This year, the Hennig meeting was held at Riverside, California, and I'm fortunate enough to be able to be there (in great part thanks to the Kurt Pickett award, given by the Willi Hennig Society). As in previous occasions, I will try to give a short review of many of talks!
23 jun
I want to remark the excellent reception given by the organizers, and the opportunity to meet some wonderful heteropteran researchers [which is huge for an heteroptera aficionado! :)]
24 Jun
The meeting start up with a plenary talk given by Quentin Wheeler, with the title of Cladistic cosmology. Basically it is about of building a “Hubble like” project for taxonomy, specifically the description of new species, and facilities to make access to museum specimens across the web, both as metadata, but using some form of virtual specimens (e.g. scans of herbaria types, 3d scans of specimens, etc.). I like his point, but I think he miss the point of sampling: we not only need better understanding of current museum data, but also, we need to go to the field and look for never seen before specimens!
The first symposium was organized by Ward Wheeler about linguistics. The first talk, was a video-conf given by Peter Whitely about the phonetic character definition used for an analysis of Uto-Aztec languages. The actual analysis was presented by Ward, that shows some of the particularities of using phonetic characters in comparison with DNA data, such as having 121 letters (against 4) and short strings (against long sequence fragments). Peter Forster talks about the using of phylogenetic networks for language data, and how it can be associated with what we know about the history inferred from mitochondrial molecular markers. You can found his program here. Joanna Nichols also uses phylogenetics networks with emphasis of using different sources of cognate data. To finish the season, John Wenzel shows a reanalysis of some previous indo-european analysis, showing some problems with the character coding, and how much of the current resolution was a by product of the errors in the codings, and the method used. I do not know much about the state of the field of phylogenetic linguistics (although I like the use of these techniques in linguistics!), I found a nice blog that usually talk about phylogenetics in linguistics here.
The next session was on phylogenomics, and was organized by Gonzalo Giribet, so are heavily biased towards invertebrates, but for a frustrated entomologist like me, it was wonderful :D! First Gonzalo talks about how new advances in sequencing technology has increased the amount of available data for phylogenetics, and how the problem was shifted from phylogenetic analysis to orthology recognition among this huge amount of new sequences. Then Torsten Struck shows how the selection of outgroups affects the position of one most mysterious group of annelids, the Myzostomida. Sebastian Kvist, explores the genomics of the blood feeding proteins used by Hirudinid leeches, and the realtionships of their host bacteria, a group related with nitrogen-fixing bacteria found in plants! Kevin Kocot was interested on orthology detection using phylogenetic trees, so he implement a program to detect the best possible set of ortholog sequences. Björn von Reumont talks about the pancrustacean phylogenomics, and how the acquisition of newer data from Remipedia is key in the problem and that results shows than remipedians are more closely related to hexapodans than to more traditional crustaceas, he also hints the existence of some apomorphies for such group based on nervous system. Vanessa González talks about the relationships among Bivalbia, that as many molluscan taxa, seems to be well known, but their phylogenetic relationships are just barely explored.
Then the poster season starts, most of the posters present a lot of entomological work on heteropterans (specially reduviids), so that makes me so happy, I like most the poster from Michael Forthman as he works with Ectrichodiins the group that I see for an small [very small!] amount of time xD, so hopefully he will construct a nice phylogeny of the group! :) The winning poster was given by Guayang Zhang and it is about the elongation of the front legs in harpactorines.
25 Jun
Students day! Most of students talks where given this day, so it will allow the judges to give the student awards with a complete overview of all the material presented by students.
