amplifies the primary siRNA forming secondary dsRNAs that feed back into the front end of the RNAi pathway ( Sijen et al., GSK2118436 chemical structure 2001). However, core RNAi machineries for siRNA production are not involved in systemic spreading of RNAi, and siRNA amplification is not necessary for the systemic RNAi effect ( Tomoyasu et al., 2008). In general, the core RNAi machineries are conserved among all insects species examined, while RdRP homologs have never been identified, even in those showing robust systemic

RNAi ( Tomoyasu et al., 2008). Nonetheless, RdRP-like activity via alternative enzymes has been reported in Drosophila cells ( Lipardi et al., 2005). SID-1 is a dsRNA-selective dsRNA-gated channel (Shih and Hunter, 2011) and its role in dsRNA uptake is the key to systemic spreading of RNAi in C. elegans. In insects, the presence of SID-1-like

(SIL) proteins appears to vary phylogenetically, e.g., being notably absent in Dipterans ( Tomoyasu et al., 2008). However, several studies cast doubts on their roles in dsRNA uptake. First, sensitivity to RNAi is not always associated with the presence of sil. For instance, the silkmoth Bombyx mori Linnaeus possesses three sid-1 orthologs but is not susceptible to experimental RNAi. However, when ectopically expressed in Bombyx cells, C. elegans SID-1 could aid dsRNA uptake thereby greatly enhance the cells’ sensitivity selleck screening library to RNAi ( Kobayashi et al., 2012). Second, for those species with robust systemic RNAi that also possess sils, the sils are actually dispensable with P-type ATPase regard to the RNAi effect ( Luo et al., 2012; Tomoyasu et al., 2008). Further, insect sils appear to share more similarity in sequence with C. elegans tag-130, which is not involved in RNAi ( Tomoyasu et al., 2008). Therefore, insects amenable to systemic RNAi must possess alternative mechanism(s) for the systemic spreading of RNAi signal. In insects other than D. melanogaster, research on RNAi has largely focused on the non-cell autonomous (environmental and

systemic) RNAi response. Until recently, most investigations of RNAi in insects have involved delivery of in vitro synthesized dsRNAs into embryos or the hemocoel by microinjection. This method of dsRNA delivery has provided a powerful reverse genetic tool for investigating gene function in species lacking well developed genetics as well as a means to evaluate the relative sensitivity of a given species to systemic RNAi. However, microinjection is obviously not a useful means to deliver dsRNA for pest control. The potential utility of RNAi for insect pest control was suggested by two studies published in 2006 demonstrating that RNAi can be elicited in insects by oral administration of dsRNA (Araujo et al., 2006; Turner et al., 2006).

10,000 00 cells were counted per samples Relative fluorescence i

10,000.00 cells were counted per samples. Relative fluorescence intensities were monitored by BD FAXSCANTO™ flow cytometer (BD Bioscience, CA, USA) and analyzed by the software Modfit and Cell-Quest (BD Biosciences, Franklin Lakes, NJ) with settings of FL1 (green)

at 530 nm and FL2 (red) at 585 nm (Liu et al., 2007). Cellular ATP was determined by means of the firefly luciferin–luciferase assay system. Cells (1 × 105) were incubated as for the viability assay and suspension was centrifuged at 50 × g for 5 min at 4 °C. The pellet was treated with 1 ml of ice-cold 1 M HClO4. After centrifugation at 2000 × g for 10 min at 4 °C, aliquots (100 μl) of the supernatants were neutralized with

70 μl selleck chemicals llc of 2 M KOH, suspended in 100 mM Tris-(hydroxymethyl) aminomethane (Tris)–HCl, pH 7.8 (1 ml final volume), and centrifuged again. Bioluminescence was measured in the supernatant with a Sigma-Aldrich assay kit according Selleck PLX3397 to the manufacturer’s instructions, using an AutoLumat LB953 Luminescence photometer (Perkin-Elmer Life Sciences, Wilbad, Germany). Intracellular oxidation of dichlorodihydrofluorescein diacetate (H2DCFDA) to 2,7-dichlorofluorescein (DCF) by ROS was monitored through fluorescence increase. HepG2 cells were seeded in a 12-well plate at a density of 1 × 105 cells/well and incubated as for the cell viability assay. After incubations, the well plates were washed with PBS and then 100 μl/well Edoxaban of 10 μmol/l H2DCFDA was added to each well, remaining incubated at 37 °C for 45 min in a 5% CO2 incubator. Fluorescence was measured in a model F-4500 Hitachi fluorescence spectrophotometer (Tokyo, Japan) at the 503/529 nm excitation/emission wavelength pair (slits 5/10 nm) (Halliwell and Whiteman, 2004). Mitochondria were isolated by standard differential centrifugation (Pedersen et al., 1978). Male Wistar rats weighing approximately 200 g were euthanized by decapitation; livers (10–15 g) were immediately removed, sliced in medium (50 ml)

