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Record W6912721255 · doi:10.5281/zenodo.5770324

Lycaea osbornae Zeidler 2021, sp. nov.

2021· article· en· W6912721255 on OpenAlexaboutno aff

Bibliographic record

VenueZenodo (CERN European Organization for Nuclear Research) · 2021
Typearticle
Languageen
FieldEarth and Planetary Sciences
TopicMarine and coastal plant biology
Canadian institutionsnot available
Fundersnot available
KeywordsNettingTaxonomy (biology)Head (geology)Bridge (graph theory)

Abstract

fetched live from OpenAlex

Lycaea osbornae sp. nov. (Figs 10–11) Material examined. Holotype: Female, 4.7 mm, USNM 1242790. North Atlantic, Georges Bank, S. of Massachusetts [39°26’N 68°03’30”W], R/VAlbatross, surface, 31 August 1885. Allotype: Male, 5.2 mm (recently moulted), NHMD-228125, Dana stn. 3563 iv, S.E. Pacific, N.E. of Marquesas Is. [07°45.5’S 131°22’W], 100 mw, 29 September 1928. Paratypes 1: 1 female, 3.7 mm, USNM 1242790, collected with holotype. 2: 1 female, 3.3 mm, SAMA C12577, N.E. Pacific, off Vancouver Island [49°15.09’N 126°40’W], “LaPerouse and Line P Monitoring Program”, stn. A 4, 250 m, September 2009 (from M. Galbraith). On the salp Cyclosalpa bakeri Ritter, 1905. 3: 1 female 5.8 mm, NHMD-619242, collected with allotype. 4: 1 female, 4.4 mm, NHMD-228132, Dana stn. 3843 iv, S.E. Indian Ocean, N. of Cocos / Keeling Is. [09°59’S 97°56’E], 200 mw, 9 October 1929. 5: 2 females, 6.1 and 6.5 mm, NHMD- 228242, Dana stn. 1208 iii, N.E. Pacific, off Panama [06°48’N 80°33’W], 300 mw, 16 January 1922. 6: 2 males about 8.6 mm, NHMD-228248, Dana stn. 3563 v, same data as allotype but 50 mw. Description of holotype. Female, 4.7 mm. Head relatively large, rounded, much deeper than long (about 1.7 x), as long as first 3 pereonites combined. Buccal mass protruded well below head. G1 and G2 sub-chelate, G1 slightly shorter than G2. G1 with slightly inflated basis; carpus rectangular with small, pointed, postero-distal tooth, reaching to about the middle of the propodus; propodus with small, slightly serrated, postero-distal corner produced very slightly posteriorly to dactylus; dactylus slender, relatively long, length 0.5 x propodus. G2 similar to G1 except for basis which is more slender and longer (1.5 x that of G1) accounting for the extra length. P3–6 with very short, stubby dactylus, those of P3 and P4 about 0.2 x as long as propodus, or slightly more. P3 and P4 morphologically similar, P4 slightly longer than P3; merus marginally inflated anteriorly, marginally longer than propodus, about 0.5 x basis; carpus marginally shorter than propodus. P5 length about 1.2 x P4 and P6; basis rectangular, length about 2 x maximum width; merus marginally inflated anteriorly, sub-equal in length to propodus, about 0.6 x basis; carpus length about 0.8 x propodus. P6 basis rectangular but slightly wider medially, length about 2 x maximum width, slightly shorter than basis of P5; merus with slightly serrated antero-distal corner, slightly inflated anteriorly, maximum width almost 0.6 x length, slightly shorter than propodus, about 0.5 x basis; carpus relatively wide but more or less rectangular, length about 0.6 x propodus; anterior and distal margin of carpus and anterior margin of propodus, slightly serrated. P7 basis with bulging posterior margin, length about 1.7 x maximum width, about 0.7 x basis of P6; remaining articles together relatively long, almost 0.7 x basis; propodus with antero-distal corner produced into small, rounded lobe; dactylus sharp, hook-like. U1 and U2; endopod not fused with peduncle. U1 peduncle relatively short, about 1.7 x length of exopod or only slightly longer; rami relatively slender, endopod slightly longer than exopod. U2 endopod slightly longer than peduncle. Telson rounded, length marginally shorter than width at base. Description of allotype. Male, 5.2 mm. Like holotype female except for the following. Head relatively large, rounded, much deeper than long (about 1.5 x), as long as first 4 pereonites combined. A1 callynophore without antero-distal corner; postero-distal corner small, rounded, separated from following article by distinct notch. Dactylus of G1 and G2 slightly longer, about 0.7 x propodus. P5 length about 1.3 x P4 and P6; basis relatively longer about 2.4 x width. P6 merus equal in length to propodus. P7 basis more rectangular, length about 2 x width; length of remaining articles together slightly less than 0.4 x basis. U1 peduncle slightly longer, about 2 x length of exopod. U2 endopod slightly shorter than peduncle. Paratype USNM 1242790. Female, 3.7 mm. This specimen is in poor condition but is like the holotype except for the morphology of G2 where the postero-distal corner of the carpus is relatively small, barely reaching to about one-third of the propodus (Fig. 10A). However, this