Literature DB >> 28630903

Comment (1) on "Formation of the Isthmus of Panama" by O'Dea et al.

Carlos Jaramillo1, Camilo Montes2, Agustín Cardona3, Daniele Silvestro4, Alexandre Antonelli4,5,6, Christine D Bacon4.   

Abstract

A review and reanalysis of geological, molecular, and paleontological data led O'Dea et al. (1) to propose (i) that reports by Montes et al. (2) and Bacon et al. (3) regarding a middle Miocene closure of the Central American Seaway (CAS) are unsupported, and (ii) a new age of the formation of the Isthmus at 2.8 million years ago (Ma). Here, we reject both of these conclusions.

Entities:  

Keywords:  Divergence; Marine environment; Vicariance; Zircon

Mesh:

Year:  2017        PMID: 28630903      PMCID: PMC5470828          DOI: 10.1126/sciadv.1602321

Source DB:  PubMed          Journal:  Sci Adv        ISSN: 2375-2548            Impact factor:   14.136


The CAS

An unambiguous definition of the CAS is critical to any discussion regarding the Isthmus of Panama, yet O’Dea et al. () failed to provide one. O’Dea et al. () appear to suggest that the CAS is any body of water connecting the Caribbean with the Pacific Ocean. In contrast, papers from our research group (–) have explicitly restricted the term CAS to the “oceanic seaway along the tectonic boundary of the South American plate and the Panamanian microplate” (). Although our definition was ignored and/or misrepresented by O’Dea et al. (), this is the definition that we maintain here when referring to the CAS. This definition is far more than a semantic issue because deepwater flow often occurs along tectonic boundaries, and both modeling and empirical data indicate that the blockage of deep and intermediate waters (>200- to 500-m depth) across the Isthmus affects global oceanography at least as much as the blockage of shallow waters ().

Montes et al. (2015)

O’Dea et al. () dismiss the geological data presented in Montes et al. () using two main lines of argument. First, O’Dea et al. () state that “sediments of the Atrato Basin were connected with the Urabá Basin entirely unaffected by the Cuchillo Hills.” Their statement is based on modeling of seismic and gravimetric data by Garzon-Varon (), which lacks empirical evidence of age and accumulation environments of strata in the Urabá Basin. O’Dea et al. () do not present any additional evidence to support their interpretation that sediments of the southern Urabá Basin are early Pliocene in age and accumulated in marine environments with Pacific connections. The Atrato hydrographic basin is characterized by high rainfall (averaging 4944 mm/year) and high water discharge (2740 m3 s−1) (). Therefore, it is equally possible that sediments observed in the seismic lines of Garzon-Varon () are fluvial deposits of the Atrato River. Furthermore, the geological interpretation of the cross section [Figure 8.2 in the study by Garzon-Varon ()] shows sedimentary cover being disrupted by the Cuchillo Hills rather than being “entirely unaffected,” as O’Dea et al. () suggest. Second, O’Dea et al. () state that “the true extent of Eocene zircons in the region [South American Block] categorically negates the assertions of Montes [that middle Eocene zircons found in Miocene sediments in the South American Block are derived from the Panama Block].” To support this statement, O’Dea et al. () present 131 ages of possible South American sources [table S2 in the study by O’Dea et al. ()] and conclude that the zircons reported in Montes et al. () could also be derived from the South American Block. This collection of ages ignores hundreds of published magmatic and detrital ages [for example, (, , –)]. Among the 131 ages presented by O’Dea et al. [table S2 in the study by O’Dea et al. ()], 118 ages cannot be considered as valid ages for a possible source rock derived from South America (Table 1). They include 41 K/Ar and Ar/Ar dates that record magmatic cooling rather than crystallization and therefore could not have affected the ages of zircons, 36 from rocks that are west of the suture and therefore belong to the Panama Block (, ), 23 are K/Ar and Ar/Ar ages in metamorphic rocks that record reheating and cooling due to intrusives older than 50 Ma (), 11 ages reported as Eocene correspond to Cretaceous ocean floor sequence basalts (, ), 4 are of an unreported rock type, 2 date veins in Cretaceous rocks, and 1 lacks geographic coordinates (Table 1 and Fig. 1). The remaining 13 ages of table S2 of O’Dea et al. () that did date South American source rocks are significantly older than the middle Eocene Panamanian signal reported in Montes et al. () (t test, P < 0.001, df = 19.8; Fig. 1). In summary, the arguments O’Dea et al. () used to dismiss Montes et al. () are not supported by the data presented or available in the literature.
Table 1

Annotated table S2 of O’Dea et al. ().