consisting of 250 mM sucrose, 1 mM ethyleneglycol-bis(β-aminoethyl)-N,N,N′,N′-tetraacetic acid (EGTA) and 10 mM HEPES-KOH, pH 7.2, and homogenized three times for 15 s at 1 min intervals using a Potter-Elvehjem homogenizer. Homogenates were centrifuged (580 × g, 5 min) and the resulting supernatant further centrifuged (10300 × g, 10 min). Pellets were then suspended in medium (10 ml) consisting of 250 mM sucrose, 0.3 mM EGTA and 10 mM HEPES-KOH, pH 7.2, and centrifuged (3400 × g, 15 min). The final mitochondrial pellet was suspended in medium (1 ml) consisting of 250 mM sucrose and 10 mM HEPES-KOH, pH 7.2, and used within 3 h. Mitochondrial protein contents were determined by the Biuret reaction. Mitochondria were energized with 5 mM potassium succinate (plus 2.

Also unlike reinforcement learning, it emphasises subjective expe

Also unlike reinforcement learning, it emphasises subjective experience of action, in addition to action performance. These features may explain our finding that intentional binding involves cortical not subcortical brain regions. To summarize, we have identified the neural correlates of an implicit measure of the sense of agency, namely the perceptual

attraction between actions and their consequences, using fMRI. We found that activation of a lateral subregion of the SMA proper correlated with the strength of the ‘intentional binding’ between actions and their effects. This area may combine a read-out from the motor areas that control intentional action, with an integration of sensory information from areas that monitor external consequences of action. This work was supported by BBSRC and ESRC project grants to P.H., and by ESF ECRP grants to P.H. Vemurafenib manufacturer and M.B. S.K. is a Postdoctoral Selleckchem EX 527 Fellow of the Research Foundation Flanders (FWO). “
“Although most healthy adults feel that they have a great deal of control over their actions, some neurological patients do not. Patients with alien hand syndrome (AHS) may involuntarily grasp objects placed within their reach, experiencing difficulty releasing objects once grasped (see e.g., Biran and Chatterjee, 2004; Della Sala et al., 1991). Despite the fact

that such individuals make seemingly deliberate and purposeful movements with their “alien” hand, 4��8C there is clear disparity between actions performed by the alien limb and the intentions of patients, who subjectively report that the hand is not under their control. Instead, they report that the alien limb behaves as though it has a mind of its own or is being controlled by an external agent (e.g., Assal et al., 2007; Biran and Chatterjee, 2004; Fitzgerald et al., 2007). Although these remarkable grasping behaviours in AHS are now well-documented, we understand very little about the mechanisms that might underlie

such behaviour. AHS is a relatively rare syndrome (for a review, see Fisher, 2000), so detailed investigation has been correspondingly sparse. Some of the most detailed experimental work comes from Riddoch and her colleagues (e.g., Humphreys and Riddoch, 2000; Riddoch et al., 1998). They instructed a patient with bilateral AHS to reach out and grasp a cup with a hand. The patient was able to do this correctly as long as the cup’s handle was on the same side as the hand they were instructed to use to grasp the cup. However, if the handle was on the opposite side, “interference” errors were generated with the patient reaching with whichever hand matched the side the cup’s handle was on. For example, if instructed to grasp a cup with the right hand when the cup’s handle was to the left, the patient would often erroneously grasp the cup with the left hand.

However, there are numerous molecules that have been categorized

However, there are numerous molecules that have been categorized as costimulatory based solely on their ability to generate a second signal when ligated with Lumacaftor purchase antibodies (Leitner et al., 2010). Recombinant proteins representing the extracellular domains of costimulatory ligands are valuable and widely used tools to study T cell activation processes. However, their generation is time consuming and costly and they might differ from

their membrane resident natural counterparts regarding their capability to modulate T cell responses. We have developed a simple cellular system to assess the role of costimulatory ligands in the activation of human T cells. This system, which we have designated T cell stimulator cells, is based on the murine thymoma cell line Bw5417 that expresses membrane-bound anti-human CD3 single chain antibody fragments at high or low densities. Upon retroviral expression of PARP inhibitor human costimulatory ligands on these cells their contribution to the activation of human T cells can readily be determined. In this study we

describe this system in detail and demonstrate that T cell stimulator cells are an efficient and versatile tool to study various aspects of human T cell costimulatory processes. 293T cells and the mouse thymoma cell line Bw5147 (short designation within this work Bw) were cultured as described (Pfistershammer et al., 2006 and Pfistershammer et al., 2008). The ethical review board of the General Hospital and the Medical University of Vienna approved the human studies performed within this work and informed consent was obtained from the donors. PBMC were isolated from heparinised whole blood of healthy volunteer donors by standard density centrifugation with Ficoll-Paque (Amersham Bioscience, Roosendaal, Netherlands). Human T cells were obtained through depletion of CD11b, CD14, CD16, CD19, CD33 and MHC-class II bearing cells with the respective mAbs by MACS (Miltenyi Biotech,

