Stability and dynamics of dark-bright soliton bound states away from the integrable limit

The existence, stability, and dynamics of bound pairs of symbiotic matter waves in the form of dark-bright soliton pairs in two-component mixtures of atomic Bose-Einstein condensates is investigated. Motivated by the tunability of the atomic interactions in recent experiments, we explore in detail the impact that changes in the interaction strengths have on these bound pairs by considering significant deviations from the Manakov (integrable) limit. It is found that dark-bright soliton pairs exist as stable configurations in a wide parametric window spanning both the miscible and the immiscible regime of interactions. Outside this parameter interval two unstable regions are identified and are associated with a supercritical and a subcritical pitchfork bifurcation, respectively. Dynamical manifestation of these instabilities gives rise to a redistribution of the bright density between the dark solitons, and also to symmetry-broken stationary states that are mass imbalanced (asymmetric) with respect to their bright soliton counterpart. The long-time dynamics of both the stable and the unstable balanced and imbalanced dark-bright soliton pairs is analyzed.


I. INTRODUCTION
After the experimental realization of Bose-Einstein condensates (BECs) in ultracold atoms, a plethora of studies has been devoted to examining and understanding the coherent structures that arise in them [1][2][3][4]. Among these structures, the formation, interactions and dynamics of matter wave dark [5][6][7] and bright solitons [2,8,9] have been a central focus of research both from the experimental and from the theoretical side. Such nonlinear waves were experimentally generated in single-component BECs over a decade ago [10][11][12][13][14]. The nature of nonlinear matter waves that can be created in a BEC background, depends on the type of the interatomic interactions. Namely, dark solitons can be created in BECs with atom-atom repulsion resulting from a positive scattering length, while bright solitons exist in single-component settings with attractive interatomic interactions resulting from a negative scattering length.
In addition to the above single-component context, soliton states can arise also in multi-component settings. Such condensates have been created as mixtures of different spin states of 87 Rb [15,16] and 23 Na [17], and triggered numerous theoretical studies involving soliton complexes. A prototypical example of the latter is a coupled dark-bright (DB) soliton state in a highly elongated (quasi-one-dimensional) condensate cloud, consisting of a dark soliton in one component and a bright soliton in the second component of a binary BEC featuring intra-and inter-species repulsion. Since bright solitons are not self-sustained structures in repulsive (self-defocusing) media, DB solitons are often called symbiotic, that is the dark soliton can be thought of as acting as an effective potential well trapping the bright soliton [18][19][20][21][22]. Such symbiotic entities were first observed, and theoretically studied in the context of nonlinear optics [23][24][25][26][27][28][29][30][31][32]. However, their experimental realization in the atomic realm [33] opened a new and highly controllable direction towards a deeper understanding of the dynamics and interactions of these states both with each other as well as with external traps [34][35][36][37][38].
Additionally, current state-of-the art experiments offer the possibility of manipulating in a controllable fashion the nonlinear interactions via the well-established technique of Feshbach resonances [39][40][41][42][43][44][45]. This motivated recent theoretical activities where the static and dynamical properties of dark-bright symbiotic matter waves have been investigated on the level of mean field theory. Mathematically, tuning the interactions corresponds to deviating from the integrable (Manakov) limit [46] of the relevant nonlinear Schrdinger system, where nonintegrability is introduced when considering arbitrary nonlinearity (i.e., interaction) coefficients. The latter nonintegrable setting forms also the main focus of the present effort. In this context, despite the nonintegrability, analytical expressions of specific single-DB soliton states and lattices thereof have been obtained in [47]. Adding a parabolic trapping potential, it was revealed how the effective restoring force acting on the DB soliton depends on the inter-atomic interactions [47], verifying that the particle-like nature [34] of the symbiotic soliton is preserved. In the same spirit, the dependence of the binding energy of a DB soliton on the inter-species interactions was found analytically in [22], where moreover a proper bound on a phase imprinted in the bright soliton constituent was obtained (i.e. considering also moving single DB states), above which a breaking of the symbiotic entity was observed.
