Classification in Baraminology:
Basic Terminology



Chad Arment (2024)



The biblical creationist will encounter different classification systems that must be properly understood in context: scientific classification schemes (Linnaean, cladistic, etc.), ethnozoological classification (how living things mentioned in the Bible were organized by ancient cultures), and creation biology’s baraminological classification of ‘created kinds.’ The latter involves approximating biological reality as revealed in the Bible: the separate creation of individual biological populations and their development through divergence and differentiation over time from Creation to the present day (or so long as they survived).


How creationists might classify living things, has been discussed ever since the modern revival of creationism, e.g. Frank Marsh in the 1940s (ReMine 1990). Specific baraminological terminology developed through discussion primarily between Walter ReMine and Dr. Kurt Wise, which led to publishing separate papers at the second International Conference on Creationism (ReMine 1990; Wise 1990). ReMine’s ‘Discontinuity Systematics’ offered an initial framework of terminology, but Dr. Wise’s approach to baraminology (Wise 1992), incorporating young-earth model criteria, has become more prevalent (expanded/revised by Wood et al. 2003). We now have a robust vocabulary for classification with which to speak about and evaluate ‘created kinds.’


Because baraminology is built upon recognizing discontinuity and continuity among groups of organisms, those concepts are built into baraminic terminology (Wise 2002). Lions and tigers exhibit continuity (through shared traits and hybridization); lions and penguins exhibit discontinuity. Lions and tigers are part of the same baramin (created kind); lions and penguins are not.


Wood et al. (2003) noted that the baramin itself is a “purely theoretical construct,” as it includes all members within a lineage, from its original created population to all descendants that developed within a ‘potentiality region’. Not all aspects of that baraminic potential will have expressed morphologically, but those that did emerge are part of the same baramin even if we are unaware of that expression (such as divergent pathways that were extirpated during the global Flood and were never fossilized for preservation to the present day). It is possible that the Fall (the curse on the natural world resulting from Adam’s sin) affected directionality within the potentiality region of baraminic lineages so that they would never fully express their potential in this fallen world.


Holobaramin: Inclusive of a group of known members (typically species, but sometimes only identifiable to genus or even family), discontinuous with all other groups, where each member demonstrates continuity with at least one other member. “[T]he complete set of known organisms that belong to a single baramin” (Wood et al. 2003). A baramin would include the holobaramin as well as any related unknown organisms, such as the original population created during the Creation Week.


Monobaramin: Inclusive of all known members of a group demonstrating continuity with each other, but may not include all members continuous with the group. ‘Bears’ and ‘flamingos’ are both monobaramins.


Apobaramin: A group in which all members are discontinuous from another group. It may contain multiple separately created baramins, or may comprise a single holobaramin. ‘Mammals’ and ‘snakes’ are both apobaramins.


Polybaramin: A designated group with members that share continuity and discontinuity with other members in the group. The group includes more than one separately created baraminic lineage. ‘Birds’ and ‘Dinosaurs’ are both polybaraminic groups.





Dinosaurs, Birds, and Penguins are each apobaramins. Dinosaurs and Birds are also polybaramins.

The family Spheniscidae (Penguins) is a monobaramin, and may or may not be a holobaramin.



While creationists utilize biological nomenclature (e.g. Panthera leo for the lion) within baraminology, scientific taxonomic levels do not directly equate to any of the baraminic levels. Scientific taxonomies utilized within an evolutionary framework have a prior commitment to universal common descent. Within creation biology, only members of the same baramin share common descent. Creationists recognize patterns in nature even above the level of baramin, but these patterns are not interpreted the same way. Individual groups sharing common descent do not imply that all groups share universal common descent. (That is a fallacy of composition: assuming that what is true for individual parts must be true for the whole.)


Within popular creationism, there is a tendency to equate the ‘Ark kinds,’ vertebrate families that survived the Flood on the Ark, with holobaramins. This is likely incorrect for most such families. Rather, these families are best considered monobaramins, as the baramin itself may be superfamilial (including fossil species not incorporated into recognized families) or multifamilial (encompassing multiple families). Additional examination of the fossil record and other factors will be necessary before any holobaraminic conclusions are drawn. At this point, I’m unaware of any possible examples of subfamilial holobaramins in Ark kinds, so I think we can dispose of that idea barring strong evidence to the contrary.


Baraminic lineages that survived outside the Ark are another issue. There are cases with microorganisms and certain other biological groups where holobaramins may encompass lower levels of scientific taxonomy than the family. That would primarily be dependent on the amount of divergence within the baramin (if any), and whether very similar organisms truly have common ancestry (which may be indeterminable). Carter (2021), for example, has posited several different ‘types’ of baramins, including one for those organisms that are asexual (and have been asexual from Creation), which could put their baramin (thus holobaramin) at the individual level.


Various criteria are used to determine placement in or outside a baramin: morphological traits, genetic traits, apparent cognita, and hybridization are commonly used (Sanders and Wise 2003; Lightner et al. 2011). Statistical baraminology is a technical methodology where data matrices with character states provide a means to calculate baraminic distance and taxonomic clustering patterns without relying on prior assumptions of common ancestry (Wood and Murray 2003). A biological trajectory is a linear or curvilinear series of organisms in biological character space, for which there is independent evidence of chronological transition (Wood and Cavanaugh 2003). All criteria used in baraminology should be used in conjunction with other criteria.





Each of 13 families (smallest circles) in the Feliformia are likely monobaramins. Each of the higher level taxa are apobaramins; but are any polybaramins? Holobaramins may not always be as obvious as we'd like to see. If the Feliformia as a whole is a holobaramin, then there are no polybaramins. Otherwise, there are a few different potential polybaraminic groupings.





The monotreme superfamily Ornithorhynchoidea contains two living families (platypus and echidna) and one fossil family. Each family is a monobaramin, but are unlikely to all be holobaramins. Evidence suggests that echidnas (Tachyglossidae) are a post-Flood derivation of the platypus family (Ornithorhynchidae). The Ornithorhynchoidea may be polybaraminic or monobaraminic, depending on further evaluation.



References:


Carter, R. 2021. Species were designed to change, part 3. CMI https://creation.com/species-designed-to-change-part-3


Lightner, J. K., T. Hennigan, G. Purdom, and B. Hodge. 2011. Determining the Ark kinds. Answers Research Journal 4: 195-201.


ReMine, W. J. 1990. Discontinuity systematics: A new methodology of biosystematics relevant to the creation model. The Proceedings of the International Conference on Creationism 2: 207-216.


Sanders, R. W., and K. P. Wise. 2003. The cognitum: A perception-dependent concept needed in baraminology. The Proceedings of the Fifth International Conference on Creationism 5: 445-456.


Wise, K. P. 1990. Baraminology: A young-earth creation biosystematics method. The Proceedings of the International Conference on Creationism 2: 345-360.


Wise, K. P. 1992. Practical baraminology. CEN Technical Journal 6(2): 122-137.


Wise, K. P. 2002. Faith, Form, and Time. Nashville, TN: Broadman & Holman.


Wood, T. C., and D. P. Cavanaugh. 2003. An evaluation of lineages and trajectories as baraminological membership criteria. Occasional Papers of the Baraminology Study Group 2: 1-6.


Wood, T. C., and M. J. Murray. 2003. Understanding the Pattern of Life. Nashville, TN: Broadman & Holman.


Wood, T. C., K. P. Wise, R. Sanders, and N. Doran. 2003. A refined baraminic concept. Occasional Papers of the Baraminology Study Group (3): 1-14.