Ansel Payne gives a wonderful talk about the general relationships of Hymenopteran superfamilies. Rebecca Dikow explores a huge data set (in term of characters) using bacterial genomes, so her trees have brutal lengths over 37 millions of steps! Ross Mounce talks about measuring support using supertrees, he also remind us about the importance of using machine readable data for phylogenetics, and that he thinks that using svg files will be great for publishing data, as you can include a lot of non-published metadata inside the files. Julieta Gallego presents a talk about the stability of molecular clocks (as I am a co-author of the talk, maybe I will talk about this in other time!). John Denton gives a talk about the usage of iterative alignments to improve the searches under likelihood approaches. Greame Oatley speaks about a cool group of birds [give me a passeriform, and I will love it ;)], and their species limits, in a work in part phylogeographic, in part taxonomic. Juanita Rodriguez (from Colombia! But she is working in Utah), talks about the phylogeny and biogeography of a group of Pompilid wasps. Fernando Gelin talks about Polybia, a wasp genus. Federico López (another colombian! And old friend of my from undergrad days! He is now at Vermont) gives a talk about the phylogenetics of a group of Vespids. To finish the first student season, I give my own talk about biogeography of amphibians.
In between student talks, there is an interesting symposium about the species problem. I'm personally no see so much in that problem, but is nice to see a lot of talk about that. Fortunatelly, I guess, although the problem is recognized, most taxonomists and systematist can continue to work, and work well, even if there is no consensus in what an species is. Brent Mischler spokes about the phylogenetic (topologic-monophyletic) species concept. Rudolf Meier talks whats about the problem of discussing the topic, and how most people skip the problem at all, and why he thinks it is important to discuss the subject. For me, this is the best talk of the symposium. Finally Kipling Will talks about the influence of the species definition in alpha-taxonomy, specifically how it is affected by some recent approaches, like bar-coding. Then a nice discussion (which includes Quentin Wheeler) was given by the four panelists of the symposium.
The second student seasson begin with a talk given by Christine Hayes about the the phylogenetic relationships of a group of phorid flies. Anna Dal Molin explore several techniques to visualize large groups of trees. Pei-Luen Li talks about a worldwide distributed (but concentrated in Hawai'i) group of asparagales, and Cecilia Waichert explore some adaptation hypothesis about nesting behavior using a phylogeny of Pomipilid wasps.
26 Jun
Pablo Goloboff, gives his talk about the implementation of Iter-PCR, focusing on the effects of changing the ingenuous algorithms, with the use of algorithms that take previous information into account, and makes feasible the use of iter-PCR in TNT. Jean DeLaet, gives an insight on his future program for phylogenetic analysis, Anagallis, that will include his algorithms for dealing with non-applicable data! I'm very curious about it [hopefully it will be open source!]. Nico Franz speaks about using taxonomy ontologies, although I think that kind of work is nice to discover some particular things, I guess that the missing thing is that they at the moment are no using character data, and I think that the key for this kind of databases will be both explicit references, and explicit data supporting each taxonomic affirmation. Lenka Drabkova talks about the plant cytokinins. Claudia Szumik shows the results of a the search of areas of endemism, using also phylogenetic information, with a huge data set of mammals. Then Santiago Catalano presents GB-to-TNT a user friendly program to build huge matrices, and also some nice taxonomy mapping tools found in the newer version of TNT. Daniel Janies, shows that super-trees are not a real solution to the uses of super-matrices, as they fails to produce approximate results of a super-matrix. In one of the most controversial talks Donald Buth argues that mitochondrial data, as non intrinsic source of data, and susceptible of the host-parasite interactions, must not be used for phylogenetic analysis. Personally I do not agree with him, but a friend of me, tells me that the same concerns have been raised in population genetics (a.k.a. Phylogeography) literature. So maybe, mitochondrial data is not good for small taxonomic levels, by the same reason of gene vs species trees, but at large levels, it will provide a nice source of evidence (as the difference between gene and species trees at this levels are no so important). This is an intriguing line of though, as it is precisely the opposite to the most received view, from at least five years ago. John Wiens gives a review of all of his papers about the use of phylogenies for study ancestral ecology. I was too tired after Jon talk, so I miss the next ones. Later Santiago gives a nice talk about the usage of morphometric data on several and different kinds of studies. Tim Crowe talks about the results of a whole life dedicated to study guinea fowls at different taxonomic levels. Dalton Amorim, shows a new analysis of phorid flies based on morphology, one of the few talks using explicit morphological data! Continuing with morphological data, and dipterans, Torsten Dikow shows its phylogenetic analysis Mydidae, he also shows interest on detecting unstable terminals. Efraín de Luna, talks about the use of morphometric data in phylogenetics. To finish the day, Nico Franz gives a talk about how his analysis of some particular group of curculionids evolve in time from the initial data matrix to the definitive one. I think this is a nice exercise, but ultimately, it is difficult to extract some information about it, except from the anecdotal experience.
