Brown Lomolino Biogeografia Pdf To Excel
The thermophilous giant centipede Scolopendra cingulata is a voracious terrestrial predator, which uses its modified first leg pair and potent venom to capture prey. The highly variable species is the most common of the genus in Europe, occurring from Portugal in the west to Iran in the east. The northernmost occurrences are in Hungary and Romania, where it abides in small isolated fringe populations. We report the rediscovery of an isolated Austrian population of Scolopendra cingulata with the first explicit specimen records for more than 80 years and provide insights into the evolutionary history of the northernmost populations utilizing fragments of two mitochondrial genes, COI and 16S, comprising 1,155 base pairs. We test the previously proposed hypothesis of a speciation by distance scenario, which argued for a simple range expansion of the species from the southeast, via Romania, Hungary and finally to Austria, based on a comprehensive taxon sampling from seven countries, including the first European mainland samples. We argue that more complex patterns must have shaped the current distribution of S. Cingulata and that the Austrian population should be viewed as an important biogeographical relict in a possible microrefugium.
The unique haplotype of the Austrian population could constitute an important part of the species genetic diversity and we hope that this discovery will initiate protective measures not only for S. Cingulata, but also for its habitat, since microrefugia are likely to host further rare thermophilous species. Furthermore, we take advantage of the unprecedented sampling to provide the first basic insights into the suitability of the COI fragment as a species identifying barcode within the centipede genus Scolopendra. IntroductionThe giant centipede Scolopendra cingulata Latreille, 1829 is Europe's largest centipede and the most common species of its genus. It is famous for its voracious habits and painful bite as well as its highly variable, often striking color pattern. Scolopendra is the only European myriapod genus that can severely harm (e.g.
), and in rare cases cause the death of humans,. Components of the potent venom were recently discovered to be of potential medical significance as a pain reliever and as an inhibitor to the proliferation of different cancer types and bacteria.S. Cingulata is widespread and common surrounding the Mediterranean Sea , and, in the past, was divided into three geographically distinct clades based on morphology: Western Europe, Italy, and Eastern Europe,. While the species, in rare cases, has been dispersed to Central Europe through commerce (e.g., a specimen found in the city of Cologne, Germany; ), the natural distribution of S. Cingulata reaches its northern limit in Romania, Hungary and Austria, where it occurs in small, isolated populations (e. Multiple recent records exist from Hungary, where it is listed as an endangered species and receives special protection. In comparison, the Austrian Scolopendra cingulata is all but forgotten, not even listed in recent species distribution maps, despite the fact that its isolated populations might be at least as endangered and localized as the populations in Hungary.
EuropeSince no referenced sequences of S. Cingulata from the European mainland are available in GenBank (but70 from Greek islands ), additional specimens were analyzed. Because of the supposed eastern origin of the Austrian populations, three Hungarian specimens (Permit: Environmental Conservation Fund No. 0) and old Museum samples (ZFMK) from Romania, the Greek mainland, and Turkey were added (see ).
To rule-out a Western origin of the Austrian population, a sample from SW France was also included. Museum specimens from Italy yielded no suitable DNA. Sequences of each of the main Aegean groups (C1, C2, C3, see ) were added from GenBank (Accession numbers: see ). OutgroupsSequences from S. Cretica Lucas, 1853 and S.
Canidens Newport, 1844 were added from GenBank (Accession numbers: see ). Because no sequences are available on GenBank, a Museum specimen (ZFMK) of S. Oraniensis Lucas, 1846 from Morocco was also added to the analysis.The total dataset included 30 terminals for the COI (21 newly added), 28 for the 16S (22 newly added), and 30 for the combined dataset (22 newly added), respectively. Locality data ( and ) is only given imprecisely because S. Cingulata is actively traded in the exotic pet market, and the continuous existence of small fringe populations could be harmed by overzealous collectors. DNA extraction, amplification, and sequencingTotal genomic DNA was extracted using the DNeasy Blood & Tissue Kit (Qiagen; Valencia, CA, USA).To study the evolutionary history of the Austrian S.
Cingulata population, fragments of the mitochondrial cytochrome c oxidase subunit I (COI) encoding gene and the mitochondrial 16S rRNA (16S) encoding gene were amplified. Both gene fragments have previously been successfully applied to study centipede evolution at both the genus (e.g.
