Slides presented on the Euler/X projected (http://taxonbytes.org/prior-work-on-concept-taxonomy-2013/ & https://bitbucket.org/eulerx/euler-project) - for the conference "The Meaning of Names: Naming Diversity in the 21st Century", CU Natural History Museum, September 30, 2014.
Franz Et Al. Using ASP to Simulate the Interplay of Taxonomic and Nomenclatur...taxonbytes
Answer Set Programming (ASP) is a declarative, stable model approach to logic programming with an under-realized potential for representing and reasoning over biological information. ASP is particularly suited to address reasoning challenges with complex starting conditions and rule sets. One such challenge is the interplay of taxonomic and nomenclatural change in biological taxonomy that often results when a taxonomy is revised based on a previously published perspective. Depending on the nature of the taxonomic changes to be undertaken, one or more Code-mandated principles will apply to regulate specific and concomitant name changes. In the case of the International Code of Zoological Nomenclature, two principles of significance include the Principles of Priority and Typification. Although the relationship between the number of taxonomic and nomenclatural adjustments under a given transition scenario is not linear, the application of the name-changing rules is usually unambiguous and therefore amenable to logic representation. Here we explore the modeling of the taxonomy/nomenclature interplay in ASP with a simple, abstract nine-taxon use case that contains four terminal species of which two are type-bearers for their respective genera. Four distinct one-taxon transfer scenarios are simulated through a transition system approach, requiring 1-7 concomitant nomenclatural changes depending (1) on the priority relationships among the terminal taxa being repositioned and (2) the type-bearing name dependencies of their higher-level parents. ASP can simulate these rules faithfully and thus reason over situations that range from a one-to-one match of taxonomic and nomenclatural changes to situations where they two kinds of change become increasingly disconnected (e.g., transfer of non-type genera among tribes without name change, or "transfer" [in reverse direction] of a single priority-carrying name/taxon into a larger yet junior entity with numerous required name changes). Our results, though very preliminary, illustrate how ASP logic approach may be utilized to perform optimizations at the taxonomy/nomenclature intersection, and generally represent a novel step towards translating Code-mandated naming rules into logic, with potential benefits for virtual taxonomic domains.
Franz Et Al - Concepts and Tools Needed to Increase Bottom-Up Taxonomic Exper...taxonbytes
We discuss the perceived requirements – conceptual, technical, and social – for the creation of a “Taxonomic Clearing House” (TCH) that will enfranchise and enhance contributions by individual taxonomic experts and collaboratives in a global, names-based infrastructure. In terms of scale, such an infrastructure must be suited to assemble, retrieve, and editing contemporary taxonomic and phylogenetic classifications that involve some 22 million name strings representing 2.3 million living and extinct species; and serve diverse contributor and user communities including 6-40 thousand experts, 400,000 biologists, and more than 100 million citizen scientists. Existing classification synthesis platforms fall short of this grand challenge because they (1) may be limited to living or fossil taxa, (2) fail to show alternative points of view or (3) integrate molecularly-defined entities (“dark taxa”), (4) do not automatically monitor new data, (5) lack scalable solutions for providing feedback and credit, (6) have slow revisionary processes, (7) lack effective machine-to-machine services, or (8) cannot represent finer-grained insights such as evolving taxonomic concepts. Jointly these factors can produce a disconnect of the expert community that leads the global, piece-meal process of advancing classifications from large-scale platforms that purport to represent and unify their individual contributions. A suitable TCH should counteract this by acting as an open communal environment allowing expert contributors to jointly assemble and edit evolving taxonomic and phylogenetic content leading to large-scale classifications. In particular, it must (1) engage major collaborating taxonomic ad phylogenetic initiatives and facilitate diverse information flow; (2) expand information acquisition capabilities to harvest names and classifications from diverse sources; (3) create a powerful interface for taxonomic editing, including a topology assembly and visualization layer, nomenclatural and taxonomic editing layers, a Filtered Push-based service (http://wiki.filteredpush.org/wiki/) for submitting, tracking and accrediting edits to expert contributors, and taxonomically intelligent alerts; and (4) leverage these efforts towards a “Union” reference classification holding two million taxa and multiple alternative perspectives as indicated. To promote the engagement and acceptance, a TCH should target existing expert communities such as contributor to the Symbiota collections or TimeTree phylogenetics platforms. The presentation will both introduce the elements of this TCH vision and assess their merits and current progress and challenges towards realization.
Franz et. al. 2012. Reconciling Succeeding Classifications, ESA 2012taxonbytes
Presentation on reconciling taxonomic concepts using the Euler approach, given at the 2012 Annual Meeting of Entomological Society of America, Knoxville, TN.
Franz 2014 BIGCB Tracking Change across Classifications and Phylogeniestaxonbytes
Slides presented on the Euler/X toolkit at the "Understanding Taxon Ranges in Space and Time" Workshop – Berkeley Initiative in Global Change Biology (BIGCB); held on November 07-09, 2014, University of California at Berkeley, CA. See also http://taxonbytes.org/bigcb-workshop-at-uc-berkeley-tackling-the-taxon-concept-problem/
Franz Et Al. Using ASP to Simulate the Interplay of Taxonomic and Nomenclatur...taxonbytes
Answer Set Programming (ASP) is a declarative, stable model approach to logic programming with an under-realized potential for representing and reasoning over biological information. ASP is particularly suited to address reasoning challenges with complex starting conditions and rule sets. One such challenge is the interplay of taxonomic and nomenclatural change in biological taxonomy that often results when a taxonomy is revised based on a previously published perspective. Depending on the nature of the taxonomic changes to be undertaken, one or more Code-mandated principles will apply to regulate specific and concomitant name changes. In the case of the International Code of Zoological Nomenclature, two principles of significance include the Principles of Priority and Typification. Although the relationship between the number of taxonomic and nomenclatural adjustments under a given transition scenario is not linear, the application of the name-changing rules is usually unambiguous and therefore amenable to logic representation. Here we explore the modeling of the taxonomy/nomenclature interplay in ASP with a simple, abstract nine-taxon use case that contains four terminal species of which two are type-bearers for their respective genera. Four distinct one-taxon transfer scenarios are simulated through a transition system approach, requiring 1-7 concomitant nomenclatural changes depending (1) on the priority relationships among the terminal taxa being repositioned and (2) the type-bearing name dependencies of their higher-level parents. ASP can simulate these rules faithfully and thus reason over situations that range from a one-to-one match of taxonomic and nomenclatural changes to situations where they two kinds of change become increasingly disconnected (e.g., transfer of non-type genera among tribes without name change, or "transfer" [in reverse direction] of a single priority-carrying name/taxon into a larger yet junior entity with numerous required name changes). Our results, though very preliminary, illustrate how ASP logic approach may be utilized to perform optimizations at the taxonomy/nomenclature intersection, and generally represent a novel step towards translating Code-mandated naming rules into logic, with potential benefits for virtual taxonomic domains.
