Pith. sign in

REVIEW 3 major objections 3 minor 72 references

Analytical solution for the polydisperse random close packing problem in 2D

T0 review · 3 major / 3 minor · reviewed 2026-08-09 · deepseek-v4-flash

Pith's one-line read The paper claims that the random close packing density of polydisperse hard disks is obtained by solving $C_0[Z(\phi_{\mathrm{RCP}})-1]=1$ with the polydisperse compressibility $Z$ from an effective-density equation of state, yielding…

desk verdict Useful first analytical 2D polydisperse RCP formula, but the central EOS transfer to jammed disks is unvalidated and one swap-MC point is too thin a benchmark. read the letter →

arxiv 2502.03354 v2 pith:SS7NCMHP submitted 2025-02-05 cond-mat.soft cond-mat.dis-nncond-mat.mtrl-scicond-mat.stat-mechphysics.chem-ph

classification cond-mat.softcond-mat.dis-nncond-mat.mtrl-scicond-mat.stat-mechphysics.chem-ph
keywords randomclosepackingpolydisperseharddiskseffectivefractionisostaticityequationofstatejammingsizepolydispersity2Ddiskpackings
verification ladder T0 review T1 audit T2 compute T3 formal

The pith

A machine-rendered reading of the paper's core claim, the machinery that carries it, and where it could break.

The reading

This paper claims that the densest disordered packing of hard disks with a spread of sizes can be computed analytically, without simulation, by solving a single algebraic equation. The equation, $C_0[Z(\phi_{\mathrm{RCP}})-1]=1$, combines the isostatic condition that each disk has on average four contacts with an equilibrium equation of state for polydisperse disks. The solution grows with the reduced standard deviation $s$ of the size distribution and saturates near $\phi_{\mathrm{RCP}}\approx 0.97$--$0.98$ at large $s$; at $s=0.25$ it gives $0.8924$, close to the recent numerical estimate $0.905$. If correct, the result turns a long-standing packing problem into a formula that depends only on the first three moments of the disk-size distribution, with consequences for granular monolayers, particle-stabilized interfaces, and two-dimensional materials.

What carries the argument

The load-bearing object is the effective-density equation of state for polydisperse hard disks, which maps a mixture at packing fraction $\phi$ onto an equivalent monodisperse fluid at $\phi_{\mathrm{eff}}=\phi/[\phi+\lambda(1-\phi)]$, with $\lambda=m_3/m_2^2$ determined by the dimensionless moments of the disk-size distribution. Its compressibility $Z(\phi)$, meaning the pressure divided by density in thermal units, enters the isostatic condition $C_0[Z(\phi_{\mathrm{RCP}})-1]=1$, obtained by writing the mean contact number as $z=4C_0[Z(\phi)-1]$ and setting $z=4$. The work this machinery does is to reduce the many-species contact problem to a one-species equation of state, so $\phi_{\mathrm{RCP}}$ becomes a function of the distribution's first three moments.

What would settle it

Simulate slow compressions or swap-based packings of log-normal polydisperse hard disks at several reduced standard deviations $s$ and compare the measured maximum disordered packing fraction with Eq. (13); a systematic gap that grows with $s$, or a non-monotone curve, would rule out the assumed mapping.

Watch

Extended reading notes

Core claim

The central claim is that random close packing in two dimensions is the rigidity-onset density, where the mean contact number reaches the isostatic value $z=4$, and that this density is the solution of $C_0[Z(\phi_{\mathrm{RCP}})-1]=1$. Here $Z$ is the compressibility of the polydisperse disk fluid obtained from the effective packing fraction mapping $\phi_{\mathrm{eff}}=\phi/[\phi+\lambda(1-\phi)]$ with $\lambda=m_3/m_2^2$, and $C_0$ is fixed by the monodisperse triangular close packing at $\phi=\pi/\sqrt{12}\approx 0.9069$. The paper evaluates $C_0$ with three standard disk equations of state to show the prediction is robust, and compares the log-normal result at $s=0.25$ ($\phi_{\mathrm{RCP}}=0.8924$) with the recent numerical estimate $0.905$ from irreversible swap Monte Carlo. This is presented as the first analytical solution to the polydisperse random close packing problem for two-dimensional disks.