Later this day was the banquet, that as is a tradition in the hennig meetings was free for students! The banquet speech was given by Dennis Stevenson, the current editor of the journal of the society (Cladistics), and it was funny, although it was somewhat small!
The winners of the awards? Ok, there is a lot of Marie Stoppes and Kurt Pickett awards for traveling students. The Don Rosen award for the best poster was given to Guayang Zhang, as I tell you before. Cecilia Waichert receives the Lars Brundin award, for the second best talk, and John Denton receives the Willi Hennig award for the best student talk! Congratulation to the winners, all are well deserved, and I think the judge have a difficult time selecting these three, because there are a lot of great talks given by students :)!
27 Jun
I think this is the most difficult day to give a talk: everyone is tired of the amount of talks in previous days, as it is the day after the banquet, a lot of people are dehydrated and overtighted, and as it is the last day, you have to check-out from the hotel...
Here this is the last symposium, this one, about molecular clocks organized by Sean Brady, who discuss several sources of error. Tracy Heath talks about how to model dating in bayesian analysis, and Elizabeth Murray has a more concrete talk on the dating of some group of Hymenoptera.
Robert Sansom presents some differences between results using hard and soft anatomy in vertebrates, and the implications for the fossil record, that is only based on hard parts. Mark Simmons shows some problems from using multiple matrices, with small overlap. He present a lot of interesting results for some particular examples, so it is important to known how general they are. Mari Källersjö gives one of the most beautiful talks of the meeting, about a working project of a particular group of plants. Everyone loves his talk :D. Veronica Pereyra talks about thysanopterans, but unfortunately I have to make the check out, so I lost it :-(. Ronald Clouse talks about the phylogeography of an opilion that lives in southeastern US, that is a remaining of a gondwanian clade (as Florida was long time ago, part of African plate!). Ulf Jondelius, talks about the acoelan worms, a poorly known taxon, that he was sampled across the world. To finish the meeting Steve Farris talks about the recent surge of the three taxon statements authors (Ebach, Williams, etc.).
General overview
The meeting was very well organized by John Hartley and Christiane Weirauch, that move around all the time to make sure everything is right. They have a full group of students that are helping with everything, so it was huge :).
On the meeting itself, it has a lot of students, with several very nice talks, and a lot of discussion, that is always welcomed :D. One of the things that I note, is in the same line of previous meetings in which few morphology is used, here I see that although most studies only use molecules for phylogenetic analysis, people is more interested in link several of their findings with well detailed morphological data, hopefully, in the next few years, fully integrative, genomic and morphological data will be used in conjunction in almost every work!
The next year, the meeting will be held in Rostock, Germany, a city on the coast of the baltic sea. Hopefully I will be able to make it, and several of my cladistists ends will be there :D Also, if any one reading this blog interested in phylogenetics, and living somewhere in Europe, I encourage you to go, even if you don't work with parsimony! [In fact, a lot of people that does not use parsimony analysis shows their results at the meeting! And nobody complains about it, at much, someone as why do you not use parsimony, but just that] So! See you there :)!
Acknowledgments
I receive a lot of funding support from several institutions that make this trip possible: CONICET, FONCyT, GBIF (well, this one in the future) provides monetary funding, whereas INSUE allows me to work at their facilities. I receive a Kurt Pickett travel award from the Willi Hennig Society. At personal level, my advisors (Pablo and Claudia) provides me a lot of support, Julí convince me to go, Santí helps me with the trip logistics, and they, with Ross, they are excellent room-mates :)!
Mostrando las entradas con la etiqueta taxonomy. Mostrar todas las entradas
Mostrando las entradas con la etiqueta taxonomy. Mostrar todas las entradas
jueves, julio 05, 2012
sábado, marzo 21, 2009
Just some links
There are some nice things on line lately :).