Franz Et Al - Concepts and Tools Needed to Increase Bottom-Up Taxonomic Exper...taxonbytes
We discuss the perceived requirements – conceptual, technical, and social – for the creation of a “Taxonomic Clearing House” (TCH) that will enfranchise and enhance contributions by individual taxonomic experts and collaboratives in a global, names-based infrastructure. In terms of scale, such an infrastructure must be suited to assemble, retrieve, and editing contemporary taxonomic and phylogenetic classifications that involve some 22 million name strings representing 2.3 million living and extinct species; and serve diverse contributor and user communities including 6-40 thousand experts, 400,000 biologists, and more than 100 million citizen scientists. Existing classification synthesis platforms fall short of this grand challenge because they (1) may be limited to living or fossil taxa, (2) fail to show alternative points of view or (3) integrate molecularly-defined entities (“dark taxa”), (4) do not automatically monitor new data, (5) lack scalable solutions for providing feedback and credit, (6) have slow revisionary processes, (7) lack effective machine-to-machine services, or (8) cannot represent finer-grained insights such as evolving taxonomic concepts. Jointly these factors can produce a disconnect of the expert community that leads the global, piece-meal process of advancing classifications from large-scale platforms that purport to represent and unify their individual contributions. A suitable TCH should counteract this by acting as an open communal environment allowing expert contributors to jointly assemble and edit evolving taxonomic and phylogenetic content leading to large-scale classifications. In particular, it must (1) engage major collaborating taxonomic ad phylogenetic initiatives and facilitate diverse information flow; (2) expand information acquisition capabilities to harvest names and classifications from diverse sources; (3) create a powerful interface for taxonomic editing, including a topology assembly and visualization layer, nomenclatural and taxonomic editing layers, a Filtered Push-based service (http://wiki.filteredpush.org/wiki/) for submitting, tracking and accrediting edits to expert contributors, and taxonomically intelligent alerts; and (4) leverage these efforts towards a “Union” reference classification holding two million taxa and multiple alternative perspectives as indicated. To promote the engagement and acceptance, a TCH should target existing expert communities such as contributor to the Symbiota collections or TimeTree phylogenetics platforms. The presentation will both introduce the elements of this TCH vision and assess their merits and current progress and challenges towards realization.
Franz et. al. 2012. Reconciling Succeeding Classifications, ESA 2012taxonbytes
Presentation on reconciling taxonomic concepts using the Euler approach, given at the 2012 Annual Meeting of Entomological Society of America, Knoxville, TN.
Franz 2014 BIGCB Tracking Change across Classifications and Phylogeniestaxonbytes
Slides presented on the Euler/X toolkit at the "Understanding Taxon Ranges in Space and Time" Workshop – Berkeley Initiative in Global Change Biology (BIGCB); held on November 07-09, 2014, University of California at Berkeley, CA. See also http://taxonbytes.org/bigcb-workshop-at-uc-berkeley-tackling-the-taxon-concept-problem/
Franz et al evol 2016 aligning multipe incongruent phylogenies with the euler...taxonbytes
Lightning talk at iEvoBio 2016 (http://www.ievobio.org/), given on June 21, 2016, at Evolution Meetings in Austin, Texas. Brief overview of using Euler/X to align phylogenies. See https://github.com/EulerProject
Franz et al ice 2016 addressing the name meaning drift challenge in open ende...taxonbytes
Presentation for the Symposium: Building the Biodiversity Knowledge Graph for Insects – Components, Progress, and Challenges; 2016 XXV International Congress of Entomology, Orlando, FL – September 26, 2016 (#ICE2016). See https://esa.confex.com/esa/ice2016/meetingapp.cgi/Session/24482
RuleML2015: User Extensible System to Identify Problems in OWL Ontologies and...RuleML
The Semantic Web uses ontologies to associate meaning to
Web content so machines can process it. One inherent problem to this
approach is that, as its popularity increases, there is an ever growing
number of ontologies available to be used, leading to difficulties in
choosing appropriate ones. With that in mind, we created a system that
allows users to evaluate ontologies/rules. It is composed by the Metadata
description For Ontologies/Rules (MetaFOR), an ontology in OWL, and
a tool to convert any OWL ontology to MetaFOR. With the MetaFOR
version of an ontology, it is possible to use SWRL rules to identify anomalies
in it. These can be problems already documented in the literature or
user defined ones. SWRL is familiar to users, so it is easier to define new
project specific anomalies. We present a case study where the system
detects 9 problems, from the literature, and two user defined ones
Franz 2017 uiuc cirss non unitary syntheses of systematic knowledgetaxonbytes
Invited Presentation given at the University of Illinois Urbana Champaign iSchool, Center for Informatics Research in Science and Scholarship, CIRSS Seminar, Friday, February 17, 2017.
Franz et al evol 2016 aligning multipe incongruent phylogenies with the euler...taxonbytes
Lightning talk at iEvoBio 2016 (http://www.ievobio.org/), given on June 21, 2016, at Evolution Meetings in Austin, Texas. Brief overview of using Euler/X to align phylogenies. See https://github.com/EulerProject
Franz et al ice 2016 addressing the name meaning drift challenge in open ende...taxonbytes
Presentation for the Symposium: Building the Biodiversity Knowledge Graph for Insects – Components, Progress, and Challenges; 2016 XXV International Congress of Entomology, Orlando, FL – September 26, 2016 (#ICE2016). See https://esa.confex.com/esa/ice2016/meetingapp.cgi/Session/24482
RuleML2015: User Extensible System to Identify Problems in OWL Ontologies and...RuleML
The Semantic Web uses ontologies to associate meaning to
Web content so machines can process it. One inherent problem to this
approach is that, as its popularity increases, there is an ever growing
number of ontologies available to be used, leading to difficulties in
choosing appropriate ones. With that in mind, we created a system that
allows users to evaluate ontologies/rules. It is composed by the Metadata
description For Ontologies/Rules (MetaFOR), an ontology in OWL, and
a tool to convert any OWL ontology to MetaFOR. With the MetaFOR
version of an ontology, it is possible to use SWRL rules to identify anomalies
in it. These can be problems already documented in the literature or
user defined ones. SWRL is familiar to users, so it is easier to define new
project specific anomalies. We present a case study where the system
detects 9 problems, from the literature, and two user defined ones
Franz 2017 uiuc cirss non unitary syntheses of systematic knowledgetaxonbytes
Invited Presentation given at the University of Illinois Urbana Champaign iSchool, Center for Informatics Research in Science and Scholarship, CIRSS Seminar, Friday, February 17, 2017.
Evolutionary tree or physlogenetic tree and it's types like rooted and unrooted labeled or unlabelled. How to construct physlogenetic tree and limitations of physlogenetic tree.
AnMicro-TBRC Seminar on Phylogenetic Analysis (EP.1).
"Evolutionary Tree: the weapon of molecular phylogeneticists"
by Asst. Prof. Pravech Ajawatanawong
Lab 12 Building Phylogenies Objectives .docxDIPESH30
Lab 12
Building Phylogenies
Objectives
In this laboratory exercise, you will examine six species of agaricomycetes and predict the evolutionary
relationships among them. After completing this exercise you will be able to
• define ancestral characteristics, derived characteristics, branch point, and phylogeny.
• predict ancestral and derived characteristics for agaricomycetes.
• construct a phylogeny (phylogenetic tree).
• support the phylogeny with data.
• explain how evolutionary biologists discover evolutionary relationships.