–) and species-level (e.g. Since the 16S fragment only provided low resolution, we decided not to include slower evolving nuclear rDNA genes in this study.The 16S fragment was amplified using the 16Sa/16Sb primer pair. The COI fragment was amplified from samples Sco01-10 (Austria) using the primer pair LCO1490/HCO2198. For the remaining samples Nancy was used as an alternative reverse primer.
Attempts were also made to amplify the region with the HCOoutout primer, but no results of sufficient quality could be obtained even though a wide range of PCR-programs were applied. All polymerase chain reactions (PCR) were carried out using the QIAGEN Multiplex PCR Kit and a T3000 Thermocycler (Biometra). All PCR setups included a positive and negative control. Detailed descriptions of temperature profiles and PCR-mixtures can be found in a previous study. The PCR products were inspected on a 1.5% agarose gel and purified using the QIAquick PCR Purification Kit (Qiagen, following the kit protocol, Valencia, CA, USA). Both strands were sequenced by Macrogen (Macrogen Europe Laboratory, Amsterdam, The Netherlands), using the PCR primers. Sequencing reads were assembled and edited using Geneious 6.0.6 (Biomatters) and Seqman II (DNASTAR, Inc.).
Sequence identities were confirmed with BLAST searches. All new sequences were deposited in GenBank (see for accession numbers). AlignmentAll sequences were aligned using the MUSCLE algorithm under the default settings as implemented in Geneious (Biomatters) and edited by hand. Missing ends were filled with N's. The following sites were deleted from the 16S dataset prior to analysis to remove regions of ambiguous homology, mostly regarding the outgroups: 487, 468, 351–353, 345–346, 332–336, 348, 149–150, 20, 1–7. The final alignments consisted of 508 bp (16S), 647 bp (COI) and 1155 bp in the combined dataset.
Fasta files of all alignments and tables containing the uncorrected p-distances for both genes can be found in the supplementary material (, and, ). Sequence analysisIn all maximum likelihood analyses the dataset was analyzed using the model suggested by the Bayesian Information Criterion (BIC), which was computed by the model test implemented in MEGA 5.1. The models with the highest fit were HKY+G for the 16S dataset (BIC = 3107.8) and GTR+G for the COI (BIC = 4855.9) and the combined dataset (BIC = 11724.8).In order to assess the phylogenetic information in our 16S and COI datasets, a likelihood mapping was conducted with TREE-PUZZLE 5.2. Hypothetical relationships of the northern Scolopendra cinuglata and phylogenetic tree recovered in maximum likelihood analysis.A: The hypothetical relationships of the northern populations as previously stated by Attems and Franz,. B: Adult Scolopendra cingulata specimen from the Austrian population in situ. Wolfram Freund.
C: Maximum likelihood tree of the combined COI and 16S dataset. Numbers represent nodal support values from the maximum likelihood (1000 bootstrap replicates), maximum parsimony analysis (1000 bootstrap replicates) and posterior probabilities from the Bayesian inference (ML/MP/BI). Sequences from GenBank marked with single asterisk in front of name. Samples with two asterisks after name include only the COI sequence. Numbers in parenthesis correspond to sample numbers in. Maximum Parsimony phylogenetic analysisAll Maximum Parsimony (MP) analyses were performed in PAUP.
4.0b10 using the TBR algorithm. Starting trees were obtained via stepwise addition and nodal support was estimated with 1000 bootstrap replicates (unlimited number of trees kept at each replicate). The combined dataset included a total of 304 (16S: 124, COI: 180) parsimony informative characters. For the 16S dataset, 1676 shortest trees with 289 steps were found. For the COI dataset, 175714 shortest trees with 568 steps were found. The analysis of the combined dataset resulted in 2101 shortest trees with 867 steps. Strict consensus trees were produced for all datasets (trees not shown).
Nodal support values of the MP bootstrap analysis are displayed in. Bayesian phylogenetic analysisBayesian inference (BI) was conducted using MrBayes 3.1.2. Each dataset was analyzed with the model suggested by the model test implemented in MEGA 5.1, as described above. The combined dataset was partitioned to allow unlinked models for the two genes.
The model parameters (priors) were left unfixed to allow estimation from the dataset, as suggested by the MrBayes manual. The analysis was performed using 3,000,000 Monte Carlo Markov Chain (MCMC) generations of three hot and one cold chain in two parallel runs, sampling trees every 100th generation. The likelihood values for the parallel runs were inspected manually and the generations prior to a stable value were discarded as burn-in. The burn-in was set to 3600, 3100 and 8400 generations for the COI, 16S and concatenated dataset, respectively.