First, Rod Page talk at NHM of London, he puts his slide-show on line, there is also a video and a pod-cast of the talk (I do not see them :P). The slide-show can give a nice idea about the talk. There are two important things on the talk: (a) the importance of the availability of data! I just agree with him: data must be freely available, and previously published data must be easy accessible; and (b) Scientific data must be readily usable, for example the “Encyclopedia of life” is just a fun site just like wikipedia or the web tree of life, they are full of nice pics and info, but cientifically irrelevant: no hard data are attached to it (i.e. morfological info, character matrices), this contrast with the most simpler ispaces of Page!
Although I do not like some of the comments, Malte Ebach made a good point against the revival of a “pragmatic” classification (for horticulture, for example). I think that the only rule of classification is the phylogeny. If an immutable classification is the objective, the only way I can thing is an “alphabetic” or “numeric” system, but the preservation of “traditional” names is not the solution. Maybe, it is better a change of the rules...
And speaking of change of the rules, I recommend the continuos checking of several of Mike Keesey posts. I do not think that phylocode is the solution (in fact I think that it is even worse than traditional Linnean classification), but he writes interesting things about databasing!
Also, it is seems to change some rules about the publication of names for taxonomy (via Evolving thoughts). I thing that only peer reviewed publication must count, at least from the last fifty years or so. Also I thing that new names, at least for species must be published on journals instead of books...
First, Rod Page talk at NHM of London, he puts his slide-show on line, there is also a video and a pod-cast of the talk (I do not see them :P). The slide-show can give a nice idea about the talk. There are two important things on the talk: (a) the importance of the availability of data! I just agree with him: data must be freely available, and previously published data must be easy accessible; and (b) Scientific data must be readily usable, for example the “Encyclopedia of life” is just a fun site just like wikipedia or the web tree of life, they are full of nice pics and info, but cientifically irrelevant: no hard data are attached to it (i.e. morfological info, character matrices), this contrast with the most simpler ispaces of Page!
Although I do not like some of the comments, Malte Ebach made a good point against the revival of a “pragmatic” classification (for horticulture, for example). I think that the only rule of classification is the phylogeny. If an immutable classification is the objective, the only way I can thing is an “alphabetic” or “numeric” system, but the preservation of “traditional” names is not the solution. Maybe, it is better a change of the rules...
And speaking of change of the rules, I recommend the continuos checking of several of Mike Keesey posts. I do not think that phylocode is the solution (in fact I think that it is even worse than traditional Linnean classification), but he writes interesting things about databasing!
Also, it is seems to change some rules about the publication of names for taxonomy (via Evolving thoughts). I thing that only peer reviewed publication must count, at least from the last fifty years or so. Also I thing that new names, at least for species must be published on journals instead of books...
Etiquetas:
databasing,
digital taxonomy,
taxonomy
viernes, abril 18, 2008
Vouchers, types and specimens
Prompted by the closure of Utrech Herbarium, Chris Taylor write two interesting posts about the nature of type specimens and vouchers (of molecular studies). In both cases Chris remarks about the importance of a comparison specimen to resolve some taxonomical problems.
In a more implicit way, the post about vouchers remarks how molecular tools can be very important, but in a some way or another, to made a proper 'molecular taxonomy' you need to rely on a proper morphological (classic) taxonomy.
I a post that I made some time ago, Chris point me some of that remarks, and actually I think that my disgust with type specimens is not the types, but the bad practice around it, specifically, that many specialist from old days (and maybe some actual ones), propose hundreds of new species based on telegraphic descriptions.
The other thing about type specimens that I do not like, is that it seems that there is an 'single specimen taxonomy', I thing that every specimen in a collection is equally valuable. For me, most important than the type speciemen information is the 'examined specimens' list, that usually include individuals of different sexes, and ontogenetic states.
But I think that new generation of taxonomists are moved into the right direction. First there are new approaches intended to store and provide access to information on an specimen basis, I specially like [1], even if the data are not made public (I prefer public data, but I understand that a taxonomist want to keep his/her data with him after a long work of several years, for at least the same amount of time!), it allows a quick reexamination of material.