Introduction
One of the most compelling pieces of evidence for evolution is that organisms have amazing similarities. An
example that almost everyone has heard before is that the limbs of birds, bats, horses, moles, cats, frogs,
humans, turtles, and other vertebrates have virtually the same skeletal plan. Furthermore, even snakes and
whales show structural remnants of the limbs of their ancestors. The evolutionary interpretation of these
similarities is that the vertebrate limb has been modified by natural selection to perform different functions
(for example, running, digging, flying). Another commonly used example is that the embryos of turtles,
mice, humans, chickens, and many other vertebrates are amazingly similar. Furthermore, the proteins and
DNA of organisms are remarkably similar. Why, do you suppose, can human diabetics use insulin extracted
from pigs to control their blood sugar levels? Well, the reason is that the chemical structure of human and
pig insulin is very similar.
In addition to these similarities, we discover that organisms that appear similar in one respect are often
similar in other respects (we can say the patterns are “concordant”). For example, organisms that are
similar morphologically (in shape) have similar protein structures. Organisms that are less similar
morphologically have less similar protein structures. This pattern holds for traits that are not easily
modified by evolution, but not so often by traits that are easily modified by selection. For example, flower
color might not be a good trait to use when looking for concordance because it is easily changed
genetically.
The concordance of traits is an important support of evolution. Imagine that we saw that organisms similar
in one set of characteristics were very different in a second set of characteristics and different again in a
third set of characteristics. This situation would be chaotic and we would be forced to question the reality
1
of evolution. The development of methods of DNA and protein analysis has shown dramatically that
organisms that are similar morphologically are also similar at the genetic level.
So, similarity among organisms provides evidence for evolution. We can then turn around and use the
similarities to try to reconstruct evolutionary relationships. That is the purpose of today’s lab: to construct a
hypothes ...
18.pdf
Taxonomy: Classifying and
Naming Organisms
After completing this exercise, you will be able to
1. define common name, scientific name, binomial, genus, specific epithet, species, taxonomy,
phylogenetic system, dichotomous key, herbarium;
2. distinguish common names from scientific names;
3. explain why scientific names are preferred over common names in biology;
4. identify the genus and specific epithet in a scientific binomial;
5. write out scientific binomials in the form appropriate to the Linnean system;
6. construct a dichotomous key;
7. explain the usefulness of an herbarium;
8. use a dichotomous key to identify plants, animals, or other organisms as provided by your
instructor.
Introduction
We are all great classifiers. Every day, we consciously or unconsciously classify and categorize the objects around
us. We recognize an organism as a cat or a dog, a pine tree or an oak tree. But there are numerous kinds of oaks,
so we refine our classification, ivin the trees distinguishing names such as "red oak," "white oak," or "bur
oak." These are examples o common name names with which you are probably iiillsHamiliar. -
---scientists are continuall exchanging information about living organisms. But not all scientists speak the
same language. Th ommon nam "white oak," familiar to an An:erican, is probably not familiar to a Spanish
~logist, even though the tree we know as white oak may exist in Spain as well as in our own backyard.
Moreover, even within our own language, the same organism can have several common names. For example,
within North America a gopher is also called a ground squirrel, a pocket mole, and a groundhog. On the other
hand, the same common name may describe many different organisms; there are more than 300 different trees
called "mahogany"! To circumvent the problems associated with common names, biologists use t[ctenti1i9
0 a§9 !hat are ni ue to each kin · and tha ar u throu hout
A cientific nam js two-parted, a bin mial. The.iirst word of the binomial designates the group to which
the organism be ongs; this is the enus arne (the plural of genus is genera). All oak trees belon to the genus
Quercus, a word derived from Latin . . ach kind of organism within a genus is given a ecific e ithe Thus, the
scientific name for white oak is Quercus alba (~Clfic ep1tljl is_Ellzg), while that of bur oa IS Quercus macrocarpa
~is macrocarl!£!1
Notice that the genus name is always capitalized; the specific e.Pithet usually is not capitalized (although
it can be if it is the proper name oi' a person or place). The binomial is written in italics (since theseare Latin
names); if italics are not available, the genus name and specific epithet are underlined.
You will hear discussion of "species" of organisms. For example, on a field trip, you may be asked "What
~ecies is this tree?" Assuming you are looking at a white oak, your reply would be "Quercus alba." .The scientific
name of the .
Biology 1108L – Laboratory Exercises
Phylogenetics
Kennesaw State University
Departments of Ecology, Evolution, and Organismal Biology
&
Molecular & Cell Biology
Lab modified from Gendron, R. P. 2000. The classification and evolution of Caminalcules.
The American Biology Teacher 62: 570-576.
Edits made by Joe Dirnberger, Sigurdur Griepsson, Paula Jackson, Thomas McElroy, Joel McNeal, and Heather Sutton.
CLASSIFICATION AND EVOLUTION
Humans classify almost everything, including each other. This habit can be quite useful.
For example, when talking about a car someone might describe it as a 4-door sedan with a
fuel injected V-8 engine. A knowledgeable listener who has not seen the car will still have
a good idea of what it is like because of certain characteristics it shares with other familiar
cars. Humans have been classifying plants and animals for a lot longer than they have
been classifying cars, but the principle is much the same. In fact, one of the central
problems in biology is the classification of organisms on the basis of shared
characteristics. As an example, biologists classify all organisms with a backbone as
"vertebrates." In this case the backbone is a characteristic that defines the group. If, in
addition to a backbone, an organism has mammary glands and hair it is a mammal, a
subcategory of the vertebrates. This mammal can be further assigned to smaller and
smaller categories down to the level of the species. The classification of organisms in this
way aids the biologist by bringing order to what would otherwise be a bewildering diversity
of species. The field devoted to the classification of organisms is called taxonomy [Greek.
taxis, to arrange, put in order + nomos, law].
The modern taxonomic system was devised by Carolus Linnaeus (1707-1778). It is a
hierarchical system because organisms are grouped into ever more inclusive categories
from species up to kingdom. Figure 1 illustrates how four species are classified using this
taxonomic system. (Note that it is standard practice to italicize the genus and species
names.)
Figure 1
Keep in mind that Linnaeus’ system of classification does not imply inherited relationships
between different taxa. Indeed Linneaus, like most other scientists of his time, considered
species to be fixed entities that had been created in their present form. According to this
view, Linnaeus' system of classification was simply a useful means of cataloging the
diversity of life.
This static view of taxonomy began to change at the 1859 publication of Charles Darwin’s
On The Origin of Species. As a consequence of Darwin's work it is now recognized that
taxonomic classifications are actually reflections of evolutionary history. For example,
Linnaeus put humans and wolves in the class Mammalia within the phylum Chordata
KINGDOM Animalia Plantae
PHYLUM Chordata Arthropoda Angiospermophyta ...
Getting Started with the Hymenoptera Anatomical OntologyKatja C. Seltmann
For Biodiversity Informatics workshop in Stockholm, Friday September 18. Describing the Hymenoptera Anatomical Ontology. Authors: Matthew Yoder, Andrew Deans, Katja Seltmann, István Mikó, Matthew Bertone
• The method of classifying organisms into monophyletic group of a common ancestor based on shared apomorphic characters is called cladistics.
