REVIEW 2 major objections 4 minor 69 references
Dark Galactic subhalos and the Gaia snail
T0 review · 2 major / 4 minor · reviewed 2026-08-11 · deepseek-v4-flash
Pith's one-line read Dark subhalos cannot explain the Gaia snail by themselves, but they should leave a persistent, detectable $0.1$–$0.5$ km/s vertical velocity signal in the solar neighborhood.
desk verdict Solid, honest model study: the Gaia snail null result is well-supported within the model, but the phenomenological diffusion kernel is the real soft spot and deserves a sensitivity analysis. read the letter →
The pith
A machine-rendered reading of the paper's core claim, the machinery that carries it, and where it could break.
The reading
What carries the argument
The engine of the calculation is a one-dimensional action-angle model of vertical stellar motion. In the equilibrium Milky Way potential, each passing satellite changes a star's vertical action $\Delta J$ by integrating the vertical force along the unperturbed orbit (Equation 4), and the perturbed distribution function is a rational isothermal-like function of the action $J$ evaluated at $J_\mathrm{eq}+\sum_i \Delta J_i$. Subhalo orbits and masses come from a semi-analytic merger-tree model that yields a kernel density estimate of the joint position-velocity distribution of present-day subhalos that passed near the Sun. A diffusion layer made of spatially varying Gaussian convolutions with kernel widths set by local action and frequency scales, calibrated to damp signals as $\exp(-\tau^3/t_0^3)$ with $t_0=0.6$ Gyr, is what lets the paper say which perturbations survive to now.
What would settle it
Search the local Gaia sample for the paper's predicted floor: fluctuations of $0.1$–$0.5$ km/s in the mean vertical velocity $\langle v_z(z)\rangle$ together with a multi-stripe pattern in frequency-angle coordinates. If the data show no such signal where the CDM abundance model says it must appear, or show a signal far stronger than the model's ceiling, then the combination of the subhalo orbit generator, the action-response calculation, or the diffusion kernel is wrong.
Extended reading notes
Core claim
The central claim is that a CDM-like population of $10^6$–$10^8\,M_\odot$ dark subhalos, the invisible low-mass end of the predicted halo mass function, cannot by itself reproduce the observed Gaia snail. Subhalos are individually and collectively too weak: for plausible abundances, the maximal mean vertical velocity perturbation stays between 0.1 and 0.5 km/s and the vertical asymmetry between about one and three percent. Only with 5–10 times more subhalos than CDM predicts, or with peak rather than bound masses assigned throughout, would the combined population match Gaia. The same model predicts that subhalo encounters produce a distinctive stochastic pattern of stripes in frequency-angle coordinates, with slopes set by encounter time, that could be mistaken for one older single disturbance.
Load-bearing premise
The whole answer depends on how long the kinematic memory of an old encounter lasts: the paper assumes molecular-cloud scattering damps spirals with the specific $\exp(-\tau^3/t_0^3)$ law with $t_0 = 0.6$ Gyr, and if that decay is wrong the verdict on subhalos could flip.
Editorial extensions
If this is right
- If subhalos cannot explain the snail, its observed amplitude requires another, more massive perturber acting in combination with the satellite population.
- If the predicted 0.1–0.5 km/s vertical-velocity signal persists, it should be detectable as a stochastic disequilibrium component in high-quality Gaia samples, independent of the snail.
- The multiple stripes in frequency-angle coordinates are a fingerprint of ongoing encounters; a single-age reconstruction of the snail will be systematically misleading when subhalos contribute.
- For subhalo abundances set by $\eta \gtrsim 3000$, dark subhalos overtake all known dwarf galaxies, including Sagittarius, as the most probable strong perturbers of the solar neighborhood.
- The factor of 5–10 gap between the abundance needed to explain the snail and the CDM prediction gives a quantitative target for future subhalo mass function constraints from streams and dwarf galaxies.
Reading between the lines
- The predicted $\sim 0.1$–$0.5$ km/s vertical-velocity floor gives next-generation astrometric surveys a concrete, testable target: measuring the fluctuation spectrum as a function of encounter time could constrain the subhalo mass function below the galaxy-formation limit.
- Because the diffusion kernel is spatially varying, old subhalo perturbations may survive selectively in phase-space regions less affected by molecular-cloud scattering, so selecting stars at higher $|z|$ or in lower-density sightlines could expose a faint, old component that the paper's summary statistics wash out.