Record #LithologyAge (Ma)Error (Ma)MethodLatitudeLongitudeComment*
1Dacite33.90.7K/Ar wr2.56−76.69Cretaceous ages
2Mandé batholith (granodiorite)34.0K/Ar Bt5.72−76.35Cooling age, west of suture
3Grupo Diabásico (dolerite)34.0K/Ar3.27−76.62Cretaceous ages
4Santa Marta batholith (granodiorite)34.21.6Ar/Ar Kfs11.24−74.02Cooling age
5Dibulla Gneiss (anorthosite)35.03.0Ar/Ar Hb10.74−74.08Metamorphic age
6Cocha Río Téllez Migmatitic Complex (gneissic granodiorite)35.00.4Ar/Ar Hb0.81−77.33Metamorphic age
7Santa Marta schist (amphibolic schist)36.25.1K/Ar Hb11.28−74.15Metamorphic age
8Paja Fm. (mineralized vein)36.40.1Ar/Ar Ms5.64−74.14Vein, unrelated to magmatism
9Cocha Río Téllez Migmatitic Complex (gneissic granodiorite)36.40.6Ar/Ar Hb0.81−77.33Metamorphic age
10Santa Cecilia–La Equis Complex (porphyritic basalt)36.711.5Ar/Ar6.74−76.39West of suture
11Patía 29-Ra-00237.11.7Ar/Ar1.98−77.15Unreported rock type
12Paja Fm. (mineralized vein)37.30.1Ar/Ar wr5.64−74.14Vein, unrelated to magmatism
13Socorro stock (granodiorite)37.81.7K/Ar Bt10.79−74.03Cooling age
14Santa Marta batholith (granodiorite)38.70.6Ar/Ar Kfs11.24−74.02Cooling age
15Santa Marta schist Fm. Concha (phyllite)38.73.4K/Ar wr11.31−74.13Metamorphic age
16Acandí batholith (quartz diorite)38.93.0K/Ar Ser8.53−77.42Cooling age, west of suture
17Timbiquí Fm. (andesite)38.94.3K/Ar2.29−77.65West of suture
18Rio Napi intrusives (Hb diorite)39.02.0K/Ar2.49−77.48Cooling age, west of suture
19Grupo Diabásico (dolerite)39.0K/Ar3.27−76.62Cretaceous ages
20Grupo Diabásico39.73.5Ar/Ar Hb1.33−77.46Cretaceous ages
21Grupo Diabásico (lava)40.02.0K/Ar wr12.23−71.69Cretaceous ages
22Piedrancha batholith (granodiorite)40.53.0K/Ar Bt1.23−77.73Cooling age
23Cocha Río Téllez Migmatitic Complex (gneissic granodiorite)40.00.5Ar/Ar Hb0.81−77.33Metamorphic age
24Grupo Diabásico (dolerite)40.0K/Ar3.27−76.62Cretaceous ages
25Santa Marta batholith (granodiorite)40.21.4Ar/Ar Kfs11.28−73.90Cooling age
26Santa Marta batholith (granodiorite)40.21.5Ar/Ar Kfs11.28−73.90Cooling age
27Santa Marta batholith (granodiorite)40.40.3Ar/Ar Kfs11.28−73.90Cooling age
28Santa Marta schist, Cinto Fm. (phyllite)40.94.7K/Ar wr11.25−74.18Metamorphic age
29Nudillales stock (quartz monzonite)41.03.0K/Ar wr7.04−76.32Cooling age, west of suture
30Timbiquí Fm. (andesite)41.01.0K/Ar2.20−77.68West of suture
31Los Cholos–Napi River pluton (Hb-bearing quartz diorite)41.04.0K/Ar2.46−77.50Cooling age, west of suture
32Basalt41.48.6Ar/Ar Pl6.02−76.26West of suture
33Llanitos latiandesite41.51.8K/Ar wr7.07−76.41West of suture
34Timbiquí Fm. (andesite)41.71.2K/Ar2.40−77.57West of suture
35Santa Marta batholith (granodiorite)41.80.8Ar/Ar Kfs11.27−74.09Cooling age
36Patía 29-Ra-00241.90.7Ar/Ar1.98−77.15Unreported rock type
37Amaime Fm.42.013.0Ar/Ar wr3.70−76.18Unreported rock type
38Balsitas pluton (andesite dike)42.61.3K/Ar2.17−77.70West of suture
39Santa Marta schist (biotite schist)42.61.7K/Ar Bt10.99−74.14Metamorphic age
40Mandé batholith (porphyritic dacite)42.70.9K/Ar Ser6.70−76.50West of suture
41Pórfido Pantanos (porphyritic dacite)42.70.9K/Ar Bt6.42−76.30West of suture
42Río Napi intrusives (Hb-bearing gabbro)43.00.4K/Ar2.53−77.45Cooling age, west of suture
43Basalt43.10.4Ar/Ar Pl6.02−76.26West of suture
44Santa Marta batholith (granodiorite)43.60.5Ar/Ar Kfs11.27−74.09Cooling age