• Cladistics is now the most commonly used and accepted method for creating phylogenetic system of classifications.
Cladistics produces a hypothesis about the relationship of organisms to predict the morphological characteristics of organism.
Similar to Franz. 2014. Explaining taxonomy's legacy to computers – how and why? (20)
De-centralized but global: Redesigning biodiversity data aggregation for impr...taxonbytes
Biodiversity data pose fundamental challenges for unification-based paradigms of data science. In particular, a hierarchical, backbone-driven approach to aggregating global biodiversity data tends to limit community engagement. Data quality, trust, fitness for use, and impact are similarly reduced. This presentation will outline an alternative, de-centralized design for aggregating biodiversity data globally. The design requires a coordinative approach to representing and reconciling evolving systematic perspectives, and further social but technologically mediated coordination between regionally and taxonomically constrained "communities of practice" (sensu Wenger, 2000, https://doi.org/10.1177/135050840072002). Important next steps in this direction include the development of use cases that quantify the benefits of a de-centralized biodiversity data aggregation - in terms of lowering costs to expert engagement, raising efficiency of curation, validating novel integration services, and improving reproducibility and provenance tracking across heterogenous data structures and portals.
Anzaldo franz 2017 ecn your daily weeviltaxonbytes
Slides of the presentation "#YourDailyWeevil - a story of modest but gratifying social media success", given at the 2017 Annual Meeting of the Entomological Collections Network, November 05, 2017, Denver, Colorado.
Franz et al tdwg 2016 new developments for libraries of lifetaxonbytes
Franz et al. @ #TDWG16 - "New developments for the Libraries of Life project and app". Talk # 1138, Friday, December 09, 2016, 02:45 pm. Session Lightning Talks. See https://mbgserv18.mobot.org/ocs/index.php/tdwg/tdwg2016/schedConf/program
Franz et al tdwg 2016 introducing lep nettaxonbytes
Franz et al. @ #TDWG16 - "Introducing LepNet – the Lepidoptera of North America Network". Talk # 1139, Friday, December 09, 2016, 02:40 pm. Session Lightning Talks. See https://mbgserv18.mobot.org/ocs/index.php/tdwg/tdwg2016/schedConf/program
Franz sterner tdwg 2016 new power balance needed for trustworthy biodiversity...taxonbytes
View a video recording here: https://vimeo.com/195024485
Franz & Sterner @ #TDWG16 - "A new power balance is needed for trustworthy biodiversity data". Talk # 1134, Friday, December 09, 2016, 11:30 am. Session Contributed Papers 05: Data Gaps, Trust, Knowledge Acquisition. See https://mbgserv18.mobot.org/ocs/index.php/tdwg/tdwg2016/schedConf/program
Zhang et al ecn 2016 building an accessible weevil tissue collection for geno...taxonbytes
Poster describing the origin and function of the ASUHIC Weevil Tissue Collection (WTC), see tinyurl.com/weeviltissuecollection; presented at the 2016 Entomological Collections Network Meeting, September 23, 2016, Orlando, Florida. ECN website: http://ecnweb.org/
Johnston ESA 2014 Trogloderus Sand Dune Speciationtaxonbytes
Andrew Johnston's presentation on Trogloderus (Coleoptera: Tenebrionidae) systematics and speciation in Southwestern United States sand dune habitat, given at the 2014 Annual Meeting of the Entomological Society of America in Portland, OR. http://www.entsoc.org/entomology2014
Arizona State University Natural History Collections - Moving to Alameda (201...taxonbytes
A collection of photos showing the transition of the Natural History Collections (School of Life Sciences, Arizona State University) from the Tempe Campus to the Alameda location. May, 2011 to August, 2014. See also http://taxonbytes.org/impressions-alameda-grand-opening/
Cobb, Seltmann, Franz. 2014. The Current State of Arthropod Biodiversity Data...taxonbytes
Cobb et al. 2014. The Current State of Arthropod Biodiversity Data: Addressing Impacts of Global Change. Presented at https://www.idigbio.org/content/collections-21st-century-symposium Program available at https://www.idigbio.org/wiki/index.php/Collections_for_the_21st_Century
Ludäscher et al. 2014 - A Hybrid Diagnosis Approach Combining Black-Box and W...taxonbytes
Presentation given at RuleML 2014 conference (http://ruleml2014.vse.cz/) with updates on the Euler/X toolkit; see also http://taxonbytes.org/prior-work-on-concept-taxonomy-2013/
The sequential stages culminating in the publication of a morphological cladistic analysis of weevils in the Exophthalmus genus complex (Coleoptera: Curculionidae: Entiminae) are reviewed, with an emphasis on how early- stage homology assessments were gradually evaluated and refined in light of intermittent phylogenetic insights. In all, 60 incremental versions of the evolving character matrix were congealed and analysed, starting with an assembly of 52 taxa and ten traditionally deployed diagnostic characters, and ending with 90 taxa and 143 characters that reflect significantly more narrow assessments of phylogenetic similarity and scope. Standard matrix properties and analytical tree statistics were traced throughout the analytical process, and series of incongruence length indifference tests were used to identify critical points of topology change among succeeding matrix versions. This kind of parsimony-contingent rescoping is generally representative of the inferential process of character individuation within individual and across multiple cladistic analyses. The expected long-term outcome is a maturing observational terminology in which precise inferences of homology are parsimony-contingent, and the notions of homology and parsimony are inextricably linked. This contingent view of cladistic character individuation is contrasted with current approaches to developing phenotype ontologies based on homology-neutral structural equivalence expressions. Recommendations are made to transparently embrace the parsimony-contingent nature of cladistic homology.
THE IMPORTANCE OF MARTIAN ATMOSPHERE SAMPLE RETURN.Sérgio Sacani
The return of a sample of near-surface atmosphere from Mars would facilitate answers to several first-order science questions surrounding the formation and evolution of the planet. One of the important aspects of terrestrial planet formation in general is the role that primary atmospheres played in influencing the chemistry and structure of the planets and their antecedents. Studies of the martian atmosphere can be used to investigate the role of a primary atmosphere in its history. Atmosphere samples would also inform our understanding of the near-surface chemistry of the planet, and ultimately the prospects for life. High-precision isotopic analyses of constituent gases are needed to address these questions, requiring that the analyses are made on returned samples rather than in situ.
Observation of Io’s Resurfacing via Plume Deposition Using Ground-based Adapt...Sérgio Sacani
Since volcanic activity was first discovered on Io from Voyager images in 1979, changes
on Io’s surface have been monitored from both spacecraft and ground-based telescopes.
Here, we present the highest spatial resolution images of Io ever obtained from a groundbased telescope. These images, acquired by the SHARK-VIS instrument on the Large
Binocular Telescope, show evidence of a major resurfacing event on Io’s trailing hemisphere. When compared to the most recent spacecraft images, the SHARK-VIS images
show that a plume deposit from a powerful eruption at Pillan Patera has covered part
of the long-lived Pele plume deposit. Although this type of resurfacing event may be common on Io, few have been detected due to the rarity of spacecraft visits and the previously low spatial resolution available from Earth-based telescopes. The SHARK-VIS instrument ushers in a new era of high resolution imaging of Io’s surface using adaptive
optics at visible wavelengths.