Load-bearing premise

The equilibrium pressure-density relation for polydisperse hard disks is assumed to remain valid for jammed, out-of-equilibrium packings near random close packing, a transfer that the paper does not test in two dimensions.

Editorial extensions

If this is right

  • The random close packing fraction of any polydisperse disk system can be estimated by solving one algebraic equation from the first three moments of its size distribution, bypassing expensive packing simulations.
  • At a fixed size spread $s=0.25$, the theory yields $\phi_{\mathrm{RCP}}=0.8924$, about 1.4 percent below the $0.905$ value from the latest irreversible swap Monte Carlo simulations.
  • Increasing polydispersity raises the predicted packing fraction monotonically toward a plateau near $\phi_{\mathrm{RCP}}\approx 0.97$--$0.98$, always below the geometric limit of 1.
  • The final formula is insensitive to which of the three standard disk equations of state is used at moderate polydispersity, so the prediction is not an artifact of a particular choice.
  • The same approach previously applied to three-dimensional polydisperse spheres now covers two-dimensional disk monolayers, connecting to interfacial, polymer, and biological packing problems.

Reading between the lines

Editorial extensions of the paper, not claims the author makes directly.

  • Because the solution depends on the size distribution only through its first three moments, two very different distributions with the same mean, variance, and skewness would be predicted to have identical $\phi_{\mathrm{RCP}}$; this moment-collapse is a direct, testable consequence not highlighted in the paper.
  • The current numerical comparison is at a single value of $s$; a stronger test would be to simulate log-normal disks over a range of $s$ and compare the whole $\phi_{\mathrm{RCP}}(s)$ curve with Eq. (13).
  • If the equilibrium-to-jammed transfer holds, the same effective-density route could likely be applied to models with soft repulsive interactions at jamming, where isostaticity and the contact number are already known to control the mechanical response.
  • The predicted saturation near 0.97--0.98 suggests an upper bound for isostatic disordered disk packings; a natural extension is to ask whether any protocol that preserves strict disorder can exceed this plateau.
Share X Bluesky LinkedIn Reddit HN

Signed reviews

No signed human review yet.

Editorial analysis

A structured set of objections, weighed in public.

Desk editor's note, referee report, and a circularity audit.

Referee Report

3 major / 3 minor

Summary. The manuscript proposes an analytical route to the random close packing density of polydisperse hard disks. It combines a jammed-state contact relation, z = 4 C0 [Z(phi) - 1], with equilibrium hard-disk equations of state, after calibrating C0 at the monodisperse triangular close-packing point. Polydispersity is introduced through the Santos effective-packing-fraction EOS, Eq. (12). Solving C0[Z(phi_RCP) - 1] = 1 yields phi_RCP as a function of the width of the size distribution; the result is compared with swap-Monte-Carlo data at s = 0.25, giving phi_RCP = 0.8924 versus 0.905.

Significance. If its assumptions held, this would be the first closed-form analytical formula for the 2D polydisperse random close packing fraction, with potential applications to granular monolayers, interfacial assemblies, and composite materials. The derivation is concise, and the s = 0.25 comparison is an external benchmark rather than a fit, because C0 is fixed at the monodisperse close-packing point. However, the two central transfers—equilibrium fluid equation of state to jammed packings, and monodisperse calibration to arbitrary polydispersity—are not validated in 2D, and Eq. (12) as printed does not reduce to the monodisperse equation of state. The paper therefore cannot be accepted without substantial revision.