In our previous work [48] the interactions between DB matter waves and the consequent formation of bound states for out-ofphase (anti-symmetric) bright soliton components has been studied. Based on a two-soliton ansatz of the hyperbolic type [37,47], the full analytical expressions for the interaction energies between two DB solitons were obtained for arbitrary nonlinear coefficients, and in the absence of a confining potential. Furthermore, the key intuition that repulsion mediated by the dark solitons at short distances, and attraction mediated by anti-symmetric bright solitons at longer distances, would be counterbalanced leading in turn to a bound state formation, has been enriched by taking into account the significant role of the cross-component interaction energy term. The crucial dependence of the latter on the inter-species interaction coefficient has been analyzed. It was shown that anti-symmetric stationary states exist and remain robust for a wide parametric window of inter-species repulsions. Importantly, an exponential instability of the anti-symmetric states was identified upon crossing a critical inter-species repulsion. The latter was found to be associated with a subcritical pitchfork bifurcation, giving rise to asymmetric stationary states with mass imbalanced bright soliton counterparts.
In the present work, we extend the aforementioned findings of [48] upon considering significant deviations from the Manakov limit, towards both the immiscible (i.e., dominated by inter-species repulsion and thus phase separated in the ground state) regime, but also towards the largely unexplored miscible (i.e., dominated by intra-species repulsion) regime. To this end, we investigate the stability and dynamics of the anti-symmetric states, the so-called "solitonic gluons" [24], as well as the abovementioned asymmetric modes covering both the miscible and immiscible parameter regime. In particular, the full excitation spectrum of these symbiotic states is explored in detail by means of a Bogolyubov-de Gennes linearization analysis [1]. It is found that for the asymmetric modes the linearization spectrum is strongly affected when crossing the immiscibility-miscibility threshold, which is in turn directly connected with a rapid change of their density profiles as observed already in [48]. As a next step, the stability and dynamics of the anti-symmetric DB pairs is explored past the immiscibility-miscibility threshold. It is found that, in addition to the destabilization in the immiscible regime reported in [48], a second critical point occurs deep in the miscible regime, rendering the anti-symmetric state unstable once more. This instability scenario is found to be associated with a supercritical pitchfork bifurcation giving rise to another family of mass imbalanced (asymmetric) symbiotic structures which are found to be stable. As the inter-species repulsion is decreased, the miscible character of this regime alters the bright soliton component, resulting into asymmetric pairs with the bright solitons "living" on top of a finite background. Comparing and contrasting the instability mechanisms in the different parameter regimes, the long-time evolution of the asymmetric and anti-symmetric states is performed numerically at different interaction ratios.
The presentation is structured as follows. In Sec. 2 a description of the theoretical model and prior results regarding the existence of the anti-symmetric DB soliton pairs is provided. Furthermore, we briefly comment on the methods to be used for the numerical analysis of our findings. Sec. 3 contains the results regarding both the stability and the dynamics of asymmetric and anti-symmetric DB soliton pairs beyond the integrable limit. Finally, in Sec. 4 we summarize our findings and discuss future perspectives.

A. Model and theoretical considerations
The model of interest is a system of a two-component BEC strongly elongated along the x-direction, subject to a tight transverse harmonic trap of frequency ω ⊥ . Such a mixture can e.g be composed of two different hyperfine states of the same alkali isotope, like 87 Rb. Within mean field theory and after integrating out the frozen transverse degrees of freedom, this mixture is described by the following two coupled (1+1)-dimensional Gross-Pitaevskii equations (GPEs) [49,50]: In the above equation, ψ j (x, t) denote the mean-field wave functions of the two components normalized to the numbers of atoms N j = +∞ −∞ |ψ j | 2 dx, while m and µ j are the atomic mass (identical for both components) and chemical potentials, respectively. The effective one-dimensional coupling constants are given by g jk = 2 ω ⊥ a jk , where a jk denote the three s-wave scattering lengths that account for collisions between atoms belonging to the same (a jj ) or different (a 12 = a 21 ) species. We restrict our considerations to purely repulsive interactions, i.e. all g jk > 0, and consider an idealized homogeneous setting with no longitudinal trapping potential along the x-axis.