Introduction:
RNA interference (RNAi) or Post-Transcriptional Gene Silencing (PTGS) is an important biological process for modulating eukaryotic gene expression.
It is highly conserved process of posttranscriptional gene silencing by which double stranded RNA (dsRNA) causes sequence-specific degradation of mRNA sequences.
dsRNA-induced gene silencing (RNAi) is reported in a wide range of eukaryotes ranging from worms, insects, mammals and plants.
This process mediates resistance to both endogenous parasitic and exogenous pathogenic nucleic acids, and regulates the expression of protein-coding genes.
What are small ncRNAs?
micro RNA (miRNA)
short interfering RNA (siRNA)
Properties of small non-coding RNA:
Involved in silencing mRNA transcripts.
Called “small” because they are usually only about 21-24 nucleotides long.
Synthesized by first cutting up longer precursor sequences (like the 61nt one that Lee discovered).
Silence an mRNA by base pairing with some sequence on the mRNA.
Discovery of siRNA?
The first small RNA:
In 1993 Rosalind Lee (Victor Ambros lab) was studying a non- coding gene in C. elegans, lin-4, that was involved in silencing of another gene, lin-14, at the appropriate time in the
development of the worm C. elegans.
Two small transcripts of lin-4 (22nt and 61nt) were found to be complementary to a sequence in the 3' UTR of lin-14.
Because lin-4 encoded no protein, she deduced that it must be these transcripts that are causing the silencing by RNA-RNA interactions.
Types of RNAi ( non coding RNA)
MiRNA
Length (23-25 nt)
Trans acting
Binds with target MRNA in mismatch
Translation inhibition
Si RNA
Length 21 nt.
Cis acting
Bind with target Mrna in perfect complementary sequence
Piwi-RNA
Length ; 25 to 36 nt.
Expressed in Germ Cells
Regulates trnasposomes activity
MECHANISM OF RNAI:
First the double-stranded RNA teams up with a protein complex named Dicer, which cuts the long RNA into short pieces.
Then another protein complex called RISC (RNA-induced silencing complex) discards one of the two RNA strands.
The RISC-docked, single-stranded RNA then pairs with the homologous mRNA and destroys it.
THE RISC COMPLEX:
RISC is large(>500kD) RNA multi- protein Binding complex which triggers MRNA degradation in response to MRNA
Unwinding of double stranded Si RNA by ATP independent Helicase
Active component of RISC is Ago proteins( ENDONUCLEASE) which cleave target MRNA.
DICER: endonuclease (RNase Family III)
Argonaute: Central Component of the RNA-Induced Silencing Complex (RISC)
One strand of the dsRNA produced by Dicer is retained in the RISC complex in association with Argonaute
ARGONAUTE PROTEIN :
1.PAZ(PIWI/Argonaute/ Zwille)- Recognition of target MRNA
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MiRNA:
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Franz. 2014. Explaining taxonomy's legacy to computers – how and why?
1. Explaining taxonomy's legacy
to computers – how and why?
Nico M. Franz 1,2
Arizona State University
http://taxonbytes.org/
1 Concepts and tools developed jointly with members of the Ludäscher Lab (UC Davis & UIUC):
Mingmin Chen, Parisa Kianmajd, Shizhuo Yu, Shawn Bowers & Bertram Ludäscher
2 The Meaning of Names: Naming Diversity in the 21st Century
September 30, 2014; Museum of Natural History, University of Colorado
On-line @ http://www.slideshare.net/taxonbytes/franz-2014-explaining-taxonomys-legacy-to-computers-how-and-why
3. Definitional preliminaries, 1
Taxonomic concept: 1
The circumscription of a perceived
(or, more accurately, hypothesized)
taxonomic group, as advocated by
a particular author and source.
1Not the same as species concepts, which are theories about what species are, and/or how they are recognized.
4. Definitional preliminaries, 2
Provenance: 1
Information describing the origin, derivation,
history, custody, or context of an entity (etc.).
Provenance establishes the authenticity, integrity
and trustworthiness of information about entities.
1 See, e.g.: http://www.w3.org/2005/Incubator/prov/wiki/What_Is_Provenance
5. Concept taxonomy in three introductory phrases
• An emerging solution to the challenge of tracking stability
and change across multiple taxonomic name usages.
6. Concept taxonomy in three introductory phrases
• An emerging solution to the challenge of tracking stability
and change across multiple taxonomic name usages.
• Fully compatible with Linnaean nomenclature (Codes).
7. Concept taxonomy in three introductory phrases
• An emerging solution to the challenge of tracking stability
and change across multiple taxonomic name usages.
• Fully compatible with Linnaean nomenclature (Codes).
• The focus is on building sound provenance chains amenable
to computational representation and reasoning; irrespective
of whether the nomenclatural/taxonomic history of a perceived
lineage of organisms was perfectly stable since the times of
Linnaeus, or continues to undergo major alterations.
8. Overview of today's presentation
• The challenge (1.0): Limitations of the name taxon reference model.
• The challenge (2.0): How to track taxonomic concept provenance?
• Introducing Euler/X – overview of workflow and user/reasoner interaction.
~ 8 mins.
9. Overview of today's presentation
• The challenge (1.0): Limitations of the name taxon reference model.
• The challenge (2.0): How to track taxonomic concept provenance?
• Introducing Euler/X – overview of workflow and user/reasoner interaction.
• How does it work?
• Use case 1: Dwarf lemur classifications sec. 1993 & 2005.
• From simple to complex merge taxonomies.
• How can we represent taxonomic concept overlap?
• Scalability & information gain: How many articulations?
• Why? Insights into the performance of names as concept identifiers.
• Use case 2: Andropogon glomeratus sec. auctorum.
• In conclusion – feasibility, accessibility, and what it means.
~ 8 mins.
~ 15 mins.
11. "Andropogon glomeratus
is a species of grass (Poaceae)
that occurs in the Southern U.S." Photo by Max Licher (ASU Herbarium); Cottonwood, Arizona.
http://swbiodiversity.org/seinet/imagelib/imgdetails.php?imgid=431755
13. Proposition 1: names refer (directly) to taxa
"Andropogon glomeratus
Taxonomic name
is a species of grass (Poaceae)
Taxon (species)
that occurs in the Southern U.S."
Biological data
Reference relation:
name refers to entity
14. Proposition 1: names refer (directly) to taxa
"Andropogon glomeratus
Taxonomic name
is a species of grass (Poaceae)
Taxon (species)
that occurs in the Southern U.S."
Biological data
Reference relation:
name refers to entity
Data transmission:
facilitated by name
15. Yet, the legacy of taxonomy is more complicated:
the name taxon relationship can change.1
This poses some representation challenges…
1 See Franz et al. 2008. On the use of taxonomic concepts in support of biodiversity research and taxonomy; pp. 63–86.
In: The New Taxonomy, Systematics Association Special Volume 74. Taylor & Francis, Boca Raton.
16. Challenge 1: by necessity, a name refers only to a type (specimen)
"Andropogon glomeratus
Taxonomic name
is a species of grass (Poaceae)
that occurs in the Southern U.S."