major comments (3)
  1. [Section 'To extend the EOS', Eq. (12)] Equation (12) as written is internally inconsistent: for a monodisperse distribution one has lambda = 1, alpha = 1, and phi_eff = phi, so the equation reduces to Z = (1 + phi) + phi^2 Z_s(phi), not to Z_s(phi). The Santos FMT mapping has the structure Z = 1/(1 - phi) + alpha [ Z_s(phi_eff) - 1/(1 - phi_eff) ], so Eq. (12) appears to contain an erroneous factor phi and to be missing the division by phi_eff (or an equivalent rearrangement). Since Eq. (13) and all polydisperse numerical values, including phi_RCP = 0.8924 and the curves in Fig. 1, are computed from Eq. (12), the polydisperse predictions must be recomputed with the correct EOS before the central claim can be assessed.
  2. [Section 'EOS', Eq. (7)] The proportionality in Eq. (7) is the pivot of the theory: it takes the equilibrium virial contact value, (Z - 1)/(2 phi), and asserts that the jammed contact value g(sigma; phi) is proportional to it. The paper justifies this by Ref. [10] for 3D hard spheres, but provides no 2D numerical or theoretical check. In a jammed disk packing near RCP, the contact peak is singular and the pressure is not given by the equilibrium virial expression; C0 absorbs the proportionality factor at one density, but the assumed functional form z proportional to Z(phi) - 1 across all densities and polydispersities is unchecked. This makes the entire phi_RCP(s) curve in Fig. 1 conditional on an unvalidated analogy.
  3. [Section 'Comparison with Ref. [69]'] The only quantitative validation of the polydisperse theory is a single point at s = 0.25, where the paper predicts phi_RCP = 0.8924 against the swap-MC value 0.905. The paper itself states that the packings in Ref. [69] are not necessarily isostatic, i.e. z may exceed 4, so the simulated phi_RCP may be set by a different criterion than z = 4. With one point and an acknowledged mismatch in the defining condition, the agreement cannot distinguish between the proposed mechanism and a systematic underestimate. The authors should compare with additional polydisperse data (e.g. bidisperse disk packings or other distribution widths) or directly measure z(phi) in simulated jammed packings to test Eq. (8).
minor comments (3)
  1. [Section 'EOS', Eq. (3)] The constant g0 in the contact-peak ansatz is said to be determined by a boundary condition, but the boundary condition is never specified; please state it explicitly.
  2. [Abstract and text] The abstract describes the comparison as a 'power-law size distribution' with s = 0.246, while the text and Fig. 1 use a log-normal distribution with sigma approximately 0.2462; please reconcile the nomenclature.
  3. [Section 'Polydisperse contacts', Eq. (2)] For polydisperse disks, the average contact relation should specify how g(r) is averaged over ij pairs and how the single mean diameter sigma follows from that average; currently the reduction from the polydisperse contact condition sigma_ij = (sigma_i + sigma_j)/2 is implicit.

Circularity Check

0 steps flagged · score 0.0 of 10

No significant circularity: the phi_RCP(s) curve follows from the calibrated crowding relation plus independent equilibrium equations of state; the swap-MC comparison is an external benchmark, not a fitted input.

full rationale

The derivation chain is non-circular. Equation (13), C0[Z(phi_RCP)-1]=1, follows by combining the isostatic definition of RCP (z_c=4, from Ref. [32]) with the crowding relation z=4C0[Z-1], where C0 is calibrated at the monodisperse CP point (phi_CP=pi/sqrt(12), z=6), not at the predicted RCP. The monodisperse values in Table I are outputs of the same equation, not fitted inputs. The EOS choices (SPT, Henderson, CS) and the Santos polydisperse mapping are independent equilibrium inputs. The s=0.25 comparison with the swap-MC value phi=0.905 (Ref. [69]) is an external benchmark; the paper explicitly concedes that those packings may have z>4 and that its prediction may therefore underestimate them, which shows the agreement is not forced. The self-citations [9,10] provide prior numerical justification of the crowding ansatz in 3D; they do not supply the 2D polydisperse result, so the central claim does not collapse into those citations. The manuscript's own limitation, namely the unvalidated transfer of the equilibrium polydisperse hard-disk EOS to jammed 2D packings, is a correctness risk rather than a circular step. No reduction of Eq. (13) to a fitted parameter or to the comparison datum can be exhibited from the paper's equations.

Assumptions & free parameters 1 free parameters · 4 assumptions · 0 invented entities

The central claim depends on four assumptions, all inherited from the author's previous crowding framework or from equilibrium EOS theory. No new physical entities are introduced, but the calibration constant C0 and the EOS choice are modeling inputs that determine the predicted values.