Bergisch Gladbach, Germany). The mAbs to CD11b (VIM12), CD14 (VIM13), CD33 (4D3), Protirelin MHC-class II (1/47), CD80 (7-480), CD58 (1-456) and the non-binding control antibody VIAP (calf intestine alkaline phosphatase specific) were produced at our institute. The mAbs to CD14 (MEM-18) was purchased from An der Grub (Kaumberg, Austria), CD19 mAb (BU12) from Ancell (Bayport, MN), and 41BB-L and CD150/SLAM (A12) from Biolegend (San Diego, CA). Goat anti-human TL1A/TNFSF15 antibodies were obtained from R&D (Minneapolis, MN). FACS analysis was performed as described previously (Pfistershammer et al., 2006). Briefly, binding of primary antibodies was detected with PE-conjugated goat anti-mouse IgG-Fcγ specific Abs or donkey anti-goat IgG (H + L) (both Jackson ImmunoResearch, West Grove, PA).

Mehrabi et al 6, numa revisão compreensiva da literatura mundial,

Mehrabi et al.6, numa revisão compreensiva da literatura mundial, englobando 434 doentes, descreveu as várias

abordagens terapêuticas. Destes, particularizando, 128 doentes foram submetidos a transplantação hepática, com sobrevida global ao primeiro e terceiro anos de 96, e 54,5%, respetivamente. Assim, a transplantação hepática permanece como uma opção terapêutica razoável, mesmo em doentes com doença extra-hepática. buy AG-014699 A sobrevida destes doentes é comparável à dos doentes transplantados por cirrose hepática22. Drogas antineoplásicas, tais como a talidomida, têm mostrado benefícios como terapêuticas adjuvantes ou como terapêutica inicial na doença irressecável23, assim como o interferon α-2 b24. A aplicação de quimioembolização transarterial poderá ser útil em doentes com doença hepática avançada, em lista de espera para transplante6, embora o seu papel como terapêutica coadjuvante no transplante hepático ainda não esteja

claramente determinado. Também doentes com localizações secundárias, tratados com esta modalidade terapêutica, parecem alcançar maior sobrevida do que Ivacaftor concentration com as modalidades cirúrgicas, poupando-os às suas comorbilidades 14. Há casos reportados de quimioterapia intra-arterial com redução do tamanho do tumor e sobrevida até 80 meses15. Os regimes quimioterapêuticos, de administração sistémica, estão longe de ser consensuais. Aqui, também múltiplos casos clínicos são reportados, utilizando múltiplos agentes, isolados ou em associação, com resultados díspares14, 25 and 26. Estas descrições apresentam-se sob a forma de casos clínicos, constituindo apenas casos descritivos, com falta Avelestat (AZD9668) de evidência constatada e de difícil interpretação, pela ausência de regimes terapêuticos uniformes e pela inexistência de estudos prospetivos. A maioria dos regimes de radioterapia (RT) foi administrada em conjunção com QT, pelo que as conclusões acerca da sua eficácia são problemáticas. Até ao momento, não estão determinados elementos prognósticos que permitam diferenciar os

doentes com HEH menos agressivos, dos indivíduos com uma doença mais agressiva, de forma a instituir uma atitude expectante ou, por outro lado, mais incisiva. Descrevemos o caso de um HEH manifestado num homem na quinta década de vida, sob a forma de desconforto no hipocôndrio direito. Apresentava-se já com um tumor de grandes dimensões, com suspeita de invasão pulmonar e óssea, e a evolução cursou com deterioração do estado geral de forma galopante, tendo falecido em menos de 2 meses após o diagnóstico. Este caso realça a imprevisibilidade do HEH, bem como a sua dificuldade diagnóstica em termos de imagem, principalmente na ausência do lollipop sign. Os autores declaram não haver conflito de interesses. “
“For decades, different cases of chronic pancreatitis associated with an important immunological component have been recognized. In 1961, Sarles et al.