(2)-(3) conserves the total energy, E, the rescaled total number of atoms in each component (N d and N b , respectively) and the rescaled total number of atoms N , where: B. Interactions of symbiotic matter waves beyond the Manakov limit In the special case where the nonlinear coefficients are all equal to each other, i.e. g 12 = g 22 = 1, Eqs. (2)-(3) correspond to the integrable Manakov model [46]. In such a case, it particularly admits exact single-DB-soliton solutions of the form [34]: subject to the boundary conditions |ψ d | 2 → 1, and |ψ b | 2 → 0 for |x| → ∞. In the aforementioned solutions, φ is the so-called soliton's phase angle which fixes the "grayness" of the dark soliton, while η denotes the amplitude of the bright component. Furthermore, x 0 (t) and D correspond to the soliton's center and inverse width respectively, while k = D tan φ is the wavenumber of the bright soliton, associated with the speedẋ 0 of the DB soliton, and θ(t) is its phase. While such a general exact expression can only be obtained in the Manakov limit, one can utilize an approximate ansatz based on the expressions given in Eqs. (6)-(7) and depart from the integrable limit. Such a method was employed in our very recent work of Ref. [48] in order to analyze effective interactions between symbiotic matter waves in the general case of different inter-atomic repulsion strengths within each and between the species. Our aim in what follows is to briefly comment on the key results obtained there, to be connected with the numerical findings that will be presented below. In particular, a pair of two equal-amplitude dark-bright solitons travelling in opposite directions was considered having the approximate form: In these expressions is the distance between the two DB solitons, while ∆θ is the relative phase between the bright solitons. If ∆θ = 0, the bright solitons are in-phase (IP), while if ∆θ = π, the bright solitons are out-of-phase (OP) or anti-symmetric. Within a Hamiltonian variational approach [3,7,37,47] the approximate ansatz of Eqs. (8)-(9) is substituted into the total energy of the system given by Eq. (4), and the relevant integrations are performed under the assumption that the soliton velocity is sufficiently small (φ ≈ 0, k ≈ 0). The total energy then can be decomposed as where E 1 corresponds to the energy of a single DB soliton, contributing twice to the total energy, while the remaining three terms, namely E dd , E bb and E db , account for the interaction between: the two dark solitons, the two bright solitons, and the cross-interaction of a dark soliton in the first component with the bright soliton of the second component, respectively. Analytical expressions for each of these energy contributions as a function of the DB soliton distance x 0 and for arbitrary nonlinear coefficients can be found in [48], together with simplified asymptotic expansions valid for large distances, Dx 0 1. Figure 1 illustrates our key findings regarding the interaction energy of two out-of-phase DB solitons as a function of their distance. Here and throughout this work the chemical potential and the intra-species interaction coefficients are fixed to µ = 2/3 and g 22 = 0.95 [51,52], respectively, while the interatomic interaction coefficient g 12 is left to widely vary. In panels (a)-(c) both the full and the asymptotic forms of the analytically obtained expressions for the total interaction energy, E tot = E dd +E bb +E db , are shown with solid green and dashed yellow lines, respectively. As it can be seen in all cases, the two results coincide at large distances as they should. Strikingly, in all three cases a pronounced local energy maximum is identified. The identification of this extremum suggests, if we further take into account the effective negative mass of the DB soliton [7], the existence of an effective stable (with respect to variations in x 0 ) fixed point, thus a bound state for the two OP dark-bright solitons. Such an anti-symmetric two-DB soliton bound state can indeed be identified also in the full Gross-Pitaevskii system (for the numerical methods used we refer the reader to the following section). The predictive strength of the variational approximation is directly checked by comparing with the full numerical computation of the respective equilibria x 0 on the level of Eqs. It is worth mentioning at this point that in order to evaluate the energy functional we need as input the width D and amplitude η occuring in Eqs. (8)- (9). These are obtained by numerically identifying the exact single-DB state at the given g 12 and fitting to it the profile known from the integrable limit, i.e. Eqs. (6)- (7). There are thus two main sources of error of this scheme, namely (i) the imperfect fit of the tanh-sech profile (strictly valid only in the integrable limit) to the single DB soliton mode and (ii) the limited accuracy of the two-DB soliton ansatz of Eqs. (8)-(9) especially at small separations x 0 . For details regarding this and also a discussion of the case of in-phase bright solitons we refer the interested reader to Ref. [48]. We note also that as g 12 increases (while µ and g 22 are kept fixed), the norm N b of the bright species is increasingly suppressed and eventually vanishes [48], beyond which point there is no bound two-soliton state anymore, since the presence of the bright component is a necessary ingredient for holding the dark solitons together [24,37]. This suppression of the bright norm is compatible with the overall decrease of the total energies from panel (a) towards (b) and (c) in Figure 1.