- The same semi-analytic machinery could be extended to radial phase mixing, where subhalo encounters would imprint a similar multi-stripe pattern in the radial frequency-angle plane, giving a three-dimensional test in the same Gaia data.
- A decisive check of the diffusion model would come from comparing the paper's subhalo-only predictions to N-body simulations that include a live giant-molecular-cloud population, testing whether the assumed $\exp(-\tau^3/t_0^3)$ decay with $t_0=0.6$ Gyr is the right description of how old spirals actually die.
Editorial analysis
A structured set of objections, weighed in public.
Referee Report
Summary. The paper models the response of the solar-neighborhood vertical phase-space distribution to perturbations from a population of low-mass (10^6-10^8 M_sun) dark subhalos, using an action-angle impulse approximation for stellar orbits and a galacticus-calibrated probabilistic model for subhalo orbits and masses. A phenomenological diffusion model, calibrated to the exp(-tau^3/t0^3) damping law of Tremaine et al. (2023), is used to erase signatures of perturbations older than ~0.6 Gyr. The paper finds that dark subhalos alone cannot explain the observed Gaia snail amplitude unless the subhalo mass-function normalization is eta > 12,000, roughly 5-10 times above the CDM-motivated range, but that subhalos do produce persistent stochastic fluctuations of ~0.1-0.5 km/s in the mean vertical velocity and a multi-stripe pattern in frequency-angle space. The methods are validated in Appendix A against direct orbit integration.
Significance. If the central null result is robust, the paper makes an important statement: the Gaia snail cannot be produced by CDM subhalos alone, so a more massive perturber (or an alternative mechanism) is required, while a stochastic subhalo signal should be present in the local vertical phase space. The paper also provides an open-source code (darkspirals) and clear documentation of a fast forward-modeling approach that resolves phase-space structure beyond N-body capabilities. The use of a semi-analytic model for subhalo orbits and the careful validation of the action-angle approximation against direct orbit integration are strengths. The main uncertainty is the phenomenological diffusion kernel, which is calibrated to a global amplitude decay but not to the phase-space pattern of diffusion; this directly affects the survivability of the coherent signal that drives the null result.
major comments (2)
- [§2.2, Eqs. (8)-(12), Fig. 3; Figs. 11-12] The central null result (eta > 12,000 required) hinges on how much subhalo-induced phase-space structure survives to the present day. The diffusion model in Section 2.2 is a Gaussian convolution in (z, v_z) with widths k_z and k_vz growing linearly in tau, calibrated only to the global amplitude decay exp(-tau^3/t0^3). This particular phase-space pattern is not validated against a physical action-diffusion calculation, and it may over-smooth the coherent large-scale stripes that contribute most to max|A(z)| and max|⟨v_z⟩|. Because the required eta is only a factor of 2-3 above the upper end of the CDM-motivated range (eta ~ 500-12,000), a modest change in the diffusion pattern could bring subhalo-only predictions into agreement with Gaia, reversing the main conclusion. Please add a robustness test: e.g., implement an action-space diffusion treatment following Tremaine et al. (2023) or Banik et al. (2023), or vary c1, c2, and t0 over their plausible ranges, and report how the inferred eta threshold shifts.
- [§3.3, Figs. 10-12] The claim that 'none of configurations ... can simultaneously match' the Gaia snail is not accompanied by a quantitative significance statement. The Gaia DR2 point in Figure 12 appears without error bars, and no confidence level is attached to the exclusion of each eta. Given the stochastic scatter among realizations at fixed eta, please report the fraction of realizations at each eta that are consistent with the Gaia measurements within their uncertainties and state the resulting uncertainty on the eta threshold. This is important for making the null result falsifiable.
minor comments (4)
- [§2.3.3] The normalization of eta is calibrated using subhalos in the range 10^7-10^8 M_sun, but the abstract and several figures (e.g., Fig. 8 and the discussion) quote 10^6-10^8 M_sun or 10^5.7-10^8 M_sun. Please clarify the mass range used for the normalization and whether the extrapolation below 10^7 M_sun is included in all reported summary statistics.
- [§3.3, Eq. (18)] The notation 'max|v_z(z)|' is used in Figures 10-12 and the text but never explicitly defined; it should be identified as the maximum of the absolute value of the mean vertical velocity profile ⟨v_z(z)⟩ from Eq. (18).