Identity of the name/reference
relation is regulated by Codes
(e.g., Typification)
17. Challenge 2: the discovery of 'true' taxon boundaries is contingent
"Andropogon glomeratus
Taxonomic name
is a species of grass (Poaceae)
Taxon (species)
that occurs in the Southern U.S."
Identity of the name/reference
relation is regulated by Codes
(e.g., Typification)
The boundaries of taxon identity
have the property of contingent,
scientific hypotheses = concepts
18. Challenge 3: name/taxon (concept) changes are semi-independent
"Andropogon glomeratus
Taxonomic name
is a species of grass (Poaceae)
Taxon (species)
that occurs in the Southern U.S."
Identity of the name/reference
relation is regulated by Codes
(e.g., Typification)
Precise,
reliable
mapping?
The boundaries of taxon identity
have the property of contingent,
scientific hypotheses = concepts
19. Consequence: the name taxon reference model is often too simple
"Andropogon glomeratus
Taxonomic name
is a species of grass (Poaceae)
Taxon (species)
that occurs in the Southern U.S."
Biological data
Identity of the name/reference
relation is regulated by Codes
(e.g., Typification)
Precise,
reliable
mapping?
The boundaries of taxon identity
have the property of contingent,
scientific hypotheses = concepts
Reference
limitations!
Name-based data transmission:
reliability is also contingent
20. If we accept a contingent, changing
name concept taxon reference model,
then perhaps we should always say this:
21. Proposition 2: concept labels refer (directly) to taxonomic concepts
"Andropogon glomeratus
..is the (Latin) name (string), nomenclaturally anchored with a
type specimen, that can participate in the (more precisely in-dividuated)
concept label "Andropogon glomeratus sec. Barkworth
et al. 2014" (reference: Manual of Grasses for North America),
which in turn refers to..
is a species of grass (Poaceae)
that occurs in the Southern U.S."
22. Proposition 2: concept labels refer (directly) to taxonomic concepts
"Andropogon glomeratus
..is the (Latin) name (string), nomenclaturally anchored with a
type specimen, that can participate in the (more precisely in-dividuated)
concept label "Andropogon glomeratus sec. Barkworth
et al. 2014" (reference: Manual of Grasses for North America),
which in turn refers to..
is a species of grass (Poaceae)
..a feature-based circumscription ("Plants cespitose, upper portion dense, …
Pedicellate spikelets vestigial or absent, sterile. 2n = 20.") – the taxonomic concept
as advocated by this reference – which may or may not align
accurately with a (presumably existing and) relatively stable
evolutionary lineage of organisms in nature for which..
that occurs in the Southern U.S."
23. Proposition 2: concept labels refer (directly) to taxonomic concepts
"Andropogon glomeratus
..is the (Latin) name (string), nomenclaturally anchored with a
type specimen, that can participate in the (more precisely in-dividuated)
concept label "Andropogon glomeratus sec. Barkworth
et al. 2014" (reference: Manual of Grasses for North America),
which in turn refers to..
is a species of grass (Poaceae)
..a feature-based circumscription ("Plants cespitose, upper portion dense, …
Pedicellate spikelets vestigial or absent, sterile. 2n = 20.") – the taxonomic concept
as advocated by this reference – which may or may not align
accurately with a (presumably existing and) relatively stable
evolutionary lineage of organisms in nature for which..
that occurs in the Southern U.S."
..biological occurrence data are on hand.
24. Hence:
The challenge (2.0):
If we individuate taxonomic concepts
and their labels consistently, ..
25. 1889
1933
1948
1950
1968
1979
1983
2006
2014
Chain of A. glomeratus concepts, 1889-2014.
50. User/reasoner interaction: achieving well-specified alignments
MIR =
Maximally Informative Relations
[==, >, <, ><, |]
for each concept pair
Yes
Yes
51. Use case 1: dwarf lemurs sec. 1993 & 2005 1
Chirogaleus furcifer sec. Mühel (1890) – Brehms Tierleben.
Public Domain: http://books.google.com/books?id=sDgQAQAAMAAJ
1 Franz et al. 2014. Two influential primate classifications logically aligned. (unpublished)
52. The 2nd & 3rd Editions of the Mammal Species of the World
1993 2005
Primates sec. Groves (1993)
317 taxonomic concepts,
233 at the species level.
Primates sec. Groves (2005)
483 taxonomic concepts,
376 at the species level.
Δ = 143
species-level
concepts
58. Microcebus murinus (et al.) sec. 2005 – "lumping / splitting" [> , <]
1. Input concepts & articulations
2. Merge visualization
Yellow octagon
Unique to T1 (1993)
Green rectangle
Unique to T2 (2005)
Merge View Legend
59. Microcebus (part) & Mirza sec. 2005 – monotypic parent concepts
1. Input concepts & articulations
Mirza & M. coquereli sec. Groves (2005)
are two co-extensional concepts in T2
60. Microcebus (part) & Mirza sec. 2005 – monotypic parent concepts
1. Input concepts & articulations
2. Merge visualization
Mirza & M. coquereli sec. Groves (2005)
are two co-extensional concepts in T2
Three concepts
are congruent!
71. Cheirogaleoidae sec. 2005 – how many articulations are sufficient?
T2: 27 concepts; T1: 14 concepts; 22 input articulations
72. Cheirogaleoidae sec. 2005 – how many articulations are sufficient?
T2: 27 concepts; T1: 14 concepts; 22 input articulations
17 'non-new' 2005 species-level concepts
Articulated to 1993 species-level concepts
73. Cheirogaleoidae sec. 2005 – how many articulations are sufficient?
T2: 27 concepts; T1: 14 concepts; 22 input articulations
4 'new' 2005 species-level concepts
Exclusion (|) from 1993 family-level
concept
74. Cheirogaleoidae sec. 2005 – how many articulations are sufficient?
T2: 27 concepts; T1: 14 concepts; 22 input articulations
1 additional highest-level articulation
2005.Cheirogaleoidae > 1993.Cheirogaleidae
Eliminates 15 additional Possible Worlds
75. Cheirogaleoidae sec. 2005 – how many articulations are sufficient?
T2: 27 concepts; T1: 14 concepts; 22 input articulations
No genus-/subfamily level
articulations are needed
76. Cheirogaleoidae sec. 2005 – how many articulations are sufficient?
Well-specified merge: 378 Maximally Informative Relations
~ 17x information gain through reasoning
77. Cheirogaleoidae sec. 2005 – how many articulations are sufficient?
Well-specified merge: 378 Maximally Informative Relations
~ 17x information gain through reasoning
Primates: 483x317 = 800 concepts
402 articulations
153,111 MIR
~ 380x information gain!
79. MSW 2nd/3rd Edition name/concept identity relations
56.4% of the paired name lineages are taxonomically reliable.
Computers need concept resolution to track taxonomic provenance.
80. Use case 2
And Andropogon glomeratus sec. auctorum? 1
"Andropogon glomeratus
is a species of grass (Poaceae)
that occurs in the Southern U.S."
Photo by Max Licher (ASU Herbarium); Cottonwood, Arizona.
http://swbiodiversity.org/seinet/imagelib/imgdetails.php?imgid=431755
1 See Franz et al. 2014. Names are not good enough: reasoning over taxonomic change in the Andropogon complex.
Semantic Web – Interoperability, Usability, Applicability – Special Issue on Semantics for Biodiversity. (in press)
82. Question 1: Which concept labels have included the name string
"Andropogon glomeratus" in past eight classifications?