Having variationally predicted and numerically confirmed the existence of anti-symmetric stationary dark-bright soliton bound states for a large interval of values of the inter-species interaction parameter g 12 (typically, we study 0.75 ≤ g 12 ≤ 1.5 in the present work), our main goal in the following is to address their stability and (where applicable) decay dynamics.

C. Numerical methods
In this section we briefly comment on the numerical methods to be used so as to obtain stationary symbiotic states consisting of two dark-bright solitons and to determine their stability and time evolution. In the numerical computations that follow, we initially obtain stationary solutions of the system of Eqs. (2)-(3) in the form of ψ d (x, t) = u d (x) and ψ b (x, t) = u b (x) by means of a fixed-point numerical iteration scheme [53]. The linear stability of the latter is adressed by using the Bogolyubov-de Gennes (BdG) analysis [7,50]. In particular to assess the stability of the obtained fixed points, we substitute the following ansatz into Eqs. (2)- (3): In the above equations the asterisk denotes complex conjugation while is the amplitude of infinitesimal perturbations. The resulting system of equations is then linearized, by keeping only terms of order O( ), and the eigenvalue problem for the eigenfrequencies ω and eigenmodes (a(x), b(x), c(x), d(x)) T is solved numerically. Note that an instability occurs if modes with purely imaginary or complex eigenfrequencies are identified [1]. Since the linearization spectrum is invariant under ω → −ω and ω → ω , only results in the first quadrant of the complex plane will be shown below. For the simulation of the time evolution based on Eqs.
(2)-(3), a fourth order Runge-Kutta algorithm is employed. In all cases, the numerical computations are performed on a spatial grid in the presence of an almost hard-wall super-Gaussian potential [48] that is chosen wide enough for boundary effects to be negligible on small and intermediate time scales.

III. NUMERICAL RESULTS
Having verified that stationary anti-symmetric pairs of symbiotic matter waves can be found in a wide range of values of the inter-species repulsion coefficient g 12 , a natural next step is to consider the fate of these solutions under small perturbations, providing information on their stability in the different regions of existence. The latter is explored by using the BdG linearization analysis discussed in Section 2.3. For the presentation of our results, we will distinguish the miscible (g 12 < g 12 th ) and immiscible (g 12 > g 12 th ) regimes, separated by the miscibility-immiscibility threshold [54] g 12 th = √ g 22 = 0.975 for our choice of g 22 = 0.95. In Figure 2, the BdG spectrum of the anti-symmetric stationary two dark-bright soliton states is shown as a function of g 12 . In particular, both the real ( (ω)) and the imaginary parts ( (ω)) of the eigenfrequencies ω are depicted in the top (a) and middle (b) panels respectively. Panels (c) and (d) depict profiles of the dark and bright wave functions at selected values of g 12 in the miscible and immiscible regime, respectively. Two general comments can be made before examining in detail the excitation spectrum. The most significant one is that within the background spectrum denoted with blue circles there exist two distinguished modes. The trajectories of the latter are illustrated with red stars. These modes are the so-called anomalous modes since they posses a so-called negative Krein signature K [55], which for the two-component system considered herein is defined as: The sign of this quantity is a topological property associated with the excited nature of this state and the eigenvectors of such anomalous modes result in a variation of the solitary waves (as opposed to a variation of the system's background). Furthermore, we note in passing that each continuous symmetry of the system corresponds to a pair of zero modes, ω = 0, in the BdG spectrum. Thus we expect three pairs of such modes related respectively with the conservation of the particle number (or the U (1) gauge invariance) in each of the two components, and with the translation invariance due to the absence of a confining potential. This is confirmed in the numerical data. Just by inspecting the trajectories of the two anomalous modes that appear in the spectrum, their very different behavior becomes apparent. As it is observed in panel (a) of Figure 2, the higher frequency mode decreases almost monotonically upon increasing g 12 . We were able not only to identify this mode but also to relate it with an out-of-phase vibration of the bound DB soliton pair around its equilibrium distance. The latter can be done by adding the corresponding eigenvector for some value of the inter-species interaction coefficient to the relevant stationary anti-symmetric state (results not shown here). Next, and also in the same panel of Figure 2, let us closely follow the trajectory of the lower-lying anomalous mode. The trajectory of this mode is more complicated than the former one. In particular, starting from the aforementioned reference point, g 12 th ≈ 1, and increasing the interspecies interactions towards the immiscible regime, i.e. for g 12 > g 12 th , it can be seen that there exists a critical point g (1) 12cr = 1.18 where this mode destabilizes. This destabilization corresponds to an eigenvalue zero crossing and signals the instability of the anti-symmetric configuration deep in the immiscible regime. Notice the non-zero imaginary part that appears past this critical point shown in panel (b) of Figure 2. The existence and destabilization of this mode was found to be related with a symmetry breaking of the bright soliton component, being linked, in turn, to other stationary states that are mass imbalanced with respect to their bright soliton counterpart. The identification of these asymmetric states which exist below g and collide with the anti-symmetric branch at g (1) 12cr in a subcritical pitchfork bifurcation was established in [48]. The following paragraphs will be devoted to a discussion of these asymmetric two-DB solutions, before we then return to an analysis of the BdG spectrum of the anti-symmetric pair, Figure 2, at small values of g 12 .