45Buriticá andesite (andesite, porphyritic diorite)43.84.3K/Ar wr6.70−75.91Cooling age
46Santa Marta batholith (granodiorite)43.90.5Ar/Ar Bt11.28−73.90Cooling age
47Santa Marta batholith (granodiorite)44.00.8Ar/Ar Bt11.28−73.90Cooling age
48Río Napi intrusives (Hb-bearing tonalite)44.04.0K/Ar2.49−77.49Cooling age, west of suture
49Timbiquí Fm. (andesite)44.01.0K/Ar2.18−77.70West of suture
50Santa Marta schist (amphibolic schist)44.12.7K/Ar Hb11.22−73.89Metamorphic age
51Santa Marta batholith (quartz diorite)44.11.6K/Ar Bt11.29−73.97Cooling age
52Mandé batholith (tonalite)44.60.9U/Pb Zr6.73−76.52West of suture
53Los Azules (ophiolite sequence + pillow lavas)44.76.0K/Ar wr1.90−77.00Cretaceous ages
54Mandé batholith (tonalite)44.81.0Ar/Ar Hb6.81−76.59Cooling age, west of suture
55Sevilla Complex (schist)44.80.4Ar/Ar Bt11.26−73.62Metamorphic age
56Mandé batholith (tonalite)45.31.2U/Pb Zr6.72−76.52West of suture
57Grupo Diabásico (lava)46.03.0K/Ar wr3.51−76.53Cretaceous ages
58Santa Marta batholith (granodiorite)46.00.4Ar/Ar Bt11.24−74.02Cooling age
59Dibulla Gneiss (anorthosite)46.11.4Ar/Ar Hb10.74−74.08Metamorphic age
60Santa Marta batholith (granodiorite)46.30.7Ar/Ar Bt11.24−74.02Cooling age
61Timbiquí Fm. (dike, andesite)46.72.0K/Ar2.18−77.70West of suture
62Sabaletas stock (gabbro, diorite)46.98.1Ar/Ar Hb3.82−76.60Cooling age
63Grupo Diabásico (dolerite)47.0K/Ar3.27−76.62Cretaceous ages
64Mandé batholith (tonalite)47.12.5K/Ar HbNANANo coordinates
65Santa Marta schist (amphibolic schist)47.42.4K/Ar Hb11.12−74.05Metamorphic age
66Santa Marta batholith (granodiorite)47.80.6Ar/Ar Hb11.28−73.90Cooling age
67Esquistos de Santa Marta (pegmatite)47.81.9K/Ar Ms11.26−74.15Cooling age
68Parashi stock (quartzodiorite)48.04.0K/Ar Hb12.23−71.74Cooling age
69Balsitas pluton (tonalite)48.01.0K/Ar2.17−77.69Cooling age
70Santa Marta batholith (granodiorite)48.00.8Ar/Ar Hb11.24−74.02Cooling age
71Acandí batholith (tonalite)48.11.0K/Ar Hb8.20−77.24Cooling age, west of suture
72Acandí batholith (tonalite)48.11.0K/Ar Ser8.46−77.36Cooling age, west of suture
73Acandí batholith (tonalite)48.12.0K/Ar Ser8.20−77.24Cooling age, west of suture
74Santa Marta batholith (granodiorite)48.30.8Ar/Ar Hb11.24−74.02Cooling age
75Santa Marta batholith (granodiorite)48.30.9Ar/Ar Hb11.28−73.90Cooling age
76Timbiquí Fm. (porphyritic andesite)48.44.8K/Ar2.29−77.64West of suture
77Buriticá pluton (quartzodiorite)48.41.8K/Ar Bt11.17−73.73Cooling age
78Santa Marta batholith (quartzodiorite)48.81.7K/Ar Hb11.29−73.97Cooling age
79Grupo Diabásico (pillow lava)49.49.8K (R)1.60−77.40Cretaceous ages
80El Bosque batholith (granodiorite)49.11.7K/Ar Bt4.44−75.08Cooling age
81Santa Marta batholith (granodiorite)49.50.8Ar/Ar Bt11.27−74.09Cooling age
82Gneis de Dibulla (anorthosite)49.81.1Ar/Ar Bt10.74−74.08Metamorphic age
83Gabro de Rodrigo (Hb-Px–bearing gabbro)49.90.2Ar/Ar Pl6.12−72.34Cooling age
84Santa Marta batholith (granodiorite-tonalite)50.10.8U/Pb Zr11.28−73.90Not Panamanian signal
85Santa Marta batholith (granodiorite)50.41.1Ar/Ar Hb11.27−74.09Cooling age
86Santa Marta batholith (granodiorite-tonalite)50.61.7U/Pb Zr11.31−73.94Not Panamanian signal
87Santa Marta batholith (granodiorite)50.70.9Ar/Ar Hb11.27−74.09Cooling age
88Santa Cecilia–La Equis Complex (porphyritic basalt)50.72.0Ar/Ar glass6.74−76.39West of suture