free parameters (1)
  • C0 (dimensionless proportionality constant) = 0.0131 (SPT), 0.0119 (Henderson), 0.0218 (CS) from Table I
    Introduced in Eq. (8) by combining the split-rdf assumption with the proportionality g(σ;φ) ∝ (Z-1)/(2φ). It is calibrated at monodisperse triangular close packing, z=6 at phi_CP=0.9069, and then used unchanged for all polydisperse predictions. It is a boundary-condition constant, not fitted to RCP data, but its value depends on the arbitrary choice of a monodisperse EOS.
assumptions (4)
  • ad hoc to paper The averaged contact value of the jammed packing rdf is proportional to the equilibrium virial contact value: g(σ;φ) ∝ (Z(phi)-1)/(2phi).
    Introduced in Eq. (7) by analogy with the equilibrium virial theorem in Eq. (6), justified only by prior 3D numerical work [10]. It is the key step that connects jammed packings to equilibrium equations of state.
  • domain assumption RCP is identified with the isostatic rigidity onset with average contact number z=4.
    Used in Eq. (13), citing Ref [32]. This defines RCP as the densest isostatic packing, one of several possible definitions.
  • domain assumption The Santos effective packing fraction mapping, phi_eff = phi/[phi+lambda(1-phi)], and the polydisperse compressibility Eq. (12) hold at jammed RCP densities.
    Imported from Refs [66-68] for equilibrium polydisperse hard-sphere fluids; no derivation or numerical check is provided for its use in 2D jammed packings.
  • ad hoc to paper C0 calibrated at monodisperse CP remains valid for arbitrary polydispersity.
    Used in Eq. (13) for all size distributions without further justification beyond the prior framework.

how reviews work

0 comments
Cite this review

Pith. "Pith review of Analytical solution for the polydisperse random close packing problem in 2D." pith.science (2026). https://pith.science/paper/SS7NCMHP

@misc{pith2026250203354,
  author       = {Pith},
  title        = {Pith review of: Analytical solution for the polydisperse random close packing problem in 2D},
  year         = {2026},
  howpublished = {\url{https://pith.science/paper/SS7NCMHP}},
  note         = {Machine review of arXiv:2502.03354}
}
abstract

An analytical theory for the random close packing density, $\phi_\textrm{RCP}$, of polydisperse hard disks is provided using an equilibrium model of crowding [A. Zaccone, Phys. Rev. Lett. 128, 028002 (2022)] which has been justified on the basis of extensive numerical analysis of the maximally random jammed (MRJ) line in the phase diagram of hard spheres [Anzivino et al., J. Chem. Phys. 158, 044901 (2023)]. The solution relies on the equations of state for the hard disk fluid and provides predictions for $\phi_\textrm{RCP}$ as a function of the ratio, $s$, of the standard deviation of the distribution of disk diameters to its mean. For a power-law size distribution with $s=0.246$, the theory yields $\phi_\textrm{RCP} =0.892$, which compares well with the most recent numerical estimate $\phi_\textrm{RCP} =0.905$ based on the Monte-Carlo swap algorithms [Ghimenti, Berthier, van Wijland, Phys. Rev. Lett. 133, 028202 (2024)].

Figures

Figures reproduced from arXiv: 2502.03354 by the authors.

Figure 1
Figure 1. FIG. 1 [PITH_FULL_IMAGE:figures/full_fig_p003_1.png] view at source ↗

Discussion (0). Continue with ORCID to comment.

Reference graph

Works this paper leans on

72 extracted references · 66 canonical work pages

  1. [10]

    Anzivino, M

    C. Anzivino, M. Casiulis, T. Zhang, A. S. Moussa, S. Martiniani, and A. Zaccone, The Journal of Chemical Physics 158 (2023)

  2. [69]

    Ghimenti, L

    F. Ghimenti, L. Berthier, and F. van Wijland, Phys. Rev. Lett. 133, 028202 (2024)

  3. [1]

    B. J. Alder and T. E. Wainwright, The Journal of chem- ical physics 27, 1208 (1957)

  4. [2]

    W. W. Wood and J. D. Jacobson, The Journal of Chem- ical Physics 27, 1207 (1957)

  5. [3]

    W. G. Hoover and F. H. Ree, The Journal of Chemical Physics 49, 3609 (1968)

  6. [4]

    Hansen and I

    J.-P. Hansen and I. R. McDonald, Theory of simple liquids (Elsevier Academic Press, 2006)

  7. [5]

    van Blaaderen and P

    A. van Blaaderen and P. Wiltzius, Science 270, 1177 (1995)

  8. [6]

    E. Sanz, C. Valeriani, E. Zaccarelli, W. C. Poon, P. N. Pusey, and M. E. Cates, Physical Review Letters 106, 215701 (2011)

Show all 72 references
  1. [7]