Even though he is no longer with us, his work, advice, and person

Even though he is no longer with us, his work, advice, and personal contributions will long

be remembered and will continue to influence our activities for many years. “
“Pesticides are considered as one of the main factors involved in environmental contamination of today’s world. These chemicals are on purpose see more designed to be toxic to pest and vectors of diseases. These compounds are among more than 1000 active ingredients that are marketed as insecticide, herbicide, and fungicide. Nevertheless, formulation of new and potent pesticides is increasingly on the order of researchers and manufacturers because of pest resistance, hygienic controls, and major human need for more food as the world population grows. Although pesticides have largely benefited the human life through enhancement

of agricultural products and controlling infectious diseases, their extensive use, in turn, has offended human health from side to side of occupational or environmental exposures. Long-term contact to pesticides can harm human life and can disturb the function of different organs in the body, including nervous, endocrine, immune, reproductive, renal, cardiovascular, and respiratory systems. In this regard, there is mounting evidence on the link of pesticide’s exposure with the incidence of human chronic diseases, including cancer, Parkinson, Alzheimer, multiple sclerosis, diabetes, aging, cardiovascular and chronic kidney disease (Abdollahi et al., 2004c, De Souza et al., 2011 and Mostafalou and Abdollahi, 2012a). In this overview, we discuss the association of pesticide’s exposure with the incidence of different types of human chronic www.selleckchem.com/products/Roscovitine.html diseases as well as general mechanisms of disease’s process, which can be involved in pesticide-induced toxicities. Chronic diseases are characterized by their generally slow progression and long term duration, which are considered as the leading cause of mortality in the new world, representing over 60% of all deaths. According to the WHO report, 36 million people died

from chronic disease in 2008, of which nine million were under 60 and 90% of these premature deaths occurred in low- and middle-income countries (http://www.who.int/topics/chronic_diseases/en/). (-)-p-Bromotetramisole Oxalate The first reports on the association of pesticides with cancer were presented around 50 years ago regarding higher prevalence of lung and skin cancer in the farmers using insecticides in grape fields (Jungmann, 1966, Roth, 1958 and Thiers et al., 1967). During the past half century, a wide spectrum of population-based studies has been carried out in this respect leading to a significant progress in understanding the relationship of pesticides to the incidence of different types of malignancies (Penel and Vansteene, 2007). The International Agency for Research on Cancer (IARC) has conducted several cohort studies on the incidence of cancers in people exposed to pesticides somehow during their lives (Baldi and Lebailly, 2007).

This variation seems to be correlated with a reduction in habitat

This variation seems to be correlated with a reduction in habitat area (Simpson, 1974) and globally, species richness in TAE is comparable to that for temperate alpine communities (Rundel et al., 1994). Understanding how TAE’s specific biogeographic features would affect plant community attributes, in particular species diversity

and endemism remains a promising area of research for both basic and applied ecologists. Only a handful of studies have focused explicitly on the patterns and/or mechanisms of plant–plant interactions in TAE. In total selleck kinase inhibitor we found 16 papers which discussed – even succinctly – plant–plant interactions in TAE worldwide. While these interactions include both intraspecific and interspecific levels (Brooker et al., 2008) most available studies EPZ015666 chemical structure in temperate and sub-polar/alpine environments have analysed the latter level. Nevertheless, we also considered studies reporting intraspecific interactions when they brought interesting insights for the scope of our review. The resulting list was used to conduct a basic meta-analysis (see Table 1 for details on meta-data). In total, 56% of publications did focus of plant–plant interactions, the rest mentioning

it in only the discussion (e.g. Smith, 1981). From a geographical viewpoint, a large majority of studies were held in the two most widespread areas of TAE, the Andes (62%) and East Africa (19%). In contrast, no studies were reported in two other widespread TAE, Mexico and Indonesia-New Guinea.

Most studies were conducted in humid TAE whereas the only studies that focused on dry TAE examined the effects of one keystone tussock grass of the Central Andes, Festuca orthophylla ( Kleier and Lambrinos, 2005, Patty et al., 2010 and Catorci et selleck chemical al., 2011). From a methodological viewpoint, all designs were observational with the exception of one series of removal experiments in the Venezuelan páramo which examined intra- and interspecific interactions with seedlings of the giant rosette E. schultzii ( Smith, 1984). In terms of results, most studies revealed patterns of spatial associations between species (69%) whereas only 31% of the papers analysed the mechanisms sustaining the interactions. We discuss both observed patterns and proposed mechanisms below. Although not all positive spatial associations reflect positive interactions (e.g. Maestre et al., 2003 and Michalet et al., 2006), many works use it as a powerful exploratory estimate – including in alpine environments (e.g. Callaway et al., 2002, Cavieres et al., 2005, Barbier et al., 2006, Dullinger et al., 2007 and Cavieres and Badano, 2009). Reports of positive spatial associations in TAE are relatively common worldwide (see Table 1 for details).