Tabular alignment of eight Andropogon classifications: 1889 to 2006
6 / 8 classifications are taxonomically unique for the concept of
A. glomeratus sec. auctorum.
No two concepts including the "A. glomeratus" name string are
taxonomically congruent.
83. Question 2: Which previously named concepts are congruent with
Andropogon glomeratus sec. Weakley (2006)?
Tabular alignment of eight Andropogon classifications: 1889 to 2006
What Weakley (2006) refers to as "A. glomeratus" was previously referred to as:
1889: A. macrourus var. hirsutior + A. macrourus var. abbreviatus
1933: A. glomeratus (in part, I)
1948: A. glomeratus (?)
1950: A. virginicus var. hisutior + A. glomeratus (in part, II)
1968: A. virginicus (in part)
1979: A. virginicus var. abbreviatus (in part)
1983: A. glomeratus (in part, I)
85. Case 1: 1948.Blomquist vs. 1950.Hitchcock & Chase (Δ = 2 years)
T2: 7 concepts (1950); T1: 7 concepts (1948) – containment view
Merge: 3 congruent regions, 3 with same name
6 unique regions, 4 with non-unique name
86. Case 1: 1948.Blomquist vs. 1950.Hitchcock & Chase (Δ = 2 years)
T2: 7 concepts (1950); T1: 7 concepts (1948) – containment view
Merge: 3 congruent regions, 3 with same name
6 unique regions, 4 with non-unique name
A. glomeratus sec. 1950 and A. glomeratus sec. 1948 are overlapping, as each concept
includes a non-congruent variety-level concept.
Interestingly, the shared concept region has no unique name in either taxonomy. It is
'un-named', at least within the context of the 1950/1948 classifications.
87. Case 1: 1948.Blomquist vs. 1950.Hitchcock & Chase (Δ = 2 years)
T2: 7 concepts (1950); T1: 7 concepts (1948) – merge concept view
Merge: 3 congruent regions, 3 with same name
6 unique regions, 4 with non-unique name
The shared, overlapping region is more informatively resolved and labeled in the merge
concept visualization; the region 1950.A._glomeratus * 1948.A_glomeratus contains no
subelements that carry the name "A. virginicus" in either classification.
88. Case 2: 1889.Hackel vs. 2006.Weakley (Δ = 117 years)
T2: 12 concepts (2006); T1: 12 concepts (1889)
Merge: 8 congruent regions, 0 with same name (!)
5 unique regions, 1 with non-unique name
89. Case 2: 1889.Hackel vs. 2006.Weakley (Δ = 117 years)
T2: 12 concepts (2006); T1: 12 concepts (1889)
Merge: 8 congruent regions, 0 with same name (!)
5 unique regions, 1 with non-unique name
Hackel & Weakley agree very substantively on what entities are
'out there in nature'; however, more than a century of Code-compliant
name changes has obscured their agreements.
90. Case 3: 1983.Campbell vs. 2006.Weakley (Δ = 23 years)
T2: 12 concepts (2006); T1: 14 concepts (1983) – containment view
Merge: 9 congruent regions, 5 with same name
6 unique regions, 4 with non-unique name
91. Case 3: 1983.Campbell vs. 2006.Weakley (Δ = 23 years)
T2: 12 concepts (2006); T1: 14 concepts (1983) – containment view
Merge: 9 congruent regions, 5 with same name
6 unique regions, 4 with non-unique name
One of the simpler merge taxonomies in this use case, although
8 / 15 merge regions have taxonomically misleading names (i.e.,
congruence/different names; non-congruence/same names).
This ratio is near-average through nine pairwise alignments.
93. In conclusion – feasibility, accessibility, and what it means.
• Feasibility of tracking taxonomic concept provenance in computational logic:
• We are making leaps and bounds in feasibility (and in scalability) right now.
• However, many interesting challenges remain (e.g., user/reasoner interaction).
94. In conclusion – feasibility, accessibility, and what it means.
• Feasibility of tracking taxonomic concept provenance in computational logic:
• We are making leaps and bounds in feasibility (and in scalability) right now.
• However, many interesting challenges remain (e.g., user/reasoner interaction).
• Accessibility and acceptance of the RCC-5/reasoning approach:
• We need more use cases, and users – the Euler/X approach works!
• It can be applied to any new or legacy systematic publication, biodiversity
database, checklist, classification, phylogeny, or other kinds of taxonomic
syntheses (print or virtual) and versions thereof; complementing the Linnaean
system while providing superior individuation of taxonomic content.
• Having a sound web service is the next critical step in advancing the approach.
95. In conclusion – feasibility, accessibility, and what it means.
• Feasibility of tracking taxonomic concept provenance in computational logic:
• We are making leaps and bounds in feasibility (and in scalability) right now.
• However, many interesting challenges remain (e.g., user/reasoner interaction).
• Accessibility and acceptance of the RCC-5/reasoning approach:
• We need more use cases, and users – the Euler/X approach works!
• It can be applied to any new or legacy systematic publication, biodiversity
database, checklist, classification, phylogeny, or other kinds of taxonomic
syntheses (print or virtual) and versions thereof; complementing the Linnaean
system while providing superior individuation of taxonomic content.
• Having a sound web service is the next critical step in advancing the approach.
• What does it all mean?
• The legacy of taxonomic name and concept authoring is amenable to
computational logic and provenance tracking. We can likely derive much data
integration power from further developments in this direction.
96. Acknowledgments
• Robert Guralnick, Susanna Drogsvold & all CU Museum of Natural History "The
Meaning of Names" conference organizers!
• Euler/X team: Mingmin Chen, Parisa Kianmajd, Shizhuo Yu, Shawn Bowers
& Bertram Ludäscher
• Juliana Cardona-Duque (weevils), Naomi Pier (primates) & AlanWeakley (grasses)
• taxonbytes lab members: Andrew Johnston & Guanyang Zhang
• NSF DEB–1155984 & DBI–1342595 (PI Franz); IIS–118088 & DBI–1147273
(PI Ludäscher)
Franz Lab: http://taxonbytes.org/ https://sols.asu.edu/
97. Select references on concept taxonomy and the Euler/X toolkit
• Franz & Peet. 2009. Towards a language for mapping relationships among
taxonomic concepts. Systematics and Biodiversity 7: 5–20. Link
• Chen et al. 2014. Euler/X: a toolkit for logic-based taxonomy integration. WFLP
2013 – 22nd International Workshop on Functional and (Constraint) Logic
Programming. Link
• Chen et al. 2014. A hybrid diagnosis approach combining Black-Box and White-
Box reasoning. Lecture Notes in Computer Science 8620: 127–141. Link
• Franz et al. 2014. Names are not good enough: reasoning over taxonomic change in
the Andropogon complex. Semantic Web – Interoperability, Usability, Applicability –
Special Issue on Semantics for Biodiversity. (in press) Link
• Franz et al. 2014. Reasoning over taxonomic change: exploring alignments for the
Perelleschus use case. PLoS ONE. (in review)
• Euler/X toolkit: https://bitbucket.org/eulerx/euler-project
• Euler web service (in progress): http://euler.asu.edu/
• Concept taxonomy @ taxonbytes: http://taxonbytes.org/tag/concept-taxonomy/
99. The good: names refer to type specimens necessarily
Source: Witteveen. 2014. Biology & Philosophy. (in press)
100. The challenge: names refer to non-type specimens contingently
Names
Non-types
Source: Dubois. 2005. Zoosystema 27: 365-426.