- [Figure 5 caption] The caption states the colors in the top panel correspond to different subhalo mass ranges, but the ranges (e.g., 10^5.7-10^6, 10^6-10^7, 10^7-10^8 M_sun) are not given in the caption or a visible legend; please add them.
- [Figure 10] The abbreviation 'dSphr.' is used in the figure key but not expanded in the caption or text; please use 'dSph' or spell out 'dwarf spheroidal'.
Circularity Check
No circular reduction: the central subhalo-versus-snail comparison is external, and the self-citations used for the diffusion timescale are non-load-bearing.
full rationale
The derivation chain does not reduce any predicted quantity to an input by construction. Subhalo perturbation amplitudes are computed from a galacticus-calibrated orbit and mass population (Section 2.3.3) and the linear response of the disk (Equation 4), and are then compared with the external Gaia DR2/DR3 snail measurements of Bennett & Bovy (2019/2021). The diffusion treatment in Section 2.2 is explicitly labeled phenomenological, and it is calibrated to the damping law exp(-tau^3/t0^3) with t0 = 0.6 Gyr from Tremaine et al. (2023); although Bovy and Frankel are co-authors of both papers, the same t0 is independently cited to Banik et al. (2023), and the calibration target is the amplitude decay, not the Gaia snail. The abundance parameter eta is fixed by matching the galacticus-predicted subhalo counts (Ngalac = 249 +/- 65 for bound masses, 1743 +/- 455 for peak masses), so the stated requirement eta > 12000 is a comparison between that predicted abundance and the abundance needed to reproduce the observed snail amplitude. The scaling relations max|vz| = A sqrt(eta/1000) are fits to the model outputs, not to the Gaia data. Appendix A checks Equation 4 against direct orbit integration, and Figures 8 and 9 show no-diffusion cases alongside diffused cases, so the damping assumption is not hidden. The identified limitations (Gaussian diffusion-kernel ansatz, one-dimensional treatment) are model-uncertainty concerns rather than circular reductions. The self-citations to galpy and Tremaine et al. are therefore not load-bearing in a circular sense.
Assumptions & free parameters
free parameters (6)
- alpha (vertical DF power-law index) =
2.34
- sigma_v (vertical velocity scale) =
15.20 km/s
- c1, c2 (diffusion kernel normalization) =
c1=0.24, c2=1.00
- eta (subhalo mass function normalization) =
500 to 12000, nominal ~770
- t0 (diffusion timescale) =
0.6 Gyr
- mass function slope alpha_mf =
1.9
assumptions (7)
- domain assumption All satellites are modeled as Navarro-Frenk-White profiles with a concentration-mass relation from Diemer & Joyce (2019) and Johnson et al. (2021).
- domain assumption MWPotential2014 in galpy approximates the equilibrium vertical potential of the solar neighborhood.
- domain assumption Small-perturbation linear response, integrating the change in vertical action along unperturbed orbits, captures the disk response.
- domain assumption Phase-spiral damping follows exp(-tau^3/t0^3) with t0 = 0.6 Gyr from Tremaine et al. (2023).
- domain assumption Subhalo orbits are independent of subhalo mass and can be resampled from a KDE of galacticus orbits.
- domain assumption The CDM subhalo mass function slope and normalization range bracket the true subhalo population.
- domain assumption Nadler et al. (2020) stellar-mass to halo-mass relation assigns infall masses to luminous satellites.
Cite this review
Pith. "Pith review of Dark Galactic subhalos and the Gaia snail." pith.science (2026). https://pith.science/paper/RFHSJLLI
@misc{pith2026241202757,
author = {Pith},
title = {Pith review of: Dark Galactic subhalos and the Gaia snail},
year = {2026},
howpublished = {\url{https://pith.science/paper/RFHSJLLI}},
note = {Machine review of arXiv:2412.02757}
}
abstract
Gaia has revealed a clear signal of disequilibrium in the solar neighborhood in the form of a spiral (or snail) feature in the vertical phase-space distribution. We investigate the possibility that this structure emerges from ongoing perturbations by dark $\left(10^{6} M_{\odot} - 10^8 M_{\odot}\right)$ Galactic subhalos. We develop a probabilistic model for generating subhalo orbits based on a semi-analytic model of structure formation, and combine this framework with an approximate prescription for calculating the response of the disk to external perturbations. We also develop a phenomenological treatment for the diffusion of phase-space spirals caused by gravitational scattering between stars and giant molecular clouds, a process that erases the kinematic signatures of old ($t \gtrsim 0.6$ Gyr) events. Perturbations caused by dark subhalos are, on average, orders of magnitude weaker than those caused by luminous satellite galaxies, but the ubiquity of dark halos predicted by cold dark matter makes them a more probable source of strong perturbation to the dynamics of the solar neighborhood. Dark subhalos alone do not cause enough disturbance to explain the Gaia snail, but they excite fluctuations of $\sim 0.1-0.5 \ \rm{km} \ \rm{s^{-1}}$ in the mean vertical velocity of stars near the Galactic midplane that should persist to the present day. Subhalos also produce correlations between vertical frequency and orbital angle that could be mistaken as originating from a single past disturbance. Our results motivate investigation of the Milky Way's dark satellites by characterizing their kinematic signatures in phase-space spirals across the Galaxy.