    Zaccarelli, C

    E. Zaccarelli, C. Valeriani, E. Sanz, W. Poon, M. Cates, and P. Pusey, Physical review letters103, 135704 (2009)

  2. [8]

    J. D. Bernal and J. Mason, Nature 188, 910 (1960)

  3. [9]

    Zaccone, Physical Review Letters 128, 028002 (2022)

    A. Zaccone, Physical Review Letters 128, 028002 (2022)

  4. [11]

    Zaccone, Theory of Disordered Solids (Springer, Cham, 2023)

    A. Zaccone, Theory of Disordered Solids (Springer, Cham, 2023)

  5. [12]

    V. L. Berezinski ˇi, Soviet Journal of Experimental and Theoretical Physics 32, 493 (1971)

  6. [13]

    V. L. Berezinski ˇi, Soviet Journal of Experimental and Theoretical Physics 34, 610 (1972)

  7. [14]

    J. M. Kosterlitz and D. J. Thouless, Journal of Physics C: Solid State Physics 6, 1181 (1973)

  8. [15]

    Gasser, C

    U. Gasser, C. Eisenmann, G. Maret, and P. Keim, ChemPhysChem 11, 963 (2010), https://chemistry- europe.onlinelibrary.wiley.com/doi/pdf/10.1002/cphc.200900755

  9. [16]

    Deutschl¨ ander, T

    S. Deutschl¨ ander, T. Horn, H. L¨ owen, G. Maret, and P. Keim, Phys. Rev. Lett. 111, 098301 (2013)

  10. [17]

    E. P. Bernard and W. Krauth, Phys. Rev. Lett. 107, 155704 (2011)

  11. [18]

    W. Qi, A. P. Gantapara, and M. Dijkstra, Soft Matter 10, 5449 (2014)

  12. [19]

    Tsiok, Y

    E. Tsiok, Y. Fomin, and V. Ryzhov, Physica A: Statis- tical Mechanics and its Applications 490, 819 (2018)

  13. [20]

    Y.-W. Li, Y. Yao, and M. P. Ciamarra, Phys. Rev. Lett. 130, 258202 (2023)

  14. [21]

    Stillinger, F

    J. Stillinger, F. H., E. A. DiMarzio, and R. L. Kornegay, The Journal of Chemical Physics 40, 1564 (1964), https://pubs.aip.org/aip/jcp/article- pdf/40/6/1564/18832883/1564 1 online.pdf

  15. [22]

    Sutherland, Journal of Colloid and Interface Science 60, 96 (1977)

    D. Sutherland, Journal of Colloid and Interface Science 60, 96 (1977)

  16. [23]

    H. J. H. Brouwers, Soft Matter 19, 8465 (2023)

  17. [24]

    B. H. J.H, Phys. Usp. 67, 510 (2024)

  18. [25]

    Sugiyama, Progress of Theoretical Physics 63, 1848 (1980), https://academic.oup.com/ptp/article- pdf/63/6/1848/5221030/63-6-1848.pdf

    M. Sugiyama, Progress of Theoretical Physics 63, 1848 (1980), https://academic.oup.com/ptp/article- pdf/63/6/1848/5221030/63-6-1848.pdf

  19. [26]

    J. G. Berryman, Phys. Rev. A 27, 1053 (1983)

  20. [27]

    Meyer, C

    S. Meyer, C. Song, Y. Jin, K. Wang, and H. A. Makse, Physica A: Statistical Mechanics and its Applications 389, 5137 (2010)

  21. [28]

    Wilken, A

    S. Wilken, A. Z. Guo, D. Levine, and P. M. Chaikin, Physical Review Letters 131, 238202 (2023)

  22. [29]

    T. M. Truskett, S. Torquato, and P. G. Debenedetti, Physical Review E 62, 993 (2000)

  23. [30]

    Ozawa, L

    M. Ozawa, L. Berthier, and D. Coslovich, SciPost Physics 3, 027 (2017)

  24. [31]

    Torquato and F

    S. Torquato and F. H. Stillinger, Reviews of modern physics 82, 2633 (2010)

  25. [32]

    Zaccone and E

    A. Zaccone and E. Scossa-Romano, Physical Review B—Condensed Matter and Materials Physics 83, 184205 (2011)

  26. [33]

    C. S. O’Hern, L. E. Silbert, A. J. Liu, and S. R. Nagel, Phys. Rev. E 68, 011306 (2003)

  27. [34]