As mentioned above, the asymmetric and the anti-symmetric two-DB states coincide at the bifurcation point g (1) 12cr . Below this critical g 12 , the anti-symmetric state is stable and there are two symmetry-broken asymmetric solutions which are unstable (as is characteristic of a subcritical pitchfork bifurcation). Indeed, these asymmetric branches can themselves be continued towards much smaller values of g 12 and exist both in the immiscible and the miscible regime, see the profiles shown in Figure 3 (c) and (d). In both panels, dashed black lines denote the wavefunction of the dark soliton component, while solid green lines depict the corresponding bright soliton counterpart. To gain further insight regarding the nature of the instability of these asymmetric states, their full BdG spectrum is illustrated in Figure 3 (a) and (b). Once more, both the real (ω) and the imaginary (ω) parts of the eigenfrequencies ω are shown as a function of the interspecies interaction. As expected from the above discussion, only one of the anomalous modes appears in the excitation spectrum of these mass imbalanced states and is depicted with stars in red. Replacing the second anomalous mode, there is now throughout a purely imaginary frequency signaling the instability of the asymmetric branch. Remarkably, as the immiscibility-miscibility threshold is crossed, the growth rate of the instability is drastically decreased, rendering these states only weakly unstable for g 12 < g 12 th . This latter observation is in close contact with the change in the spatial character of these asymmetric states, and also in line with our previous findings [48]. Namely, as the interspecies interactions decrease towards the miscible region, the asymmetric states change gradually from only weakly asymmetric (i.e. weakly mass imbalanced with respect to their bright amplitudes), to maximally asymmetric (i.e. almost purely dark/dark-bright bound states). The difference is clearly seen in the profiles provided in panels (c) and (d) of Figure 3.
Having identified the unstable linearization eigenmodes, we now turn to the associated decay dynamics. In particular, Figure 4 shows the long-time dynamics of the above-obtained stationary asymmetric states for different values of the nonlinear coefficient g 12 . Panels (a)-(d) correspond to the dark soliton component while the respective bright wave functions are depicted in panels (e)-(h). For g 12 < 1 shown in panels (a)-(c) and (e)-(g) respectively, it is observed that as a result of the instability, the solitons move towards each other forming breathing-like structures. This is accompanied by a redistribution of the bright "filling" component between the two dark solitons, in the form of almost complete tunneling back and forth. For parameter values slightly above g 12 th , as e.g. the one depicted in panels (c) and (g), a strong beating phenomenon is observed, clearly evident in the dark soliton component, with the solitons oscillating around a fixed distance from each other forming an almost stationary breather that persists till the end of the propagation. Below the above-mentioned threshold and towards the miscible region the picture becomes progressively more dramatic. The beating gets much more pronounced with the solitons experiencing more frequent collisions as shown in panels (b) and (f). Finally, when entering even deeper in the miscible side illustrated in panels (a) and (e), eventually the bound pair fully splits into an essentially empty dark and a dark-bright soliton that are released (i.e., are no longer bound by each other) and propagate towards the outer parts of the simulation domain (where they are ultimately reflected by the boundaries). However, for g 12 > 1, i.e. upon increasing g 12 towards the immiscible side depicted in panels (d) and (h) of Figure 4, a rather different picture is painted by the symbiotic entities when compared to the asymmetric states presented above. In particular, slightly after the beginning of the propagation, where the asymmetric entity looked quite robust, a dramatic redistribution of the bright soliton's mass occurs. The latter results in a strong repulsion between the single DB soliton formed and the almost empty dark one leading in turn to their subsequent separation. Note that a similar decaying mechanism was also observed in [48] but for the unstable anti-symmetric states (see also later on in the text).