Nodal support values are displayed in. Analysis of the Evolutionary History of the Austrian S. Cingulata populationIn order to further test the hypothesis of a speciation by distance scenario, as stated by previous authors, we compared the genetic and geographic distances between the Austrian S. Cingulata and those from France, Greece, Turkey, Romania and Hungary.The S.
Cingulata COI sequences and geographic distances were pooled according to populations and Kendall's Tau correlation test was performed, as the data was unsuitable for a Mantel test. Kendall's Tau allows to test for a correlation between two variables where the measurements are not equidistant and the data is non-parametric. To assess whether the data are uncorrelated or not, the two-tailed probability test was also performed. All tests were performed in PAST. Sequence DataThe sequencing was successful for most specimens, with the exception of two (one from Izmir, Turkey; and one from Kavala, Greece) of which only the COI was obtained, and of two specimens from Austria of which only the 16S sequence could be obtained.In the COI dataset, the A, T, C and G frequencies were 0.35, 0.27, 0.22 and 0.17, and in the 16S dataset, they were 0.30, 0.39, 0.09 and 0.22, respectively.
Brown Lomolino Biogeografia Pdf To Excel Online
The sequence composition in our COI dataset shows a clear bias towards A and T, which has been shown to be common within chilopods and arthropods in general –.The likelihood-mapping showed a higher amount of phylogenetic information content in the COI dataset than in the 16S. The 16S analysis resulted in 24.0% unresolved trees and a total of 11.2% partially resolved trees. The COI analysis, on the other hand, resulted in only 12.7% unresolved trees and a total of 6.1% partially resolved trees. Molecular Phylogenetic AnalysesThe trees obtained by the maximum likelihood analysis of the combined dataset, with the added support values of the MP and Bayesian analyses, are utilized for the presentation of results.In the analysis of the combined dataset, the S. Cingulata samples form a well-supported (ML = 96%, MP = 100%, PP = 100%) clade against the out-group ( S. Oraniensis).
The genetic distances between S. Cingulata and its three congeners are high (COI: 13.5–16.8%, 16S: 19.3–23.0%).
In the out-group, S. Oraniensis branches off basally, where S. Cretica and S. Canidens form a group (88% ML support). Oraniensis seems to be only slightly more closely related to S. Canidens (uncorr.
P-dist.: COI: 14.5%, 16S: 22.7%), than to S. Cretica (uncorr.
P-dist.: COI: 15.1%, 16S: 20.9%).Within S. Cingulata the basal-most branch consists of a well-supported group (99/100/100) containing two Greek island specimens, representing group C3 of previous analyses. The next split in the tree places the western European specimen outside the only weakly supported (57% ML), clade of the remaining samples. Within the clade, the sample from Nisyros (C1, ) stands basally in a well-supported (56/66/100) group with the two specimens from Turkey. The sister-group to the Greek-Turkish clade is poorly supported. Inside the latter, the Austrian S. Cingulata represent the basal-most group.
The group's monophyly receives strong support (98/100/93) and it contains only a single haplotype in both the COI and 16S gene. The sister-group of the Austrian S. Cingulata is a clade consisting of specimens from Hungary, Romania and Greece. Basally, the Hungarian specimens form a well-supported monophyletic clade (100/99/99), while their sister-groups are less well supported. The three Hungarian samples, from localities less than 1 km apart, display different COI haplotypes with small genetic distances (COI: 0.6–1.0%, 16S: 0.0%). The first weakly supported (57/-/-) split within the sister-group to the Hungarian samples, places the Romanian sample outside of a clade containing the remaining Greek samples.
Within the Greek samples (excluding the basal Greek Island C3 and the Turkish-Nisyros C1), three well-supported clades can be distinguished: (1) one specimen (red legged, ) from Port Lagos, which forms the sister-group to (2) the island samples C2 (97/100/100), and (3) the well-supported (87/92/100) Greek mainland specimens from Kavala and Port Lagos (yellow legged, ). Evolutionary History of the Austrian S. Cingulata populationThe speciation by distance scenario, as suggested by Attems and Franz, postulates that S. Cingulata could have reached Austria from an eastern refugium or point of origin via Hungary and Romania. A positive correlation between the geographic and genetic distance, as would be expected under said scenario, could not be proven.