Figures
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Reference graph
Works this paper leans on
-
[1]
2023, A&A, 673, A115, doi: 10.1051/0004-6361/202245518
Antoja, T., Ramos, P., Garc ´ ıa-Conde, B., et al. 2023, A&A, 673, A115, doi: 10.1051/0004-6361/202245518
-
[2]
2018, Nature, 561, 360, doi: 10.1038/s41586-018-0510-7 Astropy Collaboration, Robitaille, T
Antoja, T., Helmi, A., Romero-G´ omez, M., et al. 2018, Nature, 561, 360, doi: 10.1038/s41586-018-0510-7 Astropy Collaboration, Robitaille, T. P., Tollerud, E. J., et al. 2013, A&A, 558, A33, doi: 10.1051/0004-6361/201322068 Astropy Collaboration, Price-Whelan, A. M., Sip˝ ocz, B. M., et al. 2018, AJ, 156, 123, doi: 10.3847/1538-3881/aabc4f Astropy Collab...
-
[3]
Banik, N., Bovy, J., Bertone, G., Erkal, D., & de Boer, T. J. L. 2021, MNRAS, 502, 2364, doi: 10.1093/mnras/stab210
-
[4]
Banik, U., van den Bosch, F. C., & Weinberg, M. D. 2023, ApJ, 952, 65, doi: 10.3847/1538-4357/acd641
-
[5]
Banik, U., Weinberg, M. D., & van den Bosch, F. C. 2022, ApJ, 935, 135, doi: 10.3847/1538-4357/ac7ff9
-
[6]
2019, MNRAS, 482, 1417, doi: 10.1093/mnras/sty2813 —
Bennett, M., & Bovy, J. 2019, MNRAS, 482, 1417, doi: 10.1093/mnras/sty2813 —. 2021, MNRAS, 503, 376, doi: 10.1093/mnras/stab524
-
[7]
Bennett, M., Bovy, J., & Hunt, J. A. S. 2022, ApJ, 927, 131, doi: 10.3847/1538-4357/ac5021
-
[8]
Benson, A. J. 2012, NewA, 17, 175, doi: 10.1016/j.newast.2011.07.004
Show all 69 references
- [9]
-
[10]
2004, MNRAS, 351, 1215, doi: 10.1111/j.1365-2966.2004.07870.x
Cole, S. 2004, MNRAS, 351, 1215, doi: 10.1111/j.1365-2966.2004.07870.x
2004
-
[11]
2011, MNRAS, 413, 1889, doi: 10.1111/j.1365-2966.2011.18268.x
Binney, J., & McMillan, P. 2011, MNRAS, 413, 1889, doi: 10.1111/j.1365-2966.2011.18268.x
2011
-
[12]
2018, MNRAS, 481, 1501, doi: 10.1093/mnras/sty2378
Binney, J., & Sch¨ onrich, R. 2018, MNRAS, 481, 1501, doi: 10.1093/mnras/sty2378
2018 doi
-
[13]
2019, MNRAS, 486, 1167, doi: 10.1093/mnras/stz217
Bland-Hawthorn, J., Sharma, S., Tepper-Garcia, T., et al. 2019, MNRAS, 486, 1167, doi: 10.1093/mnras/stz217
2019 doi
-
[14]
2015, ApJS, 216, 29, doi: 10.1088/0067-0049/216/2/29 —
Bovy, J. 2015, ApJS, 216, 29, doi: 10.1088/0067-0049/216/2/29 —. 2016, PhRvL, 116, 121301, doi: 10.1103/PhysRevLett.116.121301
2015 doi
-
[15]
R., & Wu, C.-L
Buschmann, M., Kopp, J., Safdi, B. R., & Wu, C.-L. 2018, PhRvL, 120, 211101, doi: 10.1103/PhysRevLett.120.211101
2018 doi
-
[16]
Carlberg, R. G. 1987, ApJ, 322, 59, doi: 10.1086/165702 13 https://github.com/galacticusorg/galacticus/wiki 14 https://github.com/dangilman/darkspirals
1987 doi
-
[17]