89Timbiquí Fm. (andesite)50.72.0K/Ar2.18−77.70West of suture
90Plutón de Buriticá (tonalite, quartz diorite)50.81.5U/Pb Zr11.18−73.73Not Panamanian signal
91Santa Marta batholith (granodiorite)50.90.8Ar/Ar Bt11.27−74.09Cooling age
92Plutón El Salto (pegmatite)51.01.0K/Ar2.21−77.66Cooling age
93Esquistos de Santa Marta (amphibolic schist)51.03.6K/Ar Hb11.01−74.12Metamorphic age
94Timbiquí Fm. (porphyritic andesite)51.51.5K/Ar2.21−77.69West of suture
95Arquía Complex (garnet-bearing amphibolite)51.63.3Ar/Ar Hb4.38−75.72Metamorphic age
96Gabbronorite51.73.9Ar/Ar wr6.58−76.59Cooling age, west of suture
97Santa Marta batholith (aplite dike)52.30.7U/Pb Zr11.14−74.12Not Panamanian signal
98Gabbronorite52.73.2Ar/Ar wr6.58−76.59Cooling age, west of suture
99El Hatillo stock (quartzodiorite)53.01.8K/Ar Bt5.19−75.00Cooling age
100Río Napi intrusives (Hb-bearing tonalite)53.05.0K/Ar2.52−77.43Cooling age
101Grupo Diabásico (pillow lava)53.24.6K/Ar wr1.60−77.40Cretaceous ages
102Santa Marta batholith (aplite dike)53.31.0U/Pb Zr11.24−74.06Not Panamanian signal
103Timbiquí Fm. (andesite)53.43.0K/Ar2.19−77.71West of suture
104Gabbronorite53.62.9Ar/Ar wr6.58−76.59Cooling age, west of suture
105Gneis de Dibulla (anorthosite)53.80.7Ar/Ar Bt10.74−74.08Metamorphic age
106Sevilla Complex53.90.5Ar/Ar Bt11.26−73.62Unreported rock type
107Plutón Tucurinquita (granodiorite)54.02.2K/Ar Bt10.68−74.08Cooling age
108Sevilla Complex (schist)54.10.7Ar/Ar Bt11.26−73.62Metamorphic age
109Gneis de Dibulla (anorthosite)54.31.9Ar/Ar Hb10.74−74.08Metamorphic age
110Esquistos de Santa Marta Rodadero Fm. (amphibolite)54.32.7K/Ar Hb11.20−74.21Metamorphic age
111Esquistos de Jambaló (glaucophane blue schist)54.51.6Ar/Ar Pg2.77−76.33Metamorphic age
112Gneis de Dibulla (anorthosite)54.50.8Ar/Ar Bt10.74−74.08Metamorphic age
113El Hatillo stock (quartz diorite)54.60.7U/Pb Zr5.17−74.97Not Panamanian signal
114Santa Marta batholith (aplite dike)54.70.7U/Pb Zr11.27−74.09Not Panamanian signal
115Gneis de Dibulla (anorthosite)54.74.0Ar/Ar Hb10.74−74.08Metamorphic age
116Pórfido de Murindó (porphyry tonalite)54.71.3K/Ar Bt7.03−76.45Cooling age, west of suture
117Mandé batholith (tonalite)54.71.3K/Ar Hb7.05−76.75Cooling age, west of suture
118Florencia stock (quartz diorite)54.91.9K/Ar Bt5.53−75.05Cooling age
119Florencia stock (quartz diorite)54.91.9K/Ar Bt5.37−75.01Cooling age
120Santa Bárbara batholith (diorite)55.01.0K/Ar Bt3.37−76.13Cooling age
121Santa Cecilia–La Equis Complex (porphyritic basalt)55.11.5Ar/Ar6.74−76.39Cooling age, west of suture
122Santa Marta batholith (granodiorite-tonalite)55.11.1U/Pb Zr11.20−74.10Not Panamanian signal
123Santa Marta batholith (granodiorite-tonalite)55.30.6U/Pb Zr11.17−74.17Not Panamanian signal
124Gneis de Dibulla (anorthosite)55.40.7Ar/Ar Bt10.74−74.08Metamorphic age
125Santa Marta batholith (granodiorite-tonalite)55.50.3U/Pb Zr11.27−74.09Not Panamanian signal
126Sonsón batholith (leucogranite)55.81.0U/Pb Zr5.66−75.20Not Panamanian signal
127Dike (andesite-dacite)55.92.0K/Ar Ser6.45−74.63Cooling age
128Santa Marta batholith (dike)55.90.3U/Pb Zr11.21−74.24Not Panamanian signal
129Piedrancha batholith (microdiorite)57.73.0K/Ar Bt1.12−77.86Cooling age
130Pórfido Rio Manso (quartz diorite porphyry)58.010.0K/Ar Hb4.11−75.25Cooling age
131Manizales stock59.80.7U/Pb Zr5.12−75.29Not Panamanian signal