Although a weak positive correlation was detected (tau = 0.34213), the probability test failed to support this scenario (p = 0.1035). Sequence Data – Barcode evaluationOur analysis of the COI dataset regarding the suitability of the sequence as a species-delimiting barcode showed a clear “barcode gap” between the intra- and interspecific distances. Such a gap was also reported for the North-African representatives of the lithobiid genus Eupolybothrus, with the lowest interspecific distance of 16.61% and intraspecific distances of 1.4% and 0.3%.
However, a finer geographical sampling of all taxa would be necessary to validate our findings as high intraspecific distances have been reported for the New Caledonian endemic species Cryptops pictus, with a divergence of up to 23.8%, as well as several instances of overlapping inter- and intraspecific distances in Bavarian Chilopoda. The latter was suggested to be due to possible cryptic species or alternatively long separated haplotypes, which would concur with the findings of Wiemers & Fidler. They showed that barcode gaps could be artefacts resulting from incomplete geographical sampling of widespread species. Using the 16S fragment might pose a better option, as the highest intraspecific divergence within our S.
Cingulata samples was only 4.5%, much lower than in the COI (9.1%), and the lowest interspecific divergence was still at 10.2%, similar to the one of the COI dataset (13.5%), between the closely related S. Cretica and S. Canidens, and much higher between the other species (19.3–23.0%). The 16S fragment would likely increase the accuracy of the barcode, but at the cost of the population genetic insight. Evolutionary History of the Austrian S.
CingulataThe expected hypothetical phylogenetic tree , according to the evolutionary hypothesis by past authors, could not be recovered in any of the conducted analyses of the mitochondrial genes. Although the most interesting splits received weak statistical support in our phylogenetic analyses, it remains clear that the Austrian, Hungarian, Romanian, and northern Greek specimens are closely related. The study by Simaiakis et al.recovered the split between the eastern Aegean Islands (C1) and the northern and central Cyclades (C2) to most likely have happened approximately 10.12 Mya. In our analysis of the combined COI and 16S datasets, the Austrian population is the first to split from the branch leading to the representatives of the C1 group. This might indicate that the lineage of the Austrian population was established much earlier than the possible repopulation of the Carpathian Basin following the last glacial period. Furthermore, the fact that both of the postulated closest relatives to the Austrian Scolopendra population, the Hungarian and Romanian specimens, have a lower genetic distance to the northern Greek samples (Port Lagos) than to each other or to the Austrian population indicates that the underlying pattern is more intricate than what can be explained by a single range expansion of S.
Cingulata population founders out of a Mediterranean refugium.Our study failed to significantly prove the postulated speciation by distance scenario suggested by Attems. This implies that more complex mechanisms and/or events preceding the last glacial period could have shaped the northernmost distribution of Scolopendra cingulata in Europe. Multiple independent recolonizations would correspond with the view of Varga, who concludes that populations from multiple small meso- and microclimatically favourable sites at the fluctuating borderlines of the Mediterranean refugial and periglacial belts played a significant part in the postglacial repopulation of the Carpathian Basin in several insect groups.
Though this scenario of multiple recolonizations seems probable, further and denser sampling, especially of geographically close western populations and the populations in the regions surrounding the former periglacial belts, would be necessary to confirm our theory, as the current sampling does not provide the resolution required to draw any firm conclusions. Study of the European mainland S. Cingulata populations versus other S. Cingulata studiesMinelli proposed that S. Cingulata populated southern Europe (Iberian-, Italian and the Balkan Peninsula) quite recently. In contrast, a later study based on distributional patterns suggested that the species differentiation in the Mediterranean Basin happened less than 5.5 Mya, or, alternatively, between 9 and 12 Mya via either the Balkans or northern Africa. A recent study based on molecular data supports the latter view, suggesting the time of divergence for two main lineages of Aegean S.
Cingulata to have been approximately 10.5 Mya years ago. However, our data suggests that the Aegean islands were most likely colonized from multiple directions as supported by the fact that the representatives from the C2 group cluster within the Greek mainland samples and that the C1 sample clusters with the Turkish mainland samples.
This could imply that the formation of the mid-Aegean trench might be irrelevant to the C1/C2 split, rendering the calibration of the phylogeny in the previous analysis inaccurate.An additional study of S. Cingulata populations based on morphometric data revealed an east-west gradient within the species, suggesting a colonization of central and southern Europe from the easternmost parts of its range (Asia Minor and Middle East) via the Balkans and Northern Africa. Our analyses support the notion of separate colonization events, because the French sample is recovered in a basal position relative to the eastern European samples. If the French population had originated via the Balkans, a closer relationship with the Austrian or Greek populations would have been expected. However, given the limitations of the current sampling, our results are concurring with but not corroborating the recently proposed multiple colonizations of the European continent. Regrettably, the samples used for the present study were for the most part juveniles, prohibiting a morphometric evaluation. Two sympatric, unrelated different color morphs in Greek S.