H., Widrow, L
Chequers, M. H., Widrow, L. M., & Darling, K. 2018, MNRAS, 480, 4244, doi: 10.1093/mnras/sty2114
2018 doi
-
[18]
G., Baugh, C
Cole, S., Lacey, C. G., Baugh, C. M., & Frenk, C. S. 2000, MNRAS, 319, 168, doi: 10.1046/j.1365-8711.2000.03879.x
2000
-
[19]
Johnston, K. V. 2023, ApJ, 955, 74, doi: 10.3847/1538-4357/acf1fc
2023 doi
-
[20]
A., & Ng, K
Dekker, A., Ando, S., Correa, C. A., & Ng, K. C. Y. 2022, PhRvD, 106, 123026, doi: 10.1103/PhysRevD.106.123026
2022 doi
-
[21]
2019, ApJ, 871, 168, doi: 10.3847/1538-4357/aafad6
Diemer, B., & Joyce, M. 2019, ApJ, 871, 168, doi: 10.3847/1538-4357/aafad6
2019 doi
-
[22]
C., et al
Du, X., Benson, A., Zeng, Z. C., et al. 2024, PhRvD, 110, 023019, doi: 10.1103/PhysRevD.110.023019
2024 doi
-
[23]
2015, MNRAS, 446, 1000, doi: 10.1093/mnras/stu2147
Feldmann, R., & Spolyar, D. 2015, MNRAS, 446, 1000, doi: 10.1093/mnras/stu2147
2015 doi
-
[24]
Frankel, N., Bovy, J., Tremaine, S., & Hogg, D. W. 2023, MNRAS, 521, 5917, doi: 10.1093/mnras/stad908
2023 doi
-
[25]
W., Tremaine, S., Price-Whelan, A., & Shen, J
Frankel, N., Hogg, D. W., Tremaine, S., Price-Whelan, A., & Shen, J. 2024, arXiv e-prints, arXiv:2407.07149, doi: 10.48550/arXiv.2407.07149 Gaia Collaboration, Prusti, T., de Bruijne, J. H. J., et al. 2016, A&A, 595, A1, doi: 10.1051/0004-6361/201629272 Gaia Collaboration, Bro...
-
[26]
S., Johnston, K
Gandhi, S. S., Johnston, K. V., Hunt, J. A. S., et al. 2022, ApJ, 928, 80, doi: 10.3847/1538-4357/ac47f7 Garc ´ ıa-Conde, B., Antoja, T., Roca-F` abrega, S., et al. 2024, A&A, 683, A47, doi: 10.1051/0004-6361/202347446
2022 doi
-
[27]
S., et al
Garrison-Kimmel, S., Wetzel, A., Bullock, J. S., et al. 2017, MNRAS, 471, 1709, doi: 10.1093/mnras/stx1710
2017 doi
-
[28]
Y., Kravtsov, A
Gnedin, O. Y., Kravtsov, A. V., Klypin, A. A., & Nagai, D. 2004, ApJ, 616, 16, doi: 10.1086/424914 G´ omez, F. A., Minchev, I., O’Shea, B. W., et al. 2013, MNRAS, 429, 159, doi: 10.1093/mnras/sts327
2004 doi
-
[29]
Grand, R. J. J., Pakmor, R., Fragkoudi, F., et al. 2023, MNRAS, 524, 801, doi: 10.1093/mnras/stad1969
2023 doi
-
[30]
Grand, R. J. J., Springel, V., G´ omez, F. A., et al. 2016, MNRAS, 459, 199, doi: 10.1093/mnras/stw601 GRA VITY Collaboration, Abuter, R., Amorim, A., et al. 2019, A&A, 625, L10, doi: 10.1051/0004-6361/201935656
2016 doi
-
[31]
F., Ji, A
Griffen, B. F., Ji, A. P., Dooley, G. A., et al. 2016, ApJ, 818, 10, doi: 10.3847/0004-637X/818/1/10
2016 doi
-
[32]
R., Millman, K
Harris, C. R., Millman, K. J., van der Walt, S. J., et al. 2020, Nature, 585, 357, doi: 10.1038/s41586-020-2649-2
2020 doi
-
[33]