101. We may categorize kinds of nomenclatural
and taxonomic change, and opportunities,
to track each, as follows:
102. Nomenclatural/taxonomic change & provenance tracking square
E.g.: - A binomial name is formed incorrectly.
- A homonym is discovered, requiring name change.
103. Nomenclatural/taxonomic change & provenance tracking square
E.g.: - A type specimen is lost, a neotype must be designated.
- "One fungus (a-/sexual), one name" – Melbourne Code.
104. Nomenclatural/taxonomic change & provenance tracking square
E.g.: - A heterotypic synonymy is established (inferred).
- a Priority-carrying name is newly 'transferred'.
105. Nomenclatural/taxonomic change & provenance tracking square
E.g.: - A junior genus-level name is transferred among tribes.
- An informal clade name is redefined across treatments.
106. Nomenclatural/taxonomic change & provenance tracking square
Many
changes
Some
changes
Many
changes
MOST
CHANGES
???
Question: Which changes are most common in a particular group?
Answer: Concept-level resolution is needed to assess this.
107. Question: What is the proper scope of reference for representing our
progress in inferring the tree of life?
114. Use case 2: Perelleschus sec. 2001 & 2006 1
Perelleschus salpinflexus sec. Franz & Cardona-Duque (2013)
DOI:10.1080/14772000.2013.806371
1 Input articulations: Franz & Cardona-Duque. 2013. Description of two new species and phylogenetic reassessment of
PerelleschusWibmer & O'Brien, 1986 (Coleoptera: Curculionidae), with a complete taxonomic concept history of
Perelleschus sec. Franz & Cardona-Duque, 2013. 2013. Systematics and Biodiversity 11: 209–236.
Merge analyses: Franz et al. 2014. Reasoning over taxonomic change: exploring alignments for the Perelleschus use
case. PLoS ONE. (in press)
115. Goal: align two phylogenies with differential taxon sampling
T1: Perelleschus sec. 2001
• Phylogenetic revision
• 8 ingroup species concepts
• 2 outgroup concepts
• 18 concepts total
116. Goal: align two phylogenies with differential taxon sampling
T1: Perelleschus sec. 2001
• Phylogenetic revision
• 8 ingroup species concepts
• 2 outgroup concepts
• 18 concepts total
T2: Perelleschus sec. 2006
• Exemplar analysis
• 2 ingroup species concepts
• 1 outgroup concept
• 7 concepts total
117. Logic representation challenge:
Perelleschus sec. 2001 & 2006 concepts
have incongruent sets of subordinate members,
yet each concept has congruent synapomorphies.
118. Definitional preliminaries 1
Ostensive alignment: the congruence among higher-level
concepts is assessed in relation to their entailed members.
Ostension: giving meaning through an act of pointing out.
1 See Bird & Tobin. 2012. Natural Kinds. URL: http://plato.stanford.edu/archives/win2012/entries/natural-kinds/
119. Definitional preliminaries 1
Ostensive alignment: the congruence among higher-level
concepts is assessed in relation to their entailed members.
Ostension: giving meaning through an act of pointing out.
Intensional alignment: the congruence among higher-level
concepts is assessed in relation to their properties.
Intension: giving meaning through the specification of properties.
1 See Bird & Tobin. 2012. Natural Kinds. URL: http://plato.stanford.edu/archives/win2012/entries/natural-kinds/
120. Ostensive alignment – members are all that counts
Challenge 1: Differential outgroup sampling
(2 / 1 concepts)
T2: 2006.PHY & 2006.PHYsubcin
T1: 2006.PHY only
Input constraints
Ostensive alignment
2001 & 2006
121. Ostensive alignment – members are all that counts
Challenge 1: Differential outgroup sampling
(2 / 1 concepts)
T2: 2006.PHY & 2006.PHYsubcin
T1: 2006.PHY only
Solution: Locally relax coverage with "nc"
= "no coverage"
Input constraints
Ostensive alignment
2001 & 2006
122. Ostensive alignment – members are all that counts
Challenge 1: Differential outgroup sampling
(2 / 1 concepts)
T2: 2006.PHY & 2006.PHYsubcin
T1: 2006.PHY only
Solution: Locally relax coverage with "nc"
= "no coverage"
Result: 2006.PHY == 2001.PHY
Outgroups are held congruent.
Input constraints
Ostensive alignment
2001 & 2006
123. Ostensive alignment – members are all that counts
Input constraints Challenge 2: Ostensive alignment
Ostensive alignment
2001 & 2006
124. Ostensive alignment – members are all that counts
Challenge 2: Ostensive alignment
Solution: 11 ingroup concept articulations
are coded ostensively – either as
<, ><, or | – to represent non-congruence
in the representation
of child concepts
Input constraints
Ostensive alignment
2001 & 2006
125. Ostensive alignment – members are all that counts
Challenge 2: Ostensive alignment
Solution: 11 ingroup concept articulations
are coded ostensively – either as
<, ><, or | – to represent non-congruence
in the representation
of child concepts
Result: 2006.PER < 2001.PER
2006.PER | 2001.[5 species concepts]
etc.
Input constraints
Ostensive alignment
2001 & 2006
5 x |
2 x ><
127. Intensional alignment – representation of congruent synapomorphies
Input constraints
Challenge 3: Intensional alignment
Solution: An Implied Child (_IC) concept is
Intensional
alignment
2001 & 2006
added to the undersampled (2006)
clade concept; and the (5) "missing"
species-level concepts are included
within this Implied Child
128. Intensional alignment – representation of congruent synapomorphies
Input constraints
Challenge 3: Intensional alignment
Solution: An Implied Child (_IC) concept is
Intensional
alignment
2001 & 2006
added to the undersampled (2006)
clade concept; and the (5) "missing"
species-level concepts are included
within this Implied Child
11 ingroup concept articulations are
coded intensionally – as == or > –
to reflect congruent synapomorphies
of 2001 & 2006
129. Intensional alignment – representation of congruent synapomorphies
Input constraints
Challenge 3: Intensional alignment
Result: The genus- and ingroup clade-level
Intensional
alignment
2001 & 2006
concepts are inferred as congruent:
2006. PER == 2001.PER
2006.PcarPeve == 2001.PcarPsul
etc.
130. Review – representing ostensive versus intensional alignments
Ostensive alignment
2001.PER includes more
species-level concepts
than 2006.PER [>].
131. Review – representing ostensive versus intensional alignments
Ostensive alignment
2001.PER includes more
species-level concepts
than 2006.PER [>].
Intensional alignment
2006.PER reconfirms the
synapomorphies inferred
in 2001.PER [==].
132. The other piece in the puzzle: Concept-to-voucher identifications
Source: Baskauf & Webb. 214. Darwin-SW. URL: http://www.semantic-web-journal.net/system/files/swj635.pdf