    Wilken, R

    S. Wilken, R. E. Guerra, D. Levine, and P. M. Chaikin, Physical review letters 127, 038002 (2021). 5

  28. [35]

    Lombard and E

    O. Lombard and E. Franceschini, IEEE Transactions on Ultrasonics, Ferroelectrics, and Frequency Control 71, 572 (2024)

  29. [36]

    Kim and S

    S. Kim and S. Hilgenfeldt, Soft Matter 20, 5598 (2024)

  30. [37]

    Singh, C

    A. Singh, C. Ness, A. K. Sharma, J. J. de Pablo, and H. M. Jaeger, Phys. Rev. E 110, 034901 (2024)

  31. [38]

    Malamud, C

    U. Malamud, C. M. Sch¨ afer, I. Luciana San Sebasti´ an, M. Timpe, K. Alexander Essink, C. Kreuzig, G. Meier, J. Blum, H. B. Perets, and C. Burger, The Astrophysical Journal 974, 76 (2024)

  32. [39]

    B¨ urger, P

    J. B¨ urger, P. O. Hayne, B. Gundlach, M. L¨ auter, T. Kramer, and J. Blum, Jour- nal of Geophysical Research: Planets 129, e2023JE008152 (2024), e2023JE008152 2023JE008152, https://agupubs.onlinelibrary.wiley.com/doi/pdf/10.1029/2023JE008152

  33. [40]

    S. Yu, M. Yu, X. Xiao, J. Huang, and L. Xiao, (2024), 10.22541/essoar.173282183.30831648/v1

  34. [41]

    Mermet-Guyennet, J

    M. Mermet-Guyennet, J. Gianfelice de Castro, H. Varol, M. Habibi, B. Hosseinkhani, N. Martzel, R. Sprik, M. Denn, A. Zaccone, S. Parekh, and D. Bonn, Poly- mer 73, 170 (2015)

  35. [42]

    Krief and Y

    M. Krief and Y. Ashkenazy, Phys. Rev. Res. 6, 023253 (2024)

  36. [43]

    Zaccone, Journal of Physics: Condensed Matter 32, 203001 (2020)

    A. Zaccone, Journal of Physics: Condensed Matter 32, 203001 (2020)

  37. [44]

    D. J. Meer, I. Galoustian, J. G. d. F. Manuel, and E. R. Weeks, Physical Review E 109, 064905 (2024)

  38. [45]

    Buttinoni, Z

    I. Buttinoni, Z. A. Zell, T. M. Squires, and L. Isa, Soft Matter 11, 8313 (2015)

  39. [46]

    Maestro and A

    A. Maestro and A. Zaccone, Nanoscale 9, 18343 (2017)

  40. [47]

    E. A. Lazar, J. Lu, C. H. Rycroft, and D. Schwarcz, Modelling and Simulation in Materials Science and En- gineering 32, 085022 (2024)

  41. [48]

    Pal and S

    S. Pal and S. Keten, Soft Matter 20, 7926 (2024)

  42. [49]

    A. N. Kato, Y. Jiang, W. Chen, R. Seto, and T. Li, Journal of Colloid and Interface Science 641, 492 (2023)

  43. [50]

    Pedrosa, D

    C. Pedrosa, D. Mart ´ ınez-Fern´ andez, M. Her- ranz, K. Foteinopoulou, N. C. Karayiannis, and M. Laso, The Journal of Chemical Physics 158, 164502 (2023), https://pubs.aip.org/aip/jcp/article- pdf/doi/10.1063/5.0137115/16954588/164502 1 5.0137115.pdf

  44. [51]

    Y. Zeng, P. Gordiichuk, T. Ichihara, G. Zhang, E. Sandoz-Rosado, E. D. Wetzel, J. Tresback, J. Yang, D. Kozawa, Z. Yang, M. Kuehne, M. Quien, Z. Yuan, X. Gong, G. He, D. J. Lundberg, P. Liu, A. T. Liu, J. F. Yang, H. J. Kulik, and M. S. Strano, Nature 602, 91 (2022)

  45. [52]

    Mirigliano, F

    M. Mirigliano, F. Borghi, A. Podest` a, A. Antidormi, L. Colombo, and P. Milani, Nanoscale Adv. 1, 3119 (2019)

  46. [53]