*Comments:

1) Not Panamanian signal: These ages, although representing South American rocks, are significantly older than the middle Eocene signal. See text and Fig. 1.

2) West of suture: Rocks that are located west of the Uramita suture and therefore belong to the Panama-Choco block or oceanic terranes west of the South American realm. The suture was defined by Duque-Caro (), and its corresponding trace in the Gelogic Map of Colombia is to the south (). See Fig. 1.

3) Cooling age: Ages indicate cooling, not magmatism. For instance, table S2 of O’Dea et al. reports several ages for a single site of Santa Marta batholith including a U/Pb in zircon of 50.1 ± 0.7 Ma (record #84), as well as Ar/Ar ages of 48 to 47 Ma in hornblende (records #75 and #66), 44 to 43 Ma age in biotite (records #47 and #46), and 40 Ma in K-feldspar (records #25 to #27). This succession shows the gradual cooling of the batholith. By the time the Ar/Ar system closed in K-feldspar at 40 Ma, zircons in the same pluton were already 10 million years old. Thus, detritus derived from this body will therefore yield zircons in the 50-Ma range rather than the 40-Ma range as O’Dea wrongly assumed.

4) Metamorphic age: These ages reflect metamorphic cooling or reheating events unrelated to magmatism. These metamorphic rocks are intruded by plutonic rocks older than 50 Ma (), therefore being older.

5) Vein unrelated to magmatism: These ages date veins in Cretaceous rocks associated to deformation, not magmatism.

6) Cretaceous ages: These Eocene ages had been previously dismissed by (), because they were obtained in Cretaceous ocean floor sequence basalts. These Eocene ages are therefore unreliable and most likely related to heating and cooling by the thermal effects of well-dated Cretaceous and Miocene intrusions ().

7) Unreported rock type: Without knowledge of the rock type dated, it is impossible to assess the meaning of the age.

8) No coordinates: Without sample coordinates, it is impossible to assess the meaning of the age.

Fig. 1

Data from O’Dea et al. [table S2 plotted and categorized ()].

Colored circles show that none of the 131 localities listed in that publication could be sources for the Panamanian signal in middle Miocene sediments reported by Montes et al. (). Location of suture after Duque-Caro () mapped onto a geological map of Colombia (). One hundred eighteen of those ages do not represent valid ages for a possible source rock derived from South America. Inset shows that 13 ages that do date South American source rocks are significantly older (t test, P < 0.001, df = 19.8) than the middle Eocene Panamanian signal reported in Montes et al. ().

*Comments: 1) Not Panamanian signal: These ages, although representing South American rocks, are significantly older than the middle Eocene signal. See text and Fig. 1. 2) West of suture: Rocks that are located west of the Uramita suture and therefore belong to the Panama-Choco block or oceanic terranes west of the South American realm. The suture was defined by Duque-Caro (), and its corresponding trace in the Gelogic Map of Colombia is to the south (). See Fig. 1. 3) Cooling age: Ages indicate cooling, not magmatism. For instance, table S2 of O’Dea et al. reports several ages for a single site of Santa Marta batholith including a U/Pb in zircon of 50.1 ± 0.7 Ma (record #84), as well as Ar/Ar ages of 48 to 47 Ma in hornblende (records #75 and #66), 44 to 43 Ma age in biotite (records #47 and #46), and 40 Ma in K-feldspar (records #25 to #27). This succession shows the gradual cooling of the batholith. By the time the Ar/Ar system closed in K-feldspar at 40 Ma, zircons in the same pluton were already 10 million years old. Thus, detritus derived from this body will therefore yield zircons in the 50-Ma range rather than the 40-Ma range as O’Dea wrongly assumed. 4) Metamorphic age: These ages reflect metamorphic cooling or reheating events unrelated to magmatism. These metamorphic rocks are intruded by plutonic rocks older than 50 Ma (), therefore being older. 5) Vein unrelated to magmatism: These ages date veins in Cretaceous rocks associated to deformation, not magmatism. 6) Cretaceous ages: These Eocene ages had been previously dismissed by (), because they were obtained in Cretaceous ocean floor sequence basalts. These Eocene ages are therefore unreliable and most likely related to heating and cooling by the thermal effects of well-dated Cretaceous and Miocene intrusions (). 7) Unreported rock type: Without knowledge of the rock type dated, it is impossible to assess the meaning of the age. 8) No coordinates: Without sample coordinates, it is impossible to assess the meaning of the age.