We have now characterized the branch of asymmetric two-DB soliton modes, which were seen to bifurcate from the antisymmetric two-DB soliton branch in a subcritical pitchfork bifurcation in the immiscible regime, at g towards the miscible regime, and in particular by following once again the lower-lying anomalous BdG mode, we observe that as g 12 decreases a second critical point exists deep within the miscible side. The eigenvalue zero crossing occurs at g (2) 12cr = 0.81, and is indicated by the solid light blue box. We note here, that this latter critical point was not discussed in our previous work [48], where only larger values of g 12 were studied. The destabilization of the aforementioned mode suggests the existence of a second pitchfork bifurcation. This is, once again, related with a symmetry breaking of the bright soliton component resulting into mass imbalanced (i.e., asymmetric) two DB states.
Indeed, we were able to identify these new pairs. In contrast to the previous instability scenario, these mass imbalanced states exist past the critical point but are stable, i.e. the pitchfork deep in the miscible domain is found to be supercritical. The corresponding bifurcation diagram is shown in panel (a) of Figure 5. In order to obtain this diagram we measure the relative bright imbalance defined as Notice that four branches are identified, i.e. three stable ones consisting of two asymmetric and an anti-symmetric branch all denoted by solid blue lines, and one unstable anti-symmetric branch illustrated with dashed green line. To further demonstrate the stability of the new asymmetric symbiotic pairs in panels (b)-(d) the BdG spectra are shown for different values of the inter-species interactions below the associated critical point g (2) 12cr = 0.81. Two anomalous modes appear in the linearization spectra of these asymmetric states illustrated with red stars. The respective stationary wave profiles are depicted in panels (e)-(g), where the dark (bright) soliton wavefunction is shown with dashed black (solid green) line. We observe that upon decreasing g 12 the asymmetry between the bright solitons increases, as was also the case for the respective asymmetric but unstable states found in the immiscible regime. Furthermore, for g 12 < 0.7 a background gradually builds up for the bright solitons as is evident in the stationary state shown in panel (e) of Figure 5, revealing the miscible character of the regime supporting these states. Our detailed BdG analysis indicates that for all values within the miscible regime that we have checked, the asymmetric states exist as stable configurations and should remain dynamically robust. This result is verified and highlighted in panels (h)-(m) of Figure 5 where we use as initial condition the stationary asymmetric states depicted in panels (e)-(g). We note that in all three cases panels (h)-(j) [(k)-(m)] show the evolution of the dark (bright) soliton component. Having studied both the static and the dynamical properties of the new asymmetric structures which bifurcate from the OP dark-bright states, we now turn our attention to the dynamics of the anti-symmetric DB waveforms.
In particular, we explore the long time evolution of the OP DB states so as to reveal the decay mechanisms that such a pair suffers from. The dynamics at different values of g 12 are summarized in Figure 6, all initiated at equilibrium. As before, upper row of panels (a)-(d) shows the spatio-temporal evolution of the dark soliton counterpart, while panels (e)-(h) depict the corresponding bright component. From the stability analysis presented above it is expected that for all values of the interspecies interaction coefficient g (2) 12cr < g 12 < g (1) 12cr the anti-symmetric two dark-bright soliton states exist as stable configurations, and as such should be robust throughout the propagation. This latter result is confirmed in panels (c) and (g) of Figure 6, for From left to right the interaction is increased from g12 = 0.75 to g12 = 0.82 > g (2) 12cr , and then to g12 = 1.4 > g (1) 12cr . Panels (a)-(d) [(e)-(h)] correspond to the densities |ψ d | 2 (|ψ b | 2 ) of the dark (bright) component. g 12 = 0.82 which is slightly above the lower critical point. However, and as anticipated, a very different picture is found below the critical point g (2) 12cr depicted in panels (b) and (f), (a) and (e) respectively. Starting with the former, we observe that slightly below g (2) 12cr the initial stationary state quickly decays and in (b) and (f) we observe periodic tunneling of the bright component between the two dark solitons, while the dark solitons are only relatively weakly affected here. It is worth mentioning that similar tunneling dynamics has been identified and interpreted in terms of a bosonic Josephson junction model in [56], but with the crucial difference that the soliton pair was further supported by the restoring force of a harmonic trap in that work, while in our present setup there is no external potential that would keep the dark solitons in place. Remarkably, in this regime despite the mass exchange, the bound soliton pair does not disintegrate. Further decreasing g 12 , in panels (a) and (e) the effects of the instability are more drastic. The time scale of the bright component oscillations decreases and the dark solitons vibrate more strongly. After some time of almost periodic oscillations, a more irregular type of motion sets in, with both dark solitons (one filled by most of the bright component, the other almost empty) eventually moving towards positive x while separating and recolliding in the process, suggesting still a kind of effective attractive interaction between them. This decay mechanism deep in the miscible regime is to be contrasted to the unstable dynamics in the immiscible regime, above g (1) 12cr . In panels (d) and (h) we show the time evolution of the anti-symmetric two-DB soliton state at g 12 = 1.4. While initially almost no dynamics is visible in the densities, especially no oscillations within the bright component, on intermediate time scales a strong asymmetry in the bright filling builds up (see again [48] for a more detailed discussion) and subsequently the filled and the empty dark soliton split, showing no sign of effective attraction. Notice that the above described decaying mechanism is rather similar to the one observed for the unstable asymmetric states for g 12 > 1 (see panels (d) and (h) of Figure 4).