CingulataThe two Greek mainland samples from Port Lagos were animals of two different color morphs; one had red legs and a black body while the other had yellow legs with a green-brown body. Such extreme color variation is not rare in Scolopendra species. For example, Shelley reports that S. Viridis in North America ranges from a solid green to yellow in variations with longitudinal or transverse stripes. However, the genetic basis of these variations is completely unknown.
It is especially interesting that the two sympatrically occurring morphs do not seem to be each other's closest relatives. The gray animal clusters with the other Greek mainland samples from Kavala, which were brown with yellow legs, and the red-black animal is resolved as the sister taxon to the group containing the Greek mainland samples and the samples from the Greek islands Paros and Koufonisi. Further sampling would be required to confirm if there is any phylogenetic information behind the different morphs or if the variation is also present within one lineage.
Presently, we can only conclude that the differentiation is clearly within the intra-specific range, since the divergence between the two samples is only 2.3% (COI). Analysis problemsThe likelihood-mapping analyses we conducted show that the 16S fragment did not provide much phylogenetic information on the intraspecific level, as a large portion of the trees remained completely or at least partially unresolved. This is also evident in the trees produced by our phylogenetic analyses, where the dataset only provides some resolution in the most basal splits. The lack of intraspecific variation (highest divergence of 4.3%) prompted us to omit the gene from the analysis of the evolutionary history (but not the phylogeny, see ). A faster evolving gene than COI or 16S is needed to further elucidate the evolutionary history of the northernmost S. Cingulata and for future studies in the genus Scolopendra at the species level. While fragments of the 12S, and 28S gene – have been employed in previous centipede studies, these genes seem to be even slower evolving than 16S.
ITS (internal transcribed spacer) might be a future alternative, but it does not seem to provide more species level information than the COI-fragment.Unfortunately, a microsatellite study – often the method of choice for population genetic studies in insects (e.g. ) and vertebrates (e.g. ) – has never been conducted in Chilopoda. A cheaper and easier alternative might be using AFLPs since the method does not require specific primers or any previous knowledge about the sequences,. However, an AFLP study is not possible with old museum specimens.
As previously mentioned, a more fine-tuned and denser sampling across the whole distributional range would also vastly improve the conclusiveness of our analyses. OutlookTo test the hypothesis of multiple independent colonization events and elucidate the phylogeography of the northernmost populations of Scolopendra cingulata further, a finer geographic taxon sampling as well as the application of other molecular markers, as discussed above, is absolutely essential. Including further peripheral populations will be difficult, as they are extremely scattered and often restricted to very small areas. Within Asturia S. Cingulata is only known from the sample locality (which is.
Sep 28, 2015. Option 1) If you are an authorized Apexi tuner, then you would have access to the Power Excel software?
Option 3) Less expensive solution which is solely hardware, would be to use FC Hako interface module with what I would assume is FC Edit software that you. (Didnt download but should work). Apexi Power FC Commander Pro Software 415-X910. Product Features: - Interface cable (Serial) to allow real-time communication between the Power FC and a laptop. Home; Adam smith; capital asset; depreciation; durable; economics; s; non-renewable resource; physical capital; production; service; stock. As you may have guessed by the many hints we have dropped, FC-Datalogit was developed and is made in New Zealand. This could have been a problem for product.
Books Biogeography Ecological And Evolutionary Approach Pdf biogeography, ecological. Biogeografia ecologica: revision con enfasis enbiogeography an ecological and evolutionary approach - browse. Manual flash starblitz 320 btz radical bleach free. Moore biogeography 3rd edition by lomolino, riddle and brown. Other material will be made available.equilibrium. Classic Papers In Geriatric Medicine Buch Portofrei, Evolutionary Analysis And Ecology A M, Brown Lomolino Biogeografia Pdf, Foundations Of Ecology Classic Papers With Commentaries, Classic Papers In Geriatric Medicine Buch Portofrei, Publications Bruce Patterson S Pages, Fundamentals Of Ecology.