Hunt, J. A. S., Hong, J., Bovy, J., Kawata, D., & Grand, R. J. J. 2018, MNRAS, 481, 3794, doi: 10.1093/mnras/sty2532 Dark snails 21
2018 doi
-
[34]
2022, MNRAS, 516, L7, doi: 10.1093/mnrasl/slac082
Darragh-Ford, E. 2022, MNRAS, 516, L7, doi: 10.1093/mnrasl/slac082
2022 doi
-
[35]
Hunt, J. A. S., Price-Whelan, A. M., Johnston, K. V., et al. 2024, MNRAS, 527, 11393, doi: 10.1093/mnras/stad3918
2024 doi
-
[36]
Hunt, J. A. S., Stelea, I. A., Johnston, K. V., et al. 2021, MNRAS, 508, 1459, doi: 10.1093/mnras/stab2580
2021 doi
-
[37]
1990, MNRAS, 245, 305
Jenkins, A., & Binney, J. 1990, MNRAS, 245, 305
1990
-
[38]
J., & Grin, D
Johnson, T., Benson, A. J., & Grin, D. 2021, ApJ, 908, 33, doi: 10.3847/1538-4357/abd563
2021 doi
-
[39]
Kalnajs, A. J. 1973, ApJ, 180, 1023, doi: 10.1086/152023
1973 doi
-
[40]
2023, A&A, 674, A5, doi: 10.1051/0004-6361/202244220
Katz, D., Sartoretti, P., Guerrier, A., et al. 2023, A&A, 674, A5, doi: 10.1051/0004-6361/202244220
2023 doi
-
[41]
S., Zentner, A
Kazantzidis, S., Bullock, J. S., Zentner, A. R., Kravtsov, A. V., & Moustakas, L. A. 2008, ApJ, 688, 254, doi: 10.1086/591958
2008 doi
-
[42]
2019, A&A, 622, L6, doi: 10.1051/0004-6361/201834707
Khoperskov, S., Di Matteo, P., Gerhard, O., et al. 2019, A&A, 622, L6, doi: 10.1051/0004-6361/201834707
2019 doi
-
[43]
V., Valenzuela, O., & Prada, F
Klypin, A., Kravtsov, A. V., Valenzuela, O., & Prada, F. 1999, ApJ, 522, 82, doi: 10.1086/307643
1999 doi
-
[44]
C., & de Grijs, R
Kregel, M., van der Kruit, P. C., & de Grijs, R. 2002, MNRAS, 334, 646, doi: 10.1046/j.1365-8711.2002.05556.x
2002
-
[45]
2018, MNRAS, 481, 286, doi: 10.1093/mnras/sty1574
Garavito-Camargo, N., & Besla, G. 2018, MNRAS, 481, 286, doi: 10.1093/mnras/sty1574
2018 doi
-
[46]
Laporte, C. F. P., Minchev, I., Johnston, K. V., & G´ omez, F. A. 2019, MNRAS, 485, 3134, doi: 10.1093/mnras/stz583
2019 doi
-
[47]
W., Bovy, J., Mackereth, J
Leung, H. W., Bovy, J., Mackereth, J. T., et al. 2023, MNRAS, 519, 948, doi: 10.1093/mnras/stac3529
2023 doi
-
[48]
Li, H., & Widrow, L. M. 2021, MNRAS, 503, 1586, doi: 10.1093/mnras/stab574 —. 2023, MNRAS, 520, 3329, doi: 10.1093/mnras/stad244
2021 doi
-
[49]
2016, MNRAS, 459, 2905, doi: 10.1093/mnras/stw764
Moetazedian, R., & Just, A. 2016, MNRAS, 459, 2905, doi: 10.1093/mnras/stw764
2016 doi
-
[50]
2015, MNRAS, 452, 747, doi: 10.1093/mnras/stv1206
Monari, G., Famaey, B., & Siebert, A. 2015, MNRAS, 452, 747, doi: 10.1093/mnras/stv1206
2015 doi
-
[51]
1999, ApJL, 524, L19, doi: 10.1086/312287
Moore, B., Ghigna, S., Governato, F., et al. 1999, ApJL, 524, L19, doi: 10.1086/312287
1999 doi
-
[52]
O., Wechsler, R