Data from O’Dea et al. [table S2 plotted and categorized ()].

Colored circles show that none of the 131 localities listed in that publication could be sources for the Panamanian signal in middle Miocene sediments reported by Montes et al. (). Location of suture after Duque-Caro () mapped onto a geological map of Colombia (). One hundred eighteen of those ages do not represent valid ages for a possible source rock derived from South America. Inset shows that 13 ages that do date South American source rocks are significantly older (t test, P < 0.001, df = 19.8) than the middle Eocene Panamanian signal reported in Montes et al. ().

Bacon et al. (2015 a, b)

The goal of the study by Bacon et al. () was to test the assumption that “no vicariant date [3.5 Ma] is better dated than the Isthmus” (). O’Dea et al. () dismiss the molecular results using analysis derived from a single gene presented by Bacon et al. (, ). They further indicate disagreement with the use of a universal rate of mitochondrial DNA (mtDNA) divergence and point out that several published data sets had not been included in the study [despite the fact that the latter has already been addressed ()]. To circumvent these issues, O’Dea et al. () compiled data to examine a “corresponding concentration of [marine] divergences…to imply a common geological cause.” Here, we used the data presented in O’Dea et al. [table S3 in the study by O’Dea et al. ()] to explicitly examine the temporal distribution of vicariance events using a nonhomogeneous Poisson process to infer statistical significance of rate shifts [table S1 and Fig. 2; following Supporting Information 1.6 from the study by Bacon et al. ()]. Both our results and those shown by O’Dea et al. (Fig. 3) () fully support the conclusions of Bacon et al. (, ), showing two rate shifts of vicariance, one increase at 12 Ma (14.77 to 9.76 Ma) and another decrease at 3.01 Ma (4.65 to 1.61 Ma). These results propose a scenario of ongoing divergence of geminate species over several million years as a function of Isthmus formation. This corroboration of results clearly shows that any issues with mtDNA calibration do not affect the conclusions presented by Bacon et al. (, ).
Fig. 2

Data from O’Dea et al. [table S3 analyzed and plotted ()].

Rate through time plot showing the tempo of vicariance events (estimated number of events per million year) in marine organisms inferred from the data presented in table S3 of O’Dea et al. (). Shaded area shows the 95% confidence interval (95% CI) around the rate estimates based on 1000 replicated analyses, in which the ages of the vicariance events were resampled from the age intervals presented in O’Dea et al. (). Two statistically significant shifts in vicariance rate are detected, at 12 Ma (95% CI: 14.77 to 9.76 Ma) and 3.01 Ma (95% CI: 4.65 to 1.61 Ma). The red dashed line shows the new, 2.8-Ma date for the formation of the Isthmus of Panama proposed by O’Dea et al. ().

Data from O’Dea et al. [table S3 analyzed and plotted ()].

Rate through time plot showing the tempo of vicariance events (estimated number of events per million year) in marine organisms inferred from the data presented in table S3 of O’Dea et al. (). Shaded area shows the 95% confidence interval (95% CI) around the rate estimates based on 1000 replicated analyses, in which the ages of the vicariance events were resampled from the age intervals presented in O’Dea et al. (). Two statistically significant shifts in vicariance rate are detected, at 12 Ma (95% CI: 14.77 to 9.76 Ma) and 3.01 Ma (95% CI: 4.65 to 1.61 Ma). The red dashed line shows the new, 2.8-Ma date for the formation of the Isthmus of Panama proposed by O’Dea et al. (). Bacon et al. (, ) demonstrated that several pulses of terrestrial migration and marine vicariance occurred in the Neogene, rather than a single, time-limited event at 3.5 Ma. Can we therefore assume, a priori, that any given marine sister taxa found on either side of the Isthmus split 3.5 Ma? The answer given by Bacon et al. (, ) based on 424 data points from molecular phylogenies across multiple taxonomic groups and ecological forms, and further supported by the smaller data set (38 data points) in Figure 4 of O’Dea et al. (), is no.