The second point, but sadly it is not very popular in third world countries (and even in first world ones), is that every, I repeat every taxonomic contribution would be made under a rigurous phylogenetic framework. That is, character discussion, published data matrix, and phylogenetic tree-based classification.
Character discussions allows a more objective definition of the examined characters, as inside-study coherent terminology, because phylogenetic characters would be the same character across several species.
Data matrix, shows in a easy readable form (specially if you have a phylogenetic data editor, there are several free on the net) several characters examined for a particular terminal (that is a set of examined specimens), which shrink the usually lengthly (and bored to read) description section of the paper. That part can be reserved to particular characters that are not used under the cladistic analysis (for example, colors, measurements, proportions), or particular character scorings (explaining some particular scoring), biological information (such distribution, ecological aspects), links to figures/pictures (electronic or in print) and the list examined specimens. When a character is scored, the author of the matrix is saying that he/she view that character in the species, it also includes a list of non-seen characters (usually typed as '?'). Note that the matrix is an excellent way to fuse the information stored with the several specimens examined, so linking data from the specimens and from the matrix is direct [1].
Finally a cladogram-based classification, allows to maintain the information from the analysis, tightly binded with the taxonomy. If someone proposes a new genus, it will show that the difference with other ones is a really different group, and not a highly appomorphic group inside a previous established genus. A classification need evidence that support each proposed taxon, and the cladogram is the well know form to found evidence of grouping.
[1] Ramírez, M. J. et al. 2007. Linking of digital images to phylogenetic data matrices using a morphological ontology. Systematic Biology 56: 283-294. doi: 10.1080/10635150701313848
In a more implicit way, the post about vouchers remarks how molecular tools can be very important, but in a some way or another, to made a proper 'molecular taxonomy' you need to rely on a proper morphological (classic) taxonomy.
I a post that I made some time ago, Chris point me some of that remarks, and actually I think that my disgust with type specimens is not the types, but the bad practice around it, specifically, that many specialist from old days (and maybe some actual ones), propose hundreds of new species based on telegraphic descriptions.
The other thing about type specimens that I do not like, is that it seems that there is an 'single specimen taxonomy', I thing that every specimen in a collection is equally valuable. For me, most important than the type speciemen information is the 'examined specimens' list, that usually include individuals of different sexes, and ontogenetic states.
But I think that new generation of taxonomists are moved into the right direction. First there are new approaches intended to store and provide access to information on an specimen basis, I specially like [1], even if the data are not made public (I prefer public data, but I understand that a taxonomist want to keep his/her data with him after a long work of several years, for at least the same amount of time!), it allows a quick reexamination of material.
The second point, but sadly it is not very popular in third world countries (and even in first world ones), is that every, I repeat every taxonomic contribution would be made under a rigurous phylogenetic framework. That is, character discussion, published data matrix, and phylogenetic tree-based classification.
Character discussions allows a more objective definition of the examined characters, as inside-study coherent terminology, because phylogenetic characters would be the same character across several species.
Data matrix, shows in a easy readable form (specially if you have a phylogenetic data editor, there are several free on the net) several characters examined for a particular terminal (that is a set of examined specimens), which shrink the usually lengthly (and bored to read) description section of the paper. That part can be reserved to particular characters that are not used under the cladistic analysis (for example, colors, measurements, proportions), or particular character scorings (explaining some particular scoring), biological information (such distribution, ecological aspects), links to figures/pictures (electronic or in print) and the list examined specimens. When a character is scored, the author of the matrix is saying that he/she view that character in the species, it also includes a list of non-seen characters (usually typed as '?'). Note that the matrix is an excellent way to fuse the information stored with the several specimens examined, so linking data from the specimens and from the matrix is direct [1].
Finally a cladogram-based classification, allows to maintain the information from the analysis, tightly binded with the taxonomy. If someone proposes a new genus, it will show that the difference with other ones is a really different group, and not a highly appomorphic group inside a previous established genus. A classification need evidence that support each proposed taxon, and the cladogram is the well know form to found evidence of grouping.
[1] Ramírez, M. J. et al. 2007. Linking of digital images to phylogenetic data matrices using a morphological ontology. Systematic Biology 56: 283-294. doi: 10.1080/10635150701313848
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