Nadler, E. O., Wechsler, R. H., Bechtol, K., et al. 2020, ApJ, 893, 48, doi: 10.3847/1538-4357/ab846a
2020 doi
-
[53]
F., Frenk, C
Navarro, J. F., Frenk, C. S., & White, S. D. M. 1997, ApJ, 490, 493, doi: 10.1086/304888
1997 doi
- [54]
-
[55]
Pace, A. B. 2024, arXiv e-prints, arXiv:2411.07424, doi: 10.48550/arXiv.2411.07424
2024 doi
-
[56]
R., Benson, A
Pullen, A. R., Benson, A. J., & Moustakas, L. A. 2014, ApJ, 792, 24, doi: 10.1088/0004-637X/792/1/24
2014 doi
-
[57]
J., Hernquist, L., & Fullagar, D
Quinn, P. J., Hernquist, L., & Fullagar, D. P. 1993, ApJ, 403, 74, doi: 10.1086/172184 Sch¨ onrich, R., Binney, J., & Dehnen, W. 2010, MNRAS, 403, 1829, doi: 10.1111/j.1365-2966.2010.16253.x
1993
-
[58]
1951, ApJ, 114, 385, doi: 10.1086/145478
Spitzer, Lyman, J., & Schwarzschild, M. 1951, ApJ, 114, 385, doi: 10.1086/145478
1951 doi
-
[59]
2008, MNRAS, 391, 1685, doi: 10.1111/j.1365-2966.2008.14066.x
Springel, V., Wang, J., Vogelsberger, M., et al. 2008, MNRAS, 391, 1685, doi: 10.1111/j.1365-2966.2008.14066.x
2008
-
[60]
1999, MNRAS, 307, 877, doi: 10.1046/j.1365-8711.1999.02690.x
Tremaine, S. 1999, MNRAS, 307, 877, doi: 10.1046/j.1365-8711.1999.02690.x
1999
-
[61]
2023, MNRAS, 521, 114, doi: 10.1093/mnras/stad577
Tremaine, S., Frankel, N., & Bovy, J. 2023, MNRAS, 521, 114, doi: 10.1093/mnras/stad577
2023 doi
-
[62]
2020, MNRAS, 497, 4162, doi: 10.1093/mnras/staa2114
Vasiliev, E., & Belokurov, V. 2020, MNRAS, 497, 4162, doi: 10.1093/mnras/staa2114
2020 doi
-
[63]
Wang, W., Han, J., Cautun, M., Li, Z., & Ishigaki, M. N. 2020, Science China Physics, Mechanics, and Astronomy, 63, 109801, doi: 10.1007/s11433-019-1541-6
2020 doi
- [64]
-
[65]
Widmark, A., Laporte, C. F. P., de Salas, P. F., & Monari, G. 2021, A&A, 653, A86, doi: 10.1051/0004-6361/202141466
2021 doi
-
[66]
Widmark, A., Laporte, C. F. P., & Monari, G. 2022, A&A, 663, A15, doi: 10.1051/0004-6361/202142819
2022 doi
-
[67]
2012, ApJL, 750, L41, doi: 10.1088/2041-8205/750/2/L41
Chen, H.-Y. 2012, ApJL, 750, L41, doi: 10.1088/2041-8205/750/2/L41
2012 doi
-
[68]
J., Pullen, A
Yang, S., Du, X., Benson, A. J., Pullen, A. R., & Peter, A. H. G. 2020, MNRAS, 498, 3902, doi: 10.1093/mnras/staa2496
2020 doi
-
[69]
S., et al
Zheng, H., Bose, S., Frenk, C. S., et al. 2024, MNRAS, 528, 7300, doi: 10.1093/mnras/stae289 22 Gilman et al. 1.0 0.8 0.6 0.4 0.2 0.0 time [Gyr] 0.6 0.4 0.2 0.0 0.2 0.4 0.6 vertical force [2 GM pc 2] 2 1 0 1 2 Jtrue [km s 1kpc] 2 1 0 1 2 Jmodel [km s 1kpc] 0 20 40 60 80 |vz| [...
2024 doi
Reviewed August 11, 2026 · model on record in the stance chip above.
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