IV. DISCUSSION AND FUTURE CHALLENGES
In the present contribution we investigated in detail the stability and dynamics of bound pairs of dark-bright symbiotic solitons, which arise as nonlinear matter wave excitations in mixtures of Bose-Einstein condensates featuring inter-atomic repulsion. In particular, we explored the scenario of differently weighted inter-and intra-species interaction coefficients, breaking the integrability of the relevant nonlinear Schrdinger model. It was argued by means of a recently proposed variational approach [48] and shown numerically that upon departing from the integrable limit bound states of such symbiotic entities exist for anti-symmetric bright soliton counterparts, the so called solitonic gluons. These anti-symmetric states were found to be robust within a bounded interval of the inter-species repulsion coefficient g 12 , limited by critical points both in the miscible and in the immiscible regime of the model, associated with a supercritical and a subcritical pitchfork bifurcation respectively. Below and above these boundaries, i.e. deep in the miscible and the immiscible regime, respectively, the anti-symmetric pair becomes unstable. Long-time propagation revealed differences, but also common characteristics of the decay mechanisms in the two domains of instability. Specifically, a striking common feature is the relevance of bright mass transfer between the two dark solitons. In particular, in the miscible domain, we identified new stationary asymmetric states that bifurcate from the anti-symmetric ones in a supercritical pitchfork. The stability of the new asymmetric states was also dynamically confirmed. Moreover, it was shown that a further decrease of the interspecies repulsion, results in asymmetric states with the bright solitons living on top of a finite BEC background, highlighting in this way the miscible character of such bound pairs. In contrast to the above picture, upon entering the immiscible regime, we had found in our recent work [48] that the destabilization of the anti-symmetric dark-bright soliton pair is caused by a subcritical pitchfork bifurcation involving an unstable stationary, but as in the corresponding miscible domain also mass-imbalanced dark-bright soliton pair mode. In the present work, we further explored the range of existence and stability of this asymmetric branch, demonstrating its overall instability and its substantial deformation upon entering the miscible regime.
There are many directions that are worth considering in the future along the lines of this work. In particular, by fixing the intra-species interactions g 22 = 0.95 in this work, we have not addressed the fate of the dark-bright soliton pair states when actually approaching the Manakov (integrable) limit, which would require g 12 = g 22 = 1. In this respect it would be particularly interesting to see if the asymmetric state fully stabilizes upon restoring integrability or maintains its weakly unstable nature. Towards this direction, and since in the integrable limit exact solutions are available [31,57], one could link the antisymmetric and asymmetric states obtained here with the exact families of dark-bright soliton solutions known in the integrable case. Establishing a possible connection of this type would furthermore open a new direction of exploring and understanding the symbiotic soliton pairs, since in such a case one could depart once more from the integrable limit, but having at hand exact analytical expressions for the two-soliton problem rather than the approximate ones constructed only from the single soliton solution, as used in our present work. Furthermore, and also in this direction, in the integrable model exact closed form expressions exist not only for static symbiotic states like the ones considered here, but also for moving and scattering ones. Based on these, one could hope to get insights into the collisional dynamics of symbiotic entities at least in the vicinity of the integrable limit, paving the way of a detailed understanding of features like the breathing state formation observed here. Studies along these lines are left for future work.