The Best Free PDF Software app downloads for Windows: PDF Reader for Windows 7 PrimoPDF PDF Reader for Windows 10 PDFill Free PDF Editor Basic Foxit R.Log into Facebook to start sharing and connecting with your friends, family, and people you know.The problem with opening PDF files in Firefox is that it tends. Index of /sem201602/geo131/fuentes. Parent Directory BOCCARD-ecologia-numerica-con-R.pdf BROWN-LOMOLINO-biogeography.pdf CORREA-GONZALEZ-graficos-estadisticos-con-R.pdf EcologiaSmithSmith8vaedicionPearsoneninglesBUENO.pdf. Fix a cracked or chipped windshield yourself. If you do not fix a chip in the glass as soon as possible the chip can turn into a crack overnight! It is easy and costs $10.
A repair place will charge about $75 to fix the chip and a windshield can cost you over $500 to replace. This short diy video will save you time, money, and frustration!
Here is where I got the window repair kit: This came out WAY Better: Here is another chip repair video using a different kit: How to Super Clean a Windshield:.If the video was helpful, remember to give it a 'thumbs up' and consider subscribing. Download on iTunes Now!: Stream on Spotify Now: Subscribe to My Channel:.Lyrics are Below.For Sheet Music and Performance Tracks, click please visit:.For Licensing and use in any wedding video or video that will be posed online, please visit: // If you would like to use this song in your wedding, feel free!
I would be honored if you did! To License the rights to use this song in any wedding video that will be posted anywhere online, please visit the Licensing Page on www.ryanndarling.com. I would be honored if you did this as well! // I wrote this song and surprised my husband by singing it to him on our wedding day! I hope you enjoy:) ////// Thank you SO much for the insane amount of support & love everyone has given my songwriting and music! You can also read the thoughts written below about this video. This video demonstrates gathering or connected individuals or of human as per unremarkable intrigue.
Furthermore, concentrates all the more frequently to identities and purpose of individuals. This video assigned Rummy - Koodamela Koodavechi Lyric Imman - YouTube is assigned to allot someone`s encounter, conclusions, exercises and remarks about the point that is verbalized by its group. Subha Priya is an unselfish individual that ofcourse needs to profit us. I trust the video slaked your objective after optically peddling:). Invizimals that can allow the player to interact with their environment, as well as using the PSP (android) Camera to look for invisible creatures that lurk around every corner like pokemon GO.
By Using a PSP or android on-screen sensor, players can track the creature down the mysterious Invizimals and lay down magical traps to capture as much as possible dilikngkungan around. Invizimals Shadow Zone can also be added to the franchise with a story that takes a few months after the events of the first Invizimals in the game. And also the latest features, is in and can capture up to more than 100 new Invizimals to hunt and battle with other creatures. You can also cooperate with your friends to co-op game and capture using the meida ad hoc or Infrastructure WIRELESS connectivity. You can even modify and share your Invizimals by changing their names as you wish, and can change color. Qigong For Dummies Pdf. This game can also be menampilkanlayar heading to exotic locations that you just investigate as you investigate how the shape of creatures, the Invizimals in ancient mythology.
Powerdirector 13 Ultimate Crack Download. Installation and Set-Up GProf User Guide Supported format Installation and Set-Up Gprof plugin depends on binutils (such as addr2line, cfilt and nm). Gprof can be used on any platform as soon as these binutils are in PATH. For example, you can use it on windows with cygwin.
First of all, the user has to compile the C/C program with profiling enabled using the -pg option prior to running the tool. This can be done via the project Properties-C/C Build-Settings-Tool Settings-GCC C Compiler-Debugging tab which has a check-box 'Generate Gprof Information (-pg)'. A similar check-box can be used for CDT Autotools projects. It is found under project Properties-Autotools-Configure Settings-configure-Advanced. 2004B September 23, 1963 ♢ “Saturday Club,” BBC radio recordings, London: BO DIDDLEY (broadcast Oct. 2005A June 10, 1964 ♢ Chess Studios, Chicago: BJ and Mick Jagger interview for a local Chicago TV station. “This Hour Has Seven Days” with an extract of I'm Alright McDaniel; CBC, Nov.
Cogs and Gears This Steampunk inspired book box is a great addition to any desk or dressing table. Mixed Media Steampunk style keepsake box with VIDEO TUTORIAL by Gabrielle Pollacco using Bo Bunny mixed. Willie Dixon, Little Richard, Bo Diddley, Chuck Berry in 1986 (from the documentary 'Hail!