may be a juvenile character as noted for stage iv of L. pulex by Harbison (1976). Also, the dactylus of G1 and G2 is relatively shorter and less slender than for the holotype. Paratype SAMA C12577. Female, 3.3 mm, recently moulted, immature. It is like the holotype in all respects except that the dactylus of G1 and G2 (Fig. 10B) and P3–6 are marginally longer and sharper. However, one might expect that the dactyls of recently moulted specimens might be less worn and hence slightly longer and sharper. Collected on the salp Cyclosalpa bakeri Ritter, 1905. Paratype NHMD-619242. Female, 5.8 mm. Morphologically identical to the holotype. The dactylus of P6, on the right, is partly retracted. Paratype NHMD-228132. Female, 4.4 mm. Like the holotype. The dactylus of G2 is marginally longer. Paratypes NHMD-228242. Two females, 6.5 and 6.1 mm. Both are like the holotype except that the dactylus of G2 is slightly longer and in the smaller specimen the postero-distal corner of the carpus of G1 and G2 is worn and both are more excavate, especially on the left side. The larger specimen is ovigerous. Paratypes NHMD-228248. Two males, about 8.6 mm, one with head detached. Both with mature antennae and head with rounded knob as occurs in mature specimens of L. nasuta (Fig. 9), otherwise like the allotype. One specimen with the dactylus of P6, on the right, fully retracted (Fig. 11). Etymology. I take great pleasure in naming this species for my colleague Dr Karen Osborn, Research Zoologist/ Curator, Department of Invertebrate Zoology, Smithsonian National Museum of Natural History, Washington DC, in acknowledgement for her, and her team’s, research efforts investigating the evolutionary significance of vision and eye morphology in hyperiideans, and also for gaining the funds to enable me to spend two months at the Smithsonian in 2015, thus, in part, making this current review possible. Remarks. Lycaea osbornae is most similar to L. lilia based on the morphology of G2. It differs primarily in that the morphology of G1 is like that of G2 and in that the postero-distal corner of the carpus is pointed and the dactylus is relatively longer and slender (not stubby). In addition, the peduncle of U1 is relatively shorter, less than 2 x the length of the exopod (about 2.5 x or more in L. lilia) and the telson is wider and more rounded in L. lilia. Also, in Lycaea osbornae the peduncle of U2 is shorter than the endopod, a character only shared with L. pachypoda, L. pulex and males of L. serrata, all species from which L. osbornae is readily distinguished by the morphology of G1 and G2. An unusual character of this species is the retractile dactylus of P6 which has not been found in any other species of Lycaea except L. intermedia but, as for that species, it is not evident in all specimens and can be difficult to determine unless the dactylus is at least partly retracted. One paratype (SAMA C12577) from the N.E. Pacific was collected on the salp Cyclosalpa bakeri Ritter, 1905. Distribution. Known only from a few records, from the type locality, the north and S.E. Pacific and the S.E. Indian Ocean, as detailed above.

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame machine prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. The Gemma side is a direct model label for every work in the frame, read from the title-only record. The Codex side is a classifier learned from the 10,348 direct Codex labels and calibrated to design-weighted sample rates; fields without enough sample support carry no Codex call. Candidate is the union of the two sides; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels.

metaresearch head score (Codex)0.000
metaresearch head score (Gemma)0.001
Version: metacan-v3-hybrid-931329e0061cValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Observational · Consensus signal: none
GenreCandidate signal: Empirical · Consensus signal: none
Teacher disagreement score0.024
Threshold uncertainty score0.058

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0000.001
Meta-epidemiology (narrow)0.0020.001
Meta-epidemiology (broad)0.0010.000
Bibliometrics0.0030.002
Science and technology studies0.0020.001
Scholarly communication0.0010.005
Open science0.0010.001
Research integrity0.0020.002
Insufficient payload (model declined to judge)0.0170.011

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.025
GPT teacher head0.206
Teacher spread0.181 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one source (direct Gemma or distilled Codex), not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designObservational
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

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Citations0
Published2021
Admission routes1
Has abstractyes

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