New age for the formation of the Isthmus of Panama

O’Dea et al. () propose a new age for the formation of the Isthmus of Panama at 2.8 Ma. This new hypothesis is based on the (i) “end of surface water exchange at 2.76 Ma based on marine plankton assemblages and surface ocean salinity contrast” (Figure 3 in the study by O’Dea et al. ), (ii) absence of gene flow between shallow marine animal populations after ~3.2 Ma [Figure 4 in the study by O’Dea et al. ()], and (iii) acceleration of the dispersal rate of terrestrial mammals at ~2.7 Ma [Figure 5 and table S2 in the study by O’Dea et al. ()]. An examination of each of these points indicates that there is insufficient support for their hypothesis. First, O’Dea et al. () discuss how salinity and carbonate accumulation rates diverge at 4.2 Ma, but there is no significant change at 2.8 Ma [Figure 3 in the study by O’Dea et al. ()]. Second, Figure 3 of O’Dea et al. () provides no evidence of “marine plankton assemblages” splitting between Caribbean and Pacific waters at 2.8 Ma. Third, the youngest divergence time estimated from the molecular data set (Mellita quinquiesperforata; table S3 in the study by O’Dea et al.) has a mean age of 3.21 Ma with a 95% credible interval of 3.91 to 2.51 Ma and therefore does not define a precise split at 2.8 Ma, as O’Dea et al. () conclude. Fourth, although O’Dea et al. () show an increase in terrestrial mammal migration at ~2.7 Ma [Figure 5 and table S2 in the study by O’Dea et al. ()], this age does not necessarily reflect formation of a terrestrial land bridge. From an analysis of 1411 migrating mammal fossil records [versus 68 in O’Dea et al. ()] of 35 families and 124 genera, Bacon et al. () had already obtained a similar result. Alternative hypotheses have been proposed to explain this acceleration in mammal migration. These include habitat and environmental changes due to the onset of the Northern Hemisphere glaciation and concomitant reductions in precipitation across the Americas (–) and lower sea levels during glacial periods (, ).

Transmogrification

O’Dea et al. () published several statements that are incorrect and mislead readers. “If, on the other hand, one assumes that the Panama Arc permanently blocked all genetic exchange from 23 to 13 Ma (Montes et al. 2015)” misrepresents the data, results, and interpretation presented in Montes et al. (). That publication and additional papers from our research groups (–, ) have indicated that since the final closure of CAS ~10 to 15 Ma until 4.2 to 3.5 Ma, the Caribbean Sea and Pacific Ocean were still connected by shallow water, albeit intermittently, through other passages than CAS.

CONCLUSIONS

The rise of the Isthmus of Panama is a fascinating event in Cenozoic history that has attracted worldwide attention, mostly because it has been linked to four major events in the history of Earth: the onset of the Thermohaline Circulation, the onset of Northern Hemisphere glaciation, the birth of the Caribbean Sea, and the Great American Biotic Interchange (). Some of these links have been criticized or dismissed [for example, (, , )] and are still far from being resolved. Unfortunately, O’Dea et al. (), rather than providing a clear synthesis on the issue, have added more confusion. Further fieldwork and new data generation are needed to fully understand the implication of the rise of the Isthmus of Panama.
  7 in total

1.  Evaluating the role of contracting and expanding rainforest in initiating cycles of speciation across the Isthmus of Panama.

Authors:  Brian Tilston Smith; Amei Amei; John Klicka
Journal:  Proc Biol Sci       Date:  2012-06-06       Impact factor: 5.349

2.  Reply to Lessios and Marko et al.: Early and progressive migration across the Isthmus of Panama is robust to missing data and biases.

Authors:  Christine D Bacon; Daniele Silvestro; Carlos Jaramillo; Brian Tilston Smith; Prosanta Chakrabarty; Alexandre Antonelli
Journal:  Proc Natl Acad Sci U S A       Date:  2015-10-21       Impact factor: 11.205

Review 3.  Historical biogeography of the Isthmus of Panama.

Authors:  Egbert G Leigh; Aaron O'Dea; Geerat J Vermeij
Journal:  Biol Rev Camb Philos Soc       Date:  2013-07-19

4.  Middle Miocene closure of the Central American Seaway.

Authors:  C Montes; A Cardona; C Jaramillo; A Pardo; J C Silva; V Valencia; C Ayala; L C Pérez-Angel; L A Rodriguez-Parra; V Ramirez; H Niño
Journal:  Science       Date:  2015-04-10       Impact factor: 47.728

5.  The Great American Biotic Interchange: Dispersals, Tectonics, Climate, Sea Level and Holding Pens.

Authors:  Michael O Woodburne
Journal:  J Mamm Evol       Date:  2010-07-14       Impact factor: 2.611

6.  Biological evidence supports an early and complex emergence of the Isthmus of Panama.

Authors:  Christine D Bacon; Daniele Silvestro; Carlos Jaramillo; Brian Tilston Smith; Prosanta Chakrabarty; Alexandre Antonelli
Journal:  Proc Natl Acad Sci U S A       Date:  2015-04-27       Impact factor: 11.205

Review 7.  Formation of the Isthmus of Panama.