    S. Y. An and B. S. Kim, Electronic Materials Letters 20, 733 (2024)

  47. [54]

    Opti- mal disk packing of chloroplasts in plant cells,

    N. Schramma, E. R. Weeks, and M. Jalaal, “Opti- mal disk packing of chloroplasts in plant cells,” (2025), arXiv:2501.14335 [cond-mat.soft]

  48. [55]

    Farhadifar, J.-C

    R. Farhadifar, J.-C. R¨ oper, B. Aigouy, S. Eaton, and F. J¨ ulicher, Current Biology17, 2095 (2007)

  49. [56]

    Garcia, E

    S. Garcia, E. Hannezo, J. Elgeti, J.-F. Joanny, P. Silberzan, and N. S. Gov, Proceedings of the National Academy of Sciences 112, 15314 (2015), https://www.pnas.org/doi/pdf/10.1073/pnas.1510973112

  50. [57]

    N. I. Petridou, B. Corominas-Murtra, C.-P. Heisenberg, and E. Hannezo, Cell 184, 1914 (2021)

  51. [58]

    D. M. Sussman and M. Merkel, Soft Matter 14, 3397 (2018)

  52. [59]

    Torquato, The Journal of Chemical Physics 149, 020901 (2018)

    S. Torquato, The Journal of Chemical Physics 149, 020901 (2018)

  53. [60]

    D. G. Chae, F. H. Ree, and T. Ree, The Journal of Chemical Physics 50, 1581 (1969), https://pubs.aip.org/aip/jcp/article- pdf/50/4/1581/18860328/1581 1 online.pdf

  54. [61]

    Likos, Journal Club for Condensed Matter Physics (2022), 10.36471/JCCM-March-2022-02

    C. Likos, Journal Club for Condensed Matter Physics (2022), 10.36471/JCCM-March-2022-02

  55. [62]

    Mulero, Theory and simulation of hard-sphere fluids and related systems, Vol

    ´A. Mulero, Theory and simulation of hard-sphere fluids and related systems, Vol. 753 (Springer, 2008)

  56. [63]

    Helfand, H

    E. Helfand, H. L. Frisch, and J. L. Lebowitz, The Journal of Chemical Physics 34, 1037 (1961), https://pubs.aip.org/aip/jcp/article- pdf/34/3/1037/18821006/1037 1 online.pdf

  57. [64]

    Henderson, Molecular Physics 30, 971 (1975), https://doi.org/10.1080/00268977500102511

    D. Henderson, Molecular Physics 30, 971 (1975), https://doi.org/10.1080/00268977500102511

  58. [65]

    N. F. Carnahan and K. E. Starling, The Journal of Chem- ical Physics 51, 635 (1969)

  59. [66]

    Santos, S

    A. Santos, S. B. Yuste, M. L´ opez de Haro, and V. Oga- rko, Phys. Rev. E 96, 062603 (2017)

  60. [67]

    Santos, The Journal of Chemical Physics 136, 136102 (2012), https://pubs.aip.org/aip/jcp/article- pdf/doi/10.1063/1.3702439/14714736/136102 1 online.pdf

    A. Santos, The Journal of Chemical Physics 136, 136102 (2012), https://pubs.aip.org/aip/jcp/article- pdf/doi/10.1063/1.3702439/14714736/136102 1 online.pdf

  61. [68]

    Santos, S

    A. Santos, S. B. Yuste, and M. L´ opez de Haro, The Journal of Chemical Physics 153, 120901 (2020), https://pubs.aip.org/aip/jcp/article- pdf/doi/10.1063/5.0023903/20017843/120901 1 5.0023903.pdf

  62. [70]

    V. F. Hagh, S. R. Nagel, A. J. Liu, M. L. Man- ning, and E. I. Corwin, Proceedings of the National Academy of Sciences of the United States of America 119, 2117622119 (2022)

  63. [71]

    Bolton-Lum, R

    V. Bolton-Lum, R. C. Dennis, P. Morse, and E. Corwin, Arxiv Preprint , 2404.07492 (2024)

  64. [72]

    E. P. Bernard, W. Krauth, and D. B. Wilson, Physi- cal Review E - Statistical, Nonlinear, and Soft Matter Physics 80, 5 (2009)

Pith tools

Reviewed August 9, 2026 · model on record in the stance chip above.