Authors:  Aaron O'Dea; Harilaos A Lessios; Anthony G Coates; Ron I Eytan; Sergio A Restrepo-Moreno; Alberto L Cione; Laurel S Collins; Alan de Queiroz; David W Farris; Richard D Norris; Robert F Stallard; Michael O Woodburne; Orangel Aguilera; Marie-Pierre Aubry; William A Berggren; Ann F Budd; Mario A Cozzuol; Simon E Coppard; Herman Duque-Caro; Seth Finnegan; Germán M Gasparini; Ethan L Grossman; Kenneth G Johnson; Lloyd D Keigwin; Nancy Knowlton; Egbert G Leigh; Jill S Leonard-Pingel; Peter B Marko; Nicholas D Pyenson; Paola G Rachello-Dolmen; Esteban Soibelzon; Leopoldo Soibelzon; Jonathan A Todd; Geerat J Vermeij; Jeremy B C Jackson
Journal:  Sci Adv       Date:  2016-08-17       Impact factor: 14.136

  7 in total
  8 in total

1.  Yucatán carnivorans shed light on the Great American Biotic Interchange.

Authors:  Blaine W Schubert; James C Chatters; Joaquin Arroyo-Cabrales; Joshua X Samuels; Leopoldo H Soibelzon; Francisco J Prevosti; Christopher Widga; Alberto Nava; Dominique Rissolo; Pilar Luna Erreguerena
Journal:  Biol Lett       Date:  2019-05-31       Impact factor: 3.703

2.  Phylogenomics and biogeography of the world's thrushes (Aves, Turdus): new evidence for a more parsimonious evolutionary history.

Authors:  Romina Batista; Urban Olsson; Tobias Andermann; Alexandre Aleixo; Camila Cherem Ribas; Alexandre Antonelli
Journal:  Proc Biol Sci       Date:  2020-01-22       Impact factor: 5.349

3.  Morphological and Genetic Variation Among Populations of the Fiddler Crab Minuca burgersi (Holthuis, 1967) (Crustacea: Brachyura: Ocypodidae) from Shores of the Caribbean Basin and Western South Atlantic Ocean.

Authors:  C L Thurman; R E Alber; M J Hopkins; Hsi-Te Shih
Journal:  Zool Stud       Date:  2021-04-29       Impact factor: 2.058

4.  Historical Biogeography of endemic seed plant genera in the Caribbean: Did GAARlandia play a role?

Authors:  María Esther Nieto-Blázquez; Alexandre Antonelli; Julissa Roncal
Journal:  Ecol Evol       Date:  2017-10-24       Impact factor: 2.912

5.  Neogene Proto-Caribbean porcupinefishes (Diodontidae).

Authors:  Orangel Aguilera; Guilherme Oliveira Andrade Silva; Ricardo Tadeu Lopes; Alessandra Silveira Machado; Thaís Maria Dos Santos; Gabriela Marques; Thayse Bertucci; Thayanne Aguiar; Jorge Carrillo-Briceño; Felix Rodriguez; Carlos Jaramillo
Journal:  PLoS One       Date:  2017-07-26       Impact factor: 3.240

6.  Volcanic contribution to emergence of Central Panama in the Early Miocene.

Authors:  David M Buchs; Derek Irving; Henry Coombs; Roberto Miranda; Jian Wang; Maurylis Coronado; Rodrigo Arrocha; Mauricio Lacerda; Creed Goff; Eladio Almengor; Enier Portugal; Pastora Franceschi; Eric Chichaco; Stewart D Redwood
Journal:  Sci Rep       Date:  2019-02-05       Impact factor: 4.379

7.  Comparative genomics uncovers the evolutionary history, demography, and molecular adaptations of South American canids.

Authors:  Daniel E Chavez; Ilan Gronau; Taylor Hains; Rebecca B Dikow; Paul B Frandsen; Henrique V Figueiró; Fabrício S Garcez; Ligia Tchaicka; Rogério C de Paula; Flávio H G Rodrigues; Rodrigo S P Jorge; Edson S Lima; Nucharin Songsasen; Warren E Johnson; Eduardo Eizirik; Klaus-Peter Koepfli; Robert K Wayne
Journal:  Proc Natl Acad Sci U S A       Date:  2022-08-15       Impact factor: 12.779

8.  Shark and ray diversity in the Tropical America (Neotropics)-an examination of environmental and historical factors affecting diversity.

Authors:  Jorge Domingo Carrillo-Briceño; Juan D Carrillo; Orangel Antonio Aguilera; Marcelo R Sanchez-Villagra
Journal:  PeerJ       Date:  2018-07-20       Impact factor